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Pronunciation

sye-LAY-za-pril

Classifications

Therapeutic Classification: antihypertensives

Pharmacologic Classification: ace inhibitors

Indications

REMS


Action

  • ACE inhibitors block the conversion of angiotensin I to the vasoconstrictor angiotensin II. ACE inhibitors also prevent the degradation of bradykinin and other vasodilatory prostaglandins. ACE inhibitors also plasma renin concentrations and aldosterone concentrations. Net result is systemic vasodilation.
Therapeutic effects:
  • Lowering of BP in hypertensive patients.
  • Improved symptoms in patients with HF.

Pharmacokinetics

Absorption: Well absorbed following oral administration; rapidly converted to active metabolite, cilazaprilat (57% bioavailability for cilazaprilat).

Distribution: Unknown.

Metabolism/Excretion: Cilazaprilat is eliminated unchanged by the kidneys (91%).

Half-Life: Early elimination phase: 0.9 hr; terminal elimination phase (enzyme-bound cilazaprilat): 36–49 hr.

Time/Action Profile

(effects on hemodynamics)

ROUTEONSETPEAKDURATION
PO (hypertension)within 1 hr3–7 hr12–24 hr
PO (HF)1–2 hr2–4 hr24 hr

Contraind./Precautions

Contraindicated in:

Use Cautiously in:

Exercise Extreme Caution in:

Adv. Reactions/Side Effects

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

Metab: hyperuricemia

MS: back pain, myalgia

Neuro: dysgeusia, dizziness, drowsiness, fatigue, headache, insomnia, vertigo, weakness

Resp: cough, dyspnea

Misc: ANGIOEDEMA, fever

Interactions

Drug-drug:

Route/Dosage

Hypertension

Renal Impairment

Hepatic Impairment

Heart Failure

Renal Impairment

Availability

Assessment

Lab Test Considerations:

Implementation

Patient/Family Teaching

Evaluation/Desired Outcomes

Canadian Brand Names

Inhibace