第七十一条国家实行药品不良反应报告制度。
Article 71 The State applies a system of report on adverse drug reaction.
药品不良反应报告质量的评价与控制是药品不良反应监测工作的基本要求。
The evaluation and control for adverse drug reaction (ADR) reports quality are basic requirements for ADR monitoring.
结论从填写完整性和报告时限性上都反映出药品不良反应报告质量有待提高。
Conclusion The quality of ADR reports should be improved in integrality and reporting time limit.
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