ID: oxymetholone
Aliases: Anadrol, Anadrol-50
Type: compound
Route/form: oral
Status: approved_or_legacy_prescription
Evidence level: approved / labelled
Best data tier: approved label + human controlled/review
Support scope: human, review/regulatory
Source types: human_rct, human_trial, label, review, safety_review
Linked sources: 7
Broad outcomes: Fat loss / metabolic health, Gut / immune / inflammation, Hormones / fertility / sexual health, Muscle growth / performance / recovery, PEDs / AAS / thermogenics, Safety / regulatory
Reading note: These are curation notes anchored to linked sources, not a clinical recommendation or protocol.
Targets / mechanism
- androgen receptor agonist
- 17-alpha-alkylated oral AAS
- erythropoietic/anabolic effects
Optimization domains
- steroid
- muscle
- body composition
- anemia
- weight gain
- doping
- liver
Research basis
- Official label and human wasting/anemia literature anchor oxymetholone as a potent oral anabolic steroid in serious medical contexts.
- Phase III HIV-wasting and hemodialysis RCT data provide human anabolic/metabolic anchors beyond anecdotal mass-gain claims.
- It is a useful high-risk comparator for oral AAS discussions because efficacy and toxicity are both clinically visible.
Limits, risks, and missing evidence
- Hepatic peliosis/tumor warnings, cholestatic injury, lipid disruption, blood-pressure effects, estrogenic/progestogenic-like side effects, and endocrine suppression make risk high.
- Medical anemia/wasting/hemodialysis contexts do not justify nonmedical mass-gain extrapolation.
- As with other oral 17-alpha-alkylated AAS, stacking and long duration sharply worsen the risk interpretation.
Risk flags
- prescription only
- oral 17aa aas
- severe hepatic warning
- lipid risk
- endocrine suppression
- cardiovascular risk
Linked papers, labels, and reviews
- FDA label: Anadrol-50 oxymetholone tablets
label / fda_oxymetholone_label
Official oxymetholone label for anemia context, oral route, and serious hepatic warnings. - Oxymetholone therapy in HIV-wasting syndrome
human_trial / pubmed_oxymetholone_hiv_wasting_1996
Human HIV-wasting clinical source for oral oxymetholone anabolic effects; toxicity limits generalization. - Anabolic androgenic steroid-induced liver injury: an update
safety_review / pubmed_aas_liver_effects_2018
Class hepatic-risk review, especially relevant for 17-alpha-alkylated oral AAS such as oxymetholone, methandienone, stanozolol, and oxandrolone. - Anabolic-androgenic steroids: How do they work and what are the risks?
review / pubmed_aas_risks_2023
General AAS mechanism and risk review; used as class-level caution for nonmedical androgen/anabolic steroid entries. - Oxymetholone ameliorates insulin sensitivity in maintenance hemodialysis patients: a randomized controlled trial
human_rct / pubmed_oxymetholone_hemodialysis_insulin_2009
Hemodialysis RCT source; demonstrates systemic metabolic/anabolic relevance but in high-medical-risk disease context. - Double-blind, randomized, placebo-controlled phase III trial of oxymetholone for the treatment of HIV wasting
human_rct / pubmed_oxymetholone_hiv_wasting_phase3_2003
Phase III HIV-wasting RCT source for oxymetholone; serious indication and toxicity context, not casual mass-gain evidence. - Anabolic-androgenic steroids among recreational athletes and cardiovascular risk
safety_review / pubmed_aas_recreational_athletes_cv_review_2025
Recent cardiovascular-risk review focused on recreational athlete AAS use; class-level safety source for nonmedical androgen entries.