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:
Death;
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.There is certainly a grey area between "required" and "encouraged" reporting, as medical providers can use their discretion to claim what caused the patient to experience an illness. For example, if someone is born with a birth defect, it would be difficult for providers to trace that back to the vaccination. The website "encourages" medical providers to report any adverse event, even if they are not sure if it is tied to the vaccine, but some hospitals are actively encouraging their workers not to do so. VAERS should track any ailments within the vaccinated population to see what illnesses they’re more susceptible to contracting. The only reason not to collect such data would be to downplay the dangers of the vaccine. How can individuals and health care providers make an informed decision when the risk is unknown? This raises questions on Fauci’s "safe and effective" vaccine claims. Read more at: ArmstrongEconomics.com
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