欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Relvar Ellipta
适用类别Human
治疗领域Pulmonary Disease, Chronic Obstructive
通用名/非专利名称fluticasone furoate;vilanterol
活性成分fluticasone furoate;vilanterol
产品号EMEA/H/C/002673
患者安全信息No
许可状态Authorised
ATC编码R03AK10
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2013/11/13
上市许可开发者/申请人/持有人GlaxoSmithKline Trading Services Limited
人用药物治疗学分组Adrenergics and other drugs for obstructive airway diseases
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2025/03/12
修订号28
治疗适应症Asthma indication: Relvar Ellipta is indicated in the regular treatment of asthma in adults and adolescents aged 12 years and older, where use of a combination product (long-acting beta2-agonist and inhaled corticosteroid) is appropriate: patients not adequately controlled with inhaled corticosteroids and “as needed” inhaled short acting beta2-agonists. patients already adequately controlled on both inhaled corticosteroid and long-acting beta2-agonist. COPD indication: Relvar Ellipta is indicated for the symptomatic treatment of adults with COPD with a FEV1 <70% predicted normal (post-bronchodilator) in patients with an exacerbation history despite bronchodilator therapy.
适用物种
兽用药物ATC编码
首次发布日期2018/07/26
最后更新日期2025/04/10
产品说明书https://www.ema.europa.eu/en/documents/product-information/relvar-ellipta-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/relvar-ellipta
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