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药物评估要求的不断变化。

Changing requirements for evaluation of pharmacologic agents.

作者信息

Chesney Russell W, Christensen Michael L

机构信息

Department of Pediatrics, Center for Pediatric Pharmacokinetics and Therapeutics, University of Tennessee, Memphis, USA.

出版信息

Pediatrics. 2004 Apr;113(4 Suppl):1128-32.

Abstract

Children sadly have been excluded from some of the therapeutic advances that have marked pharmaceutical drug development during the past 100 years. Most drugs in use today lack Food and Drug Administration approval for use in children or are restricted to certain pediatric age groups, predominantly older than 12 years. Only a few of the new drugs approved each year have pediatric indications and dosing guidelines described in the drug labeling information. However, many of these drugs are used in children. The lack of suitable information places children at risk for over- or underdosing, and there is a lack of suitable dosage forms, which can result in improper drug administration. This lack of information on the safe and effective use of drugs in the most vulnerable patients--infants and neonates--is of greatest concern. Recent changes in the regulations that govern drug development has dramatically increased the number of drugs that undergo testing in children. This article reviews new laws that govern drug testing in children and the use of children in therapeutic research.

摘要

令人遗憾的是,在过去100年标志着药物研发的一些治疗进展中,儿童被排除在外。目前使用的大多数药物未获得美国食品药品监督管理局(FDA)用于儿童的批准,或仅限于某些儿科年龄组,主要是12岁以上的儿童。每年批准的新药中,只有少数在药品标签信息中描述了儿科适应症和给药指南。然而,这些药物中有许多都用于儿童。缺乏合适的信息使儿童面临用药过量或不足的风险,并且缺乏合适的剂型,这可能导致用药不当。在最脆弱的患者——婴儿和新生儿——中,缺乏关于药物安全有效使用的信息是最令人担忧的。管理药物研发的法规最近发生的变化极大地增加了在儿童中进行测试的药物数量。本文回顾了管理儿童药物测试以及儿童在治疗研究中使用的新法律。

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