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药品不良反应(ADR)是指合格药品在正常的用法用量时发生的与治疗目的无关的不良反应。这一定义把发生ADR的药品限定为质量合格,正常用法用量。可见,发生ADR是一种正常现象。开展ADR监察工作也是各级医疗卫生单位的一项法定任务。我院在各级主管部门的支持下,自2005-06始设立了A
Adverse Drug Reactions (ADRs) refer to adverse reactions that are not associated with the purpose of treatment and occur at normal usage levels of the eligible drug. This definition limits the occurrence of ADR drugs to acceptable quality and normal usage. Visible, ADR occurs is a normal phenomenon. Conducting ADR surveillance is also a statutory task for medical and health units at all levels. With the support of the competent departments at all levels, our hospital has set up A since 2005-06