Contraindicated in:
Use Cautiously in:
CV: peripheral edema, hypertension, ISCHEMIC HEART DISEASE.
Derm: hot flush, dry skin, pruritus.
EENT: epistaxis.
GI: diarrhea.
GU: hematuria, urinary frequency.
MS: arthralgia, musculoskeletal pain, fracture, muscular stiffness, muscular weakness.
Neuro: headache, weakness, anxiety, dizziness, hallucinations, hypoesthesia, insomnia, paresthesia, POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME (PRES), SEIZURES, SPINAL CORD COMPRESSION/CAUDA EQUINA SYNDROME.
Misc: falls, HYPERSENSITIVITY REACTIONS (INCLUDING ANGIOEDEMA).
Drug-Drug:
Drug-Natural Products:
Therapeutic Classification: antineoplastics
Pharmacologic Classification: androgen receptor inhibitors
Absorption: Well absorbed following oral administration.
Distribution: Widely distributed to tissues.
Protein Binding: Enzalutamide: 9798%; N-desmethylenzalutamide: 95%.
Metabolism/Excretion: Extensively metabolized by the liver via the CYP2C8 and CYP3A4 isoenzymes; one metabolite (N-desmethylenzalutamide) has antineoplastic activity. Metabolites are primarily renally excreted, only minimal amounts as unchanged drug.
Half-life: Enzalutamide: 5.8 days; N-desmethylenzalutamide: 7.88.6 days.
NDC Code*