Pediatric licensing status and the availability of suitable formulations for new medical entities approved in the United States between 1998 and 2002

被引:18
作者
Balakrishnan, Komathi [1 ]
Grieve, Joanne
Tordoff, June
Norris, Pauline
Reith, David
机构
[1] Univ Otago, Sch Pharm, Dunedin, New Zealand
[2] Univ Otago, Dunedin Sch Med, Dunedin, New Zealand
关键词
pediatric licensing; new medical entities; formulations; off-label;
D O I
10.1177/0091270006290509
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The availability of new medical entities for children in the United States was examined at the time of marketing approval and 3 years later. New medical entities approved in the United States in each of the years 1998 to 2002 were identified using the Center for Drug Evaluation and Research Web site. Each Physicians' Desk Reference published in the years 1998 to 2005 was examined to determine formulations and licensing information. For the 133 new medical entities licensed to be marketed in the period 1998 to 2002, the number licensed for children increased from 5 (4%) to 39 (29%) in the 3 years after registration. After 3 years' marketing, 79 (59%) drugs were in formulations suitable for children, and 27 (20%) of the newmedical entities were licensed and had a suitable formulation for children. Incentives to improve access for children to medicines should focus more on demonstration of improved access.
引用
收藏
页码:1038 / 1043
页数:6
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