欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Qutavina
适用类别Human
治疗领域Osteoporosis
通用名/非专利名称teriparatide
活性成分teriparatide
产品号EMEA/H/C/005388
患者安全信息No
许可状态Withdrawn
ATC编码H05AA02
是否额外监管No
是否仿制药或hybrid药物No
是否生物类似药Yes
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2020/08/27
上市许可开发者/申请人/持有人EuroGenerics Holdings B.V.
人用药物治疗学分组Calcium homeostasis
兽用药物治疗学分组
欧盟委员会决定日期2020/11/24
修订号
治疗适应症Qutavina is indicated in adults. Treatment of osteoporosis in postmenopausal women and in men at increased risk of fracture. In postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures have been demonstrated. Treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at increased risk for fracture.
适用物种
兽用药物ATC编码
首次发布日期2021/01/18
产品说明书https://www.ema.europa.eu/en/documents/product-information/qutavina-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/qutavina
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