The FDA’s Hidden System

The FDA’s Hidden System: How COVID-19 Vaccine Injuries Were Tracked and Ignored

All research and credit goes to Dr Bryan Ardis

For years, the FDA, CDC, and mainstream media have repeated the same message — that the Vaccine Adverse Event Reporting System (VAERS) couldn’t be trusted. They insisted that because VAERS is voluntary, its data couldn’t be verified.

The argument sounded simple: anyone, anywhere, could submit a report online, even multiple times, and therefore the system couldn’t be considered reliable.

But that wasn’t entirely true.

The Truth About VAERS and FDA Oversight

While VAERS does allow public reporting, all entries are screened and reviewed by the CDC and other health authorities. The data isn’t just dumped online unchecked. It’s monitored, categorized, and filtered before analysis.

So, the reason the FDA and CDC ignored the flood of reports about injuries from the COVID-19 shots wasn’t due to mistrust of VAERS. The truth was hiding in plain sight.

At the bottom of Slide 15 of the FDA’s October 2020 PowerPoint presentation — the same presentation that contained the now infamous Slide 16 — the FDA clearly stated which data system it had chosen to monitor vaccine injury reports.

It wasn’t VAERS.

The Real Data System: CMS.gov

In that October 2020 presentation, the FDA confirmed that the Centers for Medicare & Medicaid Services (CMS.gov) database would be the primary system used for their rapid cycle analysis of COVID-19 vaccine injuries.

Unlike VAERS, CMS reporting is not voluntary. It’s mandatory.

The FDA deliberately chose this system to monitor outcomes. Yet, despite knowing what the CMS data was showing — deaths and injuries among older adults soon after vaccination — the FDA never made that information public.

If you’d like to see this for yourself, Slide 15 can be found in the accompanying PDF referenced by the author.

A Chance Encounter That Uncovered the Connection

A few weeks later, at the Reawaken America Tour in Colorado Springs, Colorado, a powerful chain of events unfolded.

After speaking at the event, several presenters — including Dr. Eric Napudi, Dr. Christiane Northrup, Attorney Thomas Renz, and Dr. Robert Marsh — were invited to a mansion in town, where a film crew was setting up to record a fireside discussion for a documentary.

During the drive there, Attorney Thomas Renz mentioned that he was working with a whistleblower from CMS. That triggered an immediate realization. Dr Ardis, sitting behind him, remembered the CMS reference from the FDA’s October 2020 slide deck.

Excited, he grabbed Renz by the shoulder and showed him the FDA document on his phone, pointing out the CMS.gov reference.

Renz was stunned. He immediately downloaded Slide 16 — the one listing all the adverse events the FDA expected to see reported — and contacted his CMS whistleblower, who had direct access to CMS data.

The CMS Whistleblower and the Data Revelation

The whistleblower began pulling data state by state, compiling injury reports that matched each bullet point from Slide 16 — the very same conditions the FDA had known could occur.

Those charts, broken down by U.S. state, showing deaths and injuries reported to CMS.gov within days of vaccination, are now available for public download at www.thedrartistshow.com under Patient Resources.

The author went on to present this CMS data to elected officials in the Texas Capitol Building and several other state capitals.

The findings were undeniable: the FDA had known from the start that the COVID-19 vaccines were causing deaths and serious injuries. Yet, they did nothing to warn the public — and the mass vaccination campaign continued.

Look for the next blog in this series. This is where it starts to get crazy!!!!