Received Dec 23, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | 2 | — | — |
I had severe pain in my arm for two days; fever; difficulty breathing; chest pain; my heart rate was higher than normal; developed severe painful rash all over my face that left permanent; also have heart issues afterwards; This is a spontaneous report received from a Consumer or other non HCP. A 36-year-old female patient received BNT162b2 (BNT162B2), on 27Sep2021 as dose 2, single (Batch/Lot number: unknown) at the age of 32 years, in arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: PAIN IN EXTREMITY (hospitalization, disability, life threatening) with onset 27Sep2021, outcome "recovered with sequelae", described as "I had severe pain in my arm for two days"; CARDIAC DISORDER (hospitalization, disability, life threatening) with onset 27Sep2021, outcome "recovered with sequelae", described as "also have heart issues afterwards"; CHEST PAIN (hospitalization, disability, life threatening) with onset 27Sep2021, outcome "recovered with sequelae"; RASH (hospitalization, disability, life threatening) with onset 27Sep2021, outcome "recovered with sequelae", described as "developed severe painful rash all over my face that left permanent"; DYSPNOEA (hospitalization, disability, life threatening) with onset 27Sep2021, outcome "recovered with sequelae", described as "difficulty breathing"; PYREXIA (hospitalization, disability, life threatening) with onset 27Sep2021, outcome "recovered with sequelae", described as "fever"; HEART RATE INCREASED (hospitalization, disability, life threatening) with onset 27Sep2021, outcome "recovered with sequelae", described as "my heart rate was higher than normal". The patient was hospitalized for pain in extremity, pyrexia, dyspnoea, heart rate increased, rash, cardiac disorder (start date: 2021, discharge date: 2021, hospitalization duration: 1 day(s)); the patient was hospitalized for chest pain (start date: 2021, discharge date: 2021, hospitalization duration: 1 day(s)). The patient underwent the following laboratory tests and procedures: Heart rate: (2021) higher than normal. Therapeutic measures were taken as a result of pain in extremity, pyrexia, dyspnoea, chest pain, heart rate increased, rash, cardiac disorder. Clinical course: I had severe pain in my arm for two days. On the third day I had fever difficulty breathing chest pain my heart rate was higher than normal and I developed severe painful rash all over my face that left permanent scarring. I thought I was going to die. I had to go to the hospital and had to take antibiotics for a month. It left me very traumatized. It just felt sinister and wrong and it's sickening whatever poison this vaccine was put into my body. I also have heart issues afterwards that won't get better from the vaccine. I felt like it destroyed my life I can't do things I used to do from the scarring all over my face and my heart issues. Adverse event start date: 27Sep2021. AE resulted in: [Hospitalization, Life threatening illness (immediate risk of death from the event), Disability or permanent damage] No days hospitalization: ; If patient recovered: Recovered with lasting effects. If treatment AE: Yes; AE treatment: Antibiotics and pain medication. The information on the batch/lot number for BNT162b2 will be requested and submitted if and when received.
Test Date: 2021; Test Name: heart rate; Result Unstructured Data: Test Result:higher than normal