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Adverse drug reactions from psychotropic medicines in the paediatric population: analysis of reports to the Danish Medicines Agency over a decade

机译:小儿精神科药物引起的药物不良反应:十年来丹麦药物管理局的报告分析

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Background The prescribing of psychotropic medicines for the paediatric population is rapidly increasing. In attempts to curb the use of psychotropic medicine in the paediatric population, regulatory authorities have issued various warnings about risks associated with use of these products in childhood. Little evidence has been reported about the adverse drug reactions (ADRs) of these medicines in practice. As spontaneous reports are the main source for information about previously unknown ADRs, we analysed data submitted to a national ADR database. The objective was to characterise ADRs reported for psychotropic medicines in the Danish paediatric population over a decade. Findings All spontaneous ADR reports from 1998 to 2007 for children from birth to 17 years of age were included. The unit of analysis was one ADR. We analysed the distribution of ADRs per year, seriousness, age and gender of the child, suspected medicine and type of reported ADR. A total of 429 ADRs were reported for psychotropic medicines and 56% of these were classified as serious. Almost 20% of psychotropic ADRs were reported for children from birth up to 2 years of age and one half of ADRs were reported in adolescents, especially for antidepressants and psychostimulants. Approximately 60% of ADRs were reported for boys. Forty percent of all ADRs were from the category 'nervous and psychiatric disorders'. All but one ADR reported for children below two years were serious and two of these were fatal. A number of serious ADRs reported in children from birth up to 2 years of age were presumably caused by mothers' use of psychotropic medicines during pregnancy. Conclusion The high number of serious ADRs reported for psychotropic medicines in the paediatric population should be a concern for health care professionals and physicians. Considering the higher number of birth defects being reported greater care has to be given while prescribing these drugs for pregnant women.
机译:背景技术针对小儿科人群的精神药物处方正在迅速增加。为了限制在儿科人群中使用精神科药物,监管机构已发布各种警告,说明在儿童期使用这些产品有相关风险。在实践中,关于这些药物的不良药物反应(ADR)的报道很少。由于自发报告是有关以前未知的ADR信息的主要来源,因此我们分析了提交给国家ADR数据库的数据。目的是表征十年来丹麦儿童人群中精神药物报道的ADR。结果包括从1998年到2007年的所有自发的出生至17岁儿童的ADR报告。分析单位是一个ADR。我们分析了每年的ADR分布,儿童的严重程度,年龄和性别,可疑药物和报告的ADR类型。总共报告了429种精神药物的ADR,其中56%被归为严重药物。据报告,从出生到2岁的儿童中,精神药物ADR的比例接近20%;青少年中,特别是抗抑郁药和精神刺激药的ADR比例为一半。据报道男孩中约有60%的ADR。所有ADR的40%来自“神经和精神疾病”类别。据报道,针对一名两岁以下儿童,除一项ADR以外,其他所有疾病都是严重的,其中两项是致命的。据报道,从出生到2岁的儿童中发生了许多严重的ADR,这是由于母亲在怀孕期间使用精神药物引起的。结论儿科人群中精神药物报道的严重ADR数量很高,这应引起医疗保健专业人员和医生的关注。考虑到报告的先天缺陷数量更多,在为孕妇开这些药物时必须给予更多的照顾。

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