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Claims study estimates 0.43% 45-day serious-event risk after mifepristone use

A medRxiv preprint analysing 2017–2023 claims data reports that 0.43% of mifepristone uses in its medication-abortion cohort were followed by a serious adverse event within 45 days. The retrospective study classified outcomes using claims-based criteria aligned with FDA seriousness criteria.

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Study Links Parental Age and ART to Offspring Mutations

Whole-genome sequencing of 7,851 parent–offspring families linked distinct assisted reproductive technology procedures and parental age with de novo mutations associated with gestational duration and other birth outcomes.