......and maybe you should check this out !!
VAERS
VAERS was created in 1988 and is co-managed by the CDC and the U.S. Food and Drug Administration (FDA). The system was created “to detect possible safety problems in U.S.-licensed vaccines,”
according to its website. The website further states that It is a
“passive reporting system,” meaning that it depends on a person to report their post-vaccination experiences to the CDC and the FDA.
Anyone can report an adverse event to VAERS. Healthcare professionals must report certain adverse events, and vaccine manufacturers must report all adverse events that come to their attention.
However, it is essential to remember that “VAERS is not designed to determine if a vaccine caused a health problem.” It is simply a self-reporting tool, which helps the CDC and the FDA detect “unusual or unexpected patterns of adverse event reporting that might indicate a possible safety problem with a vaccine.”
Also this:
A disclaimer on the FAERS website
here , explains that the FDA receives over 1 million reports of adverse events with drug or biologic products each year.
The FDA explains that while the reports are a “valuable source of information”, the system allows the potential submission of reports that are
“incomplete, inaccurate, untimely, unverified”. Due to this, the FDA says that this data makes up only one part of its surveillance data and the data “does not confirm a causal relationship between the drug product and the reported adverse event(s).”
VERDICT
Misleading. The data shown for adverse events and deaths are from
FAERS and
VAERS data, which does MOT provide information on verified, causal cases. The information can be submitted by anyone and does not show causation.
https://www.reuters.com/article/factcheck-vaers-faers-idUSL2N2OE1ZA