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Comparing Existing Algorithms for Retrieving Pregnancy-related Adverse Event Reports

2026-02-18 public and global health Title + abstract only
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BackgroundPost-marketing surveillance is essential for complementing the safety profiles of medicinal products, especially for populations generally excluded from clinical trials such as pregnant individuals. However, the absence of a standardised pregnancy indicator in the electronic transmissions of adverse event reports hampers their correct identification in pharmacovigilance databases and complicates the study of safety concerns related to pregnancy exposures. Three recently developed rule-...

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