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11/28/2021 5:02:46 PM
 
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Section 4: President & Congress Subject: Covid attitudes Msg# 1144421
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The govt defines VAERS as: Vaccine Adverse Event Reporting System (VAERS) is a national early warning system to detect possible safety problems in U.S.-licensed vaccines. VAERS is co-managed by the Centers for Disease Control and Prevention (CDC) and the U.S. Food and Drug Administration (FDA).
Various sources are admitting that VAERS are underreported data. Seems its inaccuracies would be reporting too low figures of adverse events. Another govt write up describes it as : comprehensive vaccine safety monitoring program . . . to help ensure vaccines used in the United States, including COVID-19 vaccines, are closely monitored for safety. Medical critics have reported how more than 100 repetitive or elevated adverse events which ought to be receiving medical analysis were unstudied. These included many examples needing greater attention than the myocarditis and pericarditis already acknowledged by the CDC. Subtitle of report: THEY MISSED HUNDREDS OF SERIOUS ADVERSE EVENTS THAT ARE MORE ELEVATED THAN MYOCARDITIS. (their caps, not mine) |
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For reference, the above message is a reply to a message where: >>>Source is VAERS<<< Please explain why that source is reliabl. |
