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Case-Malformed Signal Detection and Prioritisation using EUROmediCAT data for Pharmacovigilance in Pregnancy

  • Hannah Johnson
  • , Helen Dolk
  • , Maria Loane
  • , Christine Damase-Michel
  • , Joanne Given
  • , Hedvig Nordeng
  • , Jorieke Bergman
  • , Iain Carey
  • , Elly Den Hond
  • , Garne Ester
  • , Florence Rouget
  • , Lea Bruneau
  • , Isabelle Monier
  • , Anke Rissmann
  • , Mary O'Mahony
  • , Miriam Gatt
  • , Renée Lutke
  • , Joanna Sichitiu
  • , Elisa Ballardini
  • , Alessio Coi
  • Clara Cavero‑Carbonell, David Tucker, Joan Morris

Research output: Contribution to journalArticlepeer-review

2 Downloads (Pure)

Abstract

Aim
Many women take medications during pregnancy. However, the risk to the fetus from most medications is uncertain. Congenital anomalies are one of the leading causes of infant death and contribute to long-term disability. Signal detection methods can be used to systematically identify possible medication–anomaly associations that require further investigation.

Methods
Data on first trimester medication exposures in pregnancies with a congenital anomaly reported to 14 EUROmediCAT registries with a birth year of 2005–2018 were analysed. Case-malformed disproportionality analysis identified medication–anomaly signals using a disproportionality signal detection method. Identified signals were then compared to previous EUROmediCAT signal detection studies and ranked based on a proxy for the severity of impact at a population level using the number of estimated excess congenital anomaly cases within the exposed population and the average additional time in hospital over the first year of life. Generalized linear mixed models were used to assess confounding by birth year and registry within the top 20 ranked signals.

Results
1611 medication–outcome pairs with at least three observations were analysed, and 153 signals for 63 different medications were identified. Of the top 20 ranked signals, 10 (involving nine medications) were prioritized for further independent investigation.

Conclusion
The signals identified here are hypothesis forming only. Independent studies that adequately account for confounding are subsequently needed to evaluate if the identified signals are causal. Further investigation of signals with low population impact, but high potential individual risk is also recommended.
Original languageEnglish
Article numbere70645
JournalBritish Journal of Clinical Pharmacology
Early online date1 Jul 2026
DOIs
Publication statusPublished online - 1 Jul 2026

Bibliographical note

© 2026 The Author(s). British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society.

Rights Retention Statement

This Author Accepted Manuscript has been made open access under a Creative Commons Attribution 4.0 International licence (CC BY 4.0) under the terms of Ulster University Rights Retention Policy for Scholarly Works.

To view a copy of this licence, visit https://creativecommons.org/licenses/by/4.0/.

Data Availability Statement

EUROmediCAT encourages the use of its data and networks for pharmacovigilance and drug safety research following study approval from the Steering Group and member registries. Information on how to request data for a study is available at: https://euromedicat.eu/research/howtoproposeorcommissionspecificstudies The data used to generate the results for this study are not publicly available due to potential disclosure

Funding

This study was funded by a PhD studentship research grant from the Medical Research council [MR/N013638/1].

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Disproportionality analysis
  • EUROmediCAT
  • Signal detection
  • Pregnancy
  • Congenital anomaly

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