Report #2867290

Overview

Sex

Male

Age

Age unknown

State

—

Recovered

Unknown

Vaccinated

—

Onset

—

Days to onset

—

Hospital days

—

Symptoms (2)

Symptom narrative

patient not receiving a full dose/a drop of FLUBLOK came out before or after the needle was pulled out with no reported adverse event; Initial information received on 16-Oct-2025 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves an unknown age male patient who did not receiving a full dose of Influenza Trivalent Recombinant Vaccine [Flublok] due to a drop of vaccine came out before or after the needle was pulled out with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received an unknown dose of suspect Influenza Trivalent Recombinant Vaccine, Solution for injection,(unknown strength and expiry date) lot number not reported via unknown route in unknown administration site for influenza immunisation, but a drop of vaccine came out before or after the needle was pulled out with no reported adverse event (incorrect dose administered) (latency same day). It was reported, "Patient said that they were not able to get the full dose and wanted to get another dose". Action taken was not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.