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>>>...