{"title":"UPA","description":null,"products":[{"product_id":"upa-test-e-300","title":"UPA Test E 300","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA=TEST E300(300MG\/ML TESTOSTERONE enanthate=10ML)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD TESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 8 days\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Androgenic\/Anabolic Steroid (For injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 200-1000mg weekly.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Yes, high due to estrogen conversion\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Yes, normally due to high water \/electrolyte retention\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Low in listed dosages\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTestosterone was generally toted as the big daddy of injectable steroids. No other steroid was consistently reported to bring such high returns as quickly in weight gain and strength increases. Due to its high anabolic\/high androgenic effects, many athletes used this drug in an off-season mass cycle. Water retention during administration of ENANTHATE was not reportedly as high as that realized during the use of OMNADREN. but darn close. Like all testosterone esters, Enanthate aromatized easily and has a high conversion rate to DHT. Those with prostate problems or who were sensitive to gyno and female pattern fat deposits, readily agreed that they should have either left it alone or taken steps to suppress estrogenic activity due to aromatization.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrugs such as PROVIRON and NOVLADEX were often utilized for this reason. DHT\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003econversion enzyme blockers such as Proscar were commonly co-administered with testosterones for the former reason.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTestosterone enanthate notably suppressed HPTA function severely. HCG\/Clomid were considered almost a must to stimulate normal endogenous (natural) testosterone production within a positive period of time at post use. My personal experience has been that if a cycle containing testosterone enanthate lasted longer than 6 weeks, HCG and usually Clomid were introduced for 10 days beginning at the end of week #4. (5000 i.u. of HCG 3 times in 10 days usually normalized sperm and endogenous testosterone production to a respectable extent) Without the use of HPTA stimulating compounds normalization did occur, only at a much slower rate. For this reason, gains made during “enanthate only” administrations were not well maintained after use was discontinued, and much was lost needlessly by most regardless. Perhaps this was why so many uninformed individuals stayed on the stuff almost year round. (There are several solutions and protocols that prevented excessive post-cycle lean mass tissue loss for the more informed athletes)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMales injected 200-1000mg weekly. Some did use much higher dosages of course. Due to a plasma half-life of 4-5 days, injections were normally administered bi­weekly. Most novice steroid should not use testosterone. Not only was considered unnecessary, it would have been foolish to diminish possible later gains when more gentle AAS were no longer providing results at reasonable dosages. Most users made excellent progress with a total weekly dosage of 200-600mg. Post-cycle use of an anti-catabolic drug was a constant agreed upon factor since it helped to maintain gains. (See Clenbuterol)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe negative side effects reported were mostly water retention and strong androgenic effects. These included gyno, accelerated hair growth, receding hair-lines, aggressiveness, higher blood pressure, acne, and increased fat deposits (due to aromatization). Since testosterones are metabolized by the liver fairly easily, alarming elevated liver enzymes occurred in very high dosages only. usually. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndrogens are derivatives of cyclopentano-perhydrophenanthrene. Endogenous androgens are C-19 steroids with a side chain at C-17, and with two angular methyl groups. Testosterone is the primary endogenous androgen.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIn their active form, all drugs in the class have a 17-beta-hydroxy group. Esterification of the 17-beta-hydroxy group produces compounds (testosterone enanthate and testosterone propionate) which have a longer duration of action and are hydrolyzed in vivo to free testosterone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndrogens are steroids that develop and maintain primary and secondary male sex characteristics.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEndogenous androgens are responsible for the normal growth and development of the male sex organs and for maintenance of secondary sex characteristics. These effects include the growth and maturation of prostate, seminal vesicles, penis, and scrotum; the development of male hair distribution, such as beard, pubic, chest and axillary hair; laryngeal enlargement, vocal chord thickening, alterations in body musculature, and fat distribution. Drugs in this class also cause retention of nitrogen, sodium, potassium, phosphorous, and decreased urinary excretion of calcium. Androgens have been reported to increase protein anabolism and decrease protein catabolism. Nitrogen balance is improved only when there is sufficient intake of calories and protein.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndrogens are responsible for the growth spurt of adolescence and for the eventual termination of linear growth which is brought about by fusion of the epiphyseal growth centers. In children, exogenous androgens accelerate linear growth rates, but may cause a disproportionate advancement in bone maturation. Use over long periods may result in fusion of the epiphyseal growth center and termination of growth process.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndrogens have been reported to stimulate the production of red blood cells by enhancing the production of erythropoietic stimulating factor.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDuring exogenous administration of androgens, endogenous testosterone release is inhibited through feedback inhibition of pituitary luteinizing hormone (LH). At large doses of exogenous androgens, spermatogenesis may also be suppressed through feedback inhibition of pituitary follicle stimulating hormone (FSH).\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53759125782820,"sku":null,"price":410.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_d6b5a7dd-3c9f-41b4-8982-b3cb0ac909ca.jpg?v=1778079609"},{"product_id":"upa-test-cyp-250","title":"UPA Test Cyp 250","description":"\u003cp\u003e\u003cspan\u003eUPA TEST CYP 250(250MG\/ML TESTOSTERONE cypionate =10ML)\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD TESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 15-16 days\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Androgenic\/Anabolic Steroid (For injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 200-1000mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Yes, common\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Yes, due to water\/electrolyte retention\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Low, except in absurd dosages\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT conversion: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Yes, severely\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePretty much all that was written about TESTOSTERONE ENANTHATE also applies to TESTOSTERONE CYPIONATE. A slight distinction was made in that they\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eeach provided a notable different half- and active-life period. For this reason, CYPIONATE injections were reduced to every 8th day by some reported users. Dosages of 200-1000mg weekly were common, but most users experienced excellent results with 200-600mg weekly. Both testosterone preparations stacked well with any other AAS and added a distinct androgenic effect. This meant improved regenerative qualities and greater training intensity with a correlating significant increase in weight-load capacity. For those who wished to use testosterone but were highly sensitive to gyno and water\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eretention, TESTOSTERONE PROPIONATE was commonly reported to be the better\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003echoice. Oddly enough, a few of those polled reported more sensitively due to Propionate’s fast action. Interesting paradox, huh? The issue was simply a matter of dosage\/administration protocols. Since PROPIONATE remained active for about 3 days a weekly administration protocol allowed circulatory clearing of the drug. It should be\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003enoted that both TESTOSTERONE ENANTHATE and CYPIONATE were said to be\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003emore anabolic and less androgenic then SUSPENSION or PROPIONATE. This is pure imagination. The truth is that suspension actually is a faster acting testosterone and contains more total testosterone per 100mg dosage than any esterfied testosterone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003etestosterone cypionate which is the oil-soluble 17 (beta)-cyclopentylpropionate ester of the androgenic hormone testosterone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEndogenous androgens are responsible for normal growth and development of the male sex organs and for maintenance of secondary sex characteristics. These effects include growth and maturation of the prostate, seminal vesicles, penis, and scrotum; development of male hair distribution, such as beard, pubic, chest, and axillary hair; laryngeal enlargement, vocal cord thickening, and alterations in body musculature and fat distribution. Drugs in this class also cause retention of nitrogen, sodium, potassium, and phosphorous, and decreased urinary excretion of calcium. Androgens have been reported to increase protein anabolism and decrease protein catabolism. Nitrogen balance is improved only when there is sufficient intake of calories and protein.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndrogens are responsible for the growth spurt of adolescence and for eventual termination of linear growth, brought about by fusion of the epiphyseal growth centers. In children, exogenous androgens accelerate linear growth rates, but may cause disproportionate advancement in bone maturation. Use over long periods may result in fusion of the epiphyseal growth centers and termination of the growth process. Androgens have been reported to stimulate production of red blood cells by enhancing production of erythropoietic stimulation factor.\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53759952912676,"sku":null,"price":410.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_8ba843fb-33c0-4ec3-bb8d-09de38c7a42b.jpg?v=1778080730"},{"product_id":"upa-anavar-15mg-50-tabs","title":"UPA Anavar 15mg\/50 Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA ANAVAR(15MG OXANDROLONE\/TAB=50TABS)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 24\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 322-630\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 8-12 hours\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anabolic\/Androgenic Steroid (Oral)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 20-50mg daily Women 10-15mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Only when administered in high dosages\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Yes, c17-alfa-alkylated steroid. Due to low dosages toxicity is low-moderate\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT conversion: Quite low\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA function: Unlikely even in high dosage use\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOxandrolone was often refereed to as an all purpose oral AAS. This drug was once marketed under the product name (still commonly used trade name) of Anavar. It has the unique quality of significantly stimulating (more than other AAS) the synthesis of phosphocreatine in muscle cells which in turn provides faster regeneration of, and a distinct elevation in, ATP. Of course all AAS have this effect to some extent. Oxandrolone is simply unmatched in this aspect.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e(See Creatine for more info) Due to this quality, a rapid build- up in strength was frequently reported and an obvious distinct hardness in muscle was obtained with little weight gain and no aromatization.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThough it is a common belief that Oxandrolone is not very anabolic, a clinical study showed a 44% increase in muscle cell protein synthesis after only 5 days of administration. Since Oxandrolone does not aromatize to estrogen, water retention is reported as quite low and gyno was of no concern. Also, for the same reason, during dieting phases fat deposits were said to be “burned away” more quickly. (Especially when the drug was co-administered with Clenbuterol).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOxandrolone was reported to stack well with so -called mass steroids such as testosterone or with high anabolic\/moderate androgenic steroids such as Equipoise or Nandrolones. Persons over 40 have reported excellent results by stacking 15-25 mg of Oxandrolone daily with 200-400 mg of Deca.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eA very hard pre-contest appearance has been achieved by males when stacked with Oxandrolone and Halotestin if a estrogen\/progesterone receptor antagonist (*See Nolvadex) had been utilized as well. As I said: “all purpose” was commonly the term of choice.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe drug Oxandrolone was originally manufactured to be used by women to prevent osteoporosis and for children as a cure for stunted growth. The low androgenic quality prevents almost all virilization for women in dosages of 15-mg daily or less. And for the same reason does not cause closure of the epiphysial plates prematurely. An interesting note: Oxandrolone does not suppress any part of the HYPOTHALAMUS-PITUITARY-TESTES AXIS (HPTA). This means Oxandrolone by itself will not significantly suppress natural testosterone production. Therefore it was not uncommon for some athletes to report post-cycle HPTA regeneration protocols that included this drug. The result was prominent lean mass retention.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAdjunctive therapy to promote weight gain after weight loss following extensive surgery, chronic infections, or severe trauma, and in some individuals who, without definite pathophysiologic reasons, fail to gain or maintain normal weight; to offset protein catabolism associated with prolonged administration of corticosteroids; for relief of bone pain frequently accompanying osteoporosis.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAlso used for Catabolic illness (eg, alcoholic liver disease, burn injury).\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53760074350884,"sku":null,"price":420.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_9d665d2c-7598-400f-ba58-f3f0d8452141.jpg?v=1778080843"},{"product_id":"upa-tb-500-and-bpc-157-hybrid","title":"UPA TB-500 and BPC-157 Hybrid","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e\n\u003cp\u003eBPC-157 \u0026amp; TB500 HYBRID\u003c\/p\u003e\n\u003cp\u003e1 x 5mg BPC-157 \u0026amp; 5mg TB500 Per Vial\u003c\/p\u003e\n\u003cp\u003e1 x 2ml Vial Bacteriostatic Water\u003c\/p\u003e\n\u003cp\u003eTB-500 is one of the more interesting peptides on the market due to its potential for directly healing injuries. Some data, although limited, has also shown the peptide may in fact have heart-healing properties, particularly that of ventricle hypertrophy. However, because full data on TB-500 is so limited, it’s very hard to give an honest review beyond “he said she said.” But it’s also difficult to ignore that many users do tend to heal much faster with it than without, and in some cases, faster than would seem possible.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eIt’s also important to note that TB-500 users often report better results when used with Human Growth Hormone (HGH) or Human Growth Hormone Releasing Hormones (HGRH) compounds. This isn’t surprising when Growth Hormone (GH) is one of the primary healing tools we have at our disposal. It’s hard to say how much faster healing will be with or without a GH product, but what we know of GH (there is massive amounts of data available on GH) it only makes sense that it would be much faster.\u003c\/p\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53760169050404,"sku":null,"price":500.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_9b5ce38c-e9e4-412d-b949-72fc39da6643.jpg?v=1778080941"},{"product_id":"upa-dianabol-15mg-50-tabs","title":"UPA Dianabol 15mg\/50 Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA DIANABOL(15MG METHANDROSTENOLONE\/TAB=50TABS) \n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 40-60\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 90-210\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD TESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 6-8 hours (Injection product remains active for about 60-72 hours) Drug Class:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAnabolic\/androgenic steroid ORAL OR INJECTABLE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 15-50 mg daily Women 5-10 mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Yes, especially in higher dosages.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Yes, similar to testosterone\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Yes, due to water retention, some experience elevated heart rate\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: Yes, strongly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Yes, 17-alfa alkylated oral\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT conversion: No\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh anabolic\/high androgenic\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA function: Yes, dose and administration period dependent\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOral Dianabol was reported to be a highly effective mass AAS which provided impressive weight and strength gains. Most users experienced a 2-4 LB bodyweight increase per week with heavy water retention. With higher dosages gynecomastia (bitch tits) was a common negative side effect. Obviously much of this was avoided by those who reported co-addministration of Proviron and\/or Novladex. When stacked with a nandrolone, some gyno problems seemed to lessen. This was probably due to Nandrolones aromatization to a weaker estrogen called Norestrogen and the resulting mild anti-estrogenic effect that results in moderate dosage administration. Methandrostenlone becomes active in 1-3 hours with a half-life of about 3.5-4.5 hours. For this reason, dosages were spread through out the day to maintain blood serum\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003econcentrations at an elevated state. Massive dosages just were not necessary since a single 10-mg dose has increase androgen anabolic activity 5 times over normal with a correlating reduction in natural cortisol activity of 50-70%. Males using 5mg per 25-LBS of body weight broken into 3-5 equal dosages throughout the day have experienced impressive results. At dosages above 50 mg per day, results were not progressively quantitative. Most first time AAS users who used a daily dosage of 20-30mg daily experience significant results over a 4-6 week period. Women should not utilize Methandrostenolone but a surprising number did report the inclusion of the drug in AAS protocols. For those who insisted, no more than 10-mg daily for 3-4 weeks stacked with a very low androgenic product minimized masculization type negative side effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSide effects such as increased liver values (toxicity) “usually” returned to normal within a short period of time after use was discontinued. High blood pressure, elevated heart rates, gyno, heavy water retention, and acne were all frequent reported negative side effects of Methandrostenlone use. Some literature on this drug supports DHT- like activity. Finasteride “usually” prevented this effect as well as possible prostate enlargement. Dianabol heavily suppresses natural testosterone production within only 10 days after continuous administration begins (dose dependent). Most note a sense of well being during use of this drug. Significant strength and weight loss follows discontinued use due to the loss of excessive water and HPTA suppression. So retained gains were only fair post-cycle.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMy personal experiences with this drug have led me to believe that no athlete should have ever stacked high dosage protocols of Dianabol with Anadrol-50 or Methyltestosterone. It is a liver killer combo. A last note: Injectable Dianabol did not have anywhere near as dramatic effects when utilized in its intended method. However, the injectable is orally active and as such was reported to be commonly used in this manner by filling gel-caps with the desired amount\/dosage and subsequent ingestion. This is probably due to the fact that oral administration of a c17-alkylated AAS results in increased liver production of IGF-1. I have also learned that it was best to avoid Russian Methandrostenlone. (It commonly contains a large amount of unconverted methyltestosterone).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003emethandrostenolone does not react strongly with the androgen receptor , instead relying on activity not mediated by the receptor for its effects. These include dramatic increases in protein synthesis , glycogenolysis , and muscle strength over a short space of time. . In high doses (30 mg or more per day), side effects such as gynaecomastia , high blood pressure , acne and male pattern baldness may begin to occur. The drug causes severe masculinising effects in women even at low doses. Without the administration of aromatase inhibitors such as Arimadex , estrogenic effects will appear over time in men. Many users will combat the estrogenic side effects with Tamoxiplex or Clomid . \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe 17α-methylation of the steroid does allow it to pass through the liver without being broken down allowing it to be taken orally. It also has the effect of decreasing the steroid’s affinity for sex hormone binding globulin , a protein that de-activates steroid molecules and prevents them from further reactions with the body. As a result, methandrostenolone is significantly more active than an equivalent quantity of testosterone , resulting in rapid growth of muscle tissue. However, the concomitant elevation in estrogen levels – a result of the aromatization of methandrostenolone – results in significant water retention. This gives the appearance of great gains in mass and strength, which prove to be temporary once the steroid is discontinued and water weight drops. Because of this, it is often used by bodybuilders only at the start of a “steroid cycle”, to facilitate rapid strength increases and the appearance of great size, while compounds such as Testosterone or Deca with long acting esters build up in the body to an appreciable amount capable of supporting anabolic function on their own.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53760211714340,"sku":null,"price":210.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_7f0410f2-1a63-4843-a098-30943e29b9bb.jpg?v=1778081030"},{"product_id":"upa-ghk-cu","title":"UPA GHK-CU","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e\n\u003cdiv\u003e\n\u003ch2 id=\"what-is-ghk-cu\" class=\"chakra-heading article-heading css-1srb9x7\" data-name=\"article-heading\"\u003e\u003cspan\u003eWhat is GHK-Cu?\u003c\/span\u003e\u003c\/h2\u003e\n\u003c\/div\u003e\n\u003cp\u003e\u003cspan\u003eGHK-Cu is a complex consisting of the tripeptide GHK (glycyl-histidyl-lysine) and copper (Cu). \u003cspan id=\"popover-trigger-26\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-26\"\u003e\u003c\/span\u003eGHK was first discovered in 1973 by Dr. Loren Pickart, who found it caused older human liver tissue to produce proteins more characteristic of younger tissue.\u003cspan id=\"popover-trigger-28\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-28\"\u003e\u003c\/span\u003e\u003cspan id=\"popover-trigger-30\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-30\"\u003e\u003c\/span\u003e This resulted in GHK being originally described, specifically, as a liver cell growth factor. However, as research continued, experts found that GHK could modulate a number of different cells besides those in the liver.\u003cspan id=\"popover-trigger-32\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-32\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eGHK is naturally found in human saliva, plasma, and urine, but its standard levels are reduced by over half once you reach age 60. As researchers note, this decline “coincides with the noticeable decrease in regenerative capacity of an organism.\u003cspan id=\"popover-trigger-34\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-34\"\u003e\u003c\/span\u003e This suggests that, for example, lower natural GHK levels may contribute to things like slower wound healing in older adults.\u003cspan id=\"popover-trigger-36\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-36\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eAccording to experts, GHK has a “strong affinity for copper” and “readily” links up with it to form GHK-Cu. In this form, the peptide complex appears to have strong protective and regenerative properties, leading to its widespread use in cosmetics.\u003cspan id=\"popover-trigger-38\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-38\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\n\u003ch2 id=\"what-is-ghk-cu-used-for\" class=\"chakra-heading article-heading css-1srb9x7\" data-name=\"article-heading\"\u003e\u003cspan\u003eWhat is GHK-Cu used for?\u003c\/span\u003e\u003c\/h2\u003e\n\u003c\/div\u003e\n\u003cp\u003e\u003cspan\u003eMost often, you’ll find GHK-Cu copper peptides (usually listed in ingredient lists under the name Copper Tripeptide-1) in various cosmetics, with skin care products being some of the most popular use cases. According to a 2018 review, GHK-Cu has demonstrated the ability to:\u003cspan id=\"popover-trigger-40\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-40\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cspan\u003eTighten loose skin\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eReverse age-related skin thinning\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eRepair the skin’s protective barrier proteins\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eImprove skin firmness and elasticity\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eReduce the appearance of fine lines and wrinkles\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eSmooth rough skin\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eStimulate wound healing\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eLessen the appearance of photodamage (sun damage), hyperpigmentation, skin spots, lesions, and more\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eReduce inflammation and damage from free radicals\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eIncrease hair growth and thickness\u003c\/span\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003cspan\u003eAdditionally, in research from 2015, the authors noted that GHK-Cu may be able to stimulate collagen, regulate the skin remodeling process, attract immune cells to the site of an injury, and restore “replicative vitality to fibroblasts” (a cell that helps form connective tissue) in patients who’ve undergone radiation therapy for cancer.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cspan id=\"popover-trigger-42\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-42\"\u003e\u003c\/span\u003eTo help you better understand how GHK-Cu works, we’ll break down some of the research behind the peptide’s potential applications for hair, skin, and other health aspects.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"css-1uf8epz\"\u003e\n\u003cp\u003e\u003cspan class=\"chakra-text split-list-title css-0\"\u003eSkin aging\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"split-list-desc css-0\"\u003e\n\u003cp\u003e\u003cspan\u003eIn a 2018 review, the authors detailed multiple positive studies and trials on the use of GHK-Cu for signs of skin aging. One trial had 71 women with “mild to advanced signs of photoaging” apply a facial cream containing GHK-Cu daily for three months and found that the treatment increased skin density and thickness while reducing sagging and the appearance of fine lines and wrinkles. In another trial, 41 women with “mild to advanced photodamage” applied GHK-Cu eye cream for three months; it reduced lines and wrinkles, improved skin density, and increased skin thickness better than both placebo and vitamin K cream.\u003cspan id=\"popover-trigger-46\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-46\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eSimilarly, in a pilot study investigating copper tripeptide topicals for aged skin, experts found that they increased skin thickness, improved hydration, boosted collagen synthesis, and increased elasticity.\u003cspan id=\"popover-trigger-48\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-48\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cdiv class=\"css-12h4rkv\"\u003e\n\u003cp\u003e\u003cspan class=\"chakra-text split-list-title css-0\"\u003eHair growth\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"split-list-desc css-0\"\u003e\n\u003cp\u003e\u003cspan\u003eIn a review from 2023, experts explained that GHK-Cu may promote hair growth in a few different ways. The first is by stimulating fibroblasts and promoting the formation of new blood vessels to help hair follicles receive the nutrients needed to grow. Second, GHK-Cu appears to inhibit growth factor beta, thereby preventing hair follicles from prematurely shrinking. And lastly, GHK-Cu may support dermal papilla cells (an important cell for healthy hair formation) to stimulate hair growth.\u003cspan id=\"popover-trigger-50\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-50\"\u003e\u003c\/span\u003e\u003cspan id=\"popover-trigger-52\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-52\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cdiv class=\"css-12h4rkv\"\u003e\n\u003cp\u003e\u003cspan class=\"chakra-text split-list-title css-0\"\u003eWound healing\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"split-list-desc css-0\"\u003e\n\u003cp\u003e\u003cspan\u003eIn animal studies, GHK-Cu has demonstrated wound-healing abilities. In one rabbit study, it improved “wound contraction and formation of granular tissue,” boosted antioxidant enzymes, and stimulated blood vessel development and growth. Also, a collagen dressing with GHK-Cu accelerated the healing of wounds in both healthy and diabetic rats.\u003cspan id=\"popover-trigger-54\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-54\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eHowever, researchers point out that GHK-Cu is “very sensitive” to breakdown by certain enzymes. Wounds like diabetic skin ulcers and bedsores often develop something called a “wound serum” that contains these enzymes. This “serum” breaks down GHK-Cu, rendering it ineffective.\u003cspan id=\"popover-trigger-56\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-56\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cdiv class=\"css-12h4rkv\"\u003e\n\u003cp\u003e\u003cspan class=\"chakra-text split-list-title css-0\"\u003eTissue regeneration\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"split-list-desc css-0\"\u003e\n\u003cp\u003e\u003cspan\u003eAn \u003cem\u003ein vitro\u003c\/em\u003e study found that treating lung fibroblasts from COPD patients with GHK-Cu helped restore their function. The researchers also suggested that GHK-Cu may be able to reverse gene expression changes associated with emphysema.\u003cspan id=\"popover-trigger-58\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-58\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cdiv class=\"css-12h4rkv\"\u003e\n\u003cp\u003e\u003cspan class=\"chakra-text split-list-title css-0\"\u003eAnti-cancer actions\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"split-list-desc css-0\"\u003e\n\u003cp\u003e\u003cspan\u003eBecause GHK-Cu can activate cell growth, tissue remodeling, and blood vessel development, experts express concerns about its potential to trigger cancer. Interestingly, though, GHK-Cu appears to possess “potent” anti-cancer properties. The peptide is one of two skin remodeling substances that may be able to downregulate the expression of “metastatic” genes.\u003cspan id=\"popover-trigger-60\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-60\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eIn an older 1983 animal study (published in 2014) that was conducted in part by Dr. Pickart, who discovered the peptide, a mixture of GHK-Cu and vitamin C suppressed the growth of a highly malignant cancer in mice called sarcoma-180.\u003cspan id=\"popover-trigger-62\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-62\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cdiv class=\"css-20wt14\"\u003e\n\u003cp\u003e\u003cspan class=\"chakra-text split-list-title css-0\"\u003eAnti-pain effects\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"split-list-desc css-0\"\u003e\n\u003cp\u003e\u003cspan\u003eGHK-Cu also appears to possess analgesic, or anti-pain, effects. In one mouse study, researchers found that the peptide reduced the pain felt by the animals in their paws when “placed on a mildly hot plate.” The authors explained that this could be because GHK is similar in structure to cimetidine, a histamine H2 receptor antagonist sometimes given to reduce pain in certain digestive conditions.\u003cspan id=\"popover-trigger-64\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-64\"\u003e\u003c\/span\u003e\u003cspan id=\"popover-trigger-66\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-66\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e\u003cspan\u003eWith all of this in mind, it’s not surprising that GHK-Cu has become a popular ingredient in topicals intended to reduce a host of skin- and hair-related concerns. And as detailed above, you may soon see this peptide being used as a part of therapy or treatment for other health conditions. As the science develops, we’ll update this guide accordingly.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\n\u003ch2 id=\"are-ghk-cu-copper-peptides-safe\" class=\"chakra-heading article-heading css-1srb9x7\" data-name=\"article-heading\"\u003e\u003cspan\u003eAre GHK-Cu copper peptides safe?\u003c\/span\u003e\u003c\/h2\u003e\n\u003c\/div\u003e\n\u003cp\u003e\u003cspan\u003eTo date, no existing research has discovered any serious safety concerns with the use of GHK-Cu copper peptides.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eIn fact, one study noted that the peptide “has a long history of safe use in wound healing and skin care; it is naturally occurring, nontoxic, and is active at a very low nanomolar concentration.”\u003cspan id=\"popover-trigger-68\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-68\"\u003e\u003c\/span\u003e In addition, another piece of research described GHK-Cu as “a safe, inexpensive, extensively studied compound.”\u003cspan id=\"popover-trigger-70\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-70\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eHowever, though this is reassuring, there are a couple of things to remain mindful of:\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"css-1uf8epz\"\u003e\n\u003cp\u003e\u003cspan class=\"chakra-text split-list-title css-0\"\u003eCopper toxicity\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"split-list-desc css-0\"\u003e\n\u003cp\u003e\u003cspan\u003eSince GHK-Cu contains copper, it’s important to only use products containing it as directed to avoid potential copper toxicity.