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Adverse drug reactions in a psychiatric department of tertiary care teaching hospital in India: Analysis of spontaneously reported cases

机译:印度三级教学医院一家精神科的药物不良反应:自发报告病例分析

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The epidemiological data are limited for the spontaneous adverse drug reaction (ADR) reporting system in psychiatry and its comparison with intensive monitoring studies in terms of causative drugs, seriousness, preventability and drug interactions. This spontaneous ADR reporting study was carried out over a period of three years in the psychiatry department. We adopted WHO definition for an ADR, Naranjo's algorithm for causality, WHO-ADR terminology for the labeling of involved organ-system, International conference on harmonisation (ICH) E2A guidelines for seriousness, modified Schumock and Thornton's criteria for preventability and Medscape drug interaction checker for drug interactions. Two subgroup analyses were performed to find out the risk factors for the serious and preventable reactions. A total of 97 ADRs from 67 patients were included for analysis. The incidence of 'overall' and 'serious ADRs were 0.69% (95% CI: 0.54%, 0.88%) and 0.18% (95% CI: 0.12-0.29%), respectively. The females experienced more ADRs than males. The most commonly reported ADR, incriminated pharmacology group and drug, were extrapyramidal movement disorders (22.68%), atypical antipsychotics (35.62%) and escitalopram (13.91%), respectively. One out of five and one out three reactions were considered as 'serious' and 'preventable', respectively. The drug interactions contributed in 34.02% reactions. The factors significantly associated with 'serious' reactions were typical antipsychotics [OR: 5.47 (1.68, 17.87)], central and peripheral nervous system disorders [OR: 24.00 (5.12,112.5)] and extrapyramidal reactions [OR: 14.03 (4.43,44.43)]. The polypharmacy [OR: 5.85 (1.90, 18.03)] was significantly associated with 'preventable' reactions. The spontaneous reporting system is efficient to detect serious reactions and preventable reactions.
机译:精神病学中自发性药物不良反应(ADR)报告系统的流行病学数据有限,并且其与致死性药物,严重性,可预防性和药物相互作用的深入监测研究的比较。这项自发的ADR报告研究是在精神病学部门进行了为期三年的研究。我们采用了WHO的ADR定义,Naranjo的因果算法,WHO-ADR的相关器官系统标签术语,国际协调统一性会议(ICH)E2A严重性指南,修改的Schumock和Thornton预防性标准以及Medscape药物相互作用检查器用于药物相互作用。进行了两个亚组分析,以找出严重和可预防反应的危险因素。纳入了来自67位患者的97个ADR进行分析。 “总体”和“严重ADR”的发生率分别为0.69%(95%CI:0.54%,0.88%)和0.18%(95%CI:0.12-0.29%)。女性的ADR比男性多。最常报告的ADR,隐含药理学组和药物分别为锥体外系运动障碍(22.68%),非典型抗精神病药(35.62%)和依他普仑(13.91%)。五分之一的反应和三分之一的反应分别被认为是“严重”和“可预防”。药物相互作用贡献了34.02%的反应。与“严重”反应显着相关的因素是典型的抗精神病药[OR:5.47(1.68,17.87)],中枢和周围神经系统疾病[OR:24.00(5.12,112.5)]和锥体束外反应[OR:14.03(4.43,44.43) )]。多元药房[OR:5.85(1.90,18.03)]与“可预防”反应显着相关。自发报告系统可有效检测严重反应和可预防反应。

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