U.S. officials are refusing to provide COVID-19 vaccine safety data to a U.S. senator.
Sen. Ron Johnson (R-Wis.) asked the U.S. Food and Drug Administration (FDA) for the results of analyses on data from the Vaccine Adverse Event Reporting System in January. The request came after the U.S. Centers for Disease Control and Prevention (CDC) said none of the safety signals it identified for the COVID-19 vaccines were “unexpected.”
The two agencies have run different types of analyses on the system’s reports, which are primarily made by health care professionals.
The first time the agency ran analyses using the method for the COVID-19 vaccines, in 2022, hundreds of signals were triggered, files obtained by The Epoch Times show.
The FDA in 2021 started a different type of analysis, called Empirical Bayesian (EB) data mining.
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