{"title":"OXYGEN LABS","description":null,"products":[{"product_id":"oxygen-labs-test-e-250-10ml","title":"Oxygen Labs Test E 250\/10ml","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB E250(250MG\/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\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\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":53647729066276,"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_e9abff89-a1da-45bd-8683-fa68d2c97cd6.png?v=1777820673"},{"product_id":"oxygen-labs-test-cyp-250mg-10ml","title":"Oxygen Labs Test CYP 250mg\/10ml","description":"\u003cp\u003e\u003cspan\u003eOXYGENSLAB 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\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":53647821111588,"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_8d0200c2-31e6-4a5f-9660-89603251f14a.png?v=1777820818"},{"product_id":"oxygen-labs-anavar-20mg-50-tabs","title":"Oxygen Labs Anavar 20mg\/50 Tabs","description":"\u003cp\u003e\u003cspan\u003eOXYGENSLAB ANAVAR 20(20MG OXANDROLONE\/TAB=50TABS)\u003c\/span\u003e\u003c\/p\u003e\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\u003eSTANDARD DIHYDROTESTOSTERONE\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\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOxandrolone 20 is typically used for\u003c\/div\u003e\n\u003cdiv\u003eCutting and hardening of skeletal muscles.\u003c\/div\u003e\n\u003cdiv\u003eThose who wish to loose weight without exercise.\u003c\/div\u003e\n\u003cdiv\u003eTreating muscle wasting diseases and osteoporosis.\u003c\/div\u003e\n\u003cdiv\u003eHelping burn victims regain muscle.\u003c\/div\u003e\n\u003cdiv\u003eContents per box:\u003c\/div\u003e\n\u003cdiv\u003e56 Green tablets in a labeled bag or labeled glass bottle.\u003c\/div\u003e\n\u003cdiv\u003eRecommended dose\u003c\/div\u003e\n\u003cdiv\u003eAlways take Oxandrolone 20 exactly as prescribed by your doctor. If you are unsure, ask your pharmacist. Unless otherwise prescribed by a doctor, the normal dose is:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMen\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFirst time users\u003c\/div\u003e\n\u003cdiv\u003eTake dose every 12 hours as follows: 20mg 30 minutes pre-training and 20mg 12 hours later for 2 weeks. Then increase daily dosage by 10 mg as follows: one 20mg 30 minutes pre training and two 20mg doses. These three doses to be taken at 8 hourly intervals.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAdvanced users\u003c\/div\u003e\n\u003cdiv\u003eTake 20mg doses 4 times per day at 6 hourly intervals. Do not exceed 20mg per dose or 80mg per 24 hour period.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWomen\u003c\/div\u003e\n\u003cdiv\u003eNot recommended for woman as 1 capsule exceeds the daily recommended dose\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDuration\u003c\/div\u003e\n\u003cdiv\u003eMinimum recommended duration is 6 weeks and maximum duration is 12 weeks.\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53647951102244,"sku":null,"price":650.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_7eacf37d-91e4-48f9-b8b6-c86e47053cf3.png?v=1777820977"},{"product_id":"oxygen-labs-cock-bomb","title":"Oxygen Labs Cock Bomb","description":"\u003cp\u003e\u003cspan\u003eOXYGENSLAB COCKBOMBS 70MG(VIAGRA 50MG SIDENAFIL CITRATE\/TAB+CIALIS 20MG TADALAFIL\/TAB=10 TABS )\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eVIAGRA\u003c\/div\u003e\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\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCIALIS\u003c\/div\u003e\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","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53648788947236,"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_fa86d625-e087-4bcf-bd46-2fbee35c28d0.png?v=1777823265"},{"product_id":"oxygen-labs-test-e-250mg-20ml","title":"Oxygen Labs Test E 250mg\/20ml","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB E250 JUMBO(250MG\/ML TESTOSTERONE ENANTHATE=20ML)\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\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\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":53671188365604,"sku":null,"price":650.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_1e925411-6239-4bec-8bbe-318f1cfb5fb3.png?v=1777862427"},{"product_id":"oxygen-labs-test-cyp-250mg-20ml","title":"Oxygen Labs Test CYP 250mg\/20ml","description":"\u003cp\u003e\u003cspan\u003eOXYGENSLAB TEST CYP 250 JUMBO(250MG\/ML TESTOSTERONE CYPIONATE=20ML)\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\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":53679423586596,"sku":null,"price":640.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_b3277473-ece9-4673-86e9-d7fed4b1c7cb.png?v=1777897119"},{"product_id":"oxygen-labs-ibutamorenmk-677","title":"Oxygen Labs Ibutamoren(MK-677)","description":"\u003cp\u003e\u003cspan\u003eOXYGENSLAB SARMS NUTROBOL(MK-677)(50G\/ML=30ML).\u003c\/span\u003e\u003c\/p\u003e\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","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53679565373732,"sku":null,"price":600.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_a76cbdbb-6496-4a86-9a0f-3894ab1670a4.png?v=1777897404"},{"product_id":"oxygen-labs-mastron-enan-200mg-10ml","title":"Oxygen Labs Mastron ENAN 200mg\/10ml","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB MASTERON ENANTHANATE 200(200MG\/ML DROSTANOLONE ENANTHATE=10ML)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 25-40\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 62-130\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 FOR PROPIONATE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e10-14 DAYS FOR ENANTHANATE\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 300-500-mg weekly Women 100-350mg 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: None\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: 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\u003eNoted Comments: High Androgenic\/Moderate Anabolic\/Moderate anti-estrogenic\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: None, DHT derivative\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Low suppression in most cases\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMasteron is a highly androgenic injectable steroid that is a synthetic derivative of DHT (dihydrotestosterone). Since DHT does not aromatize to estrogens, there was no noted water retention during administration. If a bodybuilder had achieved a low body fat level, this drug was reported to dramatically improved shape and hardness in muscle tissue while augmenting the vascular appearance of a contest ready athlete. Normally, Masteron was used only during the last 3-5 weeks before a show as part of a pre-contest stack. In this case, 100-mg was commonly injected every second or third day (2-3 times weekly) by males and at a dosage of 50mg every other day by most women whom reported use. Additionally, according to available literature, Masteron is quite anti-catabolic and anti-estrogenic in nature due to receptor inhibition. So the reported characteristics of this drug do have supportive clinical validation to consider.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCombined with so- called mass steroids, Masteron did aid in a rapid build-up of strength and mass even with its relatively moderate anabolic qualities. However, Masteron was not reported to be the best choice for this purpose by those polled. DHT can promote hair loss and prostate disorders in prone individuals though it is not well documented as to whether or not deviants of the DHT structure can in all case do the same.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMasteron has a receptor binding ability 3-5 times greater than that of testosterone. This means that the drug can hang out longer in androgen receptor-sites and is not easily displaced. The result should be increased AAS activity.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAn interesting facet of Masteron is the way it acts as an anti-estrogen. This is due to its ability to compete for the aromatase receptor. As the reader is aware of by now, many AAS are capable of conversion to estrogens. The process is caused by an enzyme called aromatase. (Of course the process of AAS conversion to estrogen is referred to as aromatization) If a drug has the ability to inhibit the enzyme at its own receptor and still act as a powerful non-aromatizing AAS, its interesting and unusual to me.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMy personal experiences with this drug have always been favorable with no negative side effects. Additionally I feel that the drug has had value as a sort of AAS moderator. Let me explain this. Masteron has a high SHBG and albumin binding rate. Since these two hormone binding proteins prevent AAS from merging with their receptors, some would assume this is a bad thing. Masteron is 3-5 times more active than testosterone, so the unbound portion circulating in the blood stream goes a long way. Since the drug binds a higher percentage of SHBG and albumin, any other AAS co-administered with it remains in an unbound\/active\/free state to a greater extent and is able to induce a greater response. This is an example of noted drug synergy common to protocols reported as most effective yet requiring lower dosages to accomplish a specific result. The implication is that lower dosages of co-administered drugs allowed a decrease in negative side effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eA point of interest is that two OTC prohormones in the United States have similar effects to Masteron (though oral administration is not the most effective delivery method and injection type administration would be illegal in most countries) (1) 5a-androst-1-en-3b,17b- dione (2) 5a-androst-en-3b,17b-diol. My personal research has shown that there is a realistic approach to an orally administered version of the latter of the two drugs that has shown great promise. We will complete the final testing soon before turning the project over to the crazies at Hazardous Materials Supplements. Personally, I am totally stoked about the project due to its vast application potential in the world OTC supplemental industry. The key is a compound from Eastman that allows lipophilic substances to become hydrophilic (Oil soluble to water soluble). This means that the high expense of effective supplements like methoxyisoflavone (and its deviants) to be reduced due to lower dosage requirements.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Since this drug clears the body quickly, it was a favorite for tested competitors.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMastaron is a synthetic derivative of dihydrotestosterone, displaying a potent androgenic effect that is responsible for increases in muscle density and hardness and a moderate anabolic effect that creates a positive nitrogen balance in humans and promotes protein synthesis. Since it is a derivative of dihydrotestosterone, dromastolone does not aromatize in any dosage and thus it cannot be converted into estrogen. Therefore, estrogen-related water retention is eliminated. Mastaplex combines the fast-acting propionate form with the longer acting enanthate form.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53679565734180,"sku":null,"price":670.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_53454169-2d48-436f-b32b-2bc8632a3d99.png?v=1777897578"},{"product_id":"oxygen-labs-winstrol-20mg-50-tabs","title":"Oxygen Labs Winstrol 20mg\/50 Tabs","description":"\u003cp\u003e\u003cspan\u003eWinstrol is the most popular and well-known brand name of the androgen and anabolic steroid Stanozolol. It is a derivative of dihydrotestosterone (DHT) which makes Winstrol like testosterone\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eImportantly, Winstrol is considered to have a more powerful anabolic to androgenic effect compared with testosterone. In the body, up to 10% of testosterone is naturally converted to DHT.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStanozolol is available in both oral and injectable forms. As to be expected, each of these Winstrol applications come with different half-lives:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOral half-life:\u003c\/div\u003e\n\u003cdiv\u003e9 hours\u003c\/div\u003e\n\u003cdiv\u003e Injection half-life:\u003c\/div\u003e\n\u003cdiv\u003e24 hours\u003c\/div\u003e\n\u003cdiv\u003eThere is no difference between the strengths of oral and injectable this compound, 0. 5mg of either type is the same amount – what does differ is how quickly they are absorbed and used up by the body which is reflected in their half-lives listed above.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDespite its negative effect on the liver, oral Winstrol is often the first choice particularly for those steroid users who are new to cycle Winstrol in order to avoid the painful injections.