VAERS Reports #FE3590

VAERS 2713154

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: TX
Alter: 41,0
Geschlecht: F
Eingang: 13.11.2023
Impfdatum: 05.10.2021
Beginn: 26.01.2022
Tage bis Beginn: 113,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 pneumonia Cough Fatigue Inflammatory marker test Vomiting Wheezing

Symptomtext

Acute hypoxic respiratory failure due to COVID-19 pneumonia: Completed course of Remdisivir. Symptoms also include nonproductive cough, wheezing, fatigue, vomiting. Received Actemra on 01/28/2022. empiric antibiotics, IV steroids, nebs, oxygen. On Lovenox for DVT prophylaxis, will switch to apixaban as outpt for 2 weeks. Monitoring COVID-19 inflammatory markers. Completed steroids

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 16,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2645187

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

kritisch

Staat: FL
Alter: 77,0
Geschlecht: M
Eingang: 14.06.2023
Impfdatum: 26.02.2021
Beginn: 19.08.2022
Tage bis Beginn: 539,0
Dosis: 3
Route/Site: - / -

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

Acute myocardial infarction Anticoagulant therapy COVID-19 COVID-19 pneumonia Cardiomyopathy Cough Diuretic therapy Dyspnoea Echocardiogram abnormal Ejection fraction decreased Pneumonia viral Pulmonary oedema SARS-CoV-2 test positive Troponin increased Vaccine breakthrough infection

Symptomtext

BREAKTHROUGH COVID: FULLY VACCINATED WITH BOOSTER BY PFIZER, COVID POSITIVE. 79-year-old gentleman who presented with complaint of cough, shortness of breath. Found to have pulmonary edema. Echo revealed cardiomyopathy. Patient had elevated troponins consistent with NSTEMI. He was started on heparin drip, IV diuresis. Cardiology was consulted. They recommend ischemic workup outpatient in light of patient's positive COVID status. Regarding COVID viral pneumonia, patient placed on oral Decadron and Albuterol, Symbicort, anticoagulation. Fortunately he had no significant hypoxia during his stay. Pt now has an ejection fracture of 20%-25%.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: UNKNONWN
Vorgeschichte: CAD, AFIB, CHF
Andere Medikamente: UNKNOWN
Allergien: PENICILLINS, GLUTEN
Vorherige Impfungen: -

VAERS 2644622

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FE3590

kritisch

Staat: PA
Alter: 52,0
Geschlecht: M
Eingang: 13.06.2023
Impfdatum: 31.10.2021
Beginn: 20.11.2021
Tage bis Beginn: 20,0
Dosis: 3
Route/Site: IM / UN

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

Coronary artery insufficiency Coronary artery thrombosis Death

Symptomtext

Death due to Acute Coronary Insufficiency due to Acute Thrombus in the Left Descending Coronary Artery

Weitere VAERSDATA-Felder

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

VAERS 2644067

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: -
Alter: 41,0
Geschlecht: M
Eingang: 12.06.2023
Impfdatum: 31.10.2021
Beginn: 07.11.2022
Tage bis Beginn: 372,0
Dosis: 2
Route/Site: IM / LA

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 2599573

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: NY
Alter: 78,0
Geschlecht: F
Eingang: 20.03.2023
Impfdatum: 18.10.2022
Beginn: 20.01.2023
Tage bis Beginn: 94,0
Dosis: 3
Route/Site: IM / RA

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

Acute kidney injury Acute respiratory failure Asthenia Blood creatinine increased Blood urea increased COVID-19 Chest X-ray normal Cough Glomerular filtration rate decreased Headache Lethargy Renal impairment SARS-CoV-2 test positive

Symptomtext

1/20/2023-Presents to ED, was seen at PCP (1/18- started on PO doxy and Paxlovid), Covid + test. C/O weakness, lethargy, cough and headache. Afebrile, HR-40. Spo2 100% RA. CXR- no evidence of acute cardiopulmonary disease. Admit acute hypoxic resp failure s/t Covid. AKI eGFR 27-hold remdesivir. Start Decadron, IV doxy and ceftriaxone. Start Combivent . Will consider remdesivir if renal function improves BUN/ Creatnine 44/1.9. On 3L Spo2 now 94%. 1/23/2023-Cont. V decadron, doxy and ceftriaxone. Start remdesivir, eGFR >60. Spo2 93% in RA. 1/30/2023-Covid downgrade awaiting d/c to snf. 2/1/2023-Finished IV antibiotics, continue decadron taper. D/c to sub acute rehab.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 12,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, Parkinsons, Fibromyalgia
Andere Medikamente: -
Allergien: Cephalosporins, PCN, Pipercillin-tazobactam and tazobactam
Vorherige Impfungen: -

VAERS 2586337

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: MI
Alter: 71,0
Geschlecht: M
Eingang: 23.02.2023
Impfdatum: 18.10.2021
Beginn: 15.01.2023
Tage bis Beginn: 454,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Angiogram pulmonary abnormal Aspiration pleural cavity Bacterial test negative Blood culture positive Blood glucose increased C-reactive protein increased COVID-19 Chills Chronic kidney disease Condition aggravated Cough Culture negative Diabetes mellitus management Dyspnoea Echocardiogram normal Fibrin D dimer Hydronephrosis

Symptomtext

"Patient with history of COVID vaccines who admitted to hospital with COVID detected PCR. Provider d/c note: ""72-year-old divorced male with past medical history significant for longstanding type 1 diabetes complicated by blindness in the setting of proliferative retinopathy, pancreatic insufficiency, hypothyroidism, primary hypertension, Gilbert's disease and hyperlipidemia with recent upper respiratory illness due to influenza A in December 2022 presented with acute onset of cough, worsening shortness of breath and fevers or chills at home found to have sepsis and acute respiratory failure with hypoxia in the setting of a right lower lobe pneumonia with associated right pleural effusion. Of note COVID-19 virus was also detected at time of admission. Procalcitonin was markedly elevated at 26.26. Patient also had marked hyperglycemia in the mid 300s. Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) Patient's sepsis in the setting of pneumonia was treated with IV fluid bolus and then maintenance IV fluids as well as starting antibiotics with IV ceftriaxone and azithromycin. CRP was markedly elevated to 19.3 and D-dimer elevated to 2170. In the setting of COVID 19 CT angiogram of chest was obtained to rule out pulmonary emboli which was ruled out. However a large right pleural effusion was noted associated with near complete consolidation of the right lower lobe and some consolidation in the lateral segment of the right middle lobe and inferior right upper lobe. There was also some characteristics consistent with possible pulmonary necrosis. Patient's ceftriaxone was brought to Unasyn to cover for oral anaerobes. MRSA nares swab was negative. Urine strep pneumoniae and urine Legionella antigens were negative. Interventional Radiology was consulted and performed a right-sided thoracentesis draining 1.2 L of transudative fluid. Pleural fluid cultures were no growth to date. With hypoxia being attributed to bacterial pneumonia it was decided to not treat COVID-19 viral infection. Patient's hypoxia resolved over several days as did his sepsis. Notably patient had 2 sets of blood cultures that both grew staph epidermidis, pansensitive. Collaborated informally with Infectious Diseases and they felt that it would be impossible to rule out this bacteria as a pathogen although it still would be most likely contaminant. Infectious diseases felt treatment for 7 days with Unasyn transition to Augmentin to cover the bacterial pneumonia would be adequate to also treat the staph epidermidis in the blood which cleared quickly with surveillance cultures. Echocardiogram was obtained which showed normal structural heart with no signs of vegetations. Plan was to complete course of antibiotics and then weight 1 additional week and then rechecked 2 sets of blood cultures to confirm no residual signs of bacteremia. Patient was discharged on Augmentin in stable condition. On separate note he was also started on vitamin-D supplementation for vitamin-D deficiency. Patient was also noted to have renal insufficiency which developed some time after October 2022. There was evidence only of minimal left hydronephrosis on imaging with no stones or other obvious pathology. Patient's renal function remained stable which suggested a somewhat chronic component to the kidney disease versus a component of acute tubular necrosis which has delayed renal recovery. Urinalysis was noninflammatory so there was felt to be no need to consult Nephrology. Of note patient was very particular about managing his diabetes because of history of hypoglycemia and so he was allowed to decide how much long and short-acting insulin he took during his hospitalization. He preferred no changes to his outpatient diabetic regimen on discharge Issues Requiring Follow Up: (Who, what, when, and how communicated?) Follow-up resolution of bacterial pneumonia with plan to repeat 2 sets of blood cultures 1 week after completing antibiotics, discussed this with primary care provider who agreed to follow-up with repeat blood cultures; follow-up renal insufficiency, mild left hydronephrosis and other medical issues with primary care provider; follow-up diabetes mellitus with endocrinology; recommend repeat CT of chest in 6-8 weeks to assess resolution of pneumonia with possible component of pulmonary necrosis."""

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: Covid PCR detected on 01/15/2023
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular Primary hypertension Mixed hyperlipidemia Digestive Pancreatic insufficiency Gastroesophageal reflux disease without esophagitis Tubular adenoma of colon Barrett's esophagus Endocrine Blindness due to type 1 diabetes mellitus Type 1 diabetes mellitus with blindness and proliferative retinopathy Hypothyroidism Proliferative diabetic retinopathy of both eyes associated with type 1 diabetes mellitus (*) Type 1 diabetes mellitus with hyperglycemia Musculoskeletal Diaphragmatic hernia Respiratory Right lower lobe pneumonia with possible gram negative and anaerobic involvement Parapneumonic effusion Pulmonary necrosis Urinary Acute kidney injury Hydronephrosis of left kidney - minimal Other History of influenza A - Dec 2022 Gilbert's disease Disorder of bilirubin excretion Family history of prostate cancer Blindness of both eyes Bilateral recurrent inguinal hernia without obstruction or gangrene Medicare annual wellness visit, subsequent Sepsis COVID-19 virus detected
Andere Medikamente: amoxicillin-clavulanate (AUGMENTIN) 875-125 mg per tablet Take 1 tablet by mouth 2 (two) times daily. aspirin 81 mg Tab Take 1 tablet by mouth twice a week Takes this Wednesday and sunday. BD ULTRA-FINE MINI PEN NEEDLE 31 gauge x 3/16" nd
Allergien: AdhesiveRash Poison Ivy ExtractRash
Vorherige Impfungen: -

VAERS 2584077

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: -
Alter: 61,0
Geschlecht: M
Eingang: 19.02.2023
Impfdatum: 02.11.2021
Beginn: 16.01.2023
Tage bis Beginn: 440,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Anticoagulant therapy Atrial fibrillation COVID-19 Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Cough Dyspnoea Glycosylated haemoglobin increased Hypercapnia Hypertension Hypervolaemia Hypoxia Lung infiltration Obesity Obstructive sleep apnoea syndrome Pickwickian syndrome

Symptomtext

Patient is a 62 y.o. male patient of Physician with history of COPD, GAD, T2DM, GERD, PAF, HTN who presented with dyspnea, found to have worsening respiratory failure, COPD exacerbation and COVID-19 infection. He improved with steroids, COPD care and was weaned back to his home 2L NC and discharged home. Acute on Chronic hypoxic/hypercarbic respiratory failure COPD with acute exacerbation Multifactorial, including COVID, volume overload, OSA/OHS Requiring 4L NC on admission, baseline O2 requirement: 2L CXR w/bilateral interstitial infiltrates, no focal consolidation Resume home Advair; add Spiriva and continue levalbuterol nebs Aggressive pulm toilet Covid-19 Virus Infection Date of onset of symptoms: 1/15 Symptoms present on admission: Dyspnea, hypoxia, cough Date of covid positive test: 1/16 Vaccination status: vaccinated, booster x1 (11/2021) Imaging: CXR w/bilateral interstitial infiltrates, no focal consolidation Oxygen requirements on admission: 4L NC Current oxygen requirements: 2L NC (baseline 2L at home) Medical therapy: remdesivir and steroids Consultants following: None Anticipated special isolation end date: 1/26 Uncontrolled Hypertension Secondary to medication non-compliance BP 220/110 on admission Improved on home regimen -- resumed on discharge Permanent AF Chronic, rate-controlled Resumed home PO Amiodarone, BB, Eliquis T2DM, non-insulin dependent A1c 6.0 Resume home metformin Morbid Obesity OSA/OHS

Weitere VAERSDATA-Felder

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

VAERS 2573265

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: -
Alter: 81,0
Geschlecht: F
Eingang: 01.02.2023
Impfdatum: 14.10.2021
Beginn: 01.01.2023
Tage bis Beginn: 444,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Blood culture negative COVID-19 Computerised tomogram thorax abnormal Dyspnoea Influenza virus test negative Lymphadenopathy Pneumonia Procalcitonin decreased SARS-CoV-2 test positive Sputum culture Streptococcus test negative Urine analysis normal Urine antigen test

Symptomtext

Patient is a 82 y.o. female patient of MD with history of breast cancer s/p left mastectomy and right lumpectomy, atrial fibrillation, chronic anticoagulation with Eliquis, DM2, HTN presented with shortness of breath with recent COVID 19 positive test results Acute COVID-19 Virus Infection Possible secondary bacterial pneumonia Acute hypoxic respiratory failure Date of onset of symptoms: 12/18/2022 Symptoms present on admission: Shortness of breath, hypoxemia Date of covid positive test: 12/19/2022; repeat for hospitalization on 1/2/2023 Vaccination status: vaccinated ? Imaging: CT pulmonary arteries - no PE; but shows Multifocal pneumonia with reactive lymph nodes in mediastinum and hilum. ? Influenza negative ? Blood culture no growth to date ? Sputum culture no growth to date ? Pro calcitonin low ? Urine Strep pneumonia Ag negative Oxygen requirements on admission:6L Oxygen saturation 95% on 2 L nasal cannula Medical therapy: ? Completed course of Decadron treatment ? Stopped Levaquin 1/5 as no clear bacterial infection ? Mucinex ? IV lasix for dry lung strategy ? Per Pulm not a candidate for Toci or other immunosuppressant The patient is clinically improved, isolation can be discontinued. Continue Mucinex, Lasix, oxygen support. OSA Continue to monitor and treat as needed. Paroxysmal atrial fibrillation Chronic HFpEF Aortic valve stenosis Hypertension, essential Follows with cardiology Previous cardioversion June 2022 12/12/2021 echo with normal EF Continue Lasix, flecainide, verapamil, and Eliquis. DM2 July 2022 A1c 6.8 Continue Lantus insulin Continue to monitor the blood sugars and treat as needed with sliding scale coverage.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 13,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2567595

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: LA
Alter: 75,0
Geschlecht: F
Eingang: 25.01.2023
Impfdatum: 19.10.2021
Beginn: 08.08.2022
Tage bis Beginn: 293,0
Dosis: 3
Route/Site: IM / LA

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

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

Symptomtext

Patient had breakthrough infection and passed away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 1,0
Labordaten: Positive COVID test on 7/28/2022 and 8/5/2022.
Aktuelle Erkrankungen: Unknow
Vorgeschichte: Dementia DM 2 HTN Dyslipidemia
Andere Medikamente: Metformin Lisinopril Estradiol Pravastatin Sodium Gabapentin Mirabegron Metoprolol Tartrate Amlodipine Aspirin Ascorbic Acid Cholecalciferol Cyanocobalamin
Allergien: Adhesive tape Latex
Vorherige Impfungen: -

VAERS 2566892

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: MN
Alter: 81,0
Geschlecht: M
Eingang: 24.01.2023
Impfdatum: 06.10.2021
Beginn: 11.11.2022
Tage bis Beginn: 401,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Chills Cough Dyspnoea Hypervolaemia Myalgia Positive airway pressure therapy Pyrexia Respiratory failure SARS-CoV-2 test positive

Symptomtext

Patient with history of atrial fibrillation, oxygen-dependent COPD, ESRD. Patient brought to the ED by EMS on 11/11 for shortness of breath for the past two days. He uses O2 at baseline, but was at 45% upon EMS arrival. EMS placed the patient on 15L via rebreather mask, sating him to 93%. In the ED, patient also reported fever, chills, myalgias, and cough, and notes he tested positive for COVID on 11/9. Patient was also tested for COVID in the ED on 11/11 and was positive. Ultimately patient admitted 11/11/2022 - 11/14/2022 for acute on chronic hypoxic respiratory failure from COVID-19 pneumonia and possible superimposed bacterial pneumonia, as well as fluid overload from missing HD. He initially required BiPAP and eventually weaned down to 3 liters (baseline). Patient has received the COVID primary vaccine series and one booster.

Weitere VAERSDATA-Felder

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

VAERS 2552616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FE3590

kritisch

Staat: NY
Alter: 68,0
Geschlecht: F
Eingang: 06.01.2023
Impfdatum: 06.10.2022
Beginn: 10.12.2022
Tage bis Beginn: 65,0
Dosis: 5
Route/Site: SYR / UN

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

Cardiac arrest Dyspnoea Fluid retention Laboratory test SARS-CoV-2 test negative

Symptomtext

I received my 5th dose of Pfizer Bivalent booster on 10/06/2022. On 12/10/2022 I experienced Cardiac arrest. I was hospitalized for 5 days. I went to the urgent care at 03:00 PM first because I was experiencing shortness of breath and fluid retention. By 08:00 I was admitted in the hospital. At the hospital they did several test. They prescribed me with furosemide, LIPITOR and baby aspirin. I got out of the hospital on 12/17/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 5,0
Labordaten: 06JAN2023 COVID-19 test negative
Aktuelle Erkrankungen: None
Vorgeschichte: GERD; High Blood Pressure
Andere Medikamente: Atenolol; omeprazole; RELAFEN; WELLBUTRIN; multivitamin; vitamin D; calcium
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2548893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 03.01.2023
Impfdatum: 14.04.2021
Beginn: 28.12.2022
Tage bis Beginn: 623,0
Dosis: 3
Route/Site: - / -

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

Acute myocardial infarction Asymptomatic COVID-19 Hypertension SARS-CoV-2 test positive

Symptomtext

Pt has a PMH of diabetes, CKD stage III, and morbid obesity. She was admitted to the hospital due to an NSTEMI and hypertension. She was also found to be asymptomatically COVID positive.

Weitere VAERSDATA-Felder

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

VAERS 2543597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: WI
Alter: 76,0
Geschlecht: M
Eingang: 27.12.2022
Impfdatum: 01.12.2021
Beginn: 12.12.2022
Tage bis Beginn: 376,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Death on 12/12/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Positive Covid-19 test on 11/29/2022
Aktuelle Erkrankungen: -
Vorgeschichte: dementia; OSC: COVID-19; HTN; HLD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2542155

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: -
Alter: 89,0
Geschlecht: M
Eingang: 23.12.2022
Impfdatum: 12.10.2021
Beginn: 21.11.2022
Tage bis Beginn: 405,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Anaemia Anticoagulant therapy Aspiration Atrial fibrillation Bladder catheter removal Bladder catheterisation Blood creatinine increased Blood folate normal Blood iron decreased Catheterisation cardiac abnormal Chest X-ray abnormal Chest discomfort Chest pain Coronary artery occlusion Delirium Electrocardiogram Q waves Electrocardiogram ST segment elevation

Symptomtext

Hospital Course: Patient is a 90 y.o. male patient of DO with a history of mild dementia but living independently presented to Hospital 12/05/2022 with chest discomfort radiating to both arms. His symptoms had begun the day before but were less specific. He was found to have ST elevation, albeit with Q waves across the anterior precordium. Due to ongoing symptomatology he was taken to the cardiac catheterization lab where he underwent intervention to the LAD successfully. He continues to have issues with sundowning, but now is in sinus rhythm and his renal function has normalized. He was then discharged home 12/10/2022 with home health assistance. He will also follow-up with cardiology. Discharge Diagnoses: Anterior STEMI Risk factors: HLD, CKD, Heart Score: 8. Presented with chest pain of unclear duration -Troponin 2,501, EKG with ST elevations V4/5/6, LHC mid/distal LAD showing complete occlusion Timi flow 0 -- > timi 3 flow after intervention. -Continue eliquis, plavix, atorvistatin, lisinopril 5 mg Paroxsymal A Fib. With RVR Likely in the setting of recent MI and volume depleted status -Received Lopressor IV 2.5 x 4 overnight with improvement of HR -transition from amio gtt to oral amio 200 mg BID, after risks and benefits discussion with family, will transition to 2.5mg of eliquis twice daily -We will arrange follow-up with cardiology as outpatient locally, Aspiration Pneumonitis In the setting of emesis, with potential chronic contributions -leukocytosis, with CXR changes per above -Transition to augmentin for 5 days therapy total, SLP consulted for swallow minor aspiration with strong cough reflex recommend pureed diet. Urinary Retention Unclear etiology, possibly underlying chronic retention exacerbated by poor intake -Foley removed 12/09 -Plan: Will encourage patient to spontaneously void on his own, may require further workup if not -patient will f/u with known urologist, Dr. CKD IV Baseline Cr 1.8-2.0, not on iHD -Cr at baseline -Continue to monitor Acute Hypoxemic Respiratory Failure, improving In the setting of an aspiration event. -CXR showing retrocardiac opacities consistent with aspiration -continue supplemental O2 wean with goal sat >88%. Patient may need homegoing O2 Anemia Likely associated with CKD, cannot rule out mineral or vitamin def playing a role. -Hgb 11.2, Iron panel showing iron def, b12/folate wnl -Continue ferrous sulfate 325 mg EOD, Continue to monitor transfuse hgb<7 Abnormal CXR Etiology unclear, primary concern would be potential underlying malginancy -Non-emergent CT chest recommended, however patient transitioned to DNR-CC GOC Due to continuing decline. -Palliative care consulted for GOC and EOL discussion. Transitioned to DNR-CC. Patient does not qualify for hospice at this time -Patient will require a hospital bed after evaluation in the hospital

Weitere VAERSDATA-Felder

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

VAERS 2510974

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: -
Alter: 68,0
Geschlecht: F
Eingang: 17.11.2022
Impfdatum: 21.10.2021
Beginn: 27.10.2022
Tage bis Beginn: 371,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Angiogram cerebral abnormal Arteriogram carotid abnormal Blood magnesium decreased Blood potassium decreased Blood pressure increased Brain natriuretic peptide increased COVID-19 Carotid artery stenosis Chest X-ray abnormal Chest pain Condition aggravated Cough Hypertension Hypokalaemia Hypomagnesaemia Lung disorder N-terminal prohormone brain natriuretic peptide increased

