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FDA: Covid Vax by Pfizer & Moderna
Causes Heart Damage
For years, parents and medical professionals have sounded the alarm about the dangerous link between mRNA COVID-19 vaccines and heart inflammation in young males – only to be dismissed as “anti-vaxxers” or conspiracy theorists. Now, in a stunning reversal, the U.S. Food and Drug Administration (FDA) has
ordered Pfizer and Moderna to strengthen their warning labels, finally admitting that these shots can cause long-lasting heart damage, particularly in adolescent boys and young men.
But this admission comes far too late – after millions of doses were administered under false pretenses, after countless young lives were altered by myocarditis, and after public health agencies actively suppressed the truth. The FDA’s belated action raises a critical question: How many more injuries could have been prevented if the government had prioritized transparency over blind vaccine promotion?
Key points:
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For years, independent researchers and medical professionals warned that mRNA vaccines posed a disproportionate risk to young, healthy individuals – especially males. Yet, public health agencies dismissed these concerns, insisting that the benefits outweighed the risks. Now, the
FDA has been forced to acknowledge what health freedom fighters have said all along: These vaccines can cause serious, sometimes permanent, heart damage.
The updated labels must now state that myocardial injury is common among those who develop post-vaccination myocarditis, with data showing persistent damage five months after vaccination. This directly contradicts the CDC’s previous assurances that cases were “mild” and “resolved quickly.”
Why did it take so long? Internal documents obtained through FOIA requests reveal that as early as May 2021, the CDC and FDA considered issuing a public warning but ultimately chose silence over transparency.
The suppression of truth and the cost of deception
The Senate’s Permanent Subcommittee on Investigations recently released a damning report exposing how federal health agencies systematically concealed the myocarditis risk linked to COVID-19 vaccines. Internal emails reveal that officials engaged in a coordinated cover-up by refusing to update the V-safe reporting system to include cardiac symptoms, ensuring countless cases were never documented. Additionally, they blocked a planned Health Alert Network warning that would have alerted doctors and the public to the dangers, prioritizing public perception over transparency.
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Despite clear evidence that myocarditis could cause long-term heart damage, officials deliberately downplayed its severity, framing it as “mild” and “resolving” to avoid undermining vaccination campaigns. The CDC and White House even held crisis meetings to craft misleading messaging, suppressing critical data while pushing narratives that emphasized rarity and safety.
This wasn’t mere negligence – it was a calculated deception, sacrificing informed consent to maintain high vaccination rates. Lawyer Ed Berkovich’s FOIA findings further corroborate this, revealing extensive redactions in CDC documents, particularly those shared with senior White House advisors, suggesting high-level involvement in obscuring the truth. The committee’s failure to act on overwhelming safety signals raises urgent questions about accountability for those who ignored irreversible harm to the public.
The FDA’s new warning is a small step toward accountability, but it doesn’t undo the damage. Millions of young people were injected with these vaccines without being told the full risks. Many now live with chronic heart conditions, while the pharmaceutical companies and government agencies responsible face no consequences.
As the truth continues to emerge, one thing is clear: The COVID-19 vaccine rollout was one of the largest medical experiments in history – and the public was never given the full story. Now, a new HHS leadership must dismantle this medical fraud, and deal with the vaccine injury fallout, one brick at a time.
This article was first published in
Vaccine News under the title of “FDA forces Pfizer, Moderna to admit COVID vaccines cause lasting heart damage in young males” on May 23, 2025
More articles by Lance D. Johnson here
But this admission comes far too late – after millions of doses were administered under false pretenses, after countless young lives were altered by myocarditis, and after public health agencies actively suppressed the truth. The FDA’s belated action raises a critical question: How many more injuries could have been prevented if the government had prioritized transparency over blind vaccine promotion?
Key points:
- The FDA has mandated that Pfizer and Moderna update their COVID-19 vaccine labels to include stronger warnings about myocarditis and pericarditis, particularly in males aged 16 to 25.
- New data reveals that myocardial injury is often long-lasting, contradicting earlier CDC claims that heart inflammation “tends to resolve quickly.”
- The highest incidence of myocarditis occurs in young males, with 38 cases per million doses—far higher than previously acknowledged.
- Internal government emails show that health officials deliberately avoided warning the public about these risks, even after detecting safety signals in 2021.
- The FDA’s action follows a Senate investigation exposing how federal agencies downplayed and hid vaccine injuries.
How many have suffered heart damage
due to vaccine lies?
The updated labels must now state that myocardial injury is common among those who develop post-vaccination myocarditis, with data showing persistent damage five months after vaccination. This directly contradicts the CDC’s previous assurances that cases were “mild” and “resolved quickly.”
Why did it take so long? Internal documents obtained through FOIA requests reveal that as early as May 2021, the CDC and FDA considered issuing a public warning but ultimately chose silence over transparency.
The suppression of truth and the cost of deception
The Senate’s Permanent Subcommittee on Investigations recently released a damning report exposing how federal health agencies systematically concealed the myocarditis risk linked to COVID-19 vaccines. Internal emails reveal that officials engaged in a coordinated cover-up by refusing to update the V-safe reporting system to include cardiac symptoms, ensuring countless cases were never documented. Additionally, they blocked a planned Health Alert Network warning that would have alerted doctors and the public to the dangers, prioritizing public perception over transparency.
The FDA now requires Pfizer & Moderna to issue warnings with their vaccines
This wasn’t mere negligence – it was a calculated deception, sacrificing informed consent to maintain high vaccination rates. Lawyer Ed Berkovich’s FOIA findings further corroborate this, revealing extensive redactions in CDC documents, particularly those shared with senior White House advisors, suggesting high-level involvement in obscuring the truth. The committee’s failure to act on overwhelming safety signals raises urgent questions about accountability for those who ignored irreversible harm to the public.
The FDA’s new warning is a small step toward accountability, but it doesn’t undo the damage. Millions of young people were injected with these vaccines without being told the full risks. Many now live with chronic heart conditions, while the pharmaceutical companies and government agencies responsible face no consequences.
As the truth continues to emerge, one thing is clear: The COVID-19 vaccine rollout was one of the largest medical experiments in history – and the public was never given the full story. Now, a new HHS leadership must dismantle this medical fraud, and deal with the vaccine injury fallout, one brick at a time.
More articles by Lance D. Johnson here
Posted May 23, 2025
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