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首页> 外文期刊>The Journal of Clinical Pharmacology: Official Journal of the American College of Clinical Pharmacology >Pharmacokinetics and pharmacodynamics of dabigatran etexilate, an oral direct thrombin inhibitor, with coadministration of digoxin
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Pharmacokinetics and pharmacodynamics of dabigatran etexilate, an oral direct thrombin inhibitor, with coadministration of digoxin

机译:口服直接凝血酶抑制剂达比加群酯与地高辛合用的药代动力学和药效学

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摘要

This study evaluated the potential impact of concomitant digoxin on the pharmacokinetics and pharmacodynamics of dabigatran etexilate, a novel oral direct thrombin inhibitor. Healthy volunteers (n = 23) received 150 mg dabigatran etexilate twice daily on days 1 to 3 and once on day 4 in 1 period. Digoxin was given in another period as a loading dose of 0.5 mg early on day 1 and 0.25 mg in the evening of day 1 and on the mornings of days 2 to 4. In a third treatment period, dabigatran etexilate together with digoxin was given on days 1 to 4. Exposure to dabigatran was not significantly altered with concomitant digoxin-the maximum concentration (Cmax,ss) and area under the concentration-time curve at steady state over 1 dosing interval (AUC τss) of dabigatran with and without digoxin were essentially unchanged. The pharmacokinetic profile of digoxin also remained unchanged in the presence of dabigatran etexilate. Dabigatran's anticoagulant effect, assessed by blood coagulation time assays, was not influenced by digoxin. Dabigatran etexilate and digoxin can be coadministered without the need for dose adjustment of either drug.
机译:这项研究评估了地高辛对新型口服直接凝血酶抑制剂达比加群酯的药代动力学和药效学的潜在影响。健康志愿者(n = 23)在第1至3天每天两次接受150 mg达比加群酯,在第1天第4天接受一次。地高辛在另一个时期的给药剂量为:第1天初期为0.5 mg,第1天晚上和第2至第4天早晨为0.25 mg。在第三个治疗阶段,达比加群酯与地高辛一起给药。第1至4天。伴随地高辛的作用,达比加群的暴露无明显改变-达比加群在有或没有地高辛的1个给药间隔(稳态)下的最大浓度(Cmax,ss)和浓度-时间曲线下的面积在稳态下为本质上不变。在达比加群酯的存在下,地高辛的药代动力学特征也保持不变。通过血液凝固时间测定评估的达比加群的抗凝作用不受地高辛的影响。达比加群酯和地高辛可以共同给药,而无需调整任何一种药物的剂量。

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