Improving drug safety with adverse event detection using natural language processing
Author:
Affiliation:
1. Department of Oncology, the Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA
Publisher
Informa UK Limited
Subject
Pharmacology (medical),General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/14740338.2023.2228197
Reference81 articles.
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2. FDA. Guidance for industry and investigators: safety reporting requirements for INDs and BA/BE studies. Silver Spring MD: Food and Drug Administration. 2012.
3. Council for International Organizations of Medical Sciences. Working Group VIII. Practical aspects of signal detection in pharmacovigilance: report of CIOMS working group VIII. Geneva: CIOMS; 2010.
4. Adverse drug event rates in pediatric pulmonary hypertension: a comparison of real-world data sources
5. Text Mining for Adverse Drug Events: the Promise, Challenges, and State of the Art
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