首页> 外文期刊>Journal of cardiovascular pharmacology and therapeutics >Pharmacokinetics/Pharmacodynamics of Dabigatran 75 mg Twice Daily in Patients With Nonvalvular Atrial Fibrillation and Severely Impaired Renal Function
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Pharmacokinetics/Pharmacodynamics of Dabigatran 75 mg Twice Daily in Patients With Nonvalvular Atrial Fibrillation and Severely Impaired Renal Function

机译:Dabigatran的药代动力学/ Pharmacy动力学每天两次,肾功能严重受损的患者每天两次,肾功能严重受损

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Introduction: Dabigatran etexilate is an oral direct thrombin inhibitor. Dabigatran excretion is 80% renal, so exposure increases with severity of renal failure. The US Food and Drug Administration-approved dabigatran etexilate 75 mg twice daily (BID) for patients with nonvalvular atrial fibrillation (NVAF) having severely impaired renal function (creatinine clearance: 15-30 mL/min), based on post hoc pharmacokinetic modeling. We assessed dabigatran exposure at trough and peak levels in patients with NVAF and severely impaired renal function and compared with model predictions.
机译:简介:Dabigatran Etexilate是口服直接凝血酶抑制剂。 Dabigatran排泄为80%肾,因此暴露随着肾衰竭的严重程度而增加。 美国食品和药物管理局批准的Dabigatran患有肾功能严重受损(肌酐清除:15-30mL / min)的非衰弱性心房颤动(NVAF)的患者每天两次(BID)两次,基于后HOC药代动力学建模。 我们评估了NVAF患者的谷胱甘肽和峰值水平,肾功能严重受损,并与模型预测相比。

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