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The U.S. Food and Drug Administration's risk-benefit assessment in connection with Pfizer's application for emergency use of its COVID vaccine for children 5 to 11 describes only relative risks in an older population. It ignores absolute risk and.

New yorkUnited statesAlex berensonJohn ioannidisAllan cunninghamRonald brownSara oliverJessica roseCathrine axforsCenters for diseaseDrug administrationBiologics products advisory committeeBiden administrationGuidance for health economics studiesAdvisory committee on immunization practicesNumber needed to vaccinated