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.
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.
FDA希望，在不良事件报告、上市后分析、器械召回和库存文档管理的情况下，该系统能够更加有效和准确地识别器械。
The FDA hopes this will lead to more efficient and accurate identifying of devices in the case of adverse event reporting, post-market analysis, managing device recalls and inventory documentation.
FDA希望，在不良事件报告、上市后分析、器械召回和库存文档管理的情况下，该系统能够更加有效和准确地识别器械。
The FDA hopes this will lead to more efficient and accurate identifying of devices in the case of adverse event reporting, post-market analysis, managing device recalls and inventory documentation.
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