Absorption: Well absorbed following oral administration, rapidly converted to active metabolite, cilazaprilat (57% bioavailability for cilazaprilat).
Distribution: Enters breast milk.
Half-Life: Early elimination phase: 0.9 hr; terminal elimination phase (enzyme-bound cilazaprilat): 3649 hr.
(effects on hemodynamics)
ROUTE | ONSET | PEAK | DURATION |
---|---|---|---|
PO (hypertension) | within 1 hr | 37 hr | 1224 hr |
PO (heart failure) | 12 hr | 24 hr | 24 hr |
Contraindicated in:
Use Cautiously in:
CV: hypotension, chest pain, edema, tachycardia
Endo: hyperuricemia
GI: taste disturbances, abdominal pain, anorexia, constipation, diarrhea, nausea, vomiting
GU: erectile dysfunction, proteinuria, renal dysfunction, renal failure
Derm: flushing, pruritis, rashes
F and E: hyperkalemia
Hemat: AGRANULOCYTOSIS
MS: back pain, muscle cramps, myalgia
Misc: ANGIOEDEMA, fever
Drug-drug:
Hypertension
Heart Failure
Renal Impairment
Hepatic Impairment
Renal Impairment
Lab Test Considerations: