VAERS Reports fcFH8028

VAERS 2673497

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: -
Alter: 49,0
Geschlecht: M
Eingang: 18.08.2023
Impfdatum: 06.11.2021
Beginn: 05.03.2023
Tage bis Beginn: 484,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Arterial disorder Cerebellar syndrome Cerebral artery occlusion Cerebral infarction Cerebrovascular accident

Symptomtext

ACUTE STROKE DUE TO OCCLUSION OF LEFT MIDDLE CEREBRAL ARTERY SUPERIOR CEREBELLAR ARTERY SYNDROME

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2645978

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: -
Alter: 46,0
Geschlecht: F
Eingang: 15.06.2023
Impfdatum: 21.11.2021
Beginn: 07.04.2023
Tage bis Beginn: 502,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acute respiratory failure Asthma-chronic obstructive pulmonary disease overlap syndrome Chronic respiratory failure Hypoxia Respiratory failure

Symptomtext

CHRONIC HYPOXEMIC RESPIRATORY FAILURE 11/28/2022 ASTHMA COPD OVERLAP SYNDROME (ASTHMA W COPD) ACUTE ON CHRONIC HYPERCAPNIC RESPIRATORY FAILURE 4/7/2023 ASTHMA COPD OVERLAP SYNDROME (ASTHMA W COPD) HYPOXIA 11/28/2022 ASTHMA COPD OVERLAP SYNDROME (ASTHMA W COPD)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2640314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: -
Alter: 22,0
Geschlecht: F
Eingang: 02.06.2023
Impfdatum: 16.12.2021
Beginn: 25.04.2022
Tage bis Beginn: 130,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure Chronic respiratory failure Obstructive sleep apnoea syndrome Respiratory failure

Symptomtext

ADULT OBSTRUCTIVE SLEEP APNEA ACUTE RESPIRATORY FAILURE CHRONIC HYPOXEMIC RESPIRATORY FAILURE CHRONIC HYPERCAPNIC RESPIRATORY FAILURE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2625830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: -
Alter: 48,0
Geschlecht: F
Eingang: 03.05.2023
Impfdatum: 28.10.2021
Beginn: 18.03.2022
Tage bis Beginn: 141,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE HYPOXEMIC RESPIRATORY FAILURE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2619788

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: -
Alter: 71,0
Geschlecht: M
Eingang: 24.04.2023
Impfdatum: 07.10.2022
Beginn: 20.01.2023
Tage bis Beginn: 105,0
Dosis: 5
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure Coagulopathy Hypotension Hypoxia Symptom recurrence

Symptomtext

COAGULOPATHY, UNSPECIFIED TYPE HYPOTENSION ACUTE RESPIRATORY FAILURE ACUTE HYPOXEMIC RESPIRATORY FAILURE HYPOXEMIA 1/21/2023 -- RECURRENCE OF SAME SYMPTOMS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2608418

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: -
Alter: 62,0
Geschlecht: F
Eingang: 03.04.2023
Impfdatum: 10.11.2021
Beginn: 18.03.2022
Tage bis Beginn: 128,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acute respiratory failure Angina unstable Arrhythmia Cardiac failure Cardiac failure congestive Condition aggravated Hypotension Idiopathic partial epilepsy Incorrect product formulation administered Status epilepticus

Symptomtext

Pfizer vaccine was given externally reported by patient. G40.001 EPILEPSY, PARTIAL IDIOPATHIC W STATUS EPILEPTICUS 9/17/2022 CHF EXACERBATION, UNSPECIFIED G40.909 EPILEPSY, UNSPECIFIED 9/17/2022 CHF EXACERBATION, UNSPECIFIED I20.8 STABLE ANGINA 3/18/2022 CHF EXACERBATION, UNSPECIFIED I95.9 HYPOTENSION 8/12/2022 CHF EXACERBATION, UNSPECIFIED J96.00 ACUTE RESPIRATORY FAILURE 10/13/2022 CHF EXACERBATION, UNSPECIFIED G40.001 EPILEPSY, PARTIAL IDIOPATHIC W STATUS EPILEPTICUS 9/17/2022 EPILEPSY, PARTIAL IDIOPATHIC W STATUS EPILEPTICUS G40.909 EPILEPSY, UNSPECIFIED 9/17/2022 EPILEPSY, PARTIAL IDIOPATHIC W STATUS EPILEPTICUS I20.8 STABLE ANGINA 3/18/2022 EPILEPSY, PARTIAL IDIOPATHIC W STATUS EPILEPTICUS I95.9 HYPOTENSION 8/12/2022 EPILEPSY, PARTIAL IDIOPATHIC W STATUS EPILEPTICUS J96.00 ACUTE RESPIRATORY FAILURE 10/13/2022 EPILEPSY, PARTIAL IDIOPATHIC W STATUS EPILEPTICUS G40.001 EPILEPSY, PARTIAL IDIOPATHIC W STATUS EPILEPTICUS 9/17/2022 HEART FAILURE W REDUCED LVEF <=30%, UNSPECIFIED ACUITY G40.909 EPILEPSY, UNSPECIFIED 9/17/2022 HEART FAILURE W REDUCED LVEF <=30%, UNSPECIFIED ACUITY I20.8 STABLE ANGINA 3/18/2022 HEART FAILURE W REDUCED LVEF <=30%, UNSPECIFIED ACUITY I95.9 HYPOTENSION 8/12/2022 HEART FAILURE W REDUCED LVEF <=30%, UNSPECIFIED ACUITY J96.00 ACUTE RESPIRATORY FAILURE 10/13/2022 HEART FAILURE W REDUCED LVEF <=30%, UNSPECIFIED ACUITY G40.001 EPILEPSY, PARTIAL IDIOPATHIC W STATUS EPILEPTICUS 9/17/2022 CHF (CONGESTIVE HEART FAILURE), UNSPECIFIED G40.909 EPILEPSY, UNSPECIFIED 9/17/2022 CHF (CONGESTIVE HEART FAILURE), UNSPECIFIED I20.8 STABLE ANGINA 3/18/2022 CHF (CONGESTIVE HEART FAILURE), UNSPECIFIED I95.9 HYPOTENSION 8/12/2022 CHF (CONGESTIVE HEART FAILURE), UNSPECIFIED J96.00 ACUTE RESPIRATORY FAILURE 10/13/2022 CHF (CONGESTIVE HEART FAILURE), UNSPECIFIED G40.001 EPILEPSY, PARTIAL IDIOPATHIC W STATUS EPILEPTICUS 9/17/2022 CARDIAC ARRHYTHMIA G40.909 EPILEPSY, UNSPECIFIED 9/17/2022 CARDIAC ARRHYTHMIA I20.8 STABLE ANGINA 3/18/2022 CARDIAC ARRHYTHMIA I95.9 HYPOTENSION 8/12/2022 CARDIAC ARRHYTHMIA J96.00 ACUTE RESPIRATORY FAILURE 10/13/2022 CARDIAC ARRHYTHMIA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2578076

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: MI
Alter: 82,0
Geschlecht: M
Eingang: 08.02.2023
Impfdatum: 24.11.2021
Beginn: 25.09.2022
Tage bis Beginn: 305,0
Dosis: 3
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Death Pyrexia SARS-CoV-2 test positive

Symptomtext

Patient presented to the hospital on 9/25/22 with fever. Tested positive for COVID on 9/26/22. Patient expired on 9/28/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 3,0
Labordaten: COVID+ by PCR on 9/26/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2447914

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: -
Alter: 89,0
Geschlecht: F
Eingang: 31.01.2023
Impfdatum: 24.03.2021
Beginn: 01.08.2022
Tage bis Beginn: 495,0
Dosis: 3
Route/Site: IM / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

Atrial fibrillation COVID-19 Chest X-ray normal Condition aggravated Death SARS-CoV-2 test positive Decubitus ulcer General physical health deterioration Hypophagia Intensive care Mental status changes Sepsis Urinary tract infection Urine analysis abnormal

Symptomtext

3rd DOSE PFIZER COVID VACCINE GIVEN 11/18/21, LOT #FH8028 to ED from SNF for AMS and poor oral intake over past few days; found to be positive for COVID although oxygenating well on RA and CXR showed no acute findings; in Atrial Fibrillation; positive for UTI; multiple decubitus ulcers on sacrum, hip, back; DNR/DNI; transferred to ICU; ABX and vasopressors; severe sepsis; critical; pt's condition worsened and she passed away in the hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: dementia, Atrial Fibrillation - on Eliquis, CAD, DMT2, HTN, PVD s/p bilateral BKA
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2569294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: TX
Alter: 55,0
Geschlecht: M
Eingang: 27.01.2023
Impfdatum: 28.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: unbekannt Erholt: nein

Cardiac monitoring Cerebrovascular accident Facial paralysis Implantable cardiac monitor insertion Laboratory test Somnolence Unresponsive to stimuli

Symptomtext

Within 36 hours of receiving this Pfizer booster shot I did not/could not wake up. My face and eye were droopy and the only way I awoke was my wife started to slap my face and I was not responding or getting up. Spent four days in the hospital and was diagnosed with a stroke.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: Saw cardiologist, neurologist and had several test during my stay. I also had a loop recorder implanted in my chest to monitor my heart.
Aktuelle Erkrankungen: Sleep Apnea Ulcerative Colitis
Vorgeschichte: Sleep Apnea Ulcerative Colitis
Andere Medikamente: HTCZ, Asacol, Zyrtec, Citalapram, Magnesium Citrate, Vit D, B and D3.
Allergien: None
Vorherige Impfungen: -

VAERS 2557599

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 11.01.2023
Impfdatum: 27.11.2021
Beginn: 04.01.2023
Tage bis Beginn: 403,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal pain Acute respiratory failure Angiogram pulmonary abnormal COVID-19 Chills Computerised tomogram abdomen normal Diuretic therapy Dyspnoea Hypervolaemia Hypophagia Hypoxia Lung consolidation Lymphadenopathy Nausea Pleural effusion Productive cough Pulmonary mass Respiratory tract congestion

Symptomtext

Discharge Provider: MD Primary Care Provider:MD Admission Date: 1/4/2023 Discharge Date: 1/7/23 COVID positive date: 01/04/2023 PRESENTING PROBLEM: Lung nodule Hypoxia Acute hypoxemic respiratory failure Nausea and vomiting, unspecified vomiting type Respiratory tract infection due to COVID-19 virus HOSPITAL COURSE: 65-year-old female with possible history of combined systolic and diastolic CHF with EF 10% status post ICD, AFib on Eliquis, hypertension, CKD 3, dyslipidemia. Patient admitted with COVID and acute hypoxic respiratory failure after presenting with shortness of breath, cough, congestion, abdominal pain, nausea and chills. She tested positive for COVID and was given a dose of Decadron. She was initially hypoxic with ambulation and required 3 L of supplemental oxygen but was weaned back to room air prior to discharge. CT abdomen and pelvis was without acute abnormality. CTA chest was without evidence of PE but noted small right pleural effusion, mildly enlarged mediastinal lymph nodes which have been stable and consolidation in the left upper lobe with spiculated nodule in the right upper lobe. Patient will need repeat CT within 3 months to re-evaluate. She was felt to have a component of fluid overload at the time of admission and was placed on IV Lasix. Cardiology was consulted but felt patient euvolemic and patient was transitioned back to home diuretics. She had some soft blood pressures and hydralazine was held at discharge. Aldactone was also decreased to 25 mg daily given poor orally intake in the setting of COVID. She was instructed to monitor her blood pressure both morning and evening and keep a log to follow-up with cardiology. She was instructed to call Cardiology if blood pressure became elevated or she had any evidence of volume overload, weight gain, worsening edema. She was set up with the transition to home program. Of note patient had productive cough so a sputum culture was sent and is pending at time of discharge. Symptoms improved without antibiotic treatment. She did culture to be followed up by transition to home program.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Snoring Pneumonia Non-ischemic cardiomyopathy Essential hypertension, benign ICD (implantable cardioverter-defibrillator) in place Raynaud's disease Chronic combined systolic and diastolic congestive heart failure Permanent atrial fibrillation Mitral valve insufficiency, unspecified etiology Coronary artery disease involving native coronary artery of native heart without angina pectoris VT (ventricular tachycardia) Chronic systolic heart failure Obesity Postoperative biliary stricture Iron deficiency anemia Chronic renal failure, stage 3 (moderate) Dyslipidemia At risk for falls Pelvic mass
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet amoxicillin-clavulanate (AUGMENTIN) 875-125 MG per tablet apixaban (ELIQUIS) 5 MG tablet Ascorbic Acid (VITAMIN C PO) atorvastatin (LIPITOR) 40 MG tablet calcium carbonate (TUMS) 500 MG chewable tablet
Allergien: Ace Inhibitors Amiodarone Angiotensin Receptor Blockers Hydromorphone
Vorherige Impfungen: -

VAERS 2544356

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: AK
Alter: 48,0
Geschlecht: M
Eingang: 27.12.2022
Impfdatum: 05.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dystonia Pulmonary embolism

Symptomtext

Pulmonary embolism, Dystonia Recovered from PE Struggling with Dystonia, Starting Treatment

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Omperazole 20MG, Irbezartan, multivitamin, vitamin D3 1000
Allergien: Aspirind\\
Vorherige Impfungen: -

VAERS 2526170

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: WA
Alter: 85,0
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 12.11.2021
Beginn: 30.11.2022
Tage bis Beginn: 383,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure COVID-19 COVID-19 pneumonia Pneumonia SARS-CoV-2 test positive

Symptomtext

Patient received Pfizer COVID vaccine on 10/14/21 and 11/12/21. On 11/30/22, patient admitted to our inpatient facility (med/surg unit) with acute hypoxic respiratory failure due to COVID-19 infection/pneumonia and multifocal PNA. As of today 12/7/22, patient is still admitted in the med/surg unit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 7,0
Labordaten: COVID status positive 11/30/22.
Aktuelle Erkrankungen: -
Vorgeschichte: history significant for aortic stenosis, SS and SVT s/p ablation, pacemaker dependence, CAD, GERD, BPH, myasthenia gravis, LUL lung cancer, and leg spasms
Andere Medikamente: acetaminophen, vitamin c, atorvastatin, calcium carbonate, chlorhexidine, vitamin d3, vitamin b12, fish oil, ferrous sulfate, lactobacillus acidophilus, lidocaine patch, melatonin, mvi, pantoprazole, prednisone, pregabalin, pyridostigmine,
Allergien: gabapentin
Vorherige Impfungen: -

VAERS 2518107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: SD
Alter: 65,0
Geschlecht: M
Eingang: 28.11.2022
Impfdatum: 01.12.2021
Beginn: 04.08.2022
Tage bis Beginn: 246,0
Dosis: 3
Route/Site: SYR / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 after which death occurred. The individual was vaccinated with the Moderna product on 03/05/2021 and 04/02/2021. They also received the Pfizer product on 12/01/2021. They tested positive for COVID-19 on 08/04/2022 and 08/05/2022, when they presented to hospital. I do not have any information regarding the reason for or circumstances of the admission . The clinical notes note a request from "Law enforcement requested blood or eye fluid to be collected." I do not have any further information about why this request was made. Some clinical notes indicate date of death is 08/04/2022 but the death certificate has 08/05/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Carpal Tunnel Syndrome, Hyperlipidemia, history of heart failure, obesity, obstructive sleep apnea
Andere Medikamente: -
Allergien: Amoxicillin (reaction: hives, rash)
Vorherige Impfungen: -

VAERS 2476294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: MA
Alter: 52,0
Geschlecht: F
Eingang: 12.10.2022
Impfdatum: 14.12.2021
Beginn: 19.09.2022
Tage bis Beginn: 279,0
Dosis: 3
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Angle closure glaucoma Visual field tests abnormal

Symptomtext

Diagnosis of Narrow Angle Glaucoma-Left 09/19/2022. I have been dealing with the migraines in the left eye which remained the same. During my annual exam, I was given a new diagnosis. The initial diagnosis was Episodic Migraines. It does not appear to cause any worsening in the original condition. I was advised to go the nearest emergency if I noticed change in my vision. I went back to the doctor on October 07 and had a Peripheral Vision Test completed which showed there was weakness in the left eye.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Angle closure glaucoma
Hospital-Tage: -
Labordaten: Eye Exam-09/19/2022-Narrow Angle Glaucoma of left eye Peripheral Vision Test-10-07-2022-left eye weakness Visual Field Test-10-07-2022-Narrow Angle OCT Optical Coherence Tomography-Narrow Angle Glaucoma of left eye
Aktuelle Erkrankungen: Migraines
Vorgeschichte: Depression; Insomnia; Low Iron
Andere Medikamente: Pantoprazole; Levothyroxine; Amitriptyline; Quetiapine; Fero Sulfate; Butalbital/Aspirin/Caffeine; Venlafaxine ER; Duloxetine; Multi Vitamin; B12; Topamax
Allergien: Zomig
Vorherige Impfungen: -

VAERS 2450862

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: TN
Alter: 78,0
Geschlecht: F
Eingang: 19.09.2022
Impfdatum: 22.11.2021
Beginn: 08.09.2022
Tage bis Beginn: 290,0
Dosis: 3
Route/Site: IM / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Covid vaccine x3, tested positive for COVID 09/08/2022, admit to local hospital from 09/08/2022-09/12/2022, expired 09/12/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2447933

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: SD
Alter: 89,0
Geschlecht: M
Eingang: 16.09.2022
Impfdatum: 05.05.2022
Beginn: 25.07.2022
Tage bis Beginn: 81,0
Dosis: 3
Route/Site: SYR / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cardio-respiratory arrest Death Fall General physical health deterioration Illness SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. The individual was vaccinated with the Pfizer product on 01/04/2021, 01/25/2021, 11/30/2021, and 05/05/2022. They tested positive for COVID-19 on 07/25/2022 at the nursing home at which they were a resident. I see no indication they were hospitalized for this illness. They experienced a cardiopulmonary arrest and died on 07/29/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: -
Labordaten: Positive COVID-19 antigen test on 07/25/2022 despite being vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: Past history of aortic aneurysm, Type II Diabetes, Acute Kidney Failure, COPD with Hypoxia (on oxygen), Chronic Respiratory Failure, Heart Failure (type not specified), Alzheimer's Dementia, Coronary Artery Disease, Past history hernias, Hypertension, Hyperlipidemia, GERD, Thrombocytopenia, Arthritis, Osteoarthritis About 2 weeks prior to the adverse event, it was noted the individual was experiencing rapidly deteriorating health status and had been falling frequently. The individual was a resident of the nursing home indicated in the Address portion of this form.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2436376

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: KY
Alter: 78,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 04.02.2021
Beginn: 19.08.2022
Tage bis Beginn: 561,0
Dosis: 3
Route/Site: - / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Chest pain Death Dyspnoea

Symptomtext

SOB, weakness, chest pain. Pt expired 08/19/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Stage IV metastatic squamous cell carcinoma of the lung; hypertension
Andere Medikamente: Benazepril; cyclobenzaprine
Allergien: N/A
Vorherige Impfungen: -

VAERS 2433664

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 08.02.2021
Beginn: 22.08.2022
Tage bis Beginn: 560,0
Dosis: 3
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 pneumonia Chest tube insertion Death Dyspnoea Endotracheal intubation Haemodynamic instability Hypoxia Mechanical ventilation Oxygen saturation decreased Pneumothorax Respiratory distress SARS-CoV-2 antibody test SARS-CoV-2 antibody test positive

Symptomtext

68y.o. female with PMH pertinent for seronegative RA on chronic prednisone recent COVID PNA presented for worsening SOB. In the ER, patient was hypoxic requiring HFNC 100% FiO2/50 L and a nonrebreather maintaining SPO2 in the early 90s. Significant increase in work of breathing. Patient was intubated. On 8/28, the patient developed resp distress. Patient had a needle decompression and then chest tube placement for right sided tension pneumothorax. Patient was unable to be weaned off ventilator and on 9/5 had a drop in SpO2 with increased WOB. Patient required multiple pressors for hemodynamic instability. Patient transitioned to comfort care, and passed peacefully that evening.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 15,0
Labordaten: 8/23/22 SARS-CoV-2 IgG (Anti-Spike) -- positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2433614

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: MI
Alter: 61,0
Geschlecht: M
Eingang: 08.09.2022
Impfdatum: 12.03.2021
Beginn: 22.08.2022
Tage bis Beginn: 528,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Catheterisation cardiac abnormal Confusional state Hypoxia Lethargy Respiratory failure SARS-CoV-2 test positive Syncope Pulmonary embolism Thrombectomy

Symptomtext

62y.o. male who recently traveled and was diagnosed with COvid about 1 week ago, treated with zithromax/ amoxicillin then atovaquone and proguanil presents with acut syncope. EMS found him quite hypoxic put on NRB and brought to ER where massive PE found. He was taken urgently to cath lab for thrombectomy- 5-6 thrombectomies were performed in both left and right sides. After, Right heart pressures were much improved. Oxygen has been weaned to room air. Evaluation on Day of Discharge: Feeling great, denies any dyspnea chest pain or bleeding, no overnight events. No lower extremity edema, lungs clear to auscultation, patient is eager to go home as soon as possible. is very lethargic and confused. Attempts to follow directions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 5,0
Labordaten: 8/23/22 SARS-COV-2 (COVID-19) by NAA, Micro -- detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2431222

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: TX
Alter: 79,0
Geschlecht: F
Eingang: 07.09.2022
Impfdatum: 02.11.2021
Beginn: 02.09.2022
Tage bis Beginn: 304,0
Dosis: 3
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Acute kidney injury COVID-19 Chronic kidney disease Death Endotracheal intubation Fungaemia Hydronephrosis Inappropriate schedule of product administration Intensive care Nephrostomy Paracentesis Pelvic mass Positive airway pressure therapy SARS-CoV-2 test positive Sepsis Shock Urinary tract infection

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization/Death. rec' Pfizer-BioNTech on 1/26/21, 2/20/21, and 11/02/21. Admitted 8/12 2/2 for pelvic mass and bil hydronephrosis c/b AKI on CKD. Found to have a UTI. Tested Covid + on 8/17. Bilateral nephrostomy tubes placed in IR on 8/19, in PACU placed on bipap. Resp status cont'd to decline requiring transfer to ICU for emergent intubation on 8/31 c/b fungemia and distributive sepsis w/shock. Paracentesis removed pus-like fluid. Transitioned to comfort care. Tx'd w/micafungin, meropenem, vancomycin, cefepime, ceftriaxone, metronidazole, zosyn, remdesivir, and decadron. Expired 09/02/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 22,0
Labordaten: covid + 8/17/22 - This assay was performed on the BioFire RP2.1 platform using PCR or equivalent Nucleic Acid Amplification (NAA) technology.
Aktuelle Erkrankungen: -
Vorgeschichte: HFpEF, paroxysmal afib, HTN, DM2
Andere Medikamente: aspirin, brimonidine, cholecalciferol, dorzolamide/timolol; felodipine, hydralazine, HC/APAP, latanoprost, omega 3, ondansetron, spironolactone
Allergien: Novacaine, codeine
Vorherige Impfungen: -

VAERS 2427588

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 02.09.2022
Impfdatum: 26.05.2022
Beginn: 21.07.2022
Tage bis Beginn: 56,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute kidney injury Agitation Angiogram abnormal Anticoagulant therapy Basal ganglia infarction COVID-19 Cardiac failure acute Cardiac failure congestive Cerebrovascular accident Confusional state Delirium Dementia Hemiparesis Magnetic resonance imaging head abnormal Mental status changes SARS-CoV-2 test positive Stenosis

Symptomtext

Patient with COVID vaccinations who admitted with incidental positive COVID test. Provider d/c note: ""73 YO M with hx afib, HTN, CKD, hx SAH, dementia, who was admitted for acute on chronic right sided weakness. He had distant history of stroke with R sided weakness, but was more weak than usual. Admitted for stroke workup. He was also found to have incidental COVID-19 infection. He was found on MRI to have acute to subacute infarct at the left corona radiata extending to the left basal ganglia. CT angiogram showed multilevel stenosis without large vessel occlusion. Neurology was consulted. He was restarted on Eliquis, aspirin and statin. His course was complicated by acute on chronic CHF and acute kidney injury. Cardiology and Nephrology were consulted early in his hospital course for assistance managing those issues with improvement. He also developed prolonged episode of confusion and agitation thought to be due to delirium in setting of advanced dementia. Over time and with assistance of Seroquel this also improved significantly. Discharge was delayed primarily due to agitation and mental status changes. As these issues resolved he was thought to be a candidate for transition to SNF with therapy. Discharged in good condition."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 20,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic heart failure with reduced ejection fraction and diastolic dysfunction (*) Vascular dementia (*) Essential (primary) hypertension Arthritis LVH (left ventricular hypertrophy) Chronic kidney disease, stage 3 unspecified (*) Obesity (BMI 30.0-34.9) Behavior related to cognitive impairment Ventricular tachycardia (paroxysmal) (*) Thyroid lesion Generalized anxiety disorder
Andere Medikamente: -
Allergien: Seasonal
Vorherige Impfungen: -

VAERS 2399352

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: WI
Alter: 86,0
Geschlecht: M
Eingang: 02.08.2022
Impfdatum: 08.12.2021
Beginn: 27.07.2022
Tage bis Beginn: 231,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure COVID-19 COVID-19 pneumonia Dizziness Dyspnoea SARS-CoV-2 test positive

Symptomtext

Patient with a significant past medical history of COPD who presented to the emergency department with his daughter today with a chief complaint of shortness of breath and dizziness in the setting of a positive home COVID-19 test. Patient admitted as observation on 7/27 due to acute respiratory failure with hypoxia due to COVID pneumonia. Patient was tested for COVID-19 and was positive on 7/27.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2393236

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: MI
Alter: 91,0
Geschlecht: F
Eingang: 27.07.2022
Impfdatum: 03.03.2021
Beginn: 24.07.2022
Tage bis Beginn: 508,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute myocardial infarction COVID-19 Hypoxia Joint dislocation SARS-CoV-2 test positive

Symptomtext

Pt found to be COVID positive after being transferred from ED due to right hip dislocation and NSTEMI. Pt had no symptoms at that time, but did develop hypoxia a day later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2319338

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: KY
Alter: 80,0
Geschlecht: F
Eingang: 14.06.2022
Impfdatum: 26.11.2021
Beginn: 23.12.2021
Tage bis Beginn: 27,0
Dosis: 1
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

COVID-19 Death SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Patient had breakthrough infection and passed away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: First positive COVID-19 test on 9/22/21 and second positive on 12/2/21.
Aktuelle Erkrankungen: -
Vorgeschichte: HTN hyperlipidemia GERD
Andere Medikamente: Aspirin furosemide gabapentin hydrocodone lisinopril duloxetine alendronate Vitamin D clonidine HCL Colace Flonase Amitiza Metoprolol succinate naproxen Patanol omeprazole pravastatin
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2267337

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: IA
Alter: 76,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 18.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute respiratory failure Alanine aminotransferase normal Anticoagulant therapy Anxiety Aspartate aminotransferase increased Asthenia Bladder catheterisation Blood alkaline phosphatase increased Blood creatinine increased Blood lactic acid Blood magnesium increased Blood potassium increased COVID-19 Cardiac failure congestive Chest X-ray abnormal Chronic obstructive pulmonary disease Computerised tomogram head normal Computerised tomogram thorax normal

Symptomtext

COVID Vaccine Breakthrough Case Pfizer Dose 1 2/26/21 (EN6203) Pfizer Dose 2 3/24/21 (ER2613) Pfizer Dose 3 11/18/21 (FH8028) COVID Positive 11/26/21 11/26/21: The patient is a 76-year-old female with past medical history atrial fibrillation on Eliquis, pacemaker, diastolic heart failure, and current tobacco use who presented to the ED today for weakness which had been progressing for the past 4 days. Last night she fell 5-6 times however denies any loss of consciousness. She has significant history of smoking 1 pack/day, and has had a chronic productive cough. She is not on any supplemental oxygen at home, and does not have an official diagnosis of COPD. She denies any chest pain or cough however does endorse some shortness of breath. ED course: Per ED note, patient was initially saturating 87% on 6 L which improved to 94% with a DuoNeb treatment. BP 95/52. Labs notable for WBC 14.44, hemoglobin 16.1, potassium 5.3, creatinine 1.41, ALT 36, AST 94, ALP 129, mg 2.7, lactate 4.0, pro BNP 5073, troponin 0.09. EKG indicated ventricular paced rhythm, no change since 2020. CXR indicated mild pulmonary venous congestion. CT head indicated no acute intracranial abnormality. She was given a DuoNeb, Solu-Medrol, azithromycin 500 mg, ceftriaxone 1g, in addition to 2 L NS. Patient continued to exhibit respiratory distress so was then placed on BiPAP for increased work of breathing without significant improvement with nebulizer. Notably she also had 3 bouts of diarrhea while in the ED. She improved significantly with use of BiPAP. She was admitted for acute hypoxic respiratory failure secondary to COPD versus CHF. Surgical history: Pacemaker placed 2010 SH: Smokes 1 pack/day FH: noncontributory 12/3/21: The patient is a 76-year-old female with past medical history atrial fibrillation on Eliquis, pacemaker, diastolic heart failure, and current tobacco use who presented to the ED today for weakness and falls. ED course: Per ED note, patient was initially saturating 87% on 6 L which improved to 94% with a DuoNeb treatment. BP 95/52. Labs notable for WBC 14.44, hemoglobin 16.1, potassium 5.3, creatinine 1.41, ALT 36, AST 94, ALP 129, mg 2.7, lactate 4.0, pro BNP 5073, troponin 0.09. EKG indicated ventricular paced rhythm, no change since 2020. CXR indicated mild pulmonary venous congestion. CT head indicated no acute intracranial abnormality. She was given a DuoNeb, Solu-Medrol, azithromycin 500 mg, ceftriaxone 1g, in addition to 2 L NS. Patient continued to exhibit respiratory distress so was then placed on BiPAP for increased work of breathing without significant improvement with nebulizer. Notably she also had 3 bouts of diarrhea while in the ED. She improved significantly with use of BiPAP. She was admitted for acute hypoxic respiratory failure secondary to COPD versus CHF. She was found to be COVID positive. She received Actemra as well as 5 day course of remdesivir and Decadron. Cardiology was consulted due to elevated troponin, troponin was trended, elevation thought to be secondary to infection. No intervention was performed, recommended outpatient ischemic workup. D-dimer was found to be elevated, CT chest negative for PE. Eliquis as was increased to 5 mg b.i.d. for more adequate DVT prophylaxis. She was diuresed with IV Lasix per Cardiology. Oxygen requirements gradually decreased, she was transitioned to room air however required supplemental oxygen not on oxygen walk test. Order was placed so she could have home O2. She did have significant anxiety during this hospitalization, her home lorazepam was continued. She also had a Foley catheter in place for a short period of time, after this was removed she was able to urinate without difficulty. Patient does have history of recurrent UTIs, urine culture was obtained and was negative. At time of discharge she was feeling much improved, vitals were stable aside from as a O2, patient had adequate help at home and felt comfortable returning. She will have visiting nurse at discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: a fib pacemaker diastolic heart failure tobacco use anxiety chronic back pain chronic UTI emphysema COPD HTN insomnia neuropathic pain spinal stenosis of lumbar region urinary incontinence
Vorgeschichte: a fib pacemaker diastolic heart failure tobacco use anxiety chronic back pain chronic UTI emphysema COPD HTN insomnia neuropathic pain spinal stenosis of lumbar region urinary incontinence
Andere Medikamente: albuterol 2 puffs Q4h PRN apixaban 5 mg PO BID duloxetine 60 mg PO QD furosemide 60 mg PO QD lorazepam 0.5 mg PO HS PRN metoprolol tartrate 25 mg PO BIFD PEG PO QD pregabalin CR 165 mg PO HS senna 17.2 mg PO QD
Allergien: nicotine patch - nausea, vomiting codeine - nausea
Vorherige Impfungen: -

VAERS 2147262

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: MD
Alter: 64,0
Geschlecht: M
Eingang: 03.05.2022
Impfdatum: 29.10.2021
Beginn: 08.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Computerised tomogram thorax abnormal Pulmonary embolism SARS-CoV-2 test

Symptomtext

Developed a pulmonary embolus

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: CHEST CT WITH CONTRAST, 10-Nov-2021, Bilateral PE
Aktuelle Erkrankungen: -
Vorgeschichte: None
Andere Medikamente: None; None
Allergien: None
Vorherige Impfungen: -

VAERS 2147262

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: MD
Alter: 64,0
Geschlecht: M
Eingang: 03.05.2022
Impfdatum: 29.10.2021
Beginn: 08.11.2021
Tage bis Beginn: 10,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Computerised tomogram thorax abnormal Pulmonary embolism SARS-CoV-2 test

Symptomtext

Developed a pulmonary embolus

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: CHEST CT WITH CONTRAST, 10-Nov-2021, Bilateral PE
Aktuelle Erkrankungen: -
Vorgeschichte: None
Andere Medikamente: None; None
Allergien: None
Vorherige Impfungen: -

VAERS 2260218

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: OH
Alter: 29,0
Geschlecht: M
Eingang: 02.05.2022
Impfdatum: 18.11.2021
Beginn: 02.12.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blindness unilateral Cerebral artery occlusion Cerebrovascular accident Computerised tomogram Headache Magnetic resonance imaging Pain Paraesthesia

Symptomtext

At 10:30 that night I had a shooting headache and about 30 seconds later lost sight in my right eye and tingling in my right arm, hand and face. Went to ER and was told I had a stroke. I have blocked artery in my brain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: CT Scan and MRI.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: None
Allergien: Seasonal; Cat Dander
Vorherige Impfungen: -

VAERS 2225888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: -
Alter: 40,0
Geschlecht: M
Eingang: 11.04.2022
Impfdatum: 31.12.2021
Beginn: 04.01.2022
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

Acute myocardial infarction Anticoagulant therapy Anticoagulation drug level below therapeutic Electrocardiogram ambulatory Ventricular extrasystoles

Symptomtext

ST elevation myocardial infarction involving right coronary artery. Today PVC's still bi and trigeminal. Will discharge with holter to assess burden. He will stay on coreg 12.5 mg BID instead of metoprolol. INR is still subtherapeutic so he will be bridged with lovenox so he can be discharged. He will continue entresto, aspirin, plavix, and warfarin. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1868616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: CA
Alter: 77,0
Geschlecht: M
Eingang: 28.03.2022
Impfdatum: 11.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: - / -

Tod: ja Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Autopsy Cerebral haemorrhage Death Histology abnormal Pericarditis Laboratory test Sudden death SARS-CoV-2 test negative

Symptomtext

2/22/2021- 1st COVID Vaccine, Pfizer lot #EN6203. 3/14/2021- 2nd Covid Vaccine, Pfizer lot #P6955S. 9/17/2021- Flu shot and Shingrix shot. 11/11/2021- 3rd COVID Vaccine, Pfizer lot #FH028. 11/14/2021- Found dead at home. 11/17/2021- Autopsy performed. 03/28/2022- Histology shows evidences of: A. Eosinophilic pericarditis B. Multi-focal peri-microvascular hemorrhages of the brain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: 11/17/2021- COVID nasal swab showed negative result. 03/28/2022- Histology confirmed diagnoses.
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic systolic congestive heart failure, atherosclerotic cardiovascular disease, dilated cardiomyopathy
Andere Medikamente: N/A
Allergien: Unknown
Vorherige Impfungen: 3/14/2021- 2nd Covid Vaccine, Pfizer lot #P6955S.

VAERS 1868616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: CA
Alter: 77,0
Geschlecht: M
Eingang: 28.03.2022
Impfdatum: 11.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / AR

Tod: ja Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Autopsy Cerebral haemorrhage Death Histology abnormal Pericarditis Laboratory test Sudden death SARS-CoV-2 test negative

Symptomtext

2/22/2021- 1st COVID Vaccine, Pfizer lot #EN6203. 3/14/2021- 2nd Covid Vaccine, Pfizer lot #P6955S. 9/17/2021- Flu shot and Shingrix shot. 11/11/2021- 3rd COVID Vaccine, Pfizer lot #FH028. 11/14/2021- Found dead at home. 11/17/2021- Autopsy performed. 03/28/2022- Histology shows evidences of: A. Eosinophilic pericarditis B. Multi-focal peri-microvascular hemorrhages of the brain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: 11/17/2021- COVID nasal swab showed negative result. 03/28/2022- Histology confirmed diagnoses.
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic systolic congestive heart failure, atherosclerotic cardiovascular disease, dilated cardiomyopathy
Andere Medikamente: N/A
Allergien: Unknown
Vorherige Impfungen: 3/14/2021- 2nd Covid Vaccine, Pfizer lot #P6955S.

VAERS 2194637

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: PA
Alter: 63,0
Geschlecht: M
Eingang: 23.03.2022
Impfdatum: 06.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Death Hyperglycaemia Hyperlipidaemia Myocardial infarction Pulmonary embolism

Symptomtext

Death. Per the death certificate the immediate cause of death was a myocardial infarction with hyperlipidemia, hyperglycemia and pulmonary embolism as contributing factors. No autopsy was performed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: The patient had a pulmonary embolism about 15 years prior. He was faithfully taking his doctor, closely monitored Jantoven every morning and having his blood checked every month to control for blood clots. He smoked cigarettes for more than 55 years.
Andere Medikamente: 8 or 9 mg of Jantoven AND 20 mg of Aciphex daily.
Allergien: None
Vorherige Impfungen: -

VAERS 2192326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: WA
Alter: 73,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 19.11.2021
Beginn: 17.03.2022
Tage bis Beginn: 118,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute kidney injury Acute respiratory failure COVID-19 COVID-19 pneumonia Colectomy Colitis ischaemic Colostomy Endotracheal intubation Inappropriate schedule of product administration Intensive care Intestinal perforation Peritonitis Respiratory failure SARS-CoV-2 test positive Septic shock

Symptomtext

Patient received Pfizer COVID vaccine on 3/17/21 (lot # EN6208), 4/13/21 (lot # ER8731), and 11/19/21 (lot # FH8028). Patient admitted to our inpatient facility on 3/14/22 for septic shock due to perforated viscus, stercoral colitis with stool contamination in the abdomen (s/p ex lab sigmoid colectomy, colostomy on 3/14), acute kidney injury, and acute respiratory failure with hypercarbia and hypoxia. COVID status was negative on admission 3/14/22, but turned positive on 3/17/22, 3/18/22, and 3/21/22. Patient was intubated from 3/14 to 3/16 and is developing COVID pneumonia. Patient was in CCU from 3/14-3/19 and still admitted in our med/surg unit from 3/19 until today (3/22).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: COVID status negative 3/14/22, and positive 3/17/22, 3/18/22, 3/21/22.
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, chronic back pain, insomnia, HCV s/p treatment, CKD stage 3, COPD, asthma/emphysema
Andere Medikamente: amlodipine, carvedilol, chlorthalidone, hydrochlorothiazide, losartan, mvi, psyllium, tramadol, zolpidem, Combivent Respimat inh
Allergien: lactose, latex, adhesive, gabapentin, procaine
Vorherige Impfungen: -

VAERS 2182879

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: OK
Alter: 23,0
Geschlecht: M
Eingang: 16.03.2022
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / AR

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Cardiac arrest Chest pain Death Dyspnoea Dyspnoea exertional Laboratory test Resuscitation Seizure

Symptomtext

Pt began having chest pain within 15 minutes post injection. Left facility and continued having shortness of breath with chest pain intermittently for two weeks. He kept stating, that he was feeling short of breath upon exertion. Pt began to have a seizure and went into cardiac arrest. CPR initiated on scene, transported to emergency room and was pronounced dead.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: Labs and testing done on 11/24/2021 at hospital.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2180694

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: HI
Alter: 37,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 03.12.2021
Beginn: 16.02.2022
Tage bis Beginn: 75,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Computerised tomogram abdomen normal Heart rate decreased Hepatobiliary scan normal Hypotension Intensive care Laboratory test normal Scan with contrast Septic shock Ultrasound abdomen normal Ultrasound pelvis normal

Symptomtext

Hospitalized for septic shock and in ICU for 2 days due to low blood pressure and low heart rate (February 17-22, 2022).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Septic shock
Hospital-Tage: 6,0
Labordaten: Pelvic ultrasound; CT abdomen with contrast; Abdominal ultrasound; HIDA scan. Lab and medical scans were normal and within normal limits. Primary hospitalization was due to profound hypotension.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Multivitamin; probiotics
Allergien: Shrimp
Vorherige Impfungen: -

VAERS 2165614

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: WI
Alter: 68,0
Geschlecht: M
Eingang: 08.03.2022
Impfdatum: 09.11.2021
Beginn: 05.03.2022
Tage bis Beginn: 116,0
Dosis: 3
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death

Symptomtext

Death related to COVID-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Other significant conditions: History of cryptococcal pneumonia, Oropharyngeal cancer (2010), Diffuse large B-cell lymphoma, HTN, COPD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2139922

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: -
Alter: 70,0
Geschlecht: M
Eingang: 25.02.2022
Impfdatum: 11.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Angiogram pulmonary abnormal Discomfort Dyspnoea Flank pain Pulmonary embolism SARS-CoV-2 test negative

Symptomtext

Patient presented to local ED with complaints of increasing dyspnea, flank pain, and discomfort for 48 hours. History of COPD, TIA, Stage 3a chronic kidney disease, hypertension, Vertigo, Atrial fibrillation, Coronary Artery Disease, AAA, and S/P aortic valve repair. COVID test was negative, however CTA showed acute PE. Previously vaccinated with Pfizer on 2/6/21, 2/27/21, and boosted on 12/11/21. Patient admitted 12/12/21 and discharged 12/20/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123018

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: MI
Alter: 62,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 27.03.2021
Beginn: 10.01.2022
Tage bis Beginn: 289,0
Dosis: 3
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Acute respiratory failure Anticoagulant therapy Atrial fibrillation COVID-19 Cardiac telemetry Condition aggravated Dyspnoea Hyperhidrosis SARS-CoV-2 test positive Tachypnoea

Symptomtext

Patient Presents to the ED with c/o SOB onset Monday and became worse today. Patient test positive Monday for Covid-19 and has received both vaccines and booster. HX: diabetes, HTN, AFib, bilateral leg swelling with discoloration. Denies fever, chills, chest pain. Patient was 61% on RA on arrival to ED, tachyonic, diaphoretic. Acute respiratory failure with hypoxia secondary to COVID-19 infection/atrial fibrillation. CONTINUE on pulmonary support included high-flow of oxygen steroid breathing treatment, rate control with telemetry with cardiology and Disease consult. Atrial fibrillation with RVR. CONTINUE BB/CC / telemetry bed, anticoagulation with Cardiology consult. On decatron to 10 days and baricitinib.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 10,0
Labordaten: see above
Aktuelle Erkrankungen: No
Vorgeschichte: OSA (obstructive sleep apnea), Acute respiratory failure with hypoxia and hypercapnia, Colon poly, Acute superficial gastritis without hemorrhage, Gastric polyp, Diabetes, CLL (chronic lymphocytic leukemia), Hypertension, Acute diastolic CHF (congestive heart failure), DOE (dyspnea on exertion), Leukocytosis (leukocytosis), Cellulitis of lower extremity, Coronary artery disease, Atrial fibrillation (CMS/HCC), Pink eye disease of left eye, Acute pain of right shoulder, CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min (CMS/HCC), Anemia, Gout, Vitamin D deficiency, Brain lesion, Sepsis (CMS/HCC), Acute kidney injury superimposed on CKD, Hyperkalemia, Elevated troponin, Demand ischemia, Leukocytosis, Thrombocytopenia, Obesity, Class III, BMI 40-49.9 (morbid obesity) (CMS/HCC), Bacteremia due to Pseudomonas, Lymphadenopathy, Erectile dysfunction due to arterial insufficiency, Hyperlipidemia, Atrial fibrillation with RVR, AKI (acute kidney injury), Obesities, morbid, MRSA infection, Chronic atrial fibrillation (CMS/HCC)
Andere Medikamente: acyclovir (ZOVIRAX) 400 MG PO Tab albuterol (PROVENTIL), allopurinol (ZYLOPRIM) 100 MG PO Tab, atorvastatin (LIPITOR) 40 MG PO Tab, carVEDilol (COREG) 25 MG PO Tab, dexamethasone 6 MG PO Tab, dilTIAZem (CARDIZEM CD) 180 MG PO CAPSULE SR 24
Allergien: Cefepime, vancomycin
Vorherige Impfungen: -

VAERS 2092895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: WI
Alter: 67,0
Geschlecht: M
Eingang: 07.02.2022
Impfdatum: 29.10.2021
Beginn: 04.02.2022
Tage bis Beginn: 98,0
Dosis: UNK
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death

Symptomtext

Death related to COVID-19 infection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: OSC: DM2; PVD; HTN; HLD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2069071

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: WI
Alter: 68,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 01.12.2021
Beginn: 25.01.2022
Tage bis Beginn: 55,0
Dosis: 3
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death

Symptomtext

Death related to complications of COVID-19 infection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: OSC: CHF; HTN; obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2065770

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: WA
Alter: 69,0
Geschlecht: M
Eingang: 26.01.2022
Impfdatum: 11.11.2021
Beginn: 24.01.2022
Tage bis Beginn: 74,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure COVID-19 COVID-19 pneumonia Hypervolaemia SARS-CoV-2 test positive

Symptomtext

Patient received Pfizer COVID vaccine on 3/25/21 (lot # EP7533), 4/17/21 (lot # ER8731), and 11/11/21 (lot # FH8028). On 1/12/22, patient tested positive for COVID. On 1/24/22, patient admitted to our inpatient facility med/surg unit with acute hypoxic respiratory failure due to COVID19 pneumonia and volume overload. On 1/25/22, patient was discharged home in good condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 1,0
Labordaten: COVID status positive 1/12/22.
Aktuelle Erkrankungen: -
Vorgeschichte: CAD with HFrEF (mild to moderate reduction in EF from 9/21) status post coronary bypass graft, CKD stage II, hypertension, A. fib with RVR (on warfarin), type 2 diabetes, CVA, stage III colon cancer status post resection and chemotherapy
Andere Medikamente: MVI, furosemide, lisinopril, metformin xr, metoprolol xl, nitroglycerin SL, simvastatin, warfarin
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2062860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: WA
Alter: 87,0
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: 26.10.2021
Beginn: 22.01.2022
Tage bis Beginn: 88,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute kidney injury Asymptomatic COVID-19 Chronic kidney disease Condition aggravated Device related infection Intensive care SARS-CoV-2 test positive Septic shock Urinary tract infection

Symptomtext

Patient received 3 Pfizer COVID vaccines on 1/19/21 (lot # EL3248), 2/9/21 (lot # EL9264), and 10/26/21 (lot # FH8028). On 1/22/22, patient admitted with septic shock (likely from complicated UTI with indwelling foley catheter), AKI on CDK III-IV, MRSA colonization with history of septic knee, and incidental COVID19 infection. As of today (1/25/22), patient is still admitted and COVID19 infection asymptomatic (not hypoxic).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Septic shock
Hospital-Tage: 3,0
Labordaten: COVID status positive 1/22/22.
Aktuelle Erkrankungen: -
Vorgeschichte: moderate to advanced dementia,, history of PE/DVT on apixaban, CKD stage III, history of septic knee with MRSA colonization on chronic doxycycline, resident of adult failure home
Andere Medikamente: acetaminophen PRN, apixaban, atorvastatin, calcium carbonate, vitamin d3, furosemide, gabapentin, lidocaine patch, melatonin, methocarbamol, metoprolol xl, MVI w/folic acid, potassium chloride, quetiapine, Tamsulosin, tramadol, trazodone
Allergien: hydrocodone, dexmedetomidine
Vorherige Impfungen: -

VAERS 2057808

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: WA
Alter: 92,0
Geschlecht: F
Eingang: 23.01.2022
Impfdatum: 06.11.2021
Beginn: 20.01.2022
Tage bis Beginn: 75,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure COVID-19 COVID-19 pneumonia Encephalopathy SARS-CoV-2 test positive

Symptomtext

Patient received Pfizer COVID vaccine on 3/13/21 (lot # EN6208), 4/3/21 (lot # ER8737), and 11/6/21 (lot # FH8028). On 1/20/22, patient admitted to our inpatient facility (med/surg unit) with acute hypoxemic respiratory failure and pneumonia due to COVID-19 and acute encephalopathy. As of today (1/22/22), patient is still admitted in our med/surg unit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: COVID status positive 1/20/22.
Aktuelle Erkrankungen: -
Vorgeschichte: alzheimer's dementia, depression
Andere Medikamente: acetaminophen PRN, alendronate, bisacodyl, calcium/magnesium, vitamin d3, duloxetine, gabapentin, haloperidol, lactobacillus acidophilus, metformin xr, MVI, polycarbophil, sennosides, trazodone
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2057209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: MT
Alter: 56,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Acute respiratory failure Immunisation SARS-CoV-2 test

Symptomtext

booster; Acute Respiratory Failure; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 03Dec2021 (Lot number: FH8028) at the age of 56 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Known allergies: Tape" (unspecified if ongoing); "Rheumatoid Arthritis" (unspecified if ongoing); "HBP" (unspecified if ongoing). Concomitant medication(s) included: ADDERALL; APIXABAN; PREDNISONE; ALLOPURINOL. Past drug history included: Demerol, reaction(s): "Known allergies: Demerol". Vaccination history included: Bnt162b2 (Dose number: 02, Administration Date: 21Jan2021, Lot No.: EL8982), administration date: 21Jan2021, when the patient was 55 years old, for Covid-19 immunization, reaction(s): "Acute respiratory failure", "Multiple unprovoked bilateral Pulmonary embolisms"; Bnt162b2 (Dose number: 01, Administration Date: 07Jan2021, Lot No.: EL3246), administration date: 07Jan2021, when the patient was 55 years old, for Covid-19 immunization. The following information was reported: ACUTE RESPIRATORY FAILURE (hospitalization, life threatening) with onset 11Dec2021, outcome "not recovered", described as "Acute Respiratory Failure"; IMMUNISATION (medically significant) with onset 03Dec2021, outcome "unknown", described as "booster". The patient was hospitalized for acute respiratory failure (start date: 11Dec2021, hospitalization duration: 16 day(s)). The event "acute respiratory failure" was evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (11Dec2021) negative; (26Dec2021) negative. Therapeutic measures were taken as a result of acute respiratory failure. No other vaccine in four weeks. Clinical course: I received my last vaccine (injection #02) on 21Jan2021. On 27Jan2021 I was admitted to the hospital with acute respiratory failure. In Jul2021 I was admitted for multiple unprovoked bilateral Pulmonary embolisms. On 03Dec2021 I received my booster (injection #03). On 11Dec2021 I was again admitted to the hospital for Acute Respiratory Failure. Prior to the vaccines, I have never had any lung or respiratory issues. Now, I have to have supplemental O2. Adverse event start date: 27Jan2021. Ae resulted in: [Emergency room/department or urgent care, Hospitalization, Life threatening illness (immediate risk of death from the event)]. No days hospitalization: 16. AE treatment: Supplemental O2 at home, Lifetime Eliquis for PE's. No covid prior vaccination. Covid tested post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: Test Date: 20211211; Test Name: Nasal swab; Test Result: Negative ; Test Date: 20211226; Test Name: Nasal swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Rheumatoid arthritis; Topical adhesive allergy
Andere Medikamente: ADDERALL; APIXABAN; PREDNISONE; ALLOPURINOL
Allergien: -
Vorherige Impfungen: -

VAERS 2031993

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: MI
Alter: 62,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 09.12.2021
Beginn: 04.01.2022
Tage bis Beginn: 26,0
Dosis: 3
Route/Site: IM / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Alanine aminotransferase increased Anticoagulant therapy Arterial catheterisation Aspartate aminotransferase increased Blood calcium decreased Blood glucose increased Brain herniation Brain stem syndrome Bundle branch block left COVID-19 Cardiac arrest Cardiomegaly Cerebellar haematoma Cerebellar haemorrhage Chest X-ray abnormal Computerised tomogram head abnormal Condition aggravated Death

Symptomtext

Deceased (1.4.22); Hospitalized/ED (1.4.22); COVID-19 positive (1.4.22); Fully vaccinated - pfizer x3 ED Note: CHIEF COMPLAINT: CARDIAC ARREST Assessment/Plan DIAGNOSIS at time of disposition: 1. Acute cerebellar hemorrhage 2. Cardiac arrest ED Disposition ED Disposition Expired Objective MEDICAL DECISION MAKING: This patient was signed out to me pending family discussion for goals of care. The family spoke with the neurosurgical team regarding prognosis as well as us. The mother and uncle were bedside and decided to make the patient comfort care only. We proceeded with extubation and stopped blood pressure supporting medication. The patient ultimately passed @ 2125. Medications etomidate (AMIDATE) injection (30 mg Intravenous Given 1/4/22 1734) EPINEPHrine 1 mg/10mL syringe (1 mg Intravenous Given 1/4/22 1808) sodium bicarbonate 8.4 % injection (50 mEq Intravenous Given 1/4/22 1751) rocuronium (ZEMURON) injection (100 mg Intravenous Given 1/4/22 1734) EPINEPHrine (ADRENALIN) 5 mg in NS 0.9% 250 mL (0.02 mg/mL) infusion premix (0 mcg/kg/min ? 111 kg Intravenous Stopped 1/4/22 2110) sodium bicarbonate 8.4 % injection CONFIRM DOSE - Pyxis Override Pull - (has no administration in time range) iopamidol (ISOVUE-370) 76 % injection 100 mL (has no administration in time range) sodium chloride 0.9% for CT injector flush 100 mL (has no administration in time range) sodium chloride flush 0.9 % syringe 10 mL (has no administration in time range) lidocaine (PF) 1 % injection CONFIRM DOSE - Pyxis Override Pull - (has no administration in time range) sodium chloride 0.9 % infusion CONFIRM DOSE - Pyxis Override Pull - (has no administration in time range) fentaNYL (SUBLIMAZE) injection 100 mcg (has no administration in time range) LORazepam (ATIVAN) injection 2 mg (has no administration in time range) anti-inhibitor coagulant complex (FEIBA) injection 5,044 Units (5,044 Units Intravenous Given 1/4/22 1829) New Prescriptions No new medications prescribed this visit. MD MRN: CSN: ED Provider Notes MD ? : Emergency Medicine MD at 1/5/2022 10:550AM Cosigned by: 1/5/2022 10:50 AM Procedure Orders 1. Insert Arterial Line ordered by MD 2. Intubation ordered by MD Signed by MD at 1/5/2022 10:50 AM ATTENDING NOTE: I have personally taken a history from and examined this patient and directed the care given in conjunction with the documenting resident. Unless otherwise indicated in a supplemental note, I agree with the resident's assessment and documentation. I was physically present for the key elements of all procedures done by those residents under my supervision. Emergency Department Attending Physician Addendum Date of service: 1/4/2022 I cared for this patient with the Resident. Please see their note for the additional details regarding this patient's encounter. Brief history, exam and Medical Decision Making: Patient seen in conjunction with the resident. Patient arrives as opposed to rest and was seen on arrival in the Trauma Bay. Did require resuscitation and several rounds of CPR. The airway was changed over to a conventional ET tube. Patient underwent head CT which showed a cerebellar hemorrhage with compression of the brainstem. Also noted to have blown pupil on the CT scanner. Blood pressure was quite labile, so an art line was established. Stat neurosurgery consult obtained. Anticoagulation reversed. Family contacted and informed of grave diagnosis and prognosis, who ventrally opted for extubation and comfort care. Critical Care Time: Critical Care time was required due to the life threatening nature of this patient's condition and I spent 95 minutes performing critical care. This excludes any procedures done during this time. Expand All Collapse All 01/04/2022 CHIEF COMPLAINT: CARDIAC ARREST Assessment/Plan DIAGNOSIS at time of disposition: 1. Acute cerebellar hemorrhage 2. Cardiac arrest Discharge Medication List as of 1/4/2022 11:13 PM ED Disposition ED Disposition Expired MEDICAL DECISION MAKING: Supervising Physician: Dr. ED Course as of 01/04/22 2344 Tue Jan 04, 2022 1911 62yo male with witnessed arrest and immediate CPR. Initial rhythm PEA, no shocks given. No meds given prior to arrival per EMS. On arrival, central pulses are palpable. He has a GCS of 3 with nonreactive pupils. Patient was intubated for airway protection. Initially, main concern was for a massive PE given reports of a respiratory arrest and patient's complaint of immediate preceding shortness of breath. EKG had been obtained and showed a LBBB without signs of ischemia using Sgarbossa criteria. LBBB is not new today. Plan is to go to CT. Will also obtain CT head, abdomen, and pelvis given patient's history of AAA. Prior to going to CT, patient had a 2nd cardiac arrest with 2 minutes of CPR and subsequent ROSC. 1916 Patient was started on epinephrine drip and then transported to CT. CT head was obtained which showed a cerebellar hemorrhage. Before additional imaging could be obtained, patient had a 3rd arrest while in CT, with given another dose of epinephrine, and underwent 1 round of CPR before ROSC. Additional imaging was forgone due to his instability and patient was returned to the resuscitation Bay where an arterial line was placed for closer blood pressure management. FEIBA was ordered for emergent reversal of his Eliquis. Neurosurgery was consulted and Dr. evaluated the patient at bedside. Patient's right pupil is now blown. GCS remains 3. According to Neurosurgery, operative intervention would be futile at this point. 1918 He began requiring increasing doses of epinephrine and was started on a norepinephrine drip as well. BP cuff readings were extremely labile and deemed unreliable, therefore a femoral arterial line was placed as below. 2339 I spoke with MICU and NSICU intensivists and patient was accepted to the NSICU. At this time, next of kin (mother) was not yet at bedside. Uncle is at bedside but does not have decision-making capacity for the patient. 2340 Mother and stepfather at bedside and updated. Mother states that patient has expressed in the past that he does not want to be on life support. Unless there is reasonable expectation of meaningful neurologic recovery, she wishes to pursue comfort care measures. I spoke with neurointensive care NPP who will also come speak to the family regarding prognosis. 2341 Following these discussions, all family at bedside is in agreement to proceed with comfort care and palliative extubation. Patient was extubated and vasopressors were stopped. He was pronounced dead at 2125. I notified ME Dr. who stated that this will not be an autopsy case and the patient's body was released to the funeral home of family's choosing. ED Course User Index MD Blood Pressure Screening: Based on last blood pressure taken in the ED of (!) 0/0, HTN (>/=140/90), recommend follow up with PCP within 1 month. Medications EPINEPHrine (ADRENALIN) 5 mg in NS 0.9% 250 mL (0.02 mg/mL) infusion premix (0 mcg/kg/min ? 111 kg Intravenous Stopped 1/4/22 2110) sodium bicarbonate 8.4 % injection CONFIRM DOSE - Pyxis Override Pull - (has no administration in time range) iopamidol (ISOVUE-370) 76 % injection 100 mL (has no administration in time range) sodium chloride 0.9% for CT injector flush 100 mL (has no administration in time range) sodium chloride flush 0.9 % syringe 10 mL (has no administration in time range) lidocaine (PF) 1 % injection CONFIRM DOSE - Pyxis Override Pull - (has no administration in time range) sodium chloride 0.9 % infusion CONFIRM DOSE - Pyxis Override Pull - (has no administration in time range) fentaNYL (SUBLIMAZE) injection 100 mcg (has no administration in time range) LORazepam (ATIVAN) injection 2 mg (has no administration in time range) etomidate (AMIDATE) injection (30 mg Intravenous Given 1/4/22 1734) EPINEPHrine 1 mg/10mL syringe (1 mg Intravenous Given 1/4/22 1808) sodium bicarbonate 8.4 % injection (50 mEq Intravenous Given 1/4/22 1751) rocuronium (ZEMURON) injection (100 mg Intravenous Given 1/4/22 1734) anti-inhibitor coagulant complex (FEIBA) injection 5,044 Units (5,044 Units Intravenous Given 1/4/22 1829) Subjective HISTORY OF PRESENT ILLNESS: HPI 62yo male working in a shop when he began acutely complaining of shortness of breath. EMS reports that they witnessed a respiratory arrest with PEA. CPR was initiated ROSC achieved after 8-12 minutes. No shocks given. No meds were given as no access was established prior to ROSC. Left tibial IO in place on arrival. Review of Systems Unable to perform ROS: patient unresponsive PAST MEDICAL HISTORY No Known Allergies Past Medical History: Diagnosis Date ? Abdominal aortic aneurysm (AAA) ? Ascending aortic aneurysm ? At risk for falls ? Bacteremia due to methicillin susceptible Staphylococcus aureus ? BPH (benign prostatic hyperplasia) ? Calcific aortic stenosis of bicuspid valve 03/08/2019 ? Congestive heart failure (CHF) 08/21/2009 ? CVA (cerebral vascular accident) ? Diastolic heart failure ? Heart disease ? HTN (hypertension) ? Hypercholesterolemia ? Left ventricular hypertrophy ? Obesity Past Surgical History Past Surgical History: Procedure Laterality Date ? HX AORTIC VALVE REPLACEMENT 10/02/2019 Willekes. AV Replacement 25 Magna, ascending aorta replacement ? HX AORTIC VALVULOPLASTY Hx of aortic stenosis / bicuspid aortic valve with valuloplasty as child ? HX ASCENDING AORTA ? HX KNEE ARTHROSCOPY Left ? HX TONSILLECTOMY Social History: reports that he has never smoked. He has never used smokeless tobacco. reports previous alcohol use of about 4.0 - 6.0 standard drinks of alcohol per week. reports no history of drug use. Family History Family History Problem Relation Age of Onset ? Breast Cancer Mother ? Cancer Father 55 brain cancer ? Anesth Problems Neg Hx Objective ED Triage Vitals Temperature Pulse Respirations BP SpO2 01/04/22 1922 01/04/22 1726 01/04/22 1726 01/04/22 1726 01/04/22 1726 36.7 ?C 90 12 (!) 115/101 98 % Temp src Heart Rate source Patient Position BP Location FIO2 (%) -- -- -- 01/04/22 1747 01/04/22 1906 Right arm 100 % Physical Exam Constitutional: Appearance: He is obese. HENT: Head: Normocephalic and atraumatic. Mouth/Throat: Mouth: Mucous membranes are moist. Eyes: Comments: Pupils 3 mm, equal, non-reactive Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Pulmonary: Comments: Bagged via I-gel LMA device. Abdominal: General: There is no distension. Palpations: Abdomen is soft. Skin: General: Skin is warm and dry. Capillary Refill: Capillary refill takes less than 2 seconds. Neurological: Comments: GCS 3. No response to noxious stimuli. No gag or cough reflexes. WORK UP: Labs: Labs Reviewed COVID-19, INFLUENZA A/B, RSV PCR - Abnormal; Notable for the following components: Result Value Ref Range Status COVID-19 PCR Detected (*) Not Detected Final Comment: COVID-19 (SARS-CoV-2) test is positive. Clinical correlation with patient history and other diagnostic information is necessary to determine infection status.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: COMPLETE BLOOD COUNT (CBC) W/DIFFERENTIAL - Abnormal; Notable for the following components: Red Blood Cell 4.38 (*) 4.60 - 6.00 x10*6/uL Final Hemoglobin 13.6 (*) 14.0 - 18.0 g/dL Final Mean Cell Hemoglobin Concentration 31.8 (*) 32.0 - 37.0 g/dL Final Immature Granulocyte Automated 1.0 (*) 0.0 - 0.6 % Final Immature Granulocyte Absolute Count 0.06 (*) 0.00 - 0.05 x10*3/uL Final All other components within normal limits COMPREHENSIVE METABOLIC PANEL - Abnormal; Notable for the following components: Glucose Level 254 (*) 70 - 99 mg/dL Final Calcium Level Total 8.4 (*) 8.6 - 10.4 mg/dL Final Alanine Aminotransferase 162 (*) 10 - 40 IU/L Final Aspartate Aminotransferase 130 (*) 10 - 40 IU/L Final All other components within normal limits HIGH SENSITIVITY TROPONIN T - Abnormal; Notable for the following components: hsTnT 25 (*) <22 ng/L Final hsTnT Interpretation Indeterminate (*) CT HEAD WITHOUT IV CONTRAST Final Result 1. Large intraparenchymal hematoma appears centered within the right cerebellum as above. There is significant resultant compression of the brainstem and supratentorial herniation of the cerebellum. 2. Intraventricular hemorrhage within the fourth ventricle and significant effacement of the fourth ventricle and cerebral aqueduct with concern for early developing supratentorial hydrocephalus. 3. Additional areas of subarachnoid hemorrhage within the basal cisterns and blood product extending along bilateral tentorial leaflets. Findings were discussed with Dr. by Dr. at 6:10 PM on 1/4/2022 DR CHEST SINGLE VIEW Final Result 1. Severe bilateral patchy airspace disease. Cardiomegaly and mediastinal prominence. Endotracheal tube 3.7 cm from the carina
Aktuelle Erkrankungen: 12/13/21 Office visit with Medical Group Infectious Disease ? long term antibiotic suppression for MV endocarditis with prosthetic aortic valve 12/26/21 - Urgent Care visit for acute right otitis media - Prescribed amoxicillin 875 mg BID
Vorgeschichte: Severe aortic stenosis Essential hypertension Dyslipidemia BPH (benign prostatic hyperplasia) NYHA class 1 heart failure with preserved ejection fraction Postoperative anemia S/P AVR, ascending aorta replacement Bilateral pulmonary embolism Bacteremia due to methicillin susceptible Staphylococcus aureus Endocarditis of mitral valve
Andere Medikamente: Acetaminophen 500 MG Take 1-2 tabs every 6 hours as needed for pain Apixaban 5 mg Oral 2 times daily Aspirin 81 mg Oral Daily Atorvastatin Calcium 40 mg Oral Nightly Carvedilol 25 mg Oral 2 times daily Cefuroxime Axetil 250 mg Oral Every 12
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2030784

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: WA
Alter: 70,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 21.12.2021
Beginn: 25.12.2021
Tage bis Beginn: 4,0
Dosis: UNK
Route/Site: SYR / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Angiogram normal Myocardial infarction Troponin increased

Symptomtext

Heart attack on 12/25/2021, Admitted to ER at 9:30 AM, Troponin levels high. Angiogram was clear, no narrowing, no blockages, no stent required. No myocardial injury.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: Troponin value at 4.138, Angiogram Negative for myocardial injury. 12/25/21.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Losartan
Allergien: None
Vorherige Impfungen: -

VAERS 2024781

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: WI
Alter: 64,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 09.11.2021
Beginn: 05.01.2022
Tage bis Beginn: 57,0
Dosis: 2
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death

Symptomtext

covid related death-vaccinated

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: DM, Ischemic cardiomyopathy, Peripheral vascular disease
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2014010

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: MI
Alter: 83,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 14.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 17,0
Dosis: 3
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Acute respiratory failure Angiogram Aortic arteriosclerosis Bronchial wall thickening Bronchitis COVID-19 Computerised tomogram thorax abnormal Haemoptysis Hilar lymphadenopathy Hyperkalaemia Hypoxia Influenza A virus test negative Influenza B virus test Influenza virus test negative Intervertebral disc degeneration Lymphadenopathy mediastinal Malaise Oxygen saturation decreased

Symptomtext

Patient hospitalized for 2 days. 83 y/o male HX of COPD on 2L at baseline who presented with acute hypoxic respiratory failure due to COVID-19. He had symptoms for about 2 weeks prior to presentation. He ultimately presented to urgent care and was sent to the ER. He required 4 L of oxygen to maintain his saturations in the ER and was started on Decadron due to his hypoxia. CT thorax with contrast showed no PE. He was weaned to his home baseline 2L easily. He was able to ambulate with minor desaturations but recovered quite quickly. Physical therapy and occupational therapy cleared him for home without services. He was discharged to home in stable condition. He was found to be hyperkalemic on admission so his potassium supplements were stopped. He remained mildly hyperkalemic, will need this rechecked outpatient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: CT ANGIO THORAX WITH IV CONTRAST [342773055]; Resulted: 12/31/21 2011. Order Status: Completed; Updated: 12/31/21 2013. Narrative: EXAMINATION: CT Angiography of the Thorax, EXAM DATE: 12/31/2021 7:44 PM. TECHNIQUE: Standard protocol CT angiogram images were obtained through the chest following the administration of intravenous contrast. Coronal and sagittal MIP 3-D reformations were performed. CONTRAST: 100 mL of Isovue-370. QPP DOCUMENTATION: At least one of the following dose reduction techniques was utilized: Iterative reconstruction, and/or Automatic Exposure Control, and/or mA/kV adjustment based on body size. INDICATION: Hemoptysis, hemoptysis. The patient is COVID-19 positive. COMPARISON: High resolution CTs of the chest performed September 23, 2021 and August 26, 2020, CTA thorax performed May 18, 2015. ENCOUNTER: Not applicable. FINDINGS: Base of Neck & Axillae: There is no lymph node enlargement. Mediastinum & Hila: Several slightly enlarged mediastinal lymph nodes and scattered nonenlarged mediastinal lymph nodes are stable compared to the study of September 23, 2021. These are nonspecific but are likely reactive or post inflammatory. The largest node resides in the caudal right paratracheal region just above the level of the carina having a short axis dimension of 16 mm. Mild bilateral hilar nodal prominence is also noted. Cardiovascular: Heart size is upper normal. There is no pericardial effusion. There is no evidence of right heart strain. The thoracic aorta is mildly atherosclerotic with no aneurysm, dissection or acute intramural hematoma. Pulmonary Arteries: The pulmonary arteries are well-opacified. No evidence of pulmonary embolism. The main pulmonary artery is upper normal in caliber at 30 mm. Lungs & Airways: The trachea and central bronchi are patent. There is mild bronchial wall thickening suggesting bronchitis that could be acute or chronic. There is no airspace disease or consolidation. There is no dominant pulmonary mass or worrisome pulmonary nodule. Pleural Space: There is no pleural effusion. There is no pneumothorax. A few calcified pleural plaques are present in the posterior left chest. These are stable. Upper Abdomen: Included portions of the upper abdomen are unremarkable. Chest Wall & Musculoskeletal: There are advanced multilevel degenerative disc changes of the thoracic spine. Impression: 1. No evidence of pulmonary embolism. 2. There is no airspace disease or consolidation. There is mild bronchial wall thickening consistent with bronchitis that could be acute or chronic. 3. No pleural effusion. No pneumothorax. 4. A few calcified pleural plaques are present in the posterior left hemithorax. These are stable and are nonspecific. Collected: 12/31/21 1822. Order Status: Completed. Specimen: Swabbed Collection from Nasopharynx Updated: 12/31/21 1943, COVID-19 PCR Detected Abnormal, Influenza A PCR Not Detected Not Detected, Influenza B PCR Not Detected Not Detected, RSV PCR Not Detected Not Detected.
Aktuelle Erkrankungen: -
Vorgeschichte: Respiratory, OSA (obstructive sleep apnea), Dyspnea, Mild intermittent asthma without complication, Restrictive ventilatory defect, On supplemental oxygen therapy, Pulmonary asbestosis (HCC), Acute on chronic respiratory failure with hypoxia (HCC), Acute on chronic respiratory failure (HCC), Circulatory TN (hypertension), Digestive GERD (gastroesophageal reflux disease), Morbid obesity (HCC), Infectious/Inflammatory. Hematologic, MGUS (monoclonal gammopathy of unknown significance), Thrombocytopenia (HCC), Genitourinary CKD (chronic kidney disease), stage III (HCC), Lower urinary tract symptoms (LUTS), Endocrine/Metabolic, Hyperlipidemia, Hypoxemia. Other: History of colon cancer, DJD (degenerative joint disease) of knee, Hypersomnia, Abnormal serum protein electrophoresis, Colonoscopy refused, History of pulmonary embolism, S/P total knee arthroplasty, left Prolonged QT interval, Abnormal CT lung screening.
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet, albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler, atenolol (TENORMIN) 100 MG tablet, atorvastatin (LIPITOR) 10 MG tablet, dexamethasone (DECADRON) 6 MG tablet, Dext
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2005680

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: WI
Alter: 64,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 29.12.2021
Beginn: 04.01.2022
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death

Symptomtext

vaccinated-covid related death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Acute UTI; cellulitis; COPD; asthma; DM2; CKD stage 3; CAD; HTN; HLD; morbid obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1999448

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 27.10.2021
Beginn: 24.12.2021
Tage bis Beginn: 58,0
Dosis: 3
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Acute respiratory failure Alanine aminotransferase normal Anion gap Aspartate aminotransferase normal Asthenia Blood albumin decreased Blood alkaline phosphatase normal Blood bicarbonate normal Blood bilirubin decreased Blood calcium decreased Blood chloride normal Blood creatinine decreased Blood glucose normal Blood potassium normal Blood sodium normal Blood urea decreased Bronchitis COVID-19

Symptomtext

Patient still hospitalized at 10 days admission. Patient is a 64 y.o. female with history of oxygen dependent COPD, chronic pain syndrome on chronic opioids, depression with anxiety, and former tobacco use who presents to the ER with worsening shortness of breath with cough in setting of COVID-19 infection. The patient lives at home with her daughter and grandson who tested positive for COVID on 12/21. The patient developed symptoms shortly after in tested positive on 12/22. She was fully vaccinated with Pfizer vaccine and booster on 10/27/2021. Patient complains of fevers, chills, generalized weakness with fatigue, worsening cough and shortness of breath. Patient reports she last had a short course of antibiotics about 1 month ago for bronchitis. She does has significant chronic obstructive pulmonary disease, on 2 L nasal cannula O2 at baseline, and former tobacco use. Patient reports chronic steroid use, typically on prednisone 7.5 mg daily, although patient self increased prednisone to 10 mg daily 3 days prior to arrival. Patient also has chronic pain, follows with pain clinic, and takes methadone 10 mg 4 times daily as well as Norco 10 daily. In the ER, patient remained afebrile, normotensive, borderline tachycardic, not tachypneic. Patient did desat to 88% on her baseline 2 L nasal cannula, bumped up to 3 L. chest x-ray showed significant emphysema with superimposed multi focal faint opacities. Labs unremarkable with normal renal function, no leukocytosis, normal procalcitonin. Patient received Solu-Medrol and remdesivir in the ER. The patient was admitted to Internal Medicine for further evaluation and treatment of acute on chronic hypoxic respiratory failure due to COVID-19 pneumonia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 10,0
Labordaten: Recent Labs 12/24/21 1932 WBC 7.24 HGB 12.2 HCT 37.7 PLATELET 366 Recent Labs 12/24/21 1932 SODIUM 136 POTASSIUM 4.2 CHLORIDE 98 HCO3 27 ANIONGAP 11 CREATININE 0.43* BUN 7* GLUCOSE 82 CALCIUM 8.2* TOTALPROTE 6.1 ALBUMIN 2.9* BILIRUBINT 0.2 AST 18 ALT 16 ALKALINEPH 74 Last EKG Result Electrocardiogram, Complete Collected: 12/24/2021 6:20 PM (Preliminary result) Narrative: Ventricular Rate 90 BPM Atrial Rate 90 BPM P-R Interval 120 ms QRS Duration 72 ms Q-T Interval 376 ms QTC Calculation(Bazett) 459 ms Calculated P Axis 77 degrees Calculated R Axis 63 degrees Calculated T Axis 63 degrees Diagnosis Sinus rhythm with occasional premature ventricular complexes Otherwise normal ECG When compared with ECG of 05-JUN-2021 15:06, premature ventricular complexes are now present Complete Results Last ECHO Study No resulted procedures found. Last Chest X-ray DR CHEST 2 VIEWS FRONTAL AND LATERAL Exam End: 12/24/2021 6:25 PM (Final result) Narrative: EXAMINATION: Frontal and Lateral View Chest EXAM DATE: 12/24/2021 6:25 PM TECHNIQUE: Frontal and lateral views INDICATION: Covid+ with shortness of breath. COMPARISON: Chest radiograph 6/30/2021. ENCOUNTER: Not applicable _________________________ FINDINGS: The cardiomediastinal silhouette is unremarkable. There are emphysematous changes with pulmonary hyperinflation. There are faint areas of opacity throughout the lungs with some of these representing chronic scarring. No pleural effusion or pneumothorax. There are anterior wedge compression deformities of 2 mid thoracic vertebral bodies resulting in exaggeration of the normal thoracic kyphosis. _________________________ Impression: Emphysematous changes with multifocal faint areas of superimposed opacity that may represent infection and/or scarring.
Aktuelle Erkrankungen: Weakness; disorders of zinc metabolism 10/26/2021
Vorgeschichte: Hospital Current chronic use of systemic steroids Chronic pain disorder Chronic, continuous use of opioids Tracheobronchitis Headache Peripheral neuropathy End stage COPD with acute exacerbation (HCC) Drug-induced constipation Unspecified severe protein-calorie malnutrition (HCC) Chronic respiratory failure with hypoxia (HCC) Pneumonia due to COVID-19 virus Goals of care, counseling/discussion Physical deconditioning Non-Hospital Hypertensive disorder Hyperlipidemia Tobacco dependence Multiple pulmonary nodules Chronic hypoxemic respiratory failure (HCC) Chronic pain Anxiety Acute sinusitis Back problem Contact dermatitis Disorder of intervertebral disc of thoracic spine Dysthymia Herniation of intervertebral disc without myelopathy Nutritional disorder Pain of right hip joint Peripheral vascular disease (HCC) Spinal stenosis of lumbar region Wrist joint pain Muscle weakness Migraine Leukocytosis Intermittent claudication (HCC) Herpes zoster Infection by Pasteurella multocida
Andere Medikamente: Acyclovir (ZOVIRAX) 5 % acyclovir (ZOVIRAX) 800 MG tablet albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler ascorbic acid (VITAMIN C) 500 MG tablet b
Allergien: Adhesive Tape Latex-Rash Penicillin [Penicillins]-Swelling Statins-Other
Vorherige Impfungen: -

VAERS 1955253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: MN
Alter: 90,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 09.11.2021
Beginn: 13.12.2021
Tage bis Beginn: 34,0
Dosis: 3
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Acute kidney injury Acute respiratory failure COVID-19 Cardiac failure congestive Chronic left ventricular failure COVID-19 pneumonia SARS-CoV-2 test positive Death Hypoxia Pulmonary embolism Pulmonary fibrosis

Symptomtext

Previously submitted E # 747322 updating with pt death 12/21/2021 Principal Problem: Acute And Chronic Respiratory Failure With Hypoxia (HCC) Active Problems: COVID-19 infection Chronic Diastolic (Congestive) Heart Failure (HCC) Fibrosis Pulmonary (HCC) Failure Renal Acute (Acute Kidney Injury) (HCC) Multiple Subsegmental Pulmonary Embolism Without Acute Cor Pulmonale (HCC)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1955253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: MN
Alter: 90,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 09.11.2021
Beginn: 13.12.2021
Tage bis Beginn: 34,0
Dosis: 3
Route/Site: SYR / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Acute kidney injury Acute respiratory failure COVID-19 Cardiac failure congestive Chronic left ventricular failure COVID-19 pneumonia SARS-CoV-2 test positive Death Hypoxia Pulmonary embolism Pulmonary fibrosis

Symptomtext

Previously submitted E # 747322 updating with pt death 12/21/2021 Principal Problem: Acute And Chronic Respiratory Failure With Hypoxia (HCC) Active Problems: COVID-19 infection Chronic Diastolic (Congestive) Heart Failure (HCC) Fibrosis Pulmonary (HCC) Failure Renal Acute (Acute Kidney Injury) (HCC) Multiple Subsegmental Pulmonary Embolism Without Acute Cor Pulmonale (HCC)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1968396

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: WA
Alter: 49,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Cardiac arrest Chest pain Death Dyspnoea Hypotension Illness Respiratory distress Resuscitation Tachycardia Tachypnoea Unresponsive to stimuli

Symptomtext

This 49 year old male was brought into MEDICAL CENTER by ambulance on 12/17/2021 at 0148 complaining of SOB and chest pains. Upon arrival he became unresponsive, CPR lasted for 1 hour with no change in rhythm until the death was pronounced. Previous visits noted for HTN, sleep apnea, cardiomegaly and obesity (350#). Unknown PCP or NOK information. Decedent told medics he got his COVID booster 3 days ago and started to exhibit SOB and chest pains since then. No signs of recent injuries, trauma or acute drug/alcohol intake. Labs put on hold for ME pick up... PER DR. at MEDICAL CENTER: Patient is a 49 y.o. male who presents with shortness of breath. History is obtained from record review paramedics and minimally from the patient due to his severe respiratory distress. Patient has reportedly been short of breath for the last 3 days it started within several hours of getting a Covid booster injection. Symptoms became severe today and he called the paramedics. Paramedics found him tachypneic hypotensive tachycardic ill-appearing placed on supplemental oxygen and transported here. Record review shows a history of obesity, obstructive sleep apnea, leg edema, nonhealing ulcer and hypertension patient reportedly came from home, history was limited due to the patient's severe respiratory distress. Patient did deny pain. Past medical history surgical history medications allergies family history social history and review of systems are all extremely limited due to the patient's severe respiratory distress on arrival and cardiac arrest several minutes after arrival.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Obesity hypertension OSA nonhealing ulcer leg edema
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1940021

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: KS
Alter: 48,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: 02.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Atherosclerotic plaque rupture Catheterisation cardiac abnormal Coronary artery thrombosis Intensive care Myocardial infarction Stent placement Ultrasound scan abnormal

Symptomtext

Had Covid-19 Virus, starting Oct 20. Asked Primary Care Physician, Dr for an exemption from getting vaccine, since just recovered from virus. Was told to get vaccine, as new studies said that the best time to get the vaccine was just after quarantine period was over. I followed his orders and had a heart attack 3 days later. I had no prior heart or other health issues other than vertigo (9/25/21) and a removed appendix (in early 20's) before receiving this vaccine. 95% blood clot to the left primary artery. To further explain: My employer was requiring the Pfizer vaccine by Nov 3. I had just returned to work Nov 1, after having Covid-19. I called Dr Nov 2 to request a 60-90 day exemption, as the Clinic had published a report recommending waiting that long after having the virus before getting the vaccine. He refused to give the exemption. It was his opinion that it would be best for me to go ahead and get the vaccine. The Clinic even had warnings about receiving the vaccine within 14 days of a Covid 19 diagnosis. When I told them about having just gotten past my quarantine, they asked what my doctor said. After I told them, they gave me the shot. Up until September 25 of this year, the only major medical I have ever experienced was having my appendix removed in my early 20's. On September 25, I went to the emergency room and was diagnosed with Vertigo (BPPV). At that time, my blood pressure and all my vital signs were completely normal. There has never been any heart related health concern prior. The CICU doctors cannot tell me what level of plaque I did have prior to the heart attack, only that the heart attack was caused because after the plaque ruptured the blood clotted in the left primary artery 95%. There are no signs that the plaque levels are above 20% anywhere else which CDC says is normal for a male my age.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 3,0
Labordaten: Heart cath & stint 11/5/2021 Sonogram of Heart 12/6/2021
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1936097

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: FL
Alter: 60,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 07.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Myocardial infarction

Symptomtext

Systemic: heart attack-Severe, Additional Details: Patient suffered from a heart attack following immunizations per pt reports

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1932306

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: MI
Alter: 42,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 29.11.2021
Beginn: 02.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Abdominal pain upper Angiogram pulmonary abnormal Arthralgia Atelectasis Chest pain Chills Computerised tomogram thorax abnormal Dyspnoea Fibrin D dimer Lung opacity Musculoskeletal chest pain Neck pain Pain Pain in extremity Painful respiration Pulmonary embolism Pulmonary thrombosis Scan with contrast abnormal

Symptomtext

On Monday, Nov. 29, 2021 I received my booster shot in my left arm. Tuesday, Nov. 30th mid af-afternoon I had a sore arm, body aches and chills for a few hours. Wednesday, Dec. 1st I felt good with the exception of having a stomach ache in the evening. Around 1am on Dec, 2nd I woke up with pain in my left shoulder, left ribs and shortness of breath. I was taken to Hospital where they did a series of tests and found a small blood clot in my left lung. Prior to my booster shot I had surgery (abdominal hysterectomy) on Friday, Nov. 12th. They believe the clot was caused from that. I asked them if this was vaccine related and they stated they do not believe so but asked me several times which vaccine I took. I asked them if they do not think this is vaccine related, why do they keep asking me what vaccine I took. They said there is a vaccine that has a history of blood clotting but would not tell me which one....Also I did ask my OBYGN if it was safe for me to get my booster shot on Tuesday, Nov. 23 and she replied it was safe encouraged me to get it ASAP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: TOO MANY TO LIST: CT chest with iv contrast pulmonary embolism - DetailsPrinter friendly page--New window will open About this test Details Study Result Narrative Patient MRN: Patient Location: Requesting Physician: Date/Time Exam Description PACS Acc # 12/2/2021 5:35 AM CT PULMONARY W/CONTRAST EXAMINATION: CTA PULMONARY WITH CONTRAST TECHNIQUE: After 100 mL of Isovue 370 was administered uneventfully, a PE Chest CTA was obtained. Axial, coronal, and sagittal MIP images were obtained. IDX EXAMINATION DATE AND TIME: 12/2/2021 5:35 AM COMPARISON/CORRELATION: None CLINICAL HISTORY: PE suspected, low/intermediate prob, positive D-dimer; Patient to ED for sudden onset left arm pain, neck pain and difficulty in breathing that awoke her.Patient states she started having chest pain and painful breathing tonight. Patient received her covid vaccine booster on Monday.. FINDINGS: Pulmonary artery tree: The pulmonary arterial tree is well-opacified with contrast. Filling defect seen in the segmental branch of the left lower lobe (series 3 image 155). MEDIASTINUM: No mediastinal or hilar lymphadenopathy. No axillary lymphadenopathy. CARDIOVASCULAR: No pericardial effusion. No cardiomegaly. LUNGS AND PLEURA: no focal consolidation. Platelike atelectasis at the left lung base. BONES/OTHER: No acute fracture. IMPRESSION: Findings concerning for a pulmonary embolus in a segmental branch of the left lower lobe. No evidence for right heart strain. Groundglass opacity at the left lung base which may reflect pulmonary infarct. Findings were discussed with Dr. by Dr. at 715 AM on 12/02/2021 with readback confirmation.
Aktuelle Erkrankungen: abdominal hysterectomy 11-12-21
Vorgeschichte: NONE
Andere Medikamente: VITAMIN C & D ZINC MULTI-VITAMIN
Allergien: MORPHINE
Vorherige Impfungen: -

VAERS 1885858

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

kritisch

Staat: CA
Alter: 88,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 06.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: UN / -

Tod: ja Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Cerebral thrombosis Cerebrovascular accident Death Fall

Symptomtext

She woke up normal, she went to her room for her prayers and that's when she fell out of her chair with a stroke. She was brought to the hospital immediately and was confirmed to have had blood clot in her brain. She was hospitalized from 11/09/2021 and passed away on 11/19/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 10,0
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Atherosclerosis Asthma
Andere Medikamente: Namenda Nanoxen Losartan
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2657380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: AZ
Alter: 53,0
Geschlecht: F
Eingang: 17.07.2023
Impfdatum: 21.11.2021
Beginn: 28.06.2023
Tage bis Beginn: 584,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein

Abdominal pain Anticoagulant therapy Computerised tomogram abdomen abnormal Magnetic resonance imaging Nausea Pyrexia Renal infarct Renal necrosis Thrombosis Ultrasound scan Vomiting

Symptomtext

Extreme abdominal pain on left side all day on June 28th, nausea, vomiting, fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 1,0
Labordaten: Admitted to ER 5pm June 28th, Ultrasound, CT Scan and MRI completed. CT Scan confirmed renal infarction, blood clot found near left kidney and left kidney indicated 30% necrosis. Admitted into hospital for overnight stay, blood thinners administered, and pain management via IV.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Vitamin C, Fish Oil, Zinc, Vitamin D, Vitamin K, Tumeric
Allergien: N/A
Vorherige Impfungen: -

VAERS 2636864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: -
Alter: 38,0
Geschlecht: M
Eingang: 25.05.2023
Impfdatum: 21.11.2021
Beginn: 20.04.2022
Tage bis Beginn: 150,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Deep vein thrombosis Neuropathy peripheral Pelvic venous thrombosis

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE CHEMOTHERAPY INDUCED PERIPHERAL NEUROPATHY, SEQUELA PERIPHERAL NEUROPATHY ACUTE DVT OF BILAT LEGS, UNSPECIFIED VEINS ACUTE DVT OF BILAT ILIOFEMORAL VEINS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2635523

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: -
Alter: 51,0
Geschlecht: F
Eingang: 23.05.2023
Impfdatum: 28.11.2021
Beginn: 13.09.2022
Tage bis Beginn: 289,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Lacunar stroke Symptom recurrence

Symptomtext

ACUTE LACUNAR STROKE, UNSPECIFIED TYPE AND ARTERY 9/27/2022 -- RECURRENCE OF SAME SYMPTOMS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lacunar stroke
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1909964

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: IN
Alter: 21,0
Geschlecht: M
Eingang: 14.03.2023
Impfdatum: 29.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Anaphylactic reaction Dysphonia Erythema Laboratory test Malaise Dyspnoea Hot flush Paraesthesia oral Pharyngeal paraesthesia Rash Oropharyngeal pain Sensory disturbance Swelling Swelling face Throat irritation Throat tightness Wheezing

Symptomtext

Within 5 minutes tingling in lips & throat 15 minutes hot flashed in face 30-45 min rash on face, arms, chest, back given Benadryl and EpiPen Some difficulty breathing that improved with EpiPen

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No ilness
Vorgeschichte: Cashews, pistacios
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2582586

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: WA
Alter: 39,0
Geschlecht: F
Eingang: 15.02.2023
Impfdatum: 02.12.2021
Beginn: 12.12.2022
Tage bis Beginn: 375,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Angiogram abnormal Cogwheel rigidity Influenza Magnetic resonance imaging abnormal Meningioma Migraine Muscular weakness Tongue paralysis

Symptomtext

Patient has developed migraines and also had lower extremity weakness. When she got influenza A she developed left deviation of the tongue and had temporary cogwheeling in the left leg

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tongue paralysis
Hospital-Tage: -
Labordaten: CT angiogram and MRI revealed Meningioma, not likely to be cause of sx
Aktuelle Erkrankungen: None
Vorgeschichte: None at time
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2560213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: NE
Alter: 68,0
Geschlecht: F
Eingang: 15.01.2023
Impfdatum: 24.02.2021
Beginn: 21.04.2021
Tage bis Beginn: 56,0
Dosis: 2
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: nein

Amnesia Angiogram Angiogram cerebral Cardiac monitoring Cognitive disorder Computerised tomogram head Echocardiogram Ischaemic stroke Magnetic resonance imaging head Speech disorder

Symptomtext

Ischemic stroke, air amublance, tomography, MRI, CT scans (mutiple), heart rythmn tracing, outcome - long term memory loss and vocabulary difficulties, cognitive loss,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: 1,0
Labordaten: ultrasound heart and neck blood flow, CT neck blood vessels. CT scan brain, CT scan blood vessels of head, long term heart rythmn tracing, MRI scan brain, hydralzaine injection, enoxaparin sodium injection,
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2553618

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: FL
Alter: 41,0
Geschlecht: F
Eingang: 08.01.2023
Impfdatum: 17.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: unbekannt Erholt: nein

Amnesia Cognitive disorder Computerised tomogram Gait inability Loss of personal independence in daily activities Magnetic resonance imaging Mental impairment Mobility decreased Shock

Symptomtext

The next morning after her vaccination date on 11-18-21 she woke up around 6:45 am with a heart rate exceeding normal levels. After taking our kids to the schools she returned home almost collapsing. I took twice her blood pressure and oxygenation level and the results were as follows: 1.- Oxygenation level : 87 2.- Heart beating rate : 116 3.- Blood pressure : less than 60 if I remember correctly(found this condition very weird). Right after taking those vitals i took her to the Hospital Emergency room where she arrived in someway already stable but in shock. After this incident , she began deteriorating mentally or cognitively to the point where she lost her life history short and long term memory. including the capacity to walk and conduct her normal occupational activities. She also lost her bearings on time and location including forgetting about essential things like eating or recognizing our two children's as her own. Her condition remains the same as of today withy a slightly improve in her mobility. During her rapid decay I took her one more time to the emergency hospital in 2021 when she failed to recognize me times in a day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Shock
Hospital-Tage: 2,0
Labordaten: Several MRI and CT scans that cab be obtained from the Hospital records
Aktuelle Erkrankungen: Multiple sclerosis
Vorgeschichte: Muiltiple Sclerosis
Andere Medikamente: Rituxumabe twice a year
Allergien: None
Vorherige Impfungen: -

VAERS 2523764

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: CA
Alter: 66,0
Geschlecht: F
Eingang: 06.12.2022
Impfdatum: 21.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein

Nasopharyngeal swab Paralysis SARS-CoV-2 test

Symptomtext

I ended up basically paralyzed; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 66-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 21Nov2021 as dose 3 (booster), single (Lot number: FH8028) at the age of 66 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hashimoto" (unspecified if ongoing), notes: Other medical history: Hashimoto; "high blood pressure" (unspecified if ongoing), notes: Other medical history: high blood pressure. The patient took concomitant medications. Vaccination history included: BNT162b2 (Dose Number: 1, Batch/Lot No: EN6198, Location of injection: Arm Left), administration date: 03Mar2021, when the patient was 65-year-old, for Covid-19 immunization; BNT162b2 (Dose Number: 2, Batch/Lot No: EP7534, Location of injection: Arm Left), administration date: 24Mar2021, when the patient was 65-year-old, for Covid-19 immunization. The following information was reported: PARALYSIS (hospitalization, disability, life threatening) with onset 30Nov2021, outcome "not recovered", described as "I ended up basically paralyzed". The event "i ended up basically paralyzed" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: Nasopharyngeal swab: (31Oct2022) Negative; SARS-CoV-2 test: (31Oct2022) Negative, notes: Nasal Swab. Therapeutic measures were not taken as a result of paralysis. Additional information: The patient had no other vaccine in four weeks and had no known allergies.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paralysis
Hospital-Tage: -
Labordaten: Test Date: 20221031; Test Name: Nasal Swab; Test Result: Negative ; Test Date: 20221031; Test Name: IHealth Antigen; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (Other medical history: high blood pressure); Hashimoto's disease (Other medical history: Hashimoto)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2501841

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: NY
Alter: 66,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 10.11.2021
Beginn: 06.01.2022
Tage bis Beginn: 57,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Adenocarcinoma Atelectasis COVID-19 Cardiac failure congestive Chest X-ray abnormal Chest pain Computerised tomogram abdomen abnormal Computerised tomogram thorax abnormal Condition aggravated Cough Dyspnoea Electrocardiogram T wave abnormal Fatigue Fibrin D dimer Haematocrit decreased Haemoglobin decreased Hyperhidrosis Hypoxia

Symptomtext

1/6/2022- Presents to ED, via ambulance family unable to care for patient, deconditioned and has fatigue, cough and SOB. Patient had IP stay 12/27-1/5/2022 for acute resp failure s/t CHF exacerbation and CAP, was on 2L NC, IV ceftriaxone and doxy. Admit Covid + test. Given IV remdesivir, decadron, baricitinib, and doxy. 02 as needed,on 1-2L sat above 98%. Afebrile. 1/9/2022- Rectal bleeding, H&H stable. Sigmoidoscopy performed rectal mass suspicious for malignancy. VSS. Currently on 2L NC 98% sat. 1/10/2022- weaned from 02 use. 1/11/2022-Rectal mass path: adenocarcinoma. D/C decadron change to prednisone. IV doxy to PO doxy. VSS 1/12/2022- Covid hypoxia improving. 1/12/2022- Will f/u with colorectal specialist post admission for surgical risk d/t antiplatelets and stenting. 1/15/2022- started on Rocephin, d/t possible UTI. 1/16/2022-BP's soft throughout day, 500cc bolus given , VSS. Rectal cancer stage IV. 1/17/2022-Had CT CAP showed liver mets. Will f/u with onc. for chemo after admission. VSS. H&H stable. 1/20/2022- H&H dropped to 7.3 1 unit given. 1/21/2022- Covid antigen negative. 1/23/2022- Hgb 9.5 improved and stable. Continues to maintain Spo2 level on 1-2L nc. 2/1/2022-Palliative Radiation tx, tolerated well. TX mon- friday. 2/6/2022-Hgb 6.8 transfused 1 unit. Pt diaphoretic, dyspenic and substernal pain. Trop indeterminate 0.027. EKG- aberrant conduction along with nonspecific T wave changes. D-Dimer 2,118. CXR- small pleural effusion noted. 60 mg Lasix given. Steroids and Bipap. Moved to CCU. BP found to be in the &0's Levophed started. Pt is extremely drowsy. 2/7/2022- Levophed now off. On 3L NC now. 2/8/2022-Chest pain resolved. Trop peaked overnight 0.136. TTE ordered. Continue DAPT. Chest CT- no definite pe, large b/l pleural effusions. Bilateral upper lobe dependent atelectasis. 2/9/2022- Stable on 3L NC. Contne intermittent albumin doses with Lasix to mobilize fluid, refused thoracentesis. 2/10/2022- Downgraded to NT3. Stable on 2L NC. 2/17/2022- VSS and Hgb stable, tolerating 2-3 L NC. 2/18/2022- D/C to SNF for deconditioning, Will follow up with oncology and GI. Surgery not an option.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 43,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CHF, HTN, Basal ganglia infarct, hyperlipidemia, Type 2 Dm, PVD,
Andere Medikamente: -
Allergien: Iodine
Vorherige Impfungen: -

VAERS 2387626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: CT
Alter: 44,0
Geschlecht: F
Eingang: 29.10.2022
Impfdatum: 30.11.2021
Beginn: 10.02.2022
Tage bis Beginn: 72,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: nein

Antinuclear antibody Back pain Biopsy skin Blood test Borrelia test Burning sensation Chest discomfort Computerised tomogram thorax Constipation Diarrhoea Dysuria Hypoaesthesia Muscle strain Muscle tightness Dyspnoea Echocardiogram Electromyogram Eye irritation

Symptomtext

right big toe hurt 02/10/2021, did cortison injection on big toe on 02/21/2021 then massive symptoms were started March 25th right buttock pain and right leg weakness, legs numbness, buttocks numbness, feet pins and needles, then 10 days later left buttocks and left legs are started then in May and June the pins and needles went upward to lower legs and thigh, like bug crawling, the middle June face numbness and arms and hands numbness then upper back pain and numbness then spread from upper back to front chest and trunk and abdominal, numbness head to toe, burning, pain almost everywhere, right big toe, legs pain, bottom feet pain, buttocks pain, upper back and upper arm pain, head, face all over body skin sensory loss some degrees, neck crunch sound, mouth tongue and gum burning, had UTI May 14th, ear ring in July, diaphragm and chest numbness more noticeable, fatigue and eye burning and eye corner shooting pain in Aug and shortness of breath, chest discomfort in Sep and high heat rate on Sep 29th, had fainting in restroom while in ER when they inject me medicine to push the lung fluid out, since then bought a BP tool AND BP are on lower side, like 95/55 - 110/74. Saw indigested salad and grapefruit 10/26/2022, still green leaves, went poo only couple of hours of eating it. Stomach gurling crazily since Sep, loose stool since beginning then constipation and diarrhea in turns since Sep.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 3,0
Labordaten: Lumbar spine MRI Cervical spine MRI BRAIN MRI X-RAY Skin biopsy Sensory Neuropathy panel EMG CT scan cheat heart and lung Heart ultrasound Blood tests Paraneoplastic test Celiac disease test Sjorens test Lyme test Thyroid test ANA test Immunofixatiom Unrine Light chain
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2387626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: CT
Alter: 44,0
Geschlecht: F
Eingang: 29.10.2022
Impfdatum: 30.11.2021
Beginn: 10.02.2022
Tage bis Beginn: 72,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: nein

Antinuclear antibody Back pain Biopsy skin Blood test Borrelia test Burning sensation Chest discomfort Computerised tomogram thorax Constipation Diarrhoea Dysuria Hypoaesthesia Muscle strain Muscle tightness Dyspnoea Echocardiogram Electromyogram Eye irritation

Symptomtext

right big toe hurt 02/10/2021, did cortison injection on big toe on 02/21/2021 then massive symptoms were started March 25th right buttock pain and right leg weakness, legs numbness, buttocks numbness, feet pins and needles, then 10 days later left buttocks and left legs are started then in May and June the pins and needles went upward to lower legs and thigh, like bug crawling, the middle June face numbness and arms and hands numbness then upper back pain and numbness then spread from upper back to front chest and trunk and abdominal, numbness head to toe, burning, pain almost everywhere, right big toe, legs pain, bottom feet pain, buttocks pain, upper back and upper arm pain, head, face all over body skin sensory loss some degrees, neck crunch sound, mouth tongue and gum burning, had UTI May 14th, ear ring in July, diaphragm and chest numbness more noticeable, fatigue and eye burning and eye corner shooting pain in Aug and shortness of breath, chest discomfort in Sep and high heat rate on Sep 29th, had fainting in restroom while in ER when they inject me medicine to push the lung fluid out, since then bought a BP tool AND BP are on lower side, like 95/55 - 110/74. Saw indigested salad and grapefruit 10/26/2022, still green leaves, went poo only couple of hours of eating it. Stomach gurling crazily since Sep, loose stool since beginning then constipation and diarrhea in turns since Sep.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 3,0
Labordaten: Lumbar spine MRI Cervical spine MRI BRAIN MRI X-RAY Skin biopsy Sensory Neuropathy panel EMG CT scan cheat heart and lung Heart ultrasound Blood tests Paraneoplastic test Celiac disease test Sjorens test Lyme test Thyroid test ANA test Immunofixatiom Unrine Light chain
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2481782

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: ME
Alter: 65,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 14.04.2022
Beginn: 21.09.2022
Tage bis Beginn: 160,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 COVID-19 pneumonia Haemoptysis Intensive care Laboratory test Pneumonia Positive airway pressure therapy SARS-CoV-2 test positive

Symptomtext

10/11 Coughing up blood, ambulance to hospital. Currently in ICU. Covid pneumonia in both lungs Antibiotics Antiviral 100%oxygen via bipap machine try nasal when possible during day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 7,0
Labordaten: Positive home test 10/10 Many hospital tests
Aktuelle Erkrankungen: Birdshot chorioretinopathy
Vorgeschichte: Birdshot chorioretinopathy
Andere Medikamente: Latanoprost 0.005% Brimonidine 0.2% Prednisone 10 mg Mycophenolate 500mg 3tabs twice a day
Allergien: Penicillin Erythromycin
Vorherige Impfungen: -

VAERS 2467296

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: MI
Alter: 50,0
Geschlecht: F
Eingang: 03.10.2022
Impfdatum: 07.12.2021
Beginn: 26.09.2022
Tage bis Beginn: 293,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Asthma Bronchial hyperreactivity COVID-19 Chest X-ray normal Dyspnoea Fibrin D dimer normal Hypertension Liver function test Myalgia Prohormone brain natriuretic peptide Renal function test Respiratory distress SARS-CoV-2 test positive Tachycardia Wheezing

Symptomtext

Discharge Provider: MD Primary Care Provider: DO Admission Date: 9/26/2022 Discharge Date: Sep 28, 2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Reactive airway disease without complication, unspecified asthma severity, unspecified whether persistent COVID-19 virus infection HOSPITAL COURSE: 51-year-old female with PMH significant for history of goiter and Hashimoto's thyroiditis (status post total thyroidectomy), subsequent hypoparathyroidism/hypothyroidism and seasonal allergies (no history of asthma or COPD) (even though uses p.r.n. albuterol an occasional steroid tapers for bronchospasm) presented to the hospital on 9/26 due to 3 day history of worsening dyspnea, myalgias.In ER, patient was noted to be tachycardic 108, hypertensive 183/81, afebrile and with normal oxygenation. Labs were all unremarkable including D-dimer and proBNP. Chest x-ray was clear of any infiltrates. She tested positive for COVID-19. Patient however appeared to be in respiratory distress, significant inspiratory/expiratory wheezing. Patient was giving breathing treatment and IV Solu-Medrol and subsequently admitted to hospitalist service for further management. Patient stayed in hospital for approximately 2 days. Patient was provided with supportive care, breathing treatment. She was continued on prednisone 40 mg daily. She was given total of 3 doses of IV remdesivir which she tolerated well with liver function, kidney function monitored. Patient remained on room air during this hospital stay. Patient's breathing much improved that she was discharged home stable.

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Praegender Schweregrund: Respiratory distress
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypocalcemia Hypoparathyroidism (HCC) Other iatrogenic hypothyroidism Hypothyroid COVID-19 virus infection Acute bronchospasm Postoperative hypothyroidism
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler butalbital-acetaminophen-caffeine (FIORICET) 50-300-40 MG CAPS calcitriol (ROCALTROL) 0.25 MCG capsule Calcium Carbonate-Vitamin D 600-400 MG-UNIT TABS Ca
Allergien: None
Vorherige Impfungen: -

VAERS 2459438

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: CA
Alter: 26,0
Geschlecht: M
Eingang: 24.09.2022
Impfdatum: 18.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 14,0
Dosis: 2
Route/Site: OT / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Bedridden COVID-19 immunisation Cardiac discomfort Chest pain Coagulopathy Deep vein thrombosis Fatigue Illness Immune system disorder Interchange of vaccine products Malaise Muscle spasms Pain Pharyngitis Post-acute COVID-19 syndrome Rhinitis SARS-CoV-2 test Vaccination site pain

Symptomtext

Left leg started cramping; left leg is having clotting; unable to get out of bed, was bedridden; just sick over and over get sick; infected in the nose and throat, constantly infected in the nose over and over again; constantly infected in the nose over and over again; injection site on arm painful; fatigue; thrombosis in legs, clotting in his legs, thighs and calves; hardening of the heart; His immunity is messed up; just a little achy; Long COVID, suffering a lot of long term COVID; lot of chest pain; Revaccination with Pfizer COVID-19 vaccine; Interchange of vaccine product; Immediately after got the Pfizer Covid Vaccine was feeling very unwell; This spontaneous case was reported by a patient and describes the occurrence of DEEP VEIN THROMBOSIS (thrombosis in legs, clotting in his legs, thighs and calves) in a 26-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 017C21A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Co-suspect product included non-company product TOZINAMERAN (COMIRNATY) for an unknown indication. The patient's past medical history included Addiction, Behavior disorder, Depression and Amphetamine abuse. On 18-Oct-2021 at 11:00 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Nov-2021, the patient received second dose of TOZINAMERAN (COMIRNATY) (unknown route) 1 dosage form. In November 2021, the patient experienced MALAISE (Immediately after got the Pfizer Covid Vaccine was feeling very unwell). On 18-Nov-2021, the patient experienced COVID-19 IMMUNISATION (Revaccination with Pfizer COVID-19 vaccine). 18-Nov-2021, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine product). On 24-Jan-2022, the patient experienced CHEST PAIN (lot of chest pain). On an unknown date, the patient experienced DEEP VEIN THROMBOSIS (thrombosis in legs, clotting in his legs, thighs and calves) (seriousness criterion medically significant), CARDIAC DISCOMFORT (hardening of the heart), IMMUNE SYSTEM DISORDER (His immunity is messed up), PAIN (just a little achy), POST-ACUTE COVID-19 SYNDROME (Long COVID, suffering a lot of long term COVID), MUSCLE SPASMS (Left leg started cramping), COAGULOPATHY (left leg is having clotting), BEDRIDDEN (unable to get out of bed, was bedridden), ILLNESS (just sick over and over get sick), PHARYNGITIS (infected in the nose and throat, constantly infected in the nose over and over again), RHINITIS (constantly infected in the nose over and over again), VACCINATION SITE PAIN (injection site on arm painful) and FATIGUE (fatigue). At the time of the report, DEEP VEIN THROMBOSIS (thrombosis in legs, clotting in his legs, thighs and calves), CARDIAC DISCOMFORT (hardening of the heart), IMMUNE SYSTEM DISORDER (His immunity is messed up), CHEST PAIN (lot of chest pain), POST-ACUTE COVID-19 SYNDROME (Long COVID, suffering a lot of long term COVID), MALAISE (Immediately after got the Pfizer Covid Vaccine was feeling very unwell), MUSCLE SPASMS (Left leg started cramping), COAGULOPATHY (left leg is having clotting), BEDRIDDEN (unable to get out of bed, was bedridden), ILLNESS (just sick over and over get sick), PHARYNGITIS (infected in the nose and throat, constantly infected in the nose over and over again), RHINITIS (constantly infected in the nose over and over again) and FATIGUE (fatigue) had not resolved and PAIN (just a little achy), VACCINATION SITE PAIN (injection site on arm painful), COVID-19 IMMUNISATION (Revaccination with Pfizer COVID-19 vaccine) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine product) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, SARS-CoV-2 test: (Negative) get sick infected but testing negative for COVID. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. This case was identified as part of a retrospective clean-up activity where certain emails received in the Moderna mailbox were missed to be booked-in. Pfizer COVID-19 vaccine time was after 15:00-15:30. Immediately after he got the Pfizer Covid Vaccine he was feeling very unwell and figured well, it was supposed to be like this because it's stronger the second round. The patient was suffering tremendously. The patient heard the booster can be any, but the first 2 were supposed to be the same. This was because he chose Pfizer Covid Vaccine. No concomitant medication was reported. No treatment medication was reported. The patient had battled with addictions and other dysfunctional behaviors. He had never felt anything past medication side effects from prescribed dose usage of psychiatric medication for treating untreatable depression and suffered a bit of those rather extreme side effects when heavily abusing methamphetamine daily. The patient had not even been using, had hardly smoked cannabis, hardly drank alcohol or cigarettes, had been very active, but he had been worsening and worsening even off of meth. Company comment: This is a spontaneous case concerning a 26-year-old male patient with medical history of depression, drug abuse and behavior disorder, who experienced the serious (medically significant) unexpected event deep vein thrombosis and the non-serious AESI COVID-19. The events occurred on an unknown date after the first dose of mRNA-1273 and after receiving the co-suspect product Tozineram as second dose of COVID-19 vaccination. DVT was reported on left leg: Clinical findings, diagnostic tests and treatment details were not provided. Event COVID-19 was described as a "long term COVID symptoms" and "repetitively infected with COVID". SARS-CoV-2 test was performed with negative result. Events seriousness captured as per IME list. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: Company comment: This is a spontaneous case concerning a 26-year-old male patient with medical history of depression, drug abuse and behavior disorder, who experienced the serious (medically significant) unexpected event deep vein thrombosis and the non-serious AESI COVID-19. The events occurred on an unknown date after the first dose of mRNA-1273 and after receiving the co-suspect product Tozineram as second dose of COVID-19 vaccination. DVT was reported on left leg: Clinical findings, diagnostic tests and treatment details were not provided. Event COVID-19 was described as a "long term COVID symptoms" and "repetitively infected with COVID". SARS-CoV-2 test was performed with negative result. Events seriousness captured as per IME list. The benefit-risk relationship of mRNA-1273 is not affected by this report.

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Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Test Name: COVID-19; Test Result: Negative ; Result Unstructured Data: get sick infected but testing negative for COVID
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Addiction; Amphetamine abuse; Behavior disorder; Depression
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2451490

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FH8028

schwer

Staat: IL
Alter: 66,0
Geschlecht: M
Eingang: 19.09.2022
Impfdatum: 15.11.2021
Beginn: 15.12.2021
Tage bis Beginn: 30,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Atrial fibrillation Atrial flutter Cardiac ablation Dizziness Electrocardiogram abnormal Heart rate increased Syncope

Symptomtext

I developed AFlutter (a form of Atrial Fibrillation) as a result of getting the Pfizer Booster. My first two vaccines were Moderna. According to my heart rate data that is tracked on my device, since 2018 my resting heart rate has been approximately 60bpm. I received the Pfizer booster on November 15, 2021. In mid-December 2021, my resting heart rate data increased to 70bpm. In March & April 2022, I started to have dizzy/fainting episodes. On my first visit to an ER on 4/12/2022, I was diagnosed with AFlutter immediately. My symptoms persisted and I had an ablation procedure on June 14, 2022 to correct the AFlutter. At my 3 week post-procedure check-up, my heart rhythm was normal again, as was my resting heart rate. On my device data, my resting heart rate has been approximately 60bpm since my ablation procedure. I have not had any additional booster vaccines since the one I had November 15, 2021.

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Praegender Schweregrund: Syncope
Hospital-Tage: 1,0
Labordaten: EKG's, both at two ER visits and at the cardiologist. 4/12/2022, May 2022, June 2022
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Levothyroxine 100 mcg daily Liothyronine 2.5 mcg daily
Allergien: None
Vorherige Impfungen: -

VAERS 2408562

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: SC
Alter: 33,0
Geschlecht: M
Eingang: 11.08.2022
Impfdatum: 11.11.2021
Beginn: 01.05.2022
Tage bis Beginn: 171,0
Dosis: 1
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Guillain-Barre syndrome Immunoglobulin therapy

Symptomtext

Guillain Barre, hospitalized, IVIG treatment

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: RA
Andere Medikamente: Humira
Allergien: -
Vorherige Impfungen: -

VAERS 2394980

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: KY
Alter: 83,0
Geschlecht: F
Eingang: 28.07.2022
Impfdatum: 28.10.2021
Beginn: 27.07.2022
Tage bis Beginn: 272,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

Abdominal discomfort Asthenia COVID-19 Diarrhoea Exposure to SARS-CoV-2 Faeces discoloured Hypophagia Illness Intensive care SARS-CoV-2 test positive

Symptomtext

She presented to the hospital today for weakness which has been getting worse progressively over the last few days.. She appeared to be ill during presentation and she was not a very great historian. Associated symptoms include abdominal discomfort which has been occurring after eating right immediately and resulting in decreased p.o. intake. She also had on and off diarrhea over the last 2 weeks up to 5 times a day, dark in color but not so foul-smelling. Vitals in ED: T-max normal; HR max 102; nadir BP 84/38. Temperature on arrival to ICU was 95.2. Patient also tested positive for COVID. She denies shortness of breath, cough or sore throat. No fever at home. She reported exposure to her son who had COVID as well but she does not recall when. She is vaccinated. Of note, patient follows with Dr. for cholecystitis and she was just seen 2 days ago and felt to be doing well. Cholecystectomy was not offered due to her multiple medical issues.

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Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2320790

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH 8028

schwer

Staat: TN
Alter: 37,0
Geschlecht: F
Eingang: 15.06.2022
Impfdatum: 18.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein

Body temperature decreased Computerised tomogram abnormal Dysstasia Electromyogram abnormal Fatigue Gait disturbance Guillain-Barre syndrome Heart rate decreased Hypoaesthesia Hypotension Immunoglobulin therapy Impaired work ability Loss of consciousness Lumbar puncture Magnetic resonance imaging abnormal Nerve conduction studies abnormal Pain Paraesthesia

Symptomtext

The morning following the vaccination, I woke up with intractable vomiting. This was followed by tingling and numbness in my hands and throughout the next several days eventually spread to my feet, then legs. This continued to worsen throughout the entire month of December along with pain as well as extreme fatigue. Ultimately, on 1/3/22 I passed out and was taken via ambulance to Hospital with hypotension, low body temp, low heart rate, inability to stand or walk. After CT, MRI, Spinal tap, EMG, Nerve conduction studies, I was diagnosed by my neurologist with Guillain Barre Syndrome. This has had to have continued treatments including IVIG infusions. I am still out of work on disability as of today and have been unable to return.

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Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 25,0
Labordaten: CT scans, MRI, Spinal Tap, EMG, Nerve conduction studies
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Lisinopril, Alprazolam, Butalbital
Allergien: Pertussis vaccine
Vorherige Impfungen: Pertussis

VAERS 2315572

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: MI
Alter: 62,0
Geschlecht: F
Eingang: 10.06.2022
Impfdatum: 08.04.2021
Beginn: 14.02.2022
Tage bis Beginn: 312,0
Dosis: 3
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Anticoagulant therapy Bladder catheterisation COVID-19 Cough Critical illness Dyspnoea Endotracheal intubation Mechanical ventilation Oxygen saturation decreased Positive airway pressure therapy Respiratory distress Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

63-year-old pt to ED for respiratory distress/shortness of breath patient states that she has a history of COPD on 2/14. COVID positive upon adm. 2/15 Pt spo2 dropped and intubation team was called. RT adjusted bi-pap FiO2 and pt spo2 climbed. Pt in obvious respiratory distress, 79% on Bipap. Heparin GTT ordered. Pt on Vanco and Cefepime. 2/17 Pt intubated, Fentanyl drip for comfort, SWRx2 to prevent pulling lines/tubes. Pt NST/ST on monitor, stable. 2/18 pt foley removed,Precedex gtt started, Fentanyl titrated off. Pt remains on vent. Critically ill; no acute cardiac issues. 2/21 pt remains on the ventilator, sedated, following simple commands. Pt discharged 2/25 with non productive congested cough noted.

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Praegender Schweregrund: Respiratory distress
Hospital-Tage: 12,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: Acute respiratory failure with hypoxia and hypercapnia (CMS/HCC) ... Acute respiratory failure with hypoxia and hypercapnia (CMS/HCC) COPD (chronic obstructive pulmonary disease) (CMS/HCC) Streptococcal pneumonia (CMS/HCC) COVID-19 Anxiety Polycythemia Agitation Alcohol abuse Alcohol withdrawal (CMS/HCC) COVID
Andere Medikamente: albuterol (PROVENTIL, VENTOLIN, PROAIR) ... albuterol (PROVENTIL, VENTOLIN, PROAIR) HFA 108 (90 Base) MCG/ACT INHAL Aero Soln albuterol-ipratropium (DUONEB) 0.5-2.5 (3) MG/3ML INHAL Solution aspirin EC (HALFPRIN) 81 MG PO Tablet Delayed Res
Allergien: codeine
Vorherige Impfungen: -

VAERS 2275677

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: OR
Alter: 54,0
Geschlecht: F
Eingang: 13.05.2022
Impfdatum: 11.11.2021
Beginn: 03.04.2022
Tage bis Beginn: 143,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Anticoagulant therapy Blood test Condition aggravated Contusion Injection site pain Injection site pruritus Injection site swelling Magnetic resonance imaging head abnormal Migraine Neurological symptom Ophthalmic migraine Pain Peripheral swelling Thrombosis Ultrasound Doppler abnormal

Symptomtext

On April 3rd, 2022, I had bruising and swelling in my lower left arm. I went to have an ultrasound done of my arm because the doctor didn't think it was an infection and it turned out to be a blood clot. The blood clot was from the length of my elbow to my wrist. I've had history of blood clots before but never in this location of the arm, which is very unusual. Symptoms were swelling and pain. Ultrasound indicated the blood clot. Physician took me of Eliquis because it failed and changed my medication to heparin injections. On April 10th, 2022. I started having migraine headaches which I've not had in decades. I had migraines when I was in my teens and 20s and I have had 7 migraines between April 10 and today, May, 13. They are ocular and again it's been decades. Don't know if it's in relation to the vaccine but its very unusual that they're suddenly back. Another note here: I've had a bump at the location site of my 2nd injection since I've gotten that vaccine (01/12/2021). There's still a bump there and it's sore. It's not always sore, sometimes it is, sometimes it isn't. About the size of a pea. Sometimes itches. Blood clot - unknown recovery. Migraines - no to recovery

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Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Ultrasound 4/3/2022 - indicated a blood clot in the left arm, MRI brain scan for migraines - resembled stroke symptoms - results were no stroke, Blood work
Aktuelle Erkrankungen: None
Vorgeschichte: Factor 5 Leiden
Andere Medikamente: Eliquis 5mg 2xday, Ropinirole HCL 0.5mg as needed, Vitamin B Complex
Allergien: Sulfa, Erythromycin, Codeine
Vorherige Impfungen: 2nd COVID Pfizer 01/12/2021 - Bump at injection site, size of pea, itchiness and soreness, still ongoing

VAERS 2235986

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: WI
Alter: 49,0
Geschlecht: F
Eingang: 15.04.2022
Impfdatum: 03.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 4,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Anticoagulant therapy Deep vein thrombosis Gait inability Laboratory test Pain in extremity Peripheral swelling Thrombectomy Ultrasound Doppler abnormal

Symptomtext

booster given on 1-3-22 and could not walk on 1-7-22. There was swelling and pain in the left leg. I had a brief pain on Thursday the 6th, but could hardly walk on Friday. I elevated my leg and took ibuprofen all day on Friday and Saturday. I had no relief after a couple days so I went to urgent care on Sunday the 9th and had an ultrasound to dx : DVT. Went on blood thinner and very little relief . On the 21st I had a CT and was scheduled for thrombectomy on the 24th. Massive bloot clot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: US on the 9th. Lab work also on the 9th. Ct on the 21st. Thromectomy and lab work on the 24th. Follow up US on 3-2-22 and lab work also.
Aktuelle Erkrankungen: none
Vorgeschichte: rt clavicle deformity varicose veins
Andere Medikamente: Sertraline
Allergien: seasonal only
Vorherige Impfungen: -

VAERS 2218326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 06.04.2022
Impfdatum: 19.11.2021
Beginn: 23.12.2021
Tage bis Beginn: 34,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Angiogram peripheral abnormal Anticoagulant therapy Catheter directed thrombolysis Foot amputation Haemoglobin decreased Red blood cell transfusion Vascular graft occlusion Vascular graft thrombosis

Symptomtext

Thrombosis of femoro-popliteal bypass graft - presented to the clinic for vascular follow-up and was found to have occlusion of his of his femoral popliteal graft. He was admitted. Interventional radiology consulted and he underwent a series of right lower extremity angiograms with catheter thrombolysis as described above in procedures. See procedure notes for details. IV heparin was transitioned to Eliquis and aspirin. He received a transfusion of 1 unit of packed red blood cells for hemoglobin of 7.2. He was seen in consultation by podiatry for consideration of right transmetatarsal amputation due to ischemic changes to the right distal foot. He was taken to the operating room by podiatry on January 3, 2022 for right transmetatarsal amputation. Hyperbaric medicine consulted and he underwent hyperbaric oxygen therapy. Discharged home. Hospital admission within 6 weeks of receiving the COVID vaccine.

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Praegender Schweregrund: Vascular graft thrombosis
Hospital-Tage: 20,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2203981

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: MI
Alter: 64,0
Geschlecht: M
Eingang: 29.03.2022
Impfdatum: 18.11.2021
Beginn: 19.03.2022
Tage bis Beginn: 121,0
Dosis: 2
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 COVID-19 pneumonia Central venous catheterisation Endotracheal intubation Gastrointestinal tube insertion Imaging procedure abnormal Interstitial lung disease Lung infiltration Pulmonary oedema SARS-CoV-2 test positive

Symptomtext

trauma pt tested positive for covid on 3/19, now with covid pneumonia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: -
Labordaten: SARS-CoV-2 (COVID-19) by NAA, Micro - detected on 3/19/22 FINDINGS: 3/18 Bilateral patchy interstitial airspace disease likely infiltrates and/or edema. Borderline cardiomegaly. Endotracheal tube, nasogastric tube and right jugular central line in place which are in satisfactory location. IMPRESSION: Worsening airspace disease likely edema. Lines and tubes in satisfactory location
Aktuelle Erkrankungen: -
Vorgeschichte: closed head injury, ARDS, cellulitis, concussion
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2116187

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: ME
Alter: 43,0
Geschlecht: M
Eingang: 02.03.2022
Impfdatum: 12.02.2022
Beginn: 13.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood pressure increased Chest pain Cough Electric shock sensation Eye pain Erythema Injection site erythema Injection site pain Muscle swelling Hypoaesthesia Injection site discolouration Injection site reaction Musculoskeletal chest pain Pain Paraesthesia Pruritus Pulmonary pain Scratch

Symptomtext

He got his vaccine, he could feel it going through his body. When he first noticed it the area was a couple inches above his vaccine site, traveled down the arm to left pectorial area of his chest. Was a darker red around it and stayed that way for 3-5 days. His head as his BP would go up on the left side from his eyeball to back top of his head, he doesn't know what blood things were going through it would stop scratching. The crown of his head is numb like pins and needles, and it starts to itch when he gets anxious and scratches like a dog with fleas and keeps himself from scratching. His chest in the center, the clavicle on the left side was sensitive to touch. The next day both sides would hurt and then it would be in the clavicles. The pains are now gone but can feel a little bit in his chest, but nothing to complain about. His lungs hurt to cough and feels like his lungs are being ripped apart. Feels like his lungs are sticking together and then they feel like they are ripping apart, still every day. Down across in front of his left eye when he was washing his face he went across it and the pain was from the right side to the left side and hit that nerve and felt like an electrical charge, which stayed like that for a day and a half. Today he is able to feel it but top of head is still numb. He called his doctor and he informed him to call us to report it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: Asthma, OCD, ADHD, bipolar, social anxiety.
Andere Medikamente: Lithium 300 mg, 8 mg of Suboxone, 0.5 Clonazepam, 25 mg Hydrochlorothiazide, 20 mg/10 mg Ritalin.
Allergien: Yellow jackets and hornets
Vorherige Impfungen: -

VAERS 2108894

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: CA
Alter: 26,0
Geschlecht: M
Eingang: 12.02.2022
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Anxiety Cardiac disorder Chest pain Deep vein thrombosis Dyspnoea Fatigue General physical health deterioration Immune system disorder Infection Interchange of vaccine products Malaise Muscle spasms Off label use Pharyngitis Rhinitis SARS-CoV-2 test Thrombosis

Symptomtext

get sick infected/Repetitive infections; Immediately after he got the Pfizer Covid Vaccine he was feeling very unwell; Left leg started cramping, clotting, definitely thrombosis in his leg and body; seems like hardening of the heart; fatigue; His immunity is messed up; being infected in the nose and throat, constantly infected in the nose over and over again; being infected in the nose and throat, constantly infected in the nose over and over again; felt uneasy; worst declined in health; he could hardly breathe; the first dose of COVID-19 vaccine (Moderna); the first dose of COVID-19 vaccine (Moderna); definitely thrombosis in his leg and body; left leg is having clotting, deep vein thrombosis; chest pain; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 26 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 18Nov2021 (Lot number: FH8028) at the age of 26 years as dose 2 (initial pfizer dose), single for covid-19 immunisation. Relevant medical history included: "Addiction" (unspecified if ongoing), notes: He has battled with addictions and other dysfunctional behaviors.; "Dysfunctional behaviors" (unspecified if ongoing), notes: He has battled with addictions and other dysfunctional behaviors. There were no concomitant medications. Vaccination history included: Moderna covid vaccine (Dose 1, Batch/lot number :017C21A, injection to left arm at 11:00), administration date: 18Oct2021, when the patient was 26 years old, for COVID-19 immunisation, reaction(s): "injection site on arm painful". The following information was reported: THROMBOSIS (disability, medically significant) with onset 2021, outcome "unknown", described as "definitely thrombosis in his leg and body"; DEEP VEIN THROMBOSIS (disability, medically significant) with onset 2021, outcome "unknown", described as "left leg is having clotting, deep vein thrombosis"; CHEST PAIN (disability) with onset 2021, outcome "not recovered", described as "chest pain"; INFECTION (disability), outcome "not recovered", described as "get sick infected/Repetitive infections"; MALAISE (disability), outcome "not recovered", described as "Immediately after he got the Pfizer Covid Vaccine he was feeling very unwell"; MUSCLE SPASMS (non-serious), outcome "not recovered", described as "Left leg started cramping, clotting, definitely thrombosis in his leg and body"; CARDIAC DISORDER (non-serious), outcome "not recovered", described as "seems like hardening of the heart"; FATIGUE (non-serious), outcome "not recovered", described as "fatigue"; IMMUNE SYSTEM DISORDER (non-serious), outcome "not recovered", described as "His immunity is messed up"; RHINITIS (non-serious), PHARYNGITIS (non-serious), outcome "not recovered" and all described as "being infected in the nose and throat, constantly infected in the nose over and over again"; DYSPNOEA (non-serious) with onset Jan2022, outcome "not recovered", described as "he could hardly breathe"; ANXIETY (non-serious), outcome "not recovered", described as "felt uneasy"; GENERAL PHYSICAL HEALTH DETERIORATION (non-serious), outcome "not recovered", described as "worst declined in health"; INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 18Nov2021, outcome "unknown", described as "the first dose of COVID-19 vaccine (Moderna)". His symptoms, which were very bad, after receiving the second dose of COVID-19 vaccine (Pfizer COVID-19 vaccine on 18Nov2021) and the first dose of COVID-19 vaccine (Moderna). Patient made a mistake, because he was going for his second primary second 2 of 2-dose follow up vaccine dose and he was not paying attention because the first one was in October, four months or three months ago, of Moderna. Patient thought he got the Pfizer patient didnt see Moderna and he had lost his vaccine card and didnt remember. The lady didn't even check, she had no way of knowing at the pharmacy nobody checked and they just administered the incorrect second dose. After patient got his second incorrect vaccine, mixed batch, patient was having severe side effects and today he was still incapacitated, his left leg was having clotting, deep vein thrombosis, and lot of chest pain, and just sick over and over patient get sick infected but testing negative for COVID. He has been testing negative for COVID but his left leg is having clotting and deep vein thrombosis and he also has chest pain over and over. He clarified that his first dose, the Moderna Covid Vaccine, was administered while he was hospitalized in a local hospital for mental health issues. The Moderna Covid Vaccine was very beneficial to him, he personally had little to no side effects. He explained that the long COVID and the repetitive infections he has had since then, he is not contagious and is testing negative; but is suffering a lot of long term COVID symptoms. Immediately after he got the Pfizer Covid Vaccine he was feeling very unwell, it is supposed to be like this because its stronger the second round. He is suffering tremendously. He still feels, like nights ago his left leg started cramping, clotting, definitely thrombosis in his leg and body. He was monitoring closely to watch after the first dose the Moderna Covid Vaccine he was quite well, just fine, hardly any, barely, just a little achy, injection site on arm painful for a few days; nothing like what he was having since Pfizer Covid Vaccine with the chest pains, thrombosis in legs, clotting in his legs, thighs and calves. He is unable to get out of bed. He is repetitively getting infected with COVID. Within minutes he felt uneasy, like why is this not cooling down already, its been 30 minutes or 1 hour and this was weeks before Christmas. He was bedridden throughout New Years and Christmas and just constantly trying to manage in mind or sight. The chest pain was so severe 24Jan2022 he could hardly breathe; he had to gather his composure because he felt like he was going to fall to the floor because the chest pain was so sharp. Then it seems like hardening of the heart and cramping in his legs, fatigue and being infected in the nose and throat, constantly infected in the nose over and over again. His immunity is messed up, not the same as when he first got the first shot, the Moderna Covid Vaccine, from before he got the Moderna Covid Vaccine his immunity was noticeably affected. To some extent he did get sick on several occasions but he noticed when he got better and recovered, he had good strong lasting effects after the Moderna Covid Vaccine. Definitely in the last few weeks he has had the absolutely worst declined in health. From his understanding, the incorrect administration scared him to a whole other level. He thinks it is just long COVID. He hopes to fix the cells incorrectly vaccinated. The symptoms every moment are agonizing and torturing. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: negative, notes: he is not contagious and is testing negative; but is suffering a lot of long term COVID symptoms. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Test Name: COVID; Test Result: Negative ; Comments: he is not contagious and is testing negative; but is suffering a lot of long term COVID symptoms.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Abnormal behavior (He has battled with addictions and other dysfunctional behaviors.); Addiction (He has battled with addictions and other dysfunctional behaviors.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2092232

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: FL
Alter: 58,0
Geschlecht: F
Eingang: 07.02.2022
Impfdatum: 20.12.2021
Beginn: 31.01.2022
Tage bis Beginn: 42,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Dyspnoea Emphysema Pain Respiratory distress Respiratory failure SARS-CoV-2 test positive Wheezing

Symptomtext

Patient was admitted for worsening respiratory failure and respiratory distress. Does have COPD and chronically wears 2-4 L nasal cannula at baseline. Did test positive for COVID-19 Chest x-ray did not show acute intrathoracic process but did show significant emphysematous changes. At most required 3 L nasal cannula to maintain oxygenation. Had significant pan expiratory and inspiratory wheezes. Received remdesivir and Solu-Medrol. Also received bronchodilator therapy. Had drastic improvement in her wheezing and her shortness of breath. Weaned to her baseline oxygenation of 2 L nasal cannula. COPD Exacerbation in addition to COVID. Discharged home 2/2/22. Previously vacc: Pfizer 3/18/21, 4/8/21, 12/20/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory distress
Hospital-Tage: 3,0
Labordaten: COVID 19 PCR + 1/31/22
Aktuelle Erkrankungen: -
Vorgeschichte: COPD on home O2, sleep apnea, hypertension, hyperlipidemia, diabetes, obesity, anxiety, peripheral neuropathy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2091168

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: NJ
Alter: 33,0
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 29.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Disorientation Dizziness Headache Irritability Meningitis Venous thrombosis

Symptomtext

meningitis; bad headache; I was like really dizzy; disoriented; I was like hearing voices kind of and just irritable; venous thrombosis; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 33 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 29Dec2021 (Lot number: FH8028) at the age of 33 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "high blood pressure" (unspecified if ongoing), notes: I am not sure I get high blood pressure once in a while. There were no concomitant medications. The following information was reported: MENINGITIS (medically significant), outcome "recovering", described as "meningitis"; HEADACHE (non-serious), outcome "recovered", described as "bad headache"; DIZZINESS (non-serious), outcome "recovering", described as "I was like really dizzy"; DISORIENTATION (non-serious), outcome "recovering", described as "disoriented"; IRRITABILITY (non-serious), outcome "recovering", described as "I was like hearing voices kind of and just irritable"; VENOUS THROMBOSIS (non-serious), outcome "recovering", described as "venous thrombosis". Therapeutic measures were not taken as a result of meningitis, headache, dizziness, disorientation, irritability, venous thrombosis. Clinical course: Patient had a "bad headache for both vaccines" and it goes away in like a day or two. After both shots, he was like really dizzy and disoriented and he was like hearing voices kind of and just irritable. No prior vaccination was taken with in four weeks. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Venous thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (I am not sure I get high blood pressure once in a while)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2082359

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: OK
Alter: 35,0
Geschlecht: M
Eingang: 02.02.2022
Impfdatum: 24.01.2022
Beginn: 25.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Bell's palsy

Symptomtext

Bell's Palsey per Dr. appt 2-1-22 provided steroid shot and pills and should recover in next 2months to 1 year

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Had COVID 12-2021
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2079226

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: VT
Alter: 16,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 31.01.2022
Beginn: 31.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Syncope

Symptomtext

Patient became light headed and fainted shortly after receiving vaccination. Patient recovered shortly after at least 10 seconds.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 2062778

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: CA
Alter: 26,0
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Fatigue Interchange of vaccine products Joint swelling Malaise Rash SARS-CoV-2 test negative Thrombosis

Symptomtext

First dose received Moderna vaccination; second dose received Pfizer. Joint swelling, joint pain, rash, fatigue, Covid symptoms, blood clot formed in leg.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: COVID - NEGATIVE
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 2057032

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 17.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test Gait inability Immunisation Interchange of vaccine products Muscle strain Thrombosis

Symptomtext

Blood clot; Booster dose after Janssen vaccine; booster; muscle pulled like sensation on each outer side of torso, below clavicle, across chest, high on the chest, same sensation left side to right side; could not walk on her right calf; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. Other Case identifier(s): 20211239219. A 72 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administration date 17Nov2021 (Lot number: FH8028) at the age of 71 years as dose 2 (booster), single for covid-19 immunisation; janssen covid-19 vaccine (JANSSEN COVID-19 VACCINE), administration date 10Mar2021 (Lot number: 180522) as dose 1, single for immunisation. Relevant medical history included: "Cigarette Smoker" (not ongoing), notes: as a teenager, stopped cigarette smoking at 18-years-old.; "Non-Alcohol User" (ongoing). The patient's concomitant medications were not reported. Past drug history included: Cipro, reaction(s): "Allergic to Cipro"; Benadryl, reaction(s): "Allergic to Benadryl". The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 17Nov2021, outcome "unknown", described as "Booster dose after Janssen vaccine"; IMMUNISATION (medically significant) with onset 17Nov2021, outcome "unknown", described as "booster"; THROMBOSIS (medically significant) with onset 27Nov2021, outcome "unknown", described as "Blood clot"; MUSCLE STRAIN (medically significant) with onset Nov2021, outcome "unknown", described as "muscle pulled like sensation on each outer side of torso, below clavicle, across chest, high on the chest, same sensation left side to right side"; GAIT INABILITY (non-serious) with onset Nov2021, outcome "unknown", described as "could not walk on her right calf". The patient underwent the following laboratory tests and procedures: blood test: (27Nov2021) blood clot, notes: Classification: UNK. Therapeutic measures were taken as a result of thrombosis. Clinical course details: First week after the Pfizer vaccine, the patient was fine. In Nov2021 (second week), on an unspecified date, the patient experienced odd things like muscle pulled like sensation on each outer side of torso, below clavicle, across chest, high on the chest, same sensation left side to right side. She woke up and could not walk on her right calf. 10 days after taking the Pfizer shot, on 27Nov2021, the patient was diagnosed with a blood clot. Treatment medications (dates unspecified) included Xarelto (rivaroxaban) for blood clot prescribed by the doctor. Additional information: Other pre-existing medical conditions included no drug abuse or illicit drug usage. This report was serious (other medically important condition). This event (s) is considered unassessable. The event (s) has a compatible/ suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s). No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Date: 20211127; Test Name: Blood Test diagnosed with a blood clot; Result Unstructured Data: Test Result:Blood Clot; Comments: Classification: UNK
Aktuelle Erkrankungen: Abstains from alcohol
Vorgeschichte: Medical History/Concurrent Conditions: Cigarette smoker (as a teenager, stopped cigarette smoking at 18-years-old.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2048181

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: ME
Alter: 32,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test Chest X-ray Chest pain Dyspnoea Electrocardiogram Pain in extremity Pericarditis

Symptomtext

Suffured chest pain, arm pain, and shortness of breath. Less then 24 hours after booster dose. Went to emergency room. Had ekg, xray, and blood work. Then saw my primary doctor.. I was diagnosed with Pericarditis. It is still an on going condition which has not resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Ekg, blood work and chest x ray - 11/5/21 Office follow up - 11/9/21 2 month follow up - 1/9/21 Still currently being seen for treatment
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Codine Oxycodone
Vorherige Impfungen: -

VAERS 2028112

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: MI
Alter: 43,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 13.11.2021
Beginn: 02.01.2022
Tage bis Beginn: 50,0
Dosis: 2
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

COVID-19 Chest X-ray normal Cough Electrolyte substitution therapy Intensive care Nausea Pain SARS-CoV-2 test positive Vomiting

Symptomtext

01/02/2022: Event occurred after 2nd vaccine. a 44-year-old female started having mild symptoms Thursday tested today positive Covid. She states that has had little bit of a cough body aches mostly nausea and vomiting for a couple of days. the patient is on insulin pump for her diabetes sugar has been under good control. no significant shortness of breath. denies: Diarrhea, fever, urinary symptoms, blurred vision, sore throat, back pain, palpitations, dizziness, rash. 01/06/2022: admitted to covid icu and dka was hammered with iv fluids insulin drip, electrolyte repletion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 4,0
Labordaten: 01/02/2022: external COVID positive as per patient report. 1/04/2022:chest xray- no evidence of acute process.
Aktuelle Erkrankungen: unknown
Vorgeschichte: hypertension diabetes high cholesterol
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2025246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: -
Alter: 39,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 10.01.2022
Beginn: 10.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Loss of consciousness Nausea Pruritus Vomiting

Symptomtext

c/o loss of consciousness, itching, nausea & vomiting which did not improve. Pt given Epi im x1 then transported to ED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 2021292

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: CA
Alter: 36,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 07.01.2022
Beginn: 09.01.2022
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue Feeling of body temperature change Thrombosis

Symptomtext

Early Sunday morning I woke up with multiple blood clots in my mouth. they were along the roof of my mouth in between my teeth. When I pulled them out one area started bleeding again - but it wasn't like normal blood it was very thick almost like a gel or that it was coagulating instantly. Saturday I had just general fatigue and hot and cold flashes. By Sunday mid morning I felt fine and no additional bleeding has occurred.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: none at this time
Aktuelle Erkrankungen: None
Vorgeschichte: Adreal adenoma
Andere Medikamente: Depo Provera
Allergien: Prozac
Vorherige Impfungen: -

VAERS 2001719

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Blood glucose increased Chest X-ray Condition aggravated Diabetes mellitus Diabetic ketoacidosis Intensive care Laboratory test SARS-CoV-2 test Staphylococcus test Urine ketone body present

Symptomtext

Three hours after receiving the booster shot, I experienced BG's in the 480 range and after multiple boluses of 14 units of Novolog, the BG's just increased. I repeated the insulin bolus twice without any change. Fell asleep and when I awoke, it was no better. Went to Urgent care later that afternoon after drinking more water didn't help. I was in full DKA which Urgent Care confirmed. Was transferred from Urgent Care to Medical facility where I was admitted and stayed for 4 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 4,0
Labordaten: Urgent Care did BG, ketone urinalysis and labs to confirm DKA. ER performed additional testing and started DKA protocol. When admitted to ICU, further testing was done along with chest xray, covid and mersa testing.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, high blood pressure, high cholesterol and anemia.
Andere Medikamente: Novolog, Victoza, Lovaza, Losartan, Fiber, Calcium, Repatha, Daily Vitamin and aspirin.
Allergien: Lortab, statins, Metformin, Lisinopril and hazelnut.
Vorherige Impfungen: -

VAERS 1999185

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: OH
Alter: 60,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 29.11.2021
Beginn: 11.12.2021
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Bell's palsy Blood thyroid stimulating hormone Glycosylated haemoglobin increased Lyme disease

Symptomtext

Bell's Palsy, partial recovery

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: TSH, Lyme pending A1c: 10
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, HTN, HLD, OSA, carpal tunnel syndrome, vitamin D deficiency
Andere Medikamente: Metformin, Glipidizide, Amlodipine, Triamterene-HCTZ, Losartan, Atorvastatin, Vit D, Omega-3
Allergien: NKA
Vorherige Impfungen: -

VAERS 1999053

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

schwer

Staat: MI
Alter: 16,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 17.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Brain natriuretic peptide normal Electrocardiogram ST segment elevation Pericarditis Troponin I increased

Symptomtext

Pericarditis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Trop i >8000 BNP >100 EKG showing diffuse ST elevation 12/23/2021
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1996957

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: NY
Alter: 39,0
Geschlecht: F
Eingang: 01.01.2022
Impfdatum: 17.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cerebral thrombosis Cough Headache Sneezing

Symptomtext

a blood clot in my brain; I started noticing a stabbing pain in the top of my head anytime I cough like sneeze, bend over, jump, I get this real bad stabbing pain in the head that lasts anywhere from 30 to 60 seconds; I started noticing a stabbing pain in the top of my head anytime I cough like sneeze, bend over, jump, I get this real bad stabbing pain in the head that lasts anywhere from 30 to 60 seconds; I started noticing a stabbing pain in the top of my head anytime I cough like sneeze, bend over, jump, I get this real bad stabbing pain in the head that lasts anywhere from 30 to 60 seconds; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. Other Case identifier(s): PFIZER INC-202101871718. A 39 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 17Dec2021 (Lot number: FH8028) at the age of 39 years as dose number unknown, single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: WELLBUTRIN; ARIMIDEX; LEXAPRO; BLUDEC; PROLIA. The following information was reported: CEREBRAL THROMBOSIS (medically significant) with onset 18Dec2021, outcome "unknown", described as "a blood clot in my brain"; HEADACHE (non-serious), SNEEZING (non-serious), COUGH (non-serious) all with onset 18Dec2021, outcome "unknown" and all described as "I started noticing a stabbing pain in the top of my head anytime I cough like sneeze, bend over, jump, I get this real bad stabbing pain in the head that lasts anywhere from 30 to 60 seconds". Therapeutic measures were taken as a result of headache, sneezing, cough. Treatment taken with Ibuprofen 800 mg. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: WELLBUTRIN; ARIMIDEX; LEXAPRO; BLUDEC; PROLIA
Allergien: -
Vorherige Impfungen: -

VAERS 1985016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: NH
Alter: 71,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 03.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 26,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cardiac failure Catheterisation cardiac Echocardiogram Myocarditis

Symptomtext

Myocarditis Heart failure Cardiac cath- takotsubo Lopressor and lisinopril. Hospitalized x2 in one week 12/1/2021 to 12/8/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Cardiac cath Echo
Aktuelle Erkrankungen: None
Vorgeschichte: Hyperimmune response post TKA 9/2019 after insertion of replacement I?m allergic to
Andere Medikamente: None
Allergien: Nickel
Vorherige Impfungen: -

VAERS 1984709

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

schwer

Staat: PA
Alter: 56,0
Geschlecht: M
Eingang: 28.12.2021
Impfdatum: 23.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Cerebral infarction Computerised tomogram head Computerised tomogram normal Dysarthria Facial paralysis Laboratory test normal Limb discomfort Magnetic resonance imaging abnormal Scan with contrast Thrombosis Transient ischaemic attack

Symptomtext

sudden onset of left droopy face associated with slurred speech and left arm pressure 4 days after injection. All symptoms resolved within 20 min and was diagnosed with a transient ischemic attack due to acute thrombotic event.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: CT scan of brain 11/27/21 without acute findings MRI w and w/o contrast 12/3/21 noted an acute/early subacute infarct of right frontal lobe all other labs were either normal or not significant
Aktuelle Erkrankungen: none
Vorgeschichte: hyperlipidemia
Andere Medikamente: rosuvastatin 5 mg daily, famotidine 20 mg prn
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1980981

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: WI
Alter: 47,0
Geschlecht: M
Eingang: 25.12.2021
Impfdatum: 19.11.2021
Beginn: 02.12.2021
Tage bis Beginn: 13,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Cardiac stress test abnormal Chest discomfort Dizziness Echocardiogram abnormal Electrocardiogram Heart rate increased Myocarditis Tinnitus

Symptomtext

Tinnitus and slight dizziness lasting approximately 24 hours One week later hospitalized for chest discomfort and rapid heart rate. Echocardiogram and nuclear stress test showed marked myocarditis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 2,0
Labordaten: EKG 12/8/2021 ECG 12/8/2021 Nuclear Stress Test 12/9/2021
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Simvastatin Daily multi vitamin Vitamin D Asprin
Allergien: Compazine
Vorherige Impfungen: -

VAERS 1916347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: CT
Alter: 72,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 17.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test Muscle strain Thrombosis Ultrasound Doppler abnormal

Symptomtext

BLOOD CLOT; MUSCLE PULLED LIKE SENSATION ON EACH OUTER SIDE OF TORSO, BELOW CLAVICLE, ACROSS CHEST,HIGH ON THE CHEST, SAME SENSATION LEFT SIDE TO RIGHT SIDE; This spontaneous report received from a patient concerned a 72-year-old female of unspecified race and ethnicity. The patient's height, and weight were not reported. The patient's past medical history included cigarette smoker (as a teenager, stopped at 18 years old) and concurrent conditions included non-alcohol user, and other pre-existing medical conditions included patient did not have drug abuse or illicit drug usage. The patient was allergic to cipro and benadryl, The patient was not pregnant at the time of report. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1), (suspension for injection, route of admin not reported, batch number: 1805022, and expiry: unknown) dose was not reported, 1 total, administered on 10-MAR-2021 for prophylactic vaccination. Then, there was a blood clot, which was almost 8 months prior to this report (dose number in series 1). No concomitant medications were reported. Non-company suspect vaccine included: BNT 162 (form of admin and route of admin were not reported, batch number: FH8028 expiry: unknown) dose was not reported, administered on 17-NOV-2021 for prophylactic vaccination (Dose number in series 2). First week after Pfizer vaccine, the patient was fine. In NOV-2021 (in second week), on an unspecified date, the patient experienced odd things like muscle pulled like sensation on each outer side of torso, below clavicle, across chest, high on the chest, same sensation left side to right side. She woke up and could not walk on their right calf. 10 days after taking the Pfizer shot on 27-NOV-2021, the patient was diagnosed with a blood clot. Treatment medications (dates unspecified) included Xarelto (rivaroxaban) for blood clot prescribed by doctor (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the blood clot and muscle pulled like sensation on each outer side of torso, below clavicle, across chest, high on the chest, same sensation left side to right side was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20211239219-covid-19 vaccine ad26.cov2.s-blood clot . This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Date: 20211127; Test Name: Blood test; Result Unstructured Data: blood clot; Comments: diagnosed with a blood clot
Aktuelle Erkrankungen: Abstains from alcohol; Allergic reaction to antibiotics; Drug allergy
Vorgeschichte: Medical History/Concurrent Conditions: Cigarette smoker (Patient said as a teenager, stopped cigarette smoking at 18 years old.); Comments: Patient did not have drug abuse or illicit drug usage.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1970835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: WV
Alter: 63,0
Geschlecht: U
Eingang: 22.12.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Amnesia Immunisation Seizure

Symptomtext

seizure; 17Nov2021: Booster Vaccine; Memory loss; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63 year-old patient received bnt162b2 (BNT162B2), administered in arm, administration date 17Nov2021 15:00 (Lot number: FH8028) at the age of 63 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Epilepsy Seizures", start date: 04May2021 (unspecified if ongoing), notes: After 2nd shot had 1st seizure in morning.; "Another seizure", start date: 02Nov2021 (unspecified if ongoing), notes: lost consciousness each time. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose: 1, Time: Afternoon, Anatomical site of injection: Arm, Lot Number: EN6208, Exp Date: 30Jun2021), administration date: 11Mar2021, for Covid-19 immunization, reaction(s): "Seizure"; Bnt162b2 (Dose: 2, Time: Afternoon, Anatomical site of injection: Arm, Lot Number: ER8737, Exp Date: 31Jul2021), administration date: 01Apr2021, for Covid-19 immunization, reaction(s): "Seizure". The following information was reported: IMMUNISATION (non-serious) with onset 17Nov2021, outcome "unknown", described as "17Nov2021: Booster Vaccine"; SEIZURE (medically significant) with onset 30Nov2021 08:00, outcome "unknown", described as "seizure"; AMNESIA (non-serious) with onset 2021, outcome "unknown", described as "Memory loss". Therapeutic measures were taken as a result of seizure. Clinical Course: Patient had reported on 30Nov2021: Drove to work (against doctor orders) around 6:00 and clocked in and recalled of stocking cigarettes. Patient came out of cigarette room and looked at the co-worker and said, "was nauseous." The co-worker said patient eyes rolled to the back of patient head and began twitching, and she grabbed before the patient hit the floor. Patient have no recall of any of this. Manager said she brought out the chair and patient was sitting in and that it took both she and other co-worker to get seated in the chair she brought out. "She said" stiffened up and grabbed onto the chair arms so tight that she was afraid patient would break one of my hands. She said that she then began rubbing patient hands and talking to patient calmly trying to get him to let go of the chair. She finally was able to get patient to let go and she then called for an ambulance. Patient recall none of this. Patient asked her how long it lasted, and she said 10-12 minutes total. When Patient started coming out of it, patient felt dazed and confused. The patient's manager drove patient to his house so patient could spend the day with his wife so she could look after me. It was patient's understanding in speaking with her that patient had another seizure while at their house, and she called patient's son to come home. She said patient was picking at clothes, rolling up pant legs, not making a whole lot of sense, etc. The patient had no recall of any of this. It was reported that on 03Dec2021, the doctor ordered patient not to drive for at least 6 months until seizure free on medication, cook, bathe, etc. These seizures did not start until after receiving the Covid vaccine. Each time the patient received a vaccination, it was shortly after that patient had a seizure. The patient had never in life had a seizure disorder of any kind and have, for the most part, been a healthy person. The patient believed the two are related. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Epilepsy (After 2nd shot had 1st seizure in morning.); Seizure (lost consciousness each time.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1963416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: TX
Alter: 39,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 04.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal distension Abdominal pain upper Angiogram Cardiac flutter Chest pain Computerised tomogram normal Dyspnoea exertional Fibrin D dimer increased Fluid retention Gait disturbance Headache Insomnia Myocarditis Pain Pericarditis Productive cough Pulmonary congestion Pulmonary oedema

Symptomtext

I began to experience a terrible headache four days and upper abdominal bloating and pain after my vaccine, so bad that I couldn't walk without feeling like I was being punched in the gut. I had never experienced anything like this. Then I began to notice phlegm in my throat and congestion in my lung. I also began to feel random shooting pains in my left chest and heart fluttering. My doctor had me get an xray which found fluid in my lungs. I somehow gained 7lbs of fluid. I couldn't walk without losing breath and couldn't sleep on my side. He said it was likely pericarditis, pneuminitis, or myocarditis, or a strange virus. He sent me to do a CTA scan to check for a pulmonary embolism - luckily they didn't find one. My bloodwork showed a high d dimer rate. My partner says that my skin was yellow during this time. It all lasted two or so weeks and then cleared on its own.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Xray - fluid in lungs, bloodwork - d dimer elevation, cta scan - normal
Aktuelle Erkrankungen: -
Vorgeschichte: I have a herniated disc and have been receiving various treatments for it over the last few years (chiro, PT, epidural injections, PRP, and prolotherapy)
Andere Medikamente: Multivitamin
Allergien: -
Vorherige Impfungen: -

VAERS 1961570

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: NC
Alter: 48,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Computerised tomogram Electrocardiogram Headache Immunisation SARS-CoV-2 test Seizure

Symptomtext

seizure; headache; booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 48 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 20Nov2021 10:30 (Lot number: FH8028) at the age of 48 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Ulcerative colitis" (unspecified if ongoing), "hypertension" (unspecified if ongoing). Concomitant medication(s) included: METOPROLOL; AMBIEN; LIALDA. Past drug history included: Known allergies: Amoxicillin, Lisinopril, Contrast Dye, Zithromycin. Vaccination history included: Bnt162b2 (Previous dose number: 2, Previous dose lot number: EW0151,, ), administration date: 12Apr2021, when the patient was 48 years old, for Covid-19 immunization; Bnt162b2 (dose number: 1, ), administration date: 15Mar2021, when the patient was 48 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (medically significant) with onset 20Nov2021, outcome "unknown", described as "booster"; SEIZURE (medically significant) with onset Dec2021, outcome "unknown", described as "seizure"; HEADACHE (non-serious) with onset 27Nov2021 21:00, outcome "unknown", described as "headache". The events "seizure" and "headache" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: computerised tomogram: (2021) showed as clear, notes: The CT scan and EKG that were done at the ER didn't show presence of mass, clot, aneurysm or stroke. The CT scan showed as clear; electrocardiogram: (2021) normal, notes: The CT scan and EKG that were done at the ER didn't show presence of mass, clot, aneurysm or stroke; sars-cov-2 test: (01Dec2021) negative, notes: Nasal Swab. It was unknown if therapeutic measures were taken as a result of seizure, headache. The patient stated that she had not suffered from headache and seizure before receiving the vaccine. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: CT scan; Result Unstructured Data: Test Result:showed as clear; Comments: The CT scan and EKG that were done at the ER didn't show presence of mass, clot, aneurysm or stroke. The CT scan showed as clear.; Test Date: 2021; Test Name: EKG; Result Unstructured Data: Test Result:normal; Comments: The CT scan and EKG that were done at the ER didn't show presence of mass, clot, aneurysm or stroke.; Test Date: 20211201; Test Name: Covid test; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Contrast media allergy; Hypertension; Ulcerative colitis
Andere Medikamente: METOPROLOL; AMBIEN; LIALDA
Allergien: -
Vorherige Impfungen: -

VAERS 1956165

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8028

schwer

Staat: CA
Alter: 31,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 18.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Aphasia Decreased appetite Dysarthria Guillain-Barre syndrome Hypoaesthesia Malaise Muscular weakness Nausea

Symptomtext

shortly after getting the first dose of Covid vaccine, patient started feeling lethargic, and sore arm. The following day, patient was unable to attend work and feel out of the ordinary. one week following the vaccine patient went to the ER due to feeling ill. Patient was told he had some swollen lymph nodes under his arm. Patient was informed by his physician that it would be ok for patient to get his second dose. Therefore, on Nov. 6, patient came into the pharmacy to receive his second dose of the covid vaccine. Patient stated that within the next few days, patient fell ill and numbness and weakness throughout his knees and legs. Patient was nauseous, had loss of appetite as well as difficulty speaking. He was unable to speak and articulate his thoughts. He informed us that he went back to the ER, and they diagnosed him with Guillen-Barr-Syndrome. Patient was told he will have a follow up with his neurologist to determine if it is GBS or other medical conditions. Patient will call us back to update with his medical situation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: none at this time
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1955305

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

schwer

Staat: NY
Alter: 23,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 23.11.2020
Beginn: 23.11.2021
Tage bis Beginn: 365,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Additional Details: ems called out of caution patient fainted patient declined further treatment

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1948053

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: WA
Alter: 43,0
Geschlecht: M
Eingang: 14.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Anaphylactic reaction Chest pain Dyspnoea

Symptomtext

Chest pain and difficulty breathing, feeling very similar to Anaphylaxis. Treatment including 50mg of Diphenhydramine HCl, and 600mg of ibuprofen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: Grastek 2800bau subligual; Testosterone Cypionate 0.33ml; Prednisolone AC 1% 5ml; Bupropion XL 300mg; Vitamin D3 1000IU; Famotidine 20mg; Lutein 20mg; Calcium Citrate Magnesium and Zinc vitamins
Allergien: None
Vorherige Impfungen: Pfizer Covid-19 vaccines, course 1 (04/21/21, lot EW0170) and course 2 (05/12/21, lot EW0182). Age 42. Symptoms, chest pain and

VAERS 1947938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: FL
Alter: 33,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 01.11.2021
Beginn: 07.12.2021
Tage bis Beginn: 36,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Blood test Dyspnoea Heart rate increased Joint range of motion decreased Laboratory test Muscle tightness Pain Thrombosis Ultrasound Doppler

Symptomtext

The first time went to ER. I experienced shortness of breath and blood clots in left leg. This past weekend on December 11, 2021, I experienced tight pain on left side, inability to lift left arm and difficulty breathing. I have been recommended to the Cardiologist have never had any heart issues before. My watch tracks my heart rate lately it's higher. The normal resting heart rate is 70 now it is 100 since second vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 1,0
Labordaten: Blood work, Ultrasound of veins, Heart test
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1941901

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: CT
Alter: 16,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 26.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Thrombosis

Symptomtext

I had been menstruating when I received my second dose and the day after I received this second dose, I found that I had a period blood clot.; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 16 year-old female patient (not pregnant) received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection), administered in arm left, administration date 26Nov2021 15:00 (Lot number: FH8028) at the age of 16 years as dose 2, single for COVID-19 immunization. The patient's relevant medical history and concomitant medications were not reported. Past drug history included: Cefcil, reaction(s): "Known allergies: Cefcil". Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: fh8028, Location of injection: Arm Left, Vaccine Administration Time: 02:30 PM), administration date: 05Nov2021, when the patient was 16 years old, for COVID-19 immunization. No any other vaccines within 4 weeks prior to the COVID vaccine. The patient not diagnosed with COVID prior to vaccination and not tested for COVID since the vaccination. The following information was reported: THROMBOSIS (medically significant) with onset 27Nov2021, outcome "unknown", described as "I had been menstruating when I received my second dose and the day after I received this second dose, I found that I had a period blood clot.". Therapeutic measures were not taken as a result of thrombosis. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1939928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: MA
Alter: 14,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Condition aggravated Muscle twitching Posture abnormal Seizure

Symptomtext

20 minutes after her second dose vaccine patient experienced a seizure. Her eyes were fluttering and head slumped. She did not lose consciousness and was fine after. Patient has a history of seizure disorder, however has not experienced a seizure in over a year.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Epilepsy and seizure disorder
Andere Medikamente: unknown
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1932240

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: -
Alter: 25,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 13.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood creatine phosphokinase increased Blood test Chest pain Dizziness Dyspnoea Dyspnoea exertional Myocarditis Palpitations

Symptomtext

Palpitations occurring 8 hours after shot. Constant chest pain and light headedness for two weeks, sometimes shortness of breath. 1 event of walking in a store and getting short of breath, heart racing and light headedness near the point of passing out. Shortness of breath doing any activity. Presumed case of myocarditis after bloodwork completed. Echocardiogram schedule 12/17 to confirm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Creatine Kinase (12/2/21) 680 U/L. Standard range is 55/170 U/L
Aktuelle Erkrankungen: None
Vorgeschichte: Exercise induced asthma
Andere Medikamente: None
Allergien: Squid ink
Vorherige Impfungen: -

VAERS 1920593

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: NY
Alter: 27,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Exposure during pregnancy Hypotension Oxygen saturation decreased Postictal state Presyncope Seizure Vomiting

Symptomtext

Pfizer COVID-19 Vaccine EUA 12/2/2021 5 PM B/P 144/90, Pulse 92, Respirations 18 Regular, pulse oximetry 98% 5:10 PM B/P 140/88, Pulse 120, Respirations16 Regular, pulse oximetry 98% 5:15 PM B/P 128/80, Pulse 138, Respirations 12 Regular, pulse oximetry 86%-98% 12/2/21 5 PM Per EMT in Vaccine Monitoring area, patient alert and oriented times four, complained of near syncope, history of near syncope with blood draws, 27 weeks pregnant, no known complications with first pregnancy, reports bouts of hypotension during office visits, eating, drinking and answering questions normally, patient reports near syncopal episode with past three vaccinations, no complications with first and second doses of Pfizer COVID-19 vaccine, 5:12 PM began to seize, EMS summoned via 911, airway patent, vital signs monitored, pulse rate tachycardia, O2 saturations dropped into mid 80's, patient began to vomit, patient placed in right recumbent position, O2 administered via nasal cannula at 6 liters per minute, cleared vomitus from mouth area to prevent aspiration, O2 saturation rose to upper 90's, discontinued O2 after a few minutes when patient regained consciousness, O2 saturation remained in upper 90's on room air, patient postictal, EMS arrived, report given with patient pedigree, vitals and emergency contacts, patient transferred to EMS for transport to Medical Center.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: History of seizures in childhood
Andere Medikamente: Zoloft and Zophran
Allergien: Sulfa, shellfish, Icy hot, Secor
Vorherige Impfungen: -

VAERS 1917549

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: GA
Alter: 20,0
Geschlecht: M
Eingang: 02.12.2021
Impfdatum: 19.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Agitation Back pain Blood pressure fluctuation Blood test normal Chest X-ray normal Chest discomfort Chest pain Decreased appetite Dizziness Electrocardiogram normal Feeling hot Headache Heart rate decreased Hyperhidrosis Hypertension Loss of consciousness Myalgia Pain in extremity

Symptomtext

HEART RACING, FLUCTUATING BLOOD PRESSURE SINCE THE PFIZER VACCINE, SWEATS, LOW BLOOD PRESSURE, LOW HEART RATE, 96% OXYGEN LEVELS, THEN RACING HEART AND THEN EXTREMELY ELEVATED BLOOD PRESSURE, DIZZINESS, CHEST TIGHTENING IN THE HEART AREA, CHEST PAINS IN GENERAL BOTH RIGHT AND LEFT, MUSCLE ACHES ALL OVER WITH PRIMARY ACHES IN LIMBS, CHEST AND BACK, HEADACHES, AGITATION, LOW-GRADE FEVER, SWEATS AND FEELING HOT AND UNABLE TO COOL CORE TEMP TO STABLE WITHOUT FEELING OVER HEATED, ALL OF THESE SYMPTOMS STARTED BY THE 3RD DAY BEFORE THE 72 HOUR MARK AT 1:00 AM 11/22/2021 AFTER PFIZER VACCINE DATE 11/19/2021 AT 12:30PM. THIS HAS CONTINUED TO WORSEN OVER THE LAST 72 HOURS. LOSING CONSCIOUSNESS AND AWARENESS WHILE FAINTING TODAY AROUND 9AM THIS MORNING 12/2/2021 - AFTER WAKING 30 MINS TO 1 HOUR PRIOR TO THE FAINTING OCCURRENCE. DECREASED APPETITE COUPLED WITH INCREASE THIRST IN THE LAST 48 TO 72 HOURS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: TODAY 12/2/2021 IN URGENT CARE DEPARTMENT COMPLETED EKG, CHEST XRAYS, BLOOD LABS AND URINE LABS, MULTIPLE BLOOD PRESSURE CHECKS WERE IN ALARMING RANGES.
Aktuelle Erkrankungen: -
Vorgeschichte: DIAGNOSED WITH GILBERT SYNDROME IN 2017; ROUTINE VISITS WHEN NECESSARY FOR LIVER ENZYMES.
Andere Medikamente: -
Allergien: ACETAMINOPHEN, ADHESIVE GLUE, PERSONALITY CHANGE XANAX
Vorherige Impfungen: -

