Pfizer documents reek of FRAUD; Big Pharma liability shield starts to unravel
(Natural News) Recently released Pfizer documents show that its Wuhan coronavirus (COVID-19) vaccine can cause systemic damage to the body. This is likely the reason why the pharma giant, through the Food and Drug Administration (FDA), previously asked a judge to keep the data from the public for as long as possible – around 55 years, to be more precise.
In the April 1 episode of “The Ben Armstrong Show,” the host talked about the Pfizer document dump. With over 55,000 pages of data to be dumped in April, a team has been assembled to go through parts of the massive document.
Pfizer obviously doesn’t want the public to know just how dangerous the COVID-19 vaccine is, and that the company has committed fraud by saying it is safe and effective. Unfortunately, also involved in the scheme are the government, the FDA, the Centers for Disease Control and Prevention and several media companies. (Related: FDA should need only ’12 weeks’ to release Pfizer data, not 75 years, plaintiff calculates.)
Pfizer and Moderna know from their studies how dangerous the vaccines are, and if independent researchers will ever prove fraud, they will lose their liability protection and people will be allowed to sue them.
When the FDA granted Pfizer the full approval for their vaccine in 2021, there are already known side effects. But there is no way to sue the drug manufacturer for vaccine injury.
“If it could be proven that Pfizer’s data shows increased all-cause mortality and that the company hid this to encourage people to take the vaccine, then there is an existence of fraud,” said former Blackrock executive and investment adviser Edward Dowd. All the protections Big Pharma is enjoying at the moment will be gone.
This is why Pfizer wants to keep its documents away from the public’s eye for as long as possible. “If you didn’t do anything wrong, you wouldn’t care if people looked at your stuff, that you know is supposed to be public record in the first place,” Armstrong said.
Armstrong also showed an interview with Dr. Naomi Wolf, whose team found how dangerous the COVID vaccines are. Wolf indicated that authorities are using these vaccines to experiment on people and use them as lab rats. She said these are not vaccines at all. According to Wolf, the mRNA injections made by Pfizer and Moderna manipulate genes – making them a form of gene therapy rather than a vaccine.
Pfizer’s efforts to conceal data indicate fraud in itself
Meanwhile, Dowd considers Pfizer’s attempt to conceal data that shows the actual risks of its COVID-19 vaccine as an obvious evidence of fraud. He pointed out the Herculean efforts of Pfizer in withholding its data despite legal challenges to release it.
Many reports have also shown that there had been more deaths in the vaccinated compared to the unvaccinated. FDA’s backing of Pfizer in its initial refusal to release the data is an attempt to conceal vaccine deaths, Dowd said.
“Pfizer got blanket immunity with EUA [emergency use authorization]. If there is fraud and it comes out, fraud eviscerates all contracts – that’s case law,” Dowd noted. (Related: Whistleblower: Pfizer FORGED signatures of trial participants, falsified and fabricated trial data.)
Another whistleblower, Dr. Jessica Rose, also obtained information from the Pfizer document dump, which shows that toxic fats have been used in the vaccine and are causing problems in people. These toxic fats apparently go to the organs.
Follow Vaccines.news for more news about Pfizer’s COVID-19 vaccine documents.
Watch the April 1 episode of “The Ben Armstrong Show” to know more about Pfizer documents showing that the company’s COVID-19 vaccine can cause system damage to the body.
This video is from The New American channel on Brighteon.com.
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Former Pfizer employee flags FDA study, warns that Pfizer vaccine increases COVID by over 300%.
COVID vaccine injury reports jump by 27,000 in one week, FDA pulls ‘bait and switch’ with Pfizer vaccine approval.
Whistleblower: Pfizer vaccine trial data was falsified, participants who experienced adverse effects were ignored.
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