Conclusion
Although data from prelicensure clinical trials revealed higher (not statistically significant) rates of KD among RotaTeq vaccines compared with placebo, our analysis of postmarketing data does not suggest an elevated risk of KD for RotaTeq or other US-licensed vaccines. Continued postmarketing monitoring for KD, including observational studies, are ongoing.
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Pediatr Infect Dis J. 2009;28(11):944-947. © 2009 Lippincott Williams & Wilkins
Cite this: Kawasaki Disease After Vaccination: Reports to the Vaccine Adverse Event Reporting System 1990-2007 - Medscape - Nov 01, 2009.
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