Secret Recordings Reveal FDA Vaccine Chief Ignored Warnings from Doctors, Injured Patients [WATCH]

A series of secretly recorded virtual meetings between former top FDA vaccine official Dr. Peter Marks and individuals reporting serious COVID-19 vaccine injuries were released this week by the Informed Consent Action Network (ICAN), raising questions about how vaccine safety concerns were handled during Marks’ tenure.

The recordings, published on a new website titled The Real Peter Marks, were unveiled during a Tuesday press conference at the National Press Club in Washington, D.C.

The videos feature several individuals, including medical professionals and vaccine trial participants, describing significant post-vaccination injuries that they say were dismissed or ignored by FDA leadership.

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Dr. Peter Marks served as Director of the FDA’s Center for Biologics Evaluation and Research until his resignation in March.

His departure, which some media outlets described as forced, came shortly before the release of these recordings.

Marks had been central to the FDA’s role in Operation Warp Speed and the approval of COVID-19 vaccines.

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In one video, San Francisco ICU physician Dr. Patricia Lee described to Marks and other FDA officials a series of vaccine-related adverse events she personally witnessed.

She said one of her pregnant patients developed transverse myelitis, went blind, required a tracheotomy, and ultimately died after a traumatic delivery and life support removal.

Lee said the events were temporally linked to the vaccine and that her nurses required a psychiatrist on-site afterward due to the trauma.

Lee told the FDA she submitted multiple VAERS reports using her own mailing address but never received follow-up.

During the call, officials listened but asked no questions after she finished speaking.

The recordings also include footage of Brianne Dressen, co-founder of vaccine injury support group REACT19, who suffered neurological injuries during the AstraZeneca clinical trial.

Her injuries were later confirmed by the NIH. Dressen repeatedly pleaded with Marks to encourage doctors to acknowledge early neurological symptoms such as paresthesia as potential precursors to vaccine-related neuropathy.

She said many patients were instead diagnosed with anxiety and sent away untreated.

“Why aren’t they treating what’s in front of them?” Marks asked in one of the virtual meetings, acknowledging the issue but not offering action. Dressen responded that doctors were afraid of losing their licenses if they labeled cases as vaccine-related.

ICAN also released footage of Dressen attending multiple virtual meetings with FDA officials between August 2021 and December 2022.

In one instance, recorded shortly after President Biden’s federal vaccine mandate for large employers, she is seen lying on a couch while speaking, visibly in pain.

ICAN founder Del Bigtree said Dressen’s group has identified 36,000 VAERS reports of neurological complications, but only a small fraction received any federal follow-up.

One video shows Marks downplaying complications, saying the worst effect seen was “mild” heart inflammation in young males, and that claims of thousands of deaths were “incredible BS.”

However, Bigtree pointed to over 38,000 deaths listed in the VAERS system and criticized Marks for dismissing concerns.

Another story presented was that of Maddie de Garay, a child participant in a Pfizer trial who was left in a wheelchair and on a feeding tube.

Her family’s attorney, Aaron Siri, said Pfizer failed to report the full extent of her injuries to regulators, listing only “abdominal pain.”

The FDA did not respond to follow-up inquiries about the allegations.

The press conference also referenced nurse Tiffany Dover, who collapsed on live TV shortly after receiving the vaccine in December 2020.

Although she later said she had a history of fainting from pain, ICAN argued her experience highlighted gaps in post-vaccination monitoring.

Senator Ron Johnson (R-WI), chair of the Permanent Subcommittee on Investigations and a vocal advocate for vaccine injury transparency, confirmed his office is reviewing the recordings.

“They will be part of the investigatory record,” his office told Just the News.

Following Marks’ departure, FDA Commissioner Dr. Marty Makary announced that Dr. Vinay Prasad, an outspoken critic of Marks’ policies, will take over the role.

The S&P Biotech ETF dropped more than 6% after Prasad’s appointment, according to STAT News, signaling concern from the pharmaceutical sector.

Prasad previously called Marks “one of the most dangerous, pro-pharma regulators of the 21st century,” and criticized him for overriding internal FDA reviewers and fast-tracking approvals of vaccines and gene therapies.

ICAN and REACT19 are calling for full transparency from the FDA, public access to the CDC’s Vaccine Safety Datalink, and a suspension of COVID-19 vaccine recommendations until a thorough safety reassessment is completed.

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