欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Integrilin
适用类别Human
治疗领域Angina, Unstable;Myocardial Infarction
通用名/非专利名称eptifibatide
活性成分eptifibatide
产品号EMEA/H/C/000230
患者安全信息No
许可状态Authorised
ATC编码B01AC16
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1999/07/01
上市许可开发者/申请人/持有人GlaxoSmithKline Trading Services Limited
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1999/07/02
欧盟委员会决定日期2021/09/24
修订号26
治疗适应症Integrilin is intended for use with acetylsalicylic acid and unfractionated heparin. Integrilin is indicated for the prevention of early myocardial infarction in patients presenting with unstable angina or non-Q-wave myocardial infarction with the last episode of chest pain occurring within 24 hours and with ECG changes and / or elevated cardiac enzymes. Patients most likely to benefit from Integrilin treatment are those at high risk of developing myocardial infarction within the first 3-4 days after onset of acute angina symptoms including for instance those that are likely to undergo an early percutaneous transluminal coronary angioplasty (PTCA).
适用物种
兽用药物ATC编码
首次发布日期2017/04/12
最后更新日期2022/03/17
产品说明书https://www.ema.europa.eu/en/documents/product-information/integrilin-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/integrilin
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