欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Sugammadex Fresenius Kabi
适用类别Human
治疗领域Neuromuscular Blockade
通用名/非专利名称sugammadex
活性成分sugammadex sodium
产品号EMEA/H/C/005760
患者安全信息no
授权状态Authorised
ATC编码V03AB35
是否额外监管no
是否仿制药yes
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
批准上市日期2022/07/15
上市许可持有人/公司名称Fresenius Kabi Deutschland GmbH
人用药物治疗分组All other therapeutic products
审评意见发布日期2022/05/19
决定日期2022/07/15
修订号
适应症Reversal of neuromuscular blockade induced by rocuronium or vecuronium in adults.For the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.
首次发布日期2022/05/17
修订日期2022/07/21
产品信息https://www.ema.europa.eu/en/documents/product-information/sugammadex-fresenius-kabi-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/sugammadex-fresenius-kabi
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