AERS：不良事件报告系统

“不良事件报告系统”（Adverse Event Reporting System）在专业领域中常被简称为AERS，这一缩写便于快速记录和日常使用。该系统主要用于收集和监测药物、医疗器械等产品的安全性数据，尤其在美国食品药品监督管理局（FDA）的监管工作中扮演着关键角色。通过标准化的报告流程，AERS有助于及时发现潜在风险，保障公共健康安全。

Adverse Event Reporting System具体释义

  • 英文缩写：AERS
  • 英语全称：Adverse Event Reporting System
  • 中文意思：不良事件报告系统
  • 中文拼音：bù liáng shì jiàn bào gào xì tǒng
  • 相关领域： aers fda

Adverse Event Reporting System的英文发音

例句

  1. Quarterly reports that list certain drugs that are being evaluated for potential safety issues, based on a review of information in the FDA's Adverse Event Reporting System(AERS) ( AERS );
  2. 季度报告列出某些被评估有潜在安全问题的药物，这是基于对FDA不良反应事件报告系统内信息的审查。
  3. Establishment and effectiveness of non-punitive adverse event reporting system
  4. 非惩罚不良事件上报系统的建立及效果
  5. The CDC's Vaccine Adverse Event Reporting System(AERS) ( VAERS ) finds no link between Gardasil and adverse events reported by doctors and vaccine recipients.
  6. CDC的疫苗不良反应事件监测中心（VAERS）没有发现加德西与医生和疫苗接种者报告的不良反应事件之间存在联系。
  7. The CDC said the Vaccine Adverse Event Reporting System(AERS) ( VAERS ) had also not detected any problems in connection with the vaccines affected by this recall.
  8. 疾病防治中心表示，疫苗不良事件报告系统(AERS)（VAERS）也没有发现受到该召回影响的疫苗相关的任何问题。
  9. The bigger issue is that the FDA's problem-ridden Adverse Event Reporting System(AERS) isn't a systematic measure of how often drugs really cause side effects.
  10. 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。

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