Eprosartan - A review of its use in the management of hypertension

被引:24
作者
Plosker, GL [1 ]
Foster, RH [1 ]
机构
[1] Adis Int Ltd, Auckland 10, New Zealand
关键词
Eprosartan; hypertension; antihypertensive; pharmacodynamics; pharmacokinetics; therapeutic use; drug interactions; tolerability;
D O I
10.2165/00003495-200060010-00009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Eprosartan is a potent and selective angiotensin II subtype 1 receptor antagonist. Results of large (n > 100) randomised double-blind studies in patients with mild, moderate or severe hypertension demonstrated that the antihypertensive efficacy of eprosartan (usually 400 to 800 mg/day as a single daily dose or in 2 divided doses) is significantly greater than that of placebo and at least as good as that of enalapril. In placebo-controlled trials, eprosartan achieved mean reductions from baseline in trough sitting systolic blood pressure of 6.3 to 15 mm Hg and in diastolic blood pressure of 4.1 to 9.7 mm Hg. Response rates associated with once daily administration of eprosartan 400 to 800mg were approximately double those with placebo. Overall, eprosartan was well tolerated with a similar tolerability profile to that of placebo. In comparative trials, in which the incidence of persistent dry cough was evaluated as the primary end-point, enalapril was several-fold more likely to induce this adverse event than eprosartan (the difference being statistically significant regardless of study population and definition of cough). In conclusion, the angiotensin II receptor antagonist eprosartan is a well tolerated and effective antihypertensive agent that is administered once or twice daily without regard to meals. Eprosartan has a low potential for serious adverse events, and the drug has not been associate with clinically significant drug interactions. Unlike ACE inhibitors such as enalapril, eprosartan does not have a high propensity to cause persistent nonproductive cough. Thus, eprosartan represents a useful therapeutic option in the management of patients with hypertension.
引用
收藏
页码:177 / 201
页数:25
相关论文
共 90 条
[1]   HUMAN AT(1) RECEPTOR IS A SINGLE-COPY GENE - CHARACTERIZATION IN A STABLE CELL-LINE [J].
AIYAR, N ;
BAKER, E ;
WU, HL ;
NAMBI, P ;
EDWARDS, RM ;
TRILL, JJ ;
ELLIS, C ;
BERGSMA, DJ .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1994, 131 (01) :75-86
[2]   CHARACTERIZATION OF [H-3] SK-AND-F-108566 AS A RADIOLIGAND FOR ANGIOTENSIN TYPE-1 RECEPTOR [J].
AIYAR, N ;
GRIFFIN, E ;
SHU, A ;
HEYS, R ;
BERGSMA, DJ ;
WEINSTOCK, J ;
EDWARDS, R .
JOURNAL OF RECEPTOR RESEARCH, 1993, 13 (05) :849-861
[3]  
[Anonymous], 1991, JAMA, V265, P3255
[4]  
[Anonymous], 1997, ARCH INTERN MED, V157, P2413, DOI [10.1001/archinte.1997.00440420033005, DOI 10.1001/ARCHINTE.1997.00440420033005]
[5]   Effect of eprosartan and enalapril in the treatment of elderly hypertensive patients: Subgroup analysis of a 26-week, double-blind, multicentre study [J].
Argenziano, L ;
Trimarco, B .
CURRENT MEDICAL RESEARCH AND OPINION, 1999, 15 (01) :9-14
[6]  
BARONE FC, 1999, J HUM HYPERTENS S3, V13, P7
[7]  
Black HR, 1999, J HYPERTENS, V17, pS49
[8]   A review of eprosartan pharmacokinetic and pharmacodynamic drug interaction studies [J].
Blum, RA ;
Kazierad, DJ ;
Tenero, DM .
PHARMACOTHERAPY, 1999, 19 (04) :79S-85S
[9]  
BOIKE S, 1993, J AM SOC NEPHROL, V54, P530
[10]   Pharmacokinetics of eprosartan in healthy subjects, patients with hypertension, and special populations [J].
Bottorff, MB ;
Tenero, DM .
PHARMACOTHERAPY, 1999, 19 (04) :73S-78S