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Report #2855717

Received Aug 26, 2025

A note on interpretation. VAERS reports are unverified and may be incomplete or coincidental. A report does not establish that a vaccine caused an event, and counts should not be used to calculate incidence or infer causation. Full disclaimer

Overview

Sex
Female
Age
Age unknown
State
MD
Recovered
Unknown
Vaccinated
Aug 4, 2025
Onset
Aug 4, 2025
Days to onset
0
Hospital days
—

Vaccines (2)

TypeNameManufacturerDoseLotRoute / Site
DTPPVHBHPBDTAP+IPV+HIB+HEPB (VAXELIS)MSP VACCINE COMPANYUNKU7829AA—
PNC15PNEUMO (VAXNEUVANCE)MERCK & CO. INC.UNKZ003633—

Symptoms (1)

Product administered to patient of inappropriate age

Symptom narrative

Inadvertent administration of a VAXNEUVANCE and VAXELIS dose to a 6-day old patient; patient did not experience ay adverse reaction to the administration of Vaxelis and Vaxneuvance after.; This non-serious spontaneous safety report, with reference number 02851064 (interaction number: 02851062), was received by partner on 05-AUG-2025 and forwarded to agency on 05-AUG-2025 from a health professional. Off-label classification was added due to Vaxelis being administered to a 6-day-old patient. Due to the nature of the event, the causality between the event 'Inadvertent administration of a VAXNEUVANCE and VAXELIS dose to a 6-day old patient' and Vaxelis was not applicable. Further information is expected. FOLLOW-UP INFORMATION was received by agency, on 11-AUG-2025 and forwarded to agency on 11-AUG-2025 from a Health professional. The case is maintained as non-serious. Due to the nature of the event, the causality between the event 'Inadvertent administration of a VAXNEUVANCE and VAXELIS dose to a 6-day old patient/patient did not experience ay adverse reaction to the administration of Vaxelis' and Vaxelis was not applicable Further information is not expected.

Current illness

Prophylaxis

Other medications

ROTARIX