The FDA posted the emails one day after the agency objected to a motion filed by Children’s Health Defense (CHD) in federal court pertaining to CHD’s 2023 Freedom of Information Act lawsuit seeking information on the agency’s monitoring of COVID-19 vaccine injuries in VAERS.
Newly posted email records on the U.S. Food and Drug Administration (FDA) website reveal that in the first 18 months after COVID-19 vaccines were rolled out to the public, the agency’s data monitoring of the Vaccine Adverse Event Reporting System (VAERS) showed consistent alerts for serious adverse events (including death) for the Janssen vaccine.
Meanwhile, the FDA’s monitoring found almost no safety signals for the Moderna and Pfizer shots, failing to detect signals even for widely recognized risks like myocarditis, pericarditis, and anaphylaxis.
The information is contained in emails sent by the FDA to key personnel in the Centers for Disease Control and Prevention’s (CDC) Immunization Safety Office between Jan. 12, 2021 and July 5, 2022.
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