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Advances and Application of a Novel Oral Anticoagulant in Specific Populations: Dabigatran Etexilate

机译:一种新的口服抗凝血剂在特定种群中的进展和应用:Dabigatran eXexilate

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Background: Dabigatran etexilate (DE) was approved by the FDA in 2010 to reduce the risk of stroke and systemic embolism in adults with Non-valvular Atrial Fibrillation (NVAF). Compared with warfarin, a traditional anticoagulant drug, DE exhibits a shorter half-life, improved dose-effect relationship, fewer food and drug interactions, and can be taken orally without monitoring the conventional coagulation index. DE can also prevent or reduce the severity of adverse events, such as attenuated drug efficacy or bleeding. It is convenient for patients to take DE due to low levels of individual variation. This review aims to application of Dabigatran etexilate in specific populations.
机译:背景:Dabigatran Etexilate(DE)于2010年被FDA批准,以降低具有非瓣膜心房颤动(NVAF)的成人中风和全身栓塞的风险。 与华法林相比,一种传统的抗凝血药物,DE表现出较短的半衰期,改善剂量效应关系,更少的食物和药物相互作用,并且可以口服,而不会监测常规凝血指数。 DE还可以预防或降低不良事件的严重程度,例如减毒药效或出血。 患者患者由于单独变化的较低而持续性方便。 该审查旨在在特定群体中申请Dabigatran eDilexilate。

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