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- Introduction on Medical Device Adverse Event Monitoring System in Canada 加拿大医疗器械不良事件监测系统
- Medical Device Adverse Event Monitoring System Development in China: Delphi Method 我国医疗器械不良事件监测体系建设之德尔菲法
- Current Situation Comparison of Medical Device Adverse Event Monitoring Among the Developed Countries 世界各国医疗器械不良事件监测现状比较
- Medical Device Adverse Event Monitoring System Development in China:Delphi Method 我国医疗器械不良事件监测体系建设之德尔菲法
- There was no iMRI-related adverse event occurred. 无iMRI相关不良事件发生。
- adverse event monitoring 不良事件监测
- 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。
- adverse events monitoring 不良事件监测
- Aim By analyzing adverse medical device event reports received in Anhui province,to promote instructional function of adverse medical device event monitoring to ensure safe use of medicine in public. 目的通过对收集到的医疗器械不良事件信息的汇总分析,发挥医疗器械不良事件监测工作的指导作用,以保障公众用械安全。
- Keyword: ZD1839 NSCLC Disease control rates Adverse events. 关键词:ZD1839非小细胞肺癌疾病控制率不良事件。
- Results. Of 25 subjects enrolled, scleral icterus was the most common adverse event (3 patients [12.5%]). 结果:在25名受试者中,巩膜黄染为最常见的副作用(3例,12.;5%25)。
- Adverse events were not significantly different in the two groups. 这两组成员在不良事件发生率方面也无明显差异。
- The adverse events during and after PCI were registered. 经PCI术的患者术后服用他汀类药物(3-6个月)及阿司匹林治疗。
- Objective Analyzed 239 cases of medical device adverse events (MDAE) and provide sugg-estion to MDAE monitoring. 目的对239例医疗器械不良事件报告进行分析,为加强医疗器械不良事件监测工作提供建议。
- Were the staff involved in the adverse event or close call properly qualified and trained to perform their functions? 牵涉不良事件当时和即将发生的员工,是否有适当的认证及训练以执行其职务?
- You can use event monitors to get a complete picture of activity. 您可以使用事件监视器来全面了解活动。
- Gynecomastia, with or without breast pain, is a frequent adverse event of treatment with this class of drugs. 这一类药物最常见的副作用,即男性女乳症或乳房疼痛。
- If I am a manufacturer, what information must I submit in my individual adverse event reports? 如果我是制造商,在我的个人不良事件报告中我必须提交什么信息?
- There was no adverse event related to the investigational product in this trial. 两组不良事件发生率无统计学差异。
- No serious adverse event data could be obtained in 6 trials enrolling a total of 2766 patients. 有共包括2766人的6个试验中没有提供关于严重不良事件的数据。