Evidence map›Paper›PMID 38615313›Full record

ArticleRheumatology international2024

The temporal association between adverse drug reactions and antirheumatic drugs utilisation in Western Australia: a retrospective study from real-world data (1995-2015).

Khalid B Almutairi, Charles A Inderjeeth, David B Preen, Helen I Keen, Johannes C Nossent

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Rheumatology international, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 36% of its field
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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Observational
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 at 1 institution in 2 countries.

Khalid B AlmutairiSchool of Medicine, The University of Western Australia, Perth, Australia. khalid.almutairi@uwa.edu.au.ORCID 0000-0003-0535-963X
Charles A InderjeethSchool of Medicine, The University of Western Australia, Perth, Australia.ORCID 0000-0002-9246-7294
David B PreenSchool of Population and Global Health, University of Western Australia, Perth, WA, Australia.ORCID 0000-0002-2982-2169
Helen I KeenSchool of Medicine, The University of Western Australia, Perth, Australia.ORCID 0000-0002-8469-2424
Johannes C NossentSchool of Medicine, The University of Western Australia, Perth, Australia.ORCID 0000-0002-2833-7997
The University of Western Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesAdverse drug reactions (ADRs) can result in morbidity, mortality, and higher healthcare costs. Given the limited information available on ADRs associated with antirheumatic medications, this study aims to analyse and compare ADR reporting for these drugs in the pharmacovigilance datasets of Western Australia (WA) and the United States (US).

methodsTherapeutic Goods Administration provided WA pharmacovigilance data of selected antirheumatic drugs to from 1995 to 2015. The proportional reporting ratio (PRR) for WA case reports was compared to corresponding USA pharmacovigilance data by assessing the disproportionality of each ADR. clinically significant or true ADRs were determined using the Evans 2001 criteria (n > 2, chi-square > 4, PRR > 2).

resultsA total of 232 reports were found in WA, mostly on sixty-nine women aged 45 to 69. Methotrexate, leflunomide, azathioprine, sulfasalazine, and infliximab had the highest reported ADRs, related to gastrointestinal disorders. Patients who used biological agents in WA had 2.7 times the likelihood of reporting true ADRs compared to conventional antirheumatic drugs. The ADR rates in the two datasets were comparable over the study period.

conclusionsThe PRR values of ADRs were consistent between WA and US databases. Methotrexate and infliximab use were commonly associated with ADR reports in WA females, with incidence rates comparable to the US; while patients using biological agents were more likely to report true ADRs than those on conventional antirheumatic drugs in WA.

Indexed as

Adverse Drug Reaction Reporting SystemsAntirheumatic AgentsPharmacovigilanceAdultAgedDatabases, FactualDrug-Related Side Effects and Adverse ReactionsFemaleHumansMaleMiddle AgedRetrospective StudiesTime FactorsUnited StatesWestern AustraliaYoung AdultAntirheumatic AgentsAdverse drug reactionsDisease-modifying antirheumatic drugsPharmacovigilanceUnited States Food and Drug Administration Adverse Event Reporting SystemWestern Australia database of adverse event notifications

Identifiers

PMID38615313
PMCPMC11108947
OpenAlexW4394793922

What OpenQuestion holds

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LicenceCC BY
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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.