Received Jul 30, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (UNKNOWN)) | UNKNOWN MANUFACTURER | 1 | — | — |
Reported Event: Myasthenia Gravis; This is a spontaneous report received from a Consumer or other non HCP. An 89-year-old male patient received BNT162b2 omicron (kp.2) (BNT162B2 OMICRON (KP.2)), on 17Sep2024 at 10:00 as dose 1, single (Batch/Lot number: unknown) at the age of 89 years, in arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: MYASTHENIA GRAVIS (disability) with onset 04Oct2024 at 10:00, outcome "not recovered", described as "Reported Event: Myasthenia Gravis". The patient underwent the following laboratory tests and procedures: Barium swallow: unknown results. Therapeutic measures were taken as a result of myasthenia gravis. The information on the batch/lot number for BNT162b2 omicron (kp.2) will be requested and submitted if and when received.
Test Name: barium swallow; Result Unstructured Data: Test Result:unknown results