VAERS Reports #FF8841

VAERS 2674915

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: -
Alter: 42,0
Geschlecht: F
Eingang: 22.08.2023
Impfdatum: 21.10.2021
Beginn: 21.01.2023
Tage bis Beginn: 457,0
Dosis: 2
Route/Site: IM / RA

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

Cerebrovascular accident

Symptomtext

ACUTE STROKE, UNSPECIFIED TYPE AND ARTERY

Weitere VAERSDATA-Felder

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

VAERS 2671496

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: -
Alter: 74,0
Geschlecht: F
Eingang: 15.08.2023
Impfdatum: 17.12.2021
Beginn: 27.01.2022
Tage bis Beginn: 41,0
Dosis: 3
Route/Site: - / -

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

Acute myocardial infarction Hypoxia

Symptomtext

ACUTE NON ST ELEVATION MI HYPOXIA

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

VAERS 2647875

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: -
Alter: 40,0
Geschlecht: F
Eingang: 21.06.2023
Impfdatum: 15.12.2021
Beginn: 18.02.2022
Tage bis Beginn: 65,0
Dosis: 3
Route/Site: IM / RA

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

Pulmonary embolism Symptom recurrence

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE PULMONARY EMBOLISM 12/3/2022 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

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

VAERS 2625678

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: -
Alter: 72,0
Geschlecht: F
Eingang: 03.05.2023
Impfdatum: 05.03.2022
Beginn: 05.04.2022
Tage bis Beginn: 31,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Hypotension Obstructive sleep apnoea syndrome Symptom recurrence

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ADULT OBSTRUCTIVE SLEEP APNEA, MODERATE HYPOTENSION ACUTE HYPOXEMIC RESPIRATORY FAILURE 5/27/2022, 6/7/2022, 6/8/2022, 6/17/2022 -- RECURRENCE OF SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2624156

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 01.05.2023
Impfdatum: 02.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: IM / RA

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

Cerebrovascular accident

Symptomtext

ACUTE STROKE, UNSPECIFIED TYPE AND ARTERY

Weitere VAERSDATA-Felder

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

VAERS 2616311

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: -
Alter: 84,0
Geschlecht: M
Eingang: 17.04.2023
Impfdatum: 09.12.2021
Beginn: 22.03.2023
Tage bis Beginn: 468,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Angiogram pulmonary normal Atelectasis Blood creatine phosphokinase increased Blood gases Blood lactic acid C-reactive protein increased COVID-19 Chest X-ray normal Computerised tomogram abdomen normal Computerised tomogram head normal Computerised tomogram spine Cough Craniocerebral injury Diuretic therapy Electrocardiogram normal Exposure to SARS-CoV-2

Symptomtext

Patient is a 85 y.o. male patient of MD with history of Parkinsons, CAD, Chronic Back and hip pain, Depression, BPH, Edema, HTN presented to Hospital with unwitnessed fall . Acute hypoxic respiratory failure d/t COVID 19 infection Atelectasis Tested + for covid 3/21/23, exposed to other residents Has mild cough and ST Febrile on arrival (Tmax 100.4), HR 76, RR 18, BP 117/73, satting mid 80s on RA CBC with mild leukopenia (Wbc 3.83). CRP 44.1. LA 1.2. VBG 7.38/46 CXR without vascular congestion or consolidation CTPA w/o PE or airspace disease. Noted atelectasis Cont PO decadron, holding off on Remdesivir IS/PEP, mucinex Now off oxygen and satting in mid 90s on RA Discharged in stable condition, return precautions discussed Patient instructed to follow up with PCP Unwitnessed mechanical fall Closed Head injury Elevated CPK Reported fell overnight and was on ground for hours CPK 402 CT head negative CT cervical, thoracic spine no acute fracture CT abdomen pelvis/chest no fractures Fall risk precautions PT/OT/CM for discharge planning Set up with home therapy Parkinsons Disease complicated by hallucinations Follows with Dr neurology Continue Carbidopa/Levodopa Continue seroquel HTN Edema CAD Follows with Dr Has moderated 3 vessel disease BP controlled on admission Troponin normal, EKG no ischemia Hold diuretics with AKI, resume when appropriate Continue metoprolol BPH with LUTS Follows with urology Continue flomax and ditropan Chronic Back Pain Follows with Dr Resume oxycodone, Gabapentin Database history reviewed

Weitere VAERSDATA-Felder

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

VAERS 2615431

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: -
Alter: 53,0
Geschlecht: M
Eingang: 14.04.2023
Impfdatum: 06.10.2021
Beginn: 14.03.2023
Tage bis Beginn: 524,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Anaemia Angiogram pulmonary abnormal Blood creatinine increased Blood iron Blood sodium decreased COVID-19 COVID-19 pneumonia Computerised tomogram thorax abnormal Dyspnoea Echocardiogram Fatigue Haemoglobin decreased Hyponatraemia Lactic acidosis Leukocytosis Liver function test increased

Symptomtext

Patient is a 54 y.o. male patient of MD with history of hypertension who presented to Hospital with shortness of breath, fatigue, recent COVID positive home test, found to have multifactorial pneumonia. Acute respiratory failure with hypoxemia Abnormal CT chest Multifocal pneumonia Respiratory failure in setting of pneumonia, likely combination of bacterial with component of COVID CTPA on admission without PE, though showed extensive bilateral lung opacity involving all lobes, most confluent in the left lung Initially required 4L supplemental O2, weaned to room air quickly Urinary antigens negative Sputum culture with mixed flora MRSA swab negative Pulm followed Initially on vanc/zosyn, transitioned to levofloxacin, planning 7 day course total Repeat CT chest in 6-8 weeks with outpatient pulmonology follow up Sepsis, POA Lactic acidosis Due to pneumonia with leukocytosis, tachycardia, lactic acidosis on admission Blood cultures 2/2 with staph hominis, suspect contaminant Repeat blood cultures without growth at 48 hours Treated with antibiotics as above CoNS positive blood cultures Blood cultures on admission 2 of 2 staph hominis, thought to be both contaminants given collection timing and not clinically relevant TTE does not show evidence of endocarditis ID followed Repeat blood cultures negative at 48 hours Covid-19 Virus Infection Date of onset of symptoms: 3/10 Symptoms present on admission: Shortness of breath, fatigue Date of covid positive test: 3/12 on home antigen test, 3/15 here Vaccination status: vaccinated without booster Imaging: CTPA as above Oxygen requirements on admission: 4L nasal cannula Current oxygen requirements: room air Medical therapy: received steroids while admitted, discontinued on discharge given on room air and only briefly required oxygen;, was taking Paxlovid at home Consultants following: pulm Anticipated special isolation end date: 3/20 AKI Metabolic acidosis Admit Cr 2.1, baseline normal, suspect prerenal with ACEi use and was taking Paxlovid Improved renal function, back to baseline Resume ACEi/diuretic on discharge Elevated LFTs In setting of COVID, though possibly related to remdesivir Improved to near normal Repeat 1 week Hyponatremia Na 123, in setting of diminished intake, but was 126 Normalized Anemia, normocytic Hgb 12.5, baseline wnl Without evidence of active bleeding Iron studies with anemia of chronic disease Repeat as outpatient Essential hypertension Home regimen: amlodipine and lisinopril/hydrochlorothiazide Held ACEi/diuretic during admission Resume home regimen on discharge

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2615344

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 14.04.2023
Impfdatum: 20.02.2022
Beginn: 01.03.2022
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / -

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

Acute respiratory failure Chronic respiratory failure Coronary artery disease Respiratory failure

Symptomtext

J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 3/28/2022 CAD (CORONARY ARTERY DISEASE) WO ANGINA J96.02 ACUTE HYPERCAPNIC RESPIRATORY FAILURE 3/28/2022 CAD (CORONARY ARTERY DISEASE) WO ANGINA J96.12 CHRONIC HYPERCAPNIC RESPIRATORY FAILURE 3/9/2022 CAD (CORONARY ARTERY DISEASE) WO ANGINA J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 3/28/2022 CAD (CORONARY ARTERY DISEASE) WO ANGINA J96.02 ACUTE HYPERCAPNIC RESPIRATORY FAILURE 3/28/2022 CAD (CORONARY ARTERY DISEASE) WO ANGINA J96.12 CHRONIC HYPERCAPNIC RESPIRATORY FAILURE 3/9/2022 CAD (CORONARY ARTERY DISEASE) WO ANGINA J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 3/28/2022 CAD (CORONARY ARTERY DISEASE) WO ANGINA J96.02 ACUTE HYPERCAPNIC RESPIRATORY FAILURE 3/28/2022 CAD (CORONARY ARTERY DISEASE) WO ANGINA J96.12 CHRONIC HYPERCAPNIC RESPIRATORY FAILURE 3/9/2022 CAD (CORONARY ARTERY DISEASE) WO ANGINA

Weitere VAERSDATA-Felder

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

VAERS 2610168

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 05.04.2023
Impfdatum: 04.10.2021
Beginn: 22.05.2022
Tage bis Beginn: 230,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure Breast cancer female Hypoxia Respiratory failure

Symptomtext

J96.00 ACUTE RESPIRATORY FAILURE 7/6/2022 FEMALE BREAST CANCER, UNSPECIFIED SITE OF LEFT BREAST J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 5/26/2022 FEMALE BREAST CANCER, UNSPECIFIED SITE OF LEFT BREAST J96.02 ACUTE HYPERCAPNIC RESPIRATORY FAILURE 7/6/2022 FEMALE BREAST CANCER, UNSPECIFIED SITE OF LEFT BREAST R09.02 HYPOXIA 5/26/2022 FEMALE BREAST CANCER, UNSPECIFIED SITE OF LEFT BREAST J96.00 ACUTE RESPIRATORY FAILURE 7/6/2022 NONTRAUMATIC ACUTE KIDNEY INJURY J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 5/26/2022 NONTRAUMATIC ACUTE KIDNEY INJURY J96.02 ACUTE HYPERCAPNIC RESPIRATORY FAILURE 7/6/2022 NONTRAUMATIC ACUTE KIDNEY INJURY R09.02 HYPOXIA 5/26/2022 NONTRAUMATIC ACUTE KIDNEY INJURY J96.00 ACUTE RESPIRATORY FAILURE 7/6/2022 HX OF LEFT BREAST CANCER J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 5/26/2022 HX OF LEFT BREAST CANCER J96.02 ACUTE HYPERCAPNIC RESPIRATORY FAILURE 7/6/2022 HX OF LEFT BREAST CANCER R09.02 HYPOXIA 5/26/2022 HX OF LEFT BREAST CANCER

Weitere VAERSDATA-Felder

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

VAERS 1797312

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: NH
Alter: 75,0
Geschlecht: F
Eingang: 05.04.2023
Impfdatum: 05.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Abdominal pain upper Ageusia Asthenia Body temperature Chills Alopecia Amnesia Blindness unilateral Condition aggravated Dyspnoea Cerebral haemorrhage Computerised tomogram head abnormal Walking aid user Extra dose administered Fatigue Fear Gastroenteritis Headache

Symptomtext

lost sight in one eye, walker, brain hemmorhage

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Praegender Schweregrund: Near death experience
Hospital-Tage: 2,0
Labordaten: ct scan
Aktuelle Erkrankungen: -
Vorgeschichte: migraines
Andere Medikamente: pheno babitol chlonazopam, zoloft, butabi
Allergien: latex, ion,
Vorherige Impfungen: -

VAERS 2607506

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: WI
Alter: 72,0
Geschlecht: M
Eingang: 31.03.2023
Impfdatum: 29.10.2021
Beginn: 16.01.2023
Tage bis Beginn: 444,0
Dosis: 3
Route/Site: UN / UN

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

Acute kidney injury Acute respiratory distress syndrome Acute respiratory failure COVID-19 COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram abdomen abnormal Computerised tomogram thorax abnormal Death Dyspnoea Fatigue General physical health deterioration Hypocalcaemia Hypokalaemia Hypomagnesaemia Lung opacity Pleural effusion Pneumonia bacterial

Symptomtext

On 1/16/2023, patient presented to the emergency department for evaluation of worsening fatigue and shortness of breath. He was initially diagnosed with COVID-19 on 1/3/2023; He had a positive COVID-19 NAA test on 1/16/2023 in the ED; his chest x-ray showed ill-defined, patchy airspace opacity in the right lower lung, concerning for pneumonia and a small right pleural effusion. Patient had oxygen saturations in the 70s on room; He was placed on 2 L supplemental oxygen with improvement. He was treated in the ED for hypokalemia, hypocalcemia and hypomagnesemia. Patient was diagnosed with acute hypoxic respiratory failure related to sepsis, COVID-19 pneumonia, possible underlying bacterial pneumonia complicated by COPD history. He was admitted to the hospital for further evaluation and treatment. During his hospital stay, patient progressed to acute respiratory distress syndrome; His CT of chest/abdomen/pelvis on 1/26/2023 showed bilateral consolidative opacities greatest in the LLL consistent with pneumonia and diffuse ground glass opacities consistent with ARDS. The patient?s condition continued to deteriorate, and he was placed on comfort care only; He died on 1/31/2023 while an inpatient at the hospital. His death abstract listed immediate cause of death as acute respiratory failure due to COVID and bacterial pneumonia, due to or as a consequence of lymphoma and acute kidney injury. Submitter does not have access to further medical information on this case. If more information is needed, please contact the admitting hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 15,0
Labordaten: 1/16/2023 - positive COVID-19 NAA test; Chest x-ray showed ill-defined, patchy airspace opacity in the right lower lung, concerning for pneumonia and a small right pleural effusion. 1/26/2023 - CT of chest/abdomen/pelvis showed bilateral consolidative opacities greatest in the LLL consistent with pneumonia and diffuse ground glass opacities consistent with ARDS.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Lymphoma, hypertension, diabetes mellitus type 2, chronic kidney disease, chronic obstructive pulmonary disease, benign prostatic hypertrophy, diastolic heart failure, peripheral vascular disease, adrenal insufficiency, coronary artery disease.
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2605039

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 28.03.2023
Impfdatum: 22.10.2021
Beginn: 18.02.2023
Tage bis Beginn: 484,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Atrial fibrillation Blood creatinine normal COVID-19 Chest pain Computerised tomogram Condition aggravated Coronary artery disease Cough Diastolic dysfunction Dyspnoea Echocardiogram abnormal Ejection fraction normal Electrocardiogram normal Glucose tolerance impaired Glycosylated haemoglobin Hypertension Pain

Symptomtext

Assessment and Plan: 77 y.o. female patient of, MD with history of respiratory failure, CHF, A-fib, CAD, CKD, COPD, DM 2, HLD, PulmHTN presented to Medical Center with dyspnea and chest pain. Acute on chronic respiratory failure with hypoxia Covid-19 Virus Infection Date of onset of symptoms: 2/17/2023 Symptoms present on admission: Dyspnea, chest pain, cough Date of covid positive test: 2/18/2023 Vaccination status: vaccinated Platelets: 115 (2/18) admitted with COVID-19 Baseline 102-115 Imaging: CT dissection without evidence of dissection or PE Oxygen requirements on admission: 4 L Current oxygen requirements: 2 L which is her baseline Medical therapy: steroids continued for 5 more days, will stop remdesivir Continue Symbicort, DuoNebs, and PRN albuterol PT/OT consulted: Pt declined consult Chest pain CAD Recent work-up including PET perfusion in November with stable CAD Pain in setting of new COVID infection Troponin minimally elevated at 16, trended flat to 15 EKG without evidence of acute ischemia Monitor symptoms Abnormal Urinalysis 15 WBC/hpf in ED Denies symptoms of UTI Hypertension BPs in the ED up to 218/86 with wide fluctuations Resume home antihypertensives COPD Without acute exacerbation Scheduled Duonebs and PRN Albuterol Continue Symbicort Prediabetes A1c 5.7 off medications Monitor glucose while on steroids, initiate SSI if needed HLD Continue home pravastatin A-fib Paroxysmal Continue metoprolol for rate control Sinus on admission Not anticoagulated CKD Creatinine stable on admission Chronic HFpEF Clinically approximately euvolemic Continue home Bumex EF 62% with grade 2 diastolic dysfunction on most recent echo

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2599510

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: WI
Alter: 15,0
Geschlecht: M
Eingang: 20.03.2023
Impfdatum: 08.10.2021
Beginn: 01.10.2022
Tage bis Beginn: 358,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain Asthenia Autopsy Blood sodium abnormal Death Drug screen negative Fluid intake reduced Full blood count abnormal Headache Histology Hypophagia Laboratory test Malaise Metabolic function test abnormal Microscopy Myocarditis Nausea Pyrexia

Symptomtext

Started feeling significantly ill 10/11/2022 with complaints of nausea, (unable to keep water or food down) weakness, and decreased food/water intake. Headache reported and sharp abdominal pain. Had a fever on admission to hospital on 10/15/22. Death 1 year after vaccine administration. Cause of death - idiopathic myocarditis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: On 10/15/22 CBC - abnormal results Comprehensive metabolic panel - abnormal results Urinalysis - abnormal results UA/microscopy - normal Sodium, serum - abnormal results Monotest - normal Respiratory panel (including COVID-19) - normal Drug screen - normal/negative Autopsy performed 10/16/22 . Toxicology - negative Histology performed Cause of death - idiopathic myocarditis
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Ariprazole, Escitalopram, Melatonin, and Ondansetron
Allergien: None known
Vorherige Impfungen: -

VAERS 2576600

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: WI
Alter: 60,0
Geschlecht: M
Eingang: 06.02.2023
Impfdatum: 12.01.2021
Beginn: 01.07.2021
Tage bis Beginn: 170,0
Dosis: 3
Route/Site: IM / RA

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

Anticoagulant therapy Cardiac operation Cardiac stress test abnormal Catheterisation cardiac abnormal Computerised tomogram coronary artery abnormal Cor pulmonale Dyspnoea Exercise tolerance decreased Heart sounds abnormal Loss of personal independence in daily activities Pulmonary embolism Pulmonary endarterectomy Pulmonary hypertension Pulmonary mass Right ventricular failure Therapeutic hypothermia Ultrasound chest Ventilation/perfusion scan abnormal

Symptomtext

I had progressive dyspnea beginning 4-6 months after first vaccine. My nightly 2 mile walk became more difficult and I could barely manage one mile. Symptoms progressed until I was found to have an oxygen saturation of 83% during a stress test in July of 2022. Diagnosed with CTEPH, with a large saddle embolus. I am very thin - 6 ft tall, 160 pounds -- no source for embolus ever found. I was on oxygen and sent to hospital for pulmonary endarterectomy of my segmental and subsegmental pulmonary vessels -- hypothermic cardiac arrest and open-heart surgery. Doing much better now, off oxygen and improving hemodynamics. All tests show normal clotting function; I'm now on coumadin for life.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 8,0
Labordaten: Stress test at my request on 7/17/21 for progressive dyspnea; Cardiac calcium scan two days later negative for coronary pathology but a large mass noted in R pulmonary artery. Further workup showed cor pulmonale of R ventricle, R ventricular gallop. U/S showed no other blood clots in my body beyond my lungs. Workup at hospital included VQ scan showing blocked small vessels in lungs. R and L heart cath showed good LV function and R heart failure. Had pulmonary endarterectomy on 8/27/2023 after fighting for coverage with insurance company.
Aktuelle Erkrankungen: none
Vorgeschichte: Reflux; anxiety
Andere Medikamente: escitalopram 20 mg, lansoprazole
Allergien: gluten
Vorherige Impfungen: -

VAERS 2563294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: -
Alter: 64,0
Geschlecht: F
Eingang: 19.01.2023
Impfdatum: 13.01.2022
Beginn: 23.12.2022
Tage bis Beginn: 344,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Angiogram pulmonary abnormal Anxiety Blood culture negative Blood lactic acid normal Bronchial wall thickening C-reactive protein increased COVID-19 pneumonia Computerised tomogram thorax abnormal Condition aggravated Culture urine negative Hypertension Legionella test Leukocytosis Pneumonia Pneumonia viral Procalcitonin normal Pulmonary mass

Symptomtext

patient is a 65 y.o. female patient of MD with history of Coronary artery disease, hypertension, hyperlipidemia, and asthma, now presented to a local Hospital with pneumonia. COVID 19 pneumonia Acute hypoxemic respiratory failure d/t above Sepsis, POA, d/t above and below Lactic acid within normal limits, no need for IVF resuscitation WBC 29K CTPA: negative PE. MF pneumonia noted. Bronchial wall thickening present as well Blood and urine cultures NGTD. Strep & legionella negative Continue remdesivir, and decadron. Will increase decadron to 10mg daily. Discontinue levaquin given negative procal and imaging suggestive of viral pna Suspect leukocytosis d/t steroid administration MRSA swab negative. PCT negative, discontinue abx. CRP markedly elevated and improving. Resume home lasix Stable on 4-5L NC with ambulation. Ready for discharge home to complete steroid therapy RX for ativan PRN for anxiety sent to pharmacy hypertension Initially low normal, now elevated. Resume home lisinopril and coreg. prescribed 40mg BID of lisinopril which is inappropriate. Change to daily Resume home lasix Continue nifedipine daily on discharge. hyperlipidemia Continue home pravastatin. Cigarette dependence without complication Counseled on cessation for 3-10 minutes. Will write for tobacco replacement patch. Solitary pulmonary nodule Incidental finding in the right upper lobe on admission CT chest. Outpatient surveillance imaging at discretion of family physician after resolution of acute presenting issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2562172

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: AL
Alter: 46,0
Geschlecht: M
Eingang: 18.01.2023
Impfdatum: 11.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 17,0
Dosis: 2
Route/Site: IM / LA

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

Blindness unilateral Cerebrovascular accident Hypoaesthesia Magnetic resonance imaging head abnormal

Symptomtext

I sustained a punctate right occipital stroke in a cortical location confirmed by MRI on brain. I suffered Left side numbness and left eye blindness for around 2 hrs and continued partial loss of left eyesight for several days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: I sustained a punctate right occipital stroke in a cortical location confirmed by MRI on brain
Aktuelle Erkrankungen: None
Vorgeschichte: Testosterone Treatment since 2009
Andere Medikamente: Zoloft 100mg
Allergien: None
Vorherige Impfungen: -

VAERS 2512316

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: -
Alter: 92,0
Geschlecht: F
Eingang: 18.11.2022
Impfdatum: 21.10.2021
Beginn: 31.10.2022
Tage bis Beginn: 375,0
Dosis: 3
Route/Site: IM / RA

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

Acute myocardial infarction Anaemia macrocytic Angiogram pulmonary abnormal Anticoagulant therapy Aortic stenosis Blood iron Bundle branch block left C-reactive protein increased COVID-19 Chest X-ray normal Condition aggravated Dyspnoea exertional Echocardiogram abnormal Ejection fraction decreased Electrocardiogram abnormal Haemoglobin decreased Left ventricular failure Pollakiuria

Symptomtext

Patient is a 93 y.o. female patient of local MD with history of CAD, HTN and AS who presented to Hospital with a cc of progressive DOE Acute pulmonary embolism with RHS COVID 19 infection P/w acute onset DOE. Etiology likely multifactorial given findings below CXR: relatively unremarkable CTPA with RLL PE w/ RHS, e/o Pulm HTN Echo outlined below LE duplex negative for DVT Started on heparin, transitioned to warfarin with lovenox bridge. CRP elevated, will monitor while in house. Decadron and remdesivir per COVID 19 protocol with plans to discharge on decadron for 10 total days of therapy Stable on RA at time of discharge Acute macrocytic anemia Baseline hgb 12-13, dropped to 10.7 today in the setting of anticoagulation Macrocytosis concerning for acute bleed however no melena, hematochezia or hematemesis iron studies, B12 level reviewed. Continue PO iron on discharge Repeat CBC in 1 week in outpatient setting New onset systolic heart failure Severe tricuspid regurgitation Severe aortic stenosis Pulmonary HTN NSTEMI, unable to determine type as refused ischemic w/u Echo obtained in the setting of PE and e/o RHS on CTPA Echo: LVEF 39% (down from 60%), severe AS, severe TR and multiple WMA noted. RVSP 80mmhg EKG w/ LBBB which is chronic Evaluated by cardiology, patient has declined any ischemic w/u at this time and has opted for medical management Continue statin, BB and ACEi as well as plavix on discharge RX for PRN lasix on discharge given EF and valve disease Cancer screening No recent mammogram. Last colonoscopy 2016. Will defer cancer screening to the outpatient setting though unlikely to change management Urinary frequency Noted today, UA pending collection Will f/u UA and send RX for abx if indicated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2476175

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: FL
Alter: 75,0
Geschlecht: M
Eingang: 12.10.2022
Impfdatum: 12.01.2022
Beginn: 24.01.2022
Tage bis Beginn: 12,0
Dosis: 2
Route/Site: SYR / AR

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

Death

Symptomtext

Death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: N/A - Pronounced dead due to natural causes on site at home.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, Heart Disease
Andere Medikamente: insulin, carvedilol
Allergien: -
Vorherige Impfungen: -

VAERS 2446485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: SD
Alter: 72,0
Geschlecht: M
Eingang: 15.09.2022
Impfdatum: 25.10.2021
Beginn: 20.07.2022
Tage bis Beginn: 268,0
Dosis: 3
Route/Site: SYR / LA

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

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

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. The individual received Pfizer vaccine on 02/12/2021, 03/05/2021, and 10/25/2021. They tested positive for COVID-19 on 07/20/2022 at the nursing home at which they were a resident. They experienced an episode of acute respiratory arrest and were diagnosed with COVID-19 pneumonia. They died later on the same day, on 07/20/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Type II Diabetes, Coronary Artery Disease, COPD, Mixed Vascular and Neurodegenerative Dementia, Hypertension The individual was a resident of the nursing home indicated in the Address portion of this form.
Andere Medikamente: -
Allergien: Flovastatin (reaction: hair loss) Simvastatin (reaction: hair loss)
Vorherige Impfungen: -

VAERS 2436935

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

kritisch

Staat: SD
Alter: 100,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 27.04.2022
Beginn: 24.07.2022
Tage bis Beginn: 88,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 COVID-19 pneumonia 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 4 times with the Pfizer product, having received vaccine on 12/30/2020, 01/20/2021, 10/13/2021, and 04/27/2022. They tested positive for COVID-19 on 07/24/2022 and died on 07/25/2022. I have no indication they were hospitalized related to the illness. Death certificate lists COVID-19 pneumonia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Positive COVID-19 test on 07/24/2022 despite being vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: Alzheimer's Dementia; History of Kidney Disease, History of Anemia; History of A-Fib The individual was a resident of the long term/rehabilitation facility indicated in the address portion of this form.
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2414890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: WI
Alter: 84,0
Geschlecht: F
Eingang: 18.08.2022
Impfdatum: 23.11.2021
Beginn: 23.07.2022
Tage bis Beginn: 242,0
Dosis: 3
Route/Site: UN / UN

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

Agonal respiration Aspiration Asthenia Blood fibrinogen increased C-reactive protein increased COVID-19 Chest X-ray Condition aggravated Cough Death Device placement issue Dizziness Dysphagia Dyspnoea Dyspnoea exertional Eating disorder Electrocardiogram Exposure to SARS-CoV-2

Symptomtext

Adverse event note: Per web report received stating the patient presented on 7/23/2022 with generalized weakness. Patient with close exposure to COVID-19, her husband was recently positive. Vague symptom onset, approximately 7/21/2022 which included generalized fatigue/weakness, cough, shortness of breath worse with exertion, headache. PCR on admission 7/23 positive. ER work-up revealing elevated CRP, fibrinogen, D-dimer. Difficulty with IV access unable to obtain CTA chest, nuclear medicine lung scan and obtained with intermediate probability PE. Patient had been on Eliquis previously without tachycardia and maintaining room air oxygen saturations. ID consulted for management given COVID-19. Patient stated improvement but reports ongoing dry cough and some fatigue. Denies fever/chills, chest pain, abdominal pain, nausea, vomiting, diarrhea, rash, joint pai n. Denies recent travel. Vaccinated against COVID-19 with Pfizer x3, last immunization 11/2021 Per report, this patient was hemo-dynamically stable and saturating well on room air. Patient was admitted given acute viral infection and weakness. The patient had a hospital course of 11 days. Her initial hospitalization focused on conservative management of COVID-19 infection. Patient had no indication for specific treatment, she was supported and remained on room air. However, she was weak and worked with PT/OT. Therapy sessions were notably limited by patient's subjective dizziness. Orthostatic vitals revealed severe and ongoing orthostatic hypotension. Patient noted to be on both metoprolol and diltiazem, and per note, numerous adjustments made to assist with symptoms. Electrophysiologist was contacted as well for support. Despite adjustments to patient's AV nodal agents, her orthostasis persisted. She was trialed on increased salt tabs, midodrine, and Florinef at different times. Despite these interventions, her symptoms and orthostasis persisted. Per note, her chronic dysphagia worsened throughout her hospitalization. Patient was unable to complete repeat video swallow studies given ongoing dizziness. Per note, later in hospital course, patient was found having difficulty with already modified dysphagia diet. Patient aspirated and developed likely aspiration pneumonia. Infectious disease contacted; patient finished a course of cefepime. Clinically, she continued to deteriorate with poor oral intake and ongoing weakness. Palliative care consulted. Family meeting occurred on 8/5/2022 with patient, husband, daughter, son on phone. After thorough discussion of progression of patient's chronic conditions without notable improvement over the course of hospital stay, family made shared decision to pursue home hospice. Patient was planning for transition to home hospice on 8/6/2022. On the evening of 8/5/2022, patient had another aspiration event leading to severe respiratory distress with hypoxemia. A rapid response was called as patient was having agonal/irregular breathing. Attempts were made to provide patient with supplemental oxygen and bedside cares. Patient was DNR/DNI. Family was contacted and ultimately decision made to make patient comfortable. Patient passed away on 8/5/2022 at 6:22 PM.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 11,0
Labordaten: Lab work Chest-XR EKG
Aktuelle Erkrankungen: unknown
Vorgeschichte: Cancer -mouth cancer ? Carotid stenosis - Left carotid occlusion. ? COPD ? Coronary artery disease (*) ? History of blood transfusion ? Hyperlipidemia ? Hypertension ? Hypothyroidism hypothyroid ? Osteoporosis (* ) alendronate 10 yrs, off 2015, ? Pseudophakia of left eye ? Pseudophakia of right eye ? Seizures ? Vitamin D deficiency ? Xerostomia due to radiotherapy
Andere Medikamente: unknown
Allergien: Biaxin [Clarithromycin ] Angioedema Nexium [Esomeprazole ] Angioedem
Vorherige Impfungen: -

VAERS 2324219

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: WI
Alter: 80,0
Geschlecht: M
Eingang: 20.06.2022
Impfdatum: 11.10.2021
Beginn: 15.06.2022
Tage bis Beginn: 247,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Chest X-ray abnormal Dyspnoea Malaise Pneumonia Renal impairment

Symptomtext

Presented to ED on 6/5/22 with COVID pneumonia and symptoms for 5 days. At that time, he was saturating well on room air with normal effort. Chest for-ray showed right middle lobe pneumonia and he was treated with doxycycline for CAP. Paxlovid was intended but unable to be used due to renal function. Presented to ED on 6/15/22 81y.o. M with PMH of Chronic mesenteric ischemia, hypertension, CAD status post CABG, PAD with SMA stenosis, chronic mesenteric ischemia status post iliac artery stent bilaterally, type 2 diabetes, CKD 3 and secondary hyperparathyroidism, normocytic anemia, and HLD who presents to the ED with complaint of shortness of breath. Admitted with acute respiratory failure 2/2 Covid

Weitere VAERSDATA-Felder

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

VAERS 2283033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: -
Alter: 81,0
Geschlecht: M
Eingang: 18.05.2022
Impfdatum: 30.09.2021
Beginn: 01.02.2022
Tage bis Beginn: 124,0
Dosis: 3
Route/Site: - / -

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

COVID-19 COVID-19 pneumonia Cardiac arrest Death General physical health deterioration Respiratory arrest SARS-CoV-2 test positive Supraventricular tachycardia

Symptomtext

COVID vaccine, Pfizer #1 given on 12/30/2021, lot # EL3246; COVID vaccine, Pfizer #2 given on 01/20/2021, lot # EL3302; 02/05/2022 pt presented to ED via EMS to be treated for COVID Pneumonia; had a positive test on 02/01/2022; pt continued to decline; was given remdesivir, zithromax, baricitinib, O2 supplementation; continued to worsen; DNR; had an episode of SVT, responded to metoprolol but was not able to maintain O2 sats above 80%; reverted back to SVT; went into respiratory arrest and asystole; he never recovered; death certificate and med records sent to VAERS website per VAERS request

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 13,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2110312

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 03.05.2022
Impfdatum: 01.10.2021
Beginn: 01.01.2022
Tage bis Beginn: 92,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Asthenia COVID-19 COVID-19 pneumonia Anticoagulant therapy Chest X-ray abnormal Chronic respiratory disease Chills Death Dizziness Dyspnoea Endotracheal intubation Computerised tomogram thorax abnormal General physical health deterioration Malaise Extubation Fall

Symptomtext

pt brought to ED via EMS after falling out of bed; c/o SOB, generalized weakness, dizziness, headache, chills; O2 supplementation, ABX, dexamethasone given; positive for COVID; COVID pneumonia; sepsis with shock; O2 demand increased; transferred to ICU; required intubation; worsening acute hypoxic respiratory distress; acute PE and UTI; AKI; code status was intubation only; transitioned to comfort measures; extubated and pt passed away

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 15,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: DMT2, HTN, COPD, Sjogren's syndrome
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2243531

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: MN
Alter: 90,0
Geschlecht: M
Eingang: 20.04.2022
Impfdatum: 01.10.2021
Beginn: 19.04.2022
Tage bis Beginn: 200,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Bronchitis Upper respiratory tract infection

Symptomtext

Patient admitted to hospital for Acute Respiratory Failure requiring O2.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Acute Bronchitis & Upper Respiratory Infection on 4/1
Vorgeschichte: Diabetes, HLD, HTN
Andere Medikamente: -
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2223909

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: SD
Alter: 81,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 13.10.2021
Beginn: 05.02.2022
Tage bis Beginn: 115,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Death Dyspnoea Endotracheal intubation Escherichia infection Hypoxia Mechanical ventilation Pneumonia staphylococcal SARS-CoV-2 test positive Urinary tract infection Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 after which death occurred. The individual was vaccinated with the Pfizer product on 01/14/2021, 02/04/2021, and 10/13/2021. They presented to Emergency Dept on 02/05/2022 with primary compliant of shortness of breath. They tested positive for COVID-19 and were admitted to hospital same day. A second COVID-19 test on 02/06/2022 was also positive. While hospitalized, they were hypoxic and found to have MSSA Pneumonia. They required intubation and mechanical ventilation. They were also found to have an E. coli urinary tract infection. They were discharged to hospice care at a nursing home facility on 02/21/2022. A COVID-19 test on 02/21/2022 was negative. They died on 03/17/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 16,0
Labordaten: Positive COVID-19 tests x2 despite being vaccinated and boosted.
Aktuelle Erkrankungen: -
Vorgeschichte: History of Breast Cancer, History of a Brain Tumor, Dementia, Obstructive Sleep Apnea, The individual was a resident of the nursing home indicated in the address field of this form.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2204005

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: -
Alter: 46,0
Geschlecht: M
Eingang: 29.03.2022
Impfdatum: 13.10.2021
Beginn: 05.01.2022
Tage bis Beginn: 84,0
Dosis: 2
Route/Site: - / -

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

Acute kidney injury COVID-19 Cardiac arrest Chills Cough Death Diabetic ketoacidosis Dyspnoea Endotracheal intubation Hypertension Hyponatraemia Nausea Resuscitation SARS-CoV-2 test positive Tachycardia Tachypnoea Vomiting

Symptomtext

pt brought to ED with increasing SOB, chills, N/V, cough; pt was hypertensive, tachycardic, tachypnic; NRB; positive for COVID; DKA, AKI, hyponatremia; pt suffered cardiac arrest; CPR; intubated; after 25 minutes of resuscitation, pt expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: DM
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2196390

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: VA
Alter: 93,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 23.03.2022
Beginn: 23.03.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Death

Symptomtext

resident expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: UTI
Vorgeschichte: HLD, HTN, dementia
Andere Medikamente: Simvastatin Latanoprost eye drops, Aspirin , colace , calcitriol , megace, HCTZ, amlodipine
Allergien: NKA
Vorherige Impfungen: -

VAERS 2151269

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: TX
Alter: 87,0
Geschlecht: M
Eingang: 01.03.2022
Impfdatum: 22.10.2021
Beginn: 23.02.2022
Tage bis Beginn: 124,0
Dosis: 3
Route/Site: IM / UN

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

Basal ganglia stroke COVID-19 Computerised tomogram head abnormal Death Depressed level of consciousness Dyspnoea Inappropriate schedule of product administration Mental status changes Oxygen saturation decreased Positive airway pressure therapy SARS-CoV-2 test positive Unresponsive to stimuli

Symptomtext

Moderna and Pfizer COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Received Moderna Vaccine on 2/22/21 and Pfizer Vaccine on 3/15/21 and 10/22/21. Presented to ED on 2/11/22 Covid+, d/c'd 2/12/22. Reported sats of 88-94% Presented to ED 2/16/22 w/increasing SOB and AMS. Placed on BiPAP. 2/23/22 not arousable. Pt began to desaturate and unresponsive. CT head with Acute left basal ganglia stroke. Transitioned to comfort care only, expired on 2/23/22. Treated with medrol dosepack, decadron, zosyn, and ceftriaxone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 7,0
Labordaten: 2/11/22: This sample was analyzed on the (Privacy) platform using RT-PCR technology.
Aktuelle Erkrankungen: -
Vorgeschichte: hx of CLL, CKD4, RA
Andere Medikamente: albuterol, amlodipine, benzonatate,calcium polycarbophil, vitamin D3, codeine/guaifenesin, dronedarone, ferrous sulfate, fluticasone, fluticasone/vilanterol, folic acid, guaifenesin, hydroxychloroquine, ibrutinib, L.acid/B.bifiddum, metopro
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1757524

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: CA
Alter: 89,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 01.10.2021
Beginn: 02.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Abdominal discomfort Abdominal pain upper Asthenia Death Dizziness Aphasia Cardiac arrest Dysstasia Atrioventricular block complete Blood lactic acid Chest X-ray Computerised tomogram abdomen Cardiac pacemaker insertion Dialysis Feeling abnormal Electrocardiogram Full blood count Laboratory test

Symptomtext

On 10/1 she received a 3rd COVID-19 vaccination (Pfizer) in her left arm at a local pharmacy. About 3 hours after the shot she began to feel dizzy and dry heaves. She continued to feel unwell experiencing weakness, GI upset, myalgia, headache and stomachache. Her family contacted her doctor and about 18 hours after the shot she was taken to the Emergency Department. En route to the hospital, she became unresponsive in PEA arrest. At the ED she was found to be hypothermic, hypoglycemic and hyperkalemic. She was admitted to the intensive care unit and later diagnosed with aspiration pneumonia. She died in the hospital on 10/13/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 11,0
Labordaten: See medical records.
Aktuelle Erkrankungen: Hypertension, atherosclerotic and valvular heart disease, chronic heart failure, chronic kidney disease, type 2 diabetes mellitus, COPD
Vorgeschichte: Hypertension, atherosclerotic and valvular heart disease, chronic heart failure, chronic kidney disease, type 2 diabetes mellitus, COPD
Andere Medikamente: Bisoprolol (ZEBETA) 5 mg Oral Tab Bumetanide (Bumex) 0.5 mg Oral Tab Fluticasone-Salmeterol (Advair Diskus) 250-50 mcg/dose Inhl Disk w/devi Meprobamate (EQUANIL/MILTOWN) 400 mg Oral Tab Pantoprazole (PROTONIX) 20 mg Oral TBEC DR Tab amLODI
Allergien: None known.
Vorherige Impfungen: -

VAERS 1757524

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: CA
Alter: 89,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 01.10.2021
Beginn: 02.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / AR

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

Abdominal discomfort Abdominal pain upper Asthenia Death Dizziness Aphasia Cardiac arrest Dysstasia Atrioventricular block complete Blood lactic acid Chest X-ray Computerised tomogram abdomen Cardiac pacemaker insertion Dialysis Feeling abnormal Electrocardiogram Full blood count Laboratory test

Symptomtext

On 10/1 she received a 3rd COVID-19 vaccination (Pfizer) in her left arm at a local pharmacy. About 3 hours after the shot she began to feel dizzy and dry heaves. She continued to feel unwell experiencing weakness, GI upset, myalgia, headache and stomachache. Her family contacted her doctor and about 18 hours after the shot she was taken to the Emergency Department. En route to the hospital, she became unresponsive in PEA arrest. At the ED she was found to be hypothermic, hypoglycemic and hyperkalemic. She was admitted to the intensive care unit and later diagnosed with aspiration pneumonia. She died in the hospital on 10/13/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 11,0
Labordaten: See medical records.
Aktuelle Erkrankungen: Hypertension, atherosclerotic and valvular heart disease, chronic heart failure, chronic kidney disease, type 2 diabetes mellitus, COPD
Vorgeschichte: Hypertension, atherosclerotic and valvular heart disease, chronic heart failure, chronic kidney disease, type 2 diabetes mellitus, COPD
Andere Medikamente: Bisoprolol (ZEBETA) 5 mg Oral Tab Bumetanide (Bumex) 0.5 mg Oral Tab Fluticasone-Salmeterol (Advair Diskus) 250-50 mcg/dose Inhl Disk w/devi Meprobamate (EQUANIL/MILTOWN) 400 mg Oral Tab Pantoprazole (PROTONIX) 20 mg Oral TBEC DR Tab amLODI
Allergien: None known.
Vorherige Impfungen: -

VAERS 1757524

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: CA
Alter: 89,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 01.10.2021
Beginn: 02.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal discomfort Abdominal pain upper Asthenia Death Dizziness Aphasia Cardiac arrest Dysstasia Atrioventricular block complete Blood lactic acid Chest X-ray Computerised tomogram abdomen Cardiac pacemaker insertion Dialysis Feeling abnormal Electrocardiogram Full blood count Laboratory test

Symptomtext

On 10/1 she received a 3rd COVID-19 vaccination (Pfizer) in her left arm at a local pharmacy. About 3 hours after the shot she began to feel dizzy and dry heaves. She continued to feel unwell experiencing weakness, GI upset, myalgia, headache and stomachache. Her family contacted her doctor and about 18 hours after the shot she was taken to the Emergency Department. En route to the hospital, she became unresponsive in PEA arrest. At the ED she was found to be hypothermic, hypoglycemic and hyperkalemic. She was admitted to the intensive care unit and later diagnosed with aspiration pneumonia. She died in the hospital on 10/13/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 11,0
Labordaten: See medical records.
Aktuelle Erkrankungen: Hypertension, atherosclerotic and valvular heart disease, chronic heart failure, chronic kidney disease, type 2 diabetes mellitus, COPD
Vorgeschichte: Hypertension, atherosclerotic and valvular heart disease, chronic heart failure, chronic kidney disease, type 2 diabetes mellitus, COPD
Andere Medikamente: Bisoprolol (ZEBETA) 5 mg Oral Tab Bumetanide (Bumex) 0.5 mg Oral Tab Fluticasone-Salmeterol (Advair Diskus) 250-50 mcg/dose Inhl Disk w/devi Meprobamate (EQUANIL/MILTOWN) 400 mg Oral Tab Pantoprazole (PROTONIX) 20 mg Oral TBEC DR Tab amLODI
Allergien: None known.
Vorherige Impfungen: -

VAERS 1757524

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: CA
Alter: 89,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 01.10.2021
Beginn: 02.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Abdominal discomfort Abdominal pain upper Asthenia Death Dizziness Aphasia Cardiac arrest Dysstasia Atrioventricular block complete Blood lactic acid Chest X-ray Computerised tomogram abdomen Cardiac pacemaker insertion Dialysis Feeling abnormal Electrocardiogram Full blood count Laboratory test

Symptomtext

On 10/1 she received a 3rd COVID-19 vaccination (Pfizer) in her left arm at a local pharmacy. About 3 hours after the shot she began to feel dizzy and dry heaves. She continued to feel unwell experiencing weakness, GI upset, myalgia, headache and stomachache. Her family contacted her doctor and about 18 hours after the shot she was taken to the Emergency Department. En route to the hospital, she became unresponsive in PEA arrest. At the ED she was found to be hypothermic, hypoglycemic and hyperkalemic. She was admitted to the intensive care unit and later diagnosed with aspiration pneumonia. She died in the hospital on 10/13/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 11,0
Labordaten: See medical records.
Aktuelle Erkrankungen: Hypertension, atherosclerotic and valvular heart disease, chronic heart failure, chronic kidney disease, type 2 diabetes mellitus, COPD
Vorgeschichte: Hypertension, atherosclerotic and valvular heart disease, chronic heart failure, chronic kidney disease, type 2 diabetes mellitus, COPD
Andere Medikamente: Bisoprolol (ZEBETA) 5 mg Oral Tab Bumetanide (Bumex) 0.5 mg Oral Tab Fluticasone-Salmeterol (Advair Diskus) 250-50 mcg/dose Inhl Disk w/devi Meprobamate (EQUANIL/MILTOWN) 400 mg Oral Tab Pantoprazole (PROTONIX) 20 mg Oral TBEC DR Tab amLODI
Allergien: None known.
Vorherige Impfungen: -

VAERS 2129257

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: AK
Alter: 71,0
Geschlecht: M
Eingang: 21.02.2022
Impfdatum: 13.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Cardiac arrest Cough Fatigue

Symptomtext

Patient got his booster on the 13th, per wife, patient was fatigued and coughing the day after the shot, on the 15th went into cardiac arrest

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: diabetes, hypertension
Andere Medikamente: amlodipine, aspirin, atorvastatin, gabapentin, glyburide, hydrochlorothiazide, losartan, metformin, metoprolol, sildenafil
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2104948

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 11.02.2022
Impfdatum: 22.10.2021
Beginn: 19.11.2021
Tage bis Beginn: 28,0
Dosis: 3
Route/Site: IM / RA

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

Cholecystectomy Cholecystitis Death Gastrointestinal haemorrhage Hepatic cancer metastatic Hepatic cirrhosis Pneumonia aspiration Procedural complication Varices oesophageal

Symptomtext

Patient admitted with cholecystitis (recent cholecystectomy with remnant remaining) s/p remnant removal with finding of new metastatic liver cancer and advanced cirrhosis. Hospital course further complicated by massive GIbleed from esophageal varices and aspiration pneumonia. ED visit, hospital admission, patient deceased. This visit was within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2102080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 10.02.2022
Impfdatum: 22.10.2021
Beginn: 16.11.2021
Tage bis Beginn: 25,0
Dosis: 3
Route/Site: IM / LA

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

Brain stem infarction Cerebrovascular accident

Symptomtext

Left pontine CVA. ED visit to hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2099742

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: MO
Alter: 96,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 09.10.2021
Beginn: 01.02.2022
Tage bis Beginn: 115,0
Dosis: 2
Route/Site: SYR / -

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

Bronchitis COVID-19 Chest scan Pulmonary embolism SARS-CoV-2 test positive

Symptomtext

SARS-COVID19PCR, NP (+) signs of COVID bronchitis bilateral pulmonary embolism dx'd during recent hospitalization

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 4,0
Labordaten: SARS COVID PCR; hospital assessment incl chest scans
Aktuelle Erkrankungen: none known
Vorgeschichte: none other than chronic sinus infections
Andere Medikamente: none reported at time of vaccination, although reports chronic sinus infections
Allergien: none known
Vorherige Impfungen: -

VAERS 2063238

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: CA
Alter: 61,0
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: 03.10.2021
Beginn: 07.12.2021
Tage bis Beginn: 65,0
Dosis: 2
Route/Site: IM / RA

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

Anticoagulant therapy Arthralgia Blood test normal Chest X-ray abnormal Computerised tomogram thorax abnormal Discomfort Dyspnoea Electrocardiogram normal Musculoskeletal chest pain Painful respiration Poor peripheral circulation Poor quality sleep Pulmonary embolism Pulmonary oedema Pulmonary thrombosis Ultrasound Doppler abnormal

Symptomtext

Experienced sharp pains in ribs area & up into shoulder (beginning Tues., Dec. 7, 2021) and started having difficulty / limited breathing. Thought I might have a rib "out." Saw chiropractor on Wed. (Dec. 8,), who made an adjustment. Felt a little better after appt. and that day. Next day (after night's sleep - (Didn't sleep well, due to discomfort a/breathing & pain - Could Not sleep on either side - Could only lay on back) - pain was much worse (next morning/day - Thurs., Dec. 9). Went to ER that afternoon. Had EKG (told it was fine), chest x-rays (showed liquid in left lung), bloodwork (told all were good), then chest CT scan (showed multiple blood clots/pulmonary embolisms in left lung). ER Dr. ordered Eliquis , to be taken as directed for at least 3-4 mos. , and told to follow up w/PCP. Dec. 14, '21 - Spoke w/PCP by phone - Dr. ordered add'l bloodwork (to check for Factor V, etc.) & ultrasound on both legs (ankles to pelvic) - He noted, there is no apparent cause for blood clots - No "smoking gun," per se. Dec. 15, '21 - Bloodwoork done - Results were all good - No problems (causes for clots) detected Dec. 17, '21 - Ultrasound(s) done on both legs - Showed (slightly?) slower blood flow on left leg (knee area?)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: See Item 18. Also....To be scheduled: Ultrasound in pelvic/abdomen area - (Advised by Dr. and PCP - Currently awaiting insurance approval
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic pain from old injuries
Andere Medikamente: Benazepril 20 mg (1/day), Simvastatin 40 mg (1/day), Terbinafine 250 (1/week), Tizanidine 4mg (prn), Eszopiclone 3mg (prn), Hydrocodone/APAP 10/325 (prn), Melatonin 5mg (prn), Tylenol Extra Strength (prn), Tylenol PM Extra Strength (prn)
Allergien: None known
Vorherige Impfungen: -

VAERS 2059319

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: KY
Alter: 95,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 05.10.2021
Beginn: 05.01.2022
Tage bis Beginn: 92,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Death

Symptomtext

Patient was fully vaccinated and boosted, developed COVID19 on 01/05/2022, and passed away on 01/12/2022. mortality review team is currently investigating this death to determine if it was COVID19 related.

Weitere VAERSDATA-Felder

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

VAERS 2043743

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: SD
Alter: 89,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 08.10.2021
Beginn: 25.12.2021
Tage bis Beginn: 78,0
Dosis: 3
Route/Site: SYR / UN

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

COVID-19 Death Fall General physical health deterioration SARS-CoV-2 test positive Surgery Vaccine breakthrough infection

Symptomtext

This is an instance of COVID-19 breakthrough disease after which death occurred. The individual was vaccinated on 01/27/2021, 02/17/2021, and 10/08/2021. The individual was admitted to hospital on 12/25/2021 for an emergency surgical procedure after a fall (the reason for admission and surgery were not related to COVID-19 or respiratory disease). They were transported via ambulance. It is not known if they experienced COVID-19 specific symptoms. They were found to be COVID-19 positive during the hospital stay. The positive specimen was collected on 12/25/2021. Their health declined rapidly during this hospital stay and they passed away on 12/26/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 1,0
Labordaten: Positive for COVID-19 via PCR despite being fully vaccinated.
Aktuelle Erkrankungen: Cardiopulmonary arrest, hypovolemic shock
Vorgeschichte: Hypertension, coronary artery disease, hyperlipidemia, hypothyroidism, gastroesophageal reflux disease
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2039576

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 17.01.2022
Impfdatum: 27.10.2021
Beginn: 21.11.2021
Tage bis Beginn: 25,0
Dosis: 2
Route/Site: IM / LA

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

Cor pulmonale acute Pulmonary embolism

Symptomtext

Acute pulmonary embolism with acute cor pulmonale. ED visit to hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1989856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: CO
Alter: 59,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Blood test Chest pain Computerised tomogram thorax abnormal Dyspnoea Fibrin D dimer increased Computerised tomogram Immunisation Pulmonary embolism Vaccination site pain Lymph node pain Pain in extremity Pulmonary thrombosis Scan with contrast abnormal

Symptomtext

Pulmonary Embolism; Upper left arm pain since the vaccine, not just at the site; 3rd Covid vaccine; This is a spontaneous report received from contactable reporter (Consumer). The reporter is the patient. A 59-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 21Oct2021 18:00 (Lot number: FF8841) at the age of 59 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine inact sag 4v (FLUCELVAX TETRA [INFLUENZA VACCINE INACT SAG 4V]), administered in arm right, administration date 18Oct2021 (Batch/Lot number: unknown) as dose 1, single for immunisation. Relevant medical history included: "breast cancer" (unspecified if ongoing), notes: breast cancer 4 years prior; "possible penicillin allergy" (unspecified if ongoing). Concomitant medication(s) included: ASPIRIN [ACETYLSALICYLIC ACID]; GABAPENTIN; LEVOTHYROXINE; LETROZOLE. Past drug history included: Neosporin, reaction(s): "Allergies: Neosporin"; Bacitracin, reaction(s): "Allergies: Bacitracin". Vaccination history included: Bnt162b2 (dose lot number: ER8732, dose administration time: 04:00PM , dose number: 2, vaccine location: Left arm), administration date: 01Apr2021, when the patient was 58 years old, for COVID-19 immunization; Bnt162b2 (dose lot number: EN6200, dose administration time: 11:00AM, dose number: 1, vaccine location: Left arm), administration date: 06Mar2021, when the patient was 58 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (life threatening) with onset 21Oct2021 18:00, outcome "unknown", described as "3rd Covid vaccine"; PULMONARY EMBOLISM (life threatening) with onset 22Oct2021 21:00, outcome "recovering", described as "Pulmonary Embolism"; VACCINATION SITE PAIN (life threatening) with onset 22Oct2021 21:00, outcome "recovering", described as "Upper left arm pain since the vaccine, not just at the site". The events "pulmonary embolism" and "upper left arm pain since the vaccine, not just at the site" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: computerised tomogram: pulmonary embolism. Therapeutic measures were taken as a result of pulmonary embolism including Eliquis for anticoagulation. About 27 hours after the 3rd Covid vaccine, the patient developed severe pain in her right chest. The following day this was confirmed by CT with contrast to be a pulmonary embolism. Additionally, the patient had upper left arm pain since the vaccine, not just at the site where the vaccine was given. The patient has no covid-19 prior vaccination has not been tested for covid-19 post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: Test Name: CT with contrast; Result Unstructured Data: Test Result:Pulmonary Embolism
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Breast cancer (breast cancer 4 years prior); Penicillin allergy
Andere Medikamente: ASPIRIN [ACETYLSALICYLIC ACID]; GABAPENTIN; LEVOTHYROXINE; LETROZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 1989856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: CO
Alter: 59,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Blood test Chest pain Computerised tomogram thorax abnormal Dyspnoea Fibrin D dimer increased Computerised tomogram Immunisation Pulmonary embolism Vaccination site pain Lymph node pain Pain in extremity Pulmonary thrombosis Scan with contrast abnormal

Symptomtext

Pulmonary Embolism; Upper left arm pain since the vaccine, not just at the site; 3rd Covid vaccine; This is a spontaneous report received from contactable reporter (Consumer). The reporter is the patient. A 59-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 21Oct2021 18:00 (Lot number: FF8841) at the age of 59 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine inact sag 4v (FLUCELVAX TETRA [INFLUENZA VACCINE INACT SAG 4V]), administered in arm right, administration date 18Oct2021 (Batch/Lot number: unknown) as dose 1, single for immunisation. Relevant medical history included: "breast cancer" (unspecified if ongoing), notes: breast cancer 4 years prior; "possible penicillin allergy" (unspecified if ongoing). Concomitant medication(s) included: ASPIRIN [ACETYLSALICYLIC ACID]; GABAPENTIN; LEVOTHYROXINE; LETROZOLE. Past drug history included: Neosporin, reaction(s): "Allergies: Neosporin"; Bacitracin, reaction(s): "Allergies: Bacitracin". Vaccination history included: Bnt162b2 (dose lot number: ER8732, dose administration time: 04:00PM , dose number: 2, vaccine location: Left arm), administration date: 01Apr2021, when the patient was 58 years old, for COVID-19 immunization; Bnt162b2 (dose lot number: EN6200, dose administration time: 11:00AM, dose number: 1, vaccine location: Left arm), administration date: 06Mar2021, when the patient was 58 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (life threatening) with onset 21Oct2021 18:00, outcome "unknown", described as "3rd Covid vaccine"; PULMONARY EMBOLISM (life threatening) with onset 22Oct2021 21:00, outcome "recovering", described as "Pulmonary Embolism"; VACCINATION SITE PAIN (life threatening) with onset 22Oct2021 21:00, outcome "recovering", described as "Upper left arm pain since the vaccine, not just at the site". The events "pulmonary embolism" and "upper left arm pain since the vaccine, not just at the site" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: computerised tomogram: pulmonary embolism. Therapeutic measures were taken as a result of pulmonary embolism including Eliquis for anticoagulation. About 27 hours after the 3rd Covid vaccine, the patient developed severe pain in her right chest. The following day this was confirmed by CT with contrast to be a pulmonary embolism. Additionally, the patient had upper left arm pain since the vaccine, not just at the site where the vaccine was given. The patient has no covid-19 prior vaccination has not been tested for covid-19 post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: Test Name: CT with contrast; Result Unstructured Data: Test Result:Pulmonary Embolism
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Breast cancer (breast cancer 4 years prior); Penicillin allergy
Andere Medikamente: ASPIRIN [ACETYLSALICYLIC ACID]; GABAPENTIN; LEVOTHYROXINE; LETROZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 1969099

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: FL
Alter: 61,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 17.10.2021
Beginn: 17.11.2021
Tage bis Beginn: 31,0
Dosis: UNK
Route/Site: IM / LA

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

Amnesia Angiogram cerebral abnormal Anticoagulant therapy Aphasia Arteriogram carotid abnormal Balance disorder Cerebral haemorrhage Cerebral thrombosis Computerised tomogram head abnormal Confusional state Dysarthria Echocardiogram Echocardiogram normal Ejection fraction normal Embolic stroke Facial paralysis Implantable cardiac monitor insertion Intensive care

Symptomtext

ADVERSE EVENT: PRT MCA Embolic Stroke (on 11/17/2021) RT small SAH (upon hospital discharge on 11/22/2021). TREATMENT: Received IV blood thinners and underwent thrombectomy. CT showed a small bleed. Monitored off antiplatelets and anticoagulants. CT was repeated. Underwent placement of loop recorder to monitor for any irregular rhythm of the heart. OUTCOME: After this stroke, I am experiencing memory loss and confusion. Still difficult to keep my balance. A detailed description of this life-threatening AE can be found on the "Continuation Page". A week prior to the AE I felt some palpitations...like tachycardia but didn't pay much attention to it. On 11/17/2021 (WEDNESDAY) Around 7:30 pm just before a board meeting at our community, my wife who was standing in front of me noticed how I abruptly lost my balance, leaning towards my left side. (This is seeing on the surveillance video camera of the clubhouse where the meeting was going to take place). She described me having slurred speech, left facial droop, left hand weakness and pale appearance. She sat me on a chair, took off my mask and immediately proceeded to have someone call 911. In the meantime, she continued to attend me, holding my head, asking me questions, and even tapping some cold water in my forehead and back of the neck. Close to 10 or 15 minutes, the paramedics (EMS) arrived. After a quick evaluation, they transported me as "stroke alert" (ASPHASIA) to the Hospital (Emergency Room). (Close to 20 minutes distance). A CTA head and neck was done which indeed showed a 5 mm clot in my brain. Alteplase was administered at 8:25 pm after consulting with us (me and my wife) the risks and benefits. We also consented to a mechanical thrombectomy. After this procedure I was then admitted to the ICU for a period of three days, where medical staff and personnel continued to run all kinds of tests including speech and memory therapy. Following days on the ICU unit included MRI, repeat CT brain which showed a small amount of subarachnoid hemorrhage. On Friday (11/29/2021) I was transferred to MICU to continue treatment as follows: On 11/19/2021 (FRIDAY) Underwent Transesophageal echo and an insertion of an implantable loop recorder was performed. (Which I will need to keep for approximately 3 years). Transferred to MICU. 11/20/2021 (SATURDAY) Still under observation. 11/21/2021 (SUNDAY) Still under observation. 11/22/2021 (MONDAY) Repeat CT brain. Small hemorrhage still present. 6 sessions of physical therapy and 6 visits from a registered nurse ordered upon hospital discharge. 12/06/2021 FOLLOW UP APPOINTMENT WITH NEUROSURGEON. Neurologically intact. MRI and non-contrast CT demonstrated a small amount of right sylvian petechial hemorrhage and right sylvian fissure subarachnoid hemorrhage asymptomatic. Cardiac Echo demonstrated no evidence of a right-to-left shunt and a normal ejection fraction. Loop recorder implanted-far no arrhythmias. Source of right middle cerebral artery thrombus is cryptogenic, although most likely cardiac, as the patient reported palpitations a few weeks earlier. PLAN: Continue Aspirin 81mg. Non-contrast CT of the brain in 1 month. Follow-up in neuro interventional clinic in 1 month.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: 5,0
Labordaten: I was hospitalized on the ICU and MICU for 5 consecutive days. A battery of tests were ran on a daily basis. 11/17/2021 to 11/22/2021. I have copies with results in detail, of every test and labs performed during my hospitalization. Please instruct me as to how and where to upload them for your evaluation.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Levothyroxine 25mg (1 tablet daily);Vitamin D (2,000 units)
Allergien: Shrimp
Vorherige Impfungen: -

VAERS 1936250

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: MO
Alter: 69,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 27.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / LA

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

Computerised tomogram thorax abnormal Dyspnoea Echocardiogram Fatigue Pulmonary embolism X-ray

Symptomtext

Approximately 5 days after vaccination patient became extremely fatigued and short of breath. Patient went to the local ER, and was transferred to a hospital with a high level of care where she was diagnosed with a pulmonary embolism. Per the patient, the hospital could not find a reason to explain the PE other than recent vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: X-rays, CT Scan to identify, Ultrasound of heart
Aktuelle Erkrankungen: None reported
Vorgeschichte: high blood pressure
Andere Medikamente: Nexium OTC, sartan blood pressure medication
Allergien: Pencillin, celebrex
Vorherige Impfungen: -

VAERS 1929539

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: NC
Alter: 79,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 11.10.2021
Beginn: 09.11.2021
Tage bis Beginn: 29,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Cardiac failure congestive Catheterisation cardiac normal Computerised tomogram thorax normal Dyspnoea Fibrin D dimer increased Myocardial infarction Pneumonia

Symptomtext

Had his booster on Oct 11,2021 . One Nov 9 he was taken by ambulance to Medical Center and diagnosed with a heart attack. He had an elevated D-Dime of 0.54 indicating clotting although a subsequent CT show no " detectable" clots. He was on a Heparin drip with three increase in dosages that we are aware of. It took 9 hours to get his vitals WNL, most notably his BP, HR and respirations. He was in the ER 4 days subsequently developing pneumonia and was admitted to the med surg unit for two additional days for a total of 6 days. He went home on oral antibiotics. Then on Dec 2 at approximately 4 am, with c/o shortness of breath, he was transported by ambulance again to and diagnosed with Congestive Heart Failure. He was on a heparin drip again. He underwent a heart catherization on Dec 3, 2021 that showed no new damage and has now been placed on two additional medications, Lasix and Potassium with an increase in his Metoprolol from 25 mg daily to 50 mg daily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 9,0
Labordaten: See note above
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1909307

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: NJ
Alter: 73,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 27.10.2021
Beginn: 16.11.2021
Tage bis Beginn: 20,0
Dosis: 3
Route/Site: IM / LA

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

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

Symptomtext

I am the epidemiologist reporting on behalf of 73-year-old male LTCF patient. The patient received their first dose of the Pfizer vaccine on 1/06/21. The patient tested positive for COVID-19 on 1/26/21 via PCR (20 days post dose 1). The patient received their second dose of the Pfizer vaccine on 5/26/21 and their third dose of the Pfizer vaccine on 10/27/21. The patient tested positive for COVID-19 a second time via PCR on 11/16/21. On 11/27/21 (one-month post dose-3 and 11 days post positive test) the patient expired (listed as COVID-19 death). The cause of death listed on the death certificate is atherosclerosis (3 years). Known patient history includes cardiovascular disease. This is the first instance I have observed within my home county of a person with a repeat infection, fully vaccinated + boosted, passing away with COVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: +PCR Covid 11/16/2021
Aktuelle Erkrankungen: Cardiovascular Disease (Known)
Vorgeschichte: Cardiovascular Disease (Known)
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1901949

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: VA
Alter: 71,0
Geschlecht: M
Eingang: 26.11.2021
Impfdatum: 20.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / -

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

Abdominal pain lower Anticoagulant therapy Atelectasis Bronchogram abnormal Computerised tomogram abdomen abnormal Computerised tomogram thorax Flank pain Lung infiltration Lung opacity Musculoskeletal pain Oedema peripheral Pain Painful respiration Pleural effusion Pulmonary embolism Scan with contrast abnormal

Symptomtext

Patient is a 71 y.o. male who presents to the ED with complaint of moderate left flank pain. Dull. Has been going on for a few of days. He thought he might have a kidney stone although he has no history of kidney stones. He walked in. Pain radiates down to his left lower quadrant. He is also had some pain in his left shoulder blade. Denies fevers cough or shortness of breath. It does hurt when he takes of breath. Has been vaccinated for Covid including the booster. He reports a little bit of bilateral leg edema. No real calf tenderness. He is not had any hematuria. He was getting an outpatient CT but was going to have to wait 48 hours to get 1 and the pain was becoming too much and nagging. Diagnosis of bilateral pulmonary embolism. treated with one dose of lovenox. eliquis 5mg Take 2 pills bid for 7 days and then 1 pill bid for 30 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 1,0
Labordaten: Radiologic Studies CT Angiogram Chest (PE) Result Date: 11/1/2021 1. Positive examination for pulmonary embolus; left greater than right. No associated right heart strain. Associated left lower lobe atelectasis/airspace disease with small left effusion. Right lung is clear. No mediastinal adenopathy. Mild wall thickening of the esophagus. 2. No acute abnormality seen in the upper abdomen. 3. Findings called to Dr. in the ED 11/1/2021, 8:10 PM. CT Abdomen Pelvis with IV Cont Result Date: 11/1/2021 1. Left lower lobe consolidative infiltrate and or atelectasis with a few air bronchograms, and hazy surrounding groundglass infiltrate. Small left pleural effusion. 2. No acute findings in the abdomen or pelvis. Recommendations: None.
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension
Andere Medikamente: valsartan-hydrochlorothiazide 320-25mg once daily
Allergien: -
Vorherige Impfungen: -

VAERS 1885663

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: -
Alter: 66,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 25.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 4,0
Dosis: UNK
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Epistaxis Pneumonia

Symptomtext

J18.9 - Pneumonia, unspecified organism J96.01 - Acute respiratory failure with hypoxia N17.9 - Acute kidney failure, unspecified R04.0 - Epistaxis

Weitere VAERSDATA-Felder

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

VAERS 1885363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 19.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 6,0
Dosis: UNK
Route/Site: - / -

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

Death Disseminated intravascular coagulation

Symptomtext

death- Disseminated intravascular coagulation (defibrination syndrome)

Weitere VAERSDATA-Felder

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

VAERS 1884233

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: MA
Alter: 46,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 15.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Chills Immunisation Near death experience Syncope Vomiting

Symptomtext

Fainted after booster.; Chills after booster; Throwing up after booster; Booster; Caller states booster almost killed him.; This is a spontaneous report from a contactable consumer (patient). A 46-year-old male patient received bnt162b2 (PFIZER BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: FF8841), via an unspecified route of administration, administered in left shoulder, on 15Oct2021 (at age of 46-year-old) as dose 3 (booster), single for covid-19 immunization. The patient medical history and concomitant medications were not reported. Historical vaccine included first dose of bnt162b2 (PFIZER BIONTECH COVID-19 VACCINE, Batch/Lot Number: EL9766), on 08Mar2021 and second dose of bnt162b2 (PFIZER BIONTECH COVID-19 VACCINE, Batch/Lot Number: EN6203), on 29Mar2021, both were received via an unspecified route of administration, administered in left shoulder (at age of 45-year-old) as dose 1 and dose 2, single for covid-19 immunization. On 15Oct2021, the patient had booster; on 16Oct2021, the patient experienced throwing up after booster; on 18Oct2021, the patient had fainted after booster, chills after booster. Caller also stated that booster almost killed him on an unknown date in Oct2021. Events fainted after booster, chills after booster, throwing up after booster, caller states booster almost killed him resulted in physician office visit. On 17Oct2021, the outcome of the event throwing up after booster was recovered. On 18Oct2021, the outcome of events fainted after booster, chills after booster were recovered. The outcome of events booster almost killed him and booster were unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Near death experience
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1873551

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: CO
Alter: 67,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 13.10.2021
Beginn: 12.11.2021
Tage bis Beginn: 30,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain lower Blood urine present Cardio-respiratory arrest General physical condition abnormal Pain Pelvic pain Resuscitation Tremor

Symptomtext

He experienced a change of condition on 11/12/21 with frank bleeding in catheter bag, pain in LLQ and worsening tremor. He reported feeling achy all over and pain in left pelvic area. The resident had a telehealth visit in the nursing home with the PA. His blood pressure was 153/99. He pending transfer to ER when his vital signs ceased and he was unable to be resuscitated with CPR.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: -
Labordaten: None- the vital signs ceased prior to transfer to ER
Aktuelle Erkrankungen: Patient was a 67 yo who admitted to nursing home on 8/4/2021. He was being treated for Parkinson's Disease, Reiter's syndrome, and incarcerated inguinal hernia. He had an indwelling foley catheter d/t urinary retention d/t BPH.
Vorgeschichte: Multiple myeloma in remission, hyperlipidemia, diverticulitis, GERD, depression, anxiety, irritable bowel syndrome
Andere Medikamente: Atorvastatin Calcium Tablet 40 MG, Azilect Tablet 1 MG, buPROPion HBr ER Tablet Extended Release 300 mg, Cholecalciferol Tablet 25 MCG, Esomeprazole Magnesium Tablet Delayed Release 20 MG, Furosemide Tablet 20 MG, Linzess Capsule 290 MCG, M
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 1867925

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: IL
Alter: 46,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 25.10.2021
Beginn: 02.11.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: SYR / LA

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

Angiogram pulmonary abnormal Blood magnesium Blood test Cardiac stress test Chest pain Dyspnoea Echocardiogram Metabolic function test Palpitations Pericarditis Pulmonary embolism Troponin

Symptomtext

Chest pains, shortness of breath, and heart palpitations began and were off and on. Symptoms gradually worsened. Shortness of breath was most pronounced symptom. Unable to lay back and it was easier to breathe when leaning forward. Went to the ER on 11/10/21. Chest Ct scan was normal and was released. Symptoms worsened and returned to ER 11/12/21. I was admitted. Cardiologist thought symptoms fell in line with pericarditis. Blood work, stress test, and echocardiogram ruled out everything else. I was given colchicine. Symptoms improved and I was released on 11/13/21. Treatment is to continue colchicine for one week and follow up with cardiologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: CTA chest pulm embolism w/ contrast?11/10/21 Comprehensive metabolic panel, 11/10/21, 11/12/21 Troponin, 11/12/21 Magnesium, 11/12/21 Multiple other lab work Stress test, 11/13/21 Echocardiogram, 11/13/21
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism, ADHD, Mitral Valve Prolapse, hypertension, GERD, kidney stones (hypocitraturia), mild fatty liver disease
Andere Medikamente: Adderrall, Hydrochlorothiazide, Levothyroxine, Losartan, Omeprazole, Potassium Citrate, Vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 1857371

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: KY
Alter: 57,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 15.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / RA

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

Cough Death Sputum increased

Symptomtext

Patient developed a cough with increase sputum production that lasted over several days starting approximately 10/22 and patient died on 10/28/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: End Stage Renal Disease requiring dialysis
Vorgeschichte: ESRD, Tracheostomy, GERD, Hyperlipidemia,
Andere Medikamente: Trazodone 150mg QHS, Famotidine 10mg QD, Hydralazine HCL 50mg BID, fluticasone propionate 50mcg/act, incruse ellipta 62.5 MCG, Nephrovite 0.8mg QD, Bupropion HCL 75mg BID, Loratadine 10mg QD, Ergocalciferol 1.25mg QWED, Metorpolol tartrate
Allergien: Aspirin
Vorherige Impfungen: -

VAERS 1850726

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: NY
Alter: 53,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 19.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: IM / AR

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

Aphasia Headache Mobility decreased Myocardial infarction Pain Resuscitation

Symptomtext

Headache, body aches, complained about not being able to get out of bed, couldn't talk, suffered heart attack.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: Epi pen, CPR- unsuccessful
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1850483

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

kritisch

Staat: FL
Alter: 51,0
Geschlecht: F
Eingang: 08.11.2021
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: nein

Chills Dyspnoea Feeling abnormal Hypopnoea Impaired work ability Malaise Pallor Pyrexia Respiratory arrest

Symptomtext

Patient participated in our Booster Clinic Wednesday 11/3/21. Thursday morning she called out due to not feeling well since the Booster has been administered and has not worked since. She stated she felt terrible all weekend with a fever and chills. The employee came to work this am; however, we had to send her out 911 this morning due to SOB, pale, shallow respirations (so shallow we couldn?t see her chest rise), she was luckily easy to arouse and was able to communicate to us she was a full code and remained alert until the ambulance came.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 1842222

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: FL
Alter: 79,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Choking Feeling abnormal Illness Joint range of motion decreased Malaise Near death experience Pain Productive cough Pruritus Rhinorrhoea

Symptomtext

feeling like she thought she was going to die; sick for 6 days, it was awful; she couldn't come to herself; producing so much phlegm she choked when speaking; body aches; running nose; did not feel well; trouble lifting her arm from so much pain; producing so much phlegm she choked when speaking; itching; This is a spontaneous report from a contactable consumer (patient). A 79-year-old female patient received BNT162B2 (COMIRNATY, Batch/Lot number was not reported), via an unspecified route of administration, administered in left arm on 14Oct2021 (at 79-year-old) as dose 3 (booster), single for COVID-19 immunisation. Medical history included allergic to a lot of things and patient didn't take medications because she was allergic to it. The patient's concomitant medications were not reported. The patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose1 and dose 2, both via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as single dose for COVID-19 immunization. The patient reported feeling like she thought she was going to die on an unspecified date and several adverse events after the dose on 14Oct2021 including: running nose, body aches, trouble lifting her arm from so much pain, producing so much phlegm she choked when speaking, and itching. She did not feel well for six days and has taken cold/flu medications to help. She was not too thrilled about it. She asked if these symptoms have been reported before. She took the Pfizer 1 and 2 shot no problem and took the booster and she thought she was going to die. 3 hours later her nose was running, her body was aching, when she tried to speak she was choking on so much phlegm. She was sick for 6 days, it was awful. She knew people that have taken it without any effects but for some reason she did. She wound up having itching since she took the shot and went to her dermatologist. She was allergic to a lot of things and they didn't ask questions or say they need to know anything about anything. She didn't know if she would take another one, it was like 6 days like that and she couldn't come to herself. She couldn't lift her arm to put on clothes she was in so much pain, it was weird. Patient thought it must be something in the shot. She said this was 6 days. She took some medication to try to ward it off and that took time and she was getting better and better. She was fine before the vaccine and was sick as a dog after. Her neighbor has been checking on her and she talked to her doctor and he told her to take cold and flu medication and that helped. Other than for itching her doctor gave her some allergy pills, she tooke allergy pills every day but he gave her something else for morning and evening. She didn't like to take medications, vitamins were ok. The outcome of the events was recovering. The lot number for BNT162B2, was not provided and will be requested during follow up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Near death experience
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy (patient didn't take medications because she was allergic to it); Drug allergy (patient didn't take medications because she was allergic to it)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1828865

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

kritisch

Staat: NY
Alter: 63,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 16.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Angiogram Cerebrovascular accident Chills Computerised tomogram head Dysarthria Malaise Echocardiogram Fatigue Magnetic resonance imaging head abnormal Muscular weakness Scan with contrast abnormal

Symptomtext

Received the Pfizer booster on 10/16/21. Experienced chills and fatigue on 10/17/21. On 10/18/21 at 6:45am she woke up and had L hand weakness, slurred speech. Last known well was at 4am that morning. Symptoms persisted and she presented to the hospital that same day where MRI brain w/wo demonstrated a small right frontal cortical stroke. She was admitted for 2 days and discharged home after completing stroke workup. She recovered completely from symptoms by the time I met her on 10/25/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 2,0
Labordaten: MRI brain w/wo contrast - 10/18/21 echocardiogram - between 10/18-10/20 (unknown). CT angiogram head and neck - 10/18/21 CT head - 10/18/21
Aktuelle Erkrankungen: Squamous Cell Carcinoma Marginal Zone Lymphoma
Vorgeschichte: Hyperlipidemia
Andere Medikamente: 1. acetaminophen (tylenol Extra Strength) 500 Mg Tablet,Take 2 tablets by mouth Every 6 Hours As Needed for Pain. Indications: Pain 2. Ascorbic Acid (vitamin C) 100 Mg Tablet, 3. aspirin 81 Mg Tablet Delayed Release,Take 81 mg by mouth Dail
Allergien: None
Vorherige Impfungen: -

VAERS 1828993

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: IN
Alter: 89,0
Geschlecht: M
Eingang: 29.10.2021
Impfdatum: 13.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

Resident passed away on 10/17/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: Prostate Cancer, Old MI, HTN ,GOUT, Hyperlipidemia
Vorgeschichte: Dementia
Andere Medikamente: cloNIDine HCl Tablet 0.1 MG Vitamin D3 Tablet ,Centrum Silver Tablet ,Fish Oil Capsule 1200 MG ,Valsartan Tablet 160 MG,hydrALAZINE HCl Tablet 50 MG,Carvedilol Tablet 12.5 MG,Atorvastatin Calcium Tablet 20 MG ,ARIPiprazole Tablet 2 MG,AmLOD
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1814957

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: NC
Alter: 90,0
Geschlecht: M
Eingang: 25.10.2021
Impfdatum: 20.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / RA

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

Cerebrovascular accident Death

Symptomtext

The patient died of a stroke 5 days after receiving the COVID-19, he was very old and it is unknown what other medical conditions they he had.

