欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Qtern
适用类别Human
治疗领域Diabetes Mellitus, Type 2;Diabetes Mellitus;Nutritional and Metabolic Diseases;Metabolic Diseases;Glucose Metabolism Disorders
通用名/非专利名称saxagliptin;dapagliflozin
活性成分saxagliptin;dapagliflozin propanediol monohydrate
产品号EMEA/H/C/004057
患者安全信息No
许可状态Authorised
ATC编码A10BD21
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2016/07/15
上市许可开发者/申请人/持有人Astra Zeneca AB
人用药物治疗学分组Drugs used in diabetes
兽用药物治疗学分组
欧盟委员会决定日期2024/07/18
修订号14
治疗适应症Qtern, fixed dose combination of saxagliptin and dapagliflozin, is indicated in adults aged 18 years and older with type 2 diabetes mellitus: to improve glycaemic control when metformin and/or sulphonylurea (SU) and one of the monocomponents of Qtern do not provide adequate glycaemic control, when already being treated with the free combination of dapagliflozin and saxagliptin. (See sections 4.2, 4.4, 4.5 and 5.1 for available data on combinations studied.)
适用物种
兽用药物ATC编码
首次发布日期2017/12/20
最后更新日期2025/12/18
产品说明书https://www.ema.europa.eu/en/documents/product-information/qtern-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/qtern
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