Low-dose drug combinations have been proposed in International Guidelines f
or use in patients with hypertension. The fixed low-dose combination of per
indopril 2mg with indapamide 0.625mg combines an angiotensin converting enz
yme (ACE) inhibitor with a non-thiazide diuretic.
Coadministration of perindopril and indapamide did not have any clinically
significant effects on the pharmacokinetic profile of either agent in healt
hy volunteers.
In experimental models of hypertension, perindopril/indapamide restored end
othelial function, improved microvascular density, reduced left ventricular
and aortic hypertrophy, and reversed renal end-organ damage.
Once daily oral perindopril 2mg/indapamide 0.625mg normalised blood pressur
e (BP) in 83.6% of elderly patients with essential hypertension (diastolic
BP was reduced to less than or equal to 90mm Hg) and 81.7% of those with is
olated systolic hypertension (systolic BP was reduced to <160mm Hg) after a
pproximate to 1 year of treatment. BP normalisation was sustained in 79.8%
of patients throughout the study.
Fixed low-dose perindopril/indapamide had a tolerability profile similar to
that of placebo in clinical trials; most adverse events were of mild to mo
derate severity. Coadministration of the 2 agents reduced the incidence of
hypokalaemia seen with indapamide alone.