Absorption: Well absorbed following oral administration; rapidly converted to active metabolite, cilazaprilat (57% bioavailability for cilazaprilat).
Distribution: Unknown.
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 (HF) | 12 hr | 24 hr | 24 hr |
Contraindicated in:
Use Cautiously in:
Exercise Extreme Caution in:
CV: hypotension, chest pain, edema, tachycardia
Derm: flushing, pruritus, rash
F and E: hyperkalemia
GI: abdominal pain, anorexia, constipation, diarrhea, nausea, vomiting
GU: erectile dysfunction, proteinuria, renal impairment
Hemat: AGRANULOCYTOSIS
MS: back pain, myalgia
Neuro: dysgeusia, dizziness, drowsiness, fatigue, headache, insomnia, vertigo, weakness
Misc: ANGIOEDEMA, fever
Drug-drug:
Hypertension
Renal Impairment
Hepatic Impairment
Renal Impairment
Lab Test Considerations: