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Duration of Follow Up for New Molecular Entities Approved in 2016

    Basic Details
    Date Posted
    Medical Product
    new molecular entities (NMEs)

    The purpose of this analysis was to describe baseline characteristics and the duration of follow-up time among new users of 22 new molecular entities (NMEs) approved in 2016 by the U.S. Food and Drug Administration in the Sentinel Distributed Database (SDD). We distributed this request to 17 Data Partners on April 26, 2019. The study period included data from January 1, 2016 to August 31, 2018.