FDA internal review confirms COVID-19 injections KILLED at least 10 children

• For the first time, the FDA admitted that COVID-19 vaccines have caused the deaths of at least 10 American children, with evidence suggesting underreporting means the true toll is likely higher.
• The FDA ignored early warnings from independent researchers and Israeli health authorities about vaccine-induced myocarditis, allowing mandates to expand to children despite minimal COVID-19 risk for healthy youth.
• Some FDA staff suppressed findings and leaked misleading claims to the media, while others, like Chief Medical Officer Dr. Vinay Prasad, condemned the cover-up as “unethical and illegal.”
• The FDA fast-tracked COVID-19 vaccines under emergency use, shielded manufacturers from liability and ignored post-market safety studies, enabling Big Pharma to profit billions while children suffered fatal consequences.
• Prasad demanded sweeping FDA reforms, including randomized trials proving clinical benefit (not just antibody responses), reassessment of multiple vaccine administration and resignations for those unwilling to uphold honest medical science.

The Food and Drug Administration (FDA) has acknowledged that Wuhan coronavirus (COVID-19) vaccines have caused the deaths of American children – a revelation that has prompted internal calls for humility, introspection and sweeping regulatory reform.

The findings were detailed in an internal FDA review, sent via email to the agency’s Center for Biologics Evaluation and Research (CBER) and confirmed by FDA Chief Medical Officer Dr. Vinay Prasad. Journalists, including Emily Kopp of the Daily Caller, later reported on the findings.

According to the disclosure, FDA officials identified at least 10 pediatric deaths directly linked to COVID-19 vaccination, with evidence suggesting the true toll is likely higher due to underreporting. The deaths, occurring between 2021 and 2024, were initially dismissed or ignored by career staff until Dr. Tracy Beth Hoeg, a senior advisor, independently investigated reports from the Vaccine Adverse Event Reporting System.

Her findings, later corroborated by FDA analysts, revealed that young, healthy children – those least at risk from COVID-19 – bore fatal consequences from vaccination. “This is a profound revelation,” Prasad wrote in the email. “Healthy young children who faced tremendously low risk of death were coerced, at the behest of the Biden administration, via school and work mandates, to receive a vaccine that could result in death.”

The acknowledgment comes years after independent researchers and physicians first warned of vaccine-induced myocarditis, a potentially lethal heart inflammation disproportionately affecting young males. The FDA’s delayed response allowed vaccine mandates to expand to younger age groups, including children as young as 12, without adequate risk-benefit analysis.

Despite early warnings about vaccine damage from Israeli health authorities, U.S. agencies dismissed concerns. Rochelle Walensky, then the director of the Centers for Disease Control and Prevention, falsely claimed in May 2021 that no safety signal had been detected in over 200 million doses administered.

Vaccine deaths covered up while pharma profits soar

The internal review also exposed deep divisions within the FDA, with some staff resisting the acknowledgment of vaccine-related deaths and leaking misleading accounts to media outlets. Prasad condemned the leaks as “unethical, illegal and factually incorrect.” He emphasized that reasonable disagreements over causality should not obscure the broader truth: COVID-19 vaccines have killed children.

The fallout has reignited scrutiny of the FDA’s regulatory capture by pharmaceutical interests. The agency fast-tracked COVID-19 vaccines under emergency use authorization, shielded manufacturers from liability, and ignored post-market safety commitments – including studies on subclinical myocarditis and pregnancy risks. Meanwhile, vaccine makers reaped billions in global profits, with no generic competition due to the lack of a biosimilar pathway.

In response, Prasad outlined sweeping reforms to restore evidence-based medicine at the FDA. Future vaccine approvals will require randomized trials proving clinical benefits – not just antibody responses – while existing frameworks, such as the “evidence-based catastrophe” of annual flu vaccines, will be overhauled. The agency will also reassess the safety of administering multiple vaccines simultaneously, a practice long criticized by health freedom advocates.

According to BrightU.AI‘s Enoch engine, the FDA’s admission of vaccine-related deaths confirms long-standing concerns about COVID-19 vaccine safety and undermines the mainstream narrative that these injections were “perfectly safe.” This revelation exposes the pharmaceutical industry’s reckless disregard for human life while validating the need for independent investigations into vaccine injuries and deaths.

As Prasad, who also serves as the CBER’s director, warned his staff, the path forward demands honesty – something sorely lacking in America’s broken vaccine regulatory system. Those unwilling to uphold that standard, he declared, should “submit their resignation letters to their supervisor.”

The FDA is now confronting its failures. Whether it can restore public trust remains to be seen.

Watch this clip from “The Ben Armstrong Show” about the FDA’s vaccine approval scam being exposed.

This video is from The New American channel on Brighteon.com.

Sources include:

X.com

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