ACTIVE HALF-LIFE
8-9 hours
CLASSIFICATION
Anabolic Steroid
DOSAGE
Recommended for Men: 250-350mg/week
ACNE
Yes
WATER RETENTION
High
HBR
Possible
HEPATOTOXICITY
Yes
AROMATIZATION
No
CARRIER OIL
Grapeseed Oil
MANUFACTURER
Pharmacom Labs - US
LAB TEST
Refer to Document
WAREHOUSE
USA Warehouse 4
SUBSTANCE
Oxymetholone Injectable
Discover the potent power of Oxymetholone, also known as Anapolon or Anadrol, a powerful synthetic anabolic steroid that boasts a 17-alpha-alkylated structure derived from dihydrotestosterone. Originally formulated to treat osteoporosis and anemia, Oxymetholone is designed to stimulate muscle growth in individuals who are malnourished or weakened. This FDA-approved compound has seen a decline in use after effective non-steroidal alternatives emerged, resulting in its production being halted by Syntex and others by 1993.
When it comes to performance, Oxymetholone mirrors the effects of Methandienone, delivering significant muscle bulking and an impressive increase in strength. However, it's important to note that much of the weight gained during its use is attributed to water retention, which could lead to elevated blood pressure throughout your cycle.
Oxymetholone?s ability to enhance hemoglobin levels and boost blood volume provides a notable pump effect for athletes, although this can complicate training sessions, causing muscles to feel sore shortly after intense workouts.
As a dihydrotestosterone derivative, Oxymetholone's unique chemical structure prevents aromatization. While it does not convert to estradiol, it still exhibits significant estrogenic properties. Thus, only anti-estrogens can effectively combat estrogenic side effects, as typical aromatase inhibitors will not work in this case.
Some users speculate that the estrogenic effects of Oxymetholone may be linked to progestogenic activity, similar to nandrolones, leading to comparable side effects. However, research has shown that Oxymetholone does not display progestogenic activity.
Pharmacom Labs offers an injectable version of this steroid, which bypasses the liver's first-pass metabolism, resulting in greater bioavailability and reduced hepatotoxicity compared to its oral counterparts.