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我们所承担的风险:审评速度和行业用户费用对新药安全性的影响。

The risk we bear: the effects of review speed and industry user fees on new drug safety.

作者信息

Olson Mary K

机构信息

Department of Economics, Tulane University, 6823 St. Charles Avenue, New Orleans, LA 70118-5698, USA.

出版信息

J Health Econ. 2008 Mar;27(2):175-200. doi: 10.1016/j.jhealeco.2007.10.007. Epub 2007 Nov 29.

Abstract

Drug review speed has increased substantially in the 1990s, largely due to industry-funded user fees. Following several drug withdrawals, however, new questions have emerged about the effects of this change on drug safety. This article examines the impact of review speed and user fees on counts of serious adverse reactions among drugs approved in 1990-2001. The analysis controls for the influence of drug utilization, patient conditions, drug novelty, black box warnings, foreign drug launch, US launch lags, patient age, and gender on drug reactions. Results show that drugs receiving faster reviews are associated with increased counts of serious adverse drug reactions. Other results show that novel drugs, drugs with black box warnings, drugs first launched abroad, and drugs with shorter US launch lags also have increased adverse drug reactions. Although any increase in risks must be weighed against benefits, the results show a trade-off between review speed and drug safety.

摘要

20世纪90年代药品审评速度大幅提高,这主要归功于行业资助的用户费。然而,在几种药物撤市后,关于这一变化对药物安全性的影响出现了新的问题。本文研究了审评速度和用户费对1990年至2001年批准药物中严重不良反应数量的影响。该分析控制了药物使用、患者病情、药物新颖性、黑框警告、国外药物上市、美国上市滞后、患者年龄和性别对药物反应的影响。结果表明,审评速度较快的药物与严重药物不良反应数量增加有关。其他结果表明,新型药物、有黑框警告的药物、首次在国外上市的药物以及美国上市滞后时间较短的药物,其药物不良反应也有所增加。尽管任何风险增加都必须与益处相权衡,但结果显示在审评速度和药物安全性之间存在权衡。

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