COMPOUNDS / STEROID / SUPERDROL
STEROID

SUPERDROL

HIGH RISK
BEST FOR:Muscle Mass●●●●●●●●○○8/10
SUPERDROL · METHASTERONE · METHASTERON · 17Β-HYDROXY-2Α,17Α-DIMETHYL-5Α-ANDROSTAN-3-ONE · METHYL-DHT · MDHT · SD
Anabolic SteroidDesigner SteroidOral 17-AlphaHepatotoxicPerformance EnhancerDHT Derivative

Potent oral designer anabolic steroid known for rapid strength and mass gains but significant hepatotoxicity.

ROUTE / DOSAGE
LOW10mg
STANDARD20-30mg
HIGH40mg+
Note: 17-alpha alkylated - highly hepatotoxic. Limit cycles to 3-4 weeks maximum. Liver support strongly advised.
CYCLE
3-4 weeks max due to hepatotoxicity no daily long-term use
BIOAVAILABILITY
~50% oral (17-alpha alkylated for oral survival)
ACTIVE DURATION
8-12h (subjective)
STORAGE
Room temperature dry away from light. Keep sealed and moisture-free.
DURATION BREAKDOWN
Total8-12h per dose; effects accumulate over 2-4 week cycle
Onset2-4h
Come up3-7 days for noticeable strength gains
Peak4-8h
Offset8-12h
After effects2-4 weeks testosterone suppression post-cycle
Duration varies by route, dose, and individual. Source: community reports.
§ 01 — EFFECTS
7 documented
Rapid strength increases
Significant lean muscle mass gain
Non-aromatizing - no water retention
Increased muscle hardness and density
Elevated blood pressure
Lethargy at higher doses
Severe lipid profile disruption
§ 02 — RISKS
Severe hepatotoxicity including cholestatic hepatitis and liver failure
Acute renal failure requiring hospitalization
IgA nephropathy
Severe dyslipidemia (crashed HDL, elevated LDL)
Hypertension and cardiovascular strain
Complete hypothalamic-pituitary-gonadal axis suppression
§ 03 — INTERACTIONS
Interaction data not yet available for this compound.
§ 04 — SCIENCE

Methasterone was marketed as an over-the-counter supplement before being identified as a potent anabolic steroid and subsequently scheduled. Case reports document severe cholestatic hepatitis, renal failure, and IgA nephropathy associated with its use. Metabolism studies in humanized mouse models and in vitro liver S9 fractions have identified multiple hydroxylated and 3-keto reduced metabolites, as well as phase II sulfation products, aiding anti-doping detection. No controlled human clinical trials exist; evidence of efficacy is limited to anecdotal reports and animal data. The hepatotoxicity profile is among the most severe of oral steroids, with multiple published cases of acute liver injury requiring hospitalization.

§ 06 — SOURCES
[1]
Severe cholestasis and renal failure associated with the use of the designer steroid Superdrol (methasteron)
pubmed.ncbi.nlm.nih.gov ↗
[2]
Cholestatic jaundice and IgA nephropathy induced by OTC muscle building agent superdrol
pubmed.ncbi.nlm.nih.gov ↗
[3]
Metabolic studies with promagnon, methylclostebol and methasterone in the uPA+/+-SCID chimeric mice
pubmed.ncbi.nlm.nih.gov ↗
[4]
Replacing PAPS: In vitro phase II sulfation of steroids with the liver S9 fraction employing ATP and sodium sulfate
pubmed.ncbi.nlm.nih.gov ↗
Disclaimer. Protokol.wiki is an informational reference. Nothing on this site is medical advice. Compounds listed may be unapproved, unregulated, or illegal in your jurisdiction. Consult a licensed physician before use. Data compiled from peer-reviewed literature.
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