欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Ivabradine JensonR
适用类别Human
治疗领域Angina Pectoris;Heart Failure
通用名/非专利名称ivabradine
活性成分ivabradine hydrochloride
产品号EMEA/H/C/004217
患者安全信息No
许可状态Withdrawn
ATC编码C01EB17
是否额外监管Nei
是否仿制药或hybrid药物
是否生物类似药Nei
是否附条件批准Nei
是否特殊情形Nei
是否加速审评Nei
是否罕用药Nei
上市许可日期2016/11/11
上市许可开发者/申请人/持有人JensonR+ Limited
人用药物治疗学分组Cardiac therapy
兽用药物治疗学分组
审评意见日期2016/06/15
欧盟委员会决定日期2016/11/11
修订号
治疗适应症Symptomatic treatment of chronic stable angina pectoris in coronary artery disease adults with normal sinus rhythm and heart rate ? 70 bpm. Ivabradine is indicated: - in adults unable to tolerate or with a contra-indication to the use of beta-blockers - or in combination with beta-blockers in patients inadequately controlled with an optimal beta-blocker dose. Treatment of chronic heart failure Ivabradine is indicated in chronic heart failure NYHA II to IV class with systolic dysfunction, in patients in sinus rhythm and whose heart rate is ? 75 bpm, in combination with standard therapy including beta-blocker therapy or when beta-blocker therapy is contraindicated or not tolerated.
适用物种
兽用药物ATC编码
首次发布日期2016/11/11
最后更新日期2018/12/20
产品说明书https://www.ema.europa.eu/en/documents/product-information/ivabradine-jensonr-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/ivabradine-jensonr
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