Weitere VAERSDATA-Felder

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

VAERS 1804391

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

kritisch

Staat: OH
Alter: 56,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 23.09.2021
Beginn: 14.10.2021
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: IM / RA

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

Angiogram pulmonary abnormal Back pain Cardiac arrest Cardiac massage Catheterisation cardiac abnormal Computerised tomogram abdomen abnormal Computerised tomogram thorax abnormal Coronary artery bypass Cough Death Deep vein thrombosis Dizziness Dyspnoea Fibrin D dimer increased Intensive care Myocardial injury Oedema Pain in extremity

Symptomtext

10/20/21 1610 patient comes into ED complaining for the past several days has had increasing shortness of breath mild cough back pain. She has had lightheaded episodes. Increasing leg pain after which she describes as possible fall. No head injury. No nausea no vomiting. No cough no hemoptysis. On arrival in the ED her room air pulse ox was between 85 and 88%. Pulse rate was 120s. Respiratory rate was in the 30 range. Lungs were clear soft nontender right extremity has some tenderness in the calf and medial thigh. Mild edema neuro intact. Patient states she had her second Pfizer vaccine on Wednesday. Symptoms started on Monday of gotten worse. Admitted for bilateral PE and right leg DVT. 10/21/21 AM taken to cath lab for pulmonary angiogram with measurement of central venous pressures, mechanical thrombectomy. Cardiac arrest at 0630 10/21/21 in cath lab during procedure. CPR performed for 45 minutes and while being transported to OR for emergent CABG. 10/21/21 1000 patient arrived to ICU with chest still cracked open and physician providing cardiac massage. Time of death called at 1005 10/21/21.

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Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 1,0
Labordaten: Dopplar US- right leg dVT ABD/PELVIS CT- Right heart strain Chest CTA- bilateral PEs DDIMER 10/20/21 13470 Platelets 10/20/21 237, 10/21/21 24
Aktuelle Erkrankungen: none that we are aware of
Vorgeschichte: copd, scoliosis, arthritis, hyperthyroid, bradycardia, tachycardia, thyrotoxicosis
Andere Medikamente: omeprazole, montelukast, methimazole, fluticasone, cyclosporine, cholecalciferol, cetrizine, nicotine, naproxen, albuterol, proventil
Allergien: gabapentin, quetiapine, acetaminophen, aspirin, caffeine, morphine, penicillin, pentazocine, propoxyphene
Vorherige Impfungen: -

VAERS 1797927

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: MA
Alter: 74,0
Geschlecht: M
Eingang: 19.10.2021
Impfdatum: 12.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / -

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

Death Hypotension Hypoxia Lethargy Muscular weakness Pyrexia

Symptomtext

Patient lived in a nursing home. The following was reported to our on-call MD. Nurse from home called to report Pt is lethargic. BP this morning 139/57, HR60. BP now 86/42. O2 sats RA 85-86%; O2 @ 1.5L applied and sats went up to 95%, temp 99.4. Pt had covid booster on 10/12/2021. At around 1:40pm, nurse found him very lethargy, can't lift his arms but responding and able to talk. He was hypotensive and hypoxia with low grade fever. He is DNR/DNI/DNH. Ambulance was called, while trying to get hold of HCP. At ~2:25pm, Patient passed away.

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: dementia bipolar disease
Vorgeschichte: dyslipidemia anxiety disorder HTN GERD DM CKD Stage 3a
Andere Medikamente: aspirin atenolol clonazepam escitalopram gabapentin geodon lipitor lisinopril mag oxide melatonin metformin omeprazole trazodone tylenol Vit D3
Allergien: rosuvastatin, linezolid, donepezil, codeine, pencillin, sulfa
Vorherige Impfungen: -

VAERS 1794122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: VT
Alter: 69,0
Geschlecht: M
Eingang: 17.10.2021
Impfdatum: 11.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RA

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

Acute respiratory failure

Symptomtext

Acute Hypoxic Respiratory Failure. Patient is still admitted to hospital

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, DM II, Prostate CA (remission), gout, hypercoagulable state
Andere Medikamente: Torsemide, metformin, cozaar, asa, Lipitor, gabapentin
Allergien: NKA
Vorherige Impfungen: -

VAERS 1771794

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

kritisch

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 08.10.2021
Impfdatum: 29.09.2021
Beginn: 02.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Computerised tomogram abnormal Dyspnoea Pulmonary embolism

Symptomtext

I experienced extreme SOB 10/02/2021. I went to hospital (Unknown Hospital), had multiple pulmonary emboli in my lungs. I never had history of that before. I was hospitalized form 10/02/2021 to 10/04/2021 and I am now on blood thinner medication. I had a chest CT scan. I am in the process of recovering.

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: CT scan of the chest; pulmonary emboli in my lungs.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Routine medication- Synthroid medication
Allergien: Minocycline
Vorherige Impfungen: -

VAERS 2629020

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 09.05.2023
Impfdatum: 19.09.2021
Beginn: 20.09.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Condition aggravated Confusional state Diarrhoea Fatigue Laboratory test Migraine Nausea Postural orthostatic tachycardia syndrome Seizure Small fibre neuropathy

Symptomtext

Nausea, diarrhea, migraine, extreme fatigue, weakness, POTS, Small fiber neuropathy, confusion, seizure, etc

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Praegender Schweregrund: Seizure
Hospital-Tage: 3,0
Labordaten: Too many to list
Aktuelle Erkrankungen: Migraines
Vorgeschichte: Migraines
Andere Medikamente: Sertraline
Allergien: Raw seeded pitted fruit, tree nuts, seasonal, bengay
Vorherige Impfungen: -

VAERS 2621424

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: -
Alter: 41,0
Geschlecht: F
Eingang: 26.04.2023
Impfdatum: 12.10.2021
Beginn: 28.11.2021
Tage bis Beginn: 47,0
Dosis: 2
Route/Site: IM / -

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

Epilepsy Generalised tonic-clonic seizure Status epilepticus

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE COMPLEX PARTIAL EPILEPSY W SECONDARY GENERALIZATION EPILEPSY, GENERALIZED CONVULSIVE, INTRACTABLE EPILEPSY, UNSPECIFIED

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Praegender Schweregrund: Generalised tonic-clonic seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2559199

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: OH
Alter: 69,0
Geschlecht: M
Eingang: 12.01.2023
Impfdatum: 11.02.2021
Beginn: 01.05.2021
Tage bis Beginn: 79,0
Dosis: 3
Route/Site: SYR / LA

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

Cardiac electrophysiologic study Cardiac flutter Cardiac monitoring Cardiac stress test Echocardiogram Electrocardiogram Implantable cardiac monitor insertion Magnetic resonance imaging heart Myocarditis Ventricular tachycardia

Symptomtext

Spring / summer of 2021 after first vaccine doses, started noticing occasional chest flutters. After many tests including a heart mri at facility, myocarditis was identified as possible / probable cause. Started on metoprolol 12.5 mg daily June 2022 - 3 days after receiving the 4th covid vaccine, I experienced a Ventricular Tachycardia event. An study was performed at Hospital in July 2022 and a specific reason for the VT was not identified. I had an ICM implanted and have not experienced any further cardiac events. Background I have CLL and started being treated with Acalabrutinib about the same time the initial heart flutters were felt (spring/summer 2021). Both Acalabrutinib and Covid vax are possible causes. Numerous tests - EKG, echocardiogram (hospital), heart mri and stress test. After MRI, cardiologist diagnosed as myocarditis and Rx metoprolol. In fall of 2021, I switched from Acalabrutinib into a clinical trial for an experiment BTK inhibitor LP-168. for my CLL. Dr is my oncologist and most familiar with this entire situation. In spring of 2022, I experienced some dizziness clinical trial personnel ordered a heart holster to determine if I was having any heart rhythm problems. A couple days into wearing this holster (6/13/22) , a VT event was recorded early in the morning when I was asleep. i did not notice anything. The EV event lasted 19 sec with a max heart rate of 157 and resolved itself. The VT occurred 3 days after having received the 4th Covid vax dose. Despite an study, the exact cause of the VT event has not been determined. There was no apparent permanent heart wiring issues from the study. It is not clear if the heart issues (myocarditis and VT event) were caused by the covid vax or something else. Some other factors which may be relevant: - I have a farm and am quite active outside in spring. It is possible I was experiencing some dehydration which was causing the dizziness and may have caused the VT. I try to drink lots of water but it had been purified bottled water. After discussion with my Drs, I started drinking Smart Water which has some of the essential nutrients added. When I started using Smart Water, the dizziness decreased. I am not sure if I started drinking the Smart Water before or after the VT event. - As noted, I have been taking an experimental BTK inhibitor LP-168 for my CLL. There had not been any issues with heart rhythm with this drug but to be cautious, I discontinued using it until the study could not identify any cause. My oncologist did not believe the LP-168 caused the issue and I restarted the drug. I also had an ICM implanted to monitor my heart rhythm. 6+ months later, there have not been any VT or other cardiac events recorded. - The VT event occurred at night when I was asleep. Earlier in the day, I was cleaning an area under a cracked shower pan which had become moldy. I was exposed to the mold and to an anti-mold agent. - I have sleep apnea and use a CPAP. My CPAP reports do not show any significant abnormal events on the day of the VT. - I have a lot of sinus congestion issues and routinely go to sleep with a Halls cough drop in my mouth. I don't know that I did but it is possible that I choked momentarily on the cough drop. - Throughout the night, I change sleeping positions several times - back, right side, left side. Other conditions and drugs: I am 71, obese, have several chronic conditions - OSA, high blood pressure, cholestrol. I take various medications to address the issues above. These include: Mucinex, Flonase (50 mcg), azelastine .15% nasal spray to address sinus congestion lisinopril 20 mg (blood pressure) lovastatin 20 mg (cholesterol) levothyrozine 50 mg (throid) valtrex 500 MG (shingles prevention) LP-168 100 mg (cll clinical trial med) metoprolol 25 mg (heart) sildenafil 50 mg (rarely used and don't remember using it during any of the events) I listed all of the covid vaccine doses above. Dates of each dose are as follows: Dose 1 - 2/11/21 Dose 2 - 3/4/21 Dose 3 - 10/1/21 Dose 4 - 6/10/22 (VT event occurred 3 days later) I participated in an study to determine antibodies created by the covid vax. I tested after the first 3 doses and did not record any antibodies. It is difficult to say definitively that the covid vax caused my cardiac issues but it is certainly one of the possible causes.

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Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: EKG, echo cardiogram, heart mri, stress test, heart monitor, study
Aktuelle Erkrankungen: -
Vorgeschichte: cll, high blood pressure, cholesterol, obstructive sleep apnea, obesity, chronic sinus congestion
Andere Medikamente: Mucinex, Flonase (50 mcg), azelastine .15% nasal spray to address sinus congestion lisinopril 20 mg (blood pressure) lovastatin 20 mg (cholesterol) levothyrozine 50 mg (throid) valtrex 500 MG (shingles prevention) LP-168 100 mg (cll clinica
Allergien: none
Vorherige Impfungen: -

VAERS 2539103

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 21.12.2022
Impfdatum: 06.02.2021
Beginn: 05.10.2022
Tage bis Beginn: 606,0
Dosis: 3
Route/Site: - / -

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

Anticoagulant therapy Atrial fibrillation COVID-19 Cardioversion Imaging procedure abnormal Intensive care Peripheral artery stenosis SARS-CoV-2 test positive Surgery

Symptomtext

This is a 75y.o. female with history of PAD with difficulty ambulating who presented on 10/5/2022 for surgery. Findings on imaging consistent with left popliteal artery stenosis. Pt underwent procedure listed above which they tolerated well without complication, see operative report for full details. She went into afib with RVR in the PACU requiring ICU admission. She was started on a cardizem gtt and converted to NSR. She was then started on a heparin gtt and transitioned to Eliquis. Patient recovered well. Hospital course significant for afib with RVR.

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Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: 10/5 SARS-CoV-2 -COVID-19 by NAA, Micro -- detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2501859

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: NY
Alter: 81,0
Geschlecht: M
Eingang: 08.11.2022
Impfdatum: 03.05.2022
Beginn: 17.05.2022
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / -

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

Acute kidney injury Angiogram Aortic aneurysm Blood creatinine normal Blood sodium increased Body temperature increased COVID-19 Computerised tomogram head normal Computerised tomogram thorax abnormal Glomerular filtration rate decreased Haemorrhage Intensive care Pneumonia SARS-CoV-2 test positive Sepsis Serum ferritin increased Staphylococcus test negative Unresponsive to stimuli

Symptomtext

5/17/2022-Presents to ED from NH, new onset unresponsiveness. Covid + on 5/7/2022-EGFR-37. WBC-13. Ferritin 626.0. 101.5 temp. Spo2 98% on 3L nc. CT head neg for subacute intracranial abnormality. CT chest-right sided PNA and AAA 6.3 cm with some wall hemorrhage, CTA bad/pelvis. Sepsis s/t r sided pna with covid infection , concern of aspiration. Ordered baricitinib , vanco, cefepime and Flagyl. Renally adjusted Decadron. 5/19/2022- D/C vanco MRSA swab neg. NA went up to 152, swithced to D5. Vascular surgery in contact with family regarding endovascular repair likely oupatient. VSS Afebrile. 5/20/2022-BP-166/111 prn hydralazine 10 given, Labetalol 5mg prn ordered, Transferred to cardiovascular ICU gtt @2L. 5/20/-2022- AKIl likely prerenal , resolving. Cont cleviprezx and titrate down, hydralazine 5mg Q6. Continue Flagy, baricitinib and decadron. 5/21/2022- Restart clonidine patch, Toprol daily. Stop hydralazine. VSS BP-115/69. Downgraded to Med/surg. 5/24/2022- Creatnine 1.2. VSS. maintain of RA. 5/25/2022- D/C to sub acute rehab. Nephro follow up. Finished Flagyl, cefepime and baricitnib.

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Praegender Schweregrund: Intensive care
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Dementia, CVA with residual L sided hemiparesis, CAD postPCI, A fib. HTN. HLD,
Andere Medikamente: -
Allergien: Diclofenac Sodium Diclofenac-misoprotsol, lisinopril-hydrochlo; misopristol
Vorherige Impfungen: -

VAERS 2475809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: AK
Alter: 16,0
Geschlecht: M
Eingang: 11.10.2022
Impfdatum: 07.12.2021
Beginn: 10.09.2022
Tage bis Beginn: 277,0
Dosis: 2
Route/Site: IM / LA

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

Blood glucose increased Glycosylated haemoglobin increased Intensive care Type 1 diabetes mellitus

Symptomtext

Developed Typed 1 diabetes with no known family history from either parent. Health prior to presenting was excellent with no adverse habits.

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Praegender Schweregrund: Intensive care
Hospital-Tage: 4,0
Labordaten: Initial diagnosis by Doctors aboard After treatment in ICU to stabilize he was released Daily injections of Humalog and Semglee are required to maintain proper glucose levels.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: All penicillin medications
Vorherige Impfungen: -

VAERS 2471959

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: MD
Alter: 76,0
Geschlecht: F
Eingang: 07.10.2022
Impfdatum: 22.06.2022
Beginn: 08.09.2022
Tage bis Beginn: 78,0
Dosis: 3
Route/Site: IM / LA

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

Blood homocysteine Blood magnesium Blood phosphorus Blood thyroid stimulating hormone Coagulation test Drug screen Glycosylated haemoglobin Intensive care Laboratory test Lipids Metabolic function test Respiratory viral panel SARS-CoV-2 test Subdural haemorrhage Toxicologic test Treponema test Urine analysis Vitamin B1

Symptomtext

I incurred Subdural Hemerage, I was in ICU

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Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: I had a metobolic pannel, I also cvcw, disc, Also had drug/tox screen, Hemoglobin A1c, Homocysteine, lipid panel, magnesium, phosphorus, Rapid plasma reagin, thyroid simulating hormones, unranalsysis pannel vitamin B1 and vitamin B!2, Covid Star/cov2, respitory panned Aids test coagulation panel.
Aktuelle Erkrankungen: None
Vorgeschichte: Controlled High blood pressure
Andere Medikamente: Crestar: Hydrochlorothiazide: Calcium:Vitamin D: Asprin:Estradiol
Allergien: None
Vorherige Impfungen: -

VAERS 2468823

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: MI
Alter: 48,0
Geschlecht: F
Eingang: 04.10.2022
Impfdatum: 02.10.2021
Beginn: 01.03.2022
Tage bis Beginn: 150,0
Dosis: 3
Route/Site: IM / AR

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

Anticoagulant therapy Blood test abnormal Deep vein thrombosis Factor II mutation Gene mutation identification test positive General physical condition abnormal Hypertension Non-alcoholic fatty liver Pain in extremity Ultrasound Doppler abnormal

Symptomtext

I started to have issues with my blood pressure in March of 2022. It was crazy high. It was I went to an urgent care and my blood pressure was 200/94. I was advised to go home and rest and stop taking ibuprofen and to follow up with my doctor. My doctor scheduled me an appointment to come in and I did on March 02, 2022. I was prescribed blood pressure medicine amlodipine. I also was diagnosed with non-alcoholic fatty liver during an annual exam in November 03, 2021. This was discovered through an annual blood panel. I was diagnosed with DVT-Deep Vein Thrombosis. I went to my doctor on July 8 because my knee was still bothering me. They did ultrasound on my knee and everything came back normal. Then on August 30, 2022 my knee was better but it was weird in appearance like kankles. I had another ultrasound and was diagnosed with DVT. I was placed on blood thinners XARELTO and advised to exercise more. I no longer have the pain in my foot. I was also Heterozygous prothrombin gene mutation G20210A. I am currently awaiting follow up from my provider regarding what this means. I am no longer having the issues with my blood pressure since being placed on the amlodipine. The last check was 128/78. I am required to take the blood thinners for 6 months and be re-evaluated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Blood panel March 02, 2022. Ultrasound 09/09/2022 diagnosed with DVT. Blood panel 09/14/2022 Heterozygous prothrombin gene mutation G20210A.
Aktuelle Erkrankungen: N/A
Vorgeschichte: PCOS; Hashimoto's Thyroiditis
Andere Medikamente: Vitamin D; women's ONE A DAY; cetirizine; levothyroxine; bupropion XL; MIRENA
Allergien: Seasonal allergies
Vorherige Impfungen: -

VAERS 2408639

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: NM
Alter: 62,0
Geschlecht: M
Eingang: 11.08.2022
Impfdatum: 29.04.2022
Beginn: 20.06.2022
Tage bis Beginn: 52,0
Dosis: 3
Route/Site: SYR / LA

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

Eyelid ptosis Facial paralysis Visual impairment

Symptomtext

Right Hand eye lid began drooping on 20Jun2022 adversely affecting my eyesight. Consulted my primary doctor at earliest opportunity on 24Jun2022. My primary Doctor referred me to an ophthalmologist which I visited on 12Jul2022. I am now awaiting my appointment to the eyelid surgical ophthalmologist which the earliest I could get was 29Sep2022.

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Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: Initial results indicated Ptosis of the right eyelid.
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure
Andere Medikamente: Valsartan 320mg, Atorvastatin 40mg, Amlodipine Besylate 5mg, Multi Vitamin , Allegra
Allergien: Cats
Vorherige Impfungen: -

VAERS 2344661

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: VA
Alter: 50,0
Geschlecht: F
Eingang: 30.06.2022
Impfdatum: 04.11.2021
Beginn: 05.04.2022
Tage bis Beginn: 152,0
Dosis: 3
Route/Site: SYR / LA

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

Antinuclear antibody negative Bundle branch block left Cardiac failure congestive Cardiomegaly Chest X-ray abnormal Computerised tomogram thorax abnormal Coxsackie virus test negative Dyspnoea Electrocardiogram abnormal Lung disorder Pleural effusion Pulmonary oedema SARS-CoV-2 test negative Sinus tachycardia

Symptomtext

I started having shortness of breath and it kept getting worse. I went to the Emergency room several times until 6/18 that I was diagnosed with Congestive Heart Failure

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Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: 4,0
Labordaten: Covid-19 test - 4/5 - Negative Covid-19 test - 4/16 - Negative X-Ray Chest - 4/16 - Mild cardiac enlargement and reticular interstitial abnormality ECG - 6/8 - SINUS TACHYCARDIA LEFT BUNDLE BRANCH BLOCK ABNORMAL ECG CT Chest - 6/8 - Pulmonary edema and small bilateral pleural effusions. DIAGNOSED with Congestive Heart Failure - 6/8 - Admitted to the hospital Coxsackie A and B - 6/11 - Negative ANA IFA - 6/11 - Negative
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Levothyroxine, multi-vitamins
Allergien: Food: Peaches, apples Other: Oak and cherry tree pollen
Vorherige Impfungen: -

VAERS 2318873

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: NY
Alter: -
Geschlecht: F
Eingang: 14.06.2022
Impfdatum: 06.03.1961
Beginn: 04.11.2021
Tage bis Beginn: 22.158,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Fall Headache Impaired driving ability Injury Loss of consciousness

Symptomtext

Headache began about 10 minutes after the injection and did not stop until May 7, 2022. During this time I also experienced dizziness upon changing positions and blackouts. I have injured myself many times by blacking out and falling without any warning. I am no longer allowed to drive, my life is greatly impacted by this.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: I am for a tilt table test to diagnose POTS on July 5, 2022
Aktuelle Erkrankungen: None.
Vorgeschichte: Diabetic, depression
Andere Medikamente: Levothyroxin 125 MCG, Duloxetine 120mg
Allergien: Penicillin, latex
Vorherige Impfungen: -

VAERS 2270869

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: -
Alter: 66,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 24.02.2021
Beginn: 10.02.2022
Tage bis Beginn: 351,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Presyncope SARS-CoV-2 test positive

Symptomtext

02/10/22 presents to ED for "Pre-syncope". PMHx of "hypothyroidism, dyslipidemia, history of CVA and dementia"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: 02/11/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2251980

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

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Staat: OH
Alter: 65,0
Geschlecht: M
Eingang: 26.04.2022
Impfdatum: 25.10.2021
Beginn: 22.01.2022
Tage bis Beginn: 89,0
Dosis: 2
Route/Site: SYR / LA

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

Akinesia Asthenia Cough Dyspnoea Fatigue Feeling abnormal Headache Hypotonia Immobile Intensive care Laboratory test Mechanical ventilation Nausea Sensory loss Walking aid user Weight decreased

Symptomtext

On 01/22/2022 I started having severe cough, fatigue, headache, nauseous, and I generally felt bad. I went to the doctor on 01/24/2022 and tested positive. Then on the 01/26/2022 I went to the Emergency room because I had trouble breathing and was coughing. On the 27th, the hospital also tested me, and I was positive, and I was put on the ventilator for a week. When I was taken off it got worse so I was put back on for over a week. After they took me out of ICU, I was not mobile. I could not move any part of my body and was completely immobile. They took me to a rehab on 02/19/2022 I had total immobility. Around 03/28/2022 I finally got to where I could stand up on parallel bars for about 30 seconds. On 04/15/2022 I was discharged from rehab and able to walk but doing outpatient care until 05/12/2022. Both inpatient and outpatient rehab could not believe how fast I could regain my ability to be mobile. I overall feel absolutely terrible. I am still walking with a walker. I get winded quickly and I don't have the strength I used to have. I lost a lot of muscle mass. I weighed 265lbs I was 207lbs upon discharge but now 225. I do have a problem with my right hand and arm is now affected with because I was kept on my right side, and I cannot feel my pinky or ring finger and numb from elbow to fingers. I believe it is from not being moved much and kept on my right side. They performed so many tests but I am not sure what they did.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 23,0
Labordaten: I don't know what they ran.
Aktuelle Erkrankungen: None.
Vorgeschichte: Stage 3 Kidney Disease; Type 2 Diabetes
Andere Medikamente: Victoza; Humalog; Farxiga; Irbesartan; Omeprazole; Fenofibric; Rosuvastatin; Multivitamin; Low Dose Bayer Aspirin 81 mg.
Allergien: Amoxycillin; Metformin.
Vorherige Impfungen: -

VAERS 2231305

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

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Staat: MT
Alter: 63,0
Geschlecht: F
Eingang: 13.04.2022
Impfdatum: 08.04.2021
Beginn: 26.06.2021
Tage bis Beginn: 79,0
Dosis: 3
Route/Site: IM / LA

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

Atrial fibrillation Cardiac stress test Electrocardiogram Intensive care

Symptomtext

I had an Afib event after the second vaccine. I have had several since then. The first event I was unsure what was happening and got to the hospital just as I slipped back into sinus rhythm. I was admitted into ICU for 2 days for observation. The second time I went to the ER and they diagnosed Afib. I have had several events since, am working with a cardiologist and electrophysicologist and will have an ablation within a few days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: ECGs, EcoStress Test, medications and soon to be ablation
Aktuelle Erkrankungen: -
Vorgeschichte: asthma, hashimotos
Andere Medikamente: synthroid, multi, melatonin
Allergien: penicillin, levothroxine
Vorherige Impfungen: -

VAERS 2206560

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

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Staat: MT
Alter: 81,0
Geschlecht: M
Eingang: 30.03.2022
Impfdatum: 12.10.2021
Beginn: 22.01.2022
Tage bis Beginn: 102,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 COVID-19 pneumonia Cardiac failure congestive Chest X-ray abnormal Hypoxia Lung infiltration Lung opacity Oropharyngeal pain Polyuria Pulmonary oedema Rhinorrhoea SARS-CoV-2 test positive Upper respiratory tract infection

Symptomtext

Case was vaccinated and boosted against Covid by October 2021, then was hospitalized for Covid in January 2022. Hospitalized at: Hospital Pneumonia due to COVID-19 virus Assessment & Plan He noted a sore throat and runny nose beginning about two weeks and resolving several days PTA. He was not tested for covid at that time but tested positive on admission. Suspect recent URI was covid. H developed mildly hypoxia after arrival. His initial CXR appeared c/w pulmonary edema due to CHF with diffuse infiltrate. He was diuresed but continued to be hypoxic. Repeat CXR on 1/23 appeared more c/w covid with patchy opacities. He has completed the Pfizer vaccine series including a booster. He was started on dexamethasone x10 days on 1/23 and we are arranging home oxygen.

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Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: 2,0
Labordaten: 1/22/2022: SARS-CoV-2 NAA: Detected Panic (Ref. Range: Not Detected) Specimen ID: 220220003LP
Aktuelle Erkrankungen: Abdominal aortic aneurysm (HCC) ? Actinic keratosis ? Arrhythmia ? CAD (coronary artery disease) ? COPD (chronic obstructive pulmonary disease) ? Hypercholesterolemia ? Hypertension ? MI (myocardial infarction) (HCC) ? Type II or unspecified type diabetes mellitus without mention of complication, not stated as uncontrolled
Vorgeschichte: Abdominal aortic aneurysm (HCC) ? Actinic keratosis ? Arrhythmia ? CAD (coronary artery disease) ? COPD (chronic obstructive pulmonary disease) ? Hypercholesterolemia ? Hypertension ? MI (myocardial infarction) (HCC) ? Type II or unspecified type diabetes mellitus without mention of complication, not stated as uncontrolled
Andere Medikamente: albuterol (VENTOLIN HFA) 90 mcg/puff inhaler INHALE 2 PUFFS INTO THE LUNGS AS NEEDED. aspirin 81 mg EC tablet Take 81 mg by mouth Daily. atorvaSTATin (LIPITOR) 80 MG tablet TAKE ONE TABLET at bedtime. calcipotriene (DOVONEX) 0.0
Allergien: Latex
Vorherige Impfungen: -

VAERS 2165441

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

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Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 08.03.2022
Impfdatum: 19.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Ischaemic stroke

Symptomtext

Acute ischemic stroke - treated and discharged. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2162840

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

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Staat: -
Alter: 39,0
Geschlecht: F
Eingang: 07.03.2022
Impfdatum: 25.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Cardiac telemetry Intensive care Intentional overdose Ventricular extrasystoles

Symptomtext

ED visit for PVC - treated and discharged. 1 month later, Patient was brought to ED after intentional overdose on Tylenol, metoprolol, and alcohol between 1900-2000. Patient was admitted to the ICU. She remained on telemetry. Patient was hemodynamically stable on day of discharge. Patient was discharged home under the care of her husband. ED visits and hospital admission within 6 weeks of receiving the COVID vaccine,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2157608

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

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Staat: -
Alter: 24,0
Geschlecht: F
Eingang: 04.03.2022
Impfdatum: 08.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia C-reactive protein increased Chest pain Cough Influenza like illness Pain Pain in jaw Painful respiration Pericarditis Pyrexia

Symptomtext

Patient experiencing mid sternal chest pain radiating up into her jaw and leftward towards her shoulder. This pain started on Sunday, which was 2 days after her 2nd Pfizer COVID-19 vaccination. On Saturday, she experienced feverishness and other flu-like symptoms, which resolved. She notes that the pain in her chest is sharp in nature and worse with movement or with deep breathing or coughing. She received 2 Norco 5 mg, which took her symptoms away completely, though they did make her feel a little bit lightheaded. Discussed the case with Dr., on-call for Cardiology. She suspects mild early atypical pericarditis. She does not see signs of myocarditis. She recommends ibuprofen 800 mg 3 times a day for a week and then a recheck of her CRP. If it is normalizing, then to taper her off from the ibuprofen. ED visit within 4 days of receiving the COVID vaccine.

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

VAERS 2119492

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

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Staat: CO
Alter: 71,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Body height Chills Lethargy Loss of consciousness Nausea Tremor

Symptomtext

Sometime that night I started getting really bad chills and I was shaking putting on lots of blankets. Do not think I ran a fever but I got sick to my stomach. It started to get worse so I got up to go to the bathroom in case of vomiting and I passed out on my bedroom floor. When I woke up I slowly got up and crawled back into bed and eventually the symptoms subsided. The next day I was lethargic but felt better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: Heart disease
Andere Medikamente: Vitamin C; calcium; zinc; vitamin D3; omega-3
Allergien: No
Vorherige Impfungen: Pfizer dose 2

VAERS 2110398

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

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Staat: VA
Alter: 70,0
Geschlecht: M
Eingang: 14.02.2022
Impfdatum: 01.08.2021
Beginn: 01.09.2021
Tage bis Beginn: 31,0
Dosis: 3
Route/Site: IM / LA

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

Anal incontinence Asthenia Bladder catheterisation Blood culture Culture urine Decubitus ulcer Demyelination Guillain-Barre syndrome Hypoaesthesia Immunoglobulin therapy Magnetic resonance imaging spinal abnormal Mobility decreased Muscular weakness Myelitis transverse Neurological symptom Nitrite urine present Paraplegia Plasmapheresis

Symptomtext

Transverse Myelitis/ Guillan Barre Syndrome, Full paraplagia LEs. Fecal/urinary incontinence.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 6,0
Labordaten: 12/7 MRI Thorax 1. Subtle areas of increased T2 signal hyperintensity within the dorsal aspect of the thoracic cord at T5-T10 remain similar to prior. No definitive progression or superimposed enhancement. 12/7 Cervical MRI Mild interval progression of ill-defined, low-level abnormal signal throughout the substance of the cervical cord. No focal mass producing lesion, cord atrophy or pathologic enhancement. Imaging findings are nonspecific but again suggestive of demyelination. Nuero Note The patient is a 70-year-old man with history of hypertension, hyperlipidemia, diabetes complicated by peripheral neuropathy, and bipolar disorder, who comes into the hospital with sepsis and stage IV sacral decubitus ulcer in the setting of paraplegia from transverse myelitis. The patient developed progressive weakness and numbness of acute onset, on November 10 through 16, 2021 was admitted with presumed diagnosis of Guillain-Barre syndrome, treated with IVIG. The patient was sent to rehabilitation, but continued to worsen, and was admitted to a HCF with worsening weakness. This was December 6, 2021. He was treated with IVIG, Solu-Medrol and plasmapheresis for presumed diagnosis of transverse myelitis. MRI imaging shows patchy signal changes in the cervical spinal cord. The patient remained completely paraplegic. Hand function improved slightly. He required a suprapubic catheter. During hospitalization at the HCF from December patient developed sacral decubitus ulcer, and has been followed up by outpatient wound care. The patient, on the day of admission, was seen by the wound care nurse. The patient was running a fever up to 101.9, and was sent to the ER for further evaluation. The patient had symptoms of sepsis, tachycardia, elevated white cell count and fever. UA showed positive nitrite, numerous white cells. Urine and blood cultures were sent. The patient received antibiotics. He was on Zosyn and vancomycin. The patient was admitted to the hospital for further evaluation. The patient says that his hand function improved a little bit, but his legs are substantially weak. He does not have feeling in his legs, with bowel and bladder incontinence. The patient was seen by Dr. and a second dr. during the previous hospitalization. The patient received Pfizer COVID vaccine two weeks prior to development of his neurological symptoms.
Aktuelle Erkrankungen: -
Vorgeschichte: DM2
Andere Medikamente: Metformin
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2087712

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

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Staat: -
Alter: 84,0
Geschlecht: M
Eingang: 04.02.2022
Impfdatum: 12.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / RA

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

Syncope

Symptomtext

Syncope and collapse. ED visit and hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 1931604

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

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Staat: CA
Alter: 75,0
Geschlecht: M
Eingang: 02.02.2022
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Aphasia Asthenia Diplopia Dysphagia Dyspnoea Blood test Chest X-ray Computerised tomogram Decreased appetite Dyspnoea exertional Echocardiogram Eyelid ptosis Eyelid disorder Gait disturbance Intensive care Laboratory test Lethargy Fatigue

Symptomtext

45 minutes after booster shot head droopy, stiff neck, double vision, droopy eyelid. Symptoms progressed: added general weakness, lethargy, unable to lift eyelid, breathing, mucous, gagging, limited ability to walk. All symptoms worsened, loss of weight. Urgent Care, 2 emergency room visits, three 911 calls. December 1st admitted on emergency basis. ICU for 7 days on ventilator (unable to speak, walk, swallow, breathe, see single image); moved to step down unit, still on vent sub-acute unit. Dec 30 moved to sub acute facility with pulmonary care.

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Praegender Schweregrund: Intensive care
Hospital-Tage: 30,0
Labordaten: Every test imaginable from 7 - 10 specialists plus others on emergency room visits
Aktuelle Erkrankungen: none
Vorgeschichte: recurring thyroid cancer (genetic), high blood pressure, obesity
Andere Medikamente: levothyroxine, atorvastatin, low-dose aspirin, multi-vitamin, D3, lisinopril
Allergien: none
Vorherige Impfungen: -

VAERS 2075058

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff8841

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Staat: CA
Alter: 35,0
Geschlecht: F
Eingang: 30.01.2022
Impfdatum: 22.10.2021
Beginn: 12.11.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: SYR / RA

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

Thrombosis Vaginal haemorrhage

Symptomtext

Exactly two weeks after the first dose, I developed severe vaginal hemorrhages/blood clots during the first day of my menstrual cycle. I have known history of blood clots. I had approximately twenty (20) within 10 hours, all the size four (4) inches or greater in diameter.

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Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: IBS
Andere Medikamente: SAM-E, glutathione reduced, vitamin D
Allergien: Septra, peanuts
Vorherige Impfungen: -

VAERS 2074936

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

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Staat: PA
Alter: 70,0
Geschlecht: F
Eingang: 30.01.2022
Impfdatum: 01.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / UN

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

Aortic dissection Aortic surgery Arteriogram coronary abnormal Arthralgia Chest discomfort Echocardiogram abnormal Electric shock sensation Musculoskeletal discomfort

Symptomtext

Sudden onset up upper shoulder pain/shock around to chest and up bil sides of neck 12/4, following additional testing--resulted in aortic dissection and surgery on 12/13/2021,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: 10,0
Labordaten: Echo, EKA, CTA
Aktuelle Erkrankungen: HTN, exertional/allergic asthma
Vorgeschichte: none
Andere Medikamente: MVI, Vit D, Calcium, Turmeric, albuterol PRN, lisinopril
Allergien: none
Vorherige Impfungen: -

VAERS 2043507

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

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Staat: MN
Alter: 49,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 01.10.2021
Beginn: 25.11.2021
Tage bis Beginn: 55,0
Dosis: 1
Route/Site: SYR / LA

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

Aphasia Brain stem haemorrhage Brain stem stroke Cranial nerve disorder Dysphagia Facial paralysis Headache Hemiplegia Immediate post-injection reaction Mechanical ventilation Palpitations Sensory loss Tracheostomy

Symptomtext

The patient suffered from a brainstem hemorrhagic stroke on November 25th, 2021 about 4 weeks after receiving the 2nd dose of the Pfizer vaccine. The patient starting having bad headaches and heart palpitations immediately after the second dose. The brain stem bleed occurred in the pons and affected the right side of the pons causing facial paralysis on the right side and left side body paralysis. Since it affected cranial nuclei and nerves of cranial nerves 5, 6, 7, 8 and 9, she lost sensation on the right side of her face and had trouble swallowing and at this point cannot speak. She was on a ventilator for 10 days, then a trach tube for 3 weeks. She is now at the rehab center, where she is receiving physical therapy, OT and Speech therapy. She remains paralyzed on the left side of her body and right face and still cannot vocalize. The relationship between the Pfizer vaccine and brain bleeds and stroke have been documented in a study of (privacy) women and with a (Privacy study showing that there were 60 cases of hemorrhagic stroke (brain bleed) for every 10 million adults receiving the Pfizer/BioNTech vaccine (published in 2021).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Brain stem stroke
Hospital-Tage: 45,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Vitamin D, Garlic pills, CQ10, Magnesium, Prozac
Allergien: -
Vorherige Impfungen: -

VAERS 2028849

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

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Staat: AZ
Alter: 36,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 30.08.2021
Beginn: 01.09.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test Computerised tomogram Dyspnoea Hypoaesthesia Pain in extremity Pyrexia Respiration abnormal Thrombosis Ultrasound scan

Symptomtext

Shortness of breath, sore arm, fever, numbness of arm. Symptoms went away except the shortness of breath. After second shot symptoms got worse. Arm and face went numb. Went to ER and they found two blood clots. Lungs aren?t filling with oxygen and now on inhalers. Symptoms are still going on since shots.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Ultrasound, CT scan, bloodwork
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2025378

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

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Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 19.11.2021
Beginn: 02.01.2022
Tage bis Beginn: 44,0
Dosis: 3
Route/Site: IM / LA

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

Areflexia Ataxia Back pain CSF test abnormal Facial paresis Guillain-Barre syndrome Hypoaesthesia Immunoglobulin therapy Ophthalmoplegia Paraesthesia

Symptomtext

Back pain that progressed to numbness and paresthesia starting 01/02/22, developed sensory ataxia, ophthalmoplegia, and areflexia. Suspect Guillain Barre Syndrome based on CSF sample. Patient received IVIG for 5 days. Symptoms improved compared to initial onset of symptoms. However, there are still facial nerve weakness as well as numbness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2015372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

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Staat: UT
Alter: 42,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 03.10.2021
Beginn: 10.12.2021
Tage bis Beginn: 68,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Deep vein thrombosis Mammogram normal Pain in extremity Smear cervix normal Ultrasound Doppler abnormal

Symptomtext

12/10/21: Developed left lower extremity pain that progressively worsened and did not improve with stretching 12/11-12/20/21: worsening left lower extremity pain 12/21/21: Doppler ultrasound with acute deep vein thrombosis involving left soleal sinus and peroneal veins. 12/21/21: initiated therapeutic anticogulation with elliquis 12/22/21: pap smear and mammogram performed, normal 12/26/21: left lower extremity pain improving.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: 12/21/21: Doppler ultrasound with acute deep vein thrombosis involving left soleal sinus and peroneal veins. 12/22/21: pap smear and mammogram performed, normal
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroid Endometriosis
Andere Medikamente: Nortel 1/35 levothyroxine, multivitamin
Allergien: Gadolinium
Vorherige Impfungen: -

VAERS 2006313

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

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Staat: MN
Alter: 93,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 08.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / RA

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

Ischaemic stroke

Symptomtext

Arterial ischemic stroke, multifocal, multiple vascular territories, acute (HCC). ED to hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1984641

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: -
Alter: 45,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 12.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Blood creatine phosphokinase Blood culture Blood thyroid stimulating hormone Brain natriuretic peptide C-reactive protein Coagulation test Condition aggravated Differential white blood cell count Dysphonia Fatigue Full blood count Influenza like illness Lipase Metabolic function test Myalgia Pericarditis Polymerase chain reaction Pyrexia

Symptomtext

Within 12-24 hours developed flu-like symptoms (fatigue, fever, myalgia, dysphonia) Within 1 month developed recurrence of pericarditis symptoms

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Respiratory PCR panel x 2 (Oct, Nov 2021) CBC w/ diff (Oct, Nov 2021) CMP (Oct, Nov 2021) ESR (Nov 2021) CRP (Nov 2021) TSH (Oct, Nov 2021) Blood cultures (Nov 2021) BNP (Nov 2021) CK (Nov 2021) Troponin T (Nov 2021) Coagulation panel (Nov 2021) Lipase (Nov 2021)
Aktuelle Erkrankungen: COVID long-haul symptoms Residual pericarditis
Vorgeschichte: COVID - August 2020 hospitalized, complicated by pericarditis Asthma - worsening since COVID Osteonecrosis of the hips RA Hypothyroidism Migraines - Botox injections Depression/ Anxiety disorder Plantar fascia B feet Obesity PTSD Insomnia Osteopenia Chronic pain syndrome R shoulder pain Avascular necrosis b/l hips
Andere Medikamente: Rilonacept (for pericarditis) - stopped prior to vaccination Aimovig (erenumab) Adalimumab Albuterol inhaler Advair Mucinex Topamax - migraines Estrogen Lexapro daily Diazepam PRN Synthroid Methotrexate- 20mg Weekly
Allergien: Dilaudid/hydromorphone (pruritus, rash) PCN (rash)
Vorherige Impfungen: -

VAERS 1970797

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: IN
Alter: 36,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 18.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: - / LA

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

Guillain-Barre syndrome Hypoaesthesia

Symptomtext

I developed Guillain-Barre syndrome; partial numbness on left leg; 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 18Oct2021 12:00 (Lot number: FF8841) at the age of 36 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EN6200, Location of injection: Right Arm, Vaccine Administration Time: 12:30 PM), administration date: 25Feb2021, when the patient was 35 years old, for COVID-19 IMMUNIZATION; Bn2162b2 (Dose Number: 1, Batch/Lot No: EL8982, Location of injection: Right Arm, Vaccine Administration Time: 12:45 PM), administration date: 04Feb2021, when the patient was 35 years old, for COVID-19 IMMUNIZATION. The following information was reported: GUILLAIN-BARRE SYNDROME (disability) with onset 29Oct2021 13:00, outcome "recovering", described as "I developed Guillain-Barre syndrome"; HYPOAESTHESIA (disability) with onset 29Oct2021 13:00, outcome "recovering", described as "partial numbness on left leg". Patient developed Guillain-Barre syndrome. Spent a lot of money on testing. Still had partial numbness on left leg. Events resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care, disability or permanent damage. No other vaccine in four weeks. No treatment for events. No covid prior vaccination. No covid tested post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1935963

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: OH
Alter: 29,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 09.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Presyncope

Symptomtext

Vasovagal within 1 minute of vaccination. Elevated legs, ice pack. Able to ambulate on own 15 mins later

Weitere VAERSDATA-Felder

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

VAERS 1932281

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

schwer

Staat: NJ
Alter: 15,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Syncope

Symptomtext

pt has hx. of fainting and fainted after vaccine while walking to charting area

Weitere VAERSDATA-Felder

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

VAERS 1928741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: WI
Alter: 57,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 26.10.2021
Beginn: 08.11.2021
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: IM / RA

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

Abdominal pain Colitis Computerised tomogram Deep vein thrombosis Laboratory test

Symptomtext

ER 11/15 FOR ACUTE ABDOMINAL PAIN DX ACUTE PANCOLITIS. ER TO ADMIT 11/23 ACUTE PE AND DVT.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 3,0
Labordaten: 11/15 FULL LABS AND CT. 11/23 FULL LABS AND CT
Aktuelle Erkrankungen: no other acute illness
Vorgeschichte: b12 defic, dysphagia, GERD, s/p gastric bypass, fatty liver, obesity, iron def anemia, major depression, chronic pain, former smoker, vit d defic, s/p lumbar fusion
Andere Medikamente: tylenol, elavil, vit b12 injections, estrace vaginal, lasix, reglan, metolazone, zoran, protonix, KCl, zanaflex, tramaxol, effexor, vitamin D
Allergien: fentanyl, latex, codeine, vicodin, adhesive tape
Vorherige Impfungen: -

VAERS 1924268

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff8841

schwer

Staat: CT
Alter: 35,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 01.09.2021
Beginn: 28.09.2021
Tage bis Beginn: 27,0
Dosis: 2
Route/Site: SC / LA

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

Heavy menstrual bleeding Thrombosis

Symptomtext

Had very unusually heavy menstrual period after the 1st dose. Bleeding through 1 Ultra Tampon every hour. Passing clots half the size of my palm. Soaking through pads and through clothing overnight. Then this month I had very heavy Bleeding for 1 day on 12/6 between my period. I had blood clots as well. Just one lone day.... never had this happen to me ever in my life.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Never went to the doctor.... I'm a nurse so I watched for symptoms. I have my annual next month and my physical this month.
Aktuelle Erkrankungen: No
Vorgeschichte: Hx of thyroid cancer; iron deficiency anemia
Andere Medikamente: Synthroid 125mcg 2 tablets daily x 6 days per week
Allergien: No
Vorherige Impfungen: -

VAERS 1923535

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: WA
Alter: 35,0
Geschlecht: M
Eingang: 04.12.2021
Impfdatum: 03.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 26,0
Dosis: 2
Route/Site: SYR / RA

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

Hypoaesthesia Laboratory test Myocarditis

Symptomtext

Myocarditis; loss of feeling in face, particularly in the forehead

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Clinic evaluation on Thursday, December 2nd with additional laboratory testing
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1917898

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: PA
Alter: 21,0
Geschlecht: M
Eingang: 02.12.2021
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

Cough Loss of consciousness Retching Seizure Skin warm Unresponsive to stimuli

Symptomtext

The patient received Pfizer vaccine in his left arm, then we reivewed his administration form about his flu shot and I gave the Flucelvax vaccine in his right arm. As soon as I pulled the needle out and reached for the band aid, he lost conciousness. A caretaker of the center called him by name many times and he was unresponsive for 15-20 seconds. She said he was having a seizure. She said he has had them in the past, but it has been a very long time since his last eipsode. He regained conciousness after 15-20 seconds and he was warm to the touch. He cough several times as if he was going to vomit, but he never did. We called 911. The patient insisted that he was fine and he did not want to go to the ER and did not want to lay down. Paramedics came and evaluated the patient. His BP was 110/70, Pulse of 76, and had an oxygen sat of 97. They waited until about 1:10 and then they left when they felt he was stable. The patient left with a caretaker.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: none
Vorgeschichte: history of epilepsy
Andere Medikamente: unknown
Allergien: none
Vorherige Impfungen: -

VAERS 1913492

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: MN
Alter: 69,0
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: 12.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Deep vein thrombosis Pain Tenderness Ultrasound scan abnormal

Symptomtext

Three days (Oct. 15) after my booster shot on Oct. 12 when I also received the FLU SHOT on the same day in my right arm, I had shooting pain down my left leg. I thought it was another episode of sciatic nerve pain and took some pain medication (at nights) to help allivieate the pain. I went in for my physical therapy appointment on Oct. 18 when I complained about the pain immediately behind my left knee. My therapist said that was not common for sciatic nerve pain and because of the tenderness wondered if I may have developed a clot. She called my physician who asked me to get to the ER/Urgent Care to get an echo of the leg and cancelled the rest of my PT appointment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: On Oct. 18. after seeing my PT, I drove to the emergency room where they did a echogram of my left extremity and was diagnosed with (radiology report follows): LEFT: Nonocclusive deep venous thrombosis at the popliteal vein. Occlusive deep venous thrombosis at the tibioperoneal trunk and posterior tibialis vein of the proximal calf. Nonocclusive deep venous thrombosis at the peroneal veins of the proximal calf. No popliteal cyst. Impression IMPRESSION: Deep venous thrombosis identified at the left leg that is nonocclusive at the popliteal vein, occlusive at the tibial peroneal trunk extending to the proximal posterior tibialis vein, and nonocclusive at the peroneal veins of the proximal left calf. These are new since the prior remote comparison from 2013. I am now the blood thinner Elequis until I see a hemaetologist in January 2022. I previously had a DVT in Dec. 2013/Jan. 2014 after a series of medical events including GI bleed, gout, and a large kidney stone in a period of three weeks. I was diagnosed with the DVT during a pre-op check for an ultrasonic procdure to remove the kidney stone that was cancelled.
Aktuelle Erkrankungen: Sciatic nerve pain, SI join pain, received steroid injection six weeks prior to Pfizer booster shot on Oct. 12.
Vorgeschichte: Low back pain, onset of chronic heart failure (not severe)
Andere Medikamente: Ramipril, Folic acid, metoprolol, allupurinol Potassium Citrate Vit B12 Omeprazole Baby aspirin Repatha (injection once every other week)
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1906095

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: CA
Alter: 17,0
Geschlecht: M
Eingang: 29.11.2021
Impfdatum: 24.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Loss of consciousness Malaise

Symptomtext

Pt?s mother stated pt having hx of syncope after needle injections. Pt?s mother and patient were advice to have pt lay down prior to vaccine admin. Pt and mother refused to have him lay and insisted on staying seated on chair while mom hugged him. Patient was vaccinated, in chair while hugging mom, pt stated he was feeling unwell, was provided a cup of water, able to drink without problems. Pt remained hugging mom while he lost consciousness sitting in chair. He was assisted to floor where he regained consciousness after a few seconds. Patient was assessed, legs were elevated, alert and oriented to name, place and situation, Vitals were taken at 18:14 read-BP:119/66, HR:60, RR-18, O2 Sat: 98%, after a few minutes was assisted to sit up on chair, pt stated feeling better. Vitals were rechecked at 18:25 and read BP:120/72, HR:80, RR:20, and O2 sat 99%. Patient stated we was feeling fine, was monitored for 30 mins. No reactions were noted, patient talking and drinking water without a problem. Patient stated feeling fine and ok to go home. Mom advise if sees a change or symptoms of reaction developing to contact PCP or ER.

Weitere VAERSDATA-Felder

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

VAERS 1869750

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: TN
Alter: 31,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Bell's palsy Facial paralysis Feeding disorder Pharyngeal swelling Swelling face

Symptomtext

11/13/2021 early morning, Right side of face swollen, cheek, jaw, and throat. Mild face droop. Sore throat. Can?t open mouth enough to eat due to swelling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: 11/15/2021 Doctor looked at face and inside mouth (what she could). Said I have Bells Palsy. Prescribed steroids for 7 days to hopefully help, if doesn?t help I have to go back to doctor.
Aktuelle Erkrankungen: -
Vorgeschichte: Fibromyalgia, malignant hyperthermia, chromosome 5q23.2-23.3 duplication disorder, Asthma, Reflux, tachycardia, Anxiety, Depression, osteoarthritis, psoriatic arthritis, PTSD, scoliosis
Andere Medikamente: Metoprolol, Topiramate, omeprazole, Aimovig, Sumatriptan (prn), dicyclomine, naproxen (prn)
Allergien: Sulfa, Zantac, Prevacid, doxycycline, clindamycin, cymbalta, adhesive tape
Vorherige Impfungen: -

VAERS 1865499

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FF8841

schwer

Staat: SC
Alter: 61,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 22.10.2021
Beginn: 09.11.2021
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: SYR / RA

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

Bell's palsy Blood test Computerised tomogram head Magnetic resonance imaging head

Symptomtext

Bell?s palsy. Treated with prednisone 60 mg for 7 days and valacyclovir 1g tablet 3 times daily for 7 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: November 11 - blood tests, brain CT, brain MRI.
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoarthritis
Andere Medikamente: Meloxicam
Allergien: Sulfa, iodine contrast used for CT scan
Vorherige Impfungen: -

VAERS 1861359

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: MN
Alter: 31,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 20.10.2021
Beginn: 11.11.2021
Tage bis Beginn: 22,0
Dosis: 3
Route/Site: IM / LA

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

Chills Syncope Tinnitus

Symptomtext

Chills for 2 hours, Syncope event during chills (unknown duration), ringing in ears

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Prenatal vitamin
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 1861242

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

schwer

Staat: UT
Alter: 33,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 05.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / RA

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

Communication disorder Coordination abnormal Dysarthria Electric shock sensation Facial paresis Fall Feeling abnormal Hemiparesis Hyperaesthesia Hypoaesthesia Lip swelling Pain Pain in extremity Paraesthesia Sensation of foreign body Swelling face Weight bearing difficulty

Symptomtext

Gradual onset of numbness, prickling or tingling in your feet or hands, which can spread upward into legs and arms Sharp, jabbing, throbbing or burning pain Extreme sensitivity to touch Pain during activities that shouldn't cause pain, such as pain in my feet when putting weight on them or when they're under a blanket Lack of coordination and falling Brainfog Problems speaking or communicating Muscle weakness on right side of the face Face and lips swelling Brainzaps Feeling as if you're wearing gloves or socks when you're not

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: pcos
Vorgeschichte: asthma
Andere Medikamente: Ibuprophen Dexametasone Albuterol Montelukast
Allergien: seasonal allergies, generalized allergies
Vorherige Impfungen: -

VAERS 1854859

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff8841

schwer

Staat: MO
Alter: 26,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 05.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Fall Head injury Loss of consciousness Nausea Pain Pruritus Syncope

Symptomtext

Itchy face and arms around 11pm Oct 5th and lasted a few hours until I went to bed around 2am. I woke up around 5am Oct 6th and was having very bad body aches and nauseousness. Within an hour, I fainted twice and I am unsure how long I was unconscious for. Caused me to fall and hit my head when I fainted the second time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: IBS
Andere Medikamente: Flonase Sensimist, 75mg (daily) of Sertraline, Tri-Sprintec (Birth Control- 1 pill daily)
Allergien: Penicillin, Amoxicillin, Erythromycin, Zithromax, Clindamycin, Doxycycline, Duloxetine, Shell Fish (minimal).
Vorherige Impfungen: -

VAERS 1853276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: NJ
Alter: 75,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 20.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

Diarrhoea Disorientation Dizziness Fatigue Lethargy Limb discomfort Malaise Nausea Oropharyngeal pain Pain Pruritus Syncope

Symptomtext

I was dizzy; Nauseousness; loose bowels not diarrhea but loose; seem to get loose bowels; Not feeling well; Lethargic, dragging, and had low energy; Felt like she would faint; Disoriented; Pain; slight discomfort pain; Sore throat; Regular arm itch/itching/This time it has been worse; itchy arm and soreness; Gets heaviness in legs and sits down; Tiredness; This is a spontaneous report from a contactable consumer (patient). A 75-year-old female patient received third dose of bnt162b2 (COMIRNATY, Formulation: Solution for injection, Lot Number: FF8841), dose 3 via an unspecified route of administration, administered in right arm on 20Oct2021 10:20 (at the age of 75-year-old), as dose 3 (booster), single for COVID-19 immunization. This was injected in the right arm.The needle was long, and she thinks it was given in the muscle, but she was not looking and cannot confirm, but it was given in the upper part of her right arm. Medical history included diabetes from 1995 (Mother had diabetes and it seems to run in family. Sister who was still living also has diabetes and young son was prediabetic), blood pressure, blood thinner and irregular heart beat. Concomitant medications included insulin lispro (HUMALOG), metformin, pravastatin sodium (PRAVASTINE), amlodipine, ezetimibe, aspirin [acetylsalicylic acid] and losartan. She had a 10:15 appt, so that morning, she took Humalog. When providing her other medications, she said she is a medicine cabinet. Over the last 5 years, she has developed the upper respiratory nasal drip. She was on CPAP machine, but that was recalled, so she is waiting on an approval for another method they will use. The patient previously took first dose of bnt162b2 (COMIRNATY, Formulation: Solution for injection, Lot Number: EL8982; Expiration date: Mar2021), dose 1 via an unspecified route of administration, administered in left arm on 24Jan2021 as dose 1, single for COVID-19 immunization (at the age of 75-year-old) and experienced itchy arm, also received second dose of bnt162b2 (COMIRNATY, Formulation: Solution for injection, Lot Number: EN5318; Expiration date: May2021), dose 2 via an unspecified route of administration, administered in left arm on 10Feb2021 as dose 2, single for COVID-19 immunization (at the age of 75-year-old) and experienced itchy arm, insulin for diabetes mellitus, flu on 04Oct2021 for immunization and experienced itchy arm. On 21Oct2021, the patient experienced felt like she would faint (medically significant), disoriented (she haven't been right, she haven't been herself really; still had the effects, the disoriented, not felling well; just the disoriented, not able to get myself together still), pain, slight discomfort pain, sore throat (When she woke up 06:00-06:30), 10:30 -11:00, regular arm itch/itching/this time it has been worse; itchy arm and soreness, nauseousness (7:00 or a little after that), loose bowels not diarrhea but loose; seem to get loose bowels, not feeling well, lethargic (at 07:30), dragging and had low energy. On 22Oct2021 07:30, the patient was dizzy. On an unspecified date in Oct2021, the patient got heaviness in legs and sits down and tiredness. She had no energy. No visits of emergency room and physician office. The patient was treated with Tylenol as a therapeutic measure of disoriented, pain; slight discomfort pain, sore throat, regular arm itch/itching/this time it has been worse; itchy arm and soreness, was dizzy, nauseousness, loose bowels not diarrhea but loose; seem to get loose bowels, not feeling well, lethargic, dragging and had low energy, got heaviness in legs and sits down and tiredness. Patient stated very ugly, still existing adverse reaction; it was horrible. The shot was given on Wednesday she took it. Thursday, when she woke up it was horrible. That all lasted all day on Thursday and then Friday she still was 'out of sort". She don't know if it was something, it's mixing with the medication (Further clarification unknown) that she took she was not really sure but she never had 'uphill' the side effect like that before, like she was dizzy, she wanted to call her doctor but she said first maybe she would check with the Pfizer, maybe other people felt maybe some, the same side effects that was similar. She never had one like that (Not clarified). She said her voice is still hoarse, but later said that she always has a hoarseness when she wakes up. Dizziness was on and off on Friday, and when she stands up, she does not know if it is the fluids, but it is still there. There is almost like there is something else going on. No relevant Tests were done. She called her doctor and said she should probably have a nose culture, but not for COVID, but to see if anything viral is going on. She has not had anything done yet. She just thought maybe others have had conditions like her. She would like to know if these symptoms are a reaction from the booster. The outcome of the events felt like she would faint, got heaviness in legs and sits down, tiredness was unknown. The outcome of the events disoriented, pain; slight discomfort pain, sore throat, was dizzy, loose bowels not diarrhea but loose; seem to get loose bowels, not feeling well, lethargic, dragging and had low energy was not recovered. The outcome of the events regular arm itch/itching/this time it has been worse; itchy arm and soreness, nauseousness was recovering. 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: Anticoagulant therapy; Arrhythmia; Blood pressure; Diabetes.
Andere Medikamente: Humalog; Metformin; Pravastine; Amlodipine; Ezetimibe; Aspirin [Acetylsalicylic Acid]; Losartan
Allergien: -
Vorherige Impfungen: -

VAERS 1847360

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: AK
Alter: 53,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Anaphylactic reaction Pharyngeal swelling

Symptomtext

Anaphylaxis with throat swelling treated with Epinephrine at 10:20am and diphenhydramine at 10:23am. Transported to ER

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: diabetes, dyslipidemia
Andere Medikamente: atorvastatin, metformin, duloxetine, zyrtec, aspirin, victoza
Allergien: moderna covid-19 vaccine, meperidine, lidocaine, promethazine, Imitrex
Vorherige Impfungen: -

VAERS 1846526

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: MI
Alter: 29,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Migraine Syncope

Symptomtext

Migraines followed by syncope. Has been occuring since 3 hours post vaccine. Still occuring as of 70 hours post vaccine

Weitere VAERSDATA-Felder

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

VAERS 1836745

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff8841

schwer

Staat: UT
Alter: 25,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Chest pain Dizziness Dyspnoea Syncope

Symptomtext

Chest pain, dizziness, fainting, shortness of breath

Weitere VAERSDATA-Felder

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

VAERS 1832990

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: NY
Alter: 20,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Hypersensitivity Intensive care Nausea Oropharyngeal discomfort Pruritus Throat tightness Tryptase Vomiting Wheezing

Symptomtext

Patient states around 5 or 6 this evening she started noticed some itching in the back of her scalp. She took 1 Benadryl, then she got home she took a second Benadryl. At that time she started feeling her throat was closing up and came to the emergency room. She did not have nausea until she arrived in the emergency room. She endorses some wheezing and throat discomfort. ED Course and Disposition: Patient was given her first dose of IM epi at about 730 this evening. Approximately 15 minutes later patient began vomiting and was given 4 mg of IV Zofran. approximately an hour later patient began feeling like her throat was closing up again. She was transferred over to the critical care bay for second round of epinephrine. She is been monitored in the critical care bay for 4 hours without requiring a third dose of epinephrine. Her blood pressure has remained stable throughout. She had no further emesis. We will plan to admit to observation for monitoring overnight Patient began feeling like her throat was closing up again. Patient transferred to the critical care bay for closer observation and second round epi You were seen today for allergic reaction. You were administered epinephrine, steroids in the ED. You can take Benadryl for itching. Admission was recommended but was declined at this time. If you have worsening swelling, increased shortness of breath or any symptoms you find concerning please turn the ED. If you feel like you mouth, tongue, throat is swelling up and you are having difficulty breathing you can administer the EpiPen and call emergency services. comirnaty

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: Ref Range & Units 2 wk ago Tryptase <=10.9 ug/L 7.5 Comment: Performed By: Lab Laboratory Director:, MD Resulting Agency
Aktuelle Erkrankungen: none
Vorgeschichte: obstructive sleep apnea, obese
Andere Medikamente: ibuprofen, iron tablets, loratadine
Allergien: brompheniramine-phenylepherine
Vorherige Impfungen: -

VAERS 1829526

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

schwer

Staat: MO
Alter: 76,0
Geschlecht: U
Eingang: 29.10.2021
Impfdatum: 14.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Blood pressure systolic increased Cardiac imaging procedure normal Computerised tomogram head normal Headache Myocarditis Pyrexia Vaccination complication

Symptomtext

sw pt wife reporting on 10/15/2021 @2am after covid 19 pfizer vaccine administered on 10/14/2021 pt went to er with chief complaint of headache, increase blood pressure(systolic 220) at urgent care, & fever of 104F. Urgent care gave fluids and recommended going to ER where pt was admitted to hospital for 4 days stay. Doctors ruled myocarditis diagnosis due to Pfizer Covid vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 4,0
Labordaten: MRI showed no evidence of heart damage and CT showed no evidence of brain bleed according to pt wife.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1829428

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: MO
Alter: 18,0
Geschlecht: M
Eingang: 29.10.2021
Impfdatum: 25.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / RA

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

Back pain Chest X-ray normal Chest discomfort Chest pain Cough Echocardiogram abnormal Left atrial enlargement Mitral valve incompetence Myocarditis Nausea Pain SARS-CoV-2 test negative Tricuspid valve incompetence Troponin increased Vomiting

Symptomtext

Pt went to walk in clinic on 10/28/21 for c/o chest discomfort and cough. Sent to local ER for eval. At ER he reported body aches, back pain, cough, n/v, on 10/27/21. On 10/28/21 started with chest pain described as heaviness, worse when laying down. Denied SOB, palpitations, etc. Troponin level elevated to 8 then increased to 10. Cardiology consult to ER and ECHO done. DX: myocarditis secondary to covid vaccine. Transferred to Hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Rapid COVID - negative (10/28/21) Echocardiogram - 10/28/21 - mild left atrial enlargement; trace mitral and trace tricuspid regurgitatio Troponin - 10/28/21 10.87 CXR - no acute cardiopulmonary process 10/28/21
Aktuelle Erkrankungen: inknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1827479

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: IL
Alter: 71,0
Geschlecht: M
Eingang: 29.10.2021
Impfdatum: 12.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Bell's palsy SARS-CoV-2 test

Symptomtext

Bell's Palsy; This is a spontaneous report from a contactable consumer (patient). A 71-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: FF8841), via an unspecified route of administration, administered in left arm on 12Oct2021 11:45 (at the of 71 years old) as dose 3 (booster), single for COVID-19 immunisation. Medical history included cancer. The patient has not had COVID prior to vaccination. The patient's concomitant medications were not reported. No other vaccine was given in four weeks. The patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in left arm on 05Mar2021 10:30 (Batch/Lot Number: En6203, at the of 70 years old) for COVID-19 immunization and the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in right arm on 26Mar2021 09:30 (Batch/Lot Number: Er8733, at the of 70 years old) for COVID-19 immunization. The patient experienced bell's palsy on 13Oct2021. No treatment was given in response to the event. The event resulted in Doctor or other healthcare professional office/clinic visit. The patient was tested for COVID post vaccination via nasal swab on an unspecified date with unknown results. The outcome of the event was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Test Name: COVID; Result Unstructured Data: Test Result:Unknown results; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cancer
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1825335

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: WV
Alter: 50,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 05.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy Blepharospasm Chills Computerised tomogram normal Facial paralysis Headache Influenza Migraine Pain Vision blurred

Symptomtext

10/05/2021 Received first Pfizer Covid shot at pharmacy 10/06/2021 Felt flu like symptoms (body ache, slight headache, chills) 10/07/2021 Severe headaches/migraines began daily 10/10/2021 Began noticing blurry vision/slow focusing and right eye lid twitching/drooping, intermittently right side of mouth would freeze 10/15/2021 Had Dr appt for severe migraines. The doctor scheduled CT scan and prescribed migraine meds ( did not have medical history of migraines until this point ). Recommended vision check also. 10/20/2021 Had CT Scan 10/22/2021 Had vision test at Eye Doctor. Right eye was drooping/fluttering and right side of mouth was froze. They confirmed seeing this during the visit. Dr and assistant got on CDC webite and suspected onset of Bells Palsey since shot after checking several symptoms. They gave me paperwork to register symptoms at CDC. 10/22/2021 Picked up migraine med prescription 10/24/2021 Had severe migraine, took first pill. Headache subsided for 2-3 hours and came back but not as bad. 10/26/2021 Had fairly severe migraine, took pill. Headache subsided for the day. 10/27/2021 Medic suggested downloading migraine monitor app to track migraines. 10/28/2021 Mild headache all day, facial paralysis began around noon and continued into next day. 11/01/2021 Have follow up visit with Dr about adverse side effects from 1st Covid shot, requesting medical exemption for second shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: 10/20/2021 CT scan results came back normal
Aktuelle Erkrankungen: none
Vorgeschichte: now have chronic migraines and Bells Palsey after 1st Covid shot
Andere Medikamente: none
Allergien: penicillian
Vorherige Impfungen: -

VAERS 1821819

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 13.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Aphasia Chest discomfort Electroencephalogram Intensive care Laboratory test Malaise Myocardial necrosis marker Pain in jaw Protein total Pruritus Rhinorrhoea Seizure Stridor Swollen tongue Unresponsive to stimuli Wheezing

Symptomtext

Itchy,,tongue swelling, running nose pain in right jar, tighten in my chest, strider breathing, wheezing, anaphylactic, unresponsive and seizure, could not speak they gave me 1 tablet of Benadryl and administer Epinephrine this is when I911 was called at the hospital that?s where I had the seizure the strider breathing there they administer again epinephrine gave me Albuterol and prednisone to opn me so I could breathe, the Allergyiest snook in with another doctor from her office who I never meet and as to listen to my lungs both of them then walked out and never to see her or him again I was in the trauma part of the hospital went to icu and was admitted there from the 13-15 I was discharged and after coming home was very sick went to my PCP who them put me on antibiotics for 7days and I?m still feeling sick. Prior to getting the vaccine I went in for skin testing and had a reaction that?s on 9-22/2021 at the same location

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: 2,0
Labordaten: EEG/ protein/ cardio enzymes and a whole punch of other test
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: Yes
Vorherige Impfungen: -

VAERS 1821667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: CA
Alter: 18,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 07.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / -

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

Blood test Feeling abnormal Loss of consciousness Muscle spasms Pregnancy test Urine analysis

Symptomtext

Felt fine Thu after injection. Friday between 9-10am she started to feel "off". She was in her college class and blacked out. She would wake up start spasming then black out again. This happened numerous times. The professor called an ambulance to take her to the hospital after numerous rounds of spasms and blackouts. They took her to the hospital where they ran urine, pregnancy and blood tests. They did not find any non-vaccine related cause for the episodes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Friday, Oct 8th after being taken to the hospital by ambulance they ran urine, pregnancy and blood tests. They did not find any non-vaccine related cause for the episodes.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birth Control Pills
Allergien: None
Vorherige Impfungen: -

VAERS 1821486

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

schwer

Staat: NY
Alter: 14,0
Geschlecht: M
Eingang: 27.10.2021
Impfdatum: 24.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Seizure

Symptomtext

Patient experience seizure 3 times.

Weitere VAERSDATA-Felder

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

VAERS 1820628

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: OH
Alter: 88,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 07.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Asthenia Body temperature Chills Culture urine Diarrhoea Electrocardiogram Feeling hot Flushing Full blood count Hyperhidrosis Loss of consciousness Metabolic function test Oxygen saturation Pollakiuria Pyrexia Urine analysis Vomiting X-ray

Symptomtext

She passed out when the diarrhea started; Diarrhea; Her cheeks are flushed, right side is worse than the left; very weak; hot; chills; Fever of 105F; Sweating profusely; having to pee; every time she thought she could go back to sleep, she had to go back to the bathroom; Vomiting; This is a spontaneous report from a contactable consumer. This consumer reported for an 88-year-old female patient (her client) received bnt162b2 (BNT162B2), dose 3 via an unspecified route of administration, administered in Arm Right on 07Oct2021 12:00 (Lot Number: FF8841) as DOSE 3 (BOOSTER), SINGLE for COVID-19 immunisation at the age of 88 years old. Medical history included ongoing cardiac failure congestive. The patient's concomitant medications were not reported. The patient previously received first dose of bnt162b2 on 23Jan2021 in upper right arm (Lot: EL9262) and second dose on 13Feb2021 in right arm (Lot: EM9809) for COVID-19 immunisation, both at the age of 88 years old. The patient had the booster on Thursday and had a reaction. It started with her having to go to the bathroom to pee; every time she thought she could go back to sleep she had to go back to the bathroom; this started at 1am on Friday 08Oct2021 and she peed until about 7am. Next, she started vomiting. She went to the hospital at around 7am on Friday 08Oct2021. After she started throwing up and sweating profusely her sons called an ambulance to take her to the hospital. When she got to the hospital, they gave her an IV, and checked her heart and her pulse ox which were both normal. She did have a fever of 105F. They gave her Oxygen for about an hour even though her pulse ox was 96-98. This morning her pulse ox was 98. They released her from the hospital about 3:45-4pm on Friday. It was verified that the patient was not admitted, she was only in the ER. While at the hospital she had a 12 lead EKG and an x-ray, which were both normal. They also did a metabolic panel, CBC with complete blood count, urinalysis and urine culture, and all came back normal. After the patient got home the diarrhea started, and she continued to throw up. She passed out when the diarrhea started. She states that today she has been resting for the most part, she is still not doing great. Her cheeks are flushed, right side is worse than the left. She is still very weak, not as weak as she was, but she will be staying in the bed today because the aide doesn't want her to be stumbling around. States that she threw up more than 10 times, which was really hard on her body, so she needs to rest. The last time she threw up or had diarrhea was on Saturday. Her fever has subsided; she went in between chills, hot, and sweating; today (12Oct2021) her temperature was 95.6F. She is able to hold food down now. Caller states that she is about to take her medication, the aide just wanted her to have food on her stomach first. The outcome of her cheeks are flushed, right side is worse than the left was not recovered, outcome of weak was recovering, the outcome of other events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 20211008; Test Name: Fever; Result Unstructured Data: Test Result:105 Fahrenheit; Test Date: 20211012; Test Name: Fever; Result Unstructured Data: Test Result:95.6 Fahrenheit; Comments: .; Test Date: 20211008; Test Name: urine culture; Result Unstructured Data: Test Result:Normal; Test Date: 20211008; Test Name: EKG; Result Unstructured Data: Test Result:Normal; Test Date: 20211008; Test Name: CBC; Result Unstructured Data: Test Result:Normal; Test Date: 20211008; Test Name: complete blood count; Result Unstructured Data: Test Result:Normal; Test Date: 20211008; Test Name: metabolic panel; Result Unstructured Data: Test Result:Normal; Test Date: 20211008; Test Name: Pulse ox; Result Unstructured Data: Test Result:pulse ox was 96-98; Comments: They gave her Oxygen for about an hour even though her pulse ox was 96-98.; Test Date: 20211012; Test Name: Pulse ox; Result Unstructured Data: Test Result:98; Comments: This morning her pulse ox was 98.; Test Date: 20211008; Test Name: urinalysis; Result Unstructured Data: Test Result:Normal; Test Date: 20211008; Test Name: X-ray; Result Unstructured Data: Test Result:Normal
Aktuelle Erkrankungen: Cardiac failure congestive
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1808053

GLAXOSMITHKLINE BIOLOGICALS · INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) · Charge FF8841

schwer

Staat: VA
Alter: 32,0
Geschlecht: U
Eingang: 26.10.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Asthenia Blood calcium normal Blood potassium decreased Chills Dizziness Dysphagia Hyperhidrosis Hypoaesthesia Dysstasia Headache Hypoaesthesia oral Immunodeficiency Paraesthesia Tremor Nausea Panic attack Paraesthesia oral Pharyngeal hypoaesthesia

Symptomtext

Per hospital event reporting system " I received Hepatitis A vaccine, flu vaccine and COVID booster shot (Pfizer) on 10/9/21 after being informed there were no contraindications in taking all 3 at the same time by Employee. I worked my 12 hours shift as scheduled, just feeling lightheaded, sweats and chills. I took tylenol during my shift. My shift ended around 1930 and I drove home. As I was driving home, I started to feel shakiness and numbness and tingling all over that started in my midsection and radiated outwards into my extremities, head, face, neck, mouth, tongue and throat. I became aware that either my blood glucose level was low, or I was having an immune reaction from the vaccines. I got home and immediately thought I was going to pass out. I tried to eat but was unable to swallow crackers. At this point, I was afraid my airway is being compromised, so my wife called 911. I was brought to the ER and was there for about 6 hours (discharged at around 0130)."

