欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Pandemic influenza vaccine H5N1 AstraZeneca (previously Pandemic influenza vaccine H5N1 Medimmune)
适用类别Human
治疗领域Influenza, Human
通用名/非专利名称pandemic influenza vaccine (H5N1) (live attenuated, nasal)
活性成分reassortant influenza virus (live attenuated) of the following strain: A/Vietnam/1203/2004 (H5N1) strain
产品号EMEA/H/C/003963
患者安全信息No
许可状态Authorised
ATC编码J07BB03
是否额外监管Yes
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Yes
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2016/05/20
上市许可开发者/申请人/持有人AstraZeneca AB
人用药物治疗学分组Vaccines
兽用药物治疗学分组
审评意见日期2016/03/31
欧盟委员会决定日期2025/12/10
修订号12
治疗适应症Prophylaxis of influenza in an officially declared pandemic situation in children and adolescents from 12 months to less than 18 years of age. Pandemic influenza vaccine H5N1 AstraZeneca should be used in accordance with official guidance
适用物种
兽用药物ATC编码
首次发布日期2017/06/23
最后更新日期2025/12/10
产品说明书https://www.ema.europa.eu/en/documents/product-information/pandemic-influenza-vaccine-h5n1-astrazeneca-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/pandemic-influenza-vaccine-h5n1-astrazeneca
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