Received Mar 18, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | UNK | Fk9896 | — |
eye injury; This is a spontaneous report received from a Consumer or other non HCP. A 50-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 31Jan2022 at 18:00 as dose number unknown (booster), single (Lot number: Fk9896), in arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for covid-19 immunisation. The following information was reported: EYE INJURY (disability) with onset 01Feb2022, outcome "not recovered". It was unknown if therapeutic measures were taken as a result of eye injury. Additional information: eye injury, ever since receiving the Covid-19 Booster vaccine. This had tremendously affected patient's ability to operate her daily activities. Just need appropriate and specialized treatments which were covered by public insurance. The patient did not receive any other vaccines on the same date as the vaccine(s) for which you are reporting. The patient did not receive any other vaccines within 4 weeks PRIOR to the vaccine(s) for which you are reporting. The patient was not taking any other medications within 2 weeks of the event starting.
Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: No