Symptomtext

Patient is a 69 y.o. female with a history of HTN, HLD, DM2, colon cancer s/p resection 2020, recent admit 10/8-10/10/22 for transient neuro symptoms and UTI, who presented to HCF 10/27/2022 with blurry vision, high BP reading, cough, congestion, sore throat. She was found to be febrile and SARS-CoV-2 positive and BP 218/68. 1. Sepsis secondary to COVID-19: Sepsis present on admit with fever, tachypnea. Symptoms present 10/26/22. Tested positive on admit. CXR on admit with bilateral coarsened lower lung bronchial markings, basilar interstitial vascular congestion. Required oxygen on admit, no hypoxia at time of discharge even with ambulating. Continue dexamethasone x 10 days at discharge 2. Acute hypoxic respiratory insufficiency: Required 2L NC on admit due to COVID-19. Resolved 10/28/2022 3. Uncontrolled HTN: blood pressure 200/60s on admit, noted history of elevated blood pressure causing transient neurologic symptoms. Changed metoprolol to carvedilol and added lisinopril (pt not taking enalapril) at discharge. 4. Chest pain: reproducible on palpation. Suspect MSK due to COVID / cough. Steroids as above. 5. Elevated BNP: Admit NT-Pro BNP 2740. CXR on admit noted vascular congestion. Consider echocardiogram outpatient 6. Hypokalemia: K 3.1 on admit, potassium 3.5 at time of discharge, replaced magnesium, added lisinopril 7. Hypomagnesemia: magnesium 1.2 10/28/2022, replaced IV 8. DM2: Controlled. A1c 6.8% 10/9/22. 9. Left ICA stenosis: 60% stenosis on recent CT angio head/neck. Continued ASA and statin. 10. Colon cancer: Patient reports resection in 2020 at HCF. Denies metastatic issues and did not require radiation or chemotherapy. Reports recent scans have been negative

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2503435

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: -
Alter: 89,0
Geschlecht: M
Eingang: 09.11.2022
Impfdatum: 20.10.2021
Beginn: 05.10.2022
Tage bis Beginn: 350,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Asthenia Blood creatine phosphokinase normal Blood culture negative Blood fibrinogen increased Blood lactate dehydrogenase normal Blood lactic acid Blood magnesium Blood potassium decreased COVID-19 Chest X-ray normal Cough Dyspnoea Fibrin D dimer Glucose tolerance impaired Glycosylated haemoglobin increased Hypertension Hypokalaemia

Symptomtext

Patient is a 90 y.o. male patient of MD with history of TN, GERD presented with generalized weakness with cough and shortness of breath. Acute Respiratory Failure with hypoxemia-resolved COVID-19 nfection Sepsis without organ dysfunction Vaccinated Presented with tachypnea and leukocytosis Hemodynamically stable, not requiring vasopressors. Lactic acid 1.9 on presentation COVID-19 symptoms: 10/4/22 COVID-19 test positive date: 10/5/22 CXR with no acute cardiopulmonary process Continue 2 liters/min via Nasal Canula; currently on room air Spo2>95% Fluid status euvolemic Blood cultures NGTD UA no evidence of infection D-dimer 0.63 , fibrinogen 484 CK 81 LDH 182 COVID-19 precautions for 10 days Albuterol via HFA q6PRN Tylenol prn for fever Continue IV Decadron; switch to oral Decadron remaining days total 10 Hypokalemia - resolved K of 3.3 and Mag 1.9 on presentation Replace and recheck Repeat K of 3.7 (10/07) HTN SBP 140s Continue home medication regime Pre -diabetes HgbA1c 6.4 month ago 6.5 on admission GERD Continue home PPI

Weitere VAERSDATA-Felder

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

VAERS 2501864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: NY
Alter: 83,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 01.04.2022
Beginn: 21.05.2022
Tage bis Beginn: 50,0
Dosis: 3
Route/Site: IM / LA

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

Acidosis Anion gap Atelectasis Blood bicarbonate decreased Blood creatinine increased Blood gases Blood potassium increased Bradycardia COVID-19 Catheter placement Chest X-ray abnormal Computerised tomogram abdomen abnormal Death Dialysis Endotracheal intubation Hypotension Intensive care Intraosseous access placement

Symptomtext

5/21/2022-Presents Ed via EMS, at home intially sinus brady hypotensive transcutaneously paced. Hr-40, systolic around 70 mmHg on norepinephrine mcg/min. Intubated. Had IO of R shoulder due to inability to place IV access. Admit hemodynamically significant bradycarida in the setting of severe mtabolic derangeent and metabolic acidosis. Potassium 7 and creatnine above 6 . CXR: bibasilar linear atelectasis. Covid + test. Hemodialsysi catheter via IJ for emergenct dislaysis. Pancreatits based on abd CTand lipase over 4000. Transfered to ICU. Temporary venous pacemaker placed along with hemodialysis catheter. Vent settings Fio2 100% resp 16 ABG: 6.9/27.2 bicarb less then 6 and anion gap more then 19 Ordered IV meropenem and pressor support. 5/22/2022-Bicarb drip started , acidosis improving. Monoclonals and steroids not recommended due to amount of renal failure. Vent settings Fio2 50% resp 10 Family discussion, Patient made palliative. Terminal exubation. Time of death 1600.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PE, Breast cancer, renal carcnoma status post nephrectomy, type 2 DM, HTN and A fib.
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 2477415

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: TX
Alter: 56,0
Geschlecht: F
Eingang: 13.10.2022
Impfdatum: 07.10.2021
Beginn: 06.10.2022
Tage bis Beginn: 364,0
Dosis: 3
Route/Site: IM / AR

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Death Laboratory test normal SARS-CoV-2 test positive

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization/Death. Rec'd Pfizer BioNTech vaccine on 1/2/22, 1/23/2021 and 10/7/2021. COVID-19+ and hypoxic w/O2 sat of 85% on 5L NC. Clinic exam and initial labs consistent w/Covid PNA, afebrile, labs wnl. Admitted, initially maintaining sats on HFNC, acutely decompensated despite standard of care Covid interventions. Transitioned to inpatient hospice and expired on 10/06/22. Tx'd w/decadron and remdesivir

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: 10/2/22 Covid 19 + - This sample was analyzed using the BioFire Torch system using PCR or equivalent Nucleic Acid Amplification (NAA) technology.
Aktuelle Erkrankungen: -
Vorgeschichte: Major Neuro-cognitive disorder
Andere Medikamente: aspirin, atorvastatin, clonazepam, clotrimazole, clozapine,
Allergien: Penicillins, Bactrim
Vorherige Impfungen: -

VAERS 2471996

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: SD
Alter: 77,0
Geschlecht: M
Eingang: 07.10.2022
Impfdatum: 26.10.2021
Beginn: 30.07.2022
Tage bis Beginn: 277,0
Dosis: 4
Route/Site: SYR / RA

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

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

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. The individual was vaccinated with the Pfizer product on 03/09/2021, 03/30/2021, and 10/26/2021. The individual also received a dose of the Moderna product on 06/24/2022. They tested positive for COVID-19 on 07/30/2022 at the nursing home at which they were a resident. They were described as having developed "weakness" as a result of the COVID-19 infection. They fell on 07/31/2022 and died in the ambulance on the way to the hospital. This individual was not admitted to hospital for this illness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Positive COVID-19 antigen test despite being vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: Congestive Heart Failure, Type II Diabetes, COPD, Hypertension, Obesity, Heart Murmur, Stage 4 Chronic Kidney Disease
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2465585

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: TX
Alter: 65,0
Geschlecht: F
Eingang: 30.09.2022
Impfdatum: 27.10.2021
Beginn: 22.09.2022
Tage bis Beginn: 330,0
Dosis: 3
Route/Site: IM / AR

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

Atrial fibrillation Blood lactic acid COVID-19 Computerised tomogram head normal Death Hypophagia Hypoxia Mental status changes SARS-CoV-2 test positive

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization/Death. Rec'd Pfizer BioNTech vaccine on 2/9/2021, 3/2/21 and 10/27/21. Presented to ED from rehab yesterday w/AMS and decreased PO intake. Prior admission to rehab after being hospitalized and tx'd for COVID, discharged 9/8/22. COVID + this admission as well. She was hypoxic on arrival to ED and placed on supplemental O2. Head CT negative for acute process. Lactate was 4.0. Admitted to the medical floor and started on decadron and Zosyn. That evening she went into Afib RVR. Transitioned to comfort care and expired on 9/22/22. Tx'd with cefepime, decadron, vancomycin, metronidazole, and zosyn.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 10,0
Labordaten: covid + 9/3/22, 9/13/22/ and 9/15/22. This sample was analyzed using the Roche LIAT SARS assay platform using PCR or equivalent Nucleic Acid Amplification (NAA) technology.
Aktuelle Erkrankungen: -
Vorgeschichte: Dementia, Parkinson's, DM, HTN, and HLD
Andere Medikamente: tylenol, carbidopa/levodopa, vitamin d3, cranberry/vit C, dexamethasone, divalproex, donepezil, memantine, metoprolol succinate, multivitamin, omega 3, pantoprazole, pioglitazone, psyllium husk, rosuvastatin, venlafaxine
Allergien: codeine, iodine
Vorherige Impfungen: -

VAERS 2460629

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: MI
Alter: 80,0
Geschlecht: M
Eingang: 26.09.2022
Impfdatum: 19.10.2021
Beginn: 15.09.2022
Tage bis Beginn: 331,0
Dosis: 3
Route/Site: - / -

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

Acute myocardial infarction COVID-19 SARS-CoV-2 test positive

Symptomtext

Patient with 3 COVID vaccines (but not up to date) who admitted to hospital with positive COVID PCR and non-STEMI. No complications from COVID noted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 4,0
Labordaten: COVID Detected PCR on 9/15/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular CAD (Coronary Artery Disease) s/p CABG Carotid stenosis PVD (peripheral vascular disease) (*) Hyperlipidemia LDL goal <70 Essential hypertension Coronary artery disease involving coronary bypass graft of native heart with other forms of angina pectoris (*) Acute ST elevation myocardial infarction (STEMI) (*) Endocrine Type 2 diabetes mellitus without complication (*) Type 2 diabetes mellitus, without long-term current use of insulin (*) Psychological Mild episode of recurrent major depressive disorder (*) Urinary Stage 3 chronic kidney disease (*) Other Color blindness Prostate cancer (*) Encounter for long-term (current) use of insulin (*)
Andere Medikamente: -
Allergien: Lisinopril, Pneumococcal Vaccine
Vorherige Impfungen: -

VAERS 2451498

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: WA
Alter: 92,0
Geschlecht: F
Eingang: 19.09.2022
Impfdatum: 04.11.2021
Beginn: 16.09.2022
Tage bis Beginn: 316,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 Condition aggravated Essential hypertension Inappropriate schedule of product administration Pneumonia SARS-CoV-2 test positive

Symptomtext

Patient received Moderna COVID vaccine on 2/28/21 (lot # 024M20A), 3/8/21 (lot # 001B21A), and Pfizer COVID vaccine on 11/4/21 (lot # FE3590). On 9/14/22, patient admitted to our inpatient facility med/surg unit with acute hypoxic respiratory failure likely due to community-acquired pneumonia as well as COVID infection and essential hypertension. Patient discharged on 9/19/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: COVID status positive on 9/14/22.
Aktuelle Erkrankungen: -
Vorgeschichte: history of atrial fibrillation on apixaban, epilepsy on levetiracetam, hypertension, COPD, CKD, osteoporosis, RA on leflunomide
Andere Medikamente: acetaminophen, albuterol inh, alendronate, apixaban, calcium/magnesium/zinc, vitamin d3, citalopram, vitamin b12, diltiazem, ferrous sulfate, furosemide, ipratropium/albuterol, irbesartan, leflunomide, levetiracetam, loperamide, Icaps Areds
Allergien: amoxicillin, azathioprine, carvedilol, hydroxychloroquine, losartan, methotrexate, infliximab, sulfasalazine, onion
Vorherige Impfungen: -

VAERS 2446223

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: MN
Alter: 77,0
Geschlecht: M
Eingang: 15.09.2022
Impfdatum: 20.04.2022
Beginn: 12.09.2022
Tage bis Beginn: 145,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory failure Bronchiolitis COVID-19 Chest pain Dyspnoea Pneumonia Pulmonary embolism SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Patient had been experiencing ongoing shortness of breath for two weeks. He was seen at urgent care on 9/11 and was diagnosed with bronchiolitis and prescribed Augmentin. Patient went to ED on 9/12 for chest pain. Rapid COVID test was done in the ED which returned positive. Patient was admitted 9/12-9/14 and diagnosed with acute hypoxic respiratory failure due to COVID-19 with bilateral large pulmonary embolism. He was on supplemental oxygen during admission, however was able to be weaned to room air. Patient also diagnosed with COVID-19 infection and pneumonia; he was placed on Augmentin for possible bacterial on top of viral infection. Patient has been vaccinated against COVID-19. This meets criteria for vaccine breakthrough case review.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Patient with history of Type II Diabetes.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2436363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: KY
Alter: 83,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 22.01.2021
Beginn: 20.08.2022
Tage bis Beginn: 575,0
Dosis: 3
Route/Site: - / RA

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

Death

Symptomtext

Pt expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 15,0
Labordaten: Pt admitted to the hospital on 08/04/2022; was d/c to Hospice on 08/19/2022. Date of death: 08/20/2022
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: Heart valve replacement
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2428504

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: KY
Alter: 83,0
Geschlecht: F
Eingang: 03.09.2022
Impfdatum: 03.11.2021
Beginn: 28.07.2022
Tage bis Beginn: 267,0
Dosis: 2
Route/Site: - / -

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

Anticoagulant therapy Asthenia COVID-19 Computerised tomogram head normal Computerised tomogram thorax abnormal Confusional state Culture urine positive Cystitis Fall Head injury Hypertension Illness Metabolic encephalopathy Pulmonary embolism Ultrasound Doppler abnormal Urinary tract infection

Symptomtext

DISCHARGE SUMMARY: MRN: Name: Age: 83 y.o. Birthday: Admit Date: 7/28/2022 2:48 PM Discharge Date: 8/4/2022 Unit: Admitting Physician: Discharge Physician: MD Discharge Diagnosis: Principal Problem: Acute metabolic encephalopathy Active Problems: HTN (hypertension) Acute cystitis without hematuria Weakness generalized COVID-19 virus infection HPI AND HOSPITAL COURSE History of Present Illness: As per admission H&P, "Patient is a 83 y.o. female with a history of neuropathy with the lot of problems with ambulation presented after a fall earlier today and she could not get up from the floor. Neighbor recommended to come to the emergency room and get evaluated. Denies any blackout. She hit her head somewhere. CT head negative. Confused here. Brother at bedside and helped with some of the history. She was diagnosed with UTI recently and was sent home on Omnicef. Urine culture came back resistant to cephalosporin and patient was started on Cipro yesterday. Not sure what makes symptoms better or worse. Patient denies any dysuria, UTI symptoms, fever, chills, pain or any other concerning symptoms. Admitted for further evaluation." Hospital Course: Patient is a 83 y.o. female who presented with confusion, weakness. She was managed for the following: * Acute metabolic encephalopathy Acute Pulmonary Embolism - likely provoked by active COVID-19 infection. CT PE study with left lower lobe segmental PE. BLE US with possible LLE DVT. Continue po eliquis, will need 6 months anticoagulation. Follow-up with PCP. COVID-19 infection - stable, on room air. Completed remdesivir 5 days. Acute UTI - completed course of macrobid during admission. Debility - PT consulted, recommend SNF. Pt will discharge to HCF for short term placement. Acute metabolic encephalopathy - delirium due to acute illness with UTI and COVID-19 infection. Confusion resolved. Physical Exam on the Date of Discharge: Blood pressure 135/53, pulse (!) 49, temperature 97.8 ?F (36.6 ?C), temperature source Oral, resp. rate 18, height 5' 2" (157.5 cm), weight 50.5 kg (111 lb 4.8 oz), SpO2 100 %. General - NAD, appears stated age, frail elderly female HEENT - EOMI, PER, MMM, Chest - lungs clear bilaterally Heart - RRR, NS1S2 Abdomen - Soft, non-tender, Extremities - warm, Psych - AAOx3, Skin - dry Discharge Condition: improved Disposition: SNF

Weitere VAERSDATA-Felder

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

VAERS 2427505

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: KY
Alter: 73,0
Geschlecht: F
Eingang: 02.09.2022
Impfdatum: 20.10.2021
Beginn: 24.07.2022
Tage bis Beginn: 277,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Anticoagulant therapy COVID-19 pneumonia Chest X-ray Chronic obstructive pulmonary disease Condition aggravated Echocardiogram Essential hypertension Fibrin D dimer increased Tobacco abuse

Symptomtext

Patient: 74 y.o. Admit Date: 7/24/2022 Discharge Date: 7/25/2022 Discharge Diagnosis: Principal Problem: Pneumonia due to COVID-19 virus Active Problems: Acute respiratory failure with hypoxemia Essential hypertension Tobacco abuse COPD with acute exacerbation S/P redo sternotomy redo AVR (aortic valve replacement) # 21 mm bovine pericardial EF 60% (2/1/2018) Hospital Course: 74 year old female with COPD was admitted with exacerbation and Covid-19 infection. She was started on antibiotics, steroids and Remdesivir. She has done well and will be discharged home today on Lovenox due to elevated d dimer. She had previously received the vaccine booster. Patient educated on appropriate level of care post-discharge. Follow up with Primary Care Doctor in 5-7 days. Physical Exam on the day of discharge: Last Recorded Vital Signs: Temp: 97.6 ?F (36.4 ?C) Heart Rate (Monitor): 85 Pulse: 75 BP: 154/86 Respirations: 18 SpO2: 90 % O2 Flow Rate (l/min): 2 l/min General Appearance: no distress Eyes: PERRLA ENT: moist mucus membranes, no adenopathy Lungs: clear to auscultation bilaterally Heart: regular rate and rhythm Abdomen: soft, non-tender Skin: No rashes or lesions Extremities: full ROM Neuro: alert, normal strength and tone Consults: IP CONSULT TO SEPSIS NURSE NAVIGATOR Significant Diagnostic Studies: TTE, CXR Operations: none Disposition: Home Discharge Condition: Fair Discharge Medications: Current Discharge Medication List START taking these medications Details cefdinir (OMNICEF) 300 mg capsule Take 1 Capsule by mouth Twice a day for 7 days. Qty: 14 Capsule, Refills: 0 Associated Diagnoses: Acute respiratory failure with hypoxemia enoxaparin (LOVENOX) 40 mg/0.4 mL injection Administer 0.4 mL subcutaneously Once Daily for 7 days. Qty: 7 Each, Refills: 0 Associated Diagnoses: Pneumonia due to COVID-19 virus CONTINUE these medications which have NOT CHANGED Details sertraline (ZOLOFT) 100 mg tablet Take 1 Tablet by mouth Daily. Qty: 90 Tablet, Refills: 3 Associated Diagnoses: Depression, unspecified depression type latanoprost (XALATAN) 0.005 % Instill 1 Drop in both eyes At bedtime. Qty: 7.5 mL, Refills: 3 Associated Diagnoses: Other specified glaucoma, unspecified laterality brimonidine (ALPHAGAN) 0.2 % ophthalmic solution Instill 1 Drop in affected eye(s) Twice a day. Qty: 15 mL, Refills: 3 Associated Diagnoses: Other specified glaucoma, unspecified laterality potassium chloride (KLOR-CON) 10 mEq tab Take 1 Tablet by mouth Twice a day. Qty: 180 Tablet, Refills: 3 Associated Diagnoses: Acute diastolic CHF (congestive heart failure) metoprolol (LOPRESSOR) 50 mg tablet Take 1 Tablet by mouth Twice a day. Qty: 180 Tablet, Refills: 3 Associated Diagnoses: Essential hypertension Ferrous Sulfate (IRON, FERROUS SULFATE,) 325 mg (65 mg iron) tablet Take 1 Tablet by mouth Twice a day. Qty: 180 Tablet, Refills: 3 Associated Diagnoses: Iron deficiency anemia secondary to inadequate dietary iron intake ipratropium-albuteroL (DUONEB) 0.5 mg-3 mg(2.5 mg base)/3 mL nebulizer solution Take 3 mL by nebulization Every 6 hours. Qty: 270 mL, Refills: 3 Associated Diagnoses: Chronic obstructive pulmonary disease, unspecified COPD type furosemide (LASIX) 40 mg tablet Take 1 Tablet by mouth Twice a day. Qty: 180 Tablet, Refills: 5 Associated Diagnoses: Acute diastolic CHF (congestive heart failure) ibuprofen (MOTRIN) 800 mg tablet Take 1 Tab by mouth Twice a day. Qty: 60 Tab, Refills: 3 Associated Diagnoses: Arthralgia, unspecified joint LORazepam (ATIVAN) 0.5 mg tablet Take 1 Tab by mouth Every 12 hours as needed. Qty: 60 Tab, Refills: 2 Associated Diagnoses: Anxiety diphenoxylate-atropine (LOMOTIL) 2.5-0.025 mg per tablet Take 1 Tab by mouth Four times a day as needed for Diarrhea. Qty: 20 Tab, Refills: 0 Associated Diagnoses: Diarrhea, unspecified type omeprazole (PRILOSEC) 40 mg DR capsule Take 1 Cap by mouth Daily. Qty: 30 Cap, Refills: 3 Associated Diagnoses: Epigastric pain aspirin (ASPIRIN) 325 mg tablet Take 0.5 Tabs by mouth Daily. Qty: 15 Tab, Refills: 11 Associated Diagnoses: Severe aortic stenosis by prior echocardiogram; S/P AVR (aortic valve replacement) cyanocobalamin 100 mcg Take 100 mcg by mouth Daily. Associated Diagnoses: Essential hypertension; White coat hypertension; Mixed hyperlipidemia; S/P AVR (aortic valve replacement) loratadine (CLARITIN) 10 mg tablet Take 1 Tab by mouth Daily. Qty: 90 Tab, Refills: 3 Associated Diagnoses: Seasonal allergic rhinitis due to pollen Ranitidine HCl 150 mg Cap Take 1 Cap by mouth Twice a day. Qty: 180 Cap, Refills: 3 Associated Diagnoses: Gastroesophageal reflux disease without esophagitis albuterol (VENTOLIN HFA) 90 mcg/Actuation inhaler Take 2 Puffs by inhalation Every 4 hours as needed. Qty: 1 Package QS, Refills: 0 Associated Diagnoses: Wheezing; COPD (chronic obstructive pulmonary disease) CALCIUM CARBONATE/VITAMIN D3 (CALCIUM + D PO) Take 1 Tab by mouth TWICE A DAY. Multivitamin Tab Take 1 Tab by mouth DAILY. VITAMIN E ACETATE (VITAMIN E PO) Take 1 Tab by mouth DAILY.

