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Description
Oxymetholone is a potent oral anabolic steroid. It was initially developed to treat osteoporosis and anemia (approved for pediatric use) and to stimulate muscle growth in malnourished and debilitated patients. Oxymetholone has clinical approval for human use, especially in pediatric cases. It exhibits low androgenic and high anabolic activity and cannot be aromatized, though it has a mild estrogenic effect.
Effects and Benefits
- Muscle Growth: Oxymetholone is considered one of the most effective oral steroids for gaining mass, with users potentially gaining up to 15 kg in a single cycle. However, there's a significant rollback phenomenon where up to 30% of the gained mass can be lost post-cycle, partly due to fluid retention.
- Strength Increase: The steroid provides a pronounced increase in strength by impacting the nervous system.
- Joint Health: It alleviates joint pain, improves joint function, and enhances joint lubrication due to fluid retention and increased synovial fluid production.
- Enhanced Effect of Other Steroids: By reducing sex hormone-binding globulin (SHBG), it amplifies the effects of other anabolic hormones when used in combination.
- Fat Burning: Particularly effective in reducing abdominal fat, making it suitable for men struggling with belly fat.
- No Significant Liver Impact Contrary to popular belief, oxymetholone does not significantly affect liver function. It is a derivative of dihydrotestosterone and lacks progestogenic activity.
Dosages
- Beginner: 50 mg per day
- Average: 50-150 mg per day
- High: 150 mg or more per day
Effects
- Significant increase in strength and muscle mass
- Water retention
- Improved recovery
- Increased glycogen levels
- Increased appetite
- Enhanced joint lubrication and healing of minor injuries
Side Effects
- Suppression of natural testosterone production
- Reduced fertility
- Increased hematocrit levels
- Increased blood pressure
- Acne
- Baldness
- Deterioration of lipid profile
- Fluid retention
- Rarely: increased prolactin levels, gynecomastia
- Hepatotoxicity (comparable to turinabol and methandrostinolone)
- Mild estrogenic effects (may require monitoring of estradiol levels and use of estrogen receptor blockers)
Profile
- Half-life: 10-12 hours
- Duration of Action: 12-15 hours
- Frequency of Intake: Twice a day
Contraindications
- Pregnancy
- Known or suspected carcinoma of the prostate or breast
- Breast-feeding
- Hypersensitivity to the active substance or any excipients
- High blood calcium levels
Storage
- Keep away from children
- Store in a cool, dry place away from direct sunlight
- Store at room temperature
- Do not use after the expiry date