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTablets are mostly available in 10mg and 50mg strengths so is easily administered for any level of user including if you’re just starting out on a low dose or are female. Steroid users wanting the maximum dosage, which might reach up to two tablets per day, for a total of 100mg\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53679569568036,"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_5b33af66-efef-4f6f-8050-0f014e0ffe5f.png?v=1777897845"},{"product_id":"oxygen-labs-dianabol-20mg-50-tabs","title":"Oxygen Labs Dianabol 20mg\/50 Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB DIANABOL(50MG 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":53679573532964,"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_8d6d2caf-21b4-47a8-9839-6d3c304a267f.png?v=1777897967"},{"product_id":"oxygen-labs-test-mix-blend-500mg-10ml","title":"Oxygen Labs Test Mix Blend 500mg\/10ml","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENS TEST BLEND 500 (500MG\/ML HYBRID MIX=10ML)\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\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53680237543716,"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_8dc8b767-e38e-4291-a8fd-497c231a6840.png?v=1777899715"},{"product_id":"oxygen-labs-primobolan-200mg-10ml","title":"Oxygen Labs Primobolan 200mg\/10ml","description":"\u003cp\u003e\u003cspan\u003eOXYGENSLAB PRIMABOLIN 200(200MG METHENOLONE ENATHATE=10ML)\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 44-57\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 88\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 10-14 DAYS\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anabolic\/Androgenic Steroid (Oral) OR (FOR INJECTION)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 200-400-mg weekly Women 50-150-mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Light at dosages of up to 200-mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Very 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\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\u003eDHT Conversion: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases: HPTA function: Only slightly in dosages over 300mg weekly and due to prolonged periods of use.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePrimobolan Depot is similar to the acetate tablets with a few differences. Though it is a predominantly anabolic steroid, being a DHT derivative it also maintains some androgenic qualities. For this reason, it does have virilizing aspects to consider. This explains the improved strength and harder appearance polled users obtained in part. Naturally since it does not convert to estrogens, induced low water retention and a distinct lack of gyno and female pattern fat deposits was noted as avoided. In fact, the drug does theoretically act as an anti-estrogen to a lesser extent.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Women reported they were able to avoid some virilizing aspects with Proscar.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMost first time male (AAS novices) users reported an 8-16 lb gain after 6-8 weeks of 200mg weekly dosages. The new muscle was of a high quality and usually was retained quite well after discontinuance. This may have been due to Primobolan depot having only a slight negative effect upon the Hypothalamic-Pituitary-Testes-Axis (HPTA). In short, this drug was noted to only slightly shut down natural testosterone production and therefore there was not a significant lack of testosterone or an elevation in circulatory estrogen post- cycle. This was especially true if dosages were kept at 200-300-mg weekly for no more than 6-8 weeks for males. (Women don’t have testes, remember?). For this reason, older males made excellent and reasonably permanent gains with little interruption in their already lower natural androgen production. For stacks focusing on this issue, Oxandrolone and Android were said to work very well with Primobolan Depot. Primobolan based stacks containing nandrolones and\/or Equipoise were commonly utilized for this purpose also.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*A point of interest: Primobolan Depot (like Winstrol Depot) has been noted to possess excellent site- injection qualities. This means that a lagging body part became the injection site for dosages. Most who used this type of\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWomen actually should not have used high dosages of any DHT product or derivative. DHT has excellent hardening effects, but also has masculinizing aspects. An often noted as safer method for use of such drugs was to also co-administer a 5-ALFA-REDUCTASE INHIBITOR such as Proscar. Its active ingredient is Finasteride which blocks testosterone’s conversion to DHT. Yes, that is the pill guys take to stop their hair -line from receding. 1mg daily was said be enough when women stayed in the 50-200mg weekly dosage range when using Primobolan Depot.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSince Primobolan Depot actually has an active-life of closer to two weeks, injections were commonly administered weekly by those whom reported lower dosage use. But due to predominantly 50-mg\/ml ampules being the most available a 4-ml\/200mg injection “hurt” to an excessive degree for those whom employed the higher dosage protocols. So twice weekly injections was the normal method chosen.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*It was my experience that Primobolan was one of the few steroids capable of increasing lean mass during calorie restricted periods therefore remaining effective even in calorie deficit induced catabolic environments. This drug is an Enanthate ester and should provide an 8 day active life. Strangely enough it does provide the above listed active-life range though the ester is an enanthate.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePrimo 100 for intramuscular injection, contains methenolone enanthate\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMethenolone Enanthate is a DHT based anabolic steroid. When it interacts with the aromatase enzyme it does not form any estrogens. It is used by people who are very succeptible to estrogenic side effects, having lower estrogenic properties than Nandrolone. Methenolone is available as an injection or as an oral. The injection is naturally regarded as having a higher bioavailability. Its an enanthate ester which is quite long-acting. Because it by-passes hepatic breakdown on the first pass, it also has a higher survival rate. The tablets are in a short-lived acetate form. Methenolone is not 17-alpha-alkylated, but 1-methylated for oral bioavailability. This reduces the stress on the liver, but also the availability. It is considered one of the safer steroids, meaning it has a very little side effects. Methenolone has no estrogenic side effects, and its effects on cholesterol levels are minimal. In doses of 200 mg or less (intramuscular) blood pressure is rarely altered.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePossibly one of the safer anabolic steroids for females due to very low virilization effects in short-term usage. Of course, this is not a blanket-statement and individual results (dependent on doses and tolereance) will vary.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMethenolone is also not overly suppressive of the HPTA axis, although how suppressive is debatable. For this reason, many bodybuilders use it in between steroid cycles during their “off-time” to help maintain their gains and strength. The long term safety of such a practice possibly dangerous and can lead to permanent suppression of the HPTA.\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53680418226468,"sku":null,"price":880.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_5954ea00-2f44-4b9b-a68e-552607d16be1.png?v=1777899954"},{"product_id":"oxygen-labs-nolvadex-25mg","title":"Oxygen Labs Nolvadex 25mg","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e\n\u003cp\u003eOXYGENSLAB NOLVADEX(25MG TAMOXIFEN CITRATE\/TAB=30TABS)\u003c\/p\u003e\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":53680539894052,"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_241120d2-44fa-4e30-b5da-8ed59a4ec6ec.png?v=1777900200"},{"product_id":"oxygen-labs-superbulk-650mg-10mltest-cyp-nandrolone-deconate-tren-e","title":"Oxygen Labs SuperBulk 650mg\/10ml(Test Cyp,Nandrolone Deconate,Tren E)","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB SUPER BULK 650 (650MG\/ML HYBRID MIX=10ML)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e250MG\/ML TESTOSTERONE CYPIONATE \u003c\/div\u003e\n\u003cdiv\u003e200MG\/ML NANDROLONE DECOANATE \u003c\/div\u003e\n\u003cdiv\u003e200MG\/ML TRENBOLONE ENANTHATE \u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53680543564068,"sku":null,"price":800.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_4d411144-c6cf-4308-8844-bd85d19574c5.png?v=1777900448"},{"product_id":"oxygen-labs-testolonerad-140","title":"Oxygen Labs Testolone(RAD-140)","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB SARMS TESTOLONE DROPS(RAD-140) 30MG\/TABLET=30ML.\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":53680544153892,"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_239daa82-8174-4de9-8ea6-989d14c80e3e.png?v=1777900566"},{"product_id":"oxygen-labs-clenbuterol-tabs","title":"Oxygen Labs Clenbuterol Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB 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":53680544350500,"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_46bd7d47-b9e5-4481-a360-569d628bcb2d.png?v=1777900722"},{"product_id":"oxygen-labs-tren-e-200mg-10ml","title":"Oxygen Labs Tren E 200mg\/10ml","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB TRENBOLONE 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\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\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\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\u003cdiv\u003ephysiological response. The hexahydrobenzylcarbonate and enanthate esters, which release at slower rates, prolong the physiological response with a relatively flat absorption curve over the duation of the injection life-cycle.\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.\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":53680546021668,"sku":null,"price":640.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_29c671a7-3b40-495d-85b5-e253be0b862e.png?v=1777900817"},{"product_id":"oxygen-labs-anapolan-50mg-50-tabs","title":"Oxygen Labs Anapolan 50mg\/50 Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e\n\u003cdiv\u003eOXYGENSLAB ANAPOLON 50(50MG OXYMETHOLONE\/TAB=50TABS)\u003c\/div\u003e\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\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe most common daily dose of Anapolon is 100mg, but even at that dosage side-effects like water-retention, elevated blood pressure, acne, hair loss, blood clotting changes, gynocomastia, liver toxicity and mood swings are very often reported. Using aromatase inhibitors to control estrogen aromatization will be ineffective as this drug does not directly convert into estrogen. It was suggested that oxymetholone can activate the estrogen receptor, similar to, but more profoundly than the estrogenic androgen methandriol. Supplements like Milk Thistle can be taken to help keep liver enzyme levels between safe ranges.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhen used correctly and responsibly Anapolon makes a great addition to any bulking cycle. The best results are seen when Anapolon is stacked in conjunction with other injectable steroids. Anapolon makes a great kickstart to a bulking cycle and is normally used during the first 3 to 4 weeks of the cycle. Avoid using other oral steroids in the same stack, because when combined with other 17-alpha alkylated compounds the hepatotoxic effects will become impossible to control and serious liver damage may occur.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEach box contains: 56 x 50mg of the active ingredient Oxymetholone (28 dark green tablets packed in a plastic bag or brown glass bottle depending on the region of distribution)\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53680547496228,"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_4f55bfe1-9c95-4dd2-a6f0-26d2a9b608e6.jpg?v=1777900950"},{"product_id":"oxygen-labs-supadrol","title":"Oxygen Labs Supadrol","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB SUPERDROL(Methasteron 10mg p\/tab=50TABS)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSuperdrol (called methasteron, and methyldrostanolone) is the name of the most popular and the well-known product to contain the 2a,17a-dimethyl-5a-androst-3-one-17b-ol (methyldrostanolone) steroid. Superdrol is probably the most effective and widely used oral anabolic steroid of the last decade. It is basically Masteron lacking the ester chain. As an oral steroid, it is equipped with a c-17aa modification allowing it to survive the first pass through the liver.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAlthough this hormone was originally researched by a pharmaceutical company called Syntex Corporation, superdrol with its c-17aa modification never made it as a prescription drug. Its counterpart drostanolone (masteron), which had an ester chain, was a commercially distributed drug. Although methasterone is first mentioned in literature in 1956, it sat in the textbooks of pharmacology for five decades until 2005 when it was rediscovered and sold under the brand name “Superdrol” by Designer Supplements LLC.