Legal steroid
If no other drugs are used, however, side effects such as gynecomastia are fairly likely. legal steroid Ben johnson steroids. Prostate enlargement, worsening of acne, and acceleration of male pattern baldness (for those genetically susceptible to it) are particularly severe because of the effectively-higher androgen levels seen in these tissues as a result of local conversion to the more-potent DHT. Synthetics which do not convert to DHT give only the same effective level of androgen in these tissues as in the body as a whole, rather than effectively three times the level. This is a significant advantage. legal steroid Steroid-oral-cycle. A particularly interesting property of testosterone is its low toxicity, exclusive of the above- mentioned side effects. Doses of two grams or four grams per week are hardly unknown in bodybuilding, and are not particularly hard on the liver. No one seems to want to take doses of any other single steroid at comparably-effective doses, and it seems that if one tried, they might be more toxic. legal steroid Steroid-use-statistics. E. g. , the hepatotoxicity of Winstrol Depot resulting from its 17a -methyl group is not severe at doses of say 350 mg/week, but might well be problematic at a dose of two grams per week - though that is speculation, since no one I have heard of uses such doses of Winstrol. Thus, at the higher dosage regimes testosterone appears to have an advantage in terms of toxicity vs. effectiveness over many of the synthetics. These doses, however, are in the pro bodybuilder range. In the dosage range more appropriate for most individuals, the reverse is often the case. Nandrolone (Deca Durabolin)This drug is unique (so far as I know) in that 5a -reductase, the enzyme which converts testosterone to the more-potent DHT, actually converts nandrolone to a less-potent compound. Therefore this AAS is somewhat deactivated in the skin, scalp, and prostate, and these tissues experience an effectively-lower androgen level than the rest of the body. Therefore, for the same amount of activity as another drug at the androgen receptors (ARs) in muscle tissue, Deca gives less activity in the scalp, skin, and prostate. Thus, it is the best choice for those particularly concerned with these things. Its effectiveness at the androgen receptor of muscle tissue is superior to that of testosterone: it binds better. Yet, it gives only about half the muscle-building results per milligram. This I think is a result of its being less effective or entirely ineffective in non-AR-mediated mechanisms for muscle growth. It also appears less effective or entirely ineffective in activity on nerve cells, certainly on the nerve cells responsible for erectile function. Use of Deca as the sole AAS often results in complete inability to perform sexually. These problems can be solved by combining with a drug that does supply the missing activity: e. g. testosterone. To some extent, nandrolone aromatizes to estrogen, and it does not appear that this can be entirely blocked by use of aromatase inhibitors - indeed, aromatase may not be involved at all in this process (there is no evidence in humans that such occurs) with the enzyme CYP 2C11 being in my opinion the more likely candidate for this activity. In any case, Cytadren, an aromatase inhibitor, has not been found effective in avoiding aromatization of nandrolone. The drug is moderately effective at doses of 400 mg/week.
Legal steroid
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