VAERS 1917033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: CA
Alter: 12,0
Geschlecht: M
Eingang: 02.12.2021
Impfdatum: 24.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Seizure Syncope

Symptomtext

Patient had no initial side effects until Day 6 after getting the vaccine. He had a seizure for the first time at around 7:10am when he was getting ready for school. He had just begun to brush his teeth when he collapsed and had a seizure. He has no medical reason to have seizures and had never had one until 6 days after getting the vaccine. Patient had to be taken the the ER to be monitored because it was his 1st seizure and then had to follow up the next day with his regular pediatrician. He will have to see Neurology, but won't see that department until January 2022. No medications were given for him to take and his was cleared to resume all normal activities again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: At this time no medical tests have been done but we are waiting for Patient to be seen by Neurology to see if they can determine why he had a seizure.
Aktuelle Erkrankungen: None
Vorgeschichte: Autism Spectrum Disorder
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1916770

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

schwer

Staat: WV
Alter: 52,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 14.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Seizure

Symptomtext

seizures

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: copd, epileptic, osteoporosis
Andere Medikamente: -
Allergien: ibprohen ,penicillin
Vorherige Impfungen: seizures with first covid vaccine-fluttering in hert-pfizer

VAERS 1912675

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: SC
Alter: 59,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 03.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: nein

Computerised tomogram Diplopia Guillain-Barre syndrome Hypoaesthesia Magnetic resonance imaging Malaise Ophthalmological examination Paraesthesia Sensory disturbance Transient ischaemic attack Visual impairment

Symptomtext

On first shot about 6to days later I had double vision on right eye for about an hour and then very bright vision followed by not feeling well for another hour.Then it all went away.Second shot about 6 days later I feel a spongy feeling in my face followed by tingling and numbness in face. Went to emergency room as they thought I had a TIA after the first shot but suggested I get the second shot anyway. I have had ct scan, mri and eye?s checked since second episode. It?s been more than a month and still have numbness on left side of face. Eye doctor suggested it might not have been a TIA but rather Gillian Barre syndrome. At my work was mandated to take the vaccine and still suffering from the second shot more than a month later. I will not take the third booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 1,0
Labordaten: I had a CT Scan at hospital, MRI as suggested by hospital Dr and then and eye exam. I cannot get to see a Neologist until later February
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lisnopril 10 Milligrams
Allergien: Avocados, bakers yeast, clams, pumkin
Vorherige Impfungen: -

VAERS 1908566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: CA
Alter: 23,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 23.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: unbekannt Erholt: ja

Seizure

Symptomtext

Seizure a day after getting the Pfizer booster. Got booster Tuesday 11/23 around 12:00 PM and seizure occured Wednesday at around 1:30 PM

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: mold
Vorherige Impfungen: -

VAERS 1904125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: MI
Alter: 16,0
Geschlecht: F
Eingang: 27.11.2021
Impfdatum: 27.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Fall Head injury Inappropriate schedule of product administration Syncope

Symptomtext

Pt received her first dose of Pfizer vaccine. She sat in chairs for approximately 10 minutes before becoming dizzy and experiencing syncopy. Her head was bumped as she fell. She recovered within a moment and was reseated. She was given orange juice and a granola bar. She stated that she frequently experiences dizziness upon standing or rising from bed. She stated she had not had anything to eat or drink prior to the vaccine. Her parents sat with her for another 1/2 hour and exited the store.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: N/a.
Aktuelle Erkrankungen: Fluvarix quadrivalent vaccine 11/19/2021
Vorgeschichte: Pt stated that she is frequently dizzy or hypotensive upon rising or standing. She stated that this is more likely if she has not eaten or is dehydrated.
Andere Medikamente: N/a
Allergien: None
Vorherige Impfungen: -

VAERS 1864803

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: MI
Alter: 33,0
Geschlecht: F
Eingang: 27.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Immunisation Syncope

Symptomtext

fainting; Dizziness; booster; This is a spontaneous report from a contactable consumer (patient). This 33-years-old female patient (non-pregnant) received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 3 via an unspecified route of administration, administered in Arm Left on 08Nov2021 16:00 (Lot Number: FH8028) as DOSE 3 (BOOSTER), SINGLE for COVID-19 immunization. Medical history included irritable bowel syndrome (IBS), gastrooesophageal reflux disease (GERD), Lichen sclerosus, Known allergies: Food dye. Concomitant medications included macrogol 3350 (GLYCOLAX); dicyclomine; omeprazole; famotidine (PEPCID); plantago ovata (METAMUCIL). Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) dose 1 on 01Apr2021 (lot number: ER8730) in Left arm at age of 33-years-old for COVID-19 Immunization, dose 2 on 22Apr2021 (lot number: EW0162) in Left arm at age of 33-years-old for COVID-19 Immunization. No other vaccine in four weeks. The patient experienced dizziness and fainting the morning after on 09Nov2021 06:00. No treatment received. The outcome of the events dizziness and fainting was recovered on an unspecified date, of event booster was unknown. No covid prior vaccination. No covid tested post vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: GERD; Irritable bowel syndrome; Lichen sclerosus; Reaction to food coloring
Andere Medikamente: GLYCOLAX; DICYCLOMINE; OMEPRAZOLE; PEPCID [FAMOTIDINE]; METAMUCIL [PLANTAGO OVATA]
Allergien: -
Vorherige Impfungen: -

VAERS 1864803

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: MI
Alter: 33,0
Geschlecht: F
Eingang: 27.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Immunisation Syncope

Symptomtext

fainting; Dizziness; booster; This is a spontaneous report from a contactable consumer (patient). This 33-years-old female patient (non-pregnant) received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 3 via an unspecified route of administration, administered in Arm Left on 08Nov2021 16:00 (Lot Number: FH8028) as DOSE 3 (BOOSTER), SINGLE for COVID-19 immunization. Medical history included irritable bowel syndrome (IBS), gastrooesophageal reflux disease (GERD), Lichen sclerosus, Known allergies: Food dye. Concomitant medications included macrogol 3350 (GLYCOLAX); dicyclomine; omeprazole; famotidine (PEPCID); plantago ovata (METAMUCIL). Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) dose 1 on 01Apr2021 (lot number: ER8730) in Left arm at age of 33-years-old for COVID-19 Immunization, dose 2 on 22Apr2021 (lot number: EW0162) in Left arm at age of 33-years-old for COVID-19 Immunization. No other vaccine in four weeks. The patient experienced dizziness and fainting the morning after on 09Nov2021 06:00. No treatment received. The outcome of the events dizziness and fainting was recovered on an unspecified date, of event booster was unknown. No covid prior vaccination. No covid tested post vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: GERD; Irritable bowel syndrome; Lichen sclerosus; Reaction to food coloring
Andere Medikamente: GLYCOLAX; DICYCLOMINE; OMEPRAZOLE; PEPCID [FAMOTIDINE]; METAMUCIL [PLANTAGO OVATA]
Allergien: -
Vorherige Impfungen: -

VAERS 1897815

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: IL
Alter: 87,0
Geschlecht: M
Eingang: 24.11.2021
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood glucose normal Dizziness Loss of consciousness

Symptomtext

After patient received his Pfizer booster, he was sitting in observation for 15 minutes. As the team was getting ready to discharge him after the 15 minutes, the team noticed the patient was leaning to the side and asked him how he was feeling. Pt stated he was lightheaded and then lost consciousness. Team immediately called 911 and checked his vitals. Pt's pulse was palpable, blood pressure - 160/100, glucose was 77. Pt then gained consciousness as EMS arrived (approximately 2 minutes later). Pt was transported to hospital via EMS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Glucose on scene was 77
Aktuelle Erkrankungen: No known
Vorgeschichte: Seizures, Dementia, Hypertension
Andere Medikamente: Unknown
Allergien: No known drug or food allergies
Vorherige Impfungen: -

VAERS 1894635

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: CA
Alter: 74,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Blood glucose normal Loss of consciousness

Symptomtext

is a 74 year old female who has completed a 45-minute observation period with the following signs and symptoms of an adverse reaction: loss of consiousness. Pfizer-BioNTech COVID-19 vaccine #3 in series administered. o Action(s) taken: Recommended transfer to higher level of care, risk and benefits explained to patient, patient declined With daughter , Family declined Per family, patient always has episodes of fainting whenever she "enters" the hospital premises Blood sugar checked 94 o Allergy to COVID-19 vaccine documented in Allergies activity: No, Vitals: 11/23/21 1050 11/23/21 1051 11/23/21 1102 11/23/21 1110 BP: (!) 201/95 (!) 203/110 (!) 191/87 (!) 175/86 BP Patient Position: SITTING SITTING BP Location: RA-RIGHT ARM RA-RIGHT ARM LA-LEFT ARM Pulse: 91 95 66 76 Resp: 18 18 18 15 SpO2: 99% 100% 100% 100% family and patient refused to go to ER or urgent care. signed

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: family and patient refused
Aktuelle Erkrankungen: ESSENTIAL HTN Other HX OF CA BREAST CANCER METASTATIC TO LN CANCER METASTATIC TO RIGHT LUNG CANCER METASTATIC TO BONE MALIGNANT PLEURAL EFFUSION ATHEROSCLEROSIS OF AORTA OSTEOPOROSIS DEMENTIA CHRONIC FATIGUE SYNDROME MAJOR DEPRESSIVE DISORDER, RECURRENT EPISODE, IN FULL REMISSION FEMALE URINARY STRESS INCONTINENCE URGE INCONTINENCE CYSTOCELE. PLEURAL EFFUSION MULTIPLE PULMONARY NODULES AXILLARY LYMPHADENOPATHY INSOMNIA FEMALE BREAST CANCER, UNSPECIFIED SITE OF LEFT BREAST NEAR SYNCOPE MILD COGNITIVE IMPAIRMENT PRESENCE OF PESSARY SYNCOPE
Vorgeschichte: ESSENTIAL HTN Other HX OF CA BREAST CANCER METASTATIC TO LN CANCER METASTATIC TO RIGHT LUNG CANCER METASTATIC TO BONE MALIGNANT PLEURAL EFFUSION ATHEROSCLEROSIS OF AORTA OSTEOPOROSIS DEMENTIA CHRONIC FATIGUE SYNDROME MAJOR DEPRESSIVE DISORDER, RECURRENT EPISODE, IN FULL REMISSION FEMALE URINARY STRESS INCONTINENCE URGE INCONTINENCE CYSTOCELE. PLEURAL EFFUSION MULTIPLE PULMONARY NODULES AXILLARY LYMPHADENOPATHY INSOMNIA FEMALE BREAST CANCER, UNSPECIFIED SITE OF LEFT BREAST NEAR SYNCOPE MILD COGNITIVE IMPAIRMENT PRESENCE OF PESSARY SYNCOPE
Andere Medikamente: Xeloda, Ativan, Namenda, Remeron, Apresoline, Aricept
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1891653

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: CA
Alter: 19,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Loss of consciousness

Symptomtext

Patient pass out for 5 minutes after getting the COVID vaccination at around noon time. Pharmacy called paramedic immediately. Patient regained consciouness before paramedic arived. Patient was oriented to time and place when asked by pharmacist and was offer drink and snack. Patient has dizzy spell and pass mout occasionally per her parent. Paramedic arrived 15-20 minutes after called and after patient regain consciousness BP and pulse was taken. Paramedic waits for patient to become stabilized then left. Patient walked with her parents to their car and left.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: BP and Pulse taken by paramedic (11/22/21)
Aktuelle Erkrankungen: Patient has occasional dizzy spells per families
Vorgeschichte: unknown
Andere Medikamente: None
Allergien: unknown
Vorherige Impfungen: -

VAERS 1890329

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: ND
Alter: 37,0
Geschlecht: M
Eingang: 22.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Fall Feeling abnormal Laboratory test Loss of consciousness

Symptomtext

Patient was "not feeling right" when walking back to chair in waiting room, patient lost consciousness and fell backwards. Patient then was transported by family to the emergency room.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: labs and ER visit
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1884649

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

schwer

Staat: MD
Alter: 57,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Anaphylactic reaction Dysphagia Hypertension Injection site swelling Lymphadenopathy Pruritus Rash Throat tightness

Symptomtext

Site: Swelling at Injection Site-Medium, Systemic: Allergic: Anaphylaxis-Severe, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Severe, Systemic: Allergic: Itch (specify: facial area, extremeties)-Severe, Systemic: Allergic: Itch Generalized-Severe, Systemic: Allergic: Rash (specify: facial area, extremeties)-Severe, Systemic: Hypertension-Severe, Systemic: Lymph Node Swelling-Severe

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1882637

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: TN
Alter: 14,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Crying Loss of consciousness Seizure

Symptomtext

Within a couple of minutes of receiving the vaccine, the patient began suffering an apparent seizure and lost consciousness. We called 911 and attended to the patient while waiting for emergency personnel to arrive. The patient regained consciousness shortly after having apparent seizure and began to cry. She was breathing and had a pulse the entire time. She was transported to a local medical facility shortly after calling. We did not administer any Epi or other medications to treat the reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: unknown at this time
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: Wheat, Corn, Peanuts
Vorherige Impfungen: -

VAERS 1880717

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: MD
Alter: 67,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 06.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Bell's palsy

Symptomtext

I developed Bells Palsy 10 days after Pfizer booster on November 16. I received the booster on November 6th. Doctor has me on an anti-viral and steroids. I started the anti-viral on Nov. 17 and the steroids on Nov. 18, 2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Autoimmune Hepatitis Type 1, Primary Biliary Cirrhosis
Andere Medikamente: Ursodiol, Azathioprine, Alendronate, Fish Oil, Calcium, PreserVision (Areds2)
Allergien: None
Vorherige Impfungen: -

VAERS 1878239

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

schwer

Staat: OR
Alter: 36,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Eye injury Head injury Nasal injury Skin laceration Syncope

Symptomtext

pt was vaccinated with both vaccines in left arm. flu on top and covid below. pt went to sit in the lobby for the 15 minutes. he reports his daughter calling him so to be polite he got up from the lobby to take his phone call. he fainted in one of our aisles, hit his head on the shelving. ended up with 3 lacerations on his head (forehead, nose bridge, under right eye). I ran over to to assist. grabbed a chair to have him sit in. tech called for store supervisor. pt started to phase out and faint, used ammonia salts. called emergency. EMT's arrived to assess. EMT released him at the scene. family came to pick him up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: -
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 1877009

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: GA
Alter: 31,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cold sweat Dizziness Hyperhidrosis Mydriasis Posture abnormal Presyncope Urinary incontinence

Symptomtext

Patient had a vasovagal response to injection. Patient stated they felt like they were going to pass out about 1 minute after shot was administered. Technician informed Pharmacist then fanned patient off and had someone bring her some water, then the patient's eyes dilated and skin became clammy and sweaty. Patient urinated herself and her head fell into her chest and she groaned. Technician called emergency number and then went to get NP on site. Another technician came in and elevated patient's feet and applied a cold rag to the back of her neck. Patient came to within a couple of seconds and NP evaluated her and then got her some juice. NP stated she was stable and didn't need emergency care but instructed the technician to call a family member to pick patient up. EMT arrived and took her vitals and established she was stable and did not need to be taken to the ER. Patient's father came to pick her up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Asthma
Vorgeschichte: Asthma
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1874656

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: CA
Alter: 23,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Feeling hot Hyperhidrosis Loss of consciousness Nausea

Symptomtext

At 12:24PM, patient received his first dose of Pfizer vaccine, alert and oriented X4, denies any allergies, pain or shortness of breath. No known medical condition but has history of fainting or passing out. At 12:27PM, 3 minutes after receiving the vaccine, per patient?s verbalization, he felt nauseous, warm and lightheaded while seated at the observation area then lost his consciousness. Patient was assisted to the floor and regained his consciousness immediately. Assessment done. Patient is alert and oriented X4. Denies any pain, able to move all extremities without difficulty. Vital signs were taken: BP: 140/82, HR:70bpm, RR:19cpm, O2 Saturation at 97% room air. He denies any pain, shortness of breath or itching. Noted sweating but denies dizziness. Patient claimed he had not taken his breakfast before coming for his vaccination. At 12:28PM EMS was called. 12:35PM, vital signs were taken, BP: 132/73, HR: 64bpm; RR:18cpm; O2 Saturation: 98% at room air. Resident is alert and oriented. At 12:39PM, EMS arrived, vital signs: 132/74, HR: 68bpm; RR:20cpm, O2 Saturation: 97% at room air. Assessment done, patient was asked if he wants to be brought to the hospital. Patient verbalized, he feels better and will just go home. Patient reported no dizziness or difficulty breathing. 12:50PM, patient went home ambulatory without complaints, accompanied by brother-in-law.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Patient reported a history of fainting. Patient reported prior episodes of fainting were not due to injections.
Andere Medikamente: Unknown
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1873723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: PA
Alter: 51,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Aphasia Chest discomfort Dysphagia Hypoaesthesia oral Loss of consciousness Paraesthesia

Symptomtext

Patient received the Pfizer COVID vaccine at 11:15am. Lips started feeling numb a few seconds later. Hands started tingling. Felt like a mask was over her face. Going down into her neck and into her chest. Unable to swallow. Lost consciousness. Niece administered 1 auto inject Epi into right thigh. Patient awakened unable to verbalize, but did follow commands. Niece administered 2nd auto inject Epi into right thigh when she lost consciousness again. Was lowered off the chair onto the ground with 3 assisting onto her left side. 911 was called. 11:21am vitals 153 heart rate, 140/64 98% on room air. Patient reports mask on face is worse. Chest feels she was kicked by a horse. HR 96. Ambulance arrived and report given to EMT. Patient transported to ED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: EpiPen 2-Pak 0.3 MG/0.3ML Injection Solution Auto-injector For a severe reaction: Inject in outer thigh following instructions on package and go to the Emergency room. metFORMIN HCl ER 500 MG Oral Tablet Extended Release 24 Hour (Glucophage
Allergien: Flu Virus Vaccine, Tetanus-diphth-acell Pertussis, Adalimumab, Clarithromycin
Vorherige Impfungen: -

VAERS 1870651

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: UT
Alter: 25,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 14.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dyspnoea Loss of consciousness Palpitations

Symptomtext

Symptomatic palpitation, shortness of breath, passing out at 5:05 am in the morning. Heart continues to race and then slowdown all today, current time is 6:05 pm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Trentinoine topical cream
Allergien: None
Vorherige Impfungen: -

VAERS 1869674

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge fh8028

schwer

Staat: SC
Alter: 45,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Amnesia Arthralgia Dysgeusia Irritability Pyrexia Thrombosis

Symptomtext

Metallic taste, 103 fever for 4 days straight and pop up fevers 2 weeks later, memory loss, Severe irratibility, severe joint pain prolonged still and it has been 2 weeks, blood clot in my arm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1869025

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 11.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Dizziness Headache Nausea Pyrexia Syncope

Symptomtext

High fever, chills, dizziness, nausea, headache, one syncopal incident.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma
Andere Medikamente: Tylenol
Allergien: No
Vorherige Impfungen: Fever

VAERS 1868399

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: MA
Alter: 30,0
Geschlecht: M
Eingang: 14.11.2021
Impfdatum: 14.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Seizure Syncope

Symptomtext

syncope, leading to fainting and mild seizure. Patient woke up without need for epinephrine and was alert and oriented. Paramedics called to check out patient. Patient declined ambulance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1866209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: CA
Alter: 31,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Immediate post-injection reaction Syncope

Symptomtext

Patient fainted after immediately getting both vaccines. Had patient sit in chair for 1 hour and monitored. Gave patient food and water.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: -
Allergien: none
Vorherige Impfungen: -

VAERS 1865602

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: AZ
Alter: 16,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Cold sweat Dizziness Feeling hot Headache Hyperhidrosis Loss of consciousness Musculoskeletal stiffness Pallor

Symptomtext

Appproximately 3-5 minutes after receiving vaccine, the patient "stiffened up", she lost consciousness for a couple of seconds while she was sitting on bench during the 15 minutes observation period. The medical assistant helped patient place her head between her legs, she immediately regained consciousness-patient did not realize what had just occured. Patient assisted to laying position, vital signs taken and PNP assessed patient. Pallor, clammy skin, diaphoretic. Patient stated that she suddenly felt a warm sensation and does not recall what happened. Patient reports she did not have breakfast or lunch and had minimal fluid intake. Juice and crackers provided. She continued to feel lightheaded-patient assisted to exam table and propped legs with pillows. Patient monitored for 55 minutes. Patient reported she felt fine and no longer lightheaded. Patient accompanied by guardian contacted Dr on 11/12/2021 by this writer. Patient had a headache the night after obtaining her vaccine-guardian adminsitered Tylenol 500 mg at 9 pm and then again on 11/10/2021 @ 6 a.m. According to guardian all symptoms have resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None found on patient's chart.
Vorgeschichte: Seasonal allergies
Andere Medikamente: None according to patient's chart.
Allergien: None according to patient's chart.
Vorherige Impfungen: -

VAERS 1850708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: MD
Alter: 58,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 02.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dysarthria Erythema Eye irritation Eye swelling Facial paralysis Headache Oral discomfort Pain in extremity Photophobia Rash Swelling face

Symptomtext

Day 1-3 Typical arm soreness, mouth burning, then both eyes burning. On 4th post vaccine woke up with severe face swelling with redness, Both eyes swollen shut. Face extremely hot to touch; could not bare light. Continued to words slurring. November 5-7 right side of mouth slightly drooping. Since vaccine, Right Eye can barely open. Burning both eyes. Dry rash around eyes and face. Cannot tolerate any light source. Headaches started with 1 day of Vaccine. *** I started getting intermittent headaches since having COVID19 in March 2020; false negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: Will not be able to see Ophthalmologist until tomorrow, November 9, 2021. My Internist, has been notified
Aktuelle Erkrankungen: None
Vorgeschichte: CFS/ME, Rosacea, Fibromyalgia, Chronic Spine Pain; Muscle/Nerve; post surgical in 08 for C-Spine Injury
Andere Medikamente: Cymbalta, LAMictal, Fentanyl Patch, Klonopin, Estradiol, Rx:Nexxium, Melatonin, VD-3, Multi-Vitamin, Biotin, OTC eye drops, OTC nose spray
Allergien: Lactose, Sulfur Antibiotics, Codeine, Demerol, Compazeine, Aspirin Products of any kind, Prednisone PO, Environmental Allergies cannot be tested due to medications
Vorherige Impfungen: -

VAERS 1847017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

schwer

Staat: ME
Alter: 36,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Loss of consciousness Seizure like phenomena

Symptomtext

Patient got the dose and left the pharmacy with his girlfriend. Few minutes later, girlfriend came back and stated that the patient just blacked out in the car and had a seizure-like episode. I asked him to have a seat and called for emergency medical services. They took his vitals and he seemed to be okay.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2685393

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: NJ
Alter: 60,0
Geschlecht: F
Eingang: 22.09.2023
Impfdatum: 09.11.2021
Beginn: 01.02.2023
Tage bis Beginn: 449,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Magnetic resonance imaging Pneumonia aspiration Renal cancer stage I Vomiting

Symptomtext

stage one kidney cancer; had aspiration pneumonia; she went in the hospital for throwing up; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61-year-old female patient received bnt162b2 (BNT162B2), on 09Nov2021 as dose 3 (booster), single (Lot number: FH8028) at the age of 60 years for covid-19 immunisation. The patient's relevant medical history included: "Cancer" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: bnt162b2 (Pfizer covid vaccine first dose: 28Feb2021, Lot: EN6203, Expiration: unknown, NDC: unknown), administration date: 28Feb2021, when the patient was 59-year-old, for COVID-19 immunization; bnt162b2 (Pfizer covid vaccine second dose: 21Mar2021, Lot: EN6208, Expiration: possibly Jun 2021, NDC: unknown), administration date: 21Mar2021, when the patient was 59-year-old, for COVID-19 immunization. The following information was reported: PNEUMONIA ASPIRATION (hospitalization, medically significant) with onset 01Feb2023, outcome "unknown", described as "had aspiration pneumonia"; VOMITING (hospitalization) with onset 01Feb2023, outcome "unknown", described as "she went in the hospital for throwing up"; RENAL CANCER STAGE I (hospitalization, medically significant) with onset 01Feb2023, outcome "unknown", described as "stage one kidney cancer". The patient was hospitalized for renal cancer stage i, pneumonia aspiration, vomiting (start date: 2023). The event "stage one kidney cancer" required physician office visit. It was reported that the patient had kidney cancer, removed 10% of her left kidney. She went in the hospital for throwing up and had aspiration pneumonia and they found a spot on her kidney. She went to a urologist and urologist told her she needed an MRI. Spot was more than 4cm and it needed to come out and was found to be stage one kidney cancer. The patient underwent the following laboratory tests and procedures: Magnetic resonance imaging (2023): Spot was more than 4cm, notes: it needed to come out and was found to be stage one kidney cancer. Therapeutic measures were taken as a result of renal cancer stage i, pneumonia aspiration, vomiting.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300306764 Same patient, same product, different event, different dose;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia aspiration
Hospital-Tage: -
Labordaten: Test Date: 2023; Test Name: MRI; Result Unstructured Data: Test Result:Spot was more than 4cm; Comments: it needed to come out and was found to be stage one kidney cancer
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cancer
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2632973

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 63,0
Geschlecht: F
Eingang: 17.05.2023
Impfdatum: 11.11.2021
Beginn: 10.04.2023
Tage bis Beginn: 515,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Chest pain Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

04/10/23 presents to EC ED for "chest pain, nausea, vomiting". PMHx of "GERD, hypothyroidism, and migraines"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 04/10/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2500264

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 89,0
Geschlecht: M
Eingang: 24.03.2023
Impfdatum: 17.11.2021
Beginn: 08.03.2023
Tage bis Beginn: 476,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Adenovirus test Adrenal adenoma Angiogram pulmonary abnormal Aortic arteriosclerosis Blood potassium decreased Back pain Blood culture COVID-19 Central venous catheterisation Bordetella test negative C-reactive protein increased Chlamydia test negative Computerised tomogram thorax abnormal Chills Computerised tomogram spine abnormal Condition aggravated Cough Culture negative

Symptomtext

Admission Date: 3/8/2023 Discharge Date: Mar 17, 2023 PRESENTING PROBLEM: T12-L1 disc space infection HOSPITAL COURSE: Patient is a 91 year old male with Hx of HTN, Afib, chronic diastolic HF, CAD, DM type II, CKD Stage III, BPH, rectal Ca, and GERD who presented to the ED with chills, shortness of breath, and cough as well as worsening back pain. He tested positive for COVID-19 and was admitted to the hospitalist service. CTA with groundglass opacities. He was requiring 3L NC O2 on admission and weaned to room air after completing 5 days of remdesivir and 6 days of dexamethasone. Pt did have steroid induced hyperglycemia, treated with insulin which improved significantly after steroids were completed. Regarding the patient's back pain, CT T/L spine concerning for T12-L1 discitis/osteomyelitis. MRI of the thoracic/lumbar spine showed discitis/osteomyelitis at T12-L1 as well as small abscess within anterior right psoas. Echo was completed showing normal EF and no valvular vegetation but pulmonic valve difficult to visualize. Spine surgery was consulted but did not recommend surgical intervention. IR was consulted and performed biopsy of T12-L1 intervertebral disc but cultures remained negative. Initial blood cultures 1/2 positive for micrococcus luteus, suspect contaminant, per ID. He was treated with ceftriaxone/vancomycin IV with all subsequent blood cultures negative. Due to improvement in back pain and negative blood cultures, ID recommended ceftriaxone/vancomycin to complete 6 weeks (3/12-4/23) with ID follow up in 4-6 weeks. His pain was controlled with tramadol, zanaflex, lidocaine patch, and gabapentin. PT/OT recommend SAR. Pt and facility were in agreement with SAR as pt desired to recover and eventually return home. They did have hospice informational meeting on 3/16 but did not yet feel that pt's goals were in alignment with hospice. PICC placed by vascular access team prior to discharge. He discharged to SAR in stable condition on 3/17/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Recurrent rectal cancer s/p radiation s/p TAMIS 8/10/21 with Benign prostatic hyperplasia with urinary frequency Hx of adenomatous colonic polyps Chronic kidney disease (CKD), stage III (moderate) (HCC) High cholesterol Gastroesophageal reflux disease Anemia due to chronic blood loss Hypertension Atherosclerosis of coronary artery History of coronary artery bypass surgery Urge incontinence of urine Peripheral vascular disease (HCC) Rectal neoplasm Atrial fibrillation Iron deficiency anemia due to chronic blood loss BPH with obstruction/lower urinary tract symptoms Posterior rectal mass, probable recurrent rectal cancer Mitral valve insufficiency Osteoarthrosis Acute on chronic anemia Diabetic neuropathy Diabetes mellitus Diastolic heart failure Rheumatic fever Ventral incisional hernia without obstruction or gangrene T12-L1 disc space infection (HCC) Chronic right shoulder pain
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet ACIDOPHILUS LACTOBACILLUS PO albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler Alcohol, USP (BEER) SOLN amLODIPine (NORVASC) 5 MG tablet atorvastatin (LIPITOR) 40 MG
Allergien: BeeSwelling Oxycodone-ibuprofenAgitation Skin AdhesivesOther
Vorherige Impfungen: -

VAERS 2500264

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 89,0
Geschlecht: M
Eingang: 24.03.2023
Impfdatum: 17.11.2021
Beginn: 08.03.2023
Tage bis Beginn: 476,0
Dosis: 3
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Adenovirus test Adrenal adenoma Angiogram pulmonary abnormal Aortic arteriosclerosis Blood potassium decreased Back pain Blood culture COVID-19 Central venous catheterisation Bordetella test negative C-reactive protein increased Chlamydia test negative Computerised tomogram thorax abnormal Chills Computerised tomogram spine abnormal Condition aggravated Cough Culture negative

Symptomtext

Admission Date: 3/8/2023 Discharge Date: Mar 17, 2023 PRESENTING PROBLEM: T12-L1 disc space infection HOSPITAL COURSE: Patient is a 91 year old male with Hx of HTN, Afib, chronic diastolic HF, CAD, DM type II, CKD Stage III, BPH, rectal Ca, and GERD who presented to the ED with chills, shortness of breath, and cough as well as worsening back pain. He tested positive for COVID-19 and was admitted to the hospitalist service. CTA with groundglass opacities. He was requiring 3L NC O2 on admission and weaned to room air after completing 5 days of remdesivir and 6 days of dexamethasone. Pt did have steroid induced hyperglycemia, treated with insulin which improved significantly after steroids were completed. Regarding the patient's back pain, CT T/L spine concerning for T12-L1 discitis/osteomyelitis. MRI of the thoracic/lumbar spine showed discitis/osteomyelitis at T12-L1 as well as small abscess within anterior right psoas. Echo was completed showing normal EF and no valvular vegetation but pulmonic valve difficult to visualize. Spine surgery was consulted but did not recommend surgical intervention. IR was consulted and performed biopsy of T12-L1 intervertebral disc but cultures remained negative. Initial blood cultures 1/2 positive for micrococcus luteus, suspect contaminant, per ID. He was treated with ceftriaxone/vancomycin IV with all subsequent blood cultures negative. Due to improvement in back pain and negative blood cultures, ID recommended ceftriaxone/vancomycin to complete 6 weeks (3/12-4/23) with ID follow up in 4-6 weeks. His pain was controlled with tramadol, zanaflex, lidocaine patch, and gabapentin. PT/OT recommend SAR. Pt and facility were in agreement with SAR as pt desired to recover and eventually return home. They did have hospice informational meeting on 3/16 but did not yet feel that pt's goals were in alignment with hospice. PICC placed by vascular access team prior to discharge. He discharged to SAR in stable condition on 3/17/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Recurrent rectal cancer s/p radiation s/p TAMIS 8/10/21 with Benign prostatic hyperplasia with urinary frequency Hx of adenomatous colonic polyps Chronic kidney disease (CKD), stage III (moderate) (HCC) High cholesterol Gastroesophageal reflux disease Anemia due to chronic blood loss Hypertension Atherosclerosis of coronary artery History of coronary artery bypass surgery Urge incontinence of urine Peripheral vascular disease (HCC) Rectal neoplasm Atrial fibrillation Iron deficiency anemia due to chronic blood loss BPH with obstruction/lower urinary tract symptoms Posterior rectal mass, probable recurrent rectal cancer Mitral valve insufficiency Osteoarthrosis Acute on chronic anemia Diabetic neuropathy Diabetes mellitus Diastolic heart failure Rheumatic fever Ventral incisional hernia without obstruction or gangrene T12-L1 disc space infection (HCC) Chronic right shoulder pain
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet ACIDOPHILUS LACTOBACILLUS PO albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler Alcohol, USP (BEER) SOLN amLODIPine (NORVASC) 5 MG tablet atorvastatin (LIPITOR) 40 MG
Allergien: BeeSwelling Oxycodone-ibuprofenAgitation Skin AdhesivesOther
Vorherige Impfungen: -

VAERS 2599927

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: WI
Alter: 45,0
Geschlecht: F
Eingang: 15.03.2023
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Chest pain Full blood count Metabolic function test Nausea Vomiting

Symptomtext

Patient was fine in clinic - Had Epipen with her. at noon she was in urgent care with chest pains, nausea vomiting - at 6:34 ED - Epi drip Patient has prior Influenza alergic reactions PPD alergic reaction Patient came with Epi pen, was observed for 20 mins after with no problems Returned to work. Reaction happened after returning to work

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: CBC BMP
Aktuelle Erkrankungen: Anxiety Castlemans Disease
Vorgeschichte: Migraines
Andere Medikamente: none
Allergien: Flu shot - PPD Sol - Nutritional Supplement amoxicillin augmentin minocycline
Vorherige Impfungen: -

VAERS 2596928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: CO
Alter: 47,0
Geschlecht: M
Eingang: 15.03.2023
Impfdatum: 13.10.2021
Beginn: 01.12.2021
Tage bis Beginn: 49,0
Dosis: 2
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Back pain Blindness Coccydynia Corrective lens user Dysstasia Magnetic resonance imaging Mobility decreased Pain Spinal X-ray

Symptomtext

I started losing my eye site and I now have to wear corrective lenses. Severe lower back/tailbone pain that started about 5 months after the second shot. Not able to sit for long periods of time. Very painful to stand from a sitting position.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: X-Rays for my back in 2022 and 2023, MRI in 2023. Vision test in 2022.
Aktuelle Erkrankungen: n/a
Vorgeschichte: Asthma, sleep apnea, issues sitting and standing from a sitting position that started in 2022 right after the vaccine
Andere Medikamente: ATORVASTATIN, CETIRIZINE, OMEPRAZOLE, FLUTICASONE, FISH OIL
Allergien: Unknown food
Vorherige Impfungen: -

VAERS 2588605

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MN
Alter: 63,0
Geschlecht: M
Eingang: 28.02.2023
Impfdatum: 30.09.2022
Beginn: 08.12.2022
Tage bis Beginn: 69,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Dyspnoea Hypoxia Pneumonia Productive cough SARS-CoV-2 test positive Superinfection

Symptomtext

Patient with history of diabetes and pulmonary emphysema. He was seen in the ED on 12/8/22 for shortness of breath and productive cough for the past four days. In the ED, patient was hypoxic into the 80's, and tested positive for COVID-19 by PCR. Ultimately, patient was admitted 12/8/22 - 12/10/22. Patient was found to be in sepsis due to COVID-19 infection superimposed with community acquired pneumonia. Patient was on supplemental O2 during admission, but was able to be weaned to room air. Patient has received the primary COVID vaccine series and two boosters.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2584314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: OR
Alter: 30,0
Geschlecht: F
Eingang: 20.02.2023
Impfdatum: 18.02.2022
Beginn: 01.08.2022
Tage bis Beginn: 164,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Nerve conduction studies Pain in extremity Paraesthesia

Symptomtext

I started having pain and tingling on the soles my feet toes that has progressed up to my ankles and shins. I am now also experiencing numbness in my feet and toes. I have been referred to a podiatrist, who then referred me to a pain management/podiatrist who ran nerve conduction study. They have referred me to another podiatrist to see if they can discover what is causing my numbness, pain and tingling in my feet and toes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Nerve Conduction Study, incon.
Aktuelle Erkrankungen: No
Vorgeschichte: Hypothyroid; GERD
Andere Medikamente: SYNTHROID; omeprazole
Allergien: Penicillin (hives)
Vorherige Impfungen: -

VAERS 2574267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: CA
Alter: 44,0
Geschlecht: F
Eingang: 02.02.2023
Impfdatum: 01.02.2022
Beginn: 01.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Aphasia Aphonia Asthma Cough Dyspnoea Fatigue Hypersensitivity Impaired work ability Loss of personal independence in daily activities Parosmia Pulmonary function test Throat irritation

Symptomtext

It started with sensitivity to smells and then having my first anaphylactic reaction was in July to spray paint and I had to use my EPI-PEN. 911 was called and I had to go to the ER. The sensitivity to smells increased. The next time I had to use the EPIPEN was in October and the reaction was to cologne, and the next reaction was to cologne as well in November. The sensitivity is continually increasing and disrupting my life. Anytime I start having a reaction I have to stay home and use my inhaler or breathing machine and rest. It will also give me a cough and irritated throat, physical exhaustion, and it effects my breathing and asthma. I have had to call off work numerous times for reactions, more than the 3x listed. My life has drastically changed, I only go to church and home because I try to limit my interactions with things. I am a triage nurse and frequently have to call out because sometimes I lose my voice, or a bad cough and am unable to speak on the phone. This is happening at least twice a week that I encounter things that cause me to react. I am frequently using my albuterol inhaler and BENADRYL. The main triggers that have the biggest reactions are cologne, spray paint and cigarette smoke. I've purchased a ventilator and a particle safe mask to help lessen the smaller attacks. I went to see my pulmonologist and my asthma has been ruled out as primary factor. I have an appointment with an allergist in March.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 2022Dec Pulmonary Function Test
Aktuelle Erkrankungen: N/A
Vorgeschichte: High blood pressure; Depression; Overactive bladder; Sleep Apnea
Andere Medikamente: Lisinopril; HCTZ; WELLBUTRIN; LEXAPRO; DETROL LA; albuterol inhaler; WOMEN'S CHOICE vitamin; BENADRYL
Allergien: Seasonal; bananas; garlic; onions; carrots; cucumbers/pickles; soy; pork; turkey; peanuts; sunflower seeds; amoxycillin; latex
Vorherige Impfungen: -

VAERS 2527799

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 60,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 03.12.2021
Beginn: 19.04.2022
Tage bis Beginn: 137,0
Dosis: 3
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Asthma COVID-19 Condition aggravated Cough Fatigue Malaise SARS-CoV-2 test positive Secretion discharge

Symptomtext

I did not have an adverse reaction to the vaccine. On 04/19/2022 I started not feeling well with a severe cough with mucus production. I thought it was due to my asthma condition. I tested positive for COVID-19 on 04/20/2022 with severe cough with mucus production and extreme fatigue. I contacted my doctor but was not prescribed additional medication. I used my asthma medication and rested for ten days. I believe in the vaccinations and that my case of COVID-19 was mild and more to do with my asthma.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 20APR2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; High Blood Pressure; Endometriosis
Andere Medikamente: N/A
Allergien: Sulfa; codeine
Vorherige Impfungen: In 1984 I had the flu after receiving the flu vaccine. Shingles and Pneumonia shot caused my arm sore at injection site.

VAERS 2516765

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 37,0
Geschlecht: F
Eingang: 25.11.2022
Impfdatum: 24.11.2021
Beginn: 17.06.2022
Tage bis Beginn: 205,0
Dosis: 3
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Dyspnoea Fatigue SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

I experienced a breakthrough case of COVID-19 that started with coughing and I later tested positive for COVID-19. I also experienced shortness of breath, fatigue and tiredness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19
Aktuelle Erkrankungen: N/A
Vorgeschichte: Chronic headaches
Andere Medikamente: Nortriptyline
Allergien: N/A
Vorherige Impfungen: -

VAERS 2507222

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 85,0
Geschlecht: M
Eingang: 14.11.2022
Impfdatum: 05.03.2021
Beginn: 19.09.2022
Tage bis Beginn: 563,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Dyspnoea Hypertension SARS-CoV-2 test positive

Symptomtext

09/19/22 presents to ED for "hypertension, shortness of breath". PMHx of "Afib, COPD, lung cancer, ascending aortic aneurysm and obesity"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 09/19/22 SARS-CoV-2 (COVID-19) detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2501875

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: NY
Alter: 90,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 23.05.2022
Beginn: 29.07.2022
Tage bis Beginn: 67,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute kidney injury Asthenia Atelectasis Blood creatinine increased Blood sodium decreased Cough SARS-CoV-2 test positive Sepsis COVID-19 Cardiac failure congestive Chest X-ray abnormal Computerised tomogram head normal Condition aggravated

Symptomtext

7/29/2022- Presents to ED, c/o weakness and cough. Afebrile, BP210/88 and RR-29. Covid + test. CXR:bibasilar linear atelectasis. Ordered remdesivir. AKI, creatnine 1.4, stop Lasix. Admit for CHF exacerbation in setting of Covid. 8/1/2022. Continue remdesivir, Creatnine down to 1.1 . VSS afebrile. No 02 use, 8/12/2022- NA level down to 123, rectal temp 94. CT head negative. Bear hugger. Ordered IV cefepime and Vacno for Septicemia. 8/15/2022- AKI resolved, VSS. Continue cefepime and vanco. 8/17/2022-D/C to SNF, 7 dasy of cefdinir and doxycycline. VSS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 20,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CAD, Type 2 DM, A Fib, HTN, Aortic valve replacement
Andere Medikamente: -
Allergien: Betaxolol, Procainamide, Shellfish, Verapamil, Aliskiren, Sulfa.
Vorherige Impfungen: -

VAERS 2493339

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: CO
Alter: 62,0
Geschlecht: F
Eingang: 29.10.2022
Impfdatum: 24.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia Chills Headache Hyperhidrosis Hypersensitivity Lip exfoliation Lip swelling Pain Palpitations Pyrexia

Symptomtext

High fever 102 + , body aches, severe joint aches, swollen and peeling lips, headache, heart palpitations, chills and sweating. This lasted 3 days. For these days I stayed home, kept hydrated and took tylenol and ibuprofen. I thought the pfizer booster may have caused this severe reaction. I am reporting this now, since I got my 4th booster recently, 11 months later and had the same reaction, but worse. I changed from Pfizer to Moderna for my last booster. I can not endure a severe reaction like this again. There must be a new ingredient in the most recent boosters causing this severe allergic reaction. I did not have a reaction to my first two Covid Pfizer vaccines that were not mRNA. From reading online, I am guessing mRNA or RNA is the culprit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: fish, fish oil, adhesives
Vorherige Impfungen: -

VAERS 2491398

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FH8028

moderat

Staat: MI
Alter: 31,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 13.04.2021
Beginn: 04.09.2022
Tage bis Beginn: 509,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Dyspnoea SARS-CoV-2 test positive

Symptomtext

09/04/22 presents to ED for "shortness of breath". PMHx of "diabetes type 2, obesity, anxiety"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 09/05/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2487925

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 65,0
Geschlecht: M
Eingang: 25.10.2022
Impfdatum: 06.12.2021
Beginn: 24.10.2022
Tage bis Beginn: 322,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Asthenia COVID-19 Cough Dyspnoea Lung infiltration Mobility decreased Nasal congestion Obesity Oropharyngeal pain Pneumonia Productive cough Respiratory tract congestion SARS-CoV-2 test positive Sputum discoloured Superinfection

Symptomtext

Chief Complaint: Cough, congestion, shortness of breath and weakness Additional Medical History: Patient is a 66-year-old morbidly obese male. He also has a history of HIV, arthritis and hypertension. He is currently on antiviral therapies for HIV. He presents to the emergency room by auto complaining of nasal congestion, worsening cough and congestion which is productive at times of a greenish tinged sputum as well as generalized weakness and shortness of breath. Patient states he started with some nasal congestion and a sore throat 4 days ago which has gradually become worse. He has been around relatives with similar symptoms however his is worse. He also states he is very weak and is having a hard time getting around at home because he feels so weak. He has not been taking his Lasix because he is afraid he cannot get to the bathroom because of his weakness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: 7:27 PM patient will have a full work-up for pneumonia including cardiac enzymes, blood cultures and lactic acid. He will also be tested for COVID. Patient will be given a fluid bolus as well as steroid and Toradol. Further recommendations are to follow. 8:26 PM patient has a right lower lobe infiltrate on x-ray and is positive for COVID. He remains oxygenating around 90 to 92% on room air and still complains of generalized weakness. He will require admission for further care and treatment. Patient will be placed on antibiotics for suspected superimposed pneumonia on top of COVID. Case was discussed with Dr. who agreed to accept the admission.
Aktuelle Erkrankungen: unknown
Vorgeschichte: HIV arthritis HTN obesity
Andere Medikamente: lasix HIV antiviral
Allergien: none known
Vorherige Impfungen: -

VAERS 2467094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 03.10.2022
Impfdatum: 14.12.2021
Beginn: 23.09.2022
Tage bis Beginn: 283,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal pain Angiogram pulmonary normal COVID-19 COVID-19 pneumonia Computerised tomogram abdomen abnormal Diverticulitis Dyspnoea Hypoxia Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Patient with 3 COVID vaccines who admitted to hospital with COVID detected PCR and COVID PNA. Provider d/c note: "75 YO female with a PMHx of hypertension, hyperlipidemia, anxiety/depression who presents with fevers, sore throat, shortness of breath, abdominal pain. Found to have COVID pneumonia and uncomplicated diverticulitis. CT PE negative for pneumonia or pulmonary embolism. CT abdomen did show sigmoid diverticulitis without abscess. She was also hypoxic requiring oxygen with ambulation. She was treated with dexamethasone and remdesivir. She was also treated with ciprofloxacin and Flagyl for diverticulitis. Hypoxia resolved the next day, even with ambulation. PT recommended home with assist and she stays with her son and his family. Patient felt well and wanted to return home. I offered the opportunity to stay in the hospital to complete remdesivir course if she wanted and she declined. Due to the fact that she received IV contrast twice in 2 days, she was given a 500 mL bolus to protect her kidneys."

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 2,0
Labordaten: COVID Detected PCR on 9/23/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular Essential hypertension, benign Mixed hyperlipidemia Internal and external bleeding hemorrhoids Psychological Anxiety and depression Respiratory Hypoxia Other Thoracic scoliosis
Andere Medikamente: -
Allergien: Tetanus Toxoid
Vorherige Impfungen: -

VAERS 2439954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: CA
Alter: -
Geschlecht: F
Eingang: 10.09.2022
Impfdatum: 20.11.2021
Beginn: 10.08.2022
Tage bis Beginn: 263,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest discomfort Dry skin Dyspepsia Dyspnoea Erythema Peripheral swelling Pruritus

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. Other Case identifier(s): MOD22-022163 (Moderna). A female patient received BNT162b2 (BNT162B2), on 20Nov2021 as dose 3 (booster), single (Lot number: FH8028) for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 08Aug2022 as dose 4 (booster), single (Lot number: 014B22A) for covid-19 immunisation. The patient's relevant medical history included: "Thyroid" (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXINE taken for thyroid disorder. Past drug history included: Cortisone, reaction(s): "Allergies (medications, food and other products) Cortisone", notes: Allergies (medications, food and other products) Cortisone. Vaccination history included: BNT162b2 (Dose 1, Single; Lot number: EN6208), administration date: 10Mar2021, for Covid-19 immunization; BNT162b2 (Dose 2, Single; Lot number: ER8737), administration date: 31Mar2021, for Covid-19 immunization. The following information was reported: PRURITUS (medically significant) with onset 10Aug2022, outcome "recovered" (12Aug2022), described as "Itching in the feet"; DYSPEPSIA (medically significant) with onset 10Aug2022, outcome "not recovered", described as "felt like heart burn"; CHEST DISCOMFORT (medically significant) with onset 10Aug2022, outcome "not recovered", described as "pressure in her chest"; ERYTHEMA (medically significant) with onset 10Aug2022, outcome "recovered" (12Aug2022), described as "redness in the hands"; DYSPNOEA (medically significant) with onset 10Aug2022, outcome "not recovered", described as "she had trouble breathing"; PRURITUS (medically significant) with onset 10Aug2022, outcome "recovered" (12Aug2022), described as "skin itching in the bottom of her hand"; PERIPHERAL SWELLING (medically significant), PERIPHERAL SWELLING (medically significant) all with onset 10Aug2022, outcome "recovered" (12Aug2022) and all described as "swollen hands/feet also started and were swelled"; DRY SKIN (medically significant) with onset 12Aug2022, outcome "not recovered", described as "patient still felt dry skin even if it wasn't because she moisturized her it". The events "swollen hands/feet also started and were swelled", "she had trouble breathing", "felt like heart burn", "pressure in her chest", "patient still felt dry skin even if it wasn't because she moisturized her it", "skin itching in the bottom of her hand", "itching in the feet" and "redness in the hands" required physician office visit. Therapeutic measures were taken as a result of peripheral swelling, peripheral swelling, dyspnoea, dyspepsia, chest discomfort, dry skin, pruritus, pruritus, erythema. Clinical course: Patient received treatment with Benadryl, a nebulizer and an inhaler Albuterol. Itchiness stopped 36 hours after it started, but patient still felt skin dry even if it was not because moisturized it. In Jan2022, patient had COVID. Had no any medical history relating to mentioned AE and both Acute and Chronic illnesses at the time of vaccination. Patient did not experienced a similar event in the past. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Thyroid disorder
Andere Medikamente: Levothyroxine
Allergien: -
Vorherige Impfungen: -

VAERS 2433460

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 90,0
Geschlecht: M
Eingang: 08.09.2022
Impfdatum: 10.03.2021
Beginn: 20.08.2022
Tage bis Beginn: 528,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal pain Anticoagulant therapy COVID-19 Chest pain Computerised tomogram abdomen normal Echocardiogram normal Ejection fraction normal Fall Haemoglobin normal SARS-CoV-2 test positive Troponin increased

Symptomtext

Patient is 91y.o. male who presented to the hospital with chest and abdominal pain. Please note that patient was seen ibn ER the day before for a fall. Patient was diagnosed with COVID, was seen by ID and completed 3 days of Remdesivir. His breathing remained stable, did not require any O2. . His troponin was elevated, peaked at 1.09, he was seen by Cardio and Eliquis was changed to IV heparin x 48 hrs. Echo did not show any WMA, EF 55%. He will continue with statin and Imdur. His chest pain resolved.His abdominal pain resolved while in the hospital, a CT a/p was done and was unremarkable. Patient had a couple of BM that were reported as black by our staff, his Hg remained stable, FOB ordered but not done as did not have any other BMs. He was seen by Gi and recommended to continue Eliquis and PPI. Patient is stable for DC with HC and 24/7 assistance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 5,0
Labordaten: 8/20 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2411149

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MN
Alter: 41,0
Geschlecht: M
Eingang: 15.08.2022
Impfdatum: 28.01.2022
Beginn: 06.07.2022
Tage bis Beginn: 159,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 COVID-19 pneumonia Cough Dehydration Pyrexia SARS-CoV-2 test positive Sneezing Vaccine breakthrough infection Vomiting

Symptomtext

Patient brought into the ED via EMS on 7/6/2022 for fever, vomiting, dry cough, and sneezing. He has a history of diabetes and DKA, and was concerned that he might be developing DKA. COVID PCR test completed in the ED was positive. Patient was admitted from 7/6-7/8/22 with COVID pneumonia with severe dehydration. Patient vaccinated with most recent vaccine administrated 1/28/22. This meets criteria for vaccine breakthrough case review.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397308

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: CA
Alter: -
Geschlecht: F
Eingang: 30.07.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Influenza like illness Pyrexia

Symptomtext

feeling like i have the flu with a full grade fever; feeling like i have the flu with a full grade fever; every time she receives the shot, the symptoms worsen; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 54-year-old female patient received BNT162b2 (BNT162B2), as dose 2, single (Lot number: FH8028) for covid-19 immunisation. The patient's relevant medical history included: "Pre-diabetes" (unspecified if ongoing); "Blood pressure" (unspecified if ongoing); "Cholesterol" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE), for Covid-19 immunization, reaction(s): "each time, the symptoms or reaction was worst", "soreness". The following information was reported: INFLUENZA LIKE ILLNESS (non-serious), PYREXIA (non-serious), outcome "unknown" and all described as "feeling like i have the flu with a full grade fever"; CONDITION AGGRAVATED (non-serious), outcome "unknown", described as "every time she receives the shot, the symptoms worsen". Additional information: As per agent (Name withheld), the patient experienced side effects from the COVID vaccine and wants to know if should proceed with the booster. Caller stated that she was solely vaccinated with the Pfizer COVID vaccine and each time, the symptoms or reaction was worst. Caller mentioned that first time 04 April, the second time it was a full blown feeling like i have the flu with a full grade fever, then the third time I had my ears swell up to the point you cannot hear in any ears now. Caller mentioned that seek urgent care and she was told never saw anything like that and to ER. Caller stated that ER said the same that they never saw anything like that. Caller added that after consultations was prescribed with a steroid drops and actually got hearing for about the week. Caller mentioned that now it is time for the second booster, is it advised to the second booster or switch to other vaccine. After providing response, caller stated that she thinks she fall under the category of those who shouldn't take the vaccine. Caller also mentioned that every time she receives the shot, the symptoms worsen. Caller also added that seek medical advise from her doctor and they didn't know what to do as well and referred to Pfizer. There were no relevant lab tests.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure; Cholesterol; Pre-diabetes
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2388130

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MO
Alter: 39,0
Geschlecht: F
Eingang: 25.07.2022
Impfdatum: 13.12.2021
Beginn: 24.06.2022
Tage bis Beginn: 193,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Dyspnoea Feeling cold Headache Mobility decreased Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

On Monday June 24, 2022, I started to have a headache. I took an at home test and I tested positive for COVID-19. The next day I could not get out of bed. I had all of the symptoms. Fevers, chills, and body aches. I also started having breathing issues so I called my doctor on June 26, 2022. My doctor prescribe me paxlovid and I took that for 5 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: At home COVID-19 test on June 24, 2022 Prescribe me Paxlovid
Aktuelle Erkrankungen: None
Vorgeschichte: Epileptic
Andere Medikamente: Lamictal
Allergien: None
Vorherige Impfungen: -

VAERS 2362574

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: -
Alter: -
Geschlecht: U
Eingang: 08.07.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Blood test Chest pain Computerised tomogram Electrocardiogram Mobility decreased Pain Polymyalgia rheumatica

Symptomtext

Daughter of patient said day after shot she woke up and couldn't get out of bed and was hurting in her chest, hurting all over. Went to see PCP and they did blood test. They gave large doses of cortisone which helped but when regime was done symptoms returned. Gave cortisone again and once meds were gone symptoms returned. Has been on cortisone since then and went to rheumatology and was diagnosed with polymyalgia rheumatica. Did have a shoulder replacement prior to shots and had to quit therapy d/t pain in shoulder starting then.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: all patient report is blood work, cat scan and ekg
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2347575

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: IA
Alter: 75,0
Geschlecht: F
Eingang: 01.07.2022
Impfdatum: 16.11.2021
Beginn: 23.01.2022
Tage bis Beginn: 68,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal pain Acute kidney injury Bladder catheterisation COVID-19 Computerised tomogram abdomen normal Cough Decreased appetite Dehydration Hypophagia Inappropriate schedule of product administration Malaise Nausea SARS-CoV-2 test positive Urine analysis abnormal Vomiting

Symptomtext

Pfizer Dose 1 4/15/21 (EW0153) Pfizer Dose 2 5/7/21 (ER8736) Pfizer Dose 3 11/16/21 (FH8028) COVID Positive 1/23/22 1/23/22: This is a 75 years old female presented to the emergency department because of nausea and vomiting. The patient has a history significant for COPD, congestive heart failure, atrial fibrillation, coronary artery disease, hypertension, diabetes mellitus, chronic anticoagulation. There is documentation that the patient is on Eliquis and previously was prescribed Coumadin. Per record it seems that she is supposed to be on Eliquis per the most recent hospitalization course The patient is not a very good historian and keeps looking at her daughter to provide answers to questions. The daughter appears exhausted in the room and is sleeping during the encounter Patient has been sick for the past week with nausea, vomiting, reduced appetite and decreased oral intake. She is also complaining of abdominal pain associated with diarrhea and cough. She denies chest pain, shortness of breath, changes in stool colors, headache, dizziness. She was found in the emergency department to be dehydrated with resultant acute kidney injury. She has a chronic indwelling Foley catheter. Urinalysis suggestive of a possible urinary tract infection. She does have a history of ESBL UTI for which she was given Invanz at the last hospitalization. CT abdomen pelvis did not show anything acute. She is up-to-date with COVID-19 vaccinations. She was given IV fluid boluses as well as Levaquin prior to being admitted to the hospitalist service for further evaluation and treatment 1/31/22: Patient is a 75-year-old female history of neurogenic bladder with chronic indwelling Foley catheter and CKD stage IV admitted to the hospital for acute complicated UTI associated with chronic indwelling Foley catheter patient was treated with IV antibiotics, her hospitalization was noted for COVID-19 infection without any respiratory symptoms. As time progressed patient clinically improved, prior to discharge patient completed IV antibiotics. Patient was evaluated by therapy recommended skilled nursing facility, however on January 31st patient requested to be discharged to home with VNA. Patient will be discharged home with VNA recommended follow-up with PCP within 1 week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD CHF a fib CAD HTN DM anticoag
Andere Medikamente: albuterol 2 pufffs Q6h PRN allopurinol 200 mg PO QD apixaban 2.5 mg PO BID atorvastatin 40 mg PO QD bumetanide 2 mg PO BID clopidogrel 75 mg PO QD glipizide 5 mg PO QD insulin glargine 12 units SQ HS isosorbide mononitrate ER 60 mg PO QD ma
Allergien: penicillin - hives - tolerates carbapenemics, tolerates cephalosporins sulfa drugs - rash, itching
Vorherige Impfungen: -

VAERS 2347383

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: AR
Alter: 68,0
Geschlecht: F
Eingang: 01.07.2022
Impfdatum: 02.12.2021
Beginn: 30.06.2022
Tage bis Beginn: 210,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Atrial fibrillation COVID-19 Condition aggravated Hypoglycaemia SARS-CoV-2 test positive

Symptomtext

The patient was admitted on 6-30-22 to our Medical/Surgical unit at 1724 from the ER department with hypoglycemia and atrial fibrillation. Patient was tested for covid-19 on arrival and was confirmed positive for covid-19 at 2353 the same day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes, hypoglycemia, Atrial Fibrillation
Andere Medikamente: Allopurinol 100mg po daily. Amlodipine Besylate/hctz 5-10mg po daily Eliquis 5 mg po bid Glimepiride 4mg po bid Jardiance 25mg po daily Levothyroxine 75 mg po daily Metoprolol 100 mg po daily
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2335888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 79,0
Geschlecht: M
Eingang: 27.06.2022
Impfdatum: 29.11.2021
Beginn: 18.06.2022
Tage bis Beginn: 201,0
Dosis: 3
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Angina pectoris Anticoagulant therapy Arteriosclerosis coronary artery Arthralgia Atrial fibrillation Benign prostatic hyperplasia COVID-19 Chronic kidney disease Computerised tomogram head normal Dyslipidaemia Emphysema Fall Gout Hypertension Magnetic resonance imaging head normal Mental status changes SARS-CoV-2 test positive Sinus arrest

Symptomtext

Provider notes "Patient had a Fall at home and suffered a Laceration of right lower extremity. After returning home after repair of the laceration he was noted to have an Altered mental status. He was evaluated for possible stroke as has a history of stroke but head CT, brain MRI negative for acute findings. Carotid artery doppler with "less than 50% bilateral internal carotid arteries" Patient mental status has returned to baseline. Patient has permanent Atrial fibrillation but was manifesting other Cardiac arrhythmias with Sinus pauses and questionable run of ventricular tachycardia. Cardiology consulted and felt there was only one pause of concern. He was kept for further monitoring and no further pauses were found. Card recommended thirty day event monitoring at discharge.Patient on ENOXAPARIN with prior to admission COUMADIN held for possible procedure. At discharge he will have three days of overlap of ENOXAPARIN and COUMADIN. Essential hypertension blood pressure controlled. Dyslipidemia, goal LDL below 70 ATORVASTATIN Gout ALLOPURINOL Type 2 diabetes mellitus, without long-term current use of insulin on sliding scale here. BPH (benign prostatic hyperplasia) FINASTERIDE, TAMSULOSIN. Ankle pain. Did not appear to be gout. Possible osteoarthritis. Short course of PREDNISONE with improvement. ."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: 5,0
Labordaten: Positive PCR COVID test 6/18/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Lumbago 11/2/2011 Thoracic or lumbosacral neuritis or radiculitis, unspecified 11/2/2011 Degeneration of thoracic or thoracolumbar intervertebral disc (Chronic) 11/2/2011 Sacroiliac joint pain 11/2/2011 GERD (gastroesophageal reflux disease) 4/16/2013 Chronic rhinitis 4/16/2013 Xerostomia 4/16/2013 OSA on CPAP (Chronic) 4/16/2013 Fatigue 2/10/2014 Atrial fibrillation (Chronic) 3/4/2015 Hyperlipidemia, unspecified (Chronic) 3/4/2015 Degenerative joint disease of hand (Chronic) 3/16/2015 Primary osteoarthritis of left knee 2/15/2016 Arterial ischemic stroke, MCA, left, acute, 2/17/16 2/17/2016 Essential hypertension (Chronic) 2/18/2016 Dyslipidemia, goal LDL below 70 (Chronic) 2/18/2016 Anemia 2/19/2016 Status post total left knee replacement/ revision 2/15/16 2/19/2016 Aphasia 2/5/2017 Paroxysmal hematoma of left hand 7/31/2017 Muscle spasms of neck 1/22/2018 Gout (Chronic) 5/13/2018 Cerumen impaction 5/14/2018 Body mass index (BMI) of 40.0-44.9 in adult 11/30/2018 Venous insufficiency of both lower extremities 4/29/2020 Sedentary lifestyle 4/29/2020 Trigger middle finger of left hand 5/20/2021 Memory changes 5/20/2021 ACE inhibitor intolerance 5/20/2021 Type 2 diabetes mellitus, without long-term current use of insulin (Chronic) 5/20/2021 Panlobular emphysema 2/24/2022 Coronary artery disease involving native coronary artery of native heart with angina pectoris 2/24/2022 Stage 3a chronic kidney disease 2/24/2022
Andere Medikamente: allopurinol 100 mg Oral 2 times daily amlodipine besylate 10 mg Oral Daily ascorbic acid 500 mg Oral NIGHTLY aspirin 81 mg Oral NIGHTLY atorvastatin calcium 20 mg Oral NIGHTLY chlorthalidone 25 mg Oral Daily enoxaparin sodium 1 mg/kg
Allergien: Ace Inhibitors Flexeril
Vorherige Impfungen: -

VAERS 2325428

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 78,0
Geschlecht: M
Eingang: 21.06.2022
Impfdatum: 09.12.2021
Beginn: 13.06.2022
Tage bis Beginn: 186,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute kidney injury Blood creatinine increased COVID-19 Cardiac failure Condition aggravated Cough Dyspnoea Left ventricular failure Malaise Polyuria Pyrexia Spinal fracture

Symptomtext

Discharge Provider: MD Primary Care Provider : DO Admission Date: 6/13/2022 Discharge Date: 6/18/2022 Admitting Diagnoses: COVID-19 CONDITION ON DISCHARGE: Stable and improved. Home Health Care Svc HOSPITAL COURSE: Presented with malaise and fever and shortness of breation. Acute exacerbation or systolic heart failure with reduced ejection fraction, precipitated by covid. Responded to diuresis and fluid restriction oxygen requirements reduced very quickly. Cough is an issue His baseline Creatinine is unknown, appears to be around 1.0 He had an AKI (cr 1.6) this admission (present on admission) that resolved with treatment. DM worsened by steroids. Recent vertebral fracture. He has history of gout and BPH.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: S/P colonoscopy with polypectomy in 1/2019, next due in 5 years Dyslipidemia Essential hypertension, benign CAD (coronary artery disease) Ischemic cardiomyopathy Aortic valve disorders AAA (abdominal aortic aneurysm) (HCC) Bilateral carotid artery disease (HCC) S/P CABG (coronary artery bypass graft) S/P ICD (internal cardiac defibrillator) procedure S/P TAVR (transcatheter aortic valve replacement) S/P coronary artery stent placement Chronic combined systolic and diastolic CHF, HA class 2 (HCC) Type 2 diabetes mellitus with diabetic neuropathy, unspecified whether long term insulin use (HCC) Chronic gout of ankle, B/L Benign prostatic hyperplasia, unspecified whether lower urinary tract symptoms present Esophagitis determined by endoscopy in 1/2019 S/P balloon dilatation of esophageal stricture in 1/2019 Hemorrhoids, internal, grade 2 s/p banding in 5/2020 BMI 28.0-28.9,adult Bilateral hearing loss, unspecified hearing loss type Peripheral polyneuropathy - suspected, no past EMG Acute systolic heart failure (HCC) COVID-19
Andere Medikamente: allopurinol (ZYLOPRIM) 100 MG tablet aspirin 81 MG tablet atorvastatin (LIPITOR) 80 MG tablet benzonatate (TESSALON) 200 MG capsule carvedilol (COREG) 12.5 MG tablet Cyanocobalamin (B-12) 1000 MCG SUBL dutasteride (AVODART) 0.5 MG cap
Allergien: None
Vorherige Impfungen: -

VAERS 2312072

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: HI
Alter: 31,0
Geschlecht: F
Eingang: 07.06.2022
Impfdatum: 03.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Biopsy thyroid gland normal COVID-19 Computerised tomogram normal Dyspnoea Exposure to SARS-CoV-2 Goitre Pain SARS-CoV-2 test positive Thyroid mass Ultrasound thyroid abnormal Vaccine breakthrough infection

Symptomtext

I had an appointment with my doctor. She advised my thyroid looked enlarged. She ordered an Ultrasound. The ultrasound showed that it was abnormally large and they recommended a biopsy. I had a biopsy completed on 01/13/2022. On 01/20/2022 I had a follow up with an Endocrinologist and the Biopsy results came back benign. Since the biopsy I have been experiencing pain in my thyroid. 04/21/2022 I went to urgent care for the pain. I was sent to the ER because the pain was impeding my breathing. They did test for COVID-19 which came back negative. They did told CT Scan which showed my airway was not blocked. I was referred to an ENT. I did have a breakthrough COVID-19 case: 04/28/2022. I was exposed I did see the ENT on 05/18/2022 and they said my thyroid nodule was enlarged and due to the size of it they can see it is pushing on my trachea. They have recommending it to be removed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 01/13/2022: Thyroid Biopsy- Benign 04/21/2022: PCR- Negative for COVID-19 04/21/2022: CT Scan: Airway Not Blocked 04/28/2022: PCR- Positive for COVID-19
Aktuelle Erkrankungen: Recovering from C-Section
Vorgeschichte: PCOS
Andere Medikamente: Serrous Sulfate 325mg once every other day Vitamin D3 plus Calcium Prenatal Vitamin Omega 369 Fatty Acid COQ10
Allergien: Eggs
Vorherige Impfungen: -

VAERS 2311915

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MA
Alter: 47,0
Geschlecht: F
Eingang: 07.06.2022
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Chills Cough Feeling abnormal Lethargy Mobility decreased Pain Pulmonary congestion Pyrexia SARS-CoV-2 test positive Vertigo

Symptomtext

After the vaccine I had 7 hours of chills. I had a bad headache and body aches for 2 days. I was not able to function after that. I was taking ibuprofen. Then I started feeling better. In May 2022 I tested positive for Covid. I had a high fever, body aches, headaches, lethargic, congestion, and a lot of coughing. I was prescribed PAXLOVID. I was in bed for 12 days and missed work. On June 10, 2022 I am going to the doctor because I have extreme vertigo. When I try to do physical activities, I feel a flutter in my chest. It feels like something is rattling and it makes me cough. I'm still having vertigo and feeling lethargic. I also still have this weird feeling in my chest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Covid Vaccine positive (5/10/2022).
Aktuelle Erkrankungen: None
Vorgeschichte: Multiple Sclerosis
Andere Medikamente: Fluoxetine 20mg 1xday; solifenacin 5mg 1xday
Allergien: Amoxicillin; penicillin; sulfa drugs
Vorherige Impfungen: Anthrax vaccine I had body aches. My body because covered with unexplained bruises. (Possibly Between 1999-2001). Anthrax Vaccin

VAERS 2302086

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: WA
Alter: 48,0
Geschlecht: F
Eingang: 30.05.2022
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Impaired work ability Injected limb mobility decreased Muscular weakness Pain Sleep disorder

Symptomtext

Severe pain, soreness, limited movement and weakness in left arm. No treatment. Resulting in sleep disruption and having to leave my 20+ year carreer as a server in high end restaurants.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoarthritis, HSV1
Andere Medikamente: Vitamin D3 , B complex, vitamin C, provitalize.
Allergien: Shrimp allergy
Vorherige Impfungen: -

VAERS 2290513

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: CA
Alter: 28,0
Geschlecht: F
Eingang: 23.05.2022
Impfdatum: 10.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: nein

Autonomic nervous system imbalance Bedridden Blood test Blood thyroid stimulating hormone increased Cardiac monitoring abnormal Computerised tomogram thorax normal Dyspnoea Dysstasia Eating disorder Echocardiogram normal Endoscopy abnormal Fibrin D dimer increased Gait inability Gastric emptying study Impaired gastric emptying Nausea Postural orthostatic tachycardia syndrome Tachycardia

Symptomtext

Within 48 hours I was experiencing severe nausea, shortness of breath, and tachycardia. These symptoms became more severe over the next few months and I have now been diagnosed with POTS syndrome, gastroparesis, and general dysautonomia. At 6 months I have seen no improvement and am completely bedridden- unable to stand, walk, or eat solid foods.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 4,0
Labordaten: 1/12/21- ER visit- transvaginal ultrasound-clear, blood panels- low vitamin D and high TSH etected 1/24/22- Echocardiogram- clear, Heart Rate Monitor determines POTS 1/28/22 ER visit- D Dimer blood test results high 2/20/22 ER visit- D Dimer blood test results abnormally high, CT scan of chest clear 3/8/22- Hospital Stay- Endoscopy shows signs of Gastroparesis 3/24/22- Gastric Emptying Scan diagnoses Gastroparesis
Aktuelle Erkrankungen: None
Vorgeschichte: None before vaccination
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2282921

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: NH
Alter: 28,0
Geschlecht: M
Eingang: 18.05.2022
Impfdatum: 29.11.2021
Beginn: 09.05.2022
Tage bis Beginn: 161,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Decreased appetite Mobility decreased Oropharyngeal pain Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I started getting symptoms of sore throat, runny nose, and fever. I was in bed all day. The next day, I took a COVID-19 test at home that was positive. My symptoms progressed to cough, congestion, and loss of appetite. I did a virtual visit with my doctor and was advised to take Mucinex. My symptoms are still lingering today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: None
Vorgeschichte: Mild asthma
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2270828

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: WI
Alter: 59,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 07.12.2021
Beginn: 05.05.2022
Tage bis Beginn: 149,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Confusional state Fatigue Hypersomnia Hypotension Hypotonia Hypoxia Lethargy Stoma site discharge

Symptomtext

59 y.o. F that lives at a group home 2/2 TBI w/ SAH, hydrocephalus shunt, G-tube dependent, seizure disorder and stoma w/o tracheostomy tube who was admitted from 4/29-5/2 w/ increased secretions and fatigue 2/2 COVID (vax x2, boosted) and was admitted for the same from 5/3-5/4. It was felt her primary issue was requiring frequent suctioning of her stoma given her increased secretions. Despite the group home providing their best efforts in this regard, she has continued to become more lethargic. She is confused at baseline but usually alert and can respond. Now, she is sleeping around the clock and has no muscle tone when they transfer her. During her initial hospitalization last week, ENT evaluated and recommended laryngoscopy for her narrowed stoma after she is out of isolation for COVID. Today in the ER she is more hypotensive than she had been previously, w/ Systolics in the 90s. She is also requiring 2L via NC to maintain saturations. During her previous hospitalizations a trach collar was used intermittently due to intermittent hypoxia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2270787

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

moderat

Staat: MI
Alter: 60,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 18.03.2021
Beginn: 18.11.2021
Tage bis Beginn: 245,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Condition aggravated Fatigue Fibromyalgia Headache Impaired work ability Influenza Laboratory test Malaise Pain Pneumonia Pneumothorax X-ray

Symptomtext

headache for 4 days, chills, malaise, all over pain. In the following few weeks I went back on my fibromyalgia pills which I had gotten off of many years previous by good diet and exercise. Fatigue that has not left me. I have had the flu shot, and pneumonia shot, yet I have had the flu 5 times in a year, resulting in pneumonia, lung infection, or collapsed lung 3 times. I have never had the flu three times in a year let alone 5. This year I have been sick, resulting in work loss more for a total of more than 3 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: x-rays, mouth swabs
Aktuelle Erkrankungen: asthma, fibromyalgia
Vorgeschichte: asthma, fibromyalgia, arthritis, neuropathy
Andere Medikamente: daily vitamin
Allergien: seasonal allergies,
Vorherige Impfungen: -

VAERS 2265957

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: FL
Alter: 32,0
Geschlecht: F
Eingang: 06.05.2022
Impfdatum: 31.10.2021
Beginn: 05.05.2022
Tage bis Beginn: 186,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Chest pain Chills Cough Nausea Seasonal allergy Vaccine breakthrough infection Vomiting

Symptomtext

COVID-19 BREAKTHROUGH: 33 y/o female presents to the ED with the CC of Cough and CP x days. Patient with no PMH presented to the ED due to worsening Cough and CP x days. Pt states that about 3 week her daughter started to have URI symptoms after returning from Daycare. Pt states that she started to have Fever, Chills, and Hoarse voice. Pt states that her symptoms continued to worsen hence she went to hospital 5/2, pt states that she was diagnosed w/ Seasonal allergies and Rx Steroids. Pt states that she continued to worsen and had N/V. Pt c/o cough and CP. Pt denies any SOB. Pt denies any fever but c/o chills.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: ASTHMA
Andere Medikamente: PEPCID
Allergien: NKA
Vorherige Impfungen: -

VAERS 2254774

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 67,0
Geschlecht: M
Eingang: 27.04.2022
Impfdatum: 29.10.2021
Beginn: 23.04.2022
Tage bis Beginn: 176,0
Dosis: 3
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia Blood creatinine increased Blood lactic acid normal Blood urine absent COVID-19 COVID-19 pneumonia Cough Dyspnoea at rest Dyspnoea exertional Exposure to SARS-CoV-2 Fatigue Feeling abnormal Flank pain Hypoxia Influenza virus test negative Laboratory test normal Nasal congestion Oxygen saturation decreased

Symptomtext

Hospitalized 04/23/2022-04/24/2022; COVID-19 positive 04/23/2022; fully vaccinated plus booste Admission Date: 4/23/2022 Discharge Date: 4/24/2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Generalized weakness Pneumonia due to COVID-19 virus HOSPITAL COURSE: Admission H and P : Patient is a 67 y.o. male past medical history schizoaffective disorder, bipolar 1, CKD stage 3, type 2 diabetes mellitus, chronic diastolic CHF who presents today with progressively worsening weakness, fever, cough. History obtained from patient who has history of dementia as spouse/MD not at bedside and unable to reach by phone. Patient endorses that yesterday a friend at his adult daycare was diagnosed with COVID. He endorses cough, fatigue, nasal congestion, and not feeling too good. He experiences pain on his left flank which started yesterday. He endorses no shortness of breath at rest of with exertion. In the Emergency Department, patient with generalized weakness he was noted to desaturate with exertion to 80%. COVID-19 PCR positive, influenza negative with abrupt symptom onset date of admission 04/23. He has noted meet sepsis criteria with fever, tachycardia, tachypnea with normal lactic acid. Serum studies with elevated creatinine at baseline with CKD stage 3. UA +, but not initiated on IV antibiotics in the emergency department. Patient did not require supplemental oxygen. He endorsed being too weak to return home for which hospitalist service was consulted for admission further evaluation. Was evaluated by physical therapy with rec for dc home with assist. Testing positive for covid with exertional hypoxia on admit started with decadron tx. No further hypoxia over night. He will be assessed for home o2 needs for exertional hypoxia prior to dc. Will dc to complete x5 day course decadron and follow up with pcp . Urine with identified pyuria , with hx dementia and of questionable historian will with x3 day cipro and rec op follow up ua to verify clearance . On day of dc tolerating oral diet ,ambulating at baseline

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: ED visit on 3/27/22 for Flank pain MEDICAL DECISION MAKING: Patient clinically looks well and in no obvious discomfort. He again contacted the ambulance without wife knowing he did so. I checked a urinalysis and no evidence of urinary tract infection with that. He has had recurrent urinary tract infections in the past. Otherwise his labs show no acute changes from baseline. He has got some chronic kidney disease but right at his baseline. With recheck he is looking and feeling well. I see no indication for imaging of the abdomen and pelvis at this time. There is no blood in the urine. I had talked with wife initially about caring for him at home she did become tearful and reports she has been talking with her case worker. Case worker recommend using some respite care that is available to her but she feels guilty using that. I encouraged her to use the resources she has for breaks. Otherwise there were no further needs with today's ER visit. Patient was discharged home and can follow up the primary care doctor. Return to ER if symptoms worsen. Patient is a 67-year-old male who presents to the ER by EMS with a chief complaint of right flank pain. His wife is at the bedside. Reportedly he woke up with this but then wife states he told her it has been ongoing for couple of days. Patient has known dementia. Reportedly he contacted the ambulance without her knowing it. He denies any nausea or vomiting. No difficulty with urination or dysuria symptoms. No fevers or chills. He looks comfortable. Wife states he has had a history of urinary tract infections in the past. She has not noted any new change in his mentation or evidence of being ill. No previous history of kidney stones.
Vorgeschichte: Nasal congestion Pneumonia due to COVID-19 virus Essential hypertension Chronic diastolic heart failure Elevated d-dimer Dementia associated with other underlying disease with behavioral disturbance Bladder atony Stage 3 chronic kidney disease Acquired hypothyroidism Type 2 diabetes mellitus without complication, without long-term current use of insulin Sepsis due to COVID-19 Bipolar 1 disorder, depressed Schizoaffective disorder, depressive type Generalized weakness
Andere Medikamente: amLODIPine (NORVASC) 10 MG tablet carvedilol (COREG) 3.125 MG tablet ciprofloxacin (CIPRO) 500 MG tablet dexamethasone (DECADRON) 6 MG tablet glimepiride (AMARYL) 1 MG tablet hydrALAZINE (APRESOLINE) 25 MG tablet levothyroxine (SYNTHROID) 2
Allergien: Codeine Latex Keflex Amoxicillin
Vorherige Impfungen: -

VAERS 2254704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: WA
Alter: 53,0
Geschlecht: M
Eingang: 27.04.2022
Impfdatum: 10.12.2021
Beginn: 10.02.2022
Tage bis Beginn: 62,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Blood 25-hydroxycholecalciferol COVID-19 Cough Dyspnoea Fatigue Gluten sensitivity Pyrexia SARS-CoV-2 test Skin discolouration

Symptomtext

I had a breakthrough of COVID-19, I couldn't breathe, horrible dry cough, fatigue, high fever, turning colors. I had to go the hospital and also received breathing treatment, steroid injections and antibody infusion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 test; Blood work
Aktuelle Erkrankungen: No
Vorgeschichte: Fibromyalgia; Chronic Fatigue; Chronic Lung Damage
Andere Medikamente: Omeprazole DR 40mg; Dicyclomine three time daily; Oxybutynin 15mg; Gabapentin 300mg; Trazadone 150mg; Cyanocobalamin; High Calcium Pill; Magnesium Citrate; Prenatal; Osteo Bi-Flex Joint; St. John's worth 30mg; Testosterones 58; Vitamin D3
Allergien: Bees; Shellfish; after vaccine Gluten allergy
Vorherige Impfungen: -

VAERS 2246827

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: WA
Alter: 64,0
Geschlecht: F
Eingang: 21.04.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Aphasia Blood test Burning sensation Cardiac flutter Chest discomfort Chest pain Chills Dyspnoea Electrocardiogram normal Eye pain Eye pruritus Fatigue Headache Hemiparesis Hyperhidrosis Hypoaesthesia Hypoaesthesia oral Injection site erythema

Symptomtext

About 20 minutes after shot left side of face started to tingle. Moved up face and grew numb. Felt like shot of novocaine from Dentist. Felt very nauseous, thought I would throw up. Hand started tingling, some numbness in arm, some pressure in chest, no pain. Called Dr., went to walk-in clinic. By that time, teeth were chattering, very fatigued and would have slept except for nausea. They did EKG. Doctor said all fine but probably related to shot. Went home. Severe headache that night, could not lie down. Arm sore, not painful. Sore throat, swollen glands. Week later, lower cheek still numb, headache better. Jan 18 - Arm starts intense itch and breaking out in rash. Spreading under arm. Left eye very sore and bloodshot. Face increasing numbness (left side). Headache back. Extreme fatigue, tinnitus. Jan 19 - Arm worse, feels like shingles, fatigued laid down and could hardly move. Husband woke me. Could not form words because of numb lips. Arm burning, extreme itch. Throat sore. Jan 21 - Face very numb, rash improving, eyes itching, throughout sore, swollen. New rash at shot site. Jan 23 - Lips tingling, numb face, headache, arm much more sore. Very nauseous. Jan 27 - Face numb, rash on face. Jan 29 - Face numb, nauseous, sweating, arm breaking out itchy. Jan 30 - Left eye very sore/bloodshot. Burning and red welt at shot site. Rash on left side of face and numb. Feb 1 - Left eye very sore, neck sore. Feb 2-4 - Can't smile the same. Left side weaker, Tongue numb. Feb 16 - Face now tingling, not as numb. Rash on arm. Nauseous. Eye painful. Feb. 24 - Woke in night - lips numb, Left eye numb into brow. April 21 - Still having original symptoms. Face numbness increase/decrease. Heart fluttering, palpitations, chest discomfort that has become painful, have trouble getting enough breath. Constant.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 2 EKGs, Blood work, heart ultrasound scheduled
Aktuelle Erkrankungen: Osteoporosis, Sjogrens (diagnosed after shot)
Vorgeschichte: Autoimmune
Andere Medikamente: Levothyroxine, Vitamin C, D/K, Zinc, Fish Oil, Algae-Cal (Calcium)
Allergien: Prednisone, Iodine scrub
Vorherige Impfungen: Shingles (original one) Itching, nauseous about 54?

