THE EFFECT OF RENAL-DISEASE ON THE DISPOSITION OF VENLAFAXINE

被引:55
作者
TROY, SM
SCHULTZ, RW
PARKER, VD
CHIANG, ST
BLUM, RA
机构
[1] MILLARD FILLMORE HOSP,DEPT MED,CLIN PHARMACOKINET LAB,BUFFALO,NY 14209
[2] SUNY BUFFALO,CTR CLIN PHARM RES,BUFFALO,NY
[3] WYETH AYERST RES,RADNOR,PA
关键词
D O I
10.1038/clpt.1994.95
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The pharmacokinetics of venlafaxine and its active metabolite O-desmethylvenlafaxine were studied in subjects with various degrees of renal dysfunction, including subjects requiring maintenance hemodialysis. Venlafaxine was administered as a single 50 mg dose, with blood and urine samples obtained at intervals up to 48 hours after administration for the subjects receiving dialysis or 72 hours for the subjects not receiving dialysis. Six subjects receiving dialysis also completed an intradialysis evaluation to estimate dialysis clearance. Concentrations of venlafaxine and O-desmethylvenlafaxine in plasma, urine, and dialysate fluid were determined by high-performance liquid chromatography. Apparent total clearance of venlafaxine and O-desmethylvenlafaxine were both significantly decreased by approximately 55% in the subjects receiving dialysis, and terminal disposition half-life was significantly prolonged for both compounds. Venlafaxine and O-desmethylvenlafaxine are poorly dialyzable. In conclusion, the disposition of venlafaxine and O-desmethylvenlafaxine is markedly altered in renal disease; therefore dosage adjustment is warranted for patients with creatinine clearance values below 30 ml/min.
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页码:14 / 21
页数:8
相关论文
共 15 条
[1]   FLUOXETINE KINETICS AND PROTEIN-BINDING IN NORMAL AND IMPAIRED RENAL-FUNCTION [J].
ARONOFF, GR ;
BERGSTROM, RF ;
POTTRATZ, ST ;
SLOAN, RS ;
WOLEN, RL ;
LEMBERGER, L .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1984, 36 (01) :138-144
[2]   NORTRIPTYLINE METABOLISM IN CHRONIC-RENAL-FAILURE - METABOLITE ELIMINATION [J].
DAWLING, S ;
LYNN, K ;
ROSSER, R ;
BRAITHWAITE, R .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1982, 32 (03) :322-329
[3]  
FABRE LF, 1987, CURR THER RES CLIN E, V42, P901
[4]  
Gibaldi M., 1982, PHARMACOKINETICS, Vsecond
[5]  
GIBSON TP, 1985, PHARMACOTHERAPY, V5, P23
[6]  
HASKINS JT, 1985, EUR J PHARMACOL, V115, P139
[7]  
HOWELL SR, IN PRESS XENOBIOTICA
[8]   INTRODUCTION OF A COMPOSITE PARAMETER TO THE PHARMACOKINETICS OF VENLAFAXINE AND ITS ACTIVE O-DESMETHYL METABOLITE [J].
KLAMERUS, KJ ;
MALONEY, K ;
RUDOLPH, RL ;
SISENWINE, SF ;
JUSKO, WJ ;
CHIANG, ST .
JOURNAL OF CLINICAL PHARMACOLOGY, 1992, 32 (08) :716-724
[9]  
METZLER CM, 1974, BIOMETRICS, V30, P562
[10]   BIOCHEMICAL, NEUROPHYSIOLOGICAL, AND BEHAVIORAL-EFFECTS OF WY-45,233 AND OTHER IDENTIFIED METABOLITES OF THE ANTIDEPRESSANT VENLAFAXINE [J].
MUTH, EA ;
MOYER, JA ;
HASKINS, JT ;
ANDREE, TH ;
HUSBANDS, GEM .
DRUG DEVELOPMENT RESEARCH, 1991, 23 (02) :191-199