Received Jun 18, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | 1 | IMM309 | — |
persistent body pain; blurry vision; I had an exacerbation of existing sciatica-related pain in my lower back that extended down to my right leg, accompanied by a pulsating sensation in my middle toes.; I had an exacerbation of existing sciatica-related pain in my lower back that extended down to my right leg, accompanied by a pulsating sensation in my middle toes.; I had an exacerbation of existing sciatica-related pain in my lower back that extended down to my right leg, accompanied by a pulsating sensation in my middle toes.; vomiting; nausea; dizziness; This is a spontaneous report received from a Consumer or other non HCP. An elderly male patient received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)), on 01May2025 at 15:30 as dose number 1, single (Lot number: IMM309) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: SCIATICA (non-serious), SENSORY DISTURBANCE (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 01May2025 at 18:00, outcome "not recovered" and all described as "I had an exacerbation of existing sciatica-related pain in my lower back that extended down to my right leg, accompanied by a pulsating sensation in my middle toes."; VISION BLURRED (non-serious) with onset 01May2025 at 18:00, outcome "not recovered", described as "blurry vision"; DIZZINESS (non-serious) with onset 01May2025 at 18:00, outcome "not recovered"; NAUSEA (non-serious) with onset 01May2025 at 18:00, outcome "not recovered"; PAIN (non-serious) with onset 01May2025 at 18:00, outcome "not recovered", described as "persistent body pain"; VOMITING (non-serious) with onset 01May2025 at 18:00, outcome "not recovered". Therapeutic measures were not taken as a result of pain, vision blurred, sciatica, sensory disturbance, pain in extremity, vomiting, nausea, dizziness. Additional information: Vaccine was administered at Doctor's office/urgent care. The patient didn't receive any other vaccines on the same date or within 4 weeks prior to Comirnaty vaccine. Device Date: 16Jun2025.