Weitere VAERSDATA-Felder

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

VAERS 2420135

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: MO
Alter: 82,0
Geschlecht: M
Eingang: 25.08.2022
Impfdatum: 15.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 17,0
Dosis: 3
Route/Site: IM / AR

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

Abdominal pain upper Anal incontinence Biopsy pancreas abnormal Death Diarrhoea Dyspepsia General physical health deterioration Insomnia Laboratory test Magnetic resonance imaging abnormal Malaise Pancreatic carcinoma Pancreatic cyst Positron emission tomogram abnormal Weight decreased

Symptomtext

The patient, my father, told me he had been having various symptoms and felt unwell for months, which he associated with the initial Moderna experimental COVID-19 gene therapy injections in March and April of 2021. After the booster dose of Pfizer's experimental COVID-19 gene therapy injection at a routine physical in December 2021, at which he was said to be in good condition for his age, he began to have digestive problems including incontinent diarrhea. He began to have pain in his "guts," to the point he could not lie on his back and sleep became difficult and later nearly impossible. He lost significant weight. Various tests were done. Doctors began to suspect a pancreatic cyst after an MRI. After a PET scan, they then suspected pancreatic cancer. After a biopsy, they finally diagnosed pancreatic cancer in June 2022. The tumor was believed to be inoperable. Chemo and radiation were not advised because of his age and severely weakened condition after months of poor digestion, severe pain, and little sleep. Hospice care was advised. Once palliative pain relief was finally prescribed he was able to eat and sleep. However, after only a few weeks of improved symptoms, he deteriorated rapidly and died July 14, 2022. While he may have had pancreatic cancer developing for a long time before the experimental injections, I am reporting this as a potential adverse event from said injections because of its rapid progression from January-July 2022. I have read about concerns that the injections impair the immune system in various ways, including negative impact on toll-like receptors and killer T cells. Thus, I am interested in the possibility that his own immune system was keeping the pancreatic tumor in check until such time as the injections damaged his immune system. I feel it is important for his case to be in VAERS in case enough other rapidly progressing cancers are reported to rise to the level of a safety signal that should be investigated, since this is the purpose of VAERS. In addition to the booster dose of Pfizer listed above, he received two doses of Moderna on 03/05/21 (Lot 011A21A) and 04/02/21 (Lot 044A21A). My understanding is that there is little to no data on the safety of mixing the different experimental COVID-19 gene therapy injections. Thus his case may also be of value in investigating outcomes following use of mixed products.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: If helpful, I can request from my father's doctors all medical records related to the events described here.
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes, high blood pressure (both mild and well controlled)
Andere Medikamente: Atorvastatin, Lisinopril, Chlorthalid, Metformin ER BID, Fluticasone Propionate
Allergien: None known
Vorherige Impfungen: -

VAERS 2412353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: MI
Alter: 88,0
Geschlecht: M
Eingang: 16.08.2022
Impfdatum: 20.10.2021
Beginn: 10.08.2022
Tage bis Beginn: 294,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Atelectasis Blood creatinine abnormal COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cystitis haemorrhagic Dyspnoea Haemoglobin Hypoxia Malaise Renal haemorrhage SARS-CoV-2 test positive Urogram abnormal

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 8/10/2022 Discharge Date: Aug 13, 2022 PRESENTING PROBLEM: Acute respiratory failure with hypoxia [J96.01] COVID-19 virus infection [U07.1] HOSPITAL COURSE: 89-year-old male with past medical history significant for chronic diastolic heart failure, persistent atrial fibrillation, hypertension, type 2 diabetes, CKD who presented to the emergency department with progressive shortness of breath. On arrival to emergency department patient is hypoxic requiring placement of 2 L nasal cannula for oxygen support. His COVID test returned positive. Chest x-ray showed left-sided basilar atelectasis. Patient was started on Decadron and admitted to the medicine service for further assessment and management. As far as acute hypoxic respiratory failure in setting of COVID pneumonia, patient improved with steroid treatment. He was able to wean from 2 L to room air and remained comfortable. He did receive 3 doses of his vaccine prior to admission. Patient's symptoms related to COVID were resolved with the time of discharge, he will complete an additional 5 days of Decadron discharge. As far as recently diagnosed renal hemorrhage/hemorrhagic cystitis from a CT urogram performed on 08/05, patient's hemoglobin was monitored in the hospital. Eliquis was held. Urology was consulted and recommended outpatient follow-up with them for eventual ureteroscopy to confirm mass followed by radical nephrectomy in the same setting. Eliquis to remain on hold until this is performed. Patient did have a mild AKI. His home torsemide and losartan were stopped in the hospital. Treated with IV fluids with improvement in his creatinine. Recommended outpatient follow-up with primary care physician in 1-2 weeks to monitor BMP and creatinine. Consider referral to Nephrology if not improving. Patient discharged home in stable and improved condition. We discussed he should call his urologist to determine when it would be safe to resume Eliquis again. From medicine standpoint this could be done over the weekend.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Personal history of colonic polyps Essential hypertension Coronary artery disease due to lipid rich plaque Hyperlipidemia Atrial fibrillation, persistent Other malaise and fatigue SOB (shortness of breath) Edema Chronic diastolic congestive heart failure Type 2 diabetes mellitus with stage 3b chronic kidney disease, without long-term current use of insulin Anemia in stage 3b chronic kidney disease Gout of multiple sites Obesity Hyperparathyroidism due to renal insufficiency Diabetic neuropathy, type II diabetes mellitus Platelets decreased
Andere Medikamente: allopurinol (ZYLOPRIM) 100 MG tablet amlodipine (NORVASC) 2.5 MG tablet Calcium Carbonate-Vitamin D (CALCIUM + D PO) Coenzyme Q10 (COQ-10) 100 MG CAPS dexamethasone (DECADRON) 6 MG tablet docusate (COLACE) 100 MG capsule (Expired) doxazosin
Allergien: Dye-contrast Iodinated Contrast MediaHives, Rash SpironolactoneOther Sulfa Drugs TramadolNausea Only
Vorherige Impfungen: -

VAERS 2400433

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: CO
Alter: 79,0
Geschlecht: F
Eingang: 03.08.2022
Impfdatum: 23.04.2022
Beginn: 08.07.2022
Tage bis Beginn: 76,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure COVID-19 Chest discomfort Chest pain Dyspnoea Electrocardiogram abnormal Fibrin D dimer Full blood count Glycosylated haemoglobin Hepatic enzyme Metabolic function test Myocardial injury Nausea Oropharyngeal pain Productive cough Respiratory tract congestion SARS-CoV-2 test positive Troponin increased

Symptomtext

Patient presented to the Emergency Department with complaints of pressure and non-radiating pain in her chest and shortness of breath. The pain sensation began 3 days after she tested positive for COVID-19. During this time, she experienced nausea with one episode of emesis, sore throat, congestion, and productive cough. On the basis of symptomatology, persistent oxygen requirements, electrocardiographic changes, and elevated troponin levels she was diagnosed with COVID-19 infection with acute hypoxemic respiratory insufficiency and non-ischemic myocardial injury. She was admitted to hospital and received one dose of dexamethasone 6mg intravenously and one dose of IV remdesivir. With symptomatic improvement, she was discharged medically stable with follow-up care plans in place.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 1,0
Labordaten: Comprehensive Metabolic Panel Complete blood count Troponin Liver enzymes Hemoglobin A1C D dimer
Aktuelle Erkrankungen: -
Vorgeschichte: Coronary heart disease, history of coronary artery bypass grafting Hyperlipidemia Type 2 diabetes Hypertension Osteoarthritis Pseudophakia
Andere Medikamente: Atorvastatin Dapagliflozin Metformin Pioglitazone Pantoprazole Aspirin Metoprolol Isosorbide dinitrate Pregabalin
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2397412

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: MI
Alter: 75,0
Geschlecht: M
Eingang: 30.07.2022
Impfdatum: 18.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Atrial fibrillation Biopsy Bradycardia Cardiac monitoring Cardiac stress test Catheterisation cardiac Cerebrovascular accident Computerised tomogram Dyspnoea Heart rate Pathology test Prostate cancer Retinal tear SARS-CoV-2 test Tachycardia Vitreous floaters

Symptomtext

Stroke; AFib; diagnosed with prostate cancer; tachy on bradycardia on the treadmill.; tachy on bradycardia on the treadmill.; Developed floater in his right eye after the stroke; They did surgery with laser to correct the hole that materialized in the retina; was like someone strapped a rope around his chest and couldn't breathe; 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 18Oct2021 as dose 3 (booster), single (Lot number: FE3590) at the age of 75 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Cholesterol" (ongoing); "prostate Cancer" (ongoing), notes: He does have prostate Cancer; "Afib" (ongoing); "cancer" (unspecified if ongoing). Concomitant medication(s) included: TAMSULOSIN taken for prostate cancer, start date: 2020 (ongoing); FINASTERIDE taken for prostate cancer, start date: 2020 (ongoing); SIMVASTATIN taken for blood cholesterol, start date: 2020 (ongoing). Vaccination history included: BNT162b2 (Suspect product:, Pfizer Covid vaccine:, First Dose: 05Feb2021 , (Facility name withheld), LOT: EL0142, he thinks, is kind of blurred , NDC, EXP: Unknown), administration date: 05Feb2021, when the patient was 74-year-old, for Covid-19 immunization; BNT162b2 (Second Dose: 24Feb2021, LOT: EL9267, NDC, EXP: Unknown), administration date: 24Feb2021, when the patient was 74-year-old, for Covid-19 immunization. The following information was reported: DYSPNOEA (non-serious) with onset Oct2021, outcome "unknown", described as "was like someone strapped a rope around his chest and couldn't breathe"; CEREBROVASCULAR ACCIDENT (hospitalization, medically significant) with onset 13Feb2022 at 09:30, outcome "unknown", described as "Stroke"; VITREOUS FLOATERS (medically significant) with onset 2022, outcome "unknown", described as "Developed floater in his right eye after the stroke"; RETINAL TEAR (medically significant) with onset 2022, outcome "unknown", described as "They did surgery with laser to correct the hole that materialized in the retina"; ATRIAL FIBRILLATION (medically significant), outcome "unknown", described as "AFib"; PROSTATE CANCER (medically significant), outcome "unknown", described as "diagnosed with prostate cancer"; BRADYCARDIA (medically significant), TACHYCARDIA (non-serious), outcome "unknown" and all described as "tachy on bradycardia on the treadmill.". The patient was hospitalized for cerebrovascular accident (start date: 13Feb2022, discharge date: 14Feb2022, hospitalization duration: 1 day(s)). The event "stroke" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: Biopsy: (13Dec2021) cancer, notes: Found out 13Dec2021 that it was definitely cancer; Cardiac monitoring: (unspecified date) Unknown results; Cardiac stress test: (26Oct2021) failed, notes: Unit: Not Provided; Catheterisation cardiac: (unspecified date) had no blockage; Computerised tomogram: (unspecified date) Unknown results; Heart rate: (unspecified date) dropped to 30; (unspecified date) go up to 167; (unspecified date) drops to 60; Pathology test: (13Oct2021) Unknown results; SARS-CoV-2 test: (25Jul2022) Positive, notes: Unit: Not Provided. Therapeutic measures were taken as a result of atrial fibrillation, bradycardia, vitreous floaters, retinal tear, tachycardia. Clinical information: Reporter mentions that her husband has to report that he had a serious reaction to the second booster shot from Pfizer. Has mentioned this to many different doctors and has had problems since Oct2021 when he had the booster. 48 hours after, almost exactly, he was walking with his wife, jogged maybe 100 yards, a slow jog, which he had been doing for many years. It was like someone strapped a rope around his chest and couldn't breathe, squeezing horribly. Draped himself over a barrier of the trail rail to keep from falling. Eventually, got his breath back, which took about 5 or 10 minutes and walked back to the house. Met with the doctor, who made appointment for stress test, which he failed and was well documented. Did a heart cath and he had no blockage. They were seeing that he had AFIB and tachy on bradycardia on the treadmill. There was no implementation other than that incident to even indicate that he had any problems. They did the heart cath, which showed there was a problem. Doctor was going to do heart ablation 15Feb2022 and he was on beta blocker Metoprolol. Clarified that he was put on that because of the stress test and had not been on it before. Went off the beta blocker and was supposed to be off it for 5 days. Went off that 12Feb2022 and 13Feb2022, the next day, he didn't take it and had stroke 13Feb2022. Survived that and they attributed it to the fact that it must have been clot. He did not have any neurological damage, thank goodness. Was in the hospital for that, for one day and they put him on the blood thinner, Eliquis, which they sent him home with and he is still taking now. Clarified that he was admitted to hospital admitted in hospital 13Feb2022 and went home 14Feb2022. Stroke started at 9:30am and he got to the hospital that afternoon. Went to the emergency room and was then sent to Hospital that afternoon. In the mean time, he has been struggling with all this stuff going on in his body. Developed floater in his right eye after the stroke: Saw that doctor again, who sent him to see an ophthalmologist. This was within a short period of time after the stroke. Was walking and doing the same things he had been doing, as he was told to do. Was not debilitated. When the ophthalmologist looked at his right eye, he said it looked like someone stuck something in his eye. They did surgery with laser to correct the hole that materialized in the retina. That was not painful, just a little painful. Went home and has been ok. Was just another manifestation of all this. Was amazing to be so healthy and have all these things happen to him. They put him on a heart monitor for 30 days. The result what they found out his heart rate dropped to 30 and would some times go up to 167, which was the highest. Was from not running or training or anything. Then, they put a pacemaker in him, which was about 2 month ago and now, he has a pacemaker. His heart rate drops to 60 all the time with no symptoms, so this is kind of frightening. To be sitting here and to take his blood pressure, it is sometimes very normal but now has Afib. When he went in for a check up, at 6 weeks, they said he had been in Afib 5 times before. They told him was 36% daily and then they put him on another medicine. 15Apr2022 was when they put the pacemaker in. The other medication they put him on, in addition to Eliquis was Sotalol and he is taking that now, also. From a person who would almost refuse to take aspirin for a headache, he is now taking 6 different pills and 4 of which, he has been taking since the booster. Unfortunate all of this has happened to him. Almost exactly 48 hours after that booster, on that Monday, all this happened on the trail rail the following Wednesday. Had the previous 3 Pfizer shots that Feb2021. Was about 6 months from then to to the booster. His world came crashing down when he found out he had cancer. Then ended up in the emergency room and they didn't let him go home. Clarified that patient was diagnosed with prostate cancer after receiving booster shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 1,0
Labordaten: Test Date: 20211213; Test Name: biopsy; Result Unstructured Data: Test Result:cancer; Comments: Found out 13Dec2021 that it was definitely cancer.; Test Name: heart monitor; Result Unstructured Data: Test Result:Unknown results; Test Date: 20211026; Test Name: Stress test; Result Unstructured Data: Test Result:failed; Comments: Unit: Not Provided; Test Name: heart cath; Result Unstructured Data: Test Result:had no blockage; Test Name: CAT scans; Result Unstructured Data: Test Result:Unknown results; Test Name: Heart rate; Result Unstructured Data: Test Result:dropped to 30; Test Name: Heart rate; Result Unstructured Data: Test Result:go up to 167; Test Name: Heart rate; Result Unstructured Data: Test Result:drops to 60; Test Date: 20211013; Test Name: Pathology tissue; Result Unstructured Data: Test Result:Unknown results; Test Date: 20220725; Test Name: Covid test; Test Result: Positive ; Comments: Unit: Not Provided
Aktuelle Erkrankungen: AFib; Cholesterol; Prostate cancer (He does have prostate Cancer)
Vorgeschichte: Medical History/Concurrent Conditions: Cancer
Andere Medikamente: TAMSULOSIN; FINASTERIDE; SIMVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2347363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: KY
Alter: 74,0
Geschlecht: M
Eingang: 01.07.2022
Impfdatum: 07.10.2021
Beginn: 28.06.2022
Tage bis Beginn: 264,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory failure Asthenia COVID-19 Fall Mobility decreased Pyrexia SARS-CoV-2 test positive

Symptomtext

has had 3 doses of covid vaccine and on 6/29/22 was admitted to hospital with covid 19 virus infection and Acute respiratory failure with hypoxia, weakness and fever from covid-19 resulting in fall and inability to get off of the floor. Was started on Remdesivir and decadron on 6/30/22

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: Covid + 6/30/22
Aktuelle Erkrankungen: allergic rhinitis, GERD, status post right hip replacement
Vorgeschichte: osteoarthritis of hip, anemia, Meniere's disease of right ear, anemia, hypogonadism male, right carotid artery stenosis
Andere Medikamente: atorvastatin 20mg, benzonatate 200mg, calcium carbonate 600mg, cetirizine 10mg, clopidogrel 75mg, denosumab 60mg/ml, fluticasone nasal spray, melatonin 5mg, pantprazole 40mg, terazosin 2mg
Allergien: hydrocodone
Vorherige Impfungen: -

VAERS 2335810

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: -
Alter: 61,0
Geschlecht: M
Eingang: 27.06.2022
Impfdatum: 09.10.2021
Beginn: 01.04.2022
Tage bis Beginn: 174,0
Dosis: 2
Route/Site: - / -

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

Autopsy COVID-19 Death Loss of consciousness Mental status changes SARS-CoV-2 test positive Syncope Unresponsive to stimuli

Symptomtext

pt to ED on 4/24/22 with AMS, syncope, unresponsive; when pt regained consciousness he requested to allow natural death; DNR; pt passed away in the ED; post-mortum testing done at Institute showed a positive COVID test

Weitere VAERSDATA-Felder

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

VAERS 2328882

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: KY
Alter: 77,0
Geschlecht: F
Eingang: 23.06.2022
Impfdatum: 21.10.2021
Beginn: 10.06.2022
Tage bis Beginn: 232,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Blood gases abnormal COVID-19 COVID-19 pneumonia Candida infection Chemotherapy Chills Condition aggravated Cough Death Dyspnoea Electrolyte imbalance Endotracheal intubation Febrile neutropenia Intensive care Pancytopenia Platelet count decreased Pneumonia

Symptomtext

Discharge Provider: MD Primary Care Physician at Discharge: DO Admission Date: 6/10/2022 PRESENTING PROBLEM: Thrombocytopenia [D69.6] Febrile neutropenia [D70.9, R50.81] Electrolyte abnormality [E87.8] Pulmonary embolism, unspecified chronicity, unspecified pulmonary embolism type, unspecified whether acute cor pulmonale present [I26.99] Pneumonia due to COVID-19 virus [U07.1, J12.82] Acute respiratory failure with hypoxia [J96.01] HOSPITAL COURSE: Patient is a 78 y.o. female with history of active small cell lung carcinoma s/p radiation therapy and was on active chemotherapy (last session completed two weeks ago), COPD, HTN who presented initially due to sepsis in the setting of febrile neutropenia who was also found to be positive for COVID-19. She was admitted on 6/10 from the infusion clinic after having 1-week of worsening shortness of breath, cough, and chills. She had sepsis due to Pseudomonas bacteremia and pneumonia. During hospitalization she declined and developed AHHRF was placed on BiPap with worsening VBG and was transferred to ICU and subsequently intubated on 6/12. During her stay she was also found to have a new acute thrombus right lower extremity and small pulmonary emolism. She had severe pancytopenia with platelets <10 so an IVC filter placed on 6/12 and unable to anticoagulate. She then suffered from worsening renal failure and required renal replacement therapy. Found to have worsening respiratory status, as well as a candida bacteremia. Shock persisted. A family meeting on 6/21/2022 with first degree relatives agreed upon comfort care measures given that her wishes were not to be kept alive on life support. Family presented at bedside and comfort care measures in place. Patient was pronounced at 6:54pm on 06/21/2022 secondary to respiratory failure in the setting of pseudomonas pneumonia, covid pneumonia, and candida bacteremia. Called and updated family over the phone

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Former smoker, Low back pain, DDD (degenerative disc disease), GERD (gastroesophageal reflux disease), DJD (degenerative joint disease), Essential hypertension, COPD (chronic obstructive pulmonary disease), Lichen sclerosus et atrophicus, Vaginal atrophy, Cystocele, midline, Osteoporosis, Requires supplemental oxygen - noc O2 - , Polycythemia secondary to hypoxia (resolved on Noc O2) , COPD with acute exacerbation, Influenza A, Acute hypoxemic respiratory failure, Small cell lung cancer, Post obstructive pneumonia, Malignant neoplasm of upper lobe, right bronchus or lung, Small cell lung cancer, right upper lobe, Febrile neutropenia, Unspecified severe protein-calorie malnutrition, Pneumonia due to COVID-19 virus, Septic shock, Atrial fibrillation with RVR, Bacteremia due to Pseudomonas, Pancytopenia, Severe anemia, Thrombocytopenia, DVT, lower extremity, distal, acute, right, Pulmonary emboli, Cerebrovascular accident (CVA) due to thrombosis of cerebral artery
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler, amlodipine-benazepril (LOTREL) 10-40 MG per capsule, apixaban (ELIQUIS) 5 MG tablet, BMX compounded suspension, budesonide/formoterol (SYMBICORT) 160-4.5
Allergien: Codeine, Diphenhydramine, Penicillins, Sulfa Drugs
Vorherige Impfungen: -

VAERS 2307129

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: TN
Alter: 77,0
Geschlecht: M
Eingang: 02.06.2022
Impfdatum: 21.10.2021
Beginn: 13.01.2022
Tage bis Beginn: 84,0
Dosis: 3
Route/Site: SYR / -

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

Acute kidney injury Bladder catheterisation COVID-19 Chronic kidney disease Death Dysphagia Dyspnoea Escherichia infection Hypothermia Oxygen saturation decreased Pneumonia aspiration SARS-CoV-2 test positive Shock Urinary tract infection

Symptomtext

Patient tested positive for Covid-19 on 01/13/2022. Patient admitted to hospital on 02/26/2022 with c/o SOB and was found to have hypothermia along with AKI/CKD. Patient was placed on antibiotics and found to have E. Coli UTI with chronic indwelling foley and had issues with dysphagia, eventually suffering from aspiration PNA with worsening oxygen requirements requiring PAP support. Patients work of breathing continued to increase and palliative measures were introduced, he developed shock which worsening despite vasopressor support and decision was made to transition to comfort measures only. Patient expired on 03/04/2022.

