MAHA BOMBSHELL: FDA Chief Officer Vinay Prasad Admits COVID-19 "Vaccines" Have Killed American Children

The Food and Drug Administration’s top vaccine regulator circulated a shocking email to staff exposing the Modified mRNA slow kill bioweapon “vaccine” as being responsible for the murder of at least ten children, adding that this represents, “[a] profound revelation.”

Except that ever since the rollout of these gene altering highly carcinogenic poison depopulation injections on the heels of the criminal FDA’s fraudulent “emergency” use authorization (EUA), magnitudes more than ten children have succumbed, not to mention the plethora of severe life-altering adverse events like myocarditis, turbo cancers, premature Alzheimer’s, and so on and so forth.

The rigged VAERS system has an underreporting factor (URF) of around 41, which is actually extremely conservative; in other words, you can multiply deaths and adverse events reported in VAERS by at very least a factor of 41, with the real URF probably closer to 100.

So, when Vinay Prasad, director of the FDA’s Center for Biologics Evaluation and Research (CBER), admitted, “a detailed analysis of deaths voluntarily reported to the VAERS system,” showed that of 96 deaths between ‘21 and ‘24, they’ve identified, “no fewer than 10,” that are related to the shot, you can multiply that by anywhere from 41 to 100 times to get a conservative iatrocide estimate, more at democide murder rate.

Here is Prasad’s bombshell email in its entirety, concluding that regulatory requirements for new vaccines would be heightened as a result of these grossly underreported deaths:

Dear Team CBER,

I am writing to report that OBPV career staff have found that at least 10 children have died after and because of receiving COVID-19 vaccination. These deaths are related to vaccination (likely/probable/possible attribution made by staff). That number is certainly an underestimate due to underreporting, and inherent bias in attribution. This safety signal has far reaching implications for Americans, the US pandemic response, and the agency itself, which I wish to discuss here. I also want to address some frequent objections.

Prior to joining the US FDA, the FDA Commissioner closely followed reports of vaccine-induced myocarditis. Unlike the COVID virus, which has a steep age gradient-- being at least 1000 times more likely to kill an 80 year old than an 8 year old-- myocarditis appeared to have the opposite pattern. Young, healthy boys and men-- those least likely to experience bad covid outcomes-- bore the greatest risk. The risk was as high as ~200-330 per million doses given in the highest risk demographic groups. Notably, the US FDA and CDC were not the first to recognize the safety signal-- instead the Israelis were-- and worse in May of 2021, then CDC director Rochelle Walensky stated, “We have not seen a signal and we’ve actually looked intentionally for the signal in the over 200 million doses we’ve given,” Many felt this statement was dishonest and manipulative.

The Commissioner, senior advisor Tracy Beth Hoeg MD PhD, myself and colleagues demonstrated that COVID-19 boosters, and the accompanying mandates by colleges, were on balance harmful to young men in a widely discussed, peer reviewed paper in 2022. Like many academic physicians, we felt the FDA and CDC abdicated their duty to the American people. These agencies did not quickly attempt mitigation strategies such as spacing doses apart, lowering doses, omitting doses among those with prior COVID-19.

Worse, the FDA delayed acknowledgement of the safety signal until after it could extend marketing authorization to younger boys 12-15. This is described by the Commissioner and I in JAMA. Had the acknowledgement come early, these younger boys, who likely did not require COVID-19 vaccination, may have chosen to avoid the products.

In the summer of 2025, Dr. Hoeg began investigating VAERS reports of children who had died after administration of the COVID-19 vaccine. By late summer, she had concluded that there were in fact deaths-- a fact this agency had never publicly admitted.

Dr. Hoeg organized a small meeting to discuss these deaths with OVRR and OBPV stakeholders. The slides she presented, emails she sent, and distorted firsthand reports was shared with media outlets. The general narrative was that OVRR staff disagreed with Dr. Hoeg’s assessment that the deaths were due to vaccine receipt. Some staff present who leaked portrayed the incident as Dr. Hoeg attempting to create a false fear regarding vaccines.

I then asked OBPV to perform a detailed analysis of deaths voluntarily reported to the VAERS system-- in full interest of balance. Causality is easy to assess in a randomized trial, but with case reports, causality is typically assessed on a subjective scale. In this scale ranging from certain to unlikely-- certain, possible/likely, and probable are broadly considered as related to the product.

