Covid-19
Exposed! Why Pfizer is desperate to rush COVID shots for infants
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.
In mid-December 2021, Pfizer admitted that two injections, at one-tenth the adult dose, failed to produce an adequate immune response in 2- to 4-year-olds. They’re now experimenting to see if three doses will produce adequate results in that age group.
As reported by The New York Times, were Pfizer to wait until the triple-dose experiment is completed, the EUA request would not be possible until late March, 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.”
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In other words, they apparently don’t care whether the shots are effective or not. They claim the shots are “safe,” so it’s OK to inject young children even though they might not gain any benefit. Does that make any sense?
According to MSN: “Pfizer and its partner BioNTech said that the submission was at the request of the FDA, which is an unusual move. Quickly after the announcement, the FDA scheduled a meeting of its vaccine advisory committee for Feb. 15 to discuss the application.
“Allowing Pfizer to submit the request now means that, if authorized, ‘parents will have the opportunity to begin a COVID-19 vaccination series for their children while awaiting potential authorization of a third dose,’ according to Pfizer CEO Albert Bourla. Data on the third dose will be submitted to the FDA ‘in the coming months,’ the company said.”
A number of medical experts, scientists and published studies have warned that COVID shots can reprogram the immune system to respond in a dysfunctional manner.
For example, a study posted on the preprint server medRxiv, May 6, 2021, found the Pfizer/BioNTech COVID jab “reprograms both adaptive and innate immune responses,” causing immune depletion.
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While the jab “induced effective humoral and cellular immunity against several SARS-CoV-2 variants,” the shot “also modulated the production of inflammatory cytokines by innate immune cells upon stimulation with both specific (SARS-CoV-2) and nonspecific (viral, fungal and bacterial) stimuli.”
People who were “fully vaccinated,” having received two doses of the Pfizer shot, also produced significantly less interferon upon stimulation, which hampers vitally important innate immune responses.
In other words, we’re looking at a horrible tradeoff. You may get some protection against SARS-CoV-2 and its variants, but you’re weakening your overall immune function, which opens the door wide to all sorts of other health problems, from bacterial, fungal and viral infections to cancer and autoimmunity.
Just because children aren’t dying within a few weeks of the shot does not mean it’s harmless and therefore safe to use. Most of the damage from these jabs will emerge far down the road, long after they’ve gotten the shot.
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 Dec. 1, 2020, and Feb. 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.
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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, to finalize the full release in about eight months.
According to Dispatches, Pfizer’s COVID jab has become the most profitable pharmaceutical product the world has ever seen.
As of the third quarter of 2021, Pfizer’s revenues were 130% above operational costs, with COVID jab revenue for 2021 reaching $36 billion. Revenue from the jab is predicted to rise to $55 billion in 2022 — equivalent to the gross domestic product (GDP) of Croatia.
One of the reasons for Pfizer’s record-breaking profits, Dispatches says, is because it has been prioritizing sales to wealthier Western nations willing and able to pay the higher cost.
Pfizer has also refused to license its patented recipe to ensure an adequate supply for poorer nations.
Its gross profit margin is estimated to be somewhere around 80%, or perhaps a little more. Pfizer, meanwhile, claims its profit margin for the jab is in the high-20%.
Article culled from The Defender
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