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国家药监局和卫生部已明确了在我国要逐步建立和完善药品不良反应监测报告制度。我们基层医疗单位应积极参与。为确保这项工作制度化的顺利实施，我们认为应当做好以下几个方面的工作： 一、明确药品不良反应报告制度的法制地位 实施药品不良反应报告制度不仅是国家的要求，更?
State Food and Drug Administration and the Ministry of Health have made it clear that in our country we should gradually establish and improve the monitoring system for adverse drug reactions. Our primary medical units should actively participate. In order to ensure the smooth implementation of this work, we think that we should do the following work: First, to clarify the legal status of the adverse drug reaction reporting system To implement the adverse drug reaction reporting system is not only a national requirement,