Evidence map›Paper›PMID 42057267›Full record

ArticlePharmacoepidemiology and drug safety2026

The EUROmediCAT Network and Databases: A Resource for Pharmacovigilance in Pregnancy.

Helen Dolk, Christine Damase-Michel, Joan Morris, Amanda Neville, Ester Garne, Sue Jordan, Anke Rissmann, Alessio Coi, Deirdre Folan, Dieuwke Broekstra and 18 more

Abstract read
In one paragraph

Article in Pharmacoepidemiology and drug safety, 2026. 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
–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

1 citing paper in PubMed.

  1. 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

28 authors.

Helen DolkSchool of Medicine, Ulster University, Londonderry, UK.ORCID https://orcid.org/0000-0001-6639-5904
Christine Damase-MichelPharmacologie, Faculté de Médecine, Université Toulouse III, Centre Hospitalier Universitaire, INSERM, Center for Epidemiology and Research in POPulation Health (CERPOP), Toulouse, France.ORCID https://orcid.org/0000-0001-5018-0108
Joan MorrisPopulation Health Research Institute, St George's University of London, London, UK.ORCID https://orcid.org/0000-0002-7164-612X
Amanda NevilleIMER Registry, Centre for Epidemiology and Clinical Research, University of Ferrara and Azienda ospedaliera e universitaria di Ferrara, Ferrara, Italy.
Ester GarneDepartment of Paediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Odense, Denmark.ORCID https://orcid.org/0000-0003-0430-2594
Sue JordanFaculty of Medicine, Health and Life Science, Swansea University, Swansea, UK.ORCID https://orcid.org/0000-0002-5691-2987
Anke RissmannMalformation Monitoring Centre Saxony-Anhalt, Medical Faculty Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.ORCID https://orcid.org/0000-0002-9437-2790
Alessio CoiUnit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology - National Research Council, Pisa, Italy.ORCID https://orcid.org/0000-0002-9816-3144
Deirdre FolanSchool of Medicine, Londonderry, Ulster University, Londonderry, UK.
Dieuwke BroekstraUniversity of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, the Netherlands.ORCID https://orcid.org/0000-0002-7134-7007
Jennifer M BroughanNational Congenital Anomaly and Rare Disease Registration Service (NCARDRS), National Disease Registration Service, Data & Analytics, Transformation Directorate, NHS England, Leeds, UK.ORCID https://orcid.org/0000-0002-4450-2147
Lea BruneauThe Reunion Registry of Congenital Malformations REMACOR and National Institute of Health and Medical Research INSERM Center for Clinical Investigation (CIC)14 10 Clinical Epidemiology, Department of Public Health and Research Support, University Hospital of La Réunion, Saint-Denis, France.ORCID https://orcid.org/0000-0002-4310-215X
Clara Cavero-CarbonellRare Diseases Research Unit, Foundation for the Promotion of the Research in Healthcare and Biomedicine, Valencia, Spain.ORCID https://orcid.org/0000-0002-4858-6456
Elly den HondProvincial Institute of Hygiene (PIH), Antwerp, Belgium.ORCID https://orcid.org/0000-0002-3909-6877
Miriam GattDirectorate for Health Information and Research, Ministry for Health, Valletta, Malta.ORCID https://orcid.org/0000-0003-1557-9919
Mika GisslerDepartment of Data and Analytics, THL Finnish Institute for Health and Welfare, Helsinki, Finland.ORCID https://orcid.org/0000-0001-8254-7525
Babak KhoshnoodCentre de Recherche Epidémiologie et Statistique - Inserm, Université de Paris, UMR 1153 DHU Risques et Grossesse Maternité Port-Royal, Paris, France.ORCID https://orcid.org/0000-0002-4031-4915
Anna Latos BielenskaChair and Department of Medical Genetics, Poznan University of Medical Sciences, Poznan, Poland.ORCID https://orcid.org/0000-0002-9152-1674
Hedvig NordengPharmacoepidemiology and Drug Safety Group, Department of Pharmacy, Faculty of Mathematics and Natural Sciences, University of Oslo, Oslo, Norway.ORCID https://orcid.org/0000-0001-6361-2918
Ljubica OdakChildren's Hospital Zagreb, Centre of Excellence for Reproductive and Regenerative Medicine, Medical School University of Zagreb, Zagreb, Croatia.ORCID https://orcid.org/0000-0001-9023-5142
Mary O'MahonyDepartment of Public Health, Health Service Executive - South, St Finbarr's Hospital, Cork, Ireland.ORCID https://orcid.org/0000-0003-0574-7579
Isabelle PerthusAuvergne Registry of Congenital Anomalies (CEMC-Auvergne), Service de Génétique Clinique, Centre de Référence des Maladies Rares, Université Clermont Auvergne, CHU Clermont-Ferrand, CNRS, SIGMA Clermont, Institut Pascal, Clermont-Ferrand, France.ORCID https://orcid.org/0000-0002-3845-6180
J Luke RichardsonUK Teratology Information Service, Newcastle upon Tyne Hospitals NHS Foundation Trust and UK Health Security Agency, Newcastle upon Tyne, UK.ORCID https://orcid.org/0000-0003-3494-9559
Florence RougetBrittany Registry of congenital anomalies, CHU Rennes, Univ Rennes, Inserm, EHESP, Irset (Institut de recherche en santé, environnement et travail) - UMR_S 1085, Rennes, France.ORCID https://orcid.org/0000-0001-5514-0893
Joanna SichitiuDepartment of Woman-Mother-Child Lausanne, University Hospital (CHUV), Lausanne, Switzerland.ORCID https://orcid.org/0000-0002-4453-1167
David TuckerCARIS, Public Health Knowledge and Research, Public Health Wales, Swansea, UK.ORCID https://orcid.org/0000-0003-3077-5918
Natalya Zymak-ZakutnyaOMNI-Net Ukraine Birth Defects Program, Rivne, Ukraine.
Maria LoaneInstitute of Nursing and Health Research, Ulster University, Belfast, UK.ORCID https://orcid.org/0000-0002-1206-3637

