TOLERABILITY AND KINETICS OF INTRAVENOUS MEDIFOXAMINE IN HEALTHY-VOLUNTEERS

被引:1
|
作者
SALEH, S
JOHNSTON, A
EDEKI, T
TURNER, P
机构
[1] Clinical Pharmacology, St. Bartholomew’s Hospital, London
关键词
D O I
10.1097/00004850-199004000-00003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Medifoxamine is a new antidepressant drug which is in clinical use in France and is undergoing clinical investigation elsewhere. We have carried out a study of its tolerance by the intraveneous route and have investigated its kinetic parameters by this route. Twelve healthy volunteers received single ascending intravenous doses of medifoxamine 5 to 10 mg. The subjects were observed for changes in haemodynamic and other vital signs. Serum samples were analyzed using a specific HPLC method. Medifoxamine was well tolerated by all volunteers. Its kinetics were described by a two-compartment open model with an elimination half-line 1-2 h, systemic clearance 1299 1/min, volume of distribution 132 I and urinary excretion of parent drug less than 1% of the dose. One subject had high serum concentrations and low clearance when compared with the other subjects. This may have been due to genetic differences in drug metabolism, as this subject was found to be a poor metabolizer of debrisoquine. © 1990 CNS (Clinical Neuroscience) Publishers.
引用
收藏
页码:97 / 102
页数:6
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