They were never even at risk before their first two injections, but now children aged 12-15 are slated for a third “booster” shot, thanks to new approval from the U.S. Food and Drug Administration (FDA).
The FDA has decided that kids need to get “boosted” immediately in order to flatten the curve because there is apparently not enough myocarditis going around these days.
Peter Marks, the FDA’s vaccines chief, says that parents should not worry about the heart effects of these injections because most inflammation in younger patients is “mild.”
Dr. Robert Malone, M.D., M.S., meanwhile, was recently banned from Twitter for saying the opposite, even though he is the guy who came up with mRNA (messenger RNA) technology in the first place.
Marks, a Big Pharma hack, insists that boosting children “may help provide better protection against both the delta and omicron variants,” especially since the latter is “slightly more resistant” to the jabs.
Israel provided the “real-world data” that FDA used to authorize boosters for children
Not only did the FDA authorize the Pfizer vaccine for children aged 12-15, it also shortened the waiting time between shots. Now, young children can get both injections in as little as five months as opposed to having to wait six months.
Children 5-11 who are considered to be “immunocompromised” will also be allowed to take a third injection along with children 12-15 who are not immunocompromised. This includes children:
“… who have undergone solid organ transplantation, or who have been diagnosed with conditions that are considered to have an equivalent level of immunocompromise, may not respond adequately to the two-dose primary vaccination series.”
The FDA insists that getting shot again and again with Pfizer syringes is the best way to provide “continued protection against COVID and the associated serious consequences that can occur including hospitalization and death.”
It turns out that Israel essentially made this decision for the FDA. According to reports, “real-world data from Israel, including safety data from more than 6,300 individuals 12 through 15 years of age who received a booster dose of the vaccine at least 5 months following completion of the primary two-dose vaccination series” is all that was needed for the FDA to green-light the next phase of the plandemic.
The U.S. Centers for Disease Control and Prevention (CDC) and its director Rochelle Walensky must also sign off on the FDA’s new “emergency use authorization” (EUA) for children, but this will be no problem at all as “this is considered largely a formality.”
The FDA claims that it also relied on “peer-reviewed data from multiple laboratories” in addition to Israel’s recommendation when making its decision.
“The plan is to get the EUA vax officially recommended on the pediatric schedule,” wrote one commenter at Zero Hedge.
“Once that happens the vaxx can be approved because the pediatric schedule is the key to obtaining legal immunity for the manufacturer. The only FDA “approved” vaxx (Comirnaty) is not available in U.S. because the lack of legal immunity. It’s all about the mystery clot shot for children.”
Another pointed out the lunacy of Peter Marks calling “mild heart inflammation” an acceptable risk for children.
“I’m so glad that I don’t have kids because my answer would be [go to hell],” this same person wrote. “Pfizer would like to thank Pfauci for his service.”
Another wrote that Pfizer “has been completely corrupt and evil for decades per witnesses.”
“At this point,” this same commenter added in speculation, “I have to ask if they are not deeply involved in sex trafficking, too.”
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