欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Teriparatide Sun
适用类别Human
治疗领域Osteoporosis;Osteoporosis, Postmenopausal
通用名/非专利名称teriparatide
活性成分teriparatide
产品号EMEA/H/C/005793
患者安全信息No
许可状态Authorised
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2022/11/18
上市许可开发者/申请人/持有人Sun Pharmaceutical Industries Europe B.V.
人用药物治疗学分组Calcium homeostasis
兽用药物治疗学分组
审评意见日期2022/09/15
欧盟委员会决定日期2025/10/09
修订号4
治疗适应症Teriparatide SUN is indicated in adults. Treatment of osteoporosis in postmenopausal women and in men at increased risk of fracture (see section 5.1). In postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures has been demonstrated. Treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at increased risk for fracture (see section 5.1).
适用物种
兽用药物ATC编码
首次发布日期2022/09/14
最后更新日期2025/10/10
产品说明书https://www.ema.europa.eu/en/documents/product-information/teriparatide-sun-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/teriparatide-sun
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