from Alison Ryan
LONDON (LifeSiteNews) – Britain’s Office for National Statistics (ONS) has released data indicating that children who received the COVID-19 jabs have suffered a death rate 54 times greater than that of their un-jabbed counterparts.
February 08, 2022
Pfizer Seeks COVID Shot Authorization for Children Under 5
Analysis by Dr. Joseph Mercola
> February 1, 2022, Pfizer/BioNTech asked the U.S. Food and Drug Administration to grant emergency use authorization (EUA) for their COVID shot to babies and children aged 6 months through 4 years
> The EUA will be for a two-dose regimen, with the possibility of extending it to a third dose, as two injections have been shown to be ineffective in 2- to 4-year-olds
> Children aged 6 months to 4 years will get a dose that is one-tenth the adult dose
> Were Pfizer to wait until the triple-dose experiment is completed, the EUA request would not be possible until late March 2022, and federal officials are reportedly “anxious to begin a vaccination program for the youngest children because the studies showed there were no safety concerns with two doses”
> Meanwhile, Pfizer’s own data raise massive safety concerns, as they received 42,086 injury reports, including 1,223 fatalities in the first 2.5 months of their COVID jab rollout for adults
Despite conclusive evidence that young children have virtually no risk of severe complications or death from COVID-19, Pfizer is hustling to get our infants and toddlers injected with their experimental gene transfer technology.
Pfizer’s own trial data, which are starting to be released in response to a Freedom of Information Act (FOIA) request to the FDA, also do nothing to assuage safety concerns. Quite the contrary. Cumulatively, between December 1, 2020, and February 28, 2021 — a period of just 2.5 months — Pfizer received 42,086 injury reports, including 1,223 fatalities.
Compare that to the 1976 swine flu vaccine, which was pulled after 25 deaths. Pfizer even acknowledges the abnormal rate of injuries. They actually had to hire more data entry and case processing personnel to handle the influx of adverse events reports. Still, they insist everything is hunky-dory and there’s absolutely no problem.
Initially, the FDA wanted 55 years to release all of Pfizer’s trial data at a rate of 500 pages per month. After finding another trove of related documents, they asked for 75 years. A judge denied both requests, ordering the agency to release the data at a rate of 55,000 pages per month, starting March 1, 2022, to finalize the full release in about eight months.
It is understandable that the FDA does not want independent scientists to review the documents it relied upon to license Pfizer’s vaccine given that it is not as effective as the FDA originally claimed, does not prevent transmission, does not prevent against certain emerging variants, can cause serious heart inflammation in younger individuals, and has numerous other undisputed safety issues.’
Why is the FDA risking our children?
As mentioned, we already know children are essentially at zero risk of dying from COVID. They might test positive. They might develop symptoms, but they get through it just like they get through the common cold or flu. There’s no reason to jeopardize their long-term health with a COVID jab. They don’t need it, and therefore ANY risk of the jab, no matter how small, is unconscionable and unacceptable.