欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Fluenz
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influenza virus A/Victoria/4897/2022  (H1N1)pdm09 - like strain (A/Norway/31694/2022, MEDI 369815), A A/Croatia/10136RV/2023 (H3N2)-like strain (A/Perth/722/2024, MEDI 392611) B/Austria/1359417/2021 - like strain (B/ Austria/1359417/2021, MEDI 355292)
产品号EMEA/H/C/006514
患者安全信息No
许可状态Authorised
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2024/06/03
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2024/05/21
欧盟委员会决定日期2025/07/09
修订号5
治疗适应症Fluenz is indicated for active immunisation for the prevention of influenza disease in children and adolescents from 2 years to less than 18 years of age.Fluenz should be used in accordance with official recommendations.
适用物种
兽用药物ATC编码
首次发布日期2024/05/31
最后更新日期2025/07/14
产品说明书https://www.ema.europa.eu/en/documents/product-information/fluenz-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/fluenz
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