Evidence map›Paper›PMID 34609719›Full record

ArticleDrug safety2021

Desloratadine Exposure and Incidence of Seizure: A Nordic Post-authorization Safety Study Using a New-User Cohort Study Design, 2001-2015.

Annette Kjær Ersbøll, Kaushik Sengupta, Eero Pukkala, Kristian Bolin, Eline Aas, Martha Emneus, Dena Rosen Ramey, Joanne E Brady, Daniel Mines, Kristian Aasbjerg and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Drug safety, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
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

14 authors at 9 institutions in 5 countries.

Annette Kjær ErsbøllNational Institute of Public Health, University of Southern Denmark, Studiestræde 6, 1455, Copenhagen, Denmark. ake@sdu.dk.ORCID 0000-0002-9407-3387
Kaushik SenguptaDrug Development Consulting, Pharma IT APS, Hvidovre, Denmark.
Eero PukkalaFinnish Cancer Registry-Institute for Statistical and Epidemiological Cancer Research, Helsinki, Finland.
Kristian BolinCentre for Health Economics and Department of Economics, University of Gothenburg, Gothenburg, Sweden.
Eline AasDepartment of Health Management and Health Economics, University of Oslo, Oslo, Norway.
Martha EmneusApplied Economic and Health Research (ApHER), Copenhagen, Denmark.
Dena Rosen RameyMerck & Co., Inc., Kenilworth, NJ, USA.
Joanne E BradyMerck & Co., Inc., Kenilworth, NJ, USA.
Daniel MinesMerck & Co., Inc., Kenilworth, NJ, USA.
Kristian AasbjergDepartment of Ophthalmology, Aalborg University Hospital, Aalborg, Denmark.
Christian VestergaardDepartment of Dermatology, Aarhus University, Aarhus, Denmark.
Gunnar GislasonNational Institute of Public Health, University of Southern Denmark, Studiestræde 6, 1455, Copenhagen, Denmark.
Alfred Peter BornDepartment of Paediatrics and Adolescents Medicine, Juliane Marie Centre, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Thora Majlund KjærulffNational Institute of Public Health, University of Southern Denmark, Studiestræde 6, 1455, Copenhagen, Denmark.
Merck & Co., Inc., Rahway, NJ, USA (United States) · USUniversity of Copenhagen · DKUniversity of Southern Denmark · DKAalborg University Hospital · DKAarhus University · DKCopenhagen University Hospital · DKTampere University · FIUniversity of Gothenburg · SEUniversity of Oslo · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionA small number of adverse events of seizure in patients using desloratadine (DL) have been reported. The European Medicines Agency requested a post-authorization safety study to investigate whether there is an association between DL exposure and seizure.

objectiveThe aim was to study the association between DL exposure and incidence of first seizure.

methodsA new-user cohort study of individuals redeeming a first-ever prescription of DL in Denmark, Finland, Norway, and Sweden in 2001-2015 was conducted. DL exposure was defined as days' supply plus a 4-week grace period. DL unexposed periods were initiated 27 weeks after DL prescription redemption. Poisson regression was used to estimate the adjusted incidence rate and adjusted incidence rate ratio (aIRR) of incident seizure.

resultsA total of 1,807,347 first-ever DL users were included in the study, with 49.3% male and a mean age of 29.5 years at inclusion; 20.3% were children aged 0-5 years. The adjusted incidence rates of seizure were 21.7 and 31.6 per 100,000 person-years during DL unexposed and exposed periods, respectively. A 46% increased incidence rate of seizure was found during DL exposed periods (aIRR = 1.46, 95% confidence interval [CI] 1.34-1.59). The aIRR ranged from 1.85 (95% CI 1.65-2.08) in children aged 0-5 years to 1.01 in adults aged 20 years or more (95% CI 0.85-1.19).

conclusionThis study found an increased incidence rate of seizure during DL exposed periods as compared to unexposed periods among individuals younger than 20 years. No difference in incidence rate of seizure was observed in adults between DL exposed and unexposed.

Indexed as

Research DesignSeizuresAdultChildCohort StudiesFemaleHumansIncidenceLoratadineMaledesloratadineLoratadine

Identifiers

PMID34609719
PMCPMC8553702
OpenAlexW3203220949

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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Registered trials

None linked

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.