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我州《药品不良反应/事件报告表》质量分析 被引量:3

Quality Analysis Report of "Adverse Drug Reaction/Event Reporting Form" in Western Hunan Autonomous Prefecture
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摘要 目的分析2008年湘西自治州《药品不良反应/事件报告表》的填写质量及存在的问题。方法采取随机抽样方法中的抽签法,以湘西自治州94家基层上报单位2008年度上报的所有类型的《药品不良反应/事件报告表》为样本总量,抽取16%的报告表作为样本,进行质量评价与分析。结果报告表分数在80分以上的为72份,占总数的59.5%。其中扣分点主要集中在患者的基本情况、不良反应情况、怀疑药品使用情况、关联性评价等项目。结论湘西自治州药品不良反应报告表总体质量一般,有表现集中的质量问题,应进行有针对性的培训,从而进一步提高报告质量。 Objective To analyze the quality filling in the "adverse drug reaction / incident report form" on 2008 in Western Hunan Autonomous Prefecture,and the existing problems.Methods A random sample of the ballot law was used,to be 94 report units in Xiangxi on 2008 to report all types of "Adverse Drug Reaction / Event Reporting Form" for the total sample,taking 16% of the reporting forms as samples for quality evaluation and analysis.Results Reports on the table scores 80 points or more were 72 reports,accounting for 59.5%.Marking the main point of which focused on the basic situation of the patient,adverse reactions,suspected drug use,relevance,evaluation and other projects.Conclusion The overall quality of Xiangxi adverse drug reaction reports is general.There are a lot of focus on quality issues arise,they should be carried out targeted training in order to further improve the quality of reports.
出处 《中国药事》 CAS 2010年第11期1105-1108,共4页 Chinese Pharmaceutical Affairs
关键词 药品不良反应/事件报告表 质量 分析 ADRs/Event Report Form quality analysis
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