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To: Buttons12

“FDA has routinely been using screening methods to monitor the safety of COVID-19 vaccines and to evaluate potential adverse events of interest (AEI) related to these vaccines. One of these methods, called near real-time surveillance, detected four potential AEIs in the Medicare healthcare claims database of persons aged 65 years and older who had received the Pfizer/BioNTech COVID-19 vaccine. The four potential AEI are pulmonary embolism, acute myocardial infarction, immune thrombocytopenia, and disseminated intravascular coagulation. The screening methods have not identified these AEI after vaccination in persons 65 years and older who received the two other authorized COVID-19 vaccines.”

“FDA strongly believes that the known and potential benefits of COVID-19 vaccination greatly outweigh the known and potential risks of COVID-19. There is no need to delay vaccination while the FDA continues its investigation.”

https://www.fda.gov/vaccines-blood-biologics/safety-availability-biologics/initial-results-near-real-time-safety-monitoring-covid-19-vaccines-persons-aged-65-years-and-older

https://www.fda.gov/vaccines-blood-biologics/safety-availability-biologics/covid-19-vaccine-safety-surveillance


62 posted on 07/18/2021 7:50:45 AM PDT by Brian Griffin
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To: Brian Griffin

I have ZERO TRUST IN THE FDA.


84 posted on 07/18/2021 8:19:41 AM PDT by goodnesswins (The issue is never the issue. The issue is always the revolution." -- Saul Alinksy)
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To: Brian Griffin

Yah, the FDA also just approved an Alzheimers’ drug which showed no benefit in clinical trials.

Because SCIENCE!™


197 posted on 07/18/2021 11:56:58 AM PDT by grey_whiskers (The opinions are solely those of the author and are subject to change with out notice.)
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