In January 2021, a contractor operating the federal Vaccine Adverse Event Reporting System (VAERS) reported that the volume of Wuhan coronavirus (COVID-19) vaccine adverse event reports had overwhelmed its processing capacity, according to a memo from General Dynamics Information Technology (GDIT) to the Centers for Disease Control and Prevention (CDC).
The memo, dated Jan. 15, 2021, stated that incoming reports “significantly exceeded the estimated maximum of 1,000 reports per day.” One month later, on Feb. 19, 2021, the CDC’s Morbidity and Mortality Weekly Report (MMWR) published an early safety review of the first COVID-19 vaccines authorized for emergency use in the United States.
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