欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Clopidogrel BMS
适用类别Human
治疗领域Stroke;Peripheral Vascular Diseases;Myocardial Infarction;Acute Coronary Syndrome
通用名/非专利名称clopidogrel
活性成分clopidogrel (as hydrogen sulfate)
产品号EMEA/H/C/000974
患者安全信息No
许可状态Withdrawn
ATC编码B01AC04
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2008/07/16
上市许可开发者/申请人/持有人Bristol-Myers Squibb Pharma EEIG
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2009/10/26
修订号3
治疗适应症Clopidogrel is indicated in adults for the prevention of atherothrombotic events in: - Patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from 7 days until less than 6 months) or established peripheral arterial disease. - Patients suffering from acute coronary syndrome: Non-ST segment elevation acute coronary syndrome (unstable angina or non-Q-wave myocardial infarction), including patients undergoing a stent placement following percutaneous coronary intervention, in combination with acetylsalicylic acid (ASA). ST segment elevation acute myocardial infarction, in combination with ASA in medically treated patients eligible for thrombolytic therapy.
适用物种
兽用药物ATC编码
首次发布日期2009/10/26
最后更新日期2010/01/26
产品说明书https://www.ema.europa.eu/en/documents/product-information/clopidogrel-bms-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/clopidogrel-bms
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