We have SO many questions!
Did you know? Healthcare providers are REQUIRED to report deaths following COVID-19 vaccination -- whether or not they think they were related to the vaccine.
Is this happening? Do all healthcare providers know this? Or do they mistakenly think that they don't have to report it if the patient is already elderly or dying? This has definitely been a problem for many decades with all other vaccines.
Here is what the government requires for COVID19 vaccine adverse event reporting:
"Healthcare providers are required to report to VAERS the following adverse events after COVID-19 vaccination [under Emergency Use Authorization (EUA)], and other adverse events if later revised by CDC:
- Vaccine administration errors, whether or not associated with an adverse event (AE)
- Serious AEs regardless of causality.
- Serious AEs per FDA are defined as:
- A life-threatening AE
- Inpatient hospitalization or prolongation of existing hospitalization
- A persistent or significant incapacity or substantial disruption of the ability to conduct normal life functions
- A congenital anomaly/birth defect
An important medical event that based on appropriate medical judgement may jeopardize the individual and may require medical or surgical intervention to prevent one of the outcomes listed above.
- Cases of Multisystem Inflammatory Syndrome
- Cases of COVID-19 that result in hospitalization or death
Healthcare providers are encouraged to report to VAERS any additional clinically significant AEs following vaccination, even if they are not sure if vaccination caused the event.
Also report any additional select AEs and/or any revised safety reporting requirements per FDA’s conditions of authorized use of vaccine(s) throughout the duration of any COVID-19 Vaccine being authorized under an Emergency Use Authorization (EUA)."
And here is what they are required to report for adverse events following other vaccines:
"Healthcare providers are required by law to report to VAERS:
Any adverse event listed in the VAERS Table of Reportable Events Following Vaccination that occurs within the specified time period after vaccination
An adverse event listed by the vaccine manufacturer as a contraindication to further doses of the vaccine."
But if you go to the VAERS Table of Reportable Events Following Vaccination, only a few reactions are listed for each specific vaccine, followed by a directive to report any reaction that the package insert classifies as a contradiction to additional doses of that vaccine.
That means that the CDC already knew that, whatever that reaction is, it's a problem.
HOW CAN THE CDC LEARN OF NEW, POTENTIALLY SERIOUS, UNANTICIPATED REACTIONS TO PREVIOUSLY FULLY-APPROVED VACCINES, IF THEY ONLY REQUIRE REPORTING OF REACTIONS THEY ALREADY KNOW ABOUT?
What could possibly go wrong here?