Evidence map›Paper›PMID 39031227›Full record

ArticleDrugs - real world outcomes2024

The Association Between Deep Vein Thrombosis, Pulmonary Embolism, and Janus Kinase Inhibitors: Reporting Status and Signal Detection in the Japanese Adverse Drug Event Report Database.

Tae Maeshima, Sayaka Aisu, Naoki Ohkura, Machiko Watanabe, Fumio Itagaki

Abstract read
In one paragraph

Article in Drugs - real world outcomes, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Recent Advances in Drug Development for Hair Loss.International journal of molecular sciences · 2025
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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

5 authors.

Tae MaeshimaDepartment of Clinical and Pharmaceutical Sciences, Faculty of Pharmaceutical Sciences, Teikyo University, Itabashi-ku, Tokyo, 173-8605, Japan. t-maeshima@pharm.teikyo-u.ac.jp.ORCID http://orcid.org/0000-0003-2179-9045
Sayaka AisuDepartment of Clinical and Pharmaceutical Sciences, Faculty of Pharmaceutical Sciences, Teikyo University, Itabashi-ku, Tokyo, 173-8605, Japan.
Naoki OhkuraDepartment of Medical and Pharmaceutical Sciences, Faculty of Pharmaceutical Sciences, Teikyo University, Itabashi-ku, Tokyo, 173-8605, Japan.
Machiko WatanabeDepartment of Clinical and Pharmaceutical Sciences, Faculty of Pharmaceutical Sciences, Teikyo University, Itabashi-ku, Tokyo, 173-8605, Japan.ORCID http://orcid.org/0000-0003-0291-5514
Fumio ItagakiDepartment of Clinical and Pharmaceutical Sciences, Faculty of Pharmaceutical Sciences, Teikyo University, Itabashi-ku, Tokyo, 173-8605, Japan.ORCID http://orcid.org/0000-0002-2816-6542

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough Janus kinase (JAK) inhibitors have expanding indications, deep vein thrombosis (DVT) and pulmonary embolism (PE) are serious adverse events associated with their use. Moreover, their analysis using the Japanese database of spontaneous adverse drug reaction reports has not yet been conducted.

objectiveThe objective of this study was to analyze the Japanese Adverse Drug Event Report database (JADER) to evaluate the association between JAK inhibitors and DVT and PE.

methodsJADER reports from April 2004 to October 2023 were analyzed. A classification of reports for the period covered was performed by drug, and an imbalance analysis was performed with oral JAK inhibitors as the target drug and DVT, PE, and "embolic and thrombotic events, venous" (Standardised MedDRA Query; SMQ) as the target adverse events. Reported odds ratios (ROR) and information components (IC) were calculated for signal detection.

resultsOverall, 6631 JAK inhibitor-related adverse events were reported, including 60 and 41 cases of DVT and PE, respectively. The ROR and IC of the JAK inhibitors for DVT were 2.52 (1.95-3.25) and 1.27 (0.41-2.13), while those of baricitinib for DVT were 4.37 (2.83-6.73) and 1.90 (0.47-3.33), respectively. ROR signals were detected for JAK inhibitors for PE and "embolic and thrombotic events, venous (SMQ)," overall and for several JAK inhibitors but none for IC.

conclusionsSeveral JAK inhibitors are under postmarketing phase vigilance, and the number of reported adverse events is low. However, when administering these drugs, care should be taken to avoid the development of thromboembolism, considering the patient's background.

Identifiers

PMID39031227
PMCPMC11365871

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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.