After years of dismissing public concerns as conspiracy theories, the FDA has now acknowledged a disturbing link between mRNA COVID-19 vaccines and a global spike in cardiac arrests—validating what critics and independent doctors have been warning about since the shots first rolled out.
What was once branded as “misinformation” is now official policy, as the FDA orders new warning labels on all Pfizer and Moderna mRNA vaccine products, explicitly citing risks of long-term heart damage and cardiac arrest.
At the center of the updated warnings: a significant risk of myocarditis, particularly in young men, and troubling new data that suggests long-term, possibly irreversible heart damage linked to the shots.
The FDA’s revised label requirements follow newly analyzed data showing that young males aged 12 to 24 continue to suffer from post-vaccination heart inflammation at higher-than-expected rates. Despite repeated claims that such cases were “rare and mild,” the evidence now paints a far grimmer picture — and the establishment is being forced to concede.
Dr. Vinay Prasad, Director of the FDA’s Center for Biologics Evaluation & Research, publicly unveiled the new findings this week, detailing how the agency’s own data revealed a myocarditis rate of 27 per million in young men — a number that independent experts say is likely much higher due to the underreporting baked into passive surveillance systems like VAERS.
But perhaps the most damning admission came in the form of cardiac MRI data. In one FDA-funded study, Prasad noted that 60% of post-vaccine myocarditis patients still showed signs of heart injury five months after diagnosis, with what’s known as late gadolinium enhancement (LGE).
LGE, a marker of permanent heart scarring, is often associated with long-term complications — something Kennedy has long accused health officials of hiding.
🚨 Dr. Vinay Prasad announces an updated FDA safety label for mRNA COVID vaccines “based on persistent and concerning cardiac MR findings” pic.twitter.com/tRqFeIsuk5
— Chief Nerd (@TheChiefNerd) July 2, 2025
The FDA’s formal statement reads:
“FDA has required and approved updates to the Prescribing Information for Comirnaty (COVID-19 Vaccine, mRNA) manufactured by Pfizer Inc. and Spikevax (COVID-19 Vaccine, mRNA) manufactured by ModernaTX, Inc. to include new safety information about the risks of myocarditis and pericarditis following administration of mRNA COVID-19 vaccines.”
The required updates include:
- The estimated unadjusted incidence of myocarditis and/or pericarditis linked to the 2023–2024 vaccine formulas
- The results of an FDA-funded MRI study showing sustained cardiac injury following vaccination
In addition, the Adverse Reactions sections and Fact Sheets for both vaccines have been updated — including those approved under emergency use for children as young as 6 months.
For Kennedy and the growing movement demanding accountability from pharmaceutical companies and captured federal agencies, this is not just a bureaucratic update — it’s proof that the wall of silence is starting to crack.
While mainstream outlets scramble to spin the news, the facts remain: the FDA has now acknowledged that serious, lasting heart injuries can and do result from mRNA COVID-19 vaccination — just as Kennedy warned.
And for Big Pharma, the days of unchecked power and legal immunity may finally be numbered.
По материалам: http://www.planet-today.com/2025/07/fda-confirms-covid-vaccines-behind.html