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAs a steroid, superdrol provides very dry and hard gains that are really noticeable after about the second week of using the product. Gains of as much as 15lbs to 30lbs of muscle mass in a short 4 week cycle were very commonly reported by users. Gains in strength are also very noticeable, with most users reporting a 15% to 25% increase in their maximum lifts after using this drug for only a couple of short weeks.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMethasterone is a oral steroid with a 17aa group; thus, it is very liver toxic. Since it was sold over the counter for so many years, there are many reported instances of people abusing this steroid by staying on the drug for more than the recommended 4 to 6 weeks.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe recommended use for this product is about 20mg to 40mg per day, depending on goals. With the cycle not being any longer than 6 weeks. Superdrol has been widely reported as being abused, with guys staying on cycle as long as 12 weeks, with devastating results on their liver functions.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe product is toxic to your liver from day one of use, but the problems only become permanent if the liver is not given a proper break and allowed to recover. Since liver support helps minimize possible risk of side effects, the use of on-cycle support like has been a mainstay for guys doing superdrol cycles.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSince using this steroid in the first 4 to 6 weeks of a cycle would ensure rapid and solid gains, superdrol became a favorite drug for bodybuilders to jump-start their cycles. This leaves the slower released injectable steroids to kick in during the later part of the cycle. Allowing users to solidify the gains made on methasterone while still making progress in strength.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis product has always stacked well with most injectable steroids or other hormones that do not have a c-17aa modification. Keep in mind, your liver would not be able to handle another oral stacked with superdrol. For bulking, Deca Durabolin and 19-Norandrosta 4,9 diene- 3,17 dione are the best stacked compounds, and for cutting, trenbolone. Since this steroid is particularly tough and hard to breakdown, this product is not recommended for use for any longer than 4 weeks due to severe liver toxicity. Though, some experienced bodybuilders who use N2Guard during the cycle report using superdrol for 6 weeks with good results.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAs with most oral steroids, the half-life of superdrol ranges between 8 to 9 hours, with users taking the product as many of 4 times per day to maintain a steady blood level.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis steroid does not aromatize, so it will not cause any estrogenic side effects, so water retention is never a problem with this product. Some users report gynacomestia symptoms that seem to come more from this hormone taking up more of the SHBG activity; thus, leaving more free testosterone to be turned into estrogen. There is no science to support this theory, but what is certain is that it’s a chemical impossibility for methyldrostanolone to turn into an estrogen.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome side effects, like oily skin and acne, seem to be reported but not as much when compared to dianabol or anadrol. The strong androgenic nature of this hormone does cause some of the most common androgen side-effects like loss of hair on the head and increased hair growth on the body. Again, this is not as bad as WInstrol or heavy Doses Of Anavar.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53680549462308,"sku":null,"price":340.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_39ae06b6-237b-4724-b7d5-bb1069bf6d2b.png?v=1777901116"},{"product_id":"oxygen-labs-anavar-10mg-30-tabs","title":"Oxygen Labs Anavar 10mg\/30 Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eAnavar is fast acting steroid derived from DHT (dihydrotestosterone) with a half-life of just 8 to 10 hours. It has been a widely used, respected and very popular steroid for a long time and is one of the few that can also be used by females because of its mild androgenic effects.\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhile Anavar is mildly toxic to the liver, as we would expect with an oral steroid, its hepatotoxicity level is minimal compared with many other steroids, making this an ideal choice for beginners.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhen looking to purchase this steroid you are not likely to find it listed or labelled using that name on any current formulations; instead, it goes by the chemical name Oxandrolone. Despite this, the name Anavar is still commonly used to describe this compound.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAnavar has a powerful anabolic rating, yet at the same time is not a steroid that is as effective for bulking for men as other steroids are. While it can contribute to bulking with high quality weight gain with no water retention, Anavar is most powerful for use as a cutting steroid as well as for enhancing athletic performance.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWomen who use Anavar will however find that it can add impressive lean muscle gains to the physique, and this is the main anabolic steroid that is suitable for woman to use for this purpose.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThere are many reasons for the popularity of Anavar:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIt is an oral steroid so it’s easy to administer It can be used by both males and females It has minimal side effects compared with many other steroids\u003c\/div\u003e\n\u003cdiv\u003eMost importantly, Anavar has exceptional benefits for people who know exactly what they’re using it for, and almost all the time this is for the purpose of improving the physique through fat loss while retaining muscle mass, and for enhancing performance.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53680551231780,"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_72c58012-43f9-4512-8349-4ea88416eb5c.png?v=1777901216"},{"product_id":"oxygen-labs-hcg-5000","title":"Oxygen Labs HCG 5000","description":"\u003cp\u003e\u003cspan\u003eOXYGENSLAB PREGNYL(HCG) 5000(5000IU CHORIONIC GONADOTROPIN\/AMP=1X 1ML 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":53680554770724,"sku":null,"price":330.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_c53921f7-cca8-4d8c-beb9-e1706edbfd0f.png?v=1777901332"},{"product_id":"oxygen-labs-cjc1295","title":"Oxygen Labs CJC1295","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB CJC-1295(2MG =1 POWDER+WATER))\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCJC-1295 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\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCJC-1295 DAC is a long acting Growth Hormone Releasing Hormone, 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 GHRP-6 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 Hexarelin or GHRP-2. 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\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCJC-1295 DAC vs. CJC-1295 No DAC\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCJC-1295 DAC and CJC-1295 (also known as Modified GRF 1-29) 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\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCJC1295\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\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\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePRODUCT DETAILS\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e2000mcg per vial\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eConstitute\u003c\/div\u003e\n\u003cdiv\u003e1ml of water depending on the brand you use.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage\u003c\/div\u003e\n\u003cdiv\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\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFunctions\u003c\/div\u003e\n\u003cdiv\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\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTIPS\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\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\/div\u003e\n\u003cdiv\u003eIntramuscular and subcutaneous routes lead to different onset times but roughly similar peaks and declines.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53684072055076,"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_b1f8b5da-dd33-4c0a-91cf-6a25129e5de1.png?v=1777912307"},{"product_id":"oxygen-labs-supersize-650mg-10mgtren-deca-test","title":"Oxygen Labs SuperSize 650mg\/10mg(tren,deca,test)","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB SUPERSIZE 650 (650MG\/ML HYBRID MIX=10ML)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e250MG\/ML TESTOSTERONE CYPIONATE \u003c\/div\u003e\n\u003cdiv\u003e200MG\/ML BOLDENONE UNDECLYNATE \u003c\/div\u003e\n\u003cdiv\u003e200MG\/ML TRENBOLONE ENANTHATE\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53684115800356,"sku":null,"price":800.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_6eeabebc-6be0-4663-8f21-3e5dae0138a1.png?v=1777912504"},{"product_id":"oxygen-labs-supercut-mix-350mg-10mltest-prop-masterone-tren-ace","title":"Oxygen Labs SuperCut Mix 350mg\/10ml(Test prop,masterone,tren ace)","description":"\u003cp\u003e\u003cspan\u003eOXYGENSLAB SUPER CUT 350(cutting blend) (350MG\/ML HYBRID MIX=10ML)\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e150MG\/ML TESTOSTERONE PROPIONATE  \u003c\/div\u003e\n\u003cdiv\u003e100MG\/ML TRENBOLONE ACETATE \u003c\/div\u003e\n\u003cdiv\u003e100MG\/ML DROSTANOLONE PROPIONATE \u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53684283343140,"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_4d42116c-3177-494a-b99c-d1c1cc45ff55.png?v=1777912690"},{"product_id":"oxygen-labs-equipoise-350mg-10ml","title":"Oxygen Labs Equipoise 350mg\/10ml","description":"\u003cp\u003e\u003cspan\u003eOXYGENSLAB EQUIPOISE 350(350MG\/ML BOLDENONE UNDECYLENATE=10ML)\u003c\/span\u003e\u003c\/p\u003e\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\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\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","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53684558758180,"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_c79c8bd6-15e0-4b94-9b93-dde33336ece6.png?v=1777913095"},{"product_id":"oxygen-labs-proviron-25mg-30-tabs","title":"Oxygen Labs Proviron 25mg\/30 Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB PROVIRION ORAL(25 MG MESTEROLONE\/TAB=30TABS)\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 PROPIONATE\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\u003ch1\u003e\u003c\/h1\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53684614496548,"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_7636424f-b682-40ce-8b29-38becb2f5ed0.png?v=1777913214"},{"product_id":"oxygen-labs-yohimbine-and-cardarine-tabs","title":"Oxygen Labs Yohimbine and Cardarine Tabs","description":"\u003cp\u003e\u003cspan\u003eOXYGENSLAB YOHIMBINE + CARDARINE ORAL(20MG\/tab 10MG YOHIMBE HCL+10MG CARDARINE=50tabs)\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eDrug Class:\u003c\/span\u003e\u003cspan\u003e sympatholytic \u003c\/span\u003e\u003cspan\u003e \u003c\/span\u003e\u003cspan\u003eantagonist (blocker) of alpha-2 adrenergic receptors\u003c\/span\u003e\u003cspan\u003e (inject)\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eAverage Reported Dosage: Men  and Women 5-20 mCg per day\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eHigh Blood Pressure: Some reported high blood pressure\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eYohimbine HCL is a sympatholytic agent, which means that its main function is to oppose stimulation of the sympathetic nervous system. In this case, it is a specific antagonist (blocker) of alpha-2 adrenergic receptors\u003csup\u003e246\u003c\/sup\u003e. Yohimbine HCL is a prescription drug in many countries, and is used, among other things, to increase low blood pressure, to dilate the pupil of the eye, treat male impotence and stimulate fat loss. Common brand names include Aphrodyne,Viritab, Yocon and Yohimex. Due to the fact that yohimbine occurs naturally, it is in somewhat of a gray area in the U.S., where it is being tolerated as on OTC supplement ingredient at this time. It is likewise readily available here, and is a very common ingredient in the enormously crowded market for fat loss products.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eTo understand how yohimbine works, you need to first understand that adrenergic lipolysis (fat loss stimulated by adrenergic or sympathomimetic hormones) in human adipose tissue is regulated in a dual nature by adrenoceptors (the receptors that respond to these hormones). Most notably, activation of the beta-1, beta-2 or beta-3 subtype increases the process of lipolysis; while activation of alpha-2 receptors diminishes it. Fat cells appear to be the only type of cells in the human body that exhibit such dual regulation by adrenoceptors\u003csup\u003e247\u003c\/sup\u003e. By antagonizing alpha 2 receptors, yohimbine can shift the balance of sympathetic activity to a place that measurably stimulates lipolysis\u003csup\u003e248\u003c\/sup\u003e. This is further enhanced by an intrinsic ability to increase synaptic norepinephrine release\u003csup\u003e249\u003c\/sup\u003e, one of the body’s own natural lipolytic hormones. In effect, it serves both beta stimulating and alpha blocking properties, an ideal combination if we want to stimulate fat loss.