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Rosiglitazone use and associated adverse event rates in Canada between 2004 and 2010

机译:2004年至2010年间加拿大使用罗格列酮的使用及相关的不良事件发生率

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Background We examined the change in the use of rosiglitazone-containing products (RCPs) Canada-wide between 2004 and 2010 and whether the rates of adverse events in association with RCP therapy in Canadian patients changed in this period to better understand the real world use of RCP medications and as part of a regulatory commitment by GlaxoSmithKline to Health Canada to assess whether there was an impact of a risk communication on cardiac safety. Methods RCP utilization data were obtained from IMS Brogan’s longitudinal de-identified patient database (known as LRx) that tracks prescription activity using store-based data collection from pharmacies in all Canadian provinces. Adverse events (AEs), serious adverse events (SAEs) and cardiac AEs associated with RCP use in Canadian patients between April 2004 and December 2010 were identified from GlaxoSmithKline’s AE database and, using the LRx data, rates per 100,000 patients were estimated. Results A total of 239,184 patients were identified as having received at least one RCP prescription between 2004 and 2010 from the LRx. After excluding those with inconsistent gender or age, only one RCP prescription at the pharmacy, a prescription from a pharmacy that had not consistently reported for the past six years or an unreasonably high number of prescriptions, 180,936 patients remained for the analysis. The number of reports identified from the AE database that occurred between April 2004 and December 2010 was 1,037. The average monthly rates of AEs, SAEs and cardiac AEs decreased by 57%, 43% and 4%, respectively, between the observed periods, April 2004-October 2007 and November 2007-December 2010. Conclusions The findings of this analysis demonstrate a significant decrease in RCP use in Canada following a meta-analysis publication suggesting harm, which has been maintained. It is not possible to disentangle whether the continuing decline can be attributed to the meta-analysis, the changes in prescribing guidelines, media attention or a combination of some or all of these factors.
机译:背景我们研究了2004年至2010年加拿大范围内含罗格列酮产品(RCP)的使用变化,以及在此期间加拿大患者中与RCP治疗相关的不良事件发生率是否发生变化,以更好地了解现实世界中使用罗格列酮的产品RCP药物是葛兰素史克(GlaxoSmithKline)向加拿大卫生部(Health Canada)监管承诺的一部分,以评估风险沟通是否对心脏安全性产生影响。方法RCP利用率数据来自IMS Brogan的纵向身份不明患者数据库(称为LRx),该数据库使用来自加拿大所有省份药房的基于商店的数据收集来跟踪处方活动。从GlaxoSmithKline的AE数据库中确定了2004年4月至2010年12月之间加拿大患者中与RCP使用相关的不良事件(AE),严重不良事件(SAE)和心脏AE,并使用LRx数据估算了每100,000名患者的发生率。结果在2004年至2010年期间,总共239,184名患者被确认接受了至少一种LRx的RCP处方。在排除性别或年龄不一致的患者之后,该药房仅保留一份RCP处方,在过去六年中未连续报告的药房处方或处方数量不合理地过多,其余180,936名患者需要进行分析。从AE数据库中识别出的2004年4月至2010年12月之间的报告数量为1,037。在观察到的2004年4月至2007年10月和2007年11月至2010年12月之间,AE,SAE和心脏AE的平均月率分别下降了57%,43%和4%。结论该分析结果表明在一项荟萃分析表明存在危害之后,加拿大的RCP使用量有所减少,这一观点一直得到维持。无法确定持续下降是否归因于荟萃分析,处方指南的变化,媒体的关注或这些因素中的一些或全部的结合。

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