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Background
The aim of this study was to evaluate the short‐term risk of adverse events associated with rotavirus vaccine (RV) in infants, overall and by vaccine formulation (three‐dose pentavalent, RV5; two‐dose monovalent, RV1).
Methods
We identified US newborns with commercial insurance during 2006‐2014 receiving a diphtheria‐tetanus‐pertussis vaccine (DTaP) dose and assessed if RV was administered...
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