LACK OF INTERACTION OF GABAPENTIN WITH CARBAMAZEPINE OR VALPROATE

被引:38
作者
RADULOVIC, LL
WILDER, BJ
LEPPIK, IE
BOCKBRADER, HN
CHANG, T
POSVAR, EL
SEDMAN, AJ
UTHMAN, BM
ERDMAN, GR
机构
[1] WARNER LAMBERT PARKE DAVIS,PARKE DAVIS PHARMACEUT RES,DEPT CLIN PHARMACOL,ANN ARBOR,MI
[2] VA MED CTR HOSP,GAINESVILLE,FL
[3] UNIV MINNESOTA,COLL PHARM,MINNEAPOLIS,MN 55455
[4] UNIV MINNESOTA,MINCEP EPILEPSY CARE PA,MINNEAPOLIS,MN
关键词
ANTICONVULSANTS; GABAPENTIN; PHARMACOKINETICS; DRUG INTERACTION; CARBAMAZEPINE; VALPROATE; DRUG TOXICITY;
D O I
10.1111/j.1528-1157.1994.tb02926.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Gabapentin (GBP) studies were conducted in patients with epilepsy receiving carbamazepine (CBZ, n = 12) or valproate (VPA, n = 14) monotherapy. The effects of GBP coadministration on steady-state CBZ or VPA concentrations and of these antiepileptic drugs (AEDs) on GBP pharmacokinetics were investigated. GBP (400 mg) was coadministered every 8 h for 31/3 days with CBZ or for 51/3 days with VPA. GBP was well tolerated. Mean steady-state plasma CBZ/CBZ-10,11-epoxide (CBZ-E) and serum VPA concentrations before, during, and after GBP administration were not significantly different. Mean steady-state GBP pharmacokinetic parameters during CBZ or VPA coadministration were similar to steady-state parameters reported in healthy subjects. Thus, no pharmacokinetic interaction exists between CBZ or VPA and GBP. No dosage adjustment is necessary when GBP and CBZ or VPA are coadministered.
引用
收藏
页码:155 / 161
页数:7
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