VAERS 2210922

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: TN
Alter: 68,0
Geschlecht: F
Eingang: 01.04.2022
Impfdatum: 10.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Alopecia Condition aggravated

Symptomtext

I am still losing hair and it's not going back; I started losing my hair and after the booster I lost even more and it's been 4 months now and I don't see any regrowth; My hair is not growing back; I am still losing hair and it's not going back; I started losing my hair and after the booster I lost even more and it's been 4 months now and I don't see any regrowth; My hair is not growing back; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 68 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 10Nov2021 (Lot number: FH8028) at the age of 68 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Diabetes" (ongoing), notes: have diabetes but I don't take medications for it. have been diagnosed with Diabetes years ago.; "Blood pressure" (unspecified if ongoing). Concomitant medication(s) included: CARDIZEM [DILTIAZEM] taken for blood pressure abnormal. Vaccination history included: Bnt162b2 (Dose 2), administration date: 16Mar2021, when the patient was 67 years old, for Covid-19 immunization, reaction(s): "burning and itchy scalp", "burning and itchy scalp"; Bnt162b2 (Dose 1), administration date: 20Feb2021, when the patient was 67 years old, for Covid-19 immunization; Flu vaccine (I have been getting the flu vaccine every year and I never had reactions with it.), administration date: Sep2021, for immunization. The following information was reported: ALOPECIA (non-serious) with onset 2021, outcome "not recovered", CONDITION AGGRAVATED (non-serious) with onset 2021, outcome "unknown" and all described as "I am still losing hair and it's not going back; I started losing my hair and after the booster I lost even more and it's been 4 months now and I don't see any regrowth; My hair is not growing back". The event "i am still losing hair and it's not going back; i started losing my hair and after the booster i lost even more and it's been 4 months now and i don't see any regrowth; my hair is not growing back" and "i am still losing hair and it's not going back; i started losing my hair and after the booster i lost even more and it's been 4 months now and i don't see any regrowth; my hair is not growing back" was evaluated at the physician office visit. Therapeutic measures were taken as a result of alopecia, condition aggravated. Additional information: Patient stated I am calling regarding a problem I have been having. I have had the 2 shots and the booster and I was thinking that this side effect would go away. But I am still losing hair and this seems to be something that the health department and the doctor seems to think that it will go back but it's not going back. When confirmed the name of the vaccine as Pfizer COVID-19 Vaccine, Patient stated I am talking about the Pfizer, I had all 3 of my shots with Pfizer and I started losing my hair and after the booster I lost even more and it's been 4 months now and I don't see any regrowth. And they are prescribing me medicines that are costing me money (general statement) and it didn't start until I had the vaccine. But they said outgoing the risk, so I am waiting. They said that they didn't have that many people that had hair loss and the ones they did their hair grow back but my hair was not growing back. Soon after I had my second vaccination and thats when I started going to the dermatologist about the burning and itchy scalp (further not clarified, hence not captured age in tab). For other medical conditions: Patient stated i have diabetes but I don't take medications for it. I don't have to take medications for it because my A1C was always under but I have been diagnosed with Diabetes years ago, but I don't take medications for it, I don't take Metformin, I don't take Insulin. I just control it with my diet, I guess its called pre-diabetes, pre-diabetes I guess. For treatment: Patient stated I am seeing a dermatologist and my medical doctor. I am using a shampoo that they prescribed and its called ketoconazole, shampoo for my scalp and I am taking, and I took vitamins (Unspecified medication) that I got over the counter thats for hair skin and nails but I am not talking that anymore because it's not helping. When probed if Patient had any vaccination 4 weeks prior to COVID-19 Vaccine, Patient stated, I have not got any other vaccine in last 4 weeks. I have not had any, I had the flu vaccine in last September before I had my booster and I have been getting the flu vaccine every year and I never had reactions with it. Follow-up attempts are completed. No further information was expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200482889 Same patient and drug, different event separated in time

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Diabetes (have diabetes but I don't take medications for it. have been diagnosed with Diabetes years ago.)
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure
Andere Medikamente: CARDIZEM [DILTIAZEM]
Allergien: -
Vorherige Impfungen: -

VAERS 2209152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 60,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 26.11.2021
Beginn: 05.01.2022
Tage bis Beginn: 40,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chest pain Dyspnoea Malaise SARS-CoV-2 test positive

Symptomtext

patient presented to emergency department on 1/5/22 with chest pain and shortness of breath patient was admitted for further management of acute chest pain patient was found to be covid-19 positive on 1/5/22 patient did requirement treatment for symptoms associated with covid-19 infection. treatment included remdesvir patient was discharge to home on 1/11/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 6,0
Labordaten: tested at healthcare - covid-19 test positive on 1/5/21
Aktuelle Erkrankungen: none known
Vorgeschichte: Cardiac and Vasculature Resistant hypertension Accelerated hypertension Acute chest pain Elevated troponin Endocrine and Metabolic Hyperthyroiditis Uncontrolled type 1 diabetes mellitus with background retinopathy and macular edema (HCC) Secondary renal hyperparathyroidism (HCC) Diabetic autonomic neuropathy associated with type 1 diabetes mellitus (HCC) Eye Mild nonproliferative diabetic retinopathy associated with type 1 diabetes mellitus, macular edema presence unspecified, unspecified laterality (HCC) Gastrointestinal and Abdominal Pharyngoesophageal dysphagia Gastroesophageal reflux disease, esophagitis presence not specified Genitourinary and Reproductive Nephrotic range proteinuria ESRD (end stage renal disease) on dialysis (HCC) End-stage renal disease on hemodialysis (HCC) Hemodialysis patient (HCC) Hematology and Neoplasia Anemia due to chronic kidney disease Kappa light chain disease (HCC) Neuro Chronic pain syndrome Headache Pulmonary and Pneumonias Acute bronchitis due to COVID-19 virus Acute hypoxemic respiratory failure (HCC) Sleep OSA (obstructive sleep apnea)
Andere Medikamente: amLODIPine (NORVASC) 10 MG tablet aspirin (HALFPRIN) 81 MG tablet calcium acetate (PHOSLO) 667 MG capsule cloNIDine (CATAPRES) 0.3 MG/24HR PTWK patch doxazosin (CARDURA) 4 MG tablet gabapentin (NEURONTIN) 400 MG capsule hydrlazine (AP
Allergien: methimazole morphine nifedipine
Vorherige Impfungen: -

VAERS 2200841

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: CO
Alter: 30,0
Geschlecht: F
Eingang: 27.03.2022
Impfdatum: 11.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Abdominal pain upper Allergy test Arthralgia Blood test Disturbance in attention Dysmenorrhoea Electrocardiogram Emotional disorder Exposure to SARS-CoV-2 Eye paraesthesia Fatigue Feeling abnormal Gait disturbance Generalised anxiety disorder Head discomfort Inflammation Muscle spasms Myalgia

Symptomtext

Neurologic; muscle pains all over body; joint in left knee hurts a lot; inflammation; hard to walk without feeling fatigued and needing to rest; nightmare; stomach aches and cramping; menstral cramping constantly; emotional; generalized anxiety; foggy brain; inability to concentrate; vitiligo; nausea; extreme pressure on left side of the head; tingling in left eye ongoing; body tingling all over; PTSD shock pains;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye paraesthesia
Hospital-Tage: -
Labordaten: antibody test confirming recent exposure to Covid; EKG; blood labs; allergy
Aktuelle Erkrankungen: Covid
Vorgeschichte: asthma
Andere Medikamente: Advair (for asthma)
Allergien: cats, dogs
Vorherige Impfungen: -

VAERS 2192321

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 50,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 17.12.2021
Beginn: 01.03.2022
Tage bis Beginn: 74,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cough Dyspnoea Fatigue Influenza virus test negative Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test negative Sinus disorder Streptococcus test negative Upper respiratory tract infection Wheezing

Symptomtext

I've had a sore throat, cough, wheezing, congestion, extreme fatigue, sob, sinus. I tested negative for COVID, strep, flu. They are calling it upper respiratory infection. They put me on doxycycline and prednisone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Negative for COVID, strep, flu.
Aktuelle Erkrankungen: No
Vorgeschichte: I have common variable immunodeficiency; Asthma; Bipolar; Gerd; Migraines; Hypertension; High Cholesterol; Lymphocytosis; Fatty Liver; Hightail Hernia; history of herbs zoster; Epidermoid Cyst
Andere Medikamente: Welchol, Fioricet, Acyclovir, Zinc, Vit C, Multivitamin (no iron), Eropranololer, Abilify, Diazepam, Vesicare, Theragran 1, Protonix, Vit D3, Zaleplon
Allergien: No
Vorherige Impfungen: -

VAERS 2190241

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 90,0
Geschlecht: F
Eingang: 21.03.2022
Impfdatum: 08.12.2021
Beginn: 16.03.2022
Tage bis Beginn: 98,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Aortic valve disease Atrial fibrillation COVID-19 Catheterisation cardiac abnormal Dyspnoea Dyspnoea at rest Dyspnoea exertional Echocardiogram abnormal Infusion Polyuria SARS-CoV-2 test positive Systolic dysfunction

Symptomtext

Patient up to date on COVID vaccines who admitted to hospital with A fib and tested detected for COVID during facility admission testing. Provider discharge summary below: "90 YO year old female with a history of Afib on Eliquis, severe aortic stenosis, and hypertension who presented to the Spectrum Health - ED on 3/16/2022 with progressive shortness of breath. Patient has had worsening shortness of breath over the past 1-2 months. Started out as dyspnea on exertion and has progressed to dyspnea at rest. She has been seen by cardiology and her PCP over the past month. Adjustments have been made to both her Amiodarone and Lasix. Prior to admission she was on Amiodarone 200mg and Lasix 20mg bid. She had an echocardiogram on 3/16/22 which revealed greatly reduced systolic dysfunction, at which point she was directed to the emergency department. On admission, cardiology was consulted and she was started on gentle diuresis. Right/Left catheterization was performed by Dr. on 3/18/22. It revealed no obstructive coronary disease, but did demonstrated an aortic valve area of 0.5 cm2. Cardiology now recommending to start process of TAVR work up - can be done as outpatient. Patient scheduled to follow-up with the valve clinic on 3/24/22. Of note, following the procedure, patient slipped into atrial fibrillation, though she later converted back into normal sinus rhythm following an amiodarone infusion. Issues Requiring Follow Up: (Who, what, when, and how communicated?) PCP - Diagnosed with incidental COVID. Not hypoxic - no treatment initiated. Was diagnosed with a 30-day supple of Metoprolol per cardiology recommendations. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: PCR detected test 03/16/22.
Aktuelle Erkrankungen: -
Vorgeschichte: HTN (hypertension) Primary osteoarthritis of right knee Beta-thalassemia Stage 3b chronic kidney disease Microcytic anemia - multifactorial Dyslipidemia Osteoporosis, post-menopausal HX: breast cancer Asthma Atrial flutter with rapid ventricular response Severe aortic stenosis Anemia in stage 3b chronic kidney disease (*) Iron deficiency anemia due to chronic blood loss Acute heart failure with reduced ejection fraction and diastolic dysfunction (*) Paroxysmal atrial fibrillation (*)
Andere Medikamente: Eliquis Os-CAL Pacerone Iron Lasix Lopressor Multivitamin Klor-Con Preservision vitamin
Allergien: Ancef [Cefazolin] Terazosin Mushroom Flavor Sulfadiazine Fosamax [Alendronate]
Vorherige Impfungen: -

VAERS 2182576

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 28,0
Geschlecht: M
Eingang: 16.03.2022
Impfdatum: 09.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Aortic dilatation Cardiac flutter Chest pain Dysgeusia Echocardiogram abnormal

Symptomtext

Ongoing Metallic taste in mouth after vaccine Feeling of chest flutters after second vaccination Burning sensation to left sternum few months after vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Echocardiogram - Noted aortic dilation not previously noted on echocardiogram in 2015
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Testosterone Cypionate .5ML subcutaneously weekly Adderall 20mg and 10mg
Allergien: None
Vorherige Impfungen: -

VAERS 2181912

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8028

moderat

Staat: CA
Alter: 31,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 07.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Contusion Migraine Muscle spasms Pain in extremity SARS-CoV-2 test Tenderness

Symptomtext

Calves of both my legs cramped up really bad as if I tore my muscles or something; felt tenderness in my left hip area and on opposite arm of the shot; felt tenderness in my left hip area and on opposite arm of the shot; There was random yellow bruising on my arms but they were small; migraine; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 31 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 07Jan2022 (Lot number: Fh8028) at the age of 31 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "allergy" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: MUSCLE SPASMS (non-serious) with onset 2022, outcome "recovered with sequelae", described as "Calves of both my legs cramped up really bad as if I tore my muscles or something"; TENDERNESS (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 2022, outcome "recovered with sequelae" and all described as "felt tenderness in my left hip area and on opposite arm of the shot"; CONTUSION (non-serious) with onset 2022, outcome "recovered with sequelae", described as "There was random yellow bruising on my arms but they were small"; MIGRAINE (non-serious) with onset 2022, outcome "recovered with sequelae", described as "migraine". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of muscle spasms, tenderness, pain in extremity, contusion, migraine. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Calves of both my legs cramped up really bad as if I tore my muscles or something. Also felt tenderness in my left hip area and on opposite arm of the shot. It lasted about four days. There was random yellow bruising on my arms but they were small. Had a massive migraine as well. No Prior to vaccination, was the patient diagnosed with COVID-19. Yes Since the vaccination, has the patient been tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Test Name: tested for COVID-19; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2176890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: VA
Alter: 60,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Alopecia Blood cholesterol Blood pressure measurement Erythema Feeling hot Heart rate Heart rate increased Hyperthyroidism Laboratory test Pain in extremity Palpitations Thyroid function test

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 60 year-old female patient received bnt162b2 (BNT162B2, solution for injection), administered in arm left, administration date 04Nov2021 (Lot number: FH8028) at the age of 60 years as dose 3 (booster), single for Covid-19 immunisation. Relevant medical history included: "high cholesterol", start date: Dec2008 (unspecified if ongoing), notes: on cholesterol meds for years. she takes Simvastatin 40mg once daily for high cholesterol.; "Barrett's esophagus", start date: Jun2019 (unspecified if ongoing). Concomitant medication(s) included: NEXIUM 24HR; SIMVASTATIN taken for blood cholesterol increased; FLUARIX QUADRIVALENT taken for immunisation, administration date 12Oct2021. Vaccination history included: Bnt162b2 (1st dose, Pfizer BioNTech Covid-19 vaccine, 0.3ml injected in left arm, lot number: EN6199), administration date: 11Mar2021, when the patient was 59 years old, for Covid-19 immunization, reaction(s): "heart pounding and fluttering", "her heart beating fast and hard", "her heart beating fast and hard", "It has affected her Thyroid"; Bnt162b2 (2nd dose; Pfizer BioNTech Covid-19 vaccine, Lot ER8732; Injected in left arm), administration date: 01Apr2021, when the patient was 59 years old, for Covid-19 immunization, reaction(s): "heart pounding and fluttering", "her heart beating fast and hard", "her heart beating fast and hard", "It has affected her Thyroid"; Fluarix quad 2021/2022 (injection was 0.5ml; Intramuscularly; NDC 58160-0887-52), administration date: 12Oct2021. The following information was reported: HYPERTHYROIDISM (medically significant) with onset 14Feb2022, outcome "unknown", described as "something has created her thyroid to be off which it never had been /her thyroid is overactive all of a sudden/thyroid problems and she's never had thyroid problems"; HEART RATE INCREASED (non-serious), outcome "unknown", described as "her heart beating fast and hard"; PALPITATIONS (non-serious), outcome "unknown", described as "Heart was beating fast and hard and pounding out of"; FEELING HOT (non-serious), ERYTHEMA (non-serious) all with onset 05Nov2021, outcome "recovering" and all described as "Warmth and redness in cheeks"; ALOPECIA (non-serious), outcome "recovering", described as "losing hair"; PAIN IN EXTREMITY (non-serious) with onset 04Nov2021, outcome "recovering", described as "arm sore". According to the caller, when she first went to her doctor on 14Jan due to her concerns about her heart beating harder since the booster vaccine, her doctor stated something has created her thyroid to be off which it never had been but the doctor does not know if it is because of the vaccine. Caller stated her doctor will do a heart monitor on her on 02Mar and her doctor will re-check her thyroid again on 10Mar. Caller stated patient got her labs done for her yearly physical and that's when it showed up about her thyroid. Patient was a pretty healthy person. Patient lost some weight, except for high cholesterol. Caller stated patient was not gonna get the booster but after she did it went all downhill since. She now has thyroid problems and she's never had thyroid problems. Patient was concerned since they are talking about a 4th vaccine and states she will not be getting anymore vaccines as she does not feel comfortable. They called in some medication, and she has not taken it. It was Atenolol 25mg. She was afraid of taking it because it lowers your blood pressure, and she didn't have high blood pressure. She took her blood pressure when her heart was beating fast, and it was 95/61, and she thought about going to the emergency room and did not. Patient got sore immediately after she got it, and got worse, but then better after 3 days. The patient underwent the following laboratory tests and procedures: blood cholesterol: (unspecified date) levels were really good; blood pressure measurement: (unspecified date) down which was at 90/61 or 95/61, notes: it had never been under 100; heart rate: (unspecified date) fast and hard; laboratory test: (unspecified date) showed up about her thyroid; thyroid function test: (11Feb2022) thyroid is out of control. Therapeutic measures were taken with atenolol as a result of heart rate increased, palpitations. Additional information: The heart beating problem is a worry and now she thinks it has affected her thyroid. She is having to go to doctor and having to do a lot of tests. Caller stated she did a lot of reading where it states the antibodies from the vaccine can attack the thyroid causing inflammation and dysfunction of the thyroid after some patients who have had the infection. The caller had her heart beating fast and hard after all of the doses but after the 1st and 2nd dose it had dissipated but after the 3rd it has not dissipated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Name: cholesterol; Result Unstructured Data: Test Result: levels were really good; Test Name: blood pressure; Result Unstructured Data: Test Result: down which was at 90/61 or 95/61; Comments: it had never been under 100; Test Name: heart beating; Result Unstructured Data: Test Result: fast and hard; Test Name: physical; Result Unstructured Data: Test Result: showed up about her thyroid; Test Date: 20220211; Test Name: thyroid; Result Unstructured Data: Test Result :thyroid is out of control.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Barrett's esophagus; High cholesterol (on cholesterol meds for years. she takes Simvastatin 40mg once daily for high cholesterol).
Andere Medikamente: NEXIUM 24HR; SIMVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2176428

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: WA
Alter: 61,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 30.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Fatigue Migraine Myalgia Pyrexia Taste disorder Vaccination site pain

Symptomtext

altered taste; Fever; chills; muscle aches; migraine; exhaustion; pain at injection site; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 30Oct2021 15:00 (Lot number: FH8028) at the age of 61 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "HBP" (unspecified if ongoing); "fibromyalgia" (unspecified if ongoing); "migraine" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Sulfa drugs, reaction(s): "allergy"; Neosporin, reaction(s): "allergy"; Penicillin, reaction(s): "allergy". Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6199, Location of injection: Arm Left), administration date: 05Mar2021, when the patient was 60 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EP7533, Location of injection: Arm Left), administration date: 27Mar2021, when the patient was 60 years old, for COVID-19 Immunization; Tetanus, reaction(s): "allergy". The following information was reported: TASTE DISORDER (non-serious) with onset 31Oct2021, outcome "recovering", described as "altered taste"; PYREXIA (non-serious) with onset 31Oct2021, outcome "recovering", described as "Fever"; CHILLS (non-serious) with onset 31Oct2021, outcome "recovering", described as "chills"; MYALGIA (non-serious) with onset 31Oct2021, outcome "recovering", described as "muscle aches"; MIGRAINE (non-serious) with onset 31Oct2021, outcome "recovering", described as "migraine"; FATIGUE (non-serious) with onset 31Oct2021, outcome "recovering", described as "exhaustion"; VACCINATION SITE PAIN (non-serious) with onset 31Oct2021, outcome "recovering", described as "pain at injection site". Therapeutic measures were not taken as a result of taste disorder, pyrexia, chills, myalgia, migraine, fatigue, vaccination site pain. Additional information: The patient had not received any other vaccine within 4 weeks. Patient had not been diagnosed with COVID-19 prior to vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Fibromyalgia; Migraine
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2176395

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: DC
Alter: 41,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain Condition aggravated Fatigue Pain Pruritus Urticaria Vaccination site irritation

Symptomtext

fatigue intensified; I began having body aches; incessant itching on the right side of my body (head to toe); The most intense itching was at the injection site; Itching/hives spread to left side of face, arm and torso; I felt sudden extreme fatigue; mild chest pains; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 41 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 28Oct2021 10:30 (Lot number: FH8028) at the age of 41 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "hypertension" (unspecified if ongoing); "HSV2" (unspecified if ongoing), notes: other medical history: hypertension, HSV2, seasonal allergies/hayfever, lichen planus; "seasonal allergies" (unspecified if ongoing), notes: other medical history: hypertension, HSV2, seasonal allergies/hayfever, lichen planus; "Hay fever" (unspecified if ongoing); "lichen planus" (unspecified if ongoing). Concomitant medication(s) included: ALLEGRA 24 HOUR; FLONASE [FLUTICASONE PROPIONATE]; VALTREX. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EN6201, Location of injection: Left Arm , Route of Administration: Intramuscular), administration date: 23Feb2021, when the patient was 40 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL8982, Location of injection: Left Arm , Route of Administration: Intramuscular), administration date: 02Feb2021, when the patient was 40 years old, for Covid-19 immunization. The following information was reported: FATIGUE (non-serious) with onset 28Oct2021 13:30, outcome "not recovered", described as "I felt sudden extreme fatigue"; CHEST PAIN (non-serious) with onset 28Oct2021 13:30, outcome "not recovered", described as "mild chest pains"; CONDITION AGGRAVATED (non-serious) with onset 28Oct2021 16:30, outcome "not recovered", described as "fatigue intensified"; PAIN (non-serious) with onset 28Oct2021 16:30, outcome "not recovered", described as "I began having body aches"; PRURITUS (non-serious) with onset 28Oct2021 16:30, outcome "not recovered", described as "incessant itching on the right side of my body (head to toe)"; VACCINATION SITE IRRITATION (non-serious) with onset 28Oct2021 16:30, outcome "not recovered", described as "The most intense itching was at the injection site"; URTICARIA (non-serious) with onset 28Oct2021 16:30, outcome "not recovered", described as "Itching/hives spread to left side of face, arm and torso". Therapeutic measures were not taken as a result of fatigue, chest pain, condition aggravated, pain, pruritus, vaccination site irritation, urticaria. Follow-Up (04Nov2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hay fever; Herpes simplex type I (other medical history: hypertension, HSV2, seasonal allergies/hayfever, lichen planus); Hypertension; Lichen planus; Seasonal allergy (other medical history: hypertension, HSV2, seasonal allergies/hayfever, lichen planus)
Andere Medikamente: ALLEGRA 24 HOUR; FLONASE [FLUTICASONE PROPIONATE]; VALTREX
Allergien: -
Vorherige Impfungen: -

VAERS 2173423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: CA
Alter: 12,0
Geschlecht: M
Eingang: 11.03.2022
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Tremor

Symptomtext

During routine visit 3months after 2nd COVID-19 vaccination mother noted that patient was shaking terribly with chattering teeth for about 2 hours, she thought he was having a seizure. Patient during this episode was alert, speaking with mother through chattering teeth while shaking. there was no eye deviation, no drooling, no stiffening, no perceived loss of consciousness. Mother gave Tylenol during the episode and symptoms resolved within 2 hours. Patient has no known history of seizure activity. Patient was not taken to Emergency Department, nor was patient was brought in for clinical care/evaluation. With this situation, mother is refusing any further vaccination of the patient for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None.
Vorgeschichte: Autism; Obesity; Hepatic Steatosis.
Andere Medikamente: None.
Allergien: Vancomycin; Milk.
Vorherige Impfungen: -

VAERS 2166081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: -
Alter: 27,0
Geschlecht: F
Eingang: 08.03.2022
Impfdatum: 01.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Angiogram normal Blood test Chest discomfort Chest pain Electrocardiogram Fibrin D dimer increased Immunisation reaction

Symptomtext

Chest pain/pressure beginning evening of 11/3/2021. Called PCP to be seen and they recommended I go to the ER because of chest discomfort. Went to the ER morning of 11/4/2021. Abnormal D Dimer, normal CTA. Discharged with a diagnosis of adverse vaccine reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 11/4/2021: EKG, blood tests, CTA. Abnormally elevated D Dimer lab result that prompted CTA. CTA was normal.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Oral contraceptive pill
Allergien: NKA
Vorherige Impfungen: -

VAERS 2155348

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: AL
Alter: 63,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 15.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test abnormal Computerised tomogram normal Heart rate increased Hyperthyroidism Malaise Tremor Ultrasound scan

Symptomtext

At first, I was sick after. About a week later, I develop tremors in my hands. I started getting rapid heart rates. I went a Cardiologist. They did blood work and that my hypothyroid turned into hyperthyroid. They also did an EKG, heart CT scan, and a ultrasound of my thyroid. The CT scan, show that my heart was fine, but I did still have an evaluated heart rate. I also have to go see an endocrinologist about my thyroid. He thinks that I have an autoimmune disorder now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Blood work; CT scan; Ultrasound
Aktuelle Erkrankungen: N/A
Vorgeschichte: MS
Andere Medikamente: Aspirin; Buclizine; Levothyroxine
Allergien: N/A
Vorherige Impfungen: -

VAERS 2147310

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8028

moderat

Staat: IL
Alter: 10,0
Geschlecht: F
Eingang: 27.02.2022
Impfdatum: 28.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal pain upper Blood test Body temperature Body temperature abnormal Chest discomfort Chills Dyspnoea Echocardiogram Fatigue Flushing Heart rate Magnetic resonance imaging Migraine Pain in extremity Palpitations Polymers allergy Still's disease Vomiting

Symptomtext

She is in remission from Systemic Jia for 1 year 7 months; Migraines; Stomach pains; Vomiting; Flushed skin; Temperature fluctuations from 99.4 to 95.0 quickly with migraines; Shivering; Chest discomfort and racing heart; Chest discomfort and racing heart; Felt out of breath; Extreme Leg pain from high thighs to ankles lasted 24 hours with moderate for the next 5-7 days.; Diagnosed with PEG allergy; Fatigue; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 10-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 28Nov2021 10:00 (Lot number: Fh8028) at the age of 10 years as dose 2, single for covid-19 immunization. Relevant medical history included: "Systemic Jia" (unspecified if ongoing), notes: Systemic Jia; "Macrophage Activation Syndrome" (unspecified if ongoing), notes: Macrophage Activation Syndrome both in remission; "Known allergy: Nsaids" (unspecified if ongoing), notes: Known allergy: Nsaids; "Known allergy: Possible wheat allergy" (unspecified if ongoing), notes: Known allergy: Possible wheat allergy; "Known allergy: adhesives" (unspecified if ongoing), notes: Known allergy: adhesives; "Known allergy: contrast" (unspecified if ongoing), notes: Known allergy: contrast. Concomitant medication(s) included: ZYRTEC [CETIRIZINE HYDROCHLORIDE]. The patient received Zyrtec as pre-treatment for possible reactions within two weeks of vaccination. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: Fl0007, Location of injection: Arm Left, Vaccine Administration Time: 10:00 AM), administration date: 07Nov2021, when the patient was 10 years old, for COVID-19 immunization, reaction(s): "Vomiting", "flushed cheeks", "Fatigue", "Migraines". The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was neither diagnosed with COVID-19 Prior to vaccination, nor been tested for COVID-19 Since the vaccination. The following information was reported: STILL'S DISEASE (medically significant) with onset 2021, outcome "recovering", described as "She is in remission from Systemic Jia for 1 year 7 months". Now 4 months out things have been started to spread out. MIGRAINE (non-serious) with onset 2021, outcome "not recovered", described as "Migraines"; ABDOMINAL PAIN UPPER (non-serious) with onset 2021, outcome "not recovered", described as "Stomach pains"; VOMITING (non-serious) with onset 2021, outcome "recovering", described as "Vomiting/Extreme vomiting"; FLUSHING (non-serious) with onset 2021, outcome "not recovered", described as "Flushed skin"; BODY TEMPERATURE ABNORMAL (non-serious) with onset 2021, outcome "recovering", described as "Temperature fluctuations from 99.4 to 95.0 quickly with migraines"; CHILLS (non-serious) with onset 2021, outcome "recovering", described as "Shivering"; CHEST DISCOMFORT (non-serious), PALPITATIONS (non-serious) all with onset 2021, outcome "recovering" and all described as "Chest discomfort and racing heart"; DYSPNOEA (non-serious) with onset 2021, outcome "recovering", described as "Felt out of breath"; PAIN IN EXTREMITY (non-serious) with onset 2021, outcome "recovering", described as "Extreme Leg pain from high thighs to ankles lasted 24 hours with moderate for the next 5-7 days."; POLYMERS ALLERGY (non-serious) with onset 2021, outcome "recovering", described as "Diagnosed with PEG allergy"; FATIGUE (non-serious) with onset 2021, outcome "not recovered", described as "Fatigue". The events "she is in remission from systemic jia for 1 year 7 months", "migraines", "stomach pains", "vomiting", "flushed skin", "temperature fluctuations from 99.4 to 95.0 quickly with migraines", "shivering", "chest discomfort and racing heart", "chest discomfort and racing heart", "felt out of breath", "extreme leg pain from high thighs to ankles lasted 24 hours with moderate for the next 5-7 days." and "diagnosed with peg allergy" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: blood test: (unspecified date) slight fluctuations, notes: Bloodwork done 3 times and only very slight fluctuations; body temperature: (08Nov2021) 99.4 to 95.0, notes: temperature fluctuations; echocardiogram: (unspecified date) unknown result; heart rate: (08Nov2021) racing, notes: racing heart; magnetic resonance imaging: (unspecified date) unknown result. Therapeutic measures were not taken as a result of still's disease, migraine, abdominal pain upper, vomiting, flushing, body temperature abnormal, chills, chest discomfort, palpitations, dyspnoea, pain in extremity, polymers allergy, fatigue. No follow-up attempts are needed. No further information is expected.; Sender's Comments: Based on available information, a possible contributory role of BNT162B2 vaccine cannot be excluded for the reported events due to temporal relationship. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: blood tests; Result Unstructured Data: Test Result:slight fluctuations; Comments: Bloodwork done 3 times and only very slight fluctuations; Test Date: 20211108; Test Name: Body temperature; Result Unstructured Data: Test Result:99.4 to 95.0; Comments: temperature fluctuations; Test Name: Echo; Result Unstructured Data: Test Result:Unknown result; Test Date: 20211108; Test Name: heart rate; Result Unstructured Data: Test Result:racing; Comments: racing heart; Test Name: Mri; Result Unstructured Data: Test Result:Unknown result
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Adhesive tape allergy (Known allergy: adhesives); Allergy to grains (Known allergy: Possible wheat allergy); Allergy to NSAIDs (Known allergy: Nsaids); Contrast media allergy (Known allergy: contrast); Macrophage activation syndrome (Macrophage Activation Syndrome both in remission); Systemic juvenile idiopathic arthritis (Systemic Jia)
Andere Medikamente: ZYRTEC [CETIRIZINE HYDROCHLORIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 2128342

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: -
Alter: 25,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 23.10.2021
Beginn: 13.02.2022
Tage bis Beginn: 113,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Mobility decreased Pain Pain in extremity

Symptomtext

It was painful to move my left arm starting Sunday afternoon 2/13/22. The pain lasted all week, each day able to do a little more with my arm but toward the end of the day it was extremely painful to move. I couldn?t lift my arm one day, then the next day I was able to lift it, but not able to lift if my arm was bent. The pain finally stopped on Friday 2/18/22. I tried taking ibuprofen to stop the pain throughout the week but it didn?t help.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2127812

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: CT
Alter: 69,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Erythema Flushing Immunisation Neuralgia Paraesthesia Pruritus Tongue dry

Symptomtext

Third dose/booster dose; some nerving sensations (tingling) all over my body.; flushing; Face got itchy, flushed, red; Face got itchy, flushed, red; Face got itchy, flushed, red; tongue got very, very dry; Felt little pricks of nerve endings all over her body, in different parts of her body; This is a spontaneous report received from contactable reporter. The reporter is the patient. Other Case identifier(s): US-PFIZER INC-202200133585. A 69 year-old female patient received bnt162b2 (BNT162B2, solution for injection), administration date 12Nov2021 (Lot number: FH8028) at the age of 69 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot: EN6201), administration date: 15Feb2021, when the patient was 69 years old, for COVID-19 immunization; Bnt162b2 (DOSE 2, SINGLE, provided as either EV6207, EU6207 or EN6207-this is handwritten on the vaccine record card.), administration date: 19Mar2021, when the patient was 69 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious), outcome "unknown", described as "Third dose/booster dose"; PARAESTHESIA (non-serious), outcome "unknown", described as "some nerving sensations (tingling) all over my body."; FLUSHING (non-serious), outcome "unknown", described as "flushing"; PRURITUS (non-serious) with onset 12Nov2021, outcome "unknown", FLUSHING (non-serious), ERYTHEMA (non-serious) all with onset 12Nov2021, outcome "recovering" and all described as "Face got itchy, flushed, red"; TONGUE DRY (non-serious) with onset 12Nov2021, outcome "unknown", described as "tongue got very, very dry"; NEURALGIA (non-serious) with onset 12Nov2021, outcome "not recovered", described as "Felt little pricks of nerve endings all over her body, in different parts of her body". Therapeutic measures were taken as a result of paraesthesia, flushing, pruritus, flushing. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2109512

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: OH
Alter: 31,0
Geschlecht: M
Eingang: 13.02.2022
Impfdatum: 01.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 30,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Abdominal pain upper Colitis ulcerative Colonoscopy abnormal Condition aggravated Haematochezia Haemorrhoids Sigmoidoscopy abnormal

Symptomtext

(Privacy) living in (Privacy) (sorry for the typos mistakes !). Apparition of a chronic disease (ulcerative colitis). After the second shot lot # EW0164 Pfizer April 11 \2021\ : blood in my stool (apparition - did not think it was linked) I was thinking the blood was due to h?morro?des, and so I did not see a doctor for this. After my 3nd dose : Nov 13 \2021\, Pfizer #FH8028 : A lot of pain in the stomach end of november. Consultation of a doctor, colonoscopy done jan 7 2022 : ulcerative colitis highlighted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Sigmoidoscopy dec 22 \2021\ in (Privacy) Colonoscopy jan 7 2022 in the (Privacy). Both confirm the diagnostic.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 2103929

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: WA
Alter: 51,0
Geschlecht: M
Eingang: 11.02.2022
Impfdatum: 09.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Blood urine Chills Dyskinesia Fatigue Feeling jittery Headache Insomnia Muscle spasms Muscle twitching Physical examination Tremor

Symptomtext

MILD HEADACHE; TIREDNESS; MUSCLES JERKED (ARMS OR HEAD FLINCHED) WHEN TRIED TO SLEEP; MUSCLE TWITCHING ON BOTH SIDES OF BODY (CALFS, THIGHS, NECK, HANDS); HAND SHAKED LIKE ESSENTIAL TREMOR; GOT ZERO HOURS OF SLEEP; FELT JITTERY; FEELING OF CRAMP IN BOTH CALFS; SHAKING IN HEAD, LEGS AND OTHER PLACES TOO (LIKE A CONSTANT CHILL); JOINT PAIN IN FOREARMS, WRISTS AND FINGERS OF BOTH SIDES; FELT FATIGUE MORE THAN NORMAL IN LEGS, PARTICULARLY IN CALFS AFTER RUNNING; MILD HEADACHE; TIREDNESS; This spontaneous report received from a patient via other manufacturer (Pfizer) concerned a 51 year old male with unspecified race and ethnic origin. The patient's height, and weight were not reported. Patient had a healthy family history and had no medical issues. Patient ran 20 miles per week and had very good annual physical results. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, intramuscular, batch number: 1808980, expiry: unknown) dose was not reported, 1 total administered to top left arm on 31-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date after the first shot of J&J, the patient experienced mild headache and tiredness for about 24 hours and then had no issues (dose number in series 1). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from mild headache, and tiredness. The patient received non-company booster BNT 162 (Pfizer) vaccine (dose number in series 2) (form of admin was not reported, intramuscular, batch number: FH8028, expiry: unknown) dose was not reported, 1 total administered to top left arm on 09-NOV-2021 at 13:00 hours for prophylactic vaccination. No concomitant medications were reported. In NOV-2021, the patient had mild headache and tiredness for 24 hours so it all seemed fine but then after 5 or 6 days after receiving Pfizer shot, Patient had weird symptoms that had started to appear. First symptom was muscle jerks he when tried to sleep (arms or head would flinch so much, it made him wake up so basically and had zero hours of sleep). The following days the muscle jerks reduced but in their place was muscle twitching on both sides of body especially at rest (calfs, thighs, neck, hands). Patient also felt like he was connected to a battery of something. Patient also felt jittery. His entire body was like this could hold hands out in front and they would shake like a essential tremor. He felt like shaking in head, legs and other places too (almost like a constant chill). This continued for about 5 weeks, reducing slightly in intensity. The next symptom was the feeling of cramp in both calfs, it felt like he always needed to stretch them. Patient also noticed that after running, he felt more fatigue than normal in the legs, particularly in calfs. Patient's final symptom was joint pain, especially in forearms, wrists and fingers of both sides. Eight weeks after Pfizer shot, Patient had some symptoms they have reduced in intensity by at least 75 percent at the time of reporting. Internal tremor was very light and hands barely shaked then and joints were not as rigid and muscle twitching was minimal when patient went to sleep. Laboratory data (dates unspecified) included: Blood urine (NR: not provided) very good, and Physical examination (NR: not provided) very good. The action taken with bnt 162 was not applicable. The patient recovered from mild headache, and tiredness, and was recovering from muscles jerked (arms or head flinched) when tried to sleep, muscle twitching on both sides of body (calfs, thighs, neck, hands), felt jittery, hand shaked like essential tremor, shaking in head, legs and other places too (like a constant chill), feeling of cramp in both calfs, felt fatigue more than normal in legs, particularly in calfs after running, joint pain in forearms, wrists and fingers of both sides, got zero hours of sleep, mild headache, and tiredness. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Name: Blood urine; Result Unstructured Data: very good; Test Name: Physical examination; Result Unstructured Data: very good
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient family history was healthy, no medical issues. Patient ran 20 miles per week and had very good annual physical results.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2095597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MN
Alter: 44,0
Geschlecht: F
Eingang: 08.02.2022
Impfdatum: 19.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Back pain Blood test normal Chest X-ray Chills Decreased appetite Dyspnoea Electrocardiogram normal Headache Influenza A virus test negative Pain in extremity Pyrexia SARS-CoV-2 test negative

Symptomtext

It started the following day of getting the vaccine. So, I got chills, low grade fever, headache, and then it got worse. Sunday I got a 102 temp and my headache got worse. I suffered with it the following next week. On 1/24/2022 I had a tele-health visit and that doctor told me that it was no way it was the vaccine and that I should get a COVID-19 and Flu test done. The next evening 1/26/2022 I notice that I was having shortness of breath, pain in my right calf, and a pain in my upper back for about three days. So I went to the ER that same evening and they said I still was having fever. They ran a lot of test and they all were negative. The fever has been intermitted on and off. I work from home and I still don't feel 100%. I also had a very bad case of COVID-19 and Pneumonia November 2020. My kidneys started shutting down and I had no appetite, not thirsty at all. I also had an anti body test in October 2021 and my body showed high anti-body and I didn't have to get it. I only took the COVID-19 because I knew that I have a lot of vacations and I didn't want to get sick.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19, Flu, A & B, EKG, Chest X-ray and Blood test, all were negative.
Aktuelle Erkrankungen: No
Vorgeschichte: Chronic Lyme Disease and Asthmas and Seasonal Allergies.
Andere Medikamente: No
Allergien: Penicillin, Morphine, Latex, Eggs, Dairy, and Gluten
Vorherige Impfungen: Flu vaccine, 19 years ago.

VAERS 2092548

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: NY
Alter: 52,0
Geschlecht: F
Eingang: 07.02.2022
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain Chills Dyspnoea Fatigue Hyperhidrosis Menstrual disorder Pain in extremity Pelvic pain

Symptomtext

Had alot of bad bad pain in right arm, Got sweats and chills. Menstrual cycle changed. Fatigued everyday. Shortness of breathe, pain in pelvic area and chest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Lyme disease.
Vorgeschichte: Lyme disease.
Andere Medikamente: No.
Allergien: No.
Vorherige Impfungen: -

VAERS 2092441

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: NJ
Alter: 37,0
Geschlecht: M
Eingang: 07.02.2022
Impfdatum: 19.11.2021
Beginn: 06.02.2022
Tage bis Beginn: 79,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

Admitted with shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: 02/06/2022 - SARS-COV-2 Antigen (++)
Aktuelle Erkrankungen: -
Vorgeschichte: Hyperlipidemia
Andere Medikamente: Atorvastatin 10 mg po daily
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2206368

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: -
Alter: 53,0
Geschlecht: M
Eingang: 04.02.2022
Impfdatum: 05.11.2021
Beginn: 23.12.2021
Tage bis Beginn: 48,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Activated partial thromboplastin time normal Ageusia Anosmia Blood fibrinogen increased Brain natriuretic peptide increased COVID-19 COVID-19 pneumonia Chest X-ray normal Cough Dyspnoea Fatigue Fibrin D dimer Headache International normalised ratio increased Myalgia Oropharyngeal pain Procalcitonin Prothrombin time normal

Symptomtext

Narrative: COVID infection following COVID vaccine series 03/25, Pfizer, dose #1 04/16, Pfizer, dose #2 11/05, Pfizer, dose #3 12/26 COVID swab, result: detected 12/23 pt cc: cough, fatigue, headache, loss of taste or smell, myalgias, rhinorrhea, sore throat exposure: unknown 12/26 pt medicine cc: cough sob dx: Covid Pneumonia LOS: 4 days APTT 35.2 12/26 SARS-COV-2 Variant Sequencing: pending 12/26 CXR impression: No acute cardiopulmonary disease. 12/26 INR; 1.11 12/26 DDIMER: 0.41 12/26 PT: 12.4 12/26 12/26 BNP: 104.8 12/27 FIBRINOGEN: 596 12/27 DDIMER: 0.26 12/27 PROCALCITONIN: <0.05 12/27 ESR: 20 12/28 FIBRINOGEN: 506 12/28 DDIMER: 0.30 12/28 ESR: 27 12/29 FIBRINOGEN: 430 12/29 DDIMER: 0.27 12/29 ESR: 24 12/29 CXR impression: No acute cardiopulmonary disease.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: 12/26 COVID swab, result: detected 12/26 APTT 35.2 12/26 SARS-COV-2 Variant Sequencing: pending 12/26 INR; 1.11 12/26 DDIMER: 0.41 12/26 PT: 12.4 12/26 12/26 BNP: 104.8 12/26 CXR impression: No acute cardiopulmonary disease. 12/27 FIBRINOGEN: 596 12/27 DDIMER: 0.26 12/27 PROCALCITONIN: <0.05 12/27 ESR: 20 12/28 FIBRINOGEN: 506 12/28 DDIMER: 0.30 12/28 ESR: 27 12/29 FIBRINOGEN: 430 12/29 DDIMER: 0.27 12/29 ESR: 24 12/29 CXR impression: No acute cardiopulmonary disease.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2085775

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: NC
Alter: 59,0
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: 13.11.2021
Beginn: 10.01.2022
Tage bis Beginn: 58,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Bed sharing Chills Condition aggravated Diarrhoea Dizziness Headache Hypertension Influenza like illness Interchange of vaccine products Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

Chllis head ache flu like symptons for 2-3 days after the JJ; Second vaccination was booster was Pfizer-BioNTech 11/13/2021 2-3 days after vaccation which ws the same experience with prior manufactor. 01/10/2022 symoptomatic covid experience chllis head ache flu like symptons for two weeks that included nausea, no vomiting and diareah, still maintained taste and smell. Positive on the 01/12/2022 new diagnoise of COVID annual flu vacciantion on same day. Periodic episodes of high blood pressure and dizziness. J and J intial vaccination and Nov. 16-18 2021 Pfizer-BioNTech Booster similar blood pressure and head aches lowe end blood pressure and she is asking her to monitor it over a period of time. Wave of nauseaness and chills are ongoing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: COVID test site PCR positive
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Mutivitamin for Seniors Calcium with D tablet Vitamin
Allergien: Coedien
Vorherige Impfungen: -

VAERS 2075937

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 17.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Condition aggravated Tinnitus

Symptomtext

Tinnitus became more severe, and has continued unrelenting at the increased level.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Tinnitus which began the day after receiving a numbing shot for dental work.
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2069103

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: -
Alter: 65,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 08.11.2021
Beginn: 23.01.2022
Tage bis Beginn: 76,0
Dosis: 3
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Chest discomfort Dyspnoea Fatigue Nausea SARS-CoV-2 test positive

Symptomtext

fatigue, chest tightness, short of breath, nausea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: + COVID test
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2057866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 23.01.2022
Impfdatum: 07.11.2021
Beginn: 17.01.2022
Tage bis Beginn: 71,0
Dosis: 3
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

short of breath

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 4,0
Labordaten: + COVID test
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2035845

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: -
Alter: 77,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 12.03.2021
Beginn: 13.01.2022
Tage bis Beginn: 307,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Anxiety Atrial fibrillation Blood gases Blood pH normal Brain natriuretic peptide increased COVID-19 Chest X-ray abnormal Condition aggravated Cough Crying Dyspnoea Emotional distress Exposure to SARS-CoV-2 Fatigue Wheezing

Symptomtext

78 y/o female with history of COPD, CHF, afib who p/w increased sob. The patient notes that she has been more tired for the last several days, acutely worsened sob today. She has been vaccinated and boosted for covid. She saw her daughter last Tuesday?, who is not vaccinated, and who tested positive for covid on Wednesday. She notes her daughter is fine, still in quarantine. The patient is covid positive. She is quite anxious and upset by this, crying, stating she got all her vaccines and it did her no good. I discussed with her that she currently is on 2L, and her CXR may be more related to some of her other issues than covid pna. Discussed that the vaccine is likely helping to keep her much better off than if she were not vaccinated. In the ER, ABG 7.44/32/52 on room air, saturating well on 2L. She is in afib with RVR, with history of afib as well. CXR shows possible edema vs atypical infection. BNP 1100. Admission is requested. Patient notes primary symptoms of cough, sob, and wheezing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028453

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 71,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 16.12.2021
Beginn: 09.01.2022
Tage bis Beginn: 24,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Atrial fibrillation COVID-19 Chest discomfort Dyspnoea Fatigue Pneumonia Pyrexia SARS-CoV-2 test positive

Symptomtext

DISCHARGED FROM HOSPITAL ON 12/29/21 WITH DIAGNOSIS OF PNEUMONIA AND A -FIB. PT SEEN IN OFFICE ON 1/11/22 WITH SYMPTOMS OF FATIGUE, CHEST TIGHTNESS, DYSPNEA, FEVER, SYMPTOMS WORSENED OVER LAST 2 DAYS ADMITTED TO HOSPITAL

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: POSITIVE COVID TEST
Aktuelle Erkrankungen: RECENT HOSPITILIZATION FOR PNEUMONIA
Vorgeschichte: COPD, CAD, HTN, CKD
Andere Medikamente: TRELEGY, ASPIRIN, ATORVASTATIN, OMEPRAZOLE, ELIQUIS, METOPROLOL, IRON, ROPINIROLE
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2021018

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: WA
Alter: 42,0
Geschlecht: M
Eingang: 10.01.2022
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypoaesthesia Immediate post-injection reaction Nerve conduction studies abnormal Paraesthesia

Symptomtext

Immediate tingling sensations in fingertips of left hand on three fingers (pointer, middle and ring fingers). Thought it would go away but it got worse over the course of a week and plateaued to a constant "pins and needles" numbness in those fingers, the same fingers in the right hand, and a couple toes in the right foot. Left hand is worst, then Right hand, then Right foot. No symptoms in Left Foot. Sought medical attention and the earliest I could see a doctor was 7 JAN 21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Medical exam included diagnostic evaluation for circulation issues but that did not present any issues. Discovered that when testing the ulnar nerve, the symptoms got slightly worse. I was prescribed prednisone 20 MG Oral to see if inflammation was indicative and could be reduced.
Aktuelle Erkrankungen: Sinus infection one month prior
Vorgeschichte: GERD - controlled; Hypertension - Controlled;
Andere Medikamente: Losartan - 100mg; Amlodipine - 5mg; Famotidine - 20 mg; Chlorpheniramine Maleate - 4mg
Allergien: None
Vorherige Impfungen: -

VAERS 2020647

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 70,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 03.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Heart rate increased Tachycardia

Symptomtext

Patient presented with Tachycardia on 12/04/2022 post Pfizer vaccination. Her caregiver stated her pulse was as high as 182 BPM.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: Patient's caregiver called an Ambulance, her pulse did go back down to within normal limits.
Aktuelle Erkrankungen: Patient was Diagnosed with Covid-19 on 12/21/2021. She isolated for the appropriate time. She was asymptomatic and stated she was feeling "fine" when asked. She received her Pfizer dose on 12/03/2022.
Vorgeschichte: Cardiac history
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 2018799

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 36,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Cognitive disorder Dizziness Echocardiogram Electrocardiogram Electrocardiogram ambulatory Immunisation Loss of personal independence in daily activities Magnetic resonance imaging heart Palpitations Speech disorder

Symptomtext

unable to cognitively understand statements and speak sentences; unable to cognitively understand statements and speak sentences; i started having intense heart palpitations; light-headed; dizzy; Booster; I am unable to exert energy from my body without becoming light-headed and dizzy; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 36 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 03Dec2021 13:00 (Lot number: FH8028) at the age of 36 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0150, Location of injection: Arm Right, Vaccine Administration Time: 01:00 PM), administration date: 02Apr2021, when the patient was 35 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: ENG6199, Location of injection: Arm Right, Vaccine Administration Time: 11:00 AM), administration date: 13Mar2021, when the patient was 35 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (hospitalization) with onset 03Dec2021 13:00, outcome "unknown", described as "Booster"; SPEECH DISORDER (hospitalization), COGNITIVE DISORDER (hospitalization) all with onset 15Dec2021 09:00, outcome "not recovered" and all described as "unable to cognitively understand statements and speak sentences"; PALPITATIONS (hospitalization) with onset 15Dec2021 09:00, outcome "not recovered", described as "i started having intense heart palpitations"; DIZZINESS (hospitalization) with onset 15Dec2021 09:00, outcome "not recovered", described as "light-headed"; DIZZINESS (hospitalization) with onset 15Dec2021 09:00, outcome "not recovered", described as "dizzy"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious), outcome "unknown", described as "I am unable to exert energy from my body without becoming light-headed and dizzy". The patient was hospitalized for immunisation, speech disorder, cognitive disorder, palpitations, dizziness, dizziness (hospitalization duration: 1 day(s)). The events "unable to cognitively understand statements and speak sentences", "unable to cognitively understand statements and speak sentences", "i started having intense heart palpitations", "light-headed" and "dizzy" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: echocardiogram: unknown result; electrocardiogram: unknown result; electrocardiogram ambulatory: wear a 48 hour holter monitor; magnetic resonance imaging heart: unknown results, notes: receive a cardiac MRI. Therapeutic measures were taken as a result of speech disorder, cognitive disorder, palpitations, dizziness, dizziness. Clinical information: 12 days after vaccine, i started having intense heart palpitations, light-headed, dizzy, and unable to cognitively understand statements and speak sentences. This has not resolved in two weeks. This has caused me to have EKG's, Echocardiogram, be prescribed a beta blocker, wear a 48 hour Holter monitor and receive a cardiac MRI. I have seen my primary care physician and also an electrophysiologist, all who have confirmed this is likely from the booster shot I received. I am unable to exert energy from my body without becoming light-headed and dizzy, with palpitations following. No other vaccine in four-weeks and also no other medications in two-weeks. No covid prior vaccination and no covid tested post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: 1,0
Labordaten: Test Name: Echocardiogram; Result Unstructured Data: Test Result:Unknown result; Test Name: EKG; Result Unstructured Data: Test Result:Unknown result; Test Name: Holter monitor; Result Unstructured Data: Test Result:wear a 48 hour Holter monitor; Test Name: MRI; Result Unstructured Data: Test Result:Unknown results; Comments: receive a cardiac MRI
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2018284

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: OH
Alter: 69,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 06.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Back pain Chest pain Fatigue Immunisation Lymphadenopathy Myalgia Pain Pain assessment SARS-CoV-2 test

Symptomtext

Pain scale=10; extreme fatique; Experiencing swollen lymph node pain in my left armpit area; Both shoulders and knee joints very painful; Chest, upper/lower back and knee joints very painful; Upper/lower back and knee joints very painful; Booster received; Muscle/ joint pain; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 06Dec2021 10:15 (Lot number: FH8028) at the age of 69 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "High Blood Pressure" (unspecified if ongoing); "IBS-D" (unspecified if ongoing). Concomitant medication(s) included: LOTRONEX; MICARDIS; HCT; ANACIN [ACETYLSALICYLIC ACID;CAFFEINE]. Past drug history included: Known allergies: codeine, reaction(s): "Known allergies: Codeine allergy". Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ED6955, Location of injection: Arm Right, Vaccine Administration Time: 09:00 AM), administration date: 27Mar2021, when the patient was 68 years old, for COVID-19 Immunization, reaction(s): "No adverse events"; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6199, Location of injection: Arm Right, Vaccine Administration Time: 01:00 PM), administration date: 06Mar2021, when the patient was 68 years old, for COVID-19 Immunization, reaction(s): "No adverse events". The following information was reported: IMMUNISATION (non-serious) with onset 06Dec2021 10:15, outcome "unknown", described as "Booster received"; PAIN (non-serious) with onset 06Dec2021 23:00, outcome "recovered with sequelae" (08Dec2021), described as "Pain scale=10"; FATIGUE (non-serious) with onset 06Dec2021 23:00, outcome "recovered" (Dec2021), described as "extreme fatique"; LYMPHADENOPATHY (non-serious) with onset 06Dec2021 23:00, outcome "not recovered", described as "Experiencing swollen lymph node pain in my left armpit area"; ARTHRALGIA (non-serious) with onset 06Dec2021 23:00, outcome "recovered with sequelae" (08Dec2021), described as "Both shoulders and knee joints very painful"; CHEST PAIN (non-serious) with onset 06Dec2021 23:00, outcome "recovered with sequelae" (08Dec2021), described as "Chest, upper/lower back and knee joints very painful"; BACK PAIN (non-serious) with onset 06Dec2021 23:00, outcome "recovered with sequelae" (08Dec2021), described as "Upper/lower back and knee joints very painful"; MYALGIA (non-serious) with onset Dec2021, outcome "recovered" (08Dec2021), described as "Muscle/ joint pain". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pain, fatigue, lymphadenopathy, arthralgia, chest pain, back pain. Additional information: Prior to the vaccination, patient not had COVID-19. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. Pain/fatigue lasted entire day & night on 07Dec2021. 08Dec2021 muscle/joint pain gone, however patient still experiencing swollen lymph node pain in my left armpit area as of 10Dec2021 four dates post booster. No adverse events post 1st and 2nd vaccine doses. This case was non serious. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20211206; Test Name: Pain scale; Result Unstructured Data: Test Result:10; Comments: Pain scale= 10; Test Date: 20211207; Test Name: BinaxNOW; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Irritable bowel syndrome
Andere Medikamente: LOTRONEX; MICARDIS; HCT; ANACIN [ACETYLSALICYLIC ACID;CAFFEINE]
Allergien: -
Vorherige Impfungen: -

VAERS 2018256

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: WA
Alter: 67,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Immunisation Vaccination site erythema Vaccination site pruritus Vaccination site swelling

Symptomtext

swelling a little bit at the injection site was reported as worsened/ a little red at the injection site was reported as worsened/ itching at the injection site was reported as worsened; swelling a little bit at the injection site; a little red at the injection site; itching at the injection site; Booster dose; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 67 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 07Dec2021 (Lot number: FH8028) at the age of 67 years as dose 3 (booster) , single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose:1, Lot,no- EN6201), administration date: 11Feb2021, when the patient was 66 years old, for COVID-19 Immunization; Bnt162b2 (Dose:2, EN6206), administration date: 06Mar2021, when the patient was 66 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 07Dec2021, outcome "unknown", described as "Booster dose"; VACCINATION SITE SWELLING (non-serious) with onset 08Dec2021, outcome "not recovered", described as "swelling a little bit at the injection site"; VACCINATION SITE ERYTHEMA (non-serious) with onset 08Dec2021, outcome "not recovered", described as "a little red at the injection site"; VACCINATION SITE PRURITUS (non-serious) with onset 08Dec2021, outcome "not recovered", described as "itching at the injection site"; CONDITION AGGRAVATED (non-serious), outcome "unknown", described as "swelling a little bit at the injection site was reported as worsened/ a little red at the injection site was reported as worsened/ itching at the injection site was reported as worsened". Therapeutic measures were not taken as a result of vaccination site swelling, vaccination site erythema, vaccination site pruritus. Additional information: No other products and no patient history. There was no investigation assessment. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2001617

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: FL
Alter: 79,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 17.02.2021
Beginn: 02.01.2022
Tage bis Beginn: 319,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Abnormal behaviour Asthenia COVID-19 Cough Exposure to SARS-CoV-2 Mental status changes Mobility decreased Muscular weakness Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st Vaccine received 01/24/2021. Pt brought to ER from ALF with AMS, generalized weakness, fever and dry cough. Per daughter, pt had recent Covid exposure and over the last 6 hours has been unable to get out of chair, left leg is weaker and she is not acting like herself. Pt receiving IV ABX and steroids. On O2 at 2L NC and O2 sat 100%.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19 -Detected 01/02/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes, HTN, Lewy Body disease, Vitamin b deficiency, Hyperlipidemia , hx of ecoli/enterococcal UTI, Thoracic fx
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2001237

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: AZ
Alter: 54,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Condition aggravated Disturbance in attention Hypoacusis Sleep disorder Tinnitus

Symptomtext

I developed worsening tinnitus after receiving the booster dose of Covid19 - Pfizer-BioNTec Vaccine. I noticed tinnitus after my second dose given on 1/7/2021 of Pfizer. After the 3rd dose I have experienced a constant higher pitched tinnitus. The symptoms have become bothersome and interferes with my normal hearing. It has also interfered with my concentration and sleep.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: I will make an appointment with an ENT as soon as possible.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Levothyroxine, Liothyronine
Allergien: NKA
Vorherige Impfungen: Covid19-Pfizer-BioNTech, 01/07/2021 (2nd Dose)

VAERS 2001081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: NY
Alter: 64,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site pain Injection site swelling Mobility decreased Pain in extremity

Symptomtext

Site: Pain at Injection Site-Severe, Site: Swelling at Injection Site-Medium, Additional Details: Patient experienced extreme pain in her left arm since her vaccination in November. Area is swollen, and marked with round circle. Patient has trouble lifting her arm. Confirmed over the phone that it was not SIRVA- vaccine was administered in mid arm, not too high to shoulder.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1997683

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

moderat

Staat: PA
Alter: 48,0
Geschlecht: M
Eingang: 02.01.2022
Impfdatum: 11.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood pressure increased Epistaxis Extrasystoles Heart rate irregular Palpitations Tinnitus

Symptomtext

pounding heart, especially in bed at night. irregular heartbeat, like skipping every 3rd beat then double-beating the 4th beat. Nose bleeds and ears are ringing. i think my blood pressure might be high now. afraid to go to a doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: one-a-day multi-vitamin
Allergien: -
Vorherige Impfungen: covid-19 pfizer, 10/6/21

VAERS 1995597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: -
Alter: 51,0
Geschlecht: M
Eingang: 31.12.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Immunisation Interchange of vaccine products Muscle fatigue Muscle twitching Tremor

Symptomtext

Muscle twitching calfs, arms, neck etc (both sides of body),; Internal tremor; some muscle fatigue in calfs and forearms; Dose 1: J&J COVID-19 vaccine and Dose 2: Pfizer COVID-19 vaccine; Dose 1: J&J COVID-19 vaccine and Dose 2: Pfizer COVID-19 vaccine; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 51-year-old male patient received bnt162b2 (BNT162B2), administered in left arm, administration date 09Nov2021 at 13:00 (Lot number: FH8028) at the age of 51 years as dose 2 (booster), single for COVID-19 immunisation. Relevant medical history included: "Penicillin allergy" (unspecified if ongoing), notes: known allergies: penicillin. There were no concomitant medications. Vaccination history included: Jnj 78436735 (DOSE 1, SINGLE, Lot Number: 1808980, Anatomical site: Left Arm), administration date: 31Mar2021, when the patient was 50 years old, for COVID-19 immunisation. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious), IMMUNISATION (non-serious) both with onset 09Nov2021 at 13:00 , outcome "unknown", and both described as "Dose 1: J&J COVID-19 vaccine and Dose 2: Pfizer COVID-19 vaccine"; MUSCLE TWITCHING (non-serious) with onset 15Nov2021, outcome "not recovered", described as "Muscle twitching calfs, arms, neck etc (both sides of body),"; TREMOR (non-serious) with onset 15Nov2021, outcome "not recovered", described as "Internal tremor"; MUSCLE FATIGUE (non-serious) with onset 15Nov2021, outcome "not recovered", described as "some muscle fatigue in calfs and forearms". The events "Muscle twitching calfs, arms, neck etc (both sides of body),", "Internal tremor" and "some muscle fatigue in calfs and forearms" were evaluated at the physician office visit. Therapeutic measures were not taken as a result of muscle twitching, tremor and muscle fatigue. Additional Information: Other medical history was reported as None, healthy. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to COVID-19 vaccine. It was reported that symptoms were still there 6 weeks after second shot and he did not have these symptoms after the first shot and its very concerning and it was reported that will those ever dissipate. Since the vaccination, the patient had not been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy (known allergies: penicillin)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1995424

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: SC
Alter: 52,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 30.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Bone pain Chills Decreased appetite Diarrhoea Immunisation Nausea Pain Pyrexia Tremor Vomiting Weight decreased

Symptomtext

High fever x2 days - 102.5; Nausea and vomiting x1 day; Nausea and vomiting x1 day; Bone and body pain x2 days; Bone and body pain x2 days; Severe body shakes, chills x1 day; Severe body shakes, chills x1 day; Anorexia x3 days; Weight loss 5 pounds; Diarrhea; Dose Number:3; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 52 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 30Nov2021 13:00 (Lot number: FH8028) at the age of 52 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Prev dose Product: COVID 19, Prev dose Brand: Pfizer, Prev dose lot number: EW 0158, Prev dose Administration time: 09:30 AM, Prev dose Vaccine location: Left arm, Dose number: 2), administration date: 20Apr2021, when the patient was 51 years old, for COVID-19 Immunization; Bnt162b2 (Prev dose Product: COVID 19, Prev dose Brand: Pfizer, Prev dose lot number: ER8727, Prev dose Administration time: 09:30 AM, Prev dose Vaccine location: Left arm, Dose number: 2), administration date: 01Apr2021, when the patient was 51 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 30Nov2021 13:00, outcome "unknown", described as "Dose Number:3"; PYREXIA (non-serious) with onset 30Nov2021 23:00, outcome "recovered" (02Dec2021), described as "High fever x2 days - 102.5"; NAUSEA (non-serious), VOMITING (non-serious) all with onset 30Nov2021 23:00, outcome "recovered" (01Dec2021) and all described as "Nausea and vomiting x1 day"; BONE PAIN (non-serious), PAIN (non-serious) all with onset 30Nov2021 23:00, outcome "recovered" (02Dec2021) and all described as "Bone and body pain x2 days"; CHILLS (non-serious), TREMOR (non-serious) all with onset 30Nov2021 23:00, outcome "recovered" (01Dec2021) and all described as "Severe body shakes, chills x1 day"; DECREASED APPETITE (non-serious) with onset 30Nov2021 23:00, outcome "recovered" (03Dec2021), described as "Anorexia x3 days"; WEIGHT DECREASED (non-serious) with onset 30Nov2021 23:00, outcome "recovered" (2021), described as "Weight loss 5 pounds"; DIARRHOEA (non-serious) with onset 30Nov2021 23:00, outcome "recovered" (2021), described as "Diarrhea". The events "high fever x2 days - 102.5", "nausea and vomiting x1 day", "nausea and vomiting x1 day", "bone and body pain x2 days", "bone and body pain x2 days", "severe body shakes, chills x1 day", "severe body shakes, chills x1 day", "anorexia x3 days", "weight loss 5 pounds" and "diarrhea" were evaluated at the physician office visit. Therapeutic measures were taken as a result of pyrexia. Additional information: The patient did not receive any other vaccine within 4 weeks prior to the COVID vaccine. Reportedly, patient was not diagnosed with COVID-19 prior to vaccination. Patient had not been tested for COVID-19 since the vaccination. No Hospitalization Prolonged. Tylenol for fevers was provided as treatment received for the adverse event. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: None known allergies: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1992356

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 60,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Abdominal pain Abdominal pain lower Adverse food reaction Asthenia Chest pain Decreased appetite Dizziness Dyspnoea Exercise tolerance decreased Fatigue Feeling abnormal Feeling cold Glossodynia Headache Heart rate abnormal Heart rate increased Impaired driving ability Injected limb mobility decreased

Symptomtext

DAY 1: Needed help walking out after shot due to dizziness within 15 minutes. Could hardly raise shot arm wihin 45 minutes. Extremely tired within an hour. Cold and achy started overnight. DAY2: cold, extremely achy, headache, dizzy, weak. Fever increased throughout day. Peaked at 101.9F at 2:45pm. Sharp pain in lower left abdomen. Rumbly tummy. Pulse spiking high with no exertion. Resting heart rate in 120's (my normal is high 60's). Out of breath without any exertion. Lungs feel like they're on fire. Oxygen varied between 85%-95% (my normal is 99-100%). Confirmed by PulseOx. Drank water or gateraide every hour or two. No appetite, but forced myself to eat light foods. DAY 3: Improving a bit, but lungs feel raw.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: X-rays of right knee, leg, ankle to see if anything mechanically wrong. All looked normal. Doctor could find no explanation for the nerve pain on the front of right shin.
Aktuelle Erkrankungen: none
Vorgeschichte: GERDS, asthma, osteopenia, fibromyalgia, endometriosis, lactose intolerance, prior history of Lyme Disease and PCOS.
Andere Medikamente: Nexium (20mg), Citracal minis, Citracal Max Plus, Lactaid
Allergien: PCN,Thimerosal, Flagyl, Cipro,Zetia, Simvastation, Prevastatin
Vorherige Impfungen: Strong reaction to Tdap immunization shot 7/1/2009 (age 48). Felt like a bad flu for 3 or 4 days.

VAERS 1984760

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH 8028

moderat

Staat: FL
Alter: 24,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 03.04.2021
Beginn: 27.12.2021
Tage bis Beginn: 268,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Arthralgia COVID-19 Chest pain Dyspnoea Exposure to SARS-CoV-2 Flank pain Pain Painful respiration Pyrexia SARS-CoV-2 test positive

Symptomtext

Pt presented to ED with c/o SOB x1 week and c/o CP with deep breath that radiates to Left side and shoulder. Febrile Tmax 101.9, HR 110's and RR 30's. Pt is fully vaccinated with booster. Had exposure to coworkers who tested positive for Covid19. Pt now Covid +. Given po/IV steroids and abx.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19 detected on 12/27/21.
Aktuelle Erkrankungen: -
Vorgeschichte: Lupus, anemia, anxiety
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 1984204

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: LA
Alter: 36,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 26.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Full blood count Hypoaesthesia Metabolic function test Paraesthesia

Symptomtext

Parasthesia (Numbness and tingling) to left leg. ER visit. Blood tests performed. Symptoms lasted 2 days then subsided, but numbness still present.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: CBC BMP on 11/28/21
Aktuelle Erkrankungen: -
Vorgeschichte: Thyroid disease
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1981745

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: OH
Alter: 39,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 02.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Abdominal distension Anxiety Chest discomfort Chills Choking sensation Dyspnoea Feeling abnormal Gastrointestinal disorder Gastrooesophageal reflux disease Headache Herpes zoster Inflammation Influenza like illness Laryngoscopy abnormal Nausea Neuralgia Pain Paraesthesia

Symptomtext

Booster Pfizer 12/02/2021 Fly like symptoms for 3 full days. Fever, chills, aches, nausea, headache 12/08/21 - string asthma like symptoms, tightness in throat, choking feeling, heaviness in chest, ( this comes in huge waves along with rushing nerve pain. I feel breathless when all of this is happening. It?s triggered if I move around too much. Any activity. My digestive system is not acting normal. My food sits in my stomach. All of my insides feel inflamed and tingly. Severe waves of brain fog. All of my symptoms come in waves and happen 2-3 times per day and then I have times where they calm down. When my symptoms flare it cause panic feelings because of the tightness in my throat. It?s very distressing. I was treated for possible asthma due to the breathing issues. Asthma meds were not relieving my symptoms like they usually would. That?s when I knew something else was going on. My steroid inhaler that she prescribed does seem to calm these odd ?episodes? I?m having and after intake mini breathe better but the tightness is non stop and unrelenting. I have also had significant bloating in my abdomen that is not normal for me. On December 23 I developed a rash that turned into blisters. I was diagnosed with shingles. I am 39. Saw pulmonologist, ENT ( did a scope), and a gastro. Leading up to my shingles diagnoses. I believe the vaccine brought on shingles for me along with these breathing issues. I feel like I have inflammation in all areas of my body. Even my thinking is effected during the flares.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/20/21-Pulmonary dr- breathing test- normal 12/22/21 ENT- scope of throat =found inflammation from acid reflux but nothing else 12/23/21 Gastro- no tests 12/23/21 -Medical facility =diagnosed Shingles (blisters)
Aktuelle Erkrankungen: -
Vorgeschichte: Mild asthma Hashimotos hypothyroid disease ( treated)
Andere Medikamente: Tirosint 150mcg Prenatal vitamin
Allergien: None
Vorherige Impfungen: H1N1 September 2009

VAERS 1981736

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: CA
Alter: 32,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 20.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Angiogram Blood test Chest X-ray Chest pain Chills Computerised tomogram Dyspnoea Electrocardiogram Fibrin D dimer increased Full blood count Injection site pain Metabolic function test Nausea Pain Pain in extremity Pregnancy test Pruritus Pyrexia

Symptomtext

Symptoms started with sore arm at injection site 1 hour after shot. Within 12 hours got chills, low fever 100.5~, sore arm, nausea, blurry vision, body pain all over, rash on left forearm that started to spread all over, day 2 rash spreading more around the arm and moving upwards on forearm and itchiness intensified even with Claritin and hydrocortisone. Thursday morning started having difficulty breathing in deeply with chest pain and throat closing up so headed to ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 12-23-21: At the ER, got blood test, CT-Scan, EKG, and Epipen. Lab tests: CBC with Differential, Comprehensive Metabolic Panel, D-Dimer, Pregnancy, Serum, Qual, Troponin I. Image Testing: CT Angio Pulmonary w Contrast, ECG 12 lead, XR Chest PA or AP. Medication given: diphenydrAMINE (Benadryl), EPHINEPHrine auto-injector, famotidine(PEPCID), HYDROcodone-acetaminophen(NORCO), iohexol, loratadine, methylpredinesolone sodium succinate, sodium chloride. NOTES: Blood test showed that I had high D-Dimer than normal so did a ct-scan to check for blood clot in lungs. Due to me moving during the scan they couldn't see a clear scan of the lung but said they didn't find a large clot. Doctor said it could have been a small clot. They injected me Prednisone, Benadryl, and IV Fluid at the end to drop my high heart beat.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1977153

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: HI
Alter: 20,0
Geschlecht: M
Eingang: 23.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chest pain Dizziness Electrocardiogram Hyperhidrosis

Symptomtext

Pt received 1st dose of Pfizer vaccine @ 1126. At appx 1133 pt c/o feeling dizzy and appeared diaphoretic. RN assisted pt to wheelchair, VS HR 47, BP 75/45, O2 99% RA. @ 1138 pt c/o chest pain, ambulance called, O2 4L NC applied. @1140 retook VS BP 117/72, HR 45. O2 99% 2L NC. @1145 retook VS BP 119/88, HR 56, 100% 2L NC, T 96.9F. EMS arrived @ 1146. EMS assessed and obtained EKG. Pt stable. Offered to take pt to ER, pt declined, was here with family. Unsure whether he will take himself to ER w/ family. Encouraged pt to follow up with PCP prior to receiving 2nd shot, pt verbalizes understanding. Profile is flagged for adverse reaction to 1st dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1975301

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: CA
Alter: 32,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Asthenia Blood test Electrocardiogram Fatigue Hot flush Hypoaesthesia Muscle spasms Myalgia Pain Paraesthesia Urine analysis

Symptomtext

After first dose, given on 11/5/2021, I had weakness, fatigue, pain in left arm/ muscle/body aches, hot flashes/chills that started the next day. Muscle aches went pretty much away after 2 weeks but weakness and fatigue never subsided and had to get second dose on 11/26/2021. After second dose weakness, fatigue, muscle/body aches and spasms, hot flashes, occasional mild tingling/numbness in legs/one arm(usually right) are still present.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Multiple blood tests on different dates, Urine, Electrocardiograms
Aktuelle Erkrankungen: N/A
Vorgeschichte: Depression, Anxiety/PTSD
Andere Medikamente: Trileptal, Buspar, Retin-A, Women's multivitamin, occasionally Ibuprofen for menstrual cramps
Allergien: Lamictal
Vorherige Impfungen: Flu vaccine, estimated age: 25, information unknown: weakness, fatigue, nausea, loss of appetite for about 2 weeks. In compari

VAERS 1974763

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: PA
Alter: 65,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Asthenia Decreased appetite Headache Hyperhidrosis Injected limb mobility decreased Pain in extremity Pyrexia

Symptomtext

My left arm was sore for about 2 weeks; I had difficulty lifting, headaches, feverish, no appetite, weak and feeling sweaty. As of present still experiencing low grade headaches and no energy and appetite has changed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: 1,0
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Fibromyalgia, High Blood Pressure
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1974730

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: GA
Alter: 47,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest discomfort Cough Dyspnoea Fatigue Pain

Symptomtext

Increasing shortness of breath with exertion, chest fullness, dry cough, increased fatigue and aches. Sx are intermittent since COVID vaccine booster on 12/07/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1974664

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: PA
Alter: 26,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 06.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Angiopathy Headache Magnetic resonance imaging Migraine

Symptomtext

Day one after first dose, started with a slight headache which later developed into a 3 day migraine type with zero relief despite medication and hydration attempts. Then resolved. Second dose then gave me a constant headache with no relief from medication and hydration attempts. At times i feel a pulse in my head when bending over. some days i cannot get out of bed due to the pounding feeling and how heavy my head feels. Went to PCP, they ordered MRI/MRA and referral to neurology.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Pending result of MRI/MRA, scheduled for 01/03/2022 Pending referral to Neurology, scheduled for 12/23/2021
Aktuelle Erkrankungen: no illnesses noted
Vorgeschichte: anxiety and depression
Andere Medikamente: Atarax 25mg, PRN Prenatal Vitamin daily Valtrex, PRN with outbreaks(none currently)
Allergien: Doxyclicline, rash.
Vorherige Impfungen: -

VAERS 1974301

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: ID
Alter: 13,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Angiogram Dyspnoea Echocardiogram Electrocardiogram Fatigue Heart rate Heart rate increased Investigation Oropharyngeal pain Pyrexia SARS-CoV-2 test

Symptomtext

Rapid resting heart rate (130-250); shortness of breath; sore throat; fever; extreme fatigue; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the parent. A 13 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 06Dec2021 17:00 (Lot number: FH8028) at the age of 13 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "low iron and low vitamin d" (unspecified if ongoing), notes: Other medical history: low iron and low vitamin d; "low iron and low vitamin d" (unspecified if ongoing), notes: Other medical history: low iron and low vitamin d. No Known allergies. No other vaccine in four weeks. No covid prior vaccination. Concomitant medication(s) included: MAGNESIUM; VITAMIN D [VITAMIN D NOS]; FERRASORB [ASCORBIC ACID;FERROUS BISGLYCINATE;LEVOMEFOLIC ACID;MECOBALAMIN;PYRIDOXAL PHOSPHATE]. Vaccination history included: Bnt162b2 (Prev dose product: COVID 19, Prev dose brand: Pfizer, Prev dose brand name unknown: False, Prev dose lot number: FF2590, Prev dose Lot unknown: false, Prev dose administration date: 15Nov2021, Prev dose administration time: 05:00 PM, prev dose dose number: 1, Prev dose vaccine location: Left arm), administration date: 15Nov2021, when the patient was 13 years old, for Covid-19 immunization. The following information was reported: HEART RATE INCREASED (medically significant) with onset 06Dec2021 23:30, outcome "not recovered", described as "Rapid resting heart rate (130-250)"; DYSPNOEA (medically significant) with onset 06Dec2021 23:30, outcome "not recovered", described as "shortness of breath"; OROPHARYNGEAL PAIN (non-serious) with onset 06Dec2021 23:30, outcome "not recovered", described as "sore throat"; PYREXIA (non-serious) with onset 06Dec2021 23:30, outcome "not recovered", described as "fever"; FATIGUE (non-serious) with onset 06Dec2021 23:30, outcome "not recovered", described as "extreme fatigue". The events "rapid resting heart rate (130-250)", "shortness of breath", "sore throat", "fever" and "extreme fatigue" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: angiogram: (unspecified date) unknown results; echocardiogram: (unspecified date) unknown results; electrocardiogram: (unspecified date) unknown results; heart rate: (unspecified date) 130-250; investigation: (unspecified date) unknown results; sars-cov-2 test (Nasal Swab): (09Dec2021) negative. Therapeutic measures were taken as a result of heart rate increased, dyspnoea, oropharyngeal pain, pyrexia, fatigue and treatment included ekg's, echocardiogram, ct angiogram, heart monitor. The events resulted in: [Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care].

