FDA Seeks Public Input on Risky COVID Vaccine Choices
Submitted by MAGA
Posted 23 days ago
**FDA Encourages Public Input on Controversial COVID-19 Vaccine Choices**
In an unprecedented move, the U.S. Food and Drug Administration (FDA) has called for public comments regarding the formulation of the 2025-2026 COVID-19 vaccines.
This announcement, made on May 8, 2025, comes amid growing concerns regarding the safety and efficacy of the vaccines approved since their inception in 2020.
CDC data shows a troubling number of vaccine-linked deaths—38,541—and alarmingly indicates that this may represent only a fraction of the true figure, as fewer than 1% of vaccine adverse events are reported.
Some estimates suggest there could be closer to 3.8 million deaths associated with the COVID vaccine in the U.S., a staggering statistic that should have every American questioning the transparency and oversight of vaccine safety protocols.
The FDA's request for public input is not merely a formality; it's a vital opportunity for citizens to express their concerns and demands regarding the ongoing vaccine initiative.
Comments can include requests for halting new vaccine formulas, citing evidence of harm, and questioning the necessity of continuing these products on the market.
This initiative comes at a time when many Americans feel their safety and health decisions have been clouded by governmental overreach and a lack of scientific transparency.
The FDA meeting, scheduled for May 22, 2025, is open for comments until May 23, and participants have the option to speak live during the meeting if they've submitted their requests by May 14.
The urgency of this opportunity cannot be overstated, especially as a growing number of medical professionals, scientists, and lawmakers worldwide are voicing skepticism about the current vaccine protocols.
Among the serious concerns raised is the assertion that the public has not received informed consent regarding the genetic contents of existing mRNA vaccines.
Critics highlight that the manufacturers have failed to provide complete plasmid DNA sequences used in producing the vaccines.
Independent studies have raised alarm over potential genomic integration risks and other health implications that have not been thoroughly investigated.
With peer-reviewed studies indicating that vaccine effectiveness diminishes over time and reports of adverse effects on health, many are rallying for a reevaluation of the current vaccination strategies.
This call for input from the FDA is a pivotal moment for Americans to voice their opinions and influence public health policy.
Failure to engage could result in another round of vaccines being authorized without complete transparency or safety assurances.
This dialogue is not just about health; it is about safeguarding personal freedoms and ensuring the integrity of medical choices in America’s public health landscape.
Citizens are encouraged to submit their comments and concerns to create a transparent discourse around one of the most pressing health issues of our time.
Sources:
modernity.news
americanthinker.com
modernity.news
In an unprecedented move, the U.S. Food and Drug Administration (FDA) has called for public comments regarding the formulation of the 2025-2026 COVID-19 vaccines.
This announcement, made on May 8, 2025, comes amid growing concerns regarding the safety and efficacy of the vaccines approved since their inception in 2020.
CDC data shows a troubling number of vaccine-linked deaths—38,541—and alarmingly indicates that this may represent only a fraction of the true figure, as fewer than 1% of vaccine adverse events are reported.
Some estimates suggest there could be closer to 3.8 million deaths associated with the COVID vaccine in the U.S., a staggering statistic that should have every American questioning the transparency and oversight of vaccine safety protocols.
The FDA's request for public input is not merely a formality; it's a vital opportunity for citizens to express their concerns and demands regarding the ongoing vaccine initiative.
Comments can include requests for halting new vaccine formulas, citing evidence of harm, and questioning the necessity of continuing these products on the market.
This initiative comes at a time when many Americans feel their safety and health decisions have been clouded by governmental overreach and a lack of scientific transparency.
The FDA meeting, scheduled for May 22, 2025, is open for comments until May 23, and participants have the option to speak live during the meeting if they've submitted their requests by May 14.
The urgency of this opportunity cannot be overstated, especially as a growing number of medical professionals, scientists, and lawmakers worldwide are voicing skepticism about the current vaccine protocols.
Among the serious concerns raised is the assertion that the public has not received informed consent regarding the genetic contents of existing mRNA vaccines.
Critics highlight that the manufacturers have failed to provide complete plasmid DNA sequences used in producing the vaccines.
Independent studies have raised alarm over potential genomic integration risks and other health implications that have not been thoroughly investigated.
With peer-reviewed studies indicating that vaccine effectiveness diminishes over time and reports of adverse effects on health, many are rallying for a reevaluation of the current vaccination strategies.
This call for input from the FDA is a pivotal moment for Americans to voice their opinions and influence public health policy.
Failure to engage could result in another round of vaccines being authorized without complete transparency or safety assurances.
This dialogue is not just about health; it is about safeguarding personal freedoms and ensuring the integrity of medical choices in America’s public health landscape.
Citizens are encouraged to submit their comments and concerns to create a transparent discourse around one of the most pressing health issues of our time.
Sources:
modernity.news
americanthinker.com
modernity.news
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