Evidence map›Paper›PMID 41482386›Full record

ArticleIn vivo (Athens, Greece)

Analysis of Onset Timing and Risk Factors for Mesalazine-related Adverse Events Using the JADER Database.

Kuninori Iwayama, Takayuki Manabe, Yuya Arai, Yuhi Wakata, Gensuke Oikawa, Mahiro Yamamoto, Mayuko Soma, Ko-Ichi Ohtaki, Ainari Konda, Maiko Machida

Abstract read
In one paragraph

Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

10 authors.

Kuninori IwayamaDepartment of Pharmacotherapy and Therapeutics, Faculty of Pharmaceutical Sciences, Hokkaido University of Science, Sapporo, Japan.
Takayuki ManabeDepartment of Nursing, Asahikawa Medical University, Asahikawa, Japan tmanabe@asahikawa-med.ac.jp.
Yuya AraiDepartment of Pharmacotherapy and Therapeutics, Faculty of Pharmaceutical Sciences, Hokkaido University of Science, Sapporo, Japan.
Yuhi WakataDepartment of Pharmacotherapy and Therapeutics, Faculty of Pharmaceutical Sciences, Hokkaido University of Science, Sapporo, Japan.
Gensuke OikawaDepartment of Pharmacotherapy and Therapeutics, Faculty of Pharmaceutical Sciences, Hokkaido University of Science, Sapporo, Japan.
Mahiro YamamotoDepartment of Pharmacotherapy and Therapeutics, Faculty of Pharmaceutical Sciences, Hokkaido University of Science, Sapporo, Japan.
Mayuko SomaDepartment of Pharmacotherapy and Therapeutics, Faculty of Pharmaceutical Sciences, Hokkaido University of Science, Sapporo, Japan.
Ko-Ichi OhtakiDepartment of Pharmacotherapy and Therapeutics, Faculty of Pharmaceutical Sciences, Hokkaido University of Science, Sapporo, Japan.
Ainari KondaDepartment of Pharmacotherapy and Therapeutics, Faculty of Pharmaceutical Sciences, Hokkaido University of Science, Sapporo, Japan.
Maiko MachidaDepartment of Pharmacotherapy and Therapeutics, Faculty of Pharmaceutical Sciences, Hokkaido University of Science, Sapporo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimMesalazine is a cornerstone therapy in the treatment of inflammatory bowel disease (IBD). Although formulated for local action, it can cause serious adverse events (AEs), such as interstitial lung disease and myocarditis, as well as mesalazine-specific drug intolerance. However, the timing of onset and associated risk factors remain insufficiently understood. This study aimed to analyze the onset timing and risk factors for mesalazine-related AEs using the Japanese Adverse Drug Event Report (JADER) database to provide pharmacists with essential information for effective monitoring of AEs. PATIENTS AND

methodsReporting odds ratios (RORs) for mesalazine-associated AEs in the JADER database were calculated to detect safety signals. Time-to-onset analyses were performed to classify patterns of mesalazine-induced AEs. Risk factors for mesalazine-induced drug intolerance were further evaluated using multivariate logistic regression analysis.

resultsAmong the 25 prespecified AEs, signals were detected for 15. Nine AEs were classified as early onset, and one as late-onset. Male sex and the concomitant use of budesonide, golimumab, vedolizumab, and upadacitinib were significantly detected signals of drug intolerance (all

conclusionMost mesalazine-associated AEs occurred shortly after treatment initiation, although some manifested later. Although direct risk quantification could not be performed from individual RORs, the indicated factors associated with mesalazine intolerance-including sex and specific concomitant drugs might be useful as items for monitoring AEs. These findings provide meaningful insights that may contribute to optimizing therapeutic strategies and improving the quality of life of patients with IBD.

Indexed as

Anti-Inflammatory Agents, Non-SteroidalDrug-Related Side Effects and Adverse ReactionsInflammatory Bowel DiseasesMesalamineAdultAdverse Drug Reaction Reporting SystemsAgedDatabases, FactualFemaleHumansJapanMaleMiddle AgedOdds RatioRisk FactorsTime FactorsAnti-Inflammatory Agents, Non-SteroidalMesalaminedrug intoleranceinflammatory bowel diseaseJADER databaseMesalazine

Identifiers

PMID41482386
PMCPMC12764213

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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.