\u003cspan id=\"popover-trigger-72\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-72\"\u003e\u003c\/span\u003eWhile it’s unlikely that using GHK-Cu products will cause copper toxicity, especially since the concentrations of the peptide are typically well within safe parameters, it’s still good to be aware of the possible risk.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eSome symptoms of copper poisoning may include abdominal pain, vomiting, chest pain, chills, cough, fever, general weakness, anemia, burning sensations, tremors, and a metallic taste in the mouth.\u003cspan id=\"popover-trigger-74\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-74\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cdiv class=\"css-20wt14\"\u003e\n\u003cp\u003e\u003cspan class=\"chakra-text split-list-title css-0\"\u003eAngiogenesis and cancer\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"split-list-desc css-0\"\u003e\n\u003cp\u003e\u003cspan\u003eGHK-Cu may promote the formation of new blood vessels, or angiogenesis.\u003cspan id=\"popover-trigger-76\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-76\"\u003e\u003c\/span\u003e As explained by the U.S. National Cancer Institute, “Angiogenesis plays a critical role in the growth of cancer because solid tumors need a blood supply if they are to grow beyond a few millimeters in size.”\u003cspan id=\"popover-trigger-78\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-78\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eSo, despite GHK-Cu’s potential anti-cancer action, those who have active or suspected cancer may still wish to avoid using products containing the peptide.\u003cspan id=\"popover-trigger-80\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-80\"\u003e\u003c\/span\u003e\u003cspan id=\"popover-trigger-82\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-82\"\u003e\u003c\/span\u003e And if you develop any symptoms of cancer while using GHK-Cu, it’s best to discontinue use and contact your doctor for their input and potential testing.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e\u003cspan\u003eIt’s also important to point out that there haven’t been any studies investigating the long-term use of this peptide in humans, so we currently don’t know if there are any potential downsides or dangers to using it for an extended period.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3 id=\"common-side-effects-of-ghk-cu\" class=\"chakra-heading css-gvl5d5\"\u003e\u003cspan\u003eCommon side effects of GHK-Cu\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eBefore adding GHK-Cu to your routine, it’s important to first conduct patch testing — as you should with any new topical product.\u003cspan id=\"popover-trigger-84\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-84\"\u003e\u003c\/span\u003e Even if GHK-Cu doesn’t cause a reaction, you may still have a sensitivity or allergy to one of the other ingredients in the product you’re using.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eIf GHK-Cu does happen to cause any adverse reactions, they’re typically mild and transient (meaning they should go away over time). Common side effects include redness, itching, or irritation at the application site. If you experience any severe reactions like hives, swelling, difficulty breathing, etc., then it’s important to stop using the product right away, gently wash it off with cool water, and either contact your doctor or seek prompt medical attention if necessary.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3 id=\"ghk-cu-and-copper-uglies\" class=\"chakra-heading css-gvl5d5\"\u003e\u003cspan\u003eGHK-Cu and “copper uglies”\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eAlbeit rare, some people may experience a side effect from using GHK-Cu or other copper peptides known as “copper uglies.” Though there aren’t any studies on this phenomenon, some users have anecdotal reports of copper peptide skin care products leading to what looks like accelerated skin \u003cem\u003eaging\u003c\/em\u003e instead of \u003cem\u003eantiaging\u003c\/em\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eThis may be due to copper’s ability to enhance the expression of metalloproteinases (MMPs). \u003cspan id=\"popover-trigger-86\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-86\"\u003e\u003c\/span\u003eNow, the degradation of collagen is normally regulated by MMPs, and a specific one, MMP-1, may be responsible for “the initiation of collagen fragmentation.” \u003cspan id=\"popover-trigger-88\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-88\"\u003e\u003c\/span\u003eSupporting this, a 2024 study noted that elevated MMP-1 levels appear to contribute to aging skin. The study authors found that higher MMP-1 levels in mice led to:\u003cspan id=\"popover-trigger-90\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-90\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cspan\u003eThe loss and fragmentation of dermal collagen fibrils\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eContracted fibroblast morphology\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eReduced collagen production\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eIncreased expression of pro-inflammatory mediators\u003c\/span\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003cspan\u003eKeeping that in mind, a 2016 study found that GHK-Cu “significantly increased gene expression of MMP-1 and MMP-2 at the lowest concentration.” The study’s authors considered this to be one of the reasons the peptide was able to \u003cem\u003eincrease\u003c\/em\u003e collagen and elastin production.\u003cspan id=\"popover-trigger-92\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-92\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eSo, what this could ultimately mean is that using \u003cem\u003etoo much\u003c\/em\u003e GHK-Cu (or other copper peptides) may — in theory — increase the skin’s MMP-1 concentration above the levels involved in healthy collagen production and take it into the “collagen fragmentation and breakdown” territory seen in older skin with naturally higher MMP-1 levels.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eAgain, the “copper uglies” are rare, but it’s still best to conduct a spot test elsewhere on your body before applying GHK-Cu peptides to the face. It could also be worth checking the ingredients of the skin care products in your daily regimen to ensure you aren’t using multiple copper peptide products all at once.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\n\u003ch2 id=\"who-are-ghk-cu-peptides-for\" class=\"chakra-heading article-heading css-1srb9x7\" data-name=\"article-heading\"\u003e\u003cspan\u003eWho are GHK-Cu peptides for?\u003c\/span\u003e\u003c\/h2\u003e\n\u003c\/div\u003e\n\u003cp\u003e\u003cspan\u003eBased on both the information we learned from knowledgeable medical professionals and what researchers have suggested GHK-Cu has the potential to do, those who’d likely benefit the most from using products containing the peptide include:\u003cspan id=\"popover-trigger-94\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-94\"\u003e\u003c\/span\u003e\u003cspan id=\"popover-trigger-96\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-96\"\u003e\u003c\/span\u003e\u003cspan id=\"popover-trigger-98\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-98\"\u003e\u003c\/span\u003e\u003cspan id=\"popover-trigger-100\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-100\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cspan\u003ePeople seeking an antiaging product for wrinkles, fine lines, and\/or sagging skin\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eThose who would prefer an alternative to other, often harsh antiaging actives like tretinoin or glycolic acid\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eIndividuals with inflammatory skin conditions (e.g., eczema, rosacea, etc.)\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003ePeople looking to reduce the appearance of striae, or stretch marks\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eThose with scarring due to injuries, surgeries, or acne\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eIndividuals dealing with hyperpigmentation concerns (e.g., melasma, dark spots)\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eAnyone seeking a proactive skin health product\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003ePeople who would like to or who need to find an alternative hair growth solution\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eIndividuals with slow-healing wounds that aren’t bedsores or due to diabetes\u003cspan id=\"popover-trigger-102\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-102\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eThose with acne, including cystic acne\u003c\/span\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003cspan\u003eWhen it comes to some of the other potential applications we detailed earlier in this guide — like pain relief and anti-cancer activity — more human research is needed before we can definitively say it should be used by individuals for those purposes. If you’re being treated for pain or cancer, it’s best to stick with what your doctor prescribes. This is especially important for cancer patients, as GHK-Cu may even increase the risk of cancer progression (more on that below).\u003cspan id=\"popover-trigger-104\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-104\"\u003e\u003c\/span\u003e\u003cspan id=\"popover-trigger-106\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-106\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3 id=\"who-should-avoid-ghk-cu\" class=\"chakra-heading css-gvl5d5\"\u003e\u003cspan\u003eWho should avoid GHK-Cu?\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eBecause of its history of safe use, there aren’t too many populations that should avoid using GHK-Cu.\u003cspan id=\"popover-trigger-108\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-108\"\u003e\u003c\/span\u003e\u003cspan id=\"popover-trigger-110\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-110\"\u003e\u003c\/span\u003e However, that doesn’t mean there aren’t any. Those who should reconsider or avoid copper peptides like GHK-Cu include:\u003c\/span\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eAnyone under the age of 18:\u003c\/strong\u003e We don’t yet know if copper peptides can have an adverse effect on young people.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eThose who are pregnant or breastfeeding:\u003c\/strong\u003e Similar to the above point, there isn’t enough research on whether or not copper peptides can affect a developing fetus or be transferred into breast milk.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003ePeople with active or suspected cancer:\u003c\/strong\u003e Even though it may have anti-cancer potential, GHK-Cu could promote the formation of new blood vessels, which can “feed” tumors.\u003cspan id=\"popover-trigger-112\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-112\"\u003e\u003c\/span\u003e\u003cspan id=\"popover-trigger-114\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-114\"\u003e\u003c\/span\u003e\u003cspan id=\"popover-trigger-116\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-116\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eIndividuals with Wilson’s disease:\u003c\/strong\u003e This rare genetic condition causes copper to build up in your body, so using copper peptides may be dangerous.\u003cspan id=\"popover-trigger-118\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-118\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cdiv\u003e\n\u003ch2 id=\"how-to-use-ghk-cu-peptides\" class=\"chakra-heading article-heading css-1srb9x7\" data-name=\"article-heading\"\u003e\u003cspan\u003eHow to use GHK-Cu peptides\u003c\/span\u003e\u003c\/h2\u003e\n\u003c\/div\u003e\n\u003cp\u003e\u003cspan\u003eUnlike many other peptide therapies, GHK-Cu typically isn’t administered as an injectable; it’s most often applied topically as a cream or serum. While some clinics may offer it as an injection or even orally, most of the research on GHK-Cu has utilized topical delivery. This is why we’ll primarily be focusing on what it’s like to use GHK-Cu peptides in the form of topicals. As the research on other administration methods develops, we’ll update this information accordingly.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eIn contrast to certain ingredients, like tretinoin or retinol, GHK-Cu won’t make your skin extra-sensitive to UV rays. In fact, GHK seems to actually block “lethal ultraviolet radiation damage” and protect the skin, per a 2014 study.\u003cspan id=\"popover-trigger-120\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-120\"\u003e\u003c\/span\u003e\u003cspan id=\"popover-trigger-122\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-122\"\u003e\u003c\/span\u003e This means that GHK-Cu doesn’t need to be applied at a certain time; you should be able to use it either during the day or at night. But if the product instructions say to apply it during a specific time — or at different times throughout the day — it’s best to follow the manufacturer’s directions.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"article_insider_tips css-166eb9r\"\u003e\n\u003cdiv class=\"article-insider-tip-image css-0\"\u003e\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cdiv class=\"article_insider_tips css-166eb9r\"\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eInsider Tip:\u003c\/strong\u003e Even though GHK-Cu may protect the skin from UV damage, you should still always use a broad-spectrum sunscreen of at least SPF 30 when you go out. Not only is sunscreen an important part of maintaining healthy skin, but the other active ingredients in the product you’re using might sensitize your skin to the sun.\u003cspan id=\"popover-trigger-124\" class=\"index-trigger css-1ywa5ey\" aria-haspopup=\"dialog\" aria-expanded=\"false\" aria-controls=\"popover-content-124\"\u003e\u003c\/span\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/div\u003e\n\u003cp\u003e\u003cspan\u003eTo lower the risk of side effects (or to relieve those that may appear), start with a small application and increase gradually over time. It may also help to use a gentle cleanser before applying GHK-Cu and follow it up with a basic, noncomedogenic moisturizer afterward.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eAdditionally, experts recommend avoiding harsh actives (e.g., retinoids, alpha-hydroxy acids, salicylic acid, etc.), vitamin C, or any active exfoliants while using GHK-Cu peptides. These ingredients could lead to irritation, reduce peptide effectiveness, or compromise the skin barrier.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3 id=\"ghk-cu-skin-care-results-timeline\" class=\"chakra-heading css-gvl5d5\"\u003e\u003cspan\u003eGHK-Cu skin care results timeline\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eAs with most skin care products, noticeable results from topical GHK-Cu copper peptides will take some time and consistent use. Based on what our team learned from communicating with medical professionals, the general timeline is as follows:\u003c\/span\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eFirst two weeks:\u003c\/strong\u003e Users may notice better skin hydration, reduced redness or irritation, and smoother skin.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eAfter 1-2 months:\u003c\/strong\u003e Fine lines and wrinkles might start to noticeably fade as skin texture and elasticity begin to improve. Those with inflammatory skin conditions may also experience improvements in symptom management.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eAfter 3-6 months:\u003c\/strong\u003e As skin elasticity and firmness continue to improve, scars and hyperpigmentation might begin to noticeably fade at this stage.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eLong-term use:\u003c\/strong\u003e Continuous use could lead to sustained collagen production, maintained skin hydration, less visible wrinkles, and better overall skin health.\u003c\/span\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003cspan\u003eOf course, everyone is different, and how your skin reacts to GHK-Cu products is no exception. For example, you might not experience the first potential benefits until after a month of using the peptide, or you could see later benefits sooner.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53760317260068,"sku":null,"price":540.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_1f81894e-c2da-417e-b631-1605d798b29a.jpg?v=1778081157"},{"product_id":"upa-hcg-5000","title":"UPA HCG 5000","description":"\u003cp\u003e\u003cspan\u003eUPA HCG 5000IU(5000IU CHORIONIC GONADOTROPIN\/AMP=1X1ML POWDER+WATER)\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePregnyl (chorionic gonadotropin) is a hormone used to cause ovulation and to treat infertility in women, and to increase sperm count in men. Human chorionic gonadotropin (HCG) is also used in young boys when their testicles have not dropped down into the scrotum normally. – Human Chorionic Gonadotropin – is the active ingredient used in “Pregnyl”.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIt is typically used as part of a PCT to “reactivate” ones natural production of testosterone post cycle. When on a heavy, long cycle it is also advisable to use it weekly at a low dose of 250 – 500iu to just keep the testicles active during the cycle. This helps with the “kick start” of natural production at the end of the cycle as the testicle will not be starting from a point of a prolonged period of zero \/ low activity.\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53760434372900,"sku":null,"price":360.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_7eca8d4d-24fa-49e3-942c-d11b51b27211.jpg?v=1778081286"},{"product_id":"upa-ultimate-test-500","title":"UPA Ultimate Test 500","description":"\u003cp\u003e\u003cspan\u003eUPA ULTIMATE TEST 500 (500MG\/ML HYBRID MIX=10ML)\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003eULTIMATE TEST 500 IS A MIXTURE OF THE 4 TESTOSTERONE ESTERS:\u003c\/div\u003e\n\u003cdiv\u003e50MG\/ML TESTOSTERONE PROPIONATE \u003c\/div\u003e\n\u003cdiv\u003e100MG\/ML TESTOSTERONE DECOANATE \u003c\/div\u003e\n\u003cdiv\u003e150MG\/ML TESTOSTERONE ENANTHATE \u003c\/div\u003e\n\u003cdiv\u003e200MG\/ML TESTOSTERONE CYPIONATE \u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD TESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: About 3 weeks\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Androgenic\/Anabolic steroid (For injection) Average Reported Dosage: Men 125-2000mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Low except in high dosages over 1000-mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Significantly after 2 weeks\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: Yes, somewhat less than testosterone cypionate or enanthate.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis is a well structured product that acts as a well timed time-released high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eanabolic\/high androgenic testosterone. In fact, due to TESTOSTERONE PROPIONATE,\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ethis product becomes active after one day, but through the series of the other 3 testosterones, remains active for 3 weeks. This mixture had a reported better over all effect milligram for milligram than any other testosterone alone. Users experienced a rapid increase in strength and an even increase in solid mass during administration. SUSTANON aromatized less and caused less water retention when compared to other single testosterones and much less than OMNADREN. Liver toxicity was low (Except in ridiculous dosages) as the liver metabolizes testosterone very efficiently. Like all testosterones, SUSTANON provided improved muscle pumps, better post-training recuperation, and an elevation in aggressiveness toward training.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSUSTANON 250\u0026amp;TEST COMBO 300 significantly suppressed the HPTA so natural testosterone production was significantly decreased as well. For this reason, HCG and CLOMID were considered mandatory after 4-6 weeks of continuous use and after the discontinuance of the drug.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMales normally utilized dosages of 250-1000mg weekly, but some used higher dosages. As a rule, excellent results were realized with a dosage of 250-500mg every 7­-10 days. Most novices and women noted that they felt that they should not use testosterone. Novices…because it was not necessary and it will limit later potential progress. Women should not use them (but a few reported doing so) due to virilizing effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome woman polled just could not leave testosterones alone. PROSCAR (FINASTERIDE, A DHT BLOCKER) was considered mandatory for co-administration\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eand TESTOSTERONE PROPIONATE 50mg 1 time weekly was noted to cause less virilizing side effects\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53760558334244,"sku":null,"price":510.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_648aa17f-3e4f-402d-ae98-d40e52267e21.jpg?v=1778081379"},{"product_id":"upa-proviron","title":"UPA Proviron","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA PROVIRION ORAL(25MG MESTEROLONE\/TAB=50TABS) \n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 30-40\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 100-150\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD TESTOSTERONE PRIOPIONATE \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 8-12 hours (effects last about 24 hours)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Androgenic Steroid\/Anti-Aromatization (Oral)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 25-200mg daily Women 25-50mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: No\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Low\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eProviron is a purely androgenic steroid with no anabolic qualities. The drug was used both as an anti-estrogen that “prevents” estrogen from being produced through the aromatization of sex steroids, and for its hardening effect upon musculature. Unlike Nolvadex (which only keeps estrogen from bonding with its receptors by blocking them), Proviron actually prevents the formation of estrogen. Due to lower estrogen levels, athletes retained less water and prevented (for the most part) the formation of gyno and female pattern fat deposits.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*If it worked perfectly, we would not see all the obvious gyno at bodybuilding shows.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eProviron was popular as a post-cycle anti-estrogen. (To keep estrogen from becoming the dominant hormone and to kick up sex drive lost due to low androgen levels) In fact, it is used in medicine as a drug to increase sperm production and eliminate sexual dysfunction in males. In some cases Proviron is prescribed to decrease flow or stop menstruation in females. For males this only replaces the androgens levels, not cures the problems of low testosterone production. Though the reader should note that the decrease in circulatory estrogen in itself promotes increased HPTA activity. At one time Proviron was commonly used year round by many appearance oriented athletes to maintain hardness. Now, according to recent polls, more athletes are using ephedrine and Clenbuterol to replaced Proviron for this purpose. By the way, frequent and sometimes painful erections are side effects of Proviron use. (So?) Actually, an erection that lasts days can cause permanent damage and erectile problems.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*I commonly extorted another physiological response provided from the use of this drug. Proviron possesses the ability to bind SHBG at a high rate. By doing so other co-administered AAS (or endogenous testosterone) remained in an unbound\/free state. This resulted in greater anabolic and androgenic activity realization with lower dosage requirements.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAs to dosages, males “usually” administered 25-200mg daily and often combined it with Nolvadex (*See Nolvadex). Women athletes commonly reported virilizing side effects when employing Proviron. It should be noted that most women who reported this side effect also co-administered other androgens. At a dosage of 25-50-mg daily combined with Nolvadex most reported good results and few side effects. Teslac was believed to be a superior anti-aromatase drug (which shuts down estrogen production) but few considered it cost effective. 50mg Proviron and 250-1000mg Teslac, or 150mg Proviron and 20mg Nolvadex daily, was said to almost totally suppress estrogens. (Both during steroid cycles and after these dosages were quite effective)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e(Mesterolone) is an androgenic\/anabolic steroid with a particularly high affinity for SHBG (sex hormone binding globulin). SHBG is a protein that acts by binding to sex hormones and preventing them from interacting within the body at places like the AR (androgen receptor). Because of its high affinity with SHBG, Proviraplex’ main use is to competitively bind with SHBG, freeing up more of the endogenous hormone to be active within the body. In effect, proviron acts as a ‘magnifier’ of the anabolic effects of steroid hormones. It also exhibits anti-aromatase activity, hence helping to prevent the conversion of certain steroids into estrogen. As a result, the intake of proviraplex whilst on a cycle of steroids, results in a ‘hardening’ of skeletal muscle – a look which is very popular amongst steroid users.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOne side effect of provirion is the increased frequency and severity of erections, particularly during sleep\/upon waking. Although provirion is an orally administered steroid, and is alkylated to survive the first pass through the liver, it is considered to be almost completely non-toxic to the liver. A typical dose of proviron might be from 25-100mg daily.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53760667779364,"sku":null,"price":450.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_83384eb9-7b7e-4ba7-8516-c5c3118f3ef3.jpg?v=1778081478"},{"product_id":"upa-nolvadex","title":"UPA Nolvadex","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA NOLVADEX(30MG TAMOXIFEN CITRATE\/TAB=30TABS)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: Less than 24 hours\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anti-estrogen\/estrogen antagonist (Oral)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: 10-30-mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: No\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Rare (not normally attributed to the drug itself)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNolvadex is a drug commonly referred to as an anti-estrogen. This would suggest less or no estrogen is produced due to the drug’s actions as in the case of Teslac. Actually, Nolvadex is an estrogen antagonist, meaning it competes with estrogen at estrogen receptor- sites. This prevents the active estrogen from entering its receptor and creating an estrogenic complex capable of activity. Since many AAS aromatize (covert to estrogen) to some degree, the control of feminizing side effects (males should pay attention here) is important. Males normally have a very low estrogen level. During AAS cycles, due to aromatization, estrogen levels rise considerably. This elevated estrogen level can cause feminizing side effects such as increased fat deposits, water retention, and gynecomastia (growth of breast gland tissue and painful tumors under the nipple). As a rule, it is more the ratio of androgens-to-estrogens than the simple increase in estrogen that actually initiates feminizing side effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIt is important that the reader realizes that Nolvadex does not decrease estrogen production and that it simply blocks estrogen receptors. For this reason the sudden discontinuance of Nolvadex will allow the increased level of circulating estrogen to merge with the newly freed receptors and do feminine things to the body.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e“Enter Proviron”. At the end of a steroid cycle, the body’s natural testosterone production can be impaired. Due to the aromatization of the AAS estrogen levels are significantly higher than normal and Nolvadex only helps by blocking the estrogen receptors. If an athlete abruptly ends an AAS protocol without regeneration of the HPTA under these conditions, much of the hard earned gains would disappear due to estrogen becoming the dominant hormone. So what did the boys (that didn’t want to be a girl) do?\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eProviron is an anti-estrogen (See “Proviron” for more info) that helps to prevent estrogen production while elevating androgen levels. During the last week of an AAS cycle, some male bodybuilders began a HCG protocol (See HCG) and administered 25-mg Proviron\/10-20-mg Novladex 1-2 times daily. This was commonly noted to almost completely suppress post-cycle estrogen and its activity. Since Nolvadex increases the body’s own testosterone production, as does HCG, much of the cycle gains were retained quite well. Nolvadex has a direct effect on the hypothalamus and therefore increases the release of Gonadotropic hormones to a minor degree. (The hormones that tell the Leydig cells in the testes to produce androgens such as testosterone are refereed to as Gonadotropics) Many added Clomid (*See Clomid) to their post-cycle stacks beginning 6-10 days after HCG and continued for the average reported two week duration. In most cases the result was athletes with normal (or above) sex drive and androgen production!\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e* High dosage use of Nolvadex can inhibit natural testosterone production. This is due to inhibition of enzymes needed for testosterone production by the testes.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNolvadex was normally layered into any protocol utilizing high aromatizing steroids such as testosterone, Dianabol, or those that are progesterone receptor stimulators such as Anadrol-50. Those who were prone to high fat deposits, water retention, and gyno consistently reported inclusion of Nolvadex. Many are were to obtain excellent estrogenic activity suppression with only 10-mg daily while others noted the need for as much as 60-mg daily (20mg 3 times daily). The best results and guidelines were obtained by starting low and increasing dosages only when necessary.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIt is important for the reader to realize that AAS must have some estrogen present in order to achieve their full positive potential effectiveness and provide the best commonly desired results. This is why many AAS lose their anabolic qualities when combined with anti-estrogens. It is also why Methandriol magnifies the effects of the same AAS. Those who used high anabolic\/moderate-low androgenic steroids such as nandrolones, Primobolan, or Winstrol, and did not combine them with high aromatizing steroids (such as testosterone) often considered not using Nolvadex during cycles the best choice when increased mass was the primary intent.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWomen who used Nolvadex usually did so because it aids in fat loss due to less estrogenic activity. I have yet to see a female compete whom was able to achieve truly cut legs with out it. Women athletes often combined 10-20mg of Nolvadex with 50-75mg Proviron daily for the last few weeks of dieting. Due to availability of Clenbuterol, Proviron dosages were reported lower as of late, at least in female fitness competitors. Women\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eshould be aware that birth control is an estrogen and Novladex will block its effectiveness. Women have note irregular menstrual cycles, weaker menstrual bleeding, and sometimes skip periods all together during Nolvadex use. I know several women who use Nolvadex for this reason and can not say I disagree with their choice. After all, the use of progestin type birth control as a means of regulating or even stopping menstruation is becoming accepted in the medical circles at last.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eA few athletes have experienced a paradox when using high dosages of Nolvadex. Instead of lowering estrogenic activity, it increased it. What happened was that the Adrenal glands went into over drive producing a pro-hormone called DHEA. DHEA is actually an adrenal androgen normally secreted in lower levels. As circulating levels increased enzymic factors came into play. Research shows DHEA readily converts into androstenedione, and to some extent, estrogens in males. (That sucks!) The female endocrine system usually favors testosterone production from converted DHEA or androstenedione. The newly formed estrogen then overwhelmed the estrogen receptors blocking the intended qualities of Novladex. In this case, Proviron, and especially Teslac where notably better choices.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Gyno that fails to react to these drugs normally must be removed by surgery. DHT derivatives can cause increases endogenous estrogen production also in some individuals. Cytadren was a commonly co-administered drug with Nolvadex.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTAMOXIfin is effective in the treatment of metastatic breast cancer in women and men. In premenopausal women with metastatic breast cancer, TAMOXIPLEX is an alternative to oophorectomy or ovarian irradiation . Available evidence indicates that patients whose tumors are estrogen receptor positive are more likely to benefit from TAMOXIfin therapy .\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAdjuvant Treatment of Breast Cancer\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTAMOXIfin is indicated for the treatment of node-positive breast cancer in women following total mastectomy or segmental mastectomy, axillary dissection , and breast irradiation. In some TAMOXIPLEX adjuvant studies, most of the benefit to date has been in the subgroup with four or more positive axillary nodes.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTAMOXIfin is indicated for the treatment of axillary node-negative breast cancer in women following total mastectomy or segmental mastectomy, axillary dissection , and breast irradiation.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe estrogen and progesterone receptor values may help to predict whether adjuvant TAMOXIPLEX therapy is likely to be beneficial.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTAMOXIfin reduces the occurrence of contralateral breast cancer in patients receiving adjuvant TAMOXIPLEX therapy for breast cancer.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDuctal Carcinoma in Situ ( DCIS )\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIn women with DCIS, following breast surgery and radiation , TAMOXIfin is indicated to reduce the risk of invasive breast cancer (see BOXED WARNING at the beginning of the label). The decision regarding therapy with TAMOXIPLEX for the reduction in breast cancer incidence should be based upon an individual assessment of the benefits and risks of TAMOXIPLEX therapy.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCurrent data from clinical trials support five years of adjuvant TAMOXIPLEX therapy for patients with breast cancer.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eReduction in Breast Cancer Incidence in High Risk Women\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTAMOXIfin is indicated to reduce the incidence of breast cancer in women at high risk for breast cancer. This effect was shown in a study of 5 years planned duration with a median follow-up of 4.2 years. Twenty-five percent of the participants received drug for 5 years. The longer-term effects are not known. In this study, there was no impact of tamoxifen on overall or breast cancer-related mortality\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53765675548964,"sku":null,"price":280.