Perindopril 2mg/Indapamide 0.625mg: Fixed Low-Dose Combination

Authors: McClellan K.J.1; Markham A.1

Source: Drugs, Volume 58, Number 2, August 1999 , pp. 297-302(6)

Publisher: Adis International

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Abstract:

utrif Low-dose drug combinations have been proposed in International Guidelines for use in patients with hypertension. The fixed low-dose combination of perindopril 2mg with indapamide 0.625mg combines an angiotensin converting enzyme (ACE) inhibitor with a non-thiazide diuretic.

utrif Coadministration of perindopril and indapamide did not have any clinically significant effects on the pharmacokinetic profile of either agent in healthy volunteers.

utrif In experimental models of hypertension, perindopril/indapamide restored endothelial function, improved microvascular density, reduced left ventricular and aortic hypertrophy, and reversed renal end-organ damage.

utrif Once daily oral perindopril 2mg/indapamide 0.625mg normalised blood pressure (BP) in 83.6% of elderly patients with essential hypertension (diastolic BP was reduced to le90mm Hg) and 81.7% of those with isolated systolic hypertension (systolic BP was reduced to <160mm Hg) after ap1 year of treatment. BP normalisation was sustained in 79.8% of patients throughout the study.

utrif Fixed low-dose perindopril/indapamide had a tolerability profile similar to that of placebo in clinical trials; most adverse events were of mild to moderate severity. Coadministration of the 2 agents reduced the incidence of hypokalaemia seen with indapamide alone.

Keywords: Reviews-on-treatment; Hypertension, treatment; Indapamide, general; Perindopril, general; Antihypertensives, general; Perindopril, therapeutic-use; Perindopril, pharmacokinetics; Perindopril, pharmacodynamics; Perindopril, adverse-reactions; Indapamide, therapeutic-use; Indapamide, pharmacodynamics; Indapamide, adverse-reactions; Indapamide, pharmacokinetics; New-drug-profiles

Language: English

Document Type: New drug profile

Affiliations: 1: Adis International Limited, Auckland, New Zealand *

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