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eThe typical dose used for fat loss is around 15-20mg, which is taken the first thing in the morning on an empty stomach. Some may opt to take a second dose later in the day, but this is an individual decision based on desired effect and tolerance to the drug’s effects. Levels do build in the body over time, so it often takes a few weeks before you really notice any effect. When used at the recommended doses yohimbine is usually well tolerated. This is supported by not only anecdotal data but medical studies, which have shown single doses as high as 21.6mg, or daily cumulative doses as high as 43.2 mg, to have no significant impact on blood pressure or heart rate.This is, of course, the exact opposite of what\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003ewould be expected of a beta-agonist like ephedrine, which is a potent stimulant. Side effects are still always possible with this drug however, and can include increased heart rate, sweating, nervousness, tremor, irritability, headache, dizziness and\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eflushing. But these effects do tend to be very dose-related, so it is important not to overuse this drug in an attempt to produce a more dramatic fat-loss effect. One of the great advantages to yohimbine is that it can be a relatively comfortable compound to use. If taken in too high a dosage, you will see that change very quickly.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eOverall I have to say that, at least as an oral product, the effects of yohimbine are not extremely dramatic. Most users notice “something” but rarely rave about a dramatic and rapid shedding of fat. It is of note that yohimbine seems to work most effectively in the fasted state, and its lipolytic action may be blocked if it is taken with a meal\u003csup\u003e250\u003c\/sup\u003e. This may account for some of the negative reports at least. Still, you are likely to notice much greater fat loss with clenbuterol or an E\/C (ephedrine, caffeine) stack than you will this agent. But then again, you would have to endure the strong stimulant properties of these drugs as well. It is also important to point out that several topical yohimbine HCL products have been introduced to the market recently, and many consumers are reporting greater success with these formulations. Some are claiming a strong “spot loss” effect, even to the point of being successfully used to locally treat lipomastia (fat buildup under the nipple that resembles\/precedes hard-tissue gynecomastia). Although this is a controversial idea, and it is premature to make sweeping judgments, I can say for certain that topical yohimbine HCL products like “Yohimburn”are gathering a small cult following of users. This is probably for good reason, as products like this are not being heavily marketed right now.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eCardarine (GW501516) The Fat Burning SARM\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\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\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\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\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eGW501516 could be a powerful way to improve performance and shed fat while maintaining muscle. Hopefully human studies will come out soon.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eSide effects of GW501516\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eShortly after it was classified as a performance-enhancing drug, reports started coming out saying that GW501516 caused cancer in lab rats.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\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\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eThat’s about 240x a normal dose, taken every day, for 104 weeks instead of 4 weeks.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\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\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eHow to dose GW501516\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\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\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\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\/span\u003e\u003c\/p\u003e\n\u003cp\u003eGW501516, or Cardarine, is said to provide incredible energy levels during workouts or training. Due to its synergistic effects of\u003cspan\u003e \u003c\/span\u003e\u003cstrong\u003eaccelerating fat loss\u003c\/strong\u003e\u003cspan\u003e \u003c\/span\u003ewhile\u003cspan\u003e \u003c\/span\u003e\u003cstrong\u003eincreasing endurance abilities\u003c\/strong\u003e, 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\/p\u003e\n\u003cul\u003e\n\u003cli\u003eTypical dose: 45-90 mg\/day\u003c\/li\u003e\n\u003cli\u003eMax: 90 mg\/day\u003c\/li\u003e\n\u003cli\u003eStacking dose: 25-45 mg\/day (depending on stack)\u003c\/li\u003e\n\u003cli\u003eHalf-life: 20-24 hours\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53684616102180,"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_aba47632-cfee-4c1a-ba7d-839f627dd240.png?v=1777913355"},{"product_id":"oxygen-labs-oxy-hyper-eca","title":"Oxygen Labs OXY-HYPER ECA","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB HYPER ECA (570MG\/CAP=60CAPSULES)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe ECA stack combines ephedrine, caffeine and aspirin in a predetermined ratio. It causes your body to target specific fat cells to be burned for energy, all the while raising your overall metabolic rate and suppressing appetite. Each ingredient in an ECA stack works in conjunction with the next. Ephedrine works as a beta agonist and stimulates production of norepinephrine, as well as circulating it through adipose tissue by way of increasing cAMP levels. The caffeine and aspirin function to inhibit the body’s natural response to halt this cAMP production, thus prolonging the effects. If you want to take an ECA stack, review your medical situation with your health care provider before you begin.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEphedrine and Caffeine work together synergistically. When stacked, the combined effects of Ephedrine, Caffeine and Aspirin are far greater than the sum of their effects when used alone. HYPER BURN assists in increasing weight loss, heightens athletic performance and boosts energy.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEphedrine dosing schedules may vary in relation to body weight and weight loss goals. Do not exceed 75-100mg dosages of Ephedrine in 24 hours. Do not take HYPER BURN on an empty stomach. Preferably take HYPER BURN 45 minutes to 1 hour before meals, but no more than 3 times per day. When starting out with HYPER BURN, the recommended dosage is one per day, preferably 30 minutes before your workout, 30 minutes before breakfast or first thing in the morning.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFAT BURNING:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTake one capsule before breakfast, lunch \u0026amp; training. Test your tolerance levels first before deciding to take more capsules throughout the day.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eENERGY:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTake one or two capsules before training.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53690937245988,"sku":null,"price":330.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_be78b38a-768a-4603-972a-15e05d0c105e.png?v=1777945039"},{"product_id":"oxygen-labs-dianabol-10mg-50-tabs","title":"Oxygen Labs Dianabol 10mg\/50 Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB DIANABOL(10MG 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":53690949959972,"sku":null,"price":180.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_790a2faa-58ba-4046-a39e-1c2b81ce0b5e.png?v=1777945154"},{"product_id":"oxygen-labs-tren-a-100mg-20ml","title":"Oxygen Labs Tren A 100mg\/20ml","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB TRENBOLONE A100 JUMBO(100MG\/ML TRENBOLONE ACETATE=20ML)\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\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\u003cdiv\u003eTrenbolone 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":53691036893476,"sku":null,"price":850.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_9bf41604-86e2-4ee3-99bd-8964b459ee93.png?v=1777945272"},{"product_id":"oxygen-labs-deca-npp-125mg-20ml","title":"Oxygen Labs DECA NPP 125mg\/20ml","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB NPP 125(125MG\/ML NANDROLONE PHENYL PROPIONATE=20ML)\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\u003eActive-Life: 1.5-3 DAYS FOR Nandrolone phenylpropionate\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 200-600mg 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\u003eNandrolone phenylpropionate 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. 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\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\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\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNandrolone phenylpropionate is a fast-acting form of nandrolone. Nandrolone is chemically related to the male hormone testosterone. Compared to testosterone, it has an enhanced anabolic and a reduced androgenic activity. This has been demonstrated in animal bioassays and explained by receptor binding studies. The low androgenicity of nandrolone is confirmed in clinical use. In the human, nandrolone has been shown to positively influence calcium metabolism and to increase bone mass in osteoporosis. In women with disseminated mammary carcinoma, nandrolone has been reported to produce objective regressions for many months. Furthermore, nandrolone has a nitrogen-saving action. This effect on protein metabolism has been established by metabolic studies and is utilised therapeutically in conditions where a protein deficiency exists such as during chronic debilitating diseases and after major surgery and severe trauma. In these conditions, nandrolone phenylpropionate serves as a supportive adjunct to specific therapies and dietary measures as well as parenteral nutrition, due to it’s faster acting nature nandrolone phenylpropionate is preffered in situations where a faster clinical response is required over it’s chemical variant nandrolone decaonate.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53691133624612,"sku":null,"price":640.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_1509bd17-16e2-46b6-8bf3-de219911f66a.png?v=1777945395"},{"product_id":"oxygen-labs-proviron-50mg-30-tabs","title":"Oxygen Labs Proviron 50mg\/30 Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB PROVIRION ORALEXTRA STRENGHT(50 MG MESTEROLONE\/TAB=30TABS)\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 PROPIONATE\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":53691222851876,"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_e2e8b183-a75a-42b5-b93f-9f4e53921fcb.jpg?v=1777945503"},{"product_id":"oxygen-labs-cyt3-tabs","title":"Oxygen Labs CYT3 Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB CYT3 TABS(40MCG CLENBUTEROL HCL 20MCG LIOTHYRONINE SODIUM,10MG YOHIMBE HCL\/TAB=50TABS\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eImportant Cycle advice – we put this first as it is critically important. Don’t think you can handle more as you probably cannot.Start low to see if you can handle it because it is a strong medication then work your-self up to see how much still is comfortable.\u003c\/div\u003e\n\u003cdiv\u003eNever go higher then 2 tablets per day! Because your receptors will degrade it is best to keep the cycles short.\u003c\/div\u003e\n\u003cdiv\u003eCombines the synergistic fat burning power of beta adrenergic agonists) and alpha adrenergic antagonists (Yohimbine HCl), all to add the T3 characteristics of increase the metabolic rate by increasing Thyroid efficiency.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eClenbuterol – 40mcg\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eT3 – 25mcg\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eYohimbine – 10mg\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEffects and Dosage\u003c\/div\u003e\n\u003cdiv\u003eThe blend is very potent combination of a beta and alpha antagonist.Clenbuterol and Yohimbine promote fat loss through the same adrenergic system, but the effects are achieved through different mechanisms. Clenbuterol is a known thermogenics shown to directly stimulate fat cells metabolism and accelerate the breakdown of triglycerides to form free fatty acids. The hormone glucagon released signals the breakdown of the triglycerides by hormone-sensitive lipase to release free fatty acids.Yohimbine, being an antagonist of alpha-2 receptors shifts the balance of sympathetic activity to ensure that lypolisis occurs. This increases synaptic Norepinephrine release, one of the body’s own natural Lipolytic hormones. In effect, it acts as beta stimulating and alpha blocking properties, an ideal combination to stimulate fat loss.