Reporte zur Charge UJ4888A

Symptomtext

Fluzone High-Dose Quadrivalent the vaccine was a bright green serum that was injected, no AE; Initial information received on 23-Jul-2021 regarding an unsolicited non-valid non-serious case from a consumer via Medical Information (Reference number- 00694840). This case involves a 72 year old female patient who was vaccinated with the bright green serum INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT]. Medical history, medical treatment, vaccination and family history were not provided. Concomitant medications included COVID (coronavirus disease)-19 VACCINE for Prophylactic vaccination. In Sep-2020, the patient received a 0.7 ml dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (lot UJ4888A and expiry date: 30-Jun-2021) (Frequency: once) via an intramuscular route in the right arm (product colour issue) for prophylactic vaccination. It was case of product colour issue. It was reported that "when they received the Fluzone High-Dose Quadrivalent the vaccine was a bright green serum that was injected. The Pharmacist does not have any knowledge of the vaccine being green and that the vaccine would not have been administered if it were bright green". At the time of reporting, no adverse event was reported. Follow-up information received on 23-Jul-2021 regarding an unsolicited non-valid non-serious case from a consumer via Medical Information (Reference number- 00694840). Case validity was updated. Based on information received on 23-Jul-2021, the report previously considered as non-case became valid: [reason for special event reported].