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首页> 外文期刊>Pharmacoepidemiology and drug safety >Quality check of spontaneous adverse drug reaction reporting forms of different countries.
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Quality check of spontaneous adverse drug reaction reporting forms of different countries.

机译:不同国家的自发不良药物反应的质量检查。

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Adverse drug reactions (ADRs) are considered as one of the leading causes of death among hospitalized patients. Thus reporting of adverse drug reactions become an important phenomenon. Spontaneous adverse drug reaction reporting form is an essential component and a major tool of the pharmacovigilance system of any country. This form is a tool to collect information of ADRs which helps in establishing the causal relationship between the suspected drug and the reaction. As different countries have different forms, our aim was to study, analyze the suspected adverse drug reaction reporting form of different countries, and assess if these forms can capture all the data regarding the adverse drug reaction. For this analysis we identified 18 points which are essential to make a good adverse drug reaction report, enabling proper causality assessment of adverse reaction to generate a safety signal. Adverse drug reaction reporting forms of 10 different countries were collected from the internet and compared for 18 points like patient information, information about dechallenge-rechallenge, adequacy of space and columns to capture necessary information required for its causality assessment, etc. Of the ADR forms that we analyzed, Malaysia was the highest scorer with 16 out of 18 points. This study reveals that there is a need to harmonize the ADR reporting forms of all the countries because there is a lot of discrepancy in data captured by the existing ADR reporting forms as the design of these forms is different for different countries. These incomplete data obtained result in inappropriate causality assessment. Copyright (c) 2010 John Wiley & Sons, Ltd.
机译:不良药物反应(ADRS)被认为是住院患者中死亡原因之一。因此,报告不良药物反应成为一个重要现象。自发的不良药物反应报告表是任何国家的药理治系统的必要组成部分和主要工具。此表格是收集ADR信息的工具,有助于建立疑似药物与反应之间的因果关系。由于不同的国家具有不同的形式,我们的目的是研究,分析不同国家的疑似不良药物反应报告形式,并评估这些形式是否可以捕获有关不良药物反应的所有数据。对于这种分析,我们确定了18个点,这对于制造良好的不利药物反应报告至关重要,可以适当地对不良反应进行不良反应来产生安全信号的原因评估。从互联网收集了10个不同国家的不良药物反应形式,并比较了18个点,如患者信息,有关Dechallenge-Rechallenge的信息,空间和专栏的充分性捕获其因果关系评估所需的必要信息。我们分析的是,马来西亚是最高的分光器,18分18分。本研究表明,需要协调所有国家的ADR报告形式,因为现有的ADR报告表格捕获的数据存在很多差异,因为这些形式的不同国家不同。这些不完整的数据获得了不适当的因果关系评估。版权所有(C)2010 John Wiley&Sons,Ltd。

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