Dianabol
Methandrostenolone / dbol · Anabolic-androgenic steroid (oral)
What it is
The original bodybuilding steroid — the oral that built the golden era and still the most common first (and most casually taken) AAS because it is cheap, oral, and fast. Rapid size and strength, much of it water.
What human evidence shows
Old, sparse clinical record; effectiveness for rapid mass is not in dispute and never was. What the decades established instead is the cost structure: heavy aromatization, liver strain, and blood-pressure elevation arriving within weeks.
Risks
17-alpha-alkylated liver load, aggressive aromatization (gyno and water/BP spikes that hit fast), lipid damage, full suppression. Its danger is sociological as much as pharmacological: it is the steroid people take WITHOUT a plan, because a bottle of pills feels casual in a way a vial does not.
Stacking interactions
Documented interactions with other things people research. A compound not listed here does not mean the combination is safe — only that no specific interaction is on file.
Each of these oral steroids has independently been associated with liver injury. Pair-specific safety data are lacking, and concurrent exposure may increase hepatic risk.
Each of these oral steroids has independently been associated with liver injury. Pair-specific safety data are lacking, and concurrent exposure may increase hepatic risk.
Each of these oral steroids has independently been associated with liver injury. Pair-specific safety data are lacking, and concurrent exposure may increase hepatic risk.
Each of these oral steroids has independently been associated with liver injury. Pair-specific safety data are lacking, and concurrent exposure may increase hepatic risk.
Each of these oral steroids has independently been associated with liver injury. Pair-specific safety data are lacking, and concurrent exposure may increase hepatic risk.
Each of these oral steroids has independently been associated with liver injury. Pair-specific safety data are lacking, and concurrent exposure may increase hepatic risk.
Each of these oral steroids has independently been associated with liver injury. Pair-specific safety data are lacking, and concurrent exposure may increase hepatic risk.
Legal status
US: Schedule III, no legitimate US pharmaceutical production — all underground.
Evidence base
established literature
Real human evidence: randomised trial reports, or review-level evidence backed by at least one human trial report.
- phase 3/4
- 0
- randomised
- 5
- reviews
- 0
- human trials
- 39
Counts are of published papers, not distinct trials, and measure how much research exists — not whether this works or is safe for you.
Research (12)
- [METHANDROSTENOLONE]Med Prom SSSR · 1964
- Methandrostenolone metabolism in humans: potential problems associated with isolation and identification of metabolitesJ Steroid Biochem · 1990
- METHANDROSTENOLONE, AN ORAL ANABOLIC AGENTSouth Med J · 1964
- [Thymolytic effects of methandrostenolone]Biull Eksp Biol Med · 1990
- Methandrostenolone in rheumatic diseases and osteoporosisGeriatrics · 1962
- DermatomyositisIndian J Pediatr · 1973
- Determination of methandrostenolone and its metabolites in equine plasma and urine by coupled-column liquid chromatography with ultraviolet detection and confirmation by tandem mass spectrometryJ Chromatogr · 1989
- HORMONE-SULPHATASE RELATIONSHIPSActa Endocrinol (Copenh) · 1965
- Methandrostenolone therapy in children with growth retardationJAMA · 1963
- [Methandrostenolone in constitutional thinness and malnutrition]Sem Med · 1961
- Neurotoxic properties of the anabolic androgenic steroids nandrolone and methandrostenolone in primary neuronal culturesJ Neurosci Res · 2011
- Quantitative fluorometric determination of methandrostenoloneJ Pharm Sci · 1962
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