Adverse Events Reported to the United States Food and Drug Administration Related to Caffeine-Containing Products.

Mayo Clinic proceedings2020Jagim AR, Harty PS, Fischer KM, et al.

Study designOther primary literature

SubjectHuman

Abstract

cc by 以外（cc by-nc / cc by-nc-nd / NONE 等）は抄録を再掲しない。DOI/PMID へのリンクのみ表示する。

MeSH

AdolescentAdultAdverse Drug Reaction Reporting SystemsAgedAged, 80 and overAnti-Obesity AgentsCaffeineCarbonated BeveragesChildChild, PreschoolCoffeeDietary SupplementsFemaleHumansInfantMaleMiddle AgedTeaUnited StatesUnited States Food and Drug AdministrationYoung Adult

DOI 10.1016/j.mayocp.2020.02.033

PMID 32753134

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