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.
Bushido, I read on Meso-rx under steroid profiles that primo has a half life of 5 days. That means that if u took an injection on day one it would be half out of ur system in 5 days, 3/4 out in 10 days, and 100% in 15 days, correct? Not 100% sure on how that works but that is what i read. When I posted this i thought it meant that 100% of the drug would be gone in ten days. So basically in order for that to work you would need to shoot everything on day one I presume, which would only give you about a week of a very high concentration. Would it be ascanine to expect ANY advantage from one week of high dosage, whilst relying on synergy with say more dianabol in the second week? Which if taken in the morning, might alow for an even faster recovery?? I imagine it would not be a great idea to shoot say 1200 mg on day one for example? Am I correct in the half life timing? With a half life of 5 days there would only be time for one shot in a two weeker? It might be a worthwhile experiment no? LOL What do u think? Better off with the anavar?
"...Body weight increased in all groups, including the group receiving placebo, during the double-blind phase ( ± , ± , ± , and ± kg in placebo and 20-, 40-, and 80-mg oxandrolone groups, respectively; all P < vs. baseline). BCM increased from baseline in all groups ( ± , ± , ± , and ± kg in placebo and 20-, 40-, and 80-mg oxandrolone groups, respectively). At 12 weeks, only the gain in weight at the 40-mg dose of oxandrolone and the gain in BCM at the 40- and 80-mg doses of oxandrolone were greater than those in the placebo group "