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_3591e874-5a3c-4881-9a46-8ca5b94391d0.jpg?v=1778087333"},{"product_id":"upa-bpc-157","title":"UPA BPC-157","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA BPC 157(PENTADECAPEPTIDE 5MG=1 POWDER+WATER))\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBPC 157 (Body Protection Compound-157) is a pentadecapeptide made up of 15 amino acids. The amino acids sequence in BPC 157 is similar to a portion of the human BPC amino acid sequence. Human BPC is found in the gastric juice. Experiments have shown that BPC 157 enhances the healing of wounds, including tendons wounds such as transected Achilles tendons of rats. The aim of this study was to investigate the probable mechanism that BPC 157 utilizes to accelerate the healing process in an injured tendon. The study used two group of tendon explants of which one group was cultured in a BPC 157-containing medium while the other group was cultured in a medium lacking BPC 157. These cultures were thereafter examined for tendon fibroblasts outgrowths. Such outgrowths indicated tendon regeneration.The results revealed that the explants’ outgrowth was significantly accelerated in the culture containing BPC 157 as compared to the culture lacking BPC 157. Also, a MTT assay did show that BPC 157 does not directly affect cellular proliferation in a culture of rat-derived Achilles tendon. However, results also showed that BPC 157 significantly increased the survival of cells under oxidative stress. Furthermore, the Transwell filter migration assay showed that BPC 157 significantly increased in-vitro fibroblast migration in a dose-dependent fashion. Moreover, BPC 157 accelerated the dispersal of the fibroblasts in culture dishes in a dose-dependent manner\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAdditionally, FITC-phalloidin staining was able to demonstrate that BPC 157 induces F-actin formation in fibroblasts. Likewise, Western blot analysis was able to detect the production and activation of paxillin and FAK proteins. The western blot analysis also showed that BPC 157 increases the extent of phosphorylation of paxillin and FAK proteins without affecting the amounts produced.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThus, it can be concluded that BPC 157 enhances the ex-vivo growth and in-vitro cellular migration of fibroblasts derived from rat tendon explants. Moreover, BPC 157 also increases the probability of a cell surviving under oxidative stress. These actions of BPC 157 are probably mediated by the activation (through phosphorylation) of the proteinic FAK-paxillin pathwa\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53765749637412,"sku":null,"price":380.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_da36cf8a-6a28-45f5-a5ee-c86094c99889.jpg?v=1778087459"},{"product_id":"upa-testolone8","title":"UPA Testolone8","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA=SARMS TESTOLONE(RAD-140) 10MG\/TABLET=50 TABLETS.\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTestolone (RAD-140) Testosterone Replacement\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTestolone (RAD-140) is designed to make hormonal receptors in the tissues act as though they are getting a strong dose of testosterone. This gives the same effect as if running a cycle of anabolics and\/or prohormones without the negative side effects that correlate with use.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBenefits:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAlong with the effects of testosterone discussed above, Testolone (RAD-140) also carries other significant benefits. Enhanced speed, stamina and endurance when doing high intensity is a key benefit shown in research tests with RAD implementation. Another huge benefit shown with RAD research is a rapid buildup of muscular tissues. Studies have also shown that RAD contains a greater anabolic effect than testosterone when used.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosing:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStudies are still being conducted to ensure the proper doses are recommended for testing to maximize the research benefits. Studies to date have implemented a method of 0.3, 3 and 30 milligrams of RAD per day based on body weight of the research subject; however, many have come to the conclusion that 20-30 milligrams per day is the proper protocol for the most benefit in the safest manner of research dosing.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSide Effects:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThere have not been any side effects found to date. This is also a breakthrough considering that regular testosterone causes drastic suppression where RAD has not shown these kinds of issue, nor has it shown any estrogen conversion or any typical testosterone, anabolic and androgenic side effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eConclusion:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBased on current findings and testing, RAD is showing to be a significant breakthrough in the medical field. While very new and still being tested, results thus far have been nothing but encouraging and as time progresses, RAD will likely become widely known as a replaced for testosterone replacement therapy or a safer alternative. Time will tell but research indicates a bright future. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDeveloped by Radius Health, RAD-140 is the newest second-gen SARM. Known also as Testalone or Testolone, it has very impressive and powerful muscle-building effects, even greater than those of LGD-4033. Despite it’s highly-anabolic profile, there are almost no reports of significant testosterone suppression or other side effects (this may be due, however, to its recency on the market). Clinical testing shows RAD-140 counteracts prostate enlargement, and also may exhibit neuro-protective and neuro-regenerative properties.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTypical dose: 15-30 mg\/day\u003c\/div\u003e\n\u003cdiv\u003eMax: 30 mg\/day\u003c\/div\u003e\n\u003cdiv\u003eStacking dose: 5-15 mg\/day (depending on stack)\u003c\/div\u003e\n\u003cdiv\u003eHalf-life: 12-18 hours\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53765855117604,"sku":null,"price":520.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_40f80ba5-ec21-4d0f-9b9d-ec2b86eb8853.jpg?v=1778087569"},{"product_id":"upa-nutrobal","title":"UPA Nutrobal","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA=SARMS NUTROBOL(MK-677)10MG\/TABLET=50 TABLETS.\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhat Is Nutrobol MK-677\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNutrobal (MK-677) is a chemical that has the characteristics of human growth hormone (HGH). It is an orally active growth hormone secretagogue. A secretagogue causes substances to be secreted. MK677 has the ability because of its ability to mimic the GH stimulating action a hormone called “ghrelin.” Ghrelin is categorized as a peptide, commonly referred to as “the hunger hormone,” which explains the drastic rise in appetite with 677 use. Ghrelin plays a large role in regulating the distribution as well as rate of energy use. It is imperative to understand all of these concepts to decipher the many capabilities that 677 has. mk677 can not only increase plasma levels of many types of hormones, but also provide sustainable increases. These are long term and not just “for the time being” types of increases. Studies show that Nutrobal can increase muscle mass and bone mineral density as well as altering the metabolism of body fat, possibly becoming a treatment for obesity.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBenefits of MK-677:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNutrobal (MK-677) studies have been conducted since the late 90’s. There is a wide array of benefits that have been found with use. The main benefit that consistently shows in study is the increase in growth hormone and IGF-levels provided with use. These have shown to be significant increases in regards to both. Below is a list of other significant benefits found through studies and implementation on humans:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIncreases in fat free mass Enhanced sleep quality A treatment for obesity and fat loss Lowering of bad cholesterol (LDL) Significant improvements in nitrogen balance Reversal of diet-induced nitrogen wasting Treatment of catabolic conditions Increase in basil metabolic rate Oral administration (no injections required) Overall sense of well-being\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIt is evident by the list of benefits that MK677 is highly desirable. These benefits, in conjunction with the very small chance of side effects show MK677 to be a breakthrough. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSide Effects:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAs stated above, MK677 carries little to no side effects however it is always important to understand the possibilities that could occur with use. \u003c\/div\u003e\n\u003cdiv\u003eThe main “side effect” associated with MK677 is the increase in appetite, which may be welcome by many research subjects. Studies show this to subside after 4-8 weeks, variant from person to person. The other side effects that showed, that were very infrequent and uncommon were mild lower extremity edema and muscle pain. Secretagogues generally carry the worry of prolactin increase, however studies with MK677 did not show any increase in prolactin levels. Cortisol levels were not increased in studies either. These traits make Nutrobal stand out amongst other chemicals that attempt to work in the same manner but carry these unwanted side effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosing:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStudies conducted had dosing between 5-25 mg per day, with 25 mg being the most common and effective dose. MK677 has a 24 hour half life and showed to be best tolerated when fed to rats each morning on an empty stomach. MK677 has extreme benefits in regards to helping with a deeper sleep however it can interfere with sleep patterns if taken too late at night or too close to bed time. MK677 can be used continuously for 1-2 years with no concern of desensitizing. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAlso known as Ibutamoren, MK-677 is often stacked with other SARM’S because it behaves differently: it stimulates the pituitary gland to release growth hormone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSARM MK-677: Growth Hormone Mimetic\u003c\/div\u003e\n\u003cdiv\u003eSARM MK-677: Growth Hormone Mimetic\u003c\/div\u003e\n\u003cdiv\u003eFor this reason, MK677 is a preferred performance enhancer and is used for bulking as well as cutting, with users consistently reporting gains in lean muscle mass. Ibutamoren is not known to be suppressive to testosterone production and, due to its affinity to oxidize fat at an accelerated rate, women looking to lose weight may prefer this SARM as well. High-dosing users have reported side effects that include numb hands, lethargy, and increased appetite.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTypical dose: 15-30 mg\/day\u003c\/div\u003e\n\u003cdiv\u003eMax: 50 mg\/day\u003c\/div\u003e\n\u003cdiv\u003eStacking dose: 10-15 mg\/day (depending on stack)\u003c\/div\u003e\n\u003cdiv\u003eHalf-life: 24 hours\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53765925896484,"sku":null,"price":550.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_7a594244-2440-4378-8d17-68931d55a363.jpg?v=1778087670"},{"product_id":"upa-clomid","title":"UPA Clomid","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA CLOMID(50MG CLOMIPHENE CITRATE TAB=50TABS)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive Life: about 8-12 hours\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Synthetic estrogen\/HPTA stimulator (Oral)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 50-100 mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: No\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Low, seldom reported.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStrong gonadotropin stimulator\/mild anti-estrogen\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eClomiphene is a synthetic estrogen clinically administered to help women ovulate. Bodybuilders, (male) following AAS cycles, seeking to jump start natural testosterone production (or those that were simply seeking a natural testosterone spike) have used this drug with great success. Clomiphene increases activity in the hypothalamus-pituitary-gonadol axis by stimulating the release of more gondotropin from the pituitary gland. Therefore, a higher\/faster level of LH (luteinizing hormone) and FSH (follicle stimulating hormone) results. This creates a signal to the leydig cells in the testes which in turn produce more testosterone and sperm. Normally with Clomiphene this took 5-15 days. Most started with 50-mg twice daily for about 5 days, then reduced intake to 50 mg once a day for 5-10 more days. Due to Clomiphene providing a fast response time, I felt it was often beneficial to use a dosage of 100 mg total daily for 5 days, mid-cycle during longer AAS protocols. This drug was seldom utilized for longer than 15 days continuously simply due to it being unnecessary. The goal was to normalize testosterone production post AAS cycle as quickly as possible so as to minimize post-cycle strength and mass loss. Not create dependency.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHCG was combined with Clomiphene (Clomid) sometimes, or Clomiphene was used after HCG administration. This is because Clomiphene acts by affecting the hypothalamus and pituitary (hypophysis) and regenerating the whole regulating system, while HCG only “imitates” LH, thus stimulating the leydig cells in the testes to produce natural testosterone. (*Also see HCG)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Some may wonder about Clomiphene being a synthetic estrogen. Yes, it is, but it works as an anti-estrogen. This is due to the fact that Clomiphene has a very low estrogenic effect. This means stronger and more active estrogen, such as those formed during the aromatization of many androgenic steroids, are blocked out of the receptor-site and less estrogenic activity results; less gyno, less water retention. Clomiphene was by no means as effective as Novladex or Proviron for estrogen suppression, but post-cycle it helped greatly.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eClomiphene is commonly used by male anabolic steroid users to bind the estrogen receptors in their bodies, thereby blocking the effects of estrogen, i.e., gynecomastia. It also restores the body’s natural production of testosterone. It is commonly used as a “recovery drug” and taken toward the end of a steroid cycle.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53766012633380,"sku":null,"price":310.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_dbd71017-c59d-4fab-ade7-8fece0579df9.jpg?v=1778087779"},{"product_id":"upa-tesamarelin","title":"UPA Tesamarelin","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e\n\u003cp\u003eTesamorelin is a synthetic peptide designed to mimic growth hormone-releasing hormone (GHRH). Its primary function is to stimulate the release of growth hormone (GH) from the pituitary gland. Tesamorelin has gained popularity in the fitness and bodybuilding community for its ability to support fat reduction, muscle growth, and overall body composition improvement.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eHow It Works\u003c\/p\u003e\n\u003cp\u003eBoosts GH Levels: Tesamorelin activates GHRH receptors in the pituitary gland, encouraging the production and release of growth hormone. This increase in GH also leads to higher levels of Insulin-Like Growth Factor 1 (IGF-1) in the bloodstream.\u003c\/p\u003e\n\u003cp\u003eElevates IGF-1 Production: By enhancing IGF-1 levels, Tesamorelin promotes anabolic processes that support muscle repair and growth.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eBenefits for Fitness and Bodybuilding\u003c\/p\u003e\n\u003cp\u003eFat Reduction: Tesamorelin is highly effective at targeting and reducing visceral fat, the type of fat stored around internal organs. This is particularly beneficial for achieving improved muscle definition and overall body aesthetics. It is especially useful for reducing abdominal fat, which is often stubborn and difficult to lose.\u003c\/p\u003e\n\u003cp\u003eEnhances Muscle Growth and Recovery: By raising GH and IGF-1 levels, Tesamorelin supports protein synthesis, crucial for muscle growth and repair. This results in increased lean muscle mass and faster recovery after intense workouts.\u003c\/p\u003e\n\u003cp\u003eImproves Recovery Rates: Higher GH levels help reduce inflammation and accelerate the repair of muscle tissues. This enables athletes to train more frequently and with greater intensity, enhancing performance and overall muscle development.\u003c\/p\u003e\n\u003cp\u003eSupports Longevity: Tesamorelin provides additional benefits such as improved skin elasticity, better bone density, and overall vitality, contributing to a healthier and more active lifestyle.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eAdministration Guidelines\u003c\/p\u003e\n\u003cp\u003eDosage: A typical dose ranges between 1 to 2 mg daily, administered via subcutaneous injection. It is often used in cycles to prevent receptor desensitization.\u003c\/p\u003e\n\u003cp\u003eTiming: The best time to administer Tesamorelin is usually before bed, aligning with the body’s natural GH production during sleep.\u003c\/p\u003e\n\u003cp\u003eStacking with Other Peptides: It can be paired with peptides such as Ipamorelin or CJC-1295 to amplify its effects on GH release and muscle development.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eKey Takeaway\u003c\/p\u003e\n\u003cp\u003eTesamorelin is an excellent option for individuals aiming to reduce fat, enhance muscle growth, and accelerate recovery. Its ability to stimulate GH and IGF-1 production makes it a valuable asset for improving physical performance and body composition.\u003c\/p\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53766124405028,"sku":null,"price":360.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_251fbc1a-7a78-43ec-bab1-a049ad8d6a4b.jpg?v=1778087916"},{"product_id":"upa-tren-e-200","title":"UPA Tren E 200","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA=TREN E200(200mg\/ml TRENBOLONE ENANTHATE=10ML)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eandrogenic 500\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eanabolic 500\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003estandard nandrolone\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 8-10 days\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anabolic\/Androgenic steroid (for injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 200-400 mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Common\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Common\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Though disputed, yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eKidney Toxic: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNoted Comments: High Anabolic\/Very high Androgenic\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Moderately\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT conversion: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTrenbolone enanthate is the most recent form of trenbolone to be developed, appearing on the market in mid-2004.This agent is essentially a new form of Parabolan, which uses the ubiquitous enanthate ester instead of the hexahydrobenzylcarbonate of the “old” product. Trenbolone enanthate is both unique and incredibly obvious at the same time. On the one hand, attaching an enanthate ester to trenbolone seems like a simple idea at best. After all, we are all familiar with testosterone and methenolone enanthate. But on the other hand, trenbolone enanthate had not been made commercially until now. With the loss of Parabolan, and only recent reemergence of a legitimate clone, the market was left with trenbolone acetate as its only readily available form of “tren”This ester of trenbolone is effective, but also very fast acting. Trenbolone enanthate is a much slower releasing drug, and offers a great alternative to the frequent injections of trenbolone acetate.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe pharmacokinetics of trenbolone enanthate should mirror those of testosterone enanthate, with peak hormone levels maintaining itself for approximately two weeks after each injection\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTHIS IS A NEWER VERSION OF TRENBOLONE.TRENBOLONE ENANTHATE IS THE LONGER ACTING FORM OF THE TRENBOLONE ESTER .IT HAS THE SAME CHARASTICHS AS DISCUSED WITH TRENBOLONE ACETATE AND TRENBOLONE HEXAHYDROBENZYLCARBONATE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNOTED POSITIVE EFFECTS OF TRENBOLONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Amazing anabolic qualities.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Rapid high quality lean tissue gains. (Dose dependent) *Maximum post-cycle lean mass retention. *Low-none water retention.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased Erythropoies (Red blood cell production) *Does not aromatize to estrogens. *Superior strength and mass gain. (Lean) *Extreme hardening of musculature and vascularity. *Excellent protein sparing\/anti-catabolic qualities. *Reduction in fat stores and favorable distribution. *Increased metabolic rate. *Low-moderate HPTA function inhibition. *Significant increase in muscle glycogen synthesis. *Increase creatine phosphate (CP) synthesis. *Improved muscle insulin receptor activity.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Remains anabolic during calorie restricted periods. (High protein intake remains necessary)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePOSSIBLE NEGATIVE EFFECTS TRENBOLONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Liver and Kidney toxicity.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Growth of prostate tissue. (PSA test is wise)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Male pattern baldness. (Accelerated genetic predisposition)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Mild hallucinations. (High dosage -prolonged use)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*High blood pressure.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53766192890148,"sku":null,"price":820.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_ebbd1e39-bd5e-4fc2-acef-b68abe5c273d.jpg?v=1778088015"},{"product_id":"upa-clenbuterol-tabs","title":"UPA Clenbuterol Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA CLENBUTEROL(40MCG CLENBUTEROL HCL\/TAB=50TABS )\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: Up to 68 hours\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Beta-2-symphatonimetic, thermalgenic\/anticatabolic (Oral)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 100-140 mcg per day Women 80-100 mcg per day\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Some reported high blood pressure\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Unknown Strong Anti-Catabolic\/Thermalgenic \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eClenbuterol is a quite strong anti-catabolic \/ thermalgenic drug that is not a steroid. During dieting periods, or post steroid cycles, this drug has reported dramatic effects on body composition. Since it suppresses the muscle wasting effects of cortisol\/cortisone, a slight increase in total muscle protein synthesis was seen. When stacked with steroids the effect were synergistic and more profound. When used as a post-cycle drug, clenbuterol helped to maintain muscle gains after AAS were discontinued. In both cases the drug acted to reduce fat deposits by elevation of thermalgenesis. It was considered very important to all polled whom had utilized this drug to start with 1-2 tabs daily (2 on -2 off) and monitor body temperature. (Increased dosages can increase body temperature to dangerous levels) Most obtained excellent results in 4-8 weeks. Many also stacked clenbuterol with thyroid drugs and \/or DNP to increase the rate of calorie expenditure.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHeadaches, high blood pressure, and elevated body temperature were among noted side effects. Many reported side effects after 8-12 days. The body quickly adapts to clenbuterol so “on\/off” periods were a must for successful results. By alternating between E\/C (Ephedrine and caffeine) stacks and Clenbuterol, the effective period was extended and results increased. Rotations weekly such as clenbuterol, week #1, ephedrine\/ caffeine week# 2, seem to have brought superior results.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe reason clenbuterol begins to lose effectiveness after only 2 weeks is that the beta-2-receptors it interacts with are quite sensitive. (These are adrenalgenic receptors) Once these receptors are over stimulated for a prolonged period of time they become insensitive. Oddly enough it appears that DNP and thyroid hormones help regenerate adrenalgenic receptor function.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSince Clenbuterol dilates blood vessels in skeletal muscle but relaxes smooth muscle blood vessels, the physical reactions are quite similar to the body’s own epinephrine and can effect heart rate. It also reduces the level of the amino acid taurine in the heart which stabilizes cardiac rhythms, or the electrical activity in the heart. Increased intake for taurine during use was noted as wise.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMost bodybuilders don’t realize that the anabolic effects of Clenbuterol are not due to increased anabolic activity. Clenbuterol is actually effective through a different mechanism. It decreases both protein synthesis and break down. The reason anti-catabolic effects result is simply because it hinders protein break down more which shifts the ratio in favor of anabolism. This means that clenbuterol had significant anti-catabolic effects when stacked with a cortisol inhibitor post or during AAS cycles. Cytadren was an often noted example. Again, since clenbuterol increases thermalgenesis, (calories released as heat) the common use of thyroid T-3 or T-4 in a stack with it caused a significant increase in body temperature. This was monitored closely by most.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eClenbuterol is utilized to treat asthma in several countries. The dosage for treatment is normally 20-30 mcg\/d.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53766261080356,"sku":null,"price":210.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_8f923fe0-f164-47a3-8c7f-c81a3a028692.jpg?v=1778088140"},{"product_id":"upa-turinabol","title":"UPA Turinabol","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eANDROGENIC N\/A\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC \u0026gt;100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 6-8 hours \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anabolic\/androgenic steroid ORAL\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003estandard: METHYLTESTOSTERONE(ORAL)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 10-50 mg daily Women 10-20 mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne:NO\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: NO\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: NO\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: NO\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Yes, 17-alfa alkylated oral\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT conversion: No\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh anabolic\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA function: NO\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOral Turinabol is an anabolic steroid developed and made famous by scientists in East Germany years ago. Actually, this is more a steroid of infamy actually, as it was one of the closely held secrets inside the “East German Doping Machine” I am referring to a state sponsored doping program, called “State Plan 14.25” that operated in East Germany for a period of time between the 1960’s and 80’s. It was an aggressive anabolic steroid administration program, designed with one goal in mind: cheating the Olympic drug test. In many cases, the Olympic athletes, both male and female, were unwitting participants, simply told by their trainers and coaches that they were being given “vitamins” Many of these blue vitamins turned out to be Oral Turinabol, a potent and undetectable (at the time) anabolic steroid. As many as 10,000 unsuspecting athletes were given anabolic steroids during the time the program was active. For a more in-depth look at this dramatic historic event, including the trials of several former East German officials for their participation, I recommend you look at the book “Faust’s Gold: Inside the East German Doping Machine”by Steven Ungerleider.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOT, as it is called, is a potent derivative of Dianabol. It is structurally a cross between methandrostenolone and clostebol (4-chlorotestosterone), having the same base structure as Dianabol with the added 4-chloro alteration of clostebol. This makes OT a “kinder, gentler Dianabol” the new steroid displaying a much lower level of androgenic activity in comparison to its more famous counterpart. Its anabolic activity of chlorodehydromethyltestosterone is somewhat lower than that of Dianabol as well, but it does maintain a much more favorable balance of anabolic to androgenic effect overall. This means that at any given level of muscle-building activity, OT will be much less likely to produce the classic androgenic side effects such as oily skin, acne, aggression, and male-pattern hair loss (if genetically prone) than would Dianabol.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe 4-chloro attachment used with this steroid also inhibits its ability to be aromatized. Therefore, OT is not going to present its user with unwanted estrogenic side effects like water retention, increased fat deposition, or gynecomastia. While Dianabol tends to produce puffiness and a little fat retention in its users, which hides muscle definition, the exact opposite effect usually happens with OT. OT tends to promote gain in lean tissue mass, accompanied by an increased look of density, hardness, and definition due to the intensified androgen to estrogen ratio. For bodybuilding purposes, this makes OT a great pre-contest or cutting steroid, not really a bulking agent of choice. Athletes in sports where speed tends to be a primary focus would also find favor in OT, obtaining a strong anabolic benefit without having to carry around any extra water or fat weight.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhen this drug was available in Western Europe, the typical daily dosages used by men were in the rage of 20mg to 40mg. Women would get by on less, usually a single 5mg tablet.That is, unless you were an East German female Olympic swimmer, in which case you could have been swallowing as many as 30 tablets per day (we can understand why long-term virilizing side effects were reported over and over again in the “doping trails”). When used in the recommended dosing levels, OT definitely proves itself as a potent lean tissue builder. Again, it will provide less overall muscle bulk than Dianabol, but with its lack of estrogen conversion, the gains obtained with OT, even if smaller in total, are visibly of better quality. Although there is a clear relationship between OT and Dianabol when it comes to molecular structure, ultimately it would be much more appropriate to be comparing the activities of this steroid to those of other mild, non-aromatizing anabolics like stanozolol, oxandrolone or methenolone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTuranabol is indicated in conditions such as chronic infections, extensive surgery, [corticosteroid-induced myopathy, decubitus ulcers, burns] , or severe trauma, which require reversal of catabolic processes or protein-sparing effects. These agents are adjuncts to, and not replacements for, conventional treatment of these disorders.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53766329205028,"sku":null,"price":270.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_399a5ead-3926-4f9f-b4a7-e46cf893a767.jpg?v=1778088247"},{"product_id":"upa-deca-330","title":"UPA Deca 330","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA DECA 330(300MG\/ML NANDROLONE DECANOATE=10ML)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 37\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 125\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD TESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 14-16 days FOR NANDROLONE DECOANATE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anabolic\/Androgenic steroid (For Injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage: Men 200-600mg weekly Women 50-100mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Yes, in higher dosages in androgen sensitive individuals\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Some, much less than testosterone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA function moderately\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Rare (When used in dosages over 600-mg weekly)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: Low, converts to less active norestrogens\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: None.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: No, converts to NOR- DHT with low activity\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNoted Comments: Highly anabolic\/moderate androgenic effects\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNandrolone Decanoate is a very anabolic, moderate androgenic form of nortestosterone that was the most commonly used drug to create a rapid build-up of lean muscle mass or as a diet “protein- sparing” drug by athletes of all kinds. This is a longer lasting nandrolone than Durabolin so some water retention resulted with long term administration (especially in higher dosages). A prominent positive nitrogen balance occurs with the use of nandrolones and therefore a high protein intake was a must for all reported users. If you read the section on protein, you know that nitrogen in its bonded form is a part of protein\/amino acids. Since nandrolone promotes nitrogen storage in muscle cells (a positive nitrogen balance) then the cell contains more protein for growth and repair than normal. Remember: This could only happen if above normal calories (with a focus on protein) were ingested. Since nandrolone is moderately androgenic, good strength gains also resulted. Another plus for nandrolone was that most users experienced a joint healing effect during cycles and a suppressed cortisol\/cortisone activity due to nandrolones ability to long-term block cortisol receptors. Since aromatization was low, in 200-400-mg weekly dosages, anti-estrogens were not commonly necessary to avoid gyno and estrogenic induced side effects. Based upon available research and information available it seems liver toxicity is unknown with nandrolone. So it was not a surprise to find that even those with liver disease have used this drug with great success.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCommon dosages for men were 200 600mg weekly. Though dosages over 400 mg weekly caused more water retention. For first time use of dosages over 400 mg weekly, I preferred to add 50-100mg Durabolin to each of the 2 weekly injections. This was because Durabolin is much faster acting and therefore creates chance for water retention and gyno. (This applied to first -time users only)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAn added benefit of this method was that nandrolone decanoate begins significant activity at 6 days and peaks at about 8 days after administration. The faster acting durabolin “kicks in” after about 1 day. This also resulted in higher “quality” muscle tissue gain.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWomen seemed to do very well with nandrolones due to the lower androgenic\/masculining effect. Women consistently reported excellent lean mass and strength gains at dosages of 50-100 mg weekly. Masculine effects usually were avoided by single weekly injections of 25-50 mg nandrolone decanoate and 25-50 mg of Durabolin (nandrolone phenylpropionate). In both men and women, this method seemed to result in more “quality” muscle, less water retention, less gyno for males, and good retention of gains after the cycle ends.