Approximately 25% of US adults have high blood pressure (BP). Selection of
effective and safe antihypertensive therapy for these individuals is an imp
ortant health-care priority. High BP can be treated with a wide range of an
tihypertensive agents from a number of different classes. These drugs may d
iffer in their suitability for administration to different subpopulations o
f patients. Results from both clinical trials and postmarketing surveillanc
e indicate that the angiotensin-converting enzyme (ACE) inhibitor perindopr
il erbumine is safe and well tolerated in a wide range of patients with hyp
ertension. Cough, the most common ACE inhibitor-associated side effect, is
also the most common clinical adverse event reported for perindopril, but <
2% of perindopril-treated patients discontinue therapy because of cough. Ot
her adverse events often associated with ACE inhibitors, first-dose hypoten
sion and hyperkalemia, appear to occur less often with perindopril than wit
h other agents in this class. The favorable safety profile for perindopril
extends to a wide range of patients, including the elderly and those with e
ither heart failure or renal disease. Perindopril has no negative effects o
n lipids in patients with hyperlipidemia or on glycemic control in patients
with type 2 diabetes mellitus, and it reduces proteinuria in patients with
renal disease. Perindopril has no known clinically significant drug-drug i
nteractions. Thus, perindopril is a safe BP-lowering agent with documented
tolerability in a wide range of patients with hypertension. (C) 2001 by Exc
erpta Medica, Inc.