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
许可状态Authorised
ATC编码J05AE30
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2022/01/28
上市许可开发者/申请人/持有人Pfizer Europe MA EEIG
人用药物治疗学分组
兽用药物治疗学分组
审评意见日期2022/01/27
欧盟委员会决定日期2025/11/26
修订号29
治疗适应症Paxlovid is indicated for the treatment of coronavirus disease 2019 (COVID-19) in adults and paediatric patients 6 years of age and older weighing at least 20 kg who do not require supplemental oxygen and who are at increased risk for progressing to severe COVID 19 (see section 5.1).
适用物种
兽用药物ATC编码
首次发布日期2022/01/28
最后更新日期2025/12/04
产品说明书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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