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- OBJECTIVE: To strengthen the ADR monitoring in medical institutions. 目的加强医疗机构药品不良反应(ADR)监测工作。
- Establishment of quantitative signal detection system can greatly enhance the efficiency of ADR monitoring. 不良反应定量信号检测系统的建立可以极大地提高药品不良反应监测工作的效率。
- We should be emphasize ADR monitoring,rational use of drug and prevention of AIAS. 应重视药品不良反应监测,合理用药,预防过敏性休克发生。
- Conclusion We should be emphasize ADR monitoring,rational use of drug and prevention of AIAS. 结论应重视药品不良反应监测,合理用药,预防过敏性休克发生。
- The evaluation and control for adverse drug reaction(ADR)reports quality are basic require-ments 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。
- 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。
- Retrospectively analysis the quality of 1 111 ADR cases in 2002 and 2 050 ADR cases in 2003 collected by ADR Monitoring Center of Jiangsu. 对江苏省药品不良反应监测中心2002年收集的1111份和2003年收集的2050份药品不良反应报告表的质量进行了回顾性分析。
- Method In virtue of Excel spreadsheet and causality assessment,463 ADR cases collected by Ningxia Center for ADR Monitoring of 2004 were analyzed. 方法应用Excel电子表格和因果关系评价方法对宁夏药品不良反应监测中心2004年收集的463份报告表进行统计分析和评价。
- Through strengthening ADR monitoring, quality of reports and ability of evaluation need to be improved to protect public health. 切实加强药品不良反应监测工作,提高报告质量和分析评价能力,为维护公众健康服务。
- Methods: 1013 ADR reports of traditional China medicines of PLA Center for ADR Monitoring in 2004 were classified andanalyzed. 方法:采用WHO的药物不良反应(ADR)因果关系判断标准,对全军药品不良反应监测中心2004年所收到的1013例抗感染药物不良反应报告进分析研究。
- Conclusion Our present ADR monitoring system needs to be improved in organization,com-munication,information and financial management. 结论我国建立药物警戒体系需要在组织机构、交流沟通、经费来源及信息技术等方面加以完善与改进。
- Objective To provide references for administration and ensure safety use of drug and provide bases for deep ADR monitoring. 目的为确保安全用药,深入开展不良反应监测工作提供依据。
- Objective To analyze the ADR reports of Panjin in 2007,bring the ADR monitoring into full play in the guarantee of medication safety. 目的汇总分析盘锦市2007年药品不良反应报告,发挥药品不良反应监测工作的指导作用,保障公众用药安全。
- In this paper, Pharmacovigilance in global perspective was reviewed in order to probe for the new tendency of the ADR monitoring. 本文论述目前药品不良反应监测工作在全球范围内的发展趋势,旨在探讨我国药品不良反应监测发展的新方向。
- Conclusion:Clinicians and pharmacists should strengthen the ADR monitoring after the medication to ensure the drug safety, effectiveness, rational drug use. 结论:临床医师与药师在患者使用药物之后要加强ADR监测,确保安全、有效、合理地用药。
- Carrying out ADR monitoring work is an important task for medical institutions, the strengthening of ADR monitoring can ensure safe drug use of patiaents. 开展ADR监测工作是医疗机构的重要任务,加强ADR监测是患者用药安全的保障。
- METHODS: 674 ADR cases induced by gatifloxacin collected in the Center of ADR Monitoring of Zhejiang Province during the recent three years were analyzed with Excel. 方法: 对浙江省药品不良反应监测中心近三年来收集的674例加替沙星ADR报告进行Excel列表分析。
- Methods: A retrospective investigation into 1 333 cases of ADR of cephalosporins collected by ADR Monitoring Centre of Shanghai from June 2003 to February 2005 was carried out. 方法:采用回顾性调查方法对2003年6月-2005年2月上海市药品不良反应中心收到的头孢菌素类抗生素所致1 333例ADR报告进行统计分折。
- Method Investigating, analyzing the construction mode of the regional ADR monitoring network by the practice of developing the regional ADR monitoring network in Shandong. 方法通过建立山东省基层药品不良反应监测网络的实践,研究、分析基层药品不良反应监测网络的建设模式。
- In order to give useful reference to the establishment of the ADR damage relief system in China, this article introduces the drug relief in Taiwan and analyses the ADR Monitoring in our country. 通过介绍台湾药害救济实践,对其有关定义、可获救济与不得救济的条件、法定鉴定机构等方面进行探讨,结合我国药品不良应监测工作的现状进行分析,以期为我国建立药品不良反应损害救济制度提供借鉴。