Danazol
- Atc Codes:G03XA01
- CAS Codes:17230-88-5
- PHARMGKB ID:17230-88-5
Table of contents
- Brand Names
- Chemistry
- Pharmacologic Category
- Mechanism of Action
- Therapeutic Use
- Pregnancy and Lactation Implications
- Contraindications
- Warnings and Precautions
- Adverse Reactions
- Genes that may be involved
- Substrate of
- Inhibits
- Drug Interactions
- Nutrition/Nutraceutical Interactions
- Dosage
- Pharmacokinetics and Pharmacodynamics
- Special Considerations
Brand Names
Europe
Austria: Danokrin; Belgium: Danatrol; Cyprus: Anargil; Czech Republic: Danoval; France: Danatrol; Greece: Danatrol; Hungary: Danoval; Italy: Danatrol; Luxembourg: Danatrol; Malta: Danol; Netherlands: Danatrol; Poland: Danazol, Danol, Danoval; Portugal: Danatrol; Slovakia: Anargil; Slovenia: Danoval; Spain: Danatrol; UK: Danol.
North America
Canada: Cyclomen; USA: Danazol.
Latin America
Argentina: Ladogal; Brazil: Ladogal; Mexico: Danalem, Ladogal, Novaprin.
Asia
Japan: Dainazol, Danan, Esdelart, Hosebon, Oyslon.
Drug combinations
Chemistry
Danazol: C~22~H~27~NO~2~. Mw: 337.46. (1) Pregna-2,4-dien-20-yno[2,3-d]isoxazol-17-ol, (17α)-; (2) 17α-Pregna-2,4-dien-20-yno[2,3-d]isoxazol-17-ol. CAS-17230-88-5 (1968).
Pharmacologic Category
Androgens. (ATC-Code: G03XA01).
Mechanism of action
Synthetic steroid analog. Suppresses pituitary output of FSH and LH which causes regression and atrophy of normal and ectopic endometrial tissue. Decreases rate of growth of abnormal breast tissue. Reduces attacks associated with hereditary angioedema by increasing levels of C4 component of complement.
Therapeutic use
Palliative treatment of endometriosis (e.g. pain relief, reduction in endometrial lesions), or fibrocystic breast disease (e.g. decreasing pain, tenderness, and nodularity). Prophylaxis in hereditary angioedema in males and females.
Pregnancy and lactiation implications
May cause androgenic effects to the female fetus. Use is contraindicated during pregnancy or breast-feeding.
Unlabeled use
Contraindications
Hypersensitivity to danazol or any component of the formulation. Undiagnosed genital bleeding. Pregnancy, breast-feeding. Porphyria. Markedly impaired hepatic, renal, or cardiac function.
Warnings and precautions
May cause nonreversible androgenic effects (e.g. weight gain, acne, seborrhea, hirsutism, edema, hair loss, voice change), benign intracranial hypertension (pseudotumor cerebri), peliosis hepatis and benign hepatic adenoma with prolonged treatment (may not be apparent until complicated by acute, potentially life-threatening intra-abdominal hemorrhage), or thromboembolic events (e.g. sagittal sinus thrombosis, stroke reported). May increase risk of atherosclerosis and coronary artery disease due to blood lipid changes (decreased HDL and increased LDL). Caution in diabetes mellitus, edematous conditions (e.g. cardiovascular disease, migraine, seizure disorder, renal impairment), hepatic impairment (use not recommended in severe hepatic impairment), renal impairment (use not recommended in severe renal impairment), or history of porphyria. Breast cancer should be ruled out prior to treatment for fibrocystic disease. May cause fluid retention.