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那格浦尔英迪拉·甘地政府医学院及医院报告的药物不良反应。

Adverse drug reactions reported in Indira Gandhi Government Medical College and Hospital, Nagpur.

作者信息

Shrivastava Meena, Uchit Ganesh, Chakravarti Ashish, Joshi Gajanan, Mahatme Mohini, Chaudhari Harshal

机构信息

Department of Pharmacology, IGGMC, Nagpur.

出版信息

J Assoc Physicians India. 2011 May;59:296-9.

Abstract

OBJECTIVE

To detect the adverse drug reactions (ADRs) through spontaneous reporting system in IGGMC&H, Nagpur and analyze them using World Health Organization (WHO) assessment scales.

METHOD

An observational, prospective study was conducted based on ADRs reported between 1st June '05 to 31st May '09 to the ADR reporting unit of the hospital. The ADRs reported by spontaneous reporting system were from patients attending outpatient department (OPD), in-patient department (IPD) and casualty of IGGMC&H Nagpur. Evaluation of the data was done for various parameters which included patient demographics, drug and reaction characteristics, and outcome of the reactions. Assessment was also done for causality and severity.

RESULT

Total 2639 ADRs were reported with in the period from 1st June '05 to 31st May '09. Antimicrobial agents (AMA) were the drug class most commonly involved and Non Steroidal Anti-inflammatory Drugs (NSAIDs) were next to AMA. Cotrimoxazole a well established agent was the individual drug most frequently reported in this study. Upon causality assessment, majority of the reports were rated as probable (55.89%).

CONCLUSION

The pattern of ADRs reported in our hospital is comparable with the results of studies conducted in hospital set up elsewhere. AMAs were causing maximum ADRs. This study provides a database of ADRs due to common drugs used in our hospital, which will help clinicians for optimum and safe use of these drugs. Hence strict vigilance is required for the use of these likely drugs and their safety assessment.

摘要

目的

通过那格浦尔政府医学院和医院(IGGMC&H)的自发报告系统检测药物不良反应(ADR),并使用世界卫生组织(WHO)评估量表对其进行分析。

方法

基于2005年6月1日至2009年5月31日期间向医院ADR报告部门报告的ADR进行一项观察性前瞻性研究。自发报告系统报告的ADR来自那格浦尔IGGMC&H的门诊患者、住院患者和急诊患者。对包括患者人口统计学、药物和反应特征以及反应结果等各种参数的数据进行评估。还对因果关系和严重程度进行了评估。

结果

在2005年6月1日至2009年5月31日期间共报告了2639例ADR。抗菌药物(AMA)是最常涉及的药物类别,非甾体抗炎药(NSAIDs)仅次于AMA。复方新诺明这种常用药物是本研究中报告最频繁的单一药物。经因果关系评估,大多数报告被评为可能(55.89%)。

结论

我院报告的ADR模式与其他地方医院开展的研究结果相当。AMA引起的ADR最多。本研究提供了我院常用药物所致ADR的数据库,这将有助于临床医生优化和安全使用这些药物。因此,对于这些可能的药物及其安全性评估需要严格警惕。

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