Received Oct 3, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | UNK | — | — |
Fever 100.4F; aches; chills; nausea; diarrhea; fatigue; This is a spontaneous report received from an Other HCP. A 67-year-old female patient (not pregnant) received BNT162b2 omicron (lp.8.1) (COMIRNATY (2025-2026 FORMULA)), on 29Sep2025 as dose number unknown, single (arm) (Batch/Lot number: unknown) at the age of 67 years for COVID-19 immunisation. The patient's relevant medical history included: "CT contrast dye" (unspecified if ongoing). There were no concomitant medications.The vaccine was administered in a Pharmacy or Drug Store. The patient did not receive any other vaccines on the same date as Comirnaty. The patient receive any other vaccines within 4 weeks prior to Comirnaty. The following information was reported: PYREXIA (non-serious) with onset 30Sep2025 at 13:00, outcome "not recovered", described as "Fever 100.4F"; PAIN (non-serious) with onset 30Sep2025 at 13:00, outcome "not recovered", described as "aches"; CHILLS (non-serious) with onset 30Sep2025 at 13:00, outcome "not recovered"; DIARRHOEA (non-serious) with onset 30Sep2025 at 13:00, outcome "not recovered", described as "diarrhea"; FATIGUE (non-serious) with onset 30Sep2025 at 13:00, outcome "not recovered"; NAUSEA (non-serious) with onset 30Sep2025 at 13:00, outcome "not recovered". Therapeutic measures were not taken as a result of pyrexia, pain, chills, nausea, diarrhoea, fatigue. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained.
Medical History/Concurrent Conditions: Contrast media allergy