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: ct angiogram; Result Unstructured Data: Test Result:Unknown Results; Test Name: echocardiogram; Result Unstructured Data: Test Result:Unknown Results; Test Name: ekg's; Result Unstructured Data: Test Result:Unknown Results; Test Name: heart rate; Result Unstructured Data: Test Result:130-250; Test Name: heart monitor; Result Unstructured Data: Test Result:Unknown Results; Test Date: 20211209; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Iron deficiency (Other medical history: low iron and low vitamin d); Vitamin D deficiency (Other medical history: low iron and low vitamin d)
Andere Medikamente: MAGNESIUM; VITAMIN D [VITAMIN D NOS]; FERRASORB [ASCORBIC ACID;FERROUS BISGLYCINATE;LEVOMEFOLIC ACID;MECOBALAMIN;PYRIDOXAL PHOSPHATE]
Allergien: -
Vorherige Impfungen: -

VAERS 1972033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MO
Alter: 20,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blindness transient Dehydration Dizziness Hyperhidrosis Hypoaesthesia Immediate post-injection reaction Paraesthesia

Symptomtext

DIaphoretic, dizzy, temporary loss of vision immediately following vaccination; obtained water for patient to sip, cold compress for forehead; patient poorly hydrated and had not recently eaten when questioned; observed patient directly for 15 minutes with additional staff and patients symptoms improved- observed for an additional 15 minutes and patient reported resolution of all symptoms and was able to drive home; patient did call later in the day and reported left hand partial numbness and tingling, as well as some facial tingling; advised to call PCP and report to ER if worsening symptoms

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1971142

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: WI
Alter: 75,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 17.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia COVID-19 Confusional state Dyspnoea SARS-CoV-2 test positive

Symptomtext

Patient is a 75 y.o. female with Parkinson's disease, dysphagia s/p G tube placement, HLD and DM who presents with worsening SOB, confusion and weakness over the last 12 hours. Patient admitted as inpatient on 12/20 due to COVID-19. Patient was tested for COVID-19 and was positive on 12/20.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1963501

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: PA
Alter: 67,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 12.11.2021
Beginn: 08.12.2021
Tage bis Beginn: 26,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Dyspnoea

Symptomtext

I had SOB return. It had gone away for months. I had not dealt with this until late September. I had to use my inhaler. I went to my doctor about this. He changed my inhaler.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Chronic back pain; long haul COVID-19
Andere Medikamente: N/A
Allergien: Diary
Vorherige Impfungen: -

VAERS 1963304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: ME
Alter: 55,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 16.11.2021
Beginn: 07.12.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Cardiac flutter Chills Migraine Pain

Symptomtext

Severe chills, total body ache, severe joint pain lasting for 3 hours, starting 24 hours after shot #1 Severe chills, total body ache, severe joint pain, sever migraine lasting for 15 hours, starting 12 hours after shot #2 Fluttering in chest continues since the shots

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Migraine
Andere Medikamente: Catalyn, Immuplex, Tuna Omega-3 oil, organically bound minerals, Lisinopril.
Allergien: None
Vorherige Impfungen: -

VAERS 1961924

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MA
Alter: 45,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 29.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain Chills Menstruation irregular Nausea Pain Pyrexia Tremor Vaccine positive rechallenge

Symptomtext

Frequent chest Pain, periods are messed up. Nausea, terrible body ache, fever, chills, shaking. Same happened after 1st and 2nd shot as well. Took Advil to get fever down for 4-5 days. Body ache- very bad for 2 weeks (after 2nd and booster - 3rd shot)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Did not go to the doctor - just kept taking Advil.
Aktuelle Erkrankungen: None
Vorgeschichte: Celiac, Hypo thyroid
Andere Medikamente: Multi-vitamins and Synthroid
Allergien: Celiac (gluten intolerant), penicillin
Vorherige Impfungen: -

VAERS 1959741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: IN
Alter: 88,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 18.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Condition aggravated Deafness unilateral

Symptomtext

The patient reports complete hearing loss in the right ear in which she previously had only partial hearing loss.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Patient previously had partial hearing loss in affected ear.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1924772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: KY
Alter: 63,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 11.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Computerised tomogram Cough Dyspnoea Immunisation SARS-CoV-2 test Echocardiogram normal Laboratory test normal SARS-CoV-2 test negative Vaccination site pain

Symptomtext

booster; I got a reaction right there and that was coughing; I can't stop coughing; Started to have trouble breathing; injection site pain; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 63 year-old female patient received bnt162b2 (BNT162B2), administered in arm, administration date 11Nov2021 (Lot number: FH8028) at the age of 63 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Arthritis" (unspecified if ongoing); "Fibromyalgia" (unspecified if ongoing); "Anxiety" (unspecified if ongoing); "Seizure" (unspecified if ongoing). Concomitant medication(s) included: LAMICTAL taken for seizure; DIAZEPAM taken for anxiety; VISTARIL [HYDROXYZINE EMBONATE] taken for anxiety. Vaccination history included: Bnt162b2 (Dose: 1, Lot Number: ENS318), administration date: 03Mar2021, when the patient was 62 years old, for Covid-19 Immunization; Bnt162b2 (Dose: 2, Lot Number: CN6707), administration date: 24Mar2021, when the patient was 62 years old, for Covid-19 Immunization. The following information was reported: IMMUNISATION (hospitalization) with onset 11Nov2021, outcome "unknown", described as "booster"; DYSPNOEA (hospitalization) with onset Nov2021, outcome "unknown", described as "Started to have trouble breathing"; COUGH (hospitalization) with onset 11Nov2021, outcome "not recovered", described as "I got a reaction right there and that was coughing; I can't stop coughing"; VACCINATION SITE PAIN (non-serious) with onset Nov2021, outcome "unknown", described as "injection site pain". The patient was hospitalized for immunisation, dyspnoea, cough (hospitalization duration: 6 day(s)). The patient underwent the following laboratory tests and procedures: computerised tomogram: unknown results; sars-cov-2 test: negative, notes: She tested negative for COVID every time. Therapeutic measures were taken as a result of dyspnoea, cough, vaccination site pain. Caller states that she is taking medication to relieve her cough and they help for a little bit but it wears off for 4 hours and is disrupting her sleep. Caller states that it's making her feel exhausted. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 6,0
Labordaten: Test Name: CT Scan; Result Unstructured Data: Test Result:Unknown results; Test Name: COVID; Test Result: Negative ; Comments: She tested negative for COVID every time.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Arthritis; Fibromyalgia; Seizures
Andere Medikamente: LAMICTAL; DIAZEPAM; VISTARIL [HYDROXYZINE EMBONATE]
Allergien: -
Vorherige Impfungen: -

VAERS 1924772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: KY
Alter: 63,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 11.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Computerised tomogram Cough Dyspnoea Immunisation SARS-CoV-2 test Echocardiogram normal Laboratory test normal SARS-CoV-2 test negative Vaccination site pain

Symptomtext

booster; I got a reaction right there and that was coughing; I can't stop coughing; Started to have trouble breathing; injection site pain; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 63 year-old female patient received bnt162b2 (BNT162B2), administered in arm, administration date 11Nov2021 (Lot number: FH8028) at the age of 63 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Arthritis" (unspecified if ongoing); "Fibromyalgia" (unspecified if ongoing); "Anxiety" (unspecified if ongoing); "Seizure" (unspecified if ongoing). Concomitant medication(s) included: LAMICTAL taken for seizure; DIAZEPAM taken for anxiety; VISTARIL [HYDROXYZINE EMBONATE] taken for anxiety. Vaccination history included: Bnt162b2 (Dose: 1, Lot Number: ENS318), administration date: 03Mar2021, when the patient was 62 years old, for Covid-19 Immunization; Bnt162b2 (Dose: 2, Lot Number: CN6707), administration date: 24Mar2021, when the patient was 62 years old, for Covid-19 Immunization. The following information was reported: IMMUNISATION (hospitalization) with onset 11Nov2021, outcome "unknown", described as "booster"; DYSPNOEA (hospitalization) with onset Nov2021, outcome "unknown", described as "Started to have trouble breathing"; COUGH (hospitalization) with onset 11Nov2021, outcome "not recovered", described as "I got a reaction right there and that was coughing; I can't stop coughing"; VACCINATION SITE PAIN (non-serious) with onset Nov2021, outcome "unknown", described as "injection site pain". The patient was hospitalized for immunisation, dyspnoea, cough (hospitalization duration: 6 day(s)). The patient underwent the following laboratory tests and procedures: computerised tomogram: unknown results; sars-cov-2 test: negative, notes: She tested negative for COVID every time. Therapeutic measures were taken as a result of dyspnoea, cough, vaccination site pain. Caller states that she is taking medication to relieve her cough and they help for a little bit but it wears off for 4 hours and is disrupting her sleep. Caller states that it's making her feel exhausted. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 6,0
Labordaten: Test Name: CT Scan; Result Unstructured Data: Test Result:Unknown results; Test Name: COVID; Test Result: Negative ; Comments: She tested negative for COVID every time.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Arthritis; Fibromyalgia; Seizures
Andere Medikamente: LAMICTAL; DIAZEPAM; VISTARIL [HYDROXYZINE EMBONATE]
Allergien: -
Vorherige Impfungen: -

VAERS 1950432

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: -
Alter: 50,0
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dizziness Fatigue Headache Heart rate irregular Myalgia Palpitations

Symptomtext

Extreme fatigue Headache Muscle aches Pounding/ Irregular heartbeat Lightheaded

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Stress test and echocardiogram pending
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Cal/Mag/Zinc/D Glucosamine/ chondritin
Allergien: None known
Vorherige Impfungen: Pfizer #1 five weeks previously

VAERS 1947666

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: WA
Alter: 65,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 12.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Condition aggravated Dizziness Feeding disorder Feeling abnormal Headache Nausea Neck pain Pain in extremity Sitting disability Spinal pain

Symptomtext

Shoulder had usual soreness but by 1:30am I also had pain in head, neck, spine and if you can imagine even in my fingers and toes! I couldn't eat anything, the smell of foods made sick to my stomach, I was dizzy and couldn't even sit up... was miserable. This is day 3 and I'm just starting to feel better. The same thing happened with my 2nd dose lot#ER8737 but more intense and was ill for a longer amount of days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Spinal injury
Andere Medikamente: None
Allergien: Sulpha antibiot
Vorherige Impfungen: See item/ine#18

VAERS 1947615

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: FL
Alter: 58,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 29.10.2021
Beginn: 12.12.2021
Tage bis Beginn: 44,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

Angiogram abnormal Blood creatinine increased COVID-19 Chest X-ray normal Dyspnoea Fibrin D dimer increased Malaise Pleural effusion Serology abnormal Tachypnoea

Symptomtext

9/6/21: The patient is a very pleasant 58 year-old female who presents to the ED with worsening shortness of breath after recent diagnosis of acute COVID-19 infection. Patient developed symptoms on Tuesday and received antibody infusion on Wednesday. She later developed severe shortness of breath yesterday and sought medical attention in the ED. Upon initial evaluation patient was tachypneic with SpO2 on room air of 90%. Serologic analysis was fairly benign only notable for elevated creatinine 1.22. Chest x-ray showed no acute cardiopulmonary findings. Due to high D-dimer a CT angio chest was done ruling out acute embolism but showing right pleural effusion. Patient received first dose Pfizer vaccine on 2/24/2021 Lot # EN6203, the second dose on 3/18/2021 Lot # EN6200 and the booster shot on 10/29/2021 Lot# FH8028

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, HLD, GERD, gastritis, RA, Hypothyroidism
Andere Medikamente: -
Allergien: Demerol HCI, Oxycontin, Penicillin, Sulfa drugs
Vorherige Impfungen: -

VAERS 1944014

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MN
Alter: 41,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Anxiety Heart rate increased Paraesthesia

Symptomtext

Felt tingly all over in pelvis, arms, face and mouth. Heart rate up a little (100) but felt anxious. It subsided with in a few minutes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: Gerd
Andere Medikamente: Prilosec, lexapro, birth control, vitamin d and b complex
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1943711

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: IL
Alter: 63,0
Geschlecht: M
Eingang: 13.12.2021
Impfdatum: 01.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: SC / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Atrial fibrillation Blood glucose Computerised tomogram Electrocardiogram Fatigue Hypotension Ultrasound scan Vomiting

Symptomtext

Day 1: Tired Day 2: Vomiting Day 3 - 5 Tired Day 6: Low blood Pressure Atrial Fibrillation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: CT Scan EKG Ultrasound Blood Sugar
Aktuelle Erkrankungen: None
Vorgeschichte: Blood pressure Cholesterol
Andere Medikamente: allopurinoL 300 mg tablet apixaban 2.5 mg Tablet atorvastatin 10 mg tablet losartan 50 mg tablet multivitamin per tablet VITAMIN B COMPLEX ORAL
Allergien: None
Vorherige Impfungen: -

VAERS 1941946

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: NH
Alter: 26,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dyspnoea Immunisation Pain

Symptomtext

Dose received: 3; Serious shortness of breath frequently during the night of receiving the Pfizer COVID-19 booster shot. I also had shortness of breath as I woke up in the morning; Very painful to stand up for about 24 hours after receiving the booster shot; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 26-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 01Dec2021 at 15:45 (Lot number: FH8028) at the age of 26 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Asthma" (ongoing) and "Seasonal allergy" (unspecified if ongoing), notes: known allergies: seasonal allergies. Concomitant medication included: FLOVENT INHALER taken for Asthma as needed. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot number: EW0182; Anatomical site: right arm; Route of administration: unspecified), administration date: 03May2021, when the patient was 25 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot number: EW0187; Anatomical site: right arm; Route of administration: unspecified), administration date: 26May2021, when the patient was 25 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 01Dec2021 at 15:45, outcome "unknown", described as "Dose received: 3"; DYSPNOEA (non-serious) with onset 01Dec2021, outcome "recovered" (an unknown date in Dec2021), described as "Serious shortness of breath frequently during the night of receiving the Pfizer COVID-19 booster shot. I also had shortness of breath as I woke up in the morning"; PAIN (non-serious) with onset 01Dec2021, outcome "recovered" (02Dec2021), described as "Very painful to stand up for about 24 hours after receiving the booster shot". Therapeutic measures were not taken as a result of dyspnoea and pain. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Asthma
Vorgeschichte: Medical History/Concurrent Conditions: Seasonal allergy (Known allergies: seasonal allergies)
Andere Medikamente: FLOVENT
Allergien: -
Vorherige Impfungen: -

VAERS 1941897

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: -
Alter: 30,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Breast enlargement Chest pain Immunisation Myalgia

Symptomtext

noticed the large difference in the size of my left breast.Again, there are no lumps or signs of lymph node swelling but my entire breast is larger; experiencing left sided chest pain; felt muscular in nature; Booster; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 30 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 23Nov2021 15:30 (Lot number: FH8028) at the age of 30 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Seasonal allergies" (unspecified if ongoing), notes: other medical history: Seasonal allergies; "if covid prior vaccination: Yes" (unspecified if ongoing), notes: if covid prior vaccination: Yes. Concomitant medication(s) included: IBUPROFEN; LARISSIA; LEVOCETIRIZINE. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0169, Location of injection: Arm Left), administration date: 21Apr2021, when the patient was 29 years old, for COVID-19 immunization, reaction(s): "left breast increased in size by 1 cup size. There are no lumps and no signs of lymph node swelling"; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8730, Location of injection: Arm Right), administration date: 31Mar2021, when the patient was 29 years old, for COVID-19 immunization, reaction(s): "left breast increased in size by 1 cup size. There are no lumps and no signs of lymph node swelling". The following information was reported: IMMUNISATION (non-serious) with onset 23Nov2021 15:30, outcome "unknown", described as "Booster"; CHEST PAIN (non-serious) with onset 24Nov2021 06:00, outcome "recovered" (25Nov2021 18:00), described as "experiencing left sided chest pain"; MYALGIA (non-serious) with onset 24Nov2021 06:00, outcome "recovered" (Nov2021), described as "felt muscular in nature"; BREAST ENLARGEMENT (non-serious) with onset 25Nov2021, outcome "not recovered", described as "noticed the large difference in the size of my left breast.Again, there are no lumps or signs of lymph node swelling but my entire breast is larger". Therapeutic measures were not taken as a result of chest pain, myalgia, breast enlargement. Follow-Up (30Nov2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (if covid prior vaccination: Yes); Seasonal allergy (other medical history: Seasonal allergies)
Andere Medikamente: IBUPROFEN; LARISSIA; LEVOCETIRIZINE
Allergien: -
Vorherige Impfungen: -

VAERS 1941614

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: OR
Alter: 44,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest pain Dizziness Painful respiration

Symptomtext

PT experience chest pain, dizziness, and pain upon breathing after vaccination. These symptoms started about a minute after vaccination. EMTs were called and pt was transported to the hospital for evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1939901

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FH8028

moderat

Staat: WA
Alter: 58,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 25.10.2021
Beginn: 30.11.2021
Tage bis Beginn: 36,0
Dosis: 3
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Arteriogram coronary abnormal Blood test normal Chest pain Coronary arterial stent insertion Coronary artery occlusion Electrocardiogram normal Sleep disorder

Symptomtext

I woke in middle of night with serious chest pain, I called 911 and was taken by ambulance to the emergency room. They did an angiogram and found that my left anterior artery was blocked 90%, they put a stent in and put me on Plavix.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: EKG - Normal; Blood Work - Normal; Angiogram - Showed blockage
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic Heart Disease, Prediabetic
Andere Medikamente: Rosuvastatin 10mg daily, Betamethasone Hand Cream, Levothyroxine 125 micrograms, Fluoxetine, Magnesium Citrate, COQ10, Turmeric 450mg 2x/day, Aspirin 81mg 1x/day, Naproxen, Mineral Supplement, Blood Sugar CinnDromeX
Allergien: Sulfa Drugs, Ace Inhibitors, Losartan
Vorherige Impfungen: -

VAERS 1935069

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: -
Alter: 39,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Axillary pain Hypoaesthesia Immunisation Lymphadenopathy Paraesthesia SARS-CoV-2 test

Symptomtext

Swelling in L axilla (L arm injection); numbness and tingling in L arm, including fingers; numbness and tingling in L arm, including fingers; Pain in L axilla; dose_received: 3; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 39 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 13Nov2021 (Lot number: FH8028) at the age of 39 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EL3302), administration date: 19Jan2021, when the patient was 38 years old, for Covid-19 Immunisation; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL0142), administration date: 30Dec2020, when the patient was 38 years old, for Covid-19 Immunisation; Flu, administration date: 06Nov2021, for Immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 13Nov2021, outcome "unknown", described as "dose_received: 3"; LYMPHADENOPATHY (non-serious) with onset 14Nov2021, outcome "not recovered", described as "Swelling in L axilla (L arm injection)"; HYPOAESTHESIA (non-serious), PARAESTHESIA (non-serious) all with onset 14Nov2021, outcome "not recovered" and all described as "numbness and tingling in L arm, including fingers"; AXILLARY PAIN (non-serious) with onset 14Nov2021, outcome "not recovered", described as "Pain in L axilla". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of lymphadenopathy, hypoaesthesia, paraesthesia, axillary pain. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19. No relevant past drug history. Device Date: 15Nov2021. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 202111; Test Name: covid tested post vaccination: Yes; Result Unstructured Data: Test Result:Unknown result
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: No known allergies: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1933799

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8028

moderat

Staat: CA
Alter: 43,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Diarrhoea Myalgia Pyrexia Tremor Vomiting

Symptomtext

Fever over 102, vomiting, shaking Ng so bad that my muscles hurt for a week, diarrhea, heat rate at 169 for two days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Called an spoke with doctor as soon as the weekend was over. Although my husband wanted me to go to the hospital, I have a son who at the time was not able to be fully vaccinated, therefore I choose to ride out the affects. Honestly I should have gone.
Aktuelle Erkrankungen: Shoulder surgery on 11/04/2021
Vorgeschichte: Asthma, migraines, back pain, shoulder pain
Andere Medikamente: Promethazine 25 mg, lodartan potassium 100 mg, melatonin 10 mg, oxycodone 5 mg
Allergien: Walnuts, sunflower seeds, iodine, iv contrast
Vorherige Impfungen: -

VAERS 1932995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: FL
Alter: 74,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 26.11.2021
Beginn: 04.12.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Magnetic resonance imaging Mobility decreased Pain in extremity Tendonitis X-ray

Symptomtext

Patient says that her arm has been in a lot of pain since receiving the shot and that she can hardly move it. She says that she tried Tylenol and Advil and it helped a little, but still couldn't move her arm. She went to the doctor and they ordered MRIs and an X-ray and diagnosed with tendonitis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1930017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: CA
Alter: 32,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 27.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest pain Injection site pain

Symptomtext

Chest pain and injection site pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: High-density lipoprotein deficiency, Prediabetes, Over weight, and Ankylosing spondylitis (HCC).
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1929586

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: ID
Alter: 34,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 29.11.2021
Beginn: 06.12.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Axillary pain Cardiac flutter Chest discomfort Dizziness Feeling cold Heavy menstrual bleeding Hot flush Hunger Muscle tightness Pain in extremity Palpitations Polymenorrhoea

Symptomtext

Woke up to an extremely heavy flow, extremely light viscosity period that lasted three hours. Note that my normal period is EXTREMELY regular, almost to the hour, and was not due for another 10 days. My normal period is very light flow, heavy viscosity. The amount of blood was almost impressive. This was followed by extreme cold and extreme hunger, with an occasional hot flash, and a lot of dizziness accompanied by some heart fluttering. All of this subsided almost entirely by 3:00 p.m., and later in the evening the heart fluttering and dizziness picked up again. It relaxed for a while then around 10:00 p.m. my heart and my left arm and back (below shoulder blade) got very, very tight. I would vacillate between tightness in my chest and extreme heart pounding - I could feel my heart beat through my whole body. When I went to bed around 11:00 p.m. my heart was pounding out of my chest and it was hard to sleep because my arm and back/under shoulder blade/underarm hurt.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None. I have not been sick even with a cold in over two years.
Vorgeschichte: None.
Andere Medikamente: A multivitamin daily.
Allergien: None that I'm aware fo
Vorherige Impfungen: -

VAERS 1924515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: PA
Alter: 43,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 30.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Axillary mass Axillary pain Fatigue Headache Immediate post-injection reaction Mobility decreased Nausea Pain Pain in extremity Palpitations Pyrexia Visual impairment

Symptomtext

Immediately after receiving the vaccine my heart started racing, and my vision started going black, like I was going to pass out. My arm hurt, and towards evening I felt exhausted. I went to bed early, but then woke up at 11:30 with severe body aches, severe arm pain, a fever, and nausea. the next day I found a baseball sized lump in my right armpit that has been extremely painful to the point that I could barely move my arm. I also started having headaches. I am still suffering with headaches and occasional nausea and severe tiredness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: COUGH, SINUS CONGESTION
Vorgeschichte: N/A
Andere Medikamente: MIRENA
Allergien: N/A
Vorherige Impfungen: fluval 2018 - annaphylactic reaction - silver floating bubbles in my eyesight, my face turned bright red, trouble breathing, se

VAERS 1923965

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: NY
Alter: 30,0
Geschlecht: F
Eingang: 05.12.2021
Impfdatum: 04.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Condition aggravated Migraine

Symptomtext

Severe migraine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Migraines
Andere Medikamente: Amyltriptaline 10mg daily, vit D, folate
Allergien: -
Vorherige Impfungen: -

VAERS 1923675

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: PA
Alter: 19,0
Geschlecht: F
Eingang: 05.12.2021
Impfdatum: 06.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test Breast swelling Chest X-ray Chest pain Computerised tomogram thorax Dyspnoea Fibrin D dimer increased Heart rate increased Musculoskeletal chest pain Pain in extremity Palpitations Scan with contrast Ultrasound scan

Symptomtext

Chest pain. Shortness of breath. Pain in left arm. Pain in left rib cage. Rapid heart-rate and feeling of irregular palpitations. Swelling of upper left breast, chest area. Elevated D-Dimer level. Pain in left calf muscle

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 11/8/2021 Chest CT scan with contrast, Chest xray. EKG. Blood work 11/10/21 Ultrasound
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1921165

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

moderat

Staat: GA
Alter: 11,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 28.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chest pain

Symptomtext

chest pain and soreness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1920323

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: NJ
Alter: 45,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Crying Emotional distress Fatigue Headache Nausea Tremor Visual impairment

Symptomtext

Headache, nausea, fatigue, seeing white with eyes closed, unexplained emotional episode (10 minutes) of crying and uncontrollable shaking/psoas tremors

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Scoliosis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1912825

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: GA
Alter: 34,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypertension Palpitations

Symptomtext

Patient experienced high blood pressure, heart palpitations,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: BP
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Vitamin c Magnesium Probiotic
Allergien: NKA
Vorherige Impfungen: -

VAERS 1909909

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH 8028

moderat

Staat: MA
Alter: 51,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 01.04.2021
Beginn: 23.08.2021
Tage bis Beginn: 144,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Electrocardiogram Hypertension

Symptomtext

High blood pressure first noticed at dermatological physician visit Aug 23, 2021. Subsequent physical Nov 11, 2021 and follow up visit Nov 19, 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: EKG Nov 11, 2021, Echo scheduled for Jan 10, 2022, manual and automatic blood pressure measurements twice daily since Nov 11. Once daily ACE inhibitor Lisinopril 2.5 mg prescription started Nov 20, 2021.
Aktuelle Erkrankungen: -
Vorgeschichte: slight heart murmur
Andere Medikamente: Daily multi vitamin (One-A-Day Men's) and Vit D 500mg
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1908499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: FL
Alter: 63,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Autoimmune disorder Burning sensation Condition aggravated Eczema Erythema Off label use Product use issue Pruritus

Symptomtext

It is an exacerbation and worsening of an existing auto-immune disorder.; my hands, inner elbows and upper arms flared with eczema; it has gotten worse over five days, now involving my left shin and my face; It is red, burning, itching; It is red, burning, itching; It is red, burning, itching; Other vaccine same date veccine date 10Nov2021; Other vaccine same date veccine date 10Nov2021; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 10Nov2021 14:30 (Lot number: FH8028) at the age of 63 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Glaucoma" (unspecified if ongoing); "eczema", start date: Oct2021 (unspecified if ongoing), notes: I recently had my first eczema episode, three weeks PRIOR to the vaccine). Concomitant medication(s) included: FLU, administration date 10Nov2021. The following information was reported: AUTOIMMUNE DISORDER (medically significant) with onset 11Nov2021, outcome "not recovered", described as "It is an exacerbation and worsening of an existing auto-immune disorder."; ECZEMA (non-serious) with onset 11Nov2021, outcome "not recovered", described as "my hands, inner elbows and upper arms flared with eczema"; CONDITION AGGRAVATED (non-serious) with onset 11Nov2021, outcome "not recovered", described as "it has gotten worse over five days, now involving my left shin and my face"; ERYTHEMA (non-serious), BURNING SENSATION (non-serious), PRURITUS (non-serious) all with onset 11Nov2021, outcome "not recovered" and all described as "It is red, burning, itching"; OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 10Nov2021 14:30, outcome "unknown" and all described as "Other vaccine same date veccine date 10Nov2021". Therapeutic measures were not taken as a result of autoimmune disorder, eczema, condition aggravated, erythema, burning sensation, pruritus. Additional information: Other medical history of Glaucoma, not related to this event. No known allergies. Facility type vaccine was pharmacy or drug store. Adverse event start time was 12:00 AM. Follow-up (17Nov2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Eczema (I recently had my first eczema episode, three weeks PRIOR to the vaccine)); Glaucoma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1906004

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: CA
Alter: 62,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest discomfort Cough Dyspnoea Eye pain Fatigue Interchange of vaccine products Nasopharyngitis Ocular hyperaemia Oral candidiasis Oropharyngeal pain Pyrexia Sneezing Stomatitis Wheezing

Symptomtext

I originally got the J&J, and got the Pfizer booster. The J&J was in March of 2021. I had vey little side effects from it. When I got the Pfizer booster on 11/9/202 which is what I reporting on here, I got immediate and terrible reactions. First, fever and fatigue, then in the evening of the first night a dry cough and sore throat. By the next day I was sneezing and wheezing, having difficulty breathing as my chest was tight and had a terrible head cold. 2 days after the vaccine my left eye filled with blood and hurt. Then on the 4th day, I got a terrible mouth infection, oral thrush. Went to see my primary doctor. She gave me cough medicine, an inhaler and a nystatin suspension for the fungal infection in my mouth. It took almost 2 weeks for me to feel better., and I'm still suffering from the fungal infection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Crohn's disease
Andere Medikamente: Amitriptyline
Allergien: latex, amoxicillin, penicillin
Vorherige Impfungen: -

VAERS 1899999

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: NC
Alter: 36,0
Geschlecht: F
Eingang: 25.11.2021
Impfdatum: 24.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Mobility decreased Pain Swelling

Symptomtext

During injection notes shoulder joint pressure. After noted severe and worsening shoulder joint pain with significant swelling and inability to utilize arm functionally. Catching intense pain with small movement.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroid
Andere Medikamente: Levothyroxine, calcium + vit D
Allergien: None
Vorherige Impfungen: -

VAERS 1899975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: ME
Alter: 48,0
Geschlecht: F
Eingang: 25.11.2021
Impfdatum: 16.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Anxiety Asthma Condition aggravated Diarrhoea Fatigue Influenza like illness Migraine Nausea Pain Poor quality sleep Pyrexia

Symptomtext

Strong reaction to vaccine. Feels like I have the flu combined with feeling like I have been in an auto accident. I have had a fever ranging from 99.0-99.6 and I normally have low body temp of 96.8 due to my connective tissue disease, EDS so a "low grade fever" for most is more significant for me. I also have had non-stop issues with my asthma and normally I only have to use it when I have a virus. I feel like this vaccine has caused system wide inflamation. Pain is not stopping, nausea, diarrhea, severe fatigue, wide spread body pain, not sleeping well, increased anxiety, 9 days post vaccine it is not letting up. Woke this morning with a migraine that did not respond to any medications. I was afraid to get this vaccine and now it seems I had good reason to be afraid of it. This needs to be studied more in those who have genetic mutation, I have MANY.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None yet
Aktuelle Erkrankungen: Hypermobile Ehlers-Danlos Syndrome, Homogenius MTHFR, COMT, Autism Spectrum disorder, ADHD, degenerative disk disease, spondolitis, Dysautonomia, Mast Cell activation Disorder, Asthma
Vorgeschichte: Hypermobile Ehlers-Danlos Syndrome, Homogenius MTHFR, COMT, Autism Spectrum disorder, ADHD, degenerative disk disease, spondolitis, Dysautonomia, Mast Cell activation Disorder, Asthma
Andere Medikamente: 300 mg gabapentin; .25 Mirapex; One loratadine; 15 mg folate; 1 mg lorazepam; 100mg levothyroxine; HRT Aravella FE 1/20; Vitamin B complex; Zinc; Ester C; Magnesium gluconate; Vitamin D3, two pills equals 10,000 units; Coenzyme Q10 600mg; 1
Allergien: ginger, clindamicin, zoloft, montelukast
Vorherige Impfungen: -

VAERS 1897247

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: IN
Alter: 60,0
Geschlecht: M
Eingang: 24.11.2021
Impfdatum: 22.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Condition aggravated Fatigue

Symptomtext

Extreme fatigue, chills, fever (100.0)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Prostate cancer
Andere Medikamente: -
Allergien: Erythromyacin
Vorherige Impfungen: Extreme fatigue

VAERS 1896967

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: -
Alter: 24,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 23.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood electrolytes normal C-reactive protein increased Chest pain Dizziness Electrocardiogram normal Headache Myocardial necrosis marker normal

Symptomtext

Reported headache, chest pain and dizziness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Mildly elevated CRP (10.5--nml=7.5) ECG normal. Cardiac enzymes negative, electrolyes within normal limits. (11/24/2021)
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1896380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MD
Alter: 41,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Arthralgia Back pain Breast pain Chest pain Decreased appetite Fatigue Immunisation Lymphadenopathy Migraine Nausea Pain Pain in extremity Skin exfoliation

Symptomtext

loss of appetite; Migraines; Nausea; Body aches and pain; Swollen lymph node under right armpit; Skin on the right breast started peeling to the white; Fatigue; Pain in right breast; Pain in right breast, right shoulder, right arm, right back, right chest and right hand; Pain in right arm/right hand; Pain in right breast, right shoulder, right arm, right back, right chest and right hand; Pain in right breast, right shoulder, right arm, right back, right chest and right hand; Dose number: 3; This is a spontaneous report from a contactable other HCP (patient). A 41-year-old non pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: FH8028), via intramuscular, administered in arm right on 28Oct2021 at 19:00 (age at vaccination was 41 years) as DOSE 3 (BOOSTER), SINGLE for covid-19 immunization; influenza vaccine (INFLUENZA VACCINE, Batch/Lot number was not reported), via an unspecified route, administered in upper right arm on 28Oct2021 as DOSE NUMBER UNKNOWN, SINGLE for immunization. The patient was not pregnant at the time of vaccination. The facility where most recent covid-19 vaccine administered was pharmacy or drug store. No other vaccines were received within four weeks prior to the administration of Covid vaccine. No other medications the patient received within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, the patient was not tested for COVID-19. Medical history included asthma from an unknown date and unknown if ongoing. There were no concomitant medications. The patient had known allergies to Codeine. The patient previously took first dose of bnt162b2 (Batch/Lot Number: EN6202), via intramuscular, administered in arm right on 24Feb2021 (age at vaccination was 40 years) as DOSE 1, SINGLE and second dose of bnt162b2 (Batch/Lot Number: ER8730), via intramuscular, administered in arm right on 24Mar2021 (age at vaccination was 40 years) as DOSE 1, SINGLE for covid-19 immunization. On 28Oct2021 19:00, booster was administered. On 29Oct2021 at 12:00 am, the patient experienced migraines; nausea; body aches and pain; swollen lymph node under right armpit; fatigue; loss of appetite; pain in right breast, right shoulder, right arm, right back, right chest and right hand and skin on the right breast started peeling to the white. The events resulted in visit to doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. The case was non-serious. Therapeutic measures were taken as a result of the events. Treatment was ongoing for the events. The outcome of the events was not recovered. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1896372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: SD
Alter: 65,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Balance disorder Bone disorder Bone pain Chest pain Eye irritation Fatigue Headache Immunisation Renal pain Skin warm Upper respiratory tract congestion

Symptomtext

Debilitating headache; chest hurts; kidneys hurt; stuffed head (but dry stuffed head); balance issues; extreme fatigue; eyeballs BURNING; body skin warm (no temp) BUT bones freezing and aching; body skin warm (no temp) BUT bones freezing and aching; body skin warm (no temp) BUT bones freezing and aching; Dose Number : 3; This is a spontaneous report from a contactable consumer (patient). A 65-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: FH8028), via an unspecified route of administration, administered in Arm Left on 03Nov2021 12:00 (at the age of 65-year-old) as dose 3 (booster), single for covid-19 immunisation. Medical history included hypothyroidism, drug hypersensitivity (known allergies: I avoid sulfa drugs). Concomitant medication(s) included levothyroxine sodium (SYNTHROID) taken for an unspecified indication, start and stop date were not reported. The patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EW0162), via an unspecified route of administration, administered in Arm Left on 15Apr2021 (at the age of 64-year-old) as dose 2, single and received dose 1 (Batch/Lot Number: ER8733), via an unspecified route of administration, administered in Arm Left on 25Mar2021 (at the age of 64-year-old) as dose 1, single for covid-19 immunisation. Patient did not have covid prior vaccination and covid was not tested post vaccination. On 04Nov2021 at 04:00, patient experienced debilitating headache, chest hurts, kidneys hurt, stuffed head (but dry stuffed head), balance issues, extreme fatigue, eyeballs burning, body skin warm (no temp) but bones freezing and aching. Patient did not receive any treatment for adverse events. The outcome of events was recovering. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism; Sulfonamide allergy (known allergies: I avoid sulfa drugs)
Andere Medikamente: SYNTHROID
Allergien: -
Vorherige Impfungen: -

VAERS 1894569

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MA
Alter: 58,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 29.10.2021
Beginn: 12.11.2021
Tage bis Beginn: 14,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chest X-ray normal Dyspnoea Fatigue Nausea SARS-CoV-2 test positive

Symptomtext

Patient presented to ED on 11/12/21 with fatigue, SOB , nausea and positve covid home test. Patient is fully vaccinated. chest x ray was unremarkable. patient was scheduled for monoclonal antibodies at other insitution. Patient was discharged on 11/17/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: covid positive test on 11/13/21 chest x ray impression on 11/12/21: no pneumonia or pulmonary edema
Aktuelle Erkrankungen: N/A
Vorgeschichte: stage II right TNBC, RA, DM2, HTN, HLD and recently diagnosed with hypothyroidism
Andere Medikamente: atenolol, azithromycin, vitamin d3, flovent, gabapentin, glimepiride, lorazepam, magnesium oxide, lovaza, zofran, prochlorperazine, rosuvastatin, tramadol, valacyclovir
Allergien: atorvastatin, amlodipine, cephalosporins, ezetimibe, iodinated contrast media, plaquenil, pravastatin, simvastatin, gadavist, lisinopril, losartan
Vorherige Impfungen: -

VAERS 1894449

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: PA
Alter: 34,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test normal Chest discomfort Dizziness Dyspnoea Dystonia Electrocardiogram normal Gait disturbance Hypoaesthesia Injection site pain Muscle spasms Muscular weakness Pain Pain in extremity Palpitations Pyrexia Vertigo Vomiting X-ray normal

Symptomtext

Right after I left the vaccine site my right arm began to hurt underneath. After a few minutes the site where I received the vaccine began to burn and I had shooting pain in my arm. As I continued to drive my arm began to spasm and my whole right side began to hurt. Suddenly after a spasm my hand closed and I could not get it to stay open. Soon after I could not feel my right foot. When I got home and got out of my vehicle I felt very dizzy and light headed and walking to my apartment was difficult. Once inside everything was spinning, my heart was racing and my chest felt tight, like I couldn't get a good breath. I then began vomiting. I had a temp of 99.8 later that evening. The next evening when I woke up, I still had the same symptoms. I called my Dr office and they told me I needed to go to the ER right away because of the extremity weakness. At the ER they did EKG, X-ray, and blood work. all came back fine. They gave me Benadryl and a medication they said was like ibuprofen. After several hours they said they didn't know why it happened but they couldn't find anything and to wait a few days and call my PCP if it worsens or goes away. Since then everything comes and goes. for the most part i know can keep my hand open, sometimes it close, chest tightness is intermittent, as well as the fever. I still can not feel my toes in my right foot and still have right arm pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG-Normal X-ray-Normal Bloodwork-normal
Aktuelle Erkrankungen: no
Vorgeschichte: GERD, Chronic migraines with aura, Major depressive disorder, PTSD, Anxiety, Anemic, Acute Cholecystic,
Andere Medikamente: Escitalopram 20mg daily, LamoTRigine 100mg daily, Topiramate 150mg PM daily, Gabapetin 100mg PRN, Sumatriptin 100mg x2 PRN, Ferrous gluconate 225mg daily, magnesium 200mg daily, lansoprazole 30mg daily, dicylomine 10mg AM daily PM PRN, Yaz
Allergien: Azithromycin, Citalopram, Hydrocodone. phentermine, flu vaccines, Gluten, Eggs,
Vorherige Impfungen: Flu vaccines

VAERS 1890953

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: FL
Alter: 53,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 19.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Back pain Chest pain Injection site erythema Injection site pain Injection site swelling Lymphadenopathy

Symptomtext

Severe swelling under the arm, at injection site and redness and painful areas around the chest and upper back.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma
Andere Medikamente: Rizatriptan, Levothyroxine
Allergien: No
Vorherige Impfungen: -

VAERS 1890654

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: SD
Alter: 64,0
Geschlecht: M
Eingang: 22.11.2021
Impfdatum: 18.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dyspnoea Mouth swelling Oral mucosal erythema Pruritus

Symptomtext

Patient had itching, mouth swelling, redness around the mouth and felt short of breath. Patient stated the symptoms started at 8 am this morning on 11/19/2021. Patient stated he got his COVID-19 shot on 11/18/2021. He took Allegra and Benadryl this morning on onset of symptoms. Patient was given a prescription for Kenalog, Aristocort (triamcinolone acetonide) 0.1 % cream and prednisone 20mg tablet to help with allergic reaction symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: History of allergic reaction, obesity
Andere Medikamente: Allegra
Allergien: Penicillin, Cefprozil, Ciprofloxacin, Clarithromycin, Clindamycin, Codeine, Levofloxacin, NSAIDS, Sulfa drugs
Vorherige Impfungen: Unknown immunization.

VAERS 1889916

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: CA
Alter: 27,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Axillary mass Axillary pain Mobility decreased

Symptomtext

2 days after vaccine she woke up with a big painful lump under her armpit. She stated that she cannot put her arm down. She will be going to the urgent care facility today because the pain has become unbearable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 1889824

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: AL
Alter: 75,0
Geschlecht: M
Eingang: 22.11.2021
Impfdatum: 13.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Asthenia Chest discomfort Chills Dizziness Dyspnoea Feeling abnormal Hyperhidrosis Nausea

Symptomtext

Patient reports he received his COVID booster on 11/13/21. States since Sunday he has been feeling poorly. Reports chills, sweats, weakness, and dizziness. Stated that on 11/18/21 he was sitting down eating an egg sandwich when he developed pressure in his midsternal chest. He does not believe it is associated with his food intake. He states it was localized to the mid chest. Reports it lasted for about an hour and the pain did not radiate. He rated it a 4 out of 10. Reports associated shortness of breath, diaphoresis, nausea, and lightheadedness. He denied any alleviating or worsening factors. States the patient spontaneously resolved after arriving to the ED, other symptoms persisted. Patient received DuoNebs, Solu-Medrol, aspirin, and nitropaste in the ER. Patient was admitted to the hospital for observation and management, cardiology was consulted. Patient was discharged on prednisone on 11/19/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: coronary artery disease, valvular heart disease, bioprosthetic mitral valve replacement, tricuspid valve repair, PAF with watchman, chronic right bundle branch block, HFpEF, pacemaker
Andere Medikamente: albuterol nebulizer, aspirin, atorvastatin, probiotic, Symbicort, cholecalciferol, cyanocobalamin, ezetimibe, fenofibric acid, Trelegy Ellipta, furosemide, guaifenesin, Combivent Respimat, levothyroxine, lisinopril, melatonin, metoprolol, p
Allergien: pseudoephedrine
Vorherige Impfungen: -

VAERS 1889801

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: NC
Alter: 52,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood magnesium Blood thyroid stimulating hormone Chest X-ray Dizziness Dyspnoea Electrocardiogram Fibrin D dimer Full blood count Hypoaesthesia Metabolic function test Palpitations Tachycardia Tremor Troponin

Symptomtext

11/12 - Dizzy and heart racing numbness in arms, shaking. Almost passed out at dinner had to be taken home. 11/14 - Symptoms started again, this time arms and hands started drawing up, couldn't breathe, called 911. Went to hospital. Since 11/14, daily occurrences with heart palpitations and can't leave my house or ride in a car. Always shaky and now have tachycardia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 11/14 at ER: CBC Troponin 1 x 2 Basic Metabolic Panel EKG Magnesium 11/16 Follow up with Doctor D-Dimer TSH Repeat Metabolic Panel Xray of chest
Aktuelle Erkrankungen: Had not been sick.
Vorgeschichte: Hereditary High Blood pressure.
Andere Medikamente: Lisinopril Hydrochlorothiazide
Allergien: Sulfa Drugs
Vorherige Impfungen: -

VAERS 1885376

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: TX
Alter: 25,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal pain Chest pain Cold sweat Hyperhidrosis Nausea

Symptomtext

Nausea, chest pain and mid-abdomen pain. Patient's skin: moist, cool and clammy. VS obtained; 88/52, 52 irregular and 99 SpO2 on RA, RR even and nonlabored. EMS called at 13:59, on scene at 14:06 to assume care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: No lab/medical tests completed.
Aktuelle Erkrankungen: Patient denied
Vorgeschichte: Patient denied
Andere Medikamente: Patient denied
Allergien: NKA
Vorherige Impfungen: -

VAERS 1880782

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: IA
Alter: 32,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 09.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Bronchitis viral Condition aggravated Cough Discharge Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test negative

Symptomtext

Viral Bronchitis (with cough, runny nose, drainage, and chest congestion). Prescribed Albuterol Sulfate Inhalation Aerosol, 90 mcg. Consult with physician if symptoms persist to prescribe an antibiotic

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Covid PCR test performed, results negative. Health, Test: Covid-19, Order Number: 97732133, Specimen Collected: 11/14/2021, Received Results: 11/16/2021, Result: Negative
Aktuelle Erkrankungen: None diagnosed, 1 week prior slight cough (for 1 day)
Vorgeschichte: Amblyopia, Obesity
Andere Medikamente: Zyrtec
Allergien: None
Vorherige Impfungen: -

VAERS 1880308

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 43,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 05.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Angina pectoris Computerised tomogram Dizziness Dyspnoea Echocardiogram

Symptomtext

Pain over heart. Shortness of breath. Dizziness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: CT scan, Echocardiogram
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1878235

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: OH
Alter: 29,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood bicarbonate Blood creatine phosphokinase Blood magnesium Bone pain Brain natriuretic peptide Chest discomfort Chest pain Computerised tomogram thorax Dizziness Dyspnoea Electrocardiogram Full blood count Heart rate increased Metabolic function test Myalgia Troponin Urine analysis

Symptomtext

Increased heart beat on the day of the vaccine Tight chest up to 2 days after Chest pain up to 2 days after Muscle and bone pain 3 days after vaccination (continued until today) Fainting feeling on the day of the vaccination Increased heart beat, tight chest , difficulty breathing on Nov 16,2021 Muscle and bone pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Brain Natriuretic peptide CBC Auto Differential CK Comprehensive Metabolic Panel w/ Reflex to MG HCG qualitative serum Magnesium Microscopic urinalysis Troponin Urinalysis Reflex to Culture CT CHEST PULMONARY EMBOLISM W/ CONTRAST EKG 12 Lead
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1877473

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

moderat

Staat: PA
Alter: 40,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Mobility decreased

Symptomtext

The patient experienced extreme shoulder pain after receiving her vaccine. She said that it is a pain scale score 10. She could not lift her left arm at all.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1877248

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: FL
Alter: 32,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Dizziness Dyspnoea Eye movement disorder Feeling hot Vomiting

Symptomtext

Once the patient was vaccinated in his left arm, I was speaking to the patient in the health room for an additional 3 minutes. I was explaining to him what V-safe is, and suddenly he stated he felt dizzy and hot. He removed his mask and repeated again that he's dizzy. I stayed with him and about 20 seconds later he said he was going to faint. I noticed his eyes roll back into his head and he had very heavy, labored breath sounds. I called out for the other pharmacist for an epipen and for a team member to call 911. Approximately 15 seconds later, the patient was alert, and said he was fine, he was only a bit dizzy. Within 1 minute, the patient vomited. We kept him in the patient health room and he stayed alert until paramedics came by. He went on a stretcher, where they checked his blood pressure, heart rate and mental alertness. He walked back to the pharmacy within 10 minutes to let us know he was doing okay. He no longer felt dizzy. His wife drove him home and was instructed to take him to urgent care or ER if he shows any signs of anaphylaxis. We also advised the patient to keep Benadryl near by.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: BP and heart rate monitoring. Leads were placed on patient by paramedics
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: Flu-like symptoms; swollen node on arm x10 days that went away on its own

VAERS 1877081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: CA
Alter: 21,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Chest X-ray normal Chest pain Differential white blood cell count abnormal Electrocardiogram Electrocardiogram ST segment abnormal Electrocardiogram abnormal Fibrin D dimer increased Full blood count abnormal Haematocrit normal Haemoglobin normal Mean cell haemoglobin concentration normal Mean cell haemoglobin normal Mean cell volume normal Mean platelet volume increased Pain Platelet count normal QRS axis abnormal Red blood cell count normal

Symptomtext

21 Years old Female presenting with chest pain for 3 days. Since then and severe proximal an hour after receiving her first dose of vaccine, denies shortness of breath at this time. Patient has no episodes of vomiting nor has had nauseating symptoms.Pain started gradually .It is described as dull and aching, radiating into nowhere. Pain is described as moderate upon onset and is currently moderate. No history of the same. Pain is not worse with exercise. Patient has no decrease in exercise tolerance recently.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Coagulation LATEST RESULTS D Dimer Qnt 11/16/21 10:56 874 High CBC and Differential LATEST RESULTS WBC 11/16/21 10:56 10.4 High RBC 11/16/21 10:56 4.47 Hgb 11/16/21 10:56 13.4 Hct 11/16/21 10:56 39.2 MCV 11/16/21 10:56 87.7 MCH 11/16/21 10:56 30.0 MCHC 11/16/21 10:56 34.2 RDW 11/16/21 10:56 13.2 Platelets 11/16/21 10:56 270 MPV 11/16/21 10:56 11.8 Diagnostic Results Imaging XR Chest Portable 11/16/21 07:48:18 IMPRESSION: No acute disease. Signed By: M.D. EKG ED ECG Provider Interpretation ECG Heart Rate: 68 bpm ECG Time Read: 11/16/21 07:22:00 ED ECG Interpretation: Right axis deviation ED ECG Interpreted By: M.D. ED ECG Rhythm: NSR ED ECG ST/T Segments: Non-specific ST changes ED ECG Stemi: No ED Normal ECG: No
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: None
Allergien: no known drug allergies
Vorherige Impfungen: -

VAERS 1876974

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: WI
Alter: 45,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Dyspnoea

Symptomtext

Approximately 1-1.5 hours following vaccine administration, patient developed shortness of breath and difficulty breathing. She was without hypotension, urticaria, wheezing, and or pharyngeal swelling. The following medications were administered in the emergency department: famotidine, diphenhydramine, dexamethasone, and epinephrine x 4 doses.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Augmentin (itching, edema) Amoxicilling (hives) Minocycline (GI intolerance only) "Moutain -ops" nutritional supplement (facial swelling and hives) Influenza vaccine (anaphylaxis)
Vorherige Impfungen: anaphylaxis to influenza vaccine in 2011

VAERS 1876742

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: IN
Alter: 44,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 02.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 6,0
Dosis: UNK
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dehydration Feeling hot Red blood cells urine Scrotal pain Testicular swelling Urine analysis X-ray

Symptomtext

pain the scrotum extreme heat in the back of the sack feeling of a cut in the back of the scrotum

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: urine test x ray dehydration - red blood cell in urine - slight swollen in the back of the testicules
Aktuelle Erkrankungen: high blood pressure
Vorgeschichte: none
Andere Medikamente: losartan
Allergien: NONE
Vorherige Impfungen: -

VAERS 1876684

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: LA
Alter: 25,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Muscle spasms Sleep disorder Tremor

Symptomtext

Uncontrollable muscle spasms, whole body shakes. Woke from sleep - unable to walk from shaking. Heart Rate @ 120 bpm. Took normal adult dose of Tylenol, symptoms ceased after 1 hour.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1873095

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: NJ
Alter: 12,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 12.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: SYR / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cardiac flutter Chest pain Heart rate increased Palpitations

Symptomtext

Feeling of having a fast-beating, fluttering or pounding heart; chest pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Levetiracetam ER Tabs 500mg
Allergien: -
Vorherige Impfungen: -

VAERS 1869429

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: VA
Alter: 55,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 29.10.2021
Beginn: 06.11.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Acute kidney injury Blood creatinine increased Blood glucose normal Blood urea increased Blood urine present Confusional state Differential white blood cell count abnormal Electrocardiogram normal Fibrin D dimer increased Gait disturbance Glomerular filtration rate normal Haematocrit decreased Haemoglobin decreased Mean platelet volume normal Metabolic function test abnormal Muscle spasms Nystagmus Palpitations

Symptomtext

I got out of bed on 11/6 with severe room spinning, almost fell. This has continued and seems to be whenever I move my head to other than vertical; I also got a severe leg cramp that lasted 3 days and some heart palpitations. By 11/9 I was sometimes not walking straight and I was getting confused and made an appointment to see my doctor; Doctors visit on 11/12 and my doctor sent me to the ER. ER Diagnoses: Vertigo with nystagmus - started 11/6/2021 and continues (now day 9) - Horizontal nystagmus when my eyes move from right to left Acute kidney injury - diagnosed at Emergency Room after testing on 11/12/2021 - Creatinine 1.7 - eGFR 33 - BUN 28

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Basic metabolic panel: BUN 28 Creatinine 1.7 eGFR: 33 Glucose: 109 CBC Auto Differential: RBC 3.77 Hemoglobin 11.5 Hemacrit 34.2 MPV 8.9 D-dimer: <500 ng/mL FEU EKG: normal Urinalysis: some blood in urine
Aktuelle Erkrankungen: None
Vorgeschichte: Mild Asthma
Andere Medikamente: Paroxetine, 10 mg daily for hot flashes; Rosuvastatin, 20 mg daily; Montelukast 10 mg daily Fexofenadine HCl 180 mg daily; Ubiquinol 100 mg daily; Calcium
Allergien: Allergic to codeine; latex; and Monistat
Vorherige Impfungen: -

VAERS 1869398

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MA
Alter: 52,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia Chills Dyspnoea Fatigue Headache Pain

Symptomtext

Headache, body aches, fatigue, sharp pain in joints (elbows and knees), chills and shortness ofbreath

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: N/a
Vorgeschichte: N/a
Andere Medikamente: One a day vitamin
Allergien: N/a
Vorherige Impfungen: -

VAERS 1867848

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: ME
Alter: 27,0
Geschlecht: M
Eingang: 13.11.2021
Impfdatum: 10.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest X-ray Computerised tomogram Echocardiogram Fibrin D dimer Full blood count Lymphadenopathy Metabolic function test Soft tissue swelling Tachycardia Troponin

Symptomtext

Atypical tachycardia, Left upper lymph node enlargement, Left axillary soft tissue edema

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: Cat Scan, Chest XRay, Echocardiogram, Troponin labs, D Dimer, BMP, CBC
Aktuelle Erkrankungen: -
Vorgeschichte: Depression, Bipolar, Anxiety
Andere Medikamente: Lamictal, Serequel, Buspirone, Famotodine, Ibprofin 800mg
Allergien: All Sufa Drugs, Zythromax
Vorherige Impfungen: -

VAERS 1865759

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: CO
Alter: 33,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 07.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood urine present Musculoskeletal chest pain Rash

Symptomtext

Blood in urine for 5 says since receiving shot . Rash on left side on torso in 3 patches. Left pain internally under ribs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Musculoskeletal chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1864997

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8028

moderat

Staat: MS
Alter: 29,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 10.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain Paraesthesia

Symptomtext

I felt chest pain for 24 hours and pain full tingling in my arm and palm of mu hand for 48 hours and it's continuing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Lupus
Vorgeschichte: Lupus
Andere Medikamente: Hair-Vit
Allergien: -
Vorherige Impfungen: -

VAERS 1864959

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: AR
Alter: 60,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 11.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Chills Confusional state Dyspnoea Gait disturbance Headache Pain Pyrexia

Symptomtext

After she left she had a splitting headache and by time she got home she could hardly breathe. She is having bad joint pains all over. It hurts when she tries to move and have a fever of 100.9 and have chills. She is also having mental confusion. She can barely walk

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no
Vorgeschichte: arthritis
Andere Medikamente: no
Allergien: penicillin and flu & chicken pox vaccine
Vorherige Impfungen: -

VAERS 1864794

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: IL
Alter: 82,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 08.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Abdominal pain Chest pain Hypotension

Symptomtext

PT C/O ABDOMINAL AND CHEST PAIN WHILE WAITING IN WAITING ROOM FOR RECOMENDED 15 MINUTE POST VACCINE WAITING PERIOD. BP CHECK REVEALED HYPOTENSION 70/40. 911 CALLED, EMS TRANSPORTED PATIENT TO MEDICAL CENTER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: UNKNOWN
Aktuelle Erkrankungen: -
Vorgeschichte: CHF, HTN, HYPERLIPIDEMIA, CAD, DEMENTIA
Andere Medikamente: COREG, LIPITOR, ASPIRIN
Allergien: STRAWBERRY, CHOCOLATE
Vorherige Impfungen: -

VAERS 1864658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

moderat

Staat: MD
Alter: 65,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia Limb injury Paraesthesia

Symptomtext

Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1858037

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

C-reactive protein increased Chest pain Dyspnoea Electrocardiogram normal Full blood count normal Pain in extremity

Symptomtext

My arm was sore that night November 4th, 2021, the next afternoon at about 4pm I had chest pain. I called my Cardiologist who refilled my Colchicine. Within thirty-six hours of taking the medication the pain is gone. I still have shortness of breath but that gets better after using my inhaler. I will see my Physician again tomorrow morning, November 11th, 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: CBC- No findings EKG- Considered relatively normal, CRP was 8.
Aktuelle Erkrankungen: No
Vorgeschichte: Type 1 Diabetes Hypertension Hyperlipidemia Acute Pancreatitis
Andere Medikamente: Prefer not to answer.
Allergien: No
Vorherige Impfungen: -

VAERS 1857898

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: LA
Alter: 55,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Cold sweat Dizziness Dyspnoea Nausea

Symptomtext

cold sweats at night, heavy breathing, severe nausea, dizziness, and weakness. This happens randomly and last for about 5 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: no
Vorgeschichte: asthma, Hypertension, eczema, DDD, Chronic pain
Andere Medikamente: alprazolam, cyclobenzaprine, depo estradiol, dextroamphetamine-amphetamine, ibuprofen, ipratropium 0.5mg- albuterol, Vyvanse
Allergien: doxycycline
Vorherige Impfungen: -

VAERS 1854224

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MI
Alter: 59,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Fatigue Pain Tremor Vomiting

Symptomtext

Fever 100.0, chills, severe shaking, severe body aches, fatigue and vomiting. Took Tylenol and Motrin. Symptoms not quite resolved as of today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1849385

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: TN
Alter: 32,0
Geschlecht: F
Eingang: 07.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Interchange of vaccine products Mobility decreased Pain

Symptomtext

I had the J&J vacc the got the Pfizer booster. I noticed the injection seemed unusually high up on my arm. By 1230 my shoulder started to hurt with movement and by 2-3 PM I couldn't lift my arm without significant pain. I iced the area for 20 minutes around 4pm. I noticed a new clicking sensation in my shoulder joint as well. I awoke this morning with the same symptoms (minor improvement, though), so I took Tylenol 650mg PO at 0930AM. If the pain does not improve I plan to see an orthopedic MD this week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma, Anxiety
Andere Medikamente: Sertraline 75mg qD, AuviQ pen PRN, Vitamin D3 2,000 iu once weekly, Metanx 3/90/314/35/2mg qD, Ventolin HFA PRN
Allergien: Shellfish, wasps/bees, birth control
Vorherige Impfungen: -

VAERS 1842640

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: MD
Alter: 43,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test Chest pain Dyspnoea Nausea Vomiting Dysphagia Throat tightness

Symptomtext

Not being able to breathe, severe chest pain, nausea, vomiting within 5-7 minutes after injection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Blood work, blood pressure at the hospital
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Sulfa containing medication
Vorherige Impfungen: -

VAERS 1842640

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8028

moderat

Staat: MD
Alter: 43,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test Chest pain Dyspnoea Nausea Vomiting Dysphagia Throat tightness

Symptomtext

Not being able to breathe, severe chest pain, nausea, vomiting within 5-7 minutes after injection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Blood work, blood pressure at the hospital
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Sulfa containing medication
Vorherige Impfungen: -

VAERS 1845494

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: CA
Alter: 40,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 01.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Genital burning sensation Genital paraesthesia

Symptomtext

Testicle burning and tingling

Weitere VAERSDATA-Felder

Praegender Schweregrund: Genital paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1843839

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: CA
Alter: 22,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 02.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Chest discomfort Cold sweat Heart rate irregular Pain Palpitations Pyrexia

Symptomtext

Pounding heart rate, body aches, chest tightness, cold sweats and fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: 1,0
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1843118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: AL
Alter: 32,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 03.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Back pain Fatigue Hypoaesthesia Impaired work ability Injection site pain Pain Paraesthesia

Symptomtext

Pt received first covid19 pfizer vaccination 11/3/2021 and woke up 11/4/2021 with R arm numbness (entire arm) and tingling. she has tenderness at injection site that is mild-moderate w/ palpation. she is experiencing moderate-severe fatigue that interferes with her ability to work today. she has entire back pain/aches as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: guaifenesin
Vorherige Impfungen: -

VAERS 1840797

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: AL
Alter: 38,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Dyspnoea Palpitations

Symptomtext

Racing heart. Shortness of breath. Onset within 90 minutes of injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Levothyroxine
Allergien: None
Vorherige Impfungen: -

VAERS 1832304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

moderat

Staat: CA
Alter: 31,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Hyperventilation Tremor

Symptomtext

pt develop tremors and hyperventilation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: none except the paramedic came
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1828697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: DC
Alter: 41,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Back pain Chest X-ray Chest pain Electrocardiogram Injection site pain Mobility decreased Myalgia Neck pain Pain Pain in extremity Troponin

Symptomtext

Unable to move arm Body aches Pain at injection site Muscle ache (From neck to right arm, back pain, chest pain)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG Chest xray Troponin lab Given benadryl
Aktuelle Erkrankungen: No
Vorgeschichte: None
Andere Medikamente: Vitamin C. Vitamin D and Zinc
Allergien: NKDA NKA
Vorherige Impfungen: -

VAERS 1828611

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

moderat

Staat: DC
Alter: 55,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 28.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Asthenia Condition aggravated Dizziness Dysphagia Fatigue Headache Lip swelling Somnolence Swelling Throat tightness Tongue disorder

Symptomtext

9 am- received COVID 19 VACCINATION IN RIGHT DELTOID AREA OF THE ARM. 9:15-16 AM- SLIGHT DIZZINESS EXPERIENCED. I WAS RECLINED IN A RECLINER CHAIR. THIS SUBSIDED. I HAD PREMEDICATED AT 8:20AM WITH BENADRYL 3/4 TAB OF 25MG. TYLENOL 250MG ES 1/2 TAB AND PEPCID 1/2 TAB 20MG ALONG WITH MY DAILY CROMOLYN SODIUM 200MG. I BECAME SLEEPY AND TIRED AT 2PM W/ INTENSE HEADACHE. AT 8:30PM, APPROXIMATELY TO 1145PM, I HAD TO USE A TOTAL OF BENADRYL 125MG, PEPCID 80MG, TYLENOLES BECAUSE OF EXPERIENCING THROAT TIGHTNESS WITH SOME DIFFICULTY SWALLOWING, TONGUE THICKNESS, WEAKNESS AND PERSISTENT STABBING HEADACHE. EXPERIENCED TONGUE THICKNESS AND LIP SWELLING SWELLING THE FOLLOWING AM.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: POTS- Mast Cell Activation Syndrome Anemia Vit B12 Deficiency Vit D Deficiency Migraines
Vorgeschichte: Anemia Vit B12 Deficiency Vit D Deficiency Migraines
Andere Medikamente: Benadryl Tyleno ES Pepcid Vitron C Vit D B12 Inj
Allergien: Flu vaccine (throat tightness, SOB, cough, acute bronchitis), prednisone (muscle fatigue, SOB, low K), Cipro (low HR, shaking, dizziness, rigors), flagyl (low HR, rigors), ASA (hives, itching, dizziness), yogurt/milk/scrambled eggs (elevated BP, dizziness, pre-sycope, shaking), nuts (itchy throat, generalized itching), peaches (urticaria), spinach (low HR, dizziness, pre-syncope), seafood including seafood smell (throat tightness, faint, cough, tach), vinegar (odor causes tongue swelling).
Vorherige Impfungen: flu vaccine (throat tightness, SOB, cough, acute bronchitis)

VAERS 2446189

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MN
Alter: 39,0
Geschlecht: F
Eingang: 18.12.2023
Impfdatum: 23.12.2021
Beginn: 16.12.2023
Tage bis Beginn: 723,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cough Oropharyngeal pain SARS-CoV-2 test positive Stomatitis COVID-19

Symptomtext

Sore throat, cough, sore in mouth

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: IDNOW
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2700840

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8028

mild

Staat: PA
Alter: 52,0
Geschlecht: F
Eingang: 24.10.2023
Impfdatum: 20.10.2023
Beginn: 20.10.2023
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Headache Joint stiffness Lethargy Pain in extremity

Symptomtext

Anticipated arm soreness plus severe headache, joint stiffness, chills, and lethargy beginning approximately seven hours after vaccination and worsening over the next 12 hours, with peak severity within 24 hours of injection and lasting approximately 12 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Joint stiffness Breast cancer 2020
Andere Medikamente: Letrozole Alendronate Vitamin D
Allergien: Penicillin Sulpha
Vorherige Impfungen: -

VAERS 2693182

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: TX
Alter: 64,0
Geschlecht: F
Eingang: 10.10.2023
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood grouping Fatigue Feeling hot Headache Vaccination site pain

Symptomtext

soreness in arm at injection site; headache; forehead feels a little warm; a little of the fatigue; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 64-year-old female patient received bnt162b2 (BNT162B2), on 01Nov2021 as dose 3 (booster), single (Lot number: FH8028, Expiration Date: 31May2022) at the age of 64 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "gastro issue" (unspecified if ongoing); "migraines" (unspecified if ongoing); "fibromyalgia" (unspecified if ongoing); "dry eyes" (unspecified if ongoing); "appendix" (ongoing); "Tonsil" (ongoing). The patient's concomitant medications were not reported. Vaccination history included: bnt162b2 (DOSE 1, SINGLE, Lot: EW0150, Expiry date 31Jul2021, Route of Administration: Intramuscular), administration date: 05Apr2021, when the patient was 63-year-old, for COVID-19 immunization, reaction(s): "a little of the fatigue", "soreness on her arm at the injection site", "has a little bit of a headache", "forehead feels a little warm"; bnt162b2 (DOSE 2, SINGLE, Lot: EW0169, Expiry date 31Aug2021), administration date: 26Apr2021, when the patient was 63-year-old, for COVID-19 immunization, reaction(s): "soreness on her arm at the injection site", "little bit of a headache", "forehead feels a little warm", "a little of the fatigue". The following information was reported: FATIGUE (non-serious) with onset Nov2021, outcome "unknown", described as "a little of the fatigue"; FEELING HOT (non-serious) with onset Nov2021, outcome "unknown", described as "forehead feels a little warm"; HEADACHE (non-serious) with onset Nov2021, outcome "unknown"; VACCINATION SITE PAIN (non-serious) with onset Nov2021, outcome "unknown", described as "soreness in arm at injection site". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The patient stated she Experienced soreness on her arm at the injection site, has a little bit of a headache, and her forehead feels a little warm, however the rest of her body doesn't feel warm. Patient stated all of the covid vaccines that she has received have been from Pfizer in which she believes her reactions are normal and thought she experienced them with the prior administrations. This isn't a fear of her safety phone call. She just wanted the gentle reminder that this is normal because she couldn't remember. She remember the soreness of the arm and remembered a little of the fatigue. She wasn't clear on the headache and is 98% certain it was normal, but she can't remember over a year ago what her symptoms were when she got the vaccination. She does trust Pfizer. When the whole thing started she was in (withheld) and she registered to get her vaccination. The state of (withheld) said register at the site and expect email. She was showing up at grocery stores and pharmacies and waiting in line and there was never anything left over. Out of fear she called her doctor at the (withheld) who said for her to call a number and get a plane ticket and head over. From that first vaccine that came out, not counting yesterday, she has had a total of 5 vaccinations during Covid period and all were Pfizer. Honestly she was hoping it would be Pfizer, but anything is better than nothing. When she got to (withheld) and found out she was getting Pfizer she was elated. She was told yesterday that it was cleared that if she had Pfizer she could switch and get Moderna, but she didn't think so and she found a (withheld) to get Pfizer. She was determined she wouldn't get anything but Pfizer. She is a retiree and is covered under (withheld) and her secondary is (withheld). She doesn't have a primary doctor. She sees gastroenterologist for gastro issues. She sees preventive cardiologist for preventive care. For dry eyes she see optometrist. She just sees a doctor for whatever ales her. She specifically remembers when she got each of her Covid vaccinations, the five she mentioned, she remembered she would get them in the morning. She would fly to (withheld) and the driver would take her to clinic and then he would take her back to airport. She knows the difference between a little bit of a headache and a migraine. This was not a migraine. Neither the headache or the warmth on the forehead have been anything that would have caused her to go to the hospital. With all her vaccination a little over 5 hours after vaccination the soreness and fatigue and little mild headache started. She had no nausea or vomiting or dizziness, nothing like that. She thinks the reason she didn't have anything like that is because of the quality of the drug. She is extremely picky about where she gets her healthcare and the doctors that she sees. Medical Conditions: she has other issues but nothing relevant. Had these issues prior to her vaccination yesterday and prior to taking first dose of Pfizer Covid vaccinations. Her gastro issue was not effected by the vaccinations. Her migraines were not effected by the vaccinations. She has fibromyalgia and it was not effected by the vaccinations. Her dry eyes were not effected. Nothing she had was effected by the vaccines. She is a blood O positive and for what it is worth she can't prove anything as she is not a scientist, she can say prior to Covid and to prior to 05Apr2021 when she got first vaccination she had never got flu shot and never got the flu. She still has tonsil and appendix. The events did not required emergency room, physician office and intensive care unit visit. Patient asked if every (pharmacy name withheld) stand alone store was offering Pfizer Covid vaccinations as she wants to make sure her family members receive Pfizer covid vaccines. The report is not related to a study or programme.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Name: Blood; Result Unstructured Data: Test Result:O positive; Comments: She is a blood O positive
Aktuelle Erkrankungen: Appendix disorder; Tonsillar disorder
Vorgeschichte: Medical History/Concurrent Conditions: Dry eyes; Fibromyalgia; Gastrointestinal disorder; Migraine
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2634849

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

mild

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 22.05.2023
Impfdatum: 13.02.2021
Beginn: 02.06.2022
Tage bis Beginn: 474,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Back pain Bacteraemia COVID-19 Computerised tomogram abdomen abnormal Hepatic cyst Hiatus hernia Leukocytosis Nephrolithiasis Pyelonephritis acute Pyrexia SARS-CoV-2 test positive Sepsis Urinary tract infection Urine leukocyte esterase positive Vaccine breakthrough infection White blood cells urine positive

Symptomtext

BREAKTHROUGH COVID: PT FULLY VACCINATED WITH BOOSTER. admitted on June 2, 2022 with lower back pain, fevers. Patient was septic on arrival leukocytosis, treat her sepsis, UTI, bacteremia. Pt tested positive for COVID-19 as she experienced a scratchy throat. She did not want to tell nursing staff so she told her family who brought in a home test kit and she tested positive. When she tested positive then the daughter relayed this information to the staff and she had a hospital test which was positive. Patient was not hypoxic however. She did not require any significant treatment for covid-19 infection without respiratory compromise.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: UA showed 3+ leukocyte esterase, positive wbc's. CT abdomen pelvis :Acute left pyelonephritis.2. Punctate nonobstructing calculi in both kidneys. 3. Moderate size hiatal hernia. 4. Hepatic cysts.
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: HLD and anxiety
Andere Medikamente: UNKNOWN
Allergien: NKA
Vorherige Impfungen: -

VAERS 2630181

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: FL
Alter: 47,0
Geschlecht: F
Eingang: 10.05.2023
Impfdatum: 13.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 14,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Breast discomfort Breast disorder female Breast pain Computerised tomogram abdomen Mammogram normal Pathology test Precancerous cells present Procedure aborted Skin odour abnormal Ultrasound breast normal Ultrasound scan vagina Uterine polyp Uterine polypectomy

Symptomtext

1. New onset change of body odor - strong onion-like more pronounced under left axilla as compared to right axilla - no treatment outcome remains unchanged 2. Pain discomfort to left breast with palpable changes matrix of breast tissue and discomfort pain voiced upon examination of left breast as compared to right breast. Treatment monitor for three months with Mammogram and ultrasound. Outcome pain and discomfort resolved on its own after three months with findings of normal diagnostic imaging. 3. New onset of Endometrial polyp with abnormal pathology upon polypectomy pre cancerous proliferation recommended laparoscopic partial hysterectomy - awaiting outcome.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Breast pain
Hospital-Tage: -
Labordaten: Mammogram with Ultrasound 12/2021 - 1/2022 Abdominal CT - 7/2022 Transvaginal Ultrasounds 2022 and 2023. Endometrial Polypectomy 1/2023 aborted procedure. Repeat endometrial polypectomy on 5/2023 with pathology.
Aktuelle Erkrankungen: N/A
Vorgeschichte: HSV Type II and infertility of unknown cause.
Andere Medikamente: Valacyclovir 500mg PO daily
Allergien: Bactrim, Sulfa
Vorherige Impfungen: -

VAERS 2605865

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: TX
Alter: 66,0
Geschlecht: F
Eingang: 29.03.2023
Impfdatum: 26.09.2022
Beginn: 08.01.2023
Tage bis Beginn: 104,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Oropharyngeal pain Pain Respiratory tract congestion SARS-CoV-2 test positive Sneezing

Symptomtext

I had a very sore throat, and unusual sneeze and a cough. I also had congestion and body aches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: at home rapid COVID-19 test- positive 1/9/2023
Aktuelle Erkrankungen: No
Vorgeschichte: High cholesterol; Pre- diabetic
Andere Medikamente: Irbesartan; Hydrochlorosiazide; Ezetimibe Woman's multivitamin; Woman's 50+ ultra; Vitamin C; Vitamin D; Vitamin A; Iron tablet; Niocin
Allergien: Statins
Vorherige Impfungen: -

VAERS 2603072

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: CA
Alter: 46,0
Geschlecht: F
Eingang: 24.03.2023
Impfdatum: 18.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blister Pemphigoid Pruritus

Symptomtext

bullous pemphigoid; itchy blisters on my skin; itchy blisters on my skin; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 47-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 18Nov2021 at 09:00 as dose 3 (booster), single (Lot number: FH8028) at the age of 46 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Dose 1, single, Unknown Manufacturer), for COVID-19 Immunization; Covid-19 vaccine (Dose 2, single, Unknown Manufacturer), for COVID-19 Immunization. The following information was reported: PEMPHIGOID (medically significant), outcome "not recovered", described as "bullous pemphigoid"; PRURITUS (non-serious), BLISTER (non-serious), outcome "not recovered" and all described as "itchy blisters on my skin". The events "bullous pemphigoid" and "itchy blisters on my skin" required physician office visit. Therapeutic measures were taken as a result of pemphigoid, pruritus, blister. Additional information: the patient received the 4th dose of Pfizer Covid-19 vaccine on 11Nov2022 at 11:00 AM in the left arm. Within a week or two of the bivalent booster she developed itchy blisters on her skin similar to what happened after her last booster dose (Dose 3). It was reported that after the first incident, it was diagnosed by a dermatologist as bullous pemphigoid, patient was given oral and topical steroid and it improved. The blisters begin as itchy and if she scratched them they would pop and turn into a scab to heal. Patient have never had any of these symptoms before receiving the covid vaccine. The patient has no known allergies.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300119722 same patient/events different vaccine doses;US-PFIZER INC-202300120267 same patient, different vaccine doses/events;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2603180

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NY
Alter: 10,0
Geschlecht: F
Eingang: 15.03.2023
Impfdatum: 15.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pain in extremity Product administered to patient of inappropriate age

Symptomtext

No abnormal side effects - sore arm (given tylenol by mother) *given adult dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2587918

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MI
Alter: 54,0
Geschlecht: F
Eingang: 27.02.2023
Impfdatum: 18.11.2021
Beginn: 12.02.2023
Tage bis Beginn: 451,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Fatigue SARS-CoV-2 test positive

Symptomtext

02/12/23 presents to ED for "fatigue". PMHx of "MS, DM II, HTN"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 02/12/23 SARS-CoV-2 (COVID-19) detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2551617

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NY
Alter: 56,0
Geschlecht: F
Eingang: 05.01.2023
Impfdatum: 16.11.2021
Beginn: 01.12.2022
Tage bis Beginn: 380,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypoaesthesia Pruritus Urticaria

Symptomtext

I broke out in hives all over my body. I have been having numbness in my right arm for 2 weeks. I used itchy cream for my hives and it did not get better. I would take a shower and they would get better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: Amlodipine; ADVIL PM
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2550343

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MI
Alter: 79,0
Geschlecht: F
Eingang: 04.01.2023
Impfdatum: 28.01.2021
Beginn: 14.11.2022
Tage bis Beginn: 655,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Asthenia COVID-19 Fatigue SARS-CoV-2 test positive

Symptomtext

11/14/22 presents to ED for "fatigue" "weakness". PMHx of "advanced dementia, rheumatoid arthritis, hypertension, PUD"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 11/14/22 SARS-CoV-2 (COVID-19) detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2524377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: FL
Alter: 57,0
Geschlecht: F
Eingang: 06.12.2022
Impfdatum: 03.12.2021
Beginn: 01.06.2022
Tage bis Beginn: 180,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chills Cough Fatigue Pyrexia SARS-CoV-2 test positive

Symptomtext

I had fatigue, fever, mild cough, and chills on and off. We were on vacation and when we got back home, I took a COVID-19 test at home and tested positive. I took doxycycline that I already had at home, and it helped to break fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension; G\ERD; Migraines; Lung are sensitive
Andere Medikamente: CRESTOR; lisinopril; PEPCID; multivitamin
Allergien: Penicillin; latex; flu shot
Vorherige Impfungen: Influenza, I couldn't rise my arm, 52

VAERS 2507558

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MD
Alter: 70,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 22.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Acupuncture Biopsy Blood test Computerised tomogram abdomen normal Computerised tomogram thorax normal Lymph node pain Lymphoma Magnetic resonance imaging head abnormal Musculoskeletal pain Neck pain Pain Positron emission tomogram Radiotherapy

Symptomtext

1. Severe pain starting at the underarm lymph gland and radiating around the scapula and up the neck. Started on 11/23/2021 and ended in June 2022. Treated with physical therapy, acupuncture and lymphatic massage. 2. On September 3, 2021 I received a great report from eye cancer specialist doctor, there was no sign of cancer. On January 13, 2022 a lymphoma recurrence in the right eye was identified by another doctor and was confirmed by the specialist via eye biopsy on April 7, 2022. Radiation treatment was performed May 23-June 8, 2022. On August 9. 2022, the specialist confirmed that the cancer was gone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: Multiple blood tests CT Chest/Abdomen 2/2/2022 negative MRI Brain 2/7/2022 - suspicious for eye lymphoma PET Scan 3/18/2022 - negative Eye biopsy 4/7/2022 - positive for lymphoma
Aktuelle Erkrankungen: NONE
Vorgeschichte: Heart Disease, High Cholesterol
Andere Medikamente: Crestor, Zetia, Rapatha, Hydroxyzine, Multivitamin, Vitamin C, Tumeric, Vitamin D3, Calcium, Estradiol, Folic Acid, Aspirin
Allergien: Mold, msg, wheat
Vorherige Impfungen: 1976-swine flu vaccine, Age 25, Guillian Barre

VAERS 2505870

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MD
Alter: 42,0
Geschlecht: F
Eingang: 11.11.2022
Impfdatum: 05.11.2021
Beginn: 26.07.2022
Tage bis Beginn: 263,0
Dosis: UNK
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chills Dizziness Fatigue Pyrexia SARS-CoV-2 test positive

Symptomtext

in the 36 hours after the vaccine, I had a high fever (102), chills, fatigues and dizzy spells. On July 26, 2022 I tested positive for COVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 26 July 2022- Dx by two home rapid tests.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism; Migraines; Obesity; Generalized anxiety disorder.
Andere Medikamente: Synthroid; Allegra; Lexapro; Rizatriptan (PRN); iIbuprofen (PRN); Acetominophen (PRN).
Allergien: Lanolin; Wool; Seasonal
Vorherige Impfungen: -

VAERS 2503192

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MI
Alter: 79,0
Geschlecht: F
Eingang: 09.11.2022
Impfdatum: 28.01.2021
Beginn: 10.09.2022
Tage bis Beginn: 590,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Fatigue SARS-CoV-2 test positive

Symptomtext

09/10/22 presents to ED for "fatigue". PMHx of "type 2 diabetes mellitus, diabetic peripheral neuropathy, diabetic nephropathy status post renal transplant, coronary artery disease"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 09/10/22 SARS-CoV-2 (COVID-19) detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2496761

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: CT
Alter: 41,0
Geschlecht: F
Eingang: 02.11.2022
Impfdatum: 03.04.2021
Beginn: 14.05.2021
Tage bis Beginn: 41,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Blood test Computerised tomogram Nephrolithiasis Pain Renal stone removal Stent removal Surgery Telemedicine Ultrasound kidney abnormal Urine analysis

Symptomtext

I have no family history of kidney stones and had never had them in my life. Have to see Urologist, Nephrologist and visited ER multiple times for pain and eventually had surgery for removal. I still am experiencing kidney stones to this day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: 4,0
Labordaten: May 14, 2021 ER visit=Ct scan, bloodwork, urine tested, pain medication May 16, 2021 ER visit=Ct scan, bloodwork, urine tested, pain medication May 19, 2021 Urologist appointment=First consult, bloodwork ordered May 21, 2021 Urologist phone call, pain medication May 23, 2021 ER visit=Ct scan, bloodwork, pain medication May 26, 2021 ER visit= Ct scan, bloodwork, urine test, pain medication May 27, 2021 Urologist telemedicine= Litholink ordered July 13, 2021 Urologist phone call=Litholink results July 15, 2021 Urologist order November 29, 2021 Urologist appointment=bloodwork order, start potassium December 27, 2021 Urologist ordered Litholink February 25, 2022 Urologist call=Litholink results March 2, 2022 Urologist order March 7, 2022 Urologist order, pain medication March 18, 2022 Urologist order pain medication, Tamsulosin March 21, 2022 Urologist order pain medication March 24, 2022 Urologist order pain medication June 7, 2022 Nephrology appointment=consult, bloodwork order September 3, 2022 ER visit=admitted, pain medication, bloodwork, urine test, Ct scan September 5, 2022 ER visit=admitted, pain medication, bloodwork, urine test, Ct scan, prep for surgery September 6, 2022=Surgery September 15, 2022= stent removal September 23, 2022= Nephrologist appointment/Urologist appointment October 20, 2022=Renal Ultrasound
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure Anxiety Depression
Andere Medikamente: Premarin Vitamin C, Vitamin D ProAir Inhaler Benadryl Montelukast Losartan Amlodipine Pravastatin Alprazolam Pantoprazole Trazodone Sertraline
Allergien: Valium Augmentin Doxycycline
Vorherige Impfungen: -

VAERS 2487454

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

mild

Staat: WI
Alter: 58,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 30.11.2021
Beginn: 01.01.2022
Tage bis Beginn: 32,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal distension Balance disorder Blood pressure increased Blood test Chest discomfort Disturbance in attention Fall Fatigue Gait disturbance Hypogeusia Hyposmia Injection site pain Joint stiffness Memory impairment Musculoskeletal stiffness Pain Paranasal sinus discomfort Stress echocardiogram

Symptomtext

injection site tenderness, slight body aches for a couple days afterward. In January 2022 began experiencing facial -sinus pressure and over ensuing months, until mid September 2022, new sxs began to arise and increase in severity: diminished sense of taste and smell (these were lost post Covid infection in Nov 2020) and never fully recovered; entire body aches and pains, muscular and joint stiffness, with resultant difficulty walking; impaired balance; extreme fatigue; bloating (abdominal and legs); chest heaviness; approx 1-month period of consistently higher than normal BPs; each ankle gave-way in 1-month timespan, resulting in falls off stairs; extreme difficulty focusing, concentrating, remembering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Normal stress ECG and routine blood work over this period of time between January and June 2022. Dr suggested acupuncture and massage therapy.
Aktuelle Erkrankungen: none
Vorgeschichte: GERD, hypercholesterolemia, depression, anxiety, esophageal dysmotility
Andere Medikamente: simvastatin, fluoxetine, omeprazole, collagen protein, Claritin, montelukast. Vit B complex, calcium, vit D, vit B12. Herbal tincture of Holy Basil (Tulsi), acetaminophen
Allergien: yellow dye
Vorherige Impfungen: loss of sense of smell and taste after 1st Covid injection on 1/23/21.

