欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Brilique
适用类别Human
治疗领域Peripheral Vascular Diseases;Acute Coronary Syndrome
通用名/非专利名称ticagrelor
活性成分ticagrelor
产品号EMEA/H/C/001241
患者安全信息No
许可状态Authorised
ATC编码B01AC24
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2010/12/03
上市许可开发者/申请人/持有人AstraZeneca AB
人用药物治疗学分组Antithrombotic agents
兽用药物治疗学分组
欧盟委员会决定日期2024/09/05
修订号23
治疗适应症Brilique, co administered with acetylsalicylic acid (ASA), is indicated for the prevention of atherothrombotic events in adult patients with acute coronary syndromes (ACS) or a history of myocardial infarction (MI) and a high risk of developing an atherothrombotic event Brilique, co-administered with acetyl salicylic acid (ASA), is indicated for the prevention of atherothrombotic events in adult patients with a history of myocardial infarction (MI occurred at least one year ago) and a high risk of developing an atherothrombotic event.
适用物种
兽用药物ATC编码
首次发布日期2017/05/18
最后更新日期2025/04/24
产品说明书https://www.ema.europa.eu/en/documents/product-information/brilique-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/brilique
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