{"title":"HD LABS","description":null,"products":[{"product_id":"hd-labs-nutrobal","title":"HD Labs Nutrobal","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eHD LABS SARMS NUTROBOL(MK-677)10MG\/TAB=50TABS\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhat Is Nutrobol MK-677\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNutrobal (MK-677) is a chemical that has the characteristics of human growth hormone (HGH). It is an orally active growth hormone secretagogue. A secretagogue causes substances to be secreted. MK677 has the ability because of its ability to mimic the GH stimulating action a hormone called “ghrelin.” Ghrelin is categorized as a peptide, commonly referred to as “the hunger hormone,” which explains the drastic rise in appetite with 677 use. Ghrelin plays a large role in regulating the distribution as well as rate of energy use. It is imperative to understand all of these concepts to decipher the many capabilities that 677 has. mk677 can not only increase plasma levels of many types of hormones, but also provide sustainable increases. These are long term and not just “for the time being” types of increases. Studies show that Nutrobal can increase muscle mass and bone mineral density as well as altering the metabolism of body fat, possibly becoming a treatment for obesity.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBenefits of MK-677:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNutrobal (MK-677) studies have been conducted since the late 90’s. There is a wide array of benefits that have been found with use. The main benefit that consistently shows in study is the increase in growth hormone and IGF-levels provided with use. These have shown to be significant increases in regards to both. Below is a list of other significant benefits found through studies and implementation on humans:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIncreases in fat free mass Enhanced sleep quality A treatment for obesity and fat loss Lowering of bad cholesterol (LDL) Significant improvements in nitrogen balance Reversal of diet-induced nitrogen wasting Treatment of catabolic conditions Increase in basil metabolic rate Oral administration (no injections required) Overall sense of well-being\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIt is evident by the list of benefits that MK677 is highly desirable. These benefits, in conjunction with the very small chance of side effects show MK677 to be a breakthrough. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSide Effects:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAs stated above, MK677 carries little to no side effects however it is always important to understand the possibilities that could occur with use. \u003c\/div\u003e\n\u003cdiv\u003eThe main “side effect” associated with MK677 is the increase in appetite, which may be welcome by many research subjects. Studies show this to subside after 4-8 weeks, variant from person to person. The other side effects that showed, that were very infrequent and uncommon were mild lower extremity edema and muscle pain. Secretagogues generally carry the worry of prolactin increase, however studies with MK677 did not show any increase in prolactin levels. Cortisol levels were not increased in studies either. These traits make Nutrobal stand out amongst other chemicals that attempt to work in the same manner but carry these unwanted side effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosing:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStudies conducted had dosing between 5-25 mg per day, with 25 mg being the most common and effective dose. MK677 has a 24 hour half life and showed to be best tolerated when fed to rats each morning on an empty stomach. MK677 has extreme benefits in regards to helping with a deeper sleep however it can interfere with sleep patterns if taken too late at night or too close to bed time. MK677 can be used continuously for 1-2 years with no concern of desensitizing. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAlso known as Ibutamoren, MK-677 is often stacked with other SARM’S because it behaves differently: it stimulates the pituitary gland to release growth hormone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSARM MK-677: Growth Hormone Mimetic\u003c\/div\u003e\n\u003cdiv\u003eSARM MK-677: Growth Hormone Mimetic\u003c\/div\u003e\n\u003cdiv\u003eFor this reason, MK677 is a preferred performance enhancer and is used for bulking as well as cutting, with users consistently reporting gains in lean muscle mass. Ibutamoren is not known to be suppressive to testosterone production and, due to its affinity to oxidize fat at an accelerated rate, women looking to lose weight may prefer this SARM as well. High-dosing users have reported side effects that include numb hands, lethargy, and increased appetite.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTypical dose: 15-30 mg\/day\u003c\/div\u003e\n\u003cdiv\u003eMax: 50 mg\/day\u003c\/div\u003e\n\u003cdiv\u003eStacking dose: 10-15 mg\/day (depending on stack)\u003c\/div\u003e\n\u003cdiv\u003eHalf-life: 24 hours\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53748807368996,"sku":null,"price":440.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_df40f806-3ff1-4501-993e-f9af6acb419a.jpg?v=1778065263"},{"product_id":"hd-labs-cialis-tabs","title":"HD Labs Cialis Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e\n\u003cp\u003e5mg Tabs\/31 Tabs\u003c\/p\u003e\n\u003cp\u003eSide Effects\u003c\/p\u003e\n\u003cp\u003ePrecautions\u003c\/p\u003e\n\u003cp\u003eInteractions\u003c\/p\u003e\n\u003cp\u003eOverdose\u003c\/p\u003e\n\u003cp\u003eImages\u003c\/p\u003e\n\u003cp\u003eReviews (438)\u003c\/p\u003e\n\u003cp\u003eUses\u003c\/p\u003e\n\u003cp\u003eTadalafil is used to treat male sexual function problems (impotence or erectile dysfunction-ED). In combination with sexual stimulation, tadalafil works by increasing blood flow to the penis to help a man get and keep an erection.Tadalafil is also used to treat the symptoms of an enlarged prostate (benign prostatic hyperplasia-BPH). It helps to relieve symptoms of BPH such as difficulty in beginning the flow of urine, weak stream, and the need to urinate often or urgently (including during the middle of the night). Tadalafil is thought to work by relaxing the smooth muscle in the prostate and bladder.This drug does not protect against sexually transmitted diseases (such as HIV, hepatitis B, gonorrhea, syphilis). Practice \"safe sex\" such as using latex condoms. Consult your doctor or pharmacist for more details.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eHow to use Cialis\u003c\/p\u003e\n\u003cp\u003eRead the Patient Information Leaflet provided by your pharmacist before you start taking tadalafil and each time you get a refill. If you have any questions, ask your doctor or pharmacist.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eTake this medication by mouth, with or without food, as directed by your doctor. Do not take tadalafil more often than once daily.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eThe manufacturer directs to swallow this medication whole. However, many similar drugs (immediate-release tablets) can be split\/crushed. Follow your doctor's directions on how to take this medication.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eThe dosage is based on your medical condition, response to treatment, and other medications you may be taking. Be sure to tell your doctor and pharmacist about all the products you use (including prescription drugs, nonprescription drugs, and herbal products).\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eTo treat the symptoms of BPH, take this medication as directed by your doctor, usually once a day. If you are also taking finasteride with this medication to treat symptoms of BPH, talk with your doctor about how long you should continue taking this medication.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eTo treat erectile dysfunction-ED, there are 2 ways that tadalafil may be prescribed. Your doctor will determine which is the best way for you to take tadalafil. Follow your doctor's directions exactly since your dosage depends on how you are taking it. The first way is to take it as needed, usually at least 30 minutes before sexual activity. Tadalafil's effect on sexual ability may last up to 36 hours.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eThe second way to treat ED is to take tadalafil regularly, once a day every day. If you take it this way, you may attempt sexual activity at any time between your doses.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eIf you are taking tadalafil to treat both ED and BPH, take it as directed by your doctor, usually once a day. You may attempt sexual activity at any time between your doses.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eIf you are taking tadalafil once daily for BPH, or for ED, or for both, take it regularly to get the most benefit from it. To help you remember, take it at the same time each day.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eTell your doctor if your condition does not improve or if it worsens.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eSide Effects\u003c\/p\u003e\n\u003cp\u003eHeadache, stomach upset, back pain, muscle pain, stuffy nose, flushing, or dizziness may occur. If any of these effects last or get worse, tell your doctor or pharmacist promptly.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eTo reduce the risk of dizziness and lightheadedness, get up slowly when rising from a sitting or lying position.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eRemember that this medication has been prescribed because your doctor has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eSexual activity may put extra strain on your heart, especially if you have heart problems. If you have heart problems and experience any of these serious side effects while having sex, stop and get medical help right away: severe dizziness, fainting, chest\/jaw\/left arm pain, nausea.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eRarely, sudden decreased vision, including permanent blindness, in one or both eyes (NAION) may occur. If this serious problem occurs, stop taking tadalafil and get medical help right away. You have a slightly greater chance of developing NAION if you have heart disease, diabetes, high cholesterol, certain other eye problems (\"crowded disk\"), high blood pressure, if you are over 50, or if you smoke.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eRarely, a sudden decrease or loss of hearing, sometimes with ringing in the ears and dizziness, may occur. Stop taking tadalafil and get medical help right away if these effects occur.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eIn the rare event you have a painful or prolonged erection lasting 4 or more hours, stop using this drug and get medical help right away, or permanent problems could occur.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003eA very serious allergic reaction to this drug is rare. However, get medical help right away if you notice any symptoms of a serious allergic reaction, including: rash, itching\/swelling (especially of the face\/tongue\/throat), severe dizziness, trouble breathing.\u003c\/p\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53748949287204,"sku":null,"price":240.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_aabf086a-7d09-4f2c-beda-6a8c3638f248.jpg?v=1778065435"},{"product_id":"hd-labs-provirion-tabs","title":"HD Labs Provirion Tabs","description":"\u003cp\u003e\u003cspan\u003eHD LABS PROVIRION(25MG MESTEROLONE\/TAB=50TABS)\u003c\/span\u003e\u003c\/p\u003e\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","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53749056471332,"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_f2fe24e5-dcf0-404a-b9c4-fdb9491e2200.jpg?v=1778065534"},{"product_id":"hd-labs-superdrol-tabs","title":"HD Labs Superdrol Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\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.\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":53749138719012,"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_9e86a2a9-156e-43fc-a9b0-c5aad8079a42.jpg?v=1778065641"},{"product_id":"hd-labs-testaject-250","title":"HD Labs Testaject 250","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eHD LABS TESTAJECT E 250(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\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTestosterone was generally toted as the big daddy of injectable steroids. No other steroid was consistently reported to bring such high returns as quickly in weight gain and strength increases. Due to its high anabolic\/high androgenic effects, many athletes used this drug in an off-season mass cycle. Water retention during administration of ENANTHATE was not reportedly as high as that realized during the use of OMNADREN. but darn close. Like all testosterone esters, Enanthate aromatized easily and has a high conversion rate to DHT. Those with prostate problems or who were sensitive to gyno and female pattern fat deposits, readily agreed that they should have either left it alone or taken steps to suppress estrogenic activity due to aromatization.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrugs such as PROVIRON and NOVLADEX were often utilized for this reason. DHT\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003econversion enzyme blockers such as Proscar were commonly co-administered with testosterones for the former reason.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTestosterone enanthate notably suppressed HPTA function severely. HCG\/Clomid were considered almost a must to stimulate normal endogenous (natural) testosterone production within a positive period of time at post use. My personal experience has been that if a cycle containing testosterone enanthate lasted longer than 6 weeks, HCG and usually Clomid were introduced for 10 days beginning at the end of week #4. (5000 i.u. of HCG 3 times in 10 days usually normalized sperm and endogenous testosterone production to a respectable extent) Without the use of HPTA stimulating compounds normalization did occur, only at a much slower rate. For this reason, gains made during “enanthate only” administrations were not well maintained after use was discontinued, and much was lost needlessly by most regardless. Perhaps this was why so many uninformed individuals stayed on the stuff almost year round. (There are several solutions and protocols that prevented excessive post-cycle lean mass tissue loss for the more informed athletes)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMales injected 200-1000mg weekly. Some did use much higher dosages of course. Due to a plasma half-life of 4-5 days, injections were normally administered bi­weekly. Most novice steroid should not use testosterone. Not only was considered unnecessary, it would have been foolish to diminish possible later gains when more gentle AAS were no longer providing results at reasonable dosages. Most users made excellent progress with a total weekly dosage of 200-600mg. Post-cycle use of an anti-catabolic drug was a constant agreed upon factor since it helped to maintain gains. (See Clenbuterol)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe negative side effects reported were mostly water retention and strong androgenic effects. These included gyno, accelerated hair growth, receding hair-lines, aggressiveness, higher blood pressure, acne, and increased fat deposits (due to aromatization). Since testosterones are metabolized by the liver fairly easily, alarming elevated liver enzymes occurred in very high dosages only. usually. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndrogens are derivatives of cyclopentano-perhydrophenanthrene. Endogenous androgens are C-19 steroids with a side chain at C-17, and with two angular methyl groups. Testosterone is the primary endogenous androgen.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIn their active form, all drugs in the class have a 17-beta-hydroxy group. Esterification of the 17-beta-hydroxy group produces compounds (testosterone enanthate and testosterone propionate) which have a longer duration of action and are hydrolyzed in vivo to free testosterone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndrogens are steroids that develop and maintain primary and secondary male sex characteristics.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEndogenous androgens are responsible for the normal growth and development of the male sex organs and for maintenance of secondary sex characteristics. These effects include the growth and maturation of prostate, seminal vesicles, penis, and scrotum; the development of male hair distribution, such as beard, pubic, chest and axillary hair; laryngeal enlargement, vocal chord thickening, alterations in body musculature, and fat distribution. Drugs in this class also cause retention of nitrogen, sodium, potassium, phosphorous, and decreased urinary excretion of calcium. Androgens have been reported to increase protein anabolism and decrease protein catabolism. Nitrogen balance is improved only when there is sufficient intake of calories and protein.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndrogens are responsible for the growth spurt of adolescence and for the eventual termination of linear growth which is brought about by fusion of the epiphyseal growth centers. In children, exogenous androgens accelerate linear growth rates, but may cause a disproportionate advancement in bone maturation. Use over long periods may result in fusion of the epiphyseal growth center and termination of growth process.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndrogens have been reported to stimulate the production of red blood cells by enhancing the production of erythropoietic stimulating factor.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDuring exogenous administration of androgens, endogenous testosterone release is inhibited through feedback inhibition of pituitary luteinizing hormone (LH). At large doses of exogenous androgens, spermatogenesis may also be suppressed through feedback inhibition of pituitary follicle stimulating hormone (FSH).\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53749214380324,"sku":null,"price":400.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_2497c825-d0b1-4a9a-819f-04c8fc639319.jpg?v=1778065762"},{"product_id":"hd-labs-clenbuterol-tabs","title":"HD Labs Clenbuterol Tabs","description":"\u003cp\u003e\u003cspan\u003eHD LABS CLENBUTEROL(40MCG CLENBUTEROL HCL\/TAB=50TABS)\u003c\/span\u003e\u003c\/p\u003e\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","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53749284274468,"sku":null,"price":220.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_0cc6eabb-c628-4d74-a188-e9105d1edfa2.jpg?v=1778065894"},{"product_id":"hd-labs-winstrol-tabs","title":"HD Labs Winstrol Tabs","description":"\u003cp\u003e\u003cspan\u003eHD LABS WINSTROL 10(10MG STANOZOLOL\/TAB=50TABS)\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eORAL VERSION\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 30\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: About 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\u003eAverage Reported Dosage: Males 20-50-mg daily Women 10-15-mg 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: 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: High in high oral dosages\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\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePretty much everything written thus far about Stanozolol injectable (*See “Winstrol Depot” under “Injectable Anabolic Androgenic Steroids” for more info) was also attributed also to the oral form. It was often said that the oral form is less effective than the injectable. In truth, it was usually due to dosages, and this in turn was due to price. Athletes usually administered a lower dosage orally because it seemed like 25 pills daily was mega dosing. In my personal opinion this was true to a point. Oral use of any 17-alfa-alkylated steroid is hard on the liver. This is because it is difficult for the liver to deactivate these modified testosterone and derivatives. Let me make it clear. Milligram for milligram oral administration of Stanozolol was reported significantly more potent than the injection product (but it is more liver toxic). Oral dosages were commonly broken into 2-3 daily dosages to maintain circulatory androgen elevation. An effective reported daily oral dosage for women was 10-15mg and for men 20-30. However, this listed male dosage was not as effective (or as toxic) as the 30-50mg daily dose range.