欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Zoonotic Influenza Vaccine Seqirus
适用类别Human
治疗领域Influenza A Virus, H5N8 Subtype
通用名/非专利名称zoonotic influenza vaccine (H5N8) (surface antigen, inactivated, adjuvanted)
活性成分A/Astrakhan/3212/2020 (H5N8)-like strain (CBER-RG8A) (clade 2.3.4.4b)
产品号EMEA/H/C/006375
患者安全信息No
许可状态Authorised
ATC编码J07BB02
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2023/10/09
上市许可开发者/申请人/持有人Seqirus S.r.l. 
人用药物治疗学分组Vaccines
兽用药物治疗学分组
欧盟委员会决定日期2025/06/12
修订号3
治疗适应症Zoonotic Influenza Vaccine Seqirus H5N8 is indicated for active immunisation against H5 subtype influenza A viruses in individuals 6 months of age and above. The use of this vaccine should be in accordance with official recommendations.
适用物种
兽用药物ATC编码
首次发布日期2023/09/14
最后更新日期2025/06/27
产品说明书https://www.ema.europa.eu/en/documents/product-information/zoonotic-influenza-vaccine-seqirus-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/zoonotic-influenza-vaccine-seqirus
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