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Metabolites can be found in urine or blood tests for 12-18 months after use of nandrolone is discontinued.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNOTED POSITIVE EFFECTS OF NORTESTOSTERONE (NANDROLONE)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Significant anabolic qualities.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*High quality (but slow) lean tissue gains.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Excellent post-cycle lean mass retention.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Low-moderate water retention.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Low aromatization to estrogens.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Does not negatively effect HDL.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Moderate strength and weight gain.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Noted improvement in joint\/soft tissue function.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Excellent protein sparing \/anti-catabolic qualities.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Inhibition of fat synthesis.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased metabolic rate.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Does not reduce to DHT (Dihydrotestosterone)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Very low-moderate HPTA function inhibition. (Dose Dependent)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased muscle glycogen synthesis.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased Creatine Phosphate (CP) synthesis.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Reduction in total triglyceride and cholesterol levels.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Beneficial\/improved insulin metabolism.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePOSSIBLE NEGATIVE EFFECTS OF NORTESTOSTERONE (NANDROLONE)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Poor protection from over training.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Some males experienced decreased libido (Not true for women) *Inhibition of HPTA function at dosages in excess of 400 MG weekly.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNandrolone binds to the androgen receptor to a greater degree than testosterone, but due to its inability to act on the muscle in ways unmediated by the receptor, has less overall effect on muscle growth. The drug is also unusual in that unlike most anabolic steroids, it is not broken down into the more reactive DHT by the enzyme 5a-reductase, but rather into a less effective product. As such, some of the negative effects associated with most such drugs are somewhat mitigated.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe positive effects of the drug include muscle growth, appetite stimulation and increased red blood cell production and bone density. Clinical studies have shown it to be effective in treating anaemia, osteoporosis and some forms of neoplasia including breast cancer, and also acts as a progestin-based contraceptive. Nandrolone is also extensively used by bodybuilders and other athletes seeking an edge in professional competition\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53766409584932,"sku":null,"price":550.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_92f2cdd8-af07-4e2f-9dd1-fbe77c95d072.jpg?v=1778088362"},{"product_id":"upa-viagra","title":"UPA Viagra","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA VIAGRA(100MG SIDENAFIL CITRATE\/TAB=10TABS )VERY GOOD QUALITY PRODUCT.\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 6-12 HOURS\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: ERECTILE DYSFUNTION(ORAL)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: 25MG-100MG- 30-60 MIN BEFORE SEXUAL ACTIVITY\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure:YES\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eVIAGRA is an oral medication for erectile dysfunction (ED).VIAGRA increases blood flow to the penis. And it helps men with erectile dysfunction (ED) get and maintain an erection. That means they are able to achieve harder erections.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTHIS IS ONE OF THE WONDER DRUGS OF THE CENTURY AND CHANGED MANY MEN’S LIFE’S AROUND THE GLOBE.VIAGRA IS SOMETIMES CALLED THE MAGICAL BLUE PILL.IMPOTENCE IS PROBALY THE BIGGEST EMBARRESMENT THAT CAN HAPPEN WITH ANY MAN .\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWho can take VIAGRA\u003c\/div\u003e\n\u003cdiv\u003eVIAGRA has an established safety profile of over 10 years. It has been shown to work safely and effectively in men with ED. This includes: Men of all ages -Men who have difficulty all the time or just some of the time -Men with other health issues such as high blood pressure, diabetes, and depression .\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWho should not take VIAGRA\u003c\/div\u003e\n\u003cdiv\u003eVIAGRA has been shown to work safely in most men. But if you take any medicines that have nitrates in them (like nitroglycerin for chest pain)—every day or even once in a while—you should NOT take VIAGRA.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLike with all medicines, some people taking VIAGRA may experience side effects. These are usually mild and don’t last longer than a few hours. The most common side effects are: Headache-Facial flushing-Upset stomach.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCERTIAN INDIVIDUALS REPORTED TRYING A MIXTURE OF VIAGRA AND CIALIS WITH GREAT SUCCESS,BUT BE VERY CAREFULL.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53766521651492,"sku":null,"price":300.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_773cdb86-38b5-4e6a-b338-8a3bb254c957.jpg?v=1778088512"},{"product_id":"upa-sustanon-350","title":"UPA Sustanon 350","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e\n\u003cdiv\u003eUPA=SUSTANON 350(350MG\/ML 4 TESTOSTERONE MIX =10ML)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD TESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: About 3 weeks\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Androgenic\/Anabolic steroid (For injection) Average Reported Dosage: Men 125-2000mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Low except in high dosages over 1000-mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Significantly after 2 weeks\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSustanon 250 is a mixture of the 4 testosterone esters:                     \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePROPIONATE -30MG\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePHENYLPROPIONATE -60MG\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eISOCAPROATE -60MG\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDECANOATE -100MG \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis is a well structured product that acts as a well timed time-released high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eanabolic\/high androgenic testosterone. In fact, due to TESTOSTERONE PROPIONATE,\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ethis product becomes active after one day, but through the series of the other 3 testosterones, remains active for 3 weeks. This mixture had a reported better over all effect milligram for milligram than any other testosterone alone. Users experienced a rapid increase in strength and an even increase in solid mass during administration. SUSTANON aromatized less and caused less water retention when compared to other single testosterones and much less than OMNADREN. Liver toxicity was low (Except in ridiculous dosages) as the liver metabolizes testosterone very efficiently. Like all testosterones, SUSTANON provided improved muscle pumps, better post-training recuperation, and an elevation in aggressiveness toward training.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSUSTANON 250\u0026amp;TEST COMBO significantly suppressed the HPTA so natural testosterone production was significantly decreased as well. For this reason, HCG and CLOMID were considered mandatory after 4-6 weeks of continuous use and after the discontinuance of the drug.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMales normally utilized dosages of 250-1000mg weekly, but some used higher dosages. As a rule, excellent results were realized with a dosage of 250-500mg every 7­-10 days. Most novices and women noted that they felt that they should not use testosterone. Novices…because it was not necessary and it will limit later potential progress. Women should not use them (but a few reported doing so) due to virilizing effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome woman polled just could not leave testosterones alone. PROSCAR (FINASTERIDE, A DHT BLOCKER) was considered mandatory for co-administration and TESTOSTERONE PROPIONATE 50mg 1 time weekly was noted to cause less virilizing side effects.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53766616383780,"sku":null,"price":430.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_0ad3bd81-a5b4-4ce6-b594-3bd7124752a7.jpg?v=1778088656"},{"product_id":"upa-enclomiphene-15mg","title":"UPA Enclomiphene 15mg","description":"","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53766707118372,"sku":null,"price":580.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_b688aea5-e7b1-4f82-baf0-3c8f406959c2.jpg?v=1778088761"},{"product_id":"upa-cjc-1295-dac","title":"UPA CJC-1295 DAC","description":"\u003cp\u003eUPA CJC-1295 DAC(2MG\/2ML VIAL)\u003c\/p\u003e\n\u003cp\u003eCJC-1295 DAC has shown some amazing results as a growth hormone releasing hormone (GHRH) analog. Not only has CJC-1295 shown the ability to increase growth hormone and IGF-I secretion and its benefits, but it has been able to do so in very large amounts. Recent research studies have shown that CJC – 1295 stimulates GH and IGF-1 Secretion, and will keep a steady increase of HGH and IGF-1 with no increase in prolactin, leading to intense fat loss, and increases protein synthesis.\u003c\/p\u003e\n\u003cp\u003eCJC-1295 DAC is a long acting \u003ca href=\"http:\/\/www.peptidesciences.com\/growth-hormone-releasing-hormone\"\u003e\u003cstrong\u003eGrowth Hormone Releasing Hormone\u003c\/strong\u003e\u003c\/a\u003e, which causes the anterior pituitary  to release more growth hormone. GHRH is released in pulses in the body, which alternate with corresponding pulses of somatostatin (growth-hormone inhibiting-hormone). Clinical Research was first conducted for CJC-1295 during the mid-2000s. The objective of the peptide was to treat visceral fat deposits in obese AIDS patients, as increased levels of exogenous hgH are presumed to increase lipolysis (fat loss). The clinical research was ultimately successful for most research subjects. Ghrelin, released from the gut, which circulates and acts as a hunger hormone, has synergistic activity in the body with GHRH and also suppresses somatostatin to make way for the GHRH pulse. Studies shows that combining a \u003ca href=\"http:\/\/www.peptidesciences.com\/ghrp-6\"\u003e\u003cstrong\u003eGHRP-6\u003c\/strong\u003e\u003c\/a\u003e with CJC 1295 DAC, significantly increase the release of GH and IGF-1 production without an increase in prolactin. An example of a GHRP (GH Releasing Peptide) is \u003ca href=\"http:\/\/www.peptidesciences.com\/hexarelin\"\u003e\u003cstrong\u003eHexarelin\u003c\/strong\u003e\u003c\/a\u003e or \u003ca href=\"http:\/\/www.peptidesciences.com\/ghrp-2\"\u003e\u003cstrong\u003eGHRP-2\u003c\/strong\u003e\u003c\/a\u003e. CJC 1295 DAC is a exceptionally designed peptide and is known for being the finest of the hGH secretogues. The DAC (Drug Affinity Complex) portion increases the half-life by binding with serum albumin and protects the CJC-1295 DAC peptide from degradation. This was formed when a lysine link was bounded to DACs to a reactive chemical called maleimidoproprionic acid (MPA).\u003c\/p\u003e\n\u003cp\u003eCJC-1295 DAC vs. CJC-1295 No DAC\u003c\/p\u003e\n\u003cp\u003eCJC-1295 DAC and CJC-1295 (also known as \u003ca href=\"http:\/\/www.peptidesciences.com\/modified-grf-1-29\"\u003e\u003cstrong\u003eModified GRF 1-29\u003c\/strong\u003e\u003c\/a\u003e) are both Growth Hormone Releasing Hormones (GHRH). Their action in the human body is identical but the difference between the two peptides are the span of the half-life. Modified GRF 1-29 and Sermorelin have a very short acting half-life of about 30 minutes, while CJC-1295 DAC has a half-life that can last up to approximately 8 days.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eCJC1295\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eCJC1295 has a very long half-life and therefore it has no dietary restrictions or specific times that you. Because of its long half-life it has long-term benefits on your body’s basal GH levels. CJC1295 is a 30 amino acid peptide hormone where synthetic growth hormone contains a 191 amino acid chain. It attaches itself to the albumim receptor and this increases its half-life oppose to the normal growth hormone releasing hormones.\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003ePRODUCT DETAILS\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e2000mcg per vial\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eConstitute\u003cbr\u003e1ml of water depending on the brand you use.\u003c\/p\u003e\n\u003cp\u003eDosage\u003cbr\u003e1000mcg (1mg) twice a week or 2000mcg (2mg) once a week. Dose per injection: 2mg or 1mg x 2 Injections per vial: 1 x 2mg dosages or 2 x 1mg dosages per week. Amount to Inject: If you have used 1ml of water for mixing then a 2mg dosage = 1ml (or 100 units on Insulin Syringe). If you want to inject 1mg twice a week and you have used 1ml of water then a 1mg dosage = 0.5ml (or 50 units). \u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eFunctions\u003cbr\u003eThis product was initially developed for AIDS patients that were obese. It increases muscle mass and decrease body fat. Increase lean muscle mass. Decrease body fat percentage. Increase growth hormone secretion of the pituitary gland.\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eTIPS\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cstrong\u003eBecause of its long acting properties this product works best in conjunction with short acting growth hormone releasing hormones like GHRP-2 and GHRP-6 to take advantage of the short-term GH pulse created after a CJC1295 injection.\u003c\/strong\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cstrong\u003eIntramuscular and subcutaneous routes lead to different onset times but roughly similar peaks and declines.\u003c\/strong\u003e\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53766752862500,"sku":null,"price":370.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_59e77284-6687-4654-ad2b-65e4f12d719b.jpg?v=1778088874"},{"product_id":"upa-tb-500","title":"UPA TB-500","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA TB500(5MG=1 POWDER+WATER)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThymosin Beta 4, or TB-500, is a synthetic version of a naturally occurring 43-amino acid peptide present in nearly all human and animal cells studied.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eA 2010 study in the Annals of the New York Academy of Sciences supported TB500’s potential for cardiac muscle repair following injury, eg, after myocardial infarction (heart attack). Recognizing the limitations of stem cell therapy for this application, TB500 was found to inhibit myocardial cell death, stimulate blood vessel growth, and activate cardiac processes that encouraged the heart to heal following injury. The investigation showed that TB500 may be the first agent which can actively recover injured cardiac muscle following heart attack. This is further supported with prior mouse studies in 2004 showing cardiomyocyte migration, survival and repair of myocardial damage. [1] [2]\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFilamentous actin (F-actin, or actin) forms polymers that thicken sputum, adversely affecting cystic fibrosis patients. TB500 was studied in a population of CF patients, showing a dose- and time-dependent decrease in cohesivity of sputum after administration of TB500 when combined with dornase alfa. The combination therapy showed a 71% improvement in mucociliary transport of mucus, and a 44% improvement in cough transport of mucus. [3\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTB500 is known to stimulate myoblasts and myocytes (muscle generating cells). Mitochondrial RNA levels of TB500 have been shown to increase following muscle injury, helping to regenerate muscle fibers and address inflammation in the injured location. The data support muscle injury causing increased local production of TB500, promoting migration of incoming myoblasts to accelerate skeletal muscle regeneration. [4]\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTB-500 is a synthetic version of the naturally occurring peptide present in virtually all human and animal cells, Thymosin Beta 4 (Tß4). It is a first-in-class peptide candidate that promotes the following*: Endothelial (blood vessels) cell differentiation Angiogenesis (growth of new blood cells from pre-existing vessels) in dermal tissues Keratinocyte migration Collagen deposition; and Decreases inflammation.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTB-500 offers many benefits to the equine world in performance racing. Recent trials by some of the world’s leading trainers on their prize winning equine members of both genders, have been credited by a huge boost in their race-day results, something long desired in the racing world. These trials along with clinical trials have indicated the following benefits associated with the use of TB-500 on mares and stallions: Increase muscle growth with huge increases in endurance and strength noted Relaxed muscle spasm Improved muscle tone Increase the exchange of substance between cells Encourage tissue repair Stretches connective tissue Helps maintain flexibility Reduces inflammation of tissue in joint Enhances nutritional components in the animal Prevents the formations of adhesions and fibrous bands in muscles, tendons and ligaments. When these proven benefits are viewed in conjunction with the fact that 60% of a horse’s body weight is muscle, it is clear to see the full potential of TB500 can be reviled in by majority of the horse’s body. In a racing era that surrounds itself around gaining that competitive edge through the use of various substances, none will deliver the results that will be experienced with the use of TB-500. Perhaps the greatest selling point of the product is that it’s 100% DRUG FREE and DOES NOT SWAB. This allows the peptide to be used right throughout racing spells in both training and competition completely free of any banned substance.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTB-500 dosage and cycle duration:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage depends on the purpose and severity of the injury \/ damage you are treating. People generally use between 4 to 8 mg of TB500 per week during the initial (loading) period of 4 to 6 weeks. Afterwards some opt to maintain the effects with a low 2 to 6 mg dose once every 2 weeks. The effects of TB-500 wear off within 2 – 3 weeks of injection.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e1. TB-500 loading phase:\u003c\/div\u003e\n\u003cdiv\u003eduration: between 4 – 6 weeks\u003c\/div\u003e\n\u003cdiv\u003edosage: between 4 – 8 mg of TB-500 per week\u003c\/div\u003e\n\u003cdiv\u003efrequency of injection:2 mg per injection, between 2 – 4 times per week (depending on the total weekly dosage)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e2. TB-500 maintainance phase:\u003c\/div\u003e\n\u003cdiv\u003eduration: as long as needed\u003c\/div\u003e\n\u003cdiv\u003edosage: between 2 – 6 mg of TB-500 per 2 weeks\u003c\/div\u003e\n\u003cdiv\u003efrequency of injection:2 mg per injection, between 2 – 3 times per 2 weeks (depending on the total bi-weekly dosage)\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53766864601380,"sku":null,"price":400.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_6d585dd5-bfc0-4b07-a02b-11d1c220aff9.jpg?v=1778089013"},{"product_id":"upa-cialis","title":"UPA Cialis","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA CICCOCIALIS (20MG TADALAFIL\/TAB=10TABS)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 12-36 HOURS\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: ERECTILE DYSFUNTION(ORAL)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: 20MG= 30-60 MIN BEFORE SEXUAL ACTIVITY\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure:YES\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTHE SAME APPLIES AS FOR VIAGRA,EXCEPT THAT ITS EFFECT LAST LONGER-FOR UP TO 36 HOURS.in my opinion viagra is the better product,but last only for 12 hours.CERTIAN INDIVIDUALS REPORTED TRYING A MIXTURE OF THE TWO WITH GREAT SUCCESS,BUT BE VERY CAREFULL.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53766937084196,"sku":null,"price":270.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_e7ea087d-9bc9-4120-b25b-9c8a7c43b167.jpg?v=1778089111"},{"product_id":"upa-ipamorelin","title":"UPA Ipamorelin","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e\n\u003cp\u003eiPamorelin\u003c\/p\u003e\n\u003cp\u003eiPamorelin is a GHRP (Growth Hormone Releasing Peptide) that is considered one of the mildest due to it being perhaps the most side effect friendly of the GHRP hormones. iPamorelin was first developed by Novo Nordisk and made its way to phase two clinical trials through Helsinn Therapeutics. However, while it showed promising results the full trials were never completed and the project was scrapped. Although it is not found in medical circles it is used in some performance based circles in lieu of Human Growth Hormone (HGH).\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eiPamorelin Functions and Traits\u003c\/p\u003e\n\u003cp\u003eiPamorelin is very similar to GHRP-6 in that it increases ghrelin and targets a specific GH pulse. However, unlike GHRP-6 there doesn’t appear to be an increase in hunger that often exists with GHRP-6. More importantly, there is no impact on cortisol and only on plasma Growth Hormone (GH) levels. Unlike many other GH peptides such as Hexarelin, there doesn’t appear to be a strong breach of desensitization. This means there is no point where a dose doesn’t improve natural GH secretion.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eAlong with powerful GH releasing abilities, iPamorelin is also one of the longest lasting GH peptides available. The release of the hormone (GH) isn’t an instant spike followed by a rapid falloff point but instead a slow steady release that is more natural to the body.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eEffects of iPamorelin\u003c\/p\u003e\n\u003cp\u003eThe effects of iPamorelin are simple, to increase natural GH production in the body. It is the increase in GH production that produces the positive benefits and effects the athlete might be after. Increased levels of GH will improve the metabolism thereby giving the individual a greater ability to burn fat or maintain a suitable fat level when trying to grow. More importantly, elevated GH levels, especially stable elevated GH levels help with recovery perhaps more than anything else. Whether we are bulking or cutting it is in the recovery stage that we improve. Recovery helps us build new lean tissue and it helps protect our existing lean tissue.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eMost iPamorelin users should also find sleep is deeper and more efficient. Many users report a better mood, which is probably due to the fact that they’re getting more out of their rest. And as with anything that increases GH levels in the body we have the anti-aging benefits. GH affects nearly all parts of the body from muscle to the skeletal structure, nervous system, skin and even hair. GH has often been called the fountain of youth hormone, and it’s not hard to understand why. When we reach our 30’s our natural GH production rapidly declines and continues to decline, and as a result we begin to age. If GH levels remain elevated, while we can’t prevent aging we can slow the effects down.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eImportant note: iPamorelin will not give as big of a boost in GH levels as HGH. However, HGH is extremely expensive, often hard to get and often counterfeited. iPamorelin, while not as effective as HGH is still better than no increase in GH levels and is one of the best GHRP options available today.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eSide Effects of iPamorelin\u003c\/p\u003e\n\u003cp\u003eThere are side effects, possible side effects of iPamorelin use, but it is one of the friendliest growth hormone or growth hormone related medications on the market. iPamorelin, while used by many athletes is not an anabolic steroid. This means side effects of iPamorelin are not anabolic steroid related.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e[1] Estrogenic:\u003c\/p\u003e\n\u003cp\u003eThere are no estrogenic side effects of iPamorelin. Gynecomastia cannot occur due to the use of this medication. Water retention cannot occur due to elevated estrogen since estrogen cannot be elevated. However, it is possible, especially during the early stages of use to experience slight water retention; the ankles and wrist are the most common areas.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e[2] Androgenic:\u003c\/p\u003e\n\u003cp\u003eThere are no androgenic side effects of iPamorelin. This GHRP cannot cause acne, hair loss or virilization symptoms inwomen.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e[3] Cardiovascular:\u003c\/p\u003e\n\u003cp\u003eThere are no known cardiovascular side effects of iPamorelin. Many users report improved cardiovascular health.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e[4] Testosterone:\u003c\/p\u003e\n\u003cp\u003eiPamorelin will not suppress natural testosterone production. It will not affect your production of Luteinizing Hormone (LH) or Follicle Stimulating Hormone (FSH). Further, iPamorelin will have no affect on Thyroid Stimulating Hormone (TSH)\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e[5] Hepatotoxicity:\u003c\/p\u003e\n\u003cp\u003eiPamorelin is not toxic to the liver at any dose.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eAlthough not highly common, possible side effects of iPamorelin most often occur during the early stages of use. You may or may not need to adjust your dose in order to find a suitable level. Possible side effects include:\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eLight Headed (diet adjustments may help)\u003c\/p\u003e\n\u003cp\u003eHeadache (diet adjustments may help)\u003c\/p\u003e\n\u003cp\u003eSore injected area (injection rotation and finding new areas to inject may help)\u003c\/p\u003e\n\u003cp\u003eIncreased levels of prolactin (very rare – Cabergoline can help if needed)\u003c\/p\u003e\n\u003cp\u003eiPamorelin Administration\u003c\/p\u003e\n\u003cp\u003eiPamorelin will be found in freeze dried powder form (lyophilized) and is reconstituted with bacteriostatic water. Once reconstituted it needs to be kept refrigerated at all times. Once prepared, while it can be injected intramuscularly (IM) or subcutaneously (SubQ) most will find SubQ the easiest since the medication is normally administered 2-3 times per day. A small insulin syringe will suffice.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eDosing ranges for iPamorelin normally fall in the 200-300mcg ranges with a frequency of 2-3 times per day. Many users will combine this with other Growth Hormone Releasing Hormones (GHRH) in order to get the most bang for their buck. Eight weeks of use is the bare minimum to get anything out of it with 12 weeks being the preferred minimum. It can also be used for indefinite periods of time.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eiPamorelin Reviews\u003c\/p\u003e\n\u003cp\u003eiPamorelin is a solid option when looking for a natural GH increasing agent and it’s side effect friendly nature makes it perhaps more appealing than some. However, very few experience too many if any side effects from any GH related product. Will the results be better with this one compared to others? Again it’s hard to say, but with the frequent administration needed, if enough is used it is possible that you might get a little more out of this one. However, you’re going to be spending approximately $20 per day to do it and that can add up quite a bit over time.\u003c\/p\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53767022477604,"sku":null,"price":360.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_939f792e-9981-4368-9803-a88aa41ba7d3.jpg?v=1778089245"},{"product_id":"hyper-upa-m1t","title":"UPA M1T","description":"\u003cp\u003e\u003cspan\u003eUPA M1T(METHYLDIHYDROBOLDENONE 15MG P\/CPS=50TABS)\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eM1T (Methyl-1-Testosterone)\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003eThis is probably the strongest oral compound ever made. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTaking one tab a day (10mg) should be sufficient for a maximum of 5 to 6 weeks. These doses might sound low but considering its potency athletes are warned to not compare it to doses being taken of other products they are familiar with. Some users reported a dose of around 20mg but this was found to be very high and the side effects of high blood pressure and toxicity at those doses became rapidly evident.\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003eSome describe M1T’s characteristics as a mix between Primabolan, Stanazol and Trenbolone. I personally like comparing it to Oxymethelone (Anapolon) by comparing its anabolic rating. Anapolon is seen as one of the strongest orals in the world and has an anabolic rating of 320. M1T has an anabolic rating of 900-1600. This is between four and five times the anabolic rating of Anapolon (Oxymethelone)\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003eThe active pharmaceutical ingredient of this agent is methyldihydroboldenone also known as Methyl-1-testosterone or in short M1T. It is a derivative of dihydrotestosterone.\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003eThis product is mostly used on a bulking cycle when rapid mass and size gains are the objective. Many athletes report some water retention on M1T. Athletes who are genetically very lean report massive pumps and extreme vascularity when working out in the gym. The toxicity of this product can be felt after a couple of days of administration.\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003eM1T is so potent as an anabolic and androgenic that it can be used on its own. Alternatively, it can be stacked with regular agents like an injectable testosterone enanthate, cypionate or even a Test 450mg Combo blend from Ciccone Pharma that will pack a serious punch and add to serious gains. One millilitre of Test 450mg Combo twice or three times per week with 2 to 3 capsules of M1T per day would be a serious stack for serious gains.\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003eM1T is not a very well-known agent and very new to the market but for athletes who want something new and different to their normal compounds this a highly-recommended bulking agent.\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003eMilligram for milligram it is also two to three times stronger than Superdrol.\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003eWARNING – Although this is listed as a Pro Hormone it is still banned by WADA (World Anti-Doping Agency) and you will test positive if you use this while competing in international sports events.\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53767097188644,"sku":null,"price":250.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_93843a38-e70b-4a61-b3aa-ec0a7731eb1b.jpg?v=1778089346"},{"product_id":"upa-melanotan","title":"UPA Melanotan","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA MELANOTAN 2(10MG\/2ML VIAL) \n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMelanotan 2 (also referred to as Melanotan II) is a synthetically produced variant of a peptide hormone naturally produced in the body that stimulates melanogenesis, a process responsible for pigmentation of the skin. This peptide hormone, called alpha-Melanocyte stimulating hormone or MSH, activates certain melanocortin receptors in the process of exerting its effects. Indeed, MSH also exerts potent influence over lipid metabolism, appetite, and sexual libido via these melanocortin receptors. As a result, Melanotan 2 has been shown in studies to exhibit appetite suppressant, lipolytic, and libido-enhancing effects in addition to promoting skin tanning. Melanotan 2 has been researched extensively for use in protecting against the harmful effects of ultraviolet radiation from sunlight due to its melanogenesis-stimulating properties. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAdditionally, Melanotan 2 and a similar synthetically produced variant, known as PT-141, have been studied at length as a potential remedy for the treatment of sexual dysfunction; specifically, male erectile dysfunction.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e PRODUCT DETAILS\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e10mg\/10000mcg per vial\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMales\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDose per Injection: 1mg of Melanotan II\u003c\/div\u003e\n\u003cdiv\u003eInjections per vial: 10 x 1mg injections\u003c\/div\u003e\n\u003cdiv\u003eAmount to Inject: If you have used 1ml of water for mixing then 1mg = 0.1ml (or 10 units on the Insulin Syringe). If you have used 2ml of water for mixing then 1mg = 0.2ml (or 20 units) and if you have used 3ml of water for mixing, then 1mg = 0.3ml (or 30 units).\u003c\/div\u003e\n\u003cdiv\u003eFemales\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDose per Injection: 0.5mg of Melanotan II\u003c\/div\u003e\n\u003cdiv\u003eInjections per vial: 20 x 0.5 mg injections\u003c\/div\u003e\n\u003cdiv\u003eAmount to Inject: If you have used 1ml of water for mixing then 1mg = 0.05ml (or 5 units on Insulin Syringe). If you have used 2ml of water for mixing then 1mg = 0.1ml (or 10 units) and if you have used 3ml of water for mixing, then 1mg = 0.15ml (or 15 units).\u003c\/div\u003e\n\u003cdiv\u003eMelanotan II Dosage Frequency\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe frequency of Melanotan II injections depends on the phase of usage you are in. If you are new to the product, or are taking it again for the first time after a period of absence, then you will begin with what is called the “loading phase” and will need to inject every day. Once you have achieved the shade of tan you are happy with, then you can switch to the “maintenance phase” which involves less frequent injections.\u003c\/div\u003e\n\u003cdiv\u003eLoading Phase\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHow often: One injection, taken every day (7 times per week) For How Long: Until you have achieved your desired shade of tan (this will take 2-6 weeks depending on how often you tan and also your skin type).\u003c\/div\u003e\n\u003cdiv\u003eMaintenance Phase\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHow often: One injection taken 2 or 3 times per week.\u003c\/div\u003e\n\u003cdiv\u003eFor How Long: As long as you want to maintain your shade of tan. Upon cessation of usage, your skin will return to its natural shade in about 1-2 months.\u003c\/div\u003e\n\u003cdiv\u003eTanning Frequency\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDespite being referred to us a “sunless tanning” agent, Melanotan II (MT2) requires UV exposure to work properly, results without it develop extremely slowly or sometimes not at all. The incidence of side effects such as hyperpigmentation also appears to be higher when Melanotan II is taken on its own and without exposure to the sun or sun beds.\u003c\/div\u003e\n\u003cdiv\u003eUV exposure recommendations\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLoading Phase: 2-3 times per week if you wish to develop your tan as quickly as possible, otherwise once per week will allow your tan to build gradually.