Received Sep 2, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | 2 | FE3590 | — |
Pains -heart-chest; Pain-chest; I had/have a heart right bundle branch block. My EKG claimed from 420 to almost 500 and anything over 500 I can die of sudden death; I had/have a heart right bundle branch block. My EKG claimed from 420 to almost 500 and anything over 500 I can die of sudden death; destroyed my heart more, left me in more pains; Brain fogs; DOSE 2 22Oct2021; This is a spontaneous report and received from Consumer or other non HCPs. A 49-year-old male patient received BNT162b2 (BNT162B2), on 22Oct2021 as dose 2, single (Lot number: FE3590) at the age of 45 years for covid-19 immunisation. The patient's relevant medical history included: "Penicillin allergy" (unspecified if ongoing); "Asthma" (unspecified if ongoing); "Previous Mild RBBB heart" (ongoing); "High Blood Pressure" (unspecified if ongoing); "Vitamin D deficiency" (unspecified if ongoing); "eczema" (unspecified if ongoing); "Schizoaffective disorder" (unspecified if ongoing); "Anxiety" (unspecified if ongoing); "Constipation" (unspecified if ongoing); "Hypertension" (unspecified if ongoing); "Bronchitis" (unspecified if ongoing); "Allergic rhinitis" (unspecified if ongoing); "Dry skin" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: influenza virus vaccine, administration date: 22Oct2020, when the patient was 44-year-old, for immunization; tetanus/diphth/pertuss (tdap) adult/adol, administration date: 13Jul2018, when the patient was 42-year-old, for Immunization; BNT162b2 (DOSE 1, SINGLE), administration date: 04Mar2021, when the patient was 44-year-old, for Covid-19 immunization, reaction(s): "Cardiac pain", "Chest pain", "Electrocardiogram abnormal", "Bundle branch block right", "Brain fog", "Heart disorder", "General body pain". The following information was reported: ANGINA PECTORIS (caused and prolonged hospitalization, disability, medically significant, life threatening), outcome "not recovered", described as "Pains -heart-chest"; CHEST PAIN (caused and prolonged hospitalization, disability, life threatening), outcome "not recovered", described as "Pain-chest"; ELECTROCARDIOGRAM ABNORMAL (caused and prolonged hospitalization, disability, life threatening), BUNDLE BRANCH BLOCK RIGHT (caused and prolonged hospitalization, disability, life threatening), outcome "not recovered" and all described as "I had/have a heart right bundle branch block. My EKG claimed from 420 to almost 500 and anything over 500 I can die of sudden death"; CONDITION AGGRAVATED (caused and prolonged hospitalization, disability, life threatening), outcome "not recovered", described as "destroyed my heart more, left me in more pains"; BRAIN FOG (non-serious), outcome "not recovered", described as "Brain fogs"; INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious), outcome "unknown", described as "DOSE 2 22Oct2021". The events "pains -heart-chest" and "i had/have a heart right bundle branch block. my ekg claimed from 420 to almost 500 and anything over 500 i can die of sudden death" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: Body height: (unspecified date) 5'8; Electrocardiogram: (unspecified date) 420-470, notes: up & down; (2021) 420 to almost 500 and anything over 500, notes: My EKG claimed from 420 to almost 500 and anything over 500 I can die of sudden death; Weight: (unspecified date) 196. Therapeutic measures were taken as a result of angina pectoris, chest pain, electrocardiogram abnormal, bundle branch block right. It was unknown if therapeutic measures were taken as a result of brain fog. Clinical course: The patient had a heart right bundle branch block. His EKG climbed from 420 to almost 500 and anything over 500, he can die of sudden death (Bundle branch block right). Prolongation of existing hospitalization (treatment received during existing hospitalization) due to consistent pains in heart/chest. The treatment received for the adverse event/incident were EKGs, Ibuprofen, breathing treatments and cardiology visit at different (name withheld) prisons over the years since that shot Pfizer covid-19 vaccine EN6204. He was made to suffer in pain. He has been in heart-chest-body pains since the first EN6204 shot. The covid-19-mrna vaccine without nothing. This was his second complaint, the first one was in 2022 for 365 million total. The patient was taking any other medication within 2 weeks prior to the event onset. The patient did not receive any other vaccines within 4 weeks prior to the first administration of the suspect vaccine.; Sender's Comments: Linked Report(s) : US-PFIZER INC-PV202200062233 same patient, different vaccine dose/event;
RBBB
Medical History/Concurrent Conditions: Allergic rhinitis; Anxiety; Asthma; Blood pressure high; Bronchitis; Constipation; Dry skin; Eczema; Hypertension; Penicillin allergy; Schizoaffective disorder; Vitamin D deficiency
Test Name: HEIGHT; Result Unstructured Data: Test Result:5'8; Test Name: EKG; Result Unstructured Data: Test Result:420-470; Comments: up & down; Test Date: 2021; Test Name: EKG; Result Unstructured Data: Test Result:420 to almost 500 and anything over 500; Comments: My EKG claimed from 420 to almost 500 and anything over 500 I can die of sudden death.; Test Name: Weight; Result Unstructured Data: Test Result:196