BOXED WARNING Fetal toxicity — discontinue as soon as pregnancy is detected; RAS-acting drugs can cause fetal injury and death.
FDA dosing
Population
Start
Target
Max
Hypertension (not adequately controlled on monotherapy)
Adults
2.5/10 mg QD
10/40 mg QD
Titration Antihypertensive effect largely attained within 2 weeks before up-titration
Renal Severe renal impairment: recommended benazepril dose is 5 mg (not available in this combination) — combination not appropriate.
Hepatic Amlodipine exposure increased in hepatic insufficiency; consider lower doses.
Instructions
Once daily; use only after failure of/edema on monotherapy or may substitute for titrated components
Available strengths
cap 2.5/10, 5/10, 5/20, 5/40, 10/20, 10/40 mg
Contraindications
Do not coadminister with aliskiren in patients with diabetes
History of angioedema (with or without prior ACE inhibitor use)
Combination with a neprilysin inhibitor (e.g., sacubitril); do not administer within 36 h of switching to/from sacubitril/valsartan
Cautions
Angioedema
Fetal toxicity
Hypotension
Hyperkalemia
Renal impairment / RAS dual blockade
Hepatic-related amlodipine accumulation
Adverse reactions
Cough
Peripheral edema
Dizziness
Headache
Pregnancy Can cause fetal harm; RAS inhibitors reduce fetal renal function and increase fetal/neonatal morbidity and death. Discontinue when pregnancy detected.
Lactation Minimal benazepril/benazeprilat excreted into breast milk.