【摘要】 通过分析2006年徐州市药品不良反应报告表存在的问题,提出在开展药品不良反应监测工作中应当采用报告表规范化、多专业合作、地区疑难报告表分析评估交流、上报人资格认定等多种方式以提高药品不良反应报告表的质量。更多还原

【Abstract】 This paper analyzes the existing problems for the quality of statements in adverse drug reac-tions reports of Xuzhou in 2006. The ADR monitoring should be more standardized,professional co-operation,regional exchanges in analysis and assessment for the difficult statements report and reported people were identified in the qualifications to improve the quality of ADR reports.更多还原