Search
Close this search box.

Action Alert

Pfizer/BioNTech has asked the Federal Food and Drug Administration (FDA) to expand the Emergency Use Authorization (EUA) of their COVID-19 vaccine for young children ages 6 months through 4 years.

The FDA’s Vaccines and Related Biological Products Advisory Committee will meet on February 15th to evaluate their EUA application. If approved, the vaccine is likely to be mandated for school attendance in many states, so we need your help.  Please tell the FDA that COVID vaccines for children under five years old is a bad idea!

TAKE ACTION

Submit your comments for consideration by the FDA by February 10 (THIS Thursday) if possible.  (The final deadline is February 14, but your comments likely won’t be provided to the advisory committee if sent after the 10th.)

You can submit comments online at: https://www.regulations.gov/commenton/FDA-2022-N-0082-0001

SAMPLE COMMENT (Feel to use this sample or customize your comments with the additional talking points below for optimum success):

I urge the FDA to deny emergency use authorization of COVID-19 vaccines for children under five years of age.

There is no reason to approve experimental vaccines for children who have extremely low risk of hospitalization and death from COVID-19.

Pfizer’s clinical trial in 2-to-5-year-olds showed that their vaccines do not work.  This is in addition to the real-world evidence that, even when the clinical trials showed effectiveness in older age groups, the vaccines have failed to protect adults and youth. 

Data from the Department of Defense shows that 70 percent of hospitalizations for COVID-19 are in fully vaccinated and boostered people.[i]

The FDA should not approve a vaccine for children when there is no data on the vaccine’s efficacy to support authorization and the vaccines are known to cause harm.

If the Pfizer vaccine is approved for children under five years old, most parents will falsely assume that it has been shown to be effective and safe.  This is not the case.

OTHER TALKING POINTS:

  • Share why this is personal to you.  Do you or a family member have a history of vaccine reactions?  Are you at risk for autoimmune conditions or other potential side effects of COVID-19 shots?
  • There is no evidence of medical necessity for COVID-19 shots in children.  A rapidly growing body of data indicates that the vaccines have serious side effects and do more harm than good in children.
  • No one knows in advance whom a vaccine will harm.  Each of us may respond differently as we have different medical histories, genes, epigenetics, and microbiomes.
  • Vaccines are medical procedures that carry risk of serious injury.  The U.S. Supreme Court recognizes vaccines to be “unavoidably unsafe” and to cause injury and death in some recipients.  The U.S. Government has paid out $4.4 billion to the victims of vaccine injury.  Hundreds of thousands have reported an adverse reaction to vaccination to VAERS. http://www.cdc.gov/vaccinesafety/ensuringsafety/monitoring/vaers/
  • COVID-19 vaccine manufacturers and providers are shielded from liability through the Public Readiness and Emergency Preparedness Act, or PREP Act.  The only option for compensating people injured by COVID-19 shots is the Countermeasures Injury Compensation program (CICP).  Only eight percent of all petitioners since 2010 have been awarded compensation through the CICP.  No legal or medical expert fees are covered, no pain and suffering is awarded, lost wages are capped at $50,000, and there is no judicial appeal. In other words, the victims will be severely undercompensated while the pharmaceutical companies get rich.
  • The claimed justification – that unvaccinated individuals pose a health risk to others – has been shown to be false.  Vaccinated individuals can become infected and transmit COVID to others.
  • COVID-19 vaccines carry the risk of injury and death for some so there must be informed consent and the right to refuse the vaccine without penalty.  As of January 21st, there had already been 740,000 COVID-19 vaccine adverse events and 10,316 COVID-19 vaccine deaths in the U.S. reported to the Vaccine Adverse Events Reporting System.
  • Vaccine manufacturers such as Pfizer, Merck and GlaxoSmithKline have paid billions of dollars in criminal penalties and settlements for research fraud, faking drug safety studies, failing to report safety problems, bribery, kickbacks and false advertising.[ii],[iii] Pfizer paid $2.3 billion in 2009 alone to resolve criminal and civil allegations. [i]
  • According to the American Academy of Pediatrics, less than 2% of children known to be infected by the coronavirus are hospitalized, and less than 0.03% of those who are infected die. The risks of vaccination do not outweigh the potential benefits.

