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Administered by: Unknown Purchased by: Unknown
Life Threatening? No
Write-up: This is a spontaneous report from a contactable consumer, the patient''s parent. This is a report received from a foreign Regulatory Agency. Regulatory authority report number ADR22389233. A 14-month-old female patient of an unspecified ethnicity received PREVENAR (Lot Number: F47829; Expiration Date: Apr2014), MMRVAXPRO (Lot Number: H0069789), MENTORIX (Lot Number: A76CA230A or A76CA176B; Expiration Date May 2015), PRIORIX (Lot Number A69DD408A: Expiration Date: Feb2015); all via the "parenteral" route of administration on 16Sep2013 at single doses. The patient''s medical history and concomitant medications were not reported. On 23Sep2013, the patient died. It was unknown if an autopsy was performed and the cause of death was reported as "death unexplained". The reporter stated that they were unsure which injections their child was given as their general practitioner (GP) provided all the above batch numbers. The reporter was given six completely different batch numbers for three injections and was unsure that their child was given the incorrect vaccine. The reporter further stated that the GP was reluctant to inform the local regulatory authority. No follow up attempts possible. No further information expected.
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