Perindopril Erbumine
A to Z Drug Facts
Perindopril Erbumine |
(per-IN-doe prill ehr-BYOO-meen) |
Aceon |
Class: Antihypertensive/Angiotensin-converting enzyme (ACE) inhibitor |
Action Competitively inhibits angiotensin I-converting enzyme, resulting in prevention of angiotensin I conversion to angiotensin II, a potent vasoconstrictor that also stimulates aldosterone release. Clinical consequences are a decrease in BP, reduced sodium resorption and potassium retention.
Indications Treatment of essential hypertension.
Contraindications Hypersensitivity or history of angioedema related to ACE inhibitor treatment.
Uncomplicated Hypertension
ADULTS: PO Initial dose 4 mg qd; then titrate upward until BP, just before the next dose, is controlled or a maximum of 16 mg/day. Usual maintenance dose is 4 to 8 mg daily. PATIENTS > 65 YRS: PO Initial dose 4 mg daily in 1 or 2 divided doses; then titrate upward until BP, just before the next dose, is controlled, or a max of 8 mg/day.
Use with Concomitant Diuretics
ADULTS: PO If BP is not adequately controlled with perindopril alone, a diuretic may be added. In patients being treated with a diuretic, to reduce the likelihood of the occurrence of symptomatic hypotension, discontinue the diuretic 2 to 3 days prior to beginning perindopril. If the diuretic cannot be discontinued, use an initial dose of 2 to 4 mg daily of perindopril and titrate the dose as above.
Impaired Renal Function
ADULTS (CREATININE CLEARANCE < 30 ML/MIN): PO Initial dose 2 mg/day (max dose 8 mg/day).
Diuretics: Increased risk of excessive reduction in BP. Potassium supplements, potassium-sparing diuretics (eg, spironolactone), drugs capable of increasing serum potassium (eg, cyclosporine, heparin, indomethacin): Increased risk of hyperkalemia. Lithium: Increased risk of lithium toxicity.
Lab Test Interferences None well documented.
CV: Palpitation; abnormal ECG. RESP: Cough; upper respiratory infection. CNS: Headache; dizziness; sleep disorder; depression; somnolence; nervousness. EENT: Sinusitis; ear infection; rhinitis; pharyngitis; seasonal allergy; tinnitus. GI: Dyspepsia; diarrhea; abdominal pain; nausea; vomiting; flatulence. GU: Proteinuria; urinary tract infection; sexual dysfunction; menstrual disorder. HEPA: Increased ALT. DERM: Rash. META: Increased triglycerides. OTHER: Asthenia; viral infection; upper and lower extremity pain; hypertonia; fever; edema; chest pain; neck pain; paresthesia; joint pain; myalgia; arthritis.
Pregnancy: Category C (first trimester); category D (second and third trimesters). Lactation: Undetermined. Children: Safety and efficacy not established. Elderly: Perindopril plasma concentrations may be increased. Angioedema: May occur and is potentially fatal if laryngeal edema occurs. Use drug with extreme caution in patients with history of angioedema. Cough: Chronic nonproductive cough may occur. Hepatic failure: Has occurred rarely with other ACE inhibitors. Hypotension: Symptomatic hypotension may occur. Neutropenia and agranulocytosis: Has occurred rarely with other ACE inhibitors; risk appears greater with renal dysfunction, heart failure, or immunosuppression. Renal impairment: Changes in renal function may occur in susceptible individuals.
PATIENT CARE CONSIDERATIONS |
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Copyright © 2003 Facts and Comparisons
David S. Tatro
A to Z Drug Facts