[i] https://childrenshealthdefense.org/defender/covid-vaccines-miscarriages-cancer-neurological-disorders-military/

[ii] www.corp-research.org/merck

[iii] https://www.theguardian.com/business/2012/jul/03/glaxosmithkline-fined-bribing-doctors-pharmaceuticals?CMP=share_btn_fb

[iv] https://abcnews.go.com/Business/pfizer-fined-23-billion-illegal-marketing-off-label/story?id=8477617

For more information visit: https://www.fda.gov/advisory-committees/advisory-committee-calendar/vaccines-and-related-biological-products-advisory-committee-february-15-2022-meeting-announcement 

The bulk of this Action Alert provided by the Weston A. Price Foundation. We thank them for their hard work compiling this information.

6 thoughts on “Action Alert”

  1. Claudia Hensley

    Data from the Department of Defense shows that 70 percent of hospitalizations for COVID-19 are in fully vaccinated and boostered people.

  2. I urge the FDA to deny emergency use authorization of COVID-19 vaccines for children under five years of age.

    There is no reason to approve experimental vaccines for children who have extremely low risk of hospitalization and death from COVID-19.

    Pfizer’s clinical trial in 2-to-5-year-olds showed that their vaccines do not work. This is in addition to the real-world evidence that, even when the clinical trials showed effectiveness in older age groups, the vaccines have failed to protect adults and youth.

    Data from the Department of Defense shows that 70 percent of hospitalizations for COVID-19 are in fully vaccinated and boostered people.[i]

    The FDA should not approve a vaccine for children when there is no data on the vaccine’s efficacy to support authorization and the vaccines are known to cause harm.

    If the Pfizer vaccine is approved for children under five years old, most parents will falsely assume that it has been shown to be effective and safe. This is not the case.

  3. I urge the FDA to deny emergency use authorization of COVID-19 vaccines for children under five years of age.

    There is no reason to approve experimental vaccines for children who have extremely low risk of hospitalization and death from COVID-19.

    Pfizer’s clinical trial in 2-to-5-year-olds showed that their vaccines do not work. This is in addition to the real-world evidence that, even when the clinical trials showed effectiveness in older age groups, the vaccines have failed to protect adults and youth.

    Data from the Department of Defense shows that 70 percent of hospitalizations for COVID-19 are in fully vaccinated and boostered people.[i]

    The FDA should not approve a vaccine for children when there is no data on the vaccine’s efficacy to support authorization and the vaccines are known to cause harm.

    If the Pfizer vaccine is approved for children under five years old, most parents will falsely assume that it has been shown to be effective and safe. This is not the case.

  4. I urge the FDA to deny emergency use authorization of COVID-19 vaccines for children under five years of age.

    There is no reason to approve experimental vaccines for children who have extremely low risk of hospitalization and death from COVID-19.

    Pfizer’s clinical trial in 2-to-5-year-olds showed that their vaccines do not work. This is in addition to the real-world evidence that, even when the clinical trials showed effectiveness in older age groups, the vaccines have failed to protect adults and youth.

    Data from the Department of Defense shows that 70 percent of hospitalizations for COVID-19 are in fully vaccinated and boostered people.[i]

    The FDA should not approve a vaccine for children when there is no data on the vaccine’s efficacy to support authorization and the vaccines are known to cause harm.

    If the Pfizer vaccine is approved for children under five years old, most parents will falsely assume that it has been shown to be effective and safe. This is not the case.

  5. When filling out the comment form – what comment category should we choose in the “What is your comment about?” dropdown?

  6. Texans-
    “Submit your comments for consideration by the FDA by February 10 (THIS Thursday) if possible. (The final deadline is February 14, but your comments likely won’t be provided to the advisory committee if sent after the 10th.)

    You can submit comments online at: https://www.regulations.gov/commenton/FDA-2022-N-0082-0001

    SAMPLE COMMENT (Feel to use this sample or customize your comments with the additional talking points below for optimum success):

    I urge the FDA to deny emergency use authorization of COVID-19 vaccines for children under five years of age.

    There is no reason to approve experimental vaccines for children who have extremely low risk of hospitalization and death from COVID-19.”

    https://texansforvaccinechoice.com/action-alert/?fbclid=IwAR18GTsOMbyO8MpcLmGu4sI1xuEVPTaUJrbwdmyMUA3IRqIbc4Ywv-1amPk

Leave a Reply to Claudia Hensley Cancel Reply

Your email address will not be published. Required fields are marked *

Scroll to Top