分为外部报告系统和内部报告系统两类。内部报告系统主要以个人为报告单位,由医院护理主管部门自行管理的报告系统。外部报告系统主要以医院护理主管部门为报告单位,由卫生行政部门或行业组织管理的报告 系统
此外,从美国FDA的“不良事件报告系统”(Adverse Events Reporting System)也能看出药物安全性问题的重大。
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疫苗不良事件报告系统 VAERS ; Vaccine Adverse Event Reporting System
的不良事件报告系统 adverse-event reporting system
截止到2006年9月,美国疫苗不良事件报告系统总共收到17份病例报告(在接种后6周发生GBS)。
As of September 2006, a total of 17 cases had been reported to the US Vaccine Adverse Event Reporting System as occurring within 6 weeks after vaccination.
疾病防治中心表示,疫苗不良事件报告系统(VAERS)也没有发现受到该召回影响的疫苗相关的任何问题。
The CDC said the vaccine Adverse Event Reporting System (VAERS) had also not detected any problems in connection with the vaccines affected by this recall.
2004年,有68%的国家报告存在监测免疫接种后不良事件的国家系统,而2001年为53%。
In 2004, 68% of countries reported the existence of a national system for the surveillance of AEFI, compared with 53% in 2001.
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