Received Oct 2, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | 1 | — | LA |
I was so dizzy; Weakness; This is a spontaneous report received from a Nurse. A 93-year-old female patient received BNT162b2 omicron (lp.8.1) (COMIRNATY (2025-2026 FORMULA)), on 26Sep2025 as dose 1, single (Batch/Lot number: unknown) at the age of 93 years, in left deltoid for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DIZZINESS (non-serious) with onset 28Sep2025, outcome "recovering", described as "I was so dizzy"; ASTHENIA (non-serious) with onset 28Sep2025, outcome "recovering", described as "Weakness". Therapeutic measures were not taken as a result of dizziness, asthenia. Additional information: the patient reported a side effect from the Pfizer covid 19 that she got on 26Sep2025. She woke up on 28Sep2025 and did not have it right away, but she woke up and she was so dizzy and she was still kind of dizzy from it and weakness. About if the events were still experiencing, patient stated, well, slightly but she could walk, but she held on to things, it was improved. The patient had dizziness and still had weakness. The patient guessed she would have to just wear off, but she was never going to take it again. The information on the batch/lot number for BNT162b2 omicron (lp.8.1) will be requested and submitted if and when received.