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将间质性肺病报告为药品不良反应的地域差异:欧洲药品管理局对EudraVigilance报告的分析结果

Geographical variation in reporting Interstitial Lung Disease as an adverse drug reaction: findings from an European Medicines Agency analysis of reports in EudraVigilance.

作者信息

Pinheiro Luis, Blake Kevin, Januskiene Justina, Yue Qun-Ying, Arlett Peter

机构信息

European Medicines Agency, Inspections and Human Medicines Pharmacovigilance Division, London, United Kingdom of Great Britain and Northern Ireland.

Läkemedelsverket (Medical Product Agency Sweden), Pharmacovigilance, Uppsala, Sweden.

出版信息

Pharmacoepidemiol Drug Saf. 2016 Jun;25(6):705-12. doi: 10.1002/pds.3998. Epub 2016 Mar 22.

Abstract

PURPOSE

Clinically, interstitial lung disease (ILD) is a heterogeneous group of over 150 respiratory disorders. In the context of its signal evaluation work, the European Medicines Agency's (EMA) Pharmacovigilance Risk Assessment Committee (PRAC) has seen geographic clustering of case reports of ILD from Japan. To explore this further, EudraVigilance (EV), the EMA's database of adverse drug reactions (ADRs), was analysed. The results have been used to inform on implications for pharmacovigilance including signal detection and evaluation activities.

METHODS

EV was queried for reports of respiratory ADRs coded using MedDRA for the period 1994-2014 for all medicinal products. Descriptive statistics and non-parametric (chi-square) independence tests were produced to compare reporting of ILD from Japan versus the rest of the world.

RESULTS

As of 31 December 2014, there were 26 551 case reports of ILD in EV of which 17 526 (66%) originated in Japan. The reporting rate of ILD for Japan has been consistently higher over the period. The odds that a case report from Japan in EV refers to ILD is OR = 20.7, 95% CI 20.2, 21.3 (p < 0.001), compared to OR = 0.60, 95% CI 0.54, 0.67 (p < 0.001) for pulmonary fibrosis.

CONCLUSIONS

A geographic imbalance between Japan and the rest of the world in reporting respiratory ADRs as ILD is confirmed. Consequently, the PRAC has developed approaches to address this in relation to signals of ILD it assesses to allow for more targeted risk minimisation including updates to the product information in the EU setting. Copyright © 2016 John Wiley & Sons, Ltd.

摘要

目的

临床上,间质性肺疾病(ILD)是一组超过150种呼吸系统疾病的异质性疾病。在其信号评估工作中,欧洲药品管理局(EMA)的药物警戒风险评估委员会(PRAC)发现来自日本的ILD病例报告存在地域聚集性。为进一步探究这一情况,对EMA的药品不良反应(ADR)数据库EudraVigilance(EV)进行了分析。研究结果已用于为药物警戒的相关影响提供信息,包括信号检测和评估活动。

方法

查询EV中1994年至2014年期间所有药品使用MedDRA编码的呼吸系统ADR报告。进行描述性统计和非参数(卡方)独立性检验,以比较日本与世界其他地区的ILD报告情况。

结果

截至2014年12月31日,EV中有26551例ILD病例报告,其中17526例(66%)来自日本。在此期间,日本的ILD报告率一直较高。与EV中来自日本的病例报告提及肺纤维化的比值比(OR)=0.60,95%置信区间(CI)0.54,0.67(p<0.001)相比,来自日本的病例报告提及ILD的比值比为OR=20.7,95%CI 20.2,21.3(p<0.001)。

结论

证实了日本与世界其他地区在将呼吸系统ADR报告为ILD方面存在地域不平衡。因此,PRAC已制定方法来解决其评估的ILD信号相关问题,以便更有针对性地降低风险,包括更新欧盟环境下的产品信息。版权所有©2016约翰威立父子有限公司。

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