The team has performed an initial analysis of 96 deaths between 2021 and 2024, and concludes that no fewer than 10 are related. If anything, this represents conservative coding, where vaccines are exculpated rather than indicted in cases of ambiguity. The real number is higher.

This is a profound revelation. For the first time, the US FDA will acknowledge that COVID-19 vaccines have killed American children. 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. In many cases, such mandates were harmful. It is difficult to read cases where kids aged 7 to 16 may be dead as a result of covid vaccines.

Did COVID-19 vaccine programs kill more healthy kids than it saved?

We do not have reliable data estimating the absolute benefit (absolute risk reduction) regarding severe disease and death in healthy children from vaccine receipt. OVRR and OBPV rely on observation cohort or case control data with notorious methodologic biases. FDA has never requested the manufacturers demonstrate in randomized fashion that vaccinating children improves these outcomes. The available randomized data in children is deeply limited, and broadly negative for symptomatic infection, as discussed in prior ad-coms. Furthermore, COVID-19 was never highly lethal for children, and now MIS-c has decreased drastically, and the harms, to kids, are comparable to many respiratory viruses for which we do not provide annual immunization.

Comparing the number of kids who died from COVID against these deaths would be a flawed comparison. We do not know how many fewer kids would have died had they been vaccinated, and we do not know how many more kids died from taking vaccines than has been voluntarily reported. Instead, the truth is we do not know if we saved lives on balance.

When it comes to vaccine deaths, VAERS is passively reported. It requires a motivated person, often a doctor, to submit the information. The submission process is tedious and most people who start the form give up along the way. Many more deaths may be unreported. Finally, the FDA has failed to properly enforce many required post market commitments for COVID-19 vaccines, including for pregnant women and to document subclinical myocarditis.

Putting these facts together, it is horrifying to consider that the US vaccine regulation, including our actions, may have harmed more children than we saved. This requires humility and introspection.

Why did it take the FDA Commissioner to identify these deaths?

There is no doubt that without this FDA commissioner, we would not have performed this investigation and identified this safety concern. This fact also demands serious introspection and reform. Why were these deaths not actively reviewed in real time? Why did it take until 2025 to perform this analysis, and take necessary further actions? Deaths were reported between 2021 and 2024, and ignored for years.

I suspect the answer is cultural and systemic. I have no doubt that many vaccines have saved millions of lives globally, and many have benefits that far exceed risks, but vaccines are like any other medical product. The right drug given to the right patient at the right time is great, but the same drug can be inappropriately given, causing harm. The same is true for vaccines. The US government’s coercive and unethical covid-19 vaccine mandates in young people may have been harmful. In contrast, there is no doubt that an elderly, un-immune American benefitted from Doses 1 and 2 in 2020. The people who might have benefit most from vaccination were those too old to be affected by workplace mandates—another Biden administration blunder.

Does COVID cause more myocarditis than covid vaccines?

A perennial argument is that COVID 19, the virus, causes more myocarditis than COVID-19 vaccines. In fact, I heard this argument made inside CBER recently when one company submitted their PMC. Here is why that argument is wrong.

In order to study how often people have myocarditis after the virus, you would want to collect everyone who got covid, and see how many get myocarditis. Yet, studies on this topic don’t do this. They take people who presented to health care systems and had covid-19 and ask how many have myocarditis. But we all know most people who get covid simply recover at home. People who seek medical care are the sickest ones. These studies use a false denominator.

Second, the demographic matters. I have no doubt COVID vaccines were life saving for an 80 year old who never had COVID, but should a 20 year old get his 6th dose this fall? These studies often fail to look at the balance in younger people.

Finally, you still get COVID anyway. No amount of covid vaccines stops a person from getting covid, so the risk is not virus vs vaccine. It is vaccine + virus vs virus alone.

I am not aware of any analysis that does this right, and we have performed an empirical review of this fact.

Thoughts on CBER staff who are leaking to the media

I have no doubt that individuals who are providing media outlets with slides, emails and personal anecdotes believe they are doing the right thing. Unfortunately, this behavior is both unethical, illegal, and, as this case illustrates, factually incorrect. COVID-19 vaccines did result in the death of children. Dr. Hoeg was correct in her assessment-- any small differences in opinion about specific cases are due only to the fact that subjective attribution of death is inherently a topic where reasonable people may have subtle disagreements. But the overall order of magnitude and directionality show concordance between Dr. Hoeg and long-time CBER staff.

