Received Feb 17, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| FLU3 | INFLUENZA (SEASONAL) (FLUARIX) | GLAXOSMITHKLINE BIOLOGICALS | N/A | ES4H5 | IM / LA |
| VARZOS | ZOSTER (SHINGRIX) | GLAXOSMITHKLINE BIOLOGICALS | 2 | B4LM4 | IM / RA |
THE ADVERSE EVENTS DESCRIBED BY THE PATIENT WERE MILD FEVER AND MILD ARM SORENESS. THESE EVENTS ARE BEING REPORTED DUE TO A WRONG VACCINE ADMINISTER FOR FLUARIX, ONE ADMINISTER ON 01/16/26 AND ANOTHER DOSE ADMINISTERED ON 01/30/26 FOR FLUARIX. PATIENT RECEIVED TWO DOSES IN A 15 DAY PERIOD.
STOMACH ILLNESS
ASTHMA, RESPIRATORY DISEASE
NO KNOW DRUGS WERE TAKEN AT THE TIME OF VACCINATION
NO KNOW ALLERGIES
NO TEST, NO LABORATORIES WERE DRAWN. PATIENT DID NOT VISIT ER, MEDICAL DOCTOR NOR CLINIC. PATIENT JUST PRESENTED MILD NORMAL SIDE EFFCTS AS REPORTED BY PATIENT. PATIENT'S DOCTOR WAS NOTIFIED.