In under a year, more than 500,000 post-COVID vaccine injuries have been reported to VAERS — nearly a third of all reports accumulated over the system’s entire three-decade lifespan — yet regulatory agencies remain silent.
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A few months before the first COVID-19 vaccines received Emergency Use Authorization (EUA) in late 2020, a global vaccine safety expert cautioned the rushed circumstances made it essential to “get [safety monitoring] right” by “intensively” and “robustly” scrutinizing adverse events following the experimental rollout.
As this expert stated, “Deploying any new vaccine based on data from expedited clinical trials into a population without a functioning safety monitoring system in place is reckless and irresponsible given the tools that are available.”
Moreover, she added, any investments needed to beef up safety monitoring would be “inexpensive in comparison” to the massive funding allocated to COVID-19 vaccine development and scale-up.
In theory, the U.S. has had a national vaccine safety monitoring system in place since 1990 — the Vaccine Adverse Event Reporting System (VAERS) — intended to function as an “early warning system.”
VAERS and its U.S. Food and Drug Administration (FDA) counterpart FAERS (FDA Adverse Event Reporting System) constitute the principal data sources that regulators rely on when pulling drugs or vaccines from the market for safety reasons.
Not only has VAERS never lived up to its promise, but there can be little doubt its glaring failures are largely, and malignantly, by design.
For example, when a government-commissioned study highlighted VAERS inadequacies in 2010 — estimating more than 99% of vaccine adverse reactions were going unreported and that one of every 39 doses of vaccine administered was linked to adverse events corroborated in vaccine package inserts — the Centers for Disease Control and Prevention (CDC) simply shut the project down.
Now, in less than a year, more than half a million reports of injuries have flooded into VAERS following experimental COVID jabs, including thousands of deaths. Yet a deafening regulatory silence has greeted this record-setting volume of adverse reactions, which accounts for nearly a third of all reports accumulated by VAERS over its entire three-decade lifespan.
How is the absence of “early warning system” alarm bells possible? In a recent commentary, “Defining Away Vaccine Safety Signals,” an experienced statistician suggested not only have safety experts’ admonitions to get COVID vaccine safety monitoring “right” not been heeded, but CDC and other public health agencies have taken steps to intentionally hide safety signals.
It’s all in the algorithm…
Read full story here: We’ve Never Seen Vaccine Injuries on This Scale — Why Are Regulatory Agencies Hiding COVID Vaccine Safety Signals? • Children’s Health Defense