Drs. Gruber and Krause resigned in 2021 as Director and Deputy Director of OVRR

Finally, one fact that must be mentioned is that disagreements by my predecessor and career staff had led to resignations in the past. Drs. Gruber and Krause ran the vaccine division for decades. They resigned over two issues: Dr. Marks insisted that annual boosters should be for all people--irrespective of age and risk-- while Gruber and Krause preferred a risk based, evidence based approach. And Dr. Marks pushed through a BLA for the COVID-19 shots, which permitted the Biden administration to administer unethical COVID-19 mandates.

As a professor, I agreed with Gruber and Krause. Furthermore, there have been prior CBER directors who have held this chair and had fundamentally different views. Some have felt the CBER director should override reviewers to approve gene therapies that do not work because of patient demand. When these products later result in post market deaths, it is difficult to take corrective action. I favor approving products with benefits that exceed risks.

Incentive in vaccine making

It is well acknowledged that the FDA does not consider the cost of drugs in our approval decisions, and similarly it is not our role to lower evidentiary standards or mask safety concerns to create artificial financial incentives to make vaccines. That said there are unique financial incentives for vaccine markers.

Covid-19 vaccines earned 100 billion dollars globally. The annual US vaccine market is estimated to be over 30 billion dollars, projected to pass 50 billion in a decade, and a single new vaccine for pregnant women has industry analysts estimating 1 billion a year in annual returns.

Additionally, vaccines do not go “generic.” There is no biosimilar pathway. You can’t show your biosimilar vaccine has the same antibody titer and get approval. This means two things: companies can expect long tails of earnings, and FDA acknowledges that cell and humoral immunity surrogates are insufficient for generic approvals-- a position I agree with.

The fact that we don’t offer generic or biosimilar vaccines because no amount of cell or humoral mediated immune surrogates would mean that a product retains efficacy has a deeper logical conclusion: how can we accept such endpoints to approve entirely novel products?

The path forward for CBER/OVRR/OBPV

I want to outline a path forward. Our general approach in CBER will be to direct vaccine regulation towards evidence based medicine. This means: we will take swift action regarding this new safety concern, we will not be granting marketing authorization to vaccines in pregnant women based on unproven surrogate endpoints (any prior promises will be null and void), and we will demand pre-market randomized trials assessing clinical endpoints for most new products. Pneumonia vaccine makers will have to show their products reduce pneumonia (at least in the post-market setting), and not merely generate antibody titers. Immunogenicity will no longer be used to expand indicated populations-- these populations should be included in premarket RCTs.

We will revise the annual flu vaccine framework, which is an evidence-based catastrophe of low quality evidence, poor surrogate assays, and uncertain vaccine effectiveness measured in case-control studies with poor methods. We will re-appraise safety and be honest in vaccine labels. I look forward to hearing your thoughts on how to do this better.

Additionally, at FDA, we have not been focused on understanding the benefits and harms of giving multiple vaccines at the same time. This is a concern shared by many Americans. The FDA’s standard has been to require randomized studies too small to draw any conclusions from-- creating a false sense of efficacy and safety.

OVRR and OBPV staff will be tasked with writing guidelines to reflect these changes, and the mission of CBER will change to reflect this worldview. Never again will the US FDA commissioner have to himself find deaths in children for staff to identify it. Vaccines will be treated like all other medication classes-- no better or worse than AAV vectors, monoclonal antibodies, or anti-sense oligonucleotides.

Insofar as vaccines have third party benefits, and many do, these will be judged just like drugs may have third party benefits-- a person who takes an appropriate psychiatric medicine may be a better parent or spouse-- but this requires data and cannot be assumed. I have seen no evidence that COVID-19 vaccines, which do not halt transmission, benefit third parties. I have no doubt that MMR vaccines do provide third party benefits when administered to high enough fractions of society.

Having said this, I remain open to vigorous discussions and debate on these topics, as I have always been. I am open minded to modifications or alterations. As you can imagine, I believe these debates should be private, internal to FDA, until they are ready to be made public. I don’t endorse selective reporting of our meetings and documents. Some staff may not agree with these core principles and operating principles. Please submit your resignation letters to your supervisor and CC my deputy Katherine Szarama.