VAERS 2481711

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: ME
Alter: 65,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 14.04.2022
Beginn: 21.09.2022
Tage bis Beginn: 160,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia Cough Diarrhoea Pyrexia Respiratory tract congestion SARS-CoV-2 test

Symptomtext

Weakness Cough Diarrhea Fever 101.5 max Congestion

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Home Covid test
Aktuelle Erkrankungen: Na
Vorgeschichte: Blood pressure Cholesterol Arthritis
Andere Medikamente: Fenofibrate 48 mg Atorvastatin calcium 10mg Lisinopril mg Voltaren 1% Acetaminophen 1000 mg Cetirizine Hydrocloride 10 mg vitamin D-3 5000iu Iron 18 mg
Allergien: No meds Environmental allergies Food allergies
Vorherige Impfungen: -

VAERS 2397271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: CA
Alter: 54,0
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 12.11.2021
Beginn: 24.02.2022
Tage bis Beginn: 104,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 SARS-CoV-2 test Vaccination failure Ear pain Ear swelling Hypoacusis Pain

Symptomtext

Positive on 25Feb2022; Positive on 25Feb2022; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 54-year-old female patient received BNT162b2 (BNT162B2), on 25Mar2021 at 12:00 as dose 1, single (Lot number: ER8730), in arm, on 22Apr2021 at 14:30 as dose 2, single (Lot number: EW0171), in arm and on 12Nov2021 at 11:40 as dose 3 (booster), single (Lot number: FH8028) at the age of 54 years, in arm, all intramuscular for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 24Feb2022, outcome "recovered" and all described as "Positive on 25Feb2022". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (22Feb2022) Negative, notes: Test: COVID Date: 22Feb2022 Result: NEG; (24Feb2022) Positive, notes: Test: COVID, Date: 24Feb2022 Result: POS; (25Feb2022) Positive, notes: confirmed positive on 25Feb2022. Lasted 13 days before testing negative on 09Mar2022; (03Mar2022) Positive, notes: Test: COVID Date: 03Mar2022 Result: POS; (08Mar2022) Negative, notes: Test: COVID Date: 08Mar2022 Result: NEG; (09Mar2022) Negative, notes: confirmed positive on 25Feb2022. Lasted 13 days before testing negative on 09Mar2022. Clinical information: Patient had not taken any other medication within two weeks of vaccination. past medical history was reported as none.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Test Date: 20220222; Test Name: Covid-19 Test; Test Result: Negative ; Comments: Test: COVID Date: 22Feb2022 Result: NEG; Test Date: 20220224; Test Name: Covid-19 Test; Test Result: Positive ; Comments: Test: COVID Date: 24Feb2022 Result: POS; Test Date: 20220225; Test Name: Covid-19 Test; Test Result: Positive ; Comments: confirmed positive on 25Feb2022. Lasted 13 days before testing negative on 09Mar2022; Test Date: 20220303; Test Name: Covid-19 Test; Test Result: Positive ; Comments: Test: COVID Date: 03Mar2022 Result: POS; Test Date: 20220308; Test Name: Covid-19 Test; Test Result: Negative ; Comments: Test: COVID Date: 08Mar2022 Result: NEG; Test Date: 20220309; Test Name: Covid-19 Test; Test Result: Negative ; Comments: confirmed positive on 25Feb2022. Lasted 13 days before testing negative on 09Mar2022
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: PATIENTS MEDICAL HISTORY (including any illness at time of vaccination): None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: CA
Alter: 54,0
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 12.11.2021
Beginn: 24.02.2022
Tage bis Beginn: 104,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 SARS-CoV-2 test Vaccination failure Ear pain Ear swelling Hypoacusis Pain

Symptomtext

Positive on 25Feb2022; Positive on 25Feb2022; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 54-year-old female patient received BNT162b2 (BNT162B2), on 25Mar2021 at 12:00 as dose 1, single (Lot number: ER8730), in arm, on 22Apr2021 at 14:30 as dose 2, single (Lot number: EW0171), in arm and on 12Nov2021 at 11:40 as dose 3 (booster), single (Lot number: FH8028) at the age of 54 years, in arm, all intramuscular for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 24Feb2022, outcome "recovered" and all described as "Positive on 25Feb2022". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (22Feb2022) Negative, notes: Test: COVID Date: 22Feb2022 Result: NEG; (24Feb2022) Positive, notes: Test: COVID, Date: 24Feb2022 Result: POS; (25Feb2022) Positive, notes: confirmed positive on 25Feb2022. Lasted 13 days before testing negative on 09Mar2022; (03Mar2022) Positive, notes: Test: COVID Date: 03Mar2022 Result: POS; (08Mar2022) Negative, notes: Test: COVID Date: 08Mar2022 Result: NEG; (09Mar2022) Negative, notes: confirmed positive on 25Feb2022. Lasted 13 days before testing negative on 09Mar2022. Clinical information: Patient had not taken any other medication within two weeks of vaccination. past medical history was reported as none.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Test Date: 20220222; Test Name: Covid-19 Test; Test Result: Negative ; Comments: Test: COVID Date: 22Feb2022 Result: NEG; Test Date: 20220224; Test Name: Covid-19 Test; Test Result: Positive ; Comments: Test: COVID Date: 24Feb2022 Result: POS; Test Date: 20220225; Test Name: Covid-19 Test; Test Result: Positive ; Comments: confirmed positive on 25Feb2022. Lasted 13 days before testing negative on 09Mar2022; Test Date: 20220303; Test Name: Covid-19 Test; Test Result: Positive ; Comments: Test: COVID Date: 03Mar2022 Result: POS; Test Date: 20220308; Test Name: Covid-19 Test; Test Result: Negative ; Comments: Test: COVID Date: 08Mar2022 Result: NEG; Test Date: 20220309; Test Name: Covid-19 Test; Test Result: Negative ; Comments: confirmed positive on 25Feb2022. Lasted 13 days before testing negative on 09Mar2022
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: PATIENTS MEDICAL HISTORY (including any illness at time of vaccination): None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2429738

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 48,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 30.11.2021
Beginn: 02.09.2022
Tage bis Beginn: 276,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Chills Cough Diarrhoea Headache Pain Sneezing

Symptomtext

Body aches, headaches, cough, sneeze, chills and diarrhea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2421053

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MI
Alter: 78,0
Geschlecht: F
Eingang: 26.08.2022
Impfdatum: 30.10.2021
Beginn: 22.08.2022
Tage bis Beginn: 296,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia Blood electrolytes Blood sodium decreased Blood thyroid stimulating hormone abnormal COVID-19 Chest X-ray normal Cough Decreased appetite Electrolyte substitution therapy Fatigue Laboratory test Malaise Memory impairment Oropharyngeal pain SARS-CoV-2 test positive Thyroid function test

Symptomtext

Discharge Physician: Primary Care Physician: Date of Admission: 8/22/2022; Discharge Date: 8/24/2022; Room Number: 2020/2020-1; PRESENTING PROBLEM: Weakness [R53.1]; Generalized weakness [R53.1]; COVID-19 [U07.1]HOSPITAL COURSE:A 79 y.o. female who presents today with weakness and fatigue. The patient is somewhat forgetful and cannot give many details about duration of symptoms. She reports that she started feeling ill two days ago however was seen in the ER at Hospital on 8/18 with report of symptoms starting a day or so before this visit. She has been having significant fatigue, weakness, a cough, sore throat and poor appetite. Many of her family members have had COVID. She tested positive on a home test and was given a prescription for paxlovid in the ER on 8/18. Her husband was admitted to the hospital last night and son had concerns about the patient's ability to care for herself at home so she was brought to the ER for evaluation. In the ER the patient had labs which were mostly unremarkable. Her sodium was a bit lower than her recent baseline at 128. She was COVID positive. Her CXR was negative. She was not hypoxic. She was admitted to the hospitalist team for PT/OT evaluation and possible placement. She was continued on IV fluid with improvement of sodium. PT/OT evaluated advised home health PT/OT and return to assisted living. Patient unable to return to assisted living until completion of quarantine for which patient's family was agreeable to watching her patient and spouse until end quarantine. Electrolytes were monitored and repleted PRN throughout the admission. TFTs were updated and she had notable improvement of TSH. Patient clinically improved and hemodynamically stable for discharge. Discussed plan of care discharge with patient including outpatient follow-up PCP within 7 days. Patient voiced understanding was agreeable with plan of care discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Microscopic colitis;Unspecified hypothyroidism;CAD (coronary artery disease); S/P coronary artery stent placement; Mixed hyperlipidemia; Moderate episode of recurrent major; Depressive disorder (HCC); Essential hypertension; Diverticulosis; Primary osteoarthritis of both knees; Age-related osteoporosis with current pathological fracture with routine healing Abnormality of gait; Falls frequently; NPH (normal pressure hydrocephalus) (HCC); Leg length difference, acquired; Slow transit constipation; GERD (gastroesophageal reflux disease); Stress-induced cardiomyopathy; Essential tremor; Mild cognitive disorder Recurrent urinary tract infection; Benign paroxysmal positional vertigo due to bilateral; vestibular disorder; Generalized anxiety disorder; Generalized weakness; COVID-19.
Andere Medikamente: Acetaminophen (TYLENOL); Alaprazolam (XANAX); Aspirin; Bupropion (WELLBUTRIN XL); Calcium-vitamin D (OSCAL-600); Cholecalciferol (VITAMIN D3); Estradiol (ESTRACE) 0.1 MG/GM vaginal cream; Fluoxetine (PROZAC); Levothyroxine (SYNTHROID); Meto
Allergien: Arthrotec [Diclofenac-misoprostol]Diarrhea; Crestor [Hmg-coa-r Inhibitors]Diarrhea; Cymbalta [Duloxetine Hcl]Rash; Methyl SalicylateDiarrhea; PravastatinDiarrhea; Sulfa DrugsRash; Zocor [Simvastatin]Diarrhea.
Vorherige Impfungen: -

VAERS 2415778

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: GA
Alter: 45,0
Geschlecht: F
Eingang: 19.08.2022
Impfdatum: 09.02.2022
Beginn: 10.08.2022
Tage bis Beginn: 182,0
Dosis: 3
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Pain Walking aid user

Symptomtext

On 08/10/2022, that morning as soon as I stood up I had a sharp pain from the knee all the way up. I have not been to the doctor, but I have been walking with a cane. The next day the sharp pain happened again and stayed. It felt as though someone had smashed my knee with a sledge hammer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetic; High Cholesterol; Fatty Liver
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: Dose 2 Pfizer, 07-01-2021, itching

VAERS 2408618

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

mild

Staat: PA
Alter: 61,0
Geschlecht: F
Eingang: 11.08.2022
Impfdatum: 02.12.2021
Beginn: 03.08.2022
Tage bis Beginn: 244,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Abdominal pain Abdominal pain upper Acute kidney injury COVID-19 Nausea Renal impairment SARS-CoV-2 test positive Vomiting

Symptomtext

Presented with epigatric pain and abdominal pain with nausea and vomiting. covid + and aqute kideny injury treated with iv fluids and bicarb. Kidney function improved pt discharged home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: DM, Htn, hld, ckd, asthma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2405620

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: SC
Alter: 51,0
Geschlecht: F
Eingang: 09.08.2022
Impfdatum: 04.05.2022
Beginn: 05.07.2022
Tage bis Beginn: 62,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Diarrhoea Fatigue Influenza like illness Nausea Oropharyngeal pain Productive cough SARS-CoV-2 test positive Throat irritation

Symptomtext

On July 5th, I woke up with a scratchy and sore throat and flu-type symptoms, exhaustion. I then took an at home test that was positive. I went and had a PCR test at an Urgent Care. I proceeded to have a productive cough for two weeks and then on July 19th I went to another Urgent Care and received another rapid test and that was a "hard positive". Prescribed an antibiotic. August 1st was the first day that I did not feel flu-like symptoms. I had experienced an abnormal sputum cough, diarrhea, and fatigue, nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: COVID-19 rapid test- negative (7/5), COVID-19 rapid test-positive (7/6), COVID-19 rapid test-positive (7/19)
Aktuelle Erkrankungen: N/A
Vorgeschichte: Congenital heart disease (HCM), Hypertension
Andere Medikamente: Jantoven; Zetia; Sertraline; Pantoprazole; Diltiazem; Skyla IUD; Flonase; Arthritis Acetaminophen; Testosterone pellets (every 3 months); Probiotic; Essential Enzymes.
Allergien: Seasonal
Vorherige Impfungen: -

VAERS 2401348

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 33,0
Geschlecht: F
Eingang: 04.08.2022
Impfdatum: 26.11.2021
Beginn: 02.08.2022
Tage bis Beginn: 249,0
Dosis: 3
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Abdominal pain Chills Diarrhoea Fatigue Hyperhidrosis Nausea Pyrexia Vomiting

Symptomtext

chills, diaphoresis, fatigue, fever, abdominal pain, diarrhea, nausea, vomiting

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2395173

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WA
Alter: 71,0
Geschlecht: M
Eingang: 28.07.2022
Impfdatum: 27.04.2022
Beginn: 16.06.2022
Tage bis Beginn: 50,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Malaise Oropharyngeal pain Pain SARS-CoV-2 test positive Somnolence

Symptomtext

On June 16, 2022 I had a sore throat and a cough that got worse by June 17, 2022 and I also wanted to sleep more and had body aches. The sore throat was worse than any strep throat I ever had. I called my Primary Care Physician and was prescribed PAXLOVID and started taking on June 18, 2022. After taking it for five days my wife and I were better then we started feeling ill again on June 28, 2022. We retested with our home COVID-19 test and were positive again so we quarantined until July 5, 2022 until were negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: Home COVID-19 test
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Levothyroxine; amlodipine; multivitamin: glucosamine sulfate
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2394962

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 95,0
Geschlecht: F
Eingang: 28.07.2022
Impfdatum: 16.11.2021
Beginn: 19.07.2022
Tage bis Beginn: 245,0
Dosis: 3
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Cough Decreased activity Fatigue

Symptomtext

activity change, fatigue, cough

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2364350

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: CO
Alter: 58,0
Geschlecht: F
Eingang: 11.07.2022
Impfdatum: 03.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 29,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: nein

Anticoagulant therapy Aortic occlusion Arterial occlusive disease Arthralgia Asthenia Computerised tomogram Computerised tomogram abdomen Dysstasia Fatigue Gait disturbance Pain Pain in extremity Ultrasound Doppler abnormal

Symptomtext

In January 2022, I began experiencing hip and leg pain and fatigue when walking or standing. It progressed over time and in April 2022, I was unable to walk any significant distance without pain and weakness. May 8, 2022, I was unable to walk and went to the ER where I was diagnosed with a partial blockage of my distal aorta and arterial occlusions in both legs, primarily my right leg. I was admitted to the hospital where I was put on a heparin IV. I came dangerously close to losing my right foot. I am now on Xeralto indefinitely and will be having surgery July 26, 2022, to attempt to open up the artery in my right leg.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: 2,0
Labordaten: May 8, 2022: CT scan of abdomen and both legs/feet May 8-10, 2022: Admitted to hospital June 7, 2022: Blood pressure tests in legs; ultrasound of right leg arteries/veins June 24, 2022: CT scan of abdomen and both legs/feet
Aktuelle Erkrankungen: -
Vorgeschichte: Myelofibrosis Diverticulosis Hiatal hernia
Andere Medikamente: Jakifi Omeprazole
Allergien: -
Vorherige Impfungen: -

VAERS 2356525

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WA
Alter: 69,0
Geschlecht: F
Eingang: 03.07.2022
Impfdatum: 15.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Influenza like illness Pain in extremity

Symptomtext

sore arm; slight flu like symptoms; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 70-year-old female patient received BNT162b2 (BNT162B2), on 15Nov2021 at 10:00 as dose 3 (booster), single (Lot number: FH8028) at the age of 69 years intramuscular, in arm for covid-19 immunisation. The patient's relevant medical history included: "Hysterectomy", start date: 1978 (unspecified if ongoing); "Illness" (unspecified if ongoing); "B/P" (unspecified if ongoing); "Depression" (unspecified if ongoing); "Cholesterol" (unspecified if ongoing); "Hormone" (unspecified if ongoing). Concomitant medication(s) included: METOPROLOL TARTRATE oral taken for blood pressure abnormal, start date: 2012 (ongoing); CITALOPRAM oral taken for depression, start date: 2019 (ongoing); ESTRADIOL oral taken for hormone therapy, start date: 1999 (ongoing); WELLBUTRIN oral taken for depression, start date: 2012 (ongoing); ATORVASTATIN oral taken for blood cholesterol, start date: 2020 (ongoing). Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Lot number: EN6208; Route of administration: Intramuscular; Anatomical site: upper arm; Vaccine administration time: 9:30), administration date: 16Mar2021, when the patient was 69-year-old, for Covid-19 immunization, reaction(s): "sore arm", "slight flu like symptoms"; BNT162b2 (DOSE 2, SINGLE; Lot number: EW0151; Route of administration: Intramuscular; Anatomical site: upper arm; Vaccine administration time: 10:00), administration date: 06Apr2021, when the patient was 69-year-old, for Covid-19 immunization, reaction(s): "sore arm", "slight flu like symptoms". The following information was reported: INFLUENZA LIKE ILLNESS (non-serious) with onset Nov2021, outcome "recovered" (2021), described as "slight flu like symptoms"; PAIN IN EXTREMITY (non-serious) with onset Nov2021, outcome "recovered" (2021), described as "sore arm". Additional information: The patient had just sore arm and slight flu like symptoms with first 3 immunizations. Lasted 2 days. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No specific relevant test for thromboembolic events with thrombocytopenia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure abnormal; Cholesterol; Depression; Hormone therapy; Hysterectomy; Illness
Andere Medikamente: METOPROLOL TARTRATE; CITALOPRAM; ESTRADIOL; WELLBUTRIN; ATORVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2347588

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: FL
Alter: 57,0
Geschlecht: F
Eingang: 01.07.2022
Impfdatum: 30.12.2021
Beginn: 21.06.2022
Tage bis Beginn: 173,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Chills Diarrhoea Fatigue Headache Malaise Pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Vomiting

Symptomtext

I contracted COVID-19 on 06/21/2022 with symptoms of fatigue, body aches, headache, fever of 101.8 at highest point, chills, congestion, and diarrhea. I was prescribed Paxlovid on 06/23/2022 and 15 to 20 I took my first dose I began violently throwing up, so I only took 4 doses of it. I was ill for 6 days before my symptoms began to resolve. I am still experiencing lingering fatigue and congestion. I am not fully recovered yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 rapid test was positive on 06/23/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: COPD; Hypertension; Celiacs Disease
Andere Medikamente: Excedrin; Gluten Intolerance Digestive Aid; THC
Allergien: Gluten; Codeine; Morphine; Oxycontin; Hydrocodone; Percocet
Vorherige Impfungen: Flu shot resulted in flu like symptoms in 2003 or 2004

VAERS 2326003

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8028

mild

Staat: NY
Alter: 63,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 12.06.2022
Beginn: 13.06.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test Electrocardiogram abnormal Fatigue Gingival discomfort Headache Mastication disorder Nausea Noninfective gingivitis Oral discomfort Oral herpes Pyrexia Rash SARS-CoV-2 test negative Stomatitis Urticaria Viral infection

Symptomtext

Nausea, 102 fever for 3 days, headache, exhaustion, irregular EKG, viral infection, rash, hives, mouth sores, cold sores, burning mouth and gums, unable to chew, sores on gums

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 6/14/2022 Covid tests at at Immediate Care and hospital result negative. EKG 6/14/2022 at Immediate Care and hospital, 6/14/2022 blood work hospital. 6//17/2022 Prednisone 20 mg prescribed by primary doctor. 6/18/2022 hospital Blood work and IV Prednisone and Benadryl, Prednisone prescription 40 mg prescribed by doctor at hospital
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure, high cholesterol, high triglycerides, migraines, arthritis
Andere Medikamente: Daily Irbesartan 300 mg daily = High BP Atorvastatin 20 mg daily = High Cholesterol Hydrochlorothiazide 25 mg daily = High BP Meloxicam 7.5 mg = Arthritis pain Levothyroxine 25 mcg daily (aka Synthroid) = Low metabolism /thyroid Nadolol
Allergien: Allergies and medications unable to tolerate Amoxicillin (oral thrush) Acyclovir (for infection, hives) Nystatin (rinse for oral thrush hives) Iodine Tramadol (extreme nausea, dizzy) Azor (headaches) Viibryd (sickly, dizzy, nightmares) Effexor (insomnia) Ultram Topamax (extreme mood swings, uncontrollable crying) Codeine (extreme nausea) Hydrocodone (extreme nausea) Oxycodone (extreme nausea) OxyContin (extreme nausea) Depakote Dilaudid (shallow breathing) Gabapentin (nauseous, dizzy) Lyrica 75 mg (extreme anger, no pain relief) Naproxen 500 mg 2 times a day with Imitrex for migraine (stomach pains, heartburn) Omeprazole 20 mg 1 pill per day while taking Naproxen (nausea, gas) Amlodpine Besylate 10 mg daily Stopped 5/4/21 Swelling Shellfish (anaphylactic shock) Walnuts (migraines) Red grapes (migraines) Alcohol any kind (migraines)
Vorherige Impfungen: -

VAERS 2311430

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NC
Alter: 51,0
Geschlecht: F
Eingang: 07.06.2022
Impfdatum: 31.05.2022
Beginn: 01.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dizziness Headache Somnolence Vaccination site pain

Symptomtext

Tenderness and aches of arm where injection was given; Tenderness and aches of arm where injection was given; Headache; Drowsiness; Light headedness; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 51-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 31May2022 at 11:45 as dose 4 (booster), single (Lot number: FH8028) at the age of 51 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hypertension" (unspecified if ongoing); "Known allergies: Whey from milk" (unspecified if ongoing), notes: Known allergies: Whey from milk; "Known allergies: Unknown fragrance" (unspecified if ongoing), notes: Known allergies: Unknown fragrance. The patient took concomitant medications. Vaccination history included: BNT162b2 (Prev dose product: COVID 19,, Prev dose brand: Pfizer,, Prev dose lot number: FF8839, Prev dose dose number: 3,, Prev dose vaccine location: Left arm), administration date: 20Oct2021, when the patient was 50-year-old, for COVID-19 Immunization; BNT162b2 (Prev dose product: COVID 19,, Prev dose brand: Pfizer,, Prev dose lot number: EL3247,, Prev dose dose number: 2,, Prev dose vaccine location: Left arm), administration date: 08Feb2021, when the patient was 49-year-old, for COVID-19 Immunization; BNT162b2 (Prev dose product: COVID 19, Prev dose brand: Pfizer,, Prev dose lot number: EL3247, Prev dose dose number: 1), administration date: 20Jan2021, when the patient was 49-year-old, for COVID-19 Immunization. The following information was reported: SOMNOLENCE (non-serious) with onset 01Jun2022 at 01:00, outcome "recovering", described as "Drowsiness"; HEADACHE (non-serious) with onset 01Jun2022 at 01:00, outcome "recovering"; DIZZINESS (non-serious) with onset 01Jun2022 at 01:00, outcome "recovering", described as "Light headedness"; VACCINATION SITE PAIN (non-serious), VACCINATION SITE PAIN (non-serious) all with onset 01Jun2022 at 01:00, outcome "recovering" and all described as "Tenderness and aches of arm where injection was given". Therapeutic measures were taken as a result of vaccination site pain, vaccination site pain, headache, somnolence, dizziness. Additional information: Patient had not received other vaccine in four weeks. Patient had received other medications in two weeks. Patient had not COVID prior vaccination. Patient had not COVID tested post vaccination. Patient had took acetaminophen treatment for AE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fragrance sensitivity (Known allergies: Unknown fragrance); Hypertension; Milk protein allergy (Known allergies: Whey from milk.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2308451

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MA
Alter: 54,0
Geschlecht: F
Eingang: 03.06.2022
Impfdatum: 10.11.2021
Beginn: 19.05.2022
Tage bis Beginn: 190,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Feeling abnormal Pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Tested positive for Covid 19. Symptoms included congestion, body aches and feeling "run down"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2306456

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NY
Alter: -
Geschlecht: U
Eingang: 02.06.2022
Impfdatum: 18.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pain in extremity Tinnitus

Symptomtext

Tinnitus; Occasional ringing; Arm is really hurting; Hearing a hissing sound in my ears; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A patient (no qualifiers provided) received BNT162b2 (BNT162B2), on 18Nov2021 as dose 3 (booster), single (Lot number: FH8028) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose 1), administration date: 21Mar2021, for COVID-19 Immunization; BNT162b2 (Dose 2, And it started from a pain in my arm and a little bit of fatigue.), administration date: 28Mar2022, for COVID-19 immunization, reaction(s): "pain in my arm", "little bit of fatigue". The following information was reported: TINNITUS (non-serious) with onset Nov2021, outcome "unknown", described as "Hearing a hissing sound in my ears"; PAIN IN EXTREMITY (non-serious) with onset 18Nov2021, outcome "unknown", described as "Arm is really hurting"; TINNITUS (non-serious), outcome "unknown"; TINNITUS (non-serious), outcome "unknown", described as "Occasional ringing". No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2305067

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MI
Alter: 49,0
Geschlecht: F
Eingang: 01.06.2022
Impfdatum: 30.11.2021
Beginn: 04.12.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Anxiety Temperature intolerance Urticaria Urticaria cholinergic

Symptomtext

Starting 12/04/2021, I got hives all over my body after exercising and getting hot. I was eventually diagnosed with cholinergic hives. I did an urgent visit, saw a dermatologist, saw my regular doctor and now going to see an allergist on Friday 06/03/2022. I take antihistamines, PEPCID and LEXAPRO (due to increased anxiety caused by the event). Its affecting me doing anything. Before the booster, I was able to go on long walks, exercise and do house work. However, now I can be in the middle of cleaning the house and break out in hives all over.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Multivitamin and Vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 2303328

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: PA
Alter: 32,0
Geschlecht: M
Eingang: 31.05.2022
Impfdatum: 23.11.2021
Beginn: 26.05.2022
Tage bis Beginn: 184,0
Dosis: 2
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

COVID-19 Cough Ear discomfort Hypoacusis Pain Respiratory tract congestion SARS-CoV-2 test positive Sneezing

Symptomtext

Initial symptom were fever 99.6 lasted two days, Cough is on 3 days that did not start with the other symptoms. Body aches that was 2 days. Congestion is 5 days. Sneezing that's 2 days and most recent that didn't start on the onset. Pressure and difficulty hearing that's been 3 days from today. They have me on an antiviral molnupiravir 200mg.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: At home Covid test, positive on this past Thursday, facility nasal shallow swap, positive on Friday.
Aktuelle Erkrankungen: No
Vorgeschichte: GERD; eczema
Andere Medikamente: Metoprolol; tenatoprazole; amlodipine; clonidine
Allergien: Penicillin
Vorherige Impfungen: MMR when I was young I couldn't get the 3rd shot because I had a bad reaction.

VAERS 2298576

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: RI
Alter: 66,0
Geschlecht: F
Eingang: 27.05.2022
Impfdatum: 24.11.2021
Beginn: 15.05.2022
Tage bis Beginn: 172,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Fatigue Nasal congestion Oropharyngeal pain Pain in extremity SARS-CoV-2 test positive

Symptomtext

Sore throat lasted less than 24 hours. The fatigue was around the same time as the sore throat and I still have it now so it's ongoing. The nasal congestion that started about 24hours the sore throat. The cough that started on the 2nd day was a dry cough that started in the evening. The 3rd day is when I had the pain in my left arm. I still have stuffiness and occasional cough. The pain in my left arm lasted 24hrs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: At home Covid test - positive; 5/25/2022 at home test Covid-negative
Aktuelle Erkrankungen: No
Vorgeschichte: Chronic kidney disease; high cholesterol and blood pressure
Andere Medikamente: Lisinipril, Atorvastatin, Lorazadine, B complex, Vitam A, C, D, E, probiotic
Allergien: Penicillin; latex
Vorherige Impfungen: -

VAERS 2294569

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: VA
Alter: 43,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 12.11.2021
Beginn: 23.12.2021
Tage bis Beginn: 41,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Balance disorder COVID-19 Fatigue Feeling drunk Gait disturbance Hypersomnia Influenza like illness Malaise Motion sickness Nasopharyngitis SARS-CoV-2 test positive Vaccine breakthrough infection Vertigo

Symptomtext

COVID break through Case I received my 1st booster shot on 11/12/2021 and my COVID symptoms started on 12/23/2021 i had extreme fatigue, i was sleeping so much, i had no fever, very severe vertigo and I had to go see an ENT. I lost balance. I was like sea sick. I felt like was drunk and i couldn't walk on an straight line. i was exhausted . it was different than what i normally do. I didn't go to a doctor. I stayed in bed and took it like a flu or cold. my husband was positive with a PCR test and was positive. So i was positive too. the vertigo lasted for 3 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: psyscoiso on my skin.
Andere Medikamente: oral birth control pill
Allergien: none
Vorherige Impfungen: -

VAERS 2290713

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 23.05.2022
Impfdatum: 05.04.2022
Beginn: 09.05.2022
Tage bis Beginn: 34,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia COVID-19 Fatigue Oropharyngeal pain Pain Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Slight sore throat first 1/2 day. Sore throat, aches, fever up to 99.3, runny nose, slightly congested chest: 2 days. No energy extremely tired on 3rd day. Tired for 5 more days. Took Ibuprofen, Vitamin C and Zinc supplements.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 5/10/22 at home Covid test; result positive. 5/10/22 PCR Covid test; result positive.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Vitamin D
Allergien: -
Vorherige Impfungen: -

VAERS 2285148

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: KS
Alter: 56,0
Geschlecht: F
Eingang: 19.05.2022
Impfdatum: 17.11.2021
Beginn: 23.04.2022
Tage bis Beginn: 157,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Chills Oropharyngeal pain Pharyngeal swelling Pyrexia SARS-CoV-2 test positive Streptococcus test negative

Symptomtext

On 4/23rd, I started to feel a slight sore throat it continued with fever and chills and a swollen sore throat through 4/25/2022. I did a home COVID-19 test and it came back positive. I waited it out on the 25th and 26th. On the 27th, I went first thing in the morning to the urgent care because I was not getting better, but not getting worse either. They saw me and did as Strep test it was negative. They prescribed me Augmentin for 10 days to avoid getting pneumonia. And they recommended Flonase. I took the medication as prescribed and started to get better. I had a COVID-19 test on May 12, 2022 and tested negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 home test on 4/25/2022 positive. COVID-19 test 5/12/2022 negative.
Aktuelle Erkrankungen: No
Vorgeschichte: Depression
Andere Medikamente: Venlafaxine
Allergien: No
Vorherige Impfungen: -

VAERS 2280734

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NH
Alter: 63,0
Geschlecht: M
Eingang: 17.05.2022
Impfdatum: 15.11.2021
Beginn: 11.05.2022
Tage bis Beginn: 177,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cough Pyrexia Throat irritation

Symptomtext

I got on 05/11/2022. I had a cough, scratchy throat and a fever. It was a mild case. I had be quarantine for about 6 days. My doctor call me Paxlovid for 5 days and I took my last one today. I am feeling fine as of today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: High Blood Pressure; Cholesterol; Prostate
Andere Medikamente: Atorvastatin 40mg; finasteride 5mg; atenolol 25mg; loratadine 10mg; aspirin 81mg and multivitamin.
Allergien: No
Vorherige Impfungen: -

VAERS 2273356

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NC
Alter: 67,0
Geschlecht: F
Eingang: 12.05.2022
Impfdatum: 04.11.2021
Beginn: 14.12.2021
Tage bis Beginn: 40,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dermatitis Dry skin Eczema Pruritus

Symptomtext

12/14/21 Dryness and discharge in and around ears. Went to Hospital ER. They say its sebaceous dermatitis and was told to wash area with anti dandruff shampoo. 1/19/22 Condition continues. Visit to Dr, primary condition confirms previous diagnosis and was advised to use Aquaphor lotion. 3/3/22 Conditions continue and worsen,with itching developing. Visit to Dr, dermatologist diagnoses me with exzema. I have never had this condition before. I was prescribed Hydrocortisone 2.5% cream, ketoconazole cream and vanicream z soap. As of today, my condition has improved but not gone away. I am currently using aveeno exzema cream.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: PSVT arrhythmia
Andere Medikamente: Propranolol Digoxin Vitamin C Omega 3 Calcium Acidophilis
Allergien: none
Vorherige Impfungen: constipation

VAERS 2268998

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WA
Alter: 38,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 08.11.2021
Beginn: 05.05.2022
Tage bis Beginn: 178,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Chest discomfort Cough Headache Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Sore throat, headache, and fever (100.7) for first 3 days. Shifted into chest and lead into coughing 5/9, Feeling better overall so far.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 5/5, home test positive; 5/6 PCR test positive; 5/8 Prescribed anti viral, started taking them.
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma; allergies to dust; IBS-D
Andere Medikamente: Zyrtec, Flonase, Benadryl, ibuprofen
Allergien: Sulfa; adhesives; bee stings
Vorherige Impfungen: -

VAERS 2268930

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: SC
Alter: 69,0
Geschlecht: M
Eingang: 10.05.2022
Impfdatum: 04.11.2021
Beginn: 19.04.2022
Tage bis Beginn: 166,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Abdominal discomfort COVID-19 Cough Diarrhoea Ear discomfort Nasopharyngitis Pain SARS-CoV-2 test positive Upper-airway cough syndrome

Symptomtext

I got COVID-19 and it was first tested at home a couple of times then went and had it done on the 22nd. The beginning was mild with a little achiness, cough, postnasal drip, slight diarrhea, minor stomach discomfort. Now, as of today, I still have coughing, postnasal drip, sometimes my ears get clogged, and feel like I have a cold (achiness) that comes and goes. Went to Urgent Care on May 5th and they checked my lungs which were clear.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: At home COVID-19 Test April 29th - light positive mark Other previous COVID-19 Tests - very positive
Aktuelle Erkrankungen: No
Vorgeschichte: High Blood Pressure Diabetic Type 2
Andere Medikamente: Plavix Zetia Xigduo Vitamin E Vitamin D Omega 3 Fiber Osteopenia medication weekly
Allergien: No
Vorherige Impfungen: -

VAERS 2268791

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MA
Alter: 51,0
Geschlecht: M
Eingang: 10.05.2022
Impfdatum: 08.11.2021
Beginn: 06.04.2022
Tage bis Beginn: 149,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Head discomfort Malaise Nasopharyngitis Rhinorrhoea SARS-CoV-2 test positive Throat irritation

Symptomtext

COVID-19 symptoms started the evening of 04/06/2022, tested positive the morning of 04/07/2022. Initial onset symptoms were scratchy throat, and a mild runny nose that was commenced on Wednesday evening. Thursday morning, I had mild head congestion and I called my PCP, and they did a telehealth appointment with me and prescribed Paxlovid but pharmacy didn't have it and so they prescribed me Molnupiravir. Symptoms never progressed beyond mild head cold. I was symptom free a week later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: COVID-19 positive 04/07/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Heart Disease
Andere Medikamente: Centrum Silver Multivitamin Vitamin D3 5000 IUs Baby Aspirin 81 mg Valsartan 8ctz 320-25 Amlodipine 10 mg Rosuvastatin 40 mg Bystolic 20 mg
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2265946

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: VA
Alter: 42,0
Geschlecht: F
Eingang: 06.05.2022
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Ageusia Anosmia Asthenia COVID-19 Chills Cough Fatigue Hypersomnia Impaired driving ability Malaise Nasopharyngitis Oropharyngeal pain Pain SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

The first thing that was notable was that within 30-35 minutes, I felt tired to the point I didn't feel safe to drive. After that, I had chills for about two days. I had severe body aches, mostly at night, three nights in a row. I didn't leave my house. I didn't drive. I slept for 3 days and it went away. Breakthrough ,COVID-19 Case: I started feeling ill on April 13th. It started with a sore throat. I felt like I had a mild cold for three days until I lost smell and taste on Sunday, the 17th. I tested at home and it was positive. The week before I had multiple negative tests because I was going to travel. I would say I was very weak through April 20th. After that, I was able to work starting on April 21st. Although, I work and live a normal life, I have a lingering cough and I feel tired all the time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 04/17/2022 - Rapid At Home Test - Positive.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Topical Cream - Tretinoin 0.05%
Allergien: Nickel Clomid
Vorherige Impfungen: -

VAERS 2263223

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: VA
Alter: 62,0
Geschlecht: M
Eingang: 04.05.2022
Impfdatum: 02.11.2021
Beginn: 15.03.2022
Tage bis Beginn: 133,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Cough Headache Influenza A virus test negative Influenza B virus test Lethargy Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive Streptococcus test negative

Symptomtext

Cough, sore throat, headache, runny nose, lethargy starting on 15 March 2022 and continuing through 25 March 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 18 March 2022: Covid-19 antigen test -- POSITIVE Influenza A -- Negative Influenza B -- Negative Strep Gp A -- Negative
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes type 2, high cholesterol, bi-lateral sensory-neural hearing loss.
Andere Medikamente: Atorvastatin 40m, Metformin HCL 500mg, Bupropion HCL XL 150mg.
Allergien: None
Vorherige Impfungen: -

VAERS 2261912

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NY
Alter: 64,0
Geschlecht: F
Eingang: 03.05.2022
Impfdatum: 04.03.2021
Beginn: 20.04.2022
Tage bis Beginn: 412,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Bone pain Cough Headache Myalgia Pyrexia

Symptomtext

Cough, fever, muscle and bone pain, headache. 5 day course of Paxlvid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bone pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2260486

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WI
Alter: 62,0
Geschlecht: M
Eingang: 02.05.2022
Impfdatum: 01.12.2021
Beginn: 04.01.2022
Tage bis Beginn: 34,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Fatigue Feeling abnormal Head discomfort SARS-CoV-2 test positive Upper-airway cough syndrome

Symptomtext

I started feeling poorly on 01/04/2022. I tried to schedule a COVID-19 test but couldn't get in until 01/06/2022. I had a lot of head congestion and postnasal drip like cough. I was also really fatigued to the point that going up the stairs winded me. On 01/06/2022, I tested positive for COVID-19. I was given an rx for cough medicine which helped (Benzonate) and allowed me to get some sleep. These symptoms lasted for about a week then resolved. By the time I got the COVID19 test results back, I was already getting better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test (01/06/2022) : positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2161423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: PA
Alter: 48,0
Geschlecht: F
Eingang: 23.04.2022
Impfdatum: 23.11.2021
Beginn: 18.04.2022
Tage bis Beginn: 146,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 SARS-CoV-2 test Vaccination failure Fatigue Nausea Pain in extremity Vaccination site pain

Symptomtext

Contracted COVID/covid test result Positive; Contracted COVID/covid test result Positive; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 48-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 23Feb2021 as dose 1, single (Lot number: EL3247), in left arm, on 16Mar2021 as dose 2, single (Lot number: EN6203), in left arm and on 23Nov2021 as dose 3 (booster), single (Lot number: FH8028) at the age of 48 years, in left arm, all intramuscular for covid-19 immunisation. The patient's relevant medical history included: "Gastric Bleed" (unspecified if ongoing); "GERD" (unspecified if ongoing); "Diverticulosis" (unspecified if ongoing); "Allergies: Dairy" (unspecified if ongoing); "Allergies: Wheat" (unspecified if ongoing). Concomitant medication(s) included: ALLEGRA. Past drug history included: Augmenting for Allergy. The following information was reported: VACCINATION FAILURE (medically significant) with onset 18Apr2022, outcome "unknown", COVID-19 (medically significant) with onset 18Apr2022, outcome "recovering" and all described as "Contracted COVID/covid test result Positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (19Apr2022) positive, notes: Nasal Swab. Therapeutic measures were not taken as a result of covid-19. Clinical course: Patient had not received any other vaccines within 4 weeks prior to the COVID vaccine. Patient received Allegra within 2 weeks of vaccination. Patient was not diagnosed with COVID-19, prior to vaccination. Patient was tested for COVID-19 after the vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Date: 20220419; Test Name: Covid-19-19Apr2022; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diverticulosis; Food allergy; Gastric bleeding; GERD; Milk allergy
Andere Medikamente: ALLEGRA
Allergien: -
Vorherige Impfungen: -

VAERS 2161423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: PA
Alter: 48,0
Geschlecht: F
Eingang: 23.04.2022
Impfdatum: 23.11.2021
Beginn: 18.04.2022
Tage bis Beginn: 146,0
Dosis: 3
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 SARS-CoV-2 test Vaccination failure Fatigue Nausea Pain in extremity Vaccination site pain

Symptomtext

Contracted COVID/covid test result Positive; Contracted COVID/covid test result Positive; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 48-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 23Feb2021 as dose 1, single (Lot number: EL3247), in left arm, on 16Mar2021 as dose 2, single (Lot number: EN6203), in left arm and on 23Nov2021 as dose 3 (booster), single (Lot number: FH8028) at the age of 48 years, in left arm, all intramuscular for covid-19 immunisation. The patient's relevant medical history included: "Gastric Bleed" (unspecified if ongoing); "GERD" (unspecified if ongoing); "Diverticulosis" (unspecified if ongoing); "Allergies: Dairy" (unspecified if ongoing); "Allergies: Wheat" (unspecified if ongoing). Concomitant medication(s) included: ALLEGRA. Past drug history included: Augmenting for Allergy. The following information was reported: VACCINATION FAILURE (medically significant) with onset 18Apr2022, outcome "unknown", COVID-19 (medically significant) with onset 18Apr2022, outcome "recovering" and all described as "Contracted COVID/covid test result Positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (19Apr2022) positive, notes: Nasal Swab. Therapeutic measures were not taken as a result of covid-19. Clinical course: Patient had not received any other vaccines within 4 weeks prior to the COVID vaccine. Patient received Allegra within 2 weeks of vaccination. Patient was not diagnosed with COVID-19, prior to vaccination. Patient was tested for COVID-19 after the vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Date: 20220419; Test Name: Covid-19-19Apr2022; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diverticulosis; Food allergy; Gastric bleeding; GERD; Milk allergy
Andere Medikamente: ALLEGRA
Allergien: -
Vorherige Impfungen: -

VAERS 2247868

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: CO
Alter: 62,0
Geschlecht: M
Eingang: 22.04.2022
Impfdatum: 04.11.2021
Beginn: 21.04.2022
Tage bis Beginn: 168,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Malaise SARS-CoV-2 test positive

Symptomtext

pt found to be COVID+ on 4/21/22 s/p 3 doses of Pfizer vax (3/11/21, 4/1/21, 11/4/21). pt symptomatic & remdesivir started

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2243814

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

mild

Staat: PA
Alter: 70,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 13.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Hypoacusis Nerve injury Pain Pyrexia Tinnitus Tonsillar hypertrophy

Symptomtext

chills, fever, aches, nerve damage to hearing swollen tonsils, tinnutis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: fiber
Allergien: sulfur
Vorherige Impfungen: -

VAERS 2241998

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WA
Alter: 23,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 28.10.2021
Beginn: 27.03.2022
Tage bis Beginn: 150,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Erythema Pruritus Rash Skin irritation Urticaria

Symptomtext

Skin irritation, hives, bumps, itching, redness, rash

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: penicillin
Vorherige Impfungen: -

VAERS 2241129

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: GA
Alter: 40,0
Geschlecht: M
Eingang: 19.04.2022
Impfdatum: 14.11.2021
Beginn: 27.12.2021
Tage bis Beginn: 43,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Asthenia COVID-19 Chills Fatigue Pyrexia SARS-CoV-2 test positive

Symptomtext

I felt weak and tired. I had chills and fever. On Dec 29th, I tested positive for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: N/A
Vorgeschichte: High blood pressure
Andere Medikamente: Olmesartan medoxomil 20mg
Allergien: N/A
Vorherige Impfungen: -

VAERS 2241120

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WA
Alter: 78,0
Geschlecht: M
Eingang: 19.04.2022
Impfdatum: 11.11.2021
Beginn: 19.02.2022
Tage bis Beginn: 100,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test normal Pruritus Sleep disorder Urticaria

Symptomtext

I woke up in the middle of the night with itching. I took an antihistamine. That helped but when it wore off the itching came back and its been persistent. It caused hives around my bellybutton, shoulders, back and chest. It does affect my arms and legs, but not as prominent. It definitely seems like an allergic reaction, but I don't know the cause. I have eliminated foods that could cause it. I even changed my laundry detergent and nothing is changing it. I think it is a reaction to the shingles vaccine and Pfizer booster being taken in close timing. On 03/06/2022, I did see my doctor. He advised to keep taking the antihistamines. On 03/10/2022, I was prescribed a topical cream for the hives. I now take antihistamines three times a day and it helps, but if I don't take it on time the itching starts all over.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: 03/21/2022 Blood panel: Normal
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic asthma through young adulthood.
Andere Medikamente: Flomax .4mg twice daily, Omeprazole 20mg once daily, Atorvastatin 20mg once daily, Wellbutrin 150mg twice daily., Multivitamin, Calcium magnesium zinc.
Allergien: None
Vorherige Impfungen: -

VAERS 2240795

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: PA
Alter: 55,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 06.11.2021
Beginn: 06.11.2001
Tage bis Beginn: -
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Feeling hot Lymphadenopathy Ultrasound scan normal

Symptomtext

11/06/2021 The night after my vaccination I ended up with glands under my left arm swelled up so bad. I was so hot and had chills. I went to to doctor and ended up in the ER. The glands under my left arm were so big and hot. This lasted for about 4 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Ultrasound, normal
Aktuelle Erkrankungen: None
Vorgeschichte: Bi Polar Asthma Hypo Thyroidism Sleep Apnea
Andere Medikamente: Geodon Lamictal Visceral Reequip Lexapro Baby aspirin Synthroid Remeron
Allergien: Penicillin Sulpha Methoprednisone Pseudoephedrine Clindamycin Metronidazole Clonazepam Methocarbamol Eudefonide-formoterol Fumarate
Vorherige Impfungen: -

VAERS 2237995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: OH
Alter: 58,0
Geschlecht: M
Eingang: 16.04.2022
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Vaccination site pain

Symptomtext

Chills; soreness at the injection site on left arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 58-year-old male patient received BNT162b2 (BNT162B2), on 30Oct2021 as dose 3 (booster), single (Lot number: FH8028, Expiration Date: 31May2022) at the age of 58 years, in left arm for covid-19 immunisation, prophylaxis. The patient's relevant medical history included: "High blood pressure" (ongoing), notes: About 20 years ago; "High Cholesterol" (ongoing), notes: About 20 years ago; "Sarcoidosis" (ongoing), notes: diagnosed maybe 12 years ago, Pertinent Details: He sees a respiratory therapist for this condition. There were no concomitant medications. Vaccination history included: BNT162b2 (First dose, Lot: E88732, Expiry: 31Jul2021, NDC: Unknown, not on the CDC vaccine record card., Dose: Unknown strength/volume/dose injection to he thinks left arm), administration date: 27Mar2021, when the patient was 57-year-old, for COVID-19 Immunization; BNT162b2 (Second dose, Lot: ER8731, Expiry: 31Jul2021, NDC: Unknown, not on the CDC vaccine record card., Dose: Unknown strength/volume/dose injection to he thinks left arm), administration date: 17Apr2021, when the patient was 57-year-old, for COVID-19 Immunization. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 30Oct2021, outcome "recovered" (Nov2021), described as "soreness at the injection site on left arm"; CHILLS (non-serious), outcome "recovered". Additional information: He also mentioned having chills and soreness at the injection site on left arm after his first booster shot of Pfizer Covid-19. There was no prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s). There was no AE(s) following prior vaccinations. Family Medical History Relevant to AE. Relevant Tests was none. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Blood pressure high (About 20 years ago); High cholesterol (About 20 years ago); Sarcoidosis (diagnosed maybe 12 years ago Pertinent Details: He sees a respiratory therapist for this condition.)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1880383

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FH8028

mild

Staat: IA
Alter: 68,0
Geschlecht: F
Eingang: 16.04.2022
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Extra dose administered Feeling abnormal Headache Pain Product storage error Factor VIII deficiency Fatigue Incorrect dose administered Overdose Poor quality product administered Product administration error

Symptomtext

severe HA; body aches; fatigue; Administered one dose each of expired vaccine; Administered one dose each of expired vaccine; Patient administered another dose of the Pfizer COVID 19 Vaccine; Patient administered another dose of the Pfizer COVID 19 Vaccine; This is a spontaneous report received from contactable reporter(s) (Nurse) from medical information team. A 68-year-old female patient received BNT162b2 (COMIRNATY), on 09Nov2021 at 08:18 as dose 3, (booster) 0.3 ml single (Lot number: FH8028, Expiration Date: 31May2022) at the age of 68 years intramuscular, in left deltoid for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (ongoing); "Fatigue" (ongoing); "Depression/Anxiety" (ongoing); "Depression/Anxiety" (ongoing); "Myalgia" (ongoing); "Cervical tension" (ongoing); "GERD" (ongoing); "Rhinitis" (ongoing); "Insomnia" (ongoing); "Obesity" (ongoing); "Osteoporosis" (ongoing); "Hypertension" (ongoing); "Hyperthyroidism" (ongoing). Concomitant medication(s) included: ALENDRONATE oral taken for osteoporosis (ongoing); FLUTICASONE PROPIONATE nasal taken for seasonal allergy (ongoing); ATORVASTATIN oral taken for blood cholesterol (ongoing); PREVACID oral taken for abdominal discomfort (ongoing); FLOVENT (ongoing); MONTELUKAST oral (ongoing); GABAPENTIN oral taken for back pain (ongoing); ZOLPIDEM oral taken for sleep disorder (ongoing); AMITRIPTYLINE oral taken for anxiety, sleep disorder (ongoing). Vaccination history included: BNT162b2 (1st dose, Lot: unknown; Expiration: unknown, Pfizer/BioNTech Covid-19 vaccine details, Dose: 1st, Date/time, Date: 16Apr2021, Site and route of injection, Route of administration: intramuscular [checked], Batch/lot number: other, please specify: given elsewhere), administration date: 16Apr2021, when the patient was 68-year-old, for Covid-19 immunization; BNT162b2 (2nd dose, Lot: unknown; Expiration: unknown, Pfizer/BioNTech Covid-19 vaccine details, Dose: 2nd, Date/time, Date: 05May2021, Site and route of injection, Route of administration: intramuscular [checked], Batch/lot number: other, please specify: given elsewhere), administration date: 05May2021, when the patient was 68-year-old, for Covid-19 immunization; flu shot, administration date: 06Jan2021, when the patient was 67-year-old, for Immunization; high dose fluzone (Lot: UJ760AC, Manufacturer: GSK, IM, Left Deltoid), administration date: 20Oct2021, when the patient was 68-year-old, for Immunization. The following information was reported: PRODUCT ADMINISTRATION ERROR (non-serious), POOR QUALITY PRODUCT ADMINISTERED (non-serious) all with onset 09Nov2021, outcome "unknown" and all described as "Administered one dose each of expired vaccine"; OVERDOSE (non-serious), INCORRECT DOSE ADMINISTERED (non-serious) all with onset 09Nov2021, outcome "unknown" and all described as "Patient administered another dose of the Pfizer COVID 19 Vaccine"; FACTOR VIII DEFICIENCY (non-serious), outcome "recovered", described as "severe HA"; PAIN (non-serious), outcome "recovered", described as "body aches"; FATIGUE (non-serious), outcome "recovered". Therapeutic measures were taken as a result of factor viii deficiency, pain, fatigue. Additional information: Prior vaccination (within 4 weeks) was Flu zone. Specific relevant test for thromboembolic event with thrombocytopenia were None. Patient in to office to receive 3rd covid-19 vaccine and medical assistant did not notice that the Pfizer in fridge were from the night before (08Nov2021). MA gave vaccine to patient at 08:18 and then went to chart vaccine she noticed time on syringe was from previous afternoon. Call was made to immune coordinator, she was advised to give another Pfizer vaccine that was drawn on 09Nov2021. 2nd Pfizer covid-19 given at 08:40. Call made to risk manager at that time. Pfizer immediately called informed AE, no need for 2nd Pfizer. Pt notified Pt 40 severe HA, body aches, fatigue after 2 Pfizer covid vaccines was treated with OTC Ibuprofen + Tylenol. No further complaints from pt. made complete recovery. There were no relevant tests. No follow-up attempts are possible. No further information is expected. Amendment: This follow-up report is being submitted to amend previous information: Recoded the event verbatim "Administered one dose each of expired vaccine" from "Expired vaccine used" to "Product administration error", and coded the new event verbatim "Administered one dose each of expired vaccine" coded as "Poor quality vaccine administered" and event verbatim "Patient administered another dose of the Pfizer COVID 19 Vaccine" coded as "Inappropriate dose of Vaccine administered". Follow-Up (25Mar2022): Follow-up attempts are completed. No further information is expected. Follow-up (12Apr2022): This is a spontaneous follow-up report received from a contactable Nurse. This Nurse reported in response to HCP letter sent which included that: Updated information included Primary reporter's middle name, Suffix and Alternate Phone, new AE: "Hemophilia A, Ache, Fatigue", dose 1, 2 details, concomitant drug, 3rd dose details, relevant medical history. Follow-up (15Apr2022): Follow-up attempts are completed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101549752 Same reporter drug AE, different patient

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Anxiety; Asthma; Cervical tension syndrome; Depression; Fatigue; GERD; Hypertension; Hyperthyroidism; Insomnia; Myalgia; Obesity; Osteoporosis; Rhinitis
Vorgeschichte: -
Andere Medikamente: ALENDRONATE; FLUTICASONE PROPIONATE; ATORVASTATIN; PREVACID; FLOVENT; MONTELUKAST; GABAPENTIN; ZOLPIDEM; AMITRIPTYLINE
Allergien: -
Vorherige Impfungen: -

VAERS 1880383

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: IA
Alter: 68,0
Geschlecht: F
Eingang: 16.04.2022
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Extra dose administered Feeling abnormal Headache Pain Product storage error Factor VIII deficiency Fatigue Incorrect dose administered Overdose Poor quality product administered Product administration error

Symptomtext

severe HA; body aches; fatigue; Administered one dose each of expired vaccine; Administered one dose each of expired vaccine; Patient administered another dose of the Pfizer COVID 19 Vaccine; Patient administered another dose of the Pfizer COVID 19 Vaccine; This is a spontaneous report received from contactable reporter(s) (Nurse) from medical information team. A 68-year-old female patient received BNT162b2 (COMIRNATY), on 09Nov2021 at 08:18 as dose 3, (booster) 0.3 ml single (Lot number: FH8028, Expiration Date: 31May2022) at the age of 68 years intramuscular, in left deltoid for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (ongoing); "Fatigue" (ongoing); "Depression/Anxiety" (ongoing); "Depression/Anxiety" (ongoing); "Myalgia" (ongoing); "Cervical tension" (ongoing); "GERD" (ongoing); "Rhinitis" (ongoing); "Insomnia" (ongoing); "Obesity" (ongoing); "Osteoporosis" (ongoing); "Hypertension" (ongoing); "Hyperthyroidism" (ongoing). Concomitant medication(s) included: ALENDRONATE oral taken for osteoporosis (ongoing); FLUTICASONE PROPIONATE nasal taken for seasonal allergy (ongoing); ATORVASTATIN oral taken for blood cholesterol (ongoing); PREVACID oral taken for abdominal discomfort (ongoing); FLOVENT (ongoing); MONTELUKAST oral (ongoing); GABAPENTIN oral taken for back pain (ongoing); ZOLPIDEM oral taken for sleep disorder (ongoing); AMITRIPTYLINE oral taken for anxiety, sleep disorder (ongoing). Vaccination history included: BNT162b2 (1st dose, Lot: unknown; Expiration: unknown, Pfizer/BioNTech Covid-19 vaccine details, Dose: 1st, Date/time, Date: 16Apr2021, Site and route of injection, Route of administration: intramuscular [checked], Batch/lot number: other, please specify: given elsewhere), administration date: 16Apr2021, when the patient was 68-year-old, for Covid-19 immunization; BNT162b2 (2nd dose, Lot: unknown; Expiration: unknown, Pfizer/BioNTech Covid-19 vaccine details, Dose: 2nd, Date/time, Date: 05May2021, Site and route of injection, Route of administration: intramuscular [checked], Batch/lot number: other, please specify: given elsewhere), administration date: 05May2021, when the patient was 68-year-old, for Covid-19 immunization; flu shot, administration date: 06Jan2021, when the patient was 67-year-old, for Immunization; high dose fluzone (Lot: UJ760AC, Manufacturer: GSK, IM, Left Deltoid), administration date: 20Oct2021, when the patient was 68-year-old, for Immunization. The following information was reported: PRODUCT ADMINISTRATION ERROR (non-serious), POOR QUALITY PRODUCT ADMINISTERED (non-serious) all with onset 09Nov2021, outcome "unknown" and all described as "Administered one dose each of expired vaccine"; OVERDOSE (non-serious), INCORRECT DOSE ADMINISTERED (non-serious) all with onset 09Nov2021, outcome "unknown" and all described as "Patient administered another dose of the Pfizer COVID 19 Vaccine"; FACTOR VIII DEFICIENCY (non-serious), outcome "recovered", described as "severe HA"; PAIN (non-serious), outcome "recovered", described as "body aches"; FATIGUE (non-serious), outcome "recovered". Therapeutic measures were taken as a result of factor viii deficiency, pain, fatigue. Additional information: Prior vaccination (within 4 weeks) was Flu zone. Specific relevant test for thromboembolic event with thrombocytopenia were None. Patient in to office to receive 3rd covid-19 vaccine and medical assistant did not notice that the Pfizer in fridge were from the night before (08Nov2021). MA gave vaccine to patient at 08:18 and then went to chart vaccine she noticed time on syringe was from previous afternoon. Call was made to immune coordinator, she was advised to give another Pfizer vaccine that was drawn on 09Nov2021. 2nd Pfizer covid-19 given at 08:40. Call made to risk manager at that time. Pfizer immediately called informed AE, no need for 2nd Pfizer. Pt notified Pt 40 severe HA, body aches, fatigue after 2 Pfizer covid vaccines was treated with OTC Ibuprofen + Tylenol. No further complaints from pt. made complete recovery. There were no relevant tests. No follow-up attempts are possible. No further information is expected. Amendment: This follow-up report is being submitted to amend previous information: Recoded the event verbatim "Administered one dose each of expired vaccine" from "Expired vaccine used" to "Product administration error", and coded the new event verbatim "Administered one dose each of expired vaccine" coded as "Poor quality vaccine administered" and event verbatim "Patient administered another dose of the Pfizer COVID 19 Vaccine" coded as "Inappropriate dose of Vaccine administered". Follow-Up (25Mar2022): Follow-up attempts are completed. No further information is expected. Follow-up (12Apr2022): This is a spontaneous follow-up report received from a contactable Nurse. This Nurse reported in response to HCP letter sent which included that: Updated information included Primary reporter's middle name, Suffix and Alternate Phone, new AE: "Hemophilia A, Ache, Fatigue", dose 1, 2 details, concomitant drug, 3rd dose details, relevant medical history. Follow-up (15Apr2022): Follow-up attempts are completed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101549752 Same reporter drug AE, different patient

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Anxiety; Asthma; Cervical tension syndrome; Depression; Fatigue; GERD; Hypertension; Hyperthyroidism; Insomnia; Myalgia; Obesity; Osteoporosis; Rhinitis
Vorgeschichte: -
Andere Medikamente: ALENDRONATE; FLUTICASONE PROPIONATE; ATORVASTATIN; PREVACID; FLOVENT; MONTELUKAST; GABAPENTIN; ZOLPIDEM; AMITRIPTYLINE
Allergien: -
Vorherige Impfungen: -

VAERS 1880383

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: IA
Alter: 68,0
Geschlecht: F
Eingang: 16.04.2022
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Extra dose administered Feeling abnormal Headache Pain Product storage error Factor VIII deficiency Fatigue Incorrect dose administered Overdose Poor quality product administered Product administration error

Symptomtext

severe HA; body aches; fatigue; Administered one dose each of expired vaccine; Administered one dose each of expired vaccine; Patient administered another dose of the Pfizer COVID 19 Vaccine; Patient administered another dose of the Pfizer COVID 19 Vaccine; This is a spontaneous report received from contactable reporter(s) (Nurse) from medical information team. A 68-year-old female patient received BNT162b2 (COMIRNATY), on 09Nov2021 at 08:18 as dose 3, (booster) 0.3 ml single (Lot number: FH8028, Expiration Date: 31May2022) at the age of 68 years intramuscular, in left deltoid for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (ongoing); "Fatigue" (ongoing); "Depression/Anxiety" (ongoing); "Depression/Anxiety" (ongoing); "Myalgia" (ongoing); "Cervical tension" (ongoing); "GERD" (ongoing); "Rhinitis" (ongoing); "Insomnia" (ongoing); "Obesity" (ongoing); "Osteoporosis" (ongoing); "Hypertension" (ongoing); "Hyperthyroidism" (ongoing). Concomitant medication(s) included: ALENDRONATE oral taken for osteoporosis (ongoing); FLUTICASONE PROPIONATE nasal taken for seasonal allergy (ongoing); ATORVASTATIN oral taken for blood cholesterol (ongoing); PREVACID oral taken for abdominal discomfort (ongoing); FLOVENT (ongoing); MONTELUKAST oral (ongoing); GABAPENTIN oral taken for back pain (ongoing); ZOLPIDEM oral taken for sleep disorder (ongoing); AMITRIPTYLINE oral taken for anxiety, sleep disorder (ongoing). Vaccination history included: BNT162b2 (1st dose, Lot: unknown; Expiration: unknown, Pfizer/BioNTech Covid-19 vaccine details, Dose: 1st, Date/time, Date: 16Apr2021, Site and route of injection, Route of administration: intramuscular [checked], Batch/lot number: other, please specify: given elsewhere), administration date: 16Apr2021, when the patient was 68-year-old, for Covid-19 immunization; BNT162b2 (2nd dose, Lot: unknown; Expiration: unknown, Pfizer/BioNTech Covid-19 vaccine details, Dose: 2nd, Date/time, Date: 05May2021, Site and route of injection, Route of administration: intramuscular [checked], Batch/lot number: other, please specify: given elsewhere), administration date: 05May2021, when the patient was 68-year-old, for Covid-19 immunization; flu shot, administration date: 06Jan2021, when the patient was 67-year-old, for Immunization; high dose fluzone (Lot: UJ760AC, Manufacturer: GSK, IM, Left Deltoid), administration date: 20Oct2021, when the patient was 68-year-old, for Immunization. The following information was reported: PRODUCT ADMINISTRATION ERROR (non-serious), POOR QUALITY PRODUCT ADMINISTERED (non-serious) all with onset 09Nov2021, outcome "unknown" and all described as "Administered one dose each of expired vaccine"; OVERDOSE (non-serious), INCORRECT DOSE ADMINISTERED (non-serious) all with onset 09Nov2021, outcome "unknown" and all described as "Patient administered another dose of the Pfizer COVID 19 Vaccine"; FACTOR VIII DEFICIENCY (non-serious), outcome "recovered", described as "severe HA"; PAIN (non-serious), outcome "recovered", described as "body aches"; FATIGUE (non-serious), outcome "recovered". Therapeutic measures were taken as a result of factor viii deficiency, pain, fatigue. Additional information: Prior vaccination (within 4 weeks) was Flu zone. Specific relevant test for thromboembolic event with thrombocytopenia were None. Patient in to office to receive 3rd covid-19 vaccine and medical assistant did not notice that the Pfizer in fridge were from the night before (08Nov2021). MA gave vaccine to patient at 08:18 and then went to chart vaccine she noticed time on syringe was from previous afternoon. Call was made to immune coordinator, she was advised to give another Pfizer vaccine that was drawn on 09Nov2021. 2nd Pfizer covid-19 given at 08:40. Call made to risk manager at that time. Pfizer immediately called informed AE, no need for 2nd Pfizer. Pt notified Pt 40 severe HA, body aches, fatigue after 2 Pfizer covid vaccines was treated with OTC Ibuprofen + Tylenol. No further complaints from pt. made complete recovery. There were no relevant tests. No follow-up attempts are possible. No further information is expected. Amendment: This follow-up report is being submitted to amend previous information: Recoded the event verbatim "Administered one dose each of expired vaccine" from "Expired vaccine used" to "Product administration error", and coded the new event verbatim "Administered one dose each of expired vaccine" coded as "Poor quality vaccine administered" and event verbatim "Patient administered another dose of the Pfizer COVID 19 Vaccine" coded as "Inappropriate dose of Vaccine administered". Follow-Up (25Mar2022): Follow-up attempts are completed. No further information is expected. Follow-up (12Apr2022): This is a spontaneous follow-up report received from a contactable Nurse. This Nurse reported in response to HCP letter sent which included that: Updated information included Primary reporter's middle name, Suffix and Alternate Phone, new AE: "Hemophilia A, Ache, Fatigue", dose 1, 2 details, concomitant drug, 3rd dose details, relevant medical history. Follow-up (15Apr2022): Follow-up attempts are completed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101549752 Same reporter drug AE, different patient

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Anxiety; Asthma; Cervical tension syndrome; Depression; Fatigue; GERD; Hypertension; Hyperthyroidism; Insomnia; Myalgia; Obesity; Osteoporosis; Rhinitis
Vorgeschichte: -
Andere Medikamente: ALENDRONATE; FLUTICASONE PROPIONATE; ATORVASTATIN; PREVACID; FLOVENT; MONTELUKAST; GABAPENTIN; ZOLPIDEM; AMITRIPTYLINE
Allergien: -
Vorherige Impfungen: -

VAERS 2226000

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: PA
Alter: 66,0
Geschlecht: F
Eingang: 11.04.2022
Impfdatum: 09.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Ear pain Neuralgia Pain in extremity

Symptomtext

Approximately 24 hours after my booster shot I experienced the following symptoms: Pain in the right side of my head (Nerve pain) 3 to 4 inches on top of my ear. It lasted for about 4 days - It was a sharp pain and I took Tylenol for treatment and it did improve my situation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Levothyroxine
Allergien: Tree Nuts; Molds
Vorherige Impfungen: -

VAERS 2223914

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: TX
Alter: 59,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 21.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Rash

Symptomtext

It started with a rash on my chest that lasted a few days and went to my back. It keep moving around it went to my neck behind my ears to my scalp. Once I have it cleared it it moves to a new location. I t was also on my face as well. As of now I got my right ear covered in rash and a little on the back of my neck. The worsen part of now is that it on my scalp.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Allergy symptoms
Vorgeschichte: Allergies
Andere Medikamente: Elderberry Syrup
Allergien: Wheat; Benzodiazepines; Celebrex; strong antibiotics the new ones: Dtap vaccine; Cats; Pollens
Vorherige Impfungen: DTap - fever, hives, soreness, fatigue 2019.

VAERS 2214515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 89,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Muscular weakness Pain in extremity

Symptomtext

She reported her arm started hurting the day after the vaccine and it has not gone away. she said her hand feels week and the pain is increasing. she feels like she is loosing strength. she has not yet seen a doctor for this issue and it was recommended she follow up with a PCP

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2210224

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: AZ
Alter: 39,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 30.10.2021
Beginn: 10.01.2022
Tage bis Beginn: 72,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Cough Fatigue Feeling abnormal Malaise

Symptomtext

Breakthrough COVID-19 infection. Extremely symptomatic for 2 weeks, though no hospitalization was necessary - no drop in O2 saturation. Lots of coughing, fatigue, malaise, brain fog; no fever. Probably one of the top 3 worst illnesses I've ever experienced, the other 2 being mono & pneumonia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Bipolar disorder, gastroparesis, migraines, asthma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2137804

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: -
Geschlecht: M
Eingang: 31.03.2022
Impfdatum: 15.02.1948
Beginn: 10.12.2021
Tage bis Beginn: 26.962,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Herpes zoster Pain

Symptomtext

the patient was diagnosed with shingles, and he stated that he had "small but painful outbreaks"; This spontaneous report has been received from a consumer through GlaxoSmithKline, and refers to a 73-year-old male patient. The patient's concurrent conditions, medical history and concomitant medications were not reported. On 19-SEP-2008, the patient was vaccinated with zoster vaccine live (ZOSTAVAX) for prophylaxis (strength, lot #, expiration date, dose, route and frequency were not reported). Then, On 29-JAN-2018 and 18-APR-2019, the patient received his first and second doses of varicella zoster vaccine rge (SHINGRIX) for prophylaxis (strength, lot #, expiration date, dose, route and frequency were not reported). Other suspect therapies included tozinameran (BNT162B2) administered intramuscularly in the arm (unspecified) administered on 25-JAN-2021 (lot # EL 3302); on 15-FEB-1948 (discrepant date)(lot # EN 6201); and on 09-NOV-2021 (FH-8028) for COVID-19 prophylaxis. On 10-DEC-2021, the patient was diagnosed with shingles, and he stated that he had "small but painful outbreaks" and considered it as severe. The patient sought medical attention and received treatment with pregabalin 75 milligram (reported as "pregamblin") The patient felt that the treatment was working, but very slow. At the reporting time, the outcome of herpes zoster was reported as recovering (reported as "ongoing"). The reporter did not provide a causality assessment between the event and the suspect vaccines. The reporter considered the event to be a medically significant event ("important medical event").

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: COVID-19 prophylaxis
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2137804

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

mild

Staat: -
Alter: -
Geschlecht: M
Eingang: 31.03.2022
Impfdatum: 15.02.1948
Beginn: 10.12.2021
Tage bis Beginn: 26.962,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Herpes zoster Pain

Symptomtext

the patient was diagnosed with shingles, and he stated that he had "small but painful outbreaks"; This spontaneous report has been received from a consumer through GlaxoSmithKline, and refers to a 73-year-old male patient. The patient's concurrent conditions, medical history and concomitant medications were not reported. On 19-SEP-2008, the patient was vaccinated with zoster vaccine live (ZOSTAVAX) for prophylaxis (strength, lot #, expiration date, dose, route and frequency were not reported). Then, On 29-JAN-2018 and 18-APR-2019, the patient received his first and second doses of varicella zoster vaccine rge (SHINGRIX) for prophylaxis (strength, lot #, expiration date, dose, route and frequency were not reported). Other suspect therapies included tozinameran (BNT162B2) administered intramuscularly in the arm (unspecified) administered on 25-JAN-2021 (lot # EL 3302); on 15-FEB-1948 (discrepant date)(lot # EN 6201); and on 09-NOV-2021 (FH-8028) for COVID-19 prophylaxis. On 10-DEC-2021, the patient was diagnosed with shingles, and he stated that he had "small but painful outbreaks" and considered it as severe. The patient sought medical attention and received treatment with pregabalin 75 milligram (reported as "pregamblin") The patient felt that the treatment was working, but very slow. At the reporting time, the outcome of herpes zoster was reported as recovering (reported as "ongoing"). The reporter did not provide a causality assessment between the event and the suspect vaccines. The reporter considered the event to be a medically significant event ("important medical event").

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: COVID-19 prophylaxis
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2201531

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: TN
Alter: 50,0
Geschlecht: F
Eingang: 28.03.2022
Impfdatum: 29.10.2021
Beginn: 22.01.2022
Tage bis Beginn: 85,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Fatigue Feeling abnormal Nausea SARS-CoV-2 antibody test positive Vomiting

Symptomtext

I had extreme nausea, vomiting and fatigue that lasted for about 3 weeks. I also have brain fog as well. I went to my gastro doctor on Feb 14th. He did a blood test and said that I recently had COVID-19. I am still having some nausea and fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Bloodwork
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multivitamin; Vitamin D
Allergien: N/A
Vorherige Impfungen: -

VAERS 2195852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: SC
Alter: 69,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 03.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Vaccination site pain

Symptomtext

pain at injection site; This is a spontaneous report received from a contactable reporter(s) (Physician). A 69 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 03Dec2021 (Lot number: FH8028) at the age of 69 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Depression" (ongoing). Concomitant medication(s) included: PRISTIQ taken for affective disorder (ongoing). Vaccination history included: Bnt162b2 (Dose: 1st, Date/Time: 16Feb2021, Site and Route of Injection: , Anatomical Site of Injection: Rt deltoid, Batch/Lot Number: EN6200), administration date: 16Feb2021, when the patient was 69 years old, for Covid-19 immunization, reaction(s): "Vaccination site pain"; Bnt162b2 (Dose: 2nd , Date/Time: 09Mar2021, Site and Route of Injection: , Anatomical Site of Injection: Lt deltoid, Batch/Lot Number: EN6204), administration date: 09Mar2021, when the patient was 69 years old, for COVID-19 Immunization. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 09Dec2021, outcome "recovering", described as "pain at injection site". Therapeutic measures were taken as a result of vaccination site pain. Additional Information: The patient provide information to you regarding the reported adverse event(s) with the use of the product. The Pfizer product had a causal effect to the adverse event. Vaccination Facility Type: Unknown, list any other vaccinations within four weeks prior to the first administration date of the sus-pect. Relevant Tests were one. Specific Relevant Test for Thromboembolic events with Thrombocy-topenia were none Autopsy Information: N/A. On 09Dec2021, 6 days after her booster shot we had an office visit, where she Complained of pain at injection site that improved with Skelaxin. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Depression
Vorgeschichte: -
Andere Medikamente: PRISTIQ
Allergien: -
Vorherige Impfungen: -

VAERS 2189299

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MA
Alter: 62,0
Geschlecht: F
Eingang: 20.03.2022
Impfdatum: 15.11.2021
Beginn: 01.01.2022
Tage bis Beginn: 47,0
Dosis: 3
Route/Site: UN / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test Polymyalgia rheumatica Vaccine breakthrough infection

Symptomtext

Got breakthrough 6 weeks later; recovered and then got Polymylagia Rhumatice immediately after recovering from breakthrough

Weitere VAERSDATA-Felder

Praegender Schweregrund: Polymyalgia rheumatica
Hospital-Tage: -
Labordaten: blood tests 3/34/22
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: opiods,
Vorherige Impfungen: -

VAERS 2189173

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge #FH8028

mild

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 19.03.2022
Impfdatum: 10.12.2021
Beginn: 21.01.2022
Tage bis Beginn: 42,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue Headache Nausea Pyrexia

Symptomtext

Headache, nausea, low fever fatigue for about four days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Tested positive for COVID a second time on 01/21/2022 I have pulmonary scarring and I am out of breath doing normal activities.
Andere Medikamente: Metformin, Glypisde
Allergien: None
Vorherige Impfungen: -

VAERS 2188294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

mild

Staat: NY
Alter: 62,0
Geschlecht: M
Eingang: 18.03.2022
Impfdatum: 07.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Pain in extremity Tinnitus

Symptomtext

sore arm and shoulder months after injection & ear rining

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: PT went to ENT
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2181828

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MA
Alter: 60,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 16.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypoaesthesia Insomnia Pain in extremity Vertigo Vomiting

Symptomtext

numbness on the arm where she got the vaccine; numbness in the place of the vaccine, started to go down her arm to her fingers; vertigo/two days after the vaccine she had vomiting that triggered an episode; vomiting; pain in the left arm; couldn't sleep all night; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A female patient in her 60's received bnt162b2 (BNT162B2), administered in arm left, administration date 16Dec2021 11:00 (Lot number: FH8028, Expiration Date: 31May2022) at the age of 7 decade as dose 1, single for covid-19 immunisation. Relevant medical history included: "Vertigo" (unspecified if ongoing), notes: Verbatim: Vertigo. There were no concomitant medications. Vaccination history included: Pneumonia vaccine, administration date: 2018, for Immunization, reaction(s): "redness". The following information was reported: HYPOAESTHESIA (non-serious) with onset 18Dec2021, outcome "recovering", described as "numbness on the arm where she got the vaccine"; VERTIGO (non-serious) with onset 17Dec2021 23:00, outcome "recovering", described as "vertigo/two days after the vaccine she had vomiting that triggered an episode"; VOMITING (non-serious) with onset 17Dec2021 23:00, outcome "recovering", described as "vomiting"; PAIN IN EXTREMITY (non-serious) with onset 16Dec2021 23:00, outcome "recovering", described as "pain in the left arm"; HYPOAESTHESIA (non-serious) with onset 18Dec2021, outcome "recovering", described as "numbness in the place of the vaccine, started to go down her arm to her fingers"; INSOMNIA (non-serious) with onset Dec2021, outcome "recovering", described as "couldn't sleep all night". The event "vertigo/two days after the vaccine she had vomiting that triggered an episode" was evaluated at the physician office visit. Therapeutic measures were not taken as a result of hypoaesthesia, vertigo, vomiting, pain in extremity, hypoaesthesia, insomnia. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient was not admitted to emergency room. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Vertigo (Verbatim: Vertigo)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2179140

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 41,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Pain

Symptomtext

body pain; shiver; This is a spontaneous report received from a non-contactable reporter(s) (Other HCP). The reporter is the patient. A 41 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 04Nov2021 19:00 (Lot number: FH8028) at the age of 41 years as dose 1, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: PAIN (non-serious) with onset 05Nov2021, outcome "recovered" (Nov2021), described as "body pain"; CHILLS (non-serious) with onset 05Nov2021, outcome "recovered" (Nov2021), described as "shiver". Therapeutic measures were not taken as a result of pain, chills. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the covid vaccine. Prior to vaccination, the patient was not diagnosed with covid-19. Since vaccination, the patient had not been tested for covid-19. No known allergies. Device date: 06Nov2021. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2176753

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: PA
Alter: 63,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 02.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia Fatigue Headache Neck pain

Symptomtext

A lot of fatigue; Shoulder pain; Neck pain; Headache; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63-year-old female patient received bnt162b2 (BNT162B2), administration date 02Dec2021 (Lot number: FH8028) at the age of 63 years as dose 2, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (1st dose, Manufacturer- Unknown), when the patient was 63 years old, for COVID-19 Immunization. The following information was reported: FATIGUE (non-serious) with onset Dec2021, outcome "recovered" (14Dec2021), described as "A lot of fatigue"; ARTHRALGIA (non-serious) with onset Dec2021, outcome "recovered" (14Dec2021), described as "Shoulder pain"; NECK PAIN (non-serious) with onset Dec2021, outcome "recovered" (14Dec2021), described as "Neck pain"; HEADACHE (non-serious) with onset Dec2021, outcome "recovered" (14Dec2021), described as "Headache". Additional information: It was really more from the second injection (Incomplete sentence). The side effects especially from the 2nd injection which the patient had 02Dec, the patient had a lot of fatigue and had shoulder and neck pain and headache for almost 2 weeks. Date of adverse event started: the patient stated, "It would have been around the 02Dec or 03Dec to 14Dec2021." Follow-Up (11Jan2022): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2176724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: TX
Alter: 63,0
Geschlecht: M
Eingang: 12.03.2022
Impfdatum: 15.11.2021
Beginn: 13.12.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood pressure measurement Cough Hypersensitivity Nasopharyngitis Pain in extremity Sneezing

Symptomtext

cold; sore arm with first dose of Covid-19 vaccine; allergic reaction after taking the first dose of the Pfizer Covid-19 vaccine; allergy symptoms of coughing and sneezing; allergy symptoms of coughing and sneezing; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 63 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 15Nov2021 (Lot number: FH8028) at the age of 63 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "blood pressure" (unspecified if ongoing); "Allergies" (unspecified if ongoing); "Cholesterol" (unspecified if ongoing). Concomitant medication(s) included: AMLODIPINE taken for hypertension (ongoing); METOPROLOL TARTRATE taken for hypertension (ongoing); OLMESARTAN MEDOXOMIL taken for hypertension, start date: 12Dec2021; CORICIDIN HBP COUGH AND COLD taken for hypersensitivity; LIPITOR taken for blood cholesterol abnormal. The following information was reported: NASOPHARYNGITIS (non-serious), outcome "unknown", described as "cold"; SNEEZING (non-serious), COUGH (non-serious) all with onset 13Dec2021, outcome "unknown" and all described as "allergy symptoms of coughing and sneezing"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "sore arm with first dose of Covid-19 vaccine"; HYPERSENSITIVITY (non-serious), outcome "unknown", described as "allergic reaction after taking the first dose of the Pfizer Covid-19 vaccine". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of nasopharyngitis, sneezing, cough, pain in extremity, hypersensitivity. Additional information: Consumer states he was fine with 1st Pfizer BTC vaccine (purple cap formula) dose and is due for his 2nd dose today. He currently is taking antihistamines for a cold. Can he still get the vaccine today. Why was the patient taking Pfizer Covid-19 vaccine (Verbatim): scared. Patient History: Unknown. The reporter was reporting an allergic reaction after taking the first dose of the Pfizer Covid-19 vaccine. He stated that he has an appointment today, to take the second dose and he does not know if he can take it or not. When clarifying the details provided by the transferring agent with the reporter, he stated that he did not have an allergic reaction to the first dose of the Pfizer Covid-19 vaccine. He stated he was fine with the first one, it went great. Right now, he has allergies, just coughing that started 2 days ago. He stated that he was due for the second dose in about an hour. He has been taking antihistamines to take away the symptoms. Reporter stated he has allergies his whole life. Reporter provides his current age as 63. Clarified that the allergy symptoms started 2 days ago, 13Dec2021. He stated that he has been taking antihistamines and he just wants to know if that was going to affect him going to get the vaccine. Reporter stated that he already took one vaccine and his arm got sore but otherwise was great. He was taking over the counter drugs to alleviate the symptoms like cough and sneezing. He does not have a fever and does not have any body aches, just coughing and sneezing. He was scheduled to take the second dose today and wants to know if he should wait or should he take it. Reporter stated he was taking prescriptions for high blood pressure right now. He was also taking an antihistamine to relieve his allergy symptoms. He stated that he was fine, he was just wondering if taking antihistamines would affect him or not or, if he was sick, if they are going to give it to him. Reporter state he has been taking Coricidin, which was for high blood pressure people which was an antihistamine he has been taking to relieve the allergies. He stated he has been taking this Coricidin since last night. It was in his blood stream right now and that was why he was trying to get information. He stated that he has to take it every 4 hours and he was just about to take it. They told him to come back at 1:00 pm. Reporter stated the blood pressure medicines he takes have ugly names. Reporter stated they are all for blood pressure. He stated they gave him one last week because the others weren't working. That medication was Olmesartan Medoxomil, 20mg, once a day. He stated that he just he just started it last week. He had his doctors appointment on 11Dec2021 and he started taking the medication 12Dec2021. He stated that all of his medications are for blood pressure. When clarifying with the reporter that his doctor started him on the Olmesartan Medoxomil because the other medications weren't working, he stated that no, it wasn't that they weren't working. His doctor added it to the other drugs he had been taking for 5 to 10 years. He stated that his blood pressure was 148 and the doctor stated that wasn't low enough so, he added this new one. Tests: Reporter stated that he has more blood work next month. Clarified that the antihistamines that reporter has been taking was Coricidin and has been taking 2 tablets every 4 hours. He stated that it says pain reliever, Acetaminophen 325mg, Chlorpheniramine 2mg, Dextromethorphan Hydrobromide 10mg, which was a cough suppressant. He stated that he does not know if those are in each individual pill, or they are combined in both pills. Clarified that the names and doses the reporter just provided were the names of the ingredients and doses that were in the antihistamine, the Coricidin and was the one medication that he has been taking as the antihistamine. Prior Vaccinations (Within 4 weeks): None. Patient's Medical History: None. Relevant Tests: None. Specific Relevant Test: None. Follow-up attempts are completed. No further information was expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Test Name: blood pressure; Result Unstructured Data: Test Result:148; Comments: his blood pressure was 148 and the doctor stated that wasn't low enough so
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Blood cholesterol abnormal; Blood pressure abnormal
Andere Medikamente: AMLODIPINE; METOPROLOL TARTRATE; OLMESARTAN MEDOXOMIL; CORICIDIN HBP COUGH AND COLD; LIPITOR
Allergien: -
Vorherige Impfungen: -

