欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Fluenz Tetra
适用类别Human
治疗领域Influenza, Human
通用名/非专利名称influenza vaccine (live attenuated, nasal)
活性成分A/Darwin/9/2021 (H3N2) - like strain (A/Norway/16606/2021, MEDI 355293) / A/Victoria/2570/2019 (H1N1)pdm09 - like strain (A/Victoria/1/2020, MEDI 340505) / B/Austria/1359417/2021 - like strain (B/Austria/1359417/2021, MEDI 355292) / B/Phuket/3073/2013 - like strain (B/Phuket/3073/2013, MEDI 306444)
产品号EMEA/H/C/002617
患者安全信息No
许可状态Withdrawn
ATC编码J07BB03
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2013/12/04
上市许可开发者/申请人/持有人AstraZeneca AB
人用药物治疗学分组Influenza vaccines;Influenza, live attenuated
兽用药物治疗学分组
审评意见日期2013/09/19
欧盟委员会决定日期2025/07/14
修订号24
治疗适应症Prophylaxis of influenza in children and adolescents from 24 months to less than 18 years of age. The use of Fluenz Tetra should be based on official recommendations.
适用物种
兽用药物ATC编码
首次发布日期2018/08/28
最后更新日期2025/08/14
产品说明书https://www.ema.europa.eu/en/documents/product-information/fluenz-tetra-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/fluenz-tetra
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