For those who choose to remain in CBER, I look forward to working with you, learning from you, discussing with you, and interacting with you on our shared mission: to elevate vaccine science to 21st century evidence based medicine.

Vinay Prasad MD MPH

CBER Director, CMSO US FDA

The admissions in Prasad’s email are as stunning as they are surprising given his governmental role, with divulgences such as, “no amount of covid vaccines stops a person from getting covid, so the risk is not virus vs vaccine. It is vaccine + virus vs virus alone,” so brutally honest and, more importantly, utterly catastrophic to BigPharma and their Intelligence-Industrial Complex partners-in-crime.

Unsurprisingly, the CIA’s main Mockingbird outlet the New York Times has been activated to go into full damage control mode; to wit:

The New York Times article unconvincingly attempts to discredit Prasad’s email:

The findings have not been published in a peer-reviewed medical journal, drawing suspicion from some critics of Health Secretary Robert F. Kennedy Jr., who has repeatedly criticized the Covid shots as deadly despite the scientific consensus that they are safe.

Of course, the article fails to mention that the entire peer-reviewed space is captured by BigPharma and the Intelligence-Industrial Complex.

And speaking of drawing suspicion, anyone paying a scintilla of attention knows full well that all of this “Trust the $cience” and “$afe and Effective” scientific consensus is just one of the many moving parts to this ongoing PSYOP-19 scamdemic program, and let us not forget that this very same scientific consensus scam is also a critical component of the PSYOP-CLIMATE-CHANGE con.

The Covid vaccine, like many other immunizations, carries some health risks in certain cases and mainstream scientists have been studying the vaccine’s effects on people for years, especially the incidence of myocarditis in teenage boys and young men.

Never mind that the Covid “vaccine” is not a vaccine proper given that it is a gene therapy replete with SV40 promotor sequences that integrate into the human genome and induce turbo cancers and other VAIDS symptoms, but as per Prasad there is absolutely no immunization offered by this eugenics shot.

In fact, there is not a single vaccine that has a quality RCT with control placebo that shows any efficacy, immunization, or attenuation of symptoms, and not a single vaccine is safe.

Also, it is scientifically impossible to inject anything into the deltoid that could prevent a respiratory infection.

“Some health risks?”

Each and every vaccine is all risk, and no reward:

While Vinay Prasad will not admit to this horrific truth about all vaccines just yet, with his important leaked email memo he has commenced the painfully glacial process of removing every single vaccine from the marketplace forever; or at least that is the hope.

And it is not just the director of the FDA’s Center for Biologics Evaluation and Research that is now eviscerating the official vaccine narratives, but it is also the FDA Commissioner dropping devastating truth bombs about all of these depopulation injections:

“Vaccine deaths are a very small minority”
That’s what News Nation’s Elizabeth Vargas just told FDA Commissioner Dr. Marty Makary…

His response left the studio silent.

Direct quotes from the interview:

- “Hundreds of thousands of Americans describe vaccine injury”

- “25% of clinicians I’ve surveyed know someone significantly disabled or died from the vaccine”

- Makary: “I know of three people who died from the COVID vaccine through first-degree physician contacts”

- Confirmed myocarditis risk in young healthy males: 1 in 2,600

- “The question isn’t ‘is it safe?’ — it’s ‘do the benefits outweigh the risks for each person?’”

Then he went further: the last administration was “rubber-stamping boosters every year with NO new clinical trials.”

No slogans. No conspiracy.
Just a Johns Hopkins surgeon and current FDA Commissioner asking for honest, nuanced science instead of blanket mandates.

Watch the full exchange below and decide for yourself.

Whether you’re triple-boosted or zero doses — should we still be allowed to talk openly about benefits vs. risks without being called “anti-science”?

Drop your thoughts below. Respectful replies only — this deserves real conversation.

Source

Profound admissions courtesy of the burgeoning MAHA movement.

And Dr. Marty Makary and Vinay Prasad can always take the opportunity to bust out a few germane charts to drive home their points:

Etc. & etc. & etc.

The MAHA movement is looking increasingly dead serious legit after all.

Do NOT comply.