Fabricator: Dragon Pharma, Europe
Unit: x1 100 tabs
Strength: 50 mg/tab
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Dragon Pharma Oxymetholon delivers 50 mg of Oxymetholone per tablet. This legendary oral agent is engineered for athletes pursuing explosive hypertrophy and immediate strength surges.
Commonly known as Anadrol or "A-Bombs," this C17-alpha alkylated compound produces dramatic weight accretion within the first few weeks of administration. Each batch is manufactured under rigorous quality protocols and verified by independent laboratory analysis.
Oxymetholone is a synthetic DHT-derived anabolic steroid with a 2-hydroxymethylene group modification. This structural alteration delivers exceptional anabolic potency alongside significant progestogenic and estrogenic activity.
The compound rapidly stimulates erythropoiesis, enhancing oxygen-carrying capacity and muscular endurance. Users frequently report a pronounced sense of well-being and heightened training aggression during the active phase.
Unlike dry cutting agents, Oxymetholon generates substantial intracellular fluid and glycogen retention. This produces a perpetually full, volumized appearance even outside the gym.
Dragon Pharma subjects every production lot to third-party analytical testing. Recent assays confirm tablet potency consistently aligns with the labeled 50 mg specification, ensuring predictable pharmacological outcomes.
Each tablet contains 50 mg of Oxymetholone as the active pharmaceutical ingredient.
Inactive excipients include microcrystalline cellulose, magnesium stearate, and pharmaceutical-grade binders to ensure tablet hardness, stability, and consistent dissolution characteristics.
All raw materials undergo identity and purity validation prior to compression and coating.
Ingest tablets with food to minimize gastrointestinal irritation. Splitting the daily total into morning and evening administrations maintains stable plasma levels.
Store the container in a cool, dry environment away from direct light and moisture. Keep the desiccant pouch intact to preserve tablet integrity.
Beginners should initiate at 50 mg daily, administered as a single tablet. This allows for assessment of individual tolerance and estrogenic response.
Intermediate users may escalate to 100 mg daily, divided into two 50 mg doses. Do not exceed this threshold, as adverse effects escalate disproportionately beyond this point.
Limit continuous administration to 4–6 weeks maximum. The hepatotoxic burden accumulates rapidly, and extended exposure significantly increases hepatic risk.
Estrogenic manifestations are prominent. Users frequently experience significant water retention, peripheral edema, elevated blood pressure, and gynecomastia. Proactive aromatase inhibitor use is essential from day one.
Hepatotoxicity is severe due to C17-alpha alkylation. Liver enzyme elevations are common even at moderate doses. Hepatoprotective agents such as TUDCA and N-acetylcysteine are mandatory.
Androgenic sequelae include acne vulgaris, accelerated scalp hair thinning in predisposed individuals, and increased sebum production.
The compound exerts a profound suppressive effect on the hypothalamic-pituitary-gonadal axis. Endogenous testosterone production declines rapidly, making structured Post-Cycle Therapy absolutely critical.
Cardiovascular strain is significant. Oxymetholone typically suppresses HDL cholesterol while elevating LDL. Regular lipid panels and heart-healthy dietary practices are required.
Other reported effects include headaches, appetite fluctuations, and general lethargy in some individuals.
This product is intended exclusively for research purposes and use by qualified male adults. It is not suitable for minors, women, or individuals with hepatic, cardiovascular, or renal conditions.
Aromatase inhibitor therapy must begin concurrently with the first dose. Blood pressure monitoring should occur at regular intervals throughout the cycle.
Comprehensive liver support supplementation is non-negotiable. Avoid alcohol, acetaminophen, and all other hepatotoxic substances during the active phase.
A structured PCT protocol using Clomiphene or Tamoxifen must follow cycle cessation. This restores natural testosterone synthesis and preserves accrued tissue.
Maintain a diet low in saturated fats and rich in omega-3 fatty acids. Regular cardiovascular exercise supports lipid management and vascular health.
Discontinue immediately and seek medical evaluation if jaundice, severe abdominal pain, dark urine, or persistent nausea develop.
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Most users notice dramatic strength increases within the first 7–10 days. Scale weight typically climbs rapidly by week 2–3, with 10–20 pounds commonly reported over a 4–6 week cycle.
No. This compound severely suppresses endogenous testosterone production. A foundational testosterone base is mandatory to maintain physiological androgen levels and prevent hypogonadal symptoms.
While Oxymetholone does not directly convert via the aromatase enzyme, it exhibits strong estrogenic activity through other mechanisms. Gynecomastia and water retention are common without estrogen management.
A significant portion of initial weight is intracellular fluid and glycogen. However, the profound strength gains facilitate real contractile tissue growth that can be retained with proper nutrition, training, and PCT.
No. The high androgenic and estrogenic activity causes rapid, irreversible virilization in female users. This compound is strictly contraindicated for women.