Canada-Approved Medicine
This monograph describes a medication approved for use in Canada by the Therapeutic Products Directorate, a division of Health Canadas Health Products and Food Branch. The medication is not approved by the United States Food and Drug Administration; however, a similar formulation carrying a different generic or brand name might be available in the US.
REMSContraindicated in:
Use Cautiously in:
CNS: fatigue, weakness, depression, MENINGIOMAS.
Resp: cough, dyspnea, pulmonary microembolism.
CV: edema, heart failure, hypotension, myocardial infarction, syncope, tachycardia, THROMBOEMBOLISM, vasovagal reactions.
GI: anorexia, constipation, diarrhea, HEPATOTOXICITY, LIVER TUMORS, nausea, vomiting.
Derm: ↑ sweating, dry skin, hot flashes, patchy hair loss.
Endo: adrenal suppression, antiandrogen withdrawal syndrome, gynecomastia.
F and E: hypercalcemia.
GU: impotence, infertility.
Hemat: anemia, thrombocytopenia.
Metab: glucose intolerance, hyperlipidemia.
MS: osteoporosis (long term use).
Misc: allergic reactions.
Drug-Drug:
Drug-Natural Products:
Absorption: Completely absorbed following oral administration. Absorption after IM depot injection is delayed and prolonged.
Distribution: Unknown.
Metabolism/Excretion: Metabolized by the CYP3A enzyme system; excreted in feces (60%) and urine (33%), as unchanged drug and metabolites.
Half-life: PO: 38 hr; IM: 4 days.