Detection of allergic transfusion‐related adverse events from electronic medical records

Author:

Whitaker Barbee1ORCID,Pizarro Jeno2,Deady Matthew2,Williams Alan1,Ezzeldin Hussein1,Belov Artur1ORCID,Kanderian Sami2,Billings Douglas2,Cook Kerry2,Hettinger Aaron Z.3,Anderson Steven1

Affiliation:

1. Office of Biostatistics and Pharmacovigilance, Center for Biologics Evaluation and Research US Food and Drug Administration Silver Spring Maryland USA

2. International Business Machines (IBM) Corporation Bethesda Maryland USA

3. Center for Biostatistics, Informatics and Data Science MedStar Health Research Institute Hyattsville Maryland USA

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Reference19 articles.

1. The Food and Drug Administration (FDA).CBER biologics effectiveness and safety (BEST) system. Available from:https://www.fda.gov/vaccines-blood-biologics/safety-availability-biologics/cber-biologics-effectiveness-and-safety-best-system

2. Centers for Disease Control and Prevention (CDC).National Healthcare Safety Network Biovigilance Component Hemovigilance Module Surveillance Protocol. 2018 [cited 2020 Jan 16]. Available from:https://www.cdc.gov/nhsn/pdfs/biovigilance/bv-hv-protocol-current.pdf

3. Risks of blood transfusion

4. The use of natural language processing to identify Tdap-related local reactions at five health care systems in the Vaccine Safety Datalink

5. Active Computerized Pharmacovigilance Using Natural Language Processing, Statistics, and Electronic Health Records: A Feasibility Study

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