The types of overseas sports dispute ADR and the cases used its ruling sports dispute have provided the model for the construction our country sports dispute ADR.
国外体育纠纷adr的类型和利用其裁决体育纠纷的案例为我国体育纠纷adr的构建提供了可借鉴的范例。
Conclusion Monitoring ADR is the effective method to prevent the occurrence of ADR, promote reasonable drug application and ensure the safety of drug use.
结论监测药品不良反应，预防药品不良反应的发生，是促进合理用药及保障用药安全的有效手段。
On the other hand, we should attach great importance to ADR, and encourage the parties to settle disputes through ADR.
另一方面也应当高度重视ADR的作用，鼓励纠纷当事人使用ADR解决纠纷。
Gene polymorphism study can provide a new reference for the prevention of ADR. Gene detection can be conducted before drug treatment to reduce the incidence of ADR.
基因多态性研究可为预防adr提供新的参考依据，临床可在药物治疗前对患者进行基因型检测，以降低adr的发生率。
METHODS: To introduce the ADR victims relief system of Japan, analyse the significance of establishment and practice of ADR victims relief system in China.
方法：介绍日本药品不良反应被害救济制度，分析药品不良反应被害救济制度在我国建立与实施的意义。
CONCLUSION: Quality of ADR report forms should be improved along with strengthening of ADR monitoring.
结论在加强adr监测的同时应采取措施，提高ADR报告的质量。
Conclusion the establishment of ADR database is beneficial to the storage and analysis of ADR information.
结论建立不良反应病案数据库有助于更好地储存分析病案信息。
Conclusion: We should strengthen the monitoring of ADR, decrease the rate of misreporting, collect other ADR cases except allergic reaction in multiple tracks and enhance the report quality.
结论：应加强ADR监测工作，降低漏报率，尤其应多途径收集过敏反应以外的药品不良反应，提高报表质量。
METHODS: 501cases of ADR reports in our city collected by ADR monitoring center in2004were classified and analyzed statistically.
方法：对我市2004年adr监测中心收集到的501例adr报告进行分类统计、分析。
Because of the limitation of ADR studies before approval market, it is very important to report ADR after approval market by regulation.
由于药品在获准上市前的不良反应研究的局限性，药品上市后依法报告药品不良反应尤其重要。
The evaluation and control for adverse drug reaction (ADR) reports quality are basic requirements for ADR monitoring.
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。
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.
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 By analyzing the relevant factor of adverse drug reaction(ADR) of Yanhuning injection in Zibo, to investigate the pattern and character of ADR.
目的了解炎琥宁注射剂不良反应发生的相关因素，探讨其不良反应发生的一般规律及特点。
The cost study includes the following3steps:defining ADR, estimating the incidence of ADR and measuring the costs of ADR.
进行成本研究具体分为3步：定义ADR、评估ADR发生率、进行ADR成本测算。
The Act demands all American Federal Courts to enforce the ADR measures of the service mode for litigants and permit the court forcing litigants to take part in the ADR procedure.
该法要求所有的美国联邦法院实施“当事人服务型”的ADR措施，并允许法院强制当事人参加ADR 程序。
METHODS: ADR compensation mechanism was analyzed; the drug injury economic systems of Taiwan region was introduced and the relation between ADR legal liability and the concerned law was proposed.
方法：分析adr补偿机制，介绍我国台湾的药害救济制度，提出adr的法律责任与有关法律关系。
Suggested that it is indispensable to carry out an ADR related knowledge training among nursing staffs, so that to enhance their recognition on the impairment of ADR.
有必要在护理人员中进行ADR监测有关知识的培训，以提高护理人员对ADR危害的认识。
CONCLUSION: We should strengthen the monitoring of ADR, extend the monitoring of ADR, decrease the factor of failing to report, improve the quality of ADR report gradually.
结论：重视ADR监测工作，不断拓展adr监测范围，尽量降低漏报率，逐步提高ADR报告质量。
Methods Discussion on how to solve ADR harm by revising the legal provision from the perspective of ADR and relief for it, and the social problems result from legal provision absence.
方法从药品不良反应、药品不良反应损害救济，以及现行《药品管理法》的法律缺失造成的社会问题出发，探讨如何从完善法律这一层面解决药品不良反应损害引发的问题。
Now, "ADR are few reported, especially new and severe ADR reports are few, the ADR reported by drug production enterprises are also few".
目前药品不良反应报告存在着“药品不良反应报告少，新的和严重的药品不良反应报告少，药品生产企业药品不良反应报告少”的现状。
Methods: 134 ADR reports of Levofloxacin collected by Taian Center for ADR Monitoring from 2006 to2007were analyzed using retrospective study method.
方法：采用回顾性分析方法对2006 ~ 2007年泰安市药品不良反应监测中心收到的134例左氧氟沙星不良反应病例报告进行统计分析。
This paper discussed problems in definition of ADR in regulation of Administrative Measures on Reporting and Monitoring of ADR, and put forward some proposals.
本文试对我国现行部门规章《药品不良反应报告和监测管理办法》中药品不良反应概念存在的问题进行探讨，提出修改建议。
OBJECTIVE: To standardize the administration of adverse drug reaction(ADR) monitoring in our hospital for the purpose of improving ADR monitoring work.
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 investigate the adverse drug reaction (ADR) induced by antineoplastics, and provide bases for deep ADR monitoring.
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 analyse the characteristics and the related factors of adverse drug reactions (ADR) occurred in our hospital, and establish the way of ADR clinical monitor in the next year.
目的分析我院药品不良反应(adr)发生特点和相关因素，制定新年度adr监测工作方向。
Objective to investigate the prevention and response of clinicians to disputes of adverse drug reactions (ADR), and explore effective ways for medical institutions to deal with disputes of ADR.
目的调查临床医师对药品不良反应(adr)纠纷的防范和应对情况，探索医疗机构防范和应对adr纠纷较为有效的方法。
Conclusion the monitoring and knowledge of ADR can be strengthened and avoid or reduce the recurrence. We will pay attention to the new or serious ADR.
结论应加强adr的监测和ADR知识的宣传，避免或减少其重复发生，对新的、严重的不良反应应引起重视。
Methods: The reports on 74 case of ADR collected by ADR monitoring group of our hospital were counted, classified and analyzed.
方法：对收集的74例不良反应报告进行统计分析及评价。
Objective to design a quantitative criterion and grading system for injury from adverse drug reaction (ADR) in order to serve the compensation system of injury from ADR.
目的设计药品不良反应(adr)伤害的量化分级标准和分级方法，为构建ADR补偿体系提供参考依据。
Objective to design a quantitative criterion and grading system for injury from adverse drug reaction (ADR) in order to serve the compensation system of injury from ADR.
目的设计药品不良反应(adr)伤害的量化分级标准和分级方法，为构建ADR补偿体系提供参考依据。
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