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAdministration and Use:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eClenbuterol should be built up and tapered off gradually with dosage increases and decreases every 3-4 days and doses never exceeding 160 µg per day for safety measures. It is administered for periods of 2-3 weeks then discontinued for equal periods of time to prevent the body’s metabolic system the ability to adapt to the metabolic effects. For fat-burning goals Clenbuterol is often stacked with another fat-burning agent for quick effect, or alternated with another fat-burning agent by people who need to stay lean for a promote period. Usually T 3 is used for such purposes, with alternating cycles of 3 weeks each. If used together, cycles will not completely overlap!!! And a new adjustment is needed. A typical cycle for Clenbuterol might be 3 weeks, with the daily amounts being:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay1-1 tablet\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay2-1 tablet\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay3-1 tablet\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay4-1 1\/2 tablets\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay5-1 1\/2 tablets\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay6-1 1\/2 tablets\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay7-2 tablets\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay8-2 tablets\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay9-2 tablets\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay10-1 1\/2 tablets\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay11-1 1\/2 tablets\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay12-1 1\/2 tablets\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay13-1 tablets\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay14-1 tablets\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay15-1 tablets\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay16-1\/2 tablet\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay17-1\/2 tablet\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay18-1\/2 tablet\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay19-1\/2 tablet\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay20-1\/4 tablet\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDay21-1\/4 tablet\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThen stopping for three weeks and recommencing.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePatients should be instructed that the expected benefits of CYT3 may only be obtained when each tablet is swallowed with plain water the first thing upon arising for the day, at least 30 minutes before the first food, beverage, or medication of the day. Even ingestion with orange juice or coffee has been shown to markedly reduce the absorption of CYT3\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTo facilitate delivery to the stomach and thus reduce the potential should be instructed to swallow CYT3 with a full glass of tap water and not to lie down for at least 30 minutes and until after their first food of the day. Patients should not chew or suck on the tablet, or retain it in the mouth for a period longer than that required for swallowing, because a potential for side effects, not to take CYT3 at bedtime or before arising for the day\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDifficulty or pain upon swallowing, retrosternal pain or new or worsening heartburn), they should stop taking CYT3\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53691301953828,"sku":null,"price":290.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_82e81230-23d0-407b-b060-f22e880e1e44.png?v=1777945613"},{"product_id":"oxygen-labs-tudca-organ-support","title":"Oxygen Labs Tudca Organ Support","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLABS TUDCA(250MG TAUROURSSODEOXYHOLIC ACID\/CAP=60 CAPS).\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eA TUDCA dose of 250mg to 750mg per day \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWHAT IS IT?\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eUpa’s answer to on cycle liver protection during any cycle of an anabolic compound is TUDCA. As a standalone ingredient, TUDCA is an incredibly well researched ingredient for improving liver health, this all round liver protection is of the highest effectiveness and quality..  \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTudca (tauroursodeoxycholic acid) is a natural compound derived from bile salts which has been scientifically proven to reduce liver enzymes, something that is commonly elevated after a cycle of anabolic compounds that can cause health issues. The problem faced with many prohormones users is the liver damage and strain from the methylated products, which can be easily defended against with the inclusion of TUDCA.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTUDCA works either by its interactions with other bile salts or by preventing cells from apoptosis.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eGALLSTONES\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTaking bile salts is a long-established way for people to prevent gallstones. TUDCA also helps to dissolve gallstones that may already be forming. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDIABETES AND HYPERGLYCEMIA\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTUDCA may help with diabetes by making the liver and the muscles more sensitive to insulin, allowing them to use glucose more effectively and cause fewer blood sugar drops and spikes.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLIVER DETOX\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTUDCA can be used as a therapy for fatty liver disease, primary biliary cirrhosis, chronic hepatitis disease, and liver problems caused by cystic fibrosis.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTUDCA also protects the liver from damage caused by sleep apnea. The lack of oxygen can damage organs by causing oxidative damage and increasing stress on cell structures – TUDCA prevents this liver damage and alleviates this stress. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eKIDNEY PROTECTION\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTUDCA reduces some of the stress on the endoplasmic reticulum protecting the kidney against injury from toxins, diseases, and normal wear and tear. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIRRITABLE BOWEL SYNDROME\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTUDCA renders IBS symptoms less intense and improves the diversity of the bacteria in the bowels and digestive system. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTROKE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhile strokes will always cause some damage, people on TUDCA experience less – nearly half as much in some studies – damage from strokes and better healing over time. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNERVE PROTECTION\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTUDCA’s protective property is mostly for the same reasons that it protects against stroke damage – much of the nerve damage is from apoptosis, which TUDCA prevents from happening. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTUDCA has been shown to slow the progression of neurodegenerative diseases and to reduce their symptoms. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHOW TUDCA WORKS\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTUDCA is water soluble, not fat soluble like other bile salts. This means that it does not have a detergent-like effect, making it less damaging. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTUDCA VS UDCA\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe advantage of TUDCA is that it is better absorbed and stored by the body, meaning that a dose of TUDCA would have a larger benefit than the same dose of UDCA. Therefore, TUDCA is better to take. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDOSAGE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIn insulin sensitivity or fatty liver, this dose can be as high as 1750mg daily.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigher doses reduce cholesterol but have few other additional benefits or side effects. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSIDE EFFECTS\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe most common, and possibly the only, side effect on record is diarrhea, which is usually not severe enough to be life-threatening. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDRUG INTERACTIONS\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTUDCA has no reported interactions with statins or other drugs,\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTUDCA vs Milk Thistle\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMilk thistle can be taken with TUDCA (with caution) or on its own. However, milk thistle has a high risk of allergic reactions, higher risk of side effects, and lower effectiveness, making TUDCA a better option to take on its own. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWHO SHOULD TAKE?\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIpharma’s TUDCA can be taken as a standalone product to raise the natural vitality of the liver, or used on cycle alongside any methylated compound to ensure optimal liver protection as an on cycle support.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHOW TO TAKE?\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTUDCA doses start at 1 capsule a day, but if desired 2 capsules may be taken, and are best digested with food.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53691416477988,"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_82fb46ee-6e2e-4e3f-8279-3fde6d7d2108.png?v=1777945921"},{"product_id":"oxygen-labs-cialis-20mg-10-tabs","title":"Oxygen Labs Cialis 20mg\/10 Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e\n\u003cp\u003e\u003cspan\u003eOXYGENSLAB CICCOCIALIS (20MG TADALAFIL\/TAB=10TABS)\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eActive-Life: 12-36 HOURS\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eDrug Class: ERECTILE DYSFUNTION(ORAL)\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eAverage Reported Dosage: 20MG= 30-60 MIN BEFORE SEXUAL ACTIVITY\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eHigh Blood Pressure:YES\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\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\/span\u003e\u003c\/p\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53691419361572,"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_437e3f74-530d-45ac-afdc-08ee7ceac3a5.png?v=1777946285"},{"product_id":"oxygen-labs-mastron-prop-125mg-20ml","title":"Oxygen Labs Mastron PROP 125mg\/20ml","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB MASTERON PROP 125 JUMBO(125MG\/ML DROSTANOLONE PROPIONATE=20ML)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 25-40\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 62-130\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 FOR PROPIONATE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e10-14 DAYS FOR ENANTHANATE\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 300-500-mg weekly Women 100-350mg 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: None\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: 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\u003eNoted Comments: High Androgenic\/Moderate Anabolic\/Moderate anti-estrogenic\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: None, DHT derivative\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Low suppression in most cases\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMasteron is a highly androgenic injectable steroid that is a synthetic derivative of DHT (dihydrotestosterone). Since DHT does not aromatize to estrogens, there was no noted water retention during administration. If a bodybuilder had achieved a low body fat level, this drug was reported to dramatically improved shape and hardness in muscle tissue while augmenting the vascular appearance of a contest ready athlete. Normally, Masteron was used only during the last 3-5 weeks before a show as part of a pre-contest stack. In this case, 100-mg was commonly injected every second or third day (2-3 times weekly) by males and at a dosage of 50mg every other day by most women whom reported use. Additionally, according to available literature, Masteron is quite anti-catabolic and anti-estrogenic in nature due to receptor inhibition. So the reported characteristics of this drug do have supportive clinical validation to consider.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCombined with so- called mass steroids, Masteron did aid in a rapid build-up of strength and mass even with its relatively moderate anabolic qualities. However, Masteron was not reported to be the best choice for this purpose by those polled. DHT can promote hair loss and prostate disorders in prone individuals though it is not well documented as to whether or not deviants of the DHT structure can in all case do the same.