Weitere VAERSDATA-Felder

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

VAERS 1808053

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: VA
Alter: 32,0
Geschlecht: U
Eingang: 26.10.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Blood calcium normal Blood potassium decreased Chills Dizziness Dysphagia Hyperhidrosis Hypoaesthesia Dysstasia Headache Hypoaesthesia oral Immunodeficiency Paraesthesia Tremor Nausea Panic attack Paraesthesia oral Pharyngeal hypoaesthesia

Symptomtext

Per hospital event reporting system " I received Hepatitis A vaccine, flu vaccine and COVID booster shot (Pfizer) on 10/9/21 after being informed there were no contraindications in taking all 3 at the same time by Employee. I worked my 12 hours shift as scheduled, just feeling lightheaded, sweats and chills. I took tylenol during my shift. My shift ended around 1930 and I drove home. As I was driving home, I started to feel shakiness and numbness and tingling all over that started in my midsection and radiated outwards into my extremities, head, face, neck, mouth, tongue and throat. I became aware that either my blood glucose level was low, or I was having an immune reaction from the vaccines. I got home and immediately thought I was going to pass out. I tried to eat but was unable to swallow crackers. At this point, I was afraid my airway is being compromised, so my wife called 911. I was brought to the ER and was there for about 6 hours (discharged at around 0130)."

Weitere VAERSDATA-Felder

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

VAERS 1813757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: FL
Alter: 19,0
Geschlecht: F
Eingang: 24.10.2021
Impfdatum: 23.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Nausea Pollakiuria Pyrexia Syncope Vomiting

Symptomtext

Fever/chills, nausea, vomiting, syncope, increased urination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Tachycardia
Andere Medikamente: Potassium citrate 15meq, daily vitamin
Allergien: N/A
Vorherige Impfungen: -

VAERS 1808771

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: CA
Alter: 25,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Nausea Pharyngeal hypoaesthesia Syncope

Symptomtext

Fainting, nausea, dizziness, numbing in throat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: penicillin V potassium trimethoprim
Vorherige Impfungen: -

VAERS 1808246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: CT
Alter: 40,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 18.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Computerised tomogram Lymphadenopathy Seizure

Symptomtext

Pt. states that after receiving the 2nd dose of Phizer 10/18/2021, started experiencing symptoms 10/20/2021 of Seizure and swollen lymphnoids. Emergency Room visit 10/20/2021 with Observation, Cat-Scan preformed. EEG recommended with Neurologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Cat-Scan 10/20/2021
Aktuelle Erkrankungen: N/A
Vorgeschichte: Siliac Disease
Andere Medikamente: N/A
Allergien: Gluten
Vorherige Impfungen: -

VAERS 1801992

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: PA
Alter: 35,0
Geschlecht: M
Eingang: 20.10.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Feeling abnormal Feeling hot Loss of consciousness Palpitations

Symptomtext

PATIENT STATED HE WAS FEELING DIZZY ABOUT 5 MINUTES AFTER RECEIVING THE VACCINE. I INFORMED HIM TO STAY SEATED IN THE CHAIR AND GOT HIM A BOTTLE OF WATER. I ASKED HIM IF HE WAS FEELING ANY BETTER AND HE SAID HE WAS GETTING HOT AND WANTED TO TAKE HIS JACKET OFF. HE SAID HE STARTED GETTING HEART PALPITATIONS AND HE SAID HE CONTRACTED HIS WIFE AND SHE WAS EN ROUTE. HE TOOK HIS JACKET OFF AND SAT BACK DOWN. HE THEN STARTED TO LOSE CONSCIOUSNESS SO I RUSHED OUT AND TOLD MY TECHNICIAN TO CALL 911. SHE CALLED AND I STAYED OUT THERE WITH HIM TRYING TO WAKE HIM AFTER HE WAS UNCONSCIOUS. HE WAS UNCONSCIOUS FOR ABOUT 20 SECONDS AND I WAS CHECKING HIS PULSE AND HE STILL HAD A PULSE. HE THEN WOKE UP AND AND SAID HE WAS STILL NOT FEELING RIGHT. I INFORMED HIM HE PASSED OUT FOR ABOUT 20 SECONDS AND WE CALLED 911 AND THEY WERE ON THEIR WAY. THE AMBULANCE ARRIVED AND TOOK OVER AND GOT HIS VITALS AND SAID THEY WERE GOOD. PATIENT STATED HE DIDN'T WANT TO GO WITH THE PARAMEDICS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: VITALS FROM THE PARAMEDIC ON 10-20-2021
Aktuelle Erkrankungen: NONE REPORTED
Vorgeschichte: ASTHMA
Andere Medikamente: NONE
Allergien: LATEX
Vorherige Impfungen: -

VAERS 1798221

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: CO
Alter: 56,0
Geschlecht: F
Eingang: 19.10.2021
Impfdatum: 19.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Adverse reaction Condition aggravated Feeling hot Nausea Presyncope Vomiting

Symptomtext

After receiving Pfizer vaccination via intramuscular injection, patient reported feelings of near syncope, nausea and vomiting, and general warmness. Patient was alert and oriented to person, time, place and event. Patient was ambulatory. Patient was waiting in her vehicle post vaccination when family member alerted crew of adverse reaction. Patients blood pressure, oximetry, and heart rate where monitored along with level of consciousness. Patient reported history of hyperlipidemia, hypotension and history of similar response to previous vaccinations. Patient was offered emergency services however she stated that she would continue to monitor herself and if condition worsened she would seek further medical help. Patient left vaccination clinic with family member.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: At 10:20: Blood pressure: 109/58 mmHg; Heart rate: 88 bpm; oximetry: 96%; respiratory rate: 18. At 10:25Blood pressure: 98/61 mmHg; Heart rate: 69 bpm; oximetry: 97%; respiratory rate: 18.
Aktuelle Erkrankungen: None reported by patient.
Vorgeschichte: Hyperlipemia, hypotension
Andere Medikamente: Crestor
Allergien: None reported by patient.
Vorherige Impfungen: -

VAERS 1795966

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

schwer

Staat: CA
Alter: 22,0
Geschlecht: M
Eingang: 18.10.2021
Impfdatum: 14.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Computerised tomogram Laboratory test Seizure

Symptomtext

seizure event ocured on 10/15/21 at work place, patient was admitted to ER facility . patient is stable and back home on 10/16.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Labs are ordered and CT -scan done in the ER
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1795516

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: IL
Alter: 45,0
Geschlecht: F
Eingang: 18.10.2021
Impfdatum: 06.10.2021
Beginn: 06.10.2021
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 pain Disturbance in attention Dizziness Echocardiogram Electrocardiogram Feeling abnormal Headache Neck pain Pain Paraesthesia Presyncope Tremor

Symptomtext

Symptoms directly following vaccination: severe dizziness, near loss of consciousness, internal trembling for 90 mins (I stayed at the facility for 2 hours until symptoms calmed down). Left side face tingling about 4 hours after shot, headache for 3 days, fogginess and unable to concentrate for 3 days. About two-three days after vaccination, i began to experience chest pains; particularly in the left side of my chest, which started as a stabbing pain and is now a dull aching constant pain which radiates up my left back and neck. My other vitals (blood pressure, heart rate and breathing) have been normal. I did see my primary care doctor for an ECK 5 days after vaccination, and she referred me to a cardiologist for further testing. I saw a cardiologist 9 days after vaccination, and I'm waiting on results from the echocardiogram the doctor ordered to check for possible pericarditis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: EKG and Echocardiogram
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Tylenol and Motrin (as needed)
Allergien: none that i am aware of
Vorherige Impfungen: -

VAERS 1794853

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: -
Alter: 37,0
Geschlecht: F
Eingang: 18.10.2021
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Seizure

Symptomtext

Was sent to hospital, vax triggered seizures.

Weitere VAERSDATA-Felder

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

VAERS 1779938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

schwer

Staat: FL
Alter: 21,0
Geschlecht: F
Eingang: 18.10.2021
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Loss of consciousness Seizure Syncope

Symptomtext

about 10min after she COVID shot my daughter had a little Seizure and we went Unconscious. Had to call 911 her BP 88/44? and heart rate was 44?

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NO
Vorgeschichte: NO
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1794107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: ME
Alter: 63,0
Geschlecht: F
Eingang: 17.10.2021
Impfdatum: 07.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hospitalisation Ventricular tachycardia

Symptomtext

PATIENT STATES WENT INTO VENTRICULAR TACHYCARDIA APPROXIMATELY 3 HOURS AFTER RECEIVING PFIZER COVID VACCINE IN COMBINATION WITH FLUBLOK VACCINE WHICH REQUIRED HOSPITALIZATION.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hospitalisation
Hospital-Tage: -
Labordaten: UNKNOWN
Aktuelle Erkrankungen: NO
Vorgeschichte: CHF, A-FIB
Andere Medikamente: ENTRESTO, GABAPENTIN, XARELTO
Allergien: UNKNOWN A-FIB MEDICATION PER PATIENT
Vorherige Impfungen: -

VAERS 1793592

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: OH
Alter: 44,0
Geschlecht: F
Eingang: 17.10.2021
Impfdatum: 10.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Bell's palsy Computerised tomogram head normal Double stranded DNA antibody Facial paralysis

Symptomtext

Acute onset of right-sided facial paralysis (Bell's palsy). Symptoms began 3 days after vaccination. Treatment was initiated with short course of steroids (prednisone 60 mg daily for 1 week).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: 2,0
Labordaten: CT head w/o contrast (10/13): negative for acute intracranial abnormality dsDNA test (10/14): normal
Aktuelle Erkrankungen: -
Vorgeschichte: lupus, lupus nephritis, kidney transplant, hypertension
Andere Medikamente: amlodipine, apixaban, losartan, metoprolol, cellcept, protonix, predisone, prograf
Allergien: cefazolin, ciprofloxacin, morphine, penicillins, cefaclor, iodine
Vorherige Impfungen: -

VAERS 1791095

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: CA
Alter: 31,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: 28.09.2021
Beginn: 28.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Blood pressure measurement Body temperature Dizziness Flushing Heart rate Laboratory test Loss of consciousness Maternal exposure during pregnancy Oxygen saturation Respiratory rate SARS-CoV-2 test Syncope Tunnel vision Vomiting

Symptomtext

Vasovagal Syncope; slight tunnel vision; closed eyes, reports passed out; flush; lightheaded; vomit; Is pregnant: Yes/ Pt is pregnant due on 01Nov2021; This is a spontaneous report from a contactable nurse. A 31-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: FF8841), intramuscular, administered in left arm on 28Sep2021 16:36 (at the age of 31 years old) as dose 1, single for COVID-19 immunisation. Medical history included Mild Anemia Due to Pregnancy and near syncopal episode. No COVID prior to vaccination and no known allergies. Concomitant medications included acetylsalicylic acid (BABY ASPIRIN); fish oil (DHA FISH OIL); iron and prenatal vitamins. No other vaccines were administered in four weeks. The patient received the vaccine at 1636, 15 minutes later, she became flush, lightheaded, slight tunnel vision, closed eyes and reported passed out. Vaccination staff observed that the patient dropped her laptop and had her head down with vomit on the floor, tapped her and she was responsive but did not realize she had vomited or dropped her laptop. V/S was T 97.0, P 92, R 20, BP 121/78 and O2 sat was 97% RA at 1650. Fire department/paramedics responded and took her to hospital's ER, treated with IV fluids while in ambulance. Multiple labs done. Diagnosis was Vasovagal Syncope. The patient reported hx of near syncopal episode after recent blood drawn for current pregnancy. The patient is pregnant and id due on 01Nov2021. The events resulted in Emergency room/department or urgent care. The patient was treated with IV fluids in response to the events. The patient was tested for COVID post vaccination. The patient underwent Binex via Nasal swab on 28Sep2021 and was negative. The outcome of the events was recovered on an unspecified date. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 20210928; Test Name: BP; Result Unstructured Data: Test Result:121/78; Test Date: 20210928; Test Name: T; Result Unstructured Data: Test Result:97.0; Test Date: 20210928; Test Name: P; Result Unstructured Data: Test Result:92; Test Date: 20210928; Test Name: Multiple labs done; Result Unstructured Data: Test Result:. Dx Vasovagal Syncope; Comments: Multiple labs done. Dx Vasovagal Syncope; Test Date: 20210928; Test Name: O2 sat; Result Unstructured Data: Test Result:97%; Test Date: 20210928; Test Name: R; Result Unstructured Data: Test Result:20; Test Date: 20210928; Test Name: Binex; Test Result: Negative ; Comments: COVID test post vaccination: COVID test type post vaccination: Nasal Swab, COVID test name post vaccination: Binex, COVID test date: 28Sep2021, COVID test result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anemia of pregnancy; Presyncope
Andere Medikamente: BABY ASPIRIN; DHA FISH OIL; IRON
Allergien: -
Vorherige Impfungen: -

VAERS 1788923

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: MI
Alter: 17,0
Geschlecht: F
Eingang: 15.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Loss of consciousness Musculoskeletal stiffness Syncope

Symptomtext

Fainting, stiffness and temporary loss of consciousness.

Weitere VAERSDATA-Felder

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

VAERS 1785941

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

schwer

Staat: -
Alter: 16,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Syncope

Symptomtext

fainting post vaccination

Weitere VAERSDATA-Felder

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

VAERS 1785295

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: FL
Alter: 35,0
Geschlecht: M
Eingang: 14.10.2021
Impfdatum: 13.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Erythema Flushing Loss of consciousness Syncope

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Medium, Additional Details: Approximately 1-2 minutes after IM administration patient developed redness on his face, flushing, blackout and felt the need to lie down on the floor. Patient remain concious during the incidence, asked for water and was provided, fan. After 15-20 minutes, patient feel better and left the store.

Weitere VAERSDATA-Felder

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

VAERS 1780338

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff8841

schwer

Staat: TX
Alter: 43,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 07.10.2021
Beginn: 10.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / RA

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

Blood test abnormal Chest X-ray normal Computerised tomogram normal Electrocardiogram normal Pericarditis

Symptomtext

Acute pericarditis. Symptoms (pain on left side of chest, going up to shoulder) began evening of 10/10, three days after Pfizer booster. Went to urgent care on 10/11. They suggested I go to an ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: 10/20/21 EKGs, chest X-rays, CT scan, blood work All except blood work were normal.
Aktuelle Erkrankungen: None
Vorgeschichte: Mal de debarquement
Andere Medikamente: Trisprintec, clonazepam, Flonase, and vitamins D, B-12, Zinc
Allergien: None
Vorherige Impfungen: -

VAERS 1779669

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: NY
Alter: 72,0
Geschlecht: M
Eingang: 12.10.2021
Impfdatum: 30.09.2021
Beginn: 05.10.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / LA

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

Bell's palsy Extra dose administered

Symptomtext

Patient developed Bell's Palsy 1 week after 3rd dose of vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKA
Vorherige Impfungen: -

VAERS 1778819

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: FL
Alter: 70,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 01.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Condition aggravated Contusion Eye contusion Fatigue Headache Memory impairment Nasal oedema Skin laceration Suture insertion Syncope

Symptomtext

Wednesday night I started experiencing pretty severe chills (had happened with dose #2 so I was expecting it). Chills off and on through Thursday. Headaches. Tiredness. At some point Friday I fainted (had not happened before), but do not remember many details. I called a friend to pick me up & take me to walk in clinic. I do not remember much from that visit. My friend would be very happy to provide additional details as my memory is foggy. The gash required 3 stitches which come out Thursday. I have a black eye, swollen nose (not broken), contusions on both elbows, and a huge bruise on one hip. My permanent damage will be an unsightly scar across my forehead.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Dr at walk-in clinic gave me a tetanus-diphtheria
Aktuelle Erkrankungen: none
Vorgeschichte: insomnia osteopenia degenerative disc disease back
Andere Medikamente: ASA 81 mg Omeprazole 20 mg Lutein 20 mg Amlodipine 2.5 mg Ambien 10 mg Gabapentin 100-300 mg bisphosphonate calcium/vitamin D azelastine flonase
Allergien: nka
Vorherige Impfungen: experienced chills, headache with dose 2

VAERS 1777960

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: MO
Alter: 36,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 08.10.2021
Beginn: 10.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Feeling hot Presyncope Sensory disturbance

Symptomtext

She was very forceful with the needle (I almost blacked out). I felt a sensation in my right upper back when she stabbed my left arm My main concern now, which started two days after the vaccination, is that I am periodically getting warm sensations on my right thigh.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None, but wrist surgery for Dequervains tendonitis two weeks prior
Vorgeschichte: None
Andere Medikamente: Amitriptyline at night, Vicodin as needed for pain post wrist surgery but had not taken any five days prior to vaccine
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1776896

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: MO
Alter: 28,0
Geschlecht: M
Eingang: 11.10.2021
Impfdatum: 05.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Hyperhidrosis Loss of consciousness Malaise Unresponsive to stimuli

Symptomtext

Patient became dizzy/diaphoretic during 15-minute post-vaccination waiting period in pharmacy waiting area; patient reported feeling unwell to pharmacy staff; this pharmacist escorted patient back to vaccination room with assistance of pharmacy manager; cold compress applied to patient's forehead, water offered- patient experienced brief loss of consciousness and became unresponsive to verbal commands for approximately 60 seconds; pulse strong; upon regaining consciousness determined patient had worked an overnight shift and had nothing to eat all day prior to vaccination; provided food/water/direct observation for at least 30 minutes, and indirect observation for additional 15 minutes- symptoms fully resolved

Weitere VAERSDATA-Felder

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

VAERS 1775850

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: MT
Alter: 46,0
Geschlecht: F
Eingang: 10.10.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Cough Dysphonia Dyspnoea Lip swelling Oropharyngeal discomfort Pallor Paraesthesia oral Pulse abnormal Throat tightness

Symptomtext

Patient had signs and symptoms of anaphylaxis approximately 10 minutes s/p administration of first Pfizer COVID-19 vaccine. Within the first 10 minutes (max) of receiving vaccine , patient reported to monitoring RN that she was having some new feelings in her throat. She was brought to the sick bay area and attended to by myself with assistance of 2 other members of the immunization team. She progressively developed additional sx: throat tightness, SOB, "tongue feels weird", hoarse voice, and onset of coughing. Lips appeared to have swelling (later confirmed when lip size lessened after Epi administration), lung sounds & throat exam were normal, pulse weak but normal rate, skin pale, warm & dry. Epinephrine administered IM to left lateral thigh, followed by 50mg Benadryl IM to R deltoid. Within 5-8minutes s/p Epi administration, patient reported improvement of symptoms. EMS was called, per protocol, patient refused their advised transport to ED, medical control at Community Medical Center was contacted by EMS, with whom patient then spoke directly. Patient again refused transport, afterwhich ED physician called in prescriptions for Epi-Pen and oral steroid for her, with instructions given to patient on home care. Vital signs remained stable, and patient was escorted with steady gait & without any signs of distress to car (picked up by a family member) . At time of departure, patient reported feeling much improved, voice was normal, skin was pink/warm/dry, respirations even & unlabored, pulse strong, and patient had drank water without problems, Pt was contacted the following day by myself, and she reported that no complications arose overnight and she was doing "good". See scanned record of event

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unknown
Vorgeschichte: Patient checked on her COVD-19 Pre-vaccination checklist that she was immunocompromised.
Andere Medikamente: unknown
Allergien: Patient stated to vaccinator, prior to adminstration of Pfizer COVID-19 vaccine, that she was allergic "to some of the ingredients in Janssen (COVID-19) vaccine".
Vorherige Impfungen: -

VAERS 1775242

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: NY
Alter: 30,0
Geschlecht: M
Eingang: 09.10.2021
Impfdatum: 09.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chills Dizziness Erythema Fall Fatigue Injection site pain Myalgia Nausea Pain in extremity Swelling Syncope

Symptomtext

The patient was fine for 15 minutes after taking the shot. However, After 25 minutes the patient fell on the chair and started calling for help. He was feeling dizzy and fainting. He was saying that he is feeling like throw up. He was feeling nauseous, had a sore arm, swelling, redness, and pain at injection site. Tiredness, muscle pain, and chills was also reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 1775171

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: NY
Alter: 22,0
Geschlecht: M
Eingang: 09.10.2021
Impfdatum: 09.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Presyncope Vision blurred

Symptomtext

Near Syncope, Blurry Vision

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: GI problems
Andere Medikamente: Multi-vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1775165

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

schwer

Staat: FL
Alter: 19,0
Geschlecht: M
Eingang: 09.10.2021
Impfdatum: 09.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Seizure

Symptomtext

seizure for 10-20 seconds right the the shot

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: no
Vorgeschichte: not available
Andere Medikamente: none
Allergien: no
Vorherige Impfungen: -

VAERS 1775145

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

schwer

Staat: MN
Alter: 14,0
Geschlecht: M
Eingang: 09.10.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Dizziness Nausea Syncope Unresponsive to stimuli Vomiting

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Nausea-Medium, Systemic: Vomiting-Medium

Weitere VAERSDATA-Felder

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

VAERS 1775085

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff8841

schwer

Staat: -
Alter: 37,0
Geschlecht: F
Eingang: 09.10.2021
Impfdatum: 02.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: SYR / LA

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

Blood chloride increased Blood creatine phosphokinase increased Chest pain Dizziness Electrocardiogram Head discomfort Hyperhidrosis Limb discomfort Night sweats Pain Presyncope

Symptomtext

Sunday 12am I was awaken by severe nights sweats that soaked my clothes and sheets. Then it happen again after 4 am. This time I developed dull pain in chest and pain and discomfort in both legs. Late afternoon went To Er with concerns about symptoms. Symptoms worsen next day. Now chest pain and dizziness and near syncope. Went back to Er. Next day Near syncope got worse! Back to ER. Currently still having near syncope and dizziness with occasionally pressure in head and nose and face.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: 10/5 10/6 10/7 Ekg borderline abnormal 10/7 Magnesium low, creatine kinase elevated chloride high
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, hashimotos, autoimmune neutropenia, pernicious anemia,
Andere Medikamente: B12 complex, B vitamin sublingual, probiotics, selenium, ashwagandha, zyflamend , vitamin D, iron, elderberry
Allergien: Percocet and prednisone
Vorherige Impfungen: -

VAERS 1772602

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

schwer

Staat: CA
Alter: 20,0
Geschlecht: F
Eingang: 08.10.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Loss of consciousness

Symptomtext

Patient was observed seated on floor. Patient's mother stated she passed out.

Weitere VAERSDATA-Felder

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

VAERS 1772077

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

schwer

Staat: TX
Alter: 13,0
Geschlecht: F
Eingang: 08.10.2021
Impfdatum: 07.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Cold sweat Dizziness Fall Pallor Syncope

Symptomtext

The patient fainted, about 1 minute after receiving her immunization. She expressed feeling nervous about "needles". She was in the lobby of the pharmacy, beginning her 15 minute post immunization observation period when the event occurred. No trauma resulted from, her fall to the floor which was slow, and assisted by her parent. She got up almost immediately and felt dizzy. She was clammy and pale. Within 10 minutes she reported feeling "fine". Her parent chose not to have medical attention at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: no
Andere Medikamente: unknown
Allergien: none
Vorherige Impfungen: -

VAERS 1769687

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: WI
Alter: 18,0
Geschlecht: M
Eingang: 07.10.2021
Impfdatum: 07.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Loss of consciousness

Symptomtext

approximately 3-5 minutes after receiving 2nd pfizer covid vaccine, patient lost consciousness. He quickly regained consciousness after putting patient on his back, elevating his feet, and placing an ice pack on his forehead. EMS was called and patient was evaluated and released.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: not known
Vorgeschichte: not known
Andere Medikamente: not known
Allergien: none listed
Vorherige Impfungen: -

VAERS 1766169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: WV
Alter: 12,0
Geschlecht: M
Eingang: 06.10.2021
Impfdatum: 06.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Pallor Syncope

Symptomtext

Patient fainted for a few seconds within a few minutes of vaccination. Within 5 seconds he was talking but still had loss of color. Removed sweatshirt. Immediately gave ice packs and stuck ammonia inhalant under his nose to help. His color improved after 5 minutes. Patient stayed in pharmacy area for thirty minutes. He then played in a soccer game a few hours later and was continuing to do fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: no
Vorherige Impfungen: -

VAERS 1765516

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 06.10.2021
Impfdatum: 06.10.2021
Beginn: 06.10.2021
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 Dysarthria Facial paralysis

Symptomtext

Pt appeared with moderate facial drooping; pt remained A&O x4 with slurred speech; pt informed nurse of seizures with vaccine administration (this being her third seizure with three vaccinations); vs taken, pt informed of severity of bp elevation, pt tolerated education; pt informed of concern and possible hospital admission to monitor bp elevation, pt declined education, stated "I'll be fine once the medication kicks in." pt reassessed 5mins after initial assessment and vs, pt A&O x4, clear speech, and no facial drooping; pt informed nurse of willingness to go home after gaining back full consciousness and no hospital admission was needed; pt ambulatory with front wheel walker independently, left the unit @1200 Vitals: 10/06/21 1147 10/06/21 1155 BP: (!) 194/77 (!) 177/56 BP Patient Position: SITTING SITTING BP Location: RL-RIGHT LEG RA-RIGHT ARM Pulse: 73 75 Resp: 20 18 SpO2: 99% 99%

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: ATHEROSCLEROSIS OF AORTA, BILATERAL MASTECTOMY DEFORMITY, CHRONIC PAIN, DERANGEMENT OF LEFT KNEE, DIVERTICULOSIS, DM TYPW 2, EPILEPSY, HTN, ASTHMA, OSTEOARTHRITIS OF BILATERAL KNEES, RIGHT OPEN ANGLE GLAUCOMA, SEVERE OBESITY
Vorgeschichte: HX OF BREAST CANCER, FATTY LIVER, COLONIC POLYPS
Andere Medikamente: N/A
Allergien: BACLOFEN, NABUMETONE, SHRIMP AGENT, BENZONATATE, LISINOPRIL, LOSARTAN POTASSIUM, AMPICILLIN, ERTHROMYCIN BASE, INDOMETHACIN, ULTRAM, GABAPENTIN, SULFA, WELLBUTRIN, LIDOCAINE, CAFFEINE, FLUOXETINE HYDROCHLORIDE, IVP DYE, IODINE CONTAINING, KETOROLAC TROMETHAMINE, LACTOSE, LEXAPRO, PROCARDIA, PROPOXYPHENE HCL
Vorherige Impfungen: -

VAERS 1765499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: NC
Alter: 39,0
Geschlecht: M
Eingang: 06.10.2021
Impfdatum: 06.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Blood pressure increased Presyncope Treatment noncompliance

Symptomtext

The patient had a near syncopal episode after receiving his 2nd Pfizer vaccine. He reports having a similar reaction with the 1st vaccine but this time it was worse. BP was 196/120. Reports not being non-compliant with BP medication has not taken today. 911 called BP was 164/98 95% 18 R when patient left with EMS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: 2nd Pfizer vaccine
Aktuelle Erkrankungen: Hypertension and 1ppd smoker
Vorgeschichte: Hypertension
Andere Medikamente: BP medication name unknown "small pink pill"
Allergien: None
Vorherige Impfungen: -

VAERS 1762527

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: NC
Alter: 29,0
Geschlecht: M
Eingang: 05.10.2021
Impfdatum: 05.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Confusional state Dyskinesia Generalised tonic-clonic seizure Speech disorder

Symptomtext

Patient discharged from clinic at 6:07pm. He returned at 6:55pm complaining of muscle jerking. He sat in a chair and began to seize. He was assisted to the floor and had a grand mal seizure that lasted approximately 1 minute. His VS remained stable. He was confused after seizure, but responded to name and had garbled speech. He was able to focus and follow simple commands. EMS arrived and his speech clear and he was oriented X 3 at that time. Patient transported to Emergency Department.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Generalised tonic-clonic seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: seizures, not on medication
Vorgeschichte: seizure disorder
Andere Medikamente: Buprenorphine 20mg SL daily
Allergien: NKA
Vorherige Impfungen: -

VAERS 1761749

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: NY
Alter: 35,0
Geschlecht: F
Eingang: 05.10.2021
Impfdatum: 29.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Blood test Computerised tomogram Pain in extremity Peripheral swelling Skin discolouration Thrombosis Ultrasound scan abnormal

Symptomtext

I am a 35 year old healthy young woman . I received the first dose of the Pfizer vaccination on September 29, 2021 in by my house. By October 1, 2021 I had excruciating pain in my right arm. I didn't think it was anything. The pain had gotten worse and I noticed that it was all black and blue and very swollen. I went to an urgent care on October 3, 2021 and they sent me to the hospital. When I got to the hospital they did a sonogram on my right arm and found that I had a blood clot. How is it that I have been very healthy with no health issues, but after I received the first dose of the vaccine I developed a blood clot?

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 2,0
Labordaten: Blood work. vitals and sonogram and cat scan
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Bactrim, ceclor, codeine
Vorherige Impfungen: -

VAERS 1756402

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: NY
Alter: 55,0
Geschlecht: F
Eingang: 02.10.2021
Impfdatum: 30.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Extra dose administered Fall Hyperhidrosis Lip injury Syncope

Symptomtext

Approximately 16 hours after receiving my third Pfizer shot, I was light headed and dizzy. I passed out approximately 5 times. I do not remember falling, I woke up on the floor. I felt sweaty at that time also. I got a fat lip from hitting the floor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Breast Cancer 2017, Radiation 2018
Andere Medikamente: Anastrozole, Fosamax, Calcium, Vitamin D, Benedryl
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1753580

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

schwer

Staat: CA
Alter: 31,0
Geschlecht: F
Eingang: 01.10.2021
Impfdatum: 28.09.2021
Beginn: 28.09.2021
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Blood test Dizziness Exposure during pregnancy Flushing Laboratory test Loss of consciousness Syncope Tunnel vision Vomiting

Symptomtext

At 1636, received vaccine Pfizer 0.3ml IM in left deltoid. She was sitting in her chair holding her laptop, dropped laptop, staff checked on her. She had her head down, large amount of vomit on the floor, tapped her on the shoulder and was responsive. Asked if she was okay and responded, "Yes and apologetic for vomiting." At 1650, DSH-Napa's dispatch/Fire Department was notified. Her vitals signs were taken T97.0-P92-R20-BP 121/78 O2 sat-97% RA. was unaware she vomited or dropped her laptop. reports, "sitting in observation area, became flush, lightheaded, then slight tunnel vision, so she closed her eyes and passed out". Fire department responded, ambulance took her to ER where she was Dx Vasovagal Syncope. She reports receiving IV fluids in ambulance, no further tx at. She reports Hx of near syncopal episode after having a blood drawn recently due to pregnancy. Patient is pregnant and her due date is 11/1/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Multiple blood work and lab test done
Aktuelle Erkrankungen: Mild Anemia due to pregnancy
Vorgeschichte: None
Andere Medikamente: Baby Aspirin, Prenatal Vitamins, DHA-Fish Oil, Iron Supplements
Allergien: None
Vorherige Impfungen: -

VAERS 2714156

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: -
Alter: 93,0
Geschlecht: M
Eingang: 15.11.2023
Impfdatum: 20.10.2021
Beginn: 03.10.2023
Tage bis Beginn: 713,0
Dosis: 3
Route/Site: - / -

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

Agitation Asthenia Back pain COVID-19 Decreased appetite Dizziness Echocardiogram Echocardiogram normal Fall Fatigue Hypoaesthesia Labile blood pressure Myalgia Neurological examination normal Orthostatic hypotension Osteoarthritis Restlessness SARS-CoV-2 test positive

Symptomtext

Patient is a 95 y.o. male PMHx AS s/p TAVR (1/3/2019) c/b CHB s/p PPM (1/9/2019), non obstructive CAD (LHC 1/2019), CKD3b (baseline cr ~ 1.5), HTN, HLD, HFpEF, prostate cancer s/p resection (1993), recent COVID infection (positive 9/27/23 s/p paxlovid) who presented from IL on 10/3/2023 with CC weakness, fatigue, myalgias. Hospital course complicated by issues with dizziness/labile blood pressures, as well as acute on chronic back pain from recent fall. Orthostasis improved with gentle IVF as well as holding BP medications. TTE 10/09/2023 showing TAVR with stable function compared to report from 10/31/2019. PT/OT recommending SNF on discharge. Patient stable for discharge on 10/09 in stable condition to SNF. COVID-19, resolved Fatigue Poor Appetite, improved - Positive 9/27 s/p paxlovid; sxs onset 9/26 - here with fatigue, weakness, myalgias, and restlessness (severe/almost akethisia like) - Continue PT/OT; appreciate CM assistance with SNF at discharge Dizziness Orthostatic hypotension - Orthostasis quite positive, noted history of HFpEF and AS s/p TAVR - Improved with gentle IVF - TTE 10/09: Unchanged/stable TAVR compared to TTE in October 2019. - Discontinue Bumex and Coreg on discharge. Continue amlodipine 5 mg daily. Follow up with Cardiology as outpatient to discuss further GDMT. Acute on Chronic Back Pain - suspect OA and in light of fall above - TTP on left SI joint, no tenderness of lumbar SP; no observed erythema; gait with walker observed without foot drop; sacral XR as below - Continue lidocaine patch, tylenol, and gabapentin; encourage PT/OT Mechanical Fall - trying to get off toilet 10/4, no LOC, did not strike head, no prodromal sxs - "toilet was too low;" neuro checks benign; no skin tears appreciated - sacral XR without fracture - PT/OT following AS s/p TAVR - continue ASA 81 HTN - Home regimen: coreg 6.25 BID, bumex 0.25 mg daily, amlodipine 5 mg daily. - Discontinue Coreg and Bumex. Increase amlodipine back to 5 mg daily. Advise accepting higher blood pressures to avoid orthostasis and falls. Chronic HFpEF - Do not see recent exacerbation (likely was related to AS history) - Holding diuresis and Coreg as above. Will discontinue on discharge. Follow up with PCP and Cardiology. CKD3b - at baseline cr(1.6-1.8) - trend BMP daily; trend UOP CHB - s/p ppm 2019 - Noted. Gout - Continue allopurinol 150 mg daily (due to CKD). Toxic metabolic encephalopathy, resolved - ED documentation showing that he is agitated and made a comment "I wish I had a gun" - s/p haldol and seroquel 10/3; no access to firearms at independent living - no further SI/HI; mentation remains intact; AMA precautions removed. - Monitor. Numbness, resolved - New 10/7/23, left face, suspect related to CKD and gabapentin - on left face, no dysarthria or dysmetria; no ringing in ears Continue gabapentin 100 mg TID (reduced dose due to CKD).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Orthostatic hypotension
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2675317

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CT
Alter: 22,0
Geschlecht: F
Eingang: 22.08.2023
Impfdatum: 20.09.2021
Beginn: 22.09.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

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

Back pain Chest X-ray normal Chest discomfort Chest pain Computerised tomogram normal Dizziness Dyspnoea Electrocardiogram normal

Symptomtext

2 days after 1st Pfizer shot: Shortness of breath at RANDOM. Felt like airway was restricted and chest tightened. Also had some mild pain in center-right region of chest and on my back is same area - not often though. Started taking my inhalers (Albuterol & Qvar) to get relief - THEY DID NOT HELP EVEN MY RESCUE INHALER. Went to walk in clinic couple days later after it didn?t go away. Took chest X-ray, oxygen checked, EKG done. All came back normal. Slowly went away fully after about week and a half. 2nd Pfizer shot: Same experiences. Took Qvar and Albuterol again just because. Saw cardiologist for another EKG - normal. Took a month and a half to go away. Had COVID in December 2021: Same experiences for about a week and then it went away. Did go on Qvar & Albuterol again. Had blood work done January 2022 - normal. August 24, 2022: took a trip to Colorado and went up high altitude to hike. Felt short of breath very badly on car ride up - almost thought I was going to pass out. Trouble sleeping that night because I could not get enough air through. Shortness of breath would come and go at random. Very uncomfortable & lasted whole trip and beyond... Went back to the doctor to get another chest x-ray to compare to a year ago - normal. Was prescribed Advair (another inhaler) - did not make a difference. Had a CT scan done in December of 2022 - normal. Took months to get (a little) better. It's been a year now and I still feel mild symptoms almost every day. Not scary, but noticeable and irritating. Terrified that it will come back strong again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: O2 levels checked: 9/30/2021 (normal) EKG: 9/30/2021 (normal) Chest x-ray: 10/4/2021 (normal) Blood work: 1/17/2022 EKG with cardiologist: 10/7/2021 (normal) Prescribed Advair: 9/22/2022 CT scan: 12/3/2022 (normal)
Aktuelle Erkrankungen: None.
Vorgeschichte: Super mild asthma as a kid - outgrew it in my teen years. Only would get when sick or playing sports outdoors in cold weather.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 2575947

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: -
Alter: 54,0
Geschlecht: M
Eingang: 13.06.2023
Impfdatum: 12.10.2022
Beginn: 27.12.2022
Tage bis Beginn: 76,0
Dosis: 3
Route/Site: SYR / LA

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

Angina pectoris Angina unstable Obstructive sleep apnoea syndrome Blood pressure increased Condition aggravated

Symptomtext

OBSTRUCTIVE SLEEP APNEA UNSTABLE ANGINA ANGINA, UNSPECIFIED

Weitere VAERSDATA-Felder

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

VAERS 2608319

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MI
Alter: 68,0
Geschlecht: F
Eingang: 03.04.2023
Impfdatum: 20.10.2021
Beginn: 08.07.2022
Tage bis Beginn: 261,0
Dosis: 3
Route/Site: SYR / LA

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

Asthenia COVID-19 Chest pain Dyspnoea Exercise tolerance decreased Fatigue Hyperhidrosis Hypersomnia Oropharyngeal pain Palpitations SARS-CoV-2 test positive Somnolence Tachycardia Throat irritation

Symptomtext

Starting 07/09/2022, I started having a scratchy sore throat and feeling kind of tired. It progressively worsened over the day. I tested myself for COVID-19 late in the afternoon that day and I was positive. I called my doctor's office and they prescribed me Paxlovid and I was started on that. I was extremely exhausted and slept most of the day for about 4 days. After that, for the rest of the month, I was weak and would intermittently test positive for COVID-19. I was having shortness of breath. Before COVID-19, I would walk about 4 miles per day. After COVID-19, I would barely be able to walk a quarter mile. I would break out in sweat and be short of breath. I started having heart palpitations and chest pain. By September, it got so bad, that I went to the ER and they sent me home. The next day the pain and heart palpitations got so bad that I went to another hospital where I was hospitalized. I was hospitalized for Tachycardia and they referred me to a cardiologist. I wasn't able to get in to see them until this past February. When I did see them in February, they put me on a medicine called Flecainide. I was on that for a month and was still having breakthrough symptoms. I went back to see them in March and they increased the dosage. The symptoms have improved a lot now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: COVID-19 test (07/09/2022): Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Fibromyalgia; Arthritis; Chronic Back Pain; Hx of Knee Replacement; High Cholesterol; High Blood Pressure; Heart Palpitations; Hypothyroidism
Andere Medikamente: Levothyroxine; Metoprolol; Montelukast; Pravastatin; Cetirizine; Lipoflavanoid; Healthy Eyes supplement; Hair, skin and nails soft gel supplement; Baby Aspirin
Allergien: None
Vorherige Impfungen: -

VAERS 2602025

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IN
Alter: 79,0
Geschlecht: F
Eingang: 22.03.2023
Impfdatum: 04.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Dizziness Fatigue Injection site pain Mobility decreased Pyrexia Retching

Symptomtext

dizzy, lightheaded. Extreme exhaustion. fever over 100. Dry heaves for a couple of hours too. lasted for 3 days. sore site for 5 days. couldnt do much of anything for the first two days. fever gone 3rd day. energy level improved some by 4th day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: COPD, post lung cancer, past aFib (both treated and cured prior years)
Andere Medikamente: Trelegy Elipta, Eliquis, Simvastatin, Amlodipine, loradine
Allergien: Penicillin, Reclast, Diltiazem
Vorherige Impfungen: sore site

VAERS 2596024

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MI
Alter: 58,0
Geschlecht: F
Eingang: 14.03.2023
Impfdatum: 22.09.2021
Beginn: 10.03.2023
Tage bis Beginn: 534,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Chest pain Dyspnoea SARS-CoV-2 test positive

Symptomtext

Pt has a PMH of HTN, HLD, CKD stage III, chronic heart failure with preserved EF, and chronic respiratory failure secondary to COPD. Pt arrived to ED due to chest pain and dyspnea and was found to be COVID-19 positive.

Weitere VAERSDATA-Felder

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

VAERS 2560155

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 60,0
Geschlecht: M
Eingang: 14.01.2023
Impfdatum: 17.11.2021
Beginn: 01.09.2022
Tage bis Beginn: 288,0
Dosis: 3
Route/Site: SYR / LA

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

Arthritis Discomfort Mobility decreased Musculoskeletal stiffness

Symptomtext

Arthritis has appeared in left and right hands. Stiffness and slight slight discomfort in moving fingers, grasping objects. Left hand arthritis is more severe, with discomfort in curling fingers to make a closed fist, and middle finger becoming slightly crooked. Right hand symptoms not nearly as bad, but noticeable. There was no sign of arthritis before vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: There have been no medical tests or lab results related to this adverse event.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 2547069

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MI
Alter: 80,0
Geschlecht: M
Eingang: 30.12.2022
Impfdatum: 15.01.2021
Beginn: 13.11.2022
Tage bis Beginn: 667,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

11/13/22 presents to ED for "breathing problem". PMHx of "Parkinson's disease, atrial fibrillation"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 1/13/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2533305

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 48,0
Geschlecht: F
Eingang: 15.12.2022
Impfdatum: 07.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Mobility decreased Pain of skin

Symptomtext

I had had a reaction of serious joint and skin pain to my second COIV dose. It was the same, but less severe. I was still in bed for 2 days, taking the same meds as the first time, which is pain meds and Benadryl, I probably took some Valium as well...

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Gabapentin, Duloxetine, Emgality, bioidentical hormones
Allergien: -
Vorherige Impfungen: A couple of years before similar, but more serious reaction to a flu shot and T-dap, then I had to go to the ER, and the previou

VAERS 2481606

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: OH
Alter: 49,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 15.10.2021
Beginn: 05.07.2022
Tage bis Beginn: 263,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Cough Dyspnoea Fatigue Impaired work ability Influenza virus test negative Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I tested positive for COVID-19 in July and had difficulty breathing, coughing, very tired, fever, body aches. I went to the clinic and was tested for COVID-19 and the Flu and I was given Teflalon pearls for the cough. I was not able to work for 2 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 test- positive; Flu- negative
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma; Migraines; Anxiety
Andere Medikamente: Pantoprazole; Fluoxetine; Bupropion; Buspirone; Tizanidine; Qlipta; Qvar
Allergien: Zonisamide; Latex; Benzalkonium fluoride
Vorherige Impfungen: Every time I get a Flu shot I have fever, coughing, asthma symptoms, and fatigue. I had that reaction with my 2 prior COVI-19 sh

VAERS 2456478

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: OH
Alter: 83,0
Geschlecht: F
Eingang: 23.09.2022
Impfdatum: 20.10.2021
Beginn: 02.09.2022
Tage bis Beginn: 317,0
Dosis: 3
Route/Site: UN / UN

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

COVID-19 Dyspnoea SARS-CoV-2 RNA SARS-CoV-2 test positive

Symptomtext

Tested COVID positive, symptoms include shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Nasopharyngeal test collected 9/02/2022 detected 2019 Coronavirus RNA on 9/02/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Type 2 diabetes mellitus, cardiovascular disease, and hypertension.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2452304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MI
Alter: 79,0
Geschlecht: M
Eingang: 20.09.2022
Impfdatum: 12.10.2021
Beginn: 09.09.2022
Tage bis Beginn: 332,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Anticoagulant therapy Atrial fibrillation Blood creatinine increased Blood potassium increased C-reactive protein increased COVID-19 Cardioversion Chest X-ray normal Chills Electrocardiogram normal Hyperkalaemia Hypotension Hypoxia Myocardial ischaemia Procalcitonin normal Pyrexia Renal impairment

Symptomtext

Discharge Provider: MD Primary Care Provider at Discharge: MD Admission Date: 9/9/2022 Discharge Date: 9/10/2022 PRESENTING PROBLEM: COVID-19 [U07.1] HOSPITAL COURSE: An 80 years old gentleman who presented to the Health emergency department on 9/9/2022 because of fever and chills after he underwent successful DC cardioversion for atrial fibrillation early in the day on the 9th. His work-up in the emergency department was found to have fever 38.9, and the initial workup showed positive COVID-19 PCR rapid test, elevated troponin 31, and elevated creatinine 1.9 with known baseline 1.2 and an elevated potassium of 5.2. The chest x-ray did not show any acute cardiopulmonary process and the urinalysis was unremarkable for any evidence of infection. He was admitted for COVID-19 with sepsis. In the ED the patient developed hypoxia with exertion down to 84% on room air. His procal was unremarkable at 0.08 and CRP only minimally elevated 12.9. He was started on decadron and IV fluids during the stay and his home lisinopril was help due to AKI/hyperkalemia and hypotension. He was started on norvasc 5mg during the stay. The patient's renal function improved however his potassium up trended to 5.5. He was given a dose of lokelma and a repeat BMP was ordered prior to discharge. Will stop decadron as this is not indicated for patients with COVID without hypoxia. Upon initial presentation troponin elevated to 31 down trended to 22. He denies chest pain. Given cardioversion prior tin the day suspect this was demand ischemia vs AKI. No evidence of ST elevation or depression on 12 lead electrocardiogram. The patient had successful DC cardioversion. The patient is still on Eliquis and will remain on the Zio patch. Recommend post-hospitalization follow-up with PCP 1-week following discharge and a repeat BMP in 1 week to reassess renal function and potassium.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Rotator cuff rupture, complete, left; Other hyperlipidemia; Erectile dysfunction Rosacea; Hx of malignant neoplasm of prostate; CAD in native artery; Essential hypertension Wears dentures; Idiopathic gout, unspecified chronicity, unspecified site; Chronotropic incompetence; Chronic left-sided low back pain without sciatica; History of smoking Frequent PVCs; History of melanoma; DOE (dyspnea on exertion); Atrial fibrillation (HCC) Elevated troponin; Acute kidney injury (nontraumatic) (HCC); COVID-19; Hyperkalemia
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 2433663

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MI
Alter: 77,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 15.01.2021
Beginn: 28.08.2022
Tage bis Beginn: 590,0
Dosis: 3
Route/Site: - / -

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

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

Symptomtext

08/28/22 presents to EC ED for "right chest pain". PMHx of "right lung transplant on chronic immunosuppression, GERD, hypothyroidism, prior bladder cancer, osteoporosis, CKD, MDD/GAD"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 08/28/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430968

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 07.09.2022
Impfdatum: 11.10.2021
Beginn: 25.08.2022
Tage bis Beginn: 318,0
Dosis: 3
Route/Site: - / -

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

Abdominal pain Acute kidney injury Asthenia Blood creatinine increased Blood potassium increased COVID-19 Chest X-ray normal Chills Cough Full blood count normal Hypophagia Hypotension Laboratory test Malaise Mobility decreased Myalgia Nausea SARS-CoV-2 test positive

Symptomtext

75-year-old female past medical history of AFib on Eliquis, hypertension, coronary artery disease, CKD 3, hyperlipidemia and insulin-dependent diabetes who presented to the Emergency Department on 08/25 for generalized weakness accompanied by nausea. Apparently, she was in the emergency department the preceding day for nausea and abdominal pain as well as cough, myalgias and chills, was tested for COVID and found to be positive but given no respiratory symptoms or hypoxia was discharged. On the subsequent visit she described her general weakness they exited the point she was unable to arise from her floor requiring transportation by EMS. Of note the patient was reportedly hypotensive for EMS at 80/30. In the emergency department, patient was placed on routine monitoring and basic laboratory studies were obtained. Her vital signs were stable and laboratory work was significant for unremarkable complete blood count menstruated demonstrated a creatinine of 2.16 up from only 1.09 the preceding day. Potassium was also elevated at 5. Given her acute kidney injury in the setting of recent COVID infection she also had a chest x-ray that was without acute process. The patient was ultimately admitted to the hospital for her AKI, felt strongly to be pre renal in this causes as the patient disclosed that she had had poor oral intake with her recent symptomatology from COVID. She was fluid resuscitated, and received frequent laboratory draws to monitor the for kidney and her serum potassium. With fluids, she continued to convalesce and is medically stable for discharge 08/28/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: CAD in native artery Edema Dyslipidemia Type II diabetes mellitus (HCC) Hypertension Preop cardiovascular exam Atrial fibrillation (HCC) AKI (acute kidney injury) (HCC
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet amLODIPine (NORVASC) 5 MG tablet atorvastatin (LIPITOR) 40 MG tablet Bacillus Coagulans-Inulin (PROBIOTIC FORMULA PO) Cholecalciferol (VITAMIN D-3 PO) dulaglutide (TRULICITY) 1.5 MG/0.5ML injection ELIQ
Allergien: Tramadol PenicillinsHives MetforminNausea Only Cats Dust
Vorherige Impfungen: -

VAERS 2427945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: HI
Alter: 57,0
Geschlecht: M
Eingang: 02.09.2022
Impfdatum: 07.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: SYR / RA

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

Hypoaesthesia Paraesthesia

Symptomtext

Tingling and numbing sensation in the left and right feet and toes (10/28/21 to 9/2/22).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Valsartan, Chlorthalidone, Mometasone Furoate
Allergien: -
Vorherige Impfungen: -

VAERS 2427593

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MI
Alter: 93,0
Geschlecht: F
Eingang: 02.09.2022
Impfdatum: 08.04.2022
Beginn: 08.08.2022
Tage bis Beginn: 122,0
Dosis: 3
Route/Site: - / -

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

Angiogram pulmonary normal Asthenia COVID-19 Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

Patient up to date on COVID vaccines who admitted with complications r/t COVID and COVID detected PCR. Provider d/c note: "94 F with PMH HLD, Anemia, HTN, OA, Mild Cognitive impairment with memory loss, Chronic Insomnia, Depression who is presenting to the ED for evaluation of worsening weakness, cough, and SOB. Patient is on chronic O2 nasal cannula at home. Was found outpatient to be COVID positive and started on Paxlovid Initial workup included a CTA that was negative for PE. Patient was found to be COVID positive. Patient was started on Decadron as well as remdesivir and monitored overnight. Patient maintained on her home O2 nasal cannula and her strength improved. Patient was discharged home to resume Paxlovid therapy and follow-up with primary care provider for continued care."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: COVID detected PCR on 08/08/22
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic obstructive pulmonary disease with acute exacerbation (*) HYPERLIPIDEMIA, MIXED (272.2) HYPERTENSION, BENIGN ESSENTIAL (401.1) Macular degeneration of both eyes Anxiety Osteoarthritis of right hip Mild cognitive impairment with memory loss Iron deficiency anemia Panlobular emphysema (*) Depression, major, in remission (*) Aortic valve stenosis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2421061

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MI
Alter: 14,0
Geschlecht: M
Eingang: 26.08.2022
Impfdatum: 02.10.2021
Beginn: 23.08.2022
Tage bis Beginn: 325,0
Dosis: 2
Route/Site: - / -

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

Asymptomatic COVID-19 Chest pain Echocardiogram normal Electrocardiogram normal SARS-CoV-2 test positive Troponin increased

Symptomtext

Primary Care Physician at Discharge: Medical doctor. Admission Date: 8/23/2022 Discharge Date: 8/23/22 PRESENTING PROBLEM: Elevated troponin HOSPITAL COURSE: The patient is a 15 y.o. who presented to hospital with sharp chest pain exacerbated with breathing a few hours after sport practice and found to have mildly elevated troponin levels. Subsequently found to be COVID positive. He was transferred to other hospital for further evaluation. Chest pain on further evaluation aligned with musculoskeletal etiology. His EKG obtained here showed no changes and he had a normal echocardiogram. Troponins have returned to normal from elevation at outside hospital. He had no elevation in his inflammatory markers to support inflammation from myocarditis. Overall, it is unlikely this patient currently has myocarditis. He currently presents with an asymptomatic COVID infection. Based on our evaluation we determined that patient did not require any further hospitalization. Will be discharge home to follow up with his PCP should COVID symptoms progress. Labs reviewed from last 24 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Reactive airway disease Overweight child with BMI >99% for age Nocturnal enuresis Obesity with body mass index (BMI) in 99th percentile for age in pediatric patient, unspecified obesity type, unspecified whether serious comorbidity present Chest pain Elevated troponin
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amitriptyline (ELAVIL) 25 MG tablet DULoxetine (CYMBALTA) 60 MG delayed release capsule DULoxetine (CYMBALTA) 60 MG delayed release capsule fexofenadine (
Allergien: ShellfishAsthma/Shortness of Breath, Cough, Hives, Itching, Shortness of Breath, Swelling GuanfacineOther, Confusion, Unknown Intuniv [Guanfacine Hcl Er]Other TrazodoneOther
Vorherige Impfungen: -

VAERS 2408483

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MN
Alter: 85,0
Geschlecht: U
Eingang: 11.08.2022
Impfdatum: -
Beginn: 12.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

COVID-19 Pneumonia SARS-CoV-2 test positive

Symptomtext

fully vaccinated. COVID positive 8/10/22. Admitted for pneumonia.

Weitere VAERSDATA-Felder

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

VAERS 2396398

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NC
Alter: 51,0
Geschlecht: F
Eingang: 29.07.2022
Impfdatum: 08.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Injection site pain Magnetic resonance imaging abnormal Muscle injury Oedema Paraesthesia

Symptomtext

Patient received vaccine on 11/8/2021. Patient reports injection site soreness worsening 2 days after receiving injection. Patient describes soreness as "a million needles" in entire right arm, into hand, and fingers. Patient followed up with Primary Care Physician. PCP referred patient to orthopedic specialist. Patient had MRI done. MRI showed "fluid" per patient. Patient got a second opinion from patient's employee's health center via phone visit with Dr.. On 7/29/2022, patient followed up with Dr., sports medicine specialist. Per patient Dr. stated he could not rule out that the vaccine injection has caused "muscle damage." Plan is to refer patient for physical therapy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: MRI
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes Hypertension High cholesterol
Andere Medikamente: Ozempic injection on Fridays Enalapril/HCTZ 10-25 mg daily Lovostatin 20 mg daily Sertraline 50 mg daily
Allergien: Percocet
Vorherige Impfungen: -

VAERS 2395016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MD
Alter: 58,0
Geschlecht: M
Eingang: 28.07.2022
Impfdatum: 01.03.2022
Beginn: 19.07.2022
Tage bis Beginn: 140,0
Dosis: 4
Route/Site: IM / LA

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

Abdominal discomfort Back pain COVID-19 Cough Discomfort Fatigue Headache Mobility decreased Nasal congestion Nasopharyngitis Nervous system disorder Pain Paranasal sinus hypersecretion Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

On July 19th while at work as I walked down the hall I noticed lower back pain a few times at work as if I had strained myself. It felt like I had "something pushing in and down". Later that evening when I arrived home from work, after sitting still in the car on commute, I had difficulty getting out of my vehicle when I arrived home. On a pain scale I would note a 3 but it was difficult. I did home a test and it was positive. I made arrangements to isolate from family. I began to have cold-like symptoms. The following day I had congestion and runny nose. I began to have a dry, irritating, cough which is worse now. I don't feel like it is going into my chest but I am coughing up drainage from my nose. I have had a dull headache and after my coughing spells my head hurts bad because of some nerve endings. The nerve endings on the top of my head seem to very sensitive to my touch. I have a pelvic pressure or front intestinal discomfort, abnormal pressure on both sides of my intestines. As of today, 10, I still have fatigue. I have the nasal congestion which is still continuing to cause my headaches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Home COVID-19
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2364393

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: FL
Alter: 39,0
Geschlecht: F
Eingang: 11.07.2022
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Biopsy Burning sensation Migraine Rash Rash pruritic

Symptomtext

Within 3 hours of first vaccine, a small rash developed on right hand. It became itchy with burning sensations as time went on. Slowly throughout the next few days, more spots appeared on the right hand. After the 2nd dose, the rash then appeared on the left hand. These rashes have been on my hands since Nov 2021. I experience flare ups at least once a week with no commonality in my environment. Also, within a week after my second dose I was admitted to the ER with a migraine that could not be resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: I have been seeing a dermatologist and they ran a biopsy on 30Dec2021. I am currently on my 5th cream to try and calm the flare ups with no success in removing the rash.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Pre-natal vitamins, Sumatriptan as needed for migraine
Allergien: Vancomycin, mold, dust mites
Vorherige Impfungen: -

VAERS 2357926

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NY
Alter: 66,0
Geschlecht: M
Eingang: 05.07.2022
Impfdatum: 06.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Arthralgia Groin pain Impaired driving ability Loss of personal independence in daily activities Mobility decreased Musculoskeletal stiffness Pain Pain in extremity Peripheral swelling

Symptomtext

Arm ache, stiffness, can't lift or move arm, swollen hand, shoulders ache, knees ache, back of legs ache, groin area hurts, can't dress self or drive anymore, can hardly move, in constant extreme pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: Atorvastatin 20 mg Metformin HCL ER 500 mg Jardiance 25mg
Allergien: -
Vorherige Impfungen: -

VAERS 2325577

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: TX
Alter: 40,0
Geschlecht: M
Eingang: 25.06.2022
Impfdatum: 02.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / UN

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

Antinuclear antibody Anxiety Asthenia Blood pressure increased Blood thyroid stimulating hormone Blood pressure measurement Depression Dizziness Fatigue C-reactive protein Condition aggravated Full blood count Headache Hypersomnia Laboratory test Lipids Loss of personal independence in daily activities Magnetic resonance imaging

Symptomtext

Migraines; dizziness; blurred vision; extreme light sensitivity; depression; hypersomnia; elevated blood pressures; palpitations; Debilitating, now cannot work; nausea; fatigue; myalgias; This is a spontaneous report received from a contactable reporter(s) (Other HCP). A 40-year-old male patient received BNT162b2 (BNT162B2), on 02Oct2021 as dose 2, single (Lot number: FF8841) at the age of 40 years intramuscular for covid-19 immunisation. The patient's relevant medical history included: "HTN" (unspecified if ongoing); "generalized anxiety since symptoms started" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number= EW0100), for Covid-19 Immunization. The following information was reported: LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (disability) with onset 08Oct2021, outcome "not recovered", described as "Debilitating, now cannot work"; VISION BLURRED (disability) with onset 08Oct2021, outcome "not recovered", described as "blurred vision"; DEPRESSION (disability) with onset 08Oct2021, outcome "not recovered"; DIZZINESS (disability) with onset 08Oct2021, outcome "not recovered"; BLOOD PRESSURE INCREASED (disability) with onset 08Oct2021, outcome "not recovered", described as "elevated blood pressures"; PHOTOPHOBIA (disability) with onset 08Oct2021, outcome "not recovered", described as "extreme light sensitivity"; FATIGUE (disability) with onset 08Oct2021, outcome "not recovered"; HYPERSOMNIA (disability) with onset 08Oct2021, outcome "not recovered"; MYALGIA (disability) with onset 08Oct2021, outcome "not recovered", described as "myalgias"; NAUSEA (disability) with onset 08Oct2021, outcome "not recovered"; PALPITATIONS (disability) with onset 08Oct2021, outcome "not recovered"; MIGRAINE (disability) with onset 09Oct2021, outcome "not recovered", described as "Migraines". The events "migraines", "dizziness", "blurred vision", "extreme light sensitivity", "depression", "hypersomnia", "elevated blood pressures", "palpitations", "debilitating, now cannot work", "nausea", "fatigue" and "myalgias" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: Blood pressure measurement: elevated; Magnetic resonance imaging: Negative. Therapeutic measures were taken as a result of migraine, dizziness, vision blurred, photophobia, depression, hypersomnia, blood pressure increased, palpitations, loss of personal independence in daily activities, nausea, fatigue, myalgia. Clinical course: Migraines started 09Oct2021; ongoing since then (current date 21Jun2022. Debilitating, now cannot work. nausea, dizziness, blurred vision, extreme light sensitivity, fatigue, depression, hypersomnia, elevated blood pressures, myalgias, palpitations. MRI negative, multiple medications tried without resolution, being treated by neurology without resolution. Patient had no known allergies. The patient was not diagnosed with COVID-19 prior to vaccination. The patient was not tested for COVID-19 since the vaccination. Other medical history: HTN and generalized anxiety since symptoms started. AE treatment: amytriptilline, sumatriptan, maxalt, propanolol, botox injections, ajovy, ibuprofen, Tylenol.; Sender's Comments: As there is limited information in the case provided, the causal association between the serious reported events and the suspect drug cannot be excluded. The case will be reassessed once new information is available. The impact of this report on the benefit/risk profile of the Pfizer drug 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: Condition aggravated
Hospital-Tage: -
Labordaten: Test Name: Blood pressure; Result Unstructured Data: Test Result:elevated; Test Name: MRI; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Hypertension
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2325577

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: TX
Alter: 40,0
Geschlecht: M
Eingang: 25.06.2022
Impfdatum: 02.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: OT / -

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

Antinuclear antibody Anxiety Asthenia Blood pressure increased Blood thyroid stimulating hormone Blood pressure measurement Depression Dizziness Fatigue C-reactive protein Condition aggravated Full blood count Headache Hypersomnia Laboratory test Lipids Loss of personal independence in daily activities Magnetic resonance imaging

Symptomtext

Migraines; dizziness; blurred vision; extreme light sensitivity; depression; hypersomnia; elevated blood pressures; palpitations; Debilitating, now cannot work; nausea; fatigue; myalgias; This is a spontaneous report received from a contactable reporter(s) (Other HCP). A 40-year-old male patient received BNT162b2 (BNT162B2), on 02Oct2021 as dose 2, single (Lot number: FF8841) at the age of 40 years intramuscular for covid-19 immunisation. The patient's relevant medical history included: "HTN" (unspecified if ongoing); "generalized anxiety since symptoms started" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number= EW0100), for Covid-19 Immunization. The following information was reported: LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (disability) with onset 08Oct2021, outcome "not recovered", described as "Debilitating, now cannot work"; VISION BLURRED (disability) with onset 08Oct2021, outcome "not recovered", described as "blurred vision"; DEPRESSION (disability) with onset 08Oct2021, outcome "not recovered"; DIZZINESS (disability) with onset 08Oct2021, outcome "not recovered"; BLOOD PRESSURE INCREASED (disability) with onset 08Oct2021, outcome "not recovered", described as "elevated blood pressures"; PHOTOPHOBIA (disability) with onset 08Oct2021, outcome "not recovered", described as "extreme light sensitivity"; FATIGUE (disability) with onset 08Oct2021, outcome "not recovered"; HYPERSOMNIA (disability) with onset 08Oct2021, outcome "not recovered"; MYALGIA (disability) with onset 08Oct2021, outcome "not recovered", described as "myalgias"; NAUSEA (disability) with onset 08Oct2021, outcome "not recovered"; PALPITATIONS (disability) with onset 08Oct2021, outcome "not recovered"; MIGRAINE (disability) with onset 09Oct2021, outcome "not recovered", described as "Migraines". The events "migraines", "dizziness", "blurred vision", "extreme light sensitivity", "depression", "hypersomnia", "elevated blood pressures", "palpitations", "debilitating, now cannot work", "nausea", "fatigue" and "myalgias" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: Blood pressure measurement: elevated; Magnetic resonance imaging: Negative. Therapeutic measures were taken as a result of migraine, dizziness, vision blurred, photophobia, depression, hypersomnia, blood pressure increased, palpitations, loss of personal independence in daily activities, nausea, fatigue, myalgia. Clinical course: Migraines started 09Oct2021; ongoing since then (current date 21Jun2022. Debilitating, now cannot work. nausea, dizziness, blurred vision, extreme light sensitivity, fatigue, depression, hypersomnia, elevated blood pressures, myalgias, palpitations. MRI negative, multiple medications tried without resolution, being treated by neurology without resolution. Patient had no known allergies. The patient was not diagnosed with COVID-19 prior to vaccination. The patient was not tested for COVID-19 since the vaccination. Other medical history: HTN and generalized anxiety since symptoms started. AE treatment: amytriptilline, sumatriptan, maxalt, propanolol, botox injections, ajovy, ibuprofen, Tylenol.; Sender's Comments: As there is limited information in the case provided, the causal association between the serious reported events and the suspect drug cannot be excluded. The case will be reassessed once new information is available. The impact of this report on the benefit/risk profile of the Pfizer drug 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: Condition aggravated
Hospital-Tage: -
Labordaten: Test Name: Blood pressure; Result Unstructured Data: Test Result:elevated; Test Name: MRI; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Hypertension
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2311682

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 62,0
Geschlecht: F
Eingang: 07.06.2022
Impfdatum: 04.12.2021
Beginn: 11.02.2022
Tage bis Beginn: 69,0
Dosis: 3
Route/Site: SYR / LA

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

Chest pain Myalgia Pain Pleural effusion Vaccination site pain X-ray

Symptomtext

Approximately 2 months after my 3rd dose I experienced the following symptoms: muscle pain, pain in my left chest, ongoing soreness in my vaccination arm (upper arm area). I had my appointment with the doctor he said he wasn't sure what was going on, they run an x-ray and there was some fluid in my right lung but not the left part. I also took some aspirin for the pain and was prescribed with MOTRIN and after taking it for a few days I noticed that it did improve my overall pain. I had a relapse after a few weeks (02/27/2022) and took aspirin (500mg), then it would stop.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: X-ray
Aktuelle Erkrankungen: N/A
Vorgeschichte: Intermittent Muscle Spasm; Asthma; Recurring Urinary Tract Infection
Andere Medikamente: Oxybutynin; ESTROVEN; fish oil; lactase; topical estrogen cream
Allergien: Antibiotics; sulfa; cheddar cheese; chilis; cayenne; shrimp; acidic food
Vorherige Impfungen: -

VAERS 2308401

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IL
Alter: 80,0
Geschlecht: M
Eingang: 03.06.2022
Impfdatum: 14.10.2021
Beginn: 13.12.2021
Tage bis Beginn: 60,0
Dosis: 2
Route/Site: IM / -

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

Anticoagulant therapy Antiplatelet therapy Atrial fibrillation Blood creatine phosphokinase MB increased Blood creatine phosphokinase increased COVID-19 Chills Cough Dyspnoea Dyspnoea exertional Fatigue Haematuria Hypoxia Laboratory test Orthopnoea Pyrexia SARS-CoV-2 test positive Troponin increased

Symptomtext

COVID Vaccine Breakthrough Case Pfizer Dose 1 9/23/21 (FE3592) Pfizer Dose 2 10/14/21 (FF8841) COVID Positive 12/16/21 12/16/21: History is obtained from patient as well as by personal review of records. Patient is 80-year-old gentleman with known history of hypertension diabetes mellitus coronary status post artery bypass, aortic aneurysm repair, bypass surgery, anxiety disorder, peripheral vascular disease and medical problems. He has received 2 doses of SARS-CoV-2 vaccination. Second dose in October 2021. He presented to emergency department worsening shortness of breath few days duration. Started off as dyspnea on exertion. Breathing is worse in last 1 day. He also reported fever, chills and extreme fatigue. He reportedly had pulse ox of 74. He required up to 10 L of oxygen in emergency department to maintain saturations. He was found to be in atrial fibrillation with rapid ventricular response. He has converted to sinus rhythm by the time of my examination. No previous history of atrial fibrillation as per records. He tested positive for SARS-CoV-2. He reported orthopnea. Worsening cough without much expectoration. Lab work showed elevated total CK, CK-MB and troponin. 1/6/22: 80-year-old male patient with history of hypertension, type 2 diabetes, CABG, aortic aneurysm repair, peripheral vascular disease the was admitted to the hospital on 12/17/2021 with complaints of shortness of breath. Patient had received 2 doses of COVID-19 vaccines. However he was very short of breath with hypoxemia and required 10 L of oxygen as his pulse ox was 74% on admission. Patient also noted to have atrial fibrillation with RVR and elevated troponins. Cardiology and pulmonology consultations were obtained and the patient was recommended outpatient evaluation for ischemic heart disease. Medications were adjusted for appropriate heart rate per Cardiology. He was maintained on aspirin, Plavix and Eliquis was started but however the patient had hematuria and hence Eliquis was on hold. The patient continued to require significant amount of oxygen to about 10 L and was able to maintain his pulse ox in the low 90s and his clinical condition was discussed in detail with the daughter. The the patient and the daughter decided for him to be discharged home with hospice. Arrangements were made per the case manager for the patient to be transferred to hospice care at home. Patient was discharged with hospice on 1/6/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 22,0
Labordaten: -
Aktuelle Erkrankungen: HTN DM type 2 CABG Aoritc aneurysm repair PVD
Vorgeschichte: HTN DM type 2 CABG Aoritc aneurysm repair PVD
Andere Medikamente: alprazolam 1 mg PO BID PRN diltiazem ER 1 180 mg PO QD furosemide 20 mg PO QD trazodone 100 mg PO HS
Allergien: contrast dye - rash morphine - AMS penicillin - rash tape - rash
Vorherige Impfungen: -

VAERS 2275742

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MN
Alter: 90,0
Geschlecht: M
Eingang: 13.05.2022
Impfdatum: 15.10.2021
Beginn: 12.05.2022
Tage bis Beginn: 209,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Dyspnoea Fatigue Hypophagia SARS-CoV-2 test positive

Symptomtext

Hospitalized 8 days post positive covid test, pt with dyspnea, fatigue, weakness, cough, decreased oral intake, weakness. Per chest xray Covid pneumonia Remdesivir, dexamethasone, O2 6L/min via nasal cannula.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CKD, HTN, Myasthenia Gravis, diabetes type 2, OSA,
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2271153

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: -
Alter: 93,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 24.02.2021
Beginn: 21.01.2022
Tage bis Beginn: 331,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

01/21/22 presents to ED for "worsening shortness of breath and cough". PMHx of "CHF, hypertension."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 01/21/22 SARS-CoV-2 (COVID-19) detected.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267891

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 67,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 20.01.2021
Beginn: 01.02.2021
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: SYR / LA

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

Condition aggravated Tinnitus

Symptomtext

My minor Tinnitus became much worse after vaccination but the condition is still getting worse over time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Levothyroxin, Zetia, Finasteride, Metropolol, Rosuvastatin, Zolpidem
Allergien: N/A
Vorherige Impfungen: -

VAERS 2258724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 66,0
Geschlecht: F
Eingang: 29.04.2022
Impfdatum: 22.10.2021
Beginn: 04.11.2021
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: IM / LA

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

Acoustic stimulation tests abnormal Audiogram abnormal Confusional state Deafness Fall Gait disturbance Head discomfort Headache Impaired driving ability Loss of personal independence in daily activities Mastocytosis Migraine Nausea Photophobia Photopsia Tinnitus Vertigo Vestibular disorder

Symptomtext

11/04/2021 - woke with severe vertigo, nausea, and confusion, trouble seeing clearly, photophobia, photophobia, greatly increased tinnitus. Headache began slowly, increasing in intensity to 7. Usual migraine abortant of sumatriptan 100 mg, taken twice, did not help. Symptoms continued for 37 hours, with a visual aura of flashing lights on the second morning. Auras almost always happen for me prior to headache onset. The second day I used hydroxyzine 50 mg, which often helps when I have neurological mastocytosis symptoms. It provided minimal help. I assumed the vertigo was a vestibular symptom of migraine, though I had never had it before, and my migraines were in a period of minimal number per month and minimal intensity. The headache slowly resolved, but the vertigo was present every morning through the end of February 2022. Throughout the days I had trouble processing visual information, had severe brain fog, trouble thinking, had to hold onto things to walk without falling, head pressure, continued increase in tinnitus such that it was constant. I had to greatly decrease my work, often could not drive, or even leave the house. I saw an osteopath with no diagnosis, a neurologist with no help, told to do Epley maneuver which made it worse, and finally saw an ENT who did hearing test, vestibular exam, and told me it was vestibular migraine and referred me to a new neurologist, who I have not yet seen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: 3/30/2022 Audiology - high frequency hearing loss. 3/30/2022 Vestibular exam - not benign positional vertigo
Aktuelle Erkrankungen: -
Vorgeschichte: Systemic mastocytosis Chronic migraine Asthma Hashimoto?s thyroiditis Grade 5 patent foramen ovale Osteopenia POTS
Andere Medikamente: Zyrtec Famotidine Armour thyroid Levothyroxine Vivelle dot patch Progesterone Monteleukast Ketotifen Arnuity Elliptica Magnesium Calcium Vitamin D
Allergien: Albuterol NSAIDs Aspirin Nor ask Nortritylene Topamax Biaxin Zithromax Ketek Skelaxin Clonidine Methadone Lunesta Gleevec Leasing Aimovig Barium Medical adhesive Nickel Pollen Mold Formaldehyde Coconut Sage Bee pollen Red wine
Vorherige Impfungen: -

VAERS 2257053

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MI
Alter: 73,0
Geschlecht: M
Eingang: 28.04.2022
Impfdatum: 13.10.2021
Beginn: 26.04.2022
Tage bis Beginn: 195,0
Dosis: 3
Route/Site: UN / UN

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

Angiogram pulmonary abnormal Aortic valve calcification Arteriosclerosis coronary artery Atelectasis Bronchial secretion retention COVID-19 COVID-19 pneumonia Chest X-ray abnormal Dyspnoea Dyspnoea exertional Fibrin D dimer increased Goitre Hypoxia Influenza A virus test negative Influenza B virus test Lung disorder Lung hypoinflation Lung opacity

Symptomtext

74 year old male presented with complaints of covid 19 infection. He came to hospital as his shortness of breath was getting worse. His oxygen saturation was low with exertion at arrival in ER. His d-dimer was elevated so CT angio and lower extremity duplex was done. His shortness of breath improved on decadron. He did not require oxygen. He was discharged home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 2,0
Labordaten: USV Venous Upper Extremity Duplex Bilateral [382527638] Resulted: 04/26/22 2130; Order Status: Completed Updated: 04/26/22 2132; Narrative: EXAMINATION: Complete Bilateral Upper Extremity Venous Duplex Doppler Ultrasound EXAM DATE: 4/26/2022 9:24 PM TECHNIQUE: Real-time B-mode imaging with and without compression was used to evaluate the right and left upper extremity for deep venous thrombosis (DVT). Duplex Doppler with color and spectral Doppler was used. INDICATION: elevated d-dimer covid COMPARISON: None Right Upper Extremity Findings: Right Internal Jugular Vein: No thrombus. Right Subclavian Vein: No thrombus. Right Axillary Vein: No thrombus. Right Brachial Vein: No thrombus. Right Radial Vein: No thrombus. Right Ulnar Vein: No thrombus. Superficial Veins: Right Basilic Vein: No thrombus. Right Cephalic Vein: No thrombus. Left Upper Extremity Findings: Left Internal Jugular Vein: No thrombus. Left Subclavian Vein: No thrombus. Left Axillary Vein: No thrombus. Left Brachial Vein: No thrombus. Left Radial Vein: No thrombus. Left Ulnar Vein: No thrombus. Superficial Veins: Left Basilic Vein: No thrombus. Left Cephalic Vein: No thrombus. ADDITIONAL FINDINGS: Normal cardiac pulsatility is present in the subclavian veins. Impression: There is no deep venous thrombosis in the visualized deep veins of the right or left upper extremity. USV Venous Lower Extremity Duplex Bilateral [382527637] Resulted: 04/26/22 2129 Order Status: Completed Updated: 04/26/22 2131 Narrative: EXAMINATION: Complete Right and Left Lower Extremity Venous Duplex Doppler Ultrasound EXAM DATE: 4/26/2022 9:23 PM TECHNIQUE: Real-time B-mode imaging with and without compression was used to evaluate the right and left lower extremity for deep venous thrombosis (DVT). Duplex Doppler with color and spectral Doppler was used. INDICATION: elevated d-dimer, covid, CTA -COMPARISON: None Right Lower Extremity Findings: Right Common Femoral Vein: No DVT. Right Femoral Vein: No DVT. Right Popliteal Vein: No DVT. Right Posterior Tibial Veins: No DVT. Right Peroneal Veins: No DVT. Right proximal Greater Saphenous Vein: No thrombus. Left Lower Extremity Findings: Left Common Femoral Vein: No DVT. Left Femoral Vein: No DVT. Left Popliteal Vein: No DVT. Left Posterior Tibial Veins: No DVT. Left Peroneal Veins: No DVT. Left proximal Greater Saphenous Vein: No thrombus. Duplex Doppler: Spectral Doppler demonstrates bilateral normal respirophasic waveforms in the common femoral veins. Additional Findings: None. Impression: There is no deep venous thrombosis in the visualized deep veins of the right or left lower extremity. CT ANGIO THORAX WITH IV CONTRAST [382514347] Resulted: 04/26/22 1957Order Status: Complete Updated: 04/26/22 1959Narrative: EXAMINATION: CT Angiography of the Thorax EXAM DATE: 4/26/2022 7:29 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: The amount and type of contrast are recorded in the medical record. 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: hypoxia, covid. COMPARISON: PET/CT 03/01/2022 ENCOUNTER: Not applicable FINDINGS: Base of Neck & Axillae: There is no lymph node enlargement. Mediastinum & Hila: Multiple mildly enlarged mediastinal lymph nodes. Multinodular thyroid goiter. Cardiovascular: Coronary artery calcification, aortic valve calcification, and the mitral annulus is calcified. There is no pericardial effusion. The thoracic aorta is not aneurysmal and there is no dissection. There is no evidence for right heart strain. Pulmonary Arteries: No pulmonary embolism is present. Lungs & Airways: Patchy groundglass airspace opacities scattered throughout both lungs. Mild mucus plugging in the lower lungs bilaterally. Pleural Space: There are no pleural effusions. There is no pneumothorax. Upper Abdomen: Nodular contour of the liver raising the possibility for cirrhosis. Splenomegaly. Chest Wall & Musculoskeletal: No significant abnormality. Impression: 1. Mild multifocal airspace disease compatible with Covid pneumonia given the patient's history. 2. Mild mediastinal lymphadenopathy, likely reactive given the above findings. 3. Mucous plugging of the peripheral bronchi in the lower lungs. 4. No evidence for pulmonary embolus. DR CHEST SINGLE VIEW [382514310] Collected: 04/26/22 1754 Order Status: Completed Updated: 04/26/22 1801 Narrative: EXAMINATION: Single View Chest EXAM DATE: 4/26/2022 5:40 PM TECHNIQUE: Single view chest INDICATION: Covid, dyspnea, COMPARISON: 8/18/2019 ENCOUNTER: Not applicable FINDINGS: There is pulmonary hypoinflation. There is subsegmental atelectasis and faint patchy atelectasis/airspace disease in bilateral lower lungs. There are no pulmonary consolidation, pleural effusions or pneumothorax. Heart size and pulmonary vascularity are within normal limits. Impression: Low lung volumes, bibasilar faint atelectasis/airspace disease. COVID-19, Influenza A/B, RSV PCR (ED ONLY) [382514309] (Abnormal) Collected: 04/26/22 1732Order Status: Completed Specimen: Swabbed Collection from NasopharynxUpdated: 04/26/22 1822COVID-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 Restrictive lung disease Lung infection Asthmatic bronchitis; Circulatory; SVT (supraventricular tachycardia) (HCC) Mitral stenosis; Left bundle branch hemiblock; Portal vein thrombosis; Cardiomyopathy, unspecified type (HCC); Nonrheumatic aortic valve stenosis Digestive; Primary pancreatic neuroendocrine tumo; Infectious/Inflammatory COVID-19; Endocrine/Metabolic; Type 2 diabetes mellitus with hyperglycemia (HCC); Other; re-operative cardiovascular examination
Andere Medikamente: Apixaban (ELIQUIS); Ascorbic acid (VITAMIN C); Benzonatate (TESSALON);Calcium carbonate (TUMS); Cetirizine (ZYRTEC); Cholecalciferol (VITAMIN D3); Chromium;Fluticasone-salmeterol (ADVAIR DISKUS); Glucosamine; Guaifenesin (HUMIBID E); Hydroc
Allergien: Sulfa Drugs-Rash
Vorherige Impfungen: -

VAERS 2254620

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: TX
Alter: 58,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 29.03.2022
Beginn: 08.04.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: SYR / LA

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

Breast discomfort Herpes zoster Paraesthesia

Symptomtext

I felt the tingling and irritation on my breast. I knew it felt like the shingles, so I called my doctor and was given meds for my shingles.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Shellfish; Iodine; Pollen
Vorherige Impfungen: -

VAERS 2252155

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IL
Alter: 86,0
Geschlecht: M
Eingang: 26.04.2022
Impfdatum: 05.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / -

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

COVID-19 COVID-19 pneumonia Cough Dyspnoea Dyspnoea exertional Hypoxia Inappropriate schedule of product administration Leukocytosis Pneumonia SARS-CoV-2 test positive Skin warm Vaccine breakthrough infection

Symptomtext

COVID Vaccine Breakthrough Case Pfizer Dose 1 3/3/21 (EL9266) Pfizer Dose 2 3/25/21 (EN6204) Pfizer Dose 3 11/5/21 (FF8841) COVID Positive 11/11/21 COVID Positive 11/13/21 11/19/21: Patient is an 86 male with pmhx of cll baseline wbc 26, rheumatoid arthritis and chronic renal insufficiency tested positive for covid 11/11/2021, given monoclonal antibodies 11/16/2021, coming in for shortness of breath of a few days duration. pateint has covid at home program following him up, and was noted ot have oxygen saturation of 85% at home. on arrival tot he er he was 87% on room air for which he was given 3l oxygen. he denies any chest pain, nausea or vomiting. minimal coughing, non bloody material.no fevers at home but felt warm. he has minimal shortness of breath with activity. no leg swelling. no bleeding. 11/23/21: 1. Pneumonia due to COVID-19 virus, COVID-19 2. Pneumonia - bilateral 3. Hypoxia, Hypoxia 4. Leukocytosis Agency Safe at Home kit- you will receive a kit in the mail that contains a blood pressure cuff, thermometer and Pulse ox- please set this equipment up and contact Agency to monitor you .

