A review of eprosartan pharmacokinetic and pharmacodynamic drug interaction studies

被引:17
作者
Blum, RA
Kazierad, DJ
Tenero, DM
机构
[1] Millard Fillmore Hosp, Clin Pharmacokinet Lab, Buffalo, NY 14209 USA
[2] SUNY Buffalo, Sch Pharm, Buffalo, NY 14260 USA
[3] Univ Penn, Presbyterian Med Ctr, SmithKline Beechan, Clin Pharmacol Unit, Philadelphia, PA 19104 USA
[4] SmithKline Beecham, Drug Metab & Pharmacokinet, King Of Prussia, PA USA
来源
PHARMACOTHERAPY | 1999年 / 19卷 / 04期
关键词
D O I
10.1592/phco.19.7.79S.30948
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A series of clinical pharmacology studies was conducted to characterize potential interactions between eprosartan and other commonly prescribed drugs. Separate studies assessed the effect of eprosartan on the pharmacokinetics of digoxin and hydrochlorothiazide (HCTZ) and the pharmacodynamics of warfarin and glyburide (glibenclamide), as well as the effects of ranitidine, HCTZ, fluconazole, and ketoconazole on eprosartan pharmacokinetics. Eprosartan had no significant effect on the pharmacokinetics of digoxin and HCTZ and the pharmacodynamics of warfarin and glyburide. Thus, no dosing adjustments are necessary during concomitant therapy with these agents. Ranitidine, HCTZ, ketoconazole, and fluconazole had no effect on eprosartan pharmacokinetics. Single or multiple oral doses of eprosartan were safe and well tolerated when coadministered with these agents.
引用
收藏
页码:79S / 85S
页数:7
相关论文
共 21 条
[1]  
ANTMAN E M, 1987, Cardiovascular Drugs and Therapy, V1, P183, DOI 10.1007/BF02125472
[2]  
COX PJ, 1996, EXP TOXICOL PATHOL, V48, P340
[3]  
Evans W, 1992, APPL THER
[4]   Irbesartan - A review of its pharmacodynamic and pharmacokinetic properties and therapeutic use in the management of hypertension [J].
Gillis, JC ;
Markham, A .
DRUGS, 1997, 54 (06) :885-902
[5]   RANITIDINE - AN UPDATED REVIEW OF ITS PHARMACODYNAMIC AND PHARMACOKINETIC PROPERTIES AND THERAPEUTIC USE IN PEPTIC-ULCER DISEASE AND OTHER ALLIED DISEASES [J].
GRANT, SM ;
LANGTRY, HD ;
BROGDEN, RN .
DRUGS, 1989, 37 (06) :801-870
[6]  
HARGREAVES JA, 1994, BR J CLIN PHARM, V38, pP175
[7]   MECHANISM OF ACTION, CLINICAL EFFECTIVENESS, AND OPTIMAL THERAPEUTIC RANGE [J].
HIRSH, J ;
DALEN, JE ;
DEYKIN, D ;
POLLER, L ;
BUSSEY, H .
CHEST, 1995, 108 (04) :S231-S246
[8]   TERFENADINE-KETOCONAZOLE INTERACTION - PHARMACOKINETIC AND ELECTROCARDIOGRAPHIC CONSEQUENCES [J].
HONIG, PK ;
WORTHAM, DC ;
ZAMANI, K ;
CONNER, DP ;
MULLIN, JC ;
CANTILENA, LR .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1993, 269 (12) :1513-1518
[9]  
*JANSS PHARM, 1996, PHYS DESK REF, P1298
[10]   Fluconazole but not itraconazole decreases the metabolism of losartan to E-3174 [J].
Kaukonen, KM ;
Olkkola, KT ;
Neuvonen, PJ .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1998, 53 (06) :445-449