by John-Michael Dumais, Childrens Health Defense:
An investigation by The BMJ into the Vaccine Adverse Event Reporting System, or VAERS, found multiple deficiencies in the system, including the revelation that the government runs two systems — one for the public, and a private back-end system that contains all of the corrections and updates, including deaths that occurred after an initial injury.
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When Dr. Robert Sullivan collapsed on his treadmill three weeks after his second COVID-19 vaccine in early 2021, he fell into a “nightmare” ordeal that he said exposed glaring deficiencies in the nation’s vaccine safety monitoring system.
Diagnosed with sudden onset pulmonary hypertension, the healthy and fit 49-year-old anesthesiologist from Maryland attempted to file a report through the government-run Vaccine Adverse Event Reporting System (VAERS).
But like others interviewed in a recent investigation by The BMJ, Sullivan hit barrier after barrier when trying to submit and update his report.
Almost three years later, still grappling with debilitating symptoms, Sullivan’s experience highlights the systemic problems with the U.S. adverse events monitoring system run jointly by the Centers for Disease Control and Prevention (CDC) and the U.S. Food and Drug Administration (FDA).
From doctors unable to file reports to disappearing data, limits on transparency and lack of resources to follow up on concerning vaccine reactions, experts warn VAERS is failing to detect critical safety signals.
According to one of those experts — VAERS researcher Albert Benavides, whose experience includes HMO claims auditing, data analytics and revenue cycle management — VAERS’ failure isn’t accidental.
“It is not broken,” Benavides wrote in his Substack coverage of The BMJ investigation. “VAERS runs cover for the big pharma cabal.”
‘They even delete legitimate reports’
Like others interviewed by The BMJ, Sullivan experienced limited follow-up after submitting his VAERS report. He received only a temporary report number months after his initial submission.
A physician named “Helen” (pseudonym) told The BMJ that fewer than 20% of concerning reports get follow-up, including many deaths she reported.
In consultation with Benavides, an audit by React19 found that 1 in 3 COVID-19 vaccine adverse events reports in VAERS were either not posted publicly or were deleted. React19 is a nonprofit that collects stories of people injured by the mRNA vaccines.
According to The BMJ, of those queried by React19, “22% had never been given a permanent VAERS ID number and 12% had disappeared from the system entirely.”
Benavides, who publishes the VAERSAware dashboards documenting many of the problems with VAERS, said there is even deeper dysfunction in the VAERS system — from inventing symptoms to deleting reports.
“VAERS does not publish all legitimate reports received,” Benavides told The Defender. “They throttle publication of reports. They even delete legitimate reports.”
For a system dependent on voluntary engagement, these restrictive policies keep critical data hidden, according to Benavides.
In 2007, the U.S. Department of Health and Human Services (HHS) contracted with Harvard Pilgrim Health Care (HPHC) to review the VAERS system. In 2010, HPHC filed its r report, which determined that 1 in 39 people experienced vaccine injuries and that only around 1% of vaccine-related injuries or deaths are ever reported to VAERS.
The CDC, which operates under HHS, scuttled the study, refused to take calls from the researchers and declined to upgrade the VAERS system when a new, much more effective system was developed.
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