Use of the Electronic Health Record for Monitoring Adverse Drug Reactions
Author:
Funder
NIH-NCATS
Publisher
Springer Science and Business Media LLC
Subject
Pulmonary and Respiratory Medicine,Immunology and Allergy,Immunology
Link
https://link.springer.com/content/pdf/10.1007/s11882-023-01087-w.pdf
Reference59 articles.
1. Khan DA, et al. Drug allergy: a 2022 practice parameter update. J Allergy Clin Immunol. 2022. https://doi.org/10.1016/j.jaci.2022.08.028.
2. Pichler WJ. Immune pathomechanism and classification of drug hypersensitivity. Allergy: Eur J Allergy Clin Immunol. Blackwell Publishing Ltd. 2019;74(8):1457–71. https://doi.org/10.1111/all.13765.
3. Schmid O, Bereznicki B, Peterson GM, Stankovich J, Bereznicki L. Persistence of adverse drug reaction-related hospitalization risk following discharge. Int J Environ Res Public Health. 2022;19(9). https://doi.org/10.3390/ijerph19095585.
4. Forster AJ, Jennings A, Chow C, Leeder C, van Walraven C. A systematic review to evaluate the accuracy of electronic adverse drug event detection. J Am Med Inform Assoc. 2012;19(1):31–8. https://doi.org/10.1136/amiajnl-2011-000454.
5. Ball R, Robb M, Anderson SA, Dal Pan G. The FDAs sentinel initiative—a comprehensive approach to medical product surveillance. Clin Pharmacol Ther. 2016;99(3):265–8. Nature Publishing Group. https://doi.org/10.1002/cpt.320.
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