Weitere VAERSDATA-Felder

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

VAERS 2304969

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: MI
Alter: 83,0
Geschlecht: F
Eingang: 01.06.2022
Impfdatum: 30.10.2021
Beginn: 22.05.2022
Tage bis Beginn: 204,0
Dosis: 3
Route/Site: UN / UN

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

Acute myocardial infarction Anticoagulant therapy Asymptomatic COVID-19 Atrioventricular block complete COVID-19 Catheterisation cardiac abnormal Contusion Ejection fraction normal Electrocardiogram ST segment elevation Haematoma Haemoglobin decreased Intensive care Percutaneous coronary intervention SARS-CoV-2 test positive

Symptomtext

Patient presented with severe heart burn symptoms and was found to have inferior ST elevation on the EKG as well as 3AVB in the ER. She was taken emergently to the cath lab by Dr. and had PCI of the RCA on 5/22/2022. Her CHB resolved - there was no recurrence. 2 days later on 5/24/2022 she underwent staged PCI of the ramus branch. Echo showed EF 55-60% with no WMA. The second cardiac cath was complicated by a groin hematoma. Pressor support with Levophed was added and she was kept in the CCU. SQ heparin was held. Her Hgb dropped from ~ 11.4 to 9.5, likely because of continuous IVF being given at 75 mL/hour. See procedure notes for complete details. Her groin was stable with significant bruising, but no firmness or swelling. On day of discharge, she was feeling well with no cardiorespiratory symptoms and was ambulating without difficulty. Vitals were stable and she was maintaining SR / ST; no recurrence of CHB. She was also incidentally found to have COVID - supportive care was recommended. She had no symptoms directly attributable to COVID during her hospitalization. The remainder of her hospital course was unremarkable. """

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 6,0
Labordaten: Positive COVID PCR test 5/22/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Hx TIA (Chronic) 8/3/2012 Type 2 diabetes mellitus with stage 4 chronic kidney disease, without long-term current use of insulin 8/3/2012 HTN (Chronic) 8/3/2012 Gastroesophageal reflux disease with hiatal hernia (Chronic) 8/3/2012 Hyperlipidemia (Chronic) 8/3/2012 Anxiety (Chronic) Unknown Osteoporosis (Chronic) Unknown History of arterial ischemic stroke 10/16/2015 Hx of renal artery stenosis status post renal artery stent (Chronic) 12/29/2015 Atrophy of right kidney (Chronic) 12/29/2015 COPD exacerbation 4/5/2017 Hypomagnesemia 4/5/2017 Chronic diastolic heart failure (Chronic) 4/5/2017 Pneumonia and Anemia 5/31/2018 Acute kidney injury superimposed on chronic kidney disease 5/31/2018 Slow transit constipation 6/9/2018 Microcytic anemia 6/10/2018 Peripheral vascular disease 6/10/2018 Pulmonary nodules 6/10/2018 Vitamin D deficiency 6/10/2018 Primary osteoarthritis of both knees 6/10/2018 Chronic pulmonary aspiration 6/10/2018 Pulmonary hypertension 6/10/2018 Hyperparathyroidism 6/10/2018 Debility 6/19/2018 Simple chronic bronchitis Unknown COPD (chronic obstructive pulmonary disease) with emphysema (Chronic) 7/21/2018 Iron deficiency anemia 7/21/2018 Chronic respiratory failure with hypoxia, on home oxygen therapy (Chronic) 7/21/2018 Coronary artery disease (Chronic) 7/21/2018 Left renal artery stenosis s/p stent 10/22/2019 HTN 10/22/2019 CAD s/p nagetive lexiscan (7/2018) 10/22/2019 GERD 10/22/2019 CKD stage 4 due to type 2 diabetes mellitus (Chronic) 7/14/2020 Coronary artery disease of native artery of native heart with stable angina pectoris 4/1/2021 STEMI involving right coronary artery 5/22/2022 Complete heart block, transient 5/22/2022 COVID-19 virus detected 5/22/2022
Andere Medikamente: EVERY 6 HOURS PRN albuterol sulfate 90 mcg/actuation 2 puffs Inhalation EVERY 6 HOURS PRN alprazolam 0.5 mg Oral DAILY PRN aspirin 81 mg Oral Daily carvedilol 6.25 mg Oral 2 TIMES DAILY WITH MEALS clopidogrel bisulfate 75 mg Oral Daily
Allergien: EVERY 6 HOURS PRN albuterol sulfate 90 mcg/actuation 2 puffs Inhalation EVERY 6 HOURS PRN alprazolam 0.5 mg Oral DAILY PRN aspirin 81 mg Oral Daily carvedilol 6.25 mg Oral 2 TIMES DAILY WITH MEALS clopidogrel bisulfate 75 mg Oral Daily docusate sodium 100 mg Oral DAILY PRN fluticasone propionate 50 mcg/actuation 2 sprays Each Nare Daily fluticasone/vilanterol 200-25 mcg/dose 1 puff Inhalation Daily loratadine 10 mg Oral DAILY PRN losartan potassium 25 mg Oral Daily oxybutynin chloride 10 mg Oral Daily pantoprazole sodium 40 mg Oral DAILY BEFORE BREAKFAST, Take on an empty stomach at least 30 minutes before food. pravastatin sodium 40 mg Oral NIGHTLY roflumilast 500 mcg TAKE 1 TABLET BY MOUTH EVERY DAY tizanidine HCl 4 mg Oral EVERY 12 HOURS PRN torsemide 20 mg Oral Daily, Take an additional 20 mg in PM for weight gain more than 2 pounds tramadol HCl 50 mg 1 tablet Oral DAILY OR AS NEEDED umeclidinium bromide 62.5 mcg/actuation 1 puff Inhalation Daily
Vorherige Impfungen: -

VAERS 2287195

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: MI
Alter: 90,0
Geschlecht: M
Eingang: 20.05.2022
Impfdatum: 06.11.2021
Beginn: 12.05.2022
Tage bis Beginn: 187,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Blood creatinine increased COVID-19 Creatinine renal clearance decreased Pancytopenia White blood cell count decreased

Symptomtext

Admission Date: 5/12/2022 Discharge Date: 5/14/2022 HOSPITAL PROBLEMS 1. AHRF secondary to Covid-19 infection 2. CKD3b 3. Pancytopenia 4. OSA 5. CAD s/p CABG 6. COPD 7. Gout 8. Barretts esophagus HOSPITAL COURSE: Patient is a 91 y.o. male who was admitted to hospital with AHRF secondary to Covid-19 infection. AHRF/Covid-19 infection: Patient required 2L NC on admission to maintain saturations. Was started on 10 day course of decadron. Did not start Remdesivir due to low CrCl. Patient improved quickly, and was weaned to room air. Observed for 24hrs to ensure no further desaturations. None noted so patient discharged home to finish course of Decadron. CKD3b: Cr mildly increased from baseline at 1.92. Remained around this level throughout admission. Pancytopenia: Patient has know anemia secondary to CKD, as well as thrombocytopenia. WCC also noted to be decreased. Likely overall pancytopenia secondary to Covid-19 infection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: History of Barrett's esophagus Dyslipidemia Anemia due to stage 3b chronic kidney disease (HCC) Idiopathic chronic gout of multiple sites without tophus Primary insomnia Moderate COPD (chronic obstructive pulmonary disease) (HCC) Hx of asbestos exposure Mycobacterium avium complex (HCC) History of bladder cancer Nocturnal hypoxemia CAD s/p CABG x 4 in 1999 without angina pectoris Stage 3b chronic kidney disease (HCC) OSA on CPAP Lung nodule Thrombocytopenia (HCC) Chronic fatigue
Andere Medikamente: allopurinol (ZYLOPRIM) 100 MG tablet aspirin 325 MG tablet atorvastatin (LIPITOR) 20 MG tablet Calcium Carbonate-Vitamin D (CALCIUM + D PO) dexamethasone (DECADRON) 6 MG tablet fish oil-omega-3 fatty acids 1000 MG capsule LORazepam (A
Allergien: Lipitor [Hmg-coa-r Inhibitors]Myalgia MorphineOther NiacinGout Nitrates, Organic [Organic Nitrates]Headache
Vorherige Impfungen: -

VAERS 2280963

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: CO
Alter: 87,0
Geschlecht: M
Eingang: 17.05.2022
Impfdatum: 30.04.2022
Beginn: 07.05.2022
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Anticoagulant therapy Blood electrolytes C-reactive protein COVID-19 Chest X-ray Chronic kidney disease Coagulation test Confusional state Deep vein thrombosis Diarrhoea Failure to thrive Fibrin D dimer Hypoglycaemia Hypophagia Illness Inflammatory marker increased Metabolic function test

Symptomtext

Symptoms of confusion and hypoglycemia associated with poor oral intake associated with acute illness with positive COVID-19 PCR test 6 days previously prompted presentation to hospital emergency department. Diagnoses included acute hypoxemic respiratory insufficiency, acute on chronic CKD, diarrhea, deep vein thrombosis, and failure to thrive in setting of increased inflammatory markers. in addition to antidiabetic medication management, patient received remdesivir, dexamethasone, and anticoagulation X 4 days. Patient was discharged medically stable to his routine home care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: Chest Xray Comprehensive Electrolyte Panel D dimer CRP Anti Xa
Aktuelle Erkrankungen: Type 2 diabetes Coronary heart disease Systolic heart failure Hyperlipidemia Chronic kidney disease Pseudophakia bilateral Hypertension
Vorgeschichte: Above
Andere Medikamente: Insulin degludec Alendronate Aspirin Atorvastatin Carvedilol Cholecalciferol Furosemide Diclofenac gel
Allergien: Penicillins
Vorherige Impfungen: -

VAERS 2266225

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: WA
Alter: 64,0
Geschlecht: M
Eingang: 06.05.2022
Impfdatum: 12.11.2021
Beginn: 25.03.2022
Tage bis Beginn: 133,0
Dosis: 3
Route/Site: IM / RA

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

Computerised tomogram Electrocardiogram Pulmonary embolism

Symptomtext

Bilateral pulmonary embolism

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: ECG 3/25/2002 CT scan
Aktuelle Erkrankungen: none
Vorgeschichte: synovial cyst on L3/L4
Andere Medikamente: Tramadol, tylenol
Allergien: none
Vorherige Impfungen: -

VAERS 2263376

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: -
Alter: 100,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 08.10.2021
Beginn: 01.12.2021
Tage bis Beginn: 54,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Pfizer COVID vac #1 - 1/14/21 - #EL3247; Pfizer COVID vac #2 - 2/4/21 - EEL9261; pt lives in a residential facility; had a positive COVID test on 12/21/21, prior to admission into the facility; DNR; slow to recover from COVID; on O2 supplementation; pt expired in the residential facility

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: dementia, HTN, DVT, hypothyroidism, dysphagia, IBS
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2258448

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: WA
Alter: 71,0
Geschlecht: F
Eingang: 29.04.2022
Impfdatum: 22.10.2021
Beginn: 11.04.2022
Tage bis Beginn: 171,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Asthenia Blood test COVID-19 Computerised tomogram thorax abnormal Cough Dyspnoea Echocardiogram Electrocardiogram Laboratory test Malaise Nasal congestion Oxygen saturation decreased Pulmonary embolism SARS-CoV-2 test positive

Symptomtext

COVID-19 symptoms started on 04/11/22, testing positive on 04/12/22. Symptoms were cough mostly, nasal congestion, and a little bit of low energy. On 04/15/22 I was extremely short of breath and had to go to urgent care where they sent me to the ER because my pulse ox was low. I was admitted for four days and was on oxygen. I'm not back to 100% but I'm close. I saw the Doctor for f/u on 04/27/22 and she made referrals for down the road. In the hospital I was put on dexamethasone for 10 days and had 4 doses for Remdesivir, as well as heparin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 4,0
Labordaten: Chest CT (Pulmonary emboli); Electrocardiogram (Non FT Change MI); Echocardiogram; Labs/Blood work. All tests done on 04/15/2022
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Tamoxifen 20 mg daily, Alendronate 70 mg once a week
Allergien: None
Vorherige Impfungen: -

VAERS 2257020

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: WI
Alter: 68,0
Geschlecht: M
Eingang: 28.04.2022
Impfdatum: 22.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure Balance disorder Computerised tomogram thorax abnormal Full blood count abnormal Hypokalaemia Lethargy Lung opacity Metabolic encephalopathy Metabolic function test abnormal Pyrexia Seizure

Symptomtext

Patient received vaccine #3 on 10/22/2021; he developed fever, unsteadiness and lethargy on 10/23/2021; he was seen in ER on 10/23/2021 and was admitted to Hospital on 10/23/2021 for acute hypoxic respiratory failure, seizure disorder and acute metabolic encephalopathy; he was discharged on 10/28/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: CBC, CMP on 10/27/2021 - findings of hypokalemia. CT of the chest 10/26/2021 - patchy geographic ground glass opacities in the upper lobes R > L.
Aktuelle Erkrankungen: URI symptoms on 9/20/2021
Vorgeschichte: Autism spectrum disorder, Intellectual disability, OCD, HTN, Remote history of seizures, history of TD and akathisia, GERD, Gastritis, Duodenal ulcer, Chronic constipation, Colon diverticulosis, Impaired vision d/t bilateral cataract and keratoconus, BPH, Osteopenia, History of pelvic fracture, History of left hip fracture, S/P hemiarthroplasty, COVID 19 viral infection 5/2020.
Andere Medikamente: Olanzapine, Sertraline, Carbamazepine, Omeprazole, Famotidine, Calcium Carbonate, Vitamin D3, Multivitamin, Amlodipine, Aspirin, ProAir inhaler as needed, Tamsulosin, Metamucil, Bisacodyl suppository as needed, Acetaminophen as needed, HC 2
Allergien: Chlorpromazine, Compazine, Dilantin.
Vorherige Impfungen: COVID 19/Pfizer 1 on 2/4/2021, on 2/5/2021 he had low grade fever, elevated BP and HR, unsteadiness, resolved after 24 hrs; sec

VAERS 2250432

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: GA
Alter: 73,0
Geschlecht: M
Eingang: 25.04.2022
Impfdatum: 12.10.2021
Beginn: 23.11.2021
Tage bis Beginn: 42,0
Dosis: UNK
Route/Site: - / -

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

Blood test Cerebrovascular accident Computerised tomogram Magnetic resonance imaging head abnormal X-ray

Symptomtext

STROKE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 10,0
Labordaten: MRI CT Xray Several blood tests
Aktuelle Erkrankungen: none known
Vorgeschichte: high blood pressure high cholesterol
Andere Medikamente: tylenol osteo biflex vitamin and mineral powdered supplemen7
Allergien: aspirin clindamycin
Vorherige Impfungen: -

VAERS 2249752

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: CA
Alter: 51,0
Geschlecht: M
Eingang: 24.04.2022
Impfdatum: 22.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Back pain Condition aggravated Death Decreased activity Somnolence Unresponsive to stimuli

Symptomtext

WAS LESS ACTIVE, SLEPT MOST OF THE TIME, COMPLAINED OF BACK PAIN ON THE DAY AFTER VACCINATION ON 10/22/2021; WAS FOUND UNRESPONSIVE/DEAD ON 10/24/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: eosinophilic esohpagitis, back pain, obesity, anxiety, asthma, memory loss
Vorgeschichte: asthma, obesity, eosinophilic esophagitis
Andere Medikamente: n/a
Allergien: none
Vorherige Impfungen: -

VAERS 2247877

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: -
Alter: 79,0
Geschlecht: M
Eingang: 22.04.2022
Impfdatum: 19.11.2021
Beginn: 29.12.2021
Tage bis Beginn: 40,0
Dosis: 3
Route/Site: - / -

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

Blood immunoglobulin G decreased Blood immunoglobulin M decreased COVID-19 Death Dyspnoea General physical health deterioration Hypoxia SARS-CoV-2 test positive

Symptomtext

pt had a positive COVID test on 12/29/21, was treated outpatient with azithromycin, Zofran, Flovent, monoclonal antibodies, Medrol Dosepak, albuterol MDI; had worsening SOB and was given Levaquin; still had worsening SOB and was given IV Rocephin and steroid injections; on 2/22/22 pt was admitted to Hospital for 2 days; dc'd to home with O2 supplementation and dexamethasone; presents to ED on 2/9/22 with worsening SOB and hypoxia; O2 supplementation; (history of lymphoma); IgG and Igm deficiency; given high dose steroids then tapered off due to no improvement; O2 requirement increased to a need of high flow via NC; DNR; pt's condition continued to worsen and he was made comfort measures; he passed away in the hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 19,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2241111

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: CO
Alter: 84,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 09.02.2021
Beginn: 24.01.2022
Tage bis Beginn: 349,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 Chest X-ray Fibrin D dimer Full blood count Metabolic function test

Symptomtext

Hospitalized for COVID-19 infection/AHRF after COVID-19 immunization. Administered oxygen and dexamethasone and discharged to home medically stable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: Blood counts Basic metabolic panel Chest X-ray D-dimer
Aktuelle Erkrankungen: Diverticulosis
Vorgeschichte: Hypothyroidism Hypertension Gastroesophageal reflux Hyperlipidemia
Andere Medikamente: Losartan Nifedipine Simvastatin Omeprazole Levothyroxine Meloxicam
Allergien: Penicillin Nitrofurantoin
Vorherige Impfungen: -

VAERS 2238643

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: CO
Alter: 84,0
Geschlecht: F
Eingang: 18.04.2022
Impfdatum: 15.10.2021
Beginn: 14.01.2022
Tage bis Beginn: 91,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 Clostridium difficile infection Clostridium test positive Culture positive SARS-CoV-2 test positive

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA: hospitalized for COVID-19 infection with acute hypoxemic respiratory failure and c. diff infection. Received oxygen, antimicrobials, and steroids and discharged to home medically stable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: GI PCR culture: c. difficile toxin AB positive; home COVID test positive
Aktuelle Erkrankungen: none known
Vorgeschichte: arthritis, cataract, cerebral infarction, dry eye, GERD heart murmur, sleep apnea, type 2 diabetes
Andere Medikamente: acetaminophen, cyclosporine, diclofenac topical, ibuprofen, levothyroxine, losartan, meloxicam, nifedepine, omeprazole, simvastatin
Allergien: nitrofurantoin, penicillin
Vorherige Impfungen: -

VAERS 2238122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: WA
Alter: 47,0
Geschlecht: M
Eingang: 16.04.2022
Impfdatum: 29.10.2021
Beginn: 11.12.2021
Tage bis Beginn: 43,0
Dosis: 3
Route/Site: SYR / UN

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

Cardiac arrest

Symptomtext

Cardiac arrest. I survived but had 3 months of recovery after the event to return to normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Busprione, bupropion
Allergien: None
Vorherige Impfungen: -

VAERS 2225863

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 11.04.2022
Impfdatum: 22.10.2021
Beginn: 01.01.2022
Tage bis Beginn: 71,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Cerebral haemorrhage Computerised tomogram head abnormal Death Diarrhoea Dizziness Endotracheal intubation Fall Head injury Hemiparesis Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

pt fell this morning and hit his head; family states he had a positive COVID test on 1/1/2022; EMS called and intubated; prior to fall pt had D/N/V and dizziness; family states they think there's right sided weakness; CT findings revealed large right sided IPH with intraventricular extension; poor prognosis; family requested extubation and comfort measures; pt passed away in the ED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: aortic dissection
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2223201

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: OH
Alter: 34,0
Geschlecht: M
Eingang: 08.04.2022
Impfdatum: 01.03.2021
Beginn: 12.10.2021
Tage bis Beginn: 225,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Cardiac arrest Epilepsy Otitis media Troponin increased

Symptomtext

Pfizer COVID vaccines on 2/8/2021 and 3/1/2021 Hospitalized on 10/12/2021 at hospital Diagnosis of epileptic seizure, COVID 19, Cardiac arrest, elevated tropinin, and otitis media Treatment included, Augmentin, Topamax 50 mg twice daily, and cardiology consult Additional Pfizer booster received on 11/18/2021 after the adverse event on 10/12/2021

Weitere VAERSDATA-Felder

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

VAERS 2214913

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: KY
Alter: 79,0
Geschlecht: M
Eingang: 04.04.2022
Impfdatum: 03.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: SYR / AR

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

Bronchitis Computerised tomogram Condition aggravated Death Laboratory test Pneumonia Pulmonary fibrosis

Symptomtext

?within a few weeks, bronchitis which went into bilateral pneumonia. Upon being admitted to hospital, it was discovered he had an acute exacerbation of pulmonary fibrosis. Previously, he was **completely** asymptomatic and incredibly active with yard work, walking, climbing stairs and ladders?no respiratory issues, whatsoever. He was in hospital four weeks before he deceased. The pneumonia had long cleared but the PF had not.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 29,0
Labordaten: January 2022- various, including CT scans at Hospital-
Aktuelle Erkrankungen: none
Vorgeschichte: none In the past, one bout with pancreatitis. My dad had no health issues and was on zero medications. He saw his physician annually.
Andere Medikamente: benadryl
Allergien: none of which I'm aware
Vorherige Impfungen: -

VAERS 2214487

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: SD
Alter: 81,0
Geschlecht: M
Eingang: 04.04.2022
Impfdatum: 19.10.2021
Beginn: 17.02.2022
Tage bis Beginn: 121,0
Dosis: 3
Route/Site: SYR / LA

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

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

Symptomtext

This is an instance of breakthrough COVID-19 after which death occurred. The individual was vaccinated with the Pfizer product on 12/30/2020 (at the Pharmacy), 01/20/2021 (at the Pharmacy) and 10/19/2021 at Clinic. They were tested via antigen test twice on 02/17/2022 at the long term care facility at which they were a resident. One result was positive and one was negative. They died on 03/06/2022. COVID-19 is listed on the death certificate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Positive COVID-19 test on 02/17/2022 despite being vaccinated and boosted.
Aktuelle Erkrankungen: -
Vorgeschichte: Primary Degenerative Dementia: Alzheimer's Type, Hypertension, Arteriosclerotic Heart Disease, Hyperlipidemia, Osteoarthritis, history of malnutrition, history of prostate cancer, history of squamous cell skin cancer The individual was a resident of the long term care facility (LTCF) indicated in the address portion of this form. Phone number is the main line for the LTCF.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2210003

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: SD
Alter: 92,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 19.10.2021
Beginn: 27.01.2022
Tage bis Beginn: 100,0
Dosis: 3
Route/Site: SYR / LA

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

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

Symptomtext

This is an instance of breakthrough COVID-19 after which death occurred. The individual was vaccinated with the Pfizer product on 12/30/2020, 01/20/2021, and 10/19/2021. The first dose was administered at the facility indicated in Item 15 of this form. The second dose was administered at a Pharmacy. The third dose was administered at a Clinic. The individual tested positive for COVID-19 on 01/27/2022 via antigen test at the long term care facility at which they were a resident. They died on 02/11/2022. It is unclear if this individual was hospitalized or not. COVID-19 is listed on the death certificate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Positive COVID-19 test on 01/27/2022 despite being vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, Coronary Artery Disease, A-Fib, Obstructive Sleep Apnea, Hypertension, Dementia (unspecified type), Hypothyroidism, Osteoporosis, The individual was a resident of a long-term care facility at the time of the adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2166010

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: SD
Alter: 72,0
Geschlecht: F
Eingang: 08.03.2022
Impfdatum: 05.11.2021
Beginn: 03.01.2022
Tage bis Beginn: 59,0
Dosis: 2
Route/Site: SYR / LA

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

COVID-19 Cough Death Dyspnoea Inappropriate schedule of product administration SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. I also uncovered a likely vaccine administration error while looking into this adverse event. The individual was vaccinated with the Pfizer product on 09/13/2021, 10/22/2021, and 11/05/2021. The first 2 doses were administered at the facility indicated in Item 17 of this form, but the third dose seems to be a deviation from protocol and was administered at a Pharmacy in a city that the individual does not live in. The individual presented to Emergency Dept for cough and shortness of breath on 01/03/2022 and was discharged 01/04/2022. The individual tested positive for COVID-19 on 01/03/2022. The individual reported a symptom onset of approx 12/29/2021. They were transported to Emergency Dept again on 01/08/2022; it appears they were dead on arrival. Death date was 01/08/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 1,0
Labordaten: Positive COVID-19 test despite being vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, Congestive Heart Failure, Hypertension, long term use of Warfrin, Type II Diabetes, Obesity, Chronic Kidney Disease, Obstructive Sleep Apnea, had presented to clinic for wound care consultation for BLE Edema about a month before the adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2166010

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: SD
Alter: 72,0
Geschlecht: F
Eingang: 08.03.2022
Impfdatum: 05.11.2021
Beginn: 03.01.2022
Tage bis Beginn: 59,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Cough Death Dyspnoea Inappropriate schedule of product administration SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. I also uncovered a likely vaccine administration error while looking into this adverse event. The individual was vaccinated with the Pfizer product on 09/13/2021, 10/22/2021, and 11/05/2021. The first 2 doses were administered at the facility indicated in Item 17 of this form, but the third dose seems to be a deviation from protocol and was administered at a Pharmacy in a city that the individual does not live in. The individual presented to Emergency Dept for cough and shortness of breath on 01/03/2022 and was discharged 01/04/2022. The individual tested positive for COVID-19 on 01/03/2022. The individual reported a symptom onset of approx 12/29/2021. They were transported to Emergency Dept again on 01/08/2022; it appears they were dead on arrival. Death date was 01/08/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 1,0
Labordaten: Positive COVID-19 test despite being vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, Congestive Heart Failure, Hypertension, long term use of Warfrin, Type II Diabetes, Obesity, Chronic Kidney Disease, Obstructive Sleep Apnea, had presented to clinic for wound care consultation for BLE Edema about a month before the adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2165527

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: WI
Alter: 76,0
Geschlecht: F
Eingang: 08.03.2022
Impfdatum: 11.10.2021
Beginn: 19.01.2022
Tage bis Beginn: 100,0
Dosis: 3
Route/Site: - / -

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

Asymptomatic COVID-19 Cardiac arrest Death Fall Femoral neck fracture Open reduction of fracture SARS-CoV-2 test positive

Symptomtext

According to System report, client admitted to hospital post fall on 1/13/2022. She was diagnosed with a left femoral neck fracture. She was taken to the OR for an ORIF left femoral neck fracture. She tested positive for COVID-19, asymptomatic. On 1/19/2022, she experienced a cardiac arrest and passed away. No other information known.

