欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Emend
适用类别Human
治疗领域Vomiting;Postoperative Nausea and Vomiting;Cancer
通用名/非专利名称aprepitant
活性成分aprepitant
产品号EMEA/H/C/000527
患者安全信息No
许可状态Authorised
ATC编码A04AD12
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2003/11/11
上市许可开发者/申请人/持有人Merck Sharp & Dohme B.V.
人用药物治疗学分组Antiemetics and antinauseants
兽用药物治疗学分组
审评意见日期2003/07/24
欧盟委员会决定日期2025/10/24
修订号33
治疗适应症Emend 40 mg hard capsules is indicated for the prevention of postoperative nausea and vomiting (PONV) in adults. Emend is also available as 80 mg and 125 mg hard capsules for the prevention of nausea and vomiting associated with highly and moderately emetogenic cancer chemotherapy in adults and adolescents from the age of 12 (see separate Summary of Product Characteristics). Emend is also available as 165 mg hard capsules for the prevention of acute and delayed nausea and vomiting associated with highly emetogenic cisplatin based cancer chemotherapy in adults and the prevention of nausea and vomiting associated with moderately emetogenic cancer chemotherapy in adults. Emend is also available as powder for oral suspension for the prevention of nausea and vomiting associated with highly and moderately emetogenic cancer chemotherapy in children, toddlers and infants from the age of 6 months to less than 12 years. Emend 80 mg, 125 mg, 165 mg hard capsules and Emend powder for oral suspension are given as part of combination therapy.
适用物种
兽用药物ATC编码
首次发布日期2018/05/24
最后更新日期2025/10/24
产品说明书https://www.ema.europa.eu/en/documents/product-information/emend-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/emend
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