欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Protopy
适用类别Human
治疗领域Dermatitis, Atopic
通用名/非专利名称tacrolimus
活性成分tacrolimus
产品号EMEA/H/C/000375
患者安全信息No
许可状态Withdrawn
ATC编码D11AX14
是否额外监管Nei
是否仿制药或hybrid药物Nei
是否生物类似药Nei
是否附条件批准Nei
是否特殊情形Nei
是否加速审评Nei
是否罕用药Nei
上市许可日期2002/02/28
上市许可开发者/申请人/持有人Astellas Pharma GmbH
人用药物治疗学分组Other dermatological preparations
兽用药物治疗学分组
欧盟委员会决定日期2007/05/03
修订号10
治疗适应症Treatment of moderate to severe atopic dermatitis in adults who are not adequately responsive to or are intolerant of conventional therapies such as topical corticosteroids. Treatment of moderate to severe atopic dermatitis in children (2 years of age and above) who failed to respond adequately to conventional therapies such as topical corticosteroids. Maintenance treatment of moderate to severe atopic dermatitis for the prevention of flares and the prolongation of flare-free intervals in patients experiencing a high frequency of disease exacerbations (i.e. occurring 4 or more times per year) who have had an initial response to a maximum of 6 weeks treatment of twice daily tacrolimus ointment (lesions cleared, almost cleared or mildly affected).
适用物种
兽用药物ATC编码
首次发布日期2007/05/03
最后更新日期2008/10/29
产品说明书https://www.ema.europa.eu/en/documents/product-information/protopy-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/protopy
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