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMale athletes reported the practice of stacking 40-50mg of Stanozolol daily with 300-400mg weekly of a nandrolone provided significant lean muscle tissue augmentation with good post-cycle retention. For “bulking” purposes many reported the use of this drug with a testosterone at an average reported dosage of 200-600mg weekly resulted in “amazing strength and weight gains” and improved post-cycle lean mass retention.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWomen athletes commonly reported the use of Stanozolol at a dosage of 10-15mg daily with 50-100mg of a nandrolone weekly resulted in a rapid increase in quality lean mass tissue with low water retention and rare virilizing negative side effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAnabolic steroids such as Stanozolol are synthetic derivatives of the male hormone testosterone. Stanozolol has a pronounced anabolic effect with fewer masculinizing side effects than testosterone and some other synthetic anabolic steroids. Anabolic steroids are used in stimulating appetite and increasing weight gain, strength, and vigor. They should be used as a part of an overall program with other supportive and nutritional therapies.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis is a very popular anabolic steroid, which is a derivative of dihydrotestosterone. Winstrol is a relatively low androgenic steroid which will not aromatise. It is moderately toxic to the liver. Very few users report any water retention or any other side effects while using Winstrol. It is a popular drug for cutting in a stack with Primobolan or Parabolan. When stacked with Testosterone it can be very effective for a size and strength gain. Women use the drug quite often, but it can cause virilising effects for some women even at low dosages. Most of the muscle gains made while taking the Winstrol are retained after the drug is discontinued. The injectable form is better than the oral. Many feel that the injectable must be administered at least twice a week: some take shots every day for better effects. Dosages range from 3 to 5 cc?s per week for men, 1 to 2 cc’s in women. .\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStanozolol is prescribed for chronic infections, for conditions such as extensive surgery, [corticosteroid-induced myopathy, decubitus ulcers, burns] , or severe trauma, which require reversal of catabolic processes or protein-sparing effects. This is used in addition to, and not as replacements for, conventional treatment of these disorders.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStanozolol is effective in raising hemoglobin concentrations in some cases of aplastic anemia (congenital or idiopathic).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStanozolol is indicated in the prophylaxis of hereditary angioedema to decrease the frequency and severity of attacks.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStanozolol is used in the treatment of hereditary angioedema.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStanozolol is indicated in the treatment of conditions associated with decreased fibrinolytic activity due to antithrombin III deficiency or excess fibrinogen. These conditions may include cutaneous vasculitis, scleroderma of Raynaud’s disease, vasculitis of Behcet’s disease, and complications of deep vein thrombosis such as venous lipodermatosclerosis. Stanozolol is indicated in the prevention of recurrent venous thrombosis associated with antithrombin III deficiency. Stanozolol may be of benefit in patients susceptible to or with a history of thromboembolism for the treatment of vascular disorders associated with these forms of reduced fibrinolytic activity.\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53749659664676,"sku":null,"price":240.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_fc402664-e379-4e7f-a16a-6b0c34de32d5.jpg?v=1778066398"},{"product_id":"hd-labs-anavar-tabs","title":"HD Labs Anavar Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eHD LABS CHINA= ANAVAR(10MG OXANDROLONE\/TAB=50 TABS) \n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 24\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 322-630\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 8-12 hours\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anabolic\/Androgenic Steroid (Oral)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 20-50mg daily Women 10-15mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Only when administered in high dosages\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Rare\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Yes, c17-alfa-alkylated steroid. Due to low dosages toxicity is low-moderate\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT conversion: Quite low\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA function: Unlikely even in high dosage use\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOxandrolone was often refereed to as an all purpose oral AAS. This drug was once marketed under the product name (still commonly used trade name) of Anavar. It has the unique quality of significantly stimulating (more than other AAS) the synthesis of phosphocreatine in muscle cells which in turn provides faster regeneration of, and a distinct elevation in, ATP. Of course all AAS have this effect to some extent. Oxandrolone is simply unmatched in this aspect.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e(See Creatine for more info) Due to this quality, a rapid build- up in strength was frequently reported and an obvious distinct hardness in muscle was obtained with little weight gain and no aromatization.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThough it is a common belief that Oxandrolone is not very anabolic, a clinical study showed a 44% increase in muscle cell protein synthesis after only 5 days of administration. Since Oxandrolone does not aromatize to estrogen, water retention is reported as quite low and gyno was of no concern. Also, for the same reason, during dieting phases fat deposits were said to be “burned away” more quickly. (Especially when the drug was co-administered with Clenbuterol).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOxandrolone was reported to stack well with so -called mass steroids such as testosterone or with high anabolic\/moderate androgenic steroids such as Equipoise or Nandrolones. Persons over 40 have reported excellent results by stacking 15-25 mg of Oxandrolone daily with 200-400 mg of Deca.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eA very hard pre-contest appearance has been achieved by males when stacked with Oxandrolone and Halotestin if a estrogen\/progesterone receptor antagonist (*See Nolvadex) had been utilized as well. As I said: “all purpose” was commonly the term of choice.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe drug Oxandrolone was originally manufactured to be used by women to prevent osteoporosis and for children as a cure for stunted growth. The low androgenic quality prevents almost all virilization for women in dosages of 15-mg daily or less. And for the same reason does not cause closure of the epiphysial plates prematurely. An interesting note: Oxandrolone does not suppress any part of the HYPOTHALAMUS-PITUITARY-TESTES AXIS (HPTA). This means Oxandrolone by itself will not significantly suppress natural testosterone production. Therefore it was not uncommon for some athletes to report post-cycle HPTA regeneration protocols that included this drug. The result was prominent lean mass retention.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAdjunctive therapy to promote weight gain after weight loss following extensive surgery, chronic infections, or severe trauma, and in some individuals who, without definite pathophysiologic reasons, fail to gain or maintain normal weight; to offset protein catabolism associated with prolonged administration of corticosteroids; for relief of bone pain frequently accompanying osteoporosis.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAlso used for Catabolic illness (eg, alcoholic liver disease, burn injury).\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53749738832164,"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_d9a8f72e-5e53-4664-935d-46bb00450b65.jpg?v=1778066527"},{"product_id":"hd-labs-ostarine","title":"HD Labs Ostarine","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eHD LABS SARMS OSTARINE(MK-2866)12.5MG\/TAB=50TABS.\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMK-2866 Builds Muscle And Burns Fat\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWith multiple published human trials under its belt, MK-2866 (also called ostarine) is one of the best-studied SARMs. Those studies found powerful results, too. Ostarine shows no meaningful side effects and is very effective at building muscle.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eElderly men and women who took modest doses of ostarine for 12 weeks grew 3 pounds of muscle and lost a pound of fat, with no changes to diet or exercise [1]. Cancer patients saw nearly identical results along a similar timeframe [2]. There were no side effects in either study.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eA pound of muscle a month is about what you would expect with a solid workout routine – but the people taking ostarine in these studies weren’t exercising. Combining the two would be even more powerful, in theory. Pretty impressive.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSide effects of MK-2866\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe studies found no side effects. Anecdotally, however, people report short-term testosterone suppression when they take high doses of ostarine for 8-12 weeks. Testosterone rebounded to normal levels within a couple weeks after they stop. The dosage I discuss below is far lower and for a shorter amount of time, but there’s still a risk of short-term T suppression, and possibly other side effects researchers don’t know about yet.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHow to dose MK-2866\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThere haven’t been official dose recommendations for SARMs because they’re so new. The doses in this article are all conservative, and based what on studies and anecdotal reports show to work.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFor ostarine, 15-20mg daily for 6 weeks. Time of day doesn’t matter. To be cautious, take at least 6 weeks off so your system balances out before starting another cycle. Ostarine, along with the other SARMs on this list, seems to pair best with regular exercise like lifting and HIIT.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAlso known as Ostarine, MK-2866 is a very popular, well-tested SARM, with no side effects observed in most users. It enhances muscle mass and helps burn fat, but Ostarine is most recognized for its unique propensity to increase bone density and aid in injury prevention \u0026amp; recovery. Most users are male, as with other SARM’s, however women choosing to adminsister SARM’S will usually prefer Ostarine for its milder overall profile. While long-term use of Ostarine can suppress testosterone production in men, the compound exhibits very low risk of this or other side effects when taken in typical dosages.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTypical dose: 15-30 mg\/day\u003c\/div\u003e\n\u003cdiv\u003eMax: 30 mg\/day\u003c\/div\u003e\n\u003cdiv\u003eStacking dose: 10-15 mg\/day (depending on stack)\u003c\/div\u003e\n\u003cdiv\u003eHalf-life: 24 hours\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53749825405220,"sku":null,"price":440.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_929c130b-13f6-4bb1-ad26-e47562b530d6.jpg?v=1778066629"},{"product_id":"hd-labs-sibutramax-tabs","title":"HD Labs Sibutramax Tabs","description":"\u003cp\u003e\u003cspan\u003eHD LABS SIBUTRA MAX(SIBUTRAMINE HCL 30MG\/TAB=30TABS)\u003c\/span\u003e\u003c\/p\u003e\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","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53749889007908,"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_621901d5-9d6c-42c7-bb02-9f10e7a8d2d6.jpg?v=1778066722"},{"product_id":"hd-labs-tren-tabs","title":"HD Labs Tren Tabs","description":"\u003cp\u003e\u003cspan\u003eHD LABS CHINA=ORAL TREN (250mCg\/TAB METHYLTRIENOLONE =50 TABS)\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndrogenic 200-300\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAnabolic 1000\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStandand methyltestosterone(oral)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: About 24 Hours\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 Dosage: Men: 100-300-mg 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: Low to None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Rarely\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\u003ehighly toxic to kidneys also\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: SEVERE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMethyldienolone (MD) is a synthetic oral anabolic steroid that was researched in the 1960’s but never sold as a prescription drug. It is fundamentally a nandrolone-based compound, modified from this base hormone in two ways. First, it has been c-17alpha-alkylated (methylated) to protect against hepatic breakdown. This alteration, in of itself, turns the mild-mannered nandrolone into the formidable oral agent methylnandrolone. Next, it has been given a second double-bond at the 9 position, which considerably increases its anabolic and androgenic potency. Methyldienolone actually differs from methyltrienolone, the most potent steroid profiled in this book, only by the lack of a third double-bond (hence the “di” part). Although not actually #2 in the book, methyldienolone is 5 times more potent than Dianabol, 10 times more potent than methyltestosterone, and 13 times more potent than Primobolan®.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOther characteristics of note include an inability to be converted into estrogen, which limits this steroid’s potential for related side effects like fat gain, water retention, and gynecomastia. This trait makes it a drug more ideally suited for cutting cycles than bulking ones. However, as a nandrolone based compound, it may have some progestational activity, which can work to intensify the effects of estrogen. Therefore, it may not be the ideal steroid to use with other aromatizable (estrogen producing) compounds, if fat loss and muscle definition are key concerns. Methyldienolone is also only moderately androgenic, with just a modest propensity to trigger oily skin and acne when used in reasonable dosages. Overall, this agent is classified as an “anabolic” and should fall somewhere between the milder nandrolone derivatives and more androgenic orals like Dianabol and Anadrol.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEffective oral daily doses are going to fall in the range of 2-1 Omg per day for men, and under 1 mg daily for women. At this level, one should expect measurable strength and lean tissue gains, which should be accompanied by decent fat loss and minimal side effects. When determining dosage one also needs to respect the fact that methyldienolone is a c-17alpha-alkylated COMPOUND AND presents some liver toxicity to its user. For optimal safety it is usually recommended to limit drug duration to no longer than 8 weeks, after which a break is taken from all methylated or ethylated steroids. One might also want to avoid stacking this drug with other liver toxic orals, and instead opt to use an injectable base instead. 5mg per day of methyldienolone combined with 400mg weekly of testosterone cypionate\/enanthate or Equipoise® would make an excellent lean-mass stack, while trenbolone (225mg) or Primobolan® (300-400mg) could be used instead for cutting.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAvailability of methyldienolone is going to be limited over the next couple of years, due to the recent scheduling of this agent as a class III controlled substance.This agent was manufactured as a nutritional supplement for a brief period of time before the 2004 amendment to the anabolic steroid act was passed, which means there should be a fair amount of leftover supplement available as people take advantage of its increasing value and sell off their pre-ban “stockpiles” The long-term future of this agent remains uncertain, however, as no legitimate drug company has yet to take an interest in it. It is unfortunate to think that this drug may no longer be available in a couple of years.This is a very powerful agent though, and may very well peak the interest of some of the companies looking for a “different” oral to sell. That is, of course, if the consumer market can get over the fact that this drug was once “legal” Although sold openly for a while, MD is indeed still one very powerful, and one very real, steroid.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMetribolone is the trade name for the drug Methyltrienolone, which is the most potent AAS produced. It is actually an orally active form of Trenbolone chemically altered into a 17-alkylated compound. Obviously, this means serious liver toxicity. In fact, even at microgram dosages, (1milligram = 1,000 micrograms) it is 15-20 times more toxic than Anadrol-50. That is toxic! Though orally active this AAS is provided in vials and meant for injection use only. But in truth, Metribolone is about 40-50 times more androgenic than Methyltestosterone, so a little goes a long way. The drug is fairly resistant to DHT conversion but does bind easily to scalp and prostate androgen receptor sites.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIn clinical research, Metribolone is used to determine receptor-site affinity \/ displacement. Let me explain that. Metribolone is a very powerful androgen receptor-site stimulator and antagonist. I doubt there is any AAS more powerful. Since it binds so strongly to the receptor-site, researchers use the drug to see if other drugs can dislocate it, or for comparison. Not even Deca can kick it out of receptor-sites!\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMetribolone is highly resistant to binding proteins such as SHBG. This means it remains highly active in the blood. If you recall, about 97-99% of our testosterone is in a “bound” state and only the remaining 1-3% is active or free. Only free or active androgens can fit into receptor-sites and trigger the anabolic mechanism. Some AAS are more resistant to these binding proteins than others. And Metribolone is the most resistant of all. Like I said, a little goes a long way. As example consider this for a moment. If all other factors of potency were equal, 1mg of unbound\/free Metribolone would have the same activity as 97-100mg of testosterone due to the effects of binding proteins.\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53750022897956,"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_fb904dd7-504f-4281-9a9c-20066044b285.jpg?v=1778066897"},{"product_id":"hd-labs-clomid-tabs","title":"HD Labs Clomid Tabs","description":"\u003cp\u003eIt is a great oral to use for when you PCT.\u003c\/p\u003e\n\u003cp\u003eYou just drink one every night before bed.\u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53750114746660,"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_f43030a3-e474-4bf0-9b96-4a799d9b421a.jpg?v=1778067013"},{"product_id":"hd-labs-dianabol-tabs","title":"HD Labs Dianabol Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eHD LABS DIANABOL10(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":53750212854052,"sku":null,"price":200.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_64d49ad3-6874-4c45-8cbe-d4267b42036d.jpg?v=1778067174"},{"product_id":"hd-labs-tamox-tabs","title":"HD Labs Tamox Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\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.\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":53751549526308,"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_f378f72e-92f3-4345-bb68-b897bf6b1777.jpg?v=1778069017"},{"product_id":"hd-labs-sustanon-250","title":"HD Labs Sustanon 250","description":"","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53751628955940,"sku":null,"price":150.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_d33254dc-3560-426c-81ee-e6e255e6e8b2.jpg?v=1778069128"},{"product_id":"hd-labs-heliost3-tabs","title":"HD Labs HeliosT3 Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eHD LABS CHINA=HELIOS\u0026amp;T3 TABS(37.5MCG Clenbuterol hcl,25 MCG LIOTHYRONINE SODIUM,5.4mg yohimbe hcl\/TAB=50 TABS)\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\u003c\/div\u003e\n\u003cdiv\u003ecycles 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 – 37.5mcg\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 5.4mg\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e Effects 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\u003e Patients should be instructed that the expected benefits of CYX 3 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 CYX 3\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e To facilitate delivery to the stomach and thus reduce the potential should be instructed to swallow CYX 3 with a full glass of tap water and not to lie down for at least 30\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eminutes 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 CYX 3 at bedtime or\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ebefore 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 CYX3\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53751692296484,"sku":null,"price":270.