Evidence map›Paper›PMID 42471477›Full record

ArticleClinical and translational science2026

Exploring Risks of Adverse Drug Events From Single Drug to Three-Drug Combination.

Yi Shi, Anna Sun, Chien-Wei Chiang, Yuedi Yang, Katherine M Hunold, Jing Xu, Mu Shan, Allison Lu, Massimiliano Russo, Jeffrey M Caterino and 5 more

Abstract read
In one paragraph

Article in Clinical and translational science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Yi ShiDepartment of Biostatistics and Health Data Science, Indiana University, Indianapolis, Indiana, USA.ORCID 0000-0003-0145-2968
Anna SunDepartment of Biostatistics and Health Data Science, Indiana University, Indianapolis, Indiana, USA.ORCID 0009-0009-0905-6469
Chien-Wei ChiangDepartment of Biomedical Informatics, The Ohio State University, Columbus, Ohio, USA.
Yuedi YangDepartment of Biostatistics and Health Data Science, Indiana University, Indianapolis, Indiana, USA.ORCID 0009-0007-5067-4387
Katherine M HunoldDepartment of Emergency Medicine, The Ohio State University, Columbus, Ohio, USA.ORCID 0000-0001-8938-0596
Jing XuDepartment of Biostatistics and Health Data Science, Indiana University, Indianapolis, Indiana, USA.ORCID 0000-0003-3673-7592
Mu ShanEli Lilly and Company, Indianapolis, Indiana, USA.
Allison LuDepartment of Computer Science, Purdue University, West Lafayette, Indiana, USA.
Massimiliano RussoDepartment of Statistics, The Ohio State University, Columbus, Ohio, USA.
Jeffrey M CaterinoDepartment of Emergency Medicine, The Ohio State University, Columbus, Ohio, USA.
Michael T EadonDepartment of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.ORCID 0000-0003-3066-2876
Lang LiDepartment of Biomedical Informatics, The Ohio State University, Columbus, Ohio, USA.
Jing SuDepartment of Biostatistics and Health Data Science, Indiana University, Indianapolis, Indiana, USA.ORCID 0000-0003-4917-6173
Macarius DonneyongCollege of Pharmacy, The Ohio State University, Columbus, Ohio, USA.ORCID 0000-0003-2710-913X
Pengyue ZhangDepartment of Biostatistics and Health Data Science, Indiana University, Indianapolis, Indiana, USA.ORCID 0000-0002-9148-5589

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Use of three-drug combinations is common and could increase the risk of adverse drug events (ADEs). Signals of ADEs from three-drug combinations could be identified from real-world data, and the risks of ADEs from single drug exposure to three-drug combination exposure could be illustrated by a graphic model. We used a US nationwide insurance claim database. We explored the relationship between drug exposure (from single drugs to three-drug combinations) and risks of ADEs (acute kidney injury, gastrointestinal bleeding, and opioid-related ADE). We used a conditional logistic regression model to estimate the odds ratios (ORs), the posterior probability of null hypothesis to control false discovery rate (FDR), and a graphic model to illustrate the ORs from single drug exposure to three-drug combination exposure. We derived approximately 1.7 million covariate-matched ADE-case-control pairs and investigated approximately 0.25 million three-drug combinations. We identified 3412 signals of adverse three-drug combinations (FDR < 0.01 and OR > 2). For the signals, we observed the medians and interquartile ranges (IQRs) of ORs increased from single drug exposure (median = 1.03, IQR: 0.95-1.15), through two-drug combination exposure (median = 1.45, IQR: 1.23-1.75), to three-drug combination exposure (median = 2.95, IQR: 2.43-3.91). We built a webpage-based tool to illustrate the ORs from single drug exposure to three-drug combination exposure. In conclusion, certain three-drug combinations are associated with an increased risk of ADE, and the risks of ADE could increase from single drug exposure to three-drug combination exposure.

Indexed as

Acute Kidney InjuryDrug-Related Side Effects and Adverse ReactionsGastrointestinal HemorrhageAnalgesics, OpioidCase-Control StudiesDatabases, FactualDrug CombinationsDrug InteractionsHumansLogistic ModelsOdds RatioRisk AssessmentRisk FactorsUnited StatesAnalgesics, OpioidDrug Combinationsacute kidney injuryadverse drug event (ADE)drug interactiongastrointestinal bleedingopioidthree‐drug combination

Identifiers

PMID42471477
PMCPMC13380602

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.