欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Recarbrio
适用类别Human
治疗领域Gram-Negative Bacterial Infections
通用名/非专利名称imipenem;cilastatin;relebactam
活性成分imipenem monohydrate;cilastatin sodium;relebactam monohydrate
产品号EMEA/H/C/004808
患者安全信息No
许可状态Authorised
ATC编码J01DH56
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2020/02/13
上市许可开发者/申请人/持有人Merck Sharp & Dohme B.V. 
人用药物治疗学分组Antibacterials for systemic use;Carbapenems
兽用药物治疗学分组
审评意见日期2019/12/12
欧盟委员会决定日期2025/01/30
修订号7
治疗适应症Recarbrio is indicated for:- Treatment of hospital-acquired pneumonia (HAP), including ventilator associated pneumonia (VAP), in adults (see sections 4.4 and 5.1).- Treatment of bacteraemia that occurs in association with, or is suspected to be associated with HAP or VAP, in adults.- Treatment of infections due to aerobic Gram-negative organisms in adults with limited treatment options (see sections 4.2, 4.4, and 5.1). Consideration should be given to official guidance on the appropriate use of antibacterial agents.
适用物种
兽用药物ATC编码
首次发布日期2020/02/26
最后更新日期2025/03/07
产品说明书https://www.ema.europa.eu/en/documents/product-information/recarbrio-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/recarbrio
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