欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Vepacel
适用类别Human
治疗领域Influenza, Human;Immunization;Disease Outbreaks
通用名/非专利名称prepandemic influenza vaccine (H5N1) (whole virion, inactivated,prepared in cell culture)
活性成分Influenza virus (whole virion, inactivated), containing antigen of: A/Vietnam/1203/2004 (H5N1)
产品号EMEA/H/C/002089
患者安全信息No
许可状态Withdrawn
ATC编码J07BB01
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2012/02/17
上市许可开发者/申请人/持有人Ology Bioservices Ireland LTD
人用药物治疗学分组Influenza vaccines
兽用药物治疗学分组
欧盟委员会决定日期2019/01/11
修订号9
治疗适应症Active immunisation against H5N1 subtype of influenza A virus. This indication is based on immunogenicity data from subjects from the age of 6 months onwards following administration of two doses of vaccine prepared with H5N1 subtype strains. Vepacel 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2017/03/10
最后更新日期2020/10/28
产品说明书https://www.ema.europa.eu/en/documents/product-information/vepacel-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/vepacel
©2006-2025 DrugFuture->European Medicines Agency Authorisation of Medicines DataBase