Miscategorization of Deaths in the US Food and Drug Administration Adverse Events Database. Academic Article uri icon

Overview

abstract

  • This database study assesses the misclassification of death reports for 2 medical devices within the US Food and Drug Administration’s Manufacturer and User Facility Device Experience database.

publication date

  • January 1, 2020

Research

keywords

  • Adverse Drug Reaction Reporting Systems
  • Drug-Related Side Effects and Adverse Reactions
  • Product Surveillance, Postmarketing
  • United States Food and Drug Administration

Identity

PubMed Central ID

  • PMC6784806

Scopus Document Identifier

  • 85073097949

Digital Object Identifier (DOI)

  • 10.1001/jamainternmed.2019.4030

PubMed ID

  • 31589249

Additional Document Info

volume

  • 180

issue

  • 1