Received Dec 11, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (MODERNA)) | MODERNA | 3 | 035C21A | — |
post-COVID; temporal arteritis; brain fog; inflammation; 104-105 fever; sjogren's; meige syndrome; tardive dystonia; small medium fiber neuropathy, acute; got very bad fever. I mean like 104 fever; This spontaneous case was reported by a consumer and describes the occurrence of POST-ACUTE COVID-19 SYNDROME (post-COVID), DYSTONIA (tardive dystonia), SMALL FIBRE NEUROPATHY (small medium fiber neuropathy, acute), GIANT CELL ARTERITIS (temporal arteritis), SJOGREN'S SYNDROME (sjogren's), MEIGE'S SYNDROME (meige syndrome), BRAIN FOG (brain fog), INFLAMMATION (inflammation) and PYREXIA (104-105 fever) in a 56-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 035C21A, 044B21A and 041321A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 19-May-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-Jun-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 03-Jan-2022, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular use) dosage was changed to 1 dosage form. In 2021, the patient experienced PYREXIA (got very bad fever. I mean like 104 fever). In January 2022, the patient experienced PYREXIA (104-105 fever) (seriousness criteria hospitalization and disability). In 2022, the patient experienced DYSTONIA (tardive dystonia) (seriousness criteria hospitalization, disability and medically significant), SMALL FIBRE NEUROPATHY (small medium fiber neuropathy, acute) (seriousness criteria hospitalization and disability), SJOGREN'S SYNDROME (sjogren's) (seriousness criteria hospitalization, disability and medically significant) and MEIGE'S SYNDROME (meige syndrome) (seriousness criteria hospitalization and disability). On an unknown date, the patient experienced POST-ACUTE COVID-19 SYNDROME (post-COVID) (seriousness criteria hospitalization and disability), GIANT CELL ARTERITIS (temporal arteritis) (seriousness criteria hospitalization and disability), BRAIN FOG (brain fog) (seriousness criteria hospitalization and disability) and INFLAMMATION (inflammation) (seriousness criteria hospitalization and disability). The patient was treated with Paracetamol (Tylenol) in January 2022 for Fever, at an unspecified dose and frequency. In 2022, PYREXIA (104-105 fever) had resolved. At the time of the report, POST-ACUTE COVID-19 SYNDROME (post-COVID), DYSTONIA (tardive dystonia), SMALL FIBRE NEUROPATHY (small medium fiber neuropathy, acute), GIANT CELL ARTERITIS (temporal arteritis), SJOGREN'S SYNDROME (sjogren's), MEIGE'S SYNDROME (meige syndrome), BRAIN FOG (brain fog) and INFLAMMATION (inflammation) had not resolved and PYREXIA (got very bad fever. I mean like 104 fever) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2021, Body temperature: 104, all three of them. On 04-Jan-2022, Body temperature: 104-105. On 12-Aug-2025, Biopsy: small medium fiber neuropathy, acute.. Patient had no vaccines in the past 4 weeks. No concomitant medication was reported. Patient had the Moderna COVID vaccines plus the boosters, and got them on 2021, but like two weeks after that booster. Patient been in and out of hospitals, doctors, and have severe things going on with her body that never had before the vaccines. The patient had so much, and she knew something was wrong after that booster, like those 3 days after the booster, she felt something wrong with her brain and her body going on. The patient was still experiencing symptoms. There were constant symptoms and different autoimmune, nerve damage, all autoimmune. All symptoms were after vaccination, afterward, and the patient also has a rare disorder called tardive dystonia. The patient had a lot going on and could not work. The patient was shaking constantly. It was very bad and that's why she needed to know about these batches, the lot numbers, if there was anything wrong. The patient did hear that one of the not one that she had, but she did look up another batch, found some particles in it, but just wanted to know about the 3 that she had because she could not find any information on it. The patient had 3 biopsies done, and she had post-COVID, due to post-COVID, the provided biopsy date was 12-Aug-2025. Patient's last test showed small medium fiber neuropathy, acute. In addition to the report on COVID, the patient had other things. The patient had 3 autoimmune diseases right after the vaccine (right after the booster) and dystonia. It started with temporal arteritis, Sjogren's was the second; and a small fiber/medium fiber neuropathy acute degenerative changes post-COVID and have Meige Syndrome, a very rare disorder/dystonia. The main thing was that that patient really wanted to know about those batch lot numbers to see if anyone had reported it. The patient had been to hospitals. The patient had to go for a spinal tap. The patient had to go for MRIs galore, CAT scans galore. Patient remembered coming home and got very bad fever, like 104 fevers from the vaccines, all three of them, but that booster one patient had very bad memory loss, very bad like brain fog. The second day, patient got like 104-105 fever. Patient was weak, she could not think right, and then everything else started. And the doctors could not figure anything out at all until recently and it, and believed it was from the booster, and have one result showing post-COVID and but everything else, have all inflammation, all autoimmune problems going on with her body and it was not going away. No additional details provided. It was unknown if the patient experienced any additional symptoms/events. Patient took the Tylenol for the fever, and it got it down but her brain and her body just, patient was falling.; Reporter's Comments: The benefit-risk relationship of product is not affected by this report.
Test Date: 20250812; Test Name: biopsy; Result Unstructured Data: small medium fiber neuropathy, acute.; Test Date: 2021; Test Name: Body temperature; Result Unstructured Data: 104, all three of them; Test Date: 20220104; Test Name: Body temperature; Result Unstructured Data: 104-105