Weitere VAERSDATA-Felder

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

VAERS 2140268

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: WI
Alter: 75,0
Geschlecht: F
Eingang: 25.02.2022
Impfdatum: 30.10.2021
Beginn: 19.02.2022
Tage bis Beginn: 112,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Death

Symptomtext

Death related to COVID 19 infection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Other significant conditions: UTI, Morbid obesity, Reactive airway disease, DM2, HTN
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2102162

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: KY
Alter: 89,0
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: 02.10.2021
Beginn: 12.01.2022
Tage bis Beginn: 102,0
Dosis: 3
Route/Site: IM / RA

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

Activated partial thromboplastin time shortened Acute respiratory failure Alanine aminotransferase increased Albumin globulin ratio Anion gap Aspartate aminotransferase increased Asthenia Atrial fibrillation Basophil count decreased Basophil percentage decreased Blood albumin decreased Blood alkaline phosphatase normal Blood bilirubin normal Blood chloride normal Blood creatinine increased Blood glucose normal Blood lactic acid Blood potassium decreased

Symptomtext

:Pt is a 89 yr/o female who presents with shortness of breath for past two days. Pt has had a cough, sneezing/tearing from eyes, body aches, and fever. Pt took home covid swab and was positive. Pt oxygen levels have been dropping despite her 2 liters continuous. Pt has had covid vaccine. No HA, sore throat, CP, abdominal pain, V/D, dysuria, or rash. Pt does bruise easily due to being on Eliquis. Pt has had covid vaccine. Review of Systems Constitutional: Negative for chills and fever. HENT: Positive for congestion and rhinorrhea. Negative for sore throat. Eyes: Negative for discharge. Respiratory: Positive for cough and shortness of breath. Cardiovascular: Negative for chest pain. Review of Systems Gastrointestinal: Negative for diarrhea and vomiting. Genitourinary: Negative for dysuria. Musculoskeletal: Positive for myalgias. Neurological: Negative for headaches. Hematological: Does not bruise/bleed easily 1/12/22 TT Echo: Physician Conclusions Any valve disease noted in the report is non-rheumatic unless otherwise specifically noted. Summary: 1. Normal biventricular chamber size and systolic function. LVEF 50 to 55%. 2. The patient is status post bioprosthetic aortic valve (#26 Evolut pro plus) with normal function.Mean gradient 8 mmHg, dimensionless index 0.52. 3. Moderate mitral annular calcification with mild to moderate mitral regurgitation. 4. Moderate tricuspid valve regurgitation. 5. RVSP estimated at 42 mmHg. 6. Dilated IVC consistent with elevated right-sided filling pressures. Findings Left Ventricle: The left ventricular chamber size, wall thickness, and systolic function are within normal limits. There are no regional wall motion abnormalities observed. Indeterminate diastolic filling pattern due to mitral annular calcification. The ejection fraction biplane was calculated at 51%. Left Atrium: Moderately dilated left atrium. Right Ventricle: The right ventricular chamber size and systolic function are within normal limits. Right Atrium: The right atrial chamber size appears normal. Aortic Valve: s/p TAVR with Evolut Pro plus 26 mm. The peak instantaneous gradient of the aortic valve is 16 mmHg. The mean gradient of the aortic valve is 8. mmHg. The aortic valve area by VTI, is calculated at 1.5 cm2.There is normal function in from the bioprosthetic aortic valve. There is no evidence of aortic valve stenosis. There is no paravalvular regurgitation appreciated. Dimensionless index is 0.52. Mitral Valve: Moderate mitral annular calcification.There is mild to moderate mitral regurgitation. There is no evidence of mitral valve stenosis. Tricuspid Valve: The tricuspid valve is normal in structure and function. There is Moderate tricuspid regurgitation. Right ventricular systolic pressure of 42 mmHg. Pulmonic Valve: The pulmonic valve is not adequately visualized but Doppler appears normal. Trivial pulmonic insufficiency. Pericardial: There is no evidence of pericardial effusion. Aorta/Great Vessels: Aortic root dimension within normal limits. There is no dilatation of the ascending aorta. The IVC appears to be dilated. CBC w/Diff Collection Time: 01/12/22 12:32 PM Result Value Ref Range White Blood Count 4.03 (L) 4.5 - 11.0 10*3/uL Red Blood Count 3.96 (L) 4.0 - 5.2 10*6/uL Hemoglobin 10.8 (L) 12.0 - 16.0 g/dL Hematocrit 35.9 (L) 36.0 - 46.0 % Mean Corpuscular Volume 90.7 80.0 - 100.0 fL Mean Corpuscular Hemoglobin 27.3 26.0 - 34.0 pg Mean Corpuscular HGB Conc 30.1 (L) 31.0 - 37.0 g/dL Red Cell Distribution Width-CV 15.4 12.0 - 16.8 % Platelet Count 143 140 - 440 10*3/uL Mean Platelet Volume 11.0 8.4 - 12.4 fL Diff Type Hospital CBC w/AutoDiff (arb'U) Neutrophils % 65.4 45 - 80 % Lymphocyte % 22.8 15 - 50 % Monocyte % 10.2 0 - 15 % Eosinophil% 0.2 0 - 7 % BASO% 0.2 0 - 2 % Immature Granulocyte% 1.2 (H) 0.0 - 1.0 % Nucleated RBC % 0 0 /100(WBC) Neutrophil Abs 2.63 2.0 - 8.8 10*3/uL Lymphocyte-Absolute 0.92 0.7 - 5.5 10*3/uL Monocyte Absolute 0.41 0.0 - 1.7 10*3/uL EOS-Absolute 0.01 0.0 - 0.8 10*3/uL Basophil Abs 0.01 0.0 - 0.2 10*3/uL Immature Granulocyte Abs 0.05 0.00 - 0.10 10*3/uL Comprehensive Metabolic Panel(CMP) Collection Time: 01/12/22 12:32 PM Result Value Ref Range Sodium 141 136 - 145 mmol/L Potassium 3.1 (L) 3.5 - 5.1 mmol/L Chloride 101 98 - 107 mmol/L Carbon Dioxide 28 22 - 29 mmol/L Anion Gap 12 5 - 13 (arb'U) Glucose 95 74 - 99 mg/dL Blood Urea Nitrogen (BUN) 55 (H) 10 - 20 mg/dL Creatinine-Blood 1.79 (H) 0.55 - 1.02 mg/dL BUN/Creatinine Ratio 30.7 RATIO Estimated GFR 27 (L) >60 /1.73 m2 Estimated GFR if (Privacy) 32 (L) >60 /1.73 m2 Total Protein 5.9 (L) 6.2 - 8.0 g/dL Albumin 3.1 (L) 3.2 - 4.6 g/dL Globulin 2.8 1.5 - 4.5 g/dL Albumin/Globulin Ratio 1.1 1.1 - 2.5 RATI Calcium 8.9 8.4 - 10.2 mg/dL Total Bilirubin 0.4 0.2 - 1.2 mg/dL AST/SGOT 55 (H) 5 - 34 U/L ALT/SGPT 52 0 - 55 U/L Alkaline Phosphatase 90 40 - 150 U/L B-Type Natriuretic Peptide Collection Time: 01/12/22 12:32 PM Result Value Ref Range B-Type Natriuretic Peptide 155.3 4 - 254 pg/mL Troponin Collection Time: 01/12/22 12:32 PM Result Value Ref Range Troponin 0.205 (HH) 0.000 - 0.034 ng/mL Partial Thromboplastin Time Collection Time: 01/12/22 12:32 PM Result Value Ref Range Partial Thromboplastin Time 33.0 25.1 - 36.5 s Protime-INR Collection Time: 01/12/22 12:32 PM Result Value Ref Range Prothrombin Time 13.6 (H) 10.3 - 13.3 s INR 1.2 INR Lactic Acid Collection Time: 01/12/22 12:33 PM Result Value Ref Range Lactic Acid 1.5 0.7 - 2.0 mmol/L 1/12/22 XR Chest 1 Vw CONCLUSION: No acute abnormality 1/17/22 Hospital Course: Patient presented to the ER with shortness of breath and weakness. She was known covid +. She was found to have acute on chronic hypoxic respiratory failure and was admitted for further management. Issues addressed this admission are detailed below. Acute hypoxic respiratory failure secondary to COVID-19 PNA On remdesivir and dexamethasone. Was increased to high flow on 1/13 and started on baricitinib but it was discontinued due to worsening leukopenia. Pt now stable on 2 liters oxygen with exertion Chronic diastolic heart failure cont torsemide Afib New diagnosis could be illness related and transient. Has been back in sinus. Already on beta blocker and AC. echo with preserved EF. F/u with cardio outpt Mild asymptomatic bradycardia Pt noted to have dips in heart rate to 50s and occassionaly 40's. Happens at rest and is asymptomatic. Recommend observatoin. If worsens may need to decrease beta blocker. Leukopenia/tcp appears to be related to baricitinib, improving with discontinuation. Recommend repeat cbc when Essential hypertension bp has been climbing on steroids. At one point prior to admission was on losartan but family unsure why it was discontinued. Recommend monitoring bp at home if persists may need further treatment. Acquired hypothyroidism Synthroid H/o DVT on eliquis, repeat dopplers with no clot 1/26/22 PCP F/u: 89 yr/o female who presents here for hospital follow-up after admission from 1/12/2022-1/17/2022 with COVID-19 infection and shortness of breath. Patient have respiratory discomfort before admission and was diagnosed with acute on chronic respiratory failure. Acute hypoxic respiratory failure secondary to COVID-19 PNA and has received remdesivir and dexamethasone. She was treated with high flow oxygen. She was started on baricitinib but it was discontinued due to worsening leukopenia. But her symptoms improved. She is currently not on oxygen when she came to the office. She still gets short of breath easily. Chronic diastolic heart failure she is doing well with the beta-blocker bisoprolol and diuretic with torsemide. No complaining of dizziness. She does have some leg swelling. Complaining of neck pain. She is sleeping with one pillow. She was also diagnosed with atrial fibrillation. She is not a candidate for anticoagulation with bleeding. She does not have any palpitation. Leukopenia/tcp appears to be related to baricitinib.I will obtain blood work again today. Hypertension she is doing well on the current regimen. Complaining of burning in the mouth. She does have poor taste. She was brought to the office by her son and history obtained from both patient and son. The following portions of the patient's history were reviewed and updated as appropriate: allergies, current medications, past family history, past medical history, past social history, past surgical history and problem list.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: 1/12/22 COVID-19 Result Detected Abnormal
Aktuelle Erkrankungen: -
Vorgeschichte: Anesthesia complication 10/2017 oct 2017 - had delirum post op o Arthritis all over o Bilateral edema of lower 1/12/22 o Bilateral edema of lower extremity off/ on o CHF (congestive heart failure) (CMS/HCC) o Chronic diastolic CHF (congestive heart failure) (CMS/HCC) 6/8/2021 o Chronic renal insufficiency, stage III (moderate) (CMS/HCC) followed by PCP o Colon cancer (CMS/HCC) 2010 has 12 inches of colon removed--no chemo/radiation o Complication of anesthesia o Constipation treated PRN o COPD (chronic obstructive pulmonary disease) (CMS/HCC) treated with meds o Coronary artery disease o Delirium, induced by drug 10/2017 combative, confused o DVT (deep venous thrombosis) (CMS/HCC) 9/14,3/2017 Admission to (Privacy) restarted after recurrent PE and DVT 3/2017 o Exercise intolerance o Fractures 08/18/2017 Comp Fx T5, broken ribs o HLD (hyperlipidemia) treated with medication o HTN (hypertension) treated with medication o Hypothyroidism treated with medication o Long term current use of anticoagulant therapy o Osteoporosis treated with medications o PE (pulmonary thromboembolism) (CMS/HCC) 9/14,3/2017 Dr. (Privacy) Admission to (Privacy), did not tolerate anticoagulation due to hematuria but restarted after recurrent PE and DVT 3/2017 o Pneumonia 2019 Hospitalized & on vent x 3-4- days o Renal cyst 10/2014 Anticoagulation was discontinued after PE and DVT-v resolved o Restless leg treatedb PRN o Skin breakdown bruises easily - large bruise right wrist. abraisions on right wrist, and rt hand d/t blood thinners o Sleep apnea pt does not use CPAP o Snoring o Vertebral compression fracture (CMS/HCC) 10/03/2017 Comp Fx T7, T8 o Vertebral compression fracture (CMS/HCC) 11/30/2017 Comp Fx T6, T10, T12
Andere Medikamente: albuterol-ipratropium (DUO-NEB) 0.5-2.5 mg/3 mL nebulizer albuterol-ipratropium (DUO-NEB) 0.5-2.5 mg/3 mL nebulizer Take 1 ampule by nebulization 4 (four) times daily. 300 mL 11 o apixaban (ELIQUIS) 5 MG tablet Take 1 tablet by mouth 2 (tw
Allergien: Bumex, Sulfa antibiotics, Xarelto, Norvasc, Trazodone
Vorherige Impfungen: -

VAERS 2095899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: MN
Alter: 83,0
Geschlecht: M
Eingang: 08.02.2022
Impfdatum: 12.10.2021
Beginn: 07.02.2022
Tage bis Beginn: 118,0
Dosis: 2
Route/Site: IM / RA

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

Acute myocardial infarction Asthenia COVID-19 pneumonia Cough Dyspnoea Fall Inappropriate schedule of product administration Pyrexia

Symptomtext

Hospitalized with COVID 19 pneumonia, fever ,cough, dyspnea, generalized weakness, and recurrent falls and NSTEMI

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 2,0
Labordaten: FYI pt received his first dose of COVID vaccine 8 months prior to his first, it is listed as given in previous 4 weeks only to give documentation of 1st dose.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2092501

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: IL
Alter: 51,0
Geschlecht: M
Eingang: 07.02.2022
Impfdatum: 12.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: - / LA

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

Angiogram Blood test Cardiac arrest Computerised tomogram head Computerised tomogram pelvis Computerised tomogram spine Echocardiogram Electrocardiogram SARS-CoV-2 test Urine analysis

Symptomtext

Unexplained cardiac arrest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 4,0
Labordaten: Every test was done. Blood, Urine, EKG, ECG ,TTE, Echocardiogram, Angiogram, CAT scan Head/Brain, CT Spine, CR Pelvis, Covid-19.
Aktuelle Erkrankungen: Diagnosed with Wolf Parkinson White Syndrome in the 90s. No issues.
Vorgeschichte: None
Andere Medikamente: None
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2075830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: TN
Alter: 37,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 23.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Computerised tomogram thorax abnormal Dyspnoea Flank pain Laboratory test Pulmonary embolism

Symptomtext

Started having sharp pain in right flank area and shortness of breath on 11-28-2021. Went to doctor on 11-30-2022, CT done on 11-30-022 which showed bilateral pulmonary emboli. Admitted to Medical Center overnight. Discharge on 12-1-2021 with Eliquis. Takes Eliquis 5mg twice daily now. No longer on birth control pills.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 1,0
Labordaten: CT of chest, lab work, etc.
Aktuelle Erkrankungen: Asthma flare and sinus issues with steroids given approx. 1 month prior to booster dose of Pfizer
Vorgeschichte: Asthma, Autoimmune d/o (unidentified)
Andere Medikamente: Drospirenone And Ethinyl Estradiol(BCP), Budesonide, Celecoxib, Albuterol inhaler, Omeprazole, Methocarbamol, Topiramate, Hydroxychloroquine,
Allergien: Rocephin
Vorherige Impfungen: -

VAERS 1936333

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: SD
Alter: -
Geschlecht: M
Eingang: 28.01.2022
Impfdatum: 08.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Arrhythmia Body temperature Body temperature increased Carbon dioxide Fatigue Autopsy Brain oedema Condition aggravated Death Myalgia Oropharyngeal pain Tachycardia Giant cell arteritis Hypersomnia Impaired work ability Inflammation Malaise Heart rate

