A systematic approach for developing a corpus of patient reported adverse drug events: A case study for SSRI and SNRI

Maryam Zolnoori1, Kin Wah Fung2, Timothy B Patrick3

  • 1Department of Health Sciences, University of Wisconsin Milwaukee, Milwaukee, WI, United States; Lister Hill National Center for Biomedical Communications, National Library of Medicine, National Institutes of Health, Bethesda, MD, United States; Section of Medical Informatics, Department of Health Science Research, Mayo Clinic, Rochester, MN, United States.

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