By Pfizer Continues to Use Babies and Children as Lab Rats to Develop More COVID-19 Vaccines – Petitions FDA for New EUA Booster for 5 to 11 Year Olds
(by Brian Shilhavy | Vaccine Impact) – Pfizer and BioNTech announced today that they have completed a submission to the U.S. Food and Drug Administration (FDA) requesting Emergency Use Authorization (EUA) of a 10-µg booster dose of the companies’ Omicron BA.4/BA.5-adapted bivalent COVID-19 vaccine for children ages 5 through 11 years of age.
They will also be making a submission to the European Medicines Agency (EMA) in the coming days.
Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) today announced they have completed a submission to the U.S. Food and Drug Administration (FDA) requesting Emergency Use Authorization (EUA) of a 10-µg booster dose of the companies’ Omicron BA.4/BA.5-adapted bivalent COVID-19 vaccine for children ages 5 through 11 years of age.
The request for Emergency Use Authorization of the Omicron BA.4/BA.5-adapted bivalent vaccine in this age group is supported by safety and immunogenicity data from the companies’ bivalent Omicron BA.1-adapted vaccine, non-clinical and manufacturing data from the companies’ 10-µg bivalent Omicron BA.4/BA.5-adapted vaccine, and pre-clinical data from the companies’ Omicron BA.4/BA.5-adapted vaccine in their decision.
An application to extend the Omicron BA.4/BA.5-adapted bivalent vaccine marketing authorization to include children ages 5 through 11 years will be submitted to the European Medicines Agency (EMA) in the coming days. (Source.)
The Press Release today also reported that they have begun Phase 1/2/3 studies on babies and young children aged 6 months through 11 years of age to test “the safety, tolerability, and immunogenicity of different doses and dosing regimens of the companies’ Omicron BA.4/BA.5-adapted bivalent COVID-19 vaccine in children 6 months through 11 years of age.” (Source.)
The Omicron BA.4/BA.5-adapted bivalent COVID-19 vaccine was already authorized for adults over the age of 18 on August 31, 2022 without any human testing, so Pfizer is using babies and children as lab rats to conduct the first human tests on this new COVID-19 vaccine.
The Press Release was published on businesswire, which is owned by Warren Buffet’s Berkshire Hathaway investment firm, and who undoubtedly is heavily invested in Pfizer stock and COVID-19 vaccine development.
Some have observed and suggested that their logo has 3 numeral 6s embedded within it, which is common in many logos used by companies owned by the Globalists today, especially in the financial world. See:
The “Mark of the Beast” and 666 Already Permeates Our Culture
Some Pro-Vaccine Heavyweights are Breaking Ranks with the FDA Over Child COVID Shots
One of the more interesting news articles to come through my newsfeed in recent days, is an interview that Dr. Paul Offit did with CNN, where he came out AGAINST giving COVID-19 booster shots to younger people.
FDA advisor and vaccine maker Paul Offit: “A healthy young person is unlikely to benefit from a booster dose… If there’s not clear evidence of benefit, then it’s not fair to ask people to take a risk.” pic.twitter.com/SgBp5WZbMS
— Max Blumenthal (@MaxBlumenthal) September 24, 2022
The reason this is interesting, is because Dr. Paul Offit is perhaps one of the most militant pro-vaccine doctors in the world. He is infamous for stating that childhood vaccines are so safe, that babies could receive up to 10,000 vaccines at one time with no harmful effects.
He owns stock in one of the childhood vaccines on the CDC childhood vaccination schedule, and in the past he has called for journalists who question vaccines to be arrested and jailed. See:
Dr. Offit Wants to Eliminate Religious and Philosophical Vaccine Exemptions
A search of his name on Health Impact News will return a result of 92 articles where we have mentioned him in the past. Dr. Offit is what we have labeled in the past as an “Extremist Pro-Vaccine Doctor,” because these kind of doctors believe that ALL vaccines are good for ALL people ALL the time, by force if necessary.
He is an advisor to the FDA for new vaccine approvals, and he voted AGAINST the approval of the COVID-19 shots for young children the first time they were submitted to the FDA, but the FDA and CDC approved them anyway, against the advice of the FDA Advisory Committee that included industry insiders such as Dr. Offit.
So why would he become so vocal against the COVID-19 shots for children, as he has touted the line “the science is settled when it comes to vaccines” for decades now in his efforts to get parents to vaccinate their children?
The only logical explanation I can think of, is that he is afraid of what potential lawsuits are coming down the road against Pfizer and the FDA, and wants to abandon a burning, sinking ship, while there is still time.
Because prior to this, it is safe to say that Dr. Offit never met a vaccine for children he didn’t like.
VAERS Data – This Should End Any Discussion of Injecting Children with COVID-19 Shots
The U.S. VAERS (Vaccine Adverse Events Reporting System) government database has just added a separate category for the newly authorized COVID-19 Bivalent vaccine, which was given emergency use authorization by the FDA as a COVID-19 “booster” shot on August 31, 2022, for adults 18 years and older. (Source.)
As of the latest update to the VAERS database on 9/16/2022, there have already been 528 cases filed of adverse reactions to this newly authorized COVID-19 booster shot, including 1 death, 1 permanent disability, 39 ER visits, 5 life threatening injuries, and 9 hospitalizations. (Source.) Read Full Article >
