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Anavar was the old U.S. brand name for the oral steroid oxandrolone, first produced in 1964 by the drug manufacturer Searle. It was designed as an extremely mild anabolic, one that could even be safely used as a growth stimulant in children. One immediately thinks of the standard worry, “steroids will stunt growth”. But it is actually the excess estrogen produced by most steroids that is the culprit, just as it is the reason why women stop growing sooner and have a shorter average stature than men. Buy Oxandrolone 10 mg 100 Tabs by Genesis Med
Oxandrolone will not aromatize, and therefore the anabolic effect of the compound can actually promote linear growth. Women usually tolerate this drug well at low doses, and at one time it was prescribed for the treatment of osteoporosis. But the atmosphere surrounding steroids began to change rapidly in the 1980s, and prescriptions for oxandrolone began to drop. Lagging sales probably led Searle to discontinue manufacture in 1989, and it had vanished from U.S. pharmacies until recently. Oxandrolone tablets are again available inside the U.S. by BTG, bearing the new brand name Oxandrin. BTG purchased rights to the drug from Searle and it is now manufactured for the new purpose of treating HIV/AIDS-related wasting syndrome. Many welcomed this announcement, as Anavar had gained a very favourable reputation among athletes over the years.
Anavar is a mild anabolic with low androgenic activity. Its reduced androgenic activity has much to due to the fact that it is a derivative of dihydrotestosterone. Although you might think at first glance this would make it a more androgenic steroid, it, in fact, creates a steroid that is less androgenic because it is already “5-alpha reduced”. In other words, it lacks the capacity to interact with the 5-alpha reductase enzyme and convert to a more potent “dihydro form. It is a simple matter of where a steroid is capable of being potentiated in the body, and with oxandrolone, we do not have the same potential as testosterone, which is several times more active in androgen-responsive tissues compared to muscle tissue due to its conversion to DHT. It essence oxandrolone has a balanced level of potency in both muscle and androgenic target tissues such as the scalp, skin and prostate. This is a similar situation as is noted with Primobolan and Winstrol, which are also derived from dihydrotestosterone yet not known to be very androgenic substances.
This steroid is known as a good agent for the promotion of strength and duality muscle mass gains, although the mild nature of this compound makes it less than ideal for bulking purposes. Among bodybuilders it is most commonly used during cutting phases of training when water retention is a concern. The standard dosage for men is in the range of 15-25mg (6-10 tablets) per day, a level that should produce noticeable results.
It can be further combined with anabolics like Primobolan and Winstrol to elicit a harder. more defined look without added water retention. Such combinations are very popular and can dramatically enhance the show physique. One can also add strong non-aromatizing androgens like Halotestin, Proviron or trenbolone. In this case, the androgen really helps to harden up the muscles, while at the same time making conditions more favourable for fat reduction. Some athletes do choose to incorporate oxandrolone into bulking stacks. but usually with standard bulking drugs like testosterone or Dianabol. The usual goal in this instance is an additional gain of strength, as well as more quality look to the androgen bulk. Women who fear the masculinizing effects of many steroids would be quite comfortable using this drug, as this is very rarely seen with low doses. Here a daily dosage of 5mg should illicit considerable growth without the noticeable androgenic side effects of other drugs. Eager females may wish to addition mild anabolics like Winstrol, Primobolan or Durabolin. When combined with such anabolics, the user should notice faster, more pronounced muscle-building effects, but may also increase the likelihood of androgenic buildup. Buy Oxandrolone 10 mg 100 Tabs by Genesis Med
Studies using low dosages of this compound note minimal interferences with natural testosterone production. Likewise, when it is used alone in small amounts there is typically no need for ancillary drugs like Clomid/Nolvadex or NCG. This has a lot to do with the fact that it does not convert to estrogen, which we know has an extremely profound effect on endogenous hormone production. Without estrogen to trigger negative feedback, we seem to note a higher threshold before inhibition is noted. But at higher dosages, of course, a suppression of natural testosterone levels will still occur with this drug as with any anabolic/androgenic steroid.
This makes clear that while estrogen is important in this regard, androgen action triggers feedback inhibition as well. In the context of the average bodybuilder using this steroid at a level to promote growth, we would probably expect that maintaining a normal level of endogenous testosterone release would likewise be very difficult.
Anavar is also a 17alpha alkylated oral steroid, carrying an alteration that is noted for putting stress on the liver. It is importar7t to point out however that to spite this alteration oxandrolone is generally very well tolerated, While liver enzyme tests will occasionally show elevated values, actual damage due to this steroid is not a statistical problem. Bio-Technology General states that oxandrolone is not as extensively metabolized by the liver as other l7aa orals are; evidenced by the fact that nearly a third of the compound is still intact when excreted in the urine. This may have to do with the understood milder nature of this agent (compared to other l7aa orals) in terms of hepatotoxicity. One study comparing the effects of oxandrolone to other agents including as methyltestosterone, norethandrolone, fluoxymesterone and methandriol clearly supports this. Here it was demonstrated that oxandrolone causes the lowest sulfobromophthalein (BSP; a marker of liver stress) retention among all. The alkylated orals tested. 20mg of oxandrolone, in fact, produced 72% less BSP retention than an equal dosage of fluoxymesterone, which is a considerable difference being that they possess the same liver-toxic alteration. With such findings, combined with the fact that athletes rarely report trouble with this drug, most feel comfortable believing it to be much safer to use during longer cycles than most of the other orals with this distinction. Although this may very well be true, the chance of liver damage still cannot be excluded, however.
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