目的利用计算机、网络技术开展药品不良反应(adr)监测。
Objective to use computer and network technologies for Adverse Drug Reaction (ADR) monitoring.
目的探讨医疗机构开展药品不良反应(adr)监测工作的模式。
Objective to discuss on the monitoring mode of adverse drug reactions (ADR) that can be used by the medical organization.
目的了解抗肿瘤药物引起的不良反应，为深入开展药品不良反应监测工作提供依据。
Objective To investigate the adverse drug reaction (ADR) induced by antineoplastics, and provide bases for deep ADR monitoring.
因此，开展药品不良反应报告和监测管理工作已成为关系民生的重要方面，是深化医药卫生体制改革的必然要求。
Therefore, the adverse drug reaction monitoring report and management has become an important aspect of the relationship between people is deepening the reform of medical care system requirement.
本文强调了建立药品不良反应监测的重要性，论述了我国开展药品不良反应监测的现状，提出了今后的工作要点。
This paper stresses the importance of establishing an monitoring system for adverse reactions of drugs, and describes the present status in China. The main points in future work are put forward.
目的了解医务人员对药品不良反应（ADR）监测相关知识的认识和掌握情况，为更好的开展ADR监测工作提供依据和参考。
Objective To conduct a survey about adverse drug reactions(ADR) knowledge among medical staff in our hospital as to improve and promote the reporting and monitoring of ADR.
处方事件监测用非干预性、观察性药品不良反应监测方法，1981年在英国最早开展。
Prescription Event monitoring (PEM) is a non-interventional observational method of adverse drug reaction monitoring, which was established first in England in 1981.
结论：通过这种方法可以及时对病因假设进行初步验证，同时也为基于药品不良反应数据库开展相关研究提供了一种新思路。
Conclusion: in this way we can timely validate a pathogenic hypothesis and find a new way for developing the study that is based on the database.
目的分析本院药品不良反应报告情况，为临床合理用药提供参考，推进我院药品不良反应监测报告工作的开展。
Aim to supply optimal reference for the rational clinical use of drugs and promote the monitoring of adverse drug reactions in Huainan First Municipal Peoples Hospital.
前言： 目的：规范我院药品不良反应（ADR）监测工作的管理，促进ADR监测工作开展。
OBJECTIVE: To standardize the administration of adverse drug reaction(ADR) monitoring in our hospital for the purpose of improving ADR monitoring work.
目的推动药品不良反应监测工作的深入开展。
Objective to promote the ADR monitoring in-depth development.
结果与结论提出进一步推动药品不良反应监测工作深入开展的建议和对策。
Results and Conclusions Many countermeasures to further promote the ADR monitoring in-depth development are proposed.
方法：回顾我国药品不良反应监测专业机构的建立，阐述其工作职责及内容，评述已开展的工作。
METHODS:To review the establishment of specialized agency for monitoring ARDs in China; to describe its working duty and content; to comment the work which has been carried out.
目的：推进我院药品不良反应(adr)监测报告工作的开展。
OBJECTIVE: to facilitate the monitoring and reporting of ADR.
目的：推进我院药品不良反应(adr)监测报告工作的开展。
OBJECTIVE: to facilitate the monitoring and reporting of ADR.
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