TEDDY EPMD: A European Paediatric Medicines Database

M. Felisi, R. Padula, F. Bartoloni, I. Grosch-Wörner, B. Kågedal, M. J. M. Peña, J. Parry, A. Stuchlík, K. Verhamme, A. Ceci
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Abstract

In line with European initiatives, TEDDY set up a new database, the European Paediatric Medicines Database, with the aim of creating a harmonised, integrated and reliable pan-European source of information. The data stored in the Database were the basis for examining the ‘state of the art’ of paediatric medicines licensed by the European Medicines Agency between October 1995 and December 2007. The results of the study show that 33% of medicinal products approved by the European Medicines Agency are intended for the paediatric population, and that this percentage has remained more or less constant in the 12 years of activity of the Agency. This trend is expected to increase rapidly in the future as a result of the adoption of the Paediatric Regulation. Nevertheless, it is essential that information on medicinal products for paediatric use are made publicly accessible and data should be verified and controllable. The European Medicines Agency has recently made public many information on medicines authorised in EU through the EudraPharm database. The TEDDY European Paediatric Medicines Database grants access also to information related to paediatric medicines, some of which are not available elsewhere. We deem this aspect a useful service to end users and a valid support to Regulatory Authorities.
TEDDY EPMD:欧洲儿科药物数据库
根据欧洲的倡议,TEDDY建立了一个新的数据库,欧洲儿科药物数据库,目的是创建一个协调、综合和可靠的泛欧信息源。存储在数据库中的数据是检查1995年10月至2007年12月期间欧洲药品管理局许可的儿科药物“最新技术”的基础。研究结果表明,欧洲药品管理局批准的药品中有33%是用于儿科人群的,并且在该机构12年的活动中,这一百分比基本保持不变。由于《儿科条例》的通过,这一趋势预计将在未来迅速增加。然而,至关重要的是,儿科用药的信息应公开可及,数据应得到核实和控制。欧洲药品管理局最近通过EudraPharm数据库公布了欧盟授权药品的许多信息。TEDDY欧洲儿科药物数据库还允许访问与儿科药物有关的信息,其中一些信息在其他地方无法获得。我们认为这方面对最终用户是有用的服务,也是对监管机构的有效支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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