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMasteron has a receptor binding ability 3-5 times greater than that of testosterone. This means that the drug can hang out longer in androgen receptor-sites and is not easily displaced. The result should be increased AAS activity.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAn interesting facet of Masteron is the way it acts as an anti-estrogen. This is due to its ability to compete for the aromatase receptor. As the reader is aware of by now, many AAS are capable of conversion to estrogens. The process is caused by an enzyme called aromatase. (Of course the process of AAS conversion to estrogen is referred to as aromatization) If a drug has the ability to inhibit the enzyme at its own receptor and still act as a powerful non-aromatizing AAS, its interesting and unusual to me.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMy personal experiences with this drug have always been favorable with no negative side effects. Additionally I feel that the drug has had value as a sort of AAS moderator. Let me explain this. Masteron has a high SHBG and albumin binding rate. Since these two hormone binding proteins prevent AAS from merging with their receptors, some would assume this is a bad thing. Masteron is 3-5 times more active than testosterone, so the unbound portion circulating in the blood stream goes a long way. Since the drug binds a higher percentage of SHBG and albumin, any other AAS co-administered with it remains in an unbound\/active\/free state to a greater extent and is able to induce a greater response. This is an example of noted drug synergy common to protocols reported as most effective yet requiring lower dosages to accomplish a specific result. The implication is that lower dosages of co-administered drugs allowed a decrease in negative side effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eA point of interest is that two OTC prohormones in the United States have similar effects to Masteron (though oral administration is not the most effective delivery method and injection type administration would be illegal in most countries) (1) 5a-androst-1-en-3b,17b- dione (2) 5a-androst-en-3b,17b-diol. My personal research has shown that there is a realistic approach to an orally administered version of the latter of the two drugs that has shown great promise. We will complete the final testing soon before turning the project over to the crazies at Hazardous Materials Supplements. Personally, I am totally stoked about the project due to its vast application potential in the world OTC supplemental industry. The key is a compound from Eastman that allows lipophilic substances to become hydrophilic (Oil soluble to water soluble). This means that the high expense of effective supplements like methoxyisoflavone (and its deviants) to be reduced due to lower dosage requirements.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Since this drug clears the body quickly, it was a favorite for tested competitors.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMastaron is a synthetic derivative of dihydrotestosterone, displaying a potent androgenic effect that is responsible for increases in muscle density and hardness and a moderate anabolic effect that creates a positive nitrogen balance in humans and promotes protein synthesis. Since it is a derivative of dihydrotestosterone, dromastolone does not aromatize in any dosage and thus it cannot be converted into estrogen. Therefore, estrogen-related water retention is eliminated. Mastaplex combines the fast-acting propionate form with the longer acting enanthate form.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53691420016932,"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_44342931-2398-49b8-96c1-da32af98bb7e.png?v=1777946408"},{"product_id":"oxygen-labs-dianabol-50mg-30-tabs","title":"Oxygen Labs Dianabol 50mg\/30 Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB DIANABOL(50MG METHANDROSTENOLONE\/TAB=30TABS)\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":53691423064356,"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_9d3f1070-d969-4358-9762-1d34a55b986c.png?v=1777946620"},{"product_id":"oxygen-labs-tren-a-100mg-10ml","title":"Oxygen Labs Tren A 100mg\/10ml","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB TRENBOLONE 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\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\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\u003cdiv\u003eTrenbolone 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":53691425521956,"sku":null,"price":570.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_653ad14e-fae7-48e0-b279-06d1582274e7.png?v=1777946759"},{"product_id":"oxygen-labs-oxy-bikini","title":"Oxygen Labs OXY-Bikini","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB OXY-BIKINI (25MG SIBUTRAMINE HCL + 30MG PHENTERMINE\/CAP=55MG=60CAPS)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage\u003c\/div\u003e\n\u003cdiv\u003eOne 30mg tablet per day every morning directly after breakfast. Sibutramine causes insomnia. Therefore, it should not be used at night.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSibutralean Slim tablets are manufactured as a big tablet with a breaker in the middle. As a result, we highly recommend that new users start with 1\/2 tablet and then work their way up to a full tablet. Sibutralean has been known for causing severe increases in heart rate. In addition it also causes feelings of anxiety. If you are not use to these kinds of side effects it is recommended that you start on 1\/2 tab.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAction\u003c\/div\u003e\n\u003cdiv\u003eSibutramine hydrochloride is a selective serotonin and noradrenaline re-uptake inhibitor. Obesity management is the main medical use of sibutramine. This is not a rapid acting drug. In other words it works rather slow and in a safe manner. This leads to a steady reduction in fat mass. Longer-term results can be maintained . This drug is most effective in conjunction with a low calorie diet and training program.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSibutralean reduces body fat via two very distinct and effective mechanisms. Firstly, it suppresses the appetite. Studies have shown people decrease their calorie intake with as much as 1300 calories a day. Secondly, Sibutralean stimulates metabolism and daily caloric expenditure. A single tablet of 30 mg sibutramine has shown an increase in basal metabolic rate by up to 30%. This increase in metabolic rate usually lasts up to six hours from taking the capsule.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSibutramine has a thermogenic action that happens in the adrenergic system. This happens mainly through the indirect support of beta 3-receptor activation. With subutralen we mainly see strong increases in brown adipose tissue thermogenesis (BAT). This increases the body temperature by 0.5 to 1 degree Celsius. As soon as the body temperature increases it is a clear indication that thermogenesis has been triggered. This means that burning is now taking place.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eClinical trials have shown that sibutramine works remarkably well with obese patients. The trials found that sibutramine also had significant improvements in serum triglyceride and HDL cholesterol levels. Patients entered into the clinical trials were obese. As a result their HDL cholesterol levels were extremely high when they started the clinical trials. For someone who is not obese the improvements in serum triglyceride and HDL cholesterol levels might not be as significant.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSide Effects\u003c\/div\u003e\n\u003cdiv\u003eThe most common side effect with sibutramine is an increase in blood pressure. For this reason patients with high blood pressure and cardiovascular problems should not be using this product. Other common side effects include dry mouth, sleeplessness, irritability, back pain, stomach upset and constipation. The side effects Sibutramine causes usually subsides in the patient as they becomes accustomed to usage. Patients who are using any form of antidepressant should also not use this product. The drug interactions between sibutramine hydrochloride and antidepressants have shown to be a very negative one.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Intake\u003c\/div\u003e\n\u003cdiv\u003eAfter taking the 30 mg tablet of sibutramine in the morning you will get instantly very thirsty. Consequently, make sure you consume as much water as possible when this thirst sets in. Some people fight this thirst. This reduces the positive effects of sibutramine. As you increase your water intake sibutramine better activated. Fat burning results are more increased. Fighting the thirst without water consumption decreases the appetite suppressing characteristics. People who consumed a lot of water get better results. Therefore, without water uptake you get very hungry late afternoon. When the product wears off you then defeat the object by consuming large amounts of food. With the increase of water late afternoon hunger is not an issue.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSibutramine affects chemicals in the brain that affect weight maintenance.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSibutramine is used together with diet and exercise to treat obesity that may be related to diabetes, high cholesterol, or high blood pressure.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSibutramine may also be used for other purposes not listed in this medication guide.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDo not use sibutramine if you have taken an MAO inhibitor such as furazolidone (Furoxone), isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam), or tranylcypromine (Parnate) in the last 14 days. Serious, life threatening side effects can occur if you use sibutramine before the MAO inhibitor has cleared from your body.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eYou should not take sibutramine if you are allergic to it, or if you have severe or uncontrolled high blood pressure, an eating disorder (anorexia or bulimia), if you are taking stimulant diet pills, or if you have a history of coronary artery disease, stroke, or heart disease.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBefore taking sibutramine, tell your doctor if you have glaucoma, high blood pressure, liver or kidney disease, depression, underactive thyroid, seizures, a bleeding disorder, a history of gallstones, or if you are older than 65 or younger than 16.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTell your doctor about all prescription and over-the-counter medications you use, especially antidepressants, cold or allergy medication, narcotic pain medicine, or migraine headache medicines.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTell your doctor if you do not lose at least 4 pounds after taking the medication for 4 weeks along with a low calorie diet.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDo not use sibutramine if you have taken an MAO inhibitor such as furazolidone (Furoxone), isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam), or tranylcypromine (Parnate) in the last 14 days. Serious, life threatening side effects can occur if you use sibutramine before the MAO inhibitor has cleared from your body.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eYou should not take this medication if you are allergic to sibutramine, or if you have:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003esevere or uncontrolled hypertension (high blood pressure);\u003c\/div\u003e\n\u003cdiv\u003ean eating disorder (anorexia or bulimia);\u003c\/div\u003e\n\u003cdiv\u003ea history of coronary artery disease (atherosclerosis);\u003c\/div\u003e\n\u003cdiv\u003ea history of heart disease (congestive heart failure, heart rhythm disorder);\u003c\/div\u003e\n\u003cdiv\u003ea history of heart attack or stroke; or\u003c\/div\u003e\n\u003cdiv\u003eif you are taking stimulant diet pills.\u003c\/div\u003e\n\u003cdiv\u003eIf you have any of these other conditions, you may need a sibutramine dose adjustment or special tests:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eglaucoma;\u003c\/div\u003e\n\u003cdiv\u003ehigh blood pressure;\u003c\/div\u003e\n\u003cdiv\u003eliver disease;\u003c\/div\u003e\n\u003cdiv\u003ekidney disease;\u003c\/div\u003e\n\u003cdiv\u003edepression;\u003c\/div\u003e\n\u003cdiv\u003eunderactive thyroid;\u003c\/div\u003e\n\u003cdiv\u003eepilepsy or seizure disorder;\u003c\/div\u003e\n\u003cdiv\u003ea bleeding or blood clotting disorder;\u003c\/div\u003e\n\u003cdiv\u003ea history of gallstones; or\u003c\/div\u003e\n\u003cdiv\u003eif you are older than 65 or younger than 16.\u003c\/div\u003e\n\u003cdiv\u003eFDA pregnancy category C. It is not known whether sibutramine will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using sibutramine.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIt is not known whether sibutramine passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDo not give this medication to anyone younger than 16 years old.