Symptomtext

Death From Myocarditis; fatal arrhythmia that killed him instantly; increased heart rate; Tachycardia; temperature was up to 100.2; fatigue; muscle soreness; sore throat; Product use for unapproved combination; left ventricular dysfunction; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program. Other Case identifier(s): US-PFIZER INC-202200065467 (Pfizer), US-PFIZER INC-202200142396 (pfizer). A 26 year-old male patient received bnt162b2 (BNT162B2), administration date 08Nov2021 (Lot number: FE3590) as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (INFLUENZA VACCINE), administration date 08Nov2021 (Batch/Lot number: unknown) for immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Pfizer 1st dose - ER8733), administration date: 26Mar2021, for COVID-19 Immunization; Bnt162b2 (Pfizer 2nd dose - EW0164), administration date: 16Apr2021, for COVID-19 immunisation. The following information was reported: MYOCARDITIS (death, medically significant) with onset 12Nov2021, outcome "fatal", described as "Death From Myocarditis"; ARRHYTHMIA (death) with onset 12Nov2021, outcome "fatal", described as "fatal arrhythmia that killed him instantly"; LEFT VENTRICULAR DYSFUNCTION (death) with onset Nov2021, outcome "fatal", described as "left ventricular dysfunction"; FATIGUE (non-serious) with onset 11Nov2021, outcome "not recovered", described as "fatigue"; MYALGIA (non-serious) with onset 11Nov2021, outcome "not recovered", described as "muscle soreness"; OROPHARYNGEAL PAIN (non-serious) with onset 11Nov2021, outcome "recovered" (2021), described as "sore throat"; HEART RATE INCREASED (non-serious) with onset 12Nov2021, outcome "not recovered", described as "increased heart rate"; TACHYCARDIA (non-serious) with onset 12Nov2021, outcome "unknown", described as "Tachycardia"; BODY TEMPERATURE INCREASED (non-serious) with onset 12Nov2021, outcome "recovered" (12Nov2021 16:30), described as "temperature was up to 100.2"; PRODUCT USE ISSUE (non-serious) with onset 08Nov2021, outcome "unknown", described as "Product use for unapproved combination". The patient underwent the following laboratory tests and procedures: body temperature: (unspecified date) 100.2 Fahrenheit, notes: his temperature was up to 100.2; carbon dioxide (0.0-1.5): (unspecified date) 0.2 %, notes: Normal; heart rate: (unspecified date) 112, notes: his heart rate was elevated to 112; (10Nov2021) 97; (10Nov2021) 85; (10Nov2021) 91; (10Nov2021) 84; (10Nov2021) 91; (10Nov2021) 89; (10Nov2021) 90; (10Nov2021) 89; (10Nov2021) 84; (10Nov2021) 85; (10Nov2021) 98; (10Nov2021) 89; (11Nov2021) 90; (11Nov2021) 120; (11Nov2021) 119; (11Nov2021) 120; (11Nov2021) 121; (11Nov2021) 127; (11Nov2021) 126; (11Nov2021) 127; (11Nov2021) 131; (11Nov2021) 128; (11Nov2021) 131; (11Nov2021) 130; (11Nov2021) 130; (11Nov2021) 128; (12Nov2021) 123; (12Nov2021) 127; (12Nov2021) 128; (12Nov2021) 135; (12Nov2021) 74; (12Nov2021) 141; (12Nov2021) 71; (12Nov2021) 146; (12Nov2021) 144; (12Nov2021) 138; (12Nov2021) 149; (12Nov2021) 148; (12Nov2021) 145; (12Nov2021) 63; (12Nov2021) 63; (12Nov2021) 119; (12Nov2021) 68; (12Nov2021) 64; (12Nov2021) 64; (12Nov2021) 64; (12Nov2021) 65; (12Nov2021) 67; (12Nov2021) 67; (12Nov2021) 67; (12Nov2021) 66; (12Nov2021) 66; (12Nov2021) 66; oxygen saturation: (unspecified date) 100 %, notes: his oxygen was at 100%. Therapeutic measures were taken as a result of oropharyngeal pain, body temperature increased. The patient date of death was 12Nov2021. The reported cause of death was myocarditis, arrhythmia, left ventricular dysfunction. Clinical course was reported as, a 26-year old (Place) man who died 12Nov2021, of myocarditis- four days after his booster dose Of Pfizer's Covid vaccine- had no idea he was experiencing a rare and supposedly "mild" heart problem after the shot. (Name) only warning signs were fatigue, muscle soreness and an increased heart rate, family members said. Reported that the pathologist performed scans of patient's heart and gathered 22 slides which confirmed that # had severe myocarditis from the Pfizer booster vaccine that led to his death. In an exclusive interview With (Show name), (Name)'s father, mother and sister said the Centers for Disease Control and Prevention (CDC) has not investigated (Name)'s death, The CDC also did not contact the pathologist who performed the autopsy or request the documents which confirmed (Name)'s death was caused by the Pfizer vaccine. According to the autopsy report and certificate of death, (Name) died from severe heart damage from "myocarditis in the left ventricle due to the recent Pfizer COVID-19 booster vaccine." (Name)'s mother, (Name), said her son was pro-vaccine and worked in an environment where he needed to be vaccinated. According to (Name)'s vaccination cards, he received his first Pfizer shot on 26Mar2021, and the second dose on 16Apr2021. (Name) said her son, who didn't experience any negative adverse events after the first two doses, received a third booster dose on 08Nov2021. "This was on a Monday," (Name) said. "Tuesday and Wednesday he was fine, but Thursday morning- 72 hours after the booster- he called and said he had a sore throat." (Name) made her son some hot apple cider and he took throat lozenges and went to work, but within two hours he called her to pick him up because he was so fatigued he couldn't work. When (Name) asked him what was wrong, (Name) told her he had some muscle soreness, exhaustion and a sore throat. 'When we searched, what are your reactions to having the Pfizer vaccine,' a lot of the results say people deal with fatigue, muscle soreness and everything, so we both just brushed it Off as reactions to the vaccine and it was no big deal," (Name) said. (Name) slept through Thursday. On Friday morning, he told his mother he would have to call into work again because he was too exhausted to go in. (Name) visited (Name)and said he appeared to be normal, other than fatigue and muscle soreness. "He wasn't really acting sick, just exhausted," she said. (Name), a critical care nurse Of 35 years, took her son's vitals and noted his temperature was up to 100.2 and his heart rate was elevated to 1 12. She thought it was related to the fever, so she gave him Tylenol. Later that day, (Name) texted his mother that his fever was down. By 4:30 p.m., his oxygen was at 100%, but his heart rate was still elevated. (Name)'s father, (Name), visited his son around 5 p.m. and they had dinner. He left at 6 p.m. Two hours later their son was dead. The family knows when (Name) died because of the fitness watch data they retrieved from his phone. (Name) had an app enabled that measured his heart rate up to the time of his death. (Name) said: "He went to sit down in his recliner and when we (the family) came the next day we were able to pull up the data from his fitness watch showing the exact time Of his death and exactly What his heart rate was doing the past two hours. "It showed he was beating at IOOs all during the day and after 6 p.m., when he sat in the recliner, his heart rate dropped into the 60s, which was low for (Name), Who always had a resting heart rate in the 80s and 90s - and then it just stopped." (Name) said When they found (Name) the next morning, there were no signs he knew he was going to die. "He was even having a two-way conversation with several of his friends before his death. The phone and remote control were on his lap," his mother said. The family called # and detectives came to make sure it wasn't a crime scene because "26-year-olds don't just die," (Name) said. When detectives separated (Name) and her husband for questioning, she told the detectives the only thing she knew was that four days prior her son had received Pfizer's vaccine and he was having adverse reactions. Four davs later he was dead. Autopsy confirms (Name) died of myocarditis After (Name) died, an autopsy had to be performed to confirm the cause of death. "When they first did the preliminaries they couldn't find anything - his heart looked normal," (Name) said. But "the pathologist said he was going to do 22 different slides to see what he could find." Meanwhile, (Name) said she started hearing stories about young males getting myocarditis from Covid vaccines. "I knew Covid could cause MIS-C (multisystem inflammatory syndrome), but nobody told me the vaccine was giving people myocarditis," (Name) said. "There's a big difference between Covid giving you myocarditis and a vaccine giving you myocarditis and actually killing you." (Name) said: When the pathologist looked at the 22 segments of (Name)'s heart, it showed the vaccine inflamed and attacked his entire heart. There was so much damage to the heart. It was full multi-focal myocarditis, and it wasn't just affecting one part of his heart, it was attacking his whole septum and ventricles." (Name) thinks her son developed so much inflammation from the booster that his heart developed a fatal arrhythmia that killed him instantly. She spoke with several cardiologists who were surprised her son never experienced any type of chest pain. "The hallmark signs as a parent that would prompt you to seek medical help were not given to me," (Name) said. "He didn't know his heart was racing, or fluttering or becoming A-fib. All he complained about was the muscle soreness and fatigue." (Name)'s private physician called the family after his autopsy results were back and told (Name) if she would have called him and informed him Of (Name)'s symptoms, he would have said it was just a side effect of the vaccine. "If we would have brought him in Thursday or Friday, nobody would have discovered it," (Name) said. (Name)'s sister, (Name), said, "My brother felt he wasn't bad enough to seek medical attention because he wasn't having any symptoms, it just came out Of nowhere." "That's What is so amazing that he didn't have any chest pain, he didn't feel his heart flutter, he didn't have any shortness of breath," (Name) said. "l mean two hours before he died he has 100 percent oxygen concentration. It just didn't show anything outside of an elevated heart rate." (Name) said she took a full set of vitals and her son just didn't feel sick. 'When you're sick, you're in bed, but he just never felt that way. He just got into a rate the heart couldn't keep up with and he died (Name) said she is thankful an autopsy was performed because it revealed her son died directly from the vaccine and the myocarditis he suffered was from the vaccine. "It's documented proof," (Name) said. "He died directly from the Pfizer booster." CDC ignores reports of death caused by myocarditis Both (Name)'s family and the pathologist submitted a report to the Vaccine Adverse Event Reporting System (VAERS), but to this day, neither have been contacted by the CDC about (Name)'s death. "You would think the death Of a child from a reaction to a Covid vaccine that's documented on the death certificate and autopsy, the CDC would have reached out to us immediately," (Name) said. "You would think the CDC would have called the pathologist." According to the CDC website, the agency contacts people who meet the case definition for myocarditis following mRNA Covid vaccine and have submitted a report to VAERS. To meet the case definition, people must have had "symptoms such as chest pain, shortness Of breath and feelings of having a fast-beating, fluttering or pounding heart, and medical tests to support the diagnosis of myocarditis and rule out other causes." This rules out deaths like (Name), Who wasn't diagnosed With myocarditis prior to death and did not experience the symptoms that would normally fall under the CDCs case definition. The CDC website does not State What happens to these cases, but there is no indication they are tracked or included in the CDC's myocarditis numbers. (Name) said the state's health department also has not investigated her son's death, as they said they first needed to be contacted by the CDC. "Nobody wants to touch it," He said. "I've been calling the health department the last few days and they keep saying they have to wait for the CDC and the facts. I told them the facts are in the autopsy, but they said they had to wait longer." (Name) said: We've heard no response. We contacted the local news station to get the word out that this happened, and they said their hands were tied_ We called the pathologist, no comment. The governor, no comment. The health department, no comment. The CDC, no comment. So, nobody's talking about it." (Name) said her main goal in sharing her son's story is to let other families know this happened Without any warning. "Thirty-five years as a registered nurse, I should have known something was happening and I didn't know," she said. "There were no signs." (Name) said: "It's sad because it's like (Name) death never occurred. I just don't get why we can't warn parents that something like this ? to watch out. He didn't have any symptoms the first two days and then he developed symptoms the third day. But I didn't put it together because he didn't have the symptoms where you think something was destroying his heart. But he was dead at four days. "(Name) been gone for two months and nobody knows that this boy gave his life for the greater good to get a booster." (Name) said he doesn't feel like anybody wants to deal With the people Who get sick or die following COVID vaccines. (Name) said her son was an innocent 26-year-old who was "doing everything right" by getting his vaccines and booster, but then died - and nobody wants to acknowledge it, accept it or tell her why. The family of 26-year-old (Name) is still grieving after a Pfizer Covid-19 vaccine booster jab led to his untimely death from myocarditis last November. The (Place) man's official exclusively obtained by the Health Defense, shows he suffered "multifocal myocarditis" just days following his third dose of the experimental mRNA shot, which his family said was required by his occupation. (Name) made her son some hot apple cider and he took throat lozenges and went to work, but within two hours he called her to pick him up because he was so fatigued he couldn't work. When (Name) asked him what was wrong, (Name) told her he had some muscle soreness, exhaustion and a sore throat. (Name) slept through Thursday. On Friday morning, he told his mother he would have to call into work again because he was too exhausted to go in. (Name) visited (Name) and said he appeared to be normal, other than fatigue and muscle soreness. "He wasn't really acting sick, just exhausted, " she said. (Name), a critical care nurse of 35 years, took her son's vitals and noted his temperature was up to 100.2 and his heart rate was elevated to 112. She thought it was related to the fever, so she gave him Tylenol. Later that day, (Name) texted his mother that his fever was down. By 4:30 p.m., his oxygen was at 100%, but his heart rate was still elevated. (Name) father, (Name), visited his son around 5 p.m. and they had dinner. He left at 6 p.m. Two hours later their son was dead. The autopsy report notes (Name) fitness watch recorded an extremely high heart rate the morning of his death: "His fitness watch recorded no cardia activity after 1959 hours. He did not respond to a text at 21:00 hours. On 13Nov he did not text his mother in the morning as he usually did and his family subsequently found him deceased in his recliner. " A death certificate issued by the State of (state name) and obtained by the (Show name) lists (Name) cause of death from "multifocal myocarditis involving the left ventricle and septum," with a second cause of death listed as "Recent Pfizer Covid-19 booster vaccine."Certificate of Death Place of death Information: Type: Decedent's Home Cause of Death Part I: Multifocal myocarditis involving the left ventricle and septum. Part II: Recent Pfizer Covid booster vaccine Coroner Contacted: Yes Autopsy Performed: Yes Autopsy Available: Y Manner of Death: Natural Causes (Name) mother says she's glad they authorized an autopsy as it's definitive proof the vaccine was what caused her son's death. "It's documented proof," (Name) told the (show name). "He died directly from the Pfizer booster." The family says despite the surprising nature of (Name) death and official documents, they have yet to be contacted by the CDC, the FDA or any other federal health agency about his death. "You would think the death of a child from a reaction to a Covid vaccine that's documented on the death certificate and autopsy, the CDC would have reached out to us immediately," (Name) bemoaned. "You would think the CDC would have called the pathologist." She added: "We've heard no response. We contacted the local news station to get the word out that this happened, and they said their hands were tied. We called the pathologist, no comment. The governor, no comment. The health department, no comment. The CDC, no comment. So, nobody s talking about it." The family is now seeking justice for their son by warning others of the potentially deadly consequences of receiving the jabs, which can evidently manifest with little, or no symptoms. "l want answers and I want Pfizer and the CDC to call me and tell me what went wrong. I want to save another child," a bereaved (Name) insists. However, this wasn't an issue for (Name), who his family described as pro-vaccine. (Name) CDC vaccine card documents his first and second doses of Pfizer's experimental gene therapy on 26Mar, and 16Apr2021, respectively. "Tuesday and Wednesday he was fine," described (Name) mother, (Name), "but Thursday morning 72 hours after the booster - he called and said he had a sore throat." The Defended s (Name) reports on how the family had no indications (Name) heart would soon fail, and believed he was experiencing mild side effects. This 26-year-old withheld male was discovered sitting in his recliner at home, He has a history Of a Of Galen malformation with multiple therapies. He had received his third Pfizer Covid shot booster and flu shot on 08Nov2021. On morning Of 11Nov, he complained of sore throat and fatigue. On morning of 12Nov2021, his apple watch recorded tachycardia. Later in the day. he had complained muscle aches and sore throat with a temperature Of 1002 F. The examination was conducted 15Nov2021 at 0915 hours. Autopsy information was reported as: Specimen: Body, General Information: Age: 26, Sex: M, Length: 69 inches, Weight: 240 pounds, Date of Death 12Nov2021, Date of autopsy: 15Nov2021; Final Diagnosis: Multifocal myocarditis involving the cardiac left ventricle and interventricular septum A. Received Pfizer Covid booster shot and flu shot on 08Nov2021 B. Pulmonary congestion C. Splenomegaly D. Cerebral edema; Il. Right cardiac ventricle; III. Vein of Galen malformation. clinical A. Multiple vessels Of varying size with refractile foreign material with giant cell inflammatory response and calcification; large caliber vessel with thrombus. Cause of death: Multifocal myocarditis involving the left ventricle and septum. Contributory: Recent Pfizer Covid booster vaccine Manner of death: Normal/Natural. Comment: Myocarditis following administration of pfizer Covid vaccine has been noted in male patients between ages of 16 and 29 Years, and most commonly presents 3 to 5 days following administration. Post Pfizer Covid vaccination myocarditis has been identified to cause left ventricle dysfunction.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200082021 Pfizer; Reported Cause(s) of Death: Death From Myocarditis; fatal arrhythmia that killed him instantly; left ventricular dysfunction

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Test Name: Body temperature; Result Unstructured Data: Test Result:100.2 Fahrenheit; Comments: his temperature was up to 100.2; Test Name: CO2; Test Result: 0.2 %; Comments: Normal; Test Name: Heart rate; Result Unstructured Data: Test Result:112; Comments: his heart rate was elevated to 112; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:97; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:85; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:91; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:84; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:91; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:89; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:90; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:89; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:84; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:85; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:98; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:89; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:90; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:120; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:119; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:120; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:121; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:127; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:126; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:127; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:131; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:128; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:131; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:130; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:130; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:128; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:123; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:127; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:128; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:135; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:74; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:141; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:71; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:146; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:144; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:138; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:149; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:148; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:145; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:63; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:63; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:119; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:68; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:64; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:64; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:64; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:65; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:67; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:67; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:67; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:66; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:66; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:66; Test Name: Oxygen level; Test Result: 100 %; Comments: his oxygen was at 100%
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1936333

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: SD
Alter: -
Geschlecht: M
Eingang: 28.01.2022
Impfdatum: 08.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / UN

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

Arrhythmia Body temperature Body temperature increased Carbon dioxide Fatigue Autopsy Brain oedema Condition aggravated Death Myalgia Oropharyngeal pain Tachycardia Giant cell arteritis Hypersomnia Impaired work ability Inflammation Malaise Heart rate

