Read through this.
https://www.fda.gov/media/144245/download
You will see that this is still an UNAPPROVED drug never used before with VERY limited testing. In other words they are using the general population as guinea pigs and they state that its critical to monitor those who take it to see what’s going to happen to them.
Read it yourself:
“In the event an EUA (Emergency Use Authorization) is issued for this product, it would still be considered unapproved and it would be under further investigation (under an Investigational New Drug Application) until it is
licensed under a Biologics License Application (BLA). Licensure of a COVID-19 vaccine will be
based on review of additional manufacturing, efficacy, and safety data, providing greater
assurance of the comparability of licensed product to product tested in the clinical trials, greater
assurance of safety based on larger numbers of vaccine recipients who have been followed for
a longer period of time, and additional information about efficacy that addresses, among other
questions, the potential for waning of protection over time”
“The EUA request should include a plan for active follow-up for safety (including deaths, hospitalizations, and other
serious or clinically significant adverse events) among individuals administered the vaccine
under an EUA in order to inform ongoing benefit-risk determinations to support continuation of
the EUA”.
Also, keep in mind if anyone chooses to participate in this ill advised experiment that the vaccine makers have ZERO liability for any injury caused by their product.