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: adjustment disorder with anxiety thoracic aortic aneurysm chronic B cell lympocytic leukemia COPD emphysema CRI h/o histoplasmosis HTN h/p pulmonary nodules LD RA DM type 2
Vorgeschichte: adjustment disorder with anxiety thoracic aortic aneurysm chronic B cell lympocytic leukemia COPD emphysema CRI h/o histoplasmosis HTN h/p pulmonary nodules LD RA DM type 2
Andere Medikamente: vitamin C 1000 mg PO QD atorvastatin 40 mg PO QD calcium-vitamin d 1 tab PO QD fluticasone nasal spray both nostrils BID folic acid 1 mg PO QD gabapentin 300 mg PO TID HCTZ 12.5 mg PO QOD probiotic 1 cap PO BID methotrexate 20 mg PO QSunday
Allergien: NKA
Vorherige Impfungen: -

VAERS 2248128

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: OH
Alter: 29,0
Geschlecht: F
Eingang: 22.04.2022
Impfdatum: 16.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test normal Chest X-ray normal Chest pain Dyspnoea Dyspnoea exertional Immunisation reaction

Symptomtext

I had chest pain and some SOB when I walked around. These lasted for about 3 days. I went to the ER on Nov 18th. They did chest x-ray, normal results. They also did blood work, normal results. They told it was a reaction to the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Chest x-ray Blood work
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Dye food can, Cats, Trees
Vorherige Impfungen: -

VAERS 2247699

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 22.04.2022
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

Chest discomfort Chest pain Condition aggravated Dizziness Dyspnoea Hypertension Hypoaesthesia Pyrexia Throat tightness

Symptomtext

Client presented at vaccination site for her Pfizer COVID booster vaccine. Client reported she received Pfizer COVID dose #1 (4/2/21; lot: EW0150) at the clinic without any issues. Client reported with Pfizer COVID dose 2 (4/23/21; lot: EW0161) at the clinic, within five minutes she had difficulty breathing with her throat closing, SOB, & facial numbness (lasted 20 minutes). Client reported at the observation area for the 2nd dose, she was laid down, and drank juice and water provided. She stated no medicines given and no emergency number called. She reported she had dizziness and lightheadedness within four hours of Pfizer COVID dose 2 and she reported she ate before received her Pfizer COVID dose 2. She reported she stayed at the observation area for 45 minutes then her son drove her home. She stated she ate today at 1100 and drinking water while waiting for approval. She said she had fever for 48 hours (took Tylenol with help) for Pfizer COVID dose 2. Client also said she had chest pressure and chest pain started the next day after Pfizer COVID dose 2. She said she followed up with PCP after day 2 of her Pfizer COVID dose 2. She said her PCP told her it was normal reactions that she had and to continue taking Tylenol for her fever as needed. Had HTN and taking Lisinopril 20 mg daily. She took Lisinopril this morning. At 1230, PHN took client?s current vitals: BP 136/86, HR 100, O2 Sat. 96%. Client reported her normal BP is 130/80. Client is requesting Pfizer booster approval today. PHN submitted a medical consult via text message to clinical project coordinator, requesting to proceed with the Pfizer COVID booster vaccine. Per the doctor, approval to proceed with Pfizer COVID booster vaccine was obtained from medical consult team via text message from clinical project coordinator. Client received Pfizer COVID vaccine, LOT#: FF8841 on 11/14/21 at 1312 by RN. The client did not report any symptoms during the 30-minute observation period. PHN educated client on possible adverse reactions and when to seek EMS. Client verbalized understanding. Client left vaccination site at 1342 unassisted and with a steady gait.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: HTN
Andere Medikamente: None
Allergien: Allergic reaction to Pfizer COVID dose #2 on 4.23.21
Vorherige Impfungen: Client presented at vaccination site for her Pfizer COVID booster vaccine. Client reported she received Pfizer COVID dose #1 (4/

VAERS 2244335

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 19.10.2021
Beginn: 09.11.2021
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: IM / RA

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

Back pain Mobility decreased Musculoskeletal pain Pain

Symptomtext

So, let's see and I am not positive about the first shot. A few weeks after the second shot instead of the soreness it seemed to come back. I would get a stabbing pain when I tried to put my hair up in a ponytail or put a shirt on. But the pain would get worse and worse. I was losing range of motion. It would also go across my back and into my shoulder blade. It was just kind of sore all over, it just took away my range of motion. I kept putting this off and did not care for myself, I put everything else first. I spoke to the nurse on call, and she recommended that I speak to my PCP and she recommended that I have the flu and shingles vaccine. Then I had the COVID-19 shot shortly thereafter. I thought I had them to close together. It just got worse and worse. When I would try to stretch, I would have this really intense pain in the same spot as the shot. On March 15, 2022 I saw my doctor in her office. She recommended an x-ray, and physical therapy. I just have not been able to do the x-ray yet and the doctor will not let me do PT until I have the x-ray. Nothing works the pain is not going away. I have been doing some stretches on my own, but I am still very limited with what I can do.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Anxiety; High Cholesterol; HBP; Vitamin D Deficiency
Andere Medikamente: Effexor XR 150mg QD; Atorvastatin 20mg QD; Lopressor 25mg BID; Losartan 50mg QD; Vitamin D3 2000 IU BID
Allergien: None
Vorherige Impfungen: -

VAERS 2243457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: -
Alter: 77,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 22.03.2021
Beginn: 02.06.2021
Tage bis Beginn: 72,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 antibody test positive SARS-CoV-2 test positive

Symptomtext

6/3/21 PMH COPD, RLL lung resection, CHF, HTN, DVT s/p IVC filter, factor V Leiden presenting for progressive dyspnea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 6/2/21 SARS-CoV-2 (COVID-19) by NAA, Micro Detected 6/2/21 SARS-CoV-2 IgG (Anti-Spike) Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2237653

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 63,0
Geschlecht: M
Eingang: 16.04.2022
Impfdatum: 08.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Blood pressure measurement Hypertension Investigation

Symptomtext

My blood pressure reading is over 200; My blood pressure was stable and controlled and suddenly after taking the booster, my systolic started going up and up; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63-year and 4-month-old male patient received BNT162b2 (BNT162B2), on 08Oct2021 as dose 3 (booster), single (Lot number: FF8841) at the age of 63 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. Vaccination history included: BNT162b2 (Dose 1, LOT# EP7534), administration date: 18Mar2021, when the patient was 62-year-old, for Covid-19 Immunization; BNT162b2 (Dose 2, Lot: EP7533), administration date: 08Apr2021, when the patient was 62-year-old, for Covid-19 Immunization. The following information was reported: HYPERTENSION (medically significant) with onset 2021, outcome "not recovered", described as "My blood pressure reading is over 200; My blood pressure was stable and controlled and suddenly after taking the booster, my systolic started going up and up". The patient underwent the following laboratory tests and procedures: Blood pressure measurement: (unspecified date) over 200; (01Apr2022) 208 over 118; lab test: (unspecified date) Unknown result. Therapeutic measures were taken as a result of hypertension. Consumer stated that he got the booster (clarified as COVID-19 booster vaccine) in Octo of last year. He had very high Blood Pressure, 200, he never used to have that. He wanted to know why after he had the booster blood pressure reading is over 200." Consumer stated that his blood pressure was stable and controlled and suddenly after taking the booster, his systolic started going up and up. He had two procedures, a foot operation and a dental implant surgery cancelled because his blood pressure is too high, over 200. He stated that he need to know all side effects from the booster. He never had blood pressure this high. Consumer stated, "he just wanted to know what side effects and how many other people have high systolic readings like him." He is on more medications than ever before in his life and he is on Clonidine, Imdur, several other Edarbi, and on lot of potent high blood pressure pills because of this." Consumer stated, "It is persisting without the medication regularly my systolic, like today 208 over 118, reflects with my medication." No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Name: Blood pressure; Result Unstructured Data: Test Result:over 200; Test Date: 20220401; Test Name: Blood pressure; Result Unstructured Data: Test Result:208 over 118; Test Name: lab test; Result Unstructured Data: Test Result:Unknown result
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2228403

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: WV
Alter: 56,0
Geschlecht: F
Eingang: 12.04.2022
Impfdatum: 01.10.2021
Beginn: 26.12.2021
Tage bis Beginn: 86,0
Dosis: 3
Route/Site: SYR / LA

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

Blood pressure increased Blood test abnormal Cardiac function test Condition aggravated Heart rate increased Hyperthyroidism Panic attack

Symptomtext

My thyroid went hyper, which is new for me because I didn't realize what it was until I ended up in the hospital, twice. My blood pressure, heart rate went up and I started getting panic attacks from my thyroid being hyper. It was high and then they kept dropping my medication dose then I ended up being hypo and sleeping for 2 months. And I'm still not where I should be.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 1,0
Labordaten: They did a heart test, bloodwork - there were a couple of things out of range but mostly my bloodwork was good.
Aktuelle Erkrankungen: no
Vorgeschichte: I have Lyme, I have hyperthyroid, asthma, high blood pressure
Andere Medikamente: NP Thyroid, Zyrtec, Carvedilol, Low dose Naltrexone
Allergien: Sudafed, Cingular, Tramadol, Bactrim
Vorherige Impfungen: -

VAERS 2221933

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 20,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 09.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Dizziness Fear Feeling cold Tremor

Symptomtext

Client received her COVID Pfizer Booster dose lot # FF8841 exp. 12.31.21 on her left arm on 12.09.21. interpreter provided to client. At 1321, client reported to EMT that she was feeling a ?cold sensation on her face and hands? and dizzy (6/10 level) and he transported client to the anti-gravity chair in a semi-fowler position. PHN came to assist with the client. Client denied shortness of breath (SOB). EMT took client?s vitals: BP 110/66, HR 132, O2 Sat. 99%. At 1328, EMT took client?s vitals: BP 111/91, HR 123, O2 95% and she reported dizziness and ?coldness.? She denied SOB or any other anaphylactic signs and symptoms. She denied any history of allergy or taking any medications. She reported had tonsils infection and took ?Doxiciclina? for 10 days which she completed the antibiotic three days ago. She told she has a primary care doctor follow-up in three weeks for the tonsils infection. At 1331, she drank a juice and ate crackers provided without any issue. At 1336, client reported she still had dizziness, but she didn?t have the ?coldness.? At 1338, EMT took client?s vitals: BP 118/73, HR 111, O2 Sat. 99% and still had dizziness and feeling a ?chill in neck only.? At 1341, client reported she felt ?cold? on her face and throat and that she has a history of dizziness with blood drawn and vaccination. At 1343, client started ?shaking and scare.? At 1351, EMT took client?s vitals except BP: HR 100, O2 Sat. 99%, and client reported no more dizziness or coldness anywhere. At 1351, her ?shaking and scare? stopped. PHN educated client on adverse reactions and when to seek EMS. At 1358, client declined to have her last vitals taken and left the vaccination site with a steady gait with her parents.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Completed antibiotic "Dociclina" for tonsils infection 3 days ago.
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2221207

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: VA
Alter: 68,0
Geschlecht: F
Eingang: 07.04.2022
Impfdatum: 14.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 17,0
Dosis: 3
Route/Site: UN / RA

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

Arthralgia Back pain Blood test Chest X-ray Dehydration Kidney infection Pain in extremity Pyrexia Spinal X-ray Ultrasound Doppler

Symptomtext

Fever, extreme dehydration, kidney infection, extreme lower body pain (back, legs, joints) requiring emergency room visits as directed by my primary physician on November 1 and on November 5

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: Blood chemistry, chest and spine x ray, ultrasound of legs for blood clots.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Maxide, Keppra, Bystolic, Vitamin D
Allergien: Sulfa, Topamax
Vorherige Impfungen: after second Pfizer booster on March 21, 2021, joint pain

VAERS 2218184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MI
Alter: 75,0
Geschlecht: F
Eingang: 06.04.2022
Impfdatum: 28.10.2021
Beginn: 03.03.2022
Tage bis Beginn: 126,0
Dosis: 3
Route/Site: IM / AR

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

Angiogram pulmonary abnormal Anticoagulant therapy Asthenia Atrial fibrillation COVID-19 Chills Clostridium test Cough Diarrhoea Dysphagia Dyspnoea Dyspnoea exertional Ear congestion Echocardiogram Ejection fraction Electrolyte imbalance Exposure to SARS-CoV-2 Headache

Symptomtext

Hospitalized (3.21.22-3.31.22); COVID-19 positive (3.3.22 and 3.24.22); fully vaccinated PLUS booster BRIEF OVERVIEW: Primary Care Physician at Discharge: Hematologist/Oncologist: Admission Date: 3/21/2022 Discharge Date: 03/31/2022 Patient's Discharge Disposition: Home in stable condition. Discharge summary: This is a 76 y.o. year old patient who was admitted on 3/21/2022 with PMH of PE, HLD, HTN, asthma, anemia, and lymphoma. Patient presented to the ED for SOB and cough x 3 weeks. Patient stated she tested positive for COVID on 3/2 and had since had worsening SOB with exertion and cough. Again positive for COVID on 3/21. CTA of chest with groundglass opacities consistent with airspace disease and tiny PE. No evidence of right heart strain. 3/22 echo with 65% LVEF and normal RV function. Pt started on rocephin and azithromycin, which was completed on 3/30. Pt also received remdesivir and steroids, which completed 3/28. Pt on xarelto at home, which was switched to lovenox. However, pt unable to afford lovenox as outpt, therefore she was discharged on eliquis. Admission complicated by diarrhea and electrolyte abnormalities. Pt negative for c diff and eletrolytes replaced. Pt also with chronic dysphagia, SLP and GI followed during inpt stay. Pt had EGD with dilation on 3/28. With pt's PCM and weakness, PT/OT consulted for assistance with discharge planning. Therapy ultimately recommended HHC PT OT and DME 4WW. Prior to discharge today, patient denies new, worsening or changes in ROS at this time, including no fevers/chills/sweats, no CP/SOB/DOE, no abd pain/N/V/D, and no neuro changes. Patient eating/drinking/voiding well and ambulating as tolerated. Patient will plan to follow up in our office with Dr.. Patient's discharge medication plan were discussed as per below and new prescriptions were sent to patient's requested pharmacy prior to discharge as per generated list below. Patient is aware to call our office should further questions or concerns arise following this discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: 3/2/2022: Seen at Urgent Care for Cough, congestion, exposure to COVID-19 positive person Comments: Patient presenting to clinic with complaints of cough, sore throat and nasal congestion. She has tried multiple over the counter medications with no relief. She denies any contact with covid positive people, however she has been around some sick people. The history is provided by the patient. COUGH This is a new problem. The current episode started in the past 7 days. The problem has been gradually worsening. The problem occurs constantly. The cough is white/clear sputum. There has been no fever. Associated symptoms include chills, ear congestion, headaches, rhinorrhea, sore throat, wheezing, nasal congestion and postnasal drip. She has tried Inhalers and decongestant for the symptoms. The treatment provided minimal relief. 3.14.22: ED visit for COVID-19 and pain of left calf - HISTORY OF PRESENT ILLNESS: Patient presents as referral from walk-in clinic for evaluation of left calf pain with clinical suspicion of possible DVT. History of DVT and she is anticoagulated with Xarelto. Currently has COVID-19 with diagnosis made on March 3rd. Has persistent cough which is causing her to not sleep much. Has persistent fevers and myalgias. No vomiting. No severe shortness of breath. Is vaccinated for COVID. She went to walk-in clinic because she was concerned about DVT. They referred her here. No chest pain or severe shortness of breath. Cough minimally productive. 3.21.22: Paroxysmal atrial fibrillation, cough
Vorgeschichte: Asthma GERD (gastroesophageal reflux disease) History of DVT of lower extremity History of stroke with residual deficit Stage 3a chronic kidney disease (HCC) Mixed hyperlipidemia Venous insufficiency Cervical spondylosis with radiculopathy Bradycardia DOE (dyspnea on exertion) Cervical spondylosis Lymphoma, small lymphocytic (HCC) Pre-operative cardiovascular examination Lumbar canal stenosis Acute cystitis without hematuria Stroke (HCC) Spondylolisthesis Lumbar radiculopathy Degeneration of lumbar intervertebral disc Hx pulmonary embolism On warfarin therapy Muscle cramp, nocturnal History of adenomatous polyp of colon Slipped Nissen fundoplication Urinary incontinence, mixed Erosive esophagitis Coronary artery disease, occlusive COPD, mild (HCC) Paroxysmal atrial fibrillation (HCC) Hypertension Cardiac pacemaker 2018 Mitral valve insufficiency Unspecified severe protein-calorie malnutrition (HCC)
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler apixaban (ELIQUIS) 5 MG tablet atorvastatin (LIPITOR) 20 MG tablet baclofen (LIORESAL) 20 MG tablet benzonatate (TESSALON) 100 MG capsule bumetanide (BUME
Allergien: NSAIDS - High cardiac risk, HTN, CKD and erosive esophagitis
Vorherige Impfungen: -

VAERS 2216068

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 41,0
Geschlecht: F
Eingang: 05.04.2022
Impfdatum: 27.12.2021
Beginn: 12.01.2022
Tage bis Beginn: 16,0
Dosis: 2
Route/Site: SYR / LA

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

Acute myeloid leukaemia recurrent Biopsy bone marrow abnormal Chemotherapy Condition aggravated Full blood count Full blood count abnormal

Symptomtext

The covid-19 vaccine caused acute myeloid leukemia to return. I received normal level blood results the day of the vaccine before the vaccine and many months prior and then after the vaccine, 16 days later all my blood counts dropped to under normal. On Feb 10, 2022 a bone marrow biopsy was done and confirmed i did have active acute myeloid leukemia in my bone marrow/blood. and again blood levels continued to drop for the next 49 days before having to start aggressive Chemotherapy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 32,0
Labordaten: Bone Marrow Biopsy on Feb 10, 2022 Blood draw to check CBC levels on 12/27/21, 01/12/22, 01/19/22, 01/27/22, 02/09/22, 02/14/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: COMPAZINE
Vorherige Impfungen: -

VAERS 2216007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: TN
Alter: 73,0
Geschlecht: F
Eingang: 05.04.2022
Impfdatum: 15.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Injection site pain Mobility decreased

Symptomtext

Site: Pain at Injection Site-Severe, Additional Details: patient has been unable to raise or lower her arm. it is difficult to use for every day use since the vaccine was given

Weitere VAERSDATA-Felder

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

VAERS 2214079

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MA
Alter: 42,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 26.09.2021
Beginn: 26.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest pain Decreased appetite Dysgeusia Dyspnoea Hypoaesthesia Laboratory test Migraine Nausea Oral discomfort Panic attack Pruritus Sensory loss Throat irritation Tongue discomfort

Symptomtext

Within 15 minutes of vaccine administration, I got a metallic taste in my mouth, itchy tongue, throat, ears, then burning of mouth, tongue throat, migraine, numbness/loss of feeling in both hands and left foot, panic attack, chest pain, SOB, extreme nausea, loss of appetite

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Labs in ER
Aktuelle Erkrankungen: -
Vorgeschichte: Sjogrens, Neuropathy, Positive Lupus titre
Andere Medikamente: Spirinactone, Vitamin D, Magnesium, Ibuprofen
Allergien: Scallops, Percocet
Vorherige Impfungen: -

VAERS 2213957

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: WV
Alter: 81,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 01.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: SYR / RA

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

Asthenia COVID-19 Condition aggravated Dizziness Eating disorder Fatigue Oropharyngeal pain SARS-CoV-2 test positive Speech disorder

Symptomtext

It occurred about 4 days after the booster. I got up dizzy, and I was extremely dizzy for at least 2 days. I took meclizine which I had on hand from the previous episode after the 2nd vaccine. I had some weakness and being tired and so on for a few days after that. I did also test positive for COVID in February 2022 after booster. The doctor gave me a prescription for dexamethasone to treat COVID which did help. Symptoms for that was the worst sore throat. Could hardly eat or talk, but I did not have to go to the hospital. Just went to the drive through to be tested. A lot of tiredness for a while after having COVID. Contacted doctor - no in person visit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: COVID test - Positive.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Atenolol 25 mg 1 1/2 tabs daily; Felodipine 5mg; Raloxifene 60mg; Omeprazole 20mg; Glucosamine Chondroitin 500/400 2x day; Aspirin 81mg; Daily Vitamin
Allergien: Penicillin; Keflex; Nubain-injected; Iodine-injected
Vorherige Impfungen: Pfizer COVID 2nd vaccine - 03/05/2021 - Dizziness and episode of high blood pressure.

VAERS 2213883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: FL
Alter: 47,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 01.10.2021
Beginn: 01.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Impaired driving ability Injected limb mobility decreased Muscle spasms Pain in extremity Weight bearing difficulty X-ray normal

Symptomtext

Constant pain in upper arm that is unresolved and does not dissipate even with Tylenol, unable to lift arm above 90 degrees, unable to carry a purse or bag on left shoulder without additional pain, unable to carry items with left arm, unable to drive with left arm. Since an Xray was ordered by my insurance instead of an MRI, I have more pain and now muscle spasms from raising my arm for an extended period of time for the images 4/1/22. This pain in my arm started the day of injection 10/1/21 and has not dissipated or lessened in any way. If anything it has continued to be more painful.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: Complained to the doctor at my annual exam Nov 1, 2021 about the pain. Had a follow up visit on 2/14/21 specifically about the pain in my arm. Two MRI were ordered and my insurance company denied coverage for the tests that were scheduled for 4/1/22. In leu of the MRI, several Xrays were performed 4/1/22: No acute fracture. Normal bone mineralization. The visualized glenohumeral joint space is preserved. The acromioclavicular joint is unremarkable. No gross soft tissue abnormality. The visualized lung is well aerated. Now waiting for scheduling of physical therapy to appease my insurance company to then be able to get an MRI and nerve induction test.
Aktuelle Erkrankungen: none
Vorgeschichte: atrial fibrillation - under control with medication.
Andere Medikamente: Lisinopril, Metoprolol, Baby Aspirin, Biotin, Vitamin C, B Complex
Allergien: Amoxicillin, Penicillin, Biaxin, Rosuvastatin, Atorvastatin
Vorherige Impfungen: -

VAERS 2204166

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CO
Alter: 65,0
Geschlecht: F
Eingang: 29.03.2022
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Atrial fibrillation Atrial flutter Cardiac ablation Echocardiogram normal Hypertension

Symptomtext

Diagnosed with high blood pressure and Afib at GP?s office on 10/25/21. Cardiologist appointment confirmed on 11/2/21. Cardiac ablation specialist seen on 12/9/21. Cardiac ablation done on 1/5/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Echocardiogram 11/26/21 normal heart function Cardiac ablation to treat afib and aflutter 1/5/22
Aktuelle Erkrankungen: None known
Vorgeschichte: Arthritis
Andere Medikamente: Multiple herbal supplements
Allergien: Shellfish
Vorherige Impfungen: -

VAERS 2204016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NY
Alter: 44,0
Geschlecht: M
Eingang: 29.03.2022
Impfdatum: 02.03.2022
Beginn: 24.03.2022
Tage bis Beginn: 22,0
Dosis: 4
Route/Site: SYR / RA

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

Blood test Chest X-ray Extra dose administered Heart rate increased Hypertension

Symptomtext

I first noticed a rapid heart rate around 114 on 03/24/2022. My blood pressure was high 238/129. I went to hospital and was in and out for 4 days. I went to the Hospital. I was having to go back in to get my blood checked. I was given Lisinopril and to only take it if I needed it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: 1,0
Labordaten: Chest x-rays 03/24/2022, Blood work 03/24/2022
Aktuelle Erkrankungen: No
Vorgeschichte: None
Andere Medikamente: Tylenol
Allergien: Aspirin, Penicillin
Vorherige Impfungen: Pfizer -dose 1, 2 and 3

VAERS 2202394

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CT
Alter: 46,0
Geschlecht: F
Eingang: 28.03.2022
Impfdatum: 21.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal distension Abdominal pain Antiphospholipid syndrome Back pain Blood test Borrelia test negative Computerised tomogram abnormal Condition aggravated Diarrhoea Diverticulum intestinal Full blood count normal Headache Heavy menstrual bleeding Impaired work ability Inflammation Liver disorder Liver function test normal Loss of personal independence in daily activities

Symptomtext

I received my booster shot on 12/21/21. I first starting noticing my symptoms in beginning of January. It started off with very mild pain in my lower back. Each day it would build and over several days, pain became severe. Pain also in my abdomen/pelvic area. I consistently have period cycles of about 25 days. My period cycle December month was 38 days. Went to GYN aptmt 1/10/22. Left ovarian cyst was palpated. Had ultrasound done 1/11/22. Confirmed large simple cyst by left ovary. No ovarian torsion. Pain seemed to correlate with period and improved with time, but then pain returned and would have days of intense pain and days of mild pain. My follow up ultrasound 2/22/22 showed simple cyst resolved completely and Yet still having pain. I went GI dr. Also have been experiencing nausea throughout this time period as well as some GI symptoms of diarrhea, bloating. Nausea feels like morning sickness and I did get prescription for Zofran. I have nausea on most days. Intermittent. Only take zofran if nausea severe. I experienced this same type of nausea as well after my first 2 Pfizer vaccines on 2/19/21 and 3/12/21. (Can see my web-based application text check in?s.) That nausea lasted for about 5-6 weeks and then resolved. With my first covid shot, I had back aches that day of injection on side I received shot in, (Aches traveled in my right arm, down my right side of my back) which then resolved. I had some minor flare up of my APS with those doses. After booster, i also have had intermittent joint pain in my knee. This is one ways I flare up with my Antiphospholipid syndrome (APS). I had strange headache which would throb for 3-4 seconds in my right temple and then go away. I would experience this between 2-6 times a day. That was in January and resolved. I had ct scan done on 3/12/22. It?s WDL with exception of fibroids, enlarged uterus, scattered sub centimeter hepatic hypodensities, and scattered colonic diverticulosis. GI Dr. cleared me. The pain I experience can be anywhere from mild to severe. One night, i woke up at 3am in severe pain. I had call out from work and not attend a couple social events due to pain intensity on certain days. My Lyme disease testing came back negative. CBC and liver enzyme panel WDL. I feel I am experiencing this due to combination of my booster shot and my autoimmune condition. Pain usually in my lower back. Last few days, more pronounced in my right mid back (behind my chest area). I can make pain increase by pressing into that area with my fingers. Pain migrated to back of my head the last couple days. Back head sore and tender with some pain continuing in my back as well. I?ve had on and off vasculitis sensation in my fingers in last couple weeks as well. I tested negative for Covid before my vaccine and after. I was not sick and did not have a cold. The only event I had was getting booster shot. Have couple more Dr. aptmts coming up. Pain overall tends to migrate in different areas of my back and lower abdomen. intensify and retreat. Some days are better than others. Nausea is consistent and pretty much daily experience. Intermittent throughout day. YES this is an adverse event. IT?s been 3 months of pain and feeling like my body is broken. I am an active person, average weight and height and I take my health very seriously. I believed in vaccines and work in healthcare. However, the third dose caused harm to my body and caused an inflammatory response that has affected my life these last 3 months. I will not get a 4th booster and I implore the government to investigate other potential inflammatory responses in patients who were otherwise status quo in their lives until covid vaccine. Check ER admissions for thyroid issues, GI inflammatory conditions, heart conditions, GYN inflammatory issues, and see if those patients received a covid vaccine dose about a month prior to their ER admissions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: ultrasounds 1/11/22 & 2/22/22, CT-Scan 3/12, Labs x2.
Aktuelle Erkrankungen: none
Vorgeschichte: Antiphospholipid Anitbody Syndrome
Andere Medikamente: Plaquenil, aspirin 81mg, New Chapter Zinc (whole foods), multivitamin
Allergien: none
Vorherige Impfungen: -

VAERS 2201742

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: PA
Alter: 60,0
Geschlecht: F
Eingang: 28.03.2022
Impfdatum: 26.09.2021
Beginn: 25.01.2022
Tage bis Beginn: 121,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Migraine Pneumonia Pyrexia SARS-CoV-2 test positive

Symptomtext

I got COVID after Dose 3 received Paxlovid it didn't work well for me after 5 days. On February 11, 2022 had a Rapid test still was testing positive which turned into Pneumonia. I started experiencing migraines and feverish from Jan 25, 2022 to March 23, 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: 3 Rapid test (results positive).
Aktuelle Erkrankungen: Arthritis flare up
Vorgeschichte: Asthma; Rheumatoid Arthritis
Andere Medikamente: Allegra, Singular, Advair 500, Flaxnil, Flonase, Caltrate D, Centrum Women's
Allergien: Penicillin, Betadine, Macrodantin, Sulfa, Bactrim, Synthetic Estrogen
Vorherige Impfungen: Shingles Dose 2-July 2019 (flared up arthritis in neck lasted a month).

VAERS 2200782

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: FL
Alter: 64,0
Geschlecht: M
Eingang: 27.03.2022
Impfdatum: 23.02.2021
Beginn: 08.09.2021
Tage bis Beginn: 197,0
Dosis: 3
Route/Site: - / LA

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

Condition aggravated Full blood count abnormal Platelet count decreased

Symptomtext

No immediate side effects. After the second dose platelets started to drop. Drop detected subsequent to second dose. Got worse after third dose. Vaccine unknown if cause. History of low platelet count but now critical low levels. Currently under medical care for low platelets.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 4,0
Labordaten: Low platelet were detected in September 2021 by lab test CBC. Hospitalized with critical low in January 2022 for three days and again in February 2022 for 4 days. In January count was down to 1 (one) . Hematologist treating ongoing currently. Not clear if vaccination is a cause or effect. History of prior low platelets but not at such extreme low levels.
Aktuelle Erkrankungen: AFFIB but no illness. History of low platelets (ITP). But platelets went down to crucial low after the the 3 series of COVID a vaccine.
Vorgeschichte: AFFIB. High Blood Pressure, ITP Low Plateletes but got worse after vaccines. Have had ITP for many years and was in a normal renege at low end. AFTER VACCINES has now reached critical low levels.
Andere Medikamente: Losartan, famotodine, troprol succinate, Eliquis but that was stopped.
Allergien: No drug allergies. Mushroom sensitive causes congestion..
Vorherige Impfungen: -

VAERS 2198634

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: IN
Alter: 65,0
Geschlecht: F
Eingang: 25.03.2022
Impfdatum: 26.10.2021
Beginn: 29.01.2022
Tage bis Beginn: 95,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Condition aggravated Cough Decreased appetite Ear infection Fatigue Headache Influenza Influenza virus test positive Myalgia Nasal congestion Nasopharyngitis Pyrexia SARS-CoV-2 test positive Throat irritation

Symptomtext

Starting 01/29/2022, I had scratchy throat, stuffy nose, some coughing, headache, muscle aches, low grade fever and fatigue. I did not lose my sense of taste or smell but food did not interest me for bout 5 days. It just felt like a bad cold. I saw my doctor and followed up at an urgent care was diagnosed with flue and COVID at the same time. I was prescribed Tamiflu. After the 5 days I was feeling better. About a week after my COVID test I got an ear infection as well. But, I have had ear infections my whole life.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: COVID -19 test - 01/31/2022 - positive, Flu test- 01/31/2022 - positive
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure, Seasonal allergies
Andere Medikamente: Hydrochlorothiazide 25mg, Atorvastatin 20mg, Lisinopril 40mg, Escitalopram 20mg, Omeprazole 40mg, Sulfa simazine 1000mg, Fluticasone spray each nostril twice daily, Calcium/vitamin d supplement twice daily, Women 50 plus Multivitamin, Dicl
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2190409

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IL
Alter: 46,0
Geschlecht: F
Eingang: 21.03.2022
Impfdatum: 27.10.2021
Beginn: 14.11.2021
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: IM / RA

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

Chest X-ray Dyspnoea Emphysema Pulmonary function test abnormal

Symptomtext

SOB stated about a few weeks after injection, no relief from 12/21/21 Flovent was prescribed and prednisone and f/u on 12/23/21 with a steroid injection. SOB was so bad I could not eat or talk. Chest X-ray, Pulmonary function test, mild emphysema. Medication was changed again to Symbicort. Now being referred to a pulmonologist. All COVID tests have been negative.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Chest X-ray, Pulmonary function test.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Dyazide 37.5/25 1 in the am; Albuterol 4x day as needed
Allergien: Penicillin; Levaquin; Bactroban ointment; Pistachos
Vorherige Impfungen: Nausea for a couple of days.

VAERS 2181587

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MI
Alter: 55,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 03.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: - / RA

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

Hypoaesthesia Motor dysfunction Paraesthesia Peripheral swelling

Symptomtext

Swelling in both arms; Numbness and tingling in arms and fingers; Unable to grasp things and dropping things for a period of time; Pins and needles sensation in feet/ numbness and tingling in arms and fingers; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 55 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 03Nov2021 08:30 (Lot number: FF8841) at the age of 55 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "hemachromatosis" (unspecified if ongoing); "known allergies: corn and corn products" (unspecified if ongoing); "known allergies: tomatoes, coconut" (unspecified if ongoing); "known allergies: pork" (unspecified if ongoing); "Known allergies: Sulpha" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 1, product: COVID 19, Brand: Pfizer, Lot number: EW0150, Administration time: 08:30 AM, Vaccine location: Left arm, Following first dose, swelling and numbness in right arm subsided within 12 hours.), administration date: 13Oct2021, when the patient was 55 years old, for COVID-19 immunization, reaction(s): "Swelling and numbness in right arm", "Swelling and numbness in right arm". The following information was reported: PERIPHERAL SWELLING (non-serious) with onset 05Nov2021, outcome "recovering", described as "Swelling in both arms"; HYPOAESTHESIA (non-serious) with onset 05Nov2021, outcome "recovering", described as "Numbness and tingling in arms and fingers"; MOTOR DYSFUNCTION (non-serious) with onset 05Nov2021, outcome "recovering", described as "Unable to grasp things and dropping things for a period of time"; PARAESTHESIA (non-serious) with onset 05Nov2021, outcome "recovering", described as "Pins and needles sensation in feet/ numbness and tingling in arms and fingers". Additional information: Other medications in two weeks include Multivitamin. No Covid prior vaccination. No Covid tested post vaccination. Follow-up attempts are completed. No further information is expected.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Food allergy; Fruit allergy; Hemochromatosis; Meat allergy; Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2176853

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NJ
Alter: 15,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 07.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / -

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

Blood test Cardiac disorder Chest discomfort Electrocardiogram Electrocardiogram ambulatory Heart rate Palpitations Tachycardia

Symptomtext

having a raise in heart rate/ heart rate was over a 150 beats per min; Heart racing; chest was heavy; having some heart issues; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the parent. A 15 year-old female patient received bnt162b2 (COMIRNATY), administration date 07Jan2022 (Lot number: FF8841) at the age of 15 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Asthmatic" (ongoing), notes: it does like exercise or allergy induced, so she does not take a normal inhaler; "fruit allergies" (ongoing). There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Manufacturer unknown, dose1), for Covid-19 immunization; Covid-19 vaccine (Manufacturer unknown, dose 2), for Covid-19 immunization. The following information was reported: CARDIAC DISORDER (non-serious) with onset 08Jan2022, outcome "unknown", described as "having some heart issues"; TACHYCARDIA (non-serious), outcome "unknown", described as "having a raise in heart rate/ heart rate was over a 150 beats per min"; PALPITATIONS (non-serious), outcome "unknown", described as "Heart racing"; CHEST DISCOMFORT (non-serious), outcome "unknown", described as "chest was heavy". The event "having a raise in heart rate/ heart rate was over a 150 beats per min" was evaluated at the emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of cardiac disorder, tachycardia, palpitations, chest discomfort. Additional information: It was reported that the patient was having some heart issues which were "intermittent" started the day after she received the dose, since then she was having a raise in heart rate, then a week after that would raise again then another week will raise again after and so on and so fort. The patient visited ER this past week because her heart rate was over a 150 beats per min. Prior vaccination (Within four weeks) was none. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Name: blood work; Result Unstructured Data: Test Result:unknown results; Test Name: EKG; Result Unstructured Data: Test Result:Normal; Comments: was okay; Test Name: heart monitor; Result Unstructured Data: Test Result:unknown results; Test Name: heart rate; Result Unstructured Data: Test Result:150; Comments: 150 beats per min
Aktuelle Erkrankungen: Asthmatic (it does like exercise or allergy induced, so she does not take a normal inhaler); Fruit allergy
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2176504

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CT
Alter: 24,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 03.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: OT / LA

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

Asthenia Dizziness Eating disorder Headache Migraine Nausea Pain Retching Vomiting

Symptomtext

headache/Headache intensified; feeling very sore/weak; feeling very sore/weak/unable to gather the strength to move or stop puking; nauseous; vomiting; I felt incredibly dizzy; I hadn't been able to eat or drink very much; full blown migraine; I was dry heaving; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 24 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 03Nov2021 14:30 (Lot number: FF8841) at the age of 24 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: FLU VACCINE VII, administration date 11Oct2021. Past drug history included: Amoxicillin, reaction(s): "Known allergies: Amoxicilin". Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EL3247, Location of injection: Arm Left, Vaccine Administration Time: 02:30 PM, Route of Administration: Intramuscular), administration date: 02Feb2021, when the patient was 24 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EL3247, Location of injection: Arm Left, Vaccine Administration Time: 02:30 PM, Route of Administration: Intramuscular), administration date: 23Feb2021, when the patient was 24 years old, for COVID-19 immunization. The following information was reported: HEADACHE (non-serious) with onset 04Nov2021 07:00, outcome "recovered with sequelae", described as "headache/Headache intensified"; PAIN (non-serious) with onset 04Nov2021 07:00, outcome "recovered with sequelae", described as "feeling very sore/weak"; ASTHENIA (non-serious) with onset 04Nov2021 07:00, outcome "recovered with sequelae", described as "feeling very sore/weak/unable to gather the strength to move or stop puking"; NAUSEA (non-serious) with onset 04Nov2021 07:00, outcome "recovered with sequelae", described as "nauseous"; MIGRAINE (non-serious) with onset 04Nov2021, outcome "recovered with sequelae", described as "full blown migraine"; RETCHING (non-serious) with onset 04Nov2021, outcome "recovered with sequelae", described as "I was dry heaving"; VOMITING (non-serious) with onset 04Nov2021 07:00, outcome "recovered with sequelae", described as "vomiting"; EATING DISORDER (non-serious) with onset 04Nov2021, outcome "recovered with sequelae", described as "I hadn't been able to eat or drink very much"; DIZZINESS (non-serious) with onset 04Nov2021 07:00, outcome "recovered with sequelae", described as "I felt incredibly dizzy". Therapeutic measures were not taken as a result of headache, pain, asthenia, nausea, migraine, retching, vomiting, eating disorder, dizziness. Additional information: Facility where the most recent COVID-19 vaccine was administered was Workplace clinic. Other medications the patient received within 2 weeks of vaccination was Birth Control Oral Pill. Prior to vaccination, the patient was not diagnosed with COVID-19; Since the vaccination, the patient has not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.

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

VAERS 2176270

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: VA
Alter: 76,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 02.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 16,0
Dosis: 3
Route/Site: OT / RA

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

Tremor

Symptomtext

she developed a tremor, a violent tremor that is controllable, she could stop it but if she didn't bother it would go on; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 76 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 02Oct2021 (Lot number: FF8841) at the age of 76 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Hypothyroidism" (ongoing); "Cancer. Rt breast", start date: 2009 (unspecified if ongoing), notes: Pertinent details: No evidence of recurrence in 11 years; "low Vitamin D" (unspecified if ongoing). Family history included: "High cholesterol" (unspecified if ongoing), notes: Pertinent details: all family runs high. Concomitant medication(s) included: LIOTHYRONINE taken for hypothyroidism, start date: 2019 (ongoing); LEVOTHYROXINE taken for hypothyroidism, start date: 1995; VITAMIN D [VITAMIN D NOS] taken for vitamin d decreased, start date: 2010 (ongoing). Vaccination history included: Bnt162b2 (Dose Number: 1, Lot Number: EN5318, 1st shot she had no symptoms, Anatomical site of Location: Left Arm, Route of administration: Intramuscular), administration date: 27Jan2021, when the patient was 76 years old, for COVID-19 immunization, reaction(s): "1st shot she had no symptoms"; Bnt162b2 (Dose Number: 2, Lot Number: EN6202, her first 2 were fine., Anatomical site of Location: Rt Arm, Lot number: EN6202, Route of administration: Intramuscular), administration date: 03Mar2021, when the patient was 76 years old, for COVID-19 immunization, reaction(s): "her first 2 were fine". The following information was reported: TREMOR (non-serious) with onset 18Oct2021, outcome "unknown", described as "she developed a tremor, a violent tremor that is controllable, she could stop it but if she didn't bother it would go on". Additional information: Reporter stated that her first 2 were fine. Stated that she got the booster sometime around 02Oct2021 and around 18Oct2021 she developed a tremor, a violent tremor that was controllable, she could stop it but if she didn't bother it would go on. Caller stated it was the arm where she got the shot and she doesn't notice it and if she puts her hand in a certain way it happens. Caller states the interesting thing was she has an identical twin sister and she got the booster and she also now has this tremor. Vaccination Facility Type was Pharmacy or Drug Store. Prior vaccination (within 4 weeks) was none. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101454872 Same reporter/drug/event, different patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hypothyroidism
Vorgeschichte: Medical History/Concurrent Conditions: Breast cancer (Pertinent details: No evidence of recurrence in 11 years); High cholesterol (Pertinent details: all family runs high); Vitamin D low
Andere Medikamente: LIOTHYRONINE; LEVOTHYROXINE; VITAMIN D [VITAMIN D NOS]
Allergien: -
Vorherige Impfungen: -

VAERS 2176215

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: NY
Alter: 26,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Headache Pain in extremity Paraesthesia

Symptomtext

Sore arm (left); Tingling down entire left side of body; Headache; This is a spontaneous report received from a non-contactable reporter(s) (Other HCP). The reporter is the patient. A 26 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 15Oct2021 15:00 (Lot number: ff8841) at the age of 26 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "PCOS" (unspecified if ongoing), notes: PCOS. Concomitant medication(s) included: ERYTHROMYCIN; VITAMIN D [ERGOCALCIFEROL]. Past drug history included: Amoxicillin, reaction(s): "Known allergies: amoxicillin", notes: Known allergies: amoxicillin; Amitriptyline, reaction(s): "Known allergies: amitriptyline", notes: Known allergies: amitriptyline. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 15Oct2021, outcome "recovered" (16Oct2021), described as "Sore arm (left)"; PARAESTHESIA (non-serious) with onset 15Oct2021, outcome "recovered" (16Oct2021), described as "Tingling down entire left side of body"; HEADACHE (non-serious) with onset 15Oct2021, outcome "recovered" (Oct2021), described as "Headache". Therapeutic measures were not taken as a result of pain in extremity, paraesthesia, headache. Additional information: The patient was non pregnant at time of Vaccination. Facility where the most recent COVID-19 vaccine was administered was Pharmacy or Drug Store. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. List of other medications the patient received within 2 weeks of vaccination included Erythromycin, Multi vitamin and vitamin d. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The patient experienced the event sore arm (left), tingling down entire left side of body for 24 hours and headache for over a week. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Polycystic ovarian syndrome (PCOS)
Andere Medikamente: ERYTHROMYCIN; VITAMIN D [ERGOCALCIFEROL]
Allergien: -
Vorherige Impfungen: -

VAERS 2176204

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: OH
Alter: 53,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 13.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Blood pressure measurement Condition aggravated Pain in extremity

Symptomtext

Her arm is still sore/Soreness in Arm/Sore arm; Soreness in Arm was reported as worsened; 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 53 year-old female patient received bnt162b2 (COMIRNATY), administered in arm left, administration date 13Oct2021 (Lot number: FF8841) at the age of 53 years as dose 3 (booster), single, administered in arm left, administration date 02Apr2021 (Lot number: ER8733) as dose 2, single and administered in arm left, administration date 12Mar2021 (Lot number: EN6206) as dose 1, single for covid-19 immunisation. Relevant medical history included: "High Blood Pressure" (ongoing). The patient's concomitant medications were not reported. Vaccination history included: Flu shot (No. of Previous Doses: 1, End of September like 29Oct2021 ), administration date: 2021, for immunisation. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 2021, outcome "not recovered", described as "Her arm is still sore/Soreness in Arm/Sore arm"; CONDITION AGGRAVATED (non-serious) with onset 2021, outcome "not recovered", described as "Soreness in Arm was reported as worsened". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pain in extremity, condition aggravated. Additional information: No additional Vaccines were administered on Same Date of the Pfizer Suspect. Family history included none. Patient took the booster dose of the Pfizer Covid-19 vaccine on 13Oct2021 and her arm was still sore. Patient states that it went over 2 weeks. Patient wants to know what to do and if this is a normal side effect. Patient states her arm was sore after her first two doses but that only lasted a couple of days, probably 3-4 days. Soreness in Arm after booster dose started on 14Oct2021. AE(s) did not require a visit to: Emergency Room or Physician Office. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: High Blood Pressure; Result Unstructured Data: Test Result:High
Aktuelle Erkrankungen: Blood pressure
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2176163

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IL
Alter: 68,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 03.10.2021
Beginn: 04.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Asthenia Fatigue Hypoaesthesia Paraesthesia

Symptomtext

Extremely week; tired; numbness and tingling in both legs and hands; numbness and tingling in both legs and hands; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 68 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 03Oct2021 11:00 (Lot number: FF8841) at the age of 68 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 Number: 1, Vaccine Administration Time: 12:00, Batch/Lot No: Lot # FC3184, Location of injection: Arm Left), administration date: 12Sep2021, when the patient was 68 years old, for COVID-19 Immunization. The following information was reported: ASTHENIA (non-serious) with onset 04Oct2021 11:00, outcome "not recovered", described as "Extremely week"; FATIGUE (non-serious) with onset 04Oct2021 11:00, outcome "not recovered", described as "tired"; HYPOAESTHESIA (non-serious), PARAESTHESIA (non-serious) all with onset 04Oct2021 11:00, outcome "not recovered" and all described as "numbness and tingling in both legs and hands". Therapeutic measures were not taken as a result of asthenia, fatigue, hypoaesthesia, paraesthesia. Additional information: Did the patient receive any other vaccines within 4 weeks prior to the COVID vaccine: No. List of any other medications the patient received within 2 weeks of vaccination: No. The event had not resulted in for death, life-threatening, prolonged hospitalisation, disabling/incapacitating or Congenital anomaly/birth defect. Adverse event Extremely week and tired, numbness and tingling in both legs and hands. Started after second dose and continued. if patient recovered: Not recovered. If treatment ae: No. Prior to vaccination, was the patient diagnosed with COVID-19: No. Since the vaccination, has the patient been tested for COVID-19: No. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2176053

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MI
Alter: 30,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 14.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: OT / LA

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

Axillary pain Blood test Headache Hepatobiliary scan Migraine Pain Ultrasound scan

Symptomtext

Headache; Migraine; Full body aches; Aching pain in my armpit of my left arm; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 30 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 14Oct2021 07:43 (Lot number: FF8841, Expiration Date: 31Mar2022) at the age of 30 years as dose 3 (booster),single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: FLU VACCINE VII, administration date 21Sep2021. Past drug history included: Flu vaccine for Influenza immunization, reaction(s): "Migraine". Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EL3248, Location of injection: Left upper arm, Route of administration: Intramuscular, Exp: Apr2021), administration date: 04Feb2021, when the patient was 30 years old, for COVID-19 immunization, reaction(s): "Migraine", "GI/Digestion Issues"; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL3248, Location of injection: Left upper arm, Route of administration: Intramuscular, Exp: Apr2021), administration date: 14Jan2021, when the patient was 30 years old, for COVID-19 immunization. The following information was reported: MIGRAINE (non-serious) with onset 15Oct2021 05:30, outcome "recovered" (18Oct2021), described as "Migraine"; PAIN (non-serious) with onset 15Oct2021 05:30, outcome "recovered" (17Oct2021), described as "Full body aches"; HEADACHE (non-serious) with onset 18Oct2021, outcome "recovered" (20Oct2021), described as "Headache"; AXILLARY PAIN (non-serious) with onset 15Oct2021, outcome "recovered" (18Oct2021), described as "Aching pain in my armpit of my left arm". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of migraine, pain, headache, axillary pain. The patient underwent the following laboratory tests and procedures: blood test: unknown results; hepatobiliary scan: unknown results, notes: HIDA scan performed to asses issue; ultrasound scan: unknown results. Therapeutic measures were not taken as a result of migraine, pain, headache, axillary pain. Additional information: The patient woke up the morning after booster was received with a migraine and full body aches. The patient treated with excedrine migraine as directed. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient was not 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: Blood work; Result Unstructured Data: Test Result:Unknown results; Test Name: HIDA scan; Result Unstructured Data: Test Result:Unknown results; Comments: HIDA scan performed to asses issue; Test Name: ultrasound; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: GI irritation (Blood work, ultrasound and HIDA scan performed to asses issue)
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy; Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2165330

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: OH
Alter: 57,0
Geschlecht: F
Eingang: 08.03.2022
Impfdatum: 06.11.2021
Beginn: 22.01.2022
Tage bis Beginn: 77,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Chest X-ray abnormal Coronavirus test positive Cough Dyspnoea Pneumonia

Symptomtext

Patient was admitted to hospital on 01/22/2022, testing positive for Covid. Patient had an abnormal chest X-ray and had developed pneumonia. Patient had a cough and was short of breath. Patient has pre-existing medical conditions: type 2 diabetes, hypertension, and severe obesity. Records were recorded by hospital. This is document is supported by those records. Number of hospital days was not charted, no discharge date given.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 2019 Novel Coronavirus RNA Detected 01/22/2022
Aktuelle Erkrankungen: type 2 diabetes, hypertension, severe obesity
Vorgeschichte: type 2 diabetes, hypertension, severe obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2162759

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: AZ
Alter: 78,0
Geschlecht: F
Eingang: 07.03.2022
Impfdatum: 12.01.2021
Beginn: 02.02.2021
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: IM / RA

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

Angiogram normal COVID-19 Cough Fibrin D dimer Hypoxia Incentive spirometry Pneumonia Pyrexia SARS-CoV-2 test positive

Symptomtext

DIAGNOSIS: Hypoxia, COVID, pneumonia -Onset date: 2/4 -presented with fevers, dry cough in ED -vaccinated x 2 with booster -initial dimer 2.14 -Admit to RCU: contact/airborne precautions -Covid test date: 2/6 + by Abbott -CTA negative -remdesivir/ dexamethasone 2/6-2/8 -titrate O2 92-94% on room air and with activity -Ambulatory O2 challenge twice daily, once per shift -incentive spirometry -isolate for 20 days 2/4/22-2/24/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: 2,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: R- Breast cancer Hyperlipidemia Hypertension Type 2 DM
Andere Medikamente: N/A
Allergien: NKA
Vorherige Impfungen: -

VAERS 2157683

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 56,0
Geschlecht: M
Eingang: 04.03.2022
Impfdatum: 29.11.2021
Beginn: 23.02.2022
Tage bis Beginn: 86,0
Dosis: 2
Route/Site: SYR / LA

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

Anxiety Asthenia Atrial fibrillation Blood test Chest pain Dyspnoea

Symptomtext

It was rapid AFIB (RVR) with classic ACS symptoms: chest pain, anxiety, shortness of breath, generalized weakness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Blood work
Aktuelle Erkrankungen: No
Vorgeschichte: Paraxsimal AFIB
Andere Medikamente: Multivitamin
Allergien: No
Vorherige Impfungen: -

VAERS 2151023

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff8841

moderat

Staat: OH
Alter: 50,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 05.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / -

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

Condition aggravated Ear pain Fatigue Neuralgia Palpitations Sinus disorder

Symptomtext

Heart palpitations Extreme sinus problems Nerve pain Extreme fatigue Ear pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Covid symptoms fever, body aches, sinus, ear ache, cough
Vorgeschichte: -
Andere Medikamente: Premarin Vyvanse
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1881223

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NY
Alter: 38,0
Geschlecht: M
Eingang: 01.03.2022
Impfdatum: 20.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Angina pectoris Burning sensation Cardiac disorder Chest discomfort Chest pain Blood test Dyspnoea Electrocardiogram normal X-ray Electrocardiogram Electrocardiogram abnormal Fatigue Heart rate Heart rate increased Injury Pain Tachycardia

Symptomtext

He had pain in his heart; patient who states that he was injured by the Pfizer Biontech COVID-19 vaccine; He had tachycardia; pressure and pain in his chest; pressure and pain in his chest; feeling like a bad feeling in his heart a few days later; rapid heart beat; there was a pressure in his chest with tightness and heaviness.; felt the pain move throughout his body; burning and aching sensation in his heart; fatigued; They did an EKG that showed something like a block barrier or something; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program. The reporter is the patient. A 38 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 20Dec2021 (Lot number: FF8841) at the age of 38 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: ANGINA PECTORIS (medically significant), outcome "unknown", described as "He had pain in his heart"; INJURY (non-serious), outcome "unknown", described as "patient who states that he was injured by the Pfizer Biontech COVID-19 vaccine"; TACHYCARDIA (non-serious), outcome "recovering", described as "He had tachycardia"; CHEST DISCOMFORT (non-serious), CHEST PAIN (non-serious), outcome "recovering" and all described as "pressure and pain in his chest"; CARDIAC DISORDER (non-serious), outcome "unknown", described as "feeling like a bad feeling in his heart a few days later"; HEART RATE INCREASED (non-serious), outcome "recovering", described as "rapid heart beat"; CHEST DISCOMFORT (non-serious), outcome "unknown", described as "there was a pressure in his chest with tightness and heaviness."; PAIN (non-serious), outcome "unknown", described as "felt the pain move throughout his body"; BURNING SENSATION (non-serious), outcome "unknown", described as "burning and aching sensation in his heart"; FATIGUE (non-serious), outcome "recovering", described as "fatigued"; ELECTROCARDIOGRAM ABNORMAL (non-serious), outcome "unknown", described as "They did an EKG that showed something like a block barrier or something". The events "he had pain in his heart", "patient who states that he was injured by the pfizer biontech covid-19 vaccine", "he had tachycardia", "pressure and pain in his chest", "pressure and pain in his chest", "feeling like a bad feeling in his heart a few days later", "rapid heart beat", "there was a pressure in his chest with tightness and heaviness.", "felt the pain move throughout his body", "burning and aching sensation in his heart", "fatigued" and "they did an ekg that showed something like a block barrier or something" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: electrocardiogram: showed something like a block barrier or something; heart rate: rapid heart beat. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Name: EKG; Result Unstructured Data: Test Result:showed something like a block barrier or something; Test Name: heart beat; Result Unstructured Data: Test Result:Rapid Heart Beat
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1881223

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NY
Alter: 38,0
Geschlecht: M
Eingang: 01.03.2022
Impfdatum: 20.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Angina pectoris Burning sensation Cardiac disorder Chest discomfort Chest pain Blood test Dyspnoea Electrocardiogram normal X-ray Electrocardiogram Electrocardiogram abnormal Fatigue Heart rate Heart rate increased Injury Pain Tachycardia

Symptomtext

He had pain in his heart; patient who states that he was injured by the Pfizer Biontech COVID-19 vaccine; He had tachycardia; pressure and pain in his chest; pressure and pain in his chest; feeling like a bad feeling in his heart a few days later; rapid heart beat; there was a pressure in his chest with tightness and heaviness.; felt the pain move throughout his body; burning and aching sensation in his heart; fatigued; They did an EKG that showed something like a block barrier or something; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program. The reporter is the patient. A 38 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 20Dec2021 (Lot number: FF8841) at the age of 38 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: ANGINA PECTORIS (medically significant), outcome "unknown", described as "He had pain in his heart"; INJURY (non-serious), outcome "unknown", described as "patient who states that he was injured by the Pfizer Biontech COVID-19 vaccine"; TACHYCARDIA (non-serious), outcome "recovering", described as "He had tachycardia"; CHEST DISCOMFORT (non-serious), CHEST PAIN (non-serious), outcome "recovering" and all described as "pressure and pain in his chest"; CARDIAC DISORDER (non-serious), outcome "unknown", described as "feeling like a bad feeling in his heart a few days later"; HEART RATE INCREASED (non-serious), outcome "recovering", described as "rapid heart beat"; CHEST DISCOMFORT (non-serious), outcome "unknown", described as "there was a pressure in his chest with tightness and heaviness."; PAIN (non-serious), outcome "unknown", described as "felt the pain move throughout his body"; BURNING SENSATION (non-serious), outcome "unknown", described as "burning and aching sensation in his heart"; FATIGUE (non-serious), outcome "recovering", described as "fatigued"; ELECTROCARDIOGRAM ABNORMAL (non-serious), outcome "unknown", described as "They did an EKG that showed something like a block barrier or something". The events "he had pain in his heart", "patient who states that he was injured by the pfizer biontech covid-19 vaccine", "he had tachycardia", "pressure and pain in his chest", "pressure and pain in his chest", "feeling like a bad feeling in his heart a few days later", "rapid heart beat", "there was a pressure in his chest with tightness and heaviness.", "felt the pain move throughout his body", "burning and aching sensation in his heart", "fatigued" and "they did an ekg that showed something like a block barrier or something" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: electrocardiogram: showed something like a block barrier or something; heart rate: rapid heart beat. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Name: EKG; Result Unstructured Data: Test Result:showed something like a block barrier or something; Test Name: heart beat; Result Unstructured Data: Test Result:Rapid Heart Beat
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2147800

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MO
Alter: 44,0
Geschlecht: F
Eingang: 28.02.2022
Impfdatum: 29.01.2021
Beginn: 26.12.2021
Tage bis Beginn: 331,0
Dosis: 3
Route/Site: IM / AR

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

Autoimmune hepatitis Biopsy liver abnormal Blood test abnormal Fatigue Hepatic enzyme increased Hepatic necrosis Hypotension Influenza virus test negative Malaise Mobility decreased SARS-CoV-2 test negative

Symptomtext

On Dec 26, 2021 I started to feel sick. I was so fatigued I could barely get out of bed. On Dec 29, 2021 I went to the urgent care and I was swabbed for COVID and flu. Both were negative. My blood pressure was extremely low so I went to the emergency dept at a local hospital. I was hospitalized until January 1, 2022 with extremely elevated liver enzymes. It was thought that I had autoimmune hepatitis but bloodwork was taking a long time to come back. I was discharged with instructions to see a hepatic specialist. It took 3 weeks for bloodwork to come back. I then got a liver biopsy on January 19, 2022. It was determined I did have autoimmune hepatitis. My liver was very necrotic so I began treatment with a high dose of Prednisone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: 4,0
Labordaten: Everything is listed above except weekly bloodwork at quest diagnostics.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin, vitamin d
Allergien: Latex, penicillin, sulfa, ibuprofen
Vorherige Impfungen: -

VAERS 2146482

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: -
Alter: -
Geschlecht: M
Eingang: 26.02.2022
Impfdatum: 23.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Asthenia Dizziness Dizziness exertional Erythema Fatigue Feeling abnormal Influenza like illness Pallor Paraesthesia Pyrexia

Symptomtext

felt like when you have the flu; dizzy/lightheaded; brain fog/really weird/felt bad; tingling on the right side of my head; when he walk, he is dizzy; cheeks turned red; cheeks have been red ever since I have gotten it; 'he turns' pale; felt weak; fever; 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 male patient received bnt162b2 (BNT162B2), administration date 23Oct2021 (Lot number: FF8841) as dose 2, 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 Number: 301308A)), administration date: 02Oct2021, for COVID-19 Immunisation. The following information was reported: INFLUENZA LIKE ILLNESS (non-serious) with onset Oct2021, outcome "unknown", described as "felt like when you have the flu"; DIZZINESS (non-serious) with onset Oct2021, outcome "unknown", described as "dizzy/lightheaded"; FEELING ABNORMAL (non-serious) with onset Oct2021, outcome "unknown", described as "brain fog/really weird/felt bad"; PARAESTHESIA (non-serious) with onset Oct2021, outcome "unknown", described as "tingling on the right side of my head"; DIZZINESS EXERTIONAL (non-serious) with onset Oct2021, outcome "unknown", described as "when he walk, he is dizzy"; ERYTHEMA (non-serious) with onset Oct2021, outcome "unknown", described as "cheeks turned red; cheeks have been red ever since I have gotten it"; PALLOR (non-serious) with onset Oct2021, outcome "unknown", described as "'he turns' pale"; ASTHENIA (non-serious) with onset Oct2021, outcome "unknown", described as "felt weak"; PYREXIA (non-serious) with onset Oct2021, outcome "unknown", described as "fever"; FATIGUE (non-serious) with onset Oct2021, outcome "unknown", described as "fatigue". Additional information: As per caller (patient) he got his first dose on 02Oct2021 and the second on 23Oct2021, he got sick after the 2nd dose (expiry date unknown). Later that night and early the next day side effects started, he felt weak, had a fever it felt like when you have the flu, been really dizzy lately, it was really weird, lightheaded, tingling on the right side of his head, brain fog. Are those common side effects"? Reporter further mentioned in another follow up call that he has taken his second Covid vaccine 3 weeks ago, Saturday which is since then he has had tingling on the right side of his head. He has had dizziness, when he walks, he is dizzy and his cheeks and 'he turns' pale and his cheeks turned red and he was wanting to speak to someone about this. "Consumer again stated, "Yeah, like real like fatigue, like brain fog type thing and then like I feel, like I feel really lightheaded a lot and it's bad and it's freaking me out. Like, I don't know what's going on and my cheeks have been red ever since I have gotten it like my cheeks. I had a temperature after I got the second one. Patient mentioned that he had his vaccination record. Patient mentioned that he read on the internet it can cause swelling of the brain. You know they are forcing the vaccine on you and when you have side effect you say go see a doctor, but the doctors don't know anything about it and some doctors are saying not to get the vaccine". Reporter seriousness was unspecified. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

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

VAERS 2146481

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: WV
Alter: 13,0
Geschlecht: M
Eingang: 26.02.2022
Impfdatum: 06.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: OT / LA

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

C-reactive protein Chest pain Dyspnoea Electrocardiogram Fatigue Nausea Red blood cell sedimentation rate Troponin T Vaccination site pain

Symptomtext

shortness of breath; chest pain; nausea; fatigue; arm pain at injection site; This is a spontaneous report received from contactable reporter(s) (Other HCP) via COVID-19 Adverse Event Self-Reporting Solution (COVAES). A 13 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 06Nov2021 10:00 (Lot number: FF8841) at the age of 13 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Seizure" (unspecified if ongoing). Concomitant medication(s) included: DEPAKOTE; STRATTERA; HYDROXYZINE; HYDROXYZINE HCL (ongoing); DIVALPROEX SODIUM (ongoing); SINGULAIR (ongoing); ATOMOXETINE HCL (ongoing). Past drug history included: Amoxicillin, reaction(s): "drug allergy". Vaccination history included: Bnt162b2 (Dose 1, single, Batch/Lot number: FF8841, via intramuscular route of administration), administration date: 16Oct2021, when the patient was 13 years old, for COVID-19 immunization. The following information was reported: DYSPNOEA (non-serious) with onset 08Nov2021, outcome "recovering", described as "shortness of breath"; CHEST PAIN (non-serious) with onset 08Nov2021, outcome "recovering", described as "chest pain"; NAUSEA (non-serious) with onset 08Nov2021, outcome "recovering", described as "nausea"; FATIGUE (non-serious) with onset 08Nov2021, outcome "recovering", described as "fatigue"; VACCINATION SITE PAIN (non-serious) with onset 08Nov2021, outcome "recovering", described as "arm pain at injection site". The events "shortness of breath", "chest pain", "nausea", "fatigue" and "arm pain at injection site" 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 dyspnoea, chest pain, nausea, fatigue, vaccination site pain. Additional information: The patient was not received other vaccine in four weeks. The patient received other medication in two weeks were DEPAKOTE, STRATTERA, HYDROXYZINE. Prior vaccination, the patient was not diagnosed with COVID-19. Post vaccination, the patient was not tested for COVID-19. The vaccine was administered at pharmacy or drug store. The vaccine was not administered at private facility. The patient underwent lab test and procedure on 08Nov2021 which includes red blood cell sedimentation rate (sed rate): 0 (Normal), C-reactive protein (CRP): unknown result, Troponin T: less than 7 (Normal), Electrocardiogram (EKG): Normal. The reporter stated that the event was related to the BNT162B2. The reporter stated, the patient normally sees doctor. The reporter stated, the patient mother wanted him to continue to see doctor for any further follow up. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20211108; Test Name: CRP; Result Unstructured Data: Test Result:Unknown result; Test Date: 20211108; Test Name: EKG; Result Unstructured Data: Test Result:Normal; Test Date: 20211108; Test Name: Sed Rate; Result Unstructured Data: Test Result:0; Comments: Normal; Test Date: 20211108; Test Name: Troponin T; Result Unstructured Data: Test Result:less than 7; Comments: Normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Seizures
Andere Medikamente: DEPAKOTE; STRATTERA; HYDROXYZINE; HYDROXYZINE HCL; DIVALPROEX SODIUM; SINGULAIR; ATOMOXETINE HCL
Allergien: -
Vorherige Impfungen: -

VAERS 2139879

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: WI
Alter: 52,0
Geschlecht: F
Eingang: 25.02.2022
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: ja Erholt: nein

Arthralgia Hypoaesthesia Insomnia Neck pain Pain Pain in extremity Paraesthesia

Symptomtext

The night after receiving the covid vaccine booster, I had body aches. I experienced numbness and tingling in my left leg and pain and aching on the left side from the neck down, including my arms elbow, and hand. (note:My left arm had remained stiff and a little sore (when used) after a shingles vaccine.) I took ibuprofen and Tylenol for two weeks. This did not work very well on the pain in my arm. After a few weeks of movement and exercise the pain in my knee receded, however the pain in my arm was so bad that I could not sleep. I have continued to take Tylenol, Aleve and ibuprofen with very little relief. The pain is so bad at night that I cannot sleep. I experience pain when dressing, trying to reach and when I am just sit-in. I have seen a doctor recently.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Zyrtec, triamterene-hydrochlorothiazide, multivitamin, lansoprazole
Allergien: penicillin
Vorherige Impfungen: The first Shingles shot may have be a part of the pain

VAERS 2137096

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MO
Alter: 22,0
Geschlecht: F
Eingang: 24.02.2022
Impfdatum: 21.01.2022
Beginn: 11.02.2022
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: IM / RA

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

Chest pain Discomfort Dyspnoea exertional Headache Nocturnal dyspnoea Pain Pain in extremity Tachycardia

Symptomtext

Follow Up of Chest pain (chief complaint). Description: The patient presents with a complaint of Follow Up of Chest pain. The symptoms began 2 weeks ago. The problem occurs intermittently. It generally lasts a variable amount of time. The symptoms have improved. The pain is in the substernal area. The patient describes the pain as pressure, stinging, jolting. It radiates to the left arm. Relevant history for this patient excludes tobacco use. Interventions the patient has tried have not provided any relief. The Follow Up of Chest pain is associated with dyspnea on exertion, headache, nocturnal dyspnea and tachycardia. The patient denies any dependent edema, dysphagia, generalized weakness or nocturia. Additional information: Of note chest pain started after first Covid vaccine 1/21 and got second 2/11 and worsened. States is slightly improved since start but is still present. Has been anxious throughout college but has never felt this before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Doxycycline
Vorherige Impfungen: -

VAERS 2134347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: -
Alter: 79,0
Geschlecht: M
Eingang: 23.02.2022
Impfdatum: 26.10.2021
Beginn: 26.11.2021
Tage bis Beginn: 31,0
Dosis: 3
Route/Site: - / -

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

Adenovirus infection Bronchitis Pneumonia

Symptomtext

Admission for Adenoviral bronchitis. empiric ceftriaxone/doxycycline started, By the following day he was feeling much better and is requesting discharge. He will discharge on cefpodoxime to complete a 7 days empiric course for pneumonia. ED visit and hospital admission were within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2119396

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: -
Alter: 89,0
Geschlecht: M
Eingang: 17.02.2022
Impfdatum: 08.10.2021
Beginn: 02.11.2021
Tage bis Beginn: 25,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain

Symptomtext

Patient with dementia, moderate persistent asthma, GERD, CAD, mild aortic stenosis, chronic pain, admitted 11/2/21 with chest pain. Known CAD with non-STEMI in 6/2021 at which time LHC showed mild atherosclerosis in the major epicardial coronary arteries as well as 100% stenosis of distal limb of a bifid rPDA likely the culprit lesion but too small and distal for revascularization. He was medically treated with dual antiplatelet therapy. ED to hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2118761

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: TX
Alter: 52,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 07.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

