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On Oct. 26, the membership of the U.S. Food and Drug Administration’s (FDA) Vaccines and Related Biological Products Advisory Committee (VRBPAC) voted 17-0 in favor of lower-dose use of Pfizer’s experimental COVID-19 vaccine in children ages 5 to 11.
The 17 individuals — including an “acting” committee chair and 11 voting members who were temporary rather than core VRBPAC members — formulaically stated the injections’ benefits outweigh the risks in that age group.
Three days later, Dr. Janet Woodcock — a 35-year FDA veteran…
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