Mosholder Andrew D, Gelperin Kate, Hammad Tarek A, Phelan Kathleen, Johann-Liang Rosemary
Office of Surveillance and Epidemiology, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, , MD 20993-0002, USA.
Pediatrics. 2009 Feb;123(2):611-6. doi: 10.1542/peds.2008-0185.
To gain a better understanding of the capacity of psychostimulant medications to induce adverse psychiatric reactions and determine the frequency of such reactions, we analyzed postmarketing surveillance data and clinical trial data for drugs, either approved or under development, for the treatment of attention-deficit/hyperactivity disorder.
The US Food and Drug Administration requested manufacturers of drugs approved for attention-deficit/hyperactivity disorder or with active clinical development programs for that indication to search their electronic clinical trial databases for cases of psychosis or mania using prespecified search terms. The manufacturers supplied descriptions of clinical trials, numbers of patients exposed to study drug, and duration of exposure to permit calculations of incidence rates. Independently, cases of psychosis or mania in children and adults for drugs used to treat attention-deficit/hyperactivity disorder from the Food and Drug Administration Adverse Event Reporting System safety database were analyzed. Manufacturers were asked to conduct similar analyses of their postmarketing surveillance databases.
We analyzed data from 49 randomized, controlled clinical trials in the pediatric development programs for these products. A total of 11 psychosis/mania adverse events occurred during 743 person-years of double-blind treatment with these drugs, and no comparable adverse events occurred in a total of 420 person-years of placebo exposure in the same trials. The rate per 100 person-years in the pooled active drug group was 1.48. The analysis of spontaneous postmarketing reports yielded >800 reports of adverse events related to psychosis or mania. In approximately 90% of the cases, there was no reported history of a similar psychiatric condition. Hallucinations involving visual and/or tactile sensations of insects, snakes, or worms were common in cases in children.
Patients and physicians should be aware that psychosis or mania arising during drug treatment of attention-deficit/hyperactivity disorder may represent adverse drug reactions.
为了更好地了解精神振奋药物引发不良精神反应的能力并确定此类反应的发生频率,我们分析了已批准或正在研发的用于治疗注意力缺陷/多动障碍的药物的上市后监测数据和临床试验数据。
美国食品药品监督管理局要求已批准用于注意力缺陷/多动障碍或有该适应症活跃临床开发项目的药物制造商,使用预先指定的搜索词在其电子临床试验数据库中搜索精神病或躁狂症病例。制造商提供了临床试验描述、接触研究药物的患者数量以及接触持续时间,以便计算发病率。独立地,对来自食品药品监督管理局不良事件报告系统安全数据库中用于治疗注意力缺陷/多动障碍的药物在儿童和成人中发生的精神病或躁狂症病例进行了分析。要求制造商对其上市后监测数据库进行类似分析。
我们分析了这些产品儿科开发项目中49项随机对照临床试验的数据。在这些药物进行的743人年双盲治疗期间,共发生了11起精神病/躁狂症不良事件,而在同一试验中总计420人年的安慰剂暴露期间未发生类似不良事件。合并活性药物组每100人年的发生率为1.48。对自发的上市后报告的分析产生了800多份与精神病或躁狂症相关的不良事件报告。在大约90%的病例中,没有报告过类似精神疾病的病史。涉及昆虫、蛇或蠕虫的视觉和/或触觉幻觉在儿童病例中很常见。
患者和医生应意识到,在注意力缺陷/多动障碍药物治疗期间出现的精神病或躁狂症可能代表药物不良反应。