Condition aggravated Cough

Symptomtext

Cannot stop coughing; worsened; 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 received bnt162b2 (BNT162B2), administered in arm right, administration date 07Oct2021 13:00 (Lot number: FF8841) at the age of 52 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Type 2 diabetes mellitus" (unspecified if ongoing); "Hypertension" (unspecified if ongoing). Concomitant medication(s) included: LANTUS; LOSARTAN. Vaccination history included: Bnt162b2 (Dose no: 1, Lot no: ER6206, The caller didn't have an side effects with the first two doses), administration date: 05Mar2021, when the patient was 52 years old, for COVID-19 immunization, reaction(s): "No reaction on previous exposure to vaccine"; Bnt162b2 (Dose no: 2, Lot no: ER8133, The caller didn't have an side effects with the first two doses), administration date: 26Mar2021, when the patient was 52 years old, for COVID-19 immunization, reaction(s): "No reaction on previous exposure to vaccine". The following information was reported: COUGH (non-serious) with onset 08Oct2021, outcome "not recovered", described as "Cannot stop coughing"; CONDITION AGGRAVATED (non-serious) with onset Oct2021, outcome "not recovered", described as "worsened". Therapeutic measures were taken as a result of cough. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypertension; Type 2 diabetes mellitus
Andere Medikamente: LANTUS; LOSARTAN
Allergien: -
Vorherige Impfungen: -

VAERS 2118572

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff8841

moderat

Staat: LA
Alter: 39,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Arthralgia Body temperature Dysgeusia Epistaxis Erythema Eye pruritus Eye swelling Flushing Headache Muscle spasms Musculoskeletal stiffness Nasal congestion Nausea Ocular hyperaemia Pain Paraesthesia Pruritus Pyrexia

Symptomtext

muscle stiffness; Metallic taste; joint pain; itching; Flushing; Low grade fever; Headache; Mild swelling of eyes; Site soreness for 8 hours; Pain for 12 hours; Orbital itching+swelling for 14 hours; Rash+Redness (flushing) across upper chest+shoulders with itching+prickle sensation; Redness (flushing) across upper chest+shoulders with itching+prickle sensation; Rash+Redness (flushing) across upper chest+shoulders with itching+prickle sensation; Nausea for 12 hours post injection; Sneezing; Rhinorrhea; congestion with clear nasal drainage; mild unilateral Epistaxis x 2 episodes; Generalised urticaria; Generalised erythema; Generalised pruritis without skin rash; Red and itchy eyes; muscle cramps; muscle spasm; This is a spontaneous report received from a contactable reporter(s) (Pharmacist). The reporter is the patient. A 39 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in deltoid left, administration date 12Oct2021 14:00 (Lot number: Ff8841) at the age of 39 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Htn" (unspecified if ongoing), notes: Htn; "Patients reports allergy to unknown red food dyes" (unspecified if ongoing), notes: Patients reports allergy to unknown red food dyes, Unknown red dye allergy (food dyes)-mild hives; "Food allergy" (unspecified if ongoing), notes: Unknown red dye allergy (food dyes)-mild hives; "Hives" (unspecified if ongoing), notes: Benadryl (Diphenhydramine) for hives+ itching due to red food dyes, Unknown red dye allergy (food dyes)-mild hives; "Itching" (unspecified if ongoing), notes: Benadryl (Diphenhydramine) for hives+ itching due to red food dyes. Concomitant medication(s) included: BENICAR; SYNTHROID; ASPIRIN 81; VIT C; VIT D [ERGOCALCIFEROL]; PROPANOLOL [PROPRANOLOL]. The following information was reported: MUSCULOSKELETAL STIFFNESS (non-serious) with onset 12Oct2021 20:00, outcome "recovering", described as "muscle stiffness"; DYSGEUSIA (non-serious) with onset 12Oct2021 20:00, outcome "recovering", described as "Metallic taste"; ARTHRALGIA (non-serious) with onset 12Oct2021 20:00, outcome "recovering", described as "joint pain"; PRURITUS (non-serious) with onset 12Oct2021 20:00, outcome "recovering", described as "itching"; FLUSHING (non-serious) with onset 12Oct2021, outcome "recovering", described as "Flushing"; PYREXIA (non-serious) with onset 12Oct2021, outcome "recovering", described as "Low grade fever"; HEADACHE (non-serious) with onset 12Oct2021, outcome "recovering", described as "Headache"; EYE SWELLING (non-serious) with onset 12Oct2021, outcome "recovering", described as "Mild swelling of eyes"; VACCINATION SITE PAIN (non-serious) with onset 12Oct2021, outcome "recovering", described as "Site soreness for 8 hours"; PAIN (non-serious) with onset 12Oct2021, outcome "recovering", described as "Pain for 12 hours"; EYE PRURITUS (non-serious) with onset 12Oct2021, outcome "recovering", described as "Orbital itching+swelling for 14 hours"; RASH (non-serious), PARAESTHESIA (non-serious) all with onset 12Oct2021, outcome "recovering" and all described as "Rash+Redness (flushing) across upper chest+shoulders with itching+prickle sensation"; ERYTHEMA (non-serious) with onset 12Oct2021, outcome "recovering", described as "Redness (flushing) across upper chest+shoulders with itching+prickle sensation"; NAUSEA (non-serious) with onset 12Oct2021, outcome "recovering", described as "Nausea for 12 hours post injection"; SNEEZING (non-serious) with onset 12Oct2021, outcome "recovering", described as "Sneezing"; RHINORRHOEA (non-serious) with onset 12Oct2021, outcome "recovering", described as "Rhinorrhea"; NASAL CONGESTION (non-serious) with onset 12Oct2021, outcome "recovering", described as "congestion with clear nasal drainage"; EPISTAXIS (non-serious) with onset 12Oct2021, outcome "recovering", described as "mild unilateral Epistaxis x 2 episodes"; URTICARIA (non-serious) with onset 12Oct2021, outcome "recovering", described as "Generalised urticaria"; ERYTHEMA (non-serious) with onset 12Oct2021, outcome "recovering", described as "Generalised erythema"; PRURITUS (non-serious) with onset 12Oct2021, outcome "recovering", described as "Generalised pruritis without skin rash"; OCULAR HYPERAEMIA (non-serious) with onset 12Oct2021, outcome "recovering", described as "Red and itchy eyes"; MUSCLE SPASMS (non-serious) with onset 12Oct2021, outcome "recovering", described as "muscle cramps"; MUSCLE SPASMS (non-serious) with onset 12Oct2021, outcome "recovering", described as "muscle spasm". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of musculoskeletal stiffness, dysgeusia, arthralgia, pruritus, flushing, pyrexia, headache, eye swelling, vaccination site pain, pain, eye pruritus, rash, erythema, paraesthesia, nausea, sneezing, rhinorrhoea, nasal congestion, epistaxis, urticaria, erythema, pruritus, ocular hyperaemia, muscle spasms, muscle spasms. Additional information included: It was reported that patient was not diagnosed with COVID-19, prior to vaccination. Patient has not been tested COVID-19 since the vaccination. Patient describe the time course of the anaphylactic reaction: Metallic taste for 10 minutes post injection; site soreness for 8 hours; joint stiffness+ pain for 12 hours; orbital itching+ swelling for 14 hours. Patient required antihistamine as medical intervention. Patient was treated with acetaminophen for fever and pain, ibuprofen for joint and moderate stiffness. Patient was not seen in emergency department. Patient was not hospitalised. Patient was not admitted to an intensive care unit. It was reported that dermatological/mucosal and other organs were also involved. Patient did not require the initiation of new medication or other treatment or procedure. Patient did not receive any recent vaccine for SARS-Cov2 other than Pfizer- BioNTech covid-19 vaccine prior to the event being reported. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20211012; Test Name: Fever; Result Unstructured Data: Test Result:Low grade fever
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to chemicals (Unknown red dye allergy (food dyes)-mild hives); Food allergy (Unknown red dye allergy (food dyes)-mild hives); Hives (hives+ itching due to red food dyes); Hypertension (Htn); Itching (Benadryl (Diphenhydramine) for hives+ itching due to red food dyes.)
Andere Medikamente: BENICAR; SYNTHROID; ASPIRIN 81; VIT C; VIT D [ERGOCALCIFEROL]; PROPANOLOL [PROPRANOLOL.]
Allergien: -
Vorherige Impfungen: -

VAERS 2118539

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 08.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / LA

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

Abdominal discomfort Asthenia Burning sensation Chills Dysphonia Fatigue Headache Heart rate abnormal Limb discomfort Malaise Myalgia Pain in extremity Peripheral swelling Pyrexia Tremor Vaccination site pain Vomiting

Symptomtext

heart started to pound; she could not stop shaking; Right arm soreness; under arm swollen all the way done; across her midsection under both breasts she felt like she was going to explode; Fatigue/Tired; not being able to pick up her arms; Injection site soreness/right arm soreness; Chills/Intense chills; She was burning up; feel sick; felt like she was going to vomit; Headache; She has a new weird hoarse raspy voice; subjective fever; profound weakness x 24 hours; myalgia; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP and Physician). The reporter is the patient. A 69 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 08Oct2021 11:14 (Lot number: FF8841) at the age of 69 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Diabetes Mellitus Type 2" (ongoing), notes: Illness /AE: Diabetes Mellitus Type 2, Onset date: few years; "Hypertension" (ongoing), notes: Illness /AE: Hypertension, Onset date: few years; "Hyperlipidaemia" (ongoing), notes: Illness /AE: Hyperlipidaemia, Onset date: few years; "Rheumatoid Arthritis" (ongoing), notes: Illness /AE: Rheumatoid Arthritis, Onset date: few years; "GERD" (ongoing), notes: Illness /AE: GERD, Onset date: few years; "Retinal anta's embolism", start date: Jul2021 (ongoing), notes: Illness /AE: Retinal anta's embolism; "Symbiotic stroke" (unspecified if ongoing), notes: Verbatim: Symbiotic stroke. Concomitant medication(s) included: JARDIANCE taken for diabetes mellitus (ongoing); ATENOLOL taken for hypertension (ongoing); AMLODIPINE taken for hypertension (ongoing); ROSUVASTATIN taken for hyperlipidaemia (ongoing); PLAVIX taken for cerebrovascular accident (ongoing); OMEPRAZOLE taken for gastroesophageal reflux disease (ongoing). Vaccination history included: Bnt162b2 (Dose 1, single, Lot: EL3261, Expiration: unknown, First two doses were administered at (withheld)Hospital, Anatomical Site of injection: Right deltoid, Route of administration: Intramuscular), administration date: 22Jan2021, when the patient was 69 years old, for Covid-19 Immunization; Bnt162b2 (Dose 2, single, Lot: EM9810, First two doses were administered at (withheld)Hospital, Anatomical Site of injection: Right Deltoid, Route of administration: Intramuscular), administration date: 12Feb2021, for COVID-19 Immunization. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 08Oct2021, outcome "recovering", described as "Right arm soreness"; PERIPHERAL SWELLING (non-serious) with onset 08Oct2021, outcome "recovering", described as "under arm swollen all the way done"; ABDOMINAL DISCOMFORT (non-serious) with onset 08Oct2021, outcome "recovered" (Oct2021), described as "across her midsection under both breasts she felt like she was going to explode"; FATIGUE (non-serious) with onset 08Oct2021, outcome "not recovered", described as "Fatigue/Tired"; LIMB DISCOMFORT (non-serious) with onset 08Oct2021, outcome "recovered" (Oct2021), described as "not being able to pick up her arms"; VOMITING (non-serious) with onset Oct2021, outcome "recovered" (Oct2021), described as "felt like she was going to vomit"; HEADACHE (non-serious) with onset Oct2021, outcome "recovered" (Oct2021), described as "Headache"; VACCINATION SITE PAIN (non-serious) with onset 08Oct2021, outcome "recovering", described as "Injection site soreness/right arm soreness"; MALAISE (non-serious) with onset Oct2021, outcome "unknown", described as "feel sick"; CHILLS (non-serious) with onset 08Oct2021, outcome "recovered" (Oct2021), described as "Chills/Intense chills"; BURNING SENSATION (non-serious) with onset Oct2021, outcome "unknown", described as "She was burning up"; TREMOR (non-serious) with onset 08Oct2021, outcome "unknown", described as "she could not stop shaking"; HEART RATE ABNORMAL (non-serious) with onset 10Oct2021, outcome "recovered" (10Oct2021), described as "heart started to pound"; DYSPHONIA (non-serious) with onset Oct2021, outcome "not recovered", described as "She has a new weird hoarse raspy voice"; PYREXIA (non-serious) with onset 2021, outcome "unknown", described as "subjective fever"; ASTHENIA (non-serious) with onset 2021, outcome "unknown", described as "profound weakness x 24 hours"; MYALGIA (non-serious) with onset 2021, outcome "unknown", described as "myalgia". Therapeutic measures were not taken as a result of pain in extremity, peripheral swelling, abdominal discomfort, limb discomfort, vomiting, vaccination site pain, malaise, tremor, heart rate abnormal, dysphonia. Therapeutic measures were taken as a result of fatigue, headache, chills, burning sensation, pyrexia, asthenia, myalgia. Additional Information: Family Medical History Relevant to AE(s) was not reported. Patient took Rosuvastatin Nopletet from months for Hyperlipidaemia oral and ongoing. It was reported that no other vaccines were given to patient within 4 weeks. Prior to vaccination, the patient was not diagnosed with COVID-19. Patient stated It was time for her flu shot and pneumonia shot, patient asks if she should wait 3 weeks to get them. Also asks if patient need another booster vaccine. Patient declined to be transferred to hospital and states patient will just ask her doctor. Patient had not visited emergency Room/Physician Office for AEs. Vaccination facility type was at Pharmacy or Drug Store for booster. Vaccine Administered at Facility was not reported. AE Term was 48 hours. For events Intense chills, myalgia, fatigue, headache, subjective fever, especially profound weakness x 24 hours was reported as Rest. No follow-up attempts are possible. No further information is expected. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Diabetes mellitus (Illness /AE: Diabetes Mellitus Type 2 Onset date: few years); GERD (Illness /AE: GERD Onset date: few years); Hyperlipidemia (Illness /AE: Hyperlipidemia Onset date: few years); Hypertension (Illness /AE: Hypertension Onset date: few years); Retinal disorder NOS (Illness /AE: Retinal antas embolism); Rheumatoid arthritis (Illness /AE: Rheumatoid Arthritis Onset date: few years)
Vorgeschichte: Medical History/Concurrent Conditions: Stroke (Verbatim: Symbiotic stroke)
Andere Medikamente: JARDIANCE; ATENOLOL; AMLODIPINE; ROSUVASTATIN; PLAVIX; OMEPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 1813646

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NY
Alter: 53,0
Geschlecht: M
Eingang: 12.02.2022
Impfdatum: 01.10.2021
Beginn: 04.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: OT / LA

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

Burning sensation Hypoaesthesia Paraesthesia SARS-CoV-2 test

Symptomtext

numbness, burning and tingling in the feet/ankles and hands; numbness, burning and tingling in the feet/ankles and hands; numbness, burning and tingling in the feet/ankles and hands; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 53 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 01Oct2021 08:00 (Lot number: FF8841) at the age of 53 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 Number: 1, Batch/Lot No: EK5730, Location of injection: Arm Left, Vaccine Administration Time: 08:00, Route of Administration: Intramuscular), administration date: 22Dec2020, when the patient was 52 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EL3246, Location of injection: Arm Left, Vaccine Administration Time: 08:00 AM, Route of Administration: Intramuscular), administration date: 12Jan2021, when the patient was 52 years old, for COVID-19 Immunization. The following information was reported: HYPOAESTHESIA (disability), PARAESTHESIA (disability), BURNING SENSATION (disability) all with onset 04Oct2021 06:00, outcome "not recovered" and all described as "numbness, burning and tingling in the feet/ankles and hands". The event "numbness, burning and tingling in the feet/ankles and hands", "numbness, burning and tingling in the feet/ankles and hands" and "numbness, burning and tingling in the feet/ankles and hands" was evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (24Dec2021) negative, notes: Nasal Swab. Therapeutic measures were taken as a result of hypoaesthesia, paraesthesia, burning sensation. Clinical course: It was reported that three days After the booster shot, the patient developed numbness, burning and tingling in the feet, ankles and hands and has persisted for four months. The patient reported that he received treatment for adverse events with Gabapentin but it has not been helpful in treating symptoms. The patient reported he had no allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested negative for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine.; Sender's Comments: As there is limited information in the case provided, the causal association between the events Hypoaesthesia, Paraesthesia, Burning sensation and the suspect drug cannot be excluded. The case will be reassessed once new information is available.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20211224; Test Name: Rapid COVID test; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2098824

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: TN
Alter: 72,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 04.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Dyspnoea

Symptomtext

Increased shortness of breath that started 1-2 days after receiving second dose. Patient was on 4 Liters O2 prior to vaccination and prescriber (PCP) increased to 6 Liters to alleviate some SOB. Patient has an appt with her pulmonologist on 2/10/22.

Weitere VAERSDATA-Felder

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

VAERS 2090078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IL
Alter: 54,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 22.09.2021
Beginn: 22.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Body temperature Chills Dysphonia Headache Mobility decreased Myalgia Nausea Oropharyngeal discomfort Pain in extremity Pyrexia Rhinorrhoea Vaccination site erythema Vaccination site pain

Symptomtext

throat is raspy; effected her voice and speech; Runny nose; Cant Lift her Left Arm; Left Arm Started Hurting; Site is Red and Hurts to the Touch and the Muscle; Shooting Pain in the Muscle; Site is Red; Left Arm Started Hurting; Site is Red and Hurts to the Touch and the Muscle; Shooting Pain in the Muscle; Shivering and Chills; Headache; Nauseous; Fever of 100.6; Site is Red and Hurts to the Touch; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 54 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 22Sep2021 12:00 (Lot number: FF8841) at the age of 54 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Covid-19", start date: 2020 (unspecified if ongoing), notes: Was hospitalized. There were no concomitant medications. The following information was reported: OROPHARYNGEAL DISCOMFORT (non-serious) with onset 22Sep2021 22:00, outcome "recovering", described as "throat is raspy"; DYSPHONIA (non-serious) with onset 22Sep2021 22:00, outcome "recovering", described as "effected her voice and speech"; RHINORRHOEA (non-serious) with onset 22Sep2021 22:00, outcome "recovering", described as "Runny nose"; MOBILITY DECREASED (non-serious) with onset 22Sep2021 22:00, outcome "recovering", described as "Cant Lift her Left Arm"; MYALGIA (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 22Sep2021 22:00, outcome "recovering" and all described as "Left Arm Started Hurting; Site is Red and Hurts to the Touch and the Muscle; Shooting Pain in the Muscle"; VACCINATION SITE ERYTHEMA (non-serious) with onset 22Sep2021 22:00, outcome "recovering", described as "Site is Red"; CHILLS (non-serious) with onset 22Sep2021 22:00, outcome "recovering", described as "Shivering and Chills"; HEADACHE (non-serious) with onset 22Sep2021 22:00, outcome "recovering", described as "Headache"; NAUSEA (non-serious) with onset 22Sep2021 22:00, outcome "recovering", described as "Nauseous"; PYREXIA (non-serious) with onset 22Sep2021 22:00, outcome "recovering", described as "Fever of 100.6"; VACCINATION SITE PAIN (non-serious) with onset 22Sep2021 22:00, outcome "recovering", described as "Site is Red and Hurts to the Touch". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia. Additional information: History of all previous immunization with the Pfizer vaccine considered as suspect were none. Additional vaccines administered on same date of the Pfizer suspect were none. The events did not require emergency room or physician office visit. Prior vaccinations (within 4 weeks) were none. AE(s) following prior vaccinations were none. Family medical history relevant to ae(s) were none. Time the vaccination was given was 22Sep2021 12:00 (Noon). The patient stated 22Sep2021 (last night), she took the Band-Aid off and she didn't see the injection site but later around 10:00-11:00 p.m. her left arm started hurting. The pharmacist suggested she massage it. The patient stated that she couldn't lift her left arm and the site was red and hurts to the touch and the muscle. She stated she can't lift her arm and there is a shooting pain in the muscle. She stated she also had shivering, headache, was nauseous and had a fever of 100.6. She took Ibuprofen, and her fever went down to 100.4, and now (23Sep2021) it was 99.6. The patient stated her throat was raspy, it affected her voice and speech. She stated she has a runny nose. She stated the chills were going away. The patient stated her side effects have improved. Time of onset of AE(s) was 22:00. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Test Date: 20210922; Test Name: Body Temperature; Result Unstructured Data: Test Result:100.6; Test Date: 20210922; Test Name: Body Temperature; Result Unstructured Data: Test Result:100.4; Test Date: 20210923; Test Name: Body Temperature; Result Unstructured Data: Test Result:99.6
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Was hopitalized)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2085485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: -
Alter: 23,0
Geschlecht: M
Eingang: 03.02.2022
Impfdatum: 08.10.2021
Beginn: 02.02.2022
Tage bis Beginn: 117,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 Cough Dyspnoea Myalgia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

cough, congestion, short of breath, myalgias

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: +Covid test 2/2/2022
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2083319

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 54,0
Geschlecht: F
Eingang: 02.02.2022
Impfdatum: 01.01.2022
Beginn: 22.01.2022
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: SYR / RA

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

Abdominal pain upper Arthralgia Condition aggravated Lymph node pain Lymphadenopathy Musculoskeletal chest pain Pain Pain in extremity

Symptomtext

Swollen lymph nodes in neck, pain moved down my body every day?neck lymph nodes day 2, shoulders day 3, rib pain day 4, stomach/hips day 5, thighs day 6, knees and calves days 7 & 8, feet day 9, toes day 10.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None. Stayed home and took Advil and Tylenol.
Aktuelle Erkrankungen: Was very sick for three weeks prior to booster. Tested negative for Covid. Fever, chills, body pain, cough, headache, nasal congestion.
Vorgeschichte: Epilepsy
Andere Medikamente: Multivitamin, Keppra
Allergien: Metroprolol
Vorherige Impfungen: -

VAERS 2082306

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 02.02.2022
Impfdatum: 13.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 15,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Small intestinal obstruction

Symptomtext

ER - chest pain, ER - small bowel obstruction. Hospital admission. These visits were within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1761867

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NC
Alter: 56,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 04.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Dyspnoea Electromyogram Hypoaesthesia Swelling Bradycardia Fatigue Hypersensitivity Paraesthesia Throat tightness

Symptomtext

Woke up the morning (10/5/2021) following the Covid vaccine (10/4/2021) the evening before with swollen airway and restricted breathing. Also, had numbness from lower neck up to bottom of mouth extending to both ears. Started losing feeling in legs & feet, arms & hands, torso, throat, and face. I contacted the pharmacy and my primary doctor to report the event. I started taking liquid Benadryl every 4 hours on 10/5/21 which helped temporarily with airway symptoms but did not help the progressive numbness and weakness throughout body. Started on low dose Prednisone during the first week of reaction. Saw Neurologist who scheduled an EMG and determined that it was small nerve fiber damage due to the Covid vaccine. Received Physical Therapy twice weekly for 6-8 week period to address damage and weakness in legs and hips. After 3 months, still experiencing some numbness in legs but improved in other areas. Still working on regaining strength and previous level of activity.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: EMG
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hashimotos
Andere Medikamente: N/A
Allergien: Allergy to soy, egg whites, peas, and Cephalosporins
Vorherige Impfungen: TDAP - possible case of mild GBS

VAERS 2071361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: FL
Alter: 76,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 23.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / RA

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

Asthenia Fatigue Gait disturbance Hypersomnia Mobility decreased

Symptomtext

she slept and had no energy; Booster Dose: Legs didn''t work and had to have help to bathroom; she was like a mop and couldn't walk; Booster Dose: Legs didn''t work and had to have help to bathroom; she was like a mop and couldn't walk; Booster Dose: Tiredness, sleeping most of the time; Booster Dose: Tiredness, sleeping most of the time; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. Other Case identifier(s): US-PFIZER INC-202200019589 (Pfizer). A 76 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 23Dec2021 (Lot number: FF8841) at the age of 76 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Bnt162b2 (Second Dose: 24Feb2021 , Lot: Unknown), administration date: 24Feb2021, when the patient was 75 years old, for COVID-19 immunization, reaction(s): "Soreness"; Bnt162b2 (First Dose: 05Feb2021 , Lot: Unknown), administration date: 05Feb2021, when the patient was 75 years old, for COVID-19 immunization, reaction(s): "Soreness". The following information was reported: MOBILITY DECREASED (non-serious), GAIT DISTURBANCE (non-serious) all with onset 24Dec2021, outcome "recovered" (27Dec2021) and all described as "Booster Dose: Legs didn''t work and had to have help to bathroom; she was like a mop and couldn't walk"; HYPERSOMNIA (non-serious), FATIGUE (non-serious) all with onset 24Dec2021, outcome "recovered" and all described as "Booster Dose: Tiredness, sleeping most of the time"; ASTHENIA (non-serious), outcome "unknown", described as "she slept and had no energy". The events "booster dose: legs didn''t work and had to have help to bathroom; she was like a mop and couldn't walk", "booster dose: legs didn''t work and had to have help to bathroom; she was like a mop and couldn't walk", "booster dose: tiredness, sleeping most of the time" and "booster dose: tiredness, sleeping most of the time" were evaluated at the physician office visit. Therapeutic measures were not taken as a result of mobility decreased, gait disturbance, hypersomnia, fatigue. Additional information: Prior Vaccinations (within 4 weeks) None. AE(s) following prior vaccinations: None. Patient's Medical History (including any illness at time of vaccination)? None. Family Medical History Relevant to AE(s): None. Relevant Tests: None. Caller states on 23Dec2021 his wife and him were in (state) for Christmas and they live in (state) , but his wife chose to have her booster shot on 23Dec2021. Caller states on the morning of 24Dec2021, she had an adverse reaction, her legs didn't work and she had to have help to the bathroom and she was sleeping most of the time and was tired. She was like a mop and couldn't walk. Caller states they actually thought about taking her to the hospital but it is full of Covid patients. Caller states they tried calling the health department who gave her the shot there, but there was no response, they tried time and time again. Caller states it seems like she had a severe reaction, has Pfizer heard of a reaction like this?. Treatment: None. Caller states the patient went to see her own doctor once she got back to and the doctor said it seems like she had a severe adverse reaction. Caller states the Doctor was asking maybe it was a live virus vs dead virus?. Caller states when they got back to (state), his wife went to see her primary physician who thought she had a serious AE and he suspected that she did not get the live vaccine. Caller would like to know if we can tell him if his wife received the live or dead vaccine based on the lot number?

Weitere VAERSDATA-Felder

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

VAERS 2069375

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: OH
Alter: 56,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Bundle branch block right Cardiac flutter Electrocardiogram Extrasystoles Hypertension

Symptomtext

The next day about 12 hours later, I felt fluttering in the middle of the chest by my heart. My husband is an ENT and he checked my pulse on my wrist as I'm feeling the fluttering in my chest and he stated that he feels my pulse skipping a beat, I went to the hospital 12/07/2021 at 03:14PM and at that time I was referred me to a cardiologist bc I had high blood pressure prior to this. I have an appointment with My PCP tomorrow, I have my EKG results and I'm taking them so we can both go over them together. Since I had the vaccination all of my family members have gotten COVID 2-3 times already. I don't know if anyone else has this but this is insane.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: 12/07/2022 EKG results incomplete right bundle branch block. No blood work done
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypothyroidism
Andere Medikamente: Levothyroxine 0.7MG 1 daily.
Allergien: N/A
Vorherige Impfungen: -

VAERS 2062551

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NJ
Alter: 46,0
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: 05.10.2021
Beginn: 22.01.2022
Tage bis Beginn: 109,0
Dosis: 2
Route/Site: - / -

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

COVID-19 COVID-19 pneumonia Cough Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

Came to ER with c/o N/V and mild cough. Found to have covid Pna.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 4,0
Labordaten: 01/22/2022 - SARS-CoV-2 Antigen (++)
Aktuelle Erkrankungen: -
Vorgeschichte: Paraplegia after C6 fracture secondary to diving accident; C6-C7 fusion with graft from his left hip, C6 paraplegia with dysreflexia; DVTs in the left leg and right thigh, s/p superior vena cava filter.C6-C7 fusion with graft from his left hip, cholecystectomy, tracheostomy. Smoking Status Former Smoker. Alcohol Use Current Current Alcohol Use Details Frequency Occasional.
Andere Medikamente: amitriptyline 10 mg Tablet Directions: 1 tablet oral daily at bedtime (Active) cholecalciferol (vitamin D3) 125 mcg (5,000 unit) Tablet Directions: 1 tablet oral daily (Active) cyanocobalamin (vitamin B-12) 1,000 mcg Tablet Directions:
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2058931

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MN
Alter: 74,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 19.10.2021
Beginn: 21.01.2022
Tage bis Beginn: 94,0
Dosis: 3
Route/Site: IM / RA

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

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

Symptomtext

Hospitalized with breakthrough COVID pneumonia

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: 1/13/22- COVID 19 positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2057767

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 36,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 05.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Chest discomfort Chest pain Dyspnoea Fatigue Hallucination Headache Hypoaesthesia Lymphadenopathy Pain Pain in extremity Rash

Symptomtext

Left arm rash on ,left arm numbness off and on since vaccine , chest pains radiating to right arm/ chest pain off and on, sob, heavy heart. Body aches chills, headache for 3 days, swollen lymph nodes since vaccination. Hallucinating.tired /weak.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Pending appt with pcp on January 26
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Latex-Rash
Vorherige Impfungen: -

VAERS 2055538

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IL
Alter: 35,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 02.09.2021
Beginn: 02.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Axillary pain Chest discomfort Chest pain Chills Headache Heart rate increased Hypertension Muscle spasms Oedema peripheral Pain Pain in extremity Palpitations Peripheral swelling Pyrexia Swelling X-ray abnormal

Symptomtext

1 dose: Legs weaknes for 1 day, sore arm for 4 days, swollen arm, 5 days, extreme weaknes for 1 week. Treatment: TYLENOL, ICEING OF SWOLLEN AND SORE ARM, A LOTS OF RESTING AND SLEEPING. Second dose 10.11.2021- chills body aches, fever,palpitations, chest pain, chest tightness. Swollen and painfull L arm left armpit, swollen left side of the chest, high heart rate, high blood pressure. Swollen both armpits .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 01. 20.22 visit in office of Dr because symptoms of headache chest pain and swollen and painfull armpits as well swollen chest in left side didn't improve. Moreover 3rd day after second dose of vaccine got extreme muscle spasm in the body and severe in the neck. Visited urgent care. Got x ray neck showing muscle spasm. Muscle relaxant didn't help. Went for physicaltherapy/ massages and hiropractor services. Symptoms improved however are comming back but less severe.
Aktuelle Erkrankungen: Migreine/ headache PCOS
Vorgeschichte: PCOS
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2053985

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 16,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea Electrocardiogram Fatigue Gait inability Hypoaesthesia Pain Paraesthesia Pyrexia Tachycardia

Symptomtext

(This HPI is from an Infectious Disease consult): Patient is a 16 yo female with no significant past medical history that was referred to clinic to discuss COVID19 vaccination. The mother reports that she believes in vaccines and everyone else in the house has gotten the primary COVID19 series, however, she feels hesitant with giving Patient the second dose because of possible adverse effects from dose #1. Patient had acute SARS-CoV2 infection in September 2021 and recovered well, she had URI symptoms x 5 days, mild myalgias and fevers x 2 days. Otherwise no other issues. In 11/14. Patient had her first dose of the vaccine. A bout 14 hours after she received the vaccine, she was sitting in class in started to feel numbness and tingling in and all of her extremities. The tingling started to spread and she also felt she was unable to walk or move her hands. She was brought to the ED where Patient also felts that she couldn't breath. She was placed on oxygen and she also felt that her face was numb. No rash or itching. She is tachycardic in the 120s and then about 4 hours later she developed a fever. After her fever came down her symptoms seem to improve. Over the next few days she felt a little bit achy and a little tired, but her symptoms have completely resolved. She had labs that were unremarkable, and a normal EKG in the ER. Mom has been extensively counseled by her PCP but mom wanted to discuss further with ID. Mom looked up the symptoms online and was concerned that Patient may have developed Guillain-Barre syndrome and is very worried that dose #2 would be worse. Patient and mom would very much like the second dose so she can travel, they just want to make sure it is safe. Pmhx Non significant pmhx. no anxiety, no panic attacks, no hosp or surg. Social hx lives with both parents and sibs. Family Hx: no hx of adverse reactions to any vaccines. No hx of autoimmune disorders. No hx of severe allergies.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG in the ER - Normal
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No.
Allergien: No
Vorherige Impfungen: -

VAERS 2052271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: VA
Alter: 25,0
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: 02.11.2021
Beginn: 11.12.2021
Tage bis Beginn: 39,0
Dosis: 1
Route/Site: SYR / RA

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

Arrhythmia Chest discomfort Chest pain Electrocardiogram abnormal Palpitations

Symptomtext

Chest pain, powerful heart-beat, chest discomfort

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: EKG - signs of arrhythmia - 12/18/2021
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2051522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NY
Alter: 48,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 28.09.2021
Beginn: 28.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Dizziness Headache Mental fatigue Myalgia Pain Palpitations Physical disability

Symptomtext

Headache, Dizziness, Muscle or body aches, Physical and mental fatigue, Racing and Palpitations..etc

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NO
Vorgeschichte: NO
Andere Medikamente: Vitamin D, C, Co Q10, and Fish oil ( However, I did not take any on 9/28/2021)
Allergien: Seasonal allergies, Fruit allergy ( Peach ..etc )
Vorherige Impfungen: -

VAERS 2050754

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MN
Alter: 89,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 18.11.2021
Beginn: 18.01.2022
Tage bis Beginn: 61,0
Dosis: 3
Route/Site: SYR / RA

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

Bacteraemia COVID-19 Dyspnoea Pleural effusion Pyrexia SARS-CoV-2 test positive

Symptomtext

Received Pfizer vaccines on 1/27, 2/17, 11/18/21 COVID-19 positive by PCR on 1/18/22 admitted to hospital on 1/19/22 d/t bacteremia, fever, dyspnea, bilateral pleural effusions

Weitere VAERSDATA-Felder

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

VAERS 2048785

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: -
Alter: 27,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Chills Headache Heart rate increased Myalgia Palpitations Postural orthostatic tachycardia syndrome Pyrexia

Symptomtext

Chills, fever, muscle ache, headache, weakness ? Tylenol 1000 mg alternating with ibuprofen 400 mg q 4 hrs, tachycardia hr 130-150 resting with chest palpitations. No SoB or chest pain noted, no adderall taken that day. Elevated hr noted second day with orthostatic tachycardia exacerbated standing. Pulse rate regular, BP 129/93. Tachycardia lasting from second day post vaccination until fourth day for total about 48+ hrs in tachycardia. No treatment was pursued at that time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: N/a did not seek treatment at that time
Aktuelle Erkrankungen: None
Vorgeschichte: Fatty liver, depression, ADHD, anxiety
Andere Medikamente: Desvenlafaxine 50 mg qhs, quetiapine 25 mg qhs, methylfolate 400 mcg daily, krill oil 300 mg daily, Adderall 30 mg daily, hydroxyzine 50 mg q12 hrs prn
Allergien: Penicillin- rash, wintergreen mint-bells palsy, mango- rash
Vorherige Impfungen: -

VAERS 2043771

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 24,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 22.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Chest pain Dizziness Dyspnoea Electrocardiogram

Symptomtext

Patient complained of chest pain (CP), approx 5 days after vaccine. Saw one of the clinic doctors before receiving 2nd vaccine but again reported worsening chest pain after second COVID vaccine, Pfizer, Lot # FF8841. Given on 11/18/21. Seen in ED approx 2 weeks after for worsening CP since second dose, also complaints of SOB and Dizzy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG performed as outpatient.
Aktuelle Erkrankungen: Unk
Vorgeschichte: Hx of anxiety
Andere Medikamente: Unk
Allergien: None
Vorherige Impfungen: -

VAERS 2037766

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NJ
Alter: 79,0
Geschlecht: M
Eingang: 15.01.2022
Impfdatum: 12.10.2021
Beginn: 13.01.2022
Tage bis Beginn: 93,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

79 yo male resident of nursing Home, tested pos for Covid 1/3, sent to ER for dyspnea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: 01/13/2022 - SARS-CoV-2 Antigen (++)
Aktuelle Erkrankungen: -
Vorgeschichte: Renal cancer, prostate cancer, CLL, Parkinsonism, dementia. Significant Surg Hx As Listed Addt'l Surgical History Kidney sx. Smoking Status Former Smoker.
Andere Medikamente: Unknown
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2035049

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: KY
Alter: 66,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 26.02.2021
Beginn: 13.01.2022
Tage bis Beginn: 321,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Cough Diarrhoea Dyspnoea Dyspnoea exertional Exposure to SARS-CoV-2 Hypophagia Nausea Pyrexia SARS-CoV-2 test negative

Symptomtext

67 y.o. female admitted 1/13/2022 with a past medical history significant for CAD, hypertension, HLD, follicular lymphoma on chemotherapy, and GERD. She present today with complaints of progressively worsening SOB going on for the past 8 days. Dyspnea worse with exertion. There is associated non productive cough, generalized weakness, decreased PO intake, nausea without vomiting, diarrhea, and subjective fever. She is fully vaccinated for COVID-19 with a booster. Patient was initially evaluated by PCP at onset of symptoms wherein she reportedly tested negative for COVID-19. She was subsequently started on tamiflu prophylactically without improvement. She called PCP today who subsequently directed her to ED for further evaluation and treatment. Patient report that she and her daughter were exposed to Covid at a new years eve party. She states he daughter had covid after this event but quickly recovered. There are no complaints of chest pain, syncope, or lower extremity pain or swelling. No abdominal pain, dysuria, or flank pain. No headache or focal weakness/parathedias. Will admit to inpatient to hospitalist service and consult nephrology and ID in the AM.

Weitere VAERSDATA-Felder

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

VAERS 2021144

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 62,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 05.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / LA

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

Chest pain Pain

Symptomtext

Dull, aching pain in right chest. Intermittent. Occurs multiple times throughout the day and lasts from minutes to hours. Was initially not concerned, as I had no shortness of breath or lightheadedness, and my radial pulse remained strong and regular. Recently contacted my physician when I felt like it wasn't getting any better, and will get an EKG this afternoon.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None yet.
Aktuelle Erkrankungen: None
Vorgeschichte: Mild asthma
Andere Medikamente: Montelukast 10mg each day
Allergien: None
Vorherige Impfungen: -

VAERS 2018782

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: WV
Alter: 36,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 17.10.2021
Beginn: 02.11.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: - / -

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

Condition aggravated Fatigue Feeling abnormal Seborrhoeic dermatitis

Symptomtext

Severe scalp flareup unlike anything I?ve seen in over a decade. Severe fatigue. Brain fog. Feels like a really severe autoimmune flare. Has been going on for almost two months now. Taking supplemental medications prescribed by Dr.s office for recovery (would love to be reimbursed for these!!)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hashimoto?s disease
Vorgeschichte: Recurrence of seborrheic dermatitis symptoms on my scalp, fatigue, brain fog - which all began within a week or so of vaccination - on a level I haven?t experienced in over 10 years. There is no other explanation for this.
Andere Medikamente: No Rx
Allergien: Gluten intolerance
Vorherige Impfungen: -

VAERS 1851002

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: FL
Alter: 30,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 28.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Angina pectoris Chest discomfort Chest pain Dyspnoea

Symptomtext

Chest pains on left side above the heart; Feels like pressure and throbbing; Shortness of breath; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 30 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 28Oct2021 10:00 (Lot number: FF8841) at the age of 30 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 Number: 1, Dose brand=PFIZER , Lot No: 30145BA, Location of injection: Arm Left, Vaccine Administration Time: 10:00 AM), administration date: 07Oct2021, when the patient was 30 years old, for COVID-19 immunization. The following information was reported: CHEST PAIN (non-serious) with onset 29Oct2021 01:00, outcome "not recovered", described as "Chest pains on left side above the heart"; CHEST DISCOMFORT (non-serious) with onset 29Oct2021 01:00, outcome "not recovered", described as "Feels like pressure and throbbing"; DYSPNOEA (non-serious) with onset 29Oct2021 01:00, outcome "not recovered", described as "Shortness of breath". Therapeutic measures were not taken as a result of chest pain, chest discomfort, dyspnoea. Additional Information: Chest pains on left side above the heart. Feels like pressure and throbbing. This is only on the left side. Issue occurs often but usually at night or in the morning. Shortness of breath. This currently occurs often. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive any other medications within 2 weeks of vaccination. The patient was not diagnosed with COVID-19 Prior to vaccination. The patient has not been tested for COVID-19, Since the vaccination. It was reported that, there were no known allergies. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
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 2010776

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: FL
Alter: 47,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 25.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / -

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

Arthralgia Burning sensation Chest pain Fatigue Heart rate increased Hypoaesthesia Muscle twitching Palpitations Paraesthesia Vision blurred

Symptomtext

I received the 2 dose Pfizer vaccine on 10/3/21 and 10/25/21. The day after my 1st dose I experienced my heart rate increase, chest pains and fatigue. The day after I received my second dose , I woke up in the am panicing bc both my hands and both feet were tingling, burning, with a sensation of pins and needles. They also felt numb, as when your arm or leg falls asleep and is limp. I experienced twitching in my eye and my vision was very blurry. I had palpitations and my heart felt like it was racing out of my chest, and chest pains. I was extremely fatigued and my joints were very painful. I am still experiencing parasthesia in both my hands and both feet. I can't hold my phone or surface laptop for long periods of time because the sensations worsen when I do this. I have intermitent episodes of chest pains and my joint feel painful still have heavy fatigue. I am setting up an appointment with a specialist in my area to consult with about my symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None available at this time
Aktuelle Erkrankungen: None
Vorgeschichte: Seasonal asthma, migraines
Andere Medikamente: N/A
Allergien: NKA
Vorherige Impfungen: -

VAERS 2010601

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NY
Alter: 80,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 01.10.2021
Beginn: 01.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal pain upper Blood glucose increased Diarrhoea Dizziness Injected limb mobility decreased Injection site erythema Pain in extremity Pyrexia Vomiting

Symptomtext

My arm was sore. I could not left it up. I had a red spot where the shot was given to me. I went to bed. I wake up and did not feel like I could eat. I had pain in my stomach and was vomiting. I had diarrhea. I started running a fever of 101. I was also very dizzy. I try to contact my doctor and could not get ahold of them. I went to an urgent care for care. They did a physical exam on me. My blood sugar was evaluated. These symptoms lasted about 12 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: N/A
Vorgeschichte: Type 2 Diabetic; DCIS; Osteoarthritis
Andere Medikamente: Levothyroxine; MCG; Metformin; Prolia; Pravastatin; Rosacea; Premarin; Vitamin D; Aspirin
Allergien: Cherries; Tea; Carmine; Morphine; Nexium; Penicillin; Tetracycline; Zyrtec; Mobic
Vorherige Impfungen: -

VAERS 2010345

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MN
Alter: 70,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 09.03.2021
Beginn: 01.01.2022
Tage bis Beginn: 298,0
Dosis: 3
Route/Site: - / -

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

Chills Cough Dyspnoea Pain Respiratory tract congestion

Symptomtext

cough, body aches, congestion, chills, shortness of breath. starting 1/1/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: hyperlipidemia, Sjogrens
Andere Medikamente: ?Hydroxychloroquine Sulfate 200 MG Tablet as directed Orally ?Simvastatin 10 MG Tablet 1 tablet in the evening Orally Once a day
Allergien: Lipitor: sore joints Botox: rash Cortisone: rash
Vorherige Impfungen: -

VAERS 2006353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: AR
Alter: 56,0
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 12.03.2021
Beginn: 03.01.2022
Tage bis Beginn: 297,0
Dosis: UNK
Route/Site: IM / LA

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

COVID-19 Cognitive disorder Fall Gait disturbance Hemiparesis Incontinence Magnetic resonance imaging head Mental status changes Metabolic encephalopathy SARS-CoV-2 test positive Tremor

Symptomtext

57-year-old male with PMH of DM 2, paranoid, seizures unspecified, autism presents to the emergency department due to a fall from the patient's bed. Patient states that he woke up on the floor after falling out of bed, does not remember the fall itself. Patient remembers getting off up after unspecified amount of time and getting himself back into bed. Patient denies losing continence or biting his tongue. Last known well time was this past Friday. Patient is reported to be altered, unstable gait, and incontinent. The weekend of event patient had hard time ambulating and had to be carried back to his bed. Patient states that he does not have a caregiver. He states that he completes his ADLs on his own Diagnosis: Metabolic encephalopathy, Likely due to COVID19 infection in the setting of baseline cognitive dysfunction, Drug induced tremor likely from anti-psychotic medications and depakote. Plan: Limited MRI brain w/o contrast to evaluate for stroke given reported left sided weakness Further stroke work up depending on MRI brain results Recommend reducing Depakote dose to 750 mg BID given mildly elevated level. Currently in hospital on 01/05/2022 in COVID stepdown unit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: COVID positive on 01/02/2022
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2006252

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge #FF8841

moderat

Staat: IL
Alter: 43,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 02.02.2021
Beginn: 01.05.2021
Tage bis Beginn: 88,0
Dosis: 3
Route/Site: SYR / AR

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

Asthenia Blood test Cardiac stress test Computerised tomogram thorax Dyspnoea Fatigue

Symptomtext

Shortness of breath that comes and goes. Lingers sometimes for two days. Feel tired and fatigued when shortness of breath occurs. Been to Emergency room since this has started. I have seen a primary care doctor, Seen Cardiologist , Seen a Pulmonoligist, seen GI doctor trying to figure out why this is occuring. It is very scary, debilitating feeling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Many test have been done. CT of chest, blood work, stress test, numerous test.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: none
Allergien: Erythromycin
Vorherige Impfungen: -

VAERS 1997995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 12,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 24.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hypoaesthesia Paraesthesia

Symptomtext

The client reported tingling diffusely on her left arm. The client denied any other symptoms. Vitals obtained at 4:12 PM were as follows: BP 100/74, HR 84, O2 99%. The client then reported the numbness was "getting better" and was only present in her hand that this time. Vitals obtained at 4:17 PM were as follows: BP 108/72, HR 88, O2 99%. The client reported her hand still felt "numb." RN provided education to the client and her mother regarding s/s of anaphylaxis and when to seek EMS. The client and her mother voiced understanding of this education. Repeat vitals obtained at 4:27PM were as follows: BP 104/70, HR 83, O2 99. RN noted the client's hand strength was equal bilaterally. The client reported a history of Lyme disease, currently under control without medications. RN asked the client how the numbness was currently and the client stated "I think it's done." Vitals obtained at 4:40 PM were as follows: BP 102/70, HR 73, O2 98%. The client stated she felt "normal." The client ambulated unassisted with a steady gait out of the vaccination site at 4:41PM.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Uknown
Vorgeschichte: Lyme Disease
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1996673

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: PR
Alter: 57,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Burning sensation Hypoaesthesia Inappropriate schedule of product administration Limb discomfort Muscular weakness Myalgia Paraesthesia SARS-CoV-2 test

Symptomtext

Burning; Tingling; Numbness; Muscle ache from shoulder, bicep, forearm and hand.; Heaviness and arm feels weak; Heaviness and arm feels weak.; Dose 1: 09Aug2021; Dose 2: 14Oct2021.; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 57 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 14Oct2021 at 09:45 (Lot number: FF8841) at the age of 57 years as dose 2, single for COVID-19 immunisation. Relevant medical history included: "None". There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number: FA7484, Anatomical Location: Left arm, Administration Time: 10:00, Route of Administration: Unknown), administration date: 09Aug2021, when the patient was 57 years old, for COVID-19 immunisation. The following information was reported: INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious) with onset 14Oct2021 at 09:45, outcome "unknown", described as "Dose 1: 09Aug2021; Dose 2: 14Oct2021"; BURNING SENSATION (non-serious) with onset 01Nov2021, outcome "not recovered", described as "Burning"; PARAESTHESIA (non-serious) with onset 01Nov2021, outcome "not recovered", described as "Tingling"; HYPOAESTHESIA (non-serious) with onset 01Nov2021, outcome "not recovered", described as "Numbness"; MYALGIA (non-serious) with onset 01Nov2021, outcome "not recovered", described as "Muscle ache from shoulder, bicep, forearm and hand"; LIMB DISCOMFORT (non-serious) with onset 01Nov2021, outcome "not recovered", described as "Heaviness and arm feels weak"; MUSCULAR WEAKNESS (non-serious) with onset 01Nov2021, outcome "not recovered", described as "Heaviness and arm feels weak". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of burning sensation, paraesthesia, hypoaesthesia, myalgia, limb discomfort and muscular weakness. Additional information: The patient had no known allergies. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient reported that the events kept getting worse daily. Since the vaccination, the patient had been tested for COVID-19 and tested negative. 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: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20211123; Test Name: BinaxNOW; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1989146

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IN
Alter: 52,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 09.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Asthma Condition aggravated Cough Dyspnoea

Symptomtext

Started feeling shortness of breath and cough 12-14 hours after taking the booster. Ended up being in an urgent care on 10/11/2021. Was put on sever asthma treatment plan. Didn't help much. Ended up being in ER on 10/18/2021 with severe asthma attack. Was given treatment and put on Prednisone and inhalers. This helps as long as I am on these medicines. As soon as I am taken off, shortness of breath and cough starts building back.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Mild Asthma
Vorgeschichte: Asthma
Andere Medikamente: Amlodipine, Losartan and Montelukast
Allergien: None
Vorherige Impfungen: -

VAERS 1989042

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IL
Alter: 40,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 01.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: SYR / RA

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

COVID-19 Cough Discomfort Fatigue Influenza virus test negative Lymph node pain Migraine SARS-CoV-2 test negative SARS-CoV-2 test positive Sinus disorder Upper respiratory tract infection

Symptomtext

STARTED ON 12/3 WILL SORENESS AND EXHAUSTION. THE PAIN WAS IN THE AREA OF MY LYMPH NODES ON THE RIGHT SIDE. THIS LASTED FOR ABOUT 1 WEEK, AND THEN AROUND 12/13 I STARTED TO HAVE SINUS TROUBLE & COUGH. ON 12/18 I HAD A TERRIBLE MIGRANE, AND EXHAUSTION. STARTED TO HAVE MORE SINUS TROUBLE AND COUGHING.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: I TOOK A COVID TEST AT WORK ON 12/22 - CAME BACK POSITIVE. ON 12/23 I WENT TO AN URGENT CARE. RECEIVED A NEGATIVE ANTIGEN AND PCR TEST. ALSO A NEGATIVE FLU TEST. THEY DIAGNOSED ME WITH ACUTE UPPER RESPIRATORY INFECTION.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: MONTELUKAST 10MG ZYTEC SERTALINE 100 MG NORTREL 1/35 TABLETS
Allergien: N/A
Vorherige Impfungen: 2ND DOSE OF COVID-19 PFIZER EN7533 ON 3/26. I EXPERIENCED SORENESS AND EXHAUSTION FOR 1-2 DAYS

VAERS 1988670

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NE
Alter: 64,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 01.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 26,0
Dosis: 3
Route/Site: IM / UN

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

Angiogram Anticoagulant therapy Atrial fibrillation Chest X-ray Chest pain Computerised tomogram thorax Cough Dyspnoea Fibrin D dimer increased Inflammation Influenza virus test negative Laboratory test Metabolic function test Procalcitonin Pyrexia Rash erythematous Rash pruritic SARS-CoV-2 test negative

Symptomtext

The patient is here with complaints of a fever, cough and shortness of breath. She said is been going on since last Tuesday. She was tested for Covid and influenza in the clinic which came back negative. She was instructed this is a viral illness and needs to pass on its own. She stated that she has been using her inhaler and her daughter's nebulizer without much relief. She also complains of right lower chest pain. She denies any swelling in any of her extremities. Her last fever was this morning. She stated that the shortness of breath just comes and goes at times. Patient was treated for UTI last Monday and was on Macrobid. She noticed over the past couple of days she had had a reddened flat rash on her bilateral lower extremities. She stated is very itchy Atrial fibrillation with RVR I48.91 The patient is not ill-appearing or toxic upon arrival to the emergency room. Her heart rate is tachycardic in the low 100s. It is sinus rhythm upon arrival. She did have clear lung sounds. Patient does have a history of asthma which she feels like is not very controlled at this time. Patient is moving air well, oxygen levels remain in the mid to upper 90s with room air. Patient's D-dimer did come back elevated at about 1700. We did do a CT of the chest to rule out a PE. There is no acute PEs noted but possible inflammation or metastasis to the bilateral lymph nodes in the hilar area. We will treat the patient with Augmentin for 10 days to see if we can help decrease the inflammation and have her rescan at that point by her primary care doctor to rule out any suspicious lesions. While she was in CAT scan and when she came back, the patient was in A. fib with RVR. She states she never had any issues like this before in the past and her shortness of breath does get worse with the faster heart rate. Otherwise she is asymptomatic. The patient was given a bolus of Cardizem and an oral dose of Cardizem with minimal relief of the elevated heart rate. I did go from the 170s/180s to the 130/140s and still in atrial fibrillation. I did contact the cardiologist and he recommended avoiding Cardizem due to lack of evidence that it will be beneficial for her in the outpatient setting and starting her on 400 mg of amiodarone twice daily for 2 weeks and then decreasing to 400 mg of amiodarone daily after the initial 2 weeks and to follow-up with him in 2 to 3 weeks for an echo and reevaluation. The patient will be started on VTE prophylaxis with Eliquis. The patient stated that she has been on this before and is unsure why. She said that she was on it when I thought she had Covid because I thought her blood looked thick. Denies any history of abnormal heart rhythms though. Her CAT scan results as well as the plan of care were discussed with the patient as well as her primary care provider. They are agreeable with the plan of care. Her PCP was comfortable with not further treating her heart rate more than what the cardiologist said due to lack of being symptomatic. The patient was instructed that she is at risk for stroke due to the atrial fibrillation and that we are trying to prevent that with the blood thinner. She verbalized understanding is agreeable. The cardiologist denied any further intervention needed. We will put her in the hospital for observation on telemetry. Patient denies any further concerns. The Doctor notified a plan of care and is agreeable. I do suspect that the patient's rash on her bilateral lower extremities is due to a medication reaction. We will continue to keep an eye on that. Chads Vasc 2 score: 1 point, 0.6% stroke risk per year

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: CXR, CT angio, cardiac markers, procalcitonin, CMP
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: famotidine, probiotic, albuterol
Allergien: Elavil, Flagyl, Lopressor, Sulfa, Macrobid
Vorherige Impfungen: -

VAERS 1975301

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

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: 1
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 1964867

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: TN
Alter: 22,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 22.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: SYR / RA

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

Asthenia Diarrhoea Dyspnoea Fatigue Impaired driving ability Impaired work ability Pyrexia

Symptomtext

Weakness, inability to work, my parents had to drive to my work site to pick me up and drive me home. I was unable to drive or carry luggage. I experienced diarrhea, difficulty breathing, high fever, weakness, and tiredness. These symptoms lasted approximately 5 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Asperger's
Andere Medikamente: None
Allergien: Ibuprofen
Vorherige Impfungen: -

VAERS 1961806

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: -
Alter: 56,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Paraesthesia oral Respiratory tract congestion

Symptomtext

Patient complained of congestion and tongue tingling while in observation area. Symptoms lasted for several minutes.

Weitere VAERSDATA-Felder

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

VAERS 1959423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 38,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 17.12.2021
Beginn: 17.12.2021
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 Flushing Paraesthesia oral Throat tightness

Symptomtext

On Friday, December 17, 2021 client received her Pfizer Covid-19 vaccine booster (LOT #: FF8841) at 12:45 PM in her left deltoid. Client also received a Fluarix Quadravalent (LOT #: 7557A) vaccine in her right deltoid. During assessment questions, client stated she has a medical history of high blood pressure and diabetes type 2 and takes Lantus and Metformin. Client states she is also allergic to nuts and cigarette smoking. Client also mentioned after her first and second Pfizer Covid-19 vaccine, she experienced slight tingling on her tongue. She stated she went home and took Benadryl and the tingling sensation subsided. Client to be observed for 30 minutes after vaccination. At approximately 12:52 PM, while in Observation Area, client stated to EMT and PHN felt "7 out of 10" throat constriction, facial flushing and lips tingling. Client was brought to anti-gravity chair and vitals started. At 12:53 PM: BP: 162/80, HR 94, O2: 97%, RR: 16. At 12:57 PM, RN administered 50 mg/ml of Diphenhydramine in client's right arm and explained the fast-acting nature and drowsiness effect. At 12:59 PM, BP: 162/80, RR: 16. client stated constriction still a "7 out of 10" but is calm and speaking full and complete sentences. At 1:09 PM, BP: 164/100, HR: 95, O2 sat: 98% client stated she felt "5 out of 10" throat constriction, lips "slightly" tingly still. Client stated she spoke to her PCP about previous reactions to Covid-19 vaccine and stated her PCP still recommended to receive her booster dose and take Benadryl or Ibuprofen as needed. Client reported similar history and baseline of tingly lips for a "few hours" after vaccination. At 1:14 PM, BP: 166/98, HR: 98, O2 sat: 98%, RR: 16. Client feels "5 out of 10" throat constriction. At 1:22 PM BP: 164/102, HR:91, O2 sat: 98%, RR: 16. At 1:25 PM, client stated she still felt "5 out of 10" throat constriction but felt stable to leave. No further interventions needed. PHN educated patient on signs and symptoms of adverse reactions and when to go to the ED/call MD. Client left vaccination site with a steady gait at approximately 1:30 PM.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: diabetes type 2, hypertension
Andere Medikamente: Lantus, Metformin
Allergien: cigarettes, nuts
Vorherige Impfungen: anaphaxlysis

VAERS 1954886

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MN
Alter: 78,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 12.02.2021
Beginn: 30.11.2021
Tage bis Beginn: 291,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Diarrhoea Dyspnoea Nausea SARS-CoV-2 test positive

Symptomtext

SOB., NAUSEA, MILD COUGH, INTERMITTENT DIARRHEA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: POSITIVE COVID DETECTED 12/14
Aktuelle Erkrankungen: -
Vorgeschichte: CAD involving native coronary artery of native heart without angina pectoris Colon polyps Diabetes mellitus type 2 DJD Dysphagia Esophageal ulcer Essential hypertension GERD HOH Hydronephrosis Hyperlipidemia Motion sickness Presbyesophagus Sarcoma of left thigh Tobacco abuse in remission SBO Diverticulosis Vertigo Renal colic Vitamin D deficiency Lumbar herniated disc Leukocytosis Primary osteoarthritis of right knee DDD, lumbar
Andere Medikamente: amLODIPine (NORVASC) 5 mg oral tablet aspirin 81 mg oral enteric coated tablet atorvastatin (LIPITOR) 10 mg oral tablet Cholecalciferol, Vitamin D3, 5,000 unit (125 mcg) oral tablet dulaglutide (TRULICITY) 1.5
Allergien: Naproxen-Pseudoephedrine Aleve [Naproxen Sodium] Triamterene
Vorherige Impfungen: -

VAERS 1952103

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 77,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 11.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Dyspnoea Palpitations

Symptomtext

Client presented to vaccination site. Client received Pfizer Booster Lot#FF8841. Client was sitting in observation area and kept putting her head down into her hands. RN asked her if she was feeling ok. Client stated she was fine. When client?s son came in. RN asked son, if mother was feeling ok. Son, asked her mother, and stated her mother was feeling dizzy. RN asked client if she had food and water and client stated she had. Client was offered water and client had a few sips. Vitals were taken 1343 BP 156/79 HR 90 02 99%. Client kept touching her chest and said she felt mild palpitations and stated she had trouble breathing. Client denied chest pain. Client was AA0X3. Son, stated mother has a history of high blood pressure and asthma. Client stated she takes all her meds for conditions. EMS were called to scene at 1349 by RN. RN asked Client how she was feeling and responded, she was better and she just wanted to ?go home and rest?. Vitals at 1347 BP 145/78 HR 81 02 99%. EMS arrived at 1349. At 1352 Client declined any services and stated she didn?t want to go to the hospital. EMS left scene at 1353.When EMS left scene Client insisted on going home and declined to stay any longer. She stated she was feeling ?better?.. Client was able to stand up with and transfer to wheelchair with no trouble. Son, was recommended by RN to seek emergency care if symptoms worsened. Son, verbalized understanding. Client left vaccination site via wheelchair with son.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: unknown
Vorgeschichte: Asthma, High blood pressure
Andere Medikamente: asthma and high blood pressure meds
Allergien: NKA
Vorherige Impfungen: -

VAERS 1947911

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FF8841

moderat

Staat: MD
Alter: 34,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 23.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / LA

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

Dysmenorrhoea Heavy menstrual bleeding Mobility decreased Sleep disorder

Symptomtext

The first dose of the vaccine caused extreme cramping and bleeding but the second dose is the one which I am reporting. Two days after receiving the second Moderna vaccine I started having the most painful menstrual cycle I have ever experienced in my life. It is also the heaviest case of bleeding that I have ever experienced. The pain was so severe, I was unable to get out of bed or do anything for a few days. I was on 800 milligrams of motrin twice per day and I had a heating pad on my stomach or lower back at all times of the day or night. I was unable to sleep due to the pain. I went through an entire tampax regular size box in less than a day and a half. Meanwhile, I was bleeding through all of my clothes for several days and soaked my sheets in blood the first night.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: I did not go to the doctor since I did not have any feeling of fainting.
Aktuelle Erkrankungen: n/a
Vorgeschichte: none
Andere Medikamente: none
Allergien: n/a
Vorherige Impfungen: -

VAERS 1947684

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: VA
Alter: 38,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 06.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Epstein-Barr virus infection reactivation Fatigue Lymph node pain Lymphadenopathy

Symptomtext

I had swollen lymph nodes under my left arm pit that were sore. This lasted about 3-5 days. I had extreme fatigue during this time as well. No fevers. I still have reactivated EBV symptoms, and it seems ongoing. This was present before my booster & flu shot, but may have started around my original vaccinations in March 2021, or possibly prior to that as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Prior to my booster & flu I received information that I had a positive EBV reactivated infection (~Oct 15th).
Aktuelle Erkrankungen: I have an active Epstein-Barr Virus (EBV) infection reactivation.
Vorgeschichte: None
Andere Medikamente: Over the counter meds: vitamin B complex, magnesium, Claritin. I also received the flu vaccine on the same day.
Allergien: Allergy to sulfa medication
Vorherige Impfungen: -

VAERS 1947007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: FL
Alter: 65,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 03.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Antibody test Body temperature Fatigue Full blood count Illness Immunisation Migraine Nausea Pyrexia Skin injury Sleep disorder Vomiting

Symptomtext

skin hurt; Vomiting; Very high fevers; Extreme fatigue; Nausea; migraine; woke up from sleep; Sick; I had The Booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program (005570). The reporter is the patient. A 65 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 03Nov2021 13:30 (Lot number: FF8841) at the age of 65 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "only have Osteoarthritis", start date: 2015 (ongoing), notes: Pertinent details: NA; "Headache", start date: 2013 (ongoing), notes: Pertinent details: NA. Concomitant medication(s) included: SUMATRIPTAN taken for headache, start date: 2018 (ongoing); TRAMADOL taken for osteoarthritis, start date: 2017 (ongoing). Vaccination history included: Bnt162b2 (Dose no: 1, The first 2 vaccines, I had minimal side effects, LOT: EL3302, Anatomical Location: left shoulder), administration date: 21Jan2021, when the patient was 64 years old, for COVID-19 immunization, reaction(s): "I had minimal side effects"; Bnt162b2 (Dose no: 2, The first 2 vaccines, I had minimal side effects, Lot number: EM9809, Exp. date: Jun2021, Anatomical Location: left shoulder), administration date: 11Feb2021, when the patient was 64 years old, for COVID-19 immunization, reaction(s): "hematoma". The following information was reported: MIGRAINE (non-serious) with onset 04Nov2021, outcome "recovered" (07Nov2021), described as "migraine"; SKIN INJURY (non-serious), outcome "unknown", described as "skin hurt"; ILLNESS (non-serious) with onset 2021, outcome "recovered", described as "Sick"; SLEEP DISORDER (non-serious) with onset 04Nov2021, outcome "recovered", described as "woke up from sleep"; VOMITING (non-serious) with onset 04Nov2021 01:30, outcome "recovered" (06Nov2021 02:00), described as "Vomiting"; PYREXIA (non-serious) with onset 04Nov2021, outcome "recovered", described as "Very high fevers"; FATIGUE (non-serious) with onset 04Nov2021, outcome "recovered" (10Nov2021), described as "Extreme fatigue"; NAUSEA (non-serious) with onset 04Nov2021, outcome "recovered" (10Nov2021), described as "Nausea"; IMMUNISATION (non-serious) with onset 2021, outcome "unknown", described as "I had The Booster". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of migraine, vomiting, pyrexia, nausea. It was unknown if therapeutic measures were taken as a result of skin injury, sleep disorder. Additional information: She received the booster 03Nov2021, around 1:30 or 2:00 in the afternoon. Around 1:30 or 2:00 in the morning, going into the next day, 04Nov2021, she started vomiting and woke up from her sleep. The vomiting continued until Saturday morning. Along with that came very high fevers of 102. That lasted until Sunday. Along with that, came severe fatigue that lasted until Wednesday, until 10Nov2021. The nausea lasted until about 10Nov2021. The fevers started around the same time that the vomiting started, around 1:30, 2:00 in the morning, 04Nov2021. She stated that her skin hurt as well. She had severe migraines and was putting ice on her forehead. It was probably from the fever. Outcome, fevers: She would say, she was pretty much back on track. Migraines: They lasted probably until around that Sunday and has recovered completely from those. Vomiting: lasted until Saturday and she has fully recovered from that. It was that night, or Wednesday morning that the vomiting started and was coming like 7 times. It was not like it was a one and done. It was horrible and she was dry heaving and she had just never been this sick. She could not even tell when was the last time she vomited before this. Nausea: She did feel nauseous until that Wednesday, it was for a week, she was nauseous. Treatment: She was taking TYLENOL and she was predisposed to migraines, so she was taking sumatriptan. Continued side effect stated the top of her head and down. She had changed shampoo and conditioner, gel. She had changed drinking coffee, changed laundry detergent, none of that has worked. She get some temporary relief with ice on her head and BENADRYL. She worked full time and could not take Rx BENADRYL so she suffered and dealt with it. Stated that prior to vaccine, she never suffered from this. It wakes her up at night its so bad, it continues throughout the day. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Test Date: 202110; Test Name: Antibody test to platelet factor IV; Result Unstructured Data: Test Result:Normal; Test Name: Fever; Result Unstructured Data: Test Result:high fevers of 102; Test Date: 202110; Test Name: CBC; Result Unstructured Data: Test Result:Normal
Aktuelle Erkrankungen: Headache (Pertinent details: NA); Osteoarthritis (Pertinent details: NA)
Vorgeschichte: -
Andere Medikamente: SUMATRIPTAN; TRAMADOL
Allergien: -
Vorherige Impfungen: -

VAERS 1944380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 51,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 09.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Feeling hot Heart rate increased Nausea Skin irritation Throat irritation Tremor

Symptomtext

After receiving the Booster COVID Pfizer vaccine client reported her "heart beating fast." RNs responded. The client ambulated unassisted and sat down in a chair. EMT responded and placed the pulse oximeter on the client's finger. Vitals obtained at 1:15 PM were as follows: BP 140/80, HR 71, and O2 99%. EMT responded with the anti-gravity chair. The client ambulated unassisted and sat down in the anti-gravity chair. RN and Interpreter responded for additional assistance. The client denied any other s/s of anaphylaxis. RN noted HR of 65 on the pulse oximeter. The client stated she felt "shaking." RN responded. The client reported feeling hot on her chest. RN visualized 3-5 red discoloration spots on the client's chest. The client denied feeling any itching on her chest. RN offered the client Benadryl. The client reported a history of hives after taking Benadryl. The client reported itchiness in her throat. RN activated EMS at 1:20PM. The client was alert and oriented to person, place, time, and situation. The client stated her throat and chest felt better, but felt like her "mandible was shaking." Repeat vitals obtained at 1:25PM were as follows: BP 135/80, HR 72, and O2 100. The client reported persistent irritation on chest. She stated that her trembling was worse. Repeat vitals obtained at 1:29PM were as follows: HR 71 and O2 99%. The client stated her heart racing was not as strong. The client reported new onset of nausea. The client received 1st dose Janssen Lot#042A21A on 04/01/21. The client denied any symptoms after the dose of Janssen. The client reported a history of hypertension controlled with Metoprolol and Hypothyroid controlled with Levothyroxine. EMS arrived at 1:34 PM and assumed care. The client was transported by Fire Department. VAERS completed. VAERS confirmation number.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Hypothyoroid and hypertension.
Andere Medikamente: Levothyroxine and Metoprolol
Allergien: Hx of urticaria with Benadryl
Vorherige Impfungen: -

VAERS 1944043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 38,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Chest pain Dysphagia Dyspnoea Urticaria

Symptomtext

Client reported chest pressure to EMT at approximately 6:40 PM. Client ambulated unassisted, sat down in the anti-gravity chair, and the chair was reclined in a semi-fowler's position by EMT. RN responded. The client reported chest pressure, shortness of breath, and feeling hot on her chest. Client denied any itchiness or feeling of swelling on her throat, lips, or tongue. EMS was activated at 6:41 PM. Client denied any history of chronic conditions or medications. Client reported a history of "bleeding inside" after taking NSAIDS. Client was alert and oriented to person, place, time, and situation. RN did not see any visible swelling of the lips or tongue. Vitals obtained at 6:44PM were as follows: manual BP 150/80, HR 106, O2 98%. Repeat automatic BP reading was 173/101. Client reported a history of hypotension. RN noted visible hives on the client's chest and recommended administration of IM Benadryl. The client reported difficulty swallowing to RN. Client stated she had previously taken Benadryl without any adverse reactions. The client provided verbal consent and RN administered 1 mL (50 mg) of Benadryl intramuscular into the right deltoid at 6:48PM. Client reported persistent chest pressure and difficulty breathing. RN did not note any signs of swelling on the client's lips or tongue. The client was alert and oriented to person and place and verbally responsive to questions. EMS arrived on site and assumed care at 6:50PM. Client was transported by

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: None
Andere Medikamente: None
Allergien: Hx of "bleeding inside" with NSAIDS
Vorherige Impfungen: -

VAERS 1943566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: DC
Alter: 43,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 19.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: SYR / AR

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

Burning sensation Condition aggravated Dermatitis Fatigue Gastrooesophageal reflux disease Laboratory test Pain Psoriasis Rash Rash macular

Symptomtext

I noticed my left leg burning about a week after the vaccine. It started off as a blotchy rash, but eventually started into turn into clusters that had liquid filled bumps that burned. I also noticed an uptick in my GERD and my dormant scalp psoriasis started to flare up. I contacted my medical practice, via email with photos of the rash, They initially suggested it could be dermatitis, but I started to develop extreme fatigue and was concerned I was having an autoimmune reaction to something. The rash clearly was not a bug bite or contact dermatitis and eventually I went to see my provider because I was struggling to exercise and my fatigue wasn't improving and was compounded with aches and pains. Because I didn't see my provider in person until the rash was mostly scabbed over, we did a swab for shingles, but she isn't confident it will test positive, although it does appear that I am suffering from shingles. I know shingles can be stressed induced, but I haven't been suffering extreme stress to trigger shingles and am concerned I am having an autoimmune reaction to my booster. I also articles about petechial rashes trigged by the COVID vaccine, which I shared with my provider in the event that is what triggered my rash/physical response.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: My provider swabbed my rash on Friday, December 10th. I don't have the results yet.
Aktuelle Erkrankungen: None
Vorgeschichte: IBS/GERD
Andere Medikamente: Prescription: Citalopram
Allergien: None known
Vorherige Impfungen: -

VAERS 1940091

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 25,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea Extra dose administered Hypoaesthesia oral Pharyngeal hypoaesthesia Throat tightness

Symptomtext

On Friday, December 10, 2021 client PRIVACY received her Pfizer Covid-19 vaccine booster (LOT #: FF8841) at 10:32 AM in her left deltoid. During assessment questions, client stated she has history of asthma with no known allergies and takes no medications. Client to be observed for 15 minutes after vaccination. At approximately 10:30 AM, while in Observation Area, client stated to EMT num. 1, she was experiencing "some tightness in her throat 8 out of 10" and felt like her breathing was "difficult and forceful." At 10:50 AM, EMT num. 2 brought client to sit in anti-gravity chair and auscultated lungs which were labored and clear in all fields. Vitals started, BP: 118/90, HR: 85, O2 sat: 99%, RR: 16, skin: normal dry and intact. At 10:58 AM BP: 124/84, HR: 75, O2 sat: 98%, RR: 16. Client stated her throat "feels numb and extends to the back of her tongue" but was still able to swallow. EMT num. 2 alerted Lead RN who offered 50 mg/mg Benadryl with water to client which she took. Client was educated of drowsiness effect and was instructed to call for a family member to come back her up and drive her home. At 11:05 AM, BP: 104/78, HR: 72, O2 sat: 99%, RR 16. Client was given juice and a snack that she ate. At 11:11 AM, BP: 104/78, HR: 79, O2 sat: 99%, lungs: clear in all fields, unlabored breathing. Client stated she felt her "throat was opening up with a 2 out of 10 tightness." At 11:16 AM, BP: 108/80, HR: 90, O2 sat: 995, RR: 16. Client states her throat "feels opened up now." At 11:25 AM, EMT num. 1 educated client to seek medical treatment if symptoms persist and signs and symptoms of adverse reactions. Client also encouraged to follow up with her PCP. At 11:27 PM, client states she feels "confident to leave" and feels "way better." No further interventions needed. At 12:00 PM, client left vaccination site with a steady gait and her sister drove her home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: hx of asthma
Andere Medikamente: none
Allergien: nka
Vorherige Impfungen: -

VAERS 1938681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: VA
Alter: 40,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Axillary pain Chest discomfort Chest pain Fatigue Immunisation Vaccination site pain

Symptomtext

My arm at injection site is much more sore than previous injections.; armpit is EXTREMELY sore; chest is tight on the same side (left) where the injection was given.; chest does not hurt as much; booster; a little more tired; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 40 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 18Nov2021 14:15 (Lot number: FF8841) at the age of 40 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included Diabetes (unspecified if ongoing); depression (unspecified if ongoing); anxiety (unspecified if ongoing); ADHD (unspecified if ongoing). Concomitant medication(s) included CELEXA; TRULICITY; SYNJARDY; BUPROPION. Past drug history included Codine, Drug Allergy. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EP7534, Location of injection: Arm Left, Reaction: arm at injection site is much more sore than previous injections), administration date: 22Mar2021, when the patient was 40 years old, for Covid-19 immunization, reaction(s) included arm at injection site is much more sore than previous injections; Bnt162b2 (Dose Number: 2, Batch/Lot No: EN0612, Location of injection Arm Left. The Reaction included arm at injection site is much more sore than previous injections, administration date: 15Apr2021, when the patient was 40 years old, for Covid-19 immunization. The following information was reported IMMUNISATION (non-serious) with onset 18Nov2021 14:15, outcome unknown; VACCINATION SITE PAIN (non-serious) with onset 19Nov2021, outcome not recovered; AXILLARY PAIN (non-serious) with onset 19Nov2021, outcome not recovered; CHEST DISCOMFORT (non-serious) with onset 19Nov2021, outcome recovering; FATIGUE (non-serious) with onset 18Nov2021, outcome recovering; CHEST PAIN (non-serious) with onset 19Nov2021, outcome recovering. Therapeutic measures were not taken as a result of vaccination site pain, axillary pain, chest discomfort, fatigue, and chest pain. Patient arm at injection site is much more sore than previous injections. Her armpit is extremely sore and chest is tight on the same side (left) where the injection was given. The same day after receiving the shot, she had no pain. She was a little more tired than usual. The next day, her chest was tight, and armpit hurt real bad. Today is day 3 and still have armpit pain and pain at the injection site, chest does not hurt as much. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination patient has not been tested for COVID-19. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Fatigue onset was same day as the vaccination, while other events onset latency was 9 hours 45 minutes. 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: ADHD; Anxiety; Depression; Diabetes
Andere Medikamente: CELEXA; TRULICITY; SYNJARDY; BUPROPION
Allergien: -
Vorherige Impfungen: -

VAERS 1936744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: OH
Alter: 59,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 09.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Immune-mediated adverse reaction Injected limb mobility decreased Lymphatic duct injury Muscle spasms Pain in extremity Vaccination complication

Symptomtext

When patient presented for second dose of COVID Pfizer vaccine in her RIGHT arm she stated that the night of her first dose her LEFT arm began hurting and had continued to hurt ever since. She demonstrated limited mobility of LEFT arm. We gave 2nd dose in RIGHT arm and advised her to see her primary physician if the problem continued. Patient visited pharmacy on 12/6/21 with update. Pain & limited mobility remains in LEFT arm. Patient has seen doctor about this problem.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: Diagnosed with 'pinched thoracic lymphatic duct caused by a muscle spasm of pectoralis minor an immune reaction set off most likely from vaccine"
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1935714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: KY
Alter: 73,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 26.02.2021
Beginn: 08.12.2021
Tage bis Beginn: 285,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Pneumonia bacterial

Symptomtext

Hospitalized for Covid-19 with superimposed bacterial Pneumonia requiring supplemental oxygen

Weitere VAERSDATA-Felder

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

VAERS 1935043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MI
Alter: 72,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 06.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / RA

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

Back pain Chills Fatigue Heart rate increased Hypoaesthesia Immunisation Malaise Nausea Pain in extremity Paraesthesia

Symptomtext

booster; was feeling a little bit of a tingling/numbness like it was about to fall asleep/Minor numbing/tingling; feeling a little bit of a tingling/numbness like it was about to fall asleep; felt very tired/ Moderate Fatigue; a little nauseous; overall not quite feeling well; back ache; arm really started to ache big time; tingling in her left upper thigh; had some chills; slight rapid heart rate/could feel my heart beating; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program. The reporter is the patient. A 72 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 06Oct2021 09:30 (Lot number: FF8841) at the age of 72 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Illness/AE: Thyroid" (unspecified if ongoing), notes: Pertinent Details: thyroid removed; "thyroid removed" (unspecified if ongoing); "Rosacea" (ongoing); "Cholesterol" (ongoing); "may-thurner" (ongoing), notes: Pertinent Details: Stint; "Gall bladder removed" (unspecified if ongoing); "Weakened immune system" (unspecified if ongoing), notes: Complete only if a third dose was administered, Weakened immune system: , Other, Please specify: Age - obesity; "obesity" (unspecified if ongoing), notes: Complete only if a third dose was administered, Weakened immune system: , Other, Please specify: Age - obesity. Concomitant medication(s) included: LEVOTHYROXINE taken for thyroidectomy (ongoing); ASPIRIN [ACETYLSALICYLIC ACID] (ongoing); DOXYCYCLINE taken for rosacea (ongoing); ATORVASTATIN taken for blood cholesterol abnormal (ongoing); CALCIUM (ongoing); VITAMIN D3 (ongoing). Vaccination history included: Bnt162b2 (1st Dose, Time: Noon , Anatomical Site of injection: Left arm, Route of administration: Intramuscular, Batch/Lot number: EN6202), administration date: 24Feb2021, when the patient was 72 years old, for Covid-19 immunization; Bnt162b2 (2nd Dose, Time: 11 AM , Anatomical Site of injection: Left arm, Route of administration: Intramuscular, Batch/Lot number: ER2613), administration date: 17Mar2021, when the patient was 72 years old, for Covid-19 immunization, reaction(s): "The caller experienced side effects noted to be tingling & numbness in her hand on the same side where she received her vaccine", "The caller experienced side effects noted to be tingling & numbness in her hand on the same side where she received her vaccine". The following information was reported: IMMUNISATION (non-serious), outcome "unknown", described as "booster"; HYPOAESTHESIA (non-serious), outcome "unknown", described as "her right hand on the arm she got the shot in was feeling a little bit of a tingling/numbness like it was about to fall asleep/Minor numbing/tingling in hand thigh upon waking up from sleep"; PARAESTHESIA (non-serious), outcome "unknown", described as "feeling a little bit of a tingling/numbness like it was about to fall asleep"; FATIGUE (non-serious), outcome "unknown", described as "felt very tired/ Moderate Fatigue"; NAUSEA (non-serious), outcome "unknown", described as "a little nauseous"; MALAISE (non-serious), outcome "unknown", described as "overall not quite feeling well"; BACK PAIN (non-serious), outcome "unknown", described as "back ache"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "arm really started to ache big time"; PARAESTHESIA (non-serious), outcome "unknown", described as "tingling in her left upper thigh"; CHILLS (non-serious), outcome "unknown", described as "had some chills"; HEART RATE INCREASED (non-serious), outcome "unknown", described as "slight rapid heart rate/could feel my heart beating". Additional info included No Prior Vaccinations within 4 weeks. Caller states she was finding and she doesn't know if this is typical, she asked her doctor about the vaccine and he seemed more in the dark and she knew more than he did. States he did say get the vaccine that will be fine and that she could get the flu shot at the same time and she opted not to. She doesn't do her dogs vaccines at the same time and spaces those out also. Caller states she has her flu shot scheduled for 3 weeks~ No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Blood cholesterol abnormal; May-Thurner syndrome (Pertinent Details: Stint); Rosacea
Vorgeschichte: Medical History/Concurrent Conditions: Gallbladder removal; Immune disorder (NOS); Obesity; Thyroid disorder (Pertinent Details: thyroid removed); Thyroidectomy
Andere Medikamente: LEVOTHYROXINE; ASPIRIN [ACETYLSALICYLIC ACID]; DOXYCYCLINE; ATORVASTATIN; CALCIUM; VITAMIN D3
Allergien: -
Vorherige Impfungen: -

VAERS 1929370

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NC
Alter: 36,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood test normal Dyspnoea Electrocardiogram normal Hypoaesthesia Impaired work ability Loss of personal independence in daily activities Malaise Palpitations Panic reaction

Symptomtext

pt stated that about 15 minutes after getting his first dose of the covid vax that the left side of his face went numb, then his body went numb, he had short of breath and heart palpitations. He felt like he was in a panic and he like he was dying. He was vaccinated on Friday and his face started going numb and by Saturday the numbness was moving to his extremities. By Tuesday he went to the local Hospital ER. He had blood work and EKG. Test Results were normal. He was told to FU w/ PCP and is scheduled for Heart Stress Test. He currently can only do 20 or 30 % of what he used to be able to do. Since he is active for his work this has changed his daily activities.

