Oxandrolone (Anavar), is especially well suited with cutting cycle and many people is using for this purpose. By using Anavar you will not notice a big difference in gain of mass, but any mass that you gain it will be lean tissue. It is knowns as well as “Girl Steroid”. Female users are more likely to see gains in tissue. Using this steroid, it means that does not aromatize to estrogen, water retention is reported as quite law and gyno is not shown at all. After 5 days of administration of Anavar, there are noticeable results as 44% increase in muscle cell protein synthesis. Benefits of Anavar BD Max:· Doesn’t aromatize· Water retention is law· Liver toxic less than other drugs· Fat burningSpecification:· Active Life - 8-12 hours· Average Dose - 15-60 mg/daily· Aromatization - No..
Since estrogen offers us no trouble, side effects are generally mild with this steroid. As discussed earlier, gynecomastia and water retention go unseen. So are problems controlling blood pressure, again usually associated with estrogen. Masteron is also not liver toxic, so there is little concern stress will be placed on this organ, even during longer cycles. The only prominent side effects stem from the basic androgenic properties of dihydrotestosterone. This includes oily skin, acne, body/facial hair growth, aggression and accelerated hair loss. Since this compound is already a synthetic DHT, Proscar® would have no impact on the level of androgenic effects. Men with a receding hairline (or those with a known familial predisposition for baldness) may therefore wish to stay away from Masteron completely, as the potent androgenic effect of this steroid can easily exacerbate such a condition.
Drostanolone propionate is a prodrug of drostanolone .  Like other AAS, drostanolone is an agonist of the androgen receptor (AR).  It is not a substrate for 5α-reductase and is a poor substrate for 3α-hydroxysteroid dehydrogenase (3α-HSD), and therefore shows a high ratio of anabolic to androgenic activity.  As a DHT derivative, drostanolone is not a substrate for aromatase and hence cannot be aromatized into estrogenic metabolites .  While no data are available on the progestogenic activity of drostanolone, it is thought to have low or no such activity similarly to other DHT derivatives.  Since the drug is not 17α-alkylated , it is not known to cause hepatotoxicity .