FDA Gives Emergency Authorization To Pfizer Booster For 12-15 Year-Olds–No Clinical Trails Cited

The FDA gave emergency authorization for 12-15-year-olds to receive the COVID vaccine.

In the FDA press release, no clinical trials are cited.

They cite data out of Israel.

From Axios:

The Food and Drug Administration expanded COVID-19 vaccine booster eligibility on Monday to allow 12- to 15-year-olds to receive a third shot of the Pfizer-BioNTech vaccine.

This comes after a study found that Pfizer’s booster shot is more likely to give young men under 40 heart inflammation.

From The Epoch Times:

Males under 40 years old are more likely to experience heart inflammation after getting a booster shot of Pfizer’s COVID-19 vaccine than COVID-19 itself, according to a recently published study.

Males in the age group had a myocarditis incidence rate ratio of 7.6 in the 28 days following receipt of a Pfizer booster, researchers with the University of Oxford and other UK institutions found.

That was higher than the ratio of 2 in the four weeks following a positive COVID-19 test result.

“For the first time, we observe an increase in myocarditis events following a third dose of BNT162b vaccine,” researchers wrote in their study, which has not been peer reviewed as of yet.

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