Fabricator: Dragon Pharma, Europe
Unit: x1 100 tabs
Strength: 10 mg
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Dragon Pharma Anavar 10 delivers 10 mg of Oxandrolone per tablet. This dihydrotestosterone-derived oral anabolic is engineered for athletes pursuing quality hypertrophy without estrogenic complications.
The compound promotes dry, defined muscle accretion and measurable strength improvements. It is particularly valued during cutting and body recomposition phases where subcutaneous water retention must be minimized.
Oxandrolone is a synthetic DHT analogue with a C2-oxygen substitution and C17-alpha alkylation. This structural profile delivers high anabolic activity with minimal androgenic expression relative to pure testosterone.
The non-aromatizing nature eliminates concerns regarding gynecomastia, bloating, or estrogen-driven blood pressure elevation. Users achieve a tight, grainy aesthetic prized during pre-contest preparation and summer conditioning.
Anavar Dragon Pharma subjects every production batch to independent third-party laboratory analysis. This ensures precise 10 mg tablet dosing and confirms the absence of contaminants or manufacturing impurities.
Each tablet contains 10 mg of Anavar Dragon Pharma (Oxandrolone) as the active pharmaceutical ingredient.
Inactive excipients include microcrystalline cellulose, magnesium stearate, and pharmaceutical-grade binders to ensure tablet integrity and consistent dissolution.
All raw materials are validated for chemical identity and purity prior to compression and packaging.
Ingest tablets with water, preferably alongside a light meal containing dietary fats to support absorption of this lipophilic steroid hormone.
Divide the daily total into two administrations—morning and evening—to maintain stable plasma concentrations across the active half-life.
For optimal recomposition results, stack with a testosterone base such as Enanthate or Cypionate. This prevents hypogonadal symptoms and amplifies lean tissue development.
Store the container in a cool, dry environment between 15–25°C (59–77°F). Protect from moisture and direct light. Keep the desiccant pouch intact.
Male beginners should initiate at 30–40 mg daily, divided into three or four 10 mg doses. This assesses individual tolerance and hepatic response.
Intermediate users typically respond well to 50–60 mg daily, administered as 5–6 tablets spread across the day.
Advanced male athletes may approach 80–100 mg daily for brief periods. Beyond this threshold, hepatotoxic risk escalates disproportionately to additional benefit.
Women may utilize 10–20 mg daily with a relatively low virilization risk. Any signs of voice deepening or clitoral enlargement require immediate cessation.
Limit continuous administration to 6–8 weeks due to C17-alpha alkylation stress on hepatic tissue.
Hepatotoxicity is the primary safety concern. The C17-aa modification protects the molecule during first-pass metabolism but elevates liver enzymes. Regular hepatic function panels are mandatory.
Lipid profiles frequently deteriorate. HDL cholesterol typically suppresses while LDL rises, creating cardiovascular strain without dietary intervention and omega-3 supplementation.
Exogenous androgens suppress hypothalamic-pituitary-gonadal axis function. Endogenous testosterone production declines during the cycle, necessitating a structured recovery phase.
Androgenic manifestations such as mild acne or increased sebum production may emerge at higher dosages. These are generally manageable and dose-dependent.
This product is intended exclusively for research purposes and use by qualified adults under appropriate supervision. It is not suitable for minors, pregnant or nursing women, or individuals with pre-existing hepatic or cardiovascular conditions.
Hepatoprotective agents such as TUDCA and N-acetylcysteine should accompany every cycle. Avoid alcohol, acetaminophen, and all other hepatotoxic substances during the active phase.
A comprehensive Post-Cycle Therapy protocol using Clomiphene or Tamoxifen must commence within days of the final tablet. This restores natural testosterone synthesis and preserves accrued tissue.
Maintain a heart-healthy diet low in saturated fats and high 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 fatigue develop.
Most users notice increased muscle hardness and strength within the first 10–14 days.
Visible physique changes typically manifest by weeks 3–4 when paired with disciplined nutrition and progressive resistance training.
For men, yes. Oxandrolone suppresses natural testosterone production. A testosterone base prevents libido collapse, fatigue, and muscle loss while amplifying anabolic results.
Yes. The mild androgenic profile makes it one of the few oral anabolics suitable for female athletes at conservative doses of 10–20 mg daily.
Close monitoring for virilization signs is essential.
No. Oxandrolone does not aromatize into estradiol. Gynecomastia, bloating, and estrogen-mediated hypertension are not concerns with this compound.
Anavar produces drier, more sustainable lean gains with fewer joint complaints. Winstrol is more aggressive for vascularity and hardness but frequently causes synovial discomfort.
Anavar is generally better tolerated for longer cutting phases.
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September 4, 2026
I tried Dragon Pharma Anavar 10 while cutting and felt like it helped me hold onto my strength as I leaned out. I wouldn’t say it was some overnight transformation, but overall I was happy with how things went for me.