Weitere VAERSDATA-Felder

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

VAERS 1925639

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: AK
Alter: 52,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 21.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RA

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

Palpitations

Symptomtext

The patient came to the clinic on 10/21/2021 to receive the 2nd dose of Pfizer COVID-19 vaccine. With her first shot, she had 3 episodes of racing heart at night for about 15-30 minutes (each time resolved on its own). She has not had any since that time. It began 2-3 days after her first immunization and occurred 3 out of 10 nights that they were out hunting. She denied any chest pain, fever or other symptoms.

Weitere VAERSDATA-Felder

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

VAERS 1923542

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: -
Alter: 34,0
Geschlecht: M
Eingang: 04.12.2021
Impfdatum: 04.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Headache

Symptomtext

Client presented to the vaccination site on 12/04/2021. The client notified PHN that he received a first dose of Pfizer COVID vaccine on 11/13/2021 and is here for the 2nd Pfizer dose. Per patient developed mild chest pain and throbbing headache on the second and fourth day only after administering Pfizer. All symptoms subsided with the use of Acetaminophen taken on the fifth day and client did not follow up with primary care provider. Patient denies underlying conditions, no known allergies and not taking any medications. PHN submitted a medical consult via text message to Vaccine Operations Leads, requesting to proceed with the COVID vaccine Pfizer 2nd dose. Approval to proceed with COVID vaccine Pfizer 2nd dose was obtained from medical consult team via text message from MD, Vaccine Operations Lead . Client received COVID vaccine Pfizer 2nd dose LOT: FF8841 on 12/04/2021. The client did not report any symptoms during the 30 minute observation period. PHN educated client on possible adverse reactions and when to seek medical care. The client left the vaccination site at 3:30pm, client left facility with a steady gait. VAERS and VERP completed.

Weitere VAERSDATA-Felder

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

VAERS 1923035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: -
Alter: 28,0
Geschlecht: F
Eingang: 04.12.2021
Impfdatum: 30.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Lymphadenopathy Mobility decreased Peripheral swelling Swelling

Symptomtext

Left axilla swelling and lymph nodes; Left upper arm swelling (injected arm). Left arm noticeably larger than right arm; Left axilla swelling; Difficult raising injected left arm; This is a spontaneous report received from a non-contactable reporter (other healthcare professional). The reporter is the patient. A 28-year-old female patient (not pregnant) received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), administered in left arm, administration date 30Nov2021 (Batch/Lot number: FF8841) at the age of 28 years as dose 2, single for COVID-19 immunisation. The patient's relevant medical history was not reported. Concomitant medications included: PRENATAL, NORETHINDRONE and IBUPROFEN. Vaccination history included: BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, DOSE 1, SINGLE, Lot Number: FF8841, Route of administration: Unspecified, Anatomical site: left arm), administration date: 09Nov2021, when the patient was 28 years old, for COVID-19 immunisation. The following information was reported: PERIPHERAL SWELLING (non-serious), SWELLING (non-serious), LYMPHADENOPATHY (non-serious), MOBILITY DECREASED (non-serious) all with onset 30 Nov2021, outcome "not recovered" and all described as "Left upper arm swelling (injected arm). Left arm noticeably larger than right arm"; "Left axilla swelling and lymph nodes"; "Difficult raising injected left arm". Therapeutic measures were not taken as a result of peripheral swelling, swelling, lymphadenopathy and joint range of mobility decreased. Additional Information: The patient had no known allergies. It was unknown whether the patient received any other vaccines within four weeks prior to COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. 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. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: NORETHINDRONE [NORETHISTERONE ACETATE]; IBUPROFEN
Allergien: -
Vorherige Impfungen: -

VAERS 1920993

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: VA
Alter: 61,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 17.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / RA

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

Blood thyroid stimulating hormone normal Chest discomfort Dyspnoea Heart rate irregular Insomnia Interchange of vaccine products Metabolic function test normal

Symptomtext

12/29/20 Moderna vaccine 1/26/21 Moderna vaccine 11/17/21 Pfizer booster 11/25/21 Episodes of chest pressure (not acute pain, non-radiating) and feeling as though my heart rate was irregular. Felt like I needed to take a deep breath. These episodes lasted for an hour or so. I had experienced a similar episode the previous day but it was of a much shorter duration and didn't register s anything abnormal until it happened again and lasted much longer. 11/30/21Same experience, this this time at night after going to bed. Pulse felt irregular @ times and it was difficult to sleep. 12/1/21Senior director informed. Encouraged to follow up with PCP. 12/1/21 PCP appointment not available 12/2/21 Saw PCP. Blood work drawn and 48 hour halter monitor ordered. 12/3/21 Went to employee health No previous cardiac history, no family history of cardiac disease, no cardiac medications, No HTN

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: TSH 12/02/2021- normal result BMP 12/02/2021- normal result
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Zyrtec
Allergien: Latex, Formaldehyde, Nickel
Vorherige Impfungen: -

VAERS 1916942

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NJ
Alter: 39,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 15.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Balance disorder Ear haemorrhage Epistaxis Fatigue Headache Hypertension Malaise Muscular weakness Rash Urticaria

Symptomtext

--Hives/rash on trunk (11/16 only) --Mild R ear bleeding & mild/moderate nose bleeding (11/16 only) --Hypertensive episodes (11/16-11/18) --Moderate to severe headache (11/16-current) --Malaise/ fatigue (11/16-11/28) --Leg weakness/ unsteadiness (~11/18- current)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Upper respiratory infection/ cold-like sxs that began Oct 27, 2021 **NOTE: All 5 COVID tests (3 antigen and 2 PCRs )taken between 10/26/2021 and 11/15/21 yielded a negative result.
Vorgeschichte: -
Andere Medikamente: Escitalopram (10mg/ 1x daily ) Omeprazole (20mg prn)
Allergien: Amoxicillan (intolerance with severe GI disturbance)
Vorherige Impfungen: -

VAERS 1906139

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: TN
Alter: 55,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Cardiac monitoring Chest X-ray Chest pain Dizziness Electrocardiogram Fatigue Headache Pyrexia

Symptomtext

Lightheaded about 15 minutes after vaccine. The next day I was tired, light headed, headache, fever. The day after that I had horrible headache, very dizzy and had bad chest pains.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Went to ER had EKG, chest xray, heart monitored.
Aktuelle Erkrankungen: frozen shoulder
Vorgeschichte: asthma, high BP
Andere Medikamente: zyrtec, omeprazole, triamterene, celecoxib, trazodone, escitalopram, fluticasone/salmeterol
Allergien: none
Vorherige Impfungen: Covid vaccine 1-short of breath, blurry vision and headache; Covid vaccine 2-headache blurry vision BP dropped, short of breath-

VAERS 1904225

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff8841

moderat

Staat: NY
Alter: 16,0
Geschlecht: F
Eingang: 28.11.2021
Impfdatum: 25.10.2021
Beginn: 12.11.2021
Tage bis Beginn: 18,0
Dosis: 1
Route/Site: IM / LA

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

Blood test Chest discomfort Dyspnoea Gastrointestinal examination Hepatic enzyme abnormal Specialist consultation Tachycardia

Symptomtext

Tachycardia, chest tightness and difficulty breathing which lasted for a day. She then had once episode of tachycardia on Saturday and one on Sunday. She had to go to the ER where they discovered that her liver enzymes were also elevated. Her PMD was able to palpate her liver on Saturday 11/13/21. She saw a Cardiologist on 11/16/21 and a GI doctor on 11/18/21. She had repeat blood tests today, the results are pending and has to follow up with GI on 12/9/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Elevated liver enzymes on 11/12/21.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Omnicef Trees Dogs Pollen
Vorherige Impfungen: -

VAERS 1813248

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: PA
Alter: 65,0
Geschlecht: F
Eingang: 27.11.2021
Impfdatum: 13.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: OT / LA

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

Influenza A virus test negative Influenza B virus test Migraine Nausea SARS-CoV-2 test negative SARS-CoV-2 test Vomiting

Symptomtext

Severe debilitating migraine type headache with nausea and vomiting; Severe debilitating migraine type headache with nausea and vomiting; Severe debilitating migraine type headache with nausea and vomiting; This is a spontaneous report from a contactable pharmacist. This 65-year-old female Pharmacist (patient) reported for herself. A 65-years-old female non-pregnant patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 3 intramuscular, administered in Arm Left on 13Oct2021 14:00 (at the age of 65 years) (Batch/Lot Number: FF8841) as DOSE 3 (BOOSTER), SINGLE for covid-19 immunisation at Pharmacy or Drug Store. The patient was not pregnant at the time of vaccination. Medical history included none from an unknown date and unknown if ongoing. Concomitant medications included levothyroxine taken for an unspecified indication; colecalciferol (VITAMIN D) taken for an unspecified indication, start and stop date were not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Historical vaccine included BNT162B2 on dose 1 intramuscular, administered in Arm Left on 23Jan2021 11:30 (Batch/Lot Number: EL3246); dose 2 intramuscular, administered in Arm Left on 13Feb2021 (Batch/Lot Number: EL8982) (at the age of 65 years) for covid-19 immunisation. On 17Oct2021 06:00 the patient experienced severe debilitating migraine type headache with nausea and vomiting. It was also reported that Symptoms started on 17Oct2021 in early morning and continued until treated with methylprednisolone. The events resulted in doctor or other healthcare professional office/clinic visit. The patient underwent lab tests and procedures which included sars-cov-2 test: negative on 19Oct2021 Post vaccination: Nasal Swab. The patient received the treatment as Methylprednisolone 4mg for the adverse events. Device date was 23Oct2021. The clinical outcome of the events was recovered on 19Oct2021. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Test Date: 20211019; Test Name: SARS-CoV-2 Antigen; Test Result: Negative ; Comments: Post vaccination: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: LEVOTHYROXINE; VITAMIN D
Allergien: -
Vorherige Impfungen: -

VAERS 1900056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: -
Alter: 37,0
Geschlecht: F
Eingang: 25.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Bladder pain Burning sensation Chills Defaecation urgency Dizziness Feeling abnormal Feeling cold Headache Hypoaesthesia Injection site haemorrhage Malaise Neck pain Paraesthesia Tremor

Symptomtext

The person who administered the vaccine said that I may get a "bruise" as I was bleeding after the vaccine. I drove out of the vaccine clinic warehouse and sat in the parking lot for the 7 minutes. I started to feel "off" and a little dizzy. The nurse came over and my BP was 109 systolic and HR was 72 - both are/have never been that low. Her pulse ox wasn't working at the time. I told her I instantly got an intense left neck pain and headache...she said that some people get that. I had to immediately go poop and used the portapotty in the parking lot. I went back to my car and still felt sick. I sat there for prob about 10 more mins and then just left as my bladder literally felt like it was on fire. It hurt SO badly....right above my pelvic bone. It was awful. I was in the fetal position as I was driving home and got numbness/tingling down my right arm. I got home and immediately went to the toilet to go poop again. I was shaking from being so cold and having the chills and had a puke bucket in front of me, which I never used, while I was sitting on the toilet. Nothing was helping my bladder from that intense burning sensation. I just went to bed because I felt so off. The next day (and following days), I just felt very weak and foggy/off. I report this to my PCP and discussed with him at my annual exam on 11.16.21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Iron 65 mg daily
Allergien: -
Vorherige Impfungen: -

VAERS 1897421

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IN
Alter: 52,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 13.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Abdominal X-ray Blood electrolytes normal Blood test normal Condition aggravated Diarrhoea Fatigue Imaging procedure Pain Weight decreased White blood cell count normal

Symptomtext

On the day after the booster shot, 10/14, I had a low fever (around 100) and felt tired and achy--all of which was in line with how I'd felt following the first two Pfizer shots I'd had in March and April 2021. But on 10/15, I started having diarrhea, and by 10/17, I had 20 episodes in a single day. Despite not eating and then moving to the BRAT diet, I averaged about 10 episodes/day of diarrhea for 3 weeks. I lost 12 pounds and bloodwork and stomach imaging revealed no other problems. 11/8 was my first day without diarrhea--and from there I improved rapidly. I'm seemingly fine now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 10/26 bloodwork to check white blood cells, electrolytes, etc 11/3 abdominal xray/imaging *no abnormal findings
Aktuelle Erkrankungen: N/A
Vorgeschichte: frozen shoulder/adhesive capsulitius (2020-21)--both shoulders Parsonage Turner Syndrome (a disorder in the long thoracic nerves)
Andere Medikamente: daily vitamin, calcium supplement
Allergien: N/A
Vorherige Impfungen: -

VAERS 1897219

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: VA
Alter: 33,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 22.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal discomfort Dyspepsia Inflammation Laboratory test normal Migraine Nausea

Symptomtext

Approximately 24 hours after I got the shot, I started to get a migraine with some pretty bad nausea. That lasted for 4 days. The migraine went away but I continued to get episodes of nausea. I experienced indigestion, severe nausea, intestinal discomfort, a little bit of acid build up, no diarrhea or vomiting. I started to track my food and I made the connection that it was triggered by a food. I went to see my doctor and she said it could be a gluten intolerance and she explained that any vaccine can cause inflammation and maybe that is what happened to me. The treatment right now is to eliminate gluten and try to reduce the inflammation. I have not had any episode in the last week because I am avoiding the foods. She said we will try again in a month to see if I can tolerate the food. We did a celiac test, and it came back negative and a physical exam. I had my flu shot after the booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Celiac test- Negative
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Breo Ventolin
Allergien: Sulfa antibiotics Fragrance allergies
Vorherige Impfungen: -

VAERS 1897144

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CO
Alter: 52,0
Geschlecht: M
Eingang: 24.11.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest pain Chills Diarrhoea Fatigue Injection site pain Lymph node pain Lymphadenopathy

Symptomtext

11/19/2021 I noticed a pain in the injection site, the entire shoulder of the left side, and I had chills that night, but no fever. 11/20/2021 Woke up to my lymph nodes swollen in the left armpit, pain was closer to the chest, diarrhea, chills and fatigue. 11/21/2021 The swelling in left armpit was now the size of a softball, the pain progressed to the shoulder area, chills and fatigue; took Advil before bed. 11/22/2021 The swelling had gone down to about baseball size, pain had mostly subsided, but still fatigue. I went to the doctor this day and told me just to take Aleve twice a day. Still just a bit of tenderness on the left side as of today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Adderall XR;
Allergien: None
Vorherige Impfungen: -

VAERS 1896424

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MI
Alter: 40,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Axillary pain Back pain Chest pain Chills Ear pain Fatigue Feeling abnormal Headache Immunisation Myalgia Pain in extremity Photosensitivity reaction Vaccination site pain

Symptomtext

Headache; Earache; Upper and lower backache; Chills; Muscle pain from head to toe; Sensitive to light; Super sore arm; Pain down my right arm near the injection site; Pain down my right arm near the injection site as well as on the opposite side of arm into armpit; Fatigue; Foggy head; Random chest pains; Dose received: 3; This is a spontaneous report from a contactable consumer, the patient. A 40-year-old non-pregnant female patient received the third (booster) dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FF8841) via an unspecified route of administration in the right arm on 16Nov2021 at 15:30 (at the age of 40-years-old) as a single dose for COVID-19 immunisation. Medical history included asthma. The patient had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications taken within two weeks of vaccination included norethisterone (NORETHINDRONE) for an unknown indication, from an unknown date and unknown if on going. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EL9261) via an unspecified route of administration in the left arm on 25Jan2021 at 15:30 (at the age of 39-years-old) and the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EL9267) via an unspecified route of administration in the left arm on 15Feb2021 at 15:30 (at the age of 39-years-old); both as single dose for COVID-19 immunisation and did not have any symptoms with the first two vaccines. On 17Nov2021 at 06:00, the patient experienced headache, earache, upper and lower backache, chills, muscle pain from head to toe, was sensitive to light, had super sore arm, pain down right arm near the injection site as well as on the opposite side of arm into armpit. The pains continued for 48 hours (as reported). The patient also had fatigue and a foggy head and random chest pains. The patient was concerned and worried that this could be more serious. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events headache, earache, upper and lower backache, chills, muscle pain from head to toe, sensitive to light, super sore arm, pain down right arm near the injection site as well as on the opposite side of arm into armpit, fatigue and a foggy head and random chest pains was resolving at the time of this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma
Andere Medikamente: NORETHINDRONE [NORETHISTERONE]
Allergien: -
Vorherige Impfungen: -

VAERS 2597368

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 24,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Dyspnoea

Symptomtext

Pt who came in for a flu vaccine and was erroniously given a covid booster vaccination, We kept Pt an extra 25-30 minutes on top of the 15 minutes required. She said she was feeling fine before she left. 11/21/2021 @ 9:00pm I recieved a call from Pt's Uncle, stating that she had difficulty breathing the night before and some chest pain as well. I told him to ask her how she was feeling now. She said that she was having a hard time catching her breath and she was having some chest pain, I advised her and her Uncle to either call 911 or go to the ER 11/22/2021 @ 11:57am Spoke with Pt's uncle, he said they took Pt to ER, ER ran some test on her and

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: KNA
Vorgeschichte: KNA
Andere Medikamente: -
Allergien: KNA
Vorherige Impfungen: -

VAERS 1890607

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: AK
Alter: 16,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 09.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: SYR / LA

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

Blood test normal Conjunctivitis Feeding disorder Headache Insomnia Migraine Nausea Paranasal sinus discomfort Visual impairment Vomiting X-ray normal

Symptomtext

2nd does of vaccine was received Tuesday November 9, 2021. On Thursday the 11th patient woke up at approximately 3pm and had decreased vision in her right eye. On Monday November 15th the patient woke up with a minor headache. When she returned from school at approximately 2:15 the headache had become a migraine, she complained of sinus pressure, nausea, and vomiting. On Tuesday November 16 the patient complained that the migraine, nausea and pressure was getting worse and vision had not gotten better. On Wednesday the 17th the patient continued to complain the symptoms were getting worse. Mother called primary care physician who instructed her to take child to emergency room to rule out blood clots. Patient arrived in the emergency room where tests were run to rule out blood clots. Patient was diagnosed with a migraine and conjunctivitis. Patient followed up with primary care physician on November 22 at 9:45 am. Patients vision was returning with the use of eye drops. However, headache and nausea remained. Patient has noted that it has been difficult to eat or drink due to nausea and headache. In addition patient complains that she is unable to sleep.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Blood work - 11/17/21 - normal Xrays - 11/17/21 - normal Eye Exam - 11/17/21 Conjunctivitis in both eyes
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma and Irritable Bowel Syndrome
Andere Medikamente: None
Allergien: Penicillan
Vorherige Impfungen: -

VAERS 1888347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 26,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Paraesthesia

Symptomtext

On Saturday, November 20, 2021 client received her Pfizer Covid-19 vaccine booster (LOT #: FF8841) at 1:33 PM in her left deltoid. During assessment questions, client stated she had no know allergies and takes no medications. Client to be observed for 15 minutes after vaccination. At approximately 1:46 PM, while in Observation Area, client stated to EMT she was experiencing "tingliness or tickleness" in her left palmar surface for less than 5 minutes only with no pain or any other symptoms. Client denied SOB. Client was brought to sit in anti-gravity chair, offered water and vitals started. Lead RN offered 50 mg oral solution Benadryl and EMS to which the patient denied. At 1:45 PM: BP 124/88, HR 69, O2 sat 98%, RR 20, skin warm and dry. At 1:52 PM, client states she was a bit anxious to get the vaccine. EMT educated client to seek medical treatment if symptoms persist and signs and symptoms of adverse reactions. At 1:57 PM, client stated the tickleness sensation was "better" and "less." No further interventions needed. At 1:58 PM, client left vaccination site with a steady gait and her husband drove her home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: NKA
Vorherige Impfungen: -

VAERS 1888136

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 61,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Paraesthesia

Symptomtext

On Friday, November 19, 2021 client received her Pfizer Covid-19 vaccine booster (LOT #: FF8841) at 4:50 PM in her left deltoid. During assessment questions, client stated she has severe allergic reaction to penicillin and experiences anaphylaxis. Client to be observed for 30 minutes after vaccination. Client's medical history included hypothyroidism and takes the medication Miccil for an unknown heart problem. At approximately 5:25 PM, while in Observation Area, client stated to EMT she was experiencing tingliness in her left hand in the palmar surface only with no pain or any other symptoms. Client denied SOB. Client was brought to sit in anti-gravity chair, offered water and vitals started. Lead RN offered 50 mg oral solution Benadryl to patient which she took with her water at 5:26 PM. At 5:26 PM: BP 126/68, HR 71, O2 sat 98%, RR 16, skin warm and dry. At 5:31 PM: BP: 124/70, HR 71, O2 sat 96%, RR 16, skin warm and dry. EMT educated client on drowsy side effect. At 5:35 PM, client stated she only felt slight tingliness in her left hand and felt stable to leave. No further interventions needed. EMT educated patient on signs and symptoms of adverse reactions and when to go to the ED/call MD. Client left vaccination site with a steady gait at approximately 5:40 PM. Client's husband drove her home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: hypothyrodism
Andere Medikamente: Miccil
Allergien: PCN
Vorherige Impfungen: -

VAERS 1888104

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MD
Alter: 45,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Back pain Chest pain Confusional state Fatigue Gait inability Headache Impaired work ability Injection site pain Injection site swelling Injection site warmth Muscle spasms Muscular weakness Pain Pyrexia Sitting disability Urine analysis

Symptomtext

On November 4, 2021, I received my second Pfizer COVID-19 vaccination lot number FF8841. The second injection was also done. The vaccination was already drawn when I entered the examining room. Before receiving the injection, I request to speak with Dr. to discuss my symptoms from the first vaccination shot so it could be properly documented. Dr. went over the list of medications that I am previously taken. The list of medications I take daily consist of Amlodipine 10mg TAB, Phentermine Hydroc 37.5mg TAB, Budesonide, and Formoterol Fumarate Dihydrate Inhalation Aerosol 160mcg/4.5mcg, and over the counter hydrocortisone cream 1%. Dr. cleared me to receive my second dosage of the Pfizer COVID-19 vaccination. After receiving my second vaccination I experience a headache, mild fever, fatigue, confusion within a one-hour time frame. The soreness, swelling, and warmth to the touch at the injection site followed hours later. I was bed resting for two days before the symptoms subsided. On November 7, 2021, walking from my bedroom to the kitchen I started experiencing shooting pain from my waist down my leg on my left side enabling me from walking. I had to rely on my daughter and fianc?? to assist me with laying down, walking, and using the restroom. My muscles on my left side became weak and begin to have spam. On November 8, 2021, I made an appointment with my healthcare provider Dr. On November 9, 2021, I followed up with Dr. concerning the pain I was experiencing. Dr. prescribe me Acetaminophen/Codeine 300-30mg TAB and Cyclobenzaprine HY 10mg TAB. The medication Dr. prescribed was not effective. I continue to have pain in my left side. On November 16, 2021, I started experiencing pain in my chest and back. November 17, 2021, I went to Urgent Care for treatment. Dr. , diagnosed me with possible sciatica. Dr. , prescribe Methocarbamol 750mg TAB and heat therapy on the affected area 4 times a day. Dr. , advise me to follow up with my healthcare provider. Dr. , also request that I be on bed rest from November 17, 2021, and return to work on November 21, 2021. The medication that Dr., prescribed allowed me to be mobile again but the pain still exists. Dr. referred me to radiology for an x-ray of the back. It?s going on three weeks since I received the second Pfizer COVID vaccination lot number FF8841. The pain on my left side has continued to be a problem since the third day of receiving the Pfizer COVID vaccination lot number FF8841. I have been suffering pain, spasms, weakness on my left side, chest, and back pain. I have trouble walking, sitting, laying, and getting up from a sitting position due to the pain. I also missed work due to my complications after receiving the COVID-19 vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: November 17, 2021, a urinalysis was performed at Urgent Care. Noted on my discharge papers is stable. I have a referral for radiology for an x-ray of the chest. I have not had the x-ray done yet.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma. and hypertension
Andere Medikamente: Hydrocortisone cream 1%
Allergien: I have allergies to mold, potatoes, and oak. I can't take any prescription containing ibuprofen due to ulcers.
Vorherige Impfungen: On October 14, 2021, I received my first Pfizer COVID-19 Vaccination, lot number FF8841. I chose to receive my vaccination from

VAERS 1885885

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NY
Alter: 56,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 05.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Mobility decreased Pain Pain in extremity X-ray limb X-ray normal

Symptomtext

Ever since this shot there has been something wrong with my right arm. It throbs like a tooth ache. I cant move my arm correctly. There is something wrong. I had an xray of my shoulder and it was negative so it mist be in the muscle

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Xray of shoulder which was negative so its mot the bone
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1885688

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 43,0
Geschlecht: F
Eingang: 19.11.2021
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

Anxiety Palpitations Tremor

Symptomtext

Client received Pfizer booster at approximately 1455 Client alerted nurse she was feeling palpitations while sitting in the observation area. She stated she wanted her vital signs to be taken. Client was AAOx3 and was breathing normally. Client denied shortness of breath or difficulty breathing. No hives or redness observed on client arms, neck or face. Client stated she had received Janssen as her first dose but had no reactions to the vaccine. Client vital signs were taken by EMT 1500 BP 140/80 HR 76 RR 14 PUPILS PERLA within normal limits. Client sat in gravity chair without assistance. Client stated she was feeling ?like a pounding feeling in her chest all the way to her ears?. At 1507 Auscultation of heart was done by EMT and confirmed palpitations every 3-5 secs. Client stated she had no medical conditions except for gastritis and takes some meds for it. She stated she had no allergies. She stated she only feels out breath when she?s in a hurry when busy. But no history of palpitations. Client stated she felt chest pressure and felt ?shaky?. 1510 BP 130/82 HR 78 with palpitations. At 1516 EMS was called for further assessment of client. Client?s Husband informed RN that two years ago an Arrythmia had been confirmed to patient, but no further follow-up was done. Client was very shaky due to being anxious about the situation and was being guided to have controlled breathing with Student nurse.. At Approximately 1525 EMS arrived at vaccination site and took over client?s care. AT 1539 Client walked with assistance by paramedics to the EMS truck. Client was taken to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: gastritis
Andere Medikamente: gastritis medications
Allergien: nka
Vorherige Impfungen: -

VAERS 1885371

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MD
Alter: 67,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 05.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 20,0
Dosis: 3
Route/Site: SYR / LA

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

Chest X-ray Cough Dyspnoea Fatigue Illness Nasal congestion Pain Physical examination Respiratory tract congestion Sinusitis

Symptomtext

Congestion, cough, fatigue, body aches, 1 night it felt like I was breathing really fast. I was pretty sick for about 2 weeks but getting better. I took Mucinex, Robitussin, soup, tea to treat myself but it wasn't getting better, and I went to get the COVID-19 test and the nurse sent me to the hospital to get a complete checkup. At the hospital they said I still had a sinus infection and gave me Augmentin antibiotic, Mucinex and Flonase. I'm improving but still with a little cough and nasal congestion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: They did the nasal test Chest X-ray Exam
Aktuelle Erkrankungen: No
Vorgeschichte: Saitic Valtrex medication injury to my liver from Losartan tingling in my hands and feet Ditropan caused difficulty swallowing in my throat
Andere Medikamente: Calcium Vitamin C Vitamin D Fish Oil Magnesium Turmeric
Allergien: Valtrex Losartan Macrobid Ditropan Dental Lidocaine Augmentin is causing diarrhea
Vorherige Impfungen: Live shingles vaccine I had shingles and was told to get the shingle shot. And after that I kept getting shingles break out over

VAERS 1881121

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: VA
Alter: 50,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 11.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: - / -

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

Blister Ear pain Headache Myalgia Neck pain Oropharyngeal pain Pain of skin Paraesthesia

Symptomtext

Was here for physical on 11/11 and had 3 vaccines. covid booster, shingles, tetanus. Then felt a little run down the next few days. Was able to do the normal routine. Then on Saturday felt like scalp was "weirdly tender." with brushing hair. Then felt prickly/tingling sensation on back of ear. Then Monday/tuesday woke up with sore throat, headache, ear ache and right neck muscles have been sore. And has been like that since then. Then yesterday started getting tingling in the eye and went to patient first. Took a look and gave valtrex. Has taken 2 pills. Gave abx drops for ear, but recommended holding off for now until seen today. Does have blisters forming.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Onychomycosis; Strabismus
Andere Medikamente: Valtrex 1000mg
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1878032

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: FL
Alter: 88,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Axillary pain Injected limb mobility decreased Myalgia

Symptomtext

patient received both flu and covid booster in left arm during at a clinic. She reports pain from armpit to elbow,muscle pain and cannot lift arm. Suggested patient check with physician.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: none yet
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1876082

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: UT
Alter: 29,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Blood test Chest pain Dizziness Dyspnoea Electrocardiogram normal Fatigue Palpitations

Symptomtext

Severe Joint Pain - 2 days Fatigue - 3 days Lightheadedness - ongoing (has lasted 7 days so far. Usually occurs when walking) Heart Palpitations - ongoing (has lasted 7 days so far. Usually occurs when walking) Mild Chest Pain - ongoing (has lasted 7 days so far) Shortness of Breath - ongoing (has lasted 7 days so far)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG (11/13/21) - appears normal Blood work (11/16/21) - results not back yet
Aktuelle Erkrankungen: -
Vorgeschichte: Mild asthma, hypothyroidism, mild IBS, severe depression
Andere Medikamente: Bupropion, Liothyronine, Levothyroxine
Allergien: -
Vorherige Impfungen: -

VAERS 1875943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: -
Alter: 30,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Back pain Chest pain Immunisation

Symptomtext

Chest pain on right side of chest.; Pain between shoulders.; Patient received third dose/ Booster dose; This is a spontaneous report from a contactable consumer, the patient. A 30-year-old non-pregnant female patient received the third booster dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FF8841) via an unspecified route of administration in the left arm on 10Nov2021 at 10:30 (at the age of 30-years-old) as a single dose for COVID-19 immunisation. Medical history included hypothyroidism. The patient had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included levothyroxine (MANUFACTURER UNKNOWN) for an unknown indication from an unknown date and unknown if ongoing. The patient did not receive any other vaccines within 4 weeks prior to the vaccination. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EP6955) via an unspecified route of administration on 27Mar2021 (at the age of 30-years-old) and also received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EV10151) via an unspecified route of administration on 17Apr2021 (at the age of 30-years-old) as a single dose for COVID-19 immunisation. On 10Nov2021 at 16:00, on the day of vaccination, the patient experienced chest pain on right side of chest and pain between shoulders. Reportedly chest pain was present the following day but was less severe. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events chest pain on right side of chest and pain between shoulders were resolving at the time of this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism
Andere Medikamente: LEVOTHYROXINE
Allergien: -
Vorherige Impfungen: -

VAERS 1873936

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NJ
Alter: 25,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Fatigue Feeling abnormal Paraesthesia

Symptomtext

patient states his left arm and right leg feel funny, tingly. patient told to stay for observation. Patient brought crackers and water, states he ate a full meal prior to vaccine. A few minutes later patient states he still feels funny, patient gets up and sits in corner, places head on wall. States he feels really tired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1872885

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF 8841

moderat

Staat: AR
Alter: 33,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 26.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Ear discomfort Erythema Feeling abnormal Impaired work ability Paraesthesia Pruritus

Symptomtext

pt reports that three days after vaccine, she was riding in the car before work, ears started burning , then a red sunburn traveled all the way down her arms , chest, abdomen, thighs legs feet , pt reports a pins and needles sensation, with itching, and the itching was worse around the neck area. No Shortness of Breath, Pt felt lightheaded, and "cloudy in my head", which last several hours, so pt left work and went home , took a Benadryl, and laid down and slept from 1000am - 100 pm. At this time all of the redness was gone.

Weitere VAERSDATA-Felder

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

VAERS 1872261

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: -
Alter: 44,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 20.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: - / -

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

Cardiac flutter Chest pain Palpitations

Symptomtext

Heart fluttering; Chest pain when exercising 3 days after shot/ continued sporadic chest pain; Heart palpitations; This is a spontaneous report from a non-contactable consumer (patient). A 44-years-old female patient (pregnant: no) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), the first dose via an unspecified route of administration on 20Oct2021 (Batch/Lot Number: FF8841) as dose 1, single for covid-19 immunisation. Medical history included polycystic ovarian syndrome from an unknown date. Concomitant medications included ethinylestradiol, levonorgestrel (LUTERA) taken for an unspecified indication, start and stop date were not reported; zinc taken for an unspecified indication, start and stop date were not reported; ascorbic acid (VIT C) taken for an unspecified indication, start and stop date were not reported; folic acid taken for an unspecified indication, start and stop date were not reported; colecalciferol (VIT D) taken for an unspecified indication, start and stop date were not reported; magnesium taken for an unspecified indication, start and stop date were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously took erythromycin and experienced allergy. The patient experienced heart fluttering on 23Oct2021 at 14:00, chest pain when exercising 3 days after shot/ continued sporadic chest pain on 23Oct2021 at 14:00, heart palpitations on 23Oct2021 at 14:00. Reported Event: Sharp chest pain when exercising 3 days after shot, continued sporadic chest pain, heart palpitations and heart fluttering still continuing 10 days after initial AE. The adverse event resulted in emergency room/department or urgent care. No treatment received for the events. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The outcome of the events was not recovered. 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: Polycystic ovarian syndrome
Andere Medikamente: LUTERA; ZINC; VIT C; FOLIC ACID; VIT D [COLECALCIFEROL]; MAGNESIUM
Allergien: -
Vorherige Impfungen: -

VAERS 1869217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: MI
Alter: 55,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 03.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: - / -

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

Grip strength decreased Hypoaesthesia Paraesthesia Peripheral swelling

Symptomtext

After first vaccination on 11/13/21 swelling in right arm and numbness lasting 12 hours. After second vaccination on 11/3/2021 swelling of both arms, and numbness, unable to hold onto things with right hand. Numbness and tingling from shoulders into fingertips, tingling and pins and needles feeling in feet. Symptoms are getting better, but there is still tingling in right arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Dr Appointment November 23, 2021 7:30 AM Unsure of outcome at this time.
Aktuelle Erkrankungen: None
Vorgeschichte: Hemochromatosis
Andere Medikamente: multi vitamin 24 hours before
Allergien: allergic to Sulpha. Food allergies: Corn any corn products, Coconut, tomatoes, pork
Vorherige Impfungen: -

VAERS 1867839

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (OTHER) · Charge FF8841

moderat

Staat: CA
Alter: 12,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hypoaesthesia oral Incorrect dose administered Paraesthesia

Symptomtext

5 min post 1st dose pfizer peds vacc: c/o tingly 15 min after c/o tongue numbness. visually no swelling Vitals normal called Dr. order to give Zyrtec 2.5ml liquid children, monitored for 30 more min. pt ok after 30 min, went home, informed to seek emergency care if worsens at home. verbalized understanding

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: none per mother
Allergien: adhesive tape
Vorherige Impfungen: -

VAERS 1867739

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: AR
Alter: 65,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 08.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Arteriogram coronary normal Chest X-ray normal Chest pain Pleurisy Troponin normal

Symptomtext

Chest pain, evaluated at Hospital Emergency Room and followed up at Doctor's office. Treated with so far two rounds of toradal anti-inflammatory shots. As of this writing chest pain is still severe and tentative diagnosis is pleurisy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Heart CT, chest x-ray, troponin levels all were normal.
Aktuelle Erkrankungen: -
Vorgeschichte: osteoarthritis, stage 1 kidney disease, hypertension
Andere Medikamente: Synthroid, amylodipene besylate, valcyclovir, vitamin D, doxycycline
Allergien: atropine, tetracycline, compazine, morphine, tramadol, codeine, reglan, mirapex, gabapentin
Vorherige Impfungen: pfizer 3/30/21 64 long term arm pain, pfizer 4/20/21 64 long term arm pain

VAERS 1865342

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CT
Alter: 32,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 29.09.2021
Beginn: 29.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Blood test Dyspnoea Echocardiogram Electrocardiogram Menstruation delayed Palpitations X-ray

Symptomtext

Shortness of breath during five days after the first dose, palpitations during more than three weeks thst have improved through time but I still experience them and 6 day delay in my period

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Blood test, x ray, electrocardiogram, ecocardiogram
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1858796

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 42,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / -

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

Arthralgia Axillary pain Musculoskeletal chest pain Pain Pain in extremity

Symptomtext

Body aches, right shoulder and armpit soreness, right side of my ribs and right arm pain from shoulder going down to my fingers tip, and headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Musculoskeletal chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: Shoulder soreness

VAERS 1858483

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: WI
Alter: 42,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 12.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Headache Hypoaesthesia Pain in extremity Paraesthesia Pruritus

Symptomtext

Within 24 hours I had severe headache and arm soreness. I started having localized tingling and numbness throughout body. It is felt like as if something is crawling under my skin. It itches slightly and then continuously moves to other localized spots all over the body. It has been persistent. I have continued to only feel this more after the 2nd dose through out hands, feet and face more. After the 2nd dose I am experience some joint pain in feet/ face and increases tingling in extremities and face.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: Vit D Zinc NAC Omega 3 Magnesium Citrate Probiotic
Allergien: no
Vorherige Impfungen: -

VAERS 1857366

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: ME
Alter: 50,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 12.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / RA

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

Chest discomfort Chest pain Dyspnoea Dyspnoea exertional Injection site reaction Miliaria

Symptomtext

During the first week I experienced prickly heat from the injection site through to the right half of my face. I experience this only the first week and it happened four times with each time the severity getting more noticeable. During the third week I experience episodes of chest pain or tightness of chest in the center of my chest. This only happened during week three and happened about four times with severity increasing with each episode. I experience shortness of breath the entire three weeks. When I walked up the stairs it was as if I had run up 10 flights of stairs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Omeprazole, Lexapro, DHEA, Vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 1854555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: WI
Alter: 53,0
Geschlecht: M
Eingang: 09.11.2021
Impfdatum: 07.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Hypoaesthesia Limb discomfort Paraesthesia

Symptomtext

It started with a tingling feeling above my right knee. After a few days, my whole quad was tingling/numb. My calf then felt like it wanted to cramp up, but never did. My root foot then became tingly/numb. After a month, parts of my leg continue to feel tingly and numb. I do have strength and range of motion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: multi-vitamins
Allergien: None
Vorherige Impfungen: -

VAERS 1854079

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: SC
Alter: 35,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 07.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: - / LA

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

Anxiety Asthenia Dizziness Headache Heavy menstrual bleeding Hypoaesthesia Nausea Paraesthesia Vomiting

Symptomtext

Dizzy, weakness, anxiety, tingling and numbness in hands and feet, nauseous, and throwing up, mensural cycle changes/hormone changes (bleed longer and heavier) headaches

Weitere VAERSDATA-Felder

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

VAERS 1853897

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MA
Alter: 30,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 30.09.2021
Beginn: 04.11.2021
Tage bis Beginn: 35,0
Dosis: 3
Route/Site: IM / RA

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

Antipsychotic drug level Anxiety Chest discomfort Computerised tomogram normal Cough Dizziness Dyspnoea Exercise tolerance decreased Fatigue Hyperventilation Laboratory test Oropharyngeal pain Paraesthesia Secretion discharge Thyroid hormones test

Symptomtext

I was biking home from work (which I usually do 1-3 times per week) and about 3-5 minutes into the ride I started feeling worse than I usually do biking (more short of breath, more tired, more chest tightness, harder to breathe, a lot of mucus in my throat, much more painful in my throat). At about 15 minutes in I was really coughing a lot and it felt very hard to breathe and I had a very sharp pain in my throat, like the muscle was spasming. The ride was about 20-30 min. I was alternating between coughing and gasping for air when I got home. I laid down but that made it harder to breathe so I stood back up. It was difficult to talk because I couldn't get enough air. I thought maybe I had developed exercise-induced asthma since it was the first time it was colder out so I went to the urgent care who sent me to the ER. I started feeling anxious and I was hyperventilating, which I think made me feel dizzy and tingly in my hands and legs. By the time I was there at the ER, I had started to feel better, and by the time I was admitted I felt completely better except for some lingering chest tightness and sore throat which I think was from the coughing - that lasted about 48 hours. Now I feel completely better, but I haven't tried biking again so I'm not sure if this is something that would happen again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 11/4/2021 or 11/5/2021 I don't have the actual results myself, but I was told that the tests were all normal except one "nonspecific marker for pulmonary embolism" that was positive, which prompted a CT scan with contrast of my lungs which was normal. I know they had done lithium levels and a thyroid panel among the tests.
Aktuelle Erkrankungen: major depression in partial remission, autism spectrum disorder, OCD, ADHD, social anxiety disorder, dissociative disorder, acne, essential tremor, migraine with aura (aura only no headache), functional dyspepsia, allergic rhinoconjunctivitis, raynaud's phenomenon
Vorgeschichte: major depression in partial remission, autism spectrum disorder, OCD, ADHD, social anxiety disorder, dissociative disorder, acne, essential tremor, migraine with aura, functional dyspepsia, allergic rhinoconjunctivitis, raynaud's phenomenon, chilblains
Andere Medikamente: lithium 300mg bid, adderall 15mg prn (don't remember if i took it that day), truvada 200/300mg qd, fiber 6 g qd, folate/vitamin B12 400mcg/300mcg qd, gabapentin 300mg bid, vitamin d 15,000 international units (375mg) once weekly (last took
Allergien: sulfa, pollen, cat dander
Vorherige Impfungen: -

VAERS 1850983

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: AZ
Alter: 66,0
Geschlecht: F
Eingang: 08.11.2021
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: ja Erholt: ja

Dry throat Dysphonia Dyspnoea

Symptomtext

shortness of breath after Pfizer booster shot #3 had history of prior reaction to a flu shot many years ago no wheezing no stridor VS stable Given 25 mg po Benadryl referred to ED for observation as has no one here to do continued observation for next 30 min. Per ED doctor's note: she feels that her voice is a bit hoarse and her throat feels dry. She has no chest pain, no rash or diaphoresis. No evidence of angioedema. She has no stomach upset. She reports that she has gotten an EpiPen before, he has not used it at home. She has been observed in the ED for allergic reactions in the past however she is not ever been admitted. She had a worse response with a flu shot and was given benadryl and observation in the past.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: unknown
Vorgeschichte: obesity mild intermittent asthma low HDL (<40)
Andere Medikamente: unknown
Allergien: aspirin - unknown ciprofloxacin - unknown penicillin - unknown
Vorherige Impfungen: influenza vaccine, can't remember reaction or when it was

VAERS 1850838

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: KY
Alter: 58,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 15.10.2021
Beginn: 02.11.2021
Tage bis Beginn: 18,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Back pain Mobility decreased

Symptomtext

An ache in the area of the left shoulder/left side of back started late Nov. 2/early Nov. 3. It was really bad to the point that it made it hard to move for about the first three days. It started improving on Nov. 6. As of the time of this report, it's barely noticeable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: detached retina; overweight
Andere Medikamente: D-amphetamine salt combo (30mg), bupropion XL (150mg), clonazepam (0.5mg), vitamin D3 (25mcg)
Allergien: none
Vorherige Impfungen: -

VAERS 1850757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NM
Alter: 42,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 20.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Breast pain Chest pain Influenza like illness Laboratory test Lymphadenopathy Mammogram Pain in extremity Pyrexia

Symptomtext

PATIENT RECEIVED VACCINE ON 10/20/2021 PATIENT STATES 24 HRS LATER SHE HAD FEVER AND FLU SYPTOMS AND ON FRIDAY 10/22/2021 SHE HAD SWELLING OF LYMPH NODES TO THE RT ARM AND ALSO HAD CHEST PAIN THAT WENT DOWN TO THE LEFT ARM, SHE WENT TO THE ER AT A DIFFERENT FACILITY TO GET CHECKED AND SHE STATES THEY DID LAB WORK. SHE SCHEDULED AN OFFICE VISIT HERE AT THE MEDICAL CLINIC ON WED 11/03/2021 WITH COMPLAINTS OF BREAST PAIN AND STATES SHE HAS HAD THE PAIN FOR THE LAST 7 DAYS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: MAM DIGITAL BILATERAL ORDERED ON 11/03/2021 LABS WERE DONE AT A DIFFERENT FACILITY PER PATIENT
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: PRILOSEC 20 MG CAPSULE
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1849604

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: PR
Alter: 42,0
Geschlecht: F
Eingang: 07.11.2021
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: unbekannt ER: unbekannt Erholt: nein

Axillary mass Dry mouth Fatigue Headache Injected limb mobility decreased Injection site erythema Injection site inflammation Injection site swelling Injection site warmth

Symptomtext

The same day head pain, excessive tiredness, dry mouth. The next day morning my arms was swollen and red in area of vaccine. The vaccine area is inflamed, red, and hot. I have a ball under my arm and I can't lift my arm today. Today Sunday 11/07/2021 I have the same symptoms. The first and second vaccine were the same symptoms but milder and didn't have the ball. Thank you for the opportunity.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Losartan 25mg
Allergien: No
Vorherige Impfungen: -

VAERS 1848924

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: TX
Alter: 35,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 10.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Angiogram cerebral Anti-thyroid antibody Dizziness Echocardiogram Gait disturbance Headache Hypoaesthesia Laboratory test Loss of personal independence in daily activities Movement disorder Muscle spasms Pain Pain in extremity Paraesthesia Pruritus Scan with contrast Urine analysis Vision blurred

Symptomtext

I started with tingling in lower limbs (legs), in the following days tingling also occurred in the upper limbs (hands) presenting numbness in extremities subsequently I started with spasms (itching) and pain in legs, arms, then tingling sensation and itching in the head, head pain, dizziness, blurred vision. Currently I have complications when walking and moving, pain, numbness and tingling in the body that prevent me from performing my daily activities.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Blood chemistry, General urine test, CT tomography A.C. of skull with contrast, ECO Doppler both legs, Thyroid with antibodies, Vitamin D
Aktuelle Erkrankungen: Fibromyalgia, Vaginal/Urinary tract infection
Vorgeschichte: Fibromyalgia
Andere Medikamente: Pregabalin of 150mg
Allergien: Do not know
Vorherige Impfungen: -

VAERS 1846796

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IL
Alter: 42,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Chest discomfort Chest pain Chills Dyspnoea Erythema Hyperhidrosis Pruritus Urticaria

Symptomtext

Pt arrived at 3pm for the pfizer booster vaccine. Three minutes following the vaccination the pt began to c/o chest tighness, hives, itching, redness and a hard time breathing. Pt was visably sweating, shivering with redness and hives present on chest upon assessment. Vitals were taken and as follow; BP 144/76, HR 115, Temp 97.2 and O2 sat 100%. An EpiPen was administered as Dr was called to assess the situation. During the evaluation, the pt chest pain began to worsen and Dr. insisted EMS Services. The on staff RN called 911 and EMS arrived within 5 mins. Pt information was given by RN and the pt was taken to ED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Morphine and Vicodin
Vorherige Impfungen: -

VAERS 1846275

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IN
Alter: 61,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 03.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Condition aggravated Fatigue Pain

Symptomtext

Symptoms occurred 15 hours after booster/3rd Pfizer vaccine shot. Minor fatigue, chills and body aches. Symptoms relieved except for fatigue by taking 500 mg Tylenol and 2-200mg Advil. Took this combination 3x on 11/4/2021. Mild fatigue continued on 11/5/2021. Experienced same symptoms on 3/20/21 with 2nd Pfizer Covid 19 vaccine; however symptoms were slightly more severe and onset was sudden (chills, fever, body aches, fatigue - similar to the flu).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 3rd Pfizer Covid 19 vaccine/booster shot on 11/3/2021.
Aktuelle Erkrankungen: Flu vaccine 2 weeks prior
Vorgeschichte: Type II diabetes
Andere Medikamente: Metformin 50 mg 2x/day. Type II diabetes
Allergien: some dairy, cheese products
Vorherige Impfungen: Milder symptoms with 3rd shot, experienced mild fever, chills, body aches, fatigue.

VAERS 1846045

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MS
Alter: 46,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Ear pain Fatigue Gait disturbance Headache Injected limb mobility decreased Myalgia Pain in extremity Peripheral swelling Pyrexia Rhinorrhoea Swelling face

Symptomtext

Could not move left arm an hour after vaccine. Joints and muscles started hurting 4 hours after vaccine. Runny nose, headache, exhausted 6 hours after vaccine. Next morning every joint and muscle hurt to the point that I could not even walk without hurting. Hip joints felt broken, ran fever 101, fingers swollen and in pain. I didn't even feel this bad when I had Covid over a year ago( I was just tired for a few weeks with a slight sore throat when I got Covid). I was in major pain for 2 days with swelling in my left cheek and my left ear hurt. I was told to take tylenol and benadryl. I don't want to take the 2nd shot now, because of the pain I felt for 2 days. I would rather just get Covid again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: none
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1845401

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IL
Alter: 31,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 07.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Chest pain Dyspnoea Inappropriate schedule of product administration Palpitations

Symptomtext

shortness of breath; heart palpitations/my heart is pounding to my chest; chest pain; Inappropriate schedule of vaccine administered; This is a spontaneous report from a contactable consumer (patient) reported for herself. A 31-years-old non pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection) via an unspecified route of administration, administered in Arm Right (reported as Right upper arm) on 07Oct2021 (Batch/Lot Number: FF8841) as DOSE 2, SINGLE and received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; Batch/Lot Number: FF8841) via an unspecified route of administration, administered in Arm Right on 07Oct2021 at 17:00 as DOSE 1, SINGLE both doses taken at age of 31-years-old for COVID-19 immunisation. The patient was not pregnant at time of vaccination. Medical history included Right bundle branch block, allergy to Shellfish, adhesive, iodine. Past Drug included Iodine and Reglan and experienced allergy. Patient took no other medications within 2 weeks of vaccination. Facility where the most recent COVID-19 vaccine was administered was Pharmacy or Drug Store, 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 the vaccination, the patient has not been tested for COVID-19. On 09Oct2021, the patient reported that she had shortness of breath, heart palpitations/my heart is pounding to my chest, chest pain and Inappropriate schedule of vaccine administered. Patient had heart palpitations at night. During the day being weekend like her heart was pounding to her chest, she had chest pain, she had the same symptoms three days after she received the vaccine. The adverse events resulted in doctor or other healthcare professional office/clinic visit and Emergency room/department or urgent care. As a treatment she was prescribed prednisone it had not helped, had been taking her inhaler for three weeks straight and it has not helped. Other treatment included for adverse events which the patient took was with Steroid. Outcome of events was not recovered. Follow-up attempts are completed. No further information is expected.; Sender's Comments: Based on the information in the case report, a possible causal association between the event dyspnea and suspect drug BNT162B2 cannot be excluded. 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: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Adhesive tape allergy; Bundle branch block right; Shellfish allergy.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1844308

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: AK
Alter: 48,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Injection site pain Injection site reaction Myalgia Pain Tremor

Symptomtext

Got my first COVID Pfizer shot since that day my deltoid has been sore for the past month, muscle continually feels tight with quivering. I have full hand strength and grip, no numbness or tingling, just myalgia and deep ache that hasn?t gone away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None so far.
Aktuelle Erkrankungen: None
Vorgeschichte: Back pain, asthma, bph
Andere Medikamente: Doxazosen- motrin- advair- proventil
Allergien: Hytrin& codeine
Vorherige Impfungen: -

VAERS 1843141

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: PA
Alter: 48,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 06.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: SYR / RA

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

Chest pain Disturbance in attention Dizziness Dyspnoea Swelling face Throat tightness Tinnitus

Symptomtext

FACIAL TIGHTNESS, SHORTNESS OF BREATH, THROAT TIGHTNESS, DIZZINESS, RINGING IN EARS, LOSS OF FOCUS, SLIGHT CHEST PAIN

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: DAILY MULTI-VITAMIN
Allergien: NONE
Vorherige Impfungen: -

VAERS 1840579

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: OH
Alter: 64,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 29.10.2021
Beginn: 03.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / LA

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

Atrial fibrillation Chest X-ray normal Chest pain Condition aggravated Dyspnoea Palpitations Tachycardia

Symptomtext

Patient presented to ED with sudden onset shortness of breath, with associated chest pain and palpitations. The patient was found to be tachycardic at 129 bpm. The patient was found to have atrial fibrillation with rapid ventricular response. The patient spontaneously converted to NSR prior to medications being given. The patient is admitted to the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 11/3/21 Chest X-ray: no acute abnormalities
Aktuelle Erkrankungen: -
Vorgeschichte: hypothyroidism, atrial fibrillation, class 2 obesity, hypertension, anxiety
Andere Medikamente: alprazolam, calcium-vitamin D, dofetilide, fluticasone nasal spray, levothyroxine, ibuprofen, loratadine, magnesium, meclizine, metformin, metoprolol succinate, multivitamin, fish oil, omeprazole, paroxetine, Xarelto, sodium chloride nasal
Allergien: sulfa antibiotics
Vorherige Impfungen: -

VAERS 1837882

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: GA
Alter: 47,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Mobility decreased Pain in extremity

Symptomtext

About 4 and a half hours later, my arm really began to hurt. It lasted for two days. I could barely bend my arm at one point.

Weitere VAERSDATA-Felder

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

VAERS 1837043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: -
Alter: 32,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 16.09.2021
Beginn: 29.10.2021
Tage bis Beginn: 43,0
Dosis: UNK
Route/Site: - / -

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

Asymptomatic COVID-19 Exposure during pregnancy Gestational hypertension SARS-CoV-2 test positive

Symptomtext

10/29/21 patient presents to a local HCF for elevated BPS, gestational hypertension, third semester, asymptomatic COVID-19 infection. No pertinent past medical history.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Gestational hypertension
Hospital-Tage: -
Labordaten: 10/29/21 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1836967

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MO
Alter: 28,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 15.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / AR

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

Palpitations

Symptomtext

Heart palpitations that started 2 days after vaccinated. Reduced caffeine intake. Contacted physician. Lasted ~12 days and resolved without treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, depression, anxiety
Andere Medikamente: Fluoxetine
Allergien: Clindamycin
Vorherige Impfungen: -

VAERS 1836351

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NE
Alter: 44,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 20.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac flutter Chest X-ray Chest pain Electrocardiogram Laboratory test Myocardial necrosis marker Palpitations

Symptomtext

Oct 23, 3 days after the vaccines I had sharp pains in my left chest area during working out, after that through now (Nov 2), I started to have more chest pain, heart palpitations and fluttering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG, Chest XRay, LabWork to check cardiac enzymes 02Nov2021
Aktuelle Erkrankungen: N/A
Vorgeschichte: Polycystic Ovarian Syndrome
Andere Medikamente: Lutera (daily), (Vitamin D, Vitamin C, Zinc, Magnesium, Folic Acid - all stopped at least 2 days prior to vaccination)
Allergien: Erythromycin
Vorherige Impfungen: 3 Days after another vaccine (MMR possibly) body aches, nausea, chills/sweats.

VAERS 1835379

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IN
Alter: 67,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 30.09.2021
Beginn: 30.09.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Asthenia Chills Headache Immunisation Off label use Tremor

Symptomtext

Extreme chills; Extreme shaking; Headache; Weakness; Off label use/ Dose number: 3; Dose number 3; This is a spontaneous report from a contactable consumer, the patient. A 67-year-old male patient received third (booster) dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FF8841) via an unspecified route of administration in the right arm on 30Sep2021 at 10:00 (at the age of 67-years-old) as a single dose for COVID-19 immunisation. Medical history included atrial fibrillation ( A fib) and known allergy to penicillin. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications were not reported. On 30Sep2021 at 22:00, the patient experienced extreme chills and shaking, headache and weakness. It was unknown whether therapeutic measures were taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events extreme chills and shaking, headache and weakness was unknown at the time of this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: AFib; Penicillin allergy (Known allergies: Penicillin)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1833603

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IN
Alter: 78,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 13.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Gait disturbance Mobility decreased Muscular weakness Walking aid user

Symptomtext

Extreme chills with intense shivering. Followed the next morning with extreme weakness so couldn't walk without help using walker. Unable to get out of chair. Weakness lasted all day after shot day till mid day of second day after shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Stage 3 kidney disease, Wild Amyloidosis
Andere Medikamente: Vyndamax, Losartan, eliquis, allopurinol, metoprolol, gabapentin, atorvastin, furosemide, tamsulosin, CoQ10, D-3, vit B complex
Allergien: Celebrex
Vorherige Impfungen: -

VAERS 1833393

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NY
Alter: 57,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Hypoaesthesia Paraesthesia

Symptomtext

About 1 hour after vaccination, patient reported feeling numbness and tingling on the right side of face and hand. Numbness described as being similar to coming off of a local anesthetic from a dental procedure. The numbness and tingling started to subside about an hour after symptoms began.

Weitere VAERSDATA-Felder

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

VAERS 1831702

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MN
Alter: 44,0
Geschlecht: M
Eingang: 30.10.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Chest pain Headache Hypoaesthesia Palpitations

Symptomtext

Systemic: Chest Tightness / Heaviness / Pain-Mild, Systemic: Headache-Mild, Systemic: Numbness (specify: facial area, extremities)-Mild, Additional Details: PATIENT EXPERIENCED NUMBNESS ON ONE SIDE OF FACE FOR A FEW DAYS AND HAD A HEADACHE AND SAID POTENTIAL RACING HEART/TIGHTNESS BUT ALL RESOLVED WITHIN A FEW DAYS TOLD HIM TO GO IN TO DOC IF IT REOCCURS

Weitere VAERSDATA-Felder

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

VAERS 1831485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IN
Alter: 73,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja 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 1825471

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: -
Alter: 45,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Feeling abnormal Palpitations Visual impairment Vitreous floaters

Symptomtext

Patient recieved pfizer-BioNtech COVID-19 doses 1 and 2 with no reactions. Patient received Pfizer-BioNtech booster dose 3 today. Two hours after the dose, patient began to see floaters and light strobes in her left eye. Patient came down to clinic, and was told to rest in the observation area. Patient felt heart palpitations and "felt worse" and was subsequently taken to the ER.

Weitere VAERSDATA-Felder

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

VAERS 1825321

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CT
Alter: 65,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 30.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Extra dose administered Genital herpes

Symptomtext

I have genital herpes and have never before had a significant out break, and never one that lasted over 1 week. The outbreak after shots 1 and 2 lasted 5 months, so far the one after shot 3 has lasted the 4 weeks since the shot. Both reactions have been bad (7+ lesions) and so far the traditional treatment (valacyclovir) has only had moderate effect. I have taken 2 courses of the medication and still am not clear.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Prediabetes, Bipolar, hypothyroidism, high cholesterol, high blood pressure, osteopenia, reflux/GERD
Andere Medikamente: Excedrin, alprazolam, amlodipine Besylate, atorvastatin, benefiber, buproprion hcl sr, calcium citrate, Tums, estradiol 0.01% cream, fluticasone propionate, folic acid, lithium carbonate er, loratidine, l-thyroxine, metformin, multivitamin,
Allergien: latex, bee stings, hay fever, Lamictal, Reglan, Gabapentin, Cefzil.
Vorherige Impfungen: -

VAERS 1825071

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: VA
Alter: 1,1
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 11.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / RA

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

Abdominal pain upper Anxiety Cardiac stress test normal Chest discomfort Chest pain Computerised tomogram abdomen normal Dizziness Dysphonia Dyspnoea Echocardiogram normal Fatigue Headache Heart rate increased Hypertension Joint stiffness Malaise Muscle spasms Myocardial necrosis marker normal

Symptomtext

Symptoms: Chest Tightness/Pain, Shortness of Breath, Raspy Voice, Elevated Heart Beat, Elevated Blood Pressure, Stomach Pain, Muscle Cramps, Joint Stiffness, Headache, Dizzy, Anxiety, Tired, Overwhelming Feeling of being Unwell. Treatment: Admitted to Hospital Emergency Room 10/21/2021 @ 10:00 AM, Released 10/23/2021 @ 12:19 PM. Treatment: STOP Amlodipine-Atorvastatin 10-40, START Amlodipine Besylate 10mg, START Atorvastatin Calcium 80mg, START Pantoprazole Sodium 40mg X2.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: Nuclear Stress Test and Echo did not demonstrate cardiac compromise; Cardiac enzymes were negative; Abdominal CT did not show anything acute.
Aktuelle Erkrankungen: See continuation page for health status
Vorgeschichte: See continuation page for health status
Andere Medikamente: See continuation page for medications
Allergien: Ranitidine
Vorherige Impfungen: -

VAERS 1823548

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MI
Alter: 52,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 29.09.2021
Beginn: 29.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Acne Dyspnoea Headache Illness Lethargy Nausea Pyrexia Rash

Symptomtext

Fever; Nauseous; Headache; broke out with pimples; Lethargic; she got really sick after the second dose; Rash; struggled to breath; This is a spontaneous report from a contactable 53 year-old female consumer (patient) communicated to a Pfizer colleague that reported a 53-year old female received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: FF8841), via an unspecified route of administration on 29Sep2021 (at the age of 52 years old) as dose 2, single for covid-19 immunisation. The patient medical history was not reported. There were no concomitant medications. Historical vaccine included first dose of BNT162B2 (Lot Number: FC3183) on 08Sep2021 (at the age of 52 years old) for covid-19 immunisation. Reporter a Pfizer employee reporting for his cousin regarding the Pfizer Covid vaccine and who explained that she received both doses. It was reported that with first shot, it was no big deal. It was explained she got really sick after the second dose. Twelve hours after the second dose she developed a rash that looked like ring worms or cigarette burns. It was all over her body but mainly on the arm she received the injection, caller thinks it was the left arm. After that when she went to lay down to sleep, she reported she struggled to breath on 29Sep2021. It felt like someone was crushing her chest. This lasted about 24 hours, the trouble breathing. She also got a fever, was nauseous and had a headache. Her head felt so heavy she couldn't not lift off her pillow. Also, she felt super lethargic, so much so she couldn't get up out of bed. In response to the breathing, she relayed she literally could not breath and this was the first time that had ever happened to her. It was absolutely horrible. She stated she will not get a booster shot. Also it was explained she broke out with pimples. The reporter's sister came over and gave her something and within 30 minutes she was feeling better. It was some herbal treatments, pine needle tea and charcoal to drink. Her sister also made her a drink of zinc mixed with lemon and grapefruit skin. Within 30 minutes of taking all this she started to feel better. It was stated that after taking all this and is getting better, she is able to pull the little blisters off her skin. No testing done. The outcome of struggled to breath was recovered on 30Sep2021, while with other events was unknown. Follow-Up (13Oct2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1821891

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: KS
Alter: 92,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 20.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / RA

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

Dyspnoea Heart rate increased Malaise Oxygen saturation decreased Pulmonary congestion Rales Terminal state

Symptomtext

low 02 sats ( 39%) increased congestion in lungs with shortness of breath crackles through out lungs increased heart rate above 100

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: did not do labs or chest x-ray due to resident on Hospice care resident is not doing well and is expected to pass
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1821333

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: KS
Alter: 98,0
Geschlecht: M
Eingang: 27.10.2021
Impfdatum: 19.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Cardiomegaly Chest X-ray abnormal Heart rate increased Oxygen saturation decreased Pneumonia Vomiting

Symptomtext

low 02 sats, increased pulse (124) vomited x 1 Chest x-ray on 10/21 showed cardiomegaly with bibaslar pneumonia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: cardiomegaly with bibaslar pneumonia
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1821218

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: TX
Alter: 43,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 24.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Chills Condition aggravated Extra dose administered Headache Influenza like illness Myalgia Nausea Pyrexia

Symptomtext

Fever, chills, muscle/joint pain, headache, nausea (flu-like symptoms). Started late on 10/24/21 and lasted until midmorning on 10/26/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: levothyroxine, duloxetine, acetaminophen, loratadine
Allergien: -
Vorherige Impfungen: Yes, some joint pain with the 2nd dose of COVID-19 vaccine on 1/18/2021.

VAERS 1819678

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: OH
Alter: 54,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 25.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Anaemia Blood ketone body Chest X-ray normal Computerised tomogram neck Dyspnoea Epiglottic oedema Full blood count abnormal HIV test negative Laryngeal oedema Laryngeal stenosis Magnetic resonance imaging Metabolic function test SARS-CoV-2 test negative Scan with contrast Stridor Urine analysis normal Wheezing

Symptomtext

54-year-old female presented to the emergency room on 10/26/21 at approximately 16:25 with complaint of shortness of breath/wheezing from outpatient MRI department. Patient stated that prior to the MRI she was feeling fine and after multiple unsuccessful IV attempts the patient started to get short of breath. IV was successfully placed and MRI completed without issues aside from the fact that patient remained short of breath. Patient was short of breath prior to IV contrast administration. She received 3 prior MRIs with IV contrast in the past without any issues or allergies. Of note the patient did receive Covid vaccination yesterday on 10/25/21 at 11:30am and is on losartan, not on any ace-inhibitors. Initially on exam the patient appeared to have an expiratory stridor. Due to the stridor we did administer 2 rounds of racemic epinephrine nebulized with no improvement. Patient then received albuterol for which she states she felt slightly better. In the meantime the patient received IV dose of steroids. We then underwent a CT of the neck which showed moderate laryngeal and epiglottic fold edema with the most narrowed area of the airway measuring 2.8mm in diameter. At this time decision was made to transfer the patient to a facility that had ENT as backup in case of the need for intubation which would be considered complicated. Spoke with Dr. at Hospital. At this time the patient had improvement of her symptoms however was still having audible expiratory stridor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: All testing on 10/26/21: COVID-19 test (negative result), CBC (stable chronic anemia), CMP (stable CKD), ketones serum (normal), rapid HIV (negative), urinalysis (normal), Chest x-ray (no acute findings), CT Neck/Soft Tissue without IV contrast (Prominent lingual tonsils abut the epiglottis. Mild aryepiglottic fold edema and laryngeal mucosal causes moderate airway stenosis at the level of the larynx with most severe level of stenosis causing diameter of 2.8mm of airway. No evidence of a drainable fluid collection.)
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, ossifying fibromyxoid tumor, obstructive sleep apnea, stage 3 chronic kidney disease, type 2 diabetes, essential hypertension, depression
Andere Medikamente: losartan, gabapentin, insulin glargine, Montelukast, melatonin, triamcinolone cream, diclofenac gel, ipratropium0albuterol nebulizer, atorvastatin, fenofibrate, albuterol HFA, cetirizine, omeprazole, liraglutide, amlodipine, amitriptyline,
Allergien: None
Vorherige Impfungen: -

VAERS 1818626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 56,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 22.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Cheilitis Chills Extra dose administered Headache Influenza like illness Lip swelling Nausea Paraesthesia oral

Symptomtext

10/25/21 @6 pm, swelling of top lip began with tingling and small red bump. I took one benadryl before bed and in the morning, my top lip had swollen to 3-4x normal size.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: Per Urgent care PA, I was given shot of Solumedrol5.5 hours ago
Aktuelle Erkrankungen: Only flu-like symptoms with headache, nausea, chills, for 30 hours after vaccine booster.
Vorgeschichte: None
Andere Medikamente: Armour Thyroid
Allergien: Pcn, Azythromycin, Vicodin, Ibuprofen, Motrin,
Vorherige Impfungen: Similar histamine reaction of left hand, wrist, forearm approximately 1.5 weeks following Shingrix booster.

