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首页> 外文期刊>The American heart journal >Edoxaban vs warfarin in patients with nonvalvular atrial fibrillation in the US Food and Drug Administration approval population: An analysis from the Effective Anticoagulation with Factor Xa Next Generation in Atrial Fibrillation-Thrombolysis in Myocardial Infarction 48 (ENGAGE AF-TIMI 48) trial
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Edoxaban vs warfarin in patients with nonvalvular atrial fibrillation in the US Food and Drug Administration approval population: An analysis from the Effective Anticoagulation with Factor Xa Next Generation in Atrial Fibrillation-Thrombolysis in Myocardial Infarction 48 (ENGAGE AF-TIMI 48) trial

机译:Edoxaban对美国食品和药物管理局批准人群的非衰弱性心房颤动患者的eDoxaban vs Warfarin:从心肌梗死心肌梗死的心房颤动溶栓中的因子Xa下一代有效抗凝的分析48(接合AF-Timi 48)试验

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摘要

Background Edoxaban is a specific anti-Xa inhibitor that, in comparison to warfarin, has been found to be noninferior for the prevention of stroke or systemic embolism (SSE) and to reduce bleeding significantly in patients with nonvalvular atrial fibrillation (AF). The US Food and Drug Administration (FDA) approved the higher-dose edoxaban regimen (60/30 mg) in patients with AF and a creatinine clearance of <= 95 mL/min. We report for the first time the clinical characteristics, efficacy, and safety of the FDA-approved population in the ENGAGE AF-TIMI 48 trial.
机译:背景技术Edoxaban是一种特异性抗XA抑制剂,与华法林相比,已被发现是防止中风或全身栓塞(SSE)的非难,并在非衰弱性心房颤动(AF)患者中显着降低出血。 美国食品和药物管理局(FDA)批准了AF的患者的较高剂量的Edoxaban方案(60/30mg)和肌酐清除率<= 95ml / min。 我们首次报告了FDA批准人口的第一次临床特征,疗效和安全性在接合AF-Timi 48审判中。

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