首页> 外文期刊>British Journal of Clinical Pharmacology >The effect of cimetidine or omeprazole on the pharmacokinetics of escitalopram in healthy subjects.
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The effect of cimetidine or omeprazole on the pharmacokinetics of escitalopram in healthy subjects.

机译:西咪替丁或奥美拉唑对健康受试者中依西酞普兰药代动力学的影响。

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Aims To investigate the effects of co-administration of cimetidine or omeprazole on the pharmacokinetics of escitalopram. Methods Two randomized placebo-controlled crossover studies were carried out. Sixteen healthy subjects were administered placebo, or cimetidine (400 mg twice daily) for 5 days (study 1) or omeprazole (30 mg once daily) for 6 days (study 2). On day 4 (study 1) or day 5 (study 2), a single dose of escitalopram (20 mg) was administered. Blood samples were taken at predetermined times for the measurement of serum concentrations of escitalopram and its demethylated metabolite (S-DCT). Treatment-emergent adverse events were also monitored. Results Co-administration with cimetidine caused a moderate increase in the systemic exposure [AUC(0, infinity)] to escitalopram (geometric mean ratio = 1.72, [95% CI 1.34, 2.21]) and a small increase in t((1/2)) from 23.7 to 29.0 h (5.24 h [3.75, 6.70]). Co-administration with omeprazole also resulted in a moderate increase in the escitalopram AUC(0, infinity) (1.51 [1.39, 1.64]) and a small increase in t((1/2)) from 26.5 to 34.8 h (8.3 h [6.44, 10.2]). There was no significant change in S-DCT AUC(0, infinity) after co-administration of either cimetidine or omeprazole. Co-administration of cimetidine or omeprazole had no effect on the incidence of treatment-emergent adverse events. Conclusions In view of the good tolerability of escitalopram, the pharmacokinetic changes observed on co-administration with cimetidine or omeprazole are unlikely to be of clinical concern.
机译:目的研究西咪替丁或奥美拉唑的共同给药对依他普仑药代动力学的影响。方法进行了两项随机安慰剂对照的交叉研究。十六名健康受试者接受安慰剂或西咪替丁(400 mg,每天两次),共5天(研究1)或奥美拉唑(奥美拉唑,每天30 mg,每天一次),共6天(研究2)。在第4天(研究1)或第5天(研究2),服用单剂量的依他普仑(20 mg)。在预定的时间采集血样以测量依他普仑及其去甲基代谢产物(S-DCT)的血清浓度。还监测了治疗中出现的不良事件。结果与西咪替丁共同给药会导致依西酞普兰的全身暴露[AUC(0,infinity)]适度增加(几何平均比率= 1.72,[95%CI 1.34,2.21]),t [(1 / 2))从23.7到29.0小时(5.24小时[3.75,6.70])。与奥美拉唑的共同给药还导致依他普仑AUC(0,infinity)适度增加(1.51 [1.39,1.64]),t((1/2))从26.5 h轻微增加至34.8 h(8.3 h [ 6.44,10.2])。西咪替丁或奥美拉唑合用后,S-DCT AUC(0,infinity)没有明显变化。西咪替丁或奥美拉唑的共同给药对紧急治疗不良事件的发生率没有影响。结论鉴于依西酞普兰具有良好的耐受性,与西咪替丁或奥美拉唑合用时观察到的药代动力学变化不太可能引起临床关注。

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