VAERS 1818242

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (OTHER) · Charge FF8841

moderat

Staat: NY
Alter: 35,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 12.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Chills Fatigue Headache Impaired work ability Lymphadenopathy Mobility decreased Pyrexia

Symptomtext

RECEIVED BOOSTER DOSE OF PFIZER VAX - HAD SEVERE SYMPTOMS THAT PATIENT WAS UNABLE TO ATTEND WORK. FEVER >102.0, CHILLS EXTREMELY SWOLLEN LYMPH NODES, EXTREME FATIGUE, HEADACHE. STAYED IN BED 5 DAYS TO RECOVER

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: EXTREME FATIGUE, FEVER 102.3, SWOLLEN LYPH NODES, CHILLS, HEADACHE LASTING 5 DAYS POST VACCINE
Vorgeschichte: CROHN'S
Andere Medikamente: APAP, OMPERZOLE
Allergien: PENICILLIIN, SULPHA, ASA
Vorherige Impfungen: -

VAERS 1815474

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NY
Alter: 34,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 18.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Chest X-ray abnormal Dyspnoea Electrocardiogram ST segment abnormal Electrocardiogram abnormal Palpitations

Symptomtext

Shortness of breath with heart palpitations

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG (ST segment changes and v1,2,3 ) and Chest X-ray (no infiltrates but poor respiratory efforts)
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: None
Allergien: none
Vorherige Impfungen: -

VAERS 1815241

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MA
Alter: 66,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 14.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Ear discomfort Extra dose administered Pain in jaw Paraesthesia oral Toothache X-ray dental normal

Symptomtext

Within minutes of third dose (booster 10 months post second dose) I felt a bit lightheaded, noted some tingling in my lips and tongue. These sensations lasted about 20 minutes. 2 1/2 days post injection (10/17/21) I experienced left lower jaw and teeth pain, with some strange sensations in my left ear. Pain became intense requiring Ibuprofen/Acetaminophen alternating every 4 hours for 24 hours. Went to my dentist following morning 10/18, full mouth exam and x-rays showing no infection, abcess or obvious problem. Pain recurred intermittently for next several days requiring Ibuprofen/Acetaminophen and then again became intense on 10/23-10/24. Returned to dentist 10/25 and exam again revealed nothing. This pain may or may not be related to vaccination but I wanted to report it. I have been reading a few reactions that sound similar to mine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: 10/18/21 Dental appt. Upper & lower left mouth x-rays and exam. No conclusive findings. Suggested mouthguard and heat. 10/25/21 Dental appt. Repeat exam. No conclusive findings. Continue to monitor.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Hydrochlorothiazide 25mg daily
Allergien: No known food or drug allergies
Vorherige Impfungen: -

VAERS 1814761

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF 8841

moderat

Staat: -
Alter: 74,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Back pain Chest discomfort Dyspnoea Immunodeficiency Pulmonary pain

Symptomtext

I was watching TV and dozing on and off, when I was jolted upright by an instantaneous and sharp pain across my upper back. I has some tightness in my chest and my breathing became a little labored. The pain was extreme and I thought maybe it was a heart attack. I called the local hospital and the person who answered the phone called the on -call doctor at my PCP's office, which is affiliated with the hospital. I was instructed to call the hospital back if I hadn't heard from the doctor within 20 minutes. The doctor called and I explained what at happened. By then the pain was slightly diminished. The doctor said she didn't know if it was related to the booster shot, and added that if it was a heart attack the pain would be constant. She said that if it got unbearable that I should come to the hospital. The pain continued to diminish, but moved from my back to the area of my right lung (front and back). It took two hours for most of the pain to subside. I did not need to go to the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Mild to moderate asthma Acid reflux
Andere Medikamente: Ibuprofen Advair inhaler Multi-vitamin Calcium and vitamin D supplement Fish oil supplement Gingko Biloba herbal supplement
Allergien: Polyethylene glycol (taken orally) I did not have a reaction to vaccine doses 1 and 2. Biaxin Sulpha drugs
Vorherige Impfungen: -

VAERS 1813836

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: WI
Alter: 44,0
Geschlecht: F
Eingang: 24.10.2021
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Asthma Burning sensation Condition aggravated Dyspnoea Feeling hot Flushing Injection site mass Injection site pruritus Injection site warmth Paraesthesia Paraesthesia ear Pruritus Rash

Symptomtext

-got a giant lump (like half baseball) at injection arm, It was hot for days. - extremely itchy (generalized and injection site) - face and ears were flushed and warm and tingly/burning yesterday -flared asthma symptoms, increased dyspnea symptoms persisting over days - facial/ ear tingling - generalized rashing, itching and flushing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Increased antihistamine use Increased asthma medication use
Aktuelle Erkrankungen: Asthma Inhalant allergies Headaches
Vorgeschichte: Patient Active Problem List Diagnosis Date Noted ? Fibromyalgia 06/22/2021 ? History of cerebral venous sinus thrombosis 02/24/2021 ? Fatty liver 11/05/2020 ? Generalized anxiety disorder 08/11/2020 ? Vitamin D deficiency 07/15/2020 ? Atypical facial pain 09/23/2019 ? Cervicogenic headache 09/23/2019 ? Palpitations 03/26/2018 ? Arthritis of right knee 11/28/2017 ? Chronic allergic rhinitis due to animal hair and dander 10/25/2017 ? Chronic seasonal allergic rhinitis due to pollen 10/25/2017 ? Contact dermatitis ? OSA (obstructive sleep apnea) ? Moderate persistent asthma without complication ? Morbid obesity with BMI of 70 and over, adult (*) ? Allergic rhinitis due to dust 11/22/2016 ? Seasonal allergic rhinitis due to pollen 11/03/2016 ? Lipoma of arm 12/04/2013 ? Dysmenorrhea 09/13/2013 ? Irregular menses 09/13/2013 ? Fibrocystic breast disease 09/13/2013 ? Irritable bowel syndrome with diarrhea
Andere Medikamente: Current Outpatient Medications on File Prior to Visit Medication Sig Dispense Refill ? aspirin, chewable, 81 mg oral tablet Take 81 mg by mouth every day. ? budesonide (PULMICORT) 0.25 mg/2 mL inhalation nebulizer suspension Take 2 mL (0.
Allergien: Carbamazepine Cephalexin Sulfa Ibuprofen Tramadol
Vorherige Impfungen: -

VAERS 1813523

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: TX
Alter: 72,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 07.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Chest X-ray Computerised tomogram head Cough Dysphagia Full blood count Myocardial necrosis marker Oropharyngeal pain Pain Pain in extremity Pneumonia SARS-CoV-2 test negative Tremor

Symptomtext

Cough and sore the following day. Day 2-soreness of right upper arm, heaviness and cough and sore throat continue. Difficulty swallowing saliva. Day 3-intense shaking (entire body) and temporary loss of awareness. EMS called and was taking to hospital. Diagnosed with pneumonia, which I was very skeptical about diagnosis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: Chest X-ray CT scan of my brain Lab-CBC of electrolytes, cardiac enzymes, Covid-19 (which was negative)
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension Diabetic
Andere Medikamente: Glipizide Losarten Lisinopril Jardiance Metformin Zanaflex Triameterene
Allergien: Dicloflenic
Vorherige Impfungen: -

VAERS 1813332

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: AR
Alter: 30,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Cough Dyspnoea Pruritus Retching Sensation of foreign body Vomiting

Symptomtext

Patient started coughing approximately 10 minutes after vaccination, stating that her throat felt like she had something in it. She then started retching, with minimal vomiting. At approximatedly 4pm, epinephrine 0.3mg was administered by intramuscular route via auto-injector. Emergency medical services were contacted, and patient was transported to local hospital, where she was admitted overnight. She states she received intravenous dexamethasone while in the hospital. She was released 10/23/21 and reports improvement in her breathing but reports diffuse itching throughout her body. Patient was prescribed a 12 day course of 5mg prednisone taper.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ProAir HFA inhaler, Vitamin D2 1.25mg, Zolpidem 10mg, Clonazepam 1mg, Bupropion ER 150mg
Allergien: latex, mushrooms, tapentadol
Vorherige Impfungen: -

VAERS 1810520

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NC
Alter: 33,0
Geschlecht: M
Eingang: 23.10.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Burning sensation Chest pain Chills Fatigue Heart rate Heart rate increased Lymphadenopathy Night sweats SARS-CoV-2 test Vaccination site pain

Symptomtext

swollen armpit (lymph nodes?); overnight sweats; elevated heartrate; chest pain; burning sensation throughout the day; fatigue; overnight chills; injection-site pain; This is a spontaneous report from a contactable consumer or other non-HCP. A 33-years-old male patient received third dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: FF8841), via an unspecified route of administration, administered in left arm on 08Oct2021 at 10:20 (at the age of 33-years-old) as DOSE 3 (BOOSTER), SINGLE for COVID-19 immunization. Patient had earlier received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution injection, lot number: EL3247) on 14Jan2021 and second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution injection, lot number: EL3247) on 04Feb2021 for COVID-19 immunization. Medical history included cholesterol, hypothyroidism and Hashimoto's Thyroiditis. Concomitant medications included levothyroxine sodium (LEVOXYL), colecalciferol, fish oil (OMEGASAN 3) and Multi-vitamins. On 08Oct2021 10:20 the patient experienced overnight chills and injection-site pain. On 09Oct2021 13:00 the patient experienced fatigue, elevated heartrate, chest pain, burning sensation throughout the day, overnight sweats. On 09Oct2021 19:00 the patient noticed swollen armpit (lymph nodes?). Facility type vaccine mentioned as Workplace clinic. No other vaccine in four weeks has been administered. Other medications in two weeks mentioned as Levoxyl, Omegas, Multi-vitamins, Other medical history: Cholesterol, Hypothyroidism, Hashimoto's Thyroiditis. The patient did not had COVID prior vaccination and post vaccination, patient had not tested with covid 19. No known allergies reported for the patient. The patient underwent lab tests and procedures which included Nasal Swab (SARS-CoV-2 test): Negative on 31Mar2021 COVID 19 Antigen/Rapid; heart rate: elevated on 09Oct2021. Therapeutic measures were taken as a result of overnight chills, injection-site pain, fatigue, elevated heartrate, chest pain, burning sensation throughout the day, swollen armpit (lymph nodes), overnight sweats. On 08Oct2021 at around 20:00 took two Tylenol PM tablets. On 09Oct2021 at around 9am took two Tylenol Gelcaps. May plan to visit Primary Care Physician this coming week reporter stated. The outcome of event overnight chills, injection-site pain was recovered on an unspecified date of Oct2021 while outcome of event fatigue recovered on 09Oct2021. The events were reported non-serious. The outcome of event overnight sweats was outcome of recovering while outcome of rest all event was not recovered. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20211009; Test Name: Heart rate; Result Unstructured Data: Test Result:elevated; Test Date: 20210331; Test Name: Nasal Swab; Test Result: Negative ; Comments: COVID 19 Antigen/Rapid.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cholesterol; Hashimoto's thyroiditis; Hypothyroidism
Andere Medikamente: LEVOXYL; OMEGASAN 3
Allergien: -
Vorherige Impfungen: -

VAERS 1808599

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: PA
Alter: 56,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 05.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / LA

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

Blood test Computerised tomogram Dizziness Extra dose administered Hyperacusis Magnetic resonance imaging Migraine Nausea Pain Photophobia Photopsia

Symptomtext

Migraines (confirmed by doctor) started within 24 hours of Covid 3rd vaccine. Pain, sensitivity to light, sounds, flashes of light in periphery of vision, dizziness, nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: MRI 10/15/2021 Bloodwork- please contact doctors office CT scan. 10/26/2021 scheduled
Aktuelle Erkrankungen: N/A
Vorgeschichte: Crohn?s Disease w/ileostomy
Andere Medikamente: Stelara-every 8weeks Omeprezole 20mg Vitamin D 2000 units daily Zyrtec 10mg Tylenol 3000mg/daily Benadryl 25mg Sudafed 30mg
Allergien: Environmental Allergies: seasonal allergies, pet dander
Vorherige Impfungen: -

VAERS 1808158

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: VA
Alter: 40,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 10.10.2021
Beginn: 10.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Angina pectoris Back pain Blood test normal Bradycardia Burning sensation Cardiac monitoring Chest X-ray normal Chest pain Dizziness Echocardiogram Headache Heart rate decreased Neuropathy peripheral Pain in extremity Pulmonary pain

Symptomtext

Felt liquid go into arm. I was able to walk and had no issues at the time of administration. By 4pm, felt burning back sensation. Next day, heart was hurting and felt burning sensation on chest as well. Have been to ER twice, but they have not found any issues. Back pain still continues to this day. Lung area feels painful. Intense headaches and dizziness. Legs hurt and fingers feel like they have neuropathy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Urgent care once. ER twice. Heart ultrasound done, but results look to be normal. Heartbeat has decreased. Hospital noted Bradycardia. Currently seeing Cardiologist and will have to carry a monitor to assure this is not an issue. Hospital did a chest Xray, results looked normal. Pain around lung area - back still hurts. Blood work done and listed abnormal. Follow up is scheduled.
Aktuelle Erkrankungen: Brain Aneurysm
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: Almonds, Nitrofurantoin, and Gabapentin
Vorherige Impfungen: -

VAERS 1804470

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: WI
Alter: 66,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 13.10.2021
Beginn: 13.10.2021
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 Nausea Pain Pyrexia Tremor Vaccination site pain

Symptomtext

The first evening after the vaccine, I had strong shaking (the "chills"). In the morning I first took my temperature and had 101.6 fever which lasted all day. My arm was extremely sore at the vaccination site and whenever raising my arm and lasted over three days. I was nauseated all day and slightly nauseated the next day. my fever subsided the next day to 99.6-100. I had a slight headache.

Weitere VAERSDATA-Felder

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

VAERS 1804346

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 14.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Blood test Chest X-ray Chest pain Dyspnoea Electrocardiogram

Symptomtext

I had chest pain and shortness of breath. I went to ER where they gave pain reliever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG Bloodwork Chest X-ray
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Levothyroxine
Allergien: None
Vorherige Impfungen: -

VAERS 1804193

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IN
Alter: 33,0
Geschlecht: M
Eingang: 21.10.2021
Impfdatum: 14.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Blood test Dizziness Fatigue Headache Hypoaesthesia Muscular weakness Myalgia Pain Pain in extremity Paraesthesia Tremor

Symptomtext

As of this date and time, I am still suffering from the following: Numbness in entire left arm and fingers tingle Hands now shake when I hold them up Dizziness Headache Soreness Fatigue Shoulder and neck muscles are sore Legs are weak/tired and hurt behind my knees and muscles

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Decided to visit Dr. Explained issues. She ordered multiple blood test labs to help determine if blood is clotting. Pending lab results
Aktuelle Erkrankungen: Confirmed test results of Covid 19 on 16 Sept 2021
Vorgeschichte: NA
Andere Medikamente: multi-vitamin
Allergien: Dihydrocodeine, bee stings, poison ivy
Vorherige Impfungen: -

VAERS 1803999

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: FL
Alter: 47,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 13.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Chills Injection site bruising Injection site erythema Injection site pain Injection site paraesthesia Injection site pruritus Injection site reaction Injection site swelling Pruritus Pyrexia Rash Rash vesicular

Symptomtext

Site: Bruising at Injection Site-Medium, Site: Itching at Injection Site-Severe, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Systemic: Allergic: Rash (specify: facial area, extremeties)-Medium, Systemic: Chills-Medium, Systemic: Fever-Medium, Additional Details: pt reported today she develop a blistered like rash at the site of injection for the past 7 days after receiving vaccine and start having tingling at the injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1803845

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: IN
Alter: 55,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia Fatigue Injection site bruising Injection site erythema Injection site pain Injection site pruritus Injection site swelling Lethargy Nausea Tremor

Symptomtext

Site: Bruising at Injection Site-Medium, Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Exhaustion / Lethargy-Severe, Systemic: Nausea-Medium, Systemic: Shakiness-Medium, Systemic: Weakness-Medium

Weitere VAERSDATA-Felder

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

VAERS 1801969

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: AZ
Alter: 26,0
Geschlecht: F
Eingang: 20.10.2021
Impfdatum: 17.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Chest pain Dizziness Dyspnoea Oropharyngeal pain Pharyngeal swelling Tachycardia

Symptomtext

Pt REPORTS tachycardia, lightheadedness within 15 minutes of her vaccine. A few hours later, at home she reported chest pain, difficulty breathing, throat pain and throat swelling. She did NOT seek medical attention. She took her kid's EpiPen and benadryl. She followed up with PCP 2 days later, symptoms were already resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None. Pt did not seek emergency medical attention. She presented to PCP office 2 days later after symptoms resolved.
Aktuelle Erkrankungen: chronic cough, asthma, allergies
Vorgeschichte: asthma, allergies, anxiety, chronic headaches, depression, chronic low back pain
Andere Medikamente: Albuterol, allergy medications, montelukast, flovent, flonase
Allergien: rocephin- pt reports anxiety, rash, sob and throat tightness Flu shot- pt reports eye swelling and SOB Both reactions are reported by patient
Vorherige Impfungen: -

VAERS 1801785

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NJ
Alter: 27,0
Geschlecht: M
Eingang: 20.10.2021
Impfdatum: 07.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 12,0
Dosis: 2
Route/Site: IM / LA

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

Blood test normal Chest X-ray Electrocardiogram Limb discomfort Palpitations Panic attack

Symptomtext

For 11 days nothing happened from 10/19/2021 I woke up at the middle of night my heart was raising, I felt like a panic attack, my right arm got very tight. Within 30 seconds to a minute I went to the emergency room. At the emergency room they gave me EKG Test, they gave me IV of fluids, they gave me a chest X-ray and they did blood work. At 7:00AM (6 hrs. after) they discharged me and said that everything is fine. I should follow with the cardiologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: 10/19/1021 Blood test was normal.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1801434

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NY
Alter: 58,0
Geschlecht: M
Eingang: 20.10.2021
Impfdatum: 19.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Arthralgia Chest discomfort Cough Dyspnoea Headache Influenza like illness Lethargy Myalgia Pain in extremity Pyrexia Respiratory tract infection Sinus disorder

Symptomtext

Chest inflammation Shortness of breath Coughing Headache Low grade fever Muscle aches & pain Joint pain Lethargic Flu like symptoms Sore arm Congestion Sinuses

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Abnormal T Waves Enlarged fatty liver Diabetes ll Cataracts Chronic Pancreatitis IBD EPI UC/Proctitis DVT/PE - Factor V Leiden Enlarged spleen Lymphedema Diverticulitis Herniated lumbar disc Rt Ankle peronious brevis tendon tear Umbilical hernia Rt inguinal hernia
Andere Medikamente: Clyndomyicin Ezetimibe 10mg Amlodipine 2.5mg Candesartan 32mg Montelukast 10mg Humulin ru 500 Breo Albuterol Eliquis 5mg Fasenra Pravastatin 40mg Vascepa 1gm Fenofibrate 145mg Metformin 500er Fluticasone Creon 36000 Pantoprazole 40er Lia
Allergien: None
Vorherige Impfungen: -

VAERS 1801210

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 45,0
Geschlecht: F
Eingang: 20.10.2021
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain upper Chest discomfort Chest pain Cold sweat Dizziness Feeling abnormal Flushing Lip swelling Rash Rash pruritic Tremor Urticaria

Symptomtext

Pruritic rash all over armpit. No SOB, No N/V 10-15 min post COVID # 3 shot. Pruritis head all over body to groin, then on feet, hives, lip swelling, tightness and chest epigastric pain. Treated with Benadryl 50 mg, Loratadine 10mg . Then pulse ox dropped to 91%. Lightheaded, dizziness, flushed hot, clammy and shaken. 14:33 138/78 95 99% 16 Benadryl 25mg 14:43 Benadryl 25mg 14:44 Loratadine 10mg 14:46 97/106 15:08 120/60 91% 58 15:35 110/90 98% 91 D/C 16:00 to home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Vitals and pulse ox monitored
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, Ankylosing spondylitis
Andere Medikamente: Trulicity, Simponi
Allergien: Penicillin-Hives
Vorherige Impfungen: -

VAERS 1797772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: TN
Alter: 54,0
Geschlecht: M
Eingang: 19.10.2021
Impfdatum: 18.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Disturbance in attention Dyspnoea Fatigue Headache Influenza like illness Injection site pain Muscular weakness Myalgia Pain

Symptomtext

Muscle pain, severe pain at injection site, flu like symptom, fatigue, headache. muscle weakness, difficulty concentrating, body as a whole pain , I only mention these because the pharmacist said they had no record of any negative side-affects from the Pfizer booster shot. this is almost as bad as shot two/three, which put me down for three days with severe flu/covid -like symptoms. no improvement yet but having minor shortness of breath. I am able to work but want it on record for the sake of others receiving the booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: planning on visiting my primary care physician if symptoms continue.
Aktuelle Erkrankungen: -
Vorgeschichte: A1C - 5.9 Pancriatits - induced by medication (I dont drink)
Andere Medikamente: Rosuvastatin Centrum Silver Plavix Atenalol Crestor Xanax Trintillix suboxone
Allergien: Iodine
Vorherige Impfungen: three-four days of severe flu like symptoms

VAERS 1795763

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MA
Alter: 82,0
Geschlecht: M
Eingang: 18.10.2021
Impfdatum: 13.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Atrial fibrillation Condition aggravated Electrocardiogram abnormal Heart rate increased

Symptomtext

Elevated heart rate, seen at hospital, EKG done, shows afib (has history), states vaccine reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: EKG
Aktuelle Erkrankungen: -
Vorgeschichte: afib, hypokalemia, history of PE, embolism and thrombosis BLE, CKD stage 3, MDD, HF, edema, intervertebral disc disorder thoracic/lumbar, BPH
Andere Medikamente: Alfuzosin 10 mg Lasix 40mg Potassium Chloride 20mEq Sertraline 25mg Eliquis 5mg Diltiazem ER 180mg
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1795435

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge FF8841

moderat

Staat: OK
Alter: 67,0
Geschlecht: M
Eingang: 18.10.2021
Impfdatum: 12.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Asthenia Dysstasia Fatigue Gait disturbance Impaired work ability Inability to crawl Mobility decreased

Symptomtext

I was very wobbly walking and the morning after the vaccine (Pfizer Booster shot and regular Flu Shot) and my wife had to assist me to get to the bathroom. As I finished urinating, I could not stay standing and didn't fall but went down to the floor by the toilet and could not get up. I could not even crawl to get out of the bathroom. I had extreme fatigue caused by trying to get up. It was like all my strength was gone. I called for my wife and she assisted me to crawl out of the bathroom but only made it to the door. After resting awhile (15 minutes), with much difficulty, my wife assisted me to get up into a rolling desk chair. I stayed in the chair for a few hours after she rolled me to my desk where I could do some work at the computer but it was really hard to sit up. After this time, I was able to stand and walk very carefully to my regular easy chair. I stayed there the rest of the day. The rest helped and I was able to walk but it was pretty unsteady. I went to bed about 10pm and when I woke up, I felt much better and could walk but I tired easily. Each day after this incident things have gotten better and better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Didn't go in for Medical Tests
Aktuelle Erkrankungen: None
Vorgeschichte: Main issues are pain over many years, Neuropathy and Pain in feet, Lower Back Pain, Neck Pain
Andere Medikamente: Allopurinol, Busiprone, Amlodopine, Tamulosin, Lisinopril, Buprenorphine, Diclofenac, Fluoxitine, Testosterone injection, Pregabalin
Allergien: none
Vorherige Impfungen: -

VAERS 1795305

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 31,0
Geschlecht: M
Eingang: 18.10.2021
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Hypoaesthesia oral Paraesthesia oral

Symptomtext

Patient started to have tingling on lips and numbness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: NA
Vorgeschichte: Syncope and collapse
Andere Medikamente: NA
Allergien: NA
Vorherige Impfungen: -

VAERS 1794359

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: WA
Alter: 29,0
Geschlecht: F
Eingang: 17.10.2021
Impfdatum: 15.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Limb discomfort Mobility decreased Oedema peripheral Pain

Symptomtext

The day after my covid booster, I woke with a large amount of swelling under my arm, in the armpit. I have heard of and experienced swelling at the injection site but not this so I thought it would be good to report it. There is almost constant discomfort, and it prevents me from letting my arm fully relax at my side or lifting my arm above my shoulder without pain. The amount of swelling is fairly large, as when I look into the mirror, my armpit no longer has a concave profile. It is now convex. I had gotten 2 other vaccines that day. They were a Tdap and a flu shot, although I do not know the brand or lot number. I selected Tdap(Boostrix) and Influenza (Seasonal)(Fluzone Quadrivalent), but that was just a guess, because I had to choose something on the list. The swelling in my armpit is on the left side, which is the same arm as where I got the covid booster and I believe the flu shot. I think the Tdap shot was in my right arm, but I might be mixing up which arms the flu and Tdap shots went into. I have not gone to my physician, because it has only been about 36-40 hours, and the swelling has gone down slightly (but not much).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: losartan, spironolactone, estradiol
Allergien: Sulfa based drugs, bee venom
Vorherige Impfungen: Previous doses of the Pfizer Covid-19 vaccine resulted in swelling at injection site and flu like symptoms

VAERS 1794259

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: TX
Alter: 74,0
Geschlecht: F
Eingang: 17.10.2021
Impfdatum: 13.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Mobility decreased Pain Pyrexia Somnolence

Symptomtext

Had chills and fever and achy. Woke up on the floor next to my bed and had a lot of trouble getting back in bed. Had fever most of the day and slept most of the day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: no
Vorgeschichte: Breast Cancer
Andere Medikamente: none
Allergien: nsaids
Vorherige Impfungen: -

VAERS 1794159

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MA
Alter: 70,0
Geschlecht: F
Eingang: 17.10.2021
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Diabetic neuropathy Disorientation Dizziness Extra dose administered Fatigue Headache Pain Pyrexia Somnolence

Symptomtext

Patient called on 10/16 to say she had a reaction to her Pfizer booster vaccine she received on 10/14/21. About 2 hours after she felt extremely exhausted, tired, fatigued and sleepy. She also had a fever, body aches, headache was dizzy and disoriented. She also said that her diabetic neuropathy was really acting up. She stated that she was feeling much better by the next day (10/15/2021). I told her that her symptoms were pretty consistent with normal vaccine reaction but to call md if she's any worse. I also advised her to stay hydrated and to take acetaminophen or ibuprofen if needed and to rest. She was also going to report reaction to VAERS

Weitere VAERSDATA-Felder

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

VAERS 1794128

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: AZ
Alter: 34,0
Geschlecht: F
Eingang: 17.10.2021
Impfdatum: 03.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal pain upper Blood lactic acid Blood test Chest pain Culture Diarrhoea Dizziness Electrocardiogram Headache Immunodeficiency Influenza A virus test Influenza B virus test Lipase Liver function test Metabolic function test Nausea Polymerase chain reaction Red blood cell count

Symptomtext

Received booster on Sunday, 10/3 at 3:00 PM (3rd dose), by Monday at 2:00 AM began to feel normal symptoms such as nausea, headache, dizziness, but by Tuesday, 10/5 at 10 PM had significant stomach pains at a 10 out of 10 (similar to feeling food poisoning). I also had chest pain. I felt dizzy and lightheaded as well. I then began to have violent diarrhea that would not stop (15+ times per day) and ended up in the emergency room on Thursday, 10/7, where I received fluids, and they monitored my heart. I was still having diarrhea at that time. They saw on EKG that I now had Long QT (at 500), which I've only had in the past secondary to medication. I did not have Long QT again prior to this event as I had an EKG in May 2021 and it did not show Long QT. They also tested me for everything including my fecal, COVID PCR test, influenza A, B, and all was negative. The ER doctor informed me that he thought it was related to the vaccine. I'm filing this report to make others aware that this could potentially happen, and there could be an impact on the QT/QTC for the heart.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: ECG while in ER at Clinic Hospital on 10/7 GIPA Screen Culture 10/5 at hospital on 10/7 Bacterial Eneteric Pathogens PCR at hospital 10/7 Influenza A,B/SARS CoV-2, PCR at hospital 10/7 Complete Blood Count at hospital 10/7 Metabolic/Electrolyte Panel at hospital 10/7 Liver Function Panel at hospital 10/7 Lactic Acid Level at hospital 10/7 Lipase Level at hospital 10/7 Troponin T at hospital 10/7 Nucleated RBC at hospital 10/7
Aktuelle Erkrankungen: none
Vorgeschichte: postural orthostatic tachycardia syndrome, asthma, history of long QT syndrome secondary to medication, circulation and blood pressure issues
Andere Medikamente: Zoloft 25 miligrams
Allergien: Methylprednisolone, thimerosal
Vorherige Impfungen: -

VAERS 1794118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IL
Alter: 34,0
Geschlecht: F
Eingang: 17.10.2021
Impfdatum: 15.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Chills Fatigue Headache Lymphadenopathy Lymphoedema Migraine Pain

Symptomtext

Lymphedema, swollen lymph nodes in left arm, armpit, left side of chest, and lower neck. Symptoms started 8 hours after injection. Headache/migraine, body aches, fatigue started 12 hours after injection, chills started 24 hours after injection. Headache/migraine, body aches, fatigue, chills subsided 24 hours later, lymphedema/swollen lymph nodes still on going.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Sinus infection
Vorgeschichte: None
Andere Medikamente: Prenatal vitamin, amoxicillin
Allergien: None
Vorherige Impfungen: -

VAERS 1793928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 37,0
Geschlecht: M
Eingang: 16.10.2021
Impfdatum: 30.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Mobility decreased Pain

Symptomtext

Significant and worsening pain in my upper left shoulder. I am unable to rotate or lift my arm above my head without significant pain. I have contacted my healthcare provider but have not been see due to lack of appointments. I am taking over-the-counter pain medication and icing constantly with little to no relief.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Spoke with nurse over the phone on Saturday October 16th. Recommended ice. Scheduled Doctor appointment on October 29th.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Cat dander, dust mites
Vorherige Impfungen: -

VAERS 1793842

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: FL
Alter: 69,0
Geschlecht: M
Eingang: 16.10.2021
Impfdatum: 13.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / RA

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

Chills Cold sweat Dry mouth Feeling abnormal Flushing Headache Hyperhidrosis Pain in extremity Piloerection Sciatica Sleep disorder Tremor

Symptomtext

One day after the Covid-19 Pfizer booster shot, my wife and I noticed that I could not finish a meal - this is extremely unusual for me. That night, October 14, 2021, I felt flushed before bed and my right arm where the shot was given was VERY sore. After going to sleep about 09:30pm, I was awakened at about 03:00am with severe chills and shaking all over, with a clammy/sweaty "goose bumped" feeling all over. Additionally, I felt severe "sciatic-like" pain extending from the middle of both right and left shoulders down both arms, and down my left leg. This was miserable. I got out of a sweaty bed and took 3 ibuprofen with a full glass of water, then sitting up until about 4:15am, at which time I went back to bed and slept through until 09:30am on the morning of October 15, 2021. I felt somewhat normal starting around Noon on October 15, but not "completely right"...my body felt "off" somehow. Around 10:00pm October 15, I went to bed and was suddenly awakened at 01:30am with SEVERE SWEATING - the whole bed was soaking wet including the pillow - and SEVERE sciatic like pain again shooting down both arms from my shoulders, but not my leg this time. I also had a mild headache and felt flushed and had dry mouth that I could not "cure" right away. Again, I took more ibuprofen and then again sat up waiting for the extreme pain to subside, which it did by the time I went to bed again around 03:45am. I then slept hard and awoke at 10:15am today, Saturday, October 16, 2021. I still do not feel "right" and at home trying to rest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: No other illnesses but being treated for neck and back injuries from car accident (no drugs)
Vorgeschichte: Adult onset asthma type 2 diabetes
Andere Medikamente: ALL TAKEN DAILY 1X DAILY EXCEPT WHERE SHOWN: Amlodipine 2.5mg Atorvastatin 80mg Bupropion 75mg Glipizide 5mg Hydrochlorothiazide 25mg Losartan 100mg Metformin 1000mg - 2x/day Metoprolol (Toprol) 25mg Plavix (Clopidogrel) 75mg Low Dose Baby
Allergien: No known allergies to anything but ketchup and pancake syrup make me sweat.
Vorherige Impfungen: -

VAERS 1793655

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IA
Alter: 12,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: 08.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / -

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

Blood creatine phosphokinase MB Blood creatine phosphokinase increased Chest pain Echocardiogram normal Electrocardiogram normal Fatigue Headache Pain Troponin increased

Symptomtext

Patient had common side effects on post-vaccination day 1 (body aches, fatigue, HA) which resolved within 24hr however patient then developed stabbing mid-sternal chest pain on the morning of 10/11 (3 days post-vaccination). Initial troponin level was 2.18 as well as CKMB at 19.6. Troponin peaked at 7.84 (roughly 24hr after symptom onset - 10/12@0400) then began declining that evening (10/12@1600). Chest pain was mild, intermittent and completely resolved within 12 hours of arrival after NSAID initiated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 2,0
Labordaten: Troponin: 2.18 -- >7.01 -- > 7.84 -- > 3.52 -- > 3.42 CKMB: 19.6, total CK 189 (normal) EKG: no abnormal rhythms noted ECHO: normal structure and function
Aktuelle Erkrankungen: asymptomatic COVID19 infection - tested positive 9/1/2021
Vorgeschichte: MCAD deficiency
Andere Medikamente: levocarnitine
Allergien: none
Vorherige Impfungen: -

VAERS 1790982

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff8841

moderat

Staat: MA
Alter: 44,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: 29.09.2021
Beginn: 29.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Anxiety Arthralgia Back pain Chills Dry mouth Dysgeusia Fatigue Inflammation Neck pain Pain Pain in extremity Palpitations Respiratory rate increased Tongue discomfort Vision blurred

Symptomtext

vision got a little fuzzy; heart started racing really fast; breathing fast; anxiety; metallic taste in my mouth; tongue felt a little funny; tired; severe dry mouth; soreness/pain in my joints; soreness/pain in fingers; soreness/pain in neck; soreness/pain in back; soreness/pain in whole body; feeling chilly; inflammation; This is a spontaneous report from a contactable consumer (patient). A 44-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration, administered in left arm on 29Sep2021 (at the of 44 years old) (Batch/Lot Number: Ff8841) as dose 1, single for covid-19 immunisation. Medical history included neutropenia, plaquepsoriasis, and endometriosis from an unknown date and unknown if ongoing, covid-19 from Feb2021 to an unknown date. The patient was not pregnant at time of vaccination. Concomitant medication included multivitamin. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced vision got a little fuzzy, heart started racing really fast, breathing fast, anxiety, metallic taste in mouth, tongue felt a little funny, tired, severe dry mouth, soreness/pain in joints, soreness/pain in joints, fingers, neck, back, whole body, feeling chilly, and inflammation on 29Sep2021. Within mins of dose, patient's vision got a little fuzzy but quickly resolved and heart started racing really fast. She was also breathing fast. About 5-10 mins it got better. She was not sure if it was anxiety or related to the medication. She was calm during injection so it was strange this happened. She also had a metallic taste in her mouth and her tongue felt a little funny. She was tired for the rest of the day. Overnight she woke up with severe dry mouth which has never happened to her. She soreness/pain in her joints, her fingers, neck, back, her whole body. She was feeling chilly but no fever as of now. She had Covid in Feb2021 and felt the same inflammation, pain/soreness in her body but not as severe. Since the vaccination, the patient has not yet been tested for COVID-19. The events were reported as non-serious. No treatment was received for the events. The outcome of a little fuzzy, heart started racing really fast, breathing fast, and anxiety was recovered in Sep2021 while the rest of the events was not recovered. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (I had Covid in Feb2021. if covid prior vaccination: Yes); Endometriosis; Neutropenia; Plaque psoriasis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1788762

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 30,0
Geschlecht: F
Eingang: 15.10.2021
Impfdatum: 13.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chest X-ray Chest pain Differential white blood cell count Electrocardiogram Full blood count Human chorionic gonadotropin Insomnia Metabolic function test Troponin I

Symptomtext

On 10/13 the night I got my shot I had difficulty sleeping, slept only 2-3 hours which is very unusual, 10/14 started experiencing mild chest pain, 10/15 went to ER doctor because chest pain persisted. My sleep returned to normal by 10/14

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: On 10/15 in the ER I was given CBC w/ diff, comprehensive metabolic panel, ER troponin-1, HCG,serum, qualitative ECG 12 lead, x ray chest AP portable
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1788636

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: TX
Alter: 19,0
Geschlecht: F
Eingang: 15.10.2021
Impfdatum: 13.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Breast pain Chest pain Lymphadenopathy

Symptomtext

lymph nodes inflamed due to the vaccine and pain protruding to her left breast causing chest pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: no
Andere Medikamente: unknown
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1788416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 93,0
Geschlecht: M
Eingang: 15.10.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Asthenia Bundle branch block right Condition aggravated Coronary arterial stent insertion Dehydration Electrocardiogram abnormal Gait inability Heart rate increased Platelet count decreased Troponin I increased

Symptomtext

93 yo M hx of HLD HTN RBBB presenting with weakness and feeling dehydrated. Patient had received covid-19 shot and was unable to walk to his car (200 ft), because he was weak. Asked another patient for help and they alerted staff, who wheeled him to the ED. Patient initially declining any intervention, not in pain, or mental confusion. Vital signs mostly normal, elevated heart rate, ran ekg and tropinin Patient Sent to cardiac unit at local Hospital then transferred to another HCF for stent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 5,0
Labordaten: Troponin I 0.77 (H) - 0.00 - 0.04 ng/mL Platelets count 95 (L) 140 - 400 K/uL ECG elevated ecg was done - elevated RBBBB on II III AVF HEART
Aktuelle Erkrankungen: None
Vorgeschichte: CHRONIC BRONCHITIS HYPERLIPIDEMIA HTN (HYPERTENSION) PREDIABETES THORACIC AORTIC ANEURYSM RIGHT BUNDLE BRANCH BLOCK BPH (BENIGN PROSTATIC HYPERTROPHY) ATHEROSCLEROSIS OF AORTA ALCOHOL PREVENTION COUNSELING RIGHT PSEUDOEXFOLIATION GLAUCOMA, SEVERE STAGE CKD STAGE 3B (GFR 30-44) LEUKOPENIA THROMBOCYTOPENIA, UNSPECIFIED
Andere Medikamente: LisinoprilaL Alvesco Lorzolimide Lumican Vitamin C, D, Zinc
Allergien: -
Vorherige Impfungen: -

VAERS 1788102

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: LA
Alter: 64,0
Geschlecht: F
Eingang: 15.10.2021
Impfdatum: 05.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Atrial fibrillation Pyrexia Tachycardia

Symptomtext

Patient reported severe tachycardia, fever over 101 degrees and atrial fibrillation.

Weitere VAERSDATA-Felder

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

VAERS 1787909

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: NY
Alter: 35,0
Geschlecht: F
Eingang: 15.10.2021
Impfdatum: 13.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Chills Headache Nausea Tremor

Symptomtext

started at 3:43 PM. body shake, chills, bad headache and a bit nauseous.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: tylenol
Allergien: none
Vorherige Impfungen: flu, 2019, 33, weak ,chills, fever, stomach cramps

VAERS 1786561

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: NV
Alter: 41,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 04.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / LA

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

Fall Hypoaesthesia Injection site pain Injection site swelling Lymphadenopathy Muscular weakness Pain Pain in extremity Paraesthesia

Symptomtext

Swelling under arm, pain and swelling in injection site, swollen lymph nodes, pain in right arm radiating upwards, severe pain and numbness in both legs from hips and ankles. Falling over from legs being weak. Tingling sensation in both legs.

Weitere VAERSDATA-Felder

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

VAERS 1785741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: TX
Alter: 43,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 11.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: IM / -

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

Hypoaesthesia Paraesthesia

Symptomtext

constant numbness, tingling on the left side (arm, hand leg) and intermittent numbness and tingling on the right side

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: asthma. ulcerative colitis
Andere Medikamente: multivitamin
Allergien: amoxicillin, azithromycin
Vorherige Impfungen: -

VAERS 1785648

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NY
Alter: 70,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 05.02.2021
Beginn: 09.10.2021
Tage bis Beginn: 246,0
Dosis: UNK
Route/Site: SYR / LA

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

Amnesia Blood test Computerised tomogram Extra dose administered Headache Hypertension Sleep disorder Urine analysis

Symptomtext

Severe headache from booster shot which require a visir to ER late morning 10/13. Headache work me up at 10/13 at Midnight. For a brief time I could not remember birth date, phone numbers, email address. My blood pressure was 180 over 90. The only they could deduce was that it was a result of high blood pressure caused the booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: All tests on 10/13. CT scan Blood work Urine test Blood pressure testing
Aktuelle Erkrankungen: -
Vorgeschichte: RA
Andere Medikamente: Omeprazole Eliquis Metroprolal Lisinopril HCTZ Budesonide Garapenton Enbrel
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1783793

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IA
Alter: 54,0
Geschlecht: F
Eingang: 13.10.2021
Impfdatum: 30.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Dehydration Extra dose administered Eye irritation Fatigue Hyperhidrosis Impaired work ability Lymph node pain Malaise Nausea Pain Palpitations Vomiting

Symptomtext

I was told by the pharmacist that whatever side effects I had from my second shot would likely be the same for my booster, so that?s what I was expecting: extreme fatigue, chills and body aches. The majority of my symptoms began 24 hours after the booster. I wasn?t feeling well when I woke up the morning after but still went to work. By 10a I was feeling unwell enough that I had to leave and come home. I was very fatigued, achy, and my eyes burned like when you have the flu. By 5p I was exponentially worse. I had nausea and could barely get my evening pills down. The lymph nodes in my armpits, neck and inguinal region were very tender, nothing like I?ve ever experienced before in past illnesses. I ached from my toenails to the hair on my head. I took my temperature and it was 98.3, normal by medical standards though I usually run 96-97. By 8p I was vomiting and kept that up until I went to bed about 11p. I was so miserable I didn?t even have the energy to cry about it. At 2p I woke up with heart palpitations, I think, brought on by dehydration. I had completely soaked the sheets and pillow with sweat. I contemplated going to the ER to get rehydrated (I avoid hospitals and doctors so to even entertain this idea is a testament to my misery), but remembered it would cost me my deductible, so I laid back in bed, chilling in the sweat-soaked sheets waiting for the grim reaper. By 3a I suddenly turned the corner and felt maybe I might survive this. I didn?t ache as bad and could hold down sips of water. By 8a (Saturday) I was eating toast and by 7p collecting my sister from the airport. Back to 85% on Sunday and 100% on Tuesday. What a ride that was, but can?t say I regret getting the booster. I?m convinced now I?d die for sure if I caught Covid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: Type II diabetes Hypertension and arrhythmia (occasional) Gout (occasional)
Andere Medikamente: Clonidine Alopurinol Metformin Lasix Bystolic Flaxseed Oil
Allergien: Penicillin ACE inhibitors ARBs
Vorherige Impfungen: Age 54, mild reaction to Pfizer Covid vaccine, see above

VAERS 1783769

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: IL
Alter: 57,0
Geschlecht: F
Eingang: 13.10.2021
Impfdatum: 13.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea

Symptomtext

Gave both vaccines flu and covid, one in each arm at about 8 pm. 10 minutes later, patient had trouble breathing. Administered Epipen. Patient started to breathe better after epipen. Fire department came and assessed her. Went home on her own.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Back surgery
Andere Medikamente: -
Allergien: aspirin, gabapentin, ibuprofen, vancomycin, erythromycin
Vorherige Impfungen: -

VAERS 1782327

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: FL
Alter: 74,0
Geschlecht: F
Eingang: 13.10.2021
Impfdatum: 04.10.2021
Beginn: 04.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Ageusia Chills Diarrhoea Dizziness Dysgeusia Eating disorder Headache Hyperhidrosis Mobility decreased Pain Pyrexia Thinking abnormal

Symptomtext

Patient stated that she has extreme diarrhea. Has been having body aches, lot taste, had a bad taste in mouth, fever, headaches, chills, lightheaded, skewed thinking, sweating, has to change clothes at least three times a night due to sweating. Patient couldn't move out of bed for at least a day and a half. Every time she eats, she has to go to the bathroom. She stated that she's unable to eat things that used to like.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: Blood pressure meds Metformin Motulukast Losartin Hydrochlrcide Nasal spray Zinc Maxi hair plus, biotin Cinnamon Ometprozole Cymbacourt
Allergien: NONE
Vorherige Impfungen: -

VAERS 1780454

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: CA
Alter: 35,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 04.10.2021
Beginn: 04.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dyspnoea Extra dose administered Wrong product administered

Symptomtext

Covid vaccine dose #4 given in error (pt was suppose to get flu shot + 1 covid 3rd dose), pt instead received 2 covid 19 vaccine and once rph realized error, pt received flu shot. Error occurred due to distraction and talking to patient. Rph followed up with patient next day and husband stated pt had some shortness of breath earlier but no problems (24 h later)

Weitere VAERSDATA-Felder

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

VAERS 1780454

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: CA
Alter: 35,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 04.10.2021
Beginn: 04.10.2021
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Dyspnoea Extra dose administered Wrong product administered

Symptomtext

Covid vaccine dose #4 given in error (pt was suppose to get flu shot + 1 covid 3rd dose), pt instead received 2 covid 19 vaccine and once rph realized error, pt received flu shot. Error occurred due to distraction and talking to patient. Rph followed up with patient next day and husband stated pt had some shortness of breath earlier but no problems (24 h later)

Weitere VAERSDATA-Felder

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

VAERS 1780126

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IA
Alter: 48,0
Geschlecht: M
Eingang: 12.10.2021
Impfdatum: 02.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / RA

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

Chest discomfort Chills Dyspnoea Fatigue Pain Pyrexia SARS-CoV-2 test negative

Symptomtext

99.5 fever started on Tuesday, Weds through Thursday sustained 102.6 fever, body aches, chills, tiredness, tightness in chest, slight shortness of breath

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID test on Weds - Negative
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Flu vaccine day before, vitamin d3, calcium, iron, anastrozole, testosterone, tadalafil, pantoprazole, clomiphene
Allergien: None
Vorherige Impfungen: -

VAERS 1779896

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 05.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: UN / LA

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

Chest pain Dyspnoea Fatigue Heart rate increased Lymph node pain Lymphadenopathy

Symptomtext

Rapid heartbeat, chest pain, shortness of breath, swollen and painful lymph nodes, extreme fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Could not be determined at ER.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Compazine, Reglan, traMADol
Vorherige Impfungen: -

VAERS 1779606

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

moderat

Staat: NJ
Alter: 83,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 09.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Decreased appetite Pain Paraesthesia Paraesthesia oral

Symptomtext

pt reports whole body aches since vaccine and as of 10/12/21 feeling of pins and needle, tingling on the tongue. Pt also reports loss of appetite.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: xarelto, metoprolol, meloxicam, glimepiride
Allergien: codeine
Vorherige Impfungen: -

VAERS 1779043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: LA
Alter: 15,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 05.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chest X-ray normal Dyspnoea Full blood count normal Headache Metabolic function test Nausea Pyrexia SARS-CoV-2 test negative

Symptomtext

FEVER 103.2, HEADACHE, NAUSEA, SHORTNESS OF BREATH

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID TEST NEGATIVE. CMP ALL NEGATIVE, , CBC NEGATIVE, CHEST XRAY NEGATIVE
Aktuelle Erkrankungen: RECENTLY DELIVERED BABY ON SEPT 22ND.
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1778775

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff8841

moderat

Staat: -
Alter: 36,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Paraesthesia Pharyngeal swelling Swollen tongue

Symptomtext

Diffuse body tingling, mild tongue and throat swelling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: -
Andere Medikamente: Lexapro, prenatal vitamin.
Allergien: Yellow jacket stings.
Vorherige Impfungen: -

VAERS 1777342

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: TN
Alter: 25,0
Geschlecht: M
Eingang: 11.10.2021
Impfdatum: 06.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Chest pain Electrocardiogram

Symptomtext

Chest Pain - taking ibuprofen - 3 days, condition seems to be improving

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG, blood pressure, heart rate
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Minocycline 100 mg
Allergien: None
Vorherige Impfungen: -

VAERS 1775357

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: TX
Alter: 53,0
Geschlecht: F
Eingang: 09.10.2021
Impfdatum: 08.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / -

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

Asthenia Blood test Diplegia Fatigue Feeling cold Full blood count Gait inability Hypothermia Incontinence Magnetic resonance imaging Mobility decreased Multiple sclerosis Muscle fatigue Myalgia Pain SARS-CoV-2 test Sleep disorder Tremor

Symptomtext

RE: COVID-19 2nd shot adverse reactions Patient 2:04 PM Woke up at 3am in hypothermic body shaking under 5 blankets but body was fine and warm. Having a psychosomatic freezing reaction. Lost all muscle functioning ability from mid back down thru toes. Completely unable to walk exactly 12 hours from shot. Incontinence w/complete voiding on the floor. Like the shot used and attacked my body using my MS as the pathway. Unable to move hips or legs, lower body paralysis, and no strength and had to crawl across the floor with my fingertips pulling me to shower. Took 1 hour to crawl. Excruciating muscle pain throughout lower half of body. My MS has never hurt. Had worse reaction than the Ocrevus infusion for MS that left me with walking issues and lost complete ability to dance and run 3 weeks after 2nd half dose. Had battled back from that with significant improvement this month. In 12 hours time while sleeping complete exhaustion, extreme muscle pain and muscle fatigue. At 24 hours past injection and still cannot sit up or prop myself over. Can barely roll over. I am in so much pain! No issues with 1st shot. All symptoms of Guillaine Barre which was not supposed to happen with the pfizer shot. Paralysis and body aches have now subsided at 1800hrs 10/9. 27 hours of agony

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Complete Viral, covid, meningitis CBC and MRIs to clear for vaccine and new long term MS therapies on 8/232021 thru 9/13/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Multiple sclerosis Raynauds Syndrome Pituitary Adenoma Hashimito's Thyroiditis All under control
Andere Medikamente: -
Allergien: Tramadol Nitrous Oxide Ocrevus verified lab results Sept 2021
Vorherige Impfungen: -

VAERS 1775271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: AZ
Alter: 20,0
Geschlecht: M
Eingang: 09.10.2021
Impfdatum: 06.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / -

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

Chest pain Troponin increased

Symptomtext

patient received vaccine within 48 to 72 hours from time of dose patient presented to the emergency department with chest pain and an elevated troponin of 6.05.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Troponin at 6.05 . Ref range of 0.00 to 0.03ng/ml
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1772977

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IN
Alter: 24,0
Geschlecht: F
Eingang: 08.10.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Dyspnoea Paraesthesia

Symptomtext

Patient experienced dizziness and tingling in extremities shortly after vaccination (within approximately 5 minutes of injection). Stated shortly after, she was also having trouble breathing at the time. Patient sat down in the waiting room with feet raised for several minutes after experiencing side effects. After approximately 5 minutes of resting patient stated symptoms were abating. Tingling in the extremities and dizziness seemed to resolve completely approximately 15 to 20 minutes after vaccine administration. Patient did not describe any issues with breathing. At 30 to 45 minutes after vaccination, patient stated she was no longer experiencing any side effects and she felt safe taking herself home.

Weitere VAERSDATA-Felder

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

VAERS 1771928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MN
Alter: 86,0
Geschlecht: M
Eingang: 08.10.2021
Impfdatum: 17.02.2021
Beginn: 07.10.2021
Tage bis Beginn: 232,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Condition aggravated Cough Fall Respiratory tract congestion Vaccine breakthrough infection

Symptomtext

This case meets vaccine breakthrough review. SxS include cough/congestion, weakness, fall.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic conditions/PMH include HTN, HLD, TIA, falls.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1770586

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: IN
Alter: 28,0
Geschlecht: F
Eingang: 08.10.2021
Impfdatum: 21.09.2021
Beginn: 22.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Back pain Chest pain Drug hypersensitivity Dyspnoea Lip swelling Pain Pruritus Swollen tongue Urticaria

Symptomtext

having an allergic reaction; Tongue and lips swelling; Tongue and lips swelling; covered in hives; itchy; trouble breathing; chest and back pains; chest and back pains; Stinging/stabbing; This is a spontaneous report from a contactable consumer (patient). A 28-year-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection Lot Number: FF8841), via an unspecified route of administration in left arm on 21Sep2021 at 13:15 (at the age of 28 years old, not pregnant at the time of vaccination) as dose 1, single for covid-19 immunisation. Medical history included asthma from an unknown date and unknown if ongoing. The patient had no known allergies. There were no concomitant medications. The patient did not receive other medications in two weeks. The patient did not receive any other vaccines within 4 weeks. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient hasn't been tested for COVID-19. On 22Sep2021 at 4:30 am she woke up around the morning after the shot having an allergic reaction. Tongue and lips swelling, covered in hives, itchy, trouble breathing. She used a primatene mist inhaler and chewed 50 mg of benedryl and began to get better shortly after. The next day she started having right side chest and back pains. Stinging/stabbing. Which have not subsided. Therapeutic measures were taken as a result of having an allergic reaction, tongue and lips swelling, covered in hives, itchy, trouble breathing, chest and back pains, stinging/stabbing. Treatment received at home from herself. No hospitalization required. Reporter considered events as non-serious. The chest and back pains, stinging/stabbing was not recovered, while with other events was recovering. Follow-Up (30Sep2021): 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 1768795

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 77,0
Geschlecht: F
Eingang: 07.10.2021
Impfdatum: 05.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Chills Fatigue Feeling abnormal Feeling hot Malaise Mobility decreased Nasal congestion Nausea Pain

Symptomtext

Began with tiredness and intermittent chills in the late afternoon, early evening. Felt very ill, very hot around 9.30 pm, and took my temperature. It was 99.0 degrees (normal for me is 93 to 94 degrees). I began to feel very slightly nauseous off and on during the night. Continued to take temperature during the night and finally, it dropped to 97.5 at 5 am in the morning. I felt very bad at 11.30 pm on the 6th. I still feel very tired and ache-y. Need to stay in bed. I also had a lot of stuffy-ness in my nose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None. I called my Dr.'s office and they said I was just experiencing side effects.
Aktuelle Erkrankungen: Prior Bronchitis. Diabetes. ILD, Sarcoidosis, Heart
Vorgeschichte: Sarcoidoses, ILD, Degenerative arthritis
Andere Medikamente: Diltiazem 120 mg; Xarelto 20 mg; Spironolactone. 25 mg; Norco with Acetaminaphin 325; Basaglar KwikPen Insulin; Fluticasone Prop Nasal Spray 50 mcg 1/day;
Allergien: Aspirin, Sulpha, Penicillins & Sporins, Preservatives AZO group,
Vorherige Impfungen: Shingles. Swollen arm, hot, rash. About 2012

VAERS 1765025

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NY
Alter: 66,0
Geschlecht: M
Eingang: 06.10.2021
Impfdatum: 06.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SC / LA

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

Dysgeusia Paraesthesia oral

Symptomtext

METALLIC TASTW, TINGLING OF LIPS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: LIPITOR, ZOLOFT
Allergien: XYVOX
Vorherige Impfungen: FLU VACCINE - SAME ADVERSE RESPONSE AS TODAY

VAERS 1759757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff8841

moderat

Staat: NY
Alter: 55,0
Geschlecht: F
Eingang: 04.10.2021
Impfdatum: 01.10.2021
Beginn: 02.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / -

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

Chills Cough Dyspnoea Headache Oropharyngeal pain Paranasal sinus discomfort Rhinorrhoea Wheezing

Symptomtext

Shortness of breath, wheezing, cough, sore throat, sinus pressure, headache, runny nose, chills

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: N
Allergien: None
Vorherige Impfungen: Influenza

VAERS 1759018

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NY
Alter: 25,0
Geschlecht: F
Eingang: 04.10.2021
Impfdatum: 01.10.2021
Beginn: 03.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Lymphadenopathy Migraine with aura

Symptomtext

Swollen axillary lymph nodes ipsilateral to injection site, experienced 2 days following injection, improving Migraine with aura (visual disturbance) evening following injection, resolved without sequalae

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine with aura
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Spironolactone
Allergien: Macrobid
Vorherige Impfungen: -

VAERS 1757136

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MA
Alter: 74,0
Geschlecht: F
Eingang: 03.10.2021
Impfdatum: 02.10.2021
Beginn: 02.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dysphagia Dyspnoea Throat tightness

Symptomtext

I woke up at 12:45 am from sleep to find my throat uncomfortably tight. I could not breathe or swallow. I took 2 OTC Benadryl and within 45 minutes I felt my throat less tight. I was more comfortable. I went back to sleep and awoke at 3:00 am. My throat felt much better. I took 2 more Benadryl at 7:45 am because my throat felt a little tight.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoporosis, high blood pressure, ASD
Andere Medikamente: Amlodipine Besylate 5mg; Calcium, Magnesium
Allergien: Eggs, Benicar, Ciprofloxacin, Hydrochlorothiazide, Hydroxyzine HCL, Influenza vaccine, Iodinated contrast media, Lisinopril, Olmesartan, Penicillin, Sulfa, Triamterene
Vorherige Impfungen: Influenza vaccine; Shingrix (shingles vaccine) 06/14/2021 and 8/30/2021.

VAERS 1757134

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: MA
Alter: 41,0
Geschlecht: F
Eingang: 03.10.2021
Impfdatum: 01.10.2021
Beginn: 01.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Anxiety Dyspnoea Erythema Pruritus Scratch Throat irritation Throat tightness Vomiting

Symptomtext

5 minutes after the administration of the Pfizer vaccine, the patient became extremely anxious and started scratching everywhere stating that she was itchy everywhere and could not breathe. She stated that her throat felt itchy and was closing. At this time, VS were unable to be obtained because the patient was flailing her arms. Her skin was red where she was scratching , but hives were not observed. A Code was called for assistance. An Epipen was administered and the patient began to vomit. Benadryl 50 mg was administered IM. She was still extremely anxious and crying and scratching her entire body. Examined by physician who noted no throat swelling and no hives, but she continued to state she could not breathe. Paramedics arrived. VSS...transported to hospital where she was seen and treated in the ER with Solumedrol and discharged with Benadryl.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma Dry eyes Reflux
Andere Medikamente: Advair Anusol Polyethylene Glycol Singulair Proair Albuterol Micotin Fluomethone Tears Renew Systene Tessalon MVI Omeprazole
Allergien: Morphine Motrin PCN Ondansetron Sulfa Tetracyclines Vancomycin
Vorherige Impfungen: -

VAERS 1757111

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: NJ
Alter: 14,0
Geschlecht: F
Eingang: 03.10.2021
Impfdatum: 02.10.2021
Beginn: 02.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Abdominal pain Dyspnoea Eye swelling Mouth swelling Swelling face Swollen tongue Tremor

Symptomtext

Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Mild, Systemic: Abdominal Pain-Medium, Systemic: Shakiness-Mild

Weitere VAERSDATA-Felder

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

VAERS 1753986

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff8841

moderat

Staat: MA
Alter: 50,0
Geschlecht: F
Eingang: 01.10.2021
Impfdatum: 30.09.2021
Beginn: 30.09.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Blood test Chest X-ray Cold sweat Dizziness Dyspnoea Electrocardiogram Feeling cold Headache Nausea Photophobia

Symptomtext

Nausea, dizziness, weakness, sharp painful headache left side behind eye/forehead, sensitivity to light, small bursts cold sweat, icy feeling across chest

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Chest X-ray 9-28-21 Blood work up 9-21-21 EKG 9-21-21 (All in response to episodes of shortness of breath)
Aktuelle Erkrankungen: None
Vorgeschichte: Type 1 diabetes Hashimotos Blood pressure- controlled Cholesterol- controlled IBS
Andere Medikamente: Insulin-Humalog-by pump Quinapril Levothyroxine Sertraline Omeprazole Atorvastatin Nortriptyline Mirena- IUD
Allergien: None
Vorherige Impfungen: -

VAERS 1753872

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CT
Alter: 65,0
Geschlecht: F
Eingang: 01.10.2021
Impfdatum: 30.09.2021
Beginn: 30.09.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Asthenia Injection site erythema Injection site pain Injection site swelling Paraesthesia

Symptomtext

Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Weakness-Severe, 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 1750396

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: CA
Alter: 28,0
Geschlecht: M
Eingang: 30.09.2021
Impfdatum: 30.09.2021
Beginn: 30.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Dizziness Dyspnoea Throat tightness

Symptomtext

1505 Patient complaint of dizziness, shortness of breath, and throat tightness after receiving pfizer vaccination. blood pressure taken 78/49 heart rate 56 1510 Benadryl 50 mg IV given times one. 1515 throat tightness, shortness of breath and dizziness still continues. Epipen 0.3 mg given times one in the left lateral thigh. blood pressure 71/38 heart rate 72. Placed patient in a trendelenburg position. 1515called 911 1517 blood pressure retaken 132/79 heart rate 73

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 1525 Ambulance transported patient to ER
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: Bently 20 mg oral tab Zofran 4 mg tablet
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1745768

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: -
Alter: 30,0
Geschlecht: F
Eingang: 29.09.2021
Impfdatum: 29.09.2021
Beginn: 29.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Pharyngeal paraesthesia Swollen tongue

Symptomtext

Patient reported tingling feeling in her throat and slight swelling of tongue with similar effect from seafood allergic reaction she had ten years ago. Patient alert and oriented, vital signs 135/83, pulse 64, O2 98%, 1525 administered benadryl 50mg IM to right deltoid. Patient tolerated it well. Patient resting in gurney monitored for 30 minutes she then stated she felt better bp 129/87, pulse 54, o2 100%. No respiratory distress noted. Patient denies swelling of tongue, throat closing and any other symptoms. Advised patient if symptoms worsened contact ER or 911.

Weitere VAERSDATA-Felder

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

VAERS 1738030

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

moderat

Staat: FL
Alter: 74,0
Geschlecht: F
Eingang: 27.09.2021
Impfdatum: 27.09.2021
Beginn: 27.09.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea

Symptomtext

Patient had Pfizer Covid -19 Vaccine at 13:15 in left deltoid and Fluad at 13:25 in the right deltoid and as she was walking to get out of the store she alerted one of the store clerk at front desk that she has trouble breathing at 13:30. She was helped by the store clerk and a fellow customer in store and alerted the pharmacist. I ran out to help her seated and she was gasping for air and kept telling me she can not breath. I immediately alerted Tech to call 911 and another tech to grab Epipen and I gave her Epipen 0.3 mg IM in left thigh and she was feeling better immediately. Paramedics arrived shortly and all her vitals were normal. Her family daughter and Husband arrived and they elected not to go to ER for observation. I have checked on patient in the evening and she is doing fine at home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: UNKOWN
Andere Medikamente: TRAMADOL 50 MG, ZOLPIDEM 5 MG, DONEPEZIL 10 MG, GLIPIZIDE 5 MG
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2713935

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: WI
Alter: 75,0
Geschlecht: M
Eingang: 14.11.2023
Impfdatum: 29.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / RA

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

Rash Rash pruritic

Symptomtext

Rash is on his legs, arms, and back; It also itches and itches.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 75-year-old male patient received bnt162b2 (BNT162B2), on 29Sep2021 as dose 3 (booster), single (Lot number: FF8841) at the age of 75 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Sleeping pill" (unspecified if ongoing). Concomitant medication(s) included: TRAZODONE taken for insomnia (ongoing). Vaccination history included: bnt162b2 (DOSE 1, SINGLE, 1st dose: , Date: 01Feb2021, Time: Unknown , Anatomical Site of injection: Administered in right arm, Route of Administration: Not provided, Batch/Lot number: EL3248), administration date: 01Feb2021, when the patient was 75-year-old, for Covid-19 Immunization; bnt162b2 (DOSE 2, SINGLE, 2nd dose: , Date: 20Mar2021, Time: Unknown , Anatomical Site of injection: Administered in arm, unknown which arm ., Batch/Lot number:EN6200), administration date: 20Mar2021, when the patient was 75-year-old, for Covid-19 Immunization. The following information was reported: RASH PRURITIC (non-serious) with onset 01Oct2021, outcome "not recovered", described as "It also itches and itches."; RASH (non-serious) with onset 01Oct2021, outcome "not recovered", described as "Rash is on his legs, arms, and back". The events "rash is on his legs, arms, and back" and "it also itches and itches." required physician office visit. Therapeutic measures were taken as a result of rash, rash pruritic.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300362828 Same patient, same drug/different dose, different event;US-PFIZER INC-202300362835 Same reporter/drug/event, different patient;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Insomnia
Andere Medikamente: TRAZODONE
Allergien: -
Vorherige Impfungen: -

VAERS 2710582

UNKNOWN MANUFACTURER · COVID19 (COVID19 (UNKNOWN)) · Charge FF8841

mild

Staat: -
Alter: -
Geschlecht: U
Eingang: 07.11.2023
Impfdatum: 30.09.2023
Beginn: 01.10.2023
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: OT / LA

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

Pain Urticaria

Symptomtext

Painful when touched; Raised, hard, warm red welt about 2 inches in diameter.; This spontaneous case was received on 26-Oct-2023 from Seqirus via Pfizer (reference number 202300315925) reported by other non-healthcare professional and concerned a patient of unknown age and gender. The patient's medical history included allergy. The patient's concomitant medications included Shingrix (varicella zoster vaccine rgE (CHO)), received on 10-Sep-2023 for unknown indication. On 30-Sep-2023, the patient was vaccinated with Flucelvax Quadrivalent (influenza vaccine inact sag 4v; anatomical location: right arm; dose, route of administration and indication: not reported). The batch number reported was 944484 (reported batch number was identified by Seqirus to be correct batch number). On the same date, the patient was vaccinated with six non-company co-suspect Covid-19 vaccines: Covid-19 vaccine (Comirnaty bivalent; route of administration: intramuscular; anatomical location: left arm; dose and indication: not reported). The batch number reported was HD9876. Four Covid-19 vaccines (Pfizer; anatomical location: left arm; route of administration, dose and indication: not reported). The batch numbers reported were GH9703, FF8841, EW0102 and EPP6955. Covid-19 vaccine (Moderna; anatomical location: left arm; route of administration, dose and indication: not reported). The batch number reported was 066K21A. On 01-Oct-2023, an unspecified amount of time after receiving Flucelvax Quadrivalent and 6 Covid-19 vaccines, the patient experienced red, hard, warm red welt about 2 inches in diameter. Painful to touch. At the time of initial reporting, the patient was recovering from the events 'welts' and 'pain'. The reporter did not provide a causality assessment. Company comment: A patient of unknown age and gender was vaccinated with Flucelvax Quadrivalent and six non-company co-suspect Covid-19 vaccines on the same day. One day following vaccination, the patient experienced urticaria and pain. Although causality was confounded by six co-suspect Covid-19 vaccines, causal role of the suspect vaccine cannot be excluded and is assessed as possibly related for events pain and urticaria due to plausible temporal relationship.; Sender's Comments: A patient of unknown age and gender was vaccinated with Flucelvax Quadrivalent and six non-company co-suspect Covid-19 vaccines on the same day. One day following vaccination, the patient experienced urticaria and pain. Although causality was confounded by six co-suspect Covid-19 vaccines, causal role of the suspect vaccine cannot be excluded and is assessed as possibly related for events pain and urticaria due to plausible temporal relationship.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy
Andere Medikamente: Shingrix
Allergien: -
Vorherige Impfungen: -

VAERS 2667116

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: GA
Alter: -
Geschlecht: F
Eingang: 07.08.2023
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Pruritus

Symptomtext

persistent, intense itching - diffuse, no rash, lasted over a year; This is a spontaneous report received from a contactable reporter(s) (Physician). A 52-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), as dose 2, single (Lot number: FF8841) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (lot number: 30145BA, dose number: 1), for Covid-19 Immunization. The following information was reported: PRURITUS (medically significant), outcome "recovering", described as "persistent, intense itching - diffuse, no rash, lasted over a year". The event "persistent, intense itching - diffuse, no rash, lasted over a year" required physician office visit. Therapeutic measures were taken as a result of pruritus which includes UV therapy and hydroxychloroquine.; Sender's Comments: On the basis of the limited information available in this report, a medically meaningful assessment of the case cannot be made. Details regarding the drug-event temporal relationship and clinical course are not provided. However on conservative basis, the possible causality cannot be excluded. 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. This case will be reassessed once additional information is available.

