VAERS Explorer
Back to explore

Report #2851455

Received Jul 28, 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
Unknown
Age
Age unknown
State
IL
Recovered
Unknown
Vaccinated
Jul 11, 2025
Onset
Jul 11, 2025
Days to onset
0
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
HIBVHIB (HIBERIX)GLAXOSMITHKLINE BIOLOGICALSUNKUNK—

Symptoms (1)

Inappropriate schedule of product administration

Symptom narrative

Differing intervals for the booster dose.; This non-serious case was reported by a other health professional via call center representative and described the occurrence of drug dose administration interval too long in a patient who received Hib (Hiberix) for prophylaxis. Previously administered products included Hiberix (previously administering another brand and switched to Hiberix). On 11-JUL-2025, the patient received Hiberix. On 11-JUL-2025, an unknown time after receiving Hiberix, the patient experienced drug dose administration interval too long (Verbatim: Differing intervals for the booster dose.). The outcome of the drug dose administration interval too long was not applicable. Additional Information: GSK receipt date: 11-JUL-2025 Other HCP reported about the administration of Hiberix's booster dose beyond the recommended interval, as they were previously administering another brand and switched to Hiberix, but were unaware of the need for an additional dose, which led to drug dose interval too long. Also asked was there any information available for the administration of Hiberix after the recommended interval. As the healthcare professional pressed on, the inquiry was escalated to global team. Also, HCP mentioned that they were not sure of how many patients were involved nor had any of their details.