Oxandrolone
Anavar. Mild 17α-alkylated DHT derivative. Popular for cutting cycles with relatively low liver stress compared to other orals.
Overview
Anavar. Mild 17α-alkylated DHT derivative. Popular for cutting cycles with relatively low liver stress compared to other orals.
Significantly lowers SHBG, mild liver stress (17-alpha alkylated but less hepatotoxic than others), worsens lipids (especially HDL suppression), can elevate LDL
Compound Guide
Ester: None -- oral 17-alpha alkylated compound. No ester; absorbed directly via GI tract.
Dosage:
- Enhancement (male): 40-80 mg/day for 6-8 weeks
- Split dose 2x/day (morning + evening) due to short half-life
Administration:
- Oral only -- no injection required
- Take with meals to reduce GI upset
Key Notes:
- Mildest oral AAS -- lowest hepatotoxicity of the 17-alpha alkylated compounds
- Despite mild reputation, still significantly suppresses HDL and can raise LDL
- Dramatically lowers SHBG -- can increase free testosterone disproportionately
- Very short detection time (3 weeks) vs other AAS
- Popular as a "finisher" in the last 6-8 weeks of a cycle
- Does not aromatise -- no direct E2 increase
- Run with a testosterone base (still suppresses natural production)
- Liver support (NAC, TUDCA) recommended even though hepatotoxicity is mild
Female-specific dose-response data, virilisation markers and stop-thresholds: Bloodwork every woman on anavar should run.
Usage History
Pairs With
How Oxandrolone behaves when it is run alongside other compounds.
Commonly stacked with
Used to offset
Stacks the risk
Marker Interactions
Compare With
Frequently Asked Questions
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Quick Reference
Category
AAS
Half-Life
8-10 hours
Detection Time
3 weeks