FDA的不良事件报告系统（adverse-event reporting system， AERS）显示，2006年共登记有91例应用他汀类药物的患者发生ALS，这一数据引起了广大临床医生和研究者的关...
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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.
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.
更大的问题是，受问题支配的FDA的不良反应事件报告系统不能系统的衡量药品引起的真实副作用的多少。
The bigger issue is that the FDA's problem-ridden Adverse Event Reporting System isn't a systematic measure of how often drugs really cause side effects.
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