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_5be5af3f-fbc2-4fbd-83a1-810be214bbdf.png?v=1778069265"},{"product_id":"hd-labs-methyl-1-t-tabs","title":"HD Labs Methyl-1-T Tabs","description":"\u003cp\u003e\u003cspan\u003eThis is probably the strongest oral compound ever made. \u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTaking one tab a day (10mg) should be sufficient for a maximum of 5 to 6 weeks. These doses might sound low but considering its potency athletes are warned to not compare it to doses being taken of other products they are familiar with. Some users reported a dose of around 20mg but this was found to be very high and the side effects of high blood pressure and toxicity at those doses became rapidly evident.\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003eSome describe M1T’s characteristics as a mix between Primabolan, Stanazol and Trenbolone. I personally like comparing it to Oxymethelone (Anapolon) by comparing its anabolic rating. Anapolon is seen as one of the strongest orals in the world and has an anabolic rating of 320. M1T has an anabolic rating of 900-1600. This is between four and five times the anabolic rating of Anapolon (Oxymethelone)\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003eThe active pharmaceutical ingredient of this agent is methyldihydroboldenone also known as Methyl-1-testosterone or in short M1T. It is a derivative of dihydrotestosterone.\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003eThis product is mostly used on a bulking cycle when rapid mass and size gains are the objective. Many athletes report some water retention on M1T. Athletes who are genetically very lean report massive pumps and extreme vascularity when working out in the gym. The toxicity of this product can be felt after a couple of days of administration.\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003eM1T is so potent as an anabolic and androgenic that it can be used on its own. Alternatively, it can be stacked with regular agents like an injectable testosterone enanthate, cypionate or even a Test 450mg Combo blend from Ciccone Pharma that will pack a serious punch and add to serious gains. One millilitre of Test 450mg Combo twice or three times per week with 2 to 3 capsules of M1T per day would be a serious stack for serious gains.\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003eM1T is not a very well-known agent and very new to the market but for athletes who want something new and different to their normal compounds this a highly-recommended bulking agent.\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003eMilligram for milligram it is also two to three times stronger than Superdrol.\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003eWARNING – Although this is listed as a Pro Hormone it is still banned by WADA (World Anti-Doping Agency) and you will test positive if you use this while competing in international sports events.\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53751777788196,"sku":null,"price":230.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_785177fd-b36e-47ec-b88b-59587e598312.jpg?v=1778069367"},{"product_id":"hd-labs-arimidex-tabs","title":"HD Labs Arimidex Tabs","description":"\u003cp\u003e\u003cspan\u003eHD LABS ARIMADEX(1MG ANASTROZOLE\/TAB=30TABS)\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 4-6 hours\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anti-estrogen \/competitive inhibitor (Oral)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: 0.5-3.0 mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: No\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Yes dosage dependent\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA function: No, the drug has been accredited with HPTA up-regulating effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eArimidex is an anti-estrogen type drug. It is usually provided in 0.5 MG tabs. The drug works in a non-steroid form by inhibiting the aromatase enzyme which converts testosterone and other androgens into estrogen. This means that there is less estrogen to cause female pattern fat deposits, gyno, and water retention. In medicine, Arimidex is utilized to treat prostate cancer. In sports chemistry, the drug has been employed as a means of preventing excessive estrogenic side effects during AAS use and to aid in creating a harder appearing musculature for competitive bodybuilders. Unlike Nolvadex, which simply block estrogen receptor-sites, this drug prevents or reduces estrogen production. Though some estrogen presence is noted as necessary for AAS to reach full effectiveness, too much can cause a layer of fat, water retention, and breast tissue growth potentially with tumors called gynecomastia or bitch tits. Arimidex has a 75-85% aromatization inhibition rate.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMales who experienced excessive aromatization of AAS or who were extremely estrogen sensitive usually utilized a dosage of 0.5-3.0 mg daily. In fact, most realized excellent estrogen control with only 0.5mg\/d (mg daily). Women usually showed excellent lean appearances (even in their legs) with 0.5-1.0 mg daily. Arimidex has a very short active-life so 0.5 mg dosages were often taken 2-6 times daily at equal intervals. Stacking 10-30 mg of Nolvadex with 1.0 mg of Arimidex has resulted in a near “0” estrogen activity situation regardless of the AAS protocol utilized. Directly following an AAS cycle, estrogen control has also become a problem (during periods intended for re­establishing HPTA function). In this case, the dosage was reduced from a higher starting dosage to a low dosage that was continued for 7-14 days after AAS discontinuance. This protocol was considered necessary to assure clearing of AAS induced estrogen build-up.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eArimidex is indicated for adjuvant treatment of postmenopausal women with hormone receptor positive early breast cancer. \u003c\/div\u003e\n\u003cdiv\u003eArimidex is indicated for the first-line treatment of postmenopausal women with hormone receptor positive or hormone receptor unknown locally advanced or metastatic breast cancer.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eArimidex is indicated for the treatment of advanced breast cancer in postmenopausal women with disease progression following tamoxifen therapy .\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53751882350884,"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_d6138c4d-c298-4153-8e04-78006e7f0fb8.jpg?v=1778069512"},{"product_id":"hd-labs-supertest-500","title":"HD Labs SuperTest 500","description":"\u003cp\u003e\u003cspan\u003eSUPER TEST 500 IS A MIXTURE OF THE 5 TESTOSTERONE ESTER:\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e30MG\/ML TESTOSTERONE PROPIONATE\u003c\/div\u003e\n\u003cdiv\u003e30MG\/ML TESTOSTERONE ISOCAPROATE\u003c\/div\u003e\n\u003cdiv\u003e40MG\/ML TESTOSTERONE DECOANATE \u003c\/div\u003e\n\u003cdiv\u003e100MG\/ML SUSTENON BLEND\u003c\/div\u003e\n\u003cdiv\u003e150MG\/ML TESTOSTERONE ENANTHATE \u003c\/div\u003e\n\u003cdiv\u003e150MG\/ML TESTOSTERONE CYPIONATE \u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD TESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: About 3 weeks\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Androgenic\/Anabolic steroid (For injection) Average Reported Dosage: Men 125-2000mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Low except in high dosages over 1000-mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Significantly after 2 weeks\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: Yes, somewhat less than testosterone cypionate or enanthate.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis is a well structured product that acts as a well timed time-released high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eanabolic\/high androgenic testosterone. In fact, due to TESTOSTERONE PROPIONATE,\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ethis product becomes active after one day, but through the series of the other 3 testosterones, remains active for 3 weeks. This mixture had a reported better over all effect milligram for milligram than any other testosterone alone. Users experienced a rapid increase in strength and an even increase in solid mass during administration. SUSTANON aromatized less and caused less water retention when compared to other single testosterones and much less than OMNADREN. Liver toxicity was low (Except in ridiculous dosages) as the liver metabolizes testosterone very efficiently. Like all testosterones, SUSTANON provided improved muscle pumps, better post-training recuperation, and an elevation in aggressiveness toward training.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSUSTANON 250\u0026amp;TEST COMBO 300 significantly suppressed the HPTA so natural testosterone production was significantly decreased as well. For this reason, HCG and CLOMID were considered mandatory after 4-6 weeks of continuous use and after the discontinuance of the drug.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMales normally utilized dosages of 250-1000mg weekly, but some used higher dosages. As a rule, excellent results were realized with a dosage of 250-500mg every 7­-10 days. Most novices and women noted that they felt that they should not use testosterone. Novices…because it was not necessary and it will limit later potential progress. Women should not use them (but a few reported doing so) due to virilizing effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome woman polled just could not leave testosterones alone. PROSCAR (FINASTERIDE, A DHT BLOCKER) was considered mandatory for co-administration\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eand TESTOSTERONE PROPIONATE 50mg 1 time weekly was noted to cause less virilizing side effects.\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53751960633636,"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_7431bb8f-1594-43e3-927e-471a63e1be04.jpg?v=1778069626"},{"product_id":"hd-labs-depoject-200","title":"HD Labs Depoject 200","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eHD LABS DEPOJECT 200(200MG\/ML TESTOSTERONE CYPIONATE=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: 15-16 days\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Androgenic\/Anabolic Steroid (For injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 200-1000mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Yes, common\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Yes, due to water\/electrolyte retention\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Low, except in absurd dosages\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT conversion: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Yes, severely\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePretty much all that was written about TESTOSTERONE ENANTHATE also applies to TESTOSTERONE CYPIONATE. A slight distinction was made in that they\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eeach provided a notable different half- and active-life period. For this reason, CYPIONATE injections were reduced to every 8th day by some reported users. Dosages of 200-1000mg weekly were common, but most users experienced excellent results with 200-600mg weekly. Both testosterone preparations stacked well with any other AAS and added a distinct androgenic effect. This meant improved regenerative qualities and greater training intensity with a correlating significant increase in weight-load capacity. For those who wished to use testosterone but were highly sensitive to gyno and water\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eretention, TESTOSTERONE PROPIONATE was commonly reported to be the better\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003echoice. Oddly enough, a few of those polled reported more sensitively due to Propionate’s fast action. Interesting paradox, huh? The issue was simply a matter of dosage\/administration protocols. Since PROPIONATE remained active for about 3 days a weekly administration protocol allowed circulatory clearing of the drug. It should be\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003enoted that both TESTOSTERONE ENANTHATE and CYPIONATE were said to be\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003emore anabolic and less androgenic then SUSPENSION or PROPIONATE. This is pure imagination. The truth is that suspension actually is a faster acting testosterone and contains more total testosterone per 100mg dosage than any esterfied testosterone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003etestosterone cypionate which is the oil-soluble 17 (beta)-cyclopentylpropionate ester of the androgenic hormone testosterone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEndogenous androgens are responsible for normal growth and development of the male sex organs and for maintenance of secondary sex characteristics. These effects include growth and maturation of the prostate, seminal vesicles, penis, and scrotum; development of male hair distribution, such as beard, pubic, chest, and axillary hair; laryngeal enlargement, vocal cord thickening, and alterations in body musculature and fat distribution. Drugs in this class also cause retention of nitrogen, sodium, potassium, and phosphorous, and decreased urinary excretion of calcium. Androgens have been reported to increase protein anabolism and decrease protein catabolism. Nitrogen balance is improved only when there is sufficient intake of calories and protein.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndrogens are responsible for the growth spurt of adolescence and for eventual termination of linear growth, brought about by fusion of the epiphyseal growth centers. In children, exogenous androgens accelerate linear growth rates, but may cause disproportionate advancement in bone maturation. Use over long periods may result in fusion of the epiphyseal growth centers and termination of the growth process. Androgens have been reported to stimulate production of red blood cells by enhancing production of erythropoietic stimulation factor.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53752068145444,"sku":null,"price":400.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_34cd9da3-2797-4d7b-bd04-83c885d27d2a.jpg?v=1778069771"},{"product_id":"hd-labs-deca-durabolin-100","title":"HD Labs Deca-Durabolin 100","description":"","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53752123293988,"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_d199fe33-3b95-4cb6-a938-0d0369a6a1ac.jpg?v=1778069885"},{"product_id":"hd-labs-andarine","title":"HD Labs Andarine","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eAndarine is widely considered to be the most potent of all SARMS that help build lean muscle mass.\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndarine has been one of the most widely tested and studied of all the SARMS. Tests have proven that Andarine helps retain lean muscle mass as well as enhancing it. However with Andarine this is not the only noted benefit. In addition to strength and lean muscle gains is its powerful fat burning properties as well.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndarine : the all-round super potent SARM for lean hard muscles\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhat to Expect\u003c\/div\u003e\n\u003cdiv\u003eWhen used for cutting, Andarine’s properties will ensure that you get similar results to what you would expect when using Anavar or Stanazol. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndarine can also minimise LPL (lipoprotein lipase) an enzyme that can cause the storing of adipose tissue or body fat.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndarine also improves vascularity, for that aesthetic chiselled look. Unlike with Stanazol, it does not affect your joints or negatively affect your cholesterol levels as with Anavar.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSide Affects\u003c\/div\u003e\n\u003cdiv\u003eAndarine is not the perfect anabolic compound and as with Anavar and Stanazol does follow the law of diminishing returns. What this means is higher dosages are required with extended use which comes with the main side effect.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe most noted negative effect of Andarine are visual issues such as the yellow tint and difficulty adjusting to night vision. This side effect is unique to Andarine and will decrease and vanish once the product leaves your system.  \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis side effect is often hyped or overblown and is noted at very high doses and cycles longer than 12 weeks. This side effect can however be managed with dosage reduction, and dosage cycling.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe Benefits of S4 over Steroids\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003every minimal growth on secondary sexual organs such as the prostate.\u003c\/div\u003e\n\u003cdiv\u003eThe LDL\/ HDL ratio is not affected which makes it a low cardiovascular risk.\u003c\/div\u003e\n\u003cdiv\u003eZERO % chance of aromatization, male breast lactation, or rise in any other female characteristic during the post cycle recovery.\u003c\/div\u003e\n\u003cdiv\u003eTestosterone is not diminished in any capacity during the post cycle recovery.\u003c\/div\u003e\n\u003cdiv\u003eVery exclusive in tissue selection and growth which means it will not cause heart enlargement or damage to neighbouring organs.\u003c\/div\u003e\n\u003cdiv\u003eAndarine does NOT require the utilization or devouring of liver enzymes to activate their anabolic effects. This eliminates any risk of hepatotoxicity or hepatitis.\u003c\/div\u003e\n\u003cdiv\u003eAlthough Andarine is not as powerful as comparable steroids such as Winstrol, they do not require the extensive post cycle therapy and can be cycled back to back throughout the year. With the possibility of obtaining the similar results.\u003c\/div\u003e\n\u003cdiv\u003eAndarine has overall presented larger increases in muscle mass than DHT.\u003c\/div\u003e\n\u003cdiv\u003eDosage\u003c\/div\u003e\n\u003cdiv\u003eWe recommend milder dosages that err on the side of caution. Higher dosages have been reported but start here. If vision side effect is a problem cycle 5 days on and 2 days off to assist with vision side.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMale athletes 2 tablets daily or cycled.\u003c\/div\u003e\n\u003cdiv\u003eFemale athletes ½ -\/ 1 tablet daily or cycled.\u003c\/div\u003e\n\u003cdiv\u003eCycle 6 weeks either 7 days on or 5 days on 2 days off depending on sensitivity.\u003c\/div\u003e\n\u003cdiv\u003e2 week off period between cycles.\u003c\/div\u003e\n\u003cdiv\u003eWhats in the box\u003c\/div\u003e\n\u003cdiv\u003e56 Tablets per box\u003c\/div\u003e\n\u003cdiv\u003e12.5mg Andarine per tablet.  \u003c\/div\u003e\n\u003cdiv\u003eStack with\u003c\/div\u003e\n\u003cdiv\u003eCardarine and\/or Nutrabol\u003c\/div\u003e\n\u003cdiv\u003eOriginally developed to help osteoporosis and muscle-wasting diseases, S4, or Andarine, is a first-gen SARM that’s been highly-tested over the years. S4 preserves and improves lean body mass. That is, it decreases body fat while increasing muscle mass. Andarine is anabolically above-average, due to strong AR (androgen receptor) affinity, with superior muscle-building and fat-reducing effects. It is also known to boost sex drive (but also reduces sperm development). Concern over vision-related side effects in one study have reportedly caused some S4 users to switch to Ostarine, which is chemically very similar.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTypical dose: 25-50 mg\/day\u003c\/div\u003e\n\u003cdiv\u003eMax: 100 mg\/day\u003c\/div\u003e\n\u003cdiv\u003eStacking dose: 15-25 mg\/day (depending on stack)\u003c\/div\u003e\n\u003cdiv\u003eHalf-life: 4-6 hours\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53752202428708,"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_01db4f72-ace3-4bc9-bbe1-2cac15daf8b7.jpg?v=1778070008"},{"product_id":"hd-labs-heliosject","title":"HD Labs Heliosject","description":"\u003cdiv\u003eHD LABS HELIOSJECT(40MCG CLENBUTEROL HCL,5.4MG YOHIMBE HCL\/ML=20ML) \u003c\/div\u003e\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.