Received Jul 7, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | 4 | FM9992 | — |
Rheumatoid arthritis; heart problems; neuropathy in my fingers; This is a spontaneous report received from a Consumer or other non HCP. A 61-year-old male patient received BNT162b2 (COMIRNATY), on 16May2022 at 12:00 as dose 4 (booster), single (Lot number: FM9992) at the age of 61 years, in arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: comirnaty (DOSE 1; Lot number: EW0162, in arm at 12:00 pm), administration date: 21Apr2021, when the patient was 60-year-old, for covid-19 immunization; comirnaty (DOSE 2; Lot number: EW0170, in arm at 12:00 pm), administration date: 07May2021, when the patient was 60-year-old, for COVID-19 immunization; comirnaty (DOSE 3; Lot number: FH8027, in arm at 12:00 pm), administration date: 09Nov2021, when the patient was 60-year-old, for COVID-19 immunization. The following information was reported: RHEUMATOID ARTHRITIS (hospitalization, disability, life threatening) with onset May2023, outcome "not recovered"; CARDIAC DISORDER (hospitalization, disability, life threatening) with onset May2023, outcome "not recovered", described as "heart problems"; NEUROPATHY PERIPHERAL (hospitalization, disability, life threatening) with onset May2023, outcome "not recovered", described as "neuropathy in my fingers". The patient was hospitalized for rheumatoid arthritis, cardiac disorder, neuropathy peripheral (hospitalization duration: 2 day(s)). Therapeutic measures were taken as a result of rheumatoid arthritis, cardiac disorder, neuropathy peripheral. Clinical course: In May2023 at 12:00 pm, the patient developed rheumatoid arthritis, heart problems, and neuropathy in his fingers. The patient received shots and unspecified medications as treatment for the events. No allergy. The patient did not receive any other vaccines on the same date as the vaccine(s). The patient did not receive any other vaccines within 4 weeks PRIOR to the vaccine(s).