Pharma OXY 50 Ampoules

ACTIVE HALF-LIFE 8-9 hours
CLASSIFICATION Anabolic Steroid
DOSAGE Men: 250-350mg/week
ACNE Yes
WATER RETENTION High
HBR Perhaps
HEPATOTOXICITY Yes
AROMATIZATION No
CARRIER OIL Grapeseed Oil
MANUFACTURER Pharmacom Labs
LAB TEST See Document
WAREHOUSE International Warehouse 3
SUBSTANCE Oxymetholone Injectable

Discover the power of Oxymetholone, also known as Anapolon or Anadrol?a formidable synthetic anabolic steroid that is a 17-alpha-alkylated derivative of dihydrotestosterone. Initially formulated to combat osteoporosis and anemia, as well as to stimulate muscle growth in those suffering from malnutrition or weakness, this FDA-approved compound has a storied past. Although its popularity waned with the rise of effective non-steroidal alternatives, Oxymetholone remains a sought-after choice among seasoned athletes and bodybuilders.

When it comes to muscle enhancement, Oxymetholone stands toe-to-toe with Methandienone. Users can expect substantial gains in muscle mass and strength; however, it?s essential to be aware that much of this weight gain is attributed to water retention, which can elevate blood pressure during use.

Thanks to its ability to boost hemoglobin levels and increase blood volume, Oxymetholone delivers an exhilarating ?pump? effect, perfect for athletes looking to maximize performance. However, this can lead to muscle soreness shortly after intense workouts, so be prepared!

As a dihydrotestosterone derivative, Oxymetholone does not aromatize, meaning it won?t convert directly to estradiol. Nonetheless, it does showcase estrogenic properties, making it crucial to manage potential side effects with antiestrogens, as aromatase inhibitors will not be effective in this case.

Some speculate that the estrogenic effects may mirror progestogenic activity, akin to Nandrolones, leading to similar side effects. However, clinical studies confirm that Oxymetholone lacks any progestogenic activity.

Pharmacom Labs has innovatively created an injectable version of this steroid, offering enhanced bioavailability and reduced hepatotoxicity compared to traditional oral formulations, thanks to the absence of first-pass metabolism in the liver.