| 商品名称 | Optruma |
|---|---|
| 适用类别 | Human |
| 治疗领域 | Osteoporosis, Postmenopausal |
| 通用名/非专利名称 | raloxifene |
| 活性成分 | raloxifene hydrochloride |
| 产品号 | EMEA/H/C/000185 |
| 患者安全信息 | No |
| 许可状态 | Authorised |
| ATC编码 | G03XC01 |
| 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 | 1998/08/05 |
| 上市许可开发者/申请人/持有人 | Eli Lilly Nederland B.V. |
| 人用药物治疗学分组 | Sex hormones and modulators of the genital system |
| 兽用药物治疗学分组 | |
| 欧盟委员会决定日期 | 2024/09/25 |
| 修订号 | 27 |
| 治疗适应症 | Optruma is indicated for the treatment and prevention of osteoporosis in post-menopausal women. A significant reduction in the incidence of vertebral, but not hip fractures has been demonstrated. When determining the choice of Optruma or other therapies, including oestrogens, for an individual postmenopausal woman, consideration should be given to menopausal symptoms, effects on uterine and breast tissues, and cardiovascular risks and benefits (see section 5.1). |
| 适用物种 | |
| 兽用药物ATC编码 | |
| 首次发布日期 | 2017/08/03 |
| 最后更新日期 | 2024/09/26 |
| 产品说明书 | https://www.ema.europa.eu/en/documents/product-information/optruma-epar-product-information_en.pdf |
| 公共评估报告 | https://www.ema.europa.eu/en/medicines/human/EPAR/optruma |