Weitere VAERSDATA-Felder

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

VAERS 2643775

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FF8841

mild

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 10.06.2023
Impfdatum: 08.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / LA

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

Amenorrhoea Arthralgia Asthma Brain fog Fatigue Inflammation Musculoskeletal stiffness Sinusitis Spinal pain Tension headache Urticaria

Symptomtext

Thoracic spine pain, stiffness, inflammation; Amenorrhea, Cervical spine stiffness, SI Joint pain, inflammation, stiffness, Tension headaches, Asthma, Brain fog, Sinusitis, Extreme Fatigue, Welts on face

Weitere VAERSDATA-Felder

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

VAERS 2633563

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 18.05.2023
Impfdatum: 29.10.2021
Beginn: 28.04.2022
Tage bis Beginn: 181,0
Dosis: 3
Route/Site: IM / RA

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

Abdominal pain Bile duct stenosis Gastrointestinal haemorrhage Neuropathy peripheral Pyrexia

Symptomtext

PERIPHERAL NEUROPATHY 11/22/2021 GI HEMORRHAGE PERIPHERAL NEUROPATHY 11/22/2021 BILE DUCT STRICTURE PERIPHERAL NEUROPATHY 11/22/2021 FEVER PERIPHERAL NEUROPATHY 11/22/2021 ABDOMINAL PAIN PERIPHERAL NEUROPATHY 11/22/2021 FEVER

Weitere VAERSDATA-Felder

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

VAERS 2623153

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 28.04.2023
Impfdatum: 04.10.2021
Beginn: 01.08.2022
Tage bis Beginn: 301,0
Dosis: 3
Route/Site: IM / AR

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

Back pain Hernia Musculoskeletal stiffness Myalgia Pain in extremity Polymyalgia rheumatica

Symptomtext

I did not have an adverse reaction to the vaccine. I was diagnosed with polymyalgia rheumatica (PMR) in 08/2022. It caused muscle pain and stiffness in my arms, legs and back. I take prednisone to help with my symptoms. I also was diagnosed with hernia recently.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Simvastatin; Metoprolol
Allergien: N/A
Vorherige Impfungen: -

VAERS 2611853

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: AZ
Alter: 52,0
Geschlecht: F
Eingang: 08.04.2023
Impfdatum: 09.10.2021
Beginn: 30.09.2022
Tage bis Beginn: 356,0
Dosis: 3
Route/Site: - / RA

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

COVID-19 Drug ineffective SARS-CoV-2 test Ear infection Myalgia Sinusitis

Symptomtext

COVID test result: Positive; COVID test result: Positive; 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), on 17Feb2021 as dose 1, single (Batch/Lot number: unknown), on 17Mar2021 as dose 2, single (Batch/Lot number: unknown) and on 09Oct2021 at 12:00 as dose 3 (booster), single (Lot number: ff8841) at the age of 52 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma, controlled" (unspecified if ongoing). Concomitant medication(s) included: ADVAIR; ALBUTEROL [SALBUTAMOL]. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 30Sep2022, outcome "unknown" and all described as "COVID test result: Positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (30Sep2022) Positive. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300146065 Same patient, same reporter, same vaccine, different dose, different events;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: Test Date: 20220930; Test Name: Nasal Swab; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma
Andere Medikamente: ADVAIR; ALBUTEROL [SALBUTAMOL]
Allergien: -
Vorherige Impfungen: -

VAERS 2610059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: UT
Alter: 71,0
Geschlecht: F
Eingang: 05.04.2023
Impfdatum: 16.10.2021
Beginn: 03.01.2022
Tage bis Beginn: 79,0
Dosis: 4
Route/Site: IM / RA

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

Biopsy skin normal Burning sensation Eye swelling Feeling abnormal Mass Pain Pruritus Urticaria

Symptomtext

On January 3rd after receiving my 4th dose, I had a huge lump on head on it was itching and burning. I awoke the next morning , !was starting to see hives spread all over my body. It was all my hips and legs they were the size of tennis balls. It was all over my chest back shoulders. They were stinging and itching, it was so bad I felt i was dying of it. They last about half a day and kind of go away. It wasn?t just in one spot, It was spreading on my eyebrow and my eye would swell up. And for half a day it was there then go away it was crazy. I contacted my doctor and he said I had the Hives. There was nothing I had changed. On the 17th he had prescribed Cetirizine for the itching. I went in and I an injection Triamcinolone Acetone on the 21st. On the 24th I called him back; it was worse he the prescribed Hydroxyzine cream. The on the next day he prescribed Prednisone and the on February 7th he gave me a injection of Methylprednisolone Acetate. By this time, it was bad and should him my hips and things. He sent me to a dermatologist Dr. ant the same facility. On February 11th, Dr. prescribed Montelukast and Claritin, he had me to continue for a month. It would be for a day or two they would come back in a big wave. Then I went back, and he prescribed Cyclosporine 100mg. I had so many side effects from that on February he added Magnesium and Vitamin D and lowered the dose. I was to have a blood draw before every visit of my next appointments. The hives were way smaller and not coming in huge spots anymore. On July 6th, I met with him and he said I should see a neurologist on August 17,2021 I had a Biopsy on the large Hive on the back of my head, to see if was cancerous or any clue. The test came back as nothing but Hives. I had to wait to see another Dr. I was put on a injection called Zolair in November, it less and less. I haven?t had any hives since December 23rd.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: 17AUG2021 Biopsy - Normal
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: Calcium; Vitamin D; Aspirin; Levothyroxin; Allendranate Sodium
Allergien: Penicillin, Amoxcicillin
Vorherige Impfungen: -

VAERS 2595640

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: MI
Alter: 75,0
Geschlecht: M
Eingang: 13.03.2023
Impfdatum: 20.11.2021
Beginn: 06.03.2023
Tage bis Beginn: 471,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Asthenia COVID-19 Chest X-ray normal Fatigue Hypernatraemia Lactic acidosis Leukocytosis Sepsis

Symptomtext

Admission Date: 3/6/2023 Discharge Date: Mar 10, 2023 PRESENTING PROBLEM: Severe sepsis AKI (acute kidney injury) COVID-19 HOSPITAL COURSE: Patient is a 77 y.o. male HTN, HLD, T2DM, Alzheimers dementia who presented to the ED from his long term care facility for 2 days of worsening weakness and fatigue, found to have severe sepsis thought to be secondary to COVID-19 and was admitted to medicine for further work-up. Initial workup in the ED revealed significant leukocytosis and lactic acidosis, as well as AKI and hypernatremia. CXR did not demonstrate any obvious signs of pneumonia. Patient initially required 2 L nasal cannula, so 10 day course of decadron was started. Patient was admitted and treated with IV fluids. AKI, hypernatremia, and sepsis quickly resolved and patient was transitioned to room air. Palliative was consulted given patient's advanced dementia and other comorbid conditions. Family ultimately elected to discharge home with hospice and patient was discharged in stable condition to his assisted living facility with hospice services.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: LVH (left ventricular hypertrophy) Right kidney stone Benign prostatic hyperplasia with urinary retention Prostate nodule- possible at right apex ED (erectile dysfunction) of organic origin Essential hypertension Type 2 diabetes mellitus with microalbuminuria, with long-term current use of insulin (HCC) Dyslipidemia Mixed Alzheimer's and vascular dementia (HCC) Weakness Pressure injury of left buttock, stage 2 (HCC) Pressure injury of right buttock, stage 2 (HCC) Counseling regarding advance care planning and goals of care Renal mass COVID-19
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet acetaminophen (TYLENOL) 650 MG suppository bisacodyl (DULCOLAX) 10 MG suppository dexamethasone (DECADRON) 6 MG tablet dutasteride (AVODART) 0.5 MG capsule haloperidol (HALDOL) 2 MG/ML solution hyoscyam
Allergien: None
Vorherige Impfungen: -

VAERS 2593155

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: MA
Alter: 66,0
Geschlecht: M
Eingang: 08.03.2023
Impfdatum: 06.09.2022
Beginn: 27.12.2022
Tage bis Beginn: 112,0
Dosis: 3
Route/Site: IM / AR

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

COVID-19 Cough Fatigue Malaise Oral pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Went on an 8-day Cruise 12/18/22-12/26/22. Began to experience early symptoms on 12/27/22. Tested with home COVID test which was negative on 12/27, Tested again on 12/28 which was positive. Symptoms developed into cough, oral mucosa pain, general malaise, low-grade fever, tiredness. Called PCP's office and was placed on antiviral (not Paxlovid, the one that starts with O). Symptoms improved by 1/8 but still tested positive. Finally tested negative on 1/15/23.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Abbot Covid-19 Ag 12/27/22 - 12/28/22 + 01/08/23 + 01/15/23 - No lab testing as recent creatinine in doctor's system.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension Gout
Andere Medikamente: Losartan 25 mg daily Allopurinol 300 mg daily ASA 81 mg daily Vitamin D3 2,000 units daily Multivitamin 1 tab daily
Allergien: None
Vorherige Impfungen: -

VAERS 2592382

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: MI
Alter: 81,0
Geschlecht: M
Eingang: 07.03.2023
Impfdatum: 19.09.2022
Beginn: 19.02.2023
Tage bis Beginn: 153,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Dysuria Fall Pyrexia SARS-CoV-2 test positive

Symptomtext

02/19/23 presents to ED for "falls" "difficulty urinating, fevers". PMHx of "CAD, HTN, hypothyroidism, DM type 2"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: 02/19/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2550298

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: CA
Alter: 47,0
Geschlecht: F
Eingang: 04.01.2023
Impfdatum: 05.12.2022
Beginn: 26.12.2022
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: IM / LA

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

Acoustic stimulation tests Dizziness Head impulse test Magnetic resonance imaging Neurological examination Vertigo

Symptomtext

3 weeks after receiving the Pfizer Bivalent vaccine, I woke up with Vertigo (dizziness).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: ENT/Neurology - hearing tests, MRI, head position testing
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: none
Allergien: amoxicillin
Vorherige Impfungen: -

VAERS 2528977

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: MD
Alter: 69,0
Geschlecht: F
Eingang: 12.12.2022
Impfdatum: 08.12.2021
Beginn: 27.07.2022
Tage bis Beginn: 231,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 Fatigue Oropharyngeal pain Pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

On Wednesday night July 27 2022 I ran a slight fever and my nose was running on the 28th I was achy with a runny nose still during the daytime of the 29th I had a sore throat and high temperature and had a positive COVID-19 test. I called my doctor this same day and was prescribed PAXLOVID I took the medication for the seven day regimen and remained at home. On the fourteenth of August I saw my kidney doctor and my function was slightly lower but within range. I was also fatigued for about three weeks as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes; High Blood Pressure; Kidney Function History
Andere Medikamente: VICTOZA; LEVEMIR; ELIQUIS; sodium bicarbonate; atorvastatin; losartan
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2527316

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: WI
Alter: 70,0
Geschlecht: M
Eingang: 09.12.2022
Impfdatum: 28.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

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

Pain in extremity

Symptomtext

little bit of a sore arm/like I've had on the other Pfizer shots; 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 70-year-old male patient received BNT162b2 (BNT162B2), on 28Oct2021 as dose 3 (booster), single (Lot number: FF8841) at the age of 70 years intramuscular for covid-19 immunisation. The patient's relevant medical history included: "blood pressure" (unspecified if ongoing), notes: He takes his regular medications, like he takes a blood pressure pill and a tablet for urinating; "urinating" (unspecified if ongoing), notes: He takes his regular medications, like he takes a blood pressure pill and a tablet for urinating. Concomitant medication(s) included: SERTRALINE taken for urinary incontinence. Past drug history included: Sertraline, notes: taking all of them for 4-5 years and didn't have neck spasms. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Route of Administration: intramuscular. , Batch/Lot number: EL9269. NDC/EXP not provide on handwritten vaccine card.), administration date: 13Feb2021, when the patient was 69-year-old, for COVID-19 Immunization, reaction(s): "little bit of a sore arm/like I've had on the other Pfizer shots"; BNT162b2 (DOSE 2, SINGLE, Route of Administration: intramuscular. , Batch/Lot number: EL9262. , NDC/EXP: not provided on handwritten vaccine card.), administration date: 07Mar2021, when the patient was 69-year-old, for COVID-19 Immunization, reaction(s): "little bit of a sore arm/like I've had on the other Pfizer shots". The following information was reported: PAIN IN EXTREMITY (non-serious), outcome "recovering", described as "little bit of a sore arm/like I've had on the other Pfizer shots". Therapeutic measures were taken as a result of pain in extremity. Additional Information: He takes his regular medications, like he takes a blood pressure pill and a tablet for urinating, and he takes Sertraline. Caller said he doesn't feel those are relevant, he had been taking all of them for 4-5 years and didn't have neck spasms.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201348782 same patient, different vaccine dose number/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure abnormal (He takes his regular medications, like he takes a blood pressure pill and a tablet for urinating); Urinary incontinence (He takes his regular medications, like he takes a blood pressure pill and a tablet for urinating)
Andere Medikamente: SERTRALINE
Allergien: -
Vorherige Impfungen: -

VAERS 2512780

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: NY
Alter: 33,0
Geschlecht: M
Eingang: 21.11.2022
Impfdatum: 03.02.2022
Beginn: 12.02.2022
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test Computerised tomogram Flank pain Gait disturbance Headache Hemiparesis Magnetic resonance imaging Speech disorder

Symptomtext

Left-side weakness, headache, walking issues, speech issues, pain in my left side,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Flank pain
Hospital-Tage: 2,0
Labordaten: Mri's, cat scans, bloodwork
Aktuelle Erkrankungen: Had a positive Covid 19 test Jan 18,2022
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2511074

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: -
Alter: 82,0
Geschlecht: F
Eingang: 17.11.2022
Impfdatum: 16.11.2021
Beginn: 21.10.2022
Tage bis Beginn: 339,0
Dosis: 3
Route/Site: IM / LA

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

Angiogram cerebral normal Arteriogram carotid normal Back pain Bladder catheterisation Blood lactate dehydrogenase normal C-reactive protein increased COVID-19 Chest X-ray normal Computerised tomogram head normal Culture urine negative Echocardiogram Ejection fraction normal Fibrin D dimer Full blood count Incentive spirometry Magnetic resonance imaging head normal Malaise Micturition disorder

Symptomtext

Patient is a 83 y.o. female patient of with history of CAD with stents ,hypertension ,anxiety, diastolic CHF, hyperlipidemia,and seizures presented to Hospital with leg weakness, fever, nasal congestin and was found to have COVID 19 infection, her husband also has COVID 19. Lower extremity weakness r/o CVA SIRS Fever-resolved Acute on Chronic low back pain T-max 101.2 CT brain - negative for acute process MRI brain-no acute intracranial process or recent infarction CTA head/neck- no acute intracranial process UA- negative Urine Cx-negative Neurology signed off- follow up as needed PT/OT Care management Monitor CBC Covid-19 Virus Infection Date of onset of symptoms: 10/21/22 Symptoms present on admission: yes Date of covid positive test: 10/21/22 Vaccination status: vaccinated Imaging: Chest x-ray-no focal pneumonia Oxygen requirements on admission: none Current oxygen requirements: none Medical therapy:Remdesivir-completed 3 days Consultants following: ID consulted Anticipated special isolation end date: 10/31/22 CRP, (86) Sedrate (41) D-dimer (0.57) ferritin(424) LDH (174) Sputum Cx-normal flora, many WBC Incentive Spirometry pen Inhalers prn Oxygen prn Encourage prone positioning CAD Hypertension Hyperlipidemia History of stents 7 years ago Continue ASA, Losartan, Plavix, Crestor Monitor BP, BP stable Chronic Diastolic CHF Echocardiogram-pending- previous Echo 3/5/21-left ventricular diastolic function is grade 1, EF 58% Continue Lasix, Spirolactone Daily weights Strict I & O's History of seizures Last seizure 15 years ago Continue Dilantin Seizure precautions Neurology -signed off follow up as needed Incomplete micturition Patient void spontaneously however has to self cath twice a day and this has prevented her from having recurrent UTIs per urology Patient remains on low-dose trimethoprim daily No urinary symptoms

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2488217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 25.10.2022
Impfdatum: 22.10.2021
Beginn: 12.10.2022
Tage bis Beginn: 355,0
Dosis: 3
Route/Site: IM / -

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

Abdominal pain upper

Symptomtext

On October 12, 2022 I started having pain in the upper part of my stomach that has not gone away. I have gone to see my doctor but he cannot figure out what is going on. Doctor scheduled a test in December 2022 for me to do.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: High blood pressure; High cholesterol
Andere Medikamente: Lisinopril; FLONASE; TYLENOL; PRESERVISION; vitamin B; vitamin D3
Allergien: Penicillin; water pills
Vorherige Impfungen: Penicillin vaccine

VAERS 2485246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: VT
Alter: 67,0
Geschlecht: F
Eingang: 21.10.2022
Impfdatum: 04.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Diarrhoea Fatigue Headache Pain Pyrexia

Symptomtext

8 hours after injection, I experienced severe diarrhea lasting about an hour. Fever peaked at 102 on day 1, day 2 fever was 99- 101, day 3 fever 99, no fever after day 4. Chills and body aches sever day 1, moderate day 2, resolving by day 3. Headache was severe on day 1 but tapered off through day 3. Fatigue was extreme until day 3, but rapidly tapered off through days 4 to 6.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: Hashimoto
Andere Medikamente: Armour Thyroid
Allergien: Bees, cashews, peanuts, gluten, doxycycline
Vorherige Impfungen: COVID19 (COVID19 (Pfizer-BioNTech)), Dose 1, 2021, age 67. Approximately 18 to 20 hours after my injection, my left arm develop

VAERS 2476157

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: IL
Alter: 73,0
Geschlecht: F
Eingang: 12.10.2022
Impfdatum: 02.10.2021
Beginn: 03.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Pyrexia Somnolence

Symptomtext

I had a fever and was tired. I took Tylenol and I slept a lot. It took 24 hours to subside. I contacted the pharmacy regarding what I was experiencing and they only recommended taking Tylenol.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension; High Cholesterol
Andere Medikamente: Levothyroxine; Trazadone; Vitamin D; Losartan; Atorvastatin; Alendronate
Allergien: N/A
Vorherige Impfungen: Flu vaccine in the 70's made me feel like I had the flu

VAERS 2473957

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: TN
Alter: 39,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 08.10.2021
Beginn: 22.08.2022
Tage bis Beginn: 318,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Chills Cough Hot flush Pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I had a congestion, coughing, body aches,chills, no fever, and heat swings. These symptoms did not happen all at once. I took at home test COVID-19 and it came back positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 test, 08/25/2022, positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Gout
Andere Medikamente: Fenofibrate; Allopurinol; Vitamin D3
Allergien: Black wool fabrics
Vorherige Impfungen: -

VAERS 2460743

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: PR
Alter: 69,0
Geschlecht: F
Eingang: 26.09.2022
Impfdatum: 24.09.2021
Beginn: 01.03.2022
Tage bis Beginn: 158,0
Dosis: 3
Route/Site: IM / LA

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

Blood test normal Burning sensation Pruritus Rash Scar Scratch

Symptomtext

In mid to late March 2022, I started having all over itching. It began on my knees. There were small bumps. I don?t have a rash that can be seen. I itch mostly at night and now have scars from the scratching. I now have itching on the sides of my breasts, under my armpits, on my lower back, my hips and buttocks and outer thighs. I used to have itching on forearms but no longer. If I feel a little bit of itch and I scratch it becomes an itching burning sensation. I was treated for scabies but that was not the case. I was also told I had dermatitis. One of the medications I was prescribed interfered with my diabetes, so I stopped taking. I have been prescribed some over the counter anti-itch medicine. I haven?t found a medication that helps with the itching. I was treated for fungus but that was not the case.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Blood tests, normal, April 2022, May 2022 and June 2022.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes Type 1
Andere Medikamente: Losartan; Lantus; Novolog; Rosuvastatin; Famotidine; Vitamin D3; Milk thistle; Ubiquitiol; Magnesium; Vitamin K
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2439716

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: NJ
Alter: 65,0
Geschlecht: F
Eingang: 10.09.2022
Impfdatum: 03.11.2021
Beginn: 28.07.2022
Tage bis Beginn: 267,0
Dosis: 3
Route/Site: - / RA

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

Investigation Rash Rash erythematous Rash pruritic Rash vesicular SARS-CoV-2 test Skin lesion Upper respiratory tract infection

Symptomtext

skin has little circles/small kind of look like pimples coming here and there; described the rashes as a blistered rash, red, itchy and painful; described the rashes as a blistered rash, red, itchy and painful; described the rashes as a blistered rash, red, itchy and painful; described the rashes as a blistered rash, red, itchy and painful; she had an upper respiratory infection/Upper respiratory infection; This is a spontaneous report received from contactable reporter (Consumer) from medical information team. The reporter is the patient. A 65-year-old female patient received BNT162b2 (COMIRNATY), on 03Nov2021 as dose 3 (booster), single (Lot number: FF8841) at the age of 65 years, in right arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication included: ROBITUSSIN [DEXTROMETHORPHAN HYDROBROMIDE] taken for cough, start date: 25Jul2022. Vaccination history included: BNT162b2 (DOSE 1; Lot number: EP6955; Administration time: 08:45; Location: Right arm), administration date: 18Mar2021, for Covid-19 immunization; BNT162b2 (DOSE 2; Lot: ER8729; Location: Arm right), administration date: 05Apr2021, for Covid-19 immunization, reactions: "Arthralgia", "Pain", "abdominal discomfort", "inappropriate schedule of vaccine administered"; Shingles vaccine (she had shingles shot a couple of years ago), for Immunization. The following information was reported: UPPER RESPIRATORY TRACT INFECTION (non-serious) with onset 28Jul2022, outcome "recovered" (Aug2022), described as "she had an upper respiratory infection/Upper respiratory infection"; RASH VESICULAR (non-serious), RASH PRURITIC (non-serious), RASH (non-serious), RASH ERYTHEMATOUS (non-serious) all with onset 10Aug2022, outcome "recovering" and all described as "described the rashes as a blistered rash, red, itchy and painful"; SKIN LESION (non-serious), outcome "unknown", described as "skin has little circles/small kind of look like pimples coming here and there". The events "she had an upper respiratory infection/upper respiratory infection" and "described the rashes as a blistered rash, red, itchy and painful" required emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of rash vesicular, rash pruritic, rash, rash erythematous, skin lesion. Additional information: the patient was not a nutritionist. She wondered about the side effects from the COVID-19 Vaccine that occurred much later. She asked if they would appear much later after having the vaccines, if it was like 6 or 8 months later. She had 2 shots and one booster. She reported having upper respiratory infection and rashes that occurred after having received 3 doses of the product. She had an upper respiratory infection most recently and had to go to urgent care and was diagnosed with it and tested negative for COVID. She saw an urgent care doctor who said this is pretty common now and that this was a viral infection. It took about a month for her to recover completely from this event. In Aug2022, she had to go to the urgent care/emergency room because of rashes and described the rashes as blistered rash red, itchy and was painful. She had some blisters on her upper body. She did not know if this was related to the vaccines or the upper respiratory infection because she had seen that you can develop rashes before or after a cold. She still gets small kind of look like pimples coming here and there so she has been applying topical creams like Benadryl or steroid creams because the urgent care doctor gave her that. She asked if this was related to COVID or vaccine in 2021. She asked if she could take HTE next booster. She was worried about the rashes and was not sure what she had. She still experience some of the rashes and it was off and on and the skin has a little circles. She took shingles shot a couple of years ago. The urgent care nurse practitioner gave her, and was prescribed steroid cream topical and prior to that, she was using anti histamine cream and also used calamine lotion. She was concerned what caused her rash. When she saw the first urgent care doctor they did a culture for strep throat which came out negative and did a PCP for COVID test which came back negative and she also did an at home COVID test which was also negative 3 days later.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021444257 same patient/vaccine, different dose/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Test Name: culture for strep throat; Test Result: Negative ; Test Name: Covid test; Test Result: Negative ; Comments: tested negative for covid; Test Name: Home Covid test; Test Result: Negative ; Comments: she also did an at home Covid test which was also negative 3 days later.; Test Name: PCP Test; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: ROBITUSSIN [DEXTROMETHORPHAN HYDROBROMIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 2433446

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: MI
Alter: 80,0
Geschlecht: M
Eingang: 08.09.2022
Impfdatum: 24.02.2021
Beginn: 18.08.2022
Tage bis Beginn: 540,0
Dosis: 3
Route/Site: - / -

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

Biliary obstruction Biliary tract dilation procedure COVID-19 Endoscopic retrograde cholangiopancreatography Fatigue Liver function test abnormal SARS-CoV-2 test positive Stent placement Surgical procedure repeated Weight decreased

Symptomtext

This is an 82-year-old male with a history of CAD with previous CABG x2 5/2017, PAF on Eliquis, HTN, T2DM, dyslipidemia, history of PPM in 2010, OSA, history of TIA 2021 originally presented to the ER on 8/18/2022 due to abnormal LFTs. Patient was noted to be having complaints of fatigue and recent 5 pound weight loss. There was concern for biliary tree obstruction. He went for ERCP on 8/22/2022 with dilation and stent placement. Repeat ERCP was performed on 8/26/2022. Patient now may require to go to the OR due to left-sided bile duct occlusion with possible left hepatectomy and Roux-en-Y reconstruction. Discharged home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: 9,0
Labordaten: 8/18 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2429760

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: FL
Alter: 72,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 19.04.2022
Beginn: 23.08.2022
Tage bis Beginn: 126,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Dizziness Nasal congestion Nausea Oropharyngeal pain SARS-CoV-2 test positive Vomiting

Symptomtext

Hospitalization: ADMITTED 8/23/2022; DISCHARGED 8/26/2022. Presentation to the ED: DIZZINESS, NAUSEA, VOMITING, SORE THROAT, NASAL CONGESTION. COVID-19 + date: 8/24/22. Treatment: Paxlovid WAS PRESCRIBEDBY THE PATIENT'S PCP, NOT DURING THE HOSPITAL STAY. Discharge to: Home or Self Care

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HYPERTENSION.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2422857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: -
Alter: 39,0
Geschlecht: F
Eingang: 29.08.2022
Impfdatum: 20.10.2021
Beginn: 21.08.2022
Tage bis Beginn: 305,0
Dosis: 2
Route/Site: UN / UN

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

Asthenia Chills Cough Pyrexia Respiratory tract congestion

Symptomtext

chills, fever, congestion, cough, weakness

Weitere VAERSDATA-Felder

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

VAERS 2419416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

mild

Staat: VA
Alter: 83,0
Geschlecht: M
Eingang: 24.08.2022
Impfdatum: 21.07.2022
Beginn: 07.08.2022
Tage bis Beginn: 17,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Foreign travel Malaise Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

While on a tour to PRIVATE I contracted COVID on or about August 7, 2022. Upon arriving in PRIVATE on August 9, 2022, for another tour in PRIVATE I became very sick with sneezing, runny nose, sore throat and dry cough. My spouse went to a local pharmacy and purchased OTC meds for my symptoms plus 4 home-style COVID antigen testing kits. I tested positive, and reported same to our tour company and to the hotel.. The tour company canceled our tour and the hotel accepted our request to remain longer in our assigned room (for up to 7 day, with no daily service and meals only by Room Service. The hotel also arranged for a nurse from a local medical facility to come to our room on August 10th.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: COVID 19 Antigen test (nasal swab) was positive on August 10th.
Aktuelle Erkrankungen: none.
Vorgeschichte: high cholesterol, diarrhea, migraine.
Andere Medikamente: rosuvastatin, aspirin, gabapentin ,losartan, atrovent, nasacort, fiorinal, lomotil, viberzi, valium, qulipta.
Allergien: none.
Vorherige Impfungen: -

VAERS 2416273

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: WA
Alter: 56,0
Geschlecht: M
Eingang: 19.08.2022
Impfdatum: 17.08.2022
Beginn: 18.08.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Hyperhidrosis Muscle spasms Myalgia Pyrexia Trismus

Symptomtext

fever, sweating, spasms in arms, legs, jaws, pain in muscles

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Covid
Vorgeschichte: back/cervical issues
Andere Medikamente: testosterone injections, benefiber, omeprazole, calcium/vitamin d, senior multivitamin, leutin
Allergien: ibuprofen
Vorherige Impfungen: -

VAERS 2370659

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: ID
Alter: 61,0
Geschlecht: M
Eingang: 15.07.2022
Impfdatum: 25.11.2021
Beginn: 30.12.2021
Tage bis Beginn: 35,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Pain

Symptomtext

Shoulder pain in the side that the vaccine between Christmas and January 1st. Now the left elbow aches. It is currently usable, but painful.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: BPH
Andere Medikamente: Finasteride; tamsulosin; multivitamin; METAMUCIL; valacyclovir
Allergien: No
Vorherige Impfungen: -

VAERS 2362999

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: CA
Alter: 70,0
Geschlecht: M
Eingang: 08.07.2022
Impfdatum: 06.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Fatigue Muscular weakness Pain in extremity

Symptomtext

Sore arm for 6 days. Right arm also sore at shoulder for 2 Days. Left Arm still somewhat weak Very tired 1 day after injection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: high blood pressure
Andere Medikamente: Atorvostatin 10mg 1/dat Olmesartin Medoximil 5mg 1/day
Allergien: None
Vorherige Impfungen: Sore arm. Very tired for 24 hours

VAERS 2313023

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: PA
Alter: 71,0
Geschlecht: F
Eingang: 08.06.2022
Impfdatum: 01.12.2021
Beginn: 09.01.2022
Tage bis Beginn: 39,0
Dosis: 3
Route/Site: SYR / LA

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

Acupuncture Arthralgia Gait inability Magnetic resonance imaging Pain in extremity Sleep disorder

Symptomtext

I received my third dose on 12/1/2021. On 01/09/2022 I woke up and had hip pain down from thigh to knee. I was unable to walk or sleep. I went to a chiropractor 2x a week for a month. I did acupuncture 2x a week for 4 weeks. Very little relief. I went to PCP and was prescribed prednisone and that did nothing. Now I started physical therapy twice a week for four weeks so far.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: MRI
Aktuelle Erkrankungen: -
Vorgeschichte: Factor 5
Andere Medikamente: Multivitamin; vitamin C; vitamin D
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2308540

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: NY
Alter: 44,0
Geschlecht: M
Eingang: 03.06.2022
Impfdatum: 30.11.2021
Beginn: 15.12.2021
Tage bis Beginn: 15,0
Dosis: 3
Route/Site: SYR / LA

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

Blood thyroid stimulating hormone increased Fatigue Weight increased Weight loss poor

Symptomtext

A couple weeks after getting my booster shot I began feeling Fatigued, tired no matter how much sleep I got. Gained weight and have hard time losing any. At the time I wasn't really thinking about it possibly being connected to the booster shot so I put off having it addressed until I seen my doctor in March at my regular check up. Testing revealed elevated TSH and was started on course of Levothyroxine for hypothyroidism. No change in symptoms as of this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: March 3, 2022 TSH results elevated.
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, Anxiety disorders, depression, GERD, IBS, allergies
Andere Medikamente: Azelastine, Buspar, Bupropion XL, Dexilant, Qvar, Oxybutynin, Allegra, Flonase, Sucralfate, Dicyclomine
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2306701

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff8841

mild

Staat: VA
Alter: 53,0
Geschlecht: F
Eingang: 02.06.2022
Impfdatum: 19.04.2022
Beginn: 26.04.2022
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Clostridium test positive Colitis Culture stool positive Magnetic resonance imaging Myalgia Nasopharyngitis SARS-CoV-2 test positive Urine analysis

Symptomtext

On April 26, 2022, I experienced cold like symptoms following by muscle aches. I saw my primary care on May 29, 2022, who prescribed amoxicillin. My doctor recommended that I test for covid during the telehealth visit and I tested positive on May 29, 2022. I started the Paxloid on May 30, 2022. I continued the amoxicillin with the Paxloid since I had already started it. On May 12, 2022, I went to the Emergency Room and was diagnosed with colitis. The hospital took stool sample and I tested positive for C Diff.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: Stool sample, urine test, and I think it was a MRI.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Sertraline, Bupropion, Linzess, Dupliexent, Multi Vitamin, Vitamin D3, Rosuvastin Calcium, and Fiber supplement.
Allergien: -
Vorherige Impfungen: -

VAERS 2296509

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: NJ
Alter: 42,0
Geschlecht: F
Eingang: 26.05.2022
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: ja Erholt: nein

Asthenia Cerumen removal Dizziness Ear discomfort Eczema Electrocardiogram normal Headache Heart rate increased Hypoacusis

Symptomtext

Within 8 hours after receiving booster, experienced fast heart rate (95-120 bpm), weakness, headache and dizziness. Heartrate was measured continuously by my watch which kept alerting me that an abnormal heart rate was detected (normal resting heart rate is 69). Went to urgent care for EKG which was inconclusive. Then went to the hospital ER, EKG found no abnormal function, given fluids, anti-inflammatory, and observed until heartrate came down below 90. Within 2 weeks eczema patches started growing on my face, neck, and ears for the first time ever. The ear eczema got so bad I had to get a prescription steriod cream (Cloderm) and the ENT doctor had to clear blocked excess wax from my left ear which was blocking hearing and creating pressure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Seasonal allergies
Vorgeschichte: asthma, seasonal allergies
Andere Medikamente: Multivitamin daily, Vitamin D 10,000 IU twice a week
Allergien: none
Vorherige Impfungen: Swollen and tender arm pit lymph node after Covid Vaccine dose 1 and 2, age 42, vaccination dates: 3/24/21 and 4/11/21, Pfizer B

VAERS 2290717

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: MA
Alter: 55,0
Geschlecht: M
Eingang: 23.05.2022
Impfdatum: 06.12.2021
Beginn: 12.05.2022
Tage bis Beginn: 157,0
Dosis: 3
Route/Site: IM / AR

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

COVID-19 Cough Fatigue Headache Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I started getting symptoms on 5/11/2022 of fatigue, headache, chest congestion, cough, and low grade fever. I received a positive COVID-19 test that was positive and also went to my doctor and did a rapid COVID-19 test that was also positive. I was prescribed Paxlovid. I did not take it. My symptoms lasted intensely for 4 days. Then the chest congestion, fatigue, and cough is still lingering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test - at home and Rapid test - positive
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: Multivitamins
Allergien: Bee stings Vancomycin
Vorherige Impfungen: -

VAERS 2290618

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: OH
Alter: 51,0
Geschlecht: F
Eingang: 23.05.2022
Impfdatum: 20.11.2021
Beginn: 09.05.2022
Tage bis Beginn: 170,0
Dosis: 3
Route/Site: IM / RA

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

Chills Cough Influenza A virus test negative Influenza B virus test Oropharyngeal pain Pyrexia SARS-CoV-2 test negative

Symptomtext

On 5/13 I woke up with a sore throat which persisted until the next day. By that evening, I had a fever, chills, and coughing. I went to a Clinic on 5/15 where they tested me for Covid, Influenza A and B and all were negative. So they stated that it was some type of virus and advised that I wait it out. It's been around a week and I feel much better with the exception of a cough that lingers.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 5/15 Covid test-neg Influenza A and B-neg
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1903760

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: CT
Alter: 46,0
Geschlecht: M
Eingang: 21.05.2022
Impfdatum: 15.11.2021
Beginn: 18.05.2022
Tage bis Beginn: 184,0
Dosis: 3
Route/Site: OT / LA

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

Chills Immunisation COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Tested positive for COVID-19 (PCR test); Tested positive for COVID-19 (PCR test); 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 (BNT162B2), on 18Mar2021 as dose 1, single (Batch/Lot number: unknown), in left arm, on 08Apr2021 as dose 2, single (Batch/Lot number: unknown), in left arm and on 15Nov2021 as dose 3 (booster), single (Batch/Lot number: unknown) at the age of 46 years, in left arm, all intramuscular for covid-19 immunization. Facility where the most recent COVID-19 vaccine was administered was reported as Other, Pfizer. The patient's relevant medical history was not reported. Concomitant medication(s) included: ESCITALOPRAM; ATORVASTATIN, also reported as other medications in two weeks. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient had not been diagnosed with COVID-19 prior to vaccination and has been tested since the vaccination. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 18May2022, outcome "recovering" and all described as "Tested positive for COVID-19 (PCR test)". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (16May2022) Positive, notes: Nasal Swab; (18May2022) Positive. Therapeutic measures were not taken as a result of vaccination failure, covid-19. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20220516; Test Name: PCR; Test Result: Positive ; Comments: Nasal Swab; Test Date: 20220518; Test Name: PCR; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ESCITALOPRAM; ATORVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2287794

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 20.05.2022
Impfdatum: 28.09.2021
Beginn: 15.05.2022
Tage bis Beginn: 229,0
Dosis: 3
Route/Site: IM / UN

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

COVID-19 Cough Myalgia Pyrexia

Symptomtext

COVID 19 that lead to hospitalization, had fever, myalgia, nonproductive cough

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2278464

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 16.05.2022
Impfdatum: 17.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Electronystagmogram abnormal Fatigue Vertigo Vestibular disorder

Symptomtext

Severe vestibular problems (lasted about 6 months) and required extensive therapy to fix it. Started as lightheadedness and severe fatigue for 3 months. The vertigo gradually got worse day by day. All symptoms began 11/18/21. I had to see an ENT and vestibular physical therapist. I had to get Video nystagmography for diagnosis as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Severe vertigo
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Effexor, propanelol, ubrelvy, baby asprin, spironalactone
Allergien: Norco and vicodin
Vorherige Impfungen: -

VAERS 2215703

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: -
Alter: 47,0
Geschlecht: F
Eingang: 15.05.2022
Impfdatum: 10.02.2021
Beginn: 25.06.2021
Tage bis Beginn: 135,0
Dosis: 3
Route/Site: - / -

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

Herpes zoster Neuralgia Pain of skin

Symptomtext

Shingles breakout with bad, lingering nerve pain. Per PCP, took Valtrex, Gabapentin, prescription ointment for skin pain/breakouts. The nerve pain continued for approximately 2 months, of which I stayed on gabapentin for relief. Additional care was with rheumatologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain of skin
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Multivitamin
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2261903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 13.05.2022
Impfdatum: 01.11.2021
Beginn: 01.05.2022
Tage bis Beginn: 181,0
Dosis: 3
Route/Site: - / -

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

Cough Fatigue Feeling abnormal Respiratory tract congestion SARS-CoV-2 test positive COVID-19 Investigation SARS-CoV-2 test Vaccination failure Throat irritation

Symptomtext

tested herself came out positive; tested herself came out positive; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group, Program ID: (172086). The reporter is the patient. A 67-year-old female patient received BNT162b2 (BNT162B2), on 28Jan2021 as dose 1, single (Lot number: EL3246), on 18Feb2021 as dose 2, single (Lot number: EL9267) and on 01Nov2021 as dose 3 (booster), single (Lot number: FF8841) at the age of 67 years for covid-19 immunisation. The patient's relevant medical history included: "Immune deficiency diagnosed 10-15 years ago, states her body does not make antibodies" (ongoing). There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 01May2022, outcome "not recovered" and all described as "tested herself came out positive". The patient underwent the following laboratory tests and procedures: vaccine challenge test: (unspecified date) Unknown result, notes: the test was they gave her a vaccine challenge test with she thinks a Pneumovax vaccine and they check your labs first,; SARS-CoV-2 test: (unspecified date) positive, notes: she initially tested herself came out positive; (05May2022) positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical information: Caller states she finished taking the 5 day course and was feeling better, but now she is on Day 12 from when she was first feeling symptoms and about a day or two ago she started feeling worse. States she initially tested herself came out positive and she thought she should go somewhere to get tested so there is a record and she could get some medication to alleviate her symptoms so she went to Pharmacy and a Nurse Practitioner saw her and prescribed the Paxlovid, she started 26Apr2022 and ended it on 30Apr2022, just tested last night again 05May2022, and she is still positive. States when she went back after she finished the course of Paxlovid she went to be tested again and they said she was still positive and the NP there said it can show up that she is positive for three months after the treatment, caller wants to know if this is true. Caller mentions she did receive three doses of the Pfizer COVID vaccines and the monoclonal antibodies twice and got Covid a month after. Caller states to diagnose her with the immune deficiency disorder, the test was they gave her a vaccine challenge test with she thinks a Pneumovax vaccine and they check your labs first, then they give you the Pneumovax and wait 6 weeks and then check the labs again to see if any of the numbers have changed and if they do not thats what they use to diagnose. States she was diagnosed 10-15 years ago she is not sure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Name: vaccine challenge test; Result Unstructured Data: Test Result:Unknown result; Comments: the test was they gave her a vaccine challenge test with she thinks a Pneumovax vaccine and they check your labs first,; Test Name: Covid; Test Result: Positive ; Comments: she initially tested herself came out positive; Test Date: 20220505; Test Name: Covid; Test Result: Positive
Aktuelle Erkrankungen: Immunocompromised
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2261903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 13.05.2022
Impfdatum: 01.11.2021
Beginn: 01.05.2022
Tage bis Beginn: 181,0
Dosis: 3
Route/Site: SYR / AR

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

Cough Fatigue Feeling abnormal Respiratory tract congestion SARS-CoV-2 test positive COVID-19 Investigation SARS-CoV-2 test Vaccination failure Throat irritation

Symptomtext

tested herself came out positive; tested herself came out positive; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group, Program ID: (172086). The reporter is the patient. A 67-year-old female patient received BNT162b2 (BNT162B2), on 28Jan2021 as dose 1, single (Lot number: EL3246), on 18Feb2021 as dose 2, single (Lot number: EL9267) and on 01Nov2021 as dose 3 (booster), single (Lot number: FF8841) at the age of 67 years for covid-19 immunisation. The patient's relevant medical history included: "Immune deficiency diagnosed 10-15 years ago, states her body does not make antibodies" (ongoing). There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 01May2022, outcome "not recovered" and all described as "tested herself came out positive". The patient underwent the following laboratory tests and procedures: vaccine challenge test: (unspecified date) Unknown result, notes: the test was they gave her a vaccine challenge test with she thinks a Pneumovax vaccine and they check your labs first,; SARS-CoV-2 test: (unspecified date) positive, notes: she initially tested herself came out positive; (05May2022) positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical information: Caller states she finished taking the 5 day course and was feeling better, but now she is on Day 12 from when she was first feeling symptoms and about a day or two ago she started feeling worse. States she initially tested herself came out positive and she thought she should go somewhere to get tested so there is a record and she could get some medication to alleviate her symptoms so she went to Pharmacy and a Nurse Practitioner saw her and prescribed the Paxlovid, she started 26Apr2022 and ended it on 30Apr2022, just tested last night again 05May2022, and she is still positive. States when she went back after she finished the course of Paxlovid she went to be tested again and they said she was still positive and the NP there said it can show up that she is positive for three months after the treatment, caller wants to know if this is true. Caller mentions she did receive three doses of the Pfizer COVID vaccines and the monoclonal antibodies twice and got Covid a month after. Caller states to diagnose her with the immune deficiency disorder, the test was they gave her a vaccine challenge test with she thinks a Pneumovax vaccine and they check your labs first, then they give you the Pneumovax and wait 6 weeks and then check the labs again to see if any of the numbers have changed and if they do not thats what they use to diagnose. States she was diagnosed 10-15 years ago she is not sure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Name: vaccine challenge test; Result Unstructured Data: Test Result:Unknown result; Comments: the test was they gave her a vaccine challenge test with she thinks a Pneumovax vaccine and they check your labs first,; Test Name: Covid; Test Result: Positive ; Comments: she initially tested herself came out positive; Test Date: 20220505; Test Name: Covid; Test Result: Positive
Aktuelle Erkrankungen: Immunocompromised
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2270933

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: -
Alter: 73,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 18.02.2021
Beginn: 28.01.2022
Tage bis Beginn: 344,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Cough Fatigue SARS-CoV-2 test positive

Symptomtext

01/28/22 presents to ED for "cough and fatigue". PMHx of "COPD with chronic hypoxic resp failure, ESRD on HD MWF, myeloma"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 01/28/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267163

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: PA
Alter: 50,0
Geschlecht: F
Eingang: 08.05.2022
Impfdatum: 14.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Chills Diarrhoea Fatigue Headache Pain Pyrexia

Symptomtext

Fever Chills Body aches Headache Fatigue Diarrhea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Wellbutrin Fish oil Green tea extract Centrum womens vitamin
Allergien: Penicillin Sulfas
Vorherige Impfungen: -

VAERS 2264711

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: IN
Alter: 74,0
Geschlecht: F
Eingang: 05.05.2022
Impfdatum: 07.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 Exposure to SARS-CoV-2 Feeling abnormal Lethargy Pain Productive cough Pyrexia SARS-CoV-2 test positive

Symptomtext

After receiving the vaccine I had a fever, pains, felt lethargic, and it made me feel worse than the flu. Every day for about a week new symptoms came up. I might of taken some acetaminophen to relieve some of the symptoms. I still have a little bit of phlegm in my throat. I had a huge tumor removed out of my sinuses about a year ago. When I went to my doctor he said that there are signs that a tumor is trying to come back. I caught COVID in January 2022. I felt a little under the weather, but I didn't really have any symptoms. I was in a nursing home where COVID was high, and I had ended up catching it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: COVID Test - negative (January 2022). PCR COVID Test - positive (January 2022).
Aktuelle Erkrankungen: none
Vorgeschichte: Kidney Stones Diabetes (The doctor said I don't have this anymore.)
Andere Medikamente: Hydrochlorothiazide 25mg 1xday Alendronate 70mg 1xweek Premarin Vaginal Cream 0.625mg 2xweek Baby Aspirin Calcium, Magnesium, Zinc Vitamin D3 Cinnamon Fish Oil Garlic Multivitamin Probiotics Vitamin B12 Complex B6 Vitamin E Zinc and Copper
Allergien: Codeine
Vorherige Impfungen: Flu shot, a long time ago I got very, very sick after receiving this vaccine.

VAERS 2260118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: OH
Alter: 69,0
Geschlecht: F
Eingang: 02.05.2022
Impfdatum: 03.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Pyrexia Rhinorrhoea SARS-CoV-2 test

Symptomtext

After received my 3rd dose I felt tired and a runny nose. It was a mild case. I did have a fever for 100 for an hour or two. I had these symptoms for only 24 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Blood Pressure; Cholesterol
Andere Medikamente: Omega 3 Triamterene/hctz 37.5/25 ml Fenofibrate 16 ML tablet Vitamin D Simvastatin 20 ML Atenolol 25 Ml
Allergien: Oxycodone; Hydrocodone; Biperiden
Vorherige Impfungen: -

VAERS 2259962

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: -
Alter: 43,0
Geschlecht: F
Eingang: 01.05.2022
Impfdatum: 03.02.2022
Beginn: 04.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / -

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

Allergy test Antinuclear antibody Blood immunoglobulin E Full blood count Rash SARS-CoV-2 test Thyroid function test Urticaria chronic

Symptomtext

Chronic urticaria that started day after vaccine - daily rash since date of vaccine (still have daily symptoms 3 months since vaccine). Treated with daily oral antihistamine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: medical testing included: allergy testing, COVID tests, Urticaria panel (ANA, CBC, Thyroid), IgE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Penicillin, Bactrim, shrimp
Vorherige Impfungen: -

VAERS 2258332

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: MN
Alter: 72,0
Geschlecht: M
Eingang: 29.04.2022
Impfdatum: 03.11.2021
Beginn: 28.04.2022
Tage bis Beginn: 176,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Fatigue Headache Malaise

Symptomtext

Hospitalized for headache, malaise, weakness, and fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: obesity, OSA
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2257111

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: GA
Alter: 61,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 09.10.2021
Beginn: 07.04.2022
Tage bis Beginn: 180,0
Dosis: 3
Route/Site: SYR / LA

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

Body temperature increased Cough Drainage Fatigue Headache Laboratory test abnormal Sinus congestion

Symptomtext

April 2022, I first noticed a headache and I didn't think much. When I awoke on the 2nd day I still having a headache and back of the throat drainage. I tested negative with a home test. That night I felt congested and took some medicine. That next Thursday night April,07/2022 I tested positive. I started running a temperature of 100. The congestion I was, head congestion and I did have a cough and low grade temp. I continued having a temp and fatigue. It was the next week I started to feela bit better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Sore throat the first week of March 2021.
Vorgeschichte: Asthma
Andere Medikamente: Calcium, Vitamin D, Cranberry, Amlodipine, Lexella, Citalopram
Allergien: Sulfates
Vorherige Impfungen: -

VAERS 2250159

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: WA
Alter: 60,0
Geschlecht: M
Eingang: 25.04.2022
Impfdatum: 12.11.2021
Beginn: 18.01.2022
Tage bis Beginn: 67,0
Dosis: 3
Route/Site: SYR / LA

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

Laboratory test Testicular pain Ultrasound testes normal

Symptomtext

Two months later, developed a persistent ache in left testicle lasting about 3 weeks. I do not think it is related to the vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Testicular pain
Hospital-Tage: -
Labordaten: Lab work, ultrasound on 11/12/2022. Later visit to urologist on 1/26/2022, said there were no health issues. Ache later resolved itself.
Aktuelle Erkrankungen: None
Vorgeschichte: Enlarged spleen from hemolytic anemia
Andere Medikamente: Pravastatin, Montelukast Sodium, Cetirizine Hydrochloride, Vitamin D, Fish oil
Allergien: Penicillin, Clindamycin, Cephalexin
Vorherige Impfungen: -

VAERS 2249714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: CO
Alter: 80,0
Geschlecht: F
Eingang: 24.04.2022
Impfdatum: 07.10.2021
Beginn: 22.04.2022
Tage bis Beginn: 197,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Malaise Mental status changes SARS-CoV-2 test positive

Symptomtext

pt admit 4/22/22 w/ AMS - found to be COVID+ with symptoms. Pt had already received 3 doses of Pfizer vax (1/3/21, 1/22/21, 10/7/21). Of note, pt had been on a steroid taper since at least 4/1/22 and lives in a facility. 1st positive COVID test on 4/13/22.

Weitere VAERSDATA-Felder

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

VAERS 2249463

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: CA
Alter: 31,0
Geschlecht: M
Eingang: 23.04.2022
Impfdatum: 28.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Abdominal discomfort Dizziness Fatigue Headache

Symptomtext

Client presented at a vaccination site on 11/28/21. The client reported he received his first dose Pfizer COIVD vaccine on 11/07/21. He reported within 15 mins he had a very ?bad headache? for two weeks straight after. Client reported tiredness for one week and a feeling of ?diarrhea like sensation? for 1.5 weeks without having the diarrhea. Client told he did have dizziness and lightheadedness within the 15 minutes after the injection. Client told he didn?t report the symptoms to the EMT in the observation station. Client told he took Ibuprofen 800 mg with help for headache for two weeks straight. Client told he has hypertension and controlling with Lisinopril 10 mg daily. Client told he didn?t follow-up with his PCP. Client told he has no known allergy. At 1110, PHN took client?s vitals: BP 126/79, HR 52, R 18, O2 Sat. 99%. Client is requesting second dose Pfizer COVID vaccine today. PHN submitted a medical consult via text message to clinical project coordinator requesting to proceed with the second dose Pfizer COVID vaccine. Per the doctor, approval to proceed with the second dose Pfizer COVID vaccine was obtained from medical consult team via text message from clinical project coordinator. Client received Pfizer COVID vaccine, LOT#: FF8841 on 11/28/21 at 1148 by vaccinating nurse. The client did not report any symptoms during the 30-minute observation period. PHN educated client on possible adverse reactions and when to seek EMS. Client verbalized understanding. Client left vaccination site at 1218 unassisted and with a steady gait.

Weitere VAERSDATA-Felder

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

VAERS 2249450

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: CA
Alter: 24,0
Geschlecht: F
Eingang: 23.04.2022
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

Dizziness Erythema Headache Injection site erythema

Symptomtext

Client presented at vaccination site on 11/28/21. The client reported she received her first dose Pfizer COIVD vaccine on 11/07/21. Client reported within 15 mins she had redness on her left side of her face with hotness and numbness on her left arm where she had her injection. Client didn?t report to the EMT in the observation station. Client told she had the headache off and on for one whole week after and lightheadedness for two days and fatigue for one week. She told she took acetaminophen 500 mg with help for headache for three days straight. Client told she didn?t follow-up with her PCP. Client told she doesn?t have any chronic illnesses or taking any medications. Client told she has no known allergy. At 1112, PHN took client?s vitals: BP 112/71, HR 64, R 20, O2 Sat. 98%. Client is requesting second dose Pfizer COVID vaccine today. PHN submitted a medical consult via text message to clinical project coordinator requesting to proceed with the second dose Pfizer COVID vaccine. Per the doctor, approval to proceed with the second dose Pfizer COVID vaccine was obtained from medical consult team via text message from clinical project coordinator. Client received the second dose Pfizer COVID vaccine, LOT#: FF8841 on 11/28/21 at 1145. The client did not report any symptoms during the 30-minute observation period. PHN educated client on possible adverse reactions and when to seek EMS. Client verbalized understanding. Client left vaccination site at 1215 unassisted and with a steady gait.

Weitere VAERSDATA-Felder

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

VAERS 2248161

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff8841

mild

Staat: MO
Alter: 75,0
Geschlecht: M
Eingang: 22.04.2022
Impfdatum: 11.10.2021
Beginn: 20.04.2022
Tage bis Beginn: 191,0
Dosis: 3
Route/Site: IM / RA

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

Fatigue Pyrexia

Symptomtext

fever and fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: 2,0
Labordaten: unknown
Aktuelle Erkrankungen: unknwon
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2248116

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: CA
Alter: 72,0
Geschlecht: F
Eingang: 22.04.2022
Impfdatum: 14.10.2021
Beginn: 26.12.2021
Tage bis Beginn: 73,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Feeling abnormal Lethargy Nasopharyngitis Oropharyngeal pain Post-acute COVID-19 syndrome SARS-CoV-2 test positive

Symptomtext

Starting 12/26/2021, I starting feeling lethargic and coming down with a cold/sore throat. I took a COVID test on 12/26/2021 and it was positive. I was in bed for a couple of weeks and constantly stayed in touch with my PCP and dermatologist. For about 3 months, I went to speech therapy, Covid Therapy and now I'm in physical therapy for long COVID symptoms. The brain fog still persists to this day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: COVID test (12/26/2021): Positive
Aktuelle Erkrankungen: None
Vorgeschichte: A-fib, Bullous Disease and arthritis
Andere Medikamente: Metoprolol 25mg, Eliquis, Cellcept 2000mg, Vitamin B12, Vitamin D3, Vitamin C and Hair, skin and Nails, Prednisone 3mg, Valacyclovir 500mg QD
Allergien: None
Vorherige Impfungen: Zosavax vaccine - caused an autoimmune skin disease

VAERS 2244299

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: CA
Alter: 37,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 15.10.2021
Beginn: 21.12.2021
Tage bis Beginn: 67,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Influenza like illness Pyrexia SARS-CoV-2 test positive

Symptomtext

Flu like symptoms without fever, Did a COVID-19 antigen and PCR (positive). Honey lemon cough drops and regular bedside paraphilias.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: 12/21 COVID-19 Test Antigen (positive). 12/22 COVID-19 Test PCR (positive).
Aktuelle Erkrankungen: None
Vorgeschichte: Congenital Adrenal Hyperplasia
Andere Medikamente: Prednisone; Fludrocortisone; VitaFusion Gummy Prenatal
Allergien: NKA
Vorherige Impfungen: -

VAERS 2243553

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: VA
Alter: 67,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 15.10.2021
Beginn: 17.01.2022
Tage bis Beginn: 94,0
Dosis: 3
Route/Site: IM / LA

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

Aphonia COVID-19 Decreased appetite Fatigue Headache Influenza virus test Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

I had a headache, sore throat, fatigue, I lost my voice for about 5 days, and lack of appetite. I tested positive for COVID on 01/17/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID Test, Flu Test.
Aktuelle Erkrankungen: None
Vorgeschichte: Arthritis; Osteoporosis
Andere Medikamente: Evista; Vitamin D; Multivitamin; Calcium
Allergien: Codeine; contact allergy to Triclosan
Vorherige Impfungen: -

VAERS 2243007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: CT
Alter: -
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 06.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Blood test Investigation Nasopharyngitis Pain Polymyalgia rheumatica Red blood cell sedimentation rate increased

Symptomtext

Illness/AE: Cold/about 3 weeks ago; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 73-year-old female patient received BNT162b2 (BNT162B2), on 06Oct2021 as dose 3 (booster), single (Lot number: FF8841), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Allergic to penicillin" (ongoing), notes: when she was a baby; "Diabetes" (ongoing), notes: About 15 years ago. The patient's family history included: "arthritis" (unspecified if ongoing), notes: Her mom has arthritis, but never told her it was PMV PMR variety. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 1, Single, Lot number: EL0142, Anatomical location: Left arm), administration date: 18Jan2021, when the patient was 72-year-old, for COVID-19 Immunization, reaction(s): "Polymyalgia Rheumatica", "She experienced pain", "Sed Rate elevated in the 60s"; BNT162b2 (Dose 2, Single, Lot number: EN6201, Anatomical location: Left arm), administration date: 09Feb2021, when the patient was 72-year-old, for COVID-19 Immunization, reaction(s): "Polymyalgia Rheumatica", "She experienced pain", "Sed Rate elevated in the 60s". The following information was reported: NASOPHARYNGITIS (non-serious) with onset 2022, outcome "unknown", described as "Illness/AE: Cold/about 3 weeks ago". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The patient received first dose on 18Jan2021. The patient has had symptoms for the past she would say year which she thought were simple arthritic concerns, clarified as pain that she had. It turns out that she has gone to a Rheumatologist and a Neurologist, and they diagnosed her with Polymyalgia rheumatica (PMR). She asked for information on PMR relative to COVID-19 Vaccine. The onset was like boom, she was like what the heck. Bloodwork populated in formal fields was done in late 2021, date otherwise unknown. Other tests were done, lupus was ruled out and whatever else done, but patient did not have any further specific details like test types, and results to provide. The patient received first dose on 09Feb2021. The patient received first dose on 06Oct2021. On an unknown date in 2022, about 3 weeks ago, the patient had Illness/AE: Cold.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Bloodwork; Result Unstructured Data: Test Result:60s; Comments: Sed Rate elevated in the 60s; Test Date: 2021; Test Name: Bloodwork; Result Unstructured Data: Test Result:Polymyalgia rheumatica; Comments: had bloodwork and it shows in the bloodwork; Test Date: 2021; Test Name: other tests; Result Unstructured Data: Test Result:ruled out lupus
Aktuelle Erkrankungen: Diabetes (About 15 years ago); Penicillin allergy (when she was a baby)
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis (Her mom has arthritis, but never told her it was PMV PMR variety)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2243007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: CT
Alter: -
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 06.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Blood test Investigation Nasopharyngitis Pain Polymyalgia rheumatica Red blood cell sedimentation rate increased

Symptomtext

Illness/AE: Cold/about 3 weeks ago; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 73-year-old female patient received BNT162b2 (BNT162B2), on 06Oct2021 as dose 3 (booster), single (Lot number: FF8841), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Allergic to penicillin" (ongoing), notes: when she was a baby; "Diabetes" (ongoing), notes: About 15 years ago. The patient's family history included: "arthritis" (unspecified if ongoing), notes: Her mom has arthritis, but never told her it was PMV PMR variety. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 1, Single, Lot number: EL0142, Anatomical location: Left arm), administration date: 18Jan2021, when the patient was 72-year-old, for COVID-19 Immunization, reaction(s): "Polymyalgia Rheumatica", "She experienced pain", "Sed Rate elevated in the 60s"; BNT162b2 (Dose 2, Single, Lot number: EN6201, Anatomical location: Left arm), administration date: 09Feb2021, when the patient was 72-year-old, for COVID-19 Immunization, reaction(s): "Polymyalgia Rheumatica", "She experienced pain", "Sed Rate elevated in the 60s". The following information was reported: NASOPHARYNGITIS (non-serious) with onset 2022, outcome "unknown", described as "Illness/AE: Cold/about 3 weeks ago". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The patient received first dose on 18Jan2021. The patient has had symptoms for the past she would say year which she thought were simple arthritic concerns, clarified as pain that she had. It turns out that she has gone to a Rheumatologist and a Neurologist, and they diagnosed her with Polymyalgia rheumatica (PMR). She asked for information on PMR relative to COVID-19 Vaccine. The onset was like boom, she was like what the heck. Bloodwork populated in formal fields was done in late 2021, date otherwise unknown. Other tests were done, lupus was ruled out and whatever else done, but patient did not have any further specific details like test types, and results to provide. The patient received first dose on 09Feb2021. The patient received first dose on 06Oct2021. On an unknown date in 2022, about 3 weeks ago, the patient had Illness/AE: Cold.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Bloodwork; Result Unstructured Data: Test Result:60s; Comments: Sed Rate elevated in the 60s; Test Date: 2021; Test Name: Bloodwork; Result Unstructured Data: Test Result:Polymyalgia rheumatica; Comments: had bloodwork and it shows in the bloodwork; Test Date: 2021; Test Name: other tests; Result Unstructured Data: Test Result:ruled out lupus
Aktuelle Erkrankungen: Diabetes (About 15 years ago); Penicillin allergy (when she was a baby)
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis (Her mom has arthritis, but never told her it was PMV PMR variety)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2242042

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: MI
Alter: 24,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 17.11.2021
Beginn: 09.04.2022
Tage bis Beginn: 143,0
Dosis: 1
Route/Site: IM / AR

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

COVID-19 Complication of pregnancy Delayed umbilical cord clamping Delivery Depression rating scale score Diarrhoea Exposure during pregnancy Labour induction Malaise Pain Perineal injury Pyrexia SARS-CoV-2 test positive Spontaneous rupture of membranes Term birth Urinary tract infection Uterine contractions during pregnancy Wound closure

Symptomtext

Hospitalized - pregnant, Term pregnancy, hospitalized for vaginal delivery; COVID-19 positive (4,9.22); Fully vaccinated (no booster) Hospitalized at Hospital OB: MD (DC summary, MD - physician, obstetrics) BRIEF OVERVIEW: Admission Date: 4/9/2022 Discharge Date: 4/11/2022 DETAILS OF HOSPITAL STAY: SUBJECTIVE: Patient is a 24 y.o. G2P2002 female at 39w4d with Estimated Date of Delivery: 4/12/22 who presents today with reported fever and body aches at home. She has also had some diarrhea. Presented to triage and tested positive for COVID. Elected to stay for IOL. Pregnancy has been complicated by recurrent UTIs. PRESENTING PROBLEM: Term pregnancy [Z34.90] SVD (spontaneous vaginal delivery) [O80] INTRAPARTUM COMPLICATIONS: Medical Problems (from 04/08/22 to present) No problems associated with this episode. PROCEDURES PERFORMED: Vaginal delivery HOSPITAL COURSE: Patient is a 24 y.o. female G2P2002 who wast admitted for IOL due to new diagnosis of COVID at term She was also vaccinated. She received one cytotec then spontaneously ruptured, making quick progress to 10/+2. She pushed with 3 ctxs to deliver a liveborn female in a compound presentation with the hand as well as a body cord. Cord clamping delayed. Placenta delivered spontaneously and was intact with 3VC. 2nd degree lac repaired with 3-0 vicryl under local anesthesia. EBL 100cc. both went home on PPD #2 in stable condition. Covid sxzs improving. Edinburgh Edinburgh Postnatal Depression Scale Total: 4 DELIVERY DETAILS: DELIVERY TYPE: Vaginal, Spontaneous ESTIMATED DUE DATE: Estimated Date of Delivery: 4/12/22 GESTATIONAL AGE AT DELIVERY: 39w4d G2P2002 DELIVERY PROVIDER: ASSISTING PROVIDER(S): FINDINGS: NEWBORN STATUS: Living NEWBORN SEX: girl Baby Girl A Delivery Date/Time: 9:40 PM WEIGHT: 3.23 kg APGAR: 1 minutes 5 minutes 10 minutes 8 9

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: Normal labor Cholelithiasis Acute gallstone pancreatitis Term pregnancy
Andere Medikamente: ferrous sulfate 325 (65 Fe) MG tablet
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2241147

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: FL
Alter: 60,0
Geschlecht: M
Eingang: 19.04.2022
Impfdatum: 08.10.2021
Beginn: 08.11.2021
Tage bis Beginn: 31,0
Dosis: 2
Route/Site: SYR / LA

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

Rash

Symptomtext

I had a rash, doctor gave me some prescription cream for it and I still have the rash.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin; Blood pressure medication; Cholesterol medication
Allergien: None
Vorherige Impfungen: -

VAERS 2226824

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FF8841

mild

Staat: CA
Alter: 41,0
Geschlecht: F
Eingang: 12.04.2022
Impfdatum: 12.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Blood test normal Urticaria

Symptomtext

I received my COVID booster (3rd Moderna shot) on Nov 12, 2021. On Nov 22, I started getting hives on my chest. These spread and moved all over my body over the course of the week, including my face (eyelids / forehead). At the advice of my doctor, I started taking antihistamines 3x/day, and this got the hives under control. However, once I stopped taking the antihistamines, the hives came back. I talked to an allergist, So, who diagnosed me with chronic hives and recommended that I continue taking the antihistamines, but just one a day. I have done this. Whenever I forget a day or two of the antihistamines, the hives come back. It has now been over 4 months. I wouldn't have thought that this was an adverse reaction to my booster, except that the exact same sequence of events happened to a friend of a friend: Booster, 10 days later: hives, developed into chronic hives.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: My doctor did some blood tests but all results were normal
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2226055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: LA
Alter: 45,0
Geschlecht: F
Eingang: 11.04.2022
Impfdatum: 01.10.2021
Beginn: 13.01.2022
Tage bis Beginn: 104,0
Dosis: 3
Route/Site: SYR / AR

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

COVID-19 Chills Fatigue Hyperhidrosis Influenza like illness Pyrexia SARS-CoV-2 test positive

Symptomtext

Breakthrough case of COVID, I had flu like symptoms, fever and chills, exhaustion, and some sweats.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID test
Aktuelle Erkrankungen: No
Vorgeschichte: High Blood Pressure
Andere Medikamente: Lisinopril 30 mg; Sertraline HCL 100 mg; Bupropion HCL XL 150 mg; Buspirone HCL 15mg; Estradiol 0.1 mg patch.
Allergien: None
Vorherige Impfungen: -

VAERS 2226036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: IL
Alter: 25,0
Geschlecht: F
Eingang: 11.04.2022
Impfdatum: 07.10.2021
Beginn: 16.01.2022
Tage bis Beginn: 101,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Headache Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Upper-airway cough syndrome

Symptomtext

1/16/2022 - Breakthrough case of COVID-19, tested positive on rapid test initially, then on RT-PCR 2 days later. Signs/Symptoms: Low grade fever, headache, fatigue, sore throat, congestion, post nasal drip, minor cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 1/16/2022: rapid home test 1/18/2022: RT PCR nasopharyngeal swab
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2220173

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: NY
Alter: 44,0
Geschlecht: F
Eingang: 07.04.2022
Impfdatum: 06.10.2021
Beginn: 31.03.2022
Tage bis Beginn: 176,0
Dosis: 3
Route/Site: SYR / RA

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

Asthenia COVID-19 Chills Fatigue Feeling abnormal Headache Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

03/31/2022, I had a sore throat. On 4/1/2022 I had the worse headache I have ever had. I had chills, fatigue and weak. On 4/2/2022 I was congested and had brain fog. Congestion and brain fog continued to the present, 6 days. Tested positive positive for COVID on 4/1/2022. I was prescribed an antiviral by the doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID test, Positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Acid Reflux; Arthritis; Endometriosis
Andere Medikamente: Omeprazole; Famotidine; Isotonix; Multivitamin with iron; Isotonix OPC 3; Isotonix Joint support formula; None
Allergien: -
Vorherige Impfungen: -

VAERS 2218270

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: TX
Alter: 70,0
Geschlecht: F
Eingang: 06.04.2022
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Injection site erythema Injection site swelling

Symptomtext

Day of the injection I started having pain in the left shoulder and I got an egg yolk size ball at the injection site with a lot of redness. The swelling resolved in about a week, but the has not gone away. It comes intermittently, but when it happens it is more intense.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None yet. They are scheduled.
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure Depression
Andere Medikamente: Irbesartan HCTZ Prozac Methyl Folate Biotin Vitamin D3 Tylenol
Allergien: Bee stings
Vorherige Impfungen: -

VAERS 2216100

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: MI
Alter: 65,0
Geschlecht: M
Eingang: 05.04.2022
Impfdatum: 04.10.2021
Beginn: 18.02.2022
Tage bis Beginn: 137,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Exposure to SARS-CoV-2 Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test negative SARS-CoV-2 test positive

Symptomtext

I had visited my son and his family, they have two young kiddos who attend daycare. The kids had been sick a week before we saw them but they had been sick but my son who was sick the same way the grandkids were tested for COVID and it was negative. After a day of skiing my wife and I started having a cough and runny nose. The next day my son tested positive for COVID and my son and one grandchild was also positive. Upon returning home we tested and we tested negative. The only symptoms we had were the cough and runny nose. On the 20th about 5 days later I did have a sore throat, but day six my symptoms did improve. I was still positive 11 days after the initial exposure and on day 16 the 25th I tested negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: COVID Test both at home and PCR tests at the doctor as well.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Triamterene HCTZ; Loratadine
Allergien: NKA
Vorherige Impfungen: -

VAERS 2216035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: MA
Alter: 68,0
Geschlecht: F
Eingang: 05.04.2022
Impfdatum: 04.10.2021
Beginn: 27.03.2022
Tage bis Beginn: 174,0
Dosis: 3
Route/Site: SYR / AR

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

COVID-19 Chills Cough Diarrhoea Fatigue Gastrointestinal disorder Headache Malaise Nausea Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive Sinus congestion Throat irritation Vomiting

Symptomtext

The morning of 03/27/2022 around 08:00 scratchy sore throat went away that morning and by afternoon around 1:30PM it came back suddenly. I ran an at-home test and positive within a minute and I did another immediately one and positive again. By that evening I wasn't feeling well and within 24 hours I had symptoms of headache, cough, chills, sinus congestion, fatigue, GI Symptom that included nausea, vomiting, and loose stools. I contacted my PCP and I was able to press an option to reach their Covid Program that was aligned with the hospital to speak to a team. They called me back an hour later and they contacted my PCP to recommend Paxlovid. I did not end up taking that. I had a few more conversions with my physician's office because the pharmacy did not have Paxlovid so I gave them another pharmacy that did. I was able to get it and because I was vomiting anytime I tried to take any pill I ended up not taking it at all. I felt like it was more important for me to stay hydrated and not vomit anymore. I did not take the medication. Today, April 5, 2022 is the first day I feel better. I am a nurse so I did not feel like I needed any additional intervention and just did saline wash for my sinuses, walk-around, and stay hydrated. I did take another government at-home Covid test today and results were also positive. I would say yes that I recovered but I still don't feel 100% because I do have some congestion and I did test positive still today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: At-home test 03/27/2022, took two both were positive. Another at-home COVID test 04/05/2022 also positive.
Aktuelle Erkrankungen: I possibly had a sinus infection around the third dose either a few weeks before or after.
Vorgeschichte: I did have a history autoimmune disease that included joint pain; asthma; headaches; I did herbal medicine; acupuncture probably around 2010 and have not have symptoms since.
Andere Medikamente: Vitamin D; biotin; B complex; Flonase; Claritin; magnesium; occasionally ibuprofen or Tylenol for pain.
Allergien: Not allergies but there are two medications I cannot take which are Percocet and Talwin.
Vorherige Impfungen: -

VAERS 2208848

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: NY
Alter: 65,0
Geschlecht: F
Eingang: 05.04.2022
Impfdatum: 06.10.2021
Beginn: 03.01.2022
Tage bis Beginn: 89,0
Dosis: 3
Route/Site: - / -

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

Body height COVID-19 SARS-CoV-2 test Vaccination failure Weight Rash Rash macular Skin haemorrhage

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 65 year-old female patient received bnt162b2 (BNT162B2), administration date 06Oct2021 (Lot number: FF8841, Expiration Date: Dec2021) at the age of 65 years as dose 3 (booster), single, administration date 03Mar2021 (Lot number: EN6203) as dose 2, single and administration date 10Feb2021 (Batch/Lot number: unknown) as dose 1, single for Covid-19 immunisation; influenza vaccine (FLU VACCINE VII), administration date 06Oct2021 (Batch/Lot number: unknown) as dose number unknown, single. Relevant medical history included: "hypothyroid", start date: 2015 (unspecified if ongoing). Concomitant medication(s) included: ARMOUR THYROID taken for hypothyroidism. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 03Jan2022, outcome "unknown" and all described as "Adds she had the booster in October and then had omicron in December". The event "adds she had the booster in October and then had omicron in December" was evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: body height: (unspecified date) 156, notes: (cm); (unspecified date) 5'1.5"; sars-cov-2 test: (03Jan2022) positive, notes: (omicron). Covid test was done in Dec2021, then resulted on 03Jan2022; weight: (unspecified date) 47.63 kg; weight: (unspecified date) 105 lbs. Therapeutic measures were taken as a result of Covid-19. Clinical course: She had the booster in Oct and then had omicron in Dec, she did not get the results because of the holiday was impossible to get a hold of them. Clarifies that the Covid test was done in Dec2021, then resulted on 03Jan2022. Facility where the most recent COVID-19 vaccine was administered was Withheld facility. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Military facility: There were soldiers there when she got the vaccine. it was a vaccination site. Emergency Room not required. Product complaint to report was Yes. The lot number for bnt162b2 was not provided and will be requested during follow up. Sender's Comments: Linked Report(s): US-PFIZER INC-202200474011 same reporter, drug, different event.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Test Name: Height; Result Unstructured Data: Test Result:156; Comments: (cm); Test Name: Height; Result Unstructured Data: Test Result:5'1.5"; Test Date: 20220103; Test Name: Covid test; Test Result: Positive; Comments: (omicron). Covid test was done in Dec2021, then resulted on 03Jan2022; Test Name: Body Weight; Test Result: 47.63 kg; Test Name: Weight; Result Unstructured Data: Test Result:105 lbs..
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism
Andere Medikamente: ARMOUR THYROID
Allergien: -
Vorherige Impfungen: -

VAERS 2214076

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: AK
Alter: 44,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 02.04.2021
Beginn: 05.04.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / RA

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

Erythema Herpes zoster Urticaria

Symptomtext

It started 3 days after being vaccine. I began to start getting red marks on my hips and it's by the size of a 5-cent piece. I start breaking out with hives and than I get the Shingles. My GP prescribes Valacyclovir each time I get the Shingles. I have gotten this each vaccines. I take it as needed.

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Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: PTSD, Sleep Apnea, Migraine and Depression
Andere Medikamente: Clonazepam 1mg x3, Duloxetine 30mg x3, Nurtec 75mg 16 days a month, Aimovig injection 1mg, Flovent Inhaler, Albuterol Inhaler, Zolpidem, Multivitamin, Vitamin C & D, Advil, Benadryl and Gas X.
Allergien: Almonds, Tylenol and Seldane
Vorherige Impfungen: Dose 1 vaccine

VAERS 2130599

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: WI
Alter: 82,0
Geschlecht: M
Eingang: 04.04.2022
Impfdatum: 07.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / RA

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

Biopsy skin Pruritus Rash Biopsy Vaccine positive rechallenge

Symptomtext

Having the last booster shot on 10/07/21, in about a week it will be 6 months I?ve been suffering the side effects from the last shot. I stayed with the Pfizer shot because all the experts kept saying, don?t switch to a different kind of shot, stay with the one you started with. The only time I had complete relief from the itching and rash was when I was on Prednisone, (4 times in the last year) but everything came back in 2-3 days when I would get off of the Prednisone. My dermatologist, Dr and my other doctors, doesn?t want to put me on Prednisone again because of the long term effect it can have on a person. She also did 2 biopsy?s on me to make sure it wasn?t a skin disease and she determined it is a reaction from the Covid shot. Just can?t seem to get it out of my system.

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Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Stomach ulcers
Andere Medikamente: Lipitor 40mg Tamsulosin 0.4mg Lutein 20mg
Allergien: NSAIDS Stomach ulcers
Vorherige Impfungen: Pfizer, 01/08/21. 02/15/21. rash and itching on all shots

VAERS 2130599

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: WI
Alter: 82,0
Geschlecht: M
Eingang: 04.04.2022
Impfdatum: 07.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Biopsy skin Pruritus Rash Biopsy Vaccine positive rechallenge

Symptomtext

Having the last booster shot on 10/07/21, in about a week it will be 6 months I?ve been suffering the side effects from the last shot. I stayed with the Pfizer shot because all the experts kept saying, don?t switch to a different kind of shot, stay with the one you started with. The only time I had complete relief from the itching and rash was when I was on Prednisone, (4 times in the last year) but everything came back in 2-3 days when I would get off of the Prednisone. My dermatologist, Dr and my other doctors, doesn?t want to put me on Prednisone again because of the long term effect it can have on a person. She also did 2 biopsy?s on me to make sure it wasn?t a skin disease and she determined it is a reaction from the Covid shot. Just can?t seem to get it out of my system.

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Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Stomach ulcers
Andere Medikamente: Lipitor 40mg Tamsulosin 0.4mg Lutein 20mg
Allergien: NSAIDS Stomach ulcers
Vorherige Impfungen: Pfizer, 01/08/21. 02/15/21. rash and itching on all shots

VAERS 2213088

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: GA
Alter: 67,0
Geschlecht: M
Eingang: 02.04.2022
Impfdatum: 06.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Blood pressure measurement Blood test Erythema Rash

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program. The reporter is the patient. A 67 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 06Oct2021 (Lot number: FF8841, Expiration Date: 30Dec2021) at the age of 67 years as dose 3 (booster ), single for Covid-19 immunisation. Relevant medical history included: "Anxiety" (unspecified if ongoing); "Blood pressure" (unspecified if ongoing); "eye infection" (unspecified if ongoing); "it was a diuretic" (unspecified if ongoing). Concomitant medication(s) included: KLONOPIN taken for anxiety; LISINOPRIL taken for blood pressure abnormal, start date: Mar2010; NIFEDIPINE taken for blood pressure abnormal, start date: Mar2010; LABETALOL taken for diuretic therapy. Vaccination history included: Bnt162b2 (Second dose: given on 17Mar2021, manufacturer: Pfizer, lot number: EP7534. Information is on a sticker on the card for second dose. Expiry: unknown. NDC: unknown. Given at the (Facility name) at drive thru in right arm.), administration date: 17Mar2021, when the patient was 66 years old, for Covid-19 immunization, reaction(s): "sore arm"; Bnt162b2 (First dose: manufacturer: Pfizer, lot number: EL9266, expiration: unknown. NDC: unknown. Information for first dose is handwritten on the card. Given at the (Facility name) at drive thru in right arm), administration date: 22Feb2021, when the patient was 66 years old, for Covid-19 immunization, reaction(s): "sore arm"; Flu vaccine (He usually get flu vaccine but he was late getting to it and the flu season was over so he didn't get flu vaccine). The following information was reported: RASH (non-serious), outcome "not recovered", described as "He indicates that a couple of months after the booster dose he noticed that both of his palms are bright red"; ERYTHEMA (non-serious), outcome "not recovered", described as "Caller's got red/all of a sudden right to the finger tips is shiny red". The events "he indicates that a couple of months after the booster dose he noticed that both of his palms are bright red" and "caller's got red/all of a sudden right to the finger tips is shiny red" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Patient noticed it two months ago. He had a doctor's appointment lined up so he followed up there. The doctor said it looked like a chemical burn, but caller wouldn't have a chemical burn for 2 months.

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Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Test Name: blood pressure; Result Unstructured Data: Test Result:220/120; Test Name: blood pressure; Result Unstructured Data: Test Result:160/70; Test Name: blood pressure; Result Unstructured Data: Test Result: fine; Test Date: 201003; Test Name: blood pressure; Result Unstructured Data: Test Result:240/140; Test Date: 20220328; Test Name: blood pressure; Result Unstructured Data: Test Result: it was good; Test Name: bloodwork; Result Unstructured Data: Test Result: normal; Comments: Caller had bloodwork done and it all came back normal.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Blood pressure abnormal; Diuretic therapy; Eye infection.
Andere Medikamente: Klonopin; Lisinopril; Nifedipine; Labetalol
Allergien: -
Vorherige Impfungen: -

VAERS 2208824

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: -
Alter: -
Geschlecht: M
Eingang: 31.03.2022
Impfdatum: 06.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Asthenia Fatigue Memory impairment Pyrexia

Symptomtext

his mind seemed to be forgetful; 2 days fever; weakness and tiredness for 2-3 months; weakness and tiredness for 2-3 months; 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): US-PFIZER INC-202200464133 (Pfizer). A 79 year-old male patient received bnt162b2 (BNT162B2), administration date 06Oct2021 (Lot number: FF8841) 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), administration date: Jan2021, for Covid-19 immunization; Bnt162b2 (Dose 2), administration date: Feb2021, for Covid-19 immunization. The following information was reported: MEMORY IMPAIRMENT (non-serious), outcome "unknown", described as "his mind seemed to be forgetful"; PYREXIA (non-serious), outcome "unknown", described as "2 days fever"; FATIGUE (non-serious), ASTHENIA (non-serious), outcome "unknown" and all described as "weakness and tiredness for 2-3 months". Additional information: Patient stated that he had his 2 shots and booster last fall and had bad reactions with the Pfizer COVID vaccine. At first he did not associate it with the shot and stated that he had 2 days fever, weakness and tiredness for 2-3 months, it probably was a lingering effect of the vaccination and ell couple times and his mind seemed to be forgetful, he did not think it is dementia. Patient scared about taking another boster shot. NDC, UPC number of Covid-19 vaccine was unknown. No follow-up attempts are possible. No further information is expected.

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

VAERS 2206458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: FL
Alter: 84,0
Geschlecht: F
Eingang: 30.03.2022
Impfdatum: 25.09.2021
Beginn: 25.12.2021
Tage bis Beginn: 91,0
Dosis: 3
Route/Site: SYR / LA

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

Cough Fatigue Mucosal discolouration Respiratory tract congestion

Symptomtext

It started with a cough, the next day I had congested too. It was a tickle cough. Then I was extreme fatigue which I never experienced fatigue that way. Then the mucus started to be yellow by the 5th day. I phoned the doctor on the 9th day and because my mucus was now green by this time he prescribed an antibiotic which I took 2 a day for 6 days, and it cleared up gradually, and by day 17, I only had a cough. This cough lasted about a month, its a tickle cough. By day 32, the cough finally went away. I was not tested for covid

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure, Chronic Kidney Disease
Andere Medikamente: Levothyroxine, Aspirin 81mg, Nifedipine, Losartan, Metoprolol, Simvastatin, Senior Vitamins
Allergien: Hydralazine
Vorherige Impfungen: -

VAERS 1782519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF8841

mild

Staat: VT
Alter: 92,0
Geschlecht: F
Eingang: 29.03.2022
Impfdatum: 09.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

Biopsy skin Injection site haematoma Insomnia Pruritus Erythema Peripheral swelling Urticaria

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 93-year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 09Oct2021 (Lot number: FF8841) at the age of 92 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: ELIQUIS taken for anticoagulant therapy; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; BENADRYL; TYLENOL; PREDNISONE taken for rash. Vaccination history included: Bnt162b2 (Her first vaccine was on 23Jan2021, with lot number EN5318., Her first two vaccines were given in her left arm), administration date: 23Jan2021, when the patient was 91 years old, for Covid-19 immunization; Bnt162b2 (Her second vaccine was on 13Feb2021 with lot number EN5318., Her first two vaccines were given in her left arm), administration date: 13Feb2021, when the patient was 91 years old, for Covid-19 immunization. The following information was reported: INSOMNIA (non-serious), outcome "unknown", described as "she hasn't been able to sleep at night"; PRURITUS (non-serious), outcome "not recovered", described as "body itching"; RASH (non-serious), outcome "not recovered", described as "rash all over her upper body, including her arms, back, and stomach"; INJECTION SITE HAEMATOMA (non-serious), outcome "recovered", described as "Her arm had a big hematoma where she had the shot in her right arm.". The events "body itching" and "rash all over her upper body, including her arms, back, and stomach" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Patient received 3 doses of the COVID shots. She doesn't had a prescribing doctor. It has been five months now, and she hadn't been able to sleep at night. She had been experiencing body itching and a rash all over her upper body, including her arms, back, and stomach. She had been to a Dermatologist 5 times, and nobody can say what it was. She had tried antihistamine, steroid ointments, and prednisone, and none of them worked for her rash. Right after her booster shot, four days later, she developed COVID arm. Her arm had a big hematoma where she had the shot in her right arm. She had recovered completely from that. Her first two vaccines were given in her left arm. The rash started about two weeks after the booster. It started with itching skin and then broke out from there. She got her first two vaccines in her senior complex. For a year and a half she had been on Eliquis a blood thinner. She takes 2.5mg in morning and 2.5mg at night. She had tried taking Zyrtec, Benadryl, and Tylenol. She doesn't know what else. She checks her medicines regularly. Patient visit dermatologist and primary Physician Office. Patient did not visit Emergency Room. Patient did not taken prior Vaccinations (within 4 weeks). Patient medical history (including any illness at time of vaccination): provide other relevant medical history including but not limited to these conditions: diagnosed allergies, compromised immune status, respiratory illness, genetic/chromosomal abnormalities, endocrine abnormalities (including diabetes) and obesity: no. Relevant Tests: List other relevant diagnostic and confirmatory test results for event(s), for example, from blood tests, cerebrospinal fluid culture, bacterial sero-type, diagnostic imaging, (e.g., chest X-ray, MRI). Description of complaint: She has tried antihistamine, steroid ointments, and prednisone, and none of them worked for her rash. She doesn't have the NDC/lot/expiration for those products. She knows she has tried Zyrtec, Benadryl, and Tylenol, but doesn't know what else right now. Is a sample of the product available to be returned, if requested (Y/N): Yes, caller was informed of a prepaid mailer in 3-10 business days. No follow-up attempts are possible. No further information is expected.

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Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: Test Name: skin biopsy; Result Unstructured Data: Test Result:Unknown Results; Comments: Dermatologist did a skin biopsy on both arms to make sure it wasn't a bug bite, and it came back as a Probable drug eruption .
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ELIQUIS; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; BENADRYL; TYLENOL; PREDNISONE.
Allergien: -
Vorherige Impfungen: -