\u003c\/div\u003e\n\u003cdiv\u003eMaintenance Phase: 1 tanning session per week is usually sufficient to maintain your color. For How Long: 5-10 minutes in a sunbed (solarium) or 20-40 minutes in the sun.\u003c\/div\u003e\n\u003cdiv\u003ePrecautions: Do not overexpose yourself to the sun, whilst Melanotan II does reduce sunburn, it only does so by approximately 50% for most users. Therefore it is still wise to apply sunscreen, especially on sensitive areas. Sunscreen will not affect Melanotan II’s ability to give you a tan.\u003c\/div\u003e\n\u003cdiv\u003eTanning Results\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIf your tan is not developing as quickly as you’d like then you simply need to increase the frequency of your UV exposure. You should never increase your Melanotan II dosage or injection frequency.??Melanotan II and UV exposure complement each other, so if you spend a lot of time tanning you will need less frequent injections of Melanotan II to obtain and maintain your tan. If you don’t spend much time in the sun or sun beds then you will need more frequent dosages of Melanotan II to develop and keep your tan\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53767182254372,"sku":null,"price":360.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_5b2f9911-8e0c-47c2-8187-378b99415840.jpg?v=1778089453"},{"product_id":"upa-cardarine","title":"UPA Cardarine","description":"\u003cp\u003e\u003cspan\u003eUPA=SARMS CARDARINE(GW501516)(10.MG\/TABLET=50 TABLETS).\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCardarine (GW501516) The Fat Burning SARM\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGW501516 (Cardarine) doesn’t have any published human studies. In rodents, though, it shows great promise as an exercise mimetic – it lights up many of the same genes you’d activate by going on a run or lifting [4]. That alone wasn’t enough to make much of a change, but when researchers had mice take GW501516 with consistent exercise, results went through the roof:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIn mice, GW501516 combined with 4 weeks of regular running increased running time by 68% and running distance by 70%, and doubled overall muscular endurance [4]. In rodents, GW501516 plus exercise increased mitochondrial growth in muscle by ~50% [5], allowing muscles to generate more power without fatiguing. It also decreased fat while preserving muscle (again, in mice) [4].\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGW501516 could be a powerful way to improve performance and shed fat while maintaining muscle. Hopefully human studies will come out soon.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSide effects of GW501516\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eShortly after it was classified as a performance-enhancing drug, reports started coming out saying that GW501516 caused cancer in lab rats.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBut as with most substances, the devil’s in the dose. Studies did find that GW501516 is carcinogenic…but the rats were taking the human equivalent of 2400 mg a day for 2 years straight [6].\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThat’s about 240x a normal dose, taken every day, for 104 weeks instead of 4 weeks.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe studies found no evidence that GW501516 causes cancer at a dose you would actually use, or even at doses considerably higher than that. Other rat studies report no side effects, and people in the online SARMs community report none either, including no testosterone suppression. Again, though, that doesn’t mean there aren’t side effects. We may just not know about them. Proceed with caution.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHow to dose GW501516\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGW501516 works best if you split it into two daily doses. Try 5 mg, morning and afternoon, for a total of 10 mg a day.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTake GW501516 for 4 weeks, then cycle off for at least 4 weeks before starting another round. It pairs well with LGD-4033 and MK-2866. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGW501516, or Cardarine, is said to provide incredible energy levels during workouts or training. Due to its synergistic effects of accelerating fat loss while increasing endurance abilities, this SARM is best known as a fat burner. Ubiquitous reports of Cardarine’s ability to raise metabolism and increase athletic stamina have also made it a favorite PED (performance enhancing drug) for endurance athletes. As with all SARMS, its anabolic properties and high specific AR affinity also stimulate increased muscle gain.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTypical dose: 45-90 mg\/day\u003c\/div\u003e\n\u003cdiv\u003eMax: 90 mg\/day\u003c\/div\u003e\n\u003cdiv\u003eStacking dose: 25-45 mg\/day (depending on stack)\u003c\/div\u003e\n\u003cdiv\u003eHalf-life: 20-24 hours\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53767251394852,"sku":null,"price":450.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_1f8a24bd-4483-4933-8d4e-d6cf84f4868a.jpg?v=1778089564"},{"product_id":"upa-anapolan","title":"UPA Anapolan","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA ANAPOLON(50MG OXYMETHOLONE\/TAB=50TABS).\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 45\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 320\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD METHYLTESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive – Life: Less than 16 hours\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Highly Androgenic \/ Anabolic Steroid (Oral) Average Reported Dosage: Men 50-400 mg daily. Women 25-mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Yes,\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003every high DHT Conversions: This is a derivative of DHT\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Yes,\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003esevere Aromatization: Debatable\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis is an oral 17-alfa-alkylated steroid that is highly androgenic and highly anabolic. Reported gains in body weight of up to 20 LBS in the first 3 weeks of use were not uncommon. Athletes using this drug experienced remarkable strength and recovery elevations. Users noted a distinct increase in aggressiveness, (which if focused on training only was noted as positive) excessive water retention, and muscular size. Oxymetholone is commonly used as an off season mass building drug, though some mass monsters have used it up to 7-10 days before competition by stacking antagonist anti-estrogens and diuretics.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eUnfortunately this drug is probably the most dangerous of all AAS when abused and utilized when not under a physician’s care. Users get huge but often feel flu-like symptoms during use. Oxymetholone abuse is linked to prostate and liver cancer, liver disease, thyroid dysfunction, leukemia, and heart disorders. Even hepatic coma can result from abuse. Not uncommon side effects included: sensitivity to anti-coagulants (the stuff that regulates bleeding internally and externally) hair loss, prostate enlargement, severe suppressions of the HPTA resulting in low sperm and endogenous (natural) androgen production, nausea, stomach aches, diarrhea, and throwing up on occasion. Women can add possible virilizing symptoms such as clitoral enlargement, facial hair growth, deeper voice, missed periods, and other androgenic linked side-effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOxymetholone negatively effects liver function such as an increase in SGPT and SGOT enzymes which are indications of hepatitis (liver infections) which can manifest itself as yellowing of the eyes and finger nails because of an increase in biliburin in the liver. Another liver enzyme, gamma -GT, is sensitive to Oxymetholone, and alkaline phosphatase is altered as well. I cannot stress the importance of monitoring by a doctor.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOxymetholone is a derivative of DHT. Many report gyno from use but this is unlikely due to this drug aromatizing because DHT does not aromatize to estrogen. The more likely reason is they purchased bogus oxymetholone from a black market dealer that actually contained methyltestosterone. There is another reason gyno is possible, but we will discuss that in a moment. Oxymetholone does cause high water retention due to electrolyte retention thus creating a massive but puffy appearance to muscles. For the same reason, the drug causes water retention and fluid build up in joints. This manifests itself in joint pain-free training for most users. In medicine Oxymetholone is used to treat low red blood cell production which means during administration red blood cell count is stimulated. For this reason the drug increases oxygen transport to the muscles resulting in an incredible muscle pump after only a few sets of training. I have often noted those who used oxymetholone recovered between sets, exercises, and work-outs at a remarkable rate. So the drug does protect against overtraining quite well, thus when it was stacked with anti-estrogen such as Nolvadex and a diuretic to cut electrolyte (aldosterone) caused water retention, and a high anabolic drug such as Deca Durabolin, quality, quantitative, muscle gain resulted. The fact that this drug’s water retention side effect responds to antagonist type anti-estrogens is interesting since, from a chemical structure stand-point, it should not aromatize to estrogen. Even the insert states edemas (water retention) may occur but does not list elevated estrogen levels under “side effects”. However, readers should realize Oxymetholone itself can merge with Progesterone receptors and may act as an estrogen in this manner.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAs to dosages, advanced bodybuilders and power lifers usually reported excellent results with 50-200 mg daily divided in 2-3 dosages. Since results begin to decline after the first 2 weeks it some reported that their protocols were more productive (and safer) when they started at 50mg daily and increase by one tab weekly until a total of 150-200 mg daily was reached at week 3. They then maintained that dosage for a total of 2-3 additional weeks. Some reported a following protocol that allowed reduced dosages by one tab weekly. My personal experience has been that liver stress becomes an issue after the 4th week of administration and as such did not personally exceed this time period for use. Replacing Oxymetholone with a high anabolic such as Deca Durabolin or Equipoise during the transitional phase was quite effective for maintaining a greater amount of the oxymetholone induced lean mass. Many reported exceptional results with a stack consisting of 50-100 mg oxymetholone daily, 152-228 mg of Parabolon weekly, and 200­500 mg of testosterone enethate weekly.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Women should not use oxymetholone, but of course some hard core types did report self administration. Novice steroid users should never use oxymetholone without a doctors supervision.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIn most cases users reported that liver values returned to normal after 1-2 months of discontinued. This seems to be supported by the available medical literature on oxymetholone. High blood pressure was common during use. High blood pressure should never go untreated. The hair loss does not reverse by the way. Post-cycle the administration of HCG and Clomid was used to return normal HPTA function in all but very rare cases. “The boys” normally began to produce normal sperm and testosterone levels after 2-3 weeks of discontinuance. Can you tell that I did not like Oxymetholone for long term personal use? Post-cycle, without the layering of a transitional phase replacement AAS such as nandrolones, Primobolan Depot, Equipoise or Winstrol Depot, gains made with Oxymetholone alone soon disappear in most cases. (See “Max Androgen Phases” in “Building The Perfect Beast” for a discussion of solutions some hard-core types have utilized)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e* A note of interest: There is not a “legit” injectable form of Oxymetholone( OXYJECT FROM KARMA WAS AVAILABLE A WHILE BACK). However, it would be very physiologically active as is the 25mg sublingual form. I have used a MEGA-MIX product that contained Oxymetholone in a 3 oil mix injectable that was a black-market product with excellent results and fewer negative side effects. However, black market manufactured AAS are often dangerous and unlikely legal anywhere.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e(Oxymetholone) is a synthetic anabolic-androgenic steroid hormone that is structurally related to the male hormone testosterone. Synthetic androgens are used to treat a variety of conditions including hypogonadism and delayed puberty. Androgens are also used to correct hereditary angioneurotic edema, manage carcinoma of the breast, promote a positive nitrogen balance following injury or surgery, and stimulate erythropoiesis.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eConsiderable amounts of androgens are consumed by athletes in attempts to improve athletic performance. Oxyplex is used to promote weight gain and counteract weakness and emaciation resulting from debilitating diseases, such as advanced HIV infection, and after serious infections, burns, trauma, or surgery. It is marketed as a human prescription drug for the treatment of bone marrow failure anemias and deficient red cell production anemias.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53767318503716,"sku":null,"price":400.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_5ad6307c-d1ff-4e7c-97dc-25fd6441bb41.jpg?v=1778089648"},{"product_id":"upa-lovers-peptide","title":"UPA Lovers Peptide","description":"\u003cp\u003e\u003cspan\u003eUPA PT141(10MG\/2ML VIAL) \u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePT-141 or Bremelanotide is the generic term for a research peptide being studied for its possible use in helping to improve sexual dysfunction in both men (erectile dysfunction or impotence) and women (sexual arousal disorder). PT-141 was developed from the tanning peptide Melanotan 2, which is a synthetically produced variant of a peptide hormone naturally produced in the body that stimulates melanogenesis that is known as alpha-Melanocyte stimulating hormone. MSH, activates certain melanocortin receptors in the process of exerting its effects. Indeed, MSH also exerts potent influence over lipid metabolism, appetite, and sexual libido. Resultantly, PT-141 has been shown in studies to exhibit libido-enhancing effects by activating the melanocortin receptors MC1R and MC4R, but not skin tanning. Melanotan 1 and Melanotan 2 have been researched for their use in protecting against the harmful effects of ultraviolet radiation from sunlight due to their melanogenesis-stimulating properties.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePT-141 is a potential remedy for the treatment of sexual dysfunction; specifically, male erectile dysfunction. Studies have shown that PT-141 does not act on the vascular system like former compounds, but allegedly works by activating melanocortin receptors in the brain, therefore helping increase ones sexual stimulation. PT-141 is a melanocortin based peptide that has shown effectiveness in clinical studies on both male and female rats. Male rats have shown erectile response with doses as low as 1-2 mgs whereas most female rats have shown positive results with higher doses around 2-3 mgs. While the dosage requirements tend to be higher for female rats, the observable results in female rats tend to be stronger.\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53767371194660,"sku":null,"price":390.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_ed9eccc2-8325-4cb2-b036-94a61d024275.jpg?v=1778089764"},{"product_id":"upa-equipoise-320","title":"UPA Equipoise 320","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA EQUIPOISE 320(320MG\/ML BOLDENONE UNDECYLENATE=10ML)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 50\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD TESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 7-9 days\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anabolic \/Androgenic steroid (for injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 150-500mg weekly Women 50-150mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Low\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: About 50% less than testosterone\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNoted comments: High anabolic\/moderate androgenic\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: Low\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA function: Moderately (Dose dependent)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBoldenone is available as a veterinary steroid under various trade names and was commonly refereed to as EQ by athletes polled. However, the quality is normally quite high due to its use in million dollar race horses. Boldenone was reported as one of the safest and most effective anabolic \/ androgenic injectable steroids used by both power lifters and bodybuilders. This drug brought slow but continuous muscle mass and strength gains over a prolonged period. Gains were mostly of a high quality lean mass nature and were maintained for several weeks after use was discontinued. Improved pumps and vascularity were normal are common attributes while low aromatization brought an improved hardness to users musculature.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMales normally reported a dosage range of 150-500mg weekly total, usually utilizing an every other day (EOD) injection schedule. Women made excellent progress with dosages of 50-150mg total weekly with a 1-2 injections weekly schedule. In this dose range, women seldom reported virilizing side effects. Most experienced an elevate libido (cool) with few other negative side effects reported. But in some cases, increased hair growth on face and legs were noted. This was usually due to higher dosages however and predominantly limited to existing hair (not new hair growth).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDue to Boldenone’s reported “non-toxic to the liver” structure, most users experienced great gains with none or few negative side effects. The appetite and red blood cell production stimulating effects of Equipoise marked this drug as a standard for those who sought few negative side effects with quality muscle mass gains. Obviously with increased red blood cell count an increase in oxygen transport was also realized, as was improved nutrient transport.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDue to a double carbon bond between carbons one and two, boldenone experiences only slight DHT conversion by the 5-alfa-reductase enzyme and is fairly resistant to aromatization to estrogens.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMale athletes commonly stacked Boldenone with testosterone and\/or Anadrol-50 for mass and strength cycles. Pre-contest cycles utilizing this drug often included Trenbolones, Winstrol, and anti-estrogens to create the ultra hard and vascular look.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Personal experiences with Boldenone have resulted in very high quality lean tissue and freaky vascularity. This quite beneficial from a competitive appearance stand-point but long term use resulted in an unfavorable CBC result. I believe my error was in protocol length.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBoldenone (1,4-androstadiene-3-one-17β-ol, available as the undecylenate ester)is an anabolic steroid developed for veterinary use, mostly for treatment of horses. It is not indicated for use in humans in the US and is only available through veterinary clinics.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe activity of boldenone is mainly anabolic, with a low androgenic potency. It has a very long half-life, with minimal blood levels present up to 8 weeks after discontinued use.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBoldenone will increase nitrogen retention, protein synthesis, increases appetite and stimulates the release of erythropoietin in the kidneys. The drug is commonly used in doping within bodybuilding. If intended to assist in bodybuilding, the drug is taken as part of a steroid stack of other anabolic steroids, usually with a potent androgen like testosterone as the ‘base’ of the stack.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBoldenone has a low rate of aromatization (about 50% of Testosterone), which means it does not convert to estrogen easily and does not cause very much water retention. Many Bodybuilders will find that it is a good replacement drug for Nandrolone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIt is a poor drug of choice for any athlete who will be subject to a blood test due to its long metabolic half-life. Trace amounts of the drug can easily be detected for months after discontinued use.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53767458652452,"sku":null,"price":520.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_18fd23f2-1e3c-4abe-ac30-a49be89b6979.jpg?v=1778089868"},{"product_id":"upa-test-prop-100","title":"UPA Test Prop 100","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA TEST PROP 100(100mg\/ml testosterone propionate =10ML)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD TESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-life: 2-3 days\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug class: Anabolic\/Androgenic steroid (For injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Male 50-200mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Low\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Yes, severely\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDue to Testosterone Propionate possessing a brief active-life of 2-3 days, many athletes involved in tested competitions liked the stuff…a lot. Testing is usually based upon testosterone \/Epitestosterone levels. Though most individuals have a much lower ratio, athletes can have natural ratios of up to 6:1. This is considered a negative test for steroids. usually. By injecting Propionate up to 36 hours before competition, plasma Testosterone levels remained elevated while urine concentrations usually fell within the 6:1 levels. Of course IOC testing protocols would detect any plant origin AAS today. But several groups still simply test for the ratio only.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTestosterone Propionate is considered a fast acting testosterone due to effects beginning in about 1 day. The drug reportedly has all the benefits of other testosterones (quick strength and muscle mass increases, increased training aggressiveness, fast post-training recovery) but caused a distinctly lower level of water retention. Users noted an improved muscle pump and increased appetite after one to two days of administration. Even with a high rate of aromatization, propionate did not cause gyno as often as other testosterone esters. Users who realize this normally did so due to less frequent injections: Not due to some special quality of the drug. I liked propionate because an increase in IGF-1 was common during liver deactivation. Also because use could be discontinued at the first sign of overt side effects (thus allowing the chemical to no longer be the cause after 2-3 days post-discontinuance).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eA high quality muscle gain has been achieved with 50-100mg Testosterone propionate every 1-2 days, 50mg Winstrol Depot every 2nd day, and 20-25mg of Oxandrolone daily. If Parabolan (76mg every other day) was substituted for Winstrol and Proviron is utilized as an anti-estrogen, this became an excellent pre-contest cycle providing superior hardness. Those who had used Primobolan only and no longer made progress at 200-400 mg weekly made consider progress by stacking 200-400mg Primobolan Depot weekly with 50-100mg of Testosterone Propionate every second day. Improved vascularity was common due to increased in red blood cell count as well.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWomen who did use testosterones considered propionate to be the superior choice over any other. 25-50mg of Propionate every 5-7 days stacked with any high anabolic such as Anadur, or especially Durabolin caused a dramatic result with less virilizing characteristics. As always, women who are extremely sensitive to androgens reported the use of 1mg Finasteride daily lowered DHT conversion of Propionate.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTestosterone propionate is a male sexual hormone with pronounced, mainly androgenic action, possessing the biological and therapeutic properties of the natural hormone. In a healthy male organism, androgens are formed by the testes and adrenal cortex. It is normally produced in women in small physiological quantities. In addition to the specific action that determines the sexual characteristics of the individual, it also has a general anabolic action, manifested in enhancement of protein synthesis. Under the effect of testosterone, body weight increases and urea excretion is reduced. High doses suppress the production of hypophyseal gonadotropin, while low doses stimulate it. It has an antitumor effect on mammary gland metastases.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*It should be noted: Propionate also severely suppresses HPTA function and HCG\/Clomid have been considered post administration stables.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53767533101348,"sku":null,"price":400.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_b02b5053-04ea-48f2-b877-5b3ed3349777.jpg?v=1778089966"},{"product_id":"upa-arimadex","title":"UPA Arimadex","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA ARIMADEX(1MG\/TAB ANASTROZOLE=30TABS)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 4-6 hours\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anti-estrogen \/competitive inhibitor (Oral)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: 0.5-3.0 mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: No\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Yes dosage dependent\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA function: No, the drug has been accredited with HPTA up-regulating effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eArimidex is an anti-estrogen type drug. It is usually provided in 0.5 MG tabs. The drug works in a non-steroid form by inhibiting the aromatase enzyme which converts testosterone and other androgens into estrogen. This means that there is less estrogen to cause female pattern fat deposits, gyno, and water retention. In medicine, Arimidex is utilized to treat prostate cancer. In sports chemistry, the drug has been employed as a means of preventing excessive estrogenic side effects during AAS use and to aid in creating a harder appearing musculature for competitive bodybuilders. Unlike Nolvadex, which simply block estrogen receptor-sites, this drug prevents or reduces estrogen production. Though some estrogen presence is noted as necessary for AAS to reach full effectiveness, too much can cause a layer of fat, water retention, and breast tissue growth potentially with tumors called gynecomastia or bitch tits. Arimidex has a 75-85% aromatization inhibition rate.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMales who experienced excessive aromatization of AAS or who were extremely estrogen sensitive usually utilized a dosage of 0.5-3.0 mg daily. In fact, most realized excellent estrogen control with only 0.5mg\/d (mg daily). Women usually showed excellent lean appearances (even in their legs) with 0.5-1.0 mg daily. Arimidex has a very short active-life so 0.5 mg dosages were often taken 2-6 times daily at equal intervals. Stacking 10-30 mg of Nolvadex with 1.0 mg of Arimidex has resulted in a near “0” estrogen activity situation regardless of the AAS protocol utilized. Directly following an AAS cycle, estrogen control has also become a problem (during periods intended for re­establishing HPTA function). In this case, the dosage was reduced from a higher starting dosage to a low dosage that was continued for 7-14 days after AAS discontinuance. This protocol was considered necessary to assure clearing of AAS induced estrogen build-up.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eArimidex is indicated for adjuvant treatment of postmenopausal women with hormone receptor positive early breast cancer.\u003c\/div\u003e\n\u003cdiv\u003eArimidex is indicated for the first-line treatment of postmenopausal women with hormone receptor positive or hormone receptor unknown locally advanced or metastatic breast cancer.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eArimidex is indicated for the treatment of advanced breast cancer in postmenopausal women with disease progression following tamoxifen therapy .\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53767621083428,"sku":null,"price":500.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_06123aab-f275-4c52-acd5-b4c248e91e07.jpg?v=1778090080"},{"product_id":"upa-ostarine","title":"UPA Ostarine","description":"\u003cp\u003e\u003cspan\u003eUPA=SARMS OSTARINE(MK-2866)10MG\/TABLET=50 TABLETS\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMK-2866 Builds Muscle And Burns Fat\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWith multiple published human trials under its belt, MK-2866 (also called ostarine) is one of the best-studied SARMs. Those studies found powerful results, too. Ostarine shows no meaningful side effects and is very effective at building muscle.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eElderly men and women who took modest doses of ostarine for 12 weeks grew 3 pounds of muscle and lost a pound of fat, with no changes to diet or exercise [1]. Cancer patients saw nearly identical results along a similar timeframe [2]. There were no side effects in either study.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eA pound of muscle a month is about what you would expect with a solid workout routine – but the people taking ostarine in these studies weren’t exercising. Combining the two would be even more powerful, in theory. Pretty impressive.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSide effects of MK-2866\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe studies found no side effects. Anecdotally, however, people report short-term testosterone suppression when they take high doses of ostarine for 8-12 weeks. Testosterone rebounded to normal levels within a couple weeks after they stop. The dosage I discuss below is far lower and for a shorter amount of time, but there’s still a risk of short-term T suppression, and possibly other side effects researchers don’t know about yet.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHow to dose MK-2866\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThere haven’t been official dose recommendations for SARMs because they’re so new. The doses in this article are all conservative, and based what on studies and anecdotal reports show to work.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFor ostarine, 15-20mg daily for 6 weeks. Time of day doesn’t matter. To be cautious, take at least 6 weeks off so your system balances out before starting another cycle. Ostarine, along with the other SARMs on this list, seems to pair best with regular exercise like lifting and HIIT.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAlso known as Ostarine, MK-2866 is a very popular, well-tested SARM, with no side effects observed in most users. It enhances muscle mass and helps burn fat, but Ostarine is most recognized for its unique propensity to increase bone density and aid in injury prevention \u0026amp; recovery. Most users are male, as with other SARM’s, however women choosing to adminsister SARM’S will usually prefer Ostarine for its milder overall profile. While long-term use of Ostarine can suppress testosterone production in men, the compound exhibits very low risk of this or other side effects when taken in typical dosages.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTypical dose: 15-30 mg\/day\u003c\/div\u003e\n\u003cdiv\u003eMax: 30 mg\/day\u003c\/div\u003e\n\u003cdiv\u003eStacking dose: 10-15 mg\/day (depending on stack)\u003c\/div\u003e\n\u003cdiv\u003eHalf-life: 24 hours\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53767699497252,"sku":null,"price":450.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_d37d196e-1d7d-4426-b663-4c9f6b4b9113.jpg?v=1778090186"},{"product_id":"upa-tren-acetate-100","title":"UPA Tren Acetate 100","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA=TREN A100(100mg\/ml TRENBOLONE ACETATE=10ML )\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eandrogenic 500\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eanabolic 500\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003estandard nandrolone\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 2-3 days\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anabolic\/Androgenic steroid (for injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 30-60 mg every other day\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Common\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Common\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Though disputed, yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eKidney Toxic: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNoted Comments: High Anabolic\/Very high Androgenic\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Moderately\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT conversion: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis was\/is a very nasty but effective steroid that was removed from the market about 1987 or so. Not all that long ago it began showing up on the black market from Australia. Upon testing the 50-ml vials, it was discovered that it actually contained 31-mg\/ml of Trenbolone acetate. Most Fina Jet now found is bogus. It contains either a testosterone ester, ground Finaplix pellets, or just oil. But the original has been discontinued. (There are several new brands of the drug trenbolone acetate)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTrenbolone acetate is a strong androgenic\/anabolic steroid that caused a fast increase in strength and increased fat burning if the athlete’s diet was right. Unless stacked with other steroids, this drug did not cause much in actual weight gain (dose dependent). Its main use was to harden the physique’s appearance once body fat levels were low enough before competition. For the most part, bodybuilders have replaced Finajet\/ Finaject with Parabolan or one of the many black market trenbolone products. Since Finajet did not cause gyno or water retention, one may assume it was fairly clean. Wrong! Even at dosages of 30-60-mg injected daily, side effects such as kidney toxicity, nose bleeds, headaches, high blood pressure, acne, and serious attitude problems were common.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome creative and brave athletes have used the Finaplix 20 mg pellets which are intended for animal use. The pellets are shot into animal tissue for a slow release of Trenbolone. However some athletes (and black market crazies) have ground the pellets into a powder, mixed it with oil or water, and injected the very un-sterile solution with 18 gauge needles. I can not stress enough how dangerous this is. The product is often labeled Finabolan. (“Finabolin” gives us a chance to discuss trenbolone in greater depth in a moment)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAnother reported method of using the Finaplix pellets was to ground them into powder, mix the powder with a 50\/50 solution of DMSO (DIMETHYL SULFOXIDE) and water. Then apply it to skin. The DMSO acts as a transporter that allows 14-18-MG of a 20MG pellet to be absorbed into the blood stream while the skin acts as a filter of sorts. Unfortunately this also allowed many toxins on the skin to enter as well.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome individuals have claimed real hard-core status by using an animal pellet implant gun and taking one in the glute. Do not try this at home. The pain would be major and compared to being shot with a .177 pellet. The interesting side of this is that the lads who did this had been told that the Finaplex pellets were readily absorbed “rectally”.