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根据国家2011年颁布《药品不良反应报告和监测管理办法》,药品不良反应(ADR)是指合格药品在正常用法用量下出现的与用药目的无关的有害反应~([1])。几乎所有的药物都可引起ADR,只是反应的程度和发生率不同。近年来,ADR的发生率呈逐年增长的态势。ADR的监测与报告是及时有效控制药品风险、保障公众用药安全的重要途径,其报告的内容和统计资料是加强药品监督管理、指导合理用药的依据。本文将我院
According to the State Administration of Drug Accident Response Reporting and Monitoring Management Measures promulgated in 2011, adverse drug reactions (ADRs) refer to the adverse reactions unrelated to the purpose of the drug (1) occurring at the normal dosage of the eligible drugs. Almost all drugs can cause ADR, but the extent of the reaction and the incidence of different. In recent years, the incidence of ADR showed a trend of increasing year by year. The monitoring and reporting of ADR is an important way to effectively and timely control the risks of medicines and ensure the safety of medicines for the public. The contents and statistical data of the reports are the basis for strengthening drug supervision and management and guiding the rational use of medicines. This article will be my hospital