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首页> 外文期刊>Drug safety: An international journal of medical toxicology and drug experience >Adverse event reporting patterns of newly approved drugs in the USA in 2006: An analysis of FDA adverse event reporting system data
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Adverse event reporting patterns of newly approved drugs in the USA in 2006: An analysis of FDA adverse event reporting system data

机译:2006年美国新批准的新批准药物的不良事件报告模式:对FDA不良事件报告系统数据的分析

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Background: The Weber effect states that adverse event (AE) reporting tends to increase in the first 2 years after a new drug is placed onto the market, peaks at the end of the second year, and then declines. However, since the Weber effect was originally described, there has been improvement in the communication of safety information and new policies regarding the reporting of AEs by healthcare professionals and consumers, prompting reassessment of the existence of the Weber effect in the current AE reporting scenario. Objectives: To determine the AE reporting patterns for new molecular entity (NME) drugs and biologics approved in 2006 and to examine these patterns for the existence of the Weber effect. Methods: Publicly available FDA Adverse Event Reporting System data were used to assess the AE reporting patterns for a 5-year period from the drug's approval date. The total number of annual reports from all sources, based on the report date, was plotted against time (in years). Results: In the period from 2006 to 2011, a total of 91,187 AE reports were submitted for 19 NMEs approved in 2006. The highest number of AE reports were submitted for varenicline tartrate (N = 47,158) and the lowest number for anidulafungin (N = 161). Anidulafungin was reported to have the highest proportion of death reports (36 %) and varenicline tartrate the lowest proportion (1.7 %). The classic Weber pattern was not observed for any of the 19 NMEs approved in 2006. While there was no one predominant pattern of AE report volume, we grouped the drugs into four general categories; the majority of drugs had either a continued increase in reports (Category A 31.6 %) or an N-pattern with reporting reaching an initial peak in year 2 or 3, declining and then beginning to climb again (Category B 42.1 %). Conclusions and relevance: There have been numerous changes in AE reporting, particularly a huge increase in overall annual report volume, since the Weber effect was first reported. Our results suggest that a Weber-type reporting pattern should not be assumed in the design or interpretation of analyses based on AE reports.
机译:背景:韦伯效应指出不良事件(AE)报告趋于在新药物被置于市场上的前2年后,第二年结束的峰值,然后拒绝。但是,由于最初描述了韦伯效应,因此在医疗保健专业人员和消费者通过医疗保健和消费者报告AE的报告,促进了对当前AE报告情景中的韦伯效应的存在的沟通。目的:确定2006年批准的新分子实体(NME)药物和生物学的AE报告模式,并检查这些模式以存在韦伯效应。方法:公开可用的FDA不良事件报告系统数据用于评估药物批准日期为5年期间的AE报告模式。根据报告日期,根据报告日期间的每年报告总数(多年)绘制。结果:在2006年至2011年期间,2006年批准的19名纽约州纳米的报告总共提交了91,187个AE报告。为anidulafungin的varenicline(n = 47,158)提交了最高的AE报告数量(n = 47,158)(n = 161)。据报道,Anidulafungin具有最高比例的死亡报告(36%)和肢体曲线比例最低(1.7%)。 2006年批准的19个纽纳斯中的任何一个未观察到经典的韦伯模式。虽然没有AE报告量的一个主要模式,我们将药物分为四个一般类别;大多数药物的报告(31.6%)或N-Pattern持续增加,报告在2或3年内达到初始峰,然后再次开始攀升(B 42.1%)。结论和相关性:AE报告中有许多变化,特别是年度报告量的巨大增加,因为韦伯效应是首次报道的。我们的结果表明,不应在基于AE报告的分析的设计或解释中假设Weber型报告模式。

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