Complementing the US Food and Drug Administration Adverse Event Reporting System With Adverse Drug Reaction Reporting From Social Media: Comparative Analysis
BackgroundAdverse drug reactions (ADRs) can occur any time someone uses a medication. ADRs are systematically tracked and cataloged, with varying degrees of success, in order to better understand their etiology and develop methods of prevention. The US Food and Drug Administr...
Main Authors: | Zhou, Zeyun, Hultgren, Kyle Emerson |
---|---|
Format: | Article |
Language: | English |
Published: |
JMIR Publications
2020-09-01
|
Series: | JMIR Public Health and Surveillance |
Online Access: | https://publichealth.jmir.org/2020/3/e19266 |
Similar Items
-
Under-reporting of Adverse Drug Reactions to the Food & Drug Administration
by: Lamb, James Alexander
Published: (2018) -
Detecting Adverse Drug Reactions in Electronic Health Records by using the Food and Drug Administration’s Adverse Event Reporting System
by: Tang, Huaxiu
Published: (2016) -
Characteristics of pediatric adverse drug reaction reports in the Japanese Adverse Drug Event Report Database
by: Aoi Noda, et al.
Published: (2020-05-01) -
Assessment of Reye’s syndrome profile with data from the US Food and Drug Administration Adverse Event Reporting System and the Japanese Adverse Drug Event Report databases using the disproportionality analysis
by: Kiyoka Matsumoto, et al.
Published: (2020-11-01) -
Automatically Recognizing Medication and Adverse Event Information From Food and Drug Administration’s Adverse Event Reporting System Narratives
by: Polepalli Ramesh, Balaji, et al.
Published: (2014-06-01)