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Benazepril

Angiotensin-converting enzyme (ACE) inhibitor (prodrug) · Antihypertensive

START
10 mg PO once daily (5 mg if elderly/on diuretic/renal)
TYPICAL MAX
80 mg/day
STOP IF
Angioedema, severe hyperkalaemia, or rising creatinine >30%
WATCH
K, creatinine baseline + 1–2 weeks after start/dose change, BP
CDSCO approvedATC C09AA07
Dose laddermg/d
5low start20usual80max/day
Renal dose adjustmenteGFR mL/min/1.73m²
FULLUsual dosing30REDUCEStart 5 mg/day; titrate cautiously90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
1hONSET1.5hPEAK10h1dDURATION
ONSET
1h · BP effect
PEAK
1.5h · Tmax
10h ·
DURATION
1d · once-daily
EXCRETION
Mainly renal — active metabolite
route + CYP
INTERACTIONS
12 major
incl. contraindicated
PREGNANCY
Contraindicated (fetotoxicity in 2nd/3rd trimesters).
FDA category + note
Top interactionssee all 12
  • Sacubitril ValsartanContraindicatedTextbookG&G 14e · p602
  • AliskirenContraindicatedDatabaseKimi deep-research + Cla
  • AlteplaseSevereTextbookG&G 14e · p600
  • AminoglycosidesSevereTextbookG&G 14e

Mechanism

Prodrug rapidly hydrolysed to benazeprilat, which competitively inhibits ACE, blocking conversion of angiotensin I to angiotensin II — reducing vasoconstriction and aldosterone secretion.

Indications

HypertensionHeart failure (adjunct)Diabetic nephropathy / proteinuric CKD

Dosing

Adult
Start 10 mg PO once daily (5 mg with diuretic or in elderly); usual 20–40 mg/day in 1–2 divided doses; max 80 mg/day.
Pediatric
≥6 y: 0.2 mg/kg once daily (max 0.6 mg/kg/day or 40 mg).
Renal adjustment
CrCl <30: start 5 mg/day; titrate cautiously.
Hepatic adjustment
Mild–moderate impairment: no adjustment; severe: caution.
Geriatric
Start 5 mg; titrate slowly.
Max dose
80 mg/day

Pharmacokinetics

Onset
BP effect 1 h; full antihypertensive effect 1–2 weeks
Peak effect
~1–2 h (Tmax of benazeprilat)
Duration
~24 h
Half-life
Benazeprilat ~10–11 h
Bioavailability
~37% (oral; food does not significantly affect)
Protein binding
~97%
Metabolism
Hepatic hydrolysis to active benazeprilat
Excretion
Mainly renal (active metabolite)

Contraindications

  • History of ACE-inhibitor angioedema
  • Bilateral renal artery stenosis
  • Concomitant aliskiren in diabetes
  • Pregnancy (second/third trimester fetotoxicity)
  • Hereditary/idiopathic angioedema
  • Hypersensitivity

Side effects

Common
Dry coughDizzinessHyperkalaemiaHeadacheFatigueFirst-dose hypotension
Serious
  • Angioedema (laryngeal — fatal)
  • Acute kidney injury (volume depletion, RAS)
  • Hyperkalaemia
  • Cholestatic jaundice (rare)
  • Neutropenia (rare)

Pregnancy & lactation

Pregnancy

Contraindicated (fetotoxicity in 2nd/3rd trimesters).

Lactation

Excreted in milk; usually compatible (low transfer) but alternative preferred.

Drug interactions

Sacubitril Valsartan
Contraindicated
Textbook

Increased risk of angioedema.

Do not use in conjunction with ACEIs.

Source: G&G 14e · p602

Aliskiren
Contraindicated
Database

Dual RAAS blockade

Avoid combination

Source: Kimi deep-research + Cla

Alteplase
Severe
Textbook

Increased risk of angioedema.

Avoid combination.

Source: G&G 14e · p600

Aminoglycosides
Severe
Textbook

Increased risk and severity of renal impairment and nephrotoxicity.

Not explicitly stated, but implies careful monitoring of renal function and cautious co-administration.

Source: G&G 14e

Angiotensin Receptor Blockers
Severe
Textbook

Greater incidence of acute kidney injury (AKI) and adverse cardiac events.

The combination of these two classes should be avoided.

Source: Harrison 22e · p2396

Azilsartan
Severe
Textbook

Increased worsening of renal function, hypotension, syncope, and hyperkalemia without increased efficacy.

Not recommended for the treatment of hypertension. Previous studies indicate more harm than benefit.

Source: G&G 14e

Candesartan
Severe
Textbook

Increased worsening of renal function, hypotension, syncope, and hyperkalemia without increased efficacy.

Not recommended for the treatment of hypertension. Previous studies indicate more harm than benefit.

Source: G&G 14e

Dipeptidyl Peptidase Iv Inhibitor
Severe
Textbook

Increased risk of angioedema.

Avoid combination.

Source: G&G 14e · p600

Losartan + Hydrochlorothiazide
Severe
Textbook

Increased worsening of renal function, hypotension, syncope, and hyperkalemia without increased efficacy.

Not recommended for the treatment of hypertension. Previous studies indicate more harm than benefit.

Source: G&G 14e

Olmesartan + Amlodipine
Severe
Textbook

Increased worsening of renal function, hypotension, syncope, and hyperkalemia without increased efficacy.

Not recommended for the treatment of hypertension. Previous studies indicate more harm than benefit.

Source: G&G 14e

Olmesartan + Hydrochlorothiazide
Severe
Textbook

Increased worsening of renal function, hypotension, syncope, and hyperkalemia without increased efficacy.

Not recommended for the treatment of hypertension. Previous studies indicate more harm than benefit.

Source: G&G 14e

Olmesartan Medoxomil
Severe
Textbook

Increased worsening of renal function, hypotension, syncope, and hyperkalemia without increased efficacy.

Not recommended for the treatment of hypertension. Previous studies indicate more harm than benefit.

Source: G&G 14e

Related guidelines

Other Angiotensin-converting enzyme (ACE) inhibitor (prodrug) drugs

Ask House about Benazepril

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: KD Tripathi 7e, Goodman & Gilman 14e, Harrison 22e, Katzung·Verified: 2026-05-20 · House clinical team·Cockpit curated: 2026-05-20