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStart low to see if you can handle it because it is a strong medication\u003c\/div\u003e\n\u003cdiv\u003estart with 0.25 – 0.5 ML in the morning and inject straight into \u003c\/div\u003e\n\u003cdiv\u003estubborn fat deposit for local fat loss. Then work your-self up to \u003c\/div\u003e\n\u003cdiv\u003esee how much still is comfortable . Never go higher then 2ML per \u003c\/div\u003e\n\u003cdiv\u003eday! Because your receptors will degrade it is best to keep the \u003c\/div\u003e\n\u003cdiv\u003ecycles short.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSample cycle: \u003c\/div\u003e\n\u003cdiv\u003eweek 1: 0.5 ML per day \u003c\/div\u003e\n\u003cdiv\u003eweek 2: 1 ML per day \u003c\/div\u003e\n\u003cdiv\u003ethen stop two weeks\u003c\/div\u003e\n\u003cdiv\u003eweek 5: 0.5 ML per day \u003c\/div\u003e\n\u003cdiv\u003eweek 6: 1 ML per day \u003c\/div\u003e\n\u003cdiv\u003erepeat breaks and repeat usage.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e The compound is a 50ml vial containing a blend of Clenbuterol HCL: 40mcg\/ml and Yohimbine HCL: 5.4mg\/ml.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCICCONE CY COMBO – Clenbuterol \u0026amp; Yohimbine HCL blend\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe compound comes in a 50ml vial containing a blend of Clenbuterol HCL: 40mcg\/ml and Yohimbine HCL: 5.4mg\/ml.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHD LABS HELIOSJECT is a blend of Clenbuterol and Yohimbine HCl. Clenbuterol is a β2 adrenergic agonist with some similarities to ephedrine, but its effects are more potent and longer-lasting as a stimulant and thermogenics drug. Thermogenics are dietary supplements used to stimulate the body’s burning of fat. Thermogenics increase the metabolism of the body’s adipose tissue, generating heat ( thermo genesis).Old practices like exposing the body to very cold temperatures to raise Basal Metabolic Rate (BMR). This is usually done by soaking the body in icy cold water until a person can not tolerate it any longer almost to the point of inducing hypothermia. This then causes a release of thyroxin from the thyroid gland by means of the sympathetic nervous system thus raising BMR resulting in an increase in body temperature back to normal.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIn HD LABS HELIOSJECT formulations we apply T3 to our CYT3 (an oral blend of t3, Yohimbine and Clenbuterol) which combines all the thermogenics properties together in one unit dose)Common thermogenics substances are Ephedra, bitter orange, capsicum, ginger and caffeine.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e The Clen Blend injectable unit dose was specially formulated for spot reduction of stubborn areas of fat tissue for muscle – fat desired proportions. The injected compound promotes fat loss through the adrenergic system. Spot fat reduction is a within your reach. The blend would act under conditions were other means including the use of traditional oral Clenbuterol and Yohimbine products could not provide the desirable effect.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eADMINISTATION: \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOne must start at a low dose to be on the watch for adverse side effects due to the high potency. 0, 5 ML is a recommended starting dose in the morning injected straight into the fat deposit for local fat loss. The dose must be adjusted cautiously. Never exceed 2ML per day! Because the adrenergic receptors will stop its responsiveness.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSample cycle: (Must be adopted personally)\u003c\/div\u003e\n\u003cdiv\u003eweek 1: 0,5 ML per day \u003c\/div\u003e\n\u003cdiv\u003eweek 2: 1 ML per day \u003c\/div\u003e\n\u003cdiv\u003ethen stop two weeks\u003c\/div\u003e\n\u003cdiv\u003eweek 5: 0,5 ML per day \u003c\/div\u003e\n\u003cdiv\u003eweek 6: 1 ML per day \u003c\/div\u003e\n\u003cdiv\u003erepeat breaks and repeat usage.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHD LABS HELIOSJECT Clen Blend (see also our oral Clen Blend with T3) contains a blend of Clenbuterol Hydrochloride and Yohimbine Hydrochloride. The 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\u003eInjecting HD LABS HELIOSJECT Clen Blend one must consider the beta-2 receptor down – regulation may\/will occur, hence the need to cycle administration just as one would oral Clenbuterol.\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCommon Uses Of Clenbuterol and Injectable Clen\u003c\/div\u003e\n\u003cdiv\u003ePost-Cycle Therapy: Clenbuterol is used post cycle to aid in recovery. It allows the user to continue eating large amounts of food, without worrying about adding body fat. It also helps the user maintain more of his strength as well as his work out intensity. Diet: Roughly the same as on cycle.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFat loss: The most popular use for Clenbuterol, it also increases muscle hardness, vascularity, strength and size on a caloric deficit. For the most significant fat loss, Clen can be stacked with T3. Diet: A high protein (1.5g per lb of bodyweight), moderate carbohydrate (0.5g to 1g per lb of bodyweight), low fat diet (0.25g per lb of bodyweight) seems to work best with Clen.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAlternative to Steroids: Clenbuterol has mild steroid-like properties and can be used by non AS allowing bodybuilder to increase LBM as well as strength and muscle hardness. Diet: A moderate carbohydrate, high protein, moderate fat diet work well.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePrecautions: \u003c\/div\u003e\n\u003cdiv\u003eThe same precautions that apply to Ephedrine must be applied to Clenbuterol, although some people find ECA – ephedrine – caffeine – aspirin stacks harsher than Clen. It should not be applied with other central nervous system stimulants such as Ephedrine. These combinations are unnecessary and potentially dangerous. Caffeine can be used in moderation before a workout for an extra energy, although its diuretic effects may shift electrolyte balance. Drink more water if one uses Caffeine.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOne should use Injectable Clen Blend carefully and pay attention not to inject too much as injecting Clen may be dangerous and if over administered it can cause a heart attack. Because it is injected it has a much stronger affect then tablet or liquid Clen\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53752300077348,"sku":null,"price":400.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_8e33f6b7-a5ee-44a8-b62f-c0c70ad04410.jpg?v=1778070106"},{"product_id":"hd-labs-sustaject-325","title":"HD Labs Sustaject 325","description":"\u003cp\u003e\u003cspan\u003eHD LABS SUSTAJECT 325(325MG\/ML 5 TESTOSTERONE MIX=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: About 3 weeks\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Androgenic\/Anabolic steroid (For injection) Average Reported Dosage: Men 125-2000mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Low except in high dosages over 1000-mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Significantly after 2 weeks\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSustaject 325 is a mixture of the 5 testosterone esters:                     \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eACETATE -30mg\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePROPIONATE -50MG\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePHENYLPROPIONATE -50MG\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCYPIONATE -90MG\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDECANOATE -100MG \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis is a well structured product that acts as a well timed time-released high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eanabolic\/high androgenic testosterone. In fact, due to TESTOSTERONE PROPIONATE,\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ethis product becomes active after one day, but through the series of the other 3 testosterones, remains active for 3 weeks. This mixture had a reported better over all effect milligram for milligram than any other testosterone alone. Users experienced a rapid increase in strength and an even increase in solid mass during administration. SUSTANON aromatized less and caused less water retention when compared to other single testosterones and much less than OMNADREN. Liver toxicity was low (Except in ridiculous dosages) as the liver metabolizes testosterone very efficiently. Like all testosterones, SUSTANON provided improved muscle pumps, better post-training recuperation, and an elevation in aggressiveness toward training.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSUSTANON 250\u0026amp;TEST COMBO 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 7­10 days. Most novices and women noted that they felt that they should not use testosterone. Novices…because it was not necessary and it will limit later potential progress. Women should not use them (but a few reported doing so) due to virilizing effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome woman polled just could not leave testosterones alone. PROSCAR (FINASTERIDE, A DHT BLOCKER) was considered mandatory for co-administration\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eand TESTOSTERONE PROPIONATE 50mg 1 time weekly was noted to cause less virilizing side effects\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53752356765988,"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_b4fa4da1-66ea-4908-b017-140bfcb826c0.jpg?v=1778070203"},{"product_id":"hd-labs-duraject-100","title":"HD Labs Duraject 100","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eNandrolone Phenylpropionate is an anabolic steroid that is very similar to the popular Nandrolone Decanoate compound. However, Nandrolone Phenylpropionate was the first Nandrolone compound ever commercially sold. Nandrolone Phenylpropionate hit the shelves in the 1950’s and was brought to the market by Organon under the name Durabolin. Soon after Organon would release its Decanoate cousin under the name Deca Durabolin.\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNandrolone Phenylpropionate is a small ester base anabolic steroid and is commonly referred to as NPP. This product has never been as popular as the larger ester Decanoate version, in part due to availability; however, in the modern era it has begun to see a resurgence in both use and availability thanks in part due to underground labs.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNandrolone Phenylpropionate carries with it numerous therapeutic and performance benefits. The Nandrolone hormone is the most commonly prescribed anabolic steroid other than testosterone, but the Decanoate version is the most commonly prescribed Nandrolone form. It is one of the most well tolerated steroids in both performance and medical settings, although possible side effects most certainly exist.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe positive functional traits of Nandrolone Phenylpropionate include:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIncreased IGF-1 Production: Insulin-Like Growth Factor-1 (IGF-1) is a potent anabolic hormone that is also essential to our body’s ability to recovery. This is a hormone that affects nearly all cells within the human body.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eInhibition of Glucocorticoids: Known as stress hormones (cortisol) these hormones are essential to our health and wellbeing. However, glucocorticoids can also promote muscle loss and fat gain when they become dominant. Vigorous activity can lead to increases in stress hormones. Hormones like Nandrolone can reduce the production of stress hormones.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIncreased Nitrogen Retention: All muscle tissue is comprised of 16% nitrogen. If retention falls we fall into a catabolic state. The more we retain the more anabolic we remain.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIncreased Protein Synthesis: This refers to the rate in which cells build proteins, the building blocks of muscle tissue.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIncreased Red Blood Cell Count: Red blood cells carry oxygen to and through the blood. Greater efficiency results in enhanced muscular endurance and recovery.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIncreased Collagen Synthesis \u0026amp; Bone Mineral Content: This refers to the strength of bones and cartilage and the ability to strengthen and provide healing relief. This will hold true in joints more so than anywhere else.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53752432689444,"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_71d9ec05-c7bb-461a-ab8b-7dd11515a61a.jpg?v=1778070302"},{"product_id":"hd-labs-venom-pre-workout","title":"HD labs Venom Pre-workout","description":"","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53752506974500,"sku":null,"price":440.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_e00a90c1-c458-4efa-8741-9f31360fb9c2.jpg?v=1778070397"},{"product_id":"hd-labs-testolone","title":"HD Labs Testolone","description":"\u003cp\u003e\u003cspan\u003eHD LABS SARMS TESTOLONE(RAD-140) 5MG\/TAB=50TABS.\u003c\/span\u003e\u003c\/p\u003e\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","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53752565989668,"sku":null,"price":470.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_025bdc81-0b7a-4e64-9e8f-3ef537d330c6.jpg?v=1778070487"},{"product_id":"hd-labs-supercutmix-300","title":"HD Labs SuperCutMix 300","description":"\u003cp\u003e\u003cspan\u003e100MG\/ML TESTOSTERONE PROPIONATE \u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e100MG\/ML NANDROLONE PHYNELPROPIONATE \u003c\/div\u003e\n\u003cdiv\u003e100MG\/ML DROSTANOLONE PROPIONATE \u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53752618746148,"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_8da7afe5-8dd0-4708-bc62-7ea9f4a152ac.jpg?v=1778070600"},{"product_id":"hd-labs-supersize-500","title":"HD Labs SuperSize 500","description":"\u003cdiv\u003e200MG\/ML NANDROLONE DECANOATE \u003c\/div\u003e\n\u003cdiv\u003e100MG\/ML TESTOSTERONE ENANTHATE\u003c\/div\u003e\n\u003cdiv\u003e100MG\/ML TESTOSTERONE CYPIONATE \u003c\/div\u003e\n\u003cdiv\u003e100MG\/ML TRENBOLONE ENANTHATE\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53753855934756,"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_c900eafe-cd76-42d6-be85-205d4fb550e9.jpg?v=1778072441"},{"product_id":"hd-labs-turanabol10","title":"HD Labs Turanabol10","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eHD LABS TURANABOL 10(10MG 4-CHLORODEHYDROMETHYLTESTOSTERONE\/TAB=50TABS)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC N\/A\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 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":53753945882916,"sku":null,"price":270.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_521bd40c-c2a9-472d-9a22-e5e67804084b.jpg?v=1778072564"},{"product_id":"hd-labs-mastaject-100","title":"HD Labs Mastaject 100","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eHD LABS MASTAJECT 100(100MG\/ML DROSTANOLONE PROPIONATE=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\u003e                   10-14 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\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 \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":53754016006436,"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_f47dd0e0-7d08-4d19-86b1-5c3000fe643f.jpg?v=1778072682"},{"product_id":"hd-labs-cardarine","title":"HD Labs Cardarine","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eHD LABS SARMS CARDARINE(GW501516)10.MG\/TAB=50TABS.\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\u003e    In 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":53754085933348,"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_93fc51c6-b7a6-4846-80b6-51708c625441.jpg?v=1778072812"},{"product_id":"hd-labs-t3-tabs","title":"HD Labs T3 Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eDrug Class: Synthetic thyroid hormone. (ORAL)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: 25-150 MCG daily.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNoted Comments: Significant suppression of Thyroid function during use.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCytomel is the synthetic form of T-3\/L-triiodothyronine and was a commonly known trade or brand name among athletes. T-3\/L-triiodothyronine is used as a form of thyroid hormone therapy mostly in Europe. Most bodybuilders favored this drug over synthetic forms of T-4\/L-thyroxine due to its vastly superior activity level.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAn advantage of T-3\/L-triiodothyronine administration over T-4\/L-thyroxine was the lack of dependence upon the liver enzyme responsible for T-4\/T-3 conversion. During diet restricted periods the liver naturally decreases the liver enzyme levels as a control measure to prevent metabolic rate induced starvation. Just as the liver increases production of this enzyme in response to elevated calorie intake it also reduces levels in response to decreased calorie intake. Remember that T-4 \/L-thyroxine is only 20% as active as T-3\/L-triiodothyronine.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe abuse of synthetic T-3\/L-triiodothyronine will result in severe suppression of natural (endogenous) thyroid function. This is especially true of this drug because it actually circumvents the normal thyroid hormone manufacturing process the body utilizes to produce endogenous forms as required. Simplified this is because T-3\/L-triiodothyronine is the most potent thyroid hormone so the body shuts down each level required for production to try to reduce circulatory T-3\/L-triiodothyronine levels. Of course this does not reduce the level if the hormone is being administered exogenously (from outside the body).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSince long term use of T-3 \/L-triiodothyronine will lead to thyroid function suppression the issue of rebound should be briefly discussed. It is commonly stated that synthetic thyroid hormone abuse will lead to permanent thyroid gland dysfunction. Though it is definitely a physiological possibility, I have not yet found a case study to support this statement. However, there is a common occurrence of thyroid gland\/function rebound in natural endogenous thyroid hormone production. It seems that it was common for individuals to realize an “increase” in endogenous thyroid hormone production of 120-130 % within 3-15 days after drug discontinuance. This means an individual would commonly see an increase in their thyroid hormone production of 20­30% above their normal pre-drug administration levels, in many cases.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe noted positive physiological effects of reasonable dosages of thyroid hormones included:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased protein synthesis rate. *Increased rate of fat oxidation.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased sensitivity of receptors for androgens, Insulin, GH, IGF-1, PGE-1, PGF-2, Clenbuterol, Ephedrine, Creatine, and others.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased metabolization of proteins, carbohydrates, fats and micronutrients. *Increased metabolic rate and calories expenditure. *Enhanced oxygen consumption by most body tissues *Improved recovery time.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe noted negative physiological effects of excessive dosages of thyroid hormones included:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Loss of lean mass tissue.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased heart rate and palpitations.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Insomnia.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Diarrhea.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Vomiting.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThyroid hormone drugs are natural or synthetic preparations containing tetraiodothyronine (T4, levothyroxine) sodium or triiodothyronine (T3, liothyronine) sodium or both. T4 and T3 are produced in the human thyroid gland by the iodination and coupling of the amino acid tyrosine T4 contains four iodine atoms and is formed by the coupling of two molecules of diiodotyrosine (DIT). T3 contains three atoms of iodine and is formed by the coupling of one molecule of DIT with one molecule of monoiodotyrosine (MIT). Both hormones are stored in the thyroid colloid as thyroglobulin.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThyroid hormone preparations belong to two categories (1) natural hormonal preparations derived from animal thyroid, and (2) synthetic preparations. Natural preparations include desiccated thyroid and thyroglobulin. Desiccated thyroid is derived from domesticated animals that are used for food by man (either beef or hog thyroid) and thyroglobulin is derived from thyroid glands of the hog. The United States Pharmacopeia (USP) has standardized the total iodine content of natural preparations. Thyroid USP contains not less than (NLT) 0.17 percent and not more than (NMT) 0.23 percent iodine, and thyroglobulin contains not less than (NLT) 0.7 percent of organically bound iodine. Iodine content is only an indirect indicator of true hormonal biologic activity.