Classes
DEA Class; Rx
Common Brand Names; Accupril
- ACE Inhibitors
Description
Oral ACE inhibitor; prodrug metabolized to active quinaprilat; used 1-2 times daily for HTN; given twice daily for CHF.
Indications
Indicated for the treatment of hypertension
Contraindications
Hypersensitivity
History of hereditary or angioedema associated with previous ACE inhibitor treatment
Coadministration of neprilysin inhibitors (eg, sacubitril) with ACE inhibitors may increase angioedema risk; do not administer ACE inhibitors within 36 hr of switching to or from sacubitril/valsartan
Do not coadminister with aliskiren in patients with diabetes mellitus
Adverse Effects
- Dizziness (7.7%)
- Coughing (4.3%)
- Fatigue (2.6%)
- Nausea and/or vomiting (2.4%)
- Hypotension (2.9%)
- Dyspnea (1.9%)
- Diarrhea (1.7%)
- Headache (1.7%)
- Myalgia (1.5%)
- Rash (1.4%)
- Back pain (1.2%)
- Angioedema
- General: Back pain, malaise, viral infections, anaphylactoid reaction
- Cardiovascular: Palpitation, vasodilation, tachycardia, heart failure, hyperkalemia, myocardial infarction, cerebrovascular accident, hypertensive crisis, angina pectoris, orthostatic hypotension, cardiac rhythm disturbances, cardiogenic shock
- Hematology: Hemolytic anemia
- Gastrointestinal: Flatulence, dry mouth or throat, constipation, gastrointestinal hemorrhage, pancreatitis, abnormal liver function tests, dyspepsia
- Metabolism and nutrition disorders: Hyponatremia
- Nervous/psychiatric: Somnolence, vertigo, syncope, nervousness, depression, insomnia, paresthesia
- Integumentary: Alopecia, increased sweating, pemphigus, pruritus, exfoliative dermatitis, photosensitivity reaction, dermatopolymyositis
- Urogenital: Urinary tract infection, impotence, acute renal failure, worsening renal failure
- Respiratory: Eosinophilic pneumonitis
- Other: Amblyopia, edema, arthralgia, pharyngitis, agranulocytosis, hepatitis, thrombocytopenia
Warnings
Discontinue STAT if pregnant (see Contraindications and Black Box Warnings)
Less effective in blacks
ACE inhibitors associated with a syndrome that starts with cholestatic jaundice and progresses to fulminant hepatic necrosis and (sometimes) death; mechanism of this syndrome is not understood; patients receiving ACE inhibitors who develop jaundice or marked elevations of hepatic enzymes should discontinue ACE inhibitor and receive appropriate medical follow-up
Use caution in severe aortic stenosis
Hyperkalemia may occur; risk factors may include renal insufficiency, diabetes mellitus, and concomitant use of other drugs that raise serum potassium levels; monitor serum potassium in such patients
Dual blockade of the renin-angiotensin system with ARBs, ACE inhibitors, or aliskiren associated with increased risk for hypotension, hyperkalemia, and renal function changes (including acute renal failure) compared to monotherapy
Anaphylactoid reactions reported in patients dialyzed with high-flux membranes and treated concomitantly with an ACE inhibitor; anaphylactoid reactions also reported in patients undergoing low-density lipoprotein apheresis with dextran sulfate absorption
Decreased absorption (25-30%) with high-fat meal
ACE inhibition also causes increased bradykinin levels which putatively mediates angioedema
Angioedema of the face, extremities, lips, tongue, glottis, and larynx reported in patients treated with angiotensin-converting enzyme inhibitors; in instances where swelling is confined to face and lips, condition generally resolves without treatment; antihistamines may be useful in relieving symptoms; when there is involvement of tongue, glottis, or larynx, likely to cause airway obstruction, administer emergency therapy including, but not limited to, subcutaneous epinephrine solution 1:1000 (0.3 to 0.5 mL)
Patients receiving coadministration of ACE inhibitor and mTOR (mammalian target of rapamycin) inhibitor (e.g. temsirolimus, sirolimus, everolimus) therapy or a neprilysin inhibitor may be at increased risk for angioedema
Intestinal angioedema has been reported in patients treated with ACE inhibitors
Presumably due to inhibition of degradation of endogenous bradykinin, persistent non-productive cough reported with all ACE inhibitors, always resolving after discontinuation of therapy; ACE inhibitor-induced cough should be considered in differential diagnosis of cough
Pregnancy and Lactation
Pregnancy Category: C (1st trimester); D (2nd & 3rd trimester)
Discontinue as soon as pregnancy detected; during the second and third trimesters of pregnancy, drugs that act directly on the renin-angiotensin have been associated with fetal injury that includes hypotension, neonatal skull hypoplasia, anuria, reversible or irreversible renal failure, and death
Lactation: excreted in breast milk; use caution
Maximum Dosage
80 mg/day PO for hypertension; 40 mg/day PO for heart failure.
80 mg/day PO for hypertension; 40 mg/day PO for heart failure.
Safety and efficacy have not been established.
Safety and efficacy have not been established.
How supplied
tablet
- 5mg
- 10mg
- 20mg
- 40mg