VAERS 2176398

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MA
Alter: 60,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Body height Chills Diarrhoea Faeces pale Fatigue Hyperhidrosis Investigation Myalgia Pain Pain in extremity Vomiting

Symptomtext

sweaty; Underneath the rib, in her diaphragm, having pain; Diarrhea was bright yellow; Underneath, the muscles are sore; Diarrhea; Joint pain and heaviness; Vomiting; Tired; Really chilly; Arm hurt; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 60-year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 28Oct2021 (Lot number: FH8028) at the age of 60 years as dose 3 (booster), single for covid-19 immunization. Relevant medical history includes block production of the aldosterone hormone, enlarged ventricle, Hyperaldosteronism, Conns Syndrome, diagnosed with a latex allergy, notes: Was diagnosed with a latex allergy, from an unknown date and unspecified if ongoing. Concomitant medication(s) includes metoprolol, spironolactone taken for blood aldosterone abnormal, entresto. Vaccination history includes Bnt162b2 (Dose:1, LOT: EN6207, Route: Injected into left arm), administration date: 15Mar2021, when the patient was 59 years old, for Covid-19 Immunization, reaction(s): chills; Bnt162b2 (Dose: 2, LOT: ER8732, Route: Injected into left arm), administration date: 05Apr2021, when the patient was 59 years old, for Covid-19 immunization, reaction(s): chills, Legs felt heavy, Hepatitis (Back in 1991 or 1992, had vaccination for Hepatitis. Had a reaction in the thigh with itchiness, redness, and bumps.), for Immunization. On 28Oct2021 the patient had experienced Really chilly, Arm hurt, on 29Oct2021 Vomiting, Tired, on 30Oct2021 Joint pain and heaviness, on 31Oct2021 Diarrhea, On an unspecified date sweaty, underneath the rib, in her diaphragm, having pain, diarrhea was bright yellow, underneath, the muscles are sore. Patient underwent lab tests and procedures on an unspecified date for body height with results of getting shrunk. Provides 5 feet 2.5 inches and bloodwork investigations of unknown results. The outcome of Really chilly, Diarrhea was recovered on 31Oct2021, Vomiting was recovered on 29Oct2021, Arm hurt, Tired, was recovering, Joint pain and heaviness, sweaty, Underneath the rib, in her diaphragm, having pain, diarrhea was bright yellow, underneath, the muscles are sore was unknown No follow-up attempts are possible. No further information is expected. Follow-Up (08Nov2021): Follow-up attempts are completed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101495427 same patient/drug, different dose/event

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Name: Height; Result Unstructured Data: Test Result:She shrunk.; Comments: Height: She shrunk. Provides 5 feet 2.5 inches; Test Name: bloodwork; Result Unstructured Data: Test Result:unknown result
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood aldosterone abnormal; Conn's syndrome; Hyperaldosteronism; Latex allergy (Was diagnosed with a latex allergy.); Ventricular hypertrophy
Andere Medikamente: METOPROLOL; SPIRONOLACTONE; ENTRESTO
Allergien: -
Vorherige Impfungen: -

VAERS 2176195

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WA
Alter: 35,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 22.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache Influenza like illness Lethargy Pain in extremity

Symptomtext

headaches; sore arm; lethargic; Had flu like symptoms; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. A 35 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 22Oct2021 (Lot number: FH8028) at the age of 35 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Root Canal", start date: 21Oct2021, stop date: 21Oct2021, notes: ibuprofen before vaccination as she had a root canal procedure the day prior.; "abscess" (unspecified if ongoing). Concomitant medication(s) included: AMOXICILLIN taken for prophylaxis, start date: 21Oct2021 (ongoing); IBUPROFEN taken for pain, prophylaxis, start date: 21Oct2021. Vaccination history included: Mmr vaccine, for immunisation. The following information was reported: HEADACHE (non-serious) with onset 23Oct2021, outcome "recovered" (Oct2021), described as "headaches"; INFLUENZA LIKE ILLNESS (non-serious) with onset Oct2021, outcome "not recovered", described as "Had flu like symptoms"; PAIN IN EXTREMITY (non-serious) with onset 22Oct2021, outcome "recovered" (25Oct2021), described as "sore arm"; LETHARGY (non-serious) with onset Oct2021, outcome "unknown", described as "lethargic". Therapeutic measures were taken as a result of headache, pain in extremity. Additional information: Caller is asking for his wife, withheld, who received her 1st dose on Friday. They were not sure whether the personnel told them not to take Ibuprofen before or after the vaccine. He mentioned that she is experiencing headaches as of now. He also mentioned that she took some ibuprofen before vaccination as she had a root canal procedure the day prior. The callers wife received first dose Pfizer Covid 19 Vaccine on 22Oct2021. Caller was asking agent if it was okay to take Ibuprofen, transfer agent addressed callers questions regarding Ibuprofen. The callers wife is having headaches after receiving the first dose Pfizer Covid 19 Vaccine. Prior to receiving the first dose Pfizer Covid 19 Vaccine, the patient had a root canal and took Ibuprofen. The patient had the root canal on 21Oct2021. The patient also took Ibuprofen on the day the patient received the first dose Pfizer Covid 19 Vaccine, 22Oct2021. Prior to receiving the first dose Pfizer Covid 19 Vaccine, the patient had a root canal and took Ibuprofen: Caller states the patient still had some abscess when the root canal took place on 21Oct2021. Did not realize abscess was still there but went ahead and did the root canal on 21Oct2021. The patient was in some pain and repercussions after the root canal on 21Oct2021. The patient was prescribed antibiotics. HCP: The caller does not wish to provide name, address, telephone number or email. The caller states in transition right now, doctors leaving clinic due to Covid and controversy. Trying to locate where the patients primary care doctor went, the primary care doctor left the clinic. Indication: The caller would like to note the patient did not receive the first dose Pfizer Covid Vaccine voluntarily. The patient was forced to receive the first dose Pfizer Covid 19 Vaccine by employer, the company that builds airplanes. Having headaches after receiving first dose vaccine: The headaches began on Saturday morning and evening, 23Oct2021. Had flu like symptoms all weekend: The patient had flu like symptoms all weekend. The patient stayed in bed and on the couch. Having headaches after receiving first dose vaccine: The caller states the headache went away. The patient took some vitamins and juice this morning and the rest of the patients antibiotics. The patient is in the bed right now. Had flu like symptoms all weekend: The patient has been pretty much lethargic all weekend. Sore arm: The patient has a sore arm. Had flu like symptoms all weekend: The patient has flu like symptoms. The patient said it felt like she was ready to have menstruation period. Sore arm: The caller states the sore arm began that morning, the caller received the first dose Pfizer Covid 19 Vaccine in the afternoon. The caller clarified the sore arm began the same day the caller received the first dose Pfizer Covid 19 Vaccine, 22Oct2021. The sore arm got worse in the morning the following day, 23Oct2021. Caller states the patient took a little bit of pain medication the caller had and the patient does not have a sore arm anymore. The patient is pretty tough. Antibiotics: Amoxicillin 500mg, every 8 hours and has 21 count, 7 days worth Lot/NDC: The caller does not see a lot or NDC. Caller clarifies the Amoxicillin is in a medication bottle from the Pharmacy with an RX number. sore arm: The sore arm went away today, 25Oct2021. Today, 25Oct2021 is the first time, the patient is not complaining of sore arm. The caller gave the patient a couple of good pain medications. The patient thought she took Amoxicillin already, patient was not sure, the caller explained to the patient the amoxicillin was for infection. The pain medication is different, the patient did not quite understand. The caller gave the patient the pain medicine because was not sure if the patient could take Ibuprofen until talking to Pfizer. Ibuprofen: The patient has been taking every 8 hours like directed. The patient got off work early at 1700. Lot: The first digit is O or 0, second digit is 8 or B, remaining digits are withheld Expiration: Nov2021. Dose: 200mg, count size 24. Caller clarifies the patient has not taken much of the Ibuprofen. Had flu like symptoms all weekend: The patient just did not feel very well, sick feeling. The caller states we already noted this earlier in the report. The caller states the first dose Pfizer Covid 19 Vaccine not being voluntary is what bothers the caller. The caller grew up in the (private) where there are rights and feels this totally is a violation of religious rights. The caller states the patient does not quite understand because the patient came from the country. This bothers the caller that an liberal dictator is telling what to do. Time the Vaccination Was Given: Afternoon. Additional Vaccines Administered on Same Date of the Pfizer Suspect If applicable, list all vaccines administered on same date with the Pfizer vaccine considered as suspect: no. Additional Information Did any AE(s) require a visit to: Emergency Room? Physician Office? No. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s): no. AE(s) following prior vaccinations: No, not that the caller knows of. The patient received vaccinations in city before coming to country. Four years ago, the patient received the MMR Vaccine and the next day did have flu like symptoms. MMR Vaccine: NDC/lot/expiration: The caller does not have this information handy to provide and does not want to wake up the patient to get the information. The caller states this information is all documented for the patient. Relevant Tests: none. Description of complaint: Caller reports his wife received first dose Pfizer Covid 19 Vaccine on 22Oct2021. Prior to receiving the patient had a root canal on 21OCT2021 and was taking Ibuprofen. Caller states the patient has not taken many Ibuprofen but reports the patient is having flu like symptoms and has been in bed or couch all weekend. The patient is still in bed right now, 25Oct2021. Caller states the patient has not taken very many Ibuprofen. Is a sample of the product available to be returned, if requested (Y/N): Yes, caller is willing to provide, informed may possibly receive mailer in 3-10 business days. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Abscess; Root canal procedure (ibuprofen before vaccination as she had a root canal procedure the day prior.)
Andere Medikamente: AMOXICILLIN; IBUPROFEN
Allergien: -
Vorherige Impfungen: -

VAERS 2161535

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: AR
Alter: 52,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood pressure measurement Heart rate Inappropriate schedule of product administration Investigation Limb discomfort Lymphadenopathy Muscle spasms Pain in extremity Peripheral swelling

Symptomtext

she couldn't put her arm down all day; it was swollen and painful underneath the arm; it was swollen and painful underneath the arm; cramp in her upper right arm; First dose: given on 16Sep2021/Second dose: Given on 23Nov2021; at least three very large swollen lymph nodes under the right arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 52 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 23Nov2021 (Lot number: FH8028) at the age of 52 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "high blood pressure" (unspecified if ongoing), notes: Additional Information for Concomitant Products Bystolic: She has been on it years. Concomitant medication(s) included: BYSTOLIC taken for hypertension (ongoing). Vaccination history included: Bnt162b2 (Dose Number:01, Lot number: FD8448), administration date: 16Sep2021, when the patient was 52 years old, for Covid-19 Immunization, reaction(s): "she thinks it did something to her heart rate/Her heart rate is usually 80 to 100 and it was around 50", "she still felt really tired". The following information was reported: MUSCLE SPASMS (non-serious) with onset 24Nov2021, outcome "not recovered", described as "cramp in her upper right arm"; LIMB DISCOMFORT (non-serious) with onset 25Nov2021, outcome "unknown", described as "she couldn't put her arm down all day"; PERIPHERAL SWELLING (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 25Nov2021, outcome "unknown" and all described as "it was swollen and painful underneath the arm"; LYMPHADENOPATHY (non-serious) with onset 2021, outcome "unknown", described as "at least three very large swollen lymph nodes under the right arm"; INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious) with onset 23Nov2021, outcome "unknown", described as "First dose: given on 16Sep2021/Second dose: Given on 23Nov2021". The events "cramp in her upper right arm", "she couldn't put her arm down all day", "it was swollen and painful underneath the arm", "it was swollen and painful underneath the arm" and "at least three very large swollen lymph nodes under the right arm" were evaluated at the physician office visit and emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of muscle spasms. Additional information: After the first shot she thinks it did something to her heart rate. She can't prove it. It was a few weeks after the first shot that she noticed she still felt really tired. She checks her blood pressure on a regular basis because she is on blood pressure medicine. Her heart rate is usually 80 to 100 and it was around 50. She went to the emergency room and they did heart test. Nothing came back. Everything seems ok now. They will do a stress test in the future on 23Dec2021. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Test Name: Blood Pressure; Result Unstructured Data: Test Result:High; Test Name: heart rate; Result Unstructured Data: Test Result:around 50; Test Name: Heart tests; Result Unstructured Data: Test Result:ok now
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypertension (Additional Information for Concomitant Products Bystolic: She has been on it years.)
Andere Medikamente: BYSTOLIC.
Allergien: -
Vorherige Impfungen: -

VAERS 2161469

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH 8028

mild

Staat: NY
Alter: 62,0
Geschlecht: U
Eingang: 05.03.2022
Impfdatum: 28.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Contusion Fatigue

Symptomtext

extreme tiredness; Have lots of purple bruising on my legs, both legs/had dark blue bruising/blushing down both legs; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 62 year-old patient received bnt162b2 (BNT162B2), administered in arm left, administration date 28Nov2021 (Lot number: FH 8028) at the age of 62 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Migraines" (ongoing). Concomitant medication(s) included: IMITREX taken for migraine (ongoing). Vaccination history included: Bnt162b2 (Dose:1,, Anatomical site of injection: left arm, Batch/lot number: ER2613), administration date: 17Mar2021, for COVID-19 Immunization; Bnt162b2 (Dose:2, Anatomical site of injection: left arm, Batch/lot number: EP7533), administration date: 08Apr2021, for COVID-19 Immunization; Flu (Anatomical site of injection: left arm, No. of previous doses:1), administration date: 05Nov2021. The following information was reported: CONTUSION (non-serious) with onset Nov2021, outcome "recovered" (Nov2021), described as "Have lots of purple bruising on my legs, both legs/had dark blue bruising/blushing down both legs"; FATIGUE (non-serious) with onset Dec2021, outcome "unknown", described as "extreme tiredness". The event "have lots of purple bruising on my legs, both legs/had dark blue bruising/blushing down both legs" was evaluated at the physician office visit. Therapeutic measures were not taken as a result of contusion. Booster dose due to high risk of frequent institutional or occupational exposure to coronavirus (and at risk of serious COVID-19 complications). After Pfizer booster had dark blue bruising/blushing down both legs. Did not hurt, no swelling. Gone the next morning waves of extreme tiredness 1 week after booster. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Migraine.
Vorgeschichte: -
Andere Medikamente: IMITREX.
Allergien: -
Vorherige Impfungen: -

VAERS 2161443

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MS
Alter: 57,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 01.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Facial pain Headache Lymph node pain Swelling face

Symptomtext

This is a spontaneous report received from contactable other HCP (patient). A 57-year-old female patient (not pregnant) received the 1st dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, batch/lot# FH8028), at the age of 57, intramuscularly, in left arm, Nov 2021, single dose, for COVID-19 immunisation. Medical history included hypothyroidism (unspecified if ongoing); pre diabetes (unspecified if ongoing) and COVID-19 (unspecified if ongoing). Concomitant medication included synthroid. The patient developed a headache (entire lower back of head very sore), swollen face, facial pain (outer edge of entire face swollen and painful) and lymph node pain (lymph nodes beneath ears very sore), onset Nov 17, 2021, with outcome of not recovered. No therapeutic measures taken as a result of headache, swelling face, facial pain and lymph node pain. Additional information: Patient did not receive any other vaccine in four weeks. Patient had COVID-19 prior to vaccination. Patient has not tested for COVID-19 post vaccination. No follow-up attempts possible. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19; hypothyroidism; pre-diabetes.
Andere Medikamente: Synthroid
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2157643

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NC
Alter: 63,0
Geschlecht: F
Eingang: 04.03.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Blood pressure increased Dizziness Headache Nausea

Symptomtext

While sitting in observation area (10 minutes after booster dose), patient felt nauseated/lightheaded and had a headache. Patient placed in recliner with lower extremities elevated. Vital signs monitored for 30 minutes. BP slightly elevated but returned to normal. Pulse Ox: 100-98%. Patient felt fine when she left.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None listed
Vorgeschichte: Diabetes, hypertension
Andere Medikamente: Unknown
Allergien: Sulfa, Penicillin
Vorherige Impfungen: -

VAERS 2157594

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NC
Alter: 55,0
Geschlecht: F
Eingang: 04.03.2022
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Pain in extremity Tenderness

Symptomtext

patient complained of tenderness on opposite deltoid(Left) from where the injection was given. Pain does not radiate down to arm. She was not having any shortness of breath or an rash at site or any discoloration. Nurse states patient was nervous prior to vaccine. Patient had great finger gripping. Vital signs were 131/84, Pulse-79, respirations-18 and Pulse ox-98%. Dr. assessed patient and patient was observed and released from clinic in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none listed
Andere Medikamente: unknown
Allergien: states she had allergic reaction years ago for a vaccine but did not list what it was.
Vorherige Impfungen: unsure of which one

VAERS 2155047

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: ID
Alter: 60,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 29.11.2021
Beginn: 03.02.2022
Tage bis Beginn: 66,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia Atrioventricular block first degree Bradycardia Dizziness Feeling abnormal

Symptomtext

02/03/2022 I started having dizziness, My BP was 75/56 and my oxygen was 43. I struggle and my husband called the ambulance. I was given an IV. I was told to follow up with my Physician. It was almost like a machine that it was unplugged and the power went out, that was me. That is exactly how I felt, They diagnosed me with bradycardia and first degree AV block. I got to go back in a few months to get lab work done.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Lisinopril 20MG 1 a day, Hydrochloride 12.5MG 1 a day
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2151909

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WA
Alter: 65,0
Geschlecht: M
Eingang: 02.03.2022
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute phase reaction Arthralgia Autoantibody negative Autoimmune disorder C-reactive protein increased Normocytic anaemia Polymyalgia rheumatica Vitiligo

Symptomtext

ASSESSMENT AND PLAN: 1. Arthralgia after vaccination (Primary), C-Reactive Protein, High Sensitivity; Future, Rheumatoid Factor, Qual.; Future, ANA Screen, Qual., Reflex; Future, Sedimentation Rate; Future, Cyclic Citrullinated Peptide Ab, IgG; Future, CBC with Differential; Future, Comprehensive Metabolic Panel; Future, TSH, Reflex Free T4; Future, predniSONE (DELTASONE) 10 mg tablet; Take 1 tablet by mouth Daily for 30 days. Dispense: 30 tablet; Refill: 0. 2. Vitiligo, C-Reactive Protein, High Sensitivity; Future, Rheumatoid Factor, Qual.; Future, ANA Screen, Qual., Reflex; Future, Sedimentation Rate; Future, Cyclic Citrullinated Peptide Ab, IgG; Future, CBC with Differential; Future, Comprehensive Metabolic Panel; Future, TSH, Reflex Free T4; Future, predniSONE (DELTASONE) 10 mg tablet; Take 1 tablet by mouth Daily for 30 days. Dispense: 30 tablet; Refill: 0. 3. History of autoimmune disorder: C-Reactive Protein, High Sensitivity; Future, Rheumatoid Factor, Qual.; Future, ANA Screen, Qual., Reflex; Future, Sedimentation Rate; Future, Cyclic Citrullinated Peptide Ab, IgG; Future, CBC with Differential; Future, Comprehensive Metabolic Panel; Future, TSH, Reflex Free T4; Future, predniSONE (DELTASONE) 10 mg tablet; Take 1 tablet by mouth Daily for 30 days. Dispense: 30 tablet; Refill: 0. 4. Polyarthralgia Assessment & Plan: U information reviewed- Polymyalgia typical findings, normocytic anemia, negative autoantibodies. Laboratory findings: Acute phase reactants are elevated in virtually all patients with PMR. Head-to-head studies of the diagnostic value of the erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) are few, but in clinical experience, the CRP is a more useful index of inflammation. The traditional laboratory finding in PMR is an elevated ESR, which ranges from mildly to markedly increased. In one study, 20 percent of patients had ESR values over 104 mm/hour [27]. Conversely, several studies have found that in approximately 5 to 20 percent of patients with PMR, the ESR is less than 40 mm/hour [28-30]. The CRP is nearly always elevated in PMR. In two reports, an elevated ESR (greater than 30 mm/hour) was noted in 92 to 94 percent of patients at the time of diagnosis of PMR, while 99 percent of such patients had an increased serum CRP level (greater than 5 mg/L) [27,31]. In another study, only 1.5 percent of patients with clinically diagnosed PMR had an ESR and CRP within normal limits (defined as less than 20 mm/hour and 10 mg/L, respectively) at the time of diagnosis [32]. The range of the CRP in PMR, like the ESR, is wide. A diagnostic cut-off value for elevations of the CRP (IE, below which the diagnosis is ruled out) has not been established, but practically speaking, a normal CRP effectively excludes the diagnosis of PMR. Other laboratory findings are nonspecific: A normocytic anemia may be present, and the white blood cell and platelet counts are usually normal, though thrombocytosis can occur as part of a general acute inflammatory response. Autoantibodies, including rheumatoid factor (RF) and anticyclic citrullinated peptide (anti-CCP) antibodies, are usually negative in PMR, and if positive, an alternative diagnosis of late-onset rheumatoid arthritis (RA) should be considered. On the other hand, it should be borne in mind that approximately 10 percent of the older adult population has a positive RF (usually at a low titer) without evidence of RA. Plan: Will get labs Since CRP elevated on labs without other concerning positive labs and patient is meeting diagnostic criteria for PMR per UTD diagnostic algorithm, will start low dose prednisone at 10mg daily due to the fact that last time he had PMR diagnosis that he developed agitation and mood changes that caused him to d/c the steroid medication. Thus will start lower than the typical recommended dosage of 15mg/daily. Will follow-up within 1 week to determine response. If in 1 week, no improvement in symptoms or no improvement in labs, would attempt to increase prednisone dose if tolerated side effects. Would also recheck labs at that point. Diagnosis and treatment of PMR.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2151066

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NH
Alter: 34,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test Ear infection Ear pain Fatigue Hypothyroidism Thyroid function test abnormal Tinnitus

Symptomtext

Approximately a few hours after my 3rd dose (booster shot) I experienced the following symptoms: When I woke up the next day I heard a really loud noise (both ears) - sounded like a really loud beep and I did not know where it was coming from. I would also get pain deep in my ear canal, I also developed Hypothyroidism (Felt very fatigued most of the time). My doctor diagnosed my ear infection as Tinnitus and nothing was prescribed as of the moment. As for my hypothyroidism I am prescribed with Levothyroxine (50mcg 1x/day).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: Physical exam, Blood work, Thyroid test.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Women's Multivitamins
Allergien: Augmentin
Vorherige Impfungen: -

VAERS 2148677

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: CA
Alter: 23,0
Geschlecht: F
Eingang: 28.02.2022
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Nausea

Symptomtext

Nausea, BP: 114/68, Pulse: 64/min - Patient lay down on gurney - Had sips of water - Stated she hasn't ate breakfast - Felt better after 10mins - Adviced to notify PHP if symptoms worsens. - Patient stated she is ok now and wants to rest at home, left with mother.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2146517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: UT
Alter: 41,0
Geschlecht: M
Eingang: 26.02.2022
Impfdatum: 16.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Lung hyperinflation Lymphadenopathy Swelling

Symptomtext

inflated in the pectoral area; pain in his joints, pains in his knees and shoulder; swelling in the lymph nodes; swelling; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 16Nov2021 (Lot number: FH8028) at the age of 41 years as dose 2, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose 1, Batch/lot number: FF2587, Anatomical location: Arm Left ), administration date: 26Oct2021, when the patient was 42 years old, for Covid-19 Immunization, reaction(s): "inflated in the pectoral area", "Discomfort". The following information was reported: LUNG HYPERINFLATION (non-serious), outcome "unknown", described as "inflated in the pectoral area"; ARTHRALGIA (non-serious) with onset 17Nov2021, outcome "unknown", described as "pain in his joints, pains in his knees and shoulder"; LYMPHADENOPATHY (non-serious) with onset Nov2021, outcome "unknown", described as "swelling in the lymph nodes"; SWELLING (non-serious) with onset Nov2021, outcome "unknown", described as "swelling". Additional info: Patient took the first dosage on the 26Oct2021 and he got inflated in the pectoral area and had discomfort and it was disturbing him. He had taken the second dosage on 16Nov2021 and the same thing happened again and was inflated in the pectoral area. It was pectoral or breast plate below the left arm. It started the next day after the first dose. It happened again after the second dose and it was ongoing and it was stronger. The symptoms are much more than the first time on the left side. . It had been more than 72 hours since he got the shot and had the swelling. It had not gone. He was a really healthy man. He doesn't do drugs or drink. He had a good diet and was healthy. He had no underlying conditions. This happening was worse with the second dose. That area was still swelling. Vaccination Facility Type: health department of withheld. No prior Vaccinations within 4 weeks. He did not have flu vaccine or any other vaccines. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient History: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2146455

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MA
Alter: 36,0
Geschlecht: M
Eingang: 26.02.2022
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Body temperature Chills Dizziness Headache Pyrexia

Symptomtext

chills; fever/Temperature was 101; dizziness; headache; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 36 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 02Nov2021 10:00 (Lot number: FH8028) at the age of 36 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (First dose, Route: Injected into his arm), administration date: 2021, for Covid-19 Immunization; Bnt162b2 (Second dose, Route: Injected into his arm, This was 6-8 months ago. He recovered completely.), administration date: 2021, for covid-19 immunization, reaction(s): "fever"; Flu shot (more than one month ago.) The following information was reported: CHILLS (non-serious) with onset 02Nov2021 20:30, outcome "recovered" (03Nov2021), described as "chills"; PYREXIA (non-serious) with onset 02Nov2021 20:30, outcome "not recovered", described as "fever/Temperature was 101"; DIZZINESS (non-serious) with onset 02Nov2021, outcome "unknown", described as "dizziness"; HEADACHE (non-serious) with onset 02Nov2021, outcome "unknown", described as "headache". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of chills, pyrexia, headache. Additional information: That evening, had chills and fever. Took Tylenol and it subsided. Fever again in the morning. Took one more Tylenol and it subsided. In the afternoon, fever came up again. Took one more Tylenol and it subsided. Temperature was 101. Family Medical History Relevant to AE(s) and Relevant Tests None. Initially caller stated he knows this is related to COVID. Clarified, that caller knows it's related to the COVID-19 Vaccine because he did not take anything else. Confirmed caller did not test positive for COVID-19. Dizziness: States it's subsided, but he still has some lightheadedness in his head because of all of the symptoms. Headache: Has subsided today, but kind of has a headache feeling. Doesn't know if it will come back again because he is on medication. The Tylenol only has a half-life of 6-8 hours. Not sure if it's going to come back. Patient underwent lab test procedures which included: On 02Nov2021 101 temperature. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20211102; Test Name: fever; Result Unstructured Data: Test Result:101 Fahrenheit
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2135184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: IL
Alter: 49,0
Geschlecht: M
Eingang: 23.02.2022
Impfdatum: 11.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal pain Arthralgia Blood test Diarrhoea Latent tuberculosis Myalgia Occupational exposure to communicable disease Systemic lupus erythematosus Vomiting

Symptomtext

Had horrible reaction to both shots that included vomiting, diarhea, severe abdominal, joint and muscular pain. Developed new-onset System Lupus after receiving these injections. NO FAMILY HISTORY OF LUPUS OR OTHER SIMILAR DISEASES. Also found latent Tuberculosis given to me from my coworkers who travel to and from another country with horrible respiratory conditions and refuse medical treatment because they feel the physicians are not smart enough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: Too many blood tests to list, as this online form timed-out when I tried to enter the results. Please call for these details.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D2
Allergien: None
Vorherige Impfungen: COVID vaccine 1 - passed out, vomiting, low blood pressure at 49 years old in April 2021

VAERS 2134777

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 24,0
Geschlecht: F
Eingang: 23.02.2022
Impfdatum: 31.01.2021
Beginn: 11.12.2021
Tage bis Beginn: 314,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Erythema Mononucleosis heterophile test negative Rash SARS-CoV-2 test negative Skin irritation Streptococcus test negative Temperature intolerance Urticaria

Symptomtext

Full body rash of small red, non-itchy welts that became irritated around heat

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Mono = negative 12/20/21 COVID = negative 12/20/21 Strep = negative 12/20/21
Aktuelle Erkrankungen: -
Vorgeschichte: PCOS, prediabetes
Andere Medikamente: Ortho-tricylin-lo
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2131204

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge FH8028

mild

Staat: TX
Alter: 56,0
Geschlecht: M
Eingang: 22.02.2022
Impfdatum: 18.11.2021
Beginn: 01.02.2022
Tage bis Beginn: 75,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Cough Headache Interchange of vaccine products SARS-CoV-2 test positive

Symptomtext

Tested positive for Covid while traveling. Got care at home with Ivermectin. Ibuprophen, loratadine, ambroxol and azotromicin. symptoms lasted for 15 days. Still have cough and light headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 02/05/2022 02/10/2022 02/12/2022 02/15/2022
Aktuelle Erkrankungen: Diabetes Bronquiectasis
Vorgeschichte: Bronquiectasis
Andere Medikamente: Metformin Lisinopril Trulicity
Allergien: Penicillin
Vorherige Impfungen: Chills, fever, headache, diarrea, cough with first Pfizer Covid Vaccine on 03/10/2022

VAERS 2127953

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NY
Alter: 57,0
Geschlecht: M
Eingang: 19.02.2022
Impfdatum: 10.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pain in extremity

Symptomtext

Right forearm pain, continuing to present

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: ITP
Andere Medikamente: Psyllium
Allergien: no
Vorherige Impfungen: -

VAERS 2125827

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8028

mild

Staat: NE
Alter: 39,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Diarrhoea Headache Pain Pyrexia Retching

Symptomtext

body aches; fever; diarrhea; Headache; chills; dry heaving first night; This is a spontaneous report received from contactable reporter (Consumer or other non HCP). The reporter is the patient. A 39 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 26Oct2021 18:15 (Lot number: Fh8028) at the age of 39 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "bradycardia" (unspecified if ongoing). Concomitant medication(s) included: MIDODRINE. Past drug history included: Penicillin, reaction(s): "allergy". Vaccination history included: Bnt162b2 (Dose 1, lot number=Er2613, administration time=12:00 PM, vaccine location=Left arm), administration date: 18Mar2021, for COVID-19 Immunization; Bnt162b2 (Dose 2, lot number=Em9809, administration time=13:00 PM, vaccine location=Left arm), administration date: 08Apr2021, for COVID-19 Immunization. The following information was reported: HEADACHE (non-serious) with onset 26Oct2021 22:00, outcome "recovering", described as "Headache"; CHILLS (non-serious) with onset 26Oct2021 22:00, outcome "recovering", described as "chills"; RETCHING (non-serious) with onset 26Oct2021 22:00, outcome "recovering", described as "dry heaving first night"; PAIN (non-serious) with onset 27Oct2021, outcome "recovering", described as "body aches"; PYREXIA (non-serious) with onset 27Oct2021, outcome "recovering", described as "fever"; DIARRHOEA (non-serious) with onset 27Oct2021, outcome "recovering", described as "diarrhea". Therapeutic measures were not taken as a result of headache, chills, retching, pain, pyrexia, diarrhoea. Additional information: Did the patient receive any other vaccines within 4 weeks prior to the COVID vaccine: No. Prior to vaccination, was the patient diagnosed with COVID-19?: No. Since the vaccination, has the patient been tested for COVID-19?: No Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bradycardia
Andere Medikamente: MIDODRINE
Allergien: -
Vorherige Impfungen: -

VAERS 2122643

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WA
Alter: -
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Body temperature Fatigue Headache Pyrexia

Symptomtext

feeling tired; has some fever/has a slight fever of 37.8 C; Headache; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A male patient received bnt162b2 (BNT162B2) (Lot number: FH8028, Expiration Date: 28Feb2022) as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose number: 1), for Covid-19 immunization; Bnt162b2 (Dose number: 2), for Covid-19 immunization. The following information was reported: FATIGUE (non-serious), outcome "unknown", described as "feeling tired"; PYREXIA (non-serious), outcome "unknown", described as "has some fever/has a slight fever of 37.8 C"; HEADACHE (non-serious), outcome "unknown", described as "Headache". Relevant laboratory tests and procedures are available in the appropriate section. Additional Information: The caller is calling about the Pfizer covid 19 vaccine. The caller and her husband took the booster shot of the Pfizer covid 19 vaccine. When they came home, the expiration date on the caller's husband's said 28Feb2022. The vaccination cards have a sticker on it with the product information on it, it is not handwritten. Both the caller and her husband's lot was FH8028. The patient is feeling tired and has some fever. The patient has a headache, is tired and has a slight fever of 37.8 C. The patient has been staying in bed. The patient has a headache and is very tired. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Name: fever; Result Unstructured Data: Test Result:37.8 Centigrade; Comments: has a slight fever of 37.8 C.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2119107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 07.12.2021
Beginn: 15.02.2022
Tage bis Beginn: 70,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Abdominal pain Brain cancer metastatic COVID-19 Chemotherapy Febrile neutropenia Liver function test increased Lung cancer metastatic Neoplasm malignant Urinary tract infection Vaccine breakthrough infection

Symptomtext

COVID BREAKTHROUGH - 58 year old female. She is Admitted to Medical Med/Tele for COVID19, Neutropenic Fever, Abdominal Pain, UTI, Metastatic Lung Cancer to Spine and Brain on Chemotherapy,and Elevated LFT's. First covid dose 4/19/21. She has recieved the booster shot on 12/7/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, COPD, Toxic Shock Syndrome, Tobacco Abuse, Lumpectomy of Left Breast, Hysterectomy, Hip Pain, Lung Cancer with
Andere Medikamente: -
Allergien: sulfADIAZINE
Vorherige Impfungen: -

VAERS 2112857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WI
Alter: 40,0
Geschlecht: M
Eingang: 15.02.2022
Impfdatum: 26.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Asthenia COVID-19 Fatigue Hepatic failure Hepatitis alcoholic Jaundice SARS-CoV-2 test positive

Symptomtext

Patient was admitted to observation level of care on 1-28 -22through 2-5-22 with marked jaundice and complaint of weakness. Receiving treatment for likely alcoholic hepatitis with liver failure. It is noted that the patient tested positive for covid on admission. Readmitted on 2/12/22 ---he reports feeling very weak and tired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2110030

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NV
Alter: 61,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 18.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pain in extremity

Symptomtext

Sore arm; has been ongoing since receiving 2nd dose of vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: Diabetes.
Andere Medikamente: None.
Allergien: Penicillin.
Vorherige Impfungen: -

VAERS 2107423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: TX
Alter: 35,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pyrexia Urticaria Vomiting

Symptomtext

large hives broke out on buttocks and have persisted for 10+ days traveling to flanks; Fever for 2 days after booster; Vomiting for 2 days after booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 35 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 05Nov2021 15:30 (Lot number: FH8028) at the age of 35 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Known allergies: Penicillin" (unspecified if ongoing); "Sulfa" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0170, Location of injection: Arm Left, Vaccine Administration Time: 04:00 PM), administration date: 23Apr2021, when the patient was 35 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8734, Location of injection: Arm Left, Vaccine Administration Time: 06:00 PM), administration date: 02Apr2021, when the patient was 35 years old, for COVID-19 immunization; Flu vaccine vii, administration date: Oct2021, for Immunisation. The following information was reported: PYREXIA (non-serious) with onset 06Nov2021 02:00, outcome "not recovered", described as "Fever for 2 days after booster"; VOMITING (non-serious) with onset 06Nov2021 02:00, outcome "not recovered", described as "Vomiting for 2 days after booster"; URTICARIA (non-serious) with onset 07Nov2021, outcome "not recovered", described as "large hives broke out on buttocks and have persisted for 10+ days traveling to flanks". The events "fever for 2 days after booster", "vomiting for 2 days after booster" and "large hives broke out on buttocks and have persisted for 10+ days traveling to flanks" were evaluated at the physician office visit. Therapeutic measures were taken as a result of pyrexia, vomiting, urticaria. Included Anti itch cream, pill. Waiting on steroids. Additional Information: Patient was not diagnosed with COVID-19, prior vaccination and since the vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy; Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2090155

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WA
Alter: 66,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Body temperature Expired product administered Fatigue Headache Pyrexia

Symptomtext

Headache; Tiredness; Slight fever of 37.8 C; Expiry Date of Pfizer covid 19 vaccine: 28Feb2021; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 66 year-old female patient received bnt162b2 (COMIRNATY), administered in arm left, administration date 27Oct2021 (Lot number: FH8028, Expiration Date: 28Feb2021) at the age of 66 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (1st dose, lot EM9810, The caller clarifies and confirms that she did not have any side effects with the first two doses of the Pfizer Covid 19 vaccine.), administration date: 06Feb2021, when the patient was 66 years old, for Covid-19 immunization, reaction(s): "No reaction on previous exposure to vaccine"; Bnt162b2 (2nd dose, lot EN6200, The caller clarifies and confirms that she did not have any side effects with the first two doses of the Pfizer Covid 19 vaccine.), administration date: 28Feb2021, when the patient was 66 years old, for Covid-19 immunization, reaction(s): "No reaction on previous exposure to vaccine". The following information was reported: HEADACHE (non-serious) with onset 28Oct2021, outcome "not recovered", described as "Headache"; FATIGUE (non-serious) with onset 28Oct2021, outcome "recovering", described as "Tiredness"; PYREXIA (non-serious) with onset 28Oct2021, outcome "not recovered", described as "Slight fever of 37.8 C"; EXPIRED PRODUCT ADMINISTERED (non-serious) with onset 27Oct2021, outcome "unknown", described as "Expiry Date of Pfizer covid 19 vaccine: 28Feb2021". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of headache. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Body temperature; Result Unstructured Data: Test Result:37.2 C; Comments: The caller's temperature was 37.2 C then 37.8 C.; Test Date: 20211028; Test Name: Body temperature; Result Unstructured Data: Test Result:37.8 C; Comments: slight fever of 37.8 C
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2085766

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: ID
Alter: 11,0
Geschlecht: M
Eingang: 03.02.2022
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Pain Pain in extremity Pyrexia

Symptomtext

patient had sore arm, low grade fever and body aches for 48 hours and then was fine, no further issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2079856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NJ
Alter: 43,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 05.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Biopsy Erythema Feeling hot Pain in extremity Peripheral swelling Pityriasis rosea Skin burning sensation

Symptomtext

After receiving the vaccine I was diagnosed with Pityriasis Rosea. I had the rash for 30 days then it went away. I also had arm pain through out the month, and it has been ongoing. I also had burning, hot, skin for about a week on my stomach and upper chest. I was prescribed a cream. I had a red swollen arm for a week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Biopsy
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Magnesium; vitamin C; zinc
Allergien: None
Vorherige Impfungen: -

VAERS 2076049

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 24,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 01.10.2021
Beginn: 29.12.2021
Tage bis Beginn: 89,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Arthralgia COVID-19 Cough Diarrhoea Pain SARS-CoV-2 test positive

Symptomtext

12/29/21 presents to antepartum for "generalized body aches and bilateral hip pain, cough, diarrhea". PMHx of "Sickle cell disease, avascular necrosis of bones of both hips, marijuana use, obesity, 31 weeks and 6 days pregnant"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 12/29/21 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2071833

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: OR
Alter: 35,0
Geschlecht: M
Eingang: 28.01.2022
Impfdatum: 24.10.2021
Beginn: 12.01.2022
Tage bis Beginn: 80,0
Dosis: UNK
Route/Site: SYR / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chills Cough Fatigue Headache Myalgia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I have since tested positive for Covid on 1/12/22. Moderate symptoms including cough, chest congestion, severe headaches, muscle aches , fatigue and chills that last for 5 days. Then I had mild symptoms for 5 more days. Currently have a residual cough and chest congestion that have improved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Home Binax Now covid test on 1/12/22.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 2069240

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MT
Alter: 45,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 28.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal pain Breast tenderness Constipation Irritability Lymph node pain Lymphadenopathy

Symptomtext

The lymph node under my arm became swollen and tender. It was roughly the size of a golf ball after the second injection and the size of a softball after the booster. Additionally, after the booster, my breasts were tender for about 2 weeks and, though I have had a hysterectomy, I had symptoms like constipation, abdominal cramps and irritability that would normally accompany a period or early pregnancy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: none
Vorgeschichte: Fibromyalgia; PMDD; PTSD; Allergies to bee venom, dust and mold; Hypertension; Chronic Sinusitis; bilateral osteoarthritis of the knees
Andere Medikamente: Lisinopril with HCTZ, Duloxetine, Mobic, Loratadine, Garlic, Vit. B, Vit. C., Vit. D and Zinc and Robaxin as needed.
Allergien: None
Vorherige Impfungen: Allergic reaction to preservative in Influenza injection in 2013. Swollen injection site about the size of a baseball that was

VAERS 2069175

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: VA
Alter: 46,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 05.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Acoustic stimulation tests Fatigue Pain Tinnitus

Symptomtext

Tinnitus. Two weeks before taking the booster, I started hearing a low pitch whirring sound in my right ear, only in very quite rooms. It actually seemed to be getting better over a couple of weeks. Then, I got the Pfizer COVID vaccine booster, which caused fatigue and aches and also made my tinnitus much worse. I now hear a louder high pitched sound in my right ear. I saw an ENT who confirmed with audiology tests that there is no hearing loss. A course of oral steroids did not help.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Audiology hearing test. Came back normal.
Aktuelle Erkrankungen: 2 weeks prior to my booster, I was hearing a low pitch whirring sound in my right ear, only in very quite rooms. It was getting better and seemed like it would go away. Then I got the Pfizer booster and soon after I stared hearing a louder high pitch sound in my right ear.
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2066890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 08.11.2021
Beginn: 15.01.2022
Tage bis Beginn: 68,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Abdominal pain upper Back pain COVID-19 Hypoxia SARS-CoV-2 test positive

Symptomtext

LOCAL TITLE: EMERGENCY STANDARD TITLE: EMERGENCY MEDICINE NOTE DATE OF NOTE: JAN 15, 2022@11:42:02 ENTRY DATE: JAN 15, 2022@11:42:02 AUTHOR: EXP COSIGNER: URGENCY: STATUS: COMPLETED *** EMERGENCY Has ADDENDA *** ER Triage Note Pt., a 69 year old FEMALE presents to Emergency Department on 01/15/22 11:28. Tetanus status: Last Tdap: Jul 29, 2019 LMP: Chief Complaint: Visit CC: + covid,back pain and stomach pain Pt. is a 69 year old FEMALE who is being admitted to the Hospital. This patient meets inpatient level of care because of need for supplemental O2 and remdesivir. ASSESSMENT/PLAN: 69 yo lady with obesity, HTN, LBBB with Covid 19 infection and ambulatory hypoxia. # Covid 19 - tested positive 1/13/22 Pt., a 69 year old FEMALE currently was admitted on JAN 16,2022 17:04.The patient is being discharged 20-Jan-2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2050326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NJ
Alter: 47,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Immunisation Vaccination site erythema Vaccination site pain

Symptomtext

booster; Pain in arm/Under that area is all red around I got the injection; red around the injection/Under that area is all red around I got the injection, I have like a red mark or the injection mark on my arm and it's kind of hurt; This is a spontaneous report received from a contactable reporter(s) (Pharmacist). The reporter is the patient. A 47 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 21Dec2021 (Lot number: FH8028, Expiration Date: 28Feb2022) at the age of 47 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Anxiety" (unspecified if ongoing). Concomitant medication(s) included: BUSPIRONE taken for anxiety. Vaccination history included: Covid-19 vaccine (Dose 1st , Lot# of First shot: EW0161., Anatomical site of administration: Left), administration date: 06May2021, when the patient was 47 years old, for COVID-19 immunization; Covid-19 vaccine (Dose 2nd, Lot# of second shot: EW0182, Anatomical site of administration: Left), administration date: 06Jun2021, when the patient was 47 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 21Dec2021, outcome "unknown", described as "booster"; VACCINATION SITE PAIN (non-serious) with onset 21Dec2021, outcome "unknown", described as "Pain in arm/Under that area is all red around I got the injection"; VACCINATION SITE ERYTHEMA (non-serious) with onset 21Dec2021, outcome "unknown", described as "red around the injection/Under that area is all red around I got the injection, I have like a red mark or the injection mark on my arm and it's kind of hurt". Therapeutic measures were taken as a result of vaccination site pain, vaccination site erythema. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety
Andere Medikamente: BUSPIRONE
Allergien: -
Vorherige Impfungen: -

VAERS 2048078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NY
Alter: 63,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 09.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Diarrhoea Fatigue Pyrexia Tinnitus

Symptomtext

Starting 24 hours after the vaccine, I developed a low grade fever and loud, whistling tinnitus in both ears. The elevated temperature abated after 1 day, but this tinnitus is still present over a month later. It has reduced in volume by about 2/3, but it has not gone away. I have NOT had this kind of tinnitus before the vaccination. Also starting at the same time as the fever was diarrhea and fatigue. The diarrhea lasted for 2 weeks then stopped, the fatigue lasted 17 days then stopped.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Autoimmune disease, hives. GERD, intestinal adhesions
Andere Medikamente: None
Allergien: Levaquin, morphine, penicillin and cephalosporins, Prilosec, milk, beef,
Vorherige Impfungen: Prophylactic rabies vaccination series, in 1992, prior to working with animals in a veterinary setting. Unknown brand of vaccine

VAERS 2043501

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

mild

Staat: MI
Alter: 80,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 06.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia Chills Incontinence Mental impairment Mental status changes Pyrexia

Symptomtext

Incontinent, impaired mental status, fever, chills, very weak

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: no
Vorgeschichte: epilepsy, history of stroke, hypoparathyroidism, pacemaker
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2035889

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: KY
Alter: 29,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Injection site pain Shoulder injury related to vaccine administration

Symptomtext

SIRVA - extreme pain at injection site, continuing for 2+ months

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: Lexapro Flonase allergy relief
Allergien: n/a
Vorherige Impfungen: -

VAERS 2554254

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 1,2
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Fatigue Headache

Symptomtext

Dizziness, Headache, Fatigue Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2554251

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

mild

Staat: -
Alter: 48,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 03.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Fatigue Injection site pain Pain in extremity

Symptomtext

Injection site soreness, right arm pain, fatigue, chills Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2552186

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 50,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Injection site pain Myalgia Pruritus Pyrexia

Symptomtext

Myalgia, Fever, Sore at injection site and itchy Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2464324

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 35,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Abnormal dreams Chills Fatigue Headache Pyrexia

Symptomtext

Headache, Fever, chills, vivid dreams, fatigued Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2464323

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 1,2
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 07.11.2021
Beginn: 02.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Headache Inappropriate schedule of product administration Nausea Vomiting

Symptomtext

Dizziness, Headache & NauseaVomiting Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2464322

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 29,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 02.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Muscle spasms Myalgia

Symptomtext

Myalgia muscle spasms Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2464320

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 33,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Lymphadenopathy Pyrexia

Symptomtext

Fever Lymph nodes swollen, - scheduled w/ PCP for assessment, Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2463056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

mild

Staat: -
Alter: 48,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Myalgia Pyrexia

Symptomtext

Dizziness, Myalgia, Fever,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2453309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 30,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Injection site mass Myalgia Pyrexia

Symptomtext

Myalgia, Fever, inj site lump (took off the 4th) Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site mass
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2021071

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: PA
Alter: 50,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 26.11.2021
Beginn: 01.01.2022
Tage bis Beginn: 36,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cough Fatigue Headache Injection site pain

Symptomtext

I had pain at the site. I was fatigued the next day. I had headache and cough. These symptoms lasted for about 2 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2021040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: SC
Alter: 13,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 07.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Erythema Pruritus Urticaria

Symptomtext

Hives(welts) on both legs appeared after the first and second covid shot. Hives were a dime size to pea size around, red and raised. Itched but not out of control itching. First time lasted 2 days. After the second shot they lasted 4 days. Controlled with Benadryl and Epstein salt baths.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Melatonin 3mg
Allergien: None
Vorherige Impfungen: -

VAERS 2020926

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 49,0
Geschlecht: M
Eingang: 10.01.2022
Impfdatum: 01.01.2022
Beginn: 02.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache

Symptomtext

I have suffered a headache since the day after I received the vaccination. I normally do not get headaches at all, certainly not ones that last this long. Tylenol does not help it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2019539

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: KY
Alter: 31,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 06.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Eye discharge Lymphadenitis Lymphadenopathy Pain Skin lesion Swelling of eyelid

Symptomtext

left sided cervical and lymphadenopathy for 10 days that self-resolved. Lymph nodes from neck up to left side of scalp including left eye lid were inflamed with serous draining and erythematous lesion that caused mild to moderate pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Only clinical findings
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Egg-based medication, coconut food allergy
Vorherige Impfungen: -

VAERS 2018839

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH 8028

mild

Staat: -
Alter: -
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 27.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Drug ineffective Fatigue Headache Immunisation Nasal congestion SARS-CoV-2 test Sinus pain

Symptomtext

Positive Bianax Now COVID test; Positive Bianax Now COVID test on 30Dec2021.; Congestion; sinus pain; headache; fatigue; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 58 year-old female patient received bnt162b2 (BNT162B2), administration date 27Nov2021 (Lot number: FH 8028) as dose number unknown (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (MANUFACTURER UNKNOWN, dose number unknown), for Covid-19 immunization. The following information was reported: DRUG INEFFECTIVE with onset 30Dec2021, outcome "unknown", described as "Positive Bianax Now COVID test"; COVID-19 with onset 30Dec2021, outcome "unknown", described as "Positive Bianax Now COVID test on 30Dec2021."; IMMUNISATION with onset 27Nov2021, outcome "unknown", described as "Booster"; NASAL CONGESTION (non-serious) with onset 27Dec2021, outcome "unknown", described as "Congestion"; SINUS PAIN (non-serious) with onset 27Dec2021, outcome "unknown", described as "sinus pain"; HEADACHE (non-serious) with onset 27Dec2021, outcome "unknown", described as "headache"; FATIGUE (non-serious) with onset 27Dec2021, outcome "unknown", described as "fatigue". The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (30Dec2021) positive, notes: Bianax. Clinical courses: Consumer was around unvaccinated individual that became sick. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Date: 20211230; Test Name: Covid-19 test; Test Result: Positive ; Comments: Bianax
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1981773

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: AZ
Alter: 30,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 03.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood iron decreased Blood test Complication associated with device Fatigue Intrauterine contraception Blood pressure measurement Haemoglobin Heart rate Heavy menstrual bleeding Immunisation

Symptomtext

heavy periods returned after that on 28Nov2021 until 02Dec2021; Booster: given on 03Nov2021; she still has fatigue; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 30 year-old female patient received bnt162b2 (BNT162B2), administration date 03Nov2021 (Lot number: FH8028) at the age of 30 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "She has been anemic her entire life" (unspecified if ongoing), notes: Verbatim: She has been anemic her entire life; "IUD", start date: 11Oct2021 (ongoing), notes: slow down menstrual, It expires in 7 years. Concomitant medication(s) included: VITAMIN D [COLECALCIFEROL]; IRON FERROUS GLUCONATE. Vaccination history included: Bnt162b2 (Dose 1 of Pfizer, lot number: EW0151.), administration date: 07Apr2021, when the patient was 30 years old, for COVID-19 Immunization, reaction(s): "one something to her menstrual cycle. She has always had heavy menstrual./Her period became worse after the vaccine", "fatigued after the vaccine", "she had low blood pressure. It was 60/80 for months", "She had low heart rate", "she was sleeping 14 to 16 hours per day", "She could barely open her eyes in the morning", "Her Hgb was low"; Bnt162b2 (Dose 2 of Pfizer, lot number: EW0177.), administration date: 07May2021, when the patient was 30 old, for COVID-19 Immunization, reaction(s): "done something to her menstrual cycle. She has always had heavy menstrual./Her period became worse after the vaccine"; Bnt162b2 (Dose 2 of Pfizer, lot number: EW0177.), administration date: 07May2021, when the patient was 30 years old, for COVID-19 Immunization, reaction(s): "still fatigued after the vaccine". The following information was reported: IMMUNISATION (non-serious) with onset 03Nov2021, outcome "unknown", described as "Booster: given on 03Nov2021"; HEAVY MENSTRUAL BLEEDING (non-serious) with onset 28Nov2021, outcome "unknown", described as "heavy periods returned after that on 28Nov2021 until 02Dec2021"; FATIGUE (non-serious) with onset Nov2021, outcome "not recovered", described as "she still has fatigue". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: She got booster on 03Nov2021 and heavy periods returned after that on 28Nov2021 until 02Dec2021. Before that they had gotten light again because of IUD. Her next period was scheduled for 23Dec2021. Since course of going to the doctor she was on daily iron pill and vitamin D. She had been taking those for her entire life. It goes up and down. They were prescription. It was iron, but different name. Vitamin D: strength 50,000 IU, one gel pill by mouth once a week. Use before 08Nov2022. Iron was Ferrous Gluc 324 mg tablet, expires in Dec2022. Caller was not an antivax and she believed medicine worked. She couldn't in good conscious recommend people to get it with how many health problems she has had this summer. Now in order for her to stop these heavy periods the chances of having a child go down. That was not fair to her. Caller stated back in May she reported that she was still fatigued after the COVID19 vaccine. Her iron couldn't get up enough to not be fatigue. All started in Apr after the vaccine. She still had fatigue and the fatigue was a by product. Essentially she was loosing too much blood every month to keep her iron. The iron was what would keep her from being fatigue. When she first got vaccine she was sleeping 14 to 16 hours per day. She could barely open her eyes in the morning. That was what made her go into the doctor. Her Hgb was low. She has been anemic her entire life, but nothing that caused disruption in her life. She would be a little tired, but she could still donate blood. It was lower average but not that she had to go see hematology prior to vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: she had low blood pressure; Result Unstructured Data: Test Result:60/80; Test Date: 2021; Test Name: Hgb; Result Unstructured Data: Test Result:Low; Test Date: 2021; Test Name: low heart rate; Result Unstructured Data: Test Result:Low
Aktuelle Erkrankungen: Device implant NOS (slow down menstrual It expires in 7 years)
Vorgeschichte: Medical History/Concurrent Conditions: Anemic (Verbatim: She has been anemic her entire life)
Andere Medikamente: VITAMIN D [COLECALCIFEROL]; IRON FERROUS GLUCONATE
Allergien: -
Vorherige Impfungen: -

VAERS 1981773

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: AZ
Alter: 30,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 03.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood iron decreased Blood test Complication associated with device Fatigue Intrauterine contraception Blood pressure measurement Haemoglobin Heart rate Heavy menstrual bleeding Immunisation

Symptomtext

heavy periods returned after that on 28Nov2021 until 02Dec2021; Booster: given on 03Nov2021; she still has fatigue; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 30 year-old female patient received bnt162b2 (BNT162B2), administration date 03Nov2021 (Lot number: FH8028) at the age of 30 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "She has been anemic her entire life" (unspecified if ongoing), notes: Verbatim: She has been anemic her entire life; "IUD", start date: 11Oct2021 (ongoing), notes: slow down menstrual, It expires in 7 years. Concomitant medication(s) included: VITAMIN D [COLECALCIFEROL]; IRON FERROUS GLUCONATE. Vaccination history included: Bnt162b2 (Dose 1 of Pfizer, lot number: EW0151.), administration date: 07Apr2021, when the patient was 30 years old, for COVID-19 Immunization, reaction(s): "one something to her menstrual cycle. She has always had heavy menstrual./Her period became worse after the vaccine", "fatigued after the vaccine", "she had low blood pressure. It was 60/80 for months", "She had low heart rate", "she was sleeping 14 to 16 hours per day", "She could barely open her eyes in the morning", "Her Hgb was low"; Bnt162b2 (Dose 2 of Pfizer, lot number: EW0177.), administration date: 07May2021, when the patient was 30 old, for COVID-19 Immunization, reaction(s): "done something to her menstrual cycle. She has always had heavy menstrual./Her period became worse after the vaccine"; Bnt162b2 (Dose 2 of Pfizer, lot number: EW0177.), administration date: 07May2021, when the patient was 30 years old, for COVID-19 Immunization, reaction(s): "still fatigued after the vaccine". The following information was reported: IMMUNISATION (non-serious) with onset 03Nov2021, outcome "unknown", described as "Booster: given on 03Nov2021"; HEAVY MENSTRUAL BLEEDING (non-serious) with onset 28Nov2021, outcome "unknown", described as "heavy periods returned after that on 28Nov2021 until 02Dec2021"; FATIGUE (non-serious) with onset Nov2021, outcome "not recovered", described as "she still has fatigue". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: She got booster on 03Nov2021 and heavy periods returned after that on 28Nov2021 until 02Dec2021. Before that they had gotten light again because of IUD. Her next period was scheduled for 23Dec2021. Since course of going to the doctor she was on daily iron pill and vitamin D. She had been taking those for her entire life. It goes up and down. They were prescription. It was iron, but different name. Vitamin D: strength 50,000 IU, one gel pill by mouth once a week. Use before 08Nov2022. Iron was Ferrous Gluc 324 mg tablet, expires in Dec2022. Caller was not an antivax and she believed medicine worked. She couldn't in good conscious recommend people to get it with how many health problems she has had this summer. Now in order for her to stop these heavy periods the chances of having a child go down. That was not fair to her. Caller stated back in May she reported that she was still fatigued after the COVID19 vaccine. Her iron couldn't get up enough to not be fatigue. All started in Apr after the vaccine. She still had fatigue and the fatigue was a by product. Essentially she was loosing too much blood every month to keep her iron. The iron was what would keep her from being fatigue. When she first got vaccine she was sleeping 14 to 16 hours per day. She could barely open her eyes in the morning. That was what made her go into the doctor. Her Hgb was low. She has been anemic her entire life, but nothing that caused disruption in her life. She would be a little tired, but she could still donate blood. It was lower average but not that she had to go see hematology prior to vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: she had low blood pressure; Result Unstructured Data: Test Result:60/80; Test Date: 2021; Test Name: Hgb; Result Unstructured Data: Test Result:Low; Test Date: 2021; Test Name: low heart rate; Result Unstructured Data: Test Result:Low
Aktuelle Erkrankungen: Device implant NOS (slow down menstrual It expires in 7 years)
Vorgeschichte: Medical History/Concurrent Conditions: Anemic (Verbatim: She has been anemic her entire life)
Andere Medikamente: VITAMIN D [COLECALCIFEROL]; IRON FERROUS GLUCONATE
Allergien: -
Vorherige Impfungen: -

VAERS 2659104

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 45,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 08.11.2021
Beginn: 20.12.2021
Tage bis Beginn: 42,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

COVID-19 Chest X-ray normal Cough Fatigue Headache Nausea Oropharyngeal pain Pharyngeal swelling Rhinorrhoea SARS-CoV-2 test SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection following COVID vaccine series 03/27 , Janssen dose #1 11/08, Pfizer, dose #2n12/20 SARS-COV-2 Variant Sequencing; pending 12/2o COVID swab, result: detected 12/20 pt cc: cough, fatigue, headache, nauseam rhinorrhea, sore throat. right-side swollen throat, exposure: unknown 12/20 CXR impression: No acute cardiopulmonary disease. 12/29 clinically resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 12/20 SARS-COV-2 Variant Sequencing: pending 12/20 CXR impression: No acute cardiopulmonary disease. 12/20 COVID swab, result: detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2019712

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: GA
Alter: -
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 29.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Hypersensitivity Injection site discolouration Injection site erythema Injection site pain Injection site swelling Pruritus Pyrexia Rhinorrhoea

Symptomtext

I got Pfizer booster on 12/29/2021. The injection site swelled up about the of a half a walnut shell and was red and swollen. The site is still raised but no longer painful. The site is still discolored. I had a fever of 100 degrees for two days. It may not be related to the injection, but for a week I have experienced an allergy attack with clear nasal discharge and itching.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site discolouration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: diabetes, asthma, high blood pressure, obesity
Andere Medikamente: gabapentin, atorvastatin, meloxicam, insulin, loratidine
Allergien: -
Vorherige Impfungen: -

VAERS 2015568

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: CA
Alter: 56,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 03.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 26,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Herpes zoster Pruritus

Symptomtext

About 10 days after the Injection my right thigh started to itch where I have some small lipomas internally the itch started. I kept wondering why and ignoring it. Then about 2 weeks later I got shingles. Was given Valacylovir 1 gram 2 times a day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Epilepsy
Vorgeschichte: Epilepsy
Andere Medikamente: Centrum Adult Pro-Biotic 25 million Vimpat 500 mg Progesterone 2.5 mg Yuvafem 10MCG Vaginal Estrogel .05% every 3 days Dymista
Allergien: Soy, All Phytoestrogen foods,
Vorherige Impfungen: -

VAERS 2010872

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MO
Alter: 59,0
Geschlecht: M
Eingang: 06.01.2022
Impfdatum: 21.12.2021
Beginn: 25.12.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Headache Injection site pain Pain in extremity Swelling

Symptomtext

After the vaccine my arm was a little sore at the injection site. 24 hours later I had a slight headache. Over the couple next days my arm was hurting more. I am taking medication for the swelling because it is still there.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: I have Hypertension and Insomnia.
Andere Medikamente: I was taking my regular prescriptions.
Allergien: I am allergic to Codeine and Walnuts. I have Seasonal Allergies as well.
Vorherige Impfungen: -

VAERS 2009856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WA
Alter: 42,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Abortion spontaneous Chills Exposure during pregnancy Human chorionic gonadotropin abnormal Myalgia Pelvic pain Ultrasound antenatal screen abnormal Vaginal haemorrhage

Symptomtext

Had no reaction to 1st or 2nd Comirnaty (Pfizer COVID-19) vaccine. Received booster 11/16/2021. On 11/17/2021, severe rigors/chills/myalgias, at 9 weeks gestation. Ultrasound at 7 weeks GA was normal. Started extremely light vaginal bleeding 11/18, continued with intermittent rigors etc. through the weekend. On 11/22, felt a sudden pain ("rip") in the pelvis during a rigor, and subsequently experienced heavier bleeding/miscarriage at 10 weeks GA. No history of prior miscarriages (3 term live births).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 29-Nov-2021: HCG 1479 Test unit MILLI INTERNATIONAL UNITS Serial hCG testing was conducted q2weeks until it was 17mlU/mL on 12/23/2021. Ultrasound 12/6/2021 confirmed miscarriage.
Aktuelle Erkrankungen: -
Vorgeschichte: None. Very healthy. History of 3 term pregnancies, no miscarriages, no abortions.
Andere Medikamente: Folic acid 0.8 mg PO daily
Allergien: None.
Vorherige Impfungen: -

VAERS 2007054

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: PA
Alter: 39,0
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 28.09.2021
Beginn: 28.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test normal Chills Dizziness Echocardiogram normal Electrocardiogram normal Fatigue Feeling abnormal Feeling hot Headache Impaired work ability Joint swelling Loss of personal independence in daily activities Malaise Pain Pain in extremity Peripheral coldness Peripheral swelling SARS-CoV-2 test negative

Symptomtext

Symptoms started several hours after the first vaccine dose: headache, sore arm, body aches, feeling nauseous, overall feeling of not being right, brain fog, weird pains in legs and arms and exhaustion. The day after my first dose I had the above symptoms but also started having additional symptoms: cold toes when sitting down, feeling like I could pass out, chills, felt like I burning up but didn't have fever. these symptoms are persistent and are drastically affecting my life in a negative way. I was so sick I was unable to go work on 9/29, 9/30 and 10/1. On October 1, 2021 I went to an Urgent Care to be checked by a doctor. The PA at urgent care thought I was having a heart attach and had a EKG performed along with a Covid test, both tests came back negative. However, the symptoms persisted. On October 6, 2021 I went to my normal doctors office, Associates,I was given a shot of Toradol-Ketorolac 15MG to assist with the non-stop headache pain. I reported all of the above symptoms to Associates. Gainer around 5# since late September. The above symptoms started to change in mid October 2021 and I had the following symptoms: Cold toes (feel ice cold) when sitting down. Exhausted all the time Brain fog Pain in legs Hard to think clearly at times. Pain in arms Overall body aches Overall don?t feel well / normal On November 19, 2021 I met with my normal doctor, Dr. at Associates. I informed him of the above symptoms and times frames. His response people have many varied side effects from the vaccine and the symptoms should go away in the near future. On the evening of December 3, 2021 I noticed that my both of my feet and ankles were swollen. On December 8, 2021 I CRNP at Associates, to discuss the above symptoms and now the swollen feet and ankles. Ms. scheduled me for some blood tests and a US Leg Bilateral Venous. On December 12, 2021 the swelling in my feet and ankles also spread to my upper thigh in my right leg. On December 13, 201 I was examined Associates. Referred to Health to obtain an Echocardiogram. On December 15, 2021 I had a another examination. No treatments have been prescribed nor recommended except for the Toradol for the headache and to elevate my feet when possible. So far no tests have shown any cause to the symptoms that immediately followed the first vaccine does I received on 9/28/2021. On January 4, 2022 Dr. with Associates, has referred me to a vascular surgeon / specialist. I have an appointment with the specialist on January 6, 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 10/1/2021: EKG and covid test - both negative for heart attack and covid 12/8/2021: blood work and US Leg Bilateral Venous - no signs of blood clots or anything else related to my symptoms 12/21/2021: Echocardiogram - heart is functioning in a normal range 1/4/2022: no results pointing to the cause of my symptoms as far as I know, waiting for review and update from Dr.
Aktuelle Erkrankungen: None that I'm aware of.
Vorgeschichte: High blood pressure; High cholesterol; Anxiety; Hypothyroidism.
Andere Medikamente: Armodafinil; Levothyroxine; Atorvastatin; Citalopram HBR; LISINOPRIL-HYDROCHLOROTHIA; OXYBUTYNIN CHLORIDE; PRILOSEC OTC; Vitamin D; Vitamin C.
Allergien: Hard Shellfish / Crabs.
Vorherige Impfungen: -

VAERS 2001575

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WA
Alter: 73,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site pain Pain

Symptomtext

Patient still reports sharp pain next to site of injection when he is moving it after 3 months of injections

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1999857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: OR
Alter: 47,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 30.11.2021
Beginn: 11.12.2021
Tage bis Beginn: 11,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Abdominal pain upper Lipase increased Pancreatitis

Symptomtext

pancreatitis, epigastric pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: elevated lipase
Aktuelle Erkrankungen: -
Vorgeschichte: diabetes, hypertension, hyperlipidemia, coronary arter disease
Andere Medikamente: lantus; metformin; soma, cialis; lipitor; aspirin
Allergien: propofol
Vorherige Impfungen: -

VAERS 1999353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: KY
Alter: 46,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 13.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Facial pain Fatigue Hypersomnia Illness Paranasal sinus discomfort Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test Sinus operation Sneezing Throat irritation Toothache

Symptomtext

12/20/2021 Covid symptoms started. I felt very exhausted and fatigued. On the 21st I woke up very sick with runny nose, sneezing, horrible sinus pressure, facial pain, teeth pain, chills with no fever, a little tickle in my throat but it wasn't persistent, and drainage and congestion. The facial pain was the worst face pain I've ever experienced. It hit all at once and I slept for 2 days, and on the 23rd I felt better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Covid
Aktuelle Erkrankungen: None
Vorgeschichte: Lupus
Andere Medikamente: Prednisone; Plaquenil; Methotrexate
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1996131

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MT
Alter: 60,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 15.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue Hyperacusis Influenza like illness Pain Pyrexia Tinnitus

Symptomtext

I felt like I had the flu for about 5 days. Low-grade fever, body aches, and fatigue. I have tinnitus and the sound level is much worse since I had the 2nd vaccine. It is so loud now that it is hard to hear the TV or people talking.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: I haven't seen a doctor yet but I plan on making an appointment.
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoarthritis, Fibromyalgia, Chronic back pain,
Andere Medikamente: Hydrochlorothiazide 25 MG, Sertaline 100 MG, Simvastatin 40 MG, Fish oil, multivitamins, Vitamin D, Acid reducer,
Allergien: Tetracycline, Keflex,
Vorherige Impfungen: -

VAERS 1995944

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: TX
Alter: 44,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 17.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Mechanical urticaria

Symptomtext

New-onset dermatographia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: Visited doctor to confirm diagnosis
Aktuelle Erkrankungen: no
Vorgeschichte: none
Andere Medikamente: Bupropion 20 mg
Allergien: no
Vorherige Impfungen: -

VAERS 1995360

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: CT
Alter: 44,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue Headache Immunisation Pain Pain in extremity

Symptomtext

aches; Sore right arm; slight headache; fatigue; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 44 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 15Dec2021 16:45 (Lot number: FH8028) at the age of 44 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Acid reflux" (unspecified if ongoing); "seasonal allergies" (unspecified if ongoing), notes: seasonal/indoor allergies; "indoor allergies" (unspecified if ongoing), notes: seasonal/indoor allergies. Concomitant medication(s) included: IUD NOS; NEXIUM MUPS [ESOMEPRAZOLE MAGNESIUM]; PROBIOTICS NOS; ALLEGRA; B12 [CYANOCOBALAMIN]; FISH OIL; TURMERIC [CURCUMA LONGA RHIZOME]. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EP6955, Location of injection: Arm Right, Vaccine Administration Time: 02:00 PM), administration date: 30Mar2021, when the patient was 44 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL3247, Location of injection: Arm Right, Vaccine Administration Time: 02:00 PM), administration date: 09Mar2021, when the patient was 44 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 15Dec2021 16:45, outcome "unknown", described as "Booster"; PAIN (non-serious) with onset 16Dec2021 07:30, outcome "not recovered", described as "aches"; PAIN IN EXTREMITY (non-serious) with onset 16Dec2021 07:30, outcome "not recovered", described as "Sore right arm"; HEADACHE (non-serious) with onset 16Dec2021 07:30, outcome "not recovered", described as "slight headache"; FATIGUE (non-serious) with onset 16Dec2021 07:30, outcome "not recovered", described as "fatigue". Therapeutic measures were not taken as a result of pain, pain in extremity, headache, fatigue. Additional Information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine, was not diagnosed, Prior to vaccination and has the patient not been test, Since the vaccination for COVID-19. known allergies: No Follow-Up (21Dec2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Acid reflux (oesophageal); Allergy (seasonal/indoor allergies); Seasonal allergy (seasonal/indoor allergies)
Andere Medikamente: IUD NOS; NEXIUM MUPS [ESOMEPRAZOLE MAGNESIUM]; PROBIOTICS NOS; ALLEGRA; B12 [CYANOCOBALAMIN]; FISH OIL; TURMERIC [CURCUMA LONGA RHIZOME]
Allergien: -
Vorherige Impfungen: -

VAERS 1995307

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: SC
Alter: 69,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 03.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia Arthropathy Body height Body height abnormal Carpal tunnel syndrome Epicondylitis Immunisation Limb discomfort Muscle disorder Myalgia Nasal congestion Pain Sneezing

Symptomtext

Muscle and joint reaction in left arm that injection of the booster shot of the Pfizer Covid Vaccine was administered; Muscle and joint reaction in left arm that injection of the booster shot of the Pfizer Covid Vaccine was administered; This event was extremely painful; event as affecting her entire left arm; It was muscle and joint and it hurt.; It was muscle and joint and it hurt.; worst carpel tunnel; worst tennis elbow; Had a reaction to the booster; reporter seemed to sneeze and then mentioned it was stuffy in there; her height has changed; reporter seemed to sneeze and then mentioned it was stuffy in there; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program. The reporter is the patient. A 69 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 03Dec2021 15:00 (Lot number: FH8028) at the age of 69 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: PRISTIQ (ongoing); TYLENOL 8 HOUR; ZYRTEC [CETIRIZINE HYDROCHLORIDE] (ongoing); ZOLPIDEM (ongoing); VITAMINS NOS (ongoing). Vaccination history included: Bnt162b2 (First dose,, to left upper arm), administration date: 16Feb2021, when the patient was 68 years old, for COVID-19 Immunization, reaction(s): "No reactions with the first 2 doses of Pfizer Covid Vaccine"; Bnt162b2 (Second dose,, Lot: EN6204,, to left upper arm), administration date: 09Mar2021, when the patient was 68 years old, for COVID-19 Immunization, reaction(s): "No reactions with the first 2 doses of Pfizer Covid Vaccine". The following information was reported: IMMUNISATION (non-serious) with onset 03Dec2021 15:00, outcome "unknown", described as "Had a reaction to the booster"; MUSCLE DISORDER (non-serious), ARTHROPATHY (non-serious) all with onset 04Dec2021 15:00, outcome "recovered" (06Dec2021 15:00) and all described as "Muscle and joint reaction in left arm that injection of the booster shot of the Pfizer Covid Vaccine was administered"; PAIN (non-serious) with onset 04Dec2021 15:00, outcome "recovered" (06Dec2021 15:00), described as "This event was extremely painful"; SNEEZING (non-serious), NASAL CONGESTION (non-serious) all with onset Dec2021, outcome "unknown" and all described as "reporter seemed to sneeze and then mentioned it was stuffy in there"; LIMB DISCOMFORT (non-serious) with onset 04Dec2021 15:00, outcome "recovered" (06Dec2021 15:00), described as "event as affecting her entire left arm"; ARTHRALGIA (non-serious), MYALGIA (non-serious) all with onset 04Dec2021 15:00, outcome "recovered" (06Dec2021 15:00) and all described as "It was muscle and joint and it hurt."; CARPAL TUNNEL SYNDROME (non-serious) with onset 04Dec2021 15:00, outcome "recovered" (06Dec2021 15:00), described as "worst carpel tunnel"; EPICONDYLITIS (non-serious) with onset 04Dec2021 15:00, outcome "recovered" (06Dec2021 15:00), described as "worst tennis elbow"; BODY HEIGHT ABNORMAL (non-serious) with onset Dec2021, outcome "unknown", described as "her height has changed". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of muscle disorder, arthropathy, pain, limb discomfort, arthralgia, myalgia. Therapeutic measures were not taken as a result of sneezing, nasal congestion. Description of Product Complaint: Consumer was patient who reported adverse event with Pfizer Covid Vaccine. During that report provided details on concomitant product: Pristiq: When Lot/NDC/Expiry queried caller mentioned she could find bottle quickly because bottle has an odd shape; mentioned she dropped the bottle and the phone during report; She mentioned holding the bottle up to the light to look for Lot/NDC/Expiry information. She was unable to locate number on the Pfizer bottle of Pristiq despite numerous attempts to assist and probe to look at different areas on the label, and caller verified that there was no pharmacy sticker over the manufacturer label on the bottle; she could not see an number anywhere on the bottle or label, but mentioned that may be just her eyesight; she was able to provide the Pristiq Lot/Expiry: Lot: ER9476, Expiry: 31Aug2023, 100mg strength pills, 90 count bottle for 3 month supply. Additional information: Patient mentioned Pfizer makes good shots for the COVID. Patient stated she had a reaction to the booster; it only lasted a couple of days, but then she was fine. Patient had no reactions with the first 2 doses of Pfizer Covid Vaccine. Patient clarified that after the booster shot of the Pfizer Covid Vaccine was administered, she had muscle and joint reaction in left arm that injection of the booster shot of the Pfizer Covid Vaccine was administered. Onset time approximately 15:00, almost exactly 24 hours after administration of the booster shot of the Pfizer Covid Vaccine. She further described event as affecting her entire left arm, not just the injection site. It was muscle and joint and it hurt. It may just be a strong immune reaction on her part which if so, makes her happy. Patient got over it and she had no other reactions to the earlier shots. This event was extremely painful, but she took Skelaxin to treat event and event went away. Caller described her symptoms of this event to her primary doctor like the worst tennis elbow and worst carpel tunnel and everything in between that hurt like crazy. She recovered completely from event by about 15:00 on 06Dec2021, almost exactly 48 hours after event onset. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Name: height; Result Unstructured Data: Test Result:changed
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient History: No
Andere Medikamente: PRISTIQ; TYLENOL 8 HOUR; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; ZOLPIDEM; VITAMINS NOS
Allergien: -
Vorherige Impfungen: -

VAERS 1995259

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

mild

Staat: SC
Alter: 58,0
Geschlecht: M
Eingang: 31.12.2021
Impfdatum: 29.11.2021
Beginn: 02.12.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache

Symptomtext

a persistent head ache that will not go away with Tylenol or other headache meds; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. AA 58 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 29Nov2021 15:45 (Lot number: fh8028) at the age of 58 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Gurd" (unspecified if ongoing); "High cholesterol" (unspecified if ongoing); "known allergies: Peppers" (unspecified if ongoing), notes: known allergies: Peppers. The patient took concomitant medications. The following information was reported: HEADACHE (medically significant) with onset 02Dec2021, outcome "not recovered", described as "a persistent head ache that will not go away with Tylenol or other headache meds". Therapeutic measures were taken as a result of headache. Facility type Vaccine: Doctor's office/urgent care. No other vaccine in four weeks. Patient had a persistent head ache that will not go away with Tylenol or other headache meds. No Covid prior vaccination.Not Covid tested post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Gastroesophageal reflux disease; High cholesterol; Spice allergy (known allergies: Peppers)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1992527

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NH
Alter: 34,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Audiogram abnormal Deafness Disturbance in attention Ear pain Emotional distress Insomnia Tinnitus

Symptomtext

Sudden onset tinnitus (never had tinnitus before) within one day of vaccination, accompanied by intermittent inner ear pain. Following an audiogram and doctor's exam, doctor determined that cause of tinnitus and inner ear pain is unknown. Tinnitus and ear pain continue, without treatment, increasing in severity, leading to loss of sleep, inability to focus at work, unable to hear some sounds, severe distress.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: Audiogram and exam: Audiogram shows high frequency hearing loss (unexplained); exam did not uncover any explanation for tinnitus and ear pain.
Aktuelle Erkrankungen: -
Vorgeschichte: IBS-D
Andere Medikamente: Prenatal vitamin daily
Allergien: Augmentin (mild itchy rash)
Vorherige Impfungen: -

VAERS 1992225

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 13.11.2021
Beginn: 19.12.2021
Tage bis Beginn: 36,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Cough Fatigue Headache Pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I had congestive, coughing, body ache, headache, and fatigue. These symptoms lasted for about 7 or 8 days. I went to a urgent care facility to get a Covid-19 test, positive results.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Covid-19 test
Aktuelle Erkrankungen: Cold
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1989020

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NY
Alter: 33,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Abdominal pain Appendicectomy Appendicitis Back pain Blood test Chills Computerised tomogram abdomen abnormal Fatigue Pyrexia Urine analysis Vomiting

Symptomtext

The night of receiving the 2nd dose of COVID vaccine I have fever, chills, severe back and abdominal pain, and fatigue that lasted 24 hours. On the evening of 12/14 I started with severe abdominal pain and vomiting. On the morning of of 12/15, I reported to a HCF ER, where it was determined I had appendicitis and I was transported to another HCF for an emergency appendectomy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: 1,0
Labordaten: CT abdomen/pelvis, bloodwork, urine, APPENDECTOMY 12/15/2021
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: multivitamin
Allergien: NKDA
Vorherige Impfungen: Only the 1st dose of the pfizer vaccine, which was also reported.