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhat is Phentermine\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe weight loss drug Phentermine is an appetite suppressant. The active ingredient within Phentermine is the generic drug phentermine. Phentermine is combined with a resin to create slow release which prolongs the effects of Phentermine.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhat does Phentermine look like?\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePhentermine capsules are available in 30mg in packs of 30 capsules.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhat is Phentermine. prescribed for?\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePhentermine is an appetite suppressant and has successfully been helping people lose weight since it was released onto the market. It is designed to be used in combination with a healthy diet and regular exercise.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWho should Phentermine be prescribed for?\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePhentermine is only recommended for use among patients who are medically classed as heavily overweight or obese. Only people with a BMI (Body Mass Index) greater than 27+ and who suffer from a related illness such as high cholesterol, high blood pressure or diabetes are normally considered as suitable candidates for the drug.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePhentermine is not recommended for:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eChildren of 18 years or younger\u003c\/div\u003e\n\u003cdiv\u003eThe elderly\u003c\/div\u003e\n\u003cdiv\u003eHow does Phentermine work?\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePhentermine is an appetite suppressant. Hunger cravings are reduced as the active chemical ingredient in Phentermine effects the parts of the central nervous system. The active ingredient in Phentermine is phentermine. Phentermine is chemically similar to amphetamine and increased energy levels are common among patients.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIt is recommended that Phentermine be taken as an accompaniment to a healthy diet and regular exercise.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePhentermine side effects\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSide effects of Phentermine can include:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eRestlessness Excess energy Insomnia\u003c\/div\u003e\n\u003cdiv\u003eEuphoria Dysphoria Difficulty in breathing\u003c\/div\u003e\n\u003cdiv\u003eLight headedness Weakness Ankle and extremity Swelling\u003c\/div\u003e\n\u003cdiv\u003eIncrease in blood pressure Fatigue Headache\u003c\/div\u003e\n\u003cdiv\u003eDryness of the mouth Unpleasant taste Diarrhea, Constipation\u003c\/div\u003e\n\u003cdiv\u003eImpotence Changes in sex drive \u003c\/div\u003e\n\u003cdiv\u003eIf used incorrectly or for excessive lengths of time, Phentermine can be habit forming. If over used or abused Phentermine patients can form a habit of perceived dependency. Phentermine should not be taken for a longer period than prescribed by your doctor. Phentermine should not be taken by anyone other than by the person it was prescribed for.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePhentermine dosages\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePhentermine capsules should be taken once daily, either before breakfast or within 2 hours of eating breakfast. It is advised to take Phentermine early in the day as it known to cause insomnia and increased energy levels.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePhentermine capsules should be swallowed whole with plenty of water.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePhentermine is not recommended for patients of 18 years old or younger. It is not recommend that the elderly be prescribed Phentermine .\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhat precautions should be taken before using Phentermine?\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eInform your Doctor of the following:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAny allergies that you may have, especially to if you have a known allergy to phentermine.\u003c\/div\u003e\n\u003cdiv\u003eAny other medicines that you are taking at the time (both prescription and over the counter)\u003c\/div\u003e\n\u003cdiv\u003eIf your medical history includes high blood pressure, a heart condition, arteriosclerosis, overactive thyroid, diabetes, glaucoma or drug abuse.\u003c\/div\u003e\n\u003cdiv\u003eIf you know or suspect that you are pregnant or plan to become pregnant. If you become pregnant while taking Phentermine tell your doctor.\u003c\/div\u003e\n\u003cdiv\u003eIf you are breastfeeding a child.\u003c\/div\u003e\n\u003cdiv\u003eIf you are prone to agitated states.\u003c\/div\u003e\n\u003cdiv\u003eOver dosage\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOverdoses of Phentermine can have serious consequences, if quantities are high enough this can include death. If an overdose is suspected seek medical help immediately.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSymptoms of overdosage can include: excess energy, tremor, hyperreflexia, increased breathing rate, confusion, assaultiveness, hallucinations, panic, excess fatigue, depression, arrhythmia, hypertension or hypotension, circulatory collapse, vomiting, diarrhea, abdominal cramps.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFatal poisoning usually terminates in convulsions and coma.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53691429486884,"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_f3a47035-2c25-44a4-9700-db8cc55a7d8b.png?v=1777946869"},{"product_id":"oxygen-labs-turanabol","title":"Oxygen labs Turanabol","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB TURANABOL 15(15MG 4-CHLORODEHYDROMETHYLTESTOSTERONE\/tab=50 tabs)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC N\/A\u003c\/div\u003e\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":53691437449508,"sku":null,"price":340.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_e5a08331-d114-4a15-b317-f222e45fe35e.png?v=1777947047"},{"product_id":"oxygen-labs-m1t","title":"Oxygen Labs M1T","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB M1T(METHYLDIHYDROBOLDENONE 15MG P\/TAB=50TABS)\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\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53691441611044,"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_9881c2b4-559d-44e9-ae9e-94ad63b47951.png?v=1777947151"},{"product_id":"oxygen-labs-deca-350mg-20ml","title":"Oxygen Labs DECA 350mg\/20ml","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eDeca Durabolin is a very famous injectable, which contains the steroidal hormone Nandrolone and is joined to the enormous Decanoate ester. This steroid is one of the most usually utilized anabolic steroids by many athletes as well as execution competitors. As a Nandrolone base, Deca Durabolin is joined to the huge Decanoate ester, which controls the hormone’s discharging action backing it off immensely. This permits the person to utilize the Nandrolone hormone without the requirement for frequent injections. Deca Durabolin conveys a moderately strong anabolic rating, somewhat more noteworthy than testosterone, be that as it may, its complete androgenic movement is a lot lower than testosterone. Deca Durabolin is an incredible steroid for muscle development and can be combined with numerous different steroids.\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDeca-Durabolin has countless benefits for bodybuilders and athletes in all the areas you’d expect from a high-quality steroid, but also for reasons that are truly unique to Deca in the area of healing and recovery.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePerfect for bulking and strength, Deca boosts collagen synthesis and bone density which strengthens joints and provides support for your mass gains while increasing capacity to continually lift heavier weights.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eInjections of this steroid promote the rapid synthesis of amino acids to muscle fibers, with simultaneous fluid retention in the muscles. The process of anabolism in the athlete’s body will proceed an order of magnitude faster under the influence of this powerful drug.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eYour joints will be significantly lubricated during your work with the fluid that Deca produces and friction delays on the course. This will greatly facilitate workouts and relieve pain.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOn a mass-building cycle, you can have the aromatization of Deca molecules, this process must be controlled and extinguished as much as possible already at the initial stage. Otherwise, your muscles can be very abundantly flooded with liquid and after a while excess of the hormone estrogen may appear.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDeca copes with these negative side effects quickly and efficiently with Proviron, an anti-estrogen drug, during a course.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIt is applied at the beginning of the course for up to four weeks. During this time, you will be completely blocked from the manifestation of various kinds of negative phenomena.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53691442626852,"sku":null,"price":870.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_6dca5ccc-2e4b-41ba-b704-86fa61ebee2f.png?v=1777947248"},{"product_id":"oxygen-labs-cardarinegw501516","title":"Oxygen Labs Cardarine(GW501516)","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB SARMS CARDARINE(GW501516)(20MG\/ML=30ML).\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\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53691443446052,"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_024ee831-c50e-4d09-90b0-17e041d1a362.png?v=1777947362"},{"product_id":"oxygen-labs-sibutramine-30-tabs","title":"Oxygen Labs Sibutramine 30 Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e\n\u003cp\u003eOXYGENSLAB SIBUTRAMINE (SIBUTRAMINE HCL 30MG\/TAB=30TABS)\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage\u003c\/div\u003e\n\u003cdiv\u003eOne to Two 20mg tablet per day every morning directly after breakfast. Sibutramine causes insomnia. Therefore, it should not be used at night.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSibutralean Slim tablets are manufactured as a big tablet with a breaker in the middle. As a result, we highly recommend that new users start with 1\/2 tablet and then work their way up to a full tablet. Sibutralean has been known for causing severe increases in heart rate. In addition it also causes feelings of anxiety. If you are not use to these kinds of side effects it is recommended that you start on 1\/2 tab.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAction\u003c\/div\u003e\n\u003cdiv\u003eSibutramine hydrochloride is a selective serotonin and noradrenaline re-uptake inhibitor. Obesity management is the main medical use of sibutramine. This is not a rapid acting drug. In other words it works rather slow and in a safe manner. This leads to a steady reduction in fat mass. Longer-term results can be maintained . This drug is most effective in conjunction with a low calorie diet and training program.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSibutralean reduces body fat via two very distinct and effective mechanisms. Firstly, it suppresses the appetite. Studies have shown people decrease their calorie intake with as much as 1300 calories a day. Secondly, Sibutralean stimulates metabolism and daily caloric expenditure. A single tablet of 30 mg sibutramine has shown an increase in basal metabolic rate by up to 30%. This increase in metabolic rate usually lasts up to six hours from taking the capsule.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSibutramine has a thermogenic action that happens in the adrenergic system. This happens mainly through the indirect support of beta 3-receptor activation. With subutralen we mainly see strong increases in brown adipose tissue thermogenesis (BAT). This increases the body temperature by 0.5 to 1 degree Celsius. As soon as the body temperature increases it is a clear indication that thermogenesis has been triggered. This means that burning is now taking place.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eClinical trials have shown that sibutramine works remarkably well with obese patients. The trials found that sibutramine also had significant improvements in serum triglyceride and HDL cholesterol levels. Patients entered into the clinical trials were obese. As a result their HDL cholesterol levels were extremely high when they started the clinical trials. For someone who is not obese the improvements in serum triglyceride and HDL cholesterol levels might not be as significant.