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53754165068068,"sku":null,"price":230.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_c71a0e13-d89c-4092-961b-d07a619fe2b3.jpg?v=1778072917"},{"product_id":"hd-labs-femara-tabs","title":"HD Labs Femara Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eHD LABS FEMARA(2.5MG LETROZOLE\/TAB=30TABS)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: Less than 24 hours\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anti-estrogen\/estrogen antagonist (Oral)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: 0.5-2.5 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\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLetrozole is a non-steroidal selective third generation aromatase inhibitor, which is being sold under the brand name Femara by the international drug-manufacturing firm Novartis. It is used to treat postmenopausal women with estrogen receptor-positive or estrogen receptor-unknown (unsure if the cancer is responsive to estrogen) breast cancer.The structure and activity of this compound are very similar to that of Arimidex (anastrozole), which is approved in the United States for the same purpose. Femara is typically used as a second line of treatment, after an estrogen-receptor antagonist like tamoxifen has failed to elicit a desirable response (although at times it is used as a first line option as well).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eFemara and Arimidex represent the newest achievements in a long line of drugs targeting aromatase inhibition. These are amongst the most potent estrogen-lowering drugs made to date, working far more effectively than the non-selective first generation aromatase inhibitors, like Teslac and Cytadren, to come before them. The dosage of each tablet of Femara is 2.5 milligrams, which according to the product insert was sufficient to lower estrogen levels by 78% during clinical trails.The drug, however, appears to still be extremely effective in much lower doses. The package insert for the product itself comments that during clinical studies doses of .1 and .5 milligram produced 75% and 78% estrogen inhibition, respectively. When it comes to a product like this, typically the recommended dose reflects what seems to work for almost everyone who takes it. A large number of people may respond extremely well to lower doses, however, to make sure each patient is receiving the proper benefit of the drug a standard effective dosage unit is ascertained and used.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIt is important to point out that there are some disadvantages to using an aromatase inhibitor over mixed estrogen agonist\/antagonists (anti-estrogen) like Nolvadex and Clomid, the most notable being unwanted (negative) alterations in cholesterol values (strong HDL suppression in particular). This is because estrogen is tied to HDL cholesterol synthesis and LDL metabolism, and aromatase inhibitors block total estrogenic action. Clomid and Nolvadex, on the other hand, tend to produce an estrogenic increase in good cholesterol values, as they are active estrogens in the liver. If I you are just trying to prevent estrogenic side effects like gynecomastia, bloating and excess water retention in general, these agents are probably better choices (they do the same job and are safer on your cholesterol levels). But if you want that really\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003etight, dry, defined look that is often so sought after when you are cutting, Nolvadex or Clomid are not quite going to cut it (excuse the unintentional pun). In such cases, I think you will find Femara to serve you well.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAt the pharmacy, 30 tablets will cost you a little under $200. This comes out to about $6.50 each tablet, roughly the same price you are going to pay for Arimidex. Like Arimidex, each tablet can be broken up if you desire to stretch out the value of the drug. In fact, with studies showing maximum inhibition in some patients with doses as low as 1\/2 milligram, each 2.5 milligram tablet can be broken up in to as many as 5 separate doses (perhaps even more). But the typical use amongst bodybuilders is to cut the tabs in half, and take one every other day (unless needed daily). In terms of overall power, Femara seems to be a little bit more potent the Arimidex, at least by most peoples’estimations. If both agents were available for the same price, Femara would probably be the one I would go for.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e(Letrozole) is an oral non-steroidal aromatase inhibitor that has been introduced for the adjuvant treatment of hormonally-responsive breast cancer.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eEstrogens are produced by the conversion of androgens through the activity of the aromatase enzyme. Letrozole blocks production of estrogens in this way by competitive, reversible binding to the heme of its cytochrome P450 unit. The action is specific, and Letroplex does not reduce production of mineralo- or corticosteroids. In contrast, the antiestrogenic action of tamoxiplex, the major medical therapy prior to the arrival of aromatase inhibitors, is due to its interfering with the estrogen receptor, rather than inhibiting estrogen production\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53754248528164,"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_fc8445f5-7742-49ea-bbf8-226914baf79c.jpg?v=1778073019"},{"product_id":"hd-labs-propioject-100","title":"HD Labs Propioject 100","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eHD LABS PROPIOJECT 100(100MG\/ML TESTOSTERONE PROPIONATE=10ML)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD TESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-life: 2-3 days\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug class: Anabolic\/Androgenic steroid (For injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Male 50-200mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Low\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Yes, severely\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDue to Testosterone Propionate possessing a brief active-life of 2-3 days, many athletes involved in tested competitions liked the stuff…a lot. Testing is usually based upon testosterone \/Epitestosterone levels. Though most individuals have a much lower ratio, athletes can have natural ratios of up to 6:1. This is considered a negative test for steroids. usually. By injecting Propionate up to 36 hours before competition, plasma Testosterone levels remained elevated while urine concentrations usually fell within the 6:1 levels. Of course IOC testing protocols would detect any plant origin AAS today. But several groups still simply test for the ratio only.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTestosterone Propionate is considered a fast acting testosterone due to effects beginning in about 1 day. The drug reportedly has all the benefits of other testosterones (quick strength and muscle mass increases, increased training aggressiveness, fast post-training recovery) but caused a distinctly lower level of water retention. Users noted an improved muscle pump and increased appetite after one to two days of administration. Even with a high rate of aromatization, propionate did not cause gyno as often as other testosterone esters. Users who realize this normally did so due to less frequent injections: Not due to some special quality of the drug. I liked propionate because an increase in IGF-1 was common during liver deactivation. Also because use could be discontinued at the first sign of overt side effects (thus allowing the chemical to no longer be the cause after 2-3 days post-discontinuance).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eA high quality muscle gain has been achieved with 50-100mg Testosterone propionate every 1-2 days, 50mg Winstrol Depot every 2nd day, and 20-25mg of Oxandrolone daily. If Parabolan (76mg every other day) was substituted for Winstrol and Proviron is utilized as an anti-estrogen, this became an excellent pre-contest cycle providing superior hardness. Those who had used Primobolan only and no longer made progress at 200-400 mg weekly made consider progress by stacking 200-400mg Primobolan Depot weekly with 50-100mg of Testosterone Propionate every second day. Improved vascularity was common due to increased in red blood cell count as well.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWomen who did use testosterones considered propionate to be the superior choice over any other. 25-50mg of Propionate every 5-7 days stacked with any high anabolic such as Anadur, or especially Durabolin caused a dramatic result with less virilizing characteristics. As always, women who are extremely sensitive to androgens reported the use of 1mg Finasteride daily lowered DHT conversion of Propionate.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTestosterone propionate is a male sexual hormone with pronounced, mainly androgenic action, possessing the biological and therapeutic properties of the natural hormone. In a healthy male organism, androgens are formed by the testes and adrenal cortex. It is normally produced in women in small physiological quantities. In addition to the specific action that determines the sexual characteristics of the individual, it also has a general anabolic action, manifested in enhancement of protein synthesis. Under the effect of testosterone, body weight increases and urea excretion is reduced. High doses suppress the production of hypophyseal gonadotropin, while low doses stimulate it. It has an antitumor effect on mammary gland metastases.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*It should be noted: Propionate also severely suppresses HPTA function and HCG\/Clomid have been considered post administration stables.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53754346832164,"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_bd2c5e13-7143-4fd7-847b-eb1ce355d804.jpg?v=1778073144"},{"product_id":"hd-labs-stenabolic","title":"HD Labs Stenabolic","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eHD LABS SARMS STENABOLIC(SR9009)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStenabolic is a Reverb Agonist SARM, code name is SR9009\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStenabolic, in current research trials has shown to increases the metabolic activity in skeletal muscle.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIt has been shown to increases Basal Meabolic Rate (BMR). Stenabolic assists with reducing obesity, and increases muscle strength.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStenabolic has shown to increase endurance\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStenabolic SR9009 Discription\u003c\/div\u003e\n\u003cdiv\u003eThe half life of Stenabolic is +\/- 2 to 4 hours so it is essential to take Stenabolic in 4 – 6 equal doses per day. This will require that you break the tablet in half. Please refer to the packaging on how to break the tablet in half and take as indicated below.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDose range is 20 – 40 mg per day for male athletes and half that for female athletes. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCycle is 8 – 12 weeks.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage :\u003c\/div\u003e\n\u003cdiv\u003eFemale Athletes 1 – 2 Tablets per day\u003c\/div\u003e\n\u003cdiv\u003eMale Athletes 2 – 4 Tablets per day.\u003c\/div\u003e\n\u003cdiv\u003eCan be stacked with any other SARM\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eStenabolic, or SR-9009, is not technically a SARM but it’s effects are similar so it’s sold on sites where peptides and SARMs are sold. It has the endurance-boosting effects of Cardarine, but also provides increased energy and enhanced metabolism to burn fat stores. It’s non-hormonal (does not target AR’s), so shut-down and PCT are not issues. The shorter half-life of a few hours means users will want to target a specific time of day, such as just before hitting the gym.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTypical dose: 20 mg\/day\u003c\/div\u003e\n\u003cdiv\u003eMax: 40 mg\/day (spaced out)\u003c\/div\u003e\n\u003cdiv\u003eStacking dose: 10-20 mg\/day (depending on stack)\u003c\/div\u003e\n\u003cdiv\u003eHalf-life: 4-6 hours\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53754438975780,"sku":null,"price":530.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_e991b67e-5e08-4cb2-9d8d-c2c1a8d5f37d.jpg?v=1778073278"},{"product_id":"hd-labs-trenaject-100","title":"HD Labs Trenaject 100","description":"\u003cp\u003e\u003cspan\u003eHD LABS TRENAJECT 100(100MG\/ML TRENBOLONE ACETATE=10ML)\u003c\/span\u003e\u003c\/p\u003e\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\u003e \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\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis was\/is a very nasty but effective steroid that was removed from the market about 1987 or so. Not all that long ago it began showing up on the black market from Australia. Upon testing the 50-ml vials, it was discovered that it actually contained 31-mg\/ml of Trenbolone acetate. Most Fina Jet now found is bogus. It contains either a testosterone ester, ground Finaplix pellets, or just oil. But the original has been discontinued. (There are several new brands of the drug trenbolone acetate)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTrenbolone acetate is a strong androgenic\/anabolic steroid that caused a fast increase in strength and increased fat burning if the athlete’s diet was right. Unless stacked with other steroids, this drug did not cause much in actual weight gain (dose dependent). Its main use was to harden the physique’s appearance once body fat levels were low enough before competition. For the most part, bodybuilders have replaced Finajet\/ Finaject with Parabolan or one of the many black market trenbolone products. Since Finajet did not cause gyno or water retention, one may assume it was fairly clean. Wrong! Even at dosages of 30-60-mg injected daily, side effects such as kidney toxicity, nose bleeds, headaches, high blood pressure, acne, and serious attitude problems were common.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome creative and brave athletes have used the Finaplix 20 mg pellets which are intended for animal use. The pellets are shot into animal tissue for a slow release of Trenbolone. However some athletes (and black market crazies) have ground the pellets into a powder, mixed it with oil or water, and injected the very un-sterile solution with 18 gauge needles. I can not stress enough how dangerous this is. The product is often labeled Finabolan. (“Finabolin” gives us a chance to discuss trenbolone in greater depth in a moment)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAnother reported method of using the Finaplix pellets was to ground them into powder, mix the powder with a 50\/50 solution of DMSO (DIMETHYL SULFOXIDE) and water. Then apply it to skin. The DMSO acts as a transporter that allows 14-18-MG of a 20MG pellet to be absorbed into the blood stream while the skin acts as a filter of sorts. Unfortunately this also allowed many toxins on the skin to enter as well.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome individuals have claimed real hard-core status by using an animal pellet implant gun and taking one in the glute. Do not try this at home. The pain would be major and compared to being shot with a .177 pellet. The interesting side of this is that the lads who did this had been told that the Finaplex pellets were readily absorbed “rectally”.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Geez! And some bodybuilders wonder why we have the stigma of dull wittedness?\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNOTED POSITIVE EFFECTS OF TRENBOLONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Amazing anabolic qualities.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Rapid high quality lean tissue gains. (Dose dependent) *Maximum post-cycle lean mass retention. *Low-none water retention.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased Erythropoies (Red blood cell production) *Does not aromatize to estrogens. *Superior strength and mass gain. (Lean) *Extreme hardening of musculature and vascularity. *Excellent protein sparing\/anti-catabolic qualities. *Reduction in fat stores and favorable distribution. *Increased metabolic rate. *Low-moderate HPTA function inhibition. *Significant increase in muscle glycogen synthesis. *Increase creatine phosphate (CP) synthesis. *Improved muscle insulin receptor activity.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Remains anabolic during calorie restricted periods. (High protein intake remains necessary)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e POSSIBLE NEGATIVE EFFECTS TRENBOLONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Liver and Kidney toxicity.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Growth of prostate tissue. (PSA test is wise)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Male pattern baldness. (Accelerated genetic predisposition)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Mild hallucinations. (High dosage -prolonged use)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*High blood pressure.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e Trenbolone Acetate is a fast acting injectable steroid.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTo increase its effective half-life, trenbolone is not used in an unrefined form, but is rather administered as trenbolone acetate ,enanthate or Hexahydrobenzylcarbonate. Trenbolone is then produced as a metabolite by the reaction of these compounds with the androgen receptor.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBodybuilders have been known to use the drug in order to increase body mass more effectively than by weight training alone. A normal bodybuilding dosage can range from 200 mg\/week up to 1400 mg\/week. Due to the relatively short metabolic half-life of trenbolone acetate, dosages should commonly be split into injections at least once every two days. Trenbolone enanthate can be injected once a week.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe 2006 book Game of Shadows alleges that baseball superstar Barry Bonds used this drug in 2001, when he set the current single-season home run record.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTrenbolone compounds have a binding affinity for the androgen receptor three times as high as that of testosterone. Once metabolised, the drugs have the effect of increasing nitrogen uptake by muscles, leading to an increase in the rate of protein synthesis. It also has the secondary effects of stimulating appetite, reducing the amount of fat being deposited in the body, and decreasing the rate of catabolism. Trenbolone has proven popular with anabolic steroid users as it is not metabolised by aromatase or 5α-reductase into estrogenic compounds such as estradiol, or into DHT. This means that it also does not cause any water retention normally associated with highly androgenic steroidal compounds like testosterone or methandrostenolone. It is also loved by many for the dramatic strength increases commonly experienced with it. Some short-term side effects include insomnia, high blood pressure, increased aggression and libido. However, since women will suffer virilization effects even at small doses, this drug should not be taken by a female. Urban wisdom\/myth in bodybuilding culture, states that the use of the drug over extended periods of time can lead to kidney damage. The kidney toxicity has not yet been proven, and scientific evidence supporting the idea is suspiciously absent from the bodybuilding community that perpetuates this idea. The origin of this myth most likely has to do with the rust colored oxidized metabolites of trenbolone which are excreted in urine and often mistaken for blood. After Schänzer (Clin Chem 1996; 42(7): 1001-1020, Metabolism of anabolic androgenic steroids) trenbolone and 17epi-trenbolone are both excreted (in urine) as conjugates that can be hydrolyzed with beta-glucuronidase. This implies that trenbolone leaves the body as beta-glucuronides or sulfates, that means mostly non metabolized\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53754528203044,"sku":null,"price":580.