LANSOPRAZOLE DOES NOT AFFECT THE BIOAVAILABILITY OF ORAL-CONTRACEPTIVES

被引:26
作者
FUCHS, W
SENNEWALD, R
KLOTZ, U
机构
[1] DR MARGARETE FISCHER BOSCH INST CLIN PHARMACOL,D-70376 STUTTGART,GERMANY
[2] TAKEDA PHARMA,AACHEN,GERMANY
[3] LAB,NEU ULM,GERMANY
关键词
LANSOPRAZOLE; ORAL CONTRACEPTIVES; HORMONES; INDUCTION; INHIBITION; DRUG INTERACTIONS;
D O I
10.1111/j.1365-2125.1994.tb04370.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effects of the proton pump inhibitor lansoprazole on the bioavailability of a low-dose oral contraceptive (OC), containing 0.03 mg ethinyloestradiol (EE) and 0.15 mg levonorgestrel (LNG), were investigated. Twenty-four healthy females (aged 19-35 years; weight 60.6 +/- 7.1 kg) participated in a multiple-dose, placebo-controlled, randomized two-way cross-over study. All subjects received the OC over 2 full menstrual cycles from day 1 to day 21 separated by a drug-free interval of 7 days. Lansoprazole (60 mg day(-1)) or placebo was coadministered for 3 weeks each. Plasma concentrations of EE and LNG were determined by GC-MS. The 90% confidence intervals for ratios of C-max and AUC after log transformation of both EE and LNG ranged between 91 and 111%, indicating that lansoprazole did not affect the bioavailability of EE and LNG.
引用
收藏
页码:376 / 380
页数:5
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