FDA: 86% of Children in Pfizer Vaccine Study Experienced Adverse Reactions

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As children become human guinea pigs in the Pfizer vaccine studies, the vast majority of them experience adverse reactions ranging from “mild to serious.”

The study included children aged 12-15, 1,127 children were given the first dose and 1,097 were given the second dose. Among the the children injected with the experimental mRNA vaccine:

  • 86% experienced side effects
  • Close to 44% experienced “moderate” effects, defined as “interfering with activity.”
  • 66% experienced fevers
  • 65% suffered headaches

Other side effects include: muscle pain, vomiting, diarrhea, joint pain, and chills. Even after 86% of the children involved in the study reported negative reactions to the vaccine, they were still subjected to a second dose.

Despite these overwhelmingly negative results, Acting FDA Commissioner, Janet Woodcock, M.D. released a statement praising Pfizer:

“Today’s action allows for a younger population to be protected from COVID-19, bringing us closer to returning to a sense of normalcy and to ending the pandemic. Parents and guardians can rest assured that the agency undertook a rigorous and thorough review of all available data, as we have with all of our COVID-19 vaccine emergency use authorizations.”

The official FDA document can be found here, and in the event of deletion, the back-up version of the document can be found here.




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1 COMMENT

  1. A non-tested vaccine granted use on a so-called “emergency basis” yet the bidenfail committee continue to promote the witch’s brew knowing the handmade-by-etsy-sellers is a toxic bioweapon intended to “thin the herd”.

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