A trove of damning documents reporting on Pfizer’s COVID vaccine has been released by the U.S. Food and Drug Administration (FDA) after a federal court ordered them to comply with a Freedom of Information Act (FOIA) request filed by a government accountability alliance called Public Health and Medical Professionals for Transparency (PHMPT). The FDA initially refused, claiming it would take them 75 years to release all 329,000 pages of documents, a first batch has been released and it reportedly shows some dire statistics. Which is strange because they approved the Vaccine in 4 months but now will take 75 years to provide the documents.
If you are wondering why the FDA and Pfizer would want to hide their test results for 75 years, well here it is…….
Pfizer was aware of 1,223 possible vaccine related deaths within the first 90 days of their COVID vaccine rollout
A document titled “Cumulative Analysis of Post-Authorization Adverse Event Records Reports” showed that within 90 days of the Pfizer COVID vaccine’s rollout in the U.S. under the FDA’s Emergency Use Approval in December 2020, there were thousands of reported adverse effects and more than 1,200 deaths following inoculation.
The document revealed that globally, there were 42,086 case reports of persons who had an adverse reaction to Pfizer’s COVID vaccine. Most of them came from the U.S. with 13,739 and the U.K. with 13,404 where the Pfizer brand of COVID jabs were being widely used. The document said that women were found to be three times more likely to experience a reaction than men, with 29,914 women reporting adverse reactions versus 9,182 men. the adverse reactions culled from the documents, including acute respiratory distress syndrome, pneumonia, Stevens-Johnson syndrome, dermatitis, Bell’s Palsy, skin allergies, paralysis, kidney and liver problems and other life-threatening side effects.
There were 42,086 case reports of persons who had an adverse reaction to Pfizer’s COVID vaccine within the first 90 days
The Pfizer document also read, “Reports are submitted voluntarily, and the magnitude of under-reporting is unknown.”
Other concerning data from the Pfizer trials was outlined by whistleblower testimony of Brooke Jackson. An article in the British Medical Journal brought light to her claims that some Pfizer COVID vaccine trial data was falsified. The company she worked for, Ventavia, one of the companies contracted to perform vaccine trials for Pfizer, even tried to discredit her claims as false by saying she did not work on the Pfizer trials. But later released documents showed Ventavia was lying.
Table 1. in Pfizer’s documents accounts 42,086 reactions to their COVID-19 vaccine over a 90-day period from December 1st. 2020 – February 28th, 2021. 25,379 reactions were ‘medically confirmed’ while 16,707 were ‘not-medically confirmed.’ Pfizer also redacted the total number of vaccine doses that had been administered up to this point.
Approximately 50 percent of vaccine injuries reported to the Vaccine Adverse Events Reporting System within the last 30 year are all from COVID shots. As of October 15, 2021, Vaccine Adverse Events Reporting System (VAERS) recorded 122,833 serious adverse events, of those 17,128 resulted in death, post administration of COVID vaccines.
The mRNA vaccine produced by both Pfizer and Moderna is a completely new type of vaccine that has never been licensed or used on humans before the Wuhan coronavirus (COVID-19) pandemic.
As such, nobody has any idea what to expect from this type of vaccine. Traditional vaccines introduce pieces of a weakened virus to stimulate an immune response, while mRNA vaccines inject molecules of synthetic genetic material from non-human sources into your cells – thus hijacking your genes and permanently reprogramming them to produce antibodies to kill SARS-CoV-2, the virus causing COVID-19.
The mRNA vaccines of Moderna and Pfizer could barely be regarded as medicine in the traditional sense. They are transhumanistic tools to synthetically alter you at the genetic level.
Vaccines usually take seven to 20 years to adequately research, test and bring to market. The slew of COVID vaccines produced by Big Pharma companies are being rushed to market in less than 12 months, which is nowhere enough time to meet established safety standards.
These vaccines are also not designed to stop transmission. Big Pharma companies admitted they didn’t design the vaccine to stop transmission. Therefore, vaccinated individuals can still transmit the virus to others – vaccinated or not.
No long-term safety studies were conducted, so no one has any real idea of the danger these vaccines could cause down the line. It is not an understatement when people say that much of the worldwide population has become Big Pharma’s guinea pigs.
WHO chief scientist Soumya Swaminathan Yadav said there is no evidence to suggest that the COVID vaccines can prevent people from getting COVID-19 or passing it on to others.