Symptomtext

Death From Myocarditis; fatal arrhythmia that killed him instantly; increased heart rate; Tachycardia; temperature was up to 100.2; fatigue; muscle soreness; sore throat; Product use for unapproved combination; left ventricular dysfunction; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program. Other Case identifier(s): US-PFIZER INC-202200065467 (Pfizer), US-PFIZER INC-202200142396 (pfizer). A 26 year-old male patient received bnt162b2 (BNT162B2), administration date 08Nov2021 (Lot number: FE3590) as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (INFLUENZA VACCINE), administration date 08Nov2021 (Batch/Lot number: unknown) for immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Pfizer 1st dose - ER8733), administration date: 26Mar2021, for COVID-19 Immunization; Bnt162b2 (Pfizer 2nd dose - EW0164), administration date: 16Apr2021, for COVID-19 immunisation. The following information was reported: MYOCARDITIS (death, medically significant) with onset 12Nov2021, outcome "fatal", described as "Death From Myocarditis"; ARRHYTHMIA (death) with onset 12Nov2021, outcome "fatal", described as "fatal arrhythmia that killed him instantly"; LEFT VENTRICULAR DYSFUNCTION (death) with onset Nov2021, outcome "fatal", described as "left ventricular dysfunction"; FATIGUE (non-serious) with onset 11Nov2021, outcome "not recovered", described as "fatigue"; MYALGIA (non-serious) with onset 11Nov2021, outcome "not recovered", described as "muscle soreness"; OROPHARYNGEAL PAIN (non-serious) with onset 11Nov2021, outcome "recovered" (2021), described as "sore throat"; HEART RATE INCREASED (non-serious) with onset 12Nov2021, outcome "not recovered", described as "increased heart rate"; TACHYCARDIA (non-serious) with onset 12Nov2021, outcome "unknown", described as "Tachycardia"; BODY TEMPERATURE INCREASED (non-serious) with onset 12Nov2021, outcome "recovered" (12Nov2021 16:30), described as "temperature was up to 100.2"; PRODUCT USE ISSUE (non-serious) with onset 08Nov2021, outcome "unknown", described as "Product use for unapproved combination". The patient underwent the following laboratory tests and procedures: body temperature: (unspecified date) 100.2 Fahrenheit, notes: his temperature was up to 100.2; carbon dioxide (0.0-1.5): (unspecified date) 0.2 %, notes: Normal; heart rate: (unspecified date) 112, notes: his heart rate was elevated to 112; (10Nov2021) 97; (10Nov2021) 85; (10Nov2021) 91; (10Nov2021) 84; (10Nov2021) 91; (10Nov2021) 89; (10Nov2021) 90; (10Nov2021) 89; (10Nov2021) 84; (10Nov2021) 85; (10Nov2021) 98; (10Nov2021) 89; (11Nov2021) 90; (11Nov2021) 120; (11Nov2021) 119; (11Nov2021) 120; (11Nov2021) 121; (11Nov2021) 127; (11Nov2021) 126; (11Nov2021) 127; (11Nov2021) 131; (11Nov2021) 128; (11Nov2021) 131; (11Nov2021) 130; (11Nov2021) 130; (11Nov2021) 128; (12Nov2021) 123; (12Nov2021) 127; (12Nov2021) 128; (12Nov2021) 135; (12Nov2021) 74; (12Nov2021) 141; (12Nov2021) 71; (12Nov2021) 146; (12Nov2021) 144; (12Nov2021) 138; (12Nov2021) 149; (12Nov2021) 148; (12Nov2021) 145; (12Nov2021) 63; (12Nov2021) 63; (12Nov2021) 119; (12Nov2021) 68; (12Nov2021) 64; (12Nov2021) 64; (12Nov2021) 64; (12Nov2021) 65; (12Nov2021) 67; (12Nov2021) 67; (12Nov2021) 67; (12Nov2021) 66; (12Nov2021) 66; (12Nov2021) 66; oxygen saturation: (unspecified date) 100 %, notes: his oxygen was at 100%. Therapeutic measures were taken as a result of oropharyngeal pain, body temperature increased. The patient date of death was 12Nov2021. The reported cause of death was myocarditis, arrhythmia, left ventricular dysfunction. Clinical course was reported as, a 26-year old (Place) man who died 12Nov2021, of myocarditis- four days after his booster dose Of Pfizer's Covid vaccine- had no idea he was experiencing a rare and supposedly "mild" heart problem after the shot. (Name) only warning signs were fatigue, muscle soreness and an increased heart rate, family members said. Reported that the pathologist performed scans of patient's heart and gathered 22 slides which confirmed that # had severe myocarditis from the Pfizer booster vaccine that led to his death. In an exclusive interview With (Show name), (Name)'s father, mother and sister said the Centers for Disease Control and Prevention (CDC) has not investigated (Name)'s death, The CDC also did not contact the pathologist who performed the autopsy or request the documents which confirmed (Name)'s death was caused by the Pfizer vaccine. According to the autopsy report and certificate of death, (Name) died from severe heart damage from "myocarditis in the left ventricle due to the recent Pfizer COVID-19 booster vaccine." (Name)'s mother, (Name), said her son was pro-vaccine and worked in an environment where he needed to be vaccinated. According to (Name)'s vaccination cards, he received his first Pfizer shot on 26Mar2021, and the second dose on 16Apr2021. (Name) said her son, who didn't experience any negative adverse events after the first two doses, received a third booster dose on 08Nov2021. "This was on a Monday," (Name) said. "Tuesday and Wednesday he was fine, but Thursday morning- 72 hours after the booster- he called and said he had a sore throat." (Name) made her son some hot apple cider and he took throat lozenges and went to work, but within two hours he called her to pick him up because he was so fatigued he couldn't work. When (Name) asked him what was wrong, (Name) told her he had some muscle soreness, exhaustion and a sore throat. 'When we searched, what are your reactions to having the Pfizer vaccine,' a lot of the results say people deal with fatigue, muscle soreness and everything, so we both just brushed it Off as reactions to the vaccine and it was no big deal," (Name) said. (Name) slept through Thursday. On Friday morning, he told his mother he would have to call into work again because he was too exhausted to go in. (Name) visited (Name)and said he appeared to be normal, other than fatigue and muscle soreness. "He wasn't really acting sick, just exhausted," she said. (Name), a critical care nurse Of 35 years, took her son's vitals and noted his temperature was up to 100.2 and his heart rate was elevated to 1 12. She thought it was related to the fever, so she gave him Tylenol. Later that day, (Name) texted his mother that his fever was down. By 4:30 p.m., his oxygen was at 100%, but his heart rate was still elevated. (Name)'s father, (Name), visited his son around 5 p.m. and they had dinner. He left at 6 p.m. Two hours later their son was dead. The family knows when (Name) died because of the fitness watch data they retrieved from his phone. (Name) had an app enabled that measured his heart rate up to the time of his death. (Name) said: "He went to sit down in his recliner and when we (the family) came the next day we were able to pull up the data from his fitness watch showing the exact time Of his death and exactly What his heart rate was doing the past two hours. "It showed he was beating at IOOs all during the day and after 6 p.m., when he sat in the recliner, his heart rate dropped into the 60s, which was low for (Name), Who always had a resting heart rate in the 80s and 90s - and then it just stopped." (Name) said When they found (Name) the next morning, there were no signs he knew he was going to die. "He was even having a two-way conversation with several of his friends before his death. The phone and remote control were on his lap," his mother said. The family called # and detectives came to make sure it wasn't a crime scene because "26-year-olds don't just die," (Name) said. When detectives separated (Name) and her husband for questioning, she told the detectives the only thing she knew was that four days prior her son had received Pfizer's vaccine and he was having adverse reactions. Four davs later he was dead. Autopsy confirms (Name) died of myocarditis After (Name) died, an autopsy had to be performed to confirm the cause of death. "When they first did the preliminaries they couldn't find anything - his heart looked normal," (Name) said. But "the pathologist said he was going to do 22 different slides to see what he could find." Meanwhile, (Name) said she started hearing stories about young males getting myocarditis from Covid vaccines. "I knew Covid could cause MIS-C (multisystem inflammatory syndrome), but nobody told me the vaccine was giving people myocarditis," (Name) said. "There's a big difference between Covid giving you myocarditis and a vaccine giving you myocarditis and actually killing you." (Name) said: When the pathologist looked at the 22 segments of (Name)'s heart, it showed the vaccine inflamed and attacked his entire heart. There was so much damage to the heart. It was full multi-focal myocarditis, and it wasn't just affecting one part of his heart, it was attacking his whole septum and ventricles." (Name) thinks her son developed so much inflammation from the booster that his heart developed a fatal arrhythmia that killed him instantly. She spoke with several cardiologists who were surprised her son never experienced any type of chest pain. "The hallmark signs as a parent that would prompt you to seek medical help were not given to me," (Name) said. "He didn't know his heart was racing, or fluttering or becoming A-fib. All he complained about was the muscle soreness and fatigue." (Name)'s private physician called the family after his autopsy results were back and told (Name) if she would have called him and informed him Of (Name)'s symptoms, he would have said it was just a side effect of the vaccine. "If we would have brought him in Thursday or Friday, nobody would have discovered it," (Name) said. (Name)'s sister, (Name), said, "My brother felt he wasn't bad enough to seek medical attention because he wasn't having any symptoms, it just came out Of nowhere." "That's What is so amazing that he didn't have any chest pain, he didn't feel his heart flutter, he didn't have any shortness of breath," (Name) said. "l mean two hours before he died he has 100 percent oxygen concentration. It just didn't show anything outside of an elevated heart rate." (Name) said she took a full set of vitals and her son just didn't feel sick. 'When you're sick, you're in bed, but he just never felt that way. He just got into a rate the heart couldn't keep up with and he died (Name) said she is thankful an autopsy was performed because it revealed her son died directly from the vaccine and the myocarditis he suffered was from the vaccine. "It's documented proof," (Name) said. "He died directly from the Pfizer booster." CDC ignores reports of death caused by myocarditis Both (Name)'s family and the pathologist submitted a report to the Vaccine Adverse Event Reporting System (VAERS), but to this day, neither have been contacted by the CDC about (Name)'s death. "You would think the death Of a child from a reaction to a Covid vaccine that's documented on the death certificate and autopsy, the CDC would have reached out to us immediately," (Name) said. "You would think the CDC would have called the pathologist." According to the CDC website, the agency contacts people who meet the case definition for myocarditis following mRNA Covid vaccine and have submitted a report to VAERS. To meet the case definition, people must have had "symptoms such as chest pain, shortness Of breath and feelings of having a fast-beating, fluttering or pounding heart, and medical tests to support the diagnosis of myocarditis and rule out other causes." This rules out deaths like (Name), Who wasn't diagnosed With myocarditis prior to death and did not experience the symptoms that would normally fall under the CDCs case definition. The CDC website does not State What happens to these cases, but there is no indication they are tracked or included in the CDC's myocarditis numbers. (Name) said the state's health department also has not investigated her son's death, as they said they first needed to be contacted by the CDC. "Nobody wants to touch it," He said. "I've been calling the health department the last few days and they keep saying they have to wait for the CDC and the facts. I told them the facts are in the autopsy, but they said they had to wait longer." (Name) said: We've heard no response. We contacted the local news station to get the word out that this happened, and they said their hands were tied_ We called the pathologist, no comment. The governor, no comment. The health department, no comment. The CDC, no comment. So, nobody's talking about it." (Name) said her main goal in sharing her son's story is to let other families know this happened Without any warning. "Thirty-five years as a registered nurse, I should have known something was happening and I didn't know," she said. "There were no signs." (Name) said: "It's sad because it's like (Name) death never occurred. I just don't get why we can't warn parents that something like this ? to watch out. He didn't have any symptoms the first two days and then he developed symptoms the third day. But I didn't put it together because he didn't have the symptoms where you think something was destroying his heart. But he was dead at four days. "(Name) been gone for two months and nobody knows that this boy gave his life for the greater good to get a booster." (Name) said he doesn't feel like anybody wants to deal With the people Who get sick or die following COVID vaccines. (Name) said her son was an innocent 26-year-old who was "doing everything right" by getting his vaccines and booster, but then died - and nobody wants to acknowledge it, accept it or tell her why. The family of 26-year-old (Name) is still grieving after a Pfizer Covid-19 vaccine booster jab led to his untimely death from myocarditis last November. The (Place) man's official exclusively obtained by the Health Defense, shows he suffered "multifocal myocarditis" just days following his third dose of the experimental mRNA shot, which his family said was required by his occupation. (Name) made her son some hot apple cider and he took throat lozenges and went to work, but within two hours he called her to pick him up because he was so fatigued he couldn't work. When (Name) asked him what was wrong, (Name) told her he had some muscle soreness, exhaustion and a sore throat. (Name) slept through Thursday. On Friday morning, he told his mother he would have to call into work again because he was too exhausted to go in. (Name) visited (Name) and said he appeared to be normal, other than fatigue and muscle soreness. "He wasn't really acting sick, just exhausted, " she said. (Name), a critical care nurse of 35 years, took her son's vitals and noted his temperature was up to 100.2 and his heart rate was elevated to 112. She thought it was related to the fever, so she gave him Tylenol. Later that day, (Name) texted his mother that his fever was down. By 4:30 p.m., his oxygen was at 100%, but his heart rate was still elevated. (Name) father, (Name), visited his son around 5 p.m. and they had dinner. He left at 6 p.m. Two hours later their son was dead. The autopsy report notes (Name) fitness watch recorded an extremely high heart rate the morning of his death: "His fitness watch recorded no cardia activity after 1959 hours. He did not respond to a text at 21:00 hours. On 13Nov he did not text his mother in the morning as he usually did and his family subsequently found him deceased in his recliner. " A death certificate issued by the State of (state name) and obtained by the (Show name) lists (Name) cause of death from "multifocal myocarditis involving the left ventricle and septum," with a second cause of death listed as "Recent Pfizer Covid-19 booster vaccine."Certificate of Death Place of death Information: Type: Decedent's Home Cause of Death Part I: Multifocal myocarditis involving the left ventricle and septum. Part II: Recent Pfizer Covid booster vaccine Coroner Contacted: Yes Autopsy Performed: Yes Autopsy Available: Y Manner of Death: Natural Causes (Name) mother says she's glad they authorized an autopsy as it's definitive proof the vaccine was what caused her son's death. "It's documented proof," (Name) told the (show name). "He died directly from the Pfizer booster." The family says despite the surprising nature of (Name) death and official documents, they have yet to be contacted by the CDC, the FDA or any other federal health agency about his death. "You would think the death of a child from a reaction to a Covid vaccine that's documented on the death certificate and autopsy, the CDC would have reached out to us immediately," (Name) bemoaned. "You would think the CDC would have called the pathologist." She added: "We've heard no response. We contacted the local news station to get the word out that this happened, and they said their hands were tied. We called the pathologist, no comment. The governor, no comment. The health department, no comment. The CDC, no comment. So, nobody s talking about it." The family is now seeking justice for their son by warning others of the potentially deadly consequences of receiving the jabs, which can evidently manifest with little, or no symptoms. "l want answers and I want Pfizer and the CDC to call me and tell me what went wrong. I want to save another child," a bereaved (Name) insists. However, this wasn't an issue for (Name), who his family described as pro-vaccine. (Name) CDC vaccine card documents his first and second doses of Pfizer's experimental gene therapy on 26Mar, and 16Apr2021, respectively. "Tuesday and Wednesday he was fine," described (Name) mother, (Name), "but Thursday morning 72 hours after the booster - he called and said he had a sore throat." The Defended s (Name) reports on how the family had no indications (Name) heart would soon fail, and believed he was experiencing mild side effects. This 26-year-old withheld male was discovered sitting in his recliner at home, He has a history Of a Of Galen malformation with multiple therapies. He had received his third Pfizer Covid shot booster and flu shot on 08Nov2021. On morning Of 11Nov, he complained of sore throat and fatigue. On morning of 12Nov2021, his apple watch recorded tachycardia. Later in the day. he had complained muscle aches and sore throat with a temperature Of 1002 F. The examination was conducted 15Nov2021 at 0915 hours. Autopsy information was reported as: Specimen: Body, General Information: Age: 26, Sex: M, Length: 69 inches, Weight: 240 pounds, Date of Death 12Nov2021, Date of autopsy: 15Nov2021; Final Diagnosis: Multifocal myocarditis involving the cardiac left ventricle and interventricular septum A. Received Pfizer Covid booster shot and flu shot on 08Nov2021 B. Pulmonary congestion C. Splenomegaly D. Cerebral edema; Il. Right cardiac ventricle; III. Vein of Galen malformation. clinical A. Multiple vessels Of varying size with refractile foreign material with giant cell inflammatory response and calcification; large caliber vessel with thrombus. Cause of death: Multifocal myocarditis involving the left ventricle and septum. Contributory: Recent Pfizer Covid booster vaccine Manner of death: Normal/Natural. Comment: Myocarditis following administration of pfizer Covid vaccine has been noted in male patients between ages of 16 and 29 Years, and most commonly presents 3 to 5 days following administration. Post Pfizer Covid vaccination myocarditis has been identified to cause left ventricle dysfunction.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200082021 Pfizer; Reported Cause(s) of Death: Death From Myocarditis; fatal arrhythmia that killed him instantly; left ventricular dysfunction

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Test Name: Body temperature; Result Unstructured Data: Test Result:100.2 Fahrenheit; Comments: his temperature was up to 100.2; Test Name: CO2; Test Result: 0.2 %; Comments: Normal; Test Name: Heart rate; Result Unstructured Data: Test Result:112; Comments: his heart rate was elevated to 112; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:97; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:85; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:91; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:84; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:91; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:89; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:90; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:89; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:84; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:85; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:98; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:89; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:90; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:120; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:119; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:120; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:121; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:127; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:126; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:127; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:131; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:128; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:131; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:130; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:130; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:128; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:123; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:127; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:128; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:135; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:74; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:141; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:71; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:146; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:144; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:138; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:149; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:148; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:145; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:63; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:63; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:119; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:68; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:64; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:64; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:64; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:65; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:67; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:67; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:67; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:66; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:66; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:66; Test Name: Oxygen level; Test Result: 100 %; Comments: his oxygen was at 100%
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1936333

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: SD
Alter: -
Geschlecht: M
Eingang: 28.01.2022
Impfdatum: 08.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: SYR / LA

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

Arrhythmia Body temperature Body temperature increased Carbon dioxide Fatigue Autopsy Brain oedema Condition aggravated Death Myalgia Oropharyngeal pain Tachycardia Giant cell arteritis Hypersomnia Impaired work ability Inflammation Malaise Heart rate

Symptomtext

Death From Myocarditis; fatal arrhythmia that killed him instantly; increased heart rate; Tachycardia; temperature was up to 100.2; fatigue; muscle soreness; sore throat; Product use for unapproved combination; left ventricular dysfunction; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program. Other Case identifier(s): US-PFIZER INC-202200065467 (Pfizer), US-PFIZER INC-202200142396 (pfizer). A 26 year-old male patient received bnt162b2 (BNT162B2), administration date 08Nov2021 (Lot number: FE3590) as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (INFLUENZA VACCINE), administration date 08Nov2021 (Batch/Lot number: unknown) for immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Pfizer 1st dose - ER8733), administration date: 26Mar2021, for COVID-19 Immunization; Bnt162b2 (Pfizer 2nd dose - EW0164), administration date: 16Apr2021, for COVID-19 immunisation. The following information was reported: MYOCARDITIS (death, medically significant) with onset 12Nov2021, outcome "fatal", described as "Death From Myocarditis"; ARRHYTHMIA (death) with onset 12Nov2021, outcome "fatal", described as "fatal arrhythmia that killed him instantly"; LEFT VENTRICULAR DYSFUNCTION (death) with onset Nov2021, outcome "fatal", described as "left ventricular dysfunction"; FATIGUE (non-serious) with onset 11Nov2021, outcome "not recovered", described as "fatigue"; MYALGIA (non-serious) with onset 11Nov2021, outcome "not recovered", described as "muscle soreness"; OROPHARYNGEAL PAIN (non-serious) with onset 11Nov2021, outcome "recovered" (2021), described as "sore throat"; HEART RATE INCREASED (non-serious) with onset 12Nov2021, outcome "not recovered", described as "increased heart rate"; TACHYCARDIA (non-serious) with onset 12Nov2021, outcome "unknown", described as "Tachycardia"; BODY TEMPERATURE INCREASED (non-serious) with onset 12Nov2021, outcome "recovered" (12Nov2021 16:30), described as "temperature was up to 100.2"; PRODUCT USE ISSUE (non-serious) with onset 08Nov2021, outcome "unknown", described as "Product use for unapproved combination". The patient underwent the following laboratory tests and procedures: body temperature: (unspecified date) 100.2 Fahrenheit, notes: his temperature was up to 100.2; carbon dioxide (0.0-1.5): (unspecified date) 0.2 %, notes: Normal; heart rate: (unspecified date) 112, notes: his heart rate was elevated to 112; (10Nov2021) 97; (10Nov2021) 85; (10Nov2021) 91; (10Nov2021) 84; (10Nov2021) 91; (10Nov2021) 89; (10Nov2021) 90; (10Nov2021) 89; (10Nov2021) 84; (10Nov2021) 85; (10Nov2021) 98; (10Nov2021) 89; (11Nov2021) 90; (11Nov2021) 120; (11Nov2021) 119; (11Nov2021) 120; (11Nov2021) 121; (11Nov2021) 127; (11Nov2021) 126; (11Nov2021) 127; (11Nov2021) 131; (11Nov2021) 128; (11Nov2021) 131; (11Nov2021) 130; (11Nov2021) 130; (11Nov2021) 128; (12Nov2021) 123; (12Nov2021) 127; (12Nov2021) 128; (12Nov2021) 135; (12Nov2021) 74; (12Nov2021) 141; (12Nov2021) 71; (12Nov2021) 146; (12Nov2021) 144; (12Nov2021) 138; (12Nov2021) 149; (12Nov2021) 148; (12Nov2021) 145; (12Nov2021) 63; (12Nov2021) 63; (12Nov2021) 119; (12Nov2021) 68; (12Nov2021) 64; (12Nov2021) 64; (12Nov2021) 64; (12Nov2021) 65; (12Nov2021) 67; (12Nov2021) 67; (12Nov2021) 67; (12Nov2021) 66; (12Nov2021) 66; (12Nov2021) 66; oxygen saturation: (unspecified date) 100 %, notes: his oxygen was at 100%. Therapeutic measures were taken as a result of oropharyngeal pain, body temperature increased. The patient date of death was 12Nov2021. The reported cause of death was myocarditis, arrhythmia, left ventricular dysfunction. Clinical course was reported as, a 26-year old (Place) man who died 12Nov2021, of myocarditis- four days after his booster dose Of Pfizer's Covid vaccine- had no idea he was experiencing a rare and supposedly "mild" heart problem after the shot. (Name) only warning signs were fatigue, muscle soreness and an increased heart rate, family members said. Reported that the pathologist performed scans of patient's heart and gathered 22 slides which confirmed that # had severe myocarditis from the Pfizer booster vaccine that led to his death. In an exclusive interview With (Show name), (Name)'s father, mother and sister said the Centers for Disease Control and Prevention (CDC) has not investigated (Name)'s death, The CDC also did not contact the pathologist who performed the autopsy or request the documents which confirmed (Name)'s death was caused by the Pfizer vaccine. According to the autopsy report and certificate of death, (Name) died from severe heart damage from "myocarditis in the left ventricle due to the recent Pfizer COVID-19 booster vaccine." (Name)'s mother, (Name), said her son was pro-vaccine and worked in an environment where he needed to be vaccinated. According to (Name)'s vaccination cards, he received his first Pfizer shot on 26Mar2021, and the second dose on 16Apr2021. (Name) said her son, who didn't experience any negative adverse events after the first two doses, received a third booster dose on 08Nov2021. "This was on a Monday," (Name) said. "Tuesday and Wednesday he was fine, but Thursday morning- 72 hours after the booster- he called and said he had a sore throat." (Name) made her son some hot apple cider and he took throat lozenges and went to work, but within two hours he called her to pick him up because he was so fatigued he couldn't work. When (Name) asked him what was wrong, (Name) told her he had some muscle soreness, exhaustion and a sore throat. 'When we searched, what are your reactions to having the Pfizer vaccine,' a lot of the results say people deal with fatigue, muscle soreness and everything, so we both just brushed it Off as reactions to the vaccine and it was no big deal," (Name) said. (Name) slept through Thursday. On Friday morning, he told his mother he would have to call into work again because he was too exhausted to go in. (Name) visited (Name)and said he appeared to be normal, other than fatigue and muscle soreness. "He wasn't really acting sick, just exhausted," she said. (Name), a critical care nurse Of 35 years, took her son's vitals and noted his temperature was up to 100.2 and his heart rate was elevated to 1 12. She thought it was related to the fever, so she gave him Tylenol. Later that day, (Name) texted his mother that his fever was down. By 4:30 p.m., his oxygen was at 100%, but his heart rate was still elevated. (Name)'s father, (Name), visited his son around 5 p.m. and they had dinner. He left at 6 p.m. Two hours later their son was dead. The family knows when (Name) died because of the fitness watch data they retrieved from his phone. (Name) had an app enabled that measured his heart rate up to the time of his death. (Name) said: "He went to sit down in his recliner and when we (the family) came the next day we were able to pull up the data from his fitness watch showing the exact time Of his death and exactly What his heart rate was doing the past two hours. "It showed he was beating at IOOs all during the day and after 6 p.m., when he sat in the recliner, his heart rate dropped into the 60s, which was low for (Name), Who always had a resting heart rate in the 80s and 90s - and then it just stopped." (Name) said When they found (Name) the next morning, there were no signs he knew he was going to die. "He was even having a two-way conversation with several of his friends before his death. The phone and remote control were on his lap," his mother said. The family called # and detectives came to make sure it wasn't a crime scene because "26-year-olds don't just die," (Name) said. When detectives separated (Name) and her husband for questioning, she told the detectives the only thing she knew was that four days prior her son had received Pfizer's vaccine and he was having adverse reactions. Four davs later he was dead. Autopsy confirms (Name) died of myocarditis After (Name) died, an autopsy had to be performed to confirm the cause of death. "When they first did the preliminaries they couldn't find anything - his heart looked normal," (Name) said. But "the pathologist said he was going to do 22 different slides to see what he could find." Meanwhile, (Name) said she started hearing stories about young males getting myocarditis from Covid vaccines. "I knew Covid could cause MIS-C (multisystem inflammatory syndrome), but nobody told me the vaccine was giving people myocarditis," (Name) said. "There's a big difference between Covid giving you myocarditis and a vaccine giving you myocarditis and actually killing you." (Name) said: When the pathologist looked at the 22 segments of (Name)'s heart, it showed the vaccine inflamed and attacked his entire heart. There was so much damage to the heart. It was full multi-focal myocarditis, and it wasn't just affecting one part of his heart, it was attacking his whole septum and ventricles." (Name) thinks her son developed so much inflammation from the booster that his heart developed a fatal arrhythmia that killed him instantly. She spoke with several cardiologists who were surprised her son never experienced any type of chest pain. "The hallmark signs as a parent that would prompt you to seek medical help were not given to me," (Name) said. "He didn't know his heart was racing, or fluttering or becoming A-fib. All he complained about was the muscle soreness and fatigue." (Name)'s private physician called the family after his autopsy results were back and told (Name) if she would have called him and informed him Of (Name)'s symptoms, he would have said it was just a side effect of the vaccine. "If we would have brought him in Thursday or Friday, nobody would have discovered it," (Name) said. (Name)'s sister, (Name), said, "My brother felt he wasn't bad enough to seek medical attention because he wasn't having any symptoms, it just came out Of nowhere." "That's What is so amazing that he didn't have any chest pain, he didn't feel his heart flutter, he didn't have any shortness of breath," (Name) said. "l mean two hours before he died he has 100 percent oxygen concentration. It just didn't show anything outside of an elevated heart rate." (Name) said she took a full set of vitals and her son just didn't feel sick. 'When you're sick, you're in bed, but he just never felt that way. He just got into a rate the heart couldn't keep up with and he died (Name) said she is thankful an autopsy was performed because it revealed her son died directly from the vaccine and the myocarditis he suffered was from the vaccine. "It's documented proof," (Name) said. "He died directly from the Pfizer booster." CDC ignores reports of death caused by myocarditis Both (Name)'s family and the pathologist submitted a report to the Vaccine Adverse Event Reporting System (VAERS), but to this day, neither have been contacted by the CDC about (Name)'s death. "You would think the death Of a child from a reaction to a Covid vaccine that's documented on the death certificate and autopsy, the CDC would have reached out to us immediately," (Name) said. "You would think the CDC would have called the pathologist." According to the CDC website, the agency contacts people who meet the case definition for myocarditis following mRNA Covid vaccine and have submitted a report to VAERS. To meet the case definition, people must have had "symptoms such as chest pain, shortness Of breath and feelings of having a fast-beating, fluttering or pounding heart, and medical tests to support the diagnosis of myocarditis and rule out other causes." This rules out deaths like (Name), Who wasn't diagnosed With myocarditis prior to death and did not experience the symptoms that would normally fall under the CDCs case definition. The CDC website does not State What happens to these cases, but there is no indication they are tracked or included in the CDC's myocarditis numbers. (Name) said the state's health department also has not investigated her son's death, as they said they first needed to be contacted by the CDC. "Nobody wants to touch it," He said. "I've been calling the health department the last few days and they keep saying they have to wait for the CDC and the facts. I told them the facts are in the autopsy, but they said they had to wait longer." (Name) said: We've heard no response. We contacted the local news station to get the word out that this happened, and they said their hands were tied_ We called the pathologist, no comment. The governor, no comment. The health department, no comment. The CDC, no comment. So, nobody's talking about it." (Name) said her main goal in sharing her son's story is to let other families know this happened Without any warning. "Thirty-five years as a registered nurse, I should have known something was happening and I didn't know," she said. "There were no signs." (Name) said: "It's sad because it's like (Name) death never occurred. I just don't get why we can't warn parents that something like this ? to watch out. He didn't have any symptoms the first two days and then he developed symptoms the third day. But I didn't put it together because he didn't have the symptoms where you think something was destroying his heart. But he was dead at four days. "(Name) been gone for two months and nobody knows that this boy gave his life for the greater good to get a booster." (Name) said he doesn't feel like anybody wants to deal With the people Who get sick or die following COVID vaccines. (Name) said her son was an innocent 26-year-old who was "doing everything right" by getting his vaccines and booster, but then died - and nobody wants to acknowledge it, accept it or tell her why. The family of 26-year-old (Name) is still grieving after a Pfizer Covid-19 vaccine booster jab led to his untimely death from myocarditis last November. The (Place) man's official exclusively obtained by the Health Defense, shows he suffered "multifocal myocarditis" just days following his third dose of the experimental mRNA shot, which his family said was required by his occupation. (Name) made her son some hot apple cider and he took throat lozenges and went to work, but within two hours he called her to pick him up because he was so fatigued he couldn't work. When (Name) asked him what was wrong, (Name) told her he had some muscle soreness, exhaustion and a sore throat. (Name) slept through Thursday. On Friday morning, he told his mother he would have to call into work again because he was too exhausted to go in. (Name) visited (Name) and said he appeared to be normal, other than fatigue and muscle soreness. "He wasn't really acting sick, just exhausted, " she said. (Name), a critical care nurse of 35 years, took her son's vitals and noted his temperature was up to 100.2 and his heart rate was elevated to 112. She thought it was related to the fever, so she gave him Tylenol. Later that day, (Name) texted his mother that his fever was down. By 4:30 p.m., his oxygen was at 100%, but his heart rate was still elevated. (Name) father, (Name), visited his son around 5 p.m. and they had dinner. He left at 6 p.m. Two hours later their son was dead. The autopsy report notes (Name) fitness watch recorded an extremely high heart rate the morning of his death: "His fitness watch recorded no cardia activity after 1959 hours. He did not respond to a text at 21:00 hours. On 13Nov he did not text his mother in the morning as he usually did and his family subsequently found him deceased in his recliner. " A death certificate issued by the State of (state name) and obtained by the (Show name) lists (Name) cause of death from "multifocal myocarditis involving the left ventricle and septum," with a second cause of death listed as "Recent Pfizer Covid-19 booster vaccine."Certificate of Death Place of death Information: Type: Decedent's Home Cause of Death Part I: Multifocal myocarditis involving the left ventricle and septum. Part II: Recent Pfizer Covid booster vaccine Coroner Contacted: Yes Autopsy Performed: Yes Autopsy Available: Y Manner of Death: Natural Causes (Name) mother says she's glad they authorized an autopsy as it's definitive proof the vaccine was what caused her son's death. "It's documented proof," (Name) told the (show name). "He died directly from the Pfizer booster." The family says despite the surprising nature of (Name) death and official documents, they have yet to be contacted by the CDC, the FDA or any other federal health agency about his death. "You would think the death of a child from a reaction to a Covid vaccine that's documented on the death certificate and autopsy, the CDC would have reached out to us immediately," (Name) bemoaned. "You would think the CDC would have called the pathologist." She added: "We've heard no response. We contacted the local news station to get the word out that this happened, and they said their hands were tied. We called the pathologist, no comment. The governor, no comment. The health department, no comment. The CDC, no comment. So, nobody s talking about it." The family is now seeking justice for their son by warning others of the potentially deadly consequences of receiving the jabs, which can evidently manifest with little, or no symptoms. "l want answers and I want Pfizer and the CDC to call me and tell me what went wrong. I want to save another child," a bereaved (Name) insists. However, this wasn't an issue for (Name), who his family described as pro-vaccine. (Name) CDC vaccine card documents his first and second doses of Pfizer's experimental gene therapy on 26Mar, and 16Apr2021, respectively. "Tuesday and Wednesday he was fine," described (Name) mother, (Name), "but Thursday morning 72 hours after the booster - he called and said he had a sore throat." The Defended s (Name) reports on how the family had no indications (Name) heart would soon fail, and believed he was experiencing mild side effects. This 26-year-old withheld male was discovered sitting in his recliner at home, He has a history Of a Of Galen malformation with multiple therapies. He had received his third Pfizer Covid shot booster and flu shot on 08Nov2021. On morning Of 11Nov, he complained of sore throat and fatigue. On morning of 12Nov2021, his apple watch recorded tachycardia. Later in the day. he had complained muscle aches and sore throat with a temperature Of 1002 F. The examination was conducted 15Nov2021 at 0915 hours. Autopsy information was reported as: Specimen: Body, General Information: Age: 26, Sex: M, Length: 69 inches, Weight: 240 pounds, Date of Death 12Nov2021, Date of autopsy: 15Nov2021; Final Diagnosis: Multifocal myocarditis involving the cardiac left ventricle and interventricular septum A. Received Pfizer Covid booster shot and flu shot on 08Nov2021 B. Pulmonary congestion C. Splenomegaly D. Cerebral edema; Il. Right cardiac ventricle; III. Vein of Galen malformation. clinical A. Multiple vessels Of varying size with refractile foreign material with giant cell inflammatory response and calcification; large caliber vessel with thrombus. Cause of death: Multifocal myocarditis involving the left ventricle and septum. Contributory: Recent Pfizer Covid booster vaccine Manner of death: Normal/Natural. Comment: Myocarditis following administration of pfizer Covid vaccine has been noted in male patients between ages of 16 and 29 Years, and most commonly presents 3 to 5 days following administration. Post Pfizer Covid vaccination myocarditis has been identified to cause left ventricle dysfunction.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200082021 Pfizer; Reported Cause(s) of Death: Death From Myocarditis; fatal arrhythmia that killed him instantly; left ventricular dysfunction

