Kingston, a former Pfizer employee, said the FDA's approval will end Pfizer and BioNTech's reign of impunity, as this will finally hold them accountable for vaccine-related injuries and deaths.
"That is to me, a red flag that Pfizer knows game over, checkmate," said Kingston. "They are already going to be held accountable for intentionally harming the American people."
The FDA approved the Pfizer/BioNTech vaccine for the Wuhan coronavirus (COVID-19) on August 23, making it the first approved COVID-19 vaccine in the country. The vaccine, now marketed as Comirnaty, is available for individuals aged 16 years and older. It also continues to be available under emergency use authorization (EUA) for adolescents aged 12 to 15, as well as for administration as a booster for people with weakened immune systems.
According to Kingston, the Pfizer/BioNTech vaccines that were granted EUA did not conform to the guidelines set by the FDA during production. But with the approval in place, Pfizer and BioNTech must now submit their final content labeling and report any deviations, complaints and adverse events associated with the approved products.
When the vaccines were initially made available under EUA, these important procedures were not followed. The quality of the vials and the consistency of the ingredients were also not checked. In addition, expiration dates were also continually extended.
"Those safety strategies, those safety protocols that were put in place, were thrown out the window," Kingston said.
The FDA approval means that Pfizer and BioNTech must now be transparent regarding any deviations in their vials – something they weren't required to disclose to the public before the approval.
So if Pfizer has had any deviations in their vaccines, there's a lot of damning information they have to report.
"If Pfizer has not been honest with the American people and with the FDA in regards to what's in these vials, they have 14 days to come clean."
When pressed by Peters on whether Pfizer was less than honest with their reporting on what's in their vaccines, Kingston noted that the lack of transparency when it comes to the side effects was suspicious. For one, the diversity of adverse effects, which range from heart inflammation to severe blood clotting, is something that does not make sense.
"The diversity of these adverse events are not consistent with a consistent product," said Kingston.
She also added that the lack of a website for the vaccine -- especially one that contains a statement regarding FDA approval and a package insert for review -- is also unusual. (Related: Pfizer will NOT mandate covid vaccines for its own employees… wonder why?)
"I've been doing this for over 20 years [and] I've launched multiple products. So going back 20 years ago, we've always had the website locked and loaded, ready to go at least six months ahead of time, literally, sometimes a year ahead of time."
Pfizer and BioNTech are keeping everyone in the dark on the specifics of the approval because they're afraid of the lawsuits that will be brought against them once this information goes public, says Kingston. What's even worse, she adds, is that the drug maker has been shilling their products, not to people, but to government institutions like the Centers for Disease Control and Prevention and the National Institutes of Health, and mainstream media.
"[Pfizer and BioNTech] have been misleading [the] American people to line themselves up, and unfortunately, in some cases, to line themselves [up] with their children to be injected with an unapproved experimental biological agent," she added.
Watch the full episode here.
The Stew Peters show airs weekdays at 6:00 p.m. on Brighteon.TV.
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