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Administered by: Other Purchased by: Other
Life Threatening? No
Write-up: This case was reported by a regulatory authority ((clinical) # 118325347) and described the occurrence of ileocolic intussusception in a 4-month-old female subject who was vaccinated with ROTARIX (GlaxoSmithKline). On 13 August 2008, the subject received unspecified dose of ROTARIX (oral). Lot number not provided. On 29 August 2008, 16 days after vaccination with ROTARIX, the subject experienced ileocolic intussusception. The subject was hospitalised. On 3 September 2008, the event was resolved. The regulatory authority reported that the event was possibly related to vaccination with ROTARIX. No further information was expected as this was the only information the foreign regulatory had, so the case has been closed.
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