Taurus Virilis
189 posts




BREAKING: Israeli PM Netanyahu announces he was diagnosed, treated for prostate cancer



New article berbarianwizard.substack.com/p/anavar-only-…






Oxandrolone (Anavar) is often cited with an anabolic-to-androgenic ratio around 322–630 : 24, with testosterone set at 100 : 100. On paper, that translates to roughly 3× to 6× more anabolic per mg than testosterone, with much lower androgenic signaling. It does not aromatize, so estrogen-related effects are limited. This removes one pathway of suppression. The second factor is its relatively low androgenicity, meaning weaker androgen receptor–mediated negative feedback compared to more androgenic compounds. In clinical settings, doses around ~20 mg/day have shown minimal suppression in some contexts, which aligns with both the lack of aromatization and its lower androgenic signaling. It also has anti-catabolic effects through glucocorticoid receptor antagonism, which is one reason it has been used in burn patients, HIV-related wasting, and post-surgical recovery. Reported effects include improved nitrogen retention, preservation of lean mass, increases in strength without significant water retention, and a lower incidence of androgenic side effects compared to many other anabolic steroids. It remains a 17α-alkylated oral compound, so hepatotoxicity is present. At lower doses it is generally considered manageable, but risk increases with dose and duration. There is a consistent gap between older reports describing it as effective and newer reports describing little effect. A major factor is product authenticity. Oxandrolone is frequently substituted with compounds like stanozolol, turinabol, or methandrostenolone, which leads to different outcomes. Pharmaceutical-grade oxandrolone is limited. Iranian pharmaceutical products have been among the known legitimate sources in certain periods. I was able to obtain Iranian oxandrolone before the war. Would you want a detailed breakdown of that experience?
