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_a2780c0a-6b93-4d21-9e44-06f48f7ce60e.jpg?v=1778073399"},{"product_id":"hd-labs-anapolan-tabs","title":"HD Labs Anapolan Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eHD LABS ANAPOLON 50(50MG OXYMETHOLONE\/TAB=50TABS)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 45\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 320\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD METHYLTESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive – Life: Less than 16 hours\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Highly Androgenic \/ Anabolic Steroid (Oral) Average Reported Dosage: Men 50-400 mg daily. Women 25-mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Yes, high\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Yes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: Yes,\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003every high DHT Conversions: This is a derivative of DHT\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA Function: Yes,\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSevere Aromatization: Debatable\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis is an oral 17-alfa-alkylated steroid that is highly androgenic and highly anabolic. Reported gains in body weight of up to 20 LBS in the first 3 weeks of use were not uncommon. Athletes using this drug experienced remarkable strength and recovery elevations. Users noted a distinct increase in aggressiveness, (which if focused on training only was noted as positive) excessive water retention, and muscular size. Oxymetholone is commonly used as an off season mass building drug, though some mass monsters have used it up to 7-10 days before competition by stacking antagonist anti-estrogens and diuretics.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eUnfortunately this drug is probably the most dangerous of all AAS when abused and utilized when not under a physician’s care. Users get huge but often feel flu-like symptoms during use. Oxymetholone abuse is linked to prostate and liver cancer, liver disease, thyroid dysfunction, leukemia, and heart disorders. Even hepatic coma can result from abuse. Not uncommon side effects included: sensitivity to anti-coagulants (the stuff that regulates bleeding internally and externally) hair loss, prostate enlargement, severe suppressions of the HPTA resulting in low sperm and endogenous (natural) androgen production, nausea, stomach aches, diarrhea, and throwing up on occasion. Women can add possible virilizing symptoms such as clitoral enlargement, facial hair growth, deeper voice, missed periods, and other androgenic linked side-effects.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOxymetholone negatively effects liver function such as an increase in SGPT and SGOT enzymes which are indications of hepatitis (liver infections) which can manifest itself as yellowing of the eyes and finger nails because of an increase in biliburin in the liver. Another liver enzyme, gamma -GT, is sensitive to Oxymetholone, and alkaline phosphatase is altered as well. I cannot stress the importance of monitoring by a doctor.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOxymetholone is a derivative of DHT. Many report gyno from use but this is unlikely due to this drug aromatizing because DHT does not aromatize to estrogen. The more likely reason is they purchased bogus oxymetholone from a black market dealer that actually contained methyltestosterone. There is another reason gyno is possible, but we will discuss that in a moment. Oxymetholone does cause high water retention due to electrolyte retention thus creating a massive but puffy appearance to muscles. For the same reason, the drug causes water retention and fluid build up in joints. This manifests itself in joint pain-free training for most users. In medicine Oxymetholone is used to treat low red blood cell production which means during administration red blood cell count is stimulated. For this reason the drug increases oxygen transport to the muscles resulting in an incredible muscle pump after only a few sets of training. I have often noted those who used oxymetholone recovered between sets, exercises, and work-outs at a remarkable rate. So the drug does protect against overtraining quite well, thus when it was stacked with anti-estrogen such as Nolvadex and a diuretic to cut electrolyte (aldosterone) caused water retention, and a high anabolic drug such as Deca Durabolin, quality, quantitative, muscle gain resulted. The fact that this drug’s water retention side effect responds to antagonist type anti-estrogens is interesting since, from a chemical structure stand-point, it should not aromatize to estrogen. Even the insert states edemas (water retention) may occur but does not list elevated estrogen levels under “side effects”. However, readers should realize Oxymetholone itself can merge with Progesterone receptors and may act as an estrogen in this manner.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAs to dosages, advanced bodybuilders and power lifers usually reported excellent results with 50-200 mg daily divided in 2-3 dosages. Since results begin to decline after the first 2 weeks it some reported that their protocols were more productive (and safer) when they started at 50mg daily and increase by one tab weekly until a total of 150-200 mg daily was reached at week 3. They then maintained that dosage for a total of 2-3 additional weeks. Some reported a following protocol that allowed reduced dosages by one tab weekly. My personal experience has been that liver stress becomes an issue after the 4th week of administration and as such did not personally exceed this time period for use. Replacing Oxymetholone with a high anabolic such as Deca Durabolin or Equipoise during the transitional phase was quite effective for maintaining a greater amount of the oxymetholone induced lean mass. Many reported exceptional results with a stack consisting of 50-100 mg oxymetholone daily, 152-228 mg of Parabolon weekly, and 200­500 mg of testosterone enethate weekly.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Women should not use oxymetholone, but of course some hard core types did report self administration. Novice steroid users should never use oxymetholone without a doctors supervision.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIn most cases users reported that liver values returned to normal after 1-2 months of discontinued. This seems to be supported by the available medical literature on oxymetholone. High blood pressure was common during use. High blood pressure should never go untreated. The hair loss does not reverse by the way. Post-cycle the administration of HCG and Clomid was used to return normal HPTA function in all but very rare cases. “The boys” normally began to produce normal sperm and testosterone levels after 2-3 weeks of discontinuance. Can you tell that I did not like Oxymetholone for long term personal use? Post-cycle, without the layering of a transitional phase replacement AAS such as nandrolones, Primobolan Depot, Equipoise or Winstrol Depot, gains made with Oxymetholone alone soon disappear in most cases. (See “Max Androgen Phases” in “Building The Perfect Beast” for a discussion of solutions some hard-core types have utilized)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e* A note of interest: There is not a “legit” injectable form of Oxymetholone( OXYJECT FROM KARMA WAS AVAILABLE A WHILE BACK). However, it would be very physiologically active as is the 25mg sublingual form. I have used a MEGA-MIX product that contained Oxymetholone in a 3 oil mix injectable that was a black-market product with excellent results and fewer negative side effects. However, black market manufactured AAS are often dangerous and unlikely legal anywhere.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e(Oxymetholone) is a synthetic anabolic-androgenic steroid hormone that is structurally related to the male hormone testosterone. Synthetic androgens are used to treat a variety of conditions including hypogonadism and delayed puberty. Androgens are also used to correct hereditary angioneurotic edema, manage carcinoma of the breast, promote a positive nitrogen balance following injury or surgery, and stimulate erythropoiesis.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eConsiderable amounts of androgens are consumed by athletes in attempts to improve athletic performance. Oxyplex is used to promote weight gain and counteract weakness and emaciation resulting from debilitating diseases, such as advanced HIV infection, and after serious infections, burns, trauma, or surgery. It is marketed as a human prescription drug for the treatment of bone marrow failure anemias and deficient red cell production anemias.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53754595115300,"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_671bf28d-a024-4992-851e-50f25c0fa24d.jpg?v=1778073504"},{"product_id":"hd-labs-superbulk-600","title":"HD Labs SuperBulk 600","description":"\u003cp\u003e\u003cspan\u003e200MG\/ML TESTOSTERONE CYPIONATE \u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e200MG\/ML BOLDENONE UNDECLYNATE \u003c\/div\u003e\n\u003cdiv\u003e200MG\/ML NANDROLONE DECANOATE\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53754672840996,"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_003e5f1b-c8f9-470b-877c-08e87ecc1367.jpg?v=1778073612"},{"product_id":"hd-labs-primo25","title":"HD Labs Primo25","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eHD LABS PRIMO 25(25MG METHENOLONE ACETATE\/ TAB=50TABS)\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: 4-6 hours\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-50-200-mg daily Women 50-100-mg 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: 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: Very low and only in very high dosages\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: None\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eModerate Anabolic\/ Low Androgenic\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\u003eDecreases HPTA function: Low\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePrimobolan tablets are a moderately anabolic and low androgenic oral steroid that was reported as limited in use by most bodybuilders. This was likely simply because alone and when it was administered in listed dosages the drug was not very effective. However, gains were made in muscle mass and strength were consistently reported to be of a very high quality and were mostly retained post-cycle. Acetates are “said” to aid in fat burning, so this drug was mostly used in a stack pre-contest.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe problem in effectiveness lies in the fact that PRIMOBOLAN ACETATE is not a c17-ALFA-ALKYLATED steroid and is therefore mostly deactivated during the first pass through the liver. As the reader is aware, oral AAS are commonly altered to decrease liver deactivation. The most common alteration is called a c-17 alfa-alkylated drug. This alteration makes the liver work over-time to deactivate it and is therefore said to be highly liver toxic. (But so are most oral birth control drugs) But another alteration in structure allows Primobolan orals to be somewhat resistant to liver deactivation. It is referred to as unsaturation in the 1-position.This alteration allows the compound to resist metabolic deactivation by significantly shifting the 17-Keto redox potential toward creation of active 17-beta hydroxyl AAS. The result is an active oral AAS that is not liver toxic except in very high dosages.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome have recalled the injectable form of Primobolan acetate with great fondness for its supposed fat burning\/lean mass building qualities. The vials contained only 20-mg\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eof METHENOLONE ACETATE (MA) yet it was reported far more effective than 150-\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003emg of the oral. A commonly reported method to obtain greater blood circulatory levels of the oral form was to mix 20-25-mg of the ground tables with either DMSO gel or a 50\/50 solution of DMSO and water. Users then simply applied the mixture to their skin (especially in areas of stubborn fat deposits). 10-20% absorbed and passed directly into the blood stream thus avoiding first pass liver deactivation. This was done 1-5 times daily.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDMSO is a solvent that carries smaller molecule structures mixed with it directly through the skin. It is said to be found at some health food stores and chemical supply warehouses.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAnother reported method was mixing ground Primobolan tabs with Vitamin-E oil. The users then ingested it orally. This caused a great deal of the active steroid to be absorbed through the lymph system like Andriol and therefore avoid first pass deactivation.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*There is a great deal of research under way in the OTC supplement industry that employs a similar pharmacological solution to liver destruction of micronutrients.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBack to reported tablet use…\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePrimobolan tabs were reportedly used most by women and steroid novices because they do not aromatize or cause water retention. Women who utilized 50-100mg daily of this drug seldom noted virilizing side effects. Most report a distinct harder look and a 3-4 LB muscle mass gain in 6-8 weeks. Obviously many females also stacked Primobolan tabs with other drugs to heighten results. Males normally ingested 100-200 mg daily in 2-4 divided doses (due to short half-life 4-6 daily divided dosages were more effective at maintaining plasma concentrations of the active drug) and report fair gains. Stacked with more androgenic steroids such as testosterone, Parabolan, or even moderate androgenics such as Deca Durabolin or Equipoise, males made high quality muscle mass and strength gains with safer low side effect results.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Since Primobolan is a derivative of dihydrotestosterone (DHT) an acceleration in hair loss can occur in those with genetic receding hair lines (but was rarely noted).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePrimabolin is indicated in the treatment of refractory deficient red cell production anemias. These may include aplastic anemia, myelofibrosis, myelosclerosis, agnogenic myeloid metaplasia, and hypoplastic anemias caused by malignancy or myelotoxic drugs.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePrimabolin 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\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePrimabolin (Methenolone Acetate) has been used in certain countries to counteract catabolic states, for example after major trauma\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53754736181540,"sku":null,"price":700.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_85dc4998-b6e2-4f0e-a31c-503806eb4e24.jpg?v=1778073688"},{"product_id":"hd-labs-anabolicum","title":"HD Labs Anabolicum","description":"\u003cp\u003e\u003cspan\u003eHD LABS SARMS ANABOLICUM(LGD-4033) 5MG\/TAB=50TABS.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLGD-4033, Also Called Ligandrol Or Anabolicum.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLGD-4033 is one of the better studied SARMs. It’s been through multiple human trials, with interesting results:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHealthy men who took LGD-4033 for 21 days saw a significant increase in lean body mass. The only side effect was short-term testosterone suppression (more on that in a second) [3]. One milligram per day was enough to cause significant muscle growth. The higher the dose, the more muscle participants put on. In another trial, participants took doses as high as 22 mg\/day with no side effects or safety issues [3]. In rats, LGD-4033 increases bone density, muscle mass, and sex drive, without damaging prostate or liver tissue [3].\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLGD-4033 does not appear to stimulate fat loss, so if you take it on its own, it won’t make you leaner – just more muscular.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSide effects of LGD-4033\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLGD-4033 will probably suppress your natural testosterone production a bit while you’re on it, although the effects seem to be short-lived [3]. Study participants saw T suppression dependent on dose, but none of them dropped out of the healthy testosterone range, and levels returned to normal within 3 weeks after they stopped taking LGD-4033.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThat said, you may want to skip this one (and SARMs in general) if your testosterone is low. Consider biohacking your testosterone instead.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHow to dose LGD-4033\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eUsers report success taking 2-5 mg of LGD-4033, in a single daily dose, for 6 weeks. It seems that the higher the dose, the more muscle you put on, and the more your testosterone dips. Some people take up to 15 mg per day for much longer timeframes, but that’s riskier. You don’t want your natural T production to tank entirely. Once your 6 weeks are up, wait at least a month before starting another cycle.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAlso known as Ligandrol, LGD-4033 is a powerful anabolic SARM known to rapidly increas muscle size and strength. LGD-4033 is not the best SARM for cutting or weight loss, but in its efforts to grow muscle mass it will burn through fat if other body fuels are unavailable. LGD-4033 is not recommended for women, and suppression of natural testosterone production is observed in men administering high doses in longer cycles.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTypical dose: 10-20 mg\/day\u003c\/div\u003e\n\u003cdiv\u003eMax dose: 30 mg\/day\u003c\/div\u003e\n\u003cdiv\u003eStacking dose: 5-10 mg\/day (depending on stack)\u003c\/div\u003e\n\u003cdiv\u003eHalf-life: 24-36 hours\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53754815021348,"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_bfb48bef-7f02-45bd-8614-c123b24ebae1.jpg?v=1778073792"},{"product_id":"hd-labs-nandroject-300","title":"HD Labs Nandroject 300","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eHD LABS NANDROJECT 300(300MG\/ML NANDROLONE DECANOATE=10ML)\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 37\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 125\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD TESTOSTERONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: 14-16 days FOR NANDROLONE DECOANATE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Anabolic\/Androgenic steroid (For Injection)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDosage: Men 200-600mg weekly Women 50-100mg weekly\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Yes, in higher dosages in androgen sensitive individuals\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Some, much less than testosterone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA function moderately\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Rare (When used in dosages over 600-mg weekly)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: Low, converts to less active norestrogens\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLiver Toxic: None.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHT Conversion: No, converts to NOR- DHT with low activity\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNoted Comments: Highly anabolic\/moderate androgenic effects\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNandrolone Decanoate is a very anabolic, moderate androgenic form of nortestosterone that was the most commonly used drug to create a rapid build-up of lean muscle mass or as a diet “protein- sparing” drug by athletes of all kinds. This is a longer lasting nandrolone than Durabolin so some water retention resulted with long term administration (especially in higher dosages). A prominent positive nitrogen balance occurs with the use of nandrolones and therefore a high protein intake was a must for all reported users. If you read the section on protein, you know that nitrogen in its bonded form is a part of protein\/amino acids. Since nandrolone promotes nitrogen storage in muscle cells (a positive nitrogen balance) then the cell contains more protein for growth and repair than normal. Remember: This could only happen if above normal calories (with a focus on protein) were ingested. Since nandrolone is moderately androgenic, good strength gains also resulted. Another plus for nandrolone was that most users experienced a joint healing effect during cycles and a suppressed cortisol\/cortisone activity due to nandrolones ability to long-term block cortisol receptors. Since aromatization was low, in 200-400-mg weekly dosages, anti-estrogens were not commonly necessary to avoid gyno and estrogenic induced side effects. Based upon available research and information available it seems liver toxicity is unknown with nandrolone. So it was not a surprise to find that even those with liver disease have used this drug with great success.