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSide Effects\u003c\/div\u003e\n\u003cdiv\u003eThe most common side effect with sibutramine is an increase in blood pressure. For this reason patients with high blood pressure and cardiovascular problems should not be using this product. Other common side effects include dry mouth, sleeplessness, irritability, back pain, stomach upset and constipation. The side effects Sibutramine causes usually subsides in the patient as they becomes accustomed to usage. Patients who are using any form of antidepressant should also not use this product. The drug interactions between sibutramine hydrochloride and antidepressants have shown to be a very negative one.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Intake\u003c\/div\u003e\n\u003cdiv\u003eAfter taking the 30 mg tablet of sibutramine in the morning you will get instantly very thirsty. Consequently, make sure you consume as much water as possible when this thirst sets in. Some people fight this thirst. This reduces the positive effects of sibutramine. As you increase your water intake sibutramine better activated. Fat burning results are more increased. Fighting the thirst without water consumption decreases the appetite suppressing characteristics. People who consumed a lot of water get better results. Therefore, without water uptake you get very hungry late afternoon. When the product wears off you then defeat the object by consuming large amounts of food. With the increase of water late afternoon hunger is not an issue.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSibutramine affects chemicals in the brain that affect weight maintenance.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSibutramine is used together with diet and exercise to treat obesity that may be related to diabetes, high cholesterol, or high blood pressure.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSibutramine may also be used for other purposes not listed in this medication guide.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDo not use sibutramine if you have taken an MAO inhibitor such as furazolidone (Furoxone), isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam), or tranylcypromine (Parnate) in the last 14 days. Serious, life threatening side effects can occur if you use sibutramine before the MAO inhibitor has cleared from your body.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eYou should not take sibutramine if you are allergic to it, or if you have severe or uncontrolled high blood pressure, an eating disorder (anorexia or bulimia), if you are taking stimulant diet pills, or if you have a history of coronary artery disease, stroke, or heart disease.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBefore taking sibutramine, tell your doctor if you have glaucoma, high blood pressure, liver or kidney disease, depression, underactive thyroid, seizures, a bleeding disorder, a history of gallstones, or if you are older than 65 or younger than 16.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTell your doctor about all prescription and over-the-counter medications you use, especially antidepressants, cold or allergy medication, narcotic pain medicine, or migraine headache medicines.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTell your doctor if you do not lose at least 4 pounds after taking the medication for 4 weeks along with a low calorie diet.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDo not use sibutramine if you have taken an MAO inhibitor such as furazolidone (Furoxone), isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam), or tranylcypromine (Parnate) in the last 14 days. Serious, life threatening side effects can occur if you use sibutramine before the MAO inhibitor has cleared from your body.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eYou should not take this medication if you are allergic to sibutramine, or if you have:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003esevere or uncontrolled hypertension (high blood pressure);\u003c\/div\u003e\n\u003cdiv\u003ean eating disorder (anorexia or bulimia);\u003c\/div\u003e\n\u003cdiv\u003ea history of coronary artery disease (atherosclerosis);\u003c\/div\u003e\n\u003cdiv\u003ea history of heart disease (congestive heart failure, heart rhythm disorder);\u003c\/div\u003e\n\u003cdiv\u003ea history of heart attack or stroke; or\u003c\/div\u003e\n\u003cdiv\u003eif you are taking stimulant diet pills.\u003c\/div\u003e\n\u003cdiv\u003eIf you have any of these other conditions, you may need a sibutramine dose adjustment or special tests:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eglaucoma;\u003c\/div\u003e\n\u003cdiv\u003ehigh blood pressure;\u003c\/div\u003e\n\u003cdiv\u003eliver disease;\u003c\/div\u003e\n\u003cdiv\u003ekidney disease;\u003c\/div\u003e\n\u003cdiv\u003edepression;\u003c\/div\u003e\n\u003cdiv\u003eunderactive thyroid;\u003c\/div\u003e\n\u003cdiv\u003eepilepsy or seizure disorder;\u003c\/div\u003e\n\u003cdiv\u003ea bleeding or blood clotting disorder;\u003c\/div\u003e\n\u003cdiv\u003ea history of gallstones; or\u003c\/div\u003e\n\u003cdiv\u003eif you are older than 65 or younger than 16.\u003c\/div\u003e\n\u003cdiv\u003eFDA pregnancy category C. It is not known whether sibutramine will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using sibutramine.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIt is not known whether sibutramine passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDo not give this medication to anyone younger than 16 years old.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53691443839268,"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_6ebac336-c8db-42d4-872c-21a42dcf949b.jpg?v=1777947476"},{"product_id":"oxygen-labs-c17-cutting","title":"Oxygen Labs C17 Cutting","description":"\u003cp\u003e\u003cspan\u003eOXYGENSLAB C17 CUTTING HYBRID 45 = 10MG TURINABOL+10MG OXANDROLONE+10MG STANOZOLOL+15MG MESTROLONE\/TAB = 50TABS\u003c\/span\u003e\u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53691444166948,"sku":null,"price":590.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_d04a4026-77ac-41fd-80c6-5e4d74b6441c.png?v=1777947596"},{"product_id":"oxygen-labs-anavar-50mg-30-tabs","title":"Oxygen Labs Anavar 50mg\/30 Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB ANAVAR 50(50MG OXANDROLONE\/TAB=30TABS)\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\u003eSTANDARD DIHYDROTESTOSTERONE\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\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOxandrolone 20 is typically used for\u003c\/div\u003e\n\u003cdiv\u003eCutting and hardening of skeletal muscles.\u003c\/div\u003e\n\u003cdiv\u003eThose who wish to loose weight without exercise.\u003c\/div\u003e\n\u003cdiv\u003eTreating muscle wasting diseases and osteoporosis.\u003c\/div\u003e\n\u003cdiv\u003eHelping burn victims regain muscle.\u003c\/div\u003e\n\u003cdiv\u003eContents per box:\u003c\/div\u003e\n\u003cdiv\u003e56 Green tablets in a labeled bag or labeled glass bottle.\u003c\/div\u003e\n\u003cdiv\u003eRecommended dose\u003c\/div\u003e\n\u003cdiv\u003eAlways take Oxandrolone 20 exactly as prescribed by your doctor. If you are unsure, ask your pharmacist. Unless otherwise prescribed by a doctor, the normal dose is:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMen\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFirst time users\u003c\/div\u003e\n\u003cdiv\u003eTake dose every 12 hours as follows: 20mg 30 minutes pre-training and 20mg 12 hours later for 2 weeks. Then increase daily dosage by 10 mg as follows: one 20mg 30 minutes pre training and two 20mg doses. These three doses to be taken at 8 hourly intervals.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAdvanced users\u003c\/div\u003e\n\u003cdiv\u003eTake 20mg doses 4 times per day at 6 hourly intervals. Do not exceed 20mg per dose or 80mg per 24 hour period.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWomen\u003c\/div\u003e\n\u003cdiv\u003eNot recommended for woman as 1 capsule exceeds the daily recommended dose\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDuration\u003c\/div\u003e\n\u003cdiv\u003eMinimum recommended duration is 6 weeks and maximum duration is 12 weeks.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53691446362404,"sku":null,"price":1000.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_546f06a1-4a26-47ce-b1a8-6179e45ce761.png?v=1777948124"},{"product_id":"oxygen-labs-c17-cutting-1","title":"Oxygen Labs C17 Cutting","description":"\u003cp\u003e\u003cspan\u003eOXYGENSLAB C17 CUTTING HYBRID 45 = 10MG TURINABOL+10MG OXANDROLONE+10MG STANOZOLOL+15MG MESTROLONE\/TAB = 50TABS\u003c\/span\u003e\u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53691457863972,"sku":null,"price":590.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_d04a4026-77ac-41fd-80c6-5e4d74b6441c.png?v=1777947596"},{"product_id":"oxygenslab-c17-cutting-hybrid-45-10mg-turinabol-10mg-oxandrolone-10mg-stanozolol-15mg-mestrolone-tab-50tabs","title":"OXYGENSLAB C17 CUTTING HYBRID 45 = 10MG TURINABOL+10MG OXANDROLONE+10MG STANOZOLOL+15MG MESTROLONE\/TAB = 50TABS","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e\n\u003cp\u003eOXYGENSLAB AROMASIN(20MG EXEMESTANE\/TAB=30TABS)\u003c\/p\u003e\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: 12.5-25 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\u003eExemestane is an oral steroidal aromatase inhibitor (but also known uniquely as an aromatase inactivator) used in the adjuvant treatment of hormonally-responsive (also called hormone-receptor-positive, estrogen-responsive) breast cancer in postmenopausal women. The aim of Exeplex is to lower estrogen levels.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eExemestane is an irreversible, steroidal aromatase inactivator, structurally related to the natural substrate androstenedione. It acts as a false substrate for the aromatase enzyme, and is processed to an intermediate that binds irreversibly to the active site of the enzyme causing its inactivation, an effect also known as “suicide inhibition.” In other words, the Exemestane, by being structurally similar to the target of the enzymes, permanently binds to those enzymes, thereby preventing them from ever completing their task of converting androgens into estrogen.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe estrogen suppression rate for exemestane varies from 85% to 95%.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53691471167780,"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_25f23ecb-702d-4b9e-a173-b3ce104bc784.png?v=1777948470"},{"product_id":"oxygen-labs-equipoise-350ml-20ml","title":"Oxygen Labs Equipoise 350ml\/20ml","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003esteroid that is based on the testosterone hormone with only a slight variation to the chemical structure, but one that it makes unique.\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe attached ester, Undecylenate, is a slow-release ester that causes Equipoise to continue being released into the body for up to three weeks after an injection. It also takes several days for the maximum blood level to be reached after you inject Boldenone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEQ is one of the few steroids that is used solely for veterinary purposes. The “equi” portion of the name indicates that this product is intended for use in horses. But like a lot of steroids, the effects of Equipoise are appealing for bodybuilders and it’s not too surprising to know that EQ shares a lot of similarities with testosterone; after all it’s only a slightly modified version of that original hormone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThese similar functions include the enhancement of both protein synthesis and muscle nitrogen retention, as well as increasing red blood cell count. EQ can also increase the output of insulin-like growth factor 1 (IGF-1) and reduce stress hormones.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEquipoise has an anabolic to androgenic ratio of 100:50, compared with testosterone having an even 100:100 ratio.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMost steroid users are familiar with the legendary compound Dianabol which EQ shares a virtually identical chemical structure with, but a slight modification allows each one to have a very different effect on the body. This makes it possible to use these very similar yet completely different acting steroids together in a cycle with great benefits.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53691471855908,"sku":null,"price":870.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_cd945a12-fe13-436a-af82-ceb999e83e3e.png?v=1777948629"},{"product_id":"oxygen-labs-deca-350mg-10ml","title":"Oxygen Labs DECA 350mg\/10ml","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eOXYGENSLAB DECA 350(350MG\/ML NANDROLONE DECOANATE=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\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\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\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\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":53691476771108,"sku":null,"price":590.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_86bfd7da-d9f0-4f1c-8548-bd4ce7069efb.png?v=1777948833"}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/collections\/rn-image_picker_lib_temp_439c6dad-4c0a-42ff-a287-d236c29511b2.png?v=1777553619","url":"https:\/\/ultrafizique.co.za\/collections\/oxygen-labs.oembed","provider":"UltraFizique","version":"1.0","type":"link"}