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“Even with respect to near-term acute adverse reactions, the study populations for these vaccines are very small, as it was only with mass vaccinations that the FDA was able to detect serious adverse reactions, particularly among young males,” read the letter.

The group demanded that the FDA answer more questions about the vaccine and its effects on children. They are also demanding that the FDA release data from pre-approval manufacturer studies, post-approval adverse events and other post-approval manufacturer data it has received from Big Pharma companies.

“We are in our third year with COVID-19, and we know vastly more about the virus than we did in 2020. One of the most important things we know is that this virus poses minimal risk for children,” said Cruz.

“Before the FDA approves an emergency use authorization for a children’s vaccine, parents should be able to see the data and paperwork they would use to justify this decision. This is the least the FDA can do for families in Texas and across the country so parents can make the best decisions for their children.”

Fifteen other Republican congressmen and one senator – Wisconsin Sen. Ron Johnson @SenRonJohnsonUS – have signed Posey and Cruz’s letter.

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