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eCommon dosages for men were 200 600mg weekly. Though dosages over 400 mg weekly caused more water retention. For first time use of dosages over 400 mg weekly, I preferred to add 50-100mg Durabolin to each of the 2 weekly injections. This was because Durabolin is much faster acting and therefore creates chance for water retention and gyno. (This applied to first -time users only)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAn added benefit of this method was that nandrolone decanoate begins significant activity at 6 days and peaks at about 8 days after administration. The faster acting durabolin “kicks in” after about 1 day. This also resulted in higher “quality” muscle tissue gain.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWomen seemed to do very well with nandrolones due to the lower androgenic\/masculining effect. Women consistently reported excellent lean mass and strength gains at dosages of 50-100 mg weekly. Masculine effects usually were avoided by single weekly injections of 25-50 mg nandrolone decanoate and 25-50 mg of Durabolin (nandrolone phenylpropionate). In both men and women, this method seemed to result in more “quality” muscle, less water retention, less gyno for males, and good retention of gains after the cycle ends.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Metabolites can be found in urine or blood tests for 12-18 months after use of nandrolone is discontinued.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNOTED POSITIVE EFFECTS OF NORTESTOSTERONE (NANDROLONE)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Significant anabolic qualities.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*High quality (but slow) lean tissue gains.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Excellent post-cycle lean mass retention.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Low-moderate water retention.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Low aromatization to estrogens.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Does not negatively effect HDL.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Moderate strength and weight gain.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Noted improvement in joint\/soft tissue function.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Excellent protein sparing \/anti-catabolic qualities.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Inhibition of fat synthesis.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased metabolic rate.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Does not reduce to DHT (Dihydrotestosterone)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Very low-moderate HPTA function inhibition. (Dose Dependent)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased muscle glycogen synthesis.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased Creatine Phosphate (CP) synthesis.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Reduction in total triglyceride and cholesterol levels.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Beneficial\/improved insulin metabolism.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ePOSSIBLE NEGATIVE EFFECTS OF NORTESTOSTERONE (NANDROLONE)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Poor protection from over training.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Some males experienced decreased libido (Not true for women) *Inhibition of HPTA function at dosages in excess of 400 MG weekly.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNandrolone binds to the androgen receptor to a greater degree than testosterone, but due to its inability to act on the muscle in ways unmediated by the receptor, has less overall effect on muscle growth. The drug is also unusual in that unlike most anabolic steroids, it is not broken down into the more reactive DHT by the enzyme 5a-reductase, but rather into a less effective product. As such, some of the negative effects associated with most such drugs are somewhat mitigated.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe positive effects of the drug include muscle growth, appetite stimulation and increased red blood cell production and bone density. Clinical studies have shown it to be effective in treating anaemia, osteoporosis and some forms of neoplasia including breast cancer, and also acts as a progestin-based contraceptive. Nandrolone is also extensively used by bodybuilders and other athletes seeking an edge in professional competition\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53757606461732,"sku":null,"price":530.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_c184ddc7-612e-4901-9133-0677fa7d233c.jpg?v=1778077641"},{"product_id":"hd-labs-equiject-200","title":"HD Labs Equiject 200","description":"\u003cp\u003e\u003cspan\u003eHD LABS EQUIJECT 200(200MG\/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\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBoldenone is available as a veterinary steroid under various trade names and was commonly refereed to as EQ by athletes polled. However, the quality is normally quite high due to its use in million dollar race horses. Boldenone was reported as one of the safest and most effective anabolic \/ androgenic injectable steroids used by both power lifters and bodybuilders. This drug brought slow but continuous muscle mass and strength gains over a prolonged period. Gains were mostly of a high quality lean mass nature and were maintained for several weeks after use was discontinued. Improved pumps and vascularity were normal are common attributes while low aromatization brought an improved hardness to users musculature.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMales normally reported a dosage range of 150-500mg weekly total, usually utilizing an every other day (EOD) injection schedule. Women made excellent progress with dosages of 50-150mg total weekly with a 1-2 injections weekly schedule. In this dose range, women seldom reported virilizing side effects. Most experienced an elevate libido (cool) with few other negative side effects reported. But in some cases, increased hair growth on face and legs were noted. This was usually due to higher dosages however and predominantly limited to existing hair (not new hair growth).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDue to Boldenone’s reported “non-toxic to the liver” structure, most users experienced great gains with none or few negative side effects. The appetite and red blood cell production stimulating effects of Equipoise marked this drug as a standard for those who sought few negative side effects with quality muscle mass gains. Obviously with increased red blood cell count an increase in oxygen transport was also realized, as was improved nutrient transport.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDue to a double carbon bond between carbons one and two, boldenone experiences only slight DHT conversion by the 5-alfa-reductase enzyme and is fairly resistant to aromatization to estrogens.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMale athletes commonly stacked Boldenone with testosterone and\/or Anadrol-50 for mass and strength cycles. Pre-contest cycles utilizing this drug often included Trenbolones, Winstrol, and anti-estrogens to create the ultra hard and vascular look.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Personal experiences with Boldenone have resulted in very high quality lean tissue and freaky vascularity. This quite beneficial from a competitive appearance stand-point but long term use resulted in an unfavorable CBC result. I believe my error was in protocol length.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBoldenone (1,4-androstadiene-3-one-17β-ol, available as the undecylenate ester)is an anabolic steroid developed for veterinary use, mostly for treatment of horses. It is not indicated for use in humans in the US and is only available through veterinary clinics.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe activity of boldenone is mainly anabolic, with a low androgenic potency. It has a very long half-life, with minimal blood levels present up to 8 weeks after discontinued use.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBoldenone will increase nitrogen retention, protein synthesis, increases appetite and stimulates the release of erythropoietin in the kidneys. The drug is commonly used in doping within bodybuilding. If intended to assist in bodybuilding, the drug is taken as part of a steroid stack of other anabolic steroids, usually with a potent androgen like testosterone as the ‘base’ of the stack.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBoldenone has a low rate of aromatization (about 50% of Testosterone), which means it does not convert to estrogen easily and does not cause very much water retention. Many Bodybuilders will find that it is a good replacement drug for Nandrolone.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIt is a poor drug of choice for any athlete who will be subject to a blood test due to its long metabolic half-life. Trace amounts of the drug can easily be detected for months after discontinued use.\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53757834297636,"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_cd4d1e12-342e-40e6-9c48-301e3bf0fdc8.jpg?v=1778077786"},{"product_id":"hd-labs-dhea25-tabs","title":"HD Labs DHEA25 Tabs","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eWhat is Dehydroepiandrosterone? \n\u003cdiv\u003eDehydroepiandrosterone (DHEA) is an important precursor hormone. Precursors are substances that are converted by the body into hormones. DHEA is the highest circulating steroid present in the human body. It does not have much biological effect on its own but is powerful when converted into hormones such as testosterone and estradiol. DHEA is produced from cholesterol by the outer layer of the adrenal glands. It is also produced in small amounts by the ovary and testes. DHEA is an important source of estrogen for women. DHEA production gradually increases from age 10, peaks during the 20s, and slowly decreases into old age. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHow Does Your Body Use DHEA? \u003c\/div\u003e\n\u003cdiv\u003eYour brain controls the production of DHEA. Your body uses a unique mechanism known as negative feedback to control the production of DHEA. Negative feedback tells your brain that once DHEA levels drop in your body, the mechanism is switched “on” and begins to produce more of the hormone. Once DHEA levels begin to rise, negative feedback is switched “off”. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDHEA and Anti-Aging\u003c\/div\u003e\n\u003cdiv\u003eThere are many rumors and claims that taking DHEA can also help slow down the process of aging. Claims include that DHEA can also increase energy and muscle strength, boosts immunity, and decrease body weight. However, these claims have yet to be medically proven. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDoes DHEA have a role in treating certain health problems?\u003c\/div\u003e\n\u003cdiv\u003eSome researchers have suggested that DHEA might be used to treat:\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAdrenal insufficiency (Addison’s disease)\u003c\/div\u003e\n\u003cdiv\u003eDepression\u003c\/div\u003e\n\u003cdiv\u003eLupus\u003c\/div\u003e\n\u003cdiv\u003eObesity\u003c\/div\u003e\n\u003cdiv\u003eAlzheimer’s disease\u003c\/div\u003e\n\u003cdiv\u003eOsteoporosis\u003c\/div\u003e\n\u003cdiv\u003eCrohn’s disease\u003c\/div\u003e\n\u003cdiv\u003eInfertility\u003c\/div\u003e\n\u003cdiv\u003eProblems linked to menopause\u003c\/div\u003e\n\u003cdiv\u003eDHEA also might help induce labor in childbirth.\u003c\/div\u003e\n\u003cdiv\u003eDHEA has not yet been approved by the FDA as a treatment for these health problems. More research is needed to study the potential benefits and the long-term risks of DHEA.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhat Problems Can Occur with DHEA? \u003c\/div\u003e\n\u003cdiv\u003eResearch has shown that women with hirsutism and polycystic ovary syndrome may have higher levels of DHEA. Children diagnosed with congenital adrenal hyperplasia also have high levels of DHEA, as well as some cancer patients. \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eLower levels of DHEA have been linked to a decreased life span in men. In women, low DHEA levels are often associated with a lower libido and osteoporosis.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome people use DHEA hoping it will increase endurance and muscle strength, increase energy, decrease fat, and boost immunity, but these effects have not been proven. Some athletes use DHEA but it is banned by the National Football League, Major League Baseball, the Olympics, and other athletic organizations.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53757921526052,"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_02f05b7f-3183-48e9-bdd8-f6b08999842a.jpg?v=1778077894"},{"product_id":"hd-labs-clenject-40","title":"HD Labs Clenject 40","description":"\u003cp\u003e\u003cspan\u003eHD LABS CLENJECT(40MCG CLENBUTEROL HCL=20ML)\u003c\/span\u003e\u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53757990568228,"sku":null,"price":400.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_a4820a80-07ab-455e-807a-b33ffa836941.jpg?v=1778078018"},{"product_id":"hd-labs-trinaject-200","title":"HD Labs Trinaject 200","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eHD LABS TRINAJECT 200(50MG\/ML TRENBOLONE ACETATE+50MG\/ML TRENBOLONE HEXAHYDROBENZYLCARBONATE+100MG\/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: 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\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\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: About 5-7 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 Dosage: Men: 76-228-mg weekly; Women: 76-mg weekly (but should not use)\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: Rare, usually 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: Yes,\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ehighly toxic to kidneys also\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: Moderately\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBLEND OF 3 TREBELONES.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThis was\/is a very nasty but effective steroid that was removed from the market about 1987 or so. Not all that long ago it began showing up on the black market from Australia. Upon testing the 50-ml vials, it was discovered that it actually contained 31-mg\/ml of Trenbolone acetate. Most Fina Jet now found is bogus. It contains either a testosterone ester, ground Finaplix pellets, or just oil. But the original has been discontinued. (There are several new brands of the drug trenbolone acetate)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTrenbolone acetate is a strong androgenic\/anabolic steroid that caused a fast increase in strength and increased fat burning if the athlete’s diet was right. Unless stacked with other steroids, this drug did not cause much in actual weight gain (dose dependent). Its main use was to harden the physique’s appearance once body fat levels were low enough before competition. For the most part, bodybuilders have replaced Finajet\/ Finaject with Parabolan or one of the many black market trenbolone products. Since Finajet did not cause gyno or water retention, one may assume it was fairly clean. Wrong! Even at dosages of 30-60-mg injected daily, side effects such as kidney toxicity, nose bleeds, headaches, high blood pressure, acne, and serious attitude problems were common.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome creative and brave athletes have used the Finaplix 20 mg pellets which are intended for animal use. The pellets are shot into animal tissue for a slow release of Trenbolone. However some athletes (and black market crazies) have ground the pellets into a powder, mixed it with oil or water, and injected the very un-sterile solution with 18 gauge needles. I can not stress enough how dangerous this is. The product is often labeled Finabolan. (“Finabolin” gives us a chance to discuss trenbolone in greater depth in a moment)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAnother reported method of using the Finaplix pellets was to ground them into powder, mix the powder with a 50\/50 solution of DMSO (DIMETHYL SULFOXIDE) and water. Then apply it to skin. The DMSO acts as a transporter that allows 14-18-MG of a 20MG pellet to be absorbed into the blood stream while the skin acts as a filter of sorts. Unfortunately this also allowed many toxins on the skin to enter as well.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSome individuals have claimed real hard-core status by using an animal pellet implant gun and taking one in the glute. Do not try this at home. The pain would be major and compared to being shot with a .177 pellet. The interesting side of this is that the lads who did this had been told that the Finaplex pellets were readily absorbed “rectally”.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Geez! And some bodybuilders wonder why we have the stigma of dull wittedness?\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eNOTED POSITIVE EFFECTS OF TRENBOLONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Amazing anabolic qualities.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Rapid high quality lean tissue gains. (Dose dependent) *Maximum post-cycle lean mass retention. *Low-none water retention.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Increased Erythropoies (Red blood cell production) *Does not aromatize to estrogens. *Superior strength and mass gain. (Lean) *Extreme hardening of musculature and vascularity. *Excellent protein sparing\/anti-catabolic qualities. *Reduction in fat stores and favorable distribution. *Increased metabolic rate. *Low-moderate HPTA function inhibition. *Significant increase in muscle glycogen synthesis. *Increase creatine phosphate (CP) synthesis. *Improved muscle insulin receptor activity.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Remains anabolic during calorie restricted periods. (High protein intake remains necessary)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e POSSIBLE NEGATIVE EFFECTS TRENBOLONE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Liver and Kidney toxicity.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Growth of prostate tissue. (PSA test is wise)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Male pattern baldness. (Accelerated genetic predisposition)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*Mild hallucinations. (High dosage -prolonged use)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e*High blood pressure.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e Trenbolone Acetate is a fast acting injectable steroid.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTo increase its effective half-life, trenbolone is not used in an unrefined form, but is rather administered as trenbolone acetate ,enanthate or Hexahydrobenzylcarbonate. Trenbolone is then produced as a metabolite by the reaction of these compounds with the androgen receptor.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBodybuilders have been known to use the drug in order to increase body mass more effectively than by weight training alone. A normal bodybuilding dosage can range from 200 mg\/week up to 1400 mg\/week. Due to the relatively short metabolic half-life of trenbolone acetate, dosages should commonly be split into injections at least once every two days. Trenbolone enanthate can be injected once a week.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe 2006 book Game of Shadows alleges that baseball superstar Barry Bonds used this drug in 2001, when he set the current single-season home run record.