Quantifying the Severity of Adverse Drug Reactions Using Social Media: Network Analysis.

adverse drug reactions drug safety machine learning network analysis pharmacovigilance social media social media for health word embeddings

Journal

Journal of medical Internet research
ISSN: 1438-8871
Titre abrégé: J Med Internet Res
Pays: Canada
ID NLM: 100959882

Informations de publication

Date de publication:
21 10 2021
Historique:
received: 03 02 2021
accepted: 14 06 2021
revised: 25 05 2021
entrez: 21 10 2021
pubmed: 22 10 2021
medline: 29 10 2021
Statut: epublish

Résumé

Adverse drug reactions (ADRs) affect the health of hundreds of thousands of individuals annually in the United States, with associated costs of hundreds of billions of dollars. The monitoring and analysis of the severity of ADRs is limited by the current qualitative and categorical systems of severity classification. Previous efforts have generated quantitative estimates for a subset of ADRs but were limited in scope because of the time and costs associated with the efforts. The aim of this study is to increase the number of ADRs for which there are quantitative severity estimates while improving the quality of these severity estimates. We present a semisupervised approach that estimates ADR severity by using social media word embeddings to construct a lexical network of ADRs and perform label propagation. We used this method to estimate the severity of 28,113 ADRs, representing 12,198 unique ADR concepts from the Medical Dictionary for Regulatory Activities. Our Severity of Adverse Events Derived from Reddit (SAEDR) scores have good correlations with real-world outcomes. The SAEDR scores had Spearman correlations of 0.595, 0.633, and -0.748 for death, serious outcome, and no outcome, respectively, with ADR case outcomes in the Food and Drug Administration Adverse Event Reporting System. We investigated different methods for defining initial seed term sets and evaluated their impact on the severity estimates. We analyzed severity distributions for ADRs based on their appearance in boxed warning drug label sections, as well as for ADRs with sex-specific associations. We found that ADRs discovered in the postmarketing period had significantly greater severity than those discovered during the clinical trial (P<.001). We created quantitative drug-risk profile (DRIP) scores for 968 drugs that had a Spearman correlation of 0.377 with drugs ranked by the Food and Drug Administration Adverse Event Reporting System cases resulting in death, where the given drug was the primary suspect. Our SAEDR and DRIP scores are well correlated with the real-world outcomes of the entities they represent and have demonstrated utility in pharmacovigilance research. We make the SAEDR scores for 12,198 ADRs and the DRIP scores for 968 drugs publicly available to enable more quantitative analysis of pharmacovigilance data.

Sections du résumé

BACKGROUND
Adverse drug reactions (ADRs) affect the health of hundreds of thousands of individuals annually in the United States, with associated costs of hundreds of billions of dollars. The monitoring and analysis of the severity of ADRs is limited by the current qualitative and categorical systems of severity classification. Previous efforts have generated quantitative estimates for a subset of ADRs but were limited in scope because of the time and costs associated with the efforts.
OBJECTIVE
The aim of this study is to increase the number of ADRs for which there are quantitative severity estimates while improving the quality of these severity estimates.
METHODS
We present a semisupervised approach that estimates ADR severity by using social media word embeddings to construct a lexical network of ADRs and perform label propagation. We used this method to estimate the severity of 28,113 ADRs, representing 12,198 unique ADR concepts from the Medical Dictionary for Regulatory Activities.
RESULTS
Our Severity of Adverse Events Derived from Reddit (SAEDR) scores have good correlations with real-world outcomes. The SAEDR scores had Spearman correlations of 0.595, 0.633, and -0.748 for death, serious outcome, and no outcome, respectively, with ADR case outcomes in the Food and Drug Administration Adverse Event Reporting System. We investigated different methods for defining initial seed term sets and evaluated their impact on the severity estimates. We analyzed severity distributions for ADRs based on their appearance in boxed warning drug label sections, as well as for ADRs with sex-specific associations. We found that ADRs discovered in the postmarketing period had significantly greater severity than those discovered during the clinical trial (P<.001). We created quantitative drug-risk profile (DRIP) scores for 968 drugs that had a Spearman correlation of 0.377 with drugs ranked by the Food and Drug Administration Adverse Event Reporting System cases resulting in death, where the given drug was the primary suspect.
CONCLUSIONS
Our SAEDR and DRIP scores are well correlated with the real-world outcomes of the entities they represent and have demonstrated utility in pharmacovigilance research. We make the SAEDR scores for 12,198 ADRs and the DRIP scores for 968 drugs publicly available to enable more quantitative analysis of pharmacovigilance data.

Identifiants

pubmed: 34673524
pii: v23i10e27714
doi: 10.2196/27714
pmc: PMC8569532
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e27714

Subventions

Organisme : NHGRI NIH HHS
ID : U24 HG010615
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI130945
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM122515
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK103358
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM102365
Pays : United States

Informations de copyright

©Adam Lavertu, Tymor Hamamsy, Russ B Altman. Originally published in the Journal of Medical Internet Research (https://www.jmir.org), 21.10.2021.

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Auteurs

Adam Lavertu (A)

Biomedical Informatics Training Program, Stanford University, Stanford, CA, United States.
Department of Biomedical Data Science, Stanford University, Stanford, CA, United States.

Tymor Hamamsy (T)

Center for Data Science, New York University, New York, NY, United States.

Russ B Altman (RB)

Department of Biomedical Data Science, Stanford University, Stanford, CA, United States.
Department of Bioengineering, Stanford University, Stanford, CA, United States.
Department of Genetics, Stanford University, Stanford, CA, United States.

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