欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Paxlovid
适用类别Human
治疗领域COVID-19 virus infection
通用名/非专利名称nirmatrelvir, ritonavir
活性成分nirmatrelvir, ritonavir
产品号EMEA/H/C/005973
患者安全信息no
授权状态Authorised
ATC编码J05AE30
是否额外监管no
是否仿制药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
批准上市日期2022/01/28
上市许可持有人/公司名称Pfizer Europe MA EEIG
审评意见发布日期2022/01/27
决定日期2023/10/26
修订号15
适应症Paxlovid is indicated for the treatment of coronavirus disease 2019 (COVID-19) in adults who do not require supplemental oxygen and who are at increased risk for progressing to severe COVID 19.
首次发布日期2022/01/28
修订日期2023/10/19
产品信息https://www.ema.europa.eu/en/documents/product-information/paxlovid-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/paxlovid
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