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTrenbolone compounds have a binding affinity for the androgen receptor three times as high as that of testosterone. Once metabolised, the drugs have the effect of increasing nitrogen uptake by muscles, leading to an increase in the rate of protein synthesis. It also has the secondary effects of stimulating appetite, reducing the amount of fat being deposited in the body, and decreasing the rate of catabolism. Trenbolone has proven popular with anabolic steroid users as it is not metabolised by aromatase or 5α-reductase into estrogenic compounds such as estradiol, or into DHT. This means that it also does not cause any water retention normally associated with highly androgenic steroidal compounds like testosterone or methandrostenolone. It is also loved by many for the dramatic strength increases commonly experienced with it. Some short-term side effects include insomnia, high blood pressure, increased aggression and libido. However, since women will suffer virilization effects even at small doses, this drug should not be taken by a female. Urban wisdom\/myth in bodybuilding culture, states that the use of the drug over extended periods of time can lead to kidney damage. The kidney toxicity has not yet been proven, and scientific evidence supporting the idea is suspiciously absent from the bodybuilding community that perpetuates this idea. The origin of this myth most likely has to do with the rust colored oxidized metabolites of trenbolone which are excreted in urine and often mistaken for blood. After Schänzer (Clin Chem 1996; 42(7): 1001-1020, Metabolism of anabolic androgenic steroids) trenbolone and 17epi-trenbolone are both excreted (in urine) as conjugates that can be hydrolyzed with beta-glucuronidase. This implies that trenbolone leaves the body as beta-glucuronides or sulfates, that means mostly non metabolized.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53758095458596,"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_781001cf-727a-43a9-979d-871682fdab4c.jpg?v=1778078145"},{"product_id":"hd-labs-ment-100","title":"HD Labs MENT 100","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003e\n\u003cdiv\u003eHD LABS TRESTOLONE MENT(TRESTOLONE ACETATE 100MG\/ML=10ML)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 650\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 2300\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSTANDARD TESTOSTERONE PRIOPIONATE\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive-Life: About 2-3 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 Dosage: Men: 100-300-mg 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: Rare, usually none\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\u003eAromatization: Low to Moderate \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: Servere\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMENT, short for methylnortestosterone, is a synthetic anabolic steroid closely related to nandrolone in structure. It was first researched back in the early 1960’s, the heyday of anabolic steroid development. Back then, there were new compounds being introduced into the journals literally every week. Like a great many of the effective steroids studied during this era, however, MENT didn’t make it’s way to becoming a commercial drug product. For about four decades it sat gathering dust on the bookshelves, next to many other effective but anonymous compounds. Historically, lack of early financial support has been a death sentence for anabolic steroids. If a company isn’t there in the beginning to spend the millions necessary to develop it into an actual prescription product, it isn’t going to go anywhere later on. The money simply wasn’t there for MENT in the 1960’s, and it died. For a long time this agent remained a “nothing” in the world of steroids.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eBut things changed for MENT around the turn of the century, in a very dramatic fashion. On October 30th in 2000, international drug giant Schering AG made a public announcement that it had entered into a partnership to research, develop, and market methylnortestosterone acetate for both male contraceptive and hormone replacement use. This followed several years of sporadic but positive studies on this agent. The ball was set in motion, and this old steroid, which scientists had ignored for over thirty years, was suddenly amidst a hotbed of new research and speculation, the likes of which it had never seen before. In their press release, Schering AG makes promise of a new androgen that offers the anabolic and endocrine benefits of an injectable testosterone, but with less prostate growth, and more patient comfort. In other words, Schering is saying that MENT looks to be an easier to administer and equally useful steroid as testosterone, yet without the same issues concerning androgenicity.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTo understand exactly why it is that Schering would be paying such interest in this steroid, we need to examine its structure and effect. While descriptive, the generic name methylnortestosterone (methylnandrolone is also appropriate) does not quite tell usenough.lt turns out that the term “methyl” which is most commonly associated with C-17 alpha alkylated androgens like methyltestosterone, methandrostenolone, or oxymetholone, is being used differently here. In this case, it refers to a modification at C-7, which gives this steroid a considerably different appearance than one might think at first. Of most obvious significance is its method of use. Although perhaps possessing a moderate level of oral bioavailability, this nandrolone derivative was really not designed for oral administration. It is much more effective when administered to the body directly, as by injection or implant.Therefore, the immediate assumption that this is the “Methyltest” of Deca is not quite accurate (that title actually belongs to Orgasteron, also profiled in this book).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eOne well understood function of 7-methylation is that is blocks steroid 5-alpha reduction (something that c-17 methylation does not accomplish). As such, this derivative of nandrolone cannot be converted to a “dihydro” metabolite”7. With nandrolone and most of its analogs, this reduction means a less androgenic steroid. Dihydronandroione is weaker than nandrolone, so relative binding is reduced in target tissues with high reductase concentrations. Not being able to convert to a weaker steroid here, MENT is going to display more relative androgenicity than nandrolone. However, this may not necessarily be a bad thing. Nandrolone is commonly too weak of an androgen, causing impotence issues in good percentage of men that try taking this steroid alone. When we are speaking of hormone replacement and contraceptive use, we can’t suppress natural testosterone and replace it with a weak androgen. In this regard MENT definitely seems to have one up on Deca-Durabolin.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e.8mg, or 1.6mg of steroid.The release rate is slowly reduced as the implant loses surface area, however, reaching approximately 200mcg per day by the one-year mark.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eThe results of the clinical trial were very promising. Four MENT implants (1.6mg\/day) suppressed spermatogenesis with similar effectiveness as testosterone implants, testosterone enanthate injections, and testosterone undecanoate injections (all of which have been investigated successfully as contraceptives). MENT was able to produce azoospermia in 82% of treated subjects, a figure that was actually higher than reported with 200mg of testosterone enanthate per week (which produced azoospermia in 65-66% of normal male subjects by 6 months). As far as negative side effects, they were few.Two subjects noted increases in blood pressure that went outside the normal range, and one was forced to discontinue the study because of it (though no ill effect was noted). Otherwise, there was generally just a very small rise in systolic pressure (+4.8), and no significant changes in lipids (including cholesterol and triglycerides) or PSA values. Furthermore, prostate volume was slightly reduced (not increased) in all groups. Liver enzymes were increased slightly, but stayed within the normal range in all subjects. The mean time to the recovery of normal sperm production after discontinuance was 3 months, similar to that reported in a 1990 World Heath Organization study with 200mg weekly of testosterone enanthate. Overall, MENT performed admirably, with a very notable (acceptable) level of effect, and minimal side effects. And what is more, the drug may be effective when being implanted an infrequently as once per year\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAnother study of interest examined the ability of MENT implants to restore sexual behavior and function in hypogonadal (having low testosterone) men128. This, of course, is one of the principle objectives of androgen replacement therapy.This investigation took place in two clinics, one based in Ireland and the other Hong Kong. Twenty men participated in total, 10 at each location.The study was a double crossover investigation comparing the effects of testosterone enanthate (200mg every 3 weeks) to that of two MENT implants (delivering .8mg of drug per day). This means that each of the twenty men had an opportunity to try both drugs, which were taken on two separate occasions between washout periods. Only minor differences in response were noted between MENT and\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003enonoptional androgen replacement therapy and both drugs were effective in restoring sexual behavior and erection frequency. MENT, at a dosage of 2 implants delivering approximately .8mg of drug per day, proved to be an effective option for androgen replacement therapy.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eIf Schering markets this drug as an implant, it will be impractical to use for bodybuilding purposes. At best it will need to be broken down and made into an injectable somehow. The clinical study discussed above used implants containing about 140mg of steroid each. Given the same in a production drug, more than one implant will be needed for a workable cycle. There is some investigation into its use as an oral129, which does seem feasible (although not ideal from a cost effectiveness standpoint). The key to this steroid’s success with bodybuilders will really be the development of a commercial injectable. This will undoubtedly follow the release of Schering’s product, perhaps even precede it.The raw powder is already available from suppliers overseas, so it should not take long for some veterinary or underground manufacturer to perceive value in this new agent. Hopefully an acetate version will even be closely followed by a slower acting MENT ester, perhaps even something basic like MENT cypionate or MENT enanthate.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAs for its use, MENT is a relatively potent steroid, so an effective dose for bodybuilders is going to be small. As a drug 10 times more anabolic than testosterone by some studies, and 20 times more effective at suppressing spermatogenesis than testosterone enanthate in others, we should commonly see daily doses of maybe 3-6mg. If prepared as an oil-based injectable (with acetate ester), this would mean shots of roughly 10-20mg every two to three days. Compare this to trenbolone, which is usually given in doses of 75-100mg per shot under the same schedule (and this is a particularly potent steroid). Some might find good effect at 10mg daily, however I suspect the number of people needing to go here will be few, and fewer still will probably venture higher. As a poorly aromatized anabolic (19-nor compounds tend to aromatize much more slowly than c-19 steroids), MENT should stack well with a variety of different steroids, possibly for both cutting and bulking phases of training. For simplicity, this would mean using it with drugs like testosterone cypionate\/enanthate (200-400mg\/week), Dianabol (20-35mg\/day), or Anadrol (50-100mg\/day) when looking for sheer size, milder anabolics like nandrolone decanoate or boldenone undecylenate (200-400mg\/week) for lean mass, or non-aromatizable drugs like Primobolan (200-300mg\/week), Winstrol (20-35mg\/day), or Anavar (15-20mg\/day) while cutting.\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53758164926756,"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_33fd57d6-564a-4792-b23a-369fa21dd89b.jpg?v=1778078275"},{"product_id":"hd-labs-primoject-100","title":"HD Labs Primoject 100","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eHD LABS PRIMOJECT 100(100MG METHENOLONE ENANTHATE=10ML)\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\u003e \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\n\u003c\/div\u003e\n\u003cp\u003e \u003c\/p\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53758273126692,"sku":null,"price":950.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_ed5c12af-2367-46bb-8469-2c7b736fc035.jpg?v=1778078397"},{"product_id":"hd-labs-nebidoject-250","title":"HD Labs Nebidoject 250","description":"\u003cdiv\u003eHD LABS NEBIDOJECT 250(250MG TESTOSTERONE UNDECANOATE\/ML=10ML)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANDROGENIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eANABOLIC 100\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eActive -Life: ORAL Less than 8 hours\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e                    INJECTABLE 50 days\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDrug Class: Androgenic\/Anabolic Steroid (Oral)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAverage Reported Dosage: Men 240-320 mg daily (Women experienced serious VIRILIZTION)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAcne: Low except if used by androgen sensitive athletes\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWater Retention: Yes, higher in dosages of 280-400mg daily\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eHigh Blood Pressure: Rare (Dosage related)\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\u003eDHT Conversion: Significant in higher dosage administration\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eDecreases HPTA functions: Low, except in higher reported dosages (above 320mg)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAromatization: Low-moderate.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAndriol is an orally active testosterone. The only other orally active testosterone is methyltestosterone. But unlike its counterpart, Andriol has a unique absorption method. When ingested with or after meals it is reabsorbed through the mucosal cells in the small intestine via the lymphatic system. This ester therefore avoids absorption through the portal vein in the liver and subsequent first pass deactivation. This means that a much higher level of Andriol enters the blood stream. Some of the drug is then converted into DHT (dihydrotestosterone) which has a high affinity for androgen receptors. Due to higher DHT conversion, Andriol does not aromatize (transform) into estrogen at a high rate like other testosterone. For this reason, water retention is much lower while gyno and female pattern fat deposits are far less likely. This drug has a reported low negative effect on the HTPA (hypothalamic pituitary testes axis) and therefore does not suppress natural (endogenous) androgen production to a significant degree in the lower reported dosages. For the most part it is due to estrogen’s negative influences that HPTA function is decreased. However, estrogen must be present in lower levels for any steroid to reach its full potential effects. Kind of a paradox huh?\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWhen stacked with other AAS, Andriol has provided a mild androgenic\/anabolic synergistic effect at dosages of 200 mg daily. However, if this drug was administered alone, this dosage did not provide much in the way of results when compared to injectable testosterone. To rival its injectable cousins, daily dosages would need to be in the above 290-320 mg range minimum. This dosage would not only be quite expensive, it also would reach a level where suppression of the HPTA would increase a great deal due to elevated aromatization. This also increases water retention significantly. Since Andriol is quickly excreted through urine release, the drug was be taken 3-6 times daily to maintain adequate circulatory levels.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eAll in all Andriol was reported as a mildly Androgenic \/ Anabolic steroid that was best used in stacks for its excellent compatibility at dosages of 240-320 mg daily. For novice steroid users, older athletes, and safety conscience individuals, a stack of 200-240\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003emg Andriol daily, 200 mg of Primobolan depot (or 200-400 mg Anadur or Deca Durabolin) weekly, and 20 mg of Oxandrolone daily was reported to provide excellent lean mass and good strength gains with minimal suppression of the HPTA and other negative side effects. The good news was that athletes retained the gains quite well after use was discontinued. (Unless they were highly psychologically influenced by off periods!)\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eTHE INJECTABLE VERSION OF TESTOSTERONE UNDECOANATE RECENTLY CAME ON THE MARKET,WHAT IS INTERESTED ABOUT THIS PRODUCT,IS THAT IT HAS A HALF LIFE OF 50 DAYS,WHICH MAKE IT ONE OF THE LONGEST ACTING INJECTABLE COMPOUNDS ON THE MARKET TODAY.\u003c\/div\u003e","brand":"UltraFizique","offers":[{"title":"Default Title","offer_id":53758399086884,"sku":null,"price":470.0,"currency_code":"ZAR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/files\/rn-image_picker_lib_temp_81e5fe98-5d53-47d5-8561-2bbeb95f74d0.jpg?v=1778078579"},{"product_id":"hd-labs-finaject","title":"HD Labs Finaject","description":"\u003cdiv class=\"product__description rte quick-add-hidden\"\u003eHD LABS FINAJECT(100MG\/ML TRENBOLONE HEXAHYDROBENZYLCARBONATE)\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: About 5-7 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 Dosage: Men: 76-228-mg weekly; Women: 76-mg weekly (but should not use)\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: Rare, usually 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: Yes,\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003ehighly toxic to kidneys also\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: Moderately\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003e \u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eParabolan was reported to be the most effective injectable anabolic\/androgenic steroid available today. Real Parabolan provided users with a rapid build-up in strength and high quality muscle mass, while increasing fat burning (even when not dieting). The drug does not aromatize to estrogen or reduce to DHT. For this reason there was no noted water retention or feminizing effects. Parabolan sped up the metabolism as well. Due to the high androgenic quality, a hard, ripped, and vascular look with a dramatic increase in quality muscle mass resulted for all that reported use. This profile is what made Parabolan appear to be another all-purpose steroid.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eSo what’s the problem? It was rare to find real Parabolan. Though the real product has a distinct odor, at least 95% seen was bogus. The real product is quite toxic to kidneys, so users mostly kept usage to 4-8 weeks and drank at least an additional gallon of water daily. Due to the high degree of potential toxicity dark urine and even blood in urine can result from high, prolonged use (as can prostate enlargement due to the drug’s structural similarity to DHT).\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eParabolan was commonly stacked with growth hormone, thyroid, and\/or Clenbuterol during diet periods for the synergistic effects. A simple stack of 20-30-mg Oxandrolone daily and 152-228-mg Parabolan weekly consistently brought excellent high quality strength and muscle mass gains while decreasing body fat.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eWomen should not use Parabolan due to a very high virilizing effect. But many competitive female athletes still did. Some stacked 76-mg of Parabolan every 5-8 days with 80-120 mcg of Clenbuterol and either 15-20-mg of Winstrol tabs or 10-15-mg of Oxandrolone tabs daily.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eI know of one female who is suffering from most of the possible side effects: missed periods, hair loss on the scalp, serious sex-drive (you should see her on an exercise bike) and clitoral hypertrophy. Facial hair growth can also result also.\u003c\/div\u003e\n\u003cdiv\u003e\u003c\/div\u003e\n\u003cdiv\u003eMales usually obtained excellent results with 76-mg every 2-3 days.(Though some doubled this amount unnecessarily)\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\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.Trenbolone hexahydrobenzylcarbonate can be injected even less frequently than trenbolone enanthate.\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.[citation needed] 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":53758504698148,"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_1119cd9e-04da-4e2a-9cb1-b0b1047e581d.jpg?v=1778078707"}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1005\/5404\/7780\/collections\/rn-image_picker_lib_temp_1a62a597-a2f6-4367-9d6a-fd867d2ba47b.png?v=1777602356","url":"https:\/\/ultrafizique.co.za\/collections\/hd-labs.oembed?page=2","provider":"UltraFizique","version":"1.0","type":"link"}