Marchand M-S, Jonville-Béra A-P, Autret-Leca E
Service de pharmacologie clinique, centre régional de pharmacovigilance et d'information sur le médicament, CHRU de Tours, 2, boulevard Tonnellé, 37044 Tours, cedex 9, France.
Arch Pediatr. 2013 Mar;20(3):269-73. doi: 10.1016/j.arcped.2012.12.006. Epub 2013 Feb 1.
Montelukast (Singulair(®)) has been the subject of post-marketing warnings about psychiatric events occurring that had not been identified during clinical trials. The objective of this study was to take stock of the adverse events (AEs) related to montelukast reported in France. Cases of psychiatric disorders reported to regional pharmacovigilance centers (CRPV) and the literature data were analyzed. The 56psychiatric AEs account for 20% of all AEs reported in the montelukast CRPV: essentially sleep disorders, behavioral disorders and depression. This risk is also found in pharmacovigilance databases in other countries, especially in the North American database, which recorded a significant number of cases of "suicidality", including suicidal ideation, suicide attempts, and suicides. Analysis of clinical efficacy studies have failed to confirm these AEs. The potential severity of these events prompts physicians to seek the existence of psychiatric disorders before prescribing the drug and to carefully monitor the occurrence of AEs during treatment.
孟鲁司特(顺尔宁®)一直是上市后有关临床试验期间未发现的精神事件警告的对象。本研究的目的是评估法国报告的与孟鲁司特相关的不良事件(AE)。分析了向地区药物警戒中心(CRPV)报告的精神障碍病例和文献数据。56例精神性AE占孟鲁司特CRPV报告的所有AE的20%:主要是睡眠障碍、行为障碍和抑郁。其他国家的药物警戒数据库中也发现了这种风险,尤其是北美数据库,其中记录了大量“自杀倾向”病例,包括自杀意念、自杀未遂和自杀。对临床疗效研究的分析未能证实这些AE。这些事件的潜在严重性促使医生在开药前寻找精神障碍的存在,并在治疗期间仔细监测AE的发生。