Most side effects are not being reported.

The only adverse events that the FDA requires providers to report are listed on the FDA’s site. They are:

Q: Are vaccine providers required to report side effects?

A: Yes. Providers administering Pfizer-BioNTech COVID-19 Vaccine must report to the Vaccine Adverse Event Reporting System (VAERS) and to Pfizer the following information associated with the vaccine of which they become aware: 

Vaccine administration errors whether or not associated with an adverse event

Serious adverse events (irrespective of attribution to vaccination)

Cases of Multisystem Inflammatory Syndrome

Cases of COVID-19 that result in hospitalization or death


Doctors who use VAERS or look at VAERS data are called “dumpster divers” in the media and they are shamed, called in to speak to administration in their hospitals, and they risk losing their jobs. But it’s the only place any safety issues are being reported.

Hospital staff are unlikely to report to VAERS. See this study: Who is unlikely to report adverse events after vaccinations to the Vaccine Adverse Event Reporting System (VAERS)?

See No More Silence for so many stories of adverse events and deaths

“There have been allegations, on federal record, by Dr. David Wiseman and colleague Dr. Josh Guetzkow that Pfizer data is obscured or simply not given to the FDA. How can the FDA consider the risk benefit analysis if data is being withheld?”

ACT NOW AMERICA: The FDA Failed Our Children. Tell the CDC That Proof Of Safety Is Not Negotiable For Children Ages 5-11.

“…it will take a Herculean effort to prove that my adverse reaction was caused by the vaccine. Correlation does not equal causation, they say. But when you are counted as a COVID-19 death, correlation ALWAYS equals causation.”

Clark County Today Administrator Heidi Wetzler shares her thoughts on the repercussions of COVID-19 vaccine mandates