Programme for Pharmacy, Faculty of Health Sciences, Oslo Metropolitan University, Oslo, Norway.
The Norwegian Medicines Agency, Grensesvingen 26, Oslo, Norway.
Eur J Clin Pharmacol. 2019 Aug;75(8):1153-1160. doi: 10.1007/s00228-019-02678-1. Epub 2019 Apr 18.
Antiepileptic drugs (AEDs) are increasingly used, and knowledge about adverse effects is scarce based on clinical studies. The purpose of the present study was to characterise adverse effects reports of AEDs in Norway relative to changes in utilisation in various indications from population-based data to elucidate important safety aspects of use of AEDs.
Aggregated data of adverse effects reported for AEDs in Norway from the EudraVigilance-database (2004-2013) in addition to indication-specific use of AEDs during 2004-2015 from the Norwegian Prescription Database were used.
The use of AEDs increased twofold the last decade due to use in psychiatry and neuropathic pain: lamotrigine, pregabalin, gabapentin, valproate, and carbamazepine. There were 1593 adverse effects reported (403 Individual Case Safety Reports, 2/3 women), 0-95 years (mean 46). Most adverse effects were reported for pregabalin (593), carbamazepine (265), lamotrigine (206), gabapentin (144), and valproate (119), where pregabalin had by far the highest reports in relation to the number of users. The most frequently reported adverse drug effects included rash, dizziness, cross-sensitivity reactions, and pyrexia. Overall, nervous system disorders constitute the largest organ class with the majority of the reports. Reporting of fatal outcomes is mandatory, and sudden unexplained death in epilepsy (SUDEP) was reported in 34 occasions.
This study demonstrates that most adverse effects reported concerned AEDs increasingly used in non-epilepsy indications: neuropathic pain (pregabalin, gabapentin, carbamazepine) and psychiatry (lamotrigine, valproate, carbamazepine). Pregabalin had the highest prevalence of adverse effects reported in relation to number of users. This elucidates an important part of pharmacovigilance for improved safety and considerations in clinical practice.
抗癫痫药物(AEDs)的应用日益增多,但基于临床研究,人们对抗癫痫药物不良反应的认识还很有限。本研究旨在通过基于人群的数据,描述挪威 AED 不良反应报告的特征,并结合各种适应证的使用变化,阐明 AED 使用的重要安全性方面。
本研究使用了挪威从 EudraVigilance 数据库(2004-2013 年)中汇总的 AED 不良反应报告数据,以及挪威处方数据库(2004-2015 年)中特定适应证 AED 使用数据。
过去十年中,由于精神科和神经病理性疼痛的应用,AED 的使用增加了两倍:拉莫三嗪、普瑞巴林、加巴喷丁、丙戊酸和卡马西平。共报告了 1593 例不良反应(403 例为个体病例安全报告,2/3 为女性),年龄 0-95 岁(平均 46 岁)。最常见的不良反应报告药物为普瑞巴林(593 例)、卡马西平(265 例)、拉莫三嗪(206 例)、加巴喷丁(144 例)和丙戊酸(119 例),其中普瑞巴林的报告数量与使用者数量之比最高。最常报告的药物不良反应包括皮疹、头晕、交叉过敏反应和发热。总体而言,神经系统疾病是最大的器官类别,占大多数报告。死亡结局的报告是强制性的,共报告了 34 例癫痫猝死(SUDEP)。
本研究表明,大多数报告的不良反应涉及在非癫痫适应证中越来越多地使用的 AED:神经病理性疼痛(普瑞巴林、加巴喷丁、卡马西平)和精神科(拉莫三嗪、丙戊酸、卡马西平)。普瑞巴林的使用者报告不良反应的比例最高。这阐明了药物警戒的一个重要方面,以提高安全性,并在临床实践中加以考虑。