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Geez! And some bodybuilders wonder why we have the stigma of dull wittedness?\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNOTED POSITIVE EFFECTS OF TRENBOLONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Amazing anabolic qualities.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Rapid high quality lean tissue gains. (Dose dependent) *Maximum post-cycle lean mass retention. *Low-none water retention.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased Erythropoies (Red blood cell production) *Does not aromatize to estrogens. *Superior strength and mass gain. (Lean) *Extreme hardening of musculature and vascularity. *Excellent protein sparing\/anti-catabolic qualities. *Reduction in fat stores and favorable distribution. *Increased metabolic rate. *Low-moderate HPTA function inhibition. *Significant increase in muscle glycogen synthesis. *Increase creatine phosphate (CP) synthesis. *Improved muscle insulin receptor activity.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Remains anabolic during calorie restricted periods. (High protein intake remains necessary)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e POSSIBLE NEGATIVE EFFECTS TRENBOLONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Liver and Kidney toxicity.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Growth of prostate tissue. (PSA test is wise)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Male pattern baldness. (Accelerated genetic predisposition)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Mild hallucinations. (High dosage -prolonged use)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*High blood pressure.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e Trenbolone Acetate is a fast acting injectable steroid.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTo increase its effective half-life, trenbolone is not used in an unrefined form, but is rather administered as trenbolone acetate ,enanthate or Hexahydrobenzylcarbonate. Trenbolone is then produced as a metabolite by the reaction of these compounds with the androgen receptor.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBodybuilders have been known to use the drug in order to increase body mass more effectively than by weight training alone. A normal bodybuilding dosage can range from 200 mg\/week up to 1400 mg\/week. Due to the relatively short metabolic half-life of trenbolone acetate, dosages should commonly be split into injections at least once every two days. Trenbolone enanthate can be injected once a week.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe 2006 book Game of Shadows alleges that baseball superstar Barry Bonds used this drug in 2001, when he set the current single-season home run record.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTrenbolone compounds have a binding affinity for the androgen receptor three times as high as that of testosterone. Once metabolised, the drugs have the effect of increasing nitrogen uptake by muscles, leading to an increase in the rate of protein synthesis. It also has the secondary effects of stimulating appetite, reducing the amount of fat being deposited in the body, and decreasing the rate of catabolism. Trenbolone has proven popular with anabolic steroid users as it is not metabolised by aromatase or 5α-reductase into estrogenic compounds such as estradiol, or into DHT. This means that it also does not cause any water retention normally associated with highly androgenic steroidal compounds like testosterone or methandrostenolone. It is also loved by many for the dramatic strength increases commonly experienced with it. Some short-term side effects include insomnia, high blood pressure, increased aggression and libido. However, since women will suffer virilization effects even at small doses, this drug should not be taken by a female. Urban wisdom\/myth in bodybuilding culture, states that the use of the drug over extended periods of time can lead to kidney damage. The kidney toxicity has not yet been proven, and scientific evidence supporting the idea is suspiciously absent from the bodybuilding community that perpetuates this idea. The origin of this myth most likely has to do with the rust colored oxidized metabolites of trenbolone which are excreted in urine and often mistaken for blood. After Schänzer (Clin Chem 1996; 42(7): 1001-1020, Metabolism of anabolic androgenic steroids) trenbolone and 17epi-trenbolone are both excreted (in urine) as conjugates that can be hydrolyzed with beta-glucuronidase. This implies that trenbolone leaves the body as beta-glucuronides or sulfates, that means mostly non metabolized\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53767766016292,"sku":null,"price":610.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_d9d5347a-2f7d-4698-8a8a-7945d4b99ef5.jpg?v=1778090330"},{"product_id":"upa-hgh-150iu","title":"UPA HGH 150iu","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA SOMATROPIN 15i0u(150iu somatropin=10x 1ml powder+water)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e191 Amino Acid Chain 99% pure \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: Varies upon injection method\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Growth Hormone\/IGF-1 Precursor (For injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: 2-16 i.u. total daily (1mg=2.7 i.u)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Very rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Very rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Anabolic\/No Androgenic Effects\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHuman Growth Hormone (GH) has been a subject of debate since I was a kid. Natural (endogenous) GH is produced by the pituitary gland. Children produce 2 i.u. “spurts” 4-7 times per day for 4-5 non-consecutive days during a 2-3 week period (during growth spurts). That would equal 32-70 i.u. in only a 4-5 day span. A healthy adult’s pituitary releases only 0.5-1.5 i.u. daily.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eUntil the mid 1980’s, the only available form of exogenous (occurring outside the body) GH was manufactured by taking the pituitary glands of dead corpses (like there are a lot of “live” corpses running around?) and grinding them up. (I am not joking!). The GH was then extracted and purified through a series of expensive procedures, packed and sold by prescription only for use by children suffering from stunted growth. About 1987, this form of GH was linked to a fatal brain disease called CREUTZFELD-JAKOB DISEASE, and removed from the market.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEnter Genetech and synthetic GH. The first synthetic GH was produced by genetically altering transformed mouse cells \/Ecoli. Natural GH has a 191 amino acid sequence where as the Protropin brand of GH produced by Genetech contains 192 amino acids in its sequence. This may have the affect of causing the body to produce GH anti­bodies which deactivate the GH. Most synthetics now contain the normal 191 amino acid sequence, of which there are over a dozen available today.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGH has 3 effects any athlete desires: GH helps the body burn more adipose (fat) tissue by promoting the release of fatty acids to be used as energy. Normally at rest, the body uses about an equal division of fat and carbohydrate calories. When the endocrine system senses a low circulatory level of glucose, the hypothalamus-pituitary-axis (HPA) reacts by releasing GH. The GH then triggers (through a series of enzymic\/chemical reactions) the release of fatty acids from adipose stores so metabolic energy requirements can be met. This means exogenous GH administration has been well documented to do the same.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGH has a very potent anabolic (protein synthesis\/tissue building) effect. In exerting anabolic effects, it can cause both hyperplasia (an increase in the number of muscle cells) and muscular hypertrophy (the enlargement of muscle cells). This change in cell number is permanent and therefore means more cells to make bigger. GH also has an anabolic effect on soft tissues such as tendons, cartilage, and other connective tissue. This means old injuries repair and strength increases due to stronger connective tissue… both at an accelerated rate. It is a well known fact that GH is a powerful anti-catabolic agent (protein sparing). This effect has allowed modern bodybuilders to retain or even add significant lean mass tissue during calorie restricted periods (cutting phases) and become the shredded monsters of the new era.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhen using GH many athletes were less than satisfied with their results. Most likely this was because they bought bogus GH. It was common to find GH for a hard-core pro bodybuilder cost about $35,000 or more, yearly. To test GH, most simply bought a pregnancy test kit, mix a vial of (hopefully) GH and place a drop or two in the test area. If the test result was “pregnant”..they had been screwed. Most pregnancy test kits test for elevated gonadoltropins (which HCG is and GH is not). For those few, whose bodies manufactured GH anti-bodies (and GH failed to work for you) sorry about your luck. GH, used properly, has overwhelmingly been renowned as a genetic equalizer if used for that purpose.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAny polled athlete chose to use GH as a performance enhancing drug should have first understand at least the basics of its actions.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGH itself is not responsible for the majority of the effects seen from GH use. Actually GH is only a precursor to the so-called “good stuff”. When GH passes through the liver, it is converted into INSULIN-LIKE GROWTH FACTORS (such as IGF-1). IGF-1 is a very active but unstable chemical, which is why the body waits until the last second to make it naturally. The liver has a limited capacity to convert excess GH into IGF-1 unless other chemical hormone levels are also elevated. Insulin, T-4\/T-3 thyroid hormones, gonadotropins, androgens\/anabolic hormones, and even estrogen and corticosteroids all play an important role in the positive effects of GH. So they too were often exogenously elevated in what was considered “the correct ratios” by the largest of the self administering athletes. For the liver to convert high levels of GH to IGF-1 several times a day and cause a high quality anabolic response, it was commonly noted that T-3 thyroid hormone and insulin also needed be increased to accomplish the desired effect. Triacana may be strong enough to increase thyroid activity, but Cytomel was considered to be a better choice. Though some seemed to disagree, most emphatically believed that a fast-acting insulin such as HUMULIN-R or Humalog was a better and safer choice of exogenous insulin since they allowed better timing and have a much shorter effective period. This allowed the athletes to time insulin activity with the active period of GH at the optimum absorption times such as upon waking and the first few hours after a work­out. The result was less chance of fat accumulation and a heightened anabolic response. Since GH suppresses natural T-3 thyroid hormone release, the exogenous administration of Triacana or Cytomel allowed for an elevated calorie intake that was utilized more for building muscle and soft tissue than for adipose tissue storage. Many pro bodybuilders used Clenbuterol and\/or ephedrine stacks with GH while dieting. Since Clenbuterol and\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEphedrine both suppress natural insulin release, they usually stacked the GH and Clenbuterol \/Ephedrine with a synthetic T-3 thyroid hormone and sometimes with insulin as well. The use of insulin was dependent upon whether it was a bulking or dieting phase and depending on how their body responded to exogenous insulin use.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*I can not stress enough how dangerous insulin use can be. Comas and death are quite possible if used wrong. If you wish to use it, please see a doctor for monitoring.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAAS and\/or Clenbuterol further enhance the anabolic effects of GH. From all but a few polled it was reported that excellent muscle mass gains resulted with the use of GH when other chosen hormone levels were also met (*also see “cycles”) and one could afford it. Also, beware of fake GH. It is more common than you may realize. It is an illegal drug and the black market is not always honest.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe question of dosage was a big one. For the purpose of stunted growth manufacturers of GH (due to pituitary hyophysially caused stunted growth) state 0.3 i.u. weekly per LB of body weight. So for a 235 LB bodybuilder that would equal 70.5 i.u. weekly, meaning a daily total of about 10-i.u. However, even 2-3i.u. daily did produce some nice results over a 6-8 week period when the other reported hormone requirements were met as well. Short high dosage burst cycles too were noted to create these results (which will be discussed later) by the more elite of those polled.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*GH is medically administered intramuscularly or subcutaneously (under the skin). *When multiple injections were utilized, I personally noted better results with subcutaneous administration.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*1-mg=2.7 i.u. of GH and some products are listed as such.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWith exception of those few whose insert states otherwise, the dry unmixed GH substance maybe stored at room temperature. Once the solution has been mixed with the dry GH powder, (SWIRLED, DO NOT SHAKEN) the mixture must be refrigerated and lasts for 24-hours before it begins to degrade. An interesting product has become available called DEPO-NUTROPIN that has an active-life of about a month. This would allow for fewer injections and a reduced price. Also, several patents run out this year so many overseas and less expensive GH preparation will soon be available in the U.S. by prescription only.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Though no negative side effects were reported, the available literature does list several serious ones: Kidneys and heart enlargement, high blood pressure, diabetes, thyroid hormone deficiency, and acromegaly. For the most part, they are rare to say the least and usually would be from extreme dosages and lengths of cycles. But like most hormones, you just do not know until it is a fact for you. Kind of scary, huh?\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhen GH was utilized with an insulin protocol, it was considered important to space injection periods between GH and insulin about an hour. Also if GH was utilized only twice daily, it was reported best to avoid natural high points of GH release such as first thing in the a.m., post-work out, and right before bed. This was if GH was utilized without insulin.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHuman Growth Hormone (somatotropin – also referred to as HGH, or HGH) is created by somatotropes in the pituitary gland of the human brain, the primary form consisting of a 191 amino acid chain. Somatotropes make up more than 50% of the pituitary gland and growth hormone is by far the most important hormone produced there. By the age of 60 most people will have approximately 80% less growth hormone in their system than when they were 20. When we are young, HGH is in big part responsible for the proper growth of bones, muscle, and other tissues. As we become adults, HGH is responsible for keeping muscles from wasting away, supports healthy immune system response, regulates aspects of our metabolic function dealing with increased fat metabolism and healthy body composition in later life, and maintains and repairs our skin and other tissues. HGH, or GH in short, is certainly an effective fat burner and anabolic agent, and is a protein secreted by the pituitary. Once secreted, it has the ability to influence various cells in the body to increase in number and size, as well as having the ability to enhance the movement of amino acids through cell membranes- thereby increasing the rate at which the cells can convert those molecules to usable proteins. It also causes cells to preferentially burn fat in lieu of carbohydrates.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003erHGH\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003erHGH is a human growth hormone produced by recombinant DNA technology derived from engineering Escherichia coli (E. coli), and is identical to the natural growth hormone in amino acid sequence and three-dimension structure. It has a molecular with of 22,125 daltons of which 191 amno acid sequence and structure are identical to the dominant form of the human pituitary growth hormone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEffects\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHGH has two distinct types of effects:\u003c\/div\u003e\n\u003cdiv\u003eDirect effects are the result of growth hormone binding its receptor on target cells. Fat cells (adipocytes), for example, have growth hormone receptors, and growth hormone stimulates them to break down triglyceride and suppresses their ability to take up and accumulate circulating lipids.\u003c\/div\u003e\n\u003cdiv\u003eIndirect effects are mediated primarily by an insulin-like growth factor-1 (IGF-1), a hormone that is secreted from the liver and other tissues in response to growth hormone. A majority of the growth promoting effects of growth hormone is actually due to IGF-1 acting on its target cells.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEffects on Growth\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGrowth is a very complex process, and requires the coordinated action of several hormones. The major role of growth hormone in stimulating body growth is to stimulate the liver and other tissues to secrete IGF-1. IGF-1 stimulates proliferation of chondrocytes (cartilage cells), resulting in bone growth. Growth hormone does seem to have a direct effect on bone growth in stimulating differentiation of chondrocytes.\u003c\/div\u003e\n\u003cdiv\u003eIGF-1 also appears to be the key player in muscle growth. It stimulates both the differentiation and proliferation of myoblasts. It also stimulates amino acid uptake and protein synthesis in muscle and other tissues.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMetabolic Effects\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGrowth hormone has important effects on protein, lipid and carbohydrate metabolism. In some cases, a direct effect of growth hormone has been clearly demonstrated, in others, IGF-1 is thought to be the critical mediator, and some cases it appears that both direct and indirect effects are at play.\u003c\/div\u003e\n\u003cdiv\u003eProtein metabolism: In general, growth hormone stimulates protein anabolism in many tissues. This effect reflects increased amino acid uptake, increased protein synthesis and decreased oxidation of proteins.\u003c\/div\u003e\n\u003cdiv\u003eFat metabolism: Growth hormone enhances the utilization of fat by stimulating triglyceride breakdown and oxidation in adipocytes.\u003c\/div\u003e\n\u003cdiv\u003eCarbohydrate metabolism: Growth hormone is one of a battery of hormones that serves to maintain blood glucose within a normal range. Growth hormone is often said to have anti-insulin activity, because it suppresses the abilities of insulin to stimulate uptake of glucose in peripheral tissues and enhance glucose synthesis in the liver. Somewhat paradoxically, administration of growth hormone stimulates insulin secretion, leading to hyperinsulinemia.\u003c\/div\u003e\n\u003cdiv\u003eHGH has been the supplement of choice for many professional athletes over the years. American football great, Lyle Alzado, claimed that 80% of all professional American football players, including himself, have taken HGH. HGH has amazing age-reversing effects that make it possibly the strongest anabolic substance available. Some of the benefits associated with HGH supplementation include the reversal of common diseases associated with aging, improved brain activity and function, it strengthens connective tissue which reduces the probability of injury, incredible weight loss without any loss in lean mass, reduces wrinkles by rejuvenating the skin, it raises energy levels and brightens mood, promotes muscle growth, improves libido, improves functions of the lungs which increases the level of oxygen in the blood stream, provides immune system support and Thymus function, and probably the most impressive characteristic is, its ability to produce more muscle cells, something no steroid can do.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePRODUCT DETAILS\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e191 amino acid chain recombinant growth hormone 10IU per vial\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePositives to taking growth hormone\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHGH does reduce body fat\u2028\u003c\/div\u003e\n\u003cdiv\u003eHGH does increase muscle mass and shape the body\u2028\u003c\/div\u003e\n\u003cdiv\u003eHGH does rejuvenate the body\u003c\/div\u003e\n\u003cdiv\u003eHGH makes your nails grow faster\u003c\/div\u003e\n\u003cdiv\u003eHGH makes your hair grow faster\u003c\/div\u003e\n\u003cdiv\u003eHGH makes your skin softer and nicer\u003c\/div\u003e\n\u003cdiv\u003eNegatives to taking growth hormone \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eProlonged HGH use does mess with your blood sugar (you need to eat more carbs if you get hypoglycemic episodes)\u2028\u003c\/div\u003e\n\u003cdiv\u003eProlonged HGH use can cause a mild carpal tunnel syndrome (which goes away when you stop taking it)\u003c\/div\u003e\n\u003cdiv\u003eHGH can cause mild water retention (which goes away when you stop taking it)\u003c\/div\u003e\n\u003cdiv\u003eHGH and temperatures\u003c\/div\u003e\n\u003cdiv\u003eCicconatropin is lyophilized (freeze dried) Growth hormone and this is how it withstands temperatures:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBefore reconstituted\u2028- if refrigerated between 2 – 8 degrees Celsius it’s good until expiration date.\u003c\/div\u003e\n\u003cdiv\u003eAt room temperature (up to 37 degrees celsius) it’s good for over 30 days.\u003c\/div\u003e\n\u003cdiv\u003eAt up to 45 degrees celsius it’s good for about a week.\u003c\/div\u003e\n\u003cdiv\u003eAfter reconstituted – it has to be refrigerated at all times. It’s good for 20 days with bacteriostatic water and 24 hours with normal water for injection.\u003c\/div\u003e\n\u003cdiv\u003eWater Bacterostatic water is sterile, has a specific pH level and contains a specific amount of benzyl alcohol as a bacteriostatic preservative, is in a specially formulated polyolefin vial to maintain it integrity and sterility, and has no adulterants that may damage\/breakdown what you are reconstituting or cause a deep tissue infection when injected. It’s what you have to use for IM and subcutaneous injections and reconstituting peptides or growth hormone. Normal water for injection will also work as a diluent for your growth and peptides but the injection is much more painful than bacteriostatic water and the active ingredient downgrade in normal water for injection is much faster than bacteriostatic water. Normal water for injection will keep your growth hormone or peptide active for only 24 hours where as bacteriostatic water will only start downgrading after 14 days. Bacteriostatic water is also much less painful to inject than water for injection. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSyringes Get the insulin type syringe with 100 markings on the side. They are very cheap and available in every local pharmacy store. They have the smallest needles. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMixing\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePull 1ml of water into the syringe and inject it into the vial with powder. GH molecules are very fragile – sensitive to heat and rapid movements. You should never shake the vial when mixing. You should not inject the water directly into the powder with force, but rather let it gently slide down the inside of the vial. If it bubbles up, you should put the vial in the refrigerator and leave it there for about 15 minutes. The bubbles will be gone by then. You should then gently turn the vial between your fingers until all of the powder has dissolved (it takes about 3-4 minutes).\u003c\/div\u003e\n\u003cdiv\u003eThe vials are under vacuum, so before you can take the GH out, you need to get rid of the vacuum. You take a fresh syringe, pull air into it and inject the air into the vial (not into liquid, but into air above the liquid). This will get rid of the vacuum. You can then pull out the GH as you need it. 10 markings on the 100-mark syringe = 1 IU.\u003c\/div\u003e\n\u003cdiv\u003eIf you want to take 2IU you will then draw 20 markings on the insulin syringe and 3IU will be 30 markings as in the picture below.\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eINJECTIONS\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome people pull the entire HGH vial content into the syringe and use the same for 5 injections. Others prefer to use a fresh syringe for every injection (which is smart in my humble opinion).\u003c\/div\u003e\n\u003cdiv\u003eThe favorite spot for HGH injections is subcutaneously, into the stomach fat – pinch some skin between your fingers and insert the needle at a 45-degree angle. Chose a different spot every time. Depending on the spot, you can either feel nothing or you can feel slight pain – you will learn your favorite spots in time. GH can also be injected into any muscle (thigh, shoulder, etc.) – it works the same either way.\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHGH DOSAGE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage depends on the purpose. People generally use 2IU per day for anti-aging purpose and 4IU per day for bodybuilding, weight loss and general fitness. In case of 4IU, people take 2IU in the morning and 2IU in the afternoon. Its best injected into stomach fat (exactly the same way as insulin).\u003c\/div\u003e\n\u003cdiv\u003eEffects are felt about a week into the first cycle (better sleep, skin improvement, etc.). Improved muscle tone is noticed about a month or two after the start (provided you do good workout and proper diet – plenty of proteins). Don’t just settle for any type of protein, because some manufacturers put in all sorts of crap (artificial flavors, sugar, etc. also some manufacturing methods produce low quality protein which is no good.). You want undenatured whey protein isolate created with micro cross flow filtration method and possibly get unflavored and unsweetened kind. I also suggest you take some good multi vitamin\/mineral supplements.\u003c\/div\u003e\n\u003cdiv\u003eThe effects are most noticeable in the initial few cycles so stay on it for as long as you can (3-4 months even).\u003c\/div\u003e\n\u003cdiv\u003eThe only noticeable side effect, which can happen to some people, is the carpal tunnel syndrome (tingling sensation in your palms and fingers. Feeling like your hands fall “asleep” sometimes, especially in the morning when you wake up). If it gets unbearable, people just stop the cycle for a few weeks and then resume when the carpal is gone. If it happens it does so only in initial few cycles when the carpal tunnel (through which nerves are passing to your palms) is too thin and doesn’t have time to adapt to the new rapid growth. Later on the tunnel adapts and in subsequent cycles the carpal is barely felt – if at all.\u003c\/div\u003e\n\u003cdiv\u003eYou can take your growth hormone once a day for example 2IU per day for anti ageing purposes. You can also split your growth and take 2IU three times per day or more for bodybuilding purposes with only one crucial rule that must apply. Not within an hour before you eat and not within two hours after you have eaten. When insulin spikes in your blood because of a meal it will destroy your growth hormone so we do not want growth hormone in the blood together with insulin from a meal.\u003c\/div\u003e\n\u003cdiv\u003e10 x 10.27iu HGH per vial (3,8mg) plus 10 x 1ml bacteriostatic water plus 10 x 1ml insulin syringes.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHGH is generally used to aid with recovery and it is recommended for use with EVERY cycle. While it is not really a stand alone anabolic product, it most certainly enhances the effect of regular anabolic’s for beyond expectation. It has also been reported that gains achieve from cycles are also for more easily maintained and the anabolic side effects are minimized. Add to this the fact that it’s also an anti-aging product so you look better in every way you possibly can!\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEutropin – Platinum Range:\u003c\/div\u003e\n\u003cdiv\u003eBeside containing high grade HGH, Eutropin contains Glycine which has been scientifically proven to stimulate the pituitary gland to release higher levels of you own, natural HGH. When you add synthetic hormone to your body there is a risk that your body may reduce production of its natural hormone and the addition of the Glycine is an attempt to reduce this phenomenon. (Please read the Product Insert for advice as to how to minimise this effect)\u003c\/div\u003e\n\u003cdiv\u003eEutropin contains additional excipients which buffer the HGH so as to allow a higher degree of effectivity. According to tests, Eutropin is ±12% more effective than most well known, reputable brands.\u003c\/div\u003e\n\u003cdiv\u003eThe bacteriostatic water contains a preservative which slows down microbial growth in the reconstituted HGH thereby extending the life thereof by up to 4 times.\u003c\/div\u003e\n\u003cdiv\u003e3.8mg HGH per vial which is 10.27iu. This takes care of the small amount one can’t draw out of the vial and ensures you get a full 10iu HGH.\u003c\/div\u003e\n\u003cdiv\u003eContains 10 x 1ml insulin syringes to get you going as soon as you get your kit. No need to run around for syringes. You can also purchase more from us.\u003c\/div\u003e\n\u003cdiv\u003eWe all know we can’t get every last drop of liquid out of the vial. We’ve worked out that this is about 0,025ml and by adding an extra 0,27iu of HGH you are ensured of getting a full 10iu out of the vial.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53767873036580,"sku":null,"price":2550.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_7a1ffc5f-4675-4e5e-93ca-ec3fda8489bc.jpg?v=1778090470"},{"product_id":"upa-test-undeconate-250","title":"UPA Test Undeconate 250","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003ethe condition, but as time goes by the symptoms will normally mount up and progressively become stronger. The primary symptoms of low testosterone, all of which can be remedied by the effects of Testosterone Undecanoate include:\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eErectile Dysfunction (inability to maintain or obtain an erection)\u003c\/div\u003e\n\u003cdiv\u003eLoss of Libido (can refer to partial or total loss)\u003c\/div\u003e\n\u003cdiv\u003eLoss of Muscle Mass (despite diet \u0026amp; exercise)\u003c\/div\u003e\n\u003cdiv\u003eLoss of Strength (despite diet \u0026amp; exercise)\u003c\/div\u003e\n\u003cdiv\u003eIncreased Body Fat (despite diet \u0026amp; exercise)\u003c\/div\u003e\n\u003cdiv\u003eInability to Lose Body Fat (despite diet \u0026amp; exercise)\u003c\/div\u003e\n\u003cdiv\u003eDeclining Memory\u003c\/div\u003e\n\u003cdiv\u003eDeclining Mental Focus\u003c\/div\u003e\n\u003cdiv\u003eDeclining Mental Clarity\u003c\/div\u003e\n\u003cdiv\u003eLethargy\u003c\/div\u003e\n\u003cdiv\u003eIrritability\u003c\/div\u003e\n\u003cdiv\u003eWeakened Immune System\u003c\/div\u003e\n\u003cdiv\u003eHigh Cholesterol\u003c\/div\u003e\n\u003cdiv\u003eLoss of Hair\u003c\/div\u003e\n\u003cdiv\u003eDepression\u003c\/div\u003e\n\u003cdiv\u003eDecreased Energy\u003c\/div\u003e\n\u003cdiv\u003eInsomnia\u003c\/div\u003e\n\u003cdiv\u003eThe symptoms of low testosterone can be very bothersome and greatly diminish your overall quality of life. The symptoms are not life threatening, not directly, but if ignored a prolonged low testosterone condition can aid in the promotion of far more serious conditions. Low testosterone has been linked to Alzheimer’s disease, diabetes, heart disease, osteoporosis and numerous other serious conditions. With exogenous testosterone so readily available and with the effects of Testosterone Undecanoate and other related compounds being so effective, there is no logical reason for suffering from a low testosterone condition.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSide Effects of Testosterone Undecanoate:\u003c\/div\u003e\n\u003cdiv\u003eThere are possible side effects of Testosterone Undecanoate, but most healthy adult men should be able to supplement with this anabolic steroid problem free. Remember, testosterone is not a foreign substance to the body; you are not introducing something to your body it is unfamiliar with. Further, you will merely be replacing what your body is lacking and nothing more. However, most men can tolerate high levels of testosterone fairly well or what is referred to as supra-physiological doses. There is a cutoff point, and supra-physiological doses of testosterone will increase the risks associated with use, but the threshold is high. As for the side effects of Testosterone Undecanoate, while possible, the threshold is even higher since we are supplementing with therapeutic level doses. In order to help you understand the possible side effects of Testosterone Undecanoate, we have broken them down into their separate categories along with all the information you’ll need.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53767994507556,"sku":null,"price":450.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_f88a71c9-32b4-403d-a48a-54082fbdb98c.jpg?v=1778090628"},{"product_id":"upa-npp-100","title":"UPA NPP 100","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eThis substance is very similar to the more common and well-known Deca Durabolin with main ingredient nandralone decanoate. The main difference between the two is the ester attached to the nandralone compound. Deca 100 Fast has a shorter phenylpriopionate attached than the more popular long acting decanoate.\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDeca Durabolin releases from the site of injection over a 2 to 3 weeks period. Deca 100 Fast releases from the injection site and lasts about a week in the system. Deca 100 Fast is therefore best when being injected every 2 to 3 days to keep the levels in the system level. Apart from the time these two substances releases and last in the system Deca Durabolin and Deca 100 Fast are virtually interchangeable.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNandralone phenylpropionate shows a sharp increase in blood serum levels of the free form of nandralone within 24 to 48 hours from the time of injection. Because of this sharp increase and quick release of nandralone this product is sometimes preferred to the longer acting version. After athletes compete and they battle with joint pain they prefer this substance because the longer acting version will take to long to kick in.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis substance is not as androgenic as testosterones but this does not mean it is not androgenic at all. At high doses it will have some androgenic effects. In other words at low doses you will have very few androgenic effects but at high doses you might experience oily skin, acne, and body\/facial hair growth. Male pattern hair loss, deepening of voice and clitoral enlargement in females is also possible. Liver toxicity with this substance is very unlikely because it is not a c-17 alpha alkylated.