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Pfizer Quietly Admits to Serious Safety Concerns on their COVID-19 Vaccine
Former Pfizer V.P. believes COVID-19 vaccine program is part of massive depopulation program
By: David Deschesne
Fort Fairfield Journal April 21, 2021
In an FDA briefing document written by COVID-19 vaccine manufacturer, Pfizer/BioNTech on December 10, 2020,1 several serious safety concerns were noted, but were buried in an otherwise glowing and cheerful report, written like sales literature by the same company who produces the vaccine.
After 40+ pages of self-aggrandizing salesmanship pitching their experimental vaccine as completely safe and “95%” effective they admit that; “Suspected COVID-19 cases that occurred within 7 days after any vaccination were 409 in the vaccine group vs. 287 in the placebo group.” They further stated that it was possible that vaccine reactogenicity with “symptoms that overlap with those of COVID-19 could have masked clinically significant adverse events that would not have otherwise been detected.”
Pfizer noted that its vaccine has not been suggested for children under 16 years of age, pregnant or lactating women or immunocompromised individuals as there is “currently insufficient data to make conclusions about the safety of the vaccine” in those subpopulations. They stated, “The representation of pediatric participants in the study population is too limited to adequately evaluate efficacy in pediatric age groups younger than 16 years. No efficacy data are available from participants ages 15 years and younger.”
But, governments are now pitching the COVID-19 vaccine to school-age children.
Previous attempts at creating a coronavirus vaccine over a decade ago resulted in severe auto-immune reactions and enhanced respiratory disease in those laboratory animals that were vaccinated with a COVID vaccine. Pfizer noted in its briefing document that this was also a concern with their vaccine. They stated that they, “identified vaccine-associated enhanced disease including vaccine-associated enhanced respiratory disease as an important potential risk.”
Pfizer also noted a statistically higher rate of appendicitis, acute myocardial infarction and cerebrovascular accident in the vaccinated group over the non-vaccinated placebo group. There were also four cases of Bells Palsy in the vaccinated group while no cases of it reported in the non-vaccinated placebo group, but the Pfizer chiefs pooh-poohed the data stating that the rate of Bells Palsy in the vaccinated group wasn’t any higher than that which occurred in the general population, anyway - downplaying their own admitted fact that none of the people in the non-vaccinated group contracted that disease.
The Pfizer/BionNTech COVID-19 vaccine has received “Emergency Use Authorization” from the US FDA to continue testing its vaccine, which is classified as “experimental,” in the human population. An EUA is not to be confused with FDA approval because the relevant long term tests have not yet been done to verify safety and adverse side effects. Those safety tests are being done now within the general population who are lining up as test subjects, believing the COVID-19 vaccines have been “approved” and certified as “safe” by the U.S. FDA, but no manufacturer’s COVID-19 vaccine has yet achieved that designation.
Furthermore, former Pfizer V.P. and Chief Science Officer, Dr. Michael Yeadon warns that there may be an evil element to the high speed rollout of an experimental mRNA that has never been used in society, before.
In an interview with America’s Frontline Doctors (AFLDS),2 Dr. Yeadon stated he believed there were more sinister ends to this rushed vaccine program.
“I’m well aware of the global crimes against humanity being perpetrated against a large proportion of the world’s population,” Dr. Yeadon told AFLDs. “I have absolutely no doubt that we are in the presence of evil (not a determination I’ve ever made before in a 40-year research career) and dangerous products.”
Dr. Yeadon further stated, “PLEASE warn every person not to go near top up vaccines. There is absolutely no need to them. As there’s no need for them, yet they’re being made in pharma, and regulators have stood aside (no safety testing), I can only deduce they will be used for nefarious purposes.”
“For example, if someone wished to harm or kill a significant proportion of the world’s population over the next few years, the systems being put in place right now will enable it. It’s my considered view that it is entirely possible that this will be used for massive-scale depopulation.”
Research by the Gateway Pundit of the FDA’s Vaccine Adverse Event Reporting System (VAERS), which all health care providers who administer vaccines must report to, showed that as of mid-March, 2021 there were 1,755 deaths attributed to the COVID-19 vaccines in the U.S. among the top three manufacturers. VAERS noted that the greatest amount of deaths (54.38%) were in Moderna’s vaccine, followed by Pfizer with 47.65% of the deaths.
There are currently 2,249 COVID-19 vaccine deaths in the U.S. reported by the VAERS. Updates on COVID vaccine deaths are compiled weekly at the National Vaccine Information Center’s website. (Continually updated chart is available here)[3]
Notes:
1. https://www.fda.gov/media/144245/download
3. https://medalerts.org/vaersdb/findfield.php?TABLE=ON&GROUP1=AGE&EVENTS=ON&VAX=COVID19&DIED=Yes