“But then clowns like your article take that high end VAERS data as gospel. Which means YOU are counting car accidents against the vaccine.”
Bingo! What you said is 100% correct. Love it, but hate that pointing out their hypocrisy won’t help them. Their heels are dug in too far.
“But then clowns like your article take that high end VAERS data as gospel. Which means YOU are counting car accidents against the vaccine.”
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V stands for vaccine. No car accidents. VAERS is specifically administered and used by CDC & FDA to monitor vaccine adverse events.
I believe the EU version is EUDRA. They also report a high incidence of deaths from the mRNA inoculation.
“EudraVigilance is the system for managing and analysing information on suspected adverse reactions to medicines which have been authorised or being studied in clinical trials in the European Economic Area (EEA). The European Medicines Agency (EMA) operates the system on behalf of the European Union (EU) medicines regulatory network.”
Meaning the EU monitors recognize this inoculation is a clinical trial.
In the UK, the system is known as the Yellow Card. Also recording a high averse event and death rate.
https://vaers.hhs.gov/about.html
About VAERS
Background and Public Health Importance
Medical professionals working with vaccines
Established in 1990, the Vaccine Adverse Event Reporting System (VAERS) is a national early warning system to detect possible safety problems in U.S.-licensed vaccines. VAERS is co-managed by the Centers for Disease Control and Prevention (CDC) and the U.S. Food and Drug Administration (FDA). VAERS accepts and analyzes reports of adverse events (possible side effects) after a person has received a vaccination. Anyone can report an adverse event to VAERS. Healthcare professionals are required to report certain adverse events and vaccine manufacturers are required to report all adverse events that come to their attention.
VAERS is a passive reporting system, meaning it relies on individuals to send in reports of their experiences to CDC and FDA. VAERS is not designed to determine if a vaccine caused a health problem, but is especially useful for detecting unusual or unexpected patterns of adverse event reporting that might indicate a possible safety problem with a vaccine. This way, VAERS can provide CDC and FDA with valuable information that additional work and evaluation is necessary to further assess a possible safety concern.
It is acknowledged globally that the passive reporting systems only catch 1%-10% of both adverse events and deaths. So: they under-report, rather than over-report.