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAll anabolic steroids have a tendency to reduce HDL (good) cholesterol and increase LDL (bad) cholesterol. The relative impact of an anabolic\/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable) type of steroid (aromatizable or non-aromatizable) and level of resistance to hepatic metabolism. With regards to nandralone at a dose of 600mg per week over 10 weeks demonstrated 26% reduction in HDL cholesterol levels. This suppression is slightly greater than an equal dose of testosterone over an equal period. In other words it shows a slightly more negative impact on HDL\/LDL ratio with nandralone than with testosterone cypionate. It’s always recommended to accompany the use of this product with a low saturated fat diet and a cardiovascular exercise program.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNandralone phenylpropionate in doses sufficient to promote muscle growth does suppress endogenous testosterone production. One 100mg nandralone phenylpropionate injection shows a rapid suppression of serum testosterone levels. After about 2 to 3 days after the injection the serum testosterone levels will decrease by approximately 30% of the initial level. Testosterone levels will increase to a normal level after about 2 to 6 months.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDoses for men vary between 200mg and 400mg over an 8 to 12 week period. The weekly dose is usually split into two doses per week due to the short acting nature of the phenylpropionate ester. Recommended dose for woman are 50mg per week (single dose once a week injection) for no longer than 4 to 6 weeks\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53768131051812,"sku":null,"price":430.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_e796fb2a-92dd-4535-b088-c42e9e89a154.jpg?v=1778090815"},{"product_id":"upa-winstrol-15mg-50-tabs","title":"UPA Winstrol 15mg\/50 Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e\n\u003cp\u003eUPA WINSTROL 15TABS(15MG STANOZOLOL\/TAB=50TABS)\u003c\/p\u003e\n\u003cp\u003eORAL VERSION\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eANDROGENIC  30\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eANABOLIC        320\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eSTANDARD       METHYLTESTOSTERONE\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eActive-Life: About 8 hours\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eDrug Class: Anabolic\/Androgenic steroid (Oral)\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eAverage Reported Dosage: Males 20-50-mg daily Women 10-15-mg daily\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eAcne: Rare\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eWater Retention: Rare\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eHigh Blood Pressure: Rare\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eLiver Toxic: High in high oral dosages\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eDHT Conversion: None, DHT derivative\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eDecreases HPTA Function: Low\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003ePretty much everything written thus far about Stanozolol injectable (*See “Winstrol Depot” under “Injectable Anabolic Androgenic Steroids” for more info) was also attributed also to the oral form. It was often said that the oral form is less effective than the injectable. In truth, it was usually due to dosages, and this in turn was due to price. Athletes usually administered a lower dosage orally because it seemed like 25 pills daily was mega dosing. In my personal opinion this was true to a point. Oral use of any 17-alfa-alkylated steroid is hard on the liver. This is because it is difficult for the liver to deactivate these modified testosterone and derivatives. Let me make it clear. Milligram for milligram oral administration of Stanozolol was reported significantly more potent than the injection product (but it is more liver toxic). Oral dosages were commonly broken into 2-3 daily dosages to maintain circulatory androgen elevation. An effective reported daily oral dosage for women was 10-15mg and for men 20-30. However, this listed male dosage was not as effective (or as toxic) as the 30-50mg daily dose range.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eMale athletes reported the practice of stacking 40-50mg of Stanozolol daily with 300-400mg weekly of a nandrolone provided significant lean muscle tissue augmentation with good post-cycle retention. For “bulking” purposes many reported the use of this drug with a testosterone at an average reported dosage of 200-600mg weekly resulted in “amazing strength and weight gains” and improved post-cycle lean mass retention.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eWomen athletes commonly reported the use of Stanozolol at a dosage of 10-15mg daily with 50-100mg of a nandrolone weekly resulted in a rapid increase in quality lean mass tissue with low water retention and rare virilizing negative side effects.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003eAnabolic steroids such as\u003cspan\u003e \u003c\/span\u003e\u003cspan\u003eStanozolol\u003c\/span\u003e\u003cspan\u003e \u003c\/span\u003eare synthetic derivatives of the male hormone testosterone. Stanozolol has a pronounced anabolic effect with fewer masculinizing side effects than testosterone and some other synthetic anabolic steroids. Anabolic steroids are used in stimulating appetite and increasing weight gain, strength, and vigor. They should be used as a part of an overall program with other supportive and nutritional therapies.\u003c\/p\u003e\n\u003cp\u003eThis is a very popular anabolic steroid, which is a derivative of dihydrotestosterone. Winstrol is a relatively low androgenic steroid which will not aromatise. It is moderately toxic to the liver. Very few users report any water retention or any other side effects while using Winstrol. It is a popular drug for cutting in a stack with Primobolan or Parabolan. When stacked with Testosterone it can be very effective for a size and strength gain. Women use the drug quite often, but it can cause virilising effects for some women even at low dosages. Most of the muscle gains made while taking the Winstrol are retained after the drug is discontinued. The injectable form is better than the oral. Many feel that the injectable must be administered at least twice a week: some take shots every day for better effects. Dosages range from 3 to 5 cc?s per week for men, 1 to 2 cc’s in women. .\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eStanozolol\u003c\/span\u003e\u003cspan\u003e \u003c\/span\u003eis prescribed for chronic infections, for conditions such as extensive surgery, [corticosteroid-induced myopathy, decubitus ulcers, burns] , or severe trauma, which require reversal of catabolic processes or protein-sparing effects. This is used in addition to, and not as replacements for, conventional treatment of these disorders.\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eStanozolol\u003c\/span\u003e\u003cspan\u003e \u003c\/span\u003eis effective in raising hemoglobin concentrations in some cases of aplastic anemia (congenital or idiopathic).\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eStanozolol\u003c\/span\u003e\u003cspan\u003e \u003c\/span\u003eis indicated in the prophylaxis of hereditary angioedema to decrease the frequency and severity of attacks.\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eStanozolol\u003c\/span\u003e\u003cspan\u003e \u003c\/span\u003eis used in the treatment of hereditary angioedema.\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eStanozolol\u003c\/span\u003e\u003cspan\u003e \u003c\/span\u003eis indicated in the treatment of conditions associated with decreased fibrinolytic activity due to antithrombin III deficiency or excess fibrinogen. These conditions may include cutaneous vasculitis, scleroderma of Raynaud’s disease, vasculitis of Behcet’s disease, and complications of deep vein thrombosis such as venous lipodermatosclerosis. Stanozolol is indicated in the prevention of recurrent venous thrombosis associated with antithrombin III deficiency. Stanozolol may be of benefit in patients susceptible to or with a history of thromboembolism for the treatment of vascular disorders associated with these forms of reduced fibrinolytic activity.\u003c\/p\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53768219099428,"sku":null,"price":260.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_7117f630-29ab-42d5-b30b-4e4ddd5dea50.jpg?v=1778090929"},{"product_id":"upa-igf-1-lr3","title":"UPA IGF-1 LR3","description":"\u003cp\u003e\u003cspan\u003eUPA IGF-1 LR3(100MCG somatomedin C\/VAIL==1x 1ml powder)\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life:10 min FOR IGF-1 to 20-30 hours for IGF-1 Long R3\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Growth Factor\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: 60-1000mcg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Diet dependent\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIGF1 LR3 allows for many of the growth-promoting effects of growth hormone insulin-like growth factors also know as IGF’s. IGF-1 LR3 comprises a family of peptides (protiens) that play important roles in mammalian growth and development. IGF1 LR3 is also known as Long R3 IGF-1 or Insulin-Like Growth Factor-I Long Arg3.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe Long R3 IGF-1 version is significantly more potent than regular IGF-1. The enhanced potency is due to the decreased binding of IGF1 LR3 to all known IGF binding proteins. These binding proteins normally inhibit the biological actions of IGF’s therefore IG-1 LR3 has been shown to have increased efficacy and function .\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis IGF-1 LR3 analog of IGF-1 has been created with the purpose of increasing the biological activity of the IGF peptide.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIGF1 LR3 is also known as Long R3 IGF-1 or Insulin-Like Growth Factor-I Long Arg3. This is a human recombinant, single, non-glycosylated, polypeptide chain containing 83 amino acids and having a molecular mass of 9200 Daltons. IGF1 mediates many of the growth-promoting effects of growth hormone (GH; MIM 139250). The LR3 is a long-term analog of human IGF-1, specifically designed and manufactured for mammalian cell culture to support large-scale manufacturing of recombinant biopharmaceuticals. Early studies showed that growth hormone did not directly stimulate the incorporation of sulfate into cartilage, but rather acted through a serum factor, termed ‘sulfation factor,’ which later became known as ‘somatomedin’.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIGF-1 LR3 is the primary protein involved in responses of cells to growth hormone (GH): that is, IGF-I is produced in response to GH and then induces cellular activities. One such example is muscle growth or hyperplasia. This compound also makes the human body more sensitive to insulin. It is the most potent growth factor found in the human body. IGF-1 causes muscle cell hyperplasia, which is an actual splitting and forming of new muscle cells.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe most effective form of IGF-1 is considered to be IGF-1 LR3. This formula has been chemically altered to avoid binding to proteins in the human body, and to increase the half life, approximately 20-30 hours.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIGF-1 is naturally produced in the liver as a result of GH (Growth Hormone) metabolism in the presence of insulin. Muscle tissue can also produce IGF-1 by way of an intracellular response. In fact, one of the benefits of training sets that result in an intense burn, or stretch position training, is the production of natural IGF-1. It is also a side effect of oral 17-ALFA ALKYLATED STEROIDS, which cause a higher release of IGF-1 from the liver. IGF-1 receptors exist throughout muscles and organs such as the heart, spleen, small intestines, and kidneys with a higher concentration of receptors exerting effects upon organs. IGF-1 is extremely anabolic, far more so than GH or Insulin.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eRecombinant IGF-1 (genetically engineered) was reported to be effective when injected intramuscularly because it causes localized growth. This was the most popular method, and the agreed wisest for the most part. The drug has a half-life of about 10 minutes, and if it is or has been bound to IGF -BP-3, (INSULIN GROWTH FACTOR BINDING PROTEIN)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ethe half- life is extended to about 12 hours. Pro’s often stacked Insulin and\/or GH with IGF-1 because IGF-1 shuts off natural GH production and GH causes Insulin resistance. IGF-1 is often referred to as Pro-insulin because it counteracts Insulin resistance and interacts with insulin. But this would actually be an untrue term for\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIGF-1.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIGF-1 can have all the side effect of GH or insulin use with an added negative: gastrointestinal (GI) growth. This is due to a higher number of IGF-1 receptors being located in the GI tract as compared to skeletal muscle. The latter has more GH receptors. This explains much of the bloat seen in pro bodybuilders of late.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIGF-1 is not stable in synthetic forms. A loud noise, shaking a vial, and sudden heat changes can render it nothing more than a bunch of expensive amino acids. Picture a piece of string folded up in a specific shape and held in that shape by a few fibers. This is what an amino acid sequence for GH or IGF-1 looks like, but the IGF-1 sequence has only 2 fibers keeping the active shape. The strand or string is a specific amino acid sequence. The shaping fibers holding the active shape are called disulfide bridges. Change the folding or break a bridge and the IGF-1 no longer fits into its receptor-site. Like a key must have a specific shape to actuate its lock, so must a drug have the right shape to actuate its receptor. Again, this explains the common noted necessity of careful preparation and site-specific injection (into the muscle group trained that day) when IGF-1 was administered.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCommon stacks have been 0.25-0.50-mg of GH per KG of body weight stacked with 60-1000mcg of IGF-1 divided into 2-5 daily injections. Many had reported improved lean mass gains by combining both with insulin and high androgen AAS (Such as testosterone or orals such as DIANABOL and \/or ANADROL-50) for 4-8 weeks. Many simply injected 40-mcg of IGF-1 directly into the muscle group trained that day after training. It is important to note that IGF-1 can cause hypoglycemia and blood sugar monitoring was considered paramount by most.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*The reader should note that IGF-1 has been used clinically on children at dosages of over 3-7mg daily. That is 3,000-7,000 mcg a day! No negative side effects were recorded, though none were expected… of course. The point being is that the 40-100 mcg of IGF-1 used by athletes is most likely insufficient, yet very expensive. However, the results some individuals have realized through IGF-1 use are amazing.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eI have personally noted amazing new growth as a result of past IGF-1 administration. However it is important that readers realize that long term negative side effects have not been well studied. Anything that possesses genetic altering potential has equally negative potential as well.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eInsulin-like growth factor (IGF-1: originally called somatomedin) has been known to be produced by live under the influence of human growth hormone (HGH). The mature systemic type of IGF-1 is a simple 70 amino acid peptide, but its gene is unexpectedly large spanning a region of over 90 kb of genomic DNA. Alternative splicing of IGF-1 gene results in different transcripts encoding several IGF-1 precursor proteins. IGF-1 has been shown to be involved in several cellular processes including tissue differentiation,maintenance of tissue mass and tissue repair . And it is known to be mitogenic and myogenic. IGF-1 is thought to be responsible for much of the anabolic activity of HGH, including nitrogen retention and protein synthesis as well as causing muscle cell hyperplasia (increase in number of muscle cells), and mitogenesis (the growth of new muscle fibers). In fact, IGF-1 acts on several different tissues (not just muscle) to enhance growth through various mechanisms. The easiest way to think about IGF is that it is a primary factor in the anabolic effects of weight training.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIGF-1 Long R3\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMany IGF-1 variations have been developed for research and bodybuilding use. IGF-1 Long R3 (or Long R3 IGF-1) is the most effective form of IGF-1. it has been chemically altered and has had amino acid changes which cause it to avoid binding to proteins in the human body and allow it to have a much longer half life, around 20-30 hours. Long R3 IGF-1 is an 83 amino acid analog of IGF-1 comprising the complete human IGF-1 sequence with the substition of an Arg(R) for the Glu(E) at position three, hence R3, and a 13 amino acid extension peptide at the N terminus. This analog of IGF-1 has been produced with the purpose of increasing the biological activity of the IGF peptide. All these alterations make IGF-1 Long R3 significantly more potent (2-3x) than IGF-1 in studies, because it has a lower affinity to be rendered inactive by IGF binding proteins. Yeah, all effects of IGF-1 still holds true for this version, but it?s just a bit more active in the body, and hence more potent. It is also not as expensive since a media grade version is available which is sufficient for bodybuilding use.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEffects\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eExperiments have been carried out using the cDNA of IGF-1(a compound which was responsible for directing over expression of IGF-1) in an adenoviral vector under the control of a muscle regulatory sequence. Results were shown by Fig.1. It was found that a single intramuscular injection of IGF-1 cDNA into a mouse muscle resulted in a 15% increase in mean muscle fibre cross section area and a 14% increase in strength in young adult mice within four months. It was concluded due to the anabolic effect of IGF-1. But those effects are not all that the researchers have found. IGF also seems to prevent aging-related muscle changes in old adult mice. These old mice experienced a 27% increase in strength as compared with uninjected old muscles. Muscle mass and fiber type distributions were maintained at levels similar to those in young adults. The researchers have speculated that these effects are primarily due to stimulation of muscle regeneration via the activation of satellite cells by IGF-I\u003c\/div\u003e\n\u003cdiv\u003eBut how effective does IGF-1 Long R3 work on bodybuilders? It’s difficult to put a number on results, since they’re so subjective, but as a general rule, experienced users have found IGF-1 Long R3 to add up to 5% to their lifts in a cycle alone, and a decent reduction in body fat coupled with an increase in muscle gain. A five to ten pound sway each way is possible. The less experienced you are with chemical enhancement, typically the greater the results you can achieve with IGF-1 Long R3 (or any body enhancement chemical). In addition, users report a steady decrease in bodyfat percentage levels due to increase in muscle tissue. Users and researchers have reported most effective results with a 6 weeks on and 4 weeks off cycle.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMechanism\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHow does IGF-1 work? To understand how IGF-1 works we have to understand how muscles grow. The ability of muscle tissue to constantly regenerate in response to activity makes it unique. It’s ability to respond to physical\/mechanical stimuli depends greatly on satellite cells. Satellite cells are muscle precursor cells which also might be thought of as “pro-muscle” cells. They are cells that reside on and around muscle cells. These cells sit dormant until called upon by growth factors such as IGF-1. Once this happens these cells divide and genetically change into cells that have nuclei identical to those of muscle cells. These new satellite cells with muscle nuclei are critical if not mandatory to muscle growth. Whenever a muscle grows in response to functional overload there is a positive correlation between the increase in the number of myonuclei and the increase in fiber cross sectional area (CSA). When satellite cells are prohibited from donating new nuclei, overloaded muscle will not grow [10, 11]. So one important key to unnatural muscle growth is the activation of satellite cells by growth factors such as IGF-1.\u003c\/div\u003e\n\u003cdiv\u003eIGF-1 stimulates both proliferation (an increase in cell number) and differentiation (a conversion to muscle specific nuclei) in an autocrine-paracrine manner, although it induces differentiation to a much greater degree. This is in agreement with the Dual Effector theory. In fact, you can inject a muscle with IGF-1 and it will grow. Studies have shown that , when injected locally, IGF-1 increases satellite cell activity, muscle DNA content, muscle protein content, muscle weight and muscle cross sectional area.\u003c\/div\u003e\n\u003cdiv\u003eScientists are now discovering the signaling pathway by which mechanical stimulation and IGF-1 activity leads to all of the above changes in satellite cells, muscle DNA content, muscle protein content, muscle weight and muscle cross sectional area just outlined above. This research is stemming from studies done to explain cardiac hypertrophy. It involves a muscle enzyme called calcineurin which is a phosphatase enzyme activated by high intracellular calcium ion concentrations. Note that overloaded muscle is characterized by chronically elevated intracellular calcium ion concentrations. Other recent research has demonstrated that IGF-1 increases intracellular calcium ion concentrations leading to the activation of the signaling pathway, and subsequent muscle fiber hypertrophy . In summary the researchers involved in these studies have explained it this way, IGF-1 as well as activated calcineurin, induces expression of the transcription factor GATA-2, which accumulates in a subset of myocyte nuclei, where it associates with calcineurin and a specific dephosphorylated isoform of the transcription factor nuclear factor of activated T cells or NF-ATc1. Thus, IGF-1 induces calcineurin-mediated signaling and activation of GATA-2, a marker of skeletal muscle hypertrophy, which cooperates with selected NF-ATc isoforms to activate gene expression programs leading to increased contractile protein synthesis and muscle hypertrophy.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage and Administration\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe magic effects happens between 60mcgs and 120mcgs per day, in divided doses. In general, people who have used less, and even up to 50mcg\/day have had mediocre results. People who have used more have suffered headaches and nausea, and generally not much more in the way of results.\u003c\/div\u003e\n\u003cdiv\u003eIt has been clearly observed in studies that when GH and IGF-1 are used together, you’ll get greater results in the accumulation of Lean Body Mass than you would by using either of them alone[15]. In addition, there is a very strong probability that testosterone would be synergistic to GH[16], and would also increase IGF levels in muscle.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDifferences between IGF-1 and HGH\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHGH is actually closely related to IGF-1, in a lot of ways. HGH, or GH in short, is certainly an effective fat burner and anabolic agent, and is a protein secreted by the pituitary. Once secreted, it has the ability to influence various cells in the body to increase in number and size, as well as having the ability to enhance the movement of amino acids through cell membranes- thereby increasing the rate at which the cells can convert those molecules to usable proteins. It also causes cells to preferentially burn fat in lieu of carbohydrates. The important thing to realize is that there is a mounting body of evidence that strongly suggests that these effects occur as a result of the IGF-1 released as a result of the pituitaries GH secretion. Scientists have discovered that many of HGH’s anabolic and regenerative effects are actually mediated by IGF-1. HGH indirectly causes muscle growth by stimulating the release of IGF-1 when it (the HGH) is destroyed in the human body. So one way you could look at it as HGH being a precursor to IGF-1. The later is more effective at directly causing muscle growth and density increases than HGH. Over the past few decades, HGH has developed quite a reputation for taking awhile (often several weeks) for the user to start seeing results. In contrast, IGF-1 often begins to product noticeable results within the first couple of weeks. With growth hormone you need to use high amounts of anabolics and often insulin to see any gains at all, this is not the case with IGF-1. IGF-1’s superiority to HGH is not only intuitive at some level, but has also been clearly elucidated clinically as well. In the following graphs taken from a rodent study comparing IGF-1 and HGH, a low dose as well as a high dose of IGF-1 was shown to be more anabolic than HGH. In comparison to HGH, IGF-1 produced an overall greater total protein content within the injected muscle as well as a greater final weight of the that muscle (called the “Tibialis Anterior” or TA)\u003c\/div\u003e\n\u003cdiv\u003eIt seems to be the case that IGF-1 would be superior to HGH as an anabolic agent. In some clinical studies, that is not always the case, but in most of bodybuilders and athletes, greater results are often seen with IGF-1 over HGH – and it should be noted that they are often seen more quickly as well.\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53768279032100,"sku":null,"price":350.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_fcd3df8a-d9ab-450b-bcee-e2006e3933d7.jpg?v=1778091101"},{"product_id":"upa-max-cut-300mg","title":"UPA Max Cut 300mg","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e100MG\/ML TESTOSTERONE PROPIONATE  \n\u003cdiv\u003e100MG\/ML TRENBOLONE ACETATE \u003c\/div\u003e\n\u003cdiv\u003e100MG\/ML DROSTANOLONE PROPIONATE\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53768510865700,"sku":null,"price":750.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_76ecd5e8-09f9-4641-b33d-aa5332b60908.jpg?v=1778091356"},{"product_id":"upa-mots-c-self-mix","title":"UPA MOTS-C Self Mix","description":"","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53768608022820,"sku":null,"price":630.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_cdeac396-03b2-4e01-a379-71a402b2006b.jpg?v=1778091482"},{"product_id":"upa-tertroxin-t3","title":"UPA Tertroxin T3","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA=T3 TERTROXIN(25 MCG LIOTHYRONINE SODIUM\/TAB=50 TABS)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Synthetic thyroid hormone. (ORAL)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: 25-150 MCG daily.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNoted Comments: Significant suppression of Thyroid function during use.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCytomel is the synthetic form of T-3\/L-triiodothyronine and was a commonly known trade or brand name among athletes. T-3\/L-triiodothyronine is used as a form of thyroid hormone therapy mostly in Europe. Most bodybuilders favored this drug over synthetic forms of T-4\/L-thyroxine due to its vastly superior activity level.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAn advantage of T-3\/L-triiodothyronine administration over T-4\/L-thyroxine was the lack of dependence upon the liver enzyme responsible for T-4\/T-3 conversion. During diet restricted periods the liver naturally decreases the liver enzyme levels as a control measure to prevent metabolic rate induced starvation. Just as the liver increases production of this enzyme in response to elevated calorie intake it also reduces levels in response to decreased calorie intake. Remember that T-4 \/L-thyroxine is only 20% as active as T-3\/L-triiodothyronine.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe abuse of synthetic T-3\/L-triiodothyronine will result in severe suppression of natural (endogenous) thyroid function. This is especially true of this drug because it actually circumvents the normal thyroid hormone manufacturing process the body utilizes to produce endogenous forms as required. Simplified this is because T-3\/L-triiodothyronine is the most potent thyroid hormone so the body shuts down each level required for production to try to reduce circulatory T-3\/L-triiodothyronine levels. Of course this does not reduce the level if the hormone is being administered exogenously (from outside the body).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSince long term use of T-3 \/L-triiodothyronine will lead to thyroid function suppression the issue of rebound should be briefly discussed. It is commonly stated that synthetic thyroid hormone abuse will lead to permanent thyroid gland dysfunction. Though it is definitely a physiological possibility, I have not yet found a case study to support this statement. However, there is a common occurrence of thyroid gland\/function rebound in natural endogenous thyroid hormone production. It seems that it was common for individuals to realize an “increase” in endogenous thyroid hormone production of 120-130 % within 3-15 days after drug discontinuance. This means an individual would commonly see an increase in their thyroid hormone production of 20­30% above their normal pre-drug administration levels, in many cases.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe noted positive physiological effects of reasonable dosages of thyroid hormones included:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased protein synthesis rate. *Increased rate of fat oxidation.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased sensitivity of receptors for androgens, Insulin, GH, IGF-1, PGE-1, PGF-2, Clenbuterol, Ephedrine, Creatine, and others.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased metabolization of proteins, carbohydrates, fats and micronutrients. *Increased metabolic rate and calories expenditure. *Enhanced oxygen consumption by most body tissues *Improved recovery time.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe noted negative physiological effects of excessive dosages of thyroid hormones included:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Loss of lean mass tissue.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased heart rate and palpitations.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Insomnia.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Diarrhea.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Vomiting.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e Thyroid hormone drugs are natural or synthetic preparations containing tetraiodothyronine (T4, levothyroxine) sodium or triiodothyronine (T3, liothyronine) sodium or both. T4 and T3 are produced in the human thyroid gland by the iodination and coupling of the amino acid tyrosine T4 contains four iodine atoms and is formed by the coupling of two molecules of diiodotyrosine (DIT). T3 contains three atoms of iodine and is formed by the coupling of one molecule of DIT with one molecule of monoiodotyrosine (MIT). Both hormones are stored in the thyroid colloid as thyroglobulin.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThyroid hormone preparations belong to two categories (1) natural hormonal preparations derived from animal thyroid, and (2) synthetic preparations. Natural preparations include desiccated thyroid and thyroglobulin. Desiccated thyroid is derived from domesticated animals that are used for food by man (either beef or hog thyroid) and thyroglobulin is derived from thyroid glands of the hog. The United States Pharmacopeia (USP) has standardized the total iodine content of natural preparations. Thyroid USP contains not less than (NLT) 0.17 percent and not more than (NMT) 0.23 percent iodine, and thyroglobulin contains not less than (NLT) 0.7 percent of organically bound iodine. Iodine content is only an indirect indicator of true hormonal biologic activity.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53768679129380,"sku":null,"price":210.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_a4999094-b99d-44d0-ae74-3ac92a636d13.jpg?v=1778091596"},{"product_id":"upa-hgh-fragment","title":"UPA HGH Fragment","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA FRAG 176-191(HGH FRAG 176-191 1x2000MCG POWDER)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHuman Growth Hormone Fragment 176-191 (HGH 176-191) is a protein peptide made from amino acids 176-191. The HGH in HGH Fragment 176-191 stands for Human Growth Hormone, and has been proven to reduce fat and help with weight loss, making it a highly desired substance. HGH 176-191 works by mimicking the way the natural HGH regulates someone’s metabolism, but without all the adverse effects on insulin sensitivity, or blood sugar, and cell proliferation, or muscle growth. This drug also promotes anti-aging.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHuman Growth Hormone Fragment 176-191 (HGH 176-191) has about 12 times the fat burning properties of normal hgh.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLike unmodified GH, the fragment stimulates the breaking down of fat and inhibits the formation of lipids, like fatty acids, in the body. HGH 176-191 is meant to be over ten times stronger than the regular growth hormone in order to prompt weight loss within the body.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMost studies have shown that the best results were given after taking doses of 500-1000 mcg split into multiple doses throughout the day. Also, many studies have shown that HGH Fragment 176-191 can be used continuously long term, as no adverse long-term side effects have been reported or found while researching.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStudies have suggested that taking 250mcg of HGH 176-191 at each meal, five days a week will get you the best results. If you are looking for a more aggressive dose, bump up your dose of HGH 176-191 to 350mcg three times a day, five days a week. Doses should be given three hours apart, and the injection should be given on an empty stomach or after eating only protein, as carbohydrates and fats stunt the release of the growth hormone within the bod\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWith HGH 176-191, results will usually start to become evident around the four-week mark, after being combined with diet and exercise in a daily routine. The best results will begin to show after a minimum of three months after the initial first injection. When buying HGH 176-191, make sure you are actually getting the real thing—you do not want to be surprised by getting a counterfeit version or some other form of steroid that isn’t what you had in mind. According to UK Peptides, fake versions of HGH 176-191, it is easy for those who are inexperienced with growth hormones to tell the difference between HGH 176-191 and something else that may or may not be similar. If you do not see any changes in your physique after a few weeks of using the HGH 176-191 you obtained, check with a medical specialist to confirm its validity.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhen you have determined that you got authentic HGH 176-191, you can begin to administer it. After administering the growth hormone, wait about half an hour before consuming a meal. At this point, the hormone has started to take effect and you are allowed to eat whatever you want, regardless of size or caloric intake.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eJust like every other steroid out there, HGH 176-191 has its side effects, even though they are short term and exist only because your body is still getting used to it. HGH 176-191 can lead to a feeling of compulsion to continue, which can be precarious for mental health. Once users stop injecting they may start to see results fade, and for some users this can create a sense of self-image dysphoria creeping in. For this reason, it is important to limit how much you come to depend on the use of this steroid for how you view your own physique.