The data used in the investigation was pulled from the publicly accessible VAERS database which can be viewed here.
 The Vaccine Adverse Event Reporting System (VAERS) is a United States 
programme for vaccine safety, co-managed by the U.S. Centers for Disease
 Control and Prevention (CDC) and the Food and Drug Administration 
(FDA). 
The programme collects information via reports made by 
doctors, nurses, and patients about adverse events (possible harmful 
side effects) that occur after the administration of vaccines to 
ascertain whether the risk-benefit ratio is high enough to justify the 
continued use of any particular vaccine. 
The reports pulled from
 the database were ones that had been submitted up to October 15th 2021 
and they included all adverse reactions reported against the Pfizer and 
Moderna mRNA Covid-19 injections, as well as all adverse reactions 
reported against the influenza vaccines; which were used to generate a 
control dataset....<<<Read More>>>...
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