US FDA vaccine advisers recommend emergency use authorization for booster dose of Moderna's COVID-19 vaccine

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Vaccine advisers to the US Food and Drug Administration voted unanimously Thursday to recommend emergency use authorization of a booster dose of Moderna's COVID-19 vaccine.

The FDA's Vaccines and Related Biological Products Advisory Committee agreed use of a booster dose would be safe and effective in some people six months out from their primary series.

Moderna's EUA request mirrored the groups authorized to receive a booster dose of Pfizer's mRNA vaccine. Third doses of the Moderna and Pfizer Covid-19 vaccines are already authorized for some immunocompromised people. "We can't afford to have health care workers, even if not sick, be positive and infected and have to stay home from work because in parts of the country there's a shortage of health care workers and there's burnout everywhere," said Dr. Stanley Perlman, a professor of pediatrics at the University of California San Diego.

 

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