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIn rare cases, the swelling of the feet and hands may occur, along with an increased heart rate and blood pressure level. Headaches and nausea may occur if too much was injected at one time, so be sure to monitor your health carefully.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTwo of the mildest side effects that are also the most common are water retention and lethargy. These occur in the early stages of using the drug, as your body is still getting used to it, and they will eventually disappear in time.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhile many of these side effects have low chances of occurrence, they can still happen for those who administer at the onset. For the reason of having low risks, many people opt for HGH 176-191 over other steroid options, claiming that it will get you the results you want without too many side affects you don’t want.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAs always, staying incredibly hydrated is key while using HGH 176-191. The more hydrated you are, the better your body works at melting fat and building muscle while on this regimen. To pair with HGH Fragment 176-191 and get the most out of it, eating a balanced diet is crucial, as well as getting enough sleep each night.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHGH Fragment 176-191 is one of the most commonly used muscle enhancements in the market and shows results in as little as four weeks. With basically no long-term side effects, it is usually the first choice for bodybuilders and anyone trying to get in shape.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDirection for use:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eInject 250mcg (0.1ml) to 500mcg(0.2ml) HGH Frag 176-191, 2 to 3 times per day. One of these injection should be done 30 minutes before cardio training for optimal effect.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eUse 5 days per week and off for 2 days\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53768783790372,"sku":null,"price":360.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_c55aad44-e6c9-4edb-aee8-814cf31349f5.jpg?v=1778091729"},{"product_id":"upa-epistane","title":"UPA Epistane","description":"\u003cp\u003e\u003cspan\u003eUPA EPISTANE(METHYLEPITIOSTANOL 10MG P\/CPS=60TABS)\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEpistane (Methylepitiostanol) \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis is the perfect pro hormone to use as cutting agent for male and female athletes who wants to avoid the androgenic effects of stronger pro hormones. It’s a anti estrogen, high anabolic, low liver toxicity compound that’s extremely versatile in gaining muscle as well as dieting.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTo put it into perspective —\u003c\/div\u003e\n\u003cdiv\u003eAnavar (Oxandrolone) has an anabolic rating of 322 – 630.\u003c\/div\u003e\n\u003cdiv\u003eEpistane (methylepitiostanol) has an anabolic rating of 1100\u003c\/div\u003e\n\u003cdiv\u003eIt’s between double and three times the anabolic rating of Anavar.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEpistane is a DHT (dihydrotestosterone also known as androstanolone) derivative that is best known for the non-aromatizing and non-progestagenic characteristics. This means very little side effects can be expected from this anabolic agent.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEpistane’s Anabolic\/Androgenic rating is 1100:91. This rating makes it the highest anabolic rated compound ever formulated with not even conventional anabolic steroids like Primobolan or Anavar matching this rating. The added benefit of this compound is that it has a very potent anti-estrogen agent that eliminates any possibilities of estrogen induced fat gain or water retention. Epistane is almost identical to a Japanese breast cancer drug called epitiostanol that blocked estrogen. Epistane however is much more anabolic than epitiostanol.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eYour gains on Epistane will be solid, lean, hard and dry gains. It will give similar effects to Primobolan, Anavar and in some cases Turinibal but it has proven to lead to greater lean muscle gains than these mentioned anabolic steroids.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEpistane is a great alternative to nolvadex, arimadex and femara when stacking with other compounds that is known for aromatizing. This means that you can stack your Epistane with your normal cycle to prevent gyno whilst still getting massive advantages from its anabolic muscle building effects. Epistane can also be taken on its own to keep the athlete anabolic while solving the gyno problem.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eJust when you think the advantages of this drug could not get any better. Epistane unlike other oral compounds Epistane (although methylated) has a very low liver toxicity and can be taken for longer periods of time and at higher doses than most orals. Epistane can easily run for 6 to 12 weeks at reasonable doses. It can be taken for longer than six weeks if it is the only oral being used at a dose of 30mg to 60mg daily split three times daily. Two doses daily is considered the minimum.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEpistane is one of the most pleasant oral steroids an athlete could ever use in their cycle considering its very low side effects and high anabolic rating. Clean solid gains with no water retention, lethargy, appetite suppression or depression when you stop the cycle.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWARNING – Although this is listed as a Pro Hormone it is still banned by WADA (World Anti-Doping Agency) and you will test positive if you use this while competing in international sports events.\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53796278206756,"sku":null,"price":440.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_e64096ea-d235-46e9-81f8-73c4c849ccee.jpg?v=1778124583"},{"product_id":"upa-anabolicum","title":"UPA Anabolicum","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA=SARMS ANABOLICUM(LGD-4033) 10MG\/TABLET=50 TABLETS.\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLGD-4033, Also Called Ligandrol Or Anabolicum.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLGD-4033 is one of the better studied SARMs. It’s been through multiple human trials, with interesting results:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHealthy men who took LGD-4033 for 21 days saw a significant increase in lean body mass. The only side effect was short-term testosterone suppression (more on that in a second) [3]. One milligram per day was enough to cause significant muscle growth. The higher the dose, the more muscle participants put on. In another trial, participants took doses as high as 22 mg\/day with no side effects or safety issues [3]. In rats, LGD-4033 increases bone density, muscle mass, and sex drive, without damaging prostate or liver tissue [3].\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLGD-4033 does not appear to stimulate fat loss, so if you take it on its own, it won’t make you leaner – just more muscular.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSide effects of LGD-4033\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLGD-4033 will probably suppress your natural testosterone production a bit while you’re on it, although the effects seem to be short-lived [3]. Study participants saw T suppression dependent on dose, but none of them dropped out of the healthy testosterone range, and levels returned to normal within 3 weeks after they stopped taking LGD-4033.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThat said, you may want to skip this one (and SARMs in general) if your testosterone is low. Consider biohacking your testosterone instead.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHow to dose LGD-4033\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eUsers report success taking 2-5 mg of LGD-4033, in a single daily dose, for 6 weeks. It seems that the higher the dose, the more muscle you put on, and the more your testosterone dips. Some people take up to 15 mg per day for much longer timeframes, but that’s riskier. You don’t want your natural T production to tank entirely. Once your 6 weeks are up, wait at least a month before starting another cycle.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAlso known as Ligandrol, LGD-4033 is a powerful anabolic SARM known to rapidly increas muscle size and strength. LGD-4033 is not the best SARM for cutting or weight loss, but in its efforts to grow muscle mass it will burn through fat if other body fuels are unavailable. LGD-4033 is not recommended for women, and suppression of natural testosterone production is observed in men administering high doses in longer cycles.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTypical dose: 10-20 mg\/day\u003c\/div\u003e\n\u003cdiv\u003eMax dose: 30 mg\/day\u003c\/div\u003e\n\u003cdiv\u003eStacking dose: 5-10 mg\/day (depending on stack)\u003c\/div\u003e\n\u003cdiv\u003eHalf-life: 24-36 hours\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53796380934436,"sku":null,"price":520.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_3ca2b285-43e7-4ac5-bc87-d072b737bad1.jpg?v=1778124716"},{"product_id":"upa-max-bulk-600mg","title":"UPA Max Bulk 600mg","description":"\u003cp\u003e\u003cspan\u003e200MG\/ML TESTOSTERONE CYPIONATE \u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e200MG\/ML NANDROLONE DECOANATE \u003c\/div\u003e\n\u003cdiv\u003e200MG\/ML TRENBOLONE ENANTHATE \u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53796467573028,"sku":null,"price":860.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_774608c2-8ac5-431f-9882-18652193e61c.jpg?v=1778124837"},{"product_id":"upa-max-size-600mg","title":"UPA Max Size 600mg","description":"\u003cp\u003e\u003cspan\u003e200MG\/ML TESTOSTERONE ENANTHATE \u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e200MG\/ML BOLDENONE UNDECLYNATE \u003c\/div\u003e\n\u003cdiv\u003e200MG\/ML TRENBOLONE ENANTHATE\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53796534583588,"sku":null,"price":860.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_4027a120-9b9b-4432-9c99-07d5abe3a786.jpg?v=1778124938"},{"product_id":"upa-hgh-100iu","title":"UPA HGH 100iu","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eUPA SOMATROPIN 10i0u(100iu somatropin=10x 1ml powder+water)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e191 Amino Acid Chain 99% pure \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: Varies upon injection method\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Growth Hormone\/IGF-1 Precursor (For injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: 2-16 i.u. total daily (1mg=2.7 i.u)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Very rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Very rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Anabolic\/No Androgenic Effects\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHuman Growth Hormone (GH) has been a subject of debate since I was a kid. Natural (endogenous) GH is produced by the pituitary gland. Children produce 2 i.u. “spurts” 4-7 times per day for 4-5 non-consecutive days during a 2-3 week period (during growth spurts). That would equal 32-70 i.u. in only a 4-5 day span. A healthy adult’s pituitary releases only 0.5-1.5 i.u. daily.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eUntil the mid 1980’s, the only available form of exogenous (occurring outside the body) GH was manufactured by taking the pituitary glands of dead corpses (like there are a lot of “live” corpses running around?) and grinding them up. (I am not joking!). The GH was then extracted and purified through a series of expensive procedures, packed and sold by prescription only for use by children suffering from stunted growth. About 1987, this form of GH was linked to a fatal brain disease called CREUTZFELD-JAKOB DISEASE, and removed from the market.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEnter Genetech and synthetic GH. The first synthetic GH was produced by genetically altering transformed mouse cells \/Ecoli. Natural GH has a 191 amino acid sequence where as the Protropin brand of GH produced by Genetech contains 192 amino acids in its sequence. This may have the affect of causing the body to produce GH anti­bodies which deactivate the GH. Most synthetics now contain the normal 191 amino acid sequence, of which there are over a dozen available today.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGH has 3 effects any athlete desires: GH helps the body burn more adipose (fat) tissue by promoting the release of fatty acids to be used as energy. Normally at rest, the body uses about an equal division of fat and carbohydrate calories. When the endocrine system senses a low circulatory level of glucose, the hypothalamus-pituitary-axis (HPA) reacts by releasing GH. The GH then triggers (through a series of enzymic\/chemical reactions) the release of fatty acids from adipose stores so metabolic energy requirements can be met. This means exogenous GH administration has been well documented to do the same.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGH has a very potent anabolic (protein synthesis\/tissue building) effect. In exerting anabolic effects, it can cause both hyperplasia (an increase in the number of muscle cells) and muscular hypertrophy (the enlargement of muscle cells). This change in cell number is permanent and therefore means more cells to make bigger. GH also has an anabolic effect on soft tissues such as tendons, cartilage, and other connective tissue. This means old injuries repair and strength increases due to stronger connective tissue… both at an accelerated rate. It is a well known fact that GH is a powerful anti-catabolic agent (protein sparing). This effect has allowed modern bodybuilders to retain or even add significant lean mass tissue during calorie restricted periods (cutting phases) and become the shredded monsters of the new era.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhen using GH many athletes were less than satisfied with their results. Most likely this was because they bought bogus GH. It was common to find GH for a hard-core pro bodybuilder cost about $35,000 or more, yearly. To test GH, most simply bought a pregnancy test kit, mix a vial of (hopefully) GH and place a drop or two in the test area. If the test result was “pregnant”..they had been screwed. Most pregnancy test kits test for elevated gonadoltropins (which HCG is and GH is not). For those few, whose bodies manufactured GH anti-bodies (and GH failed to work for you) sorry about your luck. GH, used properly, has overwhelmingly been renowned as a genetic equalizer if used for that purpose.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAny polled athlete chose to use GH as a performance enhancing drug should have first understand at least the basics of its actions.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGH itself is not responsible for the majority of the effects seen from GH use. Actually GH is only a precursor to the so-called “good stuff”. When GH passes through the liver, it is converted into INSULIN-LIKE GROWTH FACTORS (such as IGF-1). IGF-1 is a very active but unstable chemical, which is why the body waits until the last second to make it naturally. The liver has a limited capacity to convert excess GH into IGF-1 unless other chemical hormone levels are also elevated. Insulin, T-4\/T-3 thyroid hormones, gonadotropins, androgens\/anabolic hormones, and even estrogen and corticosteroids all play an important role in the positive effects of GH. So they too were often exogenously elevated in what was considered “the correct ratios” by the largest of the self administering athletes. For the liver to convert high levels of GH to IGF-1 several times a day and cause a high quality anabolic response, it was commonly noted that T-3 thyroid hormone and insulin also needed be increased to accomplish the desired effect. Triacana may be strong enough to increase thyroid activity, but Cytomel was considered to be a better choice. Though some seemed to disagree, most emphatically believed that a fast-acting insulin such as HUMULIN-R or Humalog was a better and safer choice of exogenous insulin since they allowed better timing and have a much shorter effective period. This allowed the athletes to time insulin activity with the active period of GH at the optimum absorption times such as upon waking and the first few hours after a work­out. The result was less chance of fat accumulation and a heightened anabolic response. Since GH suppresses natural T-3 thyroid hormone release, the exogenous administration of Triacana or Cytomel allowed for an elevated calorie intake that was utilized more for building muscle and soft tissue than for adipose tissue storage. Many pro bodybuilders used Clenbuterol and\/or ephedrine stacks with GH while dieting. Since Clenbuterol and\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEphedrine both suppress natural insulin release, they usually stacked the GH and Clenbuterol \/Ephedrine with a synthetic T-3 thyroid hormone and sometimes with insulin as well. The use of insulin was dependent upon whether it was a bulking or dieting phase and depending on how their body responded to exogenous insulin use.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*I can not stress enough how dangerous insulin use can be. Comas and death are quite possible if used wrong. If you wish to use it, please see a doctor for monitoring.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAAS and\/or Clenbuterol further enhance the anabolic effects of GH. From all but a few polled it was reported that excellent muscle mass gains resulted with the use of GH when other chosen hormone levels were also met (*also see “cycles”) and one could afford it. Also, beware of fake GH. It is more common than you may realize. It is an illegal drug and the black market is not always honest.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe question of dosage was a big one. For the purpose of stunted growth manufacturers of GH (due to pituitary hyophysially caused stunted growth) state 0.3 i.u. weekly per LB of body weight. So for a 235 LB bodybuilder that would equal 70.5 i.u. weekly, meaning a daily total of about 10-i.u. However, even 2-3i.u. daily did produce some nice results over a 6-8 week period when the other reported hormone requirements were met as well. Short high dosage burst cycles too were noted to create these results (which will be discussed later) by the more elite of those polled.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*GH is medically administered intramuscularly or subcutaneously (under the skin). *When multiple injections were utilized, I personally noted better results with subcutaneous administration.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*1-mg=2.7 i.u. of GH and some products are listed as such.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWith exception of those few whose insert states otherwise, the dry unmixed GH substance maybe stored at room temperature. Once the solution has been mixed with the dry GH powder, (SWIRLED, DO NOT SHAKEN) the mixture must be refrigerated and lasts for 24-hours before it begins to degrade. An interesting product has become available called DEPO-NUTROPIN that has an active-life of about a month. This would allow for fewer injections and a reduced price. Also, several patents run out this year so many overseas and less expensive GH preparation will soon be available in the U.S. by prescription only.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Though no negative side effects were reported, the available literature does list several serious ones: Kidneys and heart enlargement, high blood pressure, diabetes, thyroid hormone deficiency, and acromegaly. For the most part, they are rare to say the least and usually would be from extreme dosages and lengths of cycles. But like most hormones, you just do not know until it is a fact for you. Kind of scary, huh?\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhen GH was utilized with an insulin protocol, it was considered important to space injection periods between GH and insulin about an hour. Also if GH was utilized only twice daily, it was reported best to avoid natural high points of GH release such as first thing in the a.m., post-work out, and right before bed. This was if GH was utilized without insulin.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHuman Growth Hormone (somatotropin – also referred to as HGH, or HGH) is created by somatotropes in the pituitary gland of the human brain, the primary form consisting of a 191 amino acid chain. Somatotropes make up more than 50% of the pituitary gland and growth hormone is by far the most important hormone produced there. By the age of 60 most people will have approximately 80% less growth hormone in their system than when they were 20. When we are young, HGH is in big part responsible for the proper growth of bones, muscle, and other tissues. As we become adults, HGH is responsible for keeping muscles from wasting away, supports healthy immune system response, regulates aspects of our metabolic function dealing with increased fat metabolism and healthy body composition in later life, and maintains and repairs our skin and other tissues. HGH, or GH in short, is certainly an effective fat burner and anabolic agent, and is a protein secreted by the pituitary. Once secreted, it has the ability to influence various cells in the body to increase in number and size, as well as having the ability to enhance the movement of amino acids through cell membranes- thereby increasing the rate at which the cells can convert those molecules to usable proteins. It also causes cells to preferentially burn fat in lieu of carbohydrates.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003erHGH\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003erHGH is a human growth hormone produced by recombinant DNA technology derived from engineering Escherichia coli (E. coli), and is identical to the natural growth hormone in amino acid sequence and three-dimension structure. It has a molecular with of 22,125 daltons of which 191 amno acid sequence and structure are identical to the dominant form of the human pituitary growth hormone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEffects\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHGH has two distinct types of effects:\u003c\/div\u003e\n\u003cdiv\u003eDirect effects are the result of growth hormone binding its receptor on target cells. Fat cells (adipocytes), for example, have growth hormone receptors, and growth hormone stimulates them to break down triglyceride and suppresses their ability to take up and accumulate circulating lipids.\u003c\/div\u003e\n\u003cdiv\u003eIndirect effects are mediated primarily by an insulin-like growth factor-1 (IGF-1), a hormone that is secreted from the liver and other tissues in response to growth hormone. A majority of the growth promoting effects of growth hormone is actually due to IGF-1 acting on its target cells.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEffects on Growth\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGrowth is a very complex process, and requires the coordinated action of several hormones. The major role of growth hormone in stimulating body growth is to stimulate the liver and other tissues to secrete IGF-1. IGF-1 stimulates proliferation of chondrocytes (cartilage cells), resulting in bone growth. Growth hormone does seem to have a direct effect on bone growth in stimulating differentiation of chondrocytes.\u003c\/div\u003e\n\u003cdiv\u003eIGF-1 also appears to be the key player in muscle growth. It stimulates both the differentiation and proliferation of myoblasts. It also stimulates amino acid uptake and protein synthesis in muscle and other tissues.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMetabolic Effects\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGrowth hormone has important effects on protein, lipid and carbohydrate metabolism. In some cases, a direct effect of growth hormone has been clearly demonstrated, in others, IGF-1 is thought to be the critical mediator, and some cases it appears that both direct and indirect effects are at play.\u003c\/div\u003e\n\u003cdiv\u003eProtein metabolism: In general, growth hormone stimulates protein anabolism in many tissues. This effect reflects increased amino acid uptake, increased protein synthesis and decreased oxidation of proteins.\u003c\/div\u003e\n\u003cdiv\u003eFat metabolism: Growth hormone enhances the utilization of fat by stimulating triglyceride breakdown and oxidation in adipocytes.\u003c\/div\u003e\n\u003cdiv\u003eCarbohydrate metabolism: Growth hormone is one of a battery of hormones that serves to maintain blood glucose within a normal range. Growth hormone is often said to have anti-insulin activity, because it suppresses the abilities of insulin to stimulate uptake of glucose in peripheral tissues and enhance glucose synthesis in the liver. Somewhat paradoxically, administration of growth hormone stimulates insulin secretion, leading to hyperinsulinemia.\u003c\/div\u003e\n\u003cdiv\u003eHGH has been the supplement of choice for many professional athletes over the years. American football great, Lyle Alzado, claimed that 80% of all professional American football players, including himself, have taken HGH. HGH has amazing age-reversing effects that make it possibly the strongest anabolic substance available. Some of the benefits associated with HGH supplementation include the reversal of common diseases associated with aging, improved brain activity and function, it strengthens connective tissue which reduces the probability of injury, incredible weight loss without any loss in lean mass, reduces wrinkles by rejuvenating the skin, it raises energy levels and brightens mood, promotes muscle growth, improves libido, improves functions of the lungs which increases the level of oxygen in the blood stream, provides immune system support and Thymus function, and probably the most impressive characteristic is, its ability to produce more muscle cells, something no steroid can do.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePRODUCT DETAILS\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e191 amino acid chain recombinant growth hormone 10IU per vial\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePositives to taking growth hormone\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHGH does reduce body fat\u2028\u003c\/div\u003e\n\u003cdiv\u003eHGH does increase muscle mass and shape the body\u2028\u003c\/div\u003e\n\u003cdiv\u003eHGH does rejuvenate the body\u003c\/div\u003e\n\u003cdiv\u003eHGH makes your nails grow faster\u003c\/div\u003e\n\u003cdiv\u003eHGH makes your hair grow faster\u003c\/div\u003e\n\u003cdiv\u003eHGH makes your skin softer and nicer\u003c\/div\u003e\n\u003cdiv\u003eNegatives to taking growth hormone \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eProlonged HGH use does mess with your blood sugar (you need to eat more carbs if you get hypoglycemic episodes)\u2028\u003c\/div\u003e\n\u003cdiv\u003eProlonged HGH use can cause a mild carpal tunnel syndrome (which goes away when you stop taking it)\u003c\/div\u003e\n\u003cdiv\u003eHGH can cause mild water retention (which goes away when you stop taking it)\u003c\/div\u003e\n\u003cdiv\u003eHGH and temperatures\u003c\/div\u003e\n\u003cdiv\u003eCicconatropin is lyophilized (freeze dried) Growth hormone and this is how it withstands temperatures:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBefore reconstituted\u2028- if refrigerated between 2 – 8 degrees Celsius it’s good until expiration date.\u003c\/div\u003e\n\u003cdiv\u003eAt room temperature (up to 37 degrees celsius) it’s good for over 30 days.\u003c\/div\u003e\n\u003cdiv\u003eAt up to 45 degrees celsius it’s good for about a week.\u003c\/div\u003e\n\u003cdiv\u003eAfter reconstituted – it has to be refrigerated at all times. It’s good for 20 days with bacteriostatic water and 24 hours with normal water for injection.\u003c\/div\u003e\n\u003cdiv\u003eWater Bacterostatic water is sterile, has a specific pH level and contains a specific amount of benzyl alcohol as a bacteriostatic preservative, is in a specially formulated polyolefin vial to maintain it integrity and sterility, and has no adulterants that may damage\/breakdown what you are reconstituting or cause a deep tissue infection when injected. It’s what you have to use for IM and subcutaneous injections and reconstituting peptides or growth hormone. Normal water for injection will also work as a diluent for your growth and peptides but the injection is much more painful than bacteriostatic water and the active ingredient downgrade in normal water for injection is much faster than bacteriostatic water. Normal water for injection will keep your growth hormone or peptide active for only 24 hours where as bacteriostatic water will only start downgrading after 14 days. Bacteriostatic water is also much less painful to inject than water for injection. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSyringes Get the insulin type syringe with 100 markings on the side. They are very cheap and available in every local pharmacy store. They have the smallest needles. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMixing\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePull 1ml of water into the syringe and inject it into the vial with powder. GH molecules are very fragile – sensitive to heat and rapid movements. You should never shake the vial when mixing. You should not inject the water directly into the powder with force, but rather let it gently slide down the inside of the vial. If it bubbles up, you should put the vial in the refrigerator and leave it there for about 15 minutes. The bubbles will be gone by then. You should then gently turn the vial between your fingers until all of the powder has dissolved (it takes about 3-4 minutes).\u003c\/div\u003e\n\u003cdiv\u003eThe vials are under vacuum, so before you can take the GH out, you need to get rid of the vacuum. You take a fresh syringe, pull air into it and inject the air into the vial (not into liquid, but into air above the liquid). This will get rid of the vacuum. You can then pull out the GH as you need it. 10 markings on the 100-mark syringe = 1 IU.\u003c\/div\u003e\n\u003cdiv\u003eIf you want to take 2IU you will then draw 20 markings on the insulin syringe and 3IU will be 30 markings as in the picture below.\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eINJECTIONS\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome people pull the entire HGH vial content into the syringe and use the same for 5 injections. Others prefer to use a fresh syringe for every injection (which is smart in my humble opinion).\u003c\/div\u003e\n\u003cdiv\u003eThe favorite spot for HGH injections is subcutaneously, into the stomach fat – pinch some skin between your fingers and insert the needle at a 45-degree angle. Chose a different spot every time. Depending on the spot, you can either feel nothing or you can feel slight pain – you will learn your favorite spots in time. GH can also be injected into any muscle (thigh, shoulder, etc.) – it works the same either way.\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHGH DOSAGE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage depends on the purpose. People generally use 2IU per day for anti-aging purpose and 4IU per day for bodybuilding, weight loss and general fitness. In case of 4IU, people take 2IU in the morning and 2IU in the afternoon. Its best injected into stomach fat (exactly the same way as insulin).\u003c\/div\u003e\n\u003cdiv\u003eEffects are felt about a week into the first cycle (better sleep, skin improvement, etc.). Improved muscle tone is noticed about a month or two after the start (provided you do good workout and proper diet – plenty of proteins). Don’t just settle for any type of protein, because some manufacturers put in all sorts of crap (artificial flavors, sugar, etc. also some manufacturing methods produce low quality protein which is no good.). You want undenatured whey protein isolate created with micro cross flow filtration method and possibly get unflavored and unsweetened kind. I also suggest you take some good multi vitamin\/mineral supplements.\u003c\/div\u003e\n\u003cdiv\u003eThe effects are most noticeable in the initial few cycles so stay on it for as long as you can (3-4 months even).\u003c\/div\u003e\n\u003cdiv\u003eThe only noticeable side effect, which can happen to some people, is the carpal tunnel syndrome (tingling sensation in your palms and fingers. Feeling like your hands fall “asleep” sometimes, especially in the morning when you wake up). If it gets unbearable, people just stop the cycle for a few weeks and then resume when the carpal is gone. If it happens it does so only in initial few cycles when the carpal tunnel (through which nerves are passing to your palms) is too thin and doesn’t have time to adapt to the new rapid growth. Later on the tunnel adapts and in subsequent cycles the carpal is barely felt – if at all.\u003c\/div\u003e\n\u003cdiv\u003eYou can take your growth hormone once a day for example 2IU per day for anti ageing purposes. You can also split your growth and take 2IU three times per day or more for bodybuilding purposes with only one crucial rule that must apply. Not within an hour before you eat and not within two hours after you have eaten. When insulin spikes in your blood because of a meal it will destroy your growth hormone so we do not want growth hormone in the blood together with insulin from a meal.\u003c\/div\u003e\n\u003cdiv\u003e10 x 10.27iu HGH per vial (3,8mg) plus 10 x 1ml bacteriostatic water plus 10 x 1ml insulin syringes.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHGH is generally used to aid with recovery and it is recommended for use with EVERY cycle. While it is not really a stand alone anabolic product, it most certainly enhances the effect of regular anabolic’s for beyond expectation. It has also been reported that gains achieve from cycles are also for more easily maintained and the anabolic side effects are minimized. Add to this the fact that it’s also an anti-aging product so you look better in every way you possibly can!\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEutropin – Platinum Range:\u003c\/div\u003e\n\u003cdiv\u003eBeside containing high grade HGH, Eutropin contains Glycine which has been scientifically proven to stimulate the pituitary gland to release higher levels of you own, natural HGH. When you add synthetic hormone to your body there is a risk that your body may reduce production of its natural hormone and the addition of the Glycine is an attempt to reduce this phenomenon. (Please read the Product Insert for advice as to how to minimise this effect)\u003c\/div\u003e\n\u003cdiv\u003eEutropin contains additional excipients which buffer the HGH so as to allow a higher degree of effectivity. According to tests, Eutropin is ±12% more effective than most well known, reputable brands.\u003c\/div\u003e\n\u003cdiv\u003eThe bacteriostatic water contains a preservative which slows down microbial growth in the reconstituted HGH thereby extending the life thereof by up to 4 times.\u003c\/div\u003e\n\u003cdiv\u003e3.8mg HGH per vial which is 10.27iu. This takes care of the small amount one can’t draw out of the vial and ensures you get a full 10iu HGH.\u003c\/div\u003e\n\u003cdiv\u003eContains 10 x 1ml insulin syringes to get you going as soon as you get your kit. No need to run around for syringes. You can also purchase more from us.\u003c\/div\u003e\n\u003cdiv\u003eWe all know we can’t get every last drop of liquid out of the vial. We’ve worked out that this is about 0,025ml and by adding an extra 0,27iu of HGH you are ensured of getting a full 10iu out of the vial.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53796606443812,"sku":null,"price":2150.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_f8a03dfb-4cee-4234-96e8-e339b142d488.jpg?v=1778125023"}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/collections\/rn-image_picker_lib_temp_9f5df2ac-2d5c-4af4-a6ee-6d9ce63eae8b.png?v=1777534609","url":"https:\/\/ultrafizique.co.za\/collections\/upa.oembed","provider":"UltraFizique","version":"1.0","type":"link"}