FDA panel endorses Moderna’s COVID-19 booster vaccine for certain high risk groups
Fox News
A U.S. Food and Drug Administration (FDA) advisory panel on Thursday endorsed emergency authorization for Moderna’s half-dose COVID-19 vaccine booster shot when administered at least six months following the two-dose series among people ages 65 and older and those ages 18-64 at high risk of occupational exposure and severe COVID-19.
The FDA's Vaccines and Related Biological Products Advisory Committee, (VRBPAC) was charged with voting whether available data supported the safety and effectiveness of a 50 microgram booster dose among three high risk groups:
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