LOSARTAN DOES NOT AFFECT THE PHARMACOKINETICS AND PHARMACODYNAMICS OF WARFARIN

被引:25
作者
KONG, ANT
TOMASKO, L
WALDMAN, SA
OSBORNE, B
DEUTSCH, PJ
GOLDBERG, MR
BJORNSSON, TD
机构
[1] THOMAS JEFFERSON UNIV,JEFFERSON MED COLL,DEPT MED,DIV CLIN PHARMACOL,PHILADELPHIA,PA 19107
[2] MERCK & CO INC,RES LABS,DEPT CLIN PHARMACOL,RAHWAY,NJ 07065
关键词
D O I
10.1002/j.1552-4604.1995.tb04018.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Losartan, an orally active, nonpeptide angiotensin II receptor antagonist is being developed as a therapeutic agent for the treatment of hypertension and heart failure. Many patients requiring anticoagulant therapy with warfarin also may have hypertension or heart failure, and thus, are potential candidates for losartan therapy. This study was designed to investigate whether losartan at likely dosage levels would alter the anticoagulant response to warfarin. In a two-period, placebo-controlled, randomized, crossover study, ten healthy male subjects received a single oral dose of 30 mg warfarin sodium on the seventh day of a 13-day treatment with losartan, 100 mg daily by mouth, or placebo. Multiple plasma samples were collected over a 6-day period after both warfarin doses for the measurements of R- and S-warfarin concentrations and prothrombin times, The pharmacokinetics of R- and S-warfarin were comparable in the absence and presence of losartan (no significant effects of losartan on area under the curve, C-max, or t(max)). Losartan also had no significant effect on the anticoagulant effect of warfarin, as assessed by the area under the prothrombin time versus time curve and the maximum response for prothrombin time. The lack of pharmacokinetic or pharmacodynamic interaction between warfarin and losartan observed in this investigation suggests that a clinically important interaction between these drugs is unlikely to occur in patients requiring concomitant administration of both drugs.
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收藏
页码:1008 / 1015
页数:8
相关论文
共 29 条
  • [1] ANDREASEN PB, 1974, CLIN PHARMACOL THER, V16, P1059
  • [2] BANFIELD C, 1983, J PHARM SCI, V73, P921
  • [3] BENFIELD C, 1983, BR J CLIN PHARM, V16, P669
  • [4] BJORNSSON TD, 1979, J PHARMACOL EXP THER, V210, P316
  • [5] BJORNSSON TD, 1990, RATIONAL THERAPEUTIC, P541
  • [6] BRECKENRIDGE A, 1973, CLIN PHARMACOL THER, V14, P955
  • [7] NOMENCLATURE FOR ANGIOTENSIN RECEPTORS - A REPORT OF THE NOMENCLATURE-COMMITTEE OF THE COUNCIL-FOR-HIGH-BLOOD-PRESSURE-RESEARCH
    BUMPUS, FM
    CATT, KJ
    CHIU, AT
    DEGASPARO, M
    GOODFRIEND, T
    HUSAIN, A
    PEACH, MJ
    TAYLOR, DG
    TIMMERMANS, PBMWM
    [J]. HYPERTENSION, 1991, 17 (05) : 720 - 721
  • [8] CHIU AT, 1990, J PHARMACOL EXP THER, V252, P711
  • [9] STEREOSELECTIVE INTERACTION BETWEEN THE R-ENANTIOMER OF WARFARIN AND CIMETIDINE
    CHOONARA, IA
    CHOLERTON, S
    HAYNES, BP
    BRECKENRIDGE, AM
    PARK, BK
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1986, 21 (03) : 271 - 277
  • [10] A NATIONAL CONFERENCE SPONSORED BY THE AMERICAN-COLLEGE-OF CHEST-PHYSICIANS AND THE NATIONAL-HEART-LUNG-AND-BLOOD-INSTITUTE - INTRODUCTION
    DALEN, JE
    HIRSCH, J
    [J]. CHEST, 1986, 89 (02) : S1 - S1