Dr. Vinay Prasad, The New FDA Vaccine Chief Is Against mRNA

Dr. Vinay Prasad’s appointment as the new director of the FDA’s Center for Biologics Evaluation and Research (CBER) marks a significant shift in the agency’s approach to vaccine regulation.Prasad’s leadership is poised to influence the FDA’s future direction because of his critical stance on pharmaceutical industry practices and public health policies during the COVID-19 pandemic.

Dr. Prasad, a hematologist-oncologist and professor at the University of California, San Francisco, has been an outspoken critic of several aspects of the U.S. public health response to COVID-19.He has questioned the efficacy of certain pharmaceutical approvals, criticized mask mandates, and expressed skepticism about the accelerated approval of COVID-19 vaccine boosters, especially for younger populations.

Prasad’s appointment suggests a potential reevaluation of the FDA’s current practices, particularly concerning approving and monitoring vaccines and biologics.His leadership may lead to:

• Stricter Clinical Trial Requirements: A push for more comprehensive, placebo-controlled studies before vaccine approvals.
• Increased Transparency: Efforts to make the FDA’s decision-making processes more open to public scrutiny.
• Reassessment of Vaccine Recommendations: Particularly regarding the inclusion of COVID-19 vaccines in routine immunization schedules for children.

So far, this is the polite way of introducing Prasad, but what he actually represents is a gut punch against the vaccine industry, for he knows the truth about mRNA vaccines. Prasad has been a prominent voice in raising concerns about Myocarditis associated with mRNA COVID-19 vaccines. In 2022, he co-authored a systematic review titled “COVID-19 vaccine-induced myocarditis in young males,” published in the European Journal of Clinical Investigation. This study analyzed how myocarditis risk was reported across various studies and emphasized that the highest incidence occurred in males under 40, especially after the second dose of mRNA vaccines.

Every honest doctor worldwide should call for the Pfizer shots to be immediately halted.
So, how many doctors are calling this out? How many doctors are honest? Not many!

In the above video, Dr. Vinay Prasad reports that everyone vaccinated with genetic materials is getting higher troponin levels than normal, with the inference being that all have been injured in their hearts. Troponins are a group of proteins typically found only in skeletal muscles and the heart, but they can leak into the bloodstream if the heart becomes damaged.

The first two prospective cohort studies, where blood cardiac troponin level was measured before and after receiving mRNA injections, demonstrated unacceptably high rates of troponin elevation, indicating predictable heart damage.

Heart cells do not replicate. Once they are killed, they are lost forever. The more cells that die, the more likely the person is to have clinical Myocarditis to one degree or another. Since doctors are miserable failures in terms of knowing how to treat inflammation in the heart, most of these people could end up being part of a holocaust of death.

The latest information leads us to believe that 100 percent of the vaccinated have some level of heart damage/inflammation, making the mRNA shots the most dangerous vaccine ever conceived.

Clinical Myocarditis in kids under 18 cases up by over 100X in Canada

Large Canadian hospital: before COVID, they’d see 2 cases yearly. Now they see 27 in just 6 weeks. That’s a 117X increase. But the CDC says it’s only “slightly elevated.”

Salvation Delivers Suffering and Death

The SARS-CoV-2 virus bioweapon can directly invade the body, causing inflammation. This can impact the heart, causing Myocarditis and pericarditis — inflammation of the heart muscle or outer lining of the heart. Inflammation from COVID can also cause blood clotting, which can block a heart or brain artery, causing a heart attack or stroke.

COVID can also cause abnormal heart rhythms, blood clots in the legs and lungs, and heart failure. Our understanding of how COVID causes heart inflammation and injury to the heart muscle is becoming clearer.

One study on long COVID, published in July, found common cardiovascular symptoms include heart palpitations, fast heart rate, slow heart rate, chest pain, visible bulging veins, and fainting.

The mRNA vaccine, created to mitigate the viral COVID bioweapon, outdid the virus in terms of harm done to the public. A New Florida brand differential study shows the Pfizer vaccine likely KILLED over 470,000 Americans.

Naomi Wolf exposed devastating truths buried in Pfizer’s internal documents, revealing what she calls the “greatest crime against humanity in history.” These FDA-confidential files, shared with the FDA, expose a chilling cover-up. Here’s what Pfizer knew—and when:

1. Vaccine Failure Known Early: Just ONE MONTH after the November 2020 rollout, Pfizer’s internal records confirmed the vaccines didn’t stop COVID. Shockingly, the third most common side effect reported? COVID itself. While media and influencers pushed the jab, Pfizer knew it was failing.
2. Flood of Adverse Events: Within weeks, Pfizer was overwhelmed by reports of severe side effects. They planned to hire 2,400 full-time staff just to process the paperwork for the flood of adverse events they knew was coming. The public? Kept in the dark.
3. Heart Damage in Teens: By May 2021, Pfizer knew the vaccine caused heart damage in 35 minors within a week of injection. Yet, the FDA and U.S. government delayed warning parents until August 2021—four months later. During that time, young adults faced relentless propaganda: “Do it for grandma.” No mention of the elevated heart risks.
4. Toxic Biodistribution: The CDC claimed the vaccine’s materials (lipid nanoparticles, mRNA, spike protein) stayed at the injection site. False. Pfizer’s own data showed these materials biodistribute across the body within 48 hours, accumulating in the brain, liver, spleen, adrenals, and—most alarmingly—in women’s ovaries. These industrial fats, coated in polyethylene glycol, have no known mechanism for leaving the ovaries, building up with each dose.