Received Oct 17, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| FLU3 | INFLUENZA (SEASONAL) (FLUZONE) | SANOFI PASTEUR | N/A | UT8826KA | IM / LA |
The patient called today to report an adverse reaction following administration of the influenza vaccine. She received the vaccine on 10/15/25 at 9:13 AM. She reported that symptoms began on 10/16/25 at approximately 1:00 AM. The patient described experiencing symptoms similar to her known allergic reaction to Benadryl, including generalized tingling sensations, rapid heart rate, difficulty breathing, dizziness, and some diarrhea. She stated that the symptoms resolved spontaneously after approximately an hour and a half, and she did not seek emergency care. The following morning, she visited her primary care provider. During the call, the patient requested the name of the vaccine and the manufacturer, and this information was provided. She explained that she wanted this information in order to review the ingredients of the vaccine.
No know Medical Conditions
No know Medical Conditions
no active meds
Benadryl
none