Submitted by: Jackie Juntti
I have had to shake my head in understanding why so many folks fell for the EXPERIMENTAL part of the info on this JAB of DEATH. Why did so many become LAB RATS for any Big PHARMA outfit.
This is due to the demonic rulers holding such power on this earth right now. They don't really try to HIDE their intent but due to the DUMBING DOWN that has gone on in the PUBIC SKOOLS - only a few have any understanding of what words REALLY mean. I am of an age where I learned to QUESTION EVERYTHING and NOT BELIEVE most of what others said to me. When this so called *flu* hit the news I had a bunch of questions and all I came across raised MORE questions. But then I have been anti-vaccines since the late 1970's - Swine flu vax and first baby shots killed two family members. That told me it was a KILLER VAX being promoted. The fact that Big Pharma has protection from lawuits should alert everyone to avoid all Big Pharma poisons.
Need Anti-biotics - get some Colloidal silver and use it - no deadly side effects unless you overdue it.
Change your body pH to the alkaline side and viruses and bacterial illnesses can't take hold in your body. I did this back in the early 2000 years and haven't had even a sniffle since.
But, too many people follow the dumb sheep over the cliff rather than turn around and go the other way. You can't cure STUPID.
Jackie Juntti
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Pfizer/FDA Document: Pfizer Planned To Hire 1,800 Employees To Deal With Overwhelming Adverse Effects From Their Experimental COVID Shot
It’s incredible to me why the families of victims of the experimental COVID shots have not stormed Pfizer, Moderna, Johnson & Johnson and AstraZeneca, taken down their board, taken captive for due process (Article I, Section 8, Clause 15 US Constitution) the CEOs and others involved in the deadly experimental COVID shots these unAmerican Big Pharma corporations are engaged in, but alas, they can’t seem to get away from the “lesser of two evils, but still evil” two party system and deal with their corrupt representatives. Still, a new report out, authored by Zachary Stieber of The Epoch Times shows that Pfizer’s adverse effects due to its experimental shot was through the roof and not only did they hire 600 new employees to deal with that, but they planned to hire 1,800 employees just for the reports of adverse effects tied to their deadly poison.
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The story comes by way of Zero Hedge with emphasis added.
Pfizer hired 600 employees in the months after its COVID-19 vaccine was authorized in the United States due to the “large increase” of reports of side effects linked to the vaccine, according to a document prepared by the company.
Pfizer has “taken a multiple actions to help alleviate the large increase of adverse event reports,” according to the document. “This includes significant technology enhancements, and process and workflow solutions, as well as increasing the number of data entry and case processing colleagues.”
At the time when the document—from the first quarter of 2021—was sent to the U.S. Food and Drug Administration (FDA), Pfizer had onboarded about 600 extra full-time workers to deal with the jump.
“More are joining each month with an expected total of more than 1,800 additional resources by the end of June 2021,” Pfizer said.
The document was titled a “cumulative analysis of post-authorization adverse event reports” of Pfizer’s vaccine received through Feb. 28, 2021. It was approved by the FDA on April 30, 2021.
The document was not made public until the Public Health and Medical Professionals for Transparency sued the FDA after the agency claimed it needed decades to produce all the documents relating to the emergency use authorization granted to the company for the vaccine.
Under an agreement reached in February, the FDA must produce a certain number of pages each month.
The analysis of adverse event reports was previously disclosed to the health transparency group, but certain portions were redacted (pdf), including the number of workers Pfizer onboarded to deal with the jump in adverse event reports.
“We asked that the redactions on page 6 of this report be lifted and the FDA agreed without providing an explanation,” Aaron Siri, a lawyer representing the plaintiffs, told The Epoch Times in an email.
After the document was produced, the FDA determined that the three redactions on that page “could be lifted,” an FDA spokesperson told The Epoch Times via email.
The redactions had been made under (b) (4) of the Freedom of Information Act, which lets agencies “withhold trade secrets and commercial or financial information obtained from a person which is privileged or confidential.”
The unredacted version of the document also now shows that approximately 126 million doses of Pfizer were shipped around the world since the company received the first clearance, from U.S. regulators, on Dec. 1, 2020. The shipments took place through Feb. 28, 2021.
It was unclear how many of those doses had been administered as of that date.
Pfizer did not respond to emailed questions, including how many workers it has onboarded to deal with adverse events.
The companies that manufacture the other two COVID-19 vaccines that U.S. regulators have cleared, Moderna and Johnson & Johnson, did not respond when asked if they have seen an increase in adverse events and if they have hired more employees to deal with reports.
The number of post-vaccination adverse event reports to the Vaccine Adverse Event Reporting System, jointly run by the FDA and the Centers for Disease Control and Prevention, has spiked since the vaccines were first cleared.
Problems linked to the vaccines include heart inflammation, blood clotting, and severe allergic shock.
Federal officials say the vaccines’ benefits outweigh the risks, but some experts are increasingly questioning that assertion, particularly for certain populations.
As for his part, Dr. Bryan Ardis not only believes that Pope Francis and the Vatican are behind the entire COVID scamdemic, but he also believes it is not even a virus we’re dealing with, something we have advocated for nearly 2 years!
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