VAERS 1989007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NY
Alter: 33,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 10.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: SC / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Ageusia Anosmia Chills Decreased appetite Fatigue Pyrexia SARS-CoV-2 test negative

Symptomtext

Loss of taste, smell, appetite. Fever, chills, fatigue. Symptoms lasted a total of 2 weeks, but most severe for 4 days. During this time, I had a negative PCR and rapid COVID test 1 week apart from each other.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: multivitamin
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1985196

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: ND
Alter: 37,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site mass Maternal exposure during breast feeding Suppressed lactation

Symptomtext

I experienced a loss of breast milk production. Before the vaccine my production was 16 oz a day, after the vaccine my production wasn't over 7 oz. When I went back for the booster on 12/23/2021 I lost the remainder of my breast milk production. Was not able to express any breast milk after the booster. I also have a hard lump at the injection site that has not gone away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site mass
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetic
Andere Medikamente: Metformin Milk Thistle Prenatal vitamins
Allergien: Allergic to metal and surgical steel
Vorherige Impfungen: -

VAERS 1984671

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: IL
Alter: 18,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 18.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness

Symptomtext

PATIENT LIGHTHEADED. PATIENT WAS LAID DOWN. MOTHER AT HER SIDE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: ANXIETY ATTACKS
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1982451

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: AZ
Alter: 52,0
Geschlecht: M
Eingang: 27.12.2021
Impfdatum: 04.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test Joint swelling Pain Peripheral swelling Rash Ultrasound scan

Symptomtext

Got rashes on thighs, legs, hands and waist line. Swollen ankles, feet, legs, knees, wrists, hands and forearms and elbows. Pain associated with swollen parts mentioned. Had been to ER a couple times. They did blood tests and Ultrasound to legs to find if there were blood clots. Blood tests were normal and no blood clots were found. Doctors prescribed Steroid medicine (Prednisone). I'm still on steroid medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Blood test and Ultrasound - 12/09/2021 Blood test and Ultrasound - 12/16/2021
Aktuelle Erkrankungen: Had a Shockwave Lithotripsy (ESWL) for kidney stone on 11/23/2021.
Vorgeschichte: High Cholesterol Hypothyroidism High Blood Pressure
Andere Medikamente: ALFUZOSIN HCL SYNTHROID CRESTOR DILTIAZEM
Allergien: None
Vorherige Impfungen: -

VAERS 1982052

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WA
Alter: 45,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 04.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Biopsy Erythema Feeling hot Hypersensitivity Inflammation Pruritus Pustule Rash Swelling face

Symptomtext

7 days post shot extreme facial swelling between eyes, forehead, nose, lips. Red postulates. Heat. Inflammation. itching. Most of this occurred on vascular malformation (port wine birth mark). Symptoms continued to escalate until treated with prednisone. Problems continue to persist. Continuing prednisone (60 mgs).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: biopsy - hypersensitive reaction/eruption. Possible covid antigen allergy (type 4)
Aktuelle Erkrankungen: none
Vorgeschichte: diverticulitis
Andere Medikamente: flonase Azelastine Cetirizine
Allergien: onions
Vorherige Impfungen: -

VAERS 1981842

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: OH
Alter: 34,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 20.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test Computerised tomogram head Dizziness Electrocardiogram Eye disorder Gait disturbance Vertigo Vomiting

Symptomtext

Dizziness started exactly 24hrs after booster. Dizziness progressed over the next 3-4hrs and turned into vertigo. 30hrs after vaccine I was unable to walk unassisted, open my eyes (due to vertigo) and was uncontrollably vomiting (due to vertigo). 31hrs after vaccine I went to the hospitals emergency room and received fluids and meds. I?m 1wk since my vaccine and still suffering from ongoing dizziness and vertigo. I visited my doctor today and they confirmed it was due to the covid booster I received on 12-20-21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: 12-23-21: CT scan of head. EKG. Bloodwork. All done at the hospital.
Aktuelle Erkrankungen: Covid on November 23rd.
Vorgeschichte: -
Andere Medikamente: Multi vitamin, probiotic, vitamin C, Zinc, vitamin D
Allergien: Cillins
Vorherige Impfungen: -

VAERS 1980721

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WA
Alter: 53,0
Geschlecht: F
Eingang: 25.12.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Axillary pain Immunisation Lymph node pain Plantar fasciitis

Symptomtext

painful axial lymph nodes on same side as injection; painful axial lymph nodes on same side as injection; plantar fasciitis flare up; booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 20Nov2021 12:30 (Lot number: FH8028) at the age of 53 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8737, Location of injection: Arm Left, Vaccine Administration Time: 09:30 AM), administration date: 03Apr2021, when the patient was 53 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6204, Location of injection: Arm Left, Vaccine Administration Time: 08:00 AM), administration date: 11Mar2021, when the patient was 53 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 20Nov2021 12:30, outcome "unknown", described as "booster"; LYMPH NODE PAIN (non-serious), AXILLARY PAIN (non-serious) all with onset 21Nov2021 20:00, outcome "not recovered" and all described as "painful axial lymph nodes on same side as injection"; PLANTAR FASCIITIS (non-serious) with onset 21Nov2021 20:00, outcome "not recovered", described as "plantar fasciitis flare up". Therapeutic measures were not taken as a result of lymph node pain, axillary pain, plantar fasciitis. Additional information: The most recent COVID-19 vaccine was administered in public health clinic/veterans administration facility. The patient had not received any other vaccine within 4 weeks prior to the covid vaccine. Patient had not been diagnosed with COVID-19 prior to vaccination and had not been tested since the vaccination. The patient had No known allergies. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1978745

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: OH
Alter: 52,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 26.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dysgeusia Eating disorder Gingival bleeding Glossodynia Hypersensitivity Immunisation Interchange of vaccine products Lip blister Off label use Oral mucosal blistering Pain Swelling Taste disorder Tongue blistering

Symptomtext

Hypersensitivity of mouth and taste; Hypersensitivity of mouth and taste; Eating is painful; Eating is painful; everything tastes salty; Gums are swollen and mild bleeding; Gums are swollen and mild bleeding; Tongue is painful to move; Blisters of inside lower lip, tongue and corners of the mouth; Blisters of inside lower lip, tongue and corners of the mouth; Blisters of inside lower lip, tongue and corners of the mouth; Dose 1: Moderna, Dose 2: Moderna; Dose 1: Moderna, Dose 2: Moderna; Booster; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 52 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 26Nov2021 18:00 (Lot number: FH8028) at the age of 52 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Essential tremor" (unspecified if ongoing), notes: other medical history: Essential tremor, hypothyroidism,, dm2, hyperlipidemia, obesity; "Hypothyroidism" (unspecified if ongoing), notes: other medical history: Essential tremor, hypothyroidism,, dm2, hyperlipidemia, obesity; "dm2" (unspecified if ongoing), notes: other medical history: Essential tremor, hypothyroidism,, dm2, hyperlipidemia, obesity; "Hyperlipidemia" (unspecified if ongoing), notes: other medical history: Essential tremor, hypothyroidism,, dm2, hyperlipidemia, obesity; "Obesity" (unspecified if ongoing), notes: other medical history: Essential tremor, hypothyroidism,, dm2, hyperlipidemia, obesity; "known allergies: Penicillin" (unspecified if ongoing), notes: known allergies: Penicillin, codeine. The patient's concomitant medications were not reported. Past drug history included: Codeine, reaction(s): "known allergies: codeine", notes: known allergies: Penicillin, codeine. Vaccination history included: Moderna (Dose number: 2, Prev dose product=COVID 19, prev dose brand=Moderna, prev dose brand unknown=False, prev dose lot number=004M20A, prev dose lot unknown=False, prev dose administration date=25Jan2021, prev dose administration time=12:00 PM, prev dose dose number=2), administration date: 25Jan2021, when the patient was 52 years old, for COVID-19 Immunization; Moderna (Dose number: 1, prev dose product=COVID 19, prev dose brand=Moderna, prev dose brand unknown=False, prev dose lot number=039K20A, prev dose lot unknown=False, prev dose administration date=28Dec2020, prev dose administration time=10:00 AM, prev dose dose number=1, prev dose vaccine location=Left arm), administration date: 28Dec2020, when the patient was 52 years old, for COVID-19 Immunization. The following information was reported: OFF LABEL USE (non-serious), INTERCHANGE OF VACCINE PRODUCTS (non-serious) all with onset 26Nov2021 18:00, outcome "unknown" and all described as "Dose 1: Moderna, Dose 2: Moderna"; IMMUNISATION (non-serious) with onset 26Nov2021 18:00, outcome "unknown", described as "Booster"; HYPERSENSITIVITY (non-serious), TASTE DISORDER (non-serious) all with onset 28Nov2021, outcome "not recovered" and all described as "Hypersensitivity of mouth and taste"; EATING DISORDER (non-serious), PAIN (non-serious) all with onset 28Nov2021, outcome "not recovered" and all described as "Eating is painful"; DYSGEUSIA (non-serious) with onset 28Nov2021, outcome "not recovered", described as "everything tastes salty"; SWELLING (non-serious), GINGIVAL BLEEDING (non-serious) all with onset 28Nov2021, outcome "not recovered" and all described as "Gums are swollen and mild bleeding"; GLOSSODYNIA (non-serious) with onset 28Nov2021, outcome "not recovered", described as "Tongue is painful to move"; LIP BLISTER (non-serious), TONGUE BLISTERING (non-serious), ORAL MUCOSAL BLISTERING (non-serious) all with onset 28Nov2021, outcome "not recovered" and all described as "Blisters of inside lower lip, tongue and corners of the mouth". Therapeutic measures were not taken as a result of hypersensitivity, taste disorder, eating disorder, pain, dysgeusia, swelling, gingival bleeding, glossodynia, lip blister, tongue blistering, oral mucosal blistering. Additional information: Patient has not taken any other vaccine in four weeks. The patient took prescription medication in two weeks. Patient reported the adverse event hypersensitivity of mouth and taste. Eating is painful and everything tastes salty. Gums are swollen and mild bleeding, especially when brushing teeth. Tongue is painful to move. Blisters of inside lower lip, tongue and corners of the mouth. All start 48 hours after booster dose and still lasting at 16 days afterwards. The patient has no covid prior to vaccination and patient has not tested covid post vaccination. Follow-up attempts are completed. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Essential tremor (other medical history: Essential tremor, hypothyroidism, dm2, hyperlipidemia, obesity); Hyperlipidemia (other medical history: Essential tremor, hypothyroidism, dm2, hyperlipidemia, obesity); Hypothyroidism (other medical history: Essential tremor, hypothyroidism, dm2, hyperlipidemia, obesity); Obesity (other medical history: Essential tremor, hypothyroidism, dm2, hyperlipidemia, obesity); Penicillin allergy (known allergies: Penicillin, codeine); Type 2 diabetes mellitus (other medical history: Essential tremor, hypothyroidism, dm2, hyperlipidemia, obesity)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1972255

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

mild

Staat: IA
Alter: 22,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Rash

Symptomtext

Patient called and reported a rash a couple of hours after receiving the Pfizer COVID vaccination. Patient had previously stated that she had no allergies. She also reported to not have a Primary Care Provider. Recommended to patient to take some Benadryl and if the reaction progressed/worsened to go to the ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: No know allergies
Vorherige Impfungen: -

VAERS 1972040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WA
Alter: 31,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 12.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Balance disorder Dizziness Exposure during pregnancy Headache Nausea Vertigo Vomiting

Symptomtext

Second vaccine Friday at 9:30 am, felt fine until I went to sleep. Vomited 24hrs after second dose from extreme dizziness and nausea. Dizziness (complete spins) when laying down or turning my head to the left to this current day. Headache in my lower brain cerebellum? area, and behind my eyes all day, for multiple weeks after second dose. Vertigo feelings and equilibrium feels off still to this current day. Fourth pregnancy. Estimated due date is January 22, 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Walk in clinic diagnosed vertigo November 18, 2021.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None. I stopped taking prenatal vitamins prior to first vaccine to ensure I wasn?t mixing anything or potentially causing any side effects.
Allergien: None.
Vorherige Impfungen: -

VAERS 1970708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: CA
Alter: 82,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 09.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cough Illness Immunisation Influenza like illness Pain in extremity Rhinorrhoea

Symptomtext

Have a lot of mucous from nostrils /developing mucous/runny nose; Sore arm; Booster dose; She says she didn't get a headache at any time, but she was coughing and had a runny nose and a lot of mucus in her chest; sick; Severe flu like symptoms; This is a spontaneous report received from contactable reporter(s) (Other HCP) from medical information team. The reporter is the patient. A 82 year-old female patient received bnt162b2 (COMIRNATY), administered in arm right, administration date 09Nov2021 (Lot number: FH8028) at the age of 82 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Flu" (unspecified if ongoing), notes: She did catch it before and developed mucus before.; "Mucus" (unspecified if ongoing), notes: She did catch it before and developed mucus before. Concomitant medication(s) included: FLU taken for immunisation, administration date Oct2021. Vaccination history included: Bnt162b2 (Dose 1, Lot number: EN6203, Anatomical location: Right arm), administration date: 11Mar2021, when the patient was 81 years old, for COVID-19 immunization, reaction(s): "Sore arm"; Bnt162b2 (Dose 2, Lot number: ER8737), administration date: 01Apr2021, when the patient was 82 years old, for COVID-19 immunization, reaction(s): "Sore arm". The following information was reported: IMMUNISATION (non-serious) with onset 09Nov2021, outcome "unknown", described as "Booster dose"; RHINORRHOEA (non-serious) with onset 20Nov2021, outcome "unknown", described as "Have a lot of mucous from nostrils /developing mucous/runny nose"; INFLUENZA LIKE ILLNESS (non-serious) with onset Nov2021, outcome "unknown", described as "Severe flu like symptoms"; PAIN IN EXTREMITY (non-serious) with onset 09Nov2021, outcome "unknown", described as "Sore arm"; COUGH (non-serious) with onset Nov2021, outcome "unknown", described as "She says she didn't get a headache at any time, but she was coughing and had a runny nose and a lot of mucus in her chest"; ILLNESS (non-serious) with onset Nov2021, outcome "recovered" (2021), described as "sick". Therapeutic measures were taken as a result of rhinorrhoea, influenza like illness, cough, illness. Therapeutic measures were not taken as a result of pain in extremity. Additional information: The patient didn't have any underlying conditions like most people who have heart problems or diabetes, nothing like that. The patient takes her flu shot every year between Sep and Oct, which she already had. She caught flu like symptoms. The patient got sick and she was just now getting over being sick and she was just now feeling better. The patient had been getting a lot of mucus from her nostrils and couldn't figure out what was going on. She said she didn't know if that was one of the side effects or if the booster dose was more stronger. She said she never experienced real severe side effects like she had with the booster, so she was wondering if it was stronger than the first two that she took. She clarified for all three it hurt but not long maybe about three days each time. She was having a lot of mucus so she got some Mucinex which helped loosen up the mucus in her chest area, but it was not that effective as she thought it would be. She said she did catch it before and developed mucus before but it was not severe like with the booster. She got her flu shot back in October. She never had the mucus like that before except when she had the flu, which she doesn't have often because she always takes the flu shot before flu season between September and October.. She asked if the booster dose was a lot stronger than the other 2 shots that she took. She received the response stating that the Comirnaty or Pfizer-BioNTech COVID-19 Vaccine booster dose is the same Comirnaty or Pfizer-BioNTech COVID-19 Vaccine that was used for the primary series of Comirnaty or Pfizer-BioNTech COVID-19 Vaccine. These may not be all the possible side effects of the vaccine. Serious and unexpected side effects may occur. The possible side effects of the vaccine are still being studied in clinical trials. 1. There was a Product complaint. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Flu (She did catch it before and developed mucus before.); Mucus discharge (She did catch it before and developed mucus before.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1909705

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: ND
Alter: 34,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Bone pain Burning sensation Loss of personal independence in daily activities Myalgia Immunisation Movement disorder Vaccination site pain Pain

Symptomtext

have had excruciating pain and tenderness at the injection site; have had excruciating pain and tenderness at the injection site; I could not lift/move my arm; booster; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 34 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 19Nov2021 08:30 (Lot number: FH8028) at the age of 34 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Anxiety" (unspecified if ongoing); "occasional migraines" (unspecified if ongoing), notes: other medical history: occasional migraines; "Shellfish" (unspecified if ongoing), notes: known allergies: Shellfish. Concomitant medication(s) included: PHENTERMINE; XANAX; ZOFRAN [ONDANSETRON]; SUMATRIPTAN. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EH9899, Location of injection: Arm Left), administration date: 18Dec2020, when the patient was 33 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EL1284, Location of injection: Arm Left, Vaccine Administration Time: 10:45 AM), administration date: 08Jan2021, when the patient was 33 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 19Nov2021 08:30, outcome "unknown", described as "booster"; VACCINATION SITE PAIN (non-serious), VACCINATION SITE PAIN (non-serious) all with onset 19Nov2021 09:00, outcome "not recovered" and all described as "have had excruciating pain and tenderness at the injection site"; MOVEMENT DISORDER (non-serious) with onset 19Nov2021 09:00, outcome "not recovered", described as "I could not lift/move my arm". The events "have had excruciating pain and tenderness at the injection site", "have had excruciating pain and tenderness at the injection site" and "i could not lift/move my arm" were evaluated at the physician office visit. Therapeutic measures were taken as a result of vaccination site pain, vaccination site pain, movement disorder. Additional information: The patient has not received any other vaccines within 4 weeks prior to the COVID vaccine. Since about 30 minutes after receiving my Covid booster shot. As the day went on the pain became unbearable and to the point that I could not lift/move my arm. I went to the walk in clinic the follow day and was told it was probably a reacation to the vaccine, was put in a sling, given anti-inflamatories, put on light duty work and was told to follow up with my employee health doctor if things didnt get better. On 30Nov2021 (11 days later) I went to my employee health doctor as things still have not gotten better, he also told me it was a reaction to the booster and has put me on steriods, I will see him back on 10Dec2021, I continue to be on lifting restrictions. AE treatment- sling, medication, lifting restrictions. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Migraine (other medical history: occasional migraines); Shellfish allergy (known allergies: Shellfish)
Andere Medikamente: PHENTERMINE; XANAX; ZOFRAN [ONDANSETRON]; SUMATRIPTAN
Allergien: -
Vorherige Impfungen: -

VAERS 1909705

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: ND
Alter: 34,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Bone pain Burning sensation Loss of personal independence in daily activities Myalgia Immunisation Movement disorder Vaccination site pain Pain

Symptomtext

have had excruciating pain and tenderness at the injection site; have had excruciating pain and tenderness at the injection site; I could not lift/move my arm; booster; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 34 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 19Nov2021 08:30 (Lot number: FH8028) at the age of 34 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Anxiety" (unspecified if ongoing); "occasional migraines" (unspecified if ongoing), notes: other medical history: occasional migraines; "Shellfish" (unspecified if ongoing), notes: known allergies: Shellfish. Concomitant medication(s) included: PHENTERMINE; XANAX; ZOFRAN [ONDANSETRON]; SUMATRIPTAN. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EH9899, Location of injection: Arm Left), administration date: 18Dec2020, when the patient was 33 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EL1284, Location of injection: Arm Left, Vaccine Administration Time: 10:45 AM), administration date: 08Jan2021, when the patient was 33 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 19Nov2021 08:30, outcome "unknown", described as "booster"; VACCINATION SITE PAIN (non-serious), VACCINATION SITE PAIN (non-serious) all with onset 19Nov2021 09:00, outcome "not recovered" and all described as "have had excruciating pain and tenderness at the injection site"; MOVEMENT DISORDER (non-serious) with onset 19Nov2021 09:00, outcome "not recovered", described as "I could not lift/move my arm". The events "have had excruciating pain and tenderness at the injection site", "have had excruciating pain and tenderness at the injection site" and "i could not lift/move my arm" were evaluated at the physician office visit. Therapeutic measures were taken as a result of vaccination site pain, vaccination site pain, movement disorder. Additional information: The patient has not received any other vaccines within 4 weeks prior to the COVID vaccine. Since about 30 minutes after receiving my Covid booster shot. As the day went on the pain became unbearable and to the point that I could not lift/move my arm. I went to the walk in clinic the follow day and was told it was probably a reacation to the vaccine, was put in a sling, given anti-inflamatories, put on light duty work and was told to follow up with my employee health doctor if things didnt get better. On 30Nov2021 (11 days later) I went to my employee health doctor as things still have not gotten better, he also told me it was a reaction to the booster and has put me on steriods, I will see him back on 10Dec2021, I continue to be on lifting restrictions. AE treatment- sling, medication, lifting restrictions. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Migraine (other medical history: occasional migraines); Shellfish allergy (known allergies: Shellfish)
Andere Medikamente: PHENTERMINE; XANAX; ZOFRAN [ONDANSETRON]; SUMATRIPTAN
Allergien: -
Vorherige Impfungen: -

VAERS 1968656

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge F?H8028

mild

Staat: -
Alter: 60,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 05.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Pain Pyrexia

Symptomtext

Chills, fever, and body aches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None. Bed rest.
Aktuelle Erkrankungen: No
Vorgeschichte: Diabetes, High blood pressure, high cholesterol, and chronic kidney disease.
Andere Medikamente: All my normal Rx, over the counter meds, supplements that I take every day include: Metformin, Lisinopril, Fenofibrate, Pravastatin, Fluoxotine, Vitamin D3, Cranberry pills, and Estroven Complete.
Allergien: None known.
Vorherige Impfungen: -

VAERS 1968645

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NY
Alter: 38,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 17.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Eye pain Intraocular pressure test normal Pain Photophobia Scleral oedema Scleritis Sleep disorder Ultrasound eye abnormal Uveitis Visual acuity tests normal

Symptomtext

Approximately one week post vaccination I began to feel a dull pain behind both eyes but primarily behind my left eye. This pain very slowly increased over the course of a week and one week in to symptoms I began feeling a sharp pain with eye movement. This lead me to see my ophthalmologist (now three weeks after vaccine) After normal visual acuity and ocular pressure tests, and also noting my sensitivity to lights, he said I either had uveitis or scleritis and knowing that my symptoms had not improved with regular NSAIDS he prescribed oral prednisone. I saw him again one week later (4 weeks post vaccine) and my symptoms had not notably improved and the pain was even waking me from sleep. With an ultrasound imaging machine he documented fluid/inflammation in my posterior sclera bilaterally and prescribed continued prednisone. Over the next week pain on movement resolved but there is still severe pain behind my eyes and I still have intense light sensitivity. I am awaiting my next follow up (five weeks post vaccine).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: Probably best to consult Dr.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, poly cystic ovarian syndrome, bipolar disorder
Andere Medikamente: Lithium, venlafaxine, vyvanse, levothyroxine, l-methyl folate, metformin, azelastine, melatonin, multi vitamin, iron, vitamin D, omeprazole, dulera
Allergien: None known
Vorherige Impfungen: -

VAERS 1966893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: PA
Alter: 36,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal discomfort Chills Decreased appetite Dizziness Fatigue Feeling cold Immunisation Lymphadenopathy Nausea Nervousness Night sweats Pain Pyrexia

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP) from Regulatory Authority sponsored program (159558). The reporter is the patient. A 36-year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 22Nov2021 (Lot number: FH8028) at the age of 36 years as dose 3 (booster), single for covid-19 immunization. Relevant medical history included: "anxiety" (ongoing), notes: medical Anxiety. Concomitant medication(s) included: RISPERDAL taken for anxiety (ongoing). Vaccination history included: Bnt162b2 (DOSE 1, Lot: EL9261, Expiry: Unknown), administration date: 27Jan2021, when the patient was 35 years old, for Covid-19 immunization; Bnt162b2 (DOSE 2, Lot: EN5318, Expiry: Unknown), administration date: 17Feb2021, when the patient was 35 years old, for Covid-19 immunization; Tetanus, administration date: May2021. The following information was reported: IMMUNISATION (non-serious) with onset 22Nov2021, outcome "unknown", described as "booster dose"; FATIGUE (non-serious) with onset 24Nov2021, outcome "unknown", described as "fatigue"; LYMPHADENOPATHY (non-serious) with onset 23Nov2021, outcome "unknown", described as "swollen lymph nodes"; NIGHT SWEATS (non-serious) with onset 23Nov2021, outcome "unknown", described as "night sweats"; ABDOMINAL DISCOMFORT (non-serious) with onset 24Nov2021, outcome "unknown", described as "stomach is queasy and unsettled"; PYREXIA (non-serious) with onset 22Nov2021, outcome "recovered" (2021), described as "fever"; PAIN (non-serious) with onset 22Nov2021, outcome "recovered" (2021), described as "body aches"; DIZZINESS (non-serious) with onset 24Nov2021, outcome "unknown", described as "dizziness"; FEELING COLD (non-serious) with onset 25Nov2021, outcome "unknown", described as "very cold at times"; NERVOUSNESS (non-serious) with onset 25Nov2021, outcome "unknown", described as "shaky"; CHILLS (non-serious) with onset 25Nov2021, outcome "unknown", described as "shivers"; DECREASED APPETITE (non-serious) with onset 24Nov2021, outcome "unknown", described as "lack of appetite"; NAUSEA (non-serious) with onset 30Nov2021, outcome "unknown", described as "pretty nauseous". The event "swollen lymph nodes" was evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: pyrexia: (22Nov2021) 99.7 degrees. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20211122; Test Name: Fever; Result Unstructured Data: Test Result:99.7 degrees
Aktuelle Erkrankungen: Anxiety (medical Anxiety)
Vorgeschichte: -
Andere Medikamente: RISPERDAL
Allergien: -
Vorherige Impfungen: -

VAERS 1963860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WY
Alter: 59,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 16.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Headache Injection site erythema Injection site induration Injection site warmth

Symptomtext

Pt said she noticed a red mark on her arm on 1218/21. She did not feel ill except she had a "headache." 12/20/21 area on Right arm at the deltoid site measures 6 cm long by 7 cm wide. There is an induration in reddened area measures 2 cm Long by 4 cm wide. area is warm to the touch and red. Pt said it was much worse on 12/18/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: none
Andere Medikamente: Vitamins complete 2 a day. Zoloft 125 mg once a day. Vitamin D 3 1 time a day Cranberry 500 mcg 1 time a day Vitamin C 250 mcg 1 time a day.
Allergien: Iodine, shellfish, and contrast dye.
Vorherige Impfungen: -

VAERS 1961560

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MO
Alter: 69,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia Chills Diarrhoea Fatigue Immunisation Pyrexia Vomiting

Symptomtext

Weak; Tired; booster; Fever after booster; Diarrhea, chronic, after booster/ The caller thought her diarrhea was improving until this morning; Chills after booster; Vomiting after booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 69 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 08Nov2021 09:00 (Lot number: FH8028) at the age of 69 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose 1, single ), for COVID-19 immunization; Bnt162b2 (Dose 2, single, ), for Covid-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 08Nov2021 09:00, outcome "unknown", described as "booster"; VOMITING (non-serious) with onset 2021, outcome "recovered" (2021), described as "Vomiting after booster"; PYREXIA (non-serious) with onset 08Nov2021, outcome "recovered" (2021), described as "Fever after booster"; DIARRHOEA (non-serious) with onset 08Nov2021, outcome "recovered" (2021), described as "Diarrhea, chronic, after booster/ The caller thought her diarrhea was improving until this morning"; CHILLS (non-serious) with onset 08Nov2021, outcome "recovered" (2021), described as "Chills after booster"; ASTHENIA (non-serious) with onset 09Nov2021, outcome "recovered" (2021), described as "Weak"; FATIGUE (non-serious) with onset 09Nov2021, outcome "recovered" (2021), described as "Tired". The events "vomiting after booster", "fever after booster", "diarrhea, chronic, after booster/ the caller thought her diarrhea was improving until this morning" and "chills after booster" were evaluated at the physician office visit. Therapeutic measures were taken as a result of vomiting, diarrhoea. Additional Information: The patient stated after first two shots didn't have any reactions. There was no Product Complaint. The patient did not require Emergency Room or Physician Office visit for any adverse events. Patient had no Prior Vaccinations within 4 weeks. Patient had no adverse events prior vaccinations. Patient had no family medical history relevant to adverse events. Patient had no relevant tests. Patient stated she has a side effect that she has not reported and wants to know if this has been reported by others as well. Patient said she had very long term diarrhea which started the night she got the Comirnaty booster shot and along with this are other side effects such as vomiting, chills, and fever. Patient mentioned those all went away except the diarrhea which has been going on for 3 weeks now. The caller knows this is from the vaccine and no one else in her family had intestinal stuff go on. Finally last week the caller was able to reach her fill in doctor, they recommended her to take some things for it on the 24Nov2021 she started. The caller started on Imodium, flora stora probiotic, naproxen in case it had to do with inflammation of that area. The caller did this and by Saturday morning she had what she thought was her last episode. The caller stopped taking Imodium and was fine for the rest of the day night and the next day. This morning the diarrhea came back and the caller called the Imodium helpline and said she could go back on it. The caller thought that between having no episodes and when she went today it was something that looked familiar, a regular looking bowel movement and then some loose stuff. Then half an hour later it was water. The caller took Imodium this morning and hasn't had any issues since but who knows. This is worrying the caller because she knows it can be a side effect of the vaccine. The caller thought her diarrhea was improving until this morning but she wouldn't considered it worsened. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1959201

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 36,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 15.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Axillary mass Chills Fatigue Injection site pain Pain Tenderness

Symptomtext

Chills, aches, joint pain, tender lump in left axilla, injection site pain, fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Strep throat, other GI/cold virus
Vorgeschichte: -
Andere Medikamente: Multivitamin, ProBiotic, Cymbalta, Lorazepam
Allergien: Sulfa drugs, azithromycin, cherries
Vorherige Impfungen: -

VAERS 1959000

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 04.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Headache Hypertensive urgency Vertigo

Symptomtext

Developed severe headache and hypertensive urgency, resulted in ER visit and having ongoing vertifgo in the aftermath of the event now on 12/17/2021 - we are ordering MRI, suspect possible CVA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: pending
Aktuelle Erkrankungen: none
Vorgeschichte: migraine, GERD , Hashimoto's, insomnia, lumbar spondylosis
Andere Medikamente: misoprostol, bupropion HCl, trazodone, propranolol, PANTOPRAZO
Allergien: flexeril
Vorherige Impfungen: -

VAERS 1955732

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8028

mild

Staat: FL
Alter: 57,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 01.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Erythema Headache Induration Lymphadenopathy Nausea Pain Peripheral swelling Pyrexia Skin warm

Symptomtext

Fever chills headache nausea body aches for 72 hours. Swollen lymph nodes and red hot hard swollen arm still ongoing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroid,hypo parathyroid
Andere Medikamente: Rocaltrol,synthroid, calcium,magnesium,atorvastaten,triamterene
Allergien: Codeine
Vorherige Impfungen: Flu shot and previous second dose of Covid

VAERS 1954893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: GA
Alter: 14,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue Headache Product administered to patient of inappropriate age Pyrexia Somnolence

Symptomtext

I inadvertently ordered vaccine in this 14 year old. Not currently approved under 16 years for booster dose. He had been extremely tired for 3 days after adminisstration. Developed fever too 100.6 the day after administration. He has persistent grogginess and global headache, described much like he felt during his Long COVID. The second night after administration he awoke from sleep speaking gibberish per his Dad and he also had no recall to what he had just said.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Aware of none
Vorgeschichte: History of Long Covid in first half year of 2021, ADHD, small intestinal bacterial overgrowth, anxiety regarding health
Andere Medikamente: Bentyl, escitalopram, riboflavin, magnesium
Allergien: None
Vorherige Impfungen: -

VAERS 1954480

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: IL
Alter: 33,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 03.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Abdominal pain Dizziness Dyschezia Exposure during pregnancy Feeling hot Human chorionic gonadotropin increased Internal haemorrhage Laparoscopy Mass excision Nausea Ovarian mass Pregnancy test positive Ultrasound abdomen abnormal Ultrasound foetal Vomiting

Symptomtext

On 11/5/21 around 8 pm I went to bed and had severe abdominal cramping. I tried to defecate, and after 10 minutes of trying I felt too warm, nauseous and dizzy so I layed on the bathroom floor. After vomiting twice the pain was bearable so I went to bed. In the morning (11/6/21) I took a home pregnancy test (positive result) and scheduled a visit with my PCP's office. He felt my abdomen and recommended that I go to an emergency room. The emergency department did an ultrasound and consulted with OBGYN. The abdomen had free fluid (internal bleeding) and the ovary had a mass that could have been an ectopic pregnancy or a cyst. OBGYN did a diagnostic laparoscopy and removed the mass, excess blood, and stopped the internal bleeding. Over the next few days they monitored my hCG levels. A day after the hCG level doubled, they did an ultrasounds and detected a yolk sac. A week later they detected a fetal pole and heartbeat. My estimated due date is July 10 2022. On 11/5 I was approximately 4 weeks and 5 days pregnant.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: 1,0
Labordaten: hCG levels measured 11/6 (4,000 mIU/mL), 11/7 (5,000), 11/9 (13,000); ultrasounds 11/6, 11/10, 11/17.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Daily prenatal vitamin (Nature Made brand)
Allergien: Bee venom
Vorherige Impfungen: vasovagal response 5 days after second dose of Pfizer COVID vaccine, but could have been caused by work stress.

VAERS 1948299

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: FL
Alter: 71,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 26.10.2021
Beginn: 12.11.2021
Tage bis Beginn: 17,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Feeling abnormal Herpes zoster Nasopharyngitis Neuralgia Pain Pain in extremity Polyarteritis nodosa Skin lesion

Symptomtext

I was not feeling good after the shot. Nothing specific. Then the cold hit around 11/12/2021. I was not feeling good. I felt run down. It was a nasty cold that did not want to go away. I do not know if it has anything to do with the vaccine. I am pro-vaccine. 11/19/2021- that is when the pain started in my left shoulder and arm. The burning and firing pain. It was 2 days later when the lesions started breaking out. 11/30/2021 and 12/07/2021 I went to the doctor. The doctor diagnosed it as shingles. I talked to the nurse during the week trying to control the pain. The nerve pain that it causes is the most excruciating pain and its all the way from the center of my neck, it wraps around the left side from my spine to the center of my chest. I had lesions are on my fingertips. It feels like my fingernails are going to come off. The worse pain radiates from the shoulder. The pain is called PAN. The doctor increased the gabapentin and added the carbamazepine 200 mg twice a day and increased the dosage on hydrocodone. I would not say that it was the shot. It is just the incidental things that have happened since the 3rd dose of Pfizer. As of today, 12/14/2021- I am still under the care of a doctor for the pain of the shingles. The lesions are healing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 11/03/2021 routine visit with the cancer specialist
Aktuelle Erkrankungen: No
Vorgeschichte: Remission for Metastatic Breast Cancer and Hodgkin's Lymphoma
Andere Medikamente: B12 Supplement; Calcium; Baby Aspirin; Xanax; Fluoxetine; Gabapentin; Letrozole; Omeprazole; Rosuvastatin; Loratadine
Allergien: Flu shot - can't take it last one was 09/2016; Cephalosporin; Neosporin; Adhesive and Surgical Glues
Vorherige Impfungen: Flu shot - can't take it last one was 09/2016, flared up arm that lasted for 3 weeks.

VAERS 1947827

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NY
Alter: 48,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 01.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Rash Rash erythematous Rash pruritic

Symptomtext

I woke up to a rash on both arms. It was itchy, red and flared up when I scratched it. I took Benadryl at night and hydrocortisone and Benadryl itch cream in the evening. It went away in about 3 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: iron pills, vitamin D
Allergien: no
Vorherige Impfungen: -

VAERS 1947094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: -
Geschlecht: M
Eingang: 14.12.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Breast pain Burning sensation Hypersensitivity Injection site mass Pruritus Swelling

Symptomtext

I am having allergic reactions; I am itchy like allergic reaction in different parts of my body; I am having allergic reactions; I am itchy like allergic reaction in different parts of my body; I have a lump under my left armpit. I have a lump and it hurts, it is swelled up; I have a lump under my left armpit. I have a lump and it hurts, it is swelled up; My breast hurts as soon I received the dosage around my breast, around my areola it was burning, it burned a lot; My breast hurts as soon I received the dosage around my breast, around my areola it was burning, it burned a lot; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). A male patient received bnt162b2 (BNT162B2) (Lot number: FH8028) as dose number unknown, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: HYPERSENSITIVITY (non-serious), PRURITUS (non-serious), outcome "unknown" and all described as "I am having allergic reactions; I am itchy like allergic reaction in different parts of my body"; INJECTION SITE MASS (non-serious), SWELLING (non-serious), outcome "unknown" and all described as "I have a lump under my left armpit. I have a lump and it hurts, it is swelled up"; BREAST PAIN (non-serious), BURNING SENSATION (non-serious), outcome "unknown" and all described as "My breast hurts as soon I received the dosage around my breast, around my areola it was burning, it burned a lot". No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Breast pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1947093

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: -
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 19.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Axillary pain Breast pain Burning sensation Hypersensitivity Immunisation Mass Pain Pruritus Swelling

Symptomtext

Booster; My breast hurts as soon I received the dosage around my breast, around my areola it was burning, it burned a lot; My breast hurts as soon I received the dosage around my breast, around my areola it was burning, it burned a lot; I got this block but I did touch it but now I have seen it but it hurts me; I have a lump under my left armpit. I have a lump and it hurts, it is swelled up; I am having allergic reactions; I am itchy like allergic reaction in different parts of my body; I am having allergic reactions; I am itchy like allergic reaction in different parts of my body; I have a lump under my left armpit. I have a lump and it hurts, it is swelled up; I have a lump under my left armpit. I have a lump and it hurts, it is swelled up; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A female patient received bnt162b2 (BNT162B2), administration date 19Nov2021 (Lot number: FH8028) as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (1st Dose), for COVID-19 Immunization; Bnt162b2 (2nd Dose), for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 19Nov2021, outcome "unknown", described as "Booster"; HYPERSENSITIVITY (non-serious), PRURITUS (non-serious) all with onset Nov2021, outcome "unknown" and all described as "I am having allergic reactions; I am itchy like allergic reaction in different parts of my body"; MASS (non-serious), AXILLARY PAIN (non-serious), SWELLING (non-serious) all with onset Nov2021, outcome "unknown" and all described as "I have a lump under my left armpit. I have a lump and it hurts, it is swelled up"; BREAST PAIN (non-serious), BURNING SENSATION (non-serious) all with onset 19Nov2021, outcome "unknown" and all described as "My breast hurts as soon I received the dosage around my breast, around my areola it was burning, it burned a lot"; PAIN (non-serious) with onset 19Nov2021, outcome "unknown", described as "I got this block but I did touch it but now I have seen it but it hurts me". No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1947003

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: AZ
Alter: 47,0
Geschlecht: M
Eingang: 14.12.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Axillary pain Lymphadenopathy Mass Pain in extremity

Symptomtext

swollen lymph; lump and it is painful; lump and it is painful; pain in arm pit; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 47 year-old male patient received bnt162b2 (COMIRNATY), administered in arm right, administration date 08Nov2021 (Lot number: FH8028) at the age of 47 years as dose 2, single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose: 1, Lot Number: FF2590, Route, Anatomical Location: left arm), administration date: 16Oct2021, when the patient was 47 years old, for COVID-19 Immunisation. The following information was reported: AXILLARY PAIN (non-serious) with onset 08Nov2021, outcome "not recovered", described as "pain in arm pit"; LYMPHADENOPATHY (non-serious) with onset 09Nov2021, outcome "not recovered", described as "swollen lymph"; MASS (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 09Nov2021, outcome "not recovered" and all described as "lump and it is painful". No follow-up attempts are possible. No further information is expected. Follow-Up (15Nov2021): Follow-up attempts are completed. No further information is expected. Additional information: Time the Vaccination Was Given: between 2PM and 3PM.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1946648

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WA
Alter: -
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Autoimmune disorder Blood test Erythema Insomnia Investigation Immunisation Pain in extremity Peripheral swelling Limb discomfort Vaccination site pain Vaccination site warmth Rash Tenderness

Symptomtext

have swelling in her arm that is painful, tender and with heat; have swelling in her arm that is painful, tender and with heat/arm hurts, painful; redness; her cheeks are red even when she is not putting makeup and that may be a rash; her cheeks are red even when she is not putting makeup and that may be a rash; heat and tenderness; pain at the site; difficulty sleeping; heat and tenderness; receiving her booster dose; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 69 year-old female patient received bnt162b2 (COMIRNATY), administered in arm left, administration date Nov2021 (Lot number: FH8028) as dose number unknown (booster) 0.3 ml, single for covid-19 immunisation. Relevant medical history included: "Autoimmune issues" (unspecified if ongoing), notes: Autoimmune issues; "Stroke" (unspecified if ongoing); "Cholesterol" (unspecified if ongoing); "Blood pressure" (unspecified if ongoing). Concomitant medication(s) included: LISINOPRIL taken for blood pressure abnormal (ongoing); AMLODIPINE taken for blood pressure abnormal (ongoing); EZETIMIBE taken for blood cholesterol abnormal (ongoing). Vaccination history included: Johnson & johnson covid vaccine (Caller's first dose was the Johnson & Johnson Covid Vaccine , 0.5ml . , Date 17Mar2021 , Lot-1805022 , Exp- Did not see to provide), administration date: 17Mar2021, when the patient was 68 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset Nov2021, outcome "unknown", described as "receiving her booster dose"; PERIPHERAL SWELLING (non-serious), outcome "recovering", described as "have swelling in her arm that is painful, tender and with heat"; PAIN IN EXTREMITY (non-serious), outcome "recovering", described as "have swelling in her arm that is painful, tender and with heat/arm hurts, painful"; ERYTHEMA (non-serious), outcome "recovering", described as "redness"; ERYTHEMA (non-serious), RASH (non-serious), outcome "unknown" and all described as "her cheeks are red even when she is not putting makeup and that may be a rash"; TENDERNESS (non-serious), VACCINATION SITE WARMTH (non-serious), outcome "recovering" and all described as "heat and tenderness"; VACCINATION SITE PAIN (non-serious), outcome "recovering", described as "pain at the site"; INSOMNIA (non-serious), outcome "unknown", described as "difficulty sleeping". Additional Information: Caller was a consumer who reported that after receiving her booster dose of the Pfizer Biontech COVID19 vaccine, she still have swelling in her arm that is painful, tender and with heat, it was also swollen and there was redness. It has been 5 days already when she got the booster shot. Caller wants to know if these are normal and if she should go see a doctor about it. Caller also said that her cheeks are red even when she was not putting makeup and that may be a rash. She also mentioned about two medications that she missed to give with the DSU agent, which were progesterone and low dose naltrexone. She was having a reaction that she was not concerned about initially, but now she was more so. She was doing better, but even 5 days later she was having these events. Her arm was not huge, but she was having swelling that she would consider as moderate. Her arm hurts, painful, and it was causing difficulty sleeping, but she slept great last night. She was having pain at the site, heat, and tenderness. Her arm was swollen, and red. She confirmed this was on her left arm. Had reaction to the other one, clarified as the Johnson & Johnson Covid Vaccine. She did not know if related to the vaccine, but she had a problem with her leg. They thought she had a blood clot, but she had testing done and never found a blood clot. Later she was diagnosed with autoimmune disorder. However, she was having some blood work done even before she had the Covid Vaccine, so she cannot say this was definitely from the vaccine. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Autoimmune disorder (Autoimmune issues); Blood cholesterol abnormal; Blood pressure abnormal; Stroke
Andere Medikamente: LISINOPRIL; AMLODIPINE; EZETIMIBE
Allergien: -
Vorherige Impfungen: -

VAERS 1946648

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WA
Alter: -
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Autoimmune disorder Blood test Erythema Insomnia Investigation Immunisation Pain in extremity Peripheral swelling Limb discomfort Vaccination site pain Vaccination site warmth Rash Tenderness

Symptomtext

have swelling in her arm that is painful, tender and with heat; have swelling in her arm that is painful, tender and with heat/arm hurts, painful; redness; her cheeks are red even when she is not putting makeup and that may be a rash; her cheeks are red even when she is not putting makeup and that may be a rash; heat and tenderness; pain at the site; difficulty sleeping; heat and tenderness; receiving her booster dose; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 69 year-old female patient received bnt162b2 (COMIRNATY), administered in arm left, administration date Nov2021 (Lot number: FH8028) as dose number unknown (booster) 0.3 ml, single for covid-19 immunisation. Relevant medical history included: "Autoimmune issues" (unspecified if ongoing), notes: Autoimmune issues; "Stroke" (unspecified if ongoing); "Cholesterol" (unspecified if ongoing); "Blood pressure" (unspecified if ongoing). Concomitant medication(s) included: LISINOPRIL taken for blood pressure abnormal (ongoing); AMLODIPINE taken for blood pressure abnormal (ongoing); EZETIMIBE taken for blood cholesterol abnormal (ongoing). Vaccination history included: Johnson & johnson covid vaccine (Caller's first dose was the Johnson & Johnson Covid Vaccine , 0.5ml . , Date 17Mar2021 , Lot-1805022 , Exp- Did not see to provide), administration date: 17Mar2021, when the patient was 68 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset Nov2021, outcome "unknown", described as "receiving her booster dose"; PERIPHERAL SWELLING (non-serious), outcome "recovering", described as "have swelling in her arm that is painful, tender and with heat"; PAIN IN EXTREMITY (non-serious), outcome "recovering", described as "have swelling in her arm that is painful, tender and with heat/arm hurts, painful"; ERYTHEMA (non-serious), outcome "recovering", described as "redness"; ERYTHEMA (non-serious), RASH (non-serious), outcome "unknown" and all described as "her cheeks are red even when she is not putting makeup and that may be a rash"; TENDERNESS (non-serious), VACCINATION SITE WARMTH (non-serious), outcome "recovering" and all described as "heat and tenderness"; VACCINATION SITE PAIN (non-serious), outcome "recovering", described as "pain at the site"; INSOMNIA (non-serious), outcome "unknown", described as "difficulty sleeping". Additional Information: Caller was a consumer who reported that after receiving her booster dose of the Pfizer Biontech COVID19 vaccine, she still have swelling in her arm that is painful, tender and with heat, it was also swollen and there was redness. It has been 5 days already when she got the booster shot. Caller wants to know if these are normal and if she should go see a doctor about it. Caller also said that her cheeks are red even when she was not putting makeup and that may be a rash. She also mentioned about two medications that she missed to give with the DSU agent, which were progesterone and low dose naltrexone. She was having a reaction that she was not concerned about initially, but now she was more so. She was doing better, but even 5 days later she was having these events. Her arm was not huge, but she was having swelling that she would consider as moderate. Her arm hurts, painful, and it was causing difficulty sleeping, but she slept great last night. She was having pain at the site, heat, and tenderness. Her arm was swollen, and red. She confirmed this was on her left arm. Had reaction to the other one, clarified as the Johnson & Johnson Covid Vaccine. She did not know if related to the vaccine, but she had a problem with her leg. They thought she had a blood clot, but she had testing done and never found a blood clot. Later she was diagnosed with autoimmune disorder. However, she was having some blood work done even before she had the Covid Vaccine, so she cannot say this was definitely from the vaccine. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Autoimmune disorder (Autoimmune issues); Blood cholesterol abnormal; Blood pressure abnormal; Stroke
Andere Medikamente: LISINOPRIL; AMLODIPINE; EZETIMIBE
Allergien: -
Vorherige Impfungen: -

VAERS 1905512

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

mild

Staat: MI
Alter: 57,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 27.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Erythema Lip swelling Swelling face Swollen tongue Urticaria

Symptomtext

Bright red spot, there like a hive; I have got bright red spots; I have got them on my arms, I got 1 on my leg, I have got them on my chest and my shoulders.; Bright red spot, there like a hive; I have got bright red spots; I have got them on my arms, I got 1 on my leg, I have got them on my chest and my shoulders. This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 57 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 27Nov2021 (Lot number: FH8028) at the age of 57 years as dose 1, single for covid-19 immunisation; influenza vaccine (INFLUENZA VACCINE), administration date 20Nov2021 (Batch/Lot number: unknown) as unk, single for immunisation. Relevant medical history included: "Asthma" (unspecified if ongoing), notes: Verbatim: Asthma; "Thyroid" (unspecified if ongoing), notes: Verbatim: Thyroid. Concomitant medication(s) included: ARNUITY ELLIPTA taken for asthma; LEVOTHYROXINE taken for thyroid disorder. The following information was reported: ERYTHEMA (non-serious), URTICARIA (non-serious) all with onset 27Nov2021, outcome "unknown" and all described as "Bright red spot, there like a hive; I have got bright red spots; I have got them on my arms, I got 1 on my leg, I have got them on my chest and my shoulders.". Therapeutic measures were not taken as a result of erythema, urticaria. Follow-Up (30Nov2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma (Verbatim: Asthma); Thyroid disorder (Verbatim: Thyroid).
Andere Medikamente: ARNUITY ELLIPTA; LEVOTHYROXINE.
Allergien: -
Vorherige Impfungen: -

VAERS 1944381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8028

mild

Staat: GA
Alter: 60,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 08.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Oedema Rash Scratch

Symptomtext

leg rash, edema. scratches

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: breast cancer
Andere Medikamente: atorvastatin, omeprazole, aspirin, magnesium,
Allergien: codeine
Vorherige Impfungen: -

VAERS 1944164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WI
Alter: 38,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 08.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Rash

Symptomtext

The client's sister-in-law reported that she developed a rash (generalized, raised, erythematous) on December 12, 2021 (four days after getting the second dosage of her COVID-19 vaccine series). The client sought medical care and received a prescription for Prednisone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1943425

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WA
Alter: 28,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 11.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Axillary pain Breast pain Headache Lethargy Oropharyngeal pain Pain Pyrexia Tenderness

Symptomtext

About seven hours after the third vaccine that I received as a booster, I had a severe headache especially on my left temple, and generally felt lethargic and my whole body was hurting. This got worse the next morning when I woke up and felt feverish, with a throat ache and terrible headache. This subsided by the end of the second day. On the third day that I am filling this form (12/13/2021) my left armpit and breast are really tender and sore.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1942358

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WA
Alter: 79,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 26.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Immediate post-injection reaction Injection site erythema Injection site pain Injection site pruritus

Symptomtext

Upper right arm was achy sore immediately after injection on 11/26/29. Morning of 11/27/29 arm still was achy and the area of the injection site was painful to touch pressure. The area of the injection site was intermittently mild itchy. I iced my upper arm one time for 10 minutes. By the morning of 11/28/2021, my upper arm was less achy, but the injection site was mildly painful to touch pressure; my skin was faintly pink in the area of the injection and was still intermittently itchy. I put some Jergens lotion on the itchy area. In the morning of 11/29/2021, the injection site was less painful to touch pressure; my arm had a more noticeable pink area about 2-1/2 inches in diameter around the injection area and was more itchy. Thinking this was similar to an allergy, I took 1/2 of an over the counter Benadryl tablet (1/2 x 15 mg = 12.5 mg). Alarmed that the area had become more pink at the upper edge of the pink area, I called a pharmacy and talked with a pharmacist who suggested applying over the counter 1% cortisone cream. In the afternoon and at bedtime of 11/29/2021, I took 12.5 Benadryl, and applied the 1% cortisone cream. In the morning of 11/30 21, the area was less pink and less itchy. I applied the 1% cortisone cream in the morning and at bedtime, and took 12.5 mg Benadryl in the morning, mid-day and at bedtime. In the morning of 12/1/2021, the pinkness and itchiness were gone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoporosis; osteopenia; monoclonoal gammapothy of undetermined significance
Andere Medikamente: Fosamax 70 mg once weekly, Centrum Silver, Align
Allergien: Sulfa, sulfa-derived, aureomycin, sucralose, cortsone, crab, - Aleve [Naproxen Sodium] Affects heart rate - Allegra [Fexofenadine] Stuffy ears - Chlorpheniramine maleate Dizziness, vertigo - Erythromycin (all forms) GI nausea - Loratidine 30 mg Irregular heartbeat - Nasacort [Triamcinolone Acetonide] GI upset - Percocet [Oxycodone-Acetaminophen] Nausea - Pravastatin Muscle pain - Prevacid [Lansoprazole] GI - Prilosec [Omeprazole] GI - Pseudoephedrine Insomia - Seldane Rapid heartbeat, irregular heartbeat - Skin Tissue Adhesive Irritation, red rash - Tequin [Gatifloxacin] Nausea, GI - Vicodin [Hydrocodone-Acetaminophen] GI pain
Vorherige Impfungen: -

VAERS 1942215

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: IL
Alter: 50,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 04.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia Chills Erythema Fatigue Feeling abnormal Headache Pain Pain in extremity Peripheral swelling Pyrexia Skin warm Type III immune complex mediated reaction

Symptomtext

Developed body aches and joint pain 12/4/2021 around 6 pm, no fever presented at this time. Left arm was slightly sore with no redness or swelling. On 12/5/2021 at 12:45 am, I woke up with a fever of 101, body aches, joint pain, chills, headache and soreness in left arm. Took ibuprofen to help relieve symptoms. Continued to take ibuprofen as needed. On 12/5/2021, I was very tired, continued having body aches, joint pain, chills and headache. My arm also began to turn red and swell. Symptoms were slightly relieved with ibuprofen, however, they would return quickly once the medication wore off. On 12/6/2021 around 4 am, I awoke with a fever of 102. This was the highest temperature that I had. I continued to use ibuprofen to relieve symptoms. When I awoke on 12/7/2021 and still felt miserable, I contacted my Doctor's office. I was advised that I should come in to be seen. Dr. is the doctor who treated me. He started me on an antibiotic for my arm as it was red, hot to touch and swollen. He diagnosed me with having a arthus reaction to the Covid-19 vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: pulled muscle in back
Vorgeschichte: aortic insufficiency environmental allergies
Andere Medikamente: atorvastatin montelukast flonase zyrtec B-complex multivitamin tazoratene (topical)
Allergien: minocycline chantix
Vorherige Impfungen: -

VAERS 1941920

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: CA
Alter: 42,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 29.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Breast tenderness Immunisation Swelling Vaccination site pain

Symptomtext

she is experiencing swelling; Tenderness in the left armpit and breast area; normal site pain; booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 42 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 29Nov2021 (Lot number: FH8028) at the age of 42 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Arthritis" (unspecified if ongoing), notes: she got arthritis early. In her mid thirties; "Torn rotator cuff" (unspecified if ongoing), notes: she has a torn rotator cuff. Concomitant medication(s) included: DULOXETINE (ongoing). Vaccination history included: Bnt162b2 (Dose: 1, Lot number: ER8734.), administration date: 02Apr2021, when the patient was 42 years old, for COVID-19 immunization; Bnt162b2 (Dose: 2, Lot number: EN5318), administration date: 23Apr2021, when the patient was 42 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 29Nov2021, outcome "unknown", described as "booster"; SWELLING (non-serious) with onset 01Dec2021, outcome "unknown", described as "she is experiencing swelling"; BREAST TENDERNESS (non-serious) with onset 01Dec2021, outcome "unknown", described as "Tenderness in the left armpit and breast area"; VACCINATION SITE PAIN (non-serious) with onset 29Nov2021, outcome "unknown", described as "normal site pain". Therapeutic measures were taken as a result of swelling, breast tenderness, vaccination site pain. Additional information: She is calling about Pfizer BioNTech vaccine. She just got her six month booster. She got Pfizer BioNTech for the first two in the series six months ago. Has Pfizer heard this from anyone else. Her left arm where the breast tissue extends up into the armpit is swollen and tender there. There is a lot of lymphatic drainage in that area. That is what she is experiencing. She is wondering if anyone else has reported that. The site pain began several hours after vaccination. Caller clarified that she is having swelling and tenderness in the armpit and breast area on left side. If it was the other side she wouldn't be calling. Outcome of Event: She just noticed as she was getting in the shower. She looked in the mirror and it is definitely swollen. The first times it was given at Withheld and she had the same nurse both times. Caller thought it was done, but she was not 100 percent positive. She knew they notate it in their system. This time online it asked her preference. She picked the left arm to hurt this time. The first was six months ago, so she was not 100 percent sure which arm it was given in. The nurse this time put it in caller's arm much more gently. The pain in her arm was way less than the first time. This nurse didn't jam it in there and didn't cause trauma. The difference between the first two times is caller didn't ice the arm. This time she iced the arm. She iced it twice the same night as the vaccine. The next day she put a Salonpas patch on it so she wouldn't feel it and so it would go numb. That is the difference for what she did to relieve the discomfort. She has used Salonpas patches multiple times on her neck and shoulder before because. Caller states she doesn't have any allergic issue with Salonpas, so she doesn't think it was that thing. Caller stated she was going to get an appointment incase this was a breast issue. No Emergency Room or Physician Office visit. Caller believed it was an "H". They didn't put the line all the way down for the H and it looks like a plus sign. Expiry: Unknown. two days later, she has tenderness. Her left arm where the breast tissue extends up into the armpit is swollen and tender there. This time she iced the arm. She iced it twice the same night as the vaccine. The next day she put a Salonpas patch on it so she wouldn't feel it and so it would go numb. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis (she got arthritis early, In her mid thirties); Rotator cuff tear (she has a torn rotator cuff).
Andere Medikamente: DULOXETINE
Allergien: -
Vorherige Impfungen: -

VAERS 1941889

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: CT
Alter: 53,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Diarrhoea Dizziness Immunisation SARS-CoV-2 test

Symptomtext

Dizziness; watery diarrhea; Booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 22Nov2021 18:00 (Lot number: FH8028) at the age of 53 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Graves Disease" (unspecified if ongoing). Concomitant medication(s) included: METHIMAZOLE. Past drug history included: Cipeo, reaction(s): "Known allergies". Vaccination history included: Bnt162b2 (Dose number: 1, Brand: Pfizer, Lot number: ER8733, Administration time: 03:00 PM, location: Right arm), administration date: 26Mar2021, when the patient was 52 years old, for COVID-19 Immunization; Bnt162b2 (Dose number: 2, Brand: Pfizer, Lot number: EW0162, Administration time: 05:00 PM, location: Right arm), administration date: 16Apr2021, when the patient was 53 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 22Nov2021 18:00, outcome "unknown", described as "Booster"; DIARRHOEA (non-serious) with onset 23Nov2021 18:00, outcome "recovering", described as "watery diarrhea"; DIZZINESS (non-serious) with onset 24Nov2021, outcome "recovering", described as "Dizziness". The events "watery diarrhea" and "dizziness" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of diarrhoea, dizziness. Additional Information: Dizziness developed after two days. Severe explosive frequent watery diarrhea beginning 24 hours after the shot. Bright yellow complete liquid diarrhea. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Test Date: 20211123; Test Name: Binax Nasal swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Graves' disease
Andere Medikamente: METHIMAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 1941852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NY
Alter: 38,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Immunisation Myalgia Pain Pain in extremity Vaccination site pain

Symptomtext

Pain at injection site; Sore arm; Slight body aches; muscle aches; Chills; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 38 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 16Nov2021 13:30 (Lot number: FH8028) at the age of 38 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Migraines" (unspecified if ongoing); "Known allergies: Penicillin" (unspecified if ongoing), notes: Known allergies: Penicillin; "Known allergies: Many fruits" (unspecified if ongoing), notes: Known allergies: Many fruits (e.g., apples, pears, cherries). Concomitant medication(s) included: ALPRAZOLAM; SUMATRIPTAN. Vaccination history included: Bnt162b2 (Dose number: 1, Prev dose Product: COVID 19, Prev dose Brand: Pfizer-BioNTech, Prev dose Lot number: EL3248, Prev dose Administration date: 03Mar2021, Prev dose administrator route: Intramuscular), administration date: 03Mar2021, when the patient was 38 years old, for COVID-19 Immunization; Bnt162b2 (Dose number: 2, Prev dose Product: COVID 19, Prev dose Brand: Pfizer-BioNTech, Prev dose Lot number: EL3248, Prev dose Administration date: 23Mar2021, Prev dose administrator route: Intramuscular), administration date: 23Mar2021, when the patient was 38 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 16Nov2021, outcome "unknown", described as "Booster"; VACCINATION SITE PAIN (non-serious) with onset 17Nov2021 05:00, outcome "recovered" (18Nov2021), described as "Pain at injection site"; PAIN IN EXTREMITY (non-serious) with onset 17Nov2021 05:00, outcome "recovered" (18Nov2021), described as "Sore arm"; PAIN (non-serious) with onset 17Nov2021 05:00, outcome "recovering", described as "Slight body aches"; MYALGIA (non-serious) with onset 17Nov2021, outcome "recovered" (18Nov2021), described as "muscle aches"; CHILLS (non-serious) with onset 17Nov2021, outcome "recovered" (18Nov2021), described as "Chills". Therapeutic measures were not taken as a result of vaccination site pain, pain in extremity, pain, myalgia, chills. Additional information: Patient had no illness at time of vaccination. Facility where the most recent COVID-19 vaccine was administered: Pharmacy or Drug Store. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient did not diagnose with COVID-19 and since the vaccination, patient had not been tested for COVID-19. The events did not result in hospitalization or any other seriousness criteria. Morning after receiving shot, wake up with the reported events, they lasted about 1 day and then fully recovered. No longing effects. No relevant tests were performed with respect to the events. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fruit allergy (Known allergies: Many fruits (e.g., apples, pears, cherries)); Migraine; Penicillin allergy (Known allergies: Penicillin)
Andere Medikamente: ALPRAZOLAM; SUMATRIPTAN
Allergien: -
Vorherige Impfungen: -

VAERS 1940221

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: FL
Alter: 34,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue

Symptomtext

12 /10/2021 at 12:00 pm the patient was feeling tired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: NO
Andere Medikamente: Prozac
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1939932

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NY
Alter: 45,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 09.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache Lymph node pain Lymphadenopathy Malaise

Symptomtext

Left axillary lymphadenopathy with tenderness and swelling, headache, malaise

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic daily migraine, history of Cerebral AVM, gamma knife surgery, inflammatory dowel disease, GERD, spondylosis
Andere Medikamente: Omeprazole, Citalopram, Loryna, Promethazine, Tizanidine, Clonazepam
Allergien: Penicillins, Reglan
Vorherige Impfungen: Age 44, 3/25/21, 2nd dose Covid mRNA vaccine

VAERS 1939667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NE
Alter: 64,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Extra dose administered Headache Influenza like illness Pyrexia Rash Urinary incontinence

Symptomtext

Pt. states that after receiving the 3rd dose of Phizer 12/07/2021, started experiencing symptoms that evening of fever (100.9), chills, headache, flu-like symptoms, incontinence (urine), and rash (left calf-area) painful. Symptoms lasting 72hrs, no noted Primary visit/communications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes
Andere Medikamente: Metropalol, Glipazide, Janvia, Aspirin, Cyclobenzaprine, Tramadol, Escitalopram, Tamsulosim, Gabapentin, Magnesium, Loratadine
Allergien: Lipitor
Vorherige Impfungen: -

VAERS 1938742

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: CO
Alter: 62,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 24.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Axillary pain Breast pain Chills Fatigue Immunisation Neck pain Pain in extremity Pyrexia

Symptomtext

Fever 102 all nigh and the next day; Severe arm pain; under arm pain; breast pain; neck pain; chills; tired; booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 62 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 24Nov2021 18:00 (Lot number: FH8028) at the age of 62 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "NO" (unspecified if ongoing). There were no concomitant medications. Past drug history included: Fish oil, reaction(s): "Allergy". Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6204, Location of injection: Arm Left, Vaccine Administration Time: 16:15), administration date: 16Mar2021, when the patient was 62 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8733, Location of injection: Arm Left, Vaccine Administration Time: 16:15), administration date: 06Apr2021, when the patient was 62 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 24Nov2021 18:00, outcome "unknown", described as "booster"; PYREXIA (non-serious) with onset 24Nov2021 23:00, outcome "not recovered", described as "Fever 102 all nigh and the next day"; PAIN IN EXTREMITY (non-serious) with onset 24Nov2021 23:00, outcome "not recovered", described as "Severe arm pain"; AXILLARY PAIN (non-serious) with onset 24Nov2021 23:00, outcome "not recovered", described as "under arm pain"; BREAST PAIN (non-serious) with onset 24Nov2021 23:00, outcome "not recovered", described as "breast pain"; NECK PAIN (non-serious) with onset 24Nov2021 23:00, outcome "not recovered", described as "neck pain"; CHILLS (non-serious) with onset 24Nov2021 23:00, outcome "not recovered", described as "chills"; FATIGUE (non-serious) with onset 24Nov2021 23:00, outcome "not recovered", described as "tired". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pyrexia, pain in extremity, axillary pain, breast pain, neck pain, chills, fatigue. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: Test Date: 20211124; Test Name: fever; Result Unstructured Data: Test Result:102
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: NO
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1938688

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: WI
Alter: 54,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 12.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Dizziness Feeling abnormal Headache Immunisation Nausea Retching Vomiting

Symptomtext

On monday she started feeling light headed, felt like drinking 12 cups of coffee/Light-headed/she is really lightheaded all the time now/felt light headed it is like drank 10 pots of coffee; chills; bad headache; dry heaving, about 8 to 10 times; clarified the booster dose as for the Pfizer BioNTech Covid 19 Vaccine; she is having brain fog; felt like she wanted to vomit; nauseated; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 54 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 12Nov2021 13:00 (Lot number: FH8028) at the age of 54 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Chronic headache" (unspecified if ongoing), notes: Additional Information for Other Conditions: Has had the last 20-30 years; "migraine" (unspecified if ongoing), notes: Additional Information for Other Conditions: Has had the last 20-30 years. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number:01, Lot Number: EW0162, Dosage text: administered in left arm in muscle, Sore arm on 11Apr2021, it lasted maybe 24 hours, Outcome: Recovered), administration date: 10Apr2021, when the patient was 53 years old, for covid-19 Immunization, reaction(s): "sore arm"; Bnt162b2 (Dose Number:02, Lot Number: EW0172, Sore arm on 02May2021, it lasted maybe 24 hours, outcome: recovered), administration date: 01May2021, when the patient was 53 years old, for covid-19 Immunization, reaction(s): "sore arm"; Flu shot (Lot number: Unknown), administration date: 22Oct2021; Shingles shot (Felt bad after getting the shingles shot. It was after the second shot. This was three years ago.), reaction(s): "Felt bad", "Felt like had 24 hour flu with it.". The following information was reported: IMMUNISATION (non-serious) with onset 12Nov2021 13:00, outcome "unknown", described as "clarified the booster dose as for the Pfizer BioNTech Covid 19 Vaccine"; CHILLS (non-serious) with onset 13Nov2021, outcome "recovered" (13Nov2021), described as "chills"; HEADACHE (non-serious) with onset 13Nov2021, outcome "recovered" (13Nov2021), described as "bad headache"; VOMITING (non-serious) with onset Nov2021, outcome "unknown", described as "felt like she wanted to vomit"; DIZZINESS (non-serious) with onset 15Nov2021, outcome "not recovered", described as "On monday she started feeling light headed, felt like drinking 12 cups of coffee/Light-headed/she is really lightheaded all the time now/felt light headed it is like drank 10 pots of coffee"; NAUSEA (non-serious) with onset Nov2021, outcome "unknown", described as "nauseated"; RETCHING (non-serious) with onset 13Nov2021, outcome "recovered" (13Nov2021), described as "dry heaving, about 8 to 10 times"; FEELING ABNORMAL (non-serious) with onset Nov2021, outcome "unknown", described as "she is having brain fog". Therapeutic measures were taken as a result of headache. Additional information: Caller is consumer who received the Pfizer booster dose on 12Nov2021 around 1 in the afternoon then 12 hours she got chills and then about 6 Oclock in the morning she got bad headache then felt like she wanted to vomit. Still this lightheadedness is still being experienced up to now. She wants to know if this is something she is going to have for the rest of her life or is it temporary. The chills ended about the time when she had started dry heaving, around 6:00 AM. She would say that the chills lasted maybe 6 hours altogether. The dry heaving probably lasted about 10 to 15 minutes. She was told not to take aspirin if she happened to get a headache so she tried taking Tylenol and it did no good so she went with Excedrin and some headache powders, good's,and that's what finally helped. It was at about 3:00 that afternoon when she was feeling better with the headache. She confirmed that she recovered completely on 13Nov2021. That's when all that basically stopped but the light headedness came about on Monday, she didn't notice it on Saturday or Sunday. She says that Tylenol never works on her headaches, but the lady who gave her the shot said to try that for the headache if she were to get one. She is a production worker. she has an appointment this upcoming Friday to see the doctor regarding the light-headedness because she still feels like crap. She then added, she feels like she got something old in regard to the booster vaccine. Indication: Has a 90-year-old mom at home and a brother at home with heart issues. She works with a bunch of people not vaccinated. She wanted to do her part in getting vaccinated so does not bring any-thing home. Additional Vaccines Administered on Same Date of the Pfizer Suspect: None. Emergency Room: No. Physician Office: Has not gone yet. Has an appointment scheduled for Friday. Relevant Tests: None. At end of call, caller commented she hopes the light headedness will go away. Its dragging her down, making her feel down. She feels like she will have this the rest of her life. History/ Investigations: No, she doesn't believe there is anything else causing this light headedness other than the vaccine because as far as her heart goes, her doctor told her a few months ago that she had a heart like a 20-year-old. No follow-up attempts possible. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Chronic headaches (Additional Information for Other Conditions: Has had the last 20-30 years); Migraine (Additional Information for Other Conditions: Has had the last 20-30 years)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1909822

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: AZ
Alter: 43,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Headache Immunisation Pain Pain in extremity No adverse event Product preparation issue Poor quality product administered Product preparation error

Symptomtext

body aches; Chills; Headache; sore arm; Booster shot; booster shot was mixed with sterile water instead of normal saline; booster shot was mixed with sterile water instead of normal saline:The caller was really surprised to be called yesterday and told that the vaccine wasn't active; This is a spontaneous report received from contactable reporter(s) (Other HCP) from medical information team for a Pfizer sponsored program (159558). The reporter is the patient. A 43-year-old female patient received bnt162b2 (BNT162B2), administered in deltoid right, administration date 19Nov2021 (Lot number: FH8028) at the age of 43 years as dose 3 (booster), single for covid-19 immunization. Relevant medical history included: "COVID-19" (unspecified if ongoing), notes: she actually had COVID before and this day was worse than COVID. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose:1, Vaccine Name: First dose of the Pfizer COVID-19 vaccine , Lot Number / Expiry Date: EL0142/ unknown, She has a sticker on her vaccine record card and it only has the Lot number and where it was given , Route, Anatomical Location:Unknown, she believes the first dose was in her left deltoid), administration date: 12Jan2021, when the patient was 43 years old, for COVID-19 Immunization; Bnt162b2 (Dose:2, Vaccine Name: Second dose of the Pfizer COVID-19 Vaccine, Lot Number / Expiry Date: EL9264/ unknown , Route, Anatomical Location: Unknown, she believes it was in her right deltoid), administration date: 03Feb2021, when the patient was 43 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 19Nov2021, outcome "unknown", described as "Booster shot"; PRODUCT PREPARATION ERROR (non-serious) with onset 19Nov2021, outcome "unknown", described as "booster shot was mixed with sterile water instead of normal saline/they mistakenly used sterile water for injection instead of sterile sodium chloride as the diluent and that she needs to get the shot again."; POOR QUALITY PRODUCT ADMINISTERED (non-serious) with onset 19Nov2021, outcome "unknown", described as "booster shot was mixed with sterile water instead of normal saline: The caller was really surprised to be called yesterday and told that the vaccine wasn't active"; PAIN (non-serious) with onset 20Nov2021, outcome "recovered" (20Nov2021), described as "body aches"; CHILLS (non-serious) with onset 20Nov2021, outcome "recovered" (20Nov2021), described as "Chills"; HEADACHE (non-serious) with onset 20Nov2021, outcome "recovered" (20Nov2021), described as "Headache"; PAIN IN EXTREMITY (non-serious) with onset 20Nov2021, outcome "recovered" (20Nov2021), described as "sore arm". Additional information: NDC number of Pfizer COVID-19 vaccine was reported as Unknown, Expiry Date of Pfizer COVID-19 vaccine was reported as Unknown. Other Products was reported as No, Patient History was reported as No, Investigation Assessment was reported as No. The patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. The caller clarified she had her booster shot done at withheld last Friday, 19Nov2021. She got a call that day that it was mixed with sterile water, and it needed to be mixed with normal saline. She guessed the diluents activates the ingredients. However, she did had side effects after the shot, so she was worried about going and doing that again, but she wanted to be protected.She confirmed that she had the following side effects: body aches, chills, headache, sore arm. She confirmed she only had these side effects just on Saturday, 20Nov2021. She recovered completely from them. This was her third shot. She mentioned she actually had COVID before and this day was worse than COVID. The caller was really surprised to be called yesterday and told that the vaccine was not active, and she would need to go and do it again. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (she actually had COVID before and this day was worse than COVID.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1909822

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: AZ
Alter: 43,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Headache Immunisation Pain Pain in extremity No adverse event Product preparation issue Poor quality product administered Product preparation error

Symptomtext

body aches; Chills; Headache; sore arm; Booster shot; booster shot was mixed with sterile water instead of normal saline; booster shot was mixed with sterile water instead of normal saline:The caller was really surprised to be called yesterday and told that the vaccine wasn't active; This is a spontaneous report received from contactable reporter(s) (Other HCP) from medical information team for a Pfizer sponsored program (159558). The reporter is the patient. A 43-year-old female patient received bnt162b2 (BNT162B2), administered in deltoid right, administration date 19Nov2021 (Lot number: FH8028) at the age of 43 years as dose 3 (booster), single for covid-19 immunization. Relevant medical history included: "COVID-19" (unspecified if ongoing), notes: she actually had COVID before and this day was worse than COVID. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose:1, Vaccine Name: First dose of the Pfizer COVID-19 vaccine , Lot Number / Expiry Date: EL0142/ unknown, She has a sticker on her vaccine record card and it only has the Lot number and where it was given , Route, Anatomical Location:Unknown, she believes the first dose was in her left deltoid), administration date: 12Jan2021, when the patient was 43 years old, for COVID-19 Immunization; Bnt162b2 (Dose:2, Vaccine Name: Second dose of the Pfizer COVID-19 Vaccine, Lot Number / Expiry Date: EL9264/ unknown , Route, Anatomical Location: Unknown, she believes it was in her right deltoid), administration date: 03Feb2021, when the patient was 43 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 19Nov2021, outcome "unknown", described as "Booster shot"; PRODUCT PREPARATION ERROR (non-serious) with onset 19Nov2021, outcome "unknown", described as "booster shot was mixed with sterile water instead of normal saline/they mistakenly used sterile water for injection instead of sterile sodium chloride as the diluent and that she needs to get the shot again."; POOR QUALITY PRODUCT ADMINISTERED (non-serious) with onset 19Nov2021, outcome "unknown", described as "booster shot was mixed with sterile water instead of normal saline: The caller was really surprised to be called yesterday and told that the vaccine wasn't active"; PAIN (non-serious) with onset 20Nov2021, outcome "recovered" (20Nov2021), described as "body aches"; CHILLS (non-serious) with onset 20Nov2021, outcome "recovered" (20Nov2021), described as "Chills"; HEADACHE (non-serious) with onset 20Nov2021, outcome "recovered" (20Nov2021), described as "Headache"; PAIN IN EXTREMITY (non-serious) with onset 20Nov2021, outcome "recovered" (20Nov2021), described as "sore arm". Additional information: NDC number of Pfizer COVID-19 vaccine was reported as Unknown, Expiry Date of Pfizer COVID-19 vaccine was reported as Unknown. Other Products was reported as No, Patient History was reported as No, Investigation Assessment was reported as No. The patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. The caller clarified she had her booster shot done at withheld last Friday, 19Nov2021. She got a call that day that it was mixed with sterile water, and it needed to be mixed with normal saline. She guessed the diluents activates the ingredients. However, she did had side effects after the shot, so she was worried about going and doing that again, but she wanted to be protected.She confirmed that she had the following side effects: body aches, chills, headache, sore arm. She confirmed she only had these side effects just on Saturday, 20Nov2021. She recovered completely from them. This was her third shot. She mentioned she actually had COVID before and this day was worse than COVID. The caller was really surprised to be called yesterday and told that the vaccine was not active, and she would need to go and do it again. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (she actually had COVID before and this day was worse than COVID.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1937011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8028

mild

Staat: OH
Alter: 31,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 12.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 14,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Chillblains Dizziness Injection site erythema Musculoskeletal stiffness

Symptomtext

Dizziness developed 5 mins after shots 1 and 2 and continues for approximately 15 minutes. Pain and stiffness in shoulder for 3 days following shot. Redness at injection site. Chilblains/perniosis developed within 8 days and continued for 2+ weeks after 2nd injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetic Type 1
Andere Medikamente: Humalog Insulin
Allergien: None known
Vorherige Impfungen: -

VAERS 1935108

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: NC
Alter: 56,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 14.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Immunisation Influenza like illness Pain in extremity Pruritus Rash erythematous

Symptomtext

raised red rash; itchy; Vax 2 - Normal (flu-type) symptoms; sore to touch; location same arm as injection; Vax 3 - Normal (flu-type) symptoms; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 56-year-old female patient (not pregnant) received bnt162b2 (COMIRNATY), administered in arm left, administration date 14Nov2021 11:45 (Lot number: FH8028) at the age of 56 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "High Blood Pressure" (unspecified if ongoing). Concomitant medication(s) included: METOPROLOL SUCCINATE; AMLODIPINE BESILATE. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8736, Location of injection: Arm Left, Vaccine Administration Time: 10:00 AM), administration date: 22Apr2021, when the patient was 55 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EP7533, Location of injection: Arm Left, Vaccine Administration Time: 10:00 AM), administration date: 01Apr2021, when the patient was 55 years old, for COVID-19 Immunization, reaction(s): "Normal (flu-type) symptoms". The following information was reported: IMMUNISATION (non-serious) with onset 14Nov2021 11:45, outcome "unknown", described as "Vax 3 - Normal (flu-type) symptoms"; RASH ERYTHEMATOUS (non-serious) with onset 17Nov2021 16:00, outcome "not recovered", described as "raised red rash"; PRURITUS (non-serious) with onset 17Nov2021 16:00, outcome "not recovered", described as "itchy"; INFLUENZA LIKE ILLNESS (non-serious) with onset 17Nov2021 16:00, outcome "not recovered", described as "Vax 2 - Normal (flu-type) symptoms"; PAIN IN EXTREMITY (non-serious) with onset 17Nov2021 16:00, outcome "not recovered", described as "sore to touch; location same arm as injection". Therapeutic measures were not taken as a result of rash erythematous, pruritus, influenza like illness, pain in extremity. Additional Information: Patient covid prior vaccination was unknown. Covid tested post vaccination and known allergies was no. Device Date: 19Nov2021. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high
Andere Medikamente: METOPROLOL SUCCINATE; AMLODIPINE BESILATE
Allergien: -
Vorherige Impfungen: -

VAERS 1935078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: CA
Alter: 46,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal pain upper Arthralgia Body temperature Chills Decreased appetite Fatigue Headache Hyperhidrosis Immunisation Lymph node pain Myalgia Nausea Pyrexia Vaccination site pain

Symptomtext

This is a spontaneous report from a non-contactable consumer, the patient. A 46-year-old non-pregnant female patient received the third dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FH8028, solution for injection) via an unspecified route of administration in the left arm on 11Nov2021 at 18:00 (at the age of 46-years-old) as DOSE 3 (BOOSTER), SINGLE for COVID-19 immunisation. Medical history included iron deficiency and had known allergies to penicillin. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Concomitant medications received within two weeks of vaccination included FOCUS FACTOR at 2x/week, VITAMIN D3, and NUTRILITE at 2x/week, all taken for unknown indications from an unknown date and unknown if ongoing. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8737) via an unspecified route of administration in the left arm on 04Apr2021 at 17:00 (at the age of 46-years-old) as dose 1, single and also received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0170) via an unspecified route of administration in the left arm on 25Apr2021 at 11:00 (at the age of 46-years-old) as a dose 2, single for COVID-19 immunisation. On 11Nov2021 at 18:00, immediately after injection, the patient had pain at injection site. On 12Nov2021 at 03:00, after 9 hours (all side effects started around the same time), the patient experienced chills, fever (38 centigrade), sweating, pain in lymph nodes (left arm pit), fatigue, nausea, muscles and joints pain, light headache, and loss of appetite. After about 80 hours almost all above side effects diminished except for sweating and lymph node pain in the left arm pit. On 14Nov2021 at 06:00, after about 60 hours, mild intermittent pain started in upper left abdomen area, which got worse about 15 minutes after each meal and improved, but did not go away after about 4 hours, which was still present at 78 hours post injection. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were taken as a result of the events which included treatment with TYLENOL 1 tablet only, which did not help at all. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events pain at injection site, chills, fever (38C), fatigue, nausea, muscles and joints pain, light headache, and loss of appetite was recovering. The events sweating, pain in lymph nodes, and mild intermittent pain started in upper left abdomen area was not recovered at the time of this report. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: Test Date: 20211112; Test Name: Body temperature; Result Unstructured Data: Test Result: 38 Centigrade; Comments: at 03:00.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Iron deficiency; Penicillin allergy
Andere Medikamente: FOCUS FACTOR; VITAMIN D3; NUTRILITE
Allergien: -
Vorherige Impfungen: -

VAERS 1909674

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 55,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Fatigue Immunisation Interchange of vaccine products Off label use Pain in extremity No adverse event Product preparation issue Product preparation error

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program. The reporter is the patient. A 55 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 19Nov2021 (Lot number: FH8028) at the age of 55 years as dose 2 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: J&J vaccine (Dose 1, lot: 1805031, Route of administration: Left arm), administration date: 31Mar2021, when the patient was 54 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 19Nov2021, outcome "unknown", described as "got their booster dose"; OFF LABEL USE (non-serious), INTERCHANGE OF VACCINE PRODUCTS (non-serious) all with onset 19Nov2021, outcome "unknown" and all described as "Received First dose J&J Vaccine and booster dose Pfizer Covid 19 Vaccine"; PRODUCT PREPARATION ERROR (non-serious) with onset 19Nov2021, outcome "unknown", described as "received a notice that wrong diluent, sterile water specifically, was used in their booster shots"; PAIN IN EXTREMITY (non-serious) with onset 19Nov2021, outcome "recovered" (Nov2021), described as "sore arm"; FATIGUE (non-serious) with onset 19Nov2021, outcome "recovered" (Nov2021), described as "Exhausted". Additional information: The patient taking Pfizer Covid Vaccine because it had been 8 months. Event sore arm began three hours after receiving the booster dose Pfizer Covid 19 Vaccine on 19Nov2021 and progressively got more sore. The soreness went away after a couple of days. Exhaustion began the night of 19Nov2021 and went away. No follow-up attempts are needed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101648051 same drug/event different patient

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1909674

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: -
Alter: 55,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Fatigue Immunisation Interchange of vaccine products Off label use Pain in extremity No adverse event Product preparation issue Product preparation error

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program. The reporter is the patient. A 55 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 19Nov2021 (Lot number: FH8028) at the age of 55 years as dose 2 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: J&J vaccine (Dose 1, lot: 1805031, Route of administration: Left arm), administration date: 31Mar2021, when the patient was 54 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 19Nov2021, outcome "unknown", described as "got their booster dose"; OFF LABEL USE (non-serious), INTERCHANGE OF VACCINE PRODUCTS (non-serious) all with onset 19Nov2021, outcome "unknown" and all described as "Received First dose J&J Vaccine and booster dose Pfizer Covid 19 Vaccine"; PRODUCT PREPARATION ERROR (non-serious) with onset 19Nov2021, outcome "unknown", described as "received a notice that wrong diluent, sterile water specifically, was used in their booster shots"; PAIN IN EXTREMITY (non-serious) with onset 19Nov2021, outcome "recovered" (Nov2021), described as "sore arm"; FATIGUE (non-serious) with onset 19Nov2021, outcome "recovered" (Nov2021), described as "Exhausted". Additional information: The patient taking Pfizer Covid Vaccine because it had been 8 months. Event sore arm began three hours after receiving the booster dose Pfizer Covid 19 Vaccine on 19Nov2021 and progressively got more sore. The soreness went away after a couple of days. Exhaustion began the night of 19Nov2021 and went away. No follow-up attempts are needed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101648051 same drug/event different patient

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1925903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: CA
Alter: 16,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 04.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness

Symptomtext

Pt in for 2nd COVID vaccine states walked a long way and did not eat breakfast. After vaccine felt dizzy and faint she was put on the floor and when she felt better V/S done B/P 116/83, O2, 99%, Temp 97.7, pulse 80. First aid rendered ice pack and Trendelenburg position. Once she felt better we gave her a bag of cookies and water. Rideshare ride given to family so she would not have to walk home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: has not seen a medical provider over 2 years
Vorgeschichte: Per mom get weak after mensural periods and per mom just finished her period 2 weeks ago
Andere Medikamente: none
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1924746

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8028

mild

Staat: MI
Alter: 49,0
Geschlecht: M
Eingang: 06.12.2021
Impfdatum: 02.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Chills Myalgia Pain Pyrexia

Symptomtext

Fever Chills Sore muscles Aching body Joint pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes
Andere Medikamente: Metformin Gabapentin Allopurinol Colchicine Simvastatin Iron
Allergien: N/A
Vorherige Impfungen: -