欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Roteas
适用类别Human
治疗领域Stroke;Venous Thromboembolism
通用名/非专利名称edoxaban
活性成分edoxaban tosilate
产品号EMEA/H/C/004339
患者安全信息No
许可状态Authorised
ATC编码B01AF03
是否额外监管No
是否仿制药或hybrid药物No
是否生物类似药No
是否附条件批准No
是否特殊情形No
是否加速审评No
是否罕用药No
上市许可日期2017/04/19
上市许可开发者/申请人/持有人Berlin-Chemie AG
人用药物治疗学分组Antithrombotic agents
兽用药物治疗学分组
审评意见日期2017/02/22
欧盟委员会决定日期2023/11/20
修订号12
治疗适应症Prevention of stroke and systemic embolism in adult patients with nonvalvular atrial fibrillation (NVAF) with one or more risk factors, such as congestive heart failure, hypertension, age ? 75 years, diabetes mellitus, prior stroke or transient ischaemic attack (TIA). Treatment of deep vein thrombosis (DVT) and pulmonary embolism (PE), and prevention of recurrent DVT and PE in adults.
适用物种
兽用药物ATC编码
首次发布日期2017/11/30
最后更新日期2025/08/27
产品说明书https://www.ema.europa.eu/en/documents/product-information/roteas-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/roteas
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