FDA launches new COVID-19 EUA FAERS Public Dashboard Today, the Food and Drug Administration launched an important update to the FDA Adverse Event Reporting System (FAERS) Public Dashboard. The FAERS Public Dashboard is a user-friendly search tool that improves access to data on adverse events associated with the use of drug and therapeutic biological products submitted to FAERS. During public health emergencies, the FDA may authorize Emergency Use Authorization (EUA) to facilitate the availability and use of medical countermeasures. To expand access to adverse event safety data during the COVID-19 public health emergency, FDA has launched the COVID-19 EUA FAERS Public Dashboard. This dashboard provides weekly updates of adverse event reports submitted to FAERS for drugs and therapeutic biological products used under an EUA during the COVID-19 public health emergency. The COVID-19 EUA FAERS Public Dashboard was made available to the public to increase transparency and provide more efficient access to safety information. | 
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