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- This drug can also interact with other medications that patients may be taking and increase their risk of adverse drug events. 这种药物还会与病人服用的其他药物相互作用,增加药物不良反应的风险。
- There are a large amount of studies about MEs and Adverse Drug Events (ADEs) in some developed countries, while a few in China. 在一些发达国家已经对药物治疗错误（ME）和药物不良事件（ADE）进行了广泛研究，而在我国此类研究还非常少见。
- Abstract: The risk management for pharmaceutical products is a multidisciplinary method to document,momtor and evaluate adverse drug events （ADEs）, and plan interventions. 文章摘要: 目的简介药品风险管理的概念和方法，并附实例说明。
- Hospitals that use medication reconciliation at admission, discharge and before transfer to another care have reduced adverse drug events by up to 50%, IHI data indicate. 根据IHI统计，患者入院时、出院前及转诊前进行核对工作可以降低药物副作用达50%25。
- Adverse drug event 药物不良事件
- The rate of adverse drug reaction (ADR) in I group was 4.7%. [结果 ] 组有 194例为显效 ;显效率 82 .;6%25;不良反应发生率为 4
- Prescription Event Monitoring (PEM) is a non-interventional observational method of adverse drug reaction monitoring, which was established first in England in 1981. 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。
- METHODS 124 cases reports of Adverse Drug Reaction (ADR) were analyzed. 方法对124例药品不良反应(ADR)报告进行分析。
- Neurotoxicity is the most common adverse drug reaction seen in clinic. 神经系统毒性反应是药物常见的毒性反应。
- Adverse drug events 药品不良事件
- The literature on the Ciprofloxacin-induced adverse drug reactions (ADR) was reviewed in this article. 目的：综述环丙沙星引起的各种不良反应的文献报道。
- This study analyzes the methods, efficacy and adverse drug reactions (ADR) of domestic literatures on venlafaxine. 本文对该药的使用方法、临床疗效、不良反应等进行汇总分析。
- Lindahl K, Schvarcz, R.; Bruchfeld A.et al. Clinical pharmacology. Adverse drug interactions. BMJ 1981;282(6260):288-91. 行政院卫生署药品交互作用资料库教育训练讲义;2006.
- The analgesic effects and adverse drug reactions(ADR)after analgia 4h,8h,12h and 24h were observed and recorded. 分别于镇痛开始后4小时、8小时、12小时、24小时观察并记录镇痛效果及不良反应。
- Fluvoxamine treatment arising in the course of adverse drug reactions than clomipramine light. 氟伏沙明治疗过程中出现药物不良反应较氯米帕明轻。
- OBJECTIVE:To analyze the related factors that initiating the occurrence of adverse drug reactions (ADR). 目的 :了解我院药品不良反应 (ADR )发生及引发的相关因素。
- Objective: To evaluate adverse drug reaction (ADR) reports in Huzhou Adverse Drug Reaction Monitoring Center. 目的:对湖州市药品不良反应监测中心药品不良反应(ADR)报告进行综合评价与分析。
- He reported on the whole event to the minister. 他把整个事件向部长做了汇报。
- The clinical adverse drug reaction(ADR) rates were 5.6%(3/54) and 7.8%(4/51) in two groups respectively. 临床药物不良反应发生率分别为5.;6%25(3/54)和7
- Of 11 cases, 9 cases were classified as adverse drug resaction (ADR) , 2 cases were overdose. 11例中,9例属药物不良反应,2例属有意过量用药;