Funding

Innovative Medicines InitiativeSeventh Framework ProgrammeUlster University
6 · The paper itself

Abstract

backgroundThe evidence gap relating to the risk of congenital anomalies (CA) associated with first trimester medication exposure in pregnancy is well recognized.

aimsWe describe the EUROmediCAT network and databases, and the methodological approach to pregnancy pharmacovigilance. MATERIAL AND

methodsMultidisciplinary expertise includes CA diagnosis and epidemiology, pharmacoepidemiology, pharmacology and teratology. The EUROmediCAT central database comprises standardized data from 19 EUROCAT CA registries in 14 countries, including more than 40 000 CA cases 1995-2021 with first trimester medication exposure data recorded, and a population coverage of 14.6 million births, growing by more than 650 000 births per year. The distributed database enables federated data analysis across eight countries which can link data from CA registries to electronic healthcare data, with population coverage of up to 900 000 births per year for linkage to maternal prescriptions, of which 300 000 births per year for linkage also to data on all births.

resultsThe databases have enabled a variety of study designs: case-malformed control studies, cohort studies, disease cohort studies, signal detection studies, prevalence and ecological studies, and medication utilization studies. DISCUSSION: A key strength is that studies of CA risk can address accurately the specificity of risk by type of CA.

conclusionEUROmediCAT presents a unique data and expert resource for tackling the enormous evidence gap regarding the safety of medication during pregnancy.

Indexed as

Abnormalities, Drug-InducedAdverse Drug Reaction Reporting SystemsDatabases, FactualDrug-Related Side Effects and Adverse ReactionsPharmacovigilanceEuropeFemaleHumansPharmacoepidemiologyPregnancyPregnancy Trimester, FirstRegistriescongenital anomalydata sourcesmedication safetypharmacovigilancepregnancyregistries

Identifiers

PMID42057267
PMCPMC13129265

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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.