Because the ultimate goal of a steroid cycle is to increase strength and muscle size, the associated spike in estrogen which accompanies steroids such as Testosterone is considered undesirable. In order to disassociate the two effects, two classes of drug are used. Medications such as Nolvadex or Clomid target the estrogen receptors. They make it more difficult for the estrogen to exert it’s influence within the body thus allowing the testosterone to act more freely. The second class is aromatase inhibitors such as Femara. They target the aromatase enzyme itself in order to prevent the production of estrogen in the first place. Sometimes, it’s not always clear which option you should go with or even what the differences are between the two. Lets clear that up a little.
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Unlike many other 17-methylene, steroids oxandrolone is excreted largely unchanged and not conjugated in the urine. The major metabolites of Oxandrolons are 17-Epioxandrolon and 16-hydroxy metabolites.
On the German pharmaceutical market oxandrolone is not allowed. Under the trademarks Anavar, Lonavar or oxandrolone SPA, you can refer the drug in tablet form in the United States, Japan, Italy or Argentina relate. Doping cases in which oxandrolone have played a role and only became known in Germany for the first time by the high jumper Amewu Mensah.
The anabolic effect of oxandrolone occurs only when taken regularly over a longer period. No information has been disclosed about a performance-enhancing effect with an intake just before a competition. It can be perfectly detected over 72 hours after ingestion.