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Quinapril

ACE Inhibitor · Antihypertensive, Heart Failure Management

Also known as Quinapril hydrochloride

ACE InhibitorAntihypertensive, Heart Failure Management
CDSCO approvedSchedule H
EXCRETION
not curated
INTERACTIONS
12 major
incl. contraindicated
PREGNANCY
not curated
Top interactionssee all 12
  • Sacubitril ValsartanContraindicatedTextbookG&G 14e · p602
  • AminoglycosidesSevereTextbookG&G 14e
  • Angiotensin Receptor BlockersSevereTextbookHarrison 22e · p2396
  • AzilsartanSevereTextbookG&G 14e

Mechanism

Quinapril is an angiotensin-converting enzyme (ACE) inhibitor.

Indications

Essential hypertensionEssential hypertension if used in addition to diureticHeart failure (adjunct) (under close medical supervision)hypertensioncardiovascular diseaseheart failurediabetic nephropathyacute myocardial infarctionhigh risk of cardiovascular eventscoronary artery disease (without heart failure)Congestive heart failure (CHF)Myocardial infarction (MI)Prophylaxis in high cardiovascular risk subjectsNondiabetic nephropathyScleroderma crisis

Dosing

Adult
Essential hypertension: Initially 10 mg once daily; maintenance 20–40 mg daily in up to 2 divided doses. Essential hypertension if used in addition to diuretic: Initially 2.5 mg once daily; maintenance 20–40 mg daily in up to 2 divided doses.…
Renal adjustment
Max. initial dose 2.5 mg once daily if eGFR less than 40 mL/minute/1.73 m2.
Hepatic adjustment
Quinapril is a prodrug. Manufacturer advises caution when used in combination with a diuretic.
Geriatric
Essential hypertension: Initially 2.5 mg once daily; maintenance 20–40 mg daily in up to 2 divided doses.
Max dose
80 mg per day (for hypertension); 40 mg per day (for heart failure)

Pharmacokinetics

Peak effect
quinaprilat in plasma are achieved in about 2 h
Half-life
initial t1/2 of quinaprilat is about 2 h; a prolonged terminal t1/2 (~25 h)
Bioavailability
rate, but not extent, of oral absorption (60%) may be reduced by food
Protein binding
Q/QT: 97%
Excretion
Quinaprilat and other metabolites of quinapril are excreted in the urine (61%) and feces (37%)

Contraindications

  • Avoid in the first few weeks after delivery, particularly in preterm infants, due to the risk of profound neonatal hypotension.

Side effects

Common
Back painIncreased risk of infectionInsomniacoughhypotensionhyperkalemiaskin rashcough (5%-10%)
Serious
  • Depression
  • Generalised oedema
  • Proteinuria
  • Transient ischaemic attack
  • Balance impaired
  • Glossitis
  • Arthritis
  • Hypersensitivity
  • Jaundice cholestatic
  • Leucocytosis
  • Pulmonary oedema
  • Serositis
  • Toxic epidermal necrolysis
  • Vasculitis necrotising
  • angioedema
  • acute renal failure
  • fetopathic syndrome
  • neutropenia
  • glycosuria
  • anemia
  • hepatotoxicity
  • dysgeusia
  • hepatic failure (rare)
  • agranulocytosis (rare)

Pregnancy & lactation

Lactation

Avoid in the first few weeks after delivery, particularly in preterm infants, due to the risk of profound neonatal hypotension; if essential, may be used in mothers breast-feeding older infants—the infant’s blood pressure should be monitored.

Drug interactions

Sacubitril Valsartan
Contraindicated
Textbook

Increased risk of angioedema.

Do not use in conjunction with ACEIs.

Source: G&G 14e · p602

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

Sacubitril With Valsartan
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

Telmisartan + 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

Related guidelines

Other ACE Inhibitor drugs

Ask House about Quinapril

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

Sources: KD Tripathi 7e, Goodman & Gilman 14e, Katzung, BNF·Verified: 2026-05-13 · House clinical team