Back to Search Start Over

Calcitonin gene-related peptide antagonists in pregnancy: a disproportionality analysis in VigiBase®.

Authors :
Noseda, Roberta
Bedussi, Francesca
Gobbi, Claudio
Ceschi, Alessandro
Zecca, Chiara
Source :
Journal of Headache & Pain. 1/19/2024, Vol. 25 Issue 1, p1-6. 6p.
Publication Year :
2024

Abstract

Background: Current evidence on the safety of calcitonin gene–related peptide antagonists (CGRP-A) in pregnancy for the treatment of both episodic and chronic migraine is scarce and does not yet provide definitive information. By querying VigiBase®, the World Health Organization global pharmacovigilance database, this study aimed to detect differences in the reporting frequency between CGRP-A and triptans in relation to pregnancy. Methods: Disproportionality analyses on de-duplicated safety reports collected in VigiBase® as of 31.05.2023 reporting exposure to CGRP-A in pregnancy with or without pregnancy outcomes. A Reporting Odds Ratio (ROR) with a 95% confidence interval (CI) was used as a measure of disproportionality and the threshold for the detection of a signal of disproportionate reporting was set with a 95% CI lower limit > 1. Findings: Four hundred sixty-seven safety reports reported exposure to CGRP-A in pregnancy, mostly originating from the United States of America (360/467, 77%), more frequently reported by patients (225/467, 48%), who were mainly females (431/467, 92%), and more frequently reported exposure to CGRP-A during pregnancy (400/467, 86%). Compared to triptans, no signals of disproportionate reporting were detected with CGRP-A either for the overall reporting of pregnancy-related safety reports (ROR 0.91, 95% CI 0.78–1.06), for the reporting of pregnancy outcomes (maternal and/or foetal/neonatal, ROR 0.54, 95% CI 0.45–0.66), or for the reporting of foetal/neonatal outcomes (ROR 0.53, 95% CI 0.41–0.68). Conclusions: This study showed that, to date, there are no signals of increased reporting with CGRP-A compared to triptans in relation to pregnancy in VigiBase®. Future pharmacovigilance studies are needed to confirm these findings. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
11292369
Volume :
25
Issue :
1
Database :
Academic Search Index
Journal :
Journal of Headache & Pain
Publication Type :
Academic Journal
Accession number :
174919599
Full Text :
https://doi.org/10.1186/s10194-024-01715-4