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Test Name: Body temperature; Result Unstructured Data: Test Result:100.2 Fahrenheit; Comments: his temperature was up to 100.2; Test Name: CO2; Test Result: 0.2 %; Comments: Normal; Test Name: Heart rate; Result Unstructured Data: Test Result:112; Comments: his heart rate was elevated to 112; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:97; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:85; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:91; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:84; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:91; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:89; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:90; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:89; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:84; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:85; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:98; Test Date: 20211110; Test Name: Heart rate; Result Unstructured Data: Test Result:89; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:90; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:120; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:119; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:120; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:121; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:127; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:126; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:127; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:131; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:128; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:131; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:130; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:130; Test Date: 20211111; Test Name: Heart rate; Result Unstructured Data: Test Result:128; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:123; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:127; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:128; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:135; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:74; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:141; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:71; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:146; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:144; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:138; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:149; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:148; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:145; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:63; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:63; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:119; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:68; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:64; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:64; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:64; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:65; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:67; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:67; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:67; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:66; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:66; Test Date: 20211112; Test Name: Heart rate; Result Unstructured Data: Test Result:66; Test Name: Oxygen level; Test Result: 100 %; Comments: his oxygen was at 100%
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2061885

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: MA
Alter: 53,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 16.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Chest X-ray Chest discomfort Chest pain Coagulation test Contusion Echocardiogram Electrocardiogram Fall Fatigue Fibrin D dimer Heart rate Immunisation Interchange of vaccine products Loss of consciousness Myocardial infarction Oxygen saturation PO2 decreased Pain

Symptomtext

thought she was having a heart attack; collapsed to the floor; had bruises to her elbows and knees; felt like puking or throwing up; oxygen level was horrible; Passed out/ collapsed to the floor; she couldn't speak or say full words because the pain was debilitating; extreme exhaustion; her first and second doses of COVID-19 vaccine were Moderna and third dose Pfizer; booster; Pericarditis; pressure in her upper chest.; Pain; soreness to her upper chest; 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 received bnt162b2 (BNT162B2), administered in arm, administration date 16Dec2021 (Lot number: FE3590) at the age of 53 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Heart attack", start date: 2016 (unspecified if ongoing), notes: she had a heart attack 5 years ago; "Electrocardiogram QT prolonged" (unspecified if ongoing), notes: Verbatim: QT interval prolonged; "Cardiac issue" (unspecified if ongoing); "broken her hand" (unspecified if ongoing); "acid reflux" (unspecified if ongoing). Family history included: "Mother almost died due to COVID" (unspecified if ongoing), notes: Caller says because her mother almost died of COVID, and was in the ICU for a month. Concomitant medication(s) included: ASPIRIN [ACETYLSALICYLIC ACID], start date: 2016; METOPROLOL taken for heart rate, start date: 2016; DILTIAZEM taken for cardiac disorder, start date: 2016; LANSOPRAZOLE taken for gastrooesophageal reflux disease. Vaccination history included: Moderna covid-19 vaccine (First Dose, LOT: 023 then E or C, she can't tell, then Z then IA or 1A), administration date: 11May2021, when the patient was 52 years old, for COVID-19 Immunization; Moderna covid-19 vaccine (Second dose, LOT that she says is illegible but she can try to read it. She says it looks like: 007), administration date: 08Jun2021, when the patient was 52 years old, for COVID-19 Immunization. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 16Dec2021, outcome "unknown", described as "her first and second doses of COVID-19 vaccine were Moderna and third dose Pfizer"; IMMUNISATION (medically significant) with onset 16Dec2021, outcome "unknown", described as "booster"; MYOCARDIAL INFARCTION (medically significant) with onset 04Jan2022, outcome "unknown", described as "thought she was having a heart attack"; PERICARDITIS (medically significant) with onset Dec2021, outcome "not recovered", described as "Pericarditis"; LOSS OF CONSCIOUSNESS (medically significant) with onset 04Jan2022, outcome "unknown", described as "Passed out/ collapsed to the floor"; PAIN (medically significant) with onset Dec2021, outcome "not recovered", described as "Pain"; CHEST PAIN (medically significant) with onset Dec2021, outcome "not recovered", described as "soreness to her upper chest"; FALL (medically significant) with onset 04Jan2022, outcome "unknown", described as "collapsed to the floor"; CONTUSION (medically significant) with onset 04Jan2022, outcome "recovering", described as "had bruises to her elbows and knees"; VOMITING (medically significant) with onset 04Jan2022, outcome "unknown", described as "felt like puking or throwing up"; PO2 DECREASED (medically significant) with onset 04Jan2022, outcome "recovered" (Jan2022), described as "oxygen level was horrible"; FATIGUE (medically significant) with onset Jan2022, outcome "not recovered", described as "extreme exhaustion"; CHEST DISCOMFORT (medically significant) with onset Dec2021, outcome "not recovered", described as "pressure in her upper chest."; SPEECH DISORDER (medically significant) with onset Jan2022, outcome "unknown", described as "she couldn't speak or say full words because the pain was debilitating". The events "thought she was having a heart attack", "pericarditis", "passed out/ collapsed to the floor", "pain", "soreness to her upper chest", "collapsed to the floor", "had bruises to her elbows and knees", "felt like puking or throwing up", "oxygen level was horrible", "extreme exhaustion", "pressure in her upper chest." and "she couldn't speak or say full words because the pain was debilitating" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: chest x-ray: (Jan2022) unknown results; coagulation test: (Jan2022) no blood clots; echocardiogram: (Jan2022) unknown results; electrocardiogram: (Jan2022) unknown results; fibrin d dimer: (Jan2022) normal; heart rate: (Jan2022) unknown results; oxygen saturation: (Jan2022) 90; (Jan2022) 98-100; sars-cov-2 test: (Jan2022) negative, notes: All ok; troponin: (Jan2022) normal. Therapeutic measures were taken as a result of myocardial infarction, pericarditis, loss of consciousness, pain, chest pain, fall, contusion, vomiting, po2 decreased and it was mentioned as the Tylenol dose she had took she didn't know, and they gave her Fentanyl IV and all kinds of pain meds while she was in the hospital, and they gave her an anti-inflammatory in the hospital. The patient said they did not admit her to the hospital due to her Troponin level and D-dimer being ok. She said that she had had other cardiac issues in the past, so she didn't know how they would not want to monitor her, she had a heart attack 5 years ago, but that didn't feel like this constant horrific pain. Caller clarified that she was taking Dual Action Advil with Acetaminophen, 250mg, and she was taking two pills, two to three times a day. She clarified they were tablets, Dual Action Advil with Acetaminophen NDC/UPC/LOT/EXP: Unknown. Caller said at the hospital they tried 3-4 different things, she couldn't speak or felt her arm because she was in so much horrific pain and she was presenting like from the pain for all different things. She said they gave her an EKG, and a chest x-ray, but they didn't do a CT scan, they did a resting heart rate, but did not do MRI to find out if there was fluid around her heart, which she had a complaint at the hospital about that. Clinical course: Caller says the adverse effect was pericarditis, which started a day to two days later after the dose. She says she had soreness to her upper chest that was prominent all day long and didn't go away, but she ignored it. She says it never went away, so she took Tylenol and stuff. Caller says on Tuesday of last week she woke up from a sound sleep and thought she was having a heart attack. She says she collapsed on the floor and had bruises to her elbows and knees, and felt like puking or throwing up, and passed out. Caller says she taken by ambulance out of the house, her oxygen level was horrible. She says her oxygen came back up, and they did tests on her. She says right now they had her get an echocardiogram this morning. She says while she was at the hospital she was inundated with tests including COVID, D-dimer, and Troponin, which were all ok, so they said they could handle her care out patient, but now she has results from the echocardiogram which she will have soon, and her primary doctor called in steroids, because she was still in so much pain, to see if that would alleviate it. Caller says her primary doctor said if the steroids ended up working, she would be pretty sure that she has pericarditis, and the steroids are working two days later. She says they had questioned if it could be esophageal spasms, but those wouldn't keep going like this, and the steroids are working to help alleviate pain. She says that she still has extreme exhaustion and pressure in her upper chest. Caller clarifies that it was on 04Jan2022 when she went by ambulance because the pain in her chest had gotten worse. She says at first for a week it stayed the same and then it became more intense, and she is a total procrastinator with a high pain tolerance. She provides examples of previously having an eardrum almost ready to perforate and her doctor asking why she waited to come in because it had to have been like that for a week and she told her doctor that she didn't feel it. She says she also had broken her hand twice in the past and didn't go to the doctor right away either time. She says these things occurred prior to her recent vaccinations. She says her point is that this recent pain had been nagging her all day long and she was like I can breath and is not a whistleblower, so she had waited to be seen for it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: Test Date: 202201; Test Name: Chest X-ray; Result Unstructured Data: Test Result:Unknown Results; Test Date: 202201; Test Name: Blood clots; Result Unstructured Data: Test Result:No blood clots; Test Date: 202201; Test Name: Echocardiogram; Result Unstructured Data: Test Result:Unknown Results; Test Date: 202201; Test Name: EKG; Result Unstructured Data: Test Result:Unknown Results; Test Date: 202201; Test Name: D-Dimer; Result Unstructured Data: Test Result:Normal; Test Date: 202201; Test Name: Resting Heart rate; Result Unstructured Data: Test Result:Unknown Results; Test Date: 202201; Test Name: O2 Level; Result Unstructured Data: Test Result:90; Test Date: 202201; Test Name: O2 Level; Result Unstructured Data: Test Result:98-100; Test Date: 202201; Test Name: COVID test; Test Result: Negative ; Comments: All ok; Test Date: 202201; Test Name: Troponin; Result Unstructured Data: Test Result:Normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Acid reflux (oesophageal); Broken hand; Cardiac disorder; COVID-19 (Caller says because her mother almost died of COVID, and was in the ICU for a month.); Heart attack (she had a heart attack 5 years ago); QT interval prolonged (Verbatim: QT interval prolonged)
Andere Medikamente: ASPIRIN [ACETYLSALICYLIC ACID]; METOPROLOL; DILTIAZEM; LANSOPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2059136

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: TX
Alter: 70,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 30.11.2021
Beginn: 12.01.2022
Tage bis Beginn: 43,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure COVID-19 COVID-19 pneumonia Cardiomegaly Chest X-ray abnormal Condition aggravated Death General physical health deterioration Hypoxia Lung consolidation Mental status changes Multiple organ dysfunction syndrome Osteomyelitis SARS-CoV-2 test positive Septic shock

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 2/27/2021, 4/6/2021, and 11/30/2021. Presented to Emergency Department for altered mental status and hypoxia. Per nursing home, patient tested positive for COVID on 1/9/2022. Admitted for COVID-19 pneumonia w/acute hypoxic respiratory failure, osteomyelitis, AKI, and septic shock. Treated with supplemental oxygen, pressors, vitamin C, steroids, antibiotics, and zinc. Continued to decompensate requiring higher doses of oxygen and pressor support with multi-organ failure. Expired on 1/13/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 1,0
Labordaten: 1/12/2022: COVID positive; 1/12/2022: Chest x-ray demonstrated enlarged cardiac silhouette and bilateral lung consolidation could reflect CHF or pneumonia
Aktuelle Erkrankungen: -
Vorgeschichte: Osteomyelitis, COPD, cirrhosis, hypertension, diabetes, anxiety, bipolar, CAD, hyperlipidemia, GERD, lymphedema
Andere Medikamente: vitamin C, collagenase, doxycycline, duo-neb, multivitamin, propranolol, zosyn, spironolactone, vitamin A, zinc, furosemide, albuterol, aspirin, cyanocobalamin, dicyclomine, lomotil, ferrous gluconate, gabapenetin, norco, hydroxyzine, lorat
Allergien: Caffeine, codeine, adhesive, feldene, fluoxetine, formaldehde analogs, gold salts, silver, alprazolam
Vorherige Impfungen: -

VAERS 2054518

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: GA
Alter: 36,0
Geschlecht: M
Eingang: 21.01.2022
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: nein

Angioedema Angiogram pulmonary normal Blood follicle stimulating hormone normal Blood luteinising hormone normal Blood oestrogen increased Blood testosterone Blood testosterone free increased Blood thyroid stimulating hormone decreased Breast mass C-reactive protein decreased Chills Differential white blood cell count Dyspnoea exertional Fatigue Free androgen index Full blood count normal Gynaecomastia Human chorionic gonadotropin negative

Symptomtext

Approx 12 hours after administration pt developed extreme arm pain, axillary lymphadenopathy, severe fevers and chills. Lymphadenopathy spread into his ipsilateral torso and he developed a painful subareolar lump. Experienced same symptoms on the right side when administered dose 2 in the right arm (same Lot #). Also experienced extreme fatigue and dyspnea on exertion that patient says was not present prior to the vaccination, even when he was isolating with COVID. Recovered from COVID 12-14 days prior to vaccine administration. Did not receive monoclonal antibody infusion or other similar treatment. Continues to have significant fatigue, dyspnea on exertion, and subareolar masses.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Gynaecomastia
Hospital-Tage: -
Labordaten: 16 Nov 2021: CBC w/ diff - normal, CMP non-fasting - normal, ESR - 19, CRP - 0.2 17 Dec 2021: TSH - 1.8, Free T4 - 6.6, Estrogen - 62, serum hCG Quant - <1, FSH - 7.0, LH 5.7, Testosterone 309, Sex hormone binding globulin 15, testosterone free - 8.44, Androgen free - 71.48 16 Nov 2021 - Chest PA/Lateral - No acute cardiopulmonary disease 15 Dec 2021 - Bilateral mammogram - benign gynecomastia, no evidence of malignancy
Aktuelle Erkrankungen: COVID-19 diagnosed on 02 Sep 2021 by PCR
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillins (anaphylaxis), azithromycin (unknown reaction)
Vorherige Impfungen: -

VAERS 2006473

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: MO
Alter: 60,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 30.09.2021
Beginn: 29.12.2021
Tage bis Beginn: 90,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Arthralgia Chest pain Computerised tomogram thorax abnormal Dyspnoea Full blood count Pulmonary embolism Thrombotic thrombocytopenic purpura Ultrasound Doppler Electrocardiogram Heparin-induced thrombocytopenia Impaired work ability Pain in extremity Pulmonary thrombosis Scan with contrast abnormal

Symptomtext

Massive bilateral pulmonary emboli/Vaccine Induced Thrombotic Thrombocytopenia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 7,0
Labordaten: CBC, CT Chest, Venous US legs.
Aktuelle Erkrankungen: microcytic anemia
Vorgeschichte: Hypertension, anxiety, degenerative cervical disc disease, insomnia, chronic low back pain, migraines, seasonal allergies.
Andere Medikamente: Zyrtec. Flexeril. Benadryl. Lisinopril. Tramadol. Trazodone. Ambien.
Allergien: Codeine. Mango. Penicillin.
Vorherige Impfungen: -

VAERS 2006473

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: MO
Alter: 60,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 30.09.2021
Beginn: 29.12.2021
Tage bis Beginn: 90,0
Dosis: 3
Route/Site: SYR / LA

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

Anticoagulant therapy Arthralgia Chest pain Computerised tomogram thorax abnormal Dyspnoea Full blood count Pulmonary embolism Thrombotic thrombocytopenic purpura Ultrasound Doppler Electrocardiogram Heparin-induced thrombocytopenia Impaired work ability Pain in extremity Pulmonary thrombosis Scan with contrast abnormal

Symptomtext

Massive bilateral pulmonary emboli/Vaccine Induced Thrombotic Thrombocytopenia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 7,0
Labordaten: CBC, CT Chest, Venous US legs.
Aktuelle Erkrankungen: microcytic anemia
Vorgeschichte: Hypertension, anxiety, degenerative cervical disc disease, insomnia, chronic low back pain, migraines, seasonal allergies.
Andere Medikamente: Zyrtec. Flexeril. Benadryl. Lisinopril. Tramadol. Trazodone. Ambien.
Allergien: Codeine. Mango. Penicillin.
Vorherige Impfungen: -

VAERS 2047469

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: MI
Alter: 83,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 15.10.2021
Beginn: 11.01.2022
Tage bis Beginn: 88,0
Dosis: 3
Route/Site: IM / AR

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

Acute kidney injury Acute respiratory failure Brain natriuretic peptide increased COVID-19 pneumonia Cardiac failure congestive Chest X-ray abnormal Electrocardiogram abnormal Lung infiltration Pulmonary congestion Troponin

Symptomtext

Hospitalized 01/11/2022-still currently admitted; COVID-19 positive 01/11/2022; fully vaccinated plus booster CHIEF COMPLAINT: Acute respiratory failure with hypoxia (HCC) Assessment/Plan ASSESSMENT / PLAN: Acute Respiratory failure with hypoxia Pneumonia due to COVID 19 Virus Immunosuppressed status Vaccinated: 2 doses and booster Symptom onset: 1/4 CXR w/ scattered scattered left peripheral infiltrates and vascular congestion with possible small bilateral effusions Decadron Check procal, consider abx if elevated Not candidate for remdisivr due to renal disease Already on coumadin, check INR to ensure therapeutic Wean O2 as tolerated Acute CHF exacerbation, unspecified type and chronicity Elevated Troponins Hx of CAD s/p stenting Hx of Aortic Valve stenosis s/p TAVR (bioprosthetic) Hx of Complete Heart Block s/p PPM Hx of Subclavian Veinoplasty Trop 143-- >142 BNP 5790 ECG is ventricular paced but does appear to have some increased ST elevation No previous Hx of CHF Will obtain Echo, Consider cardiology consult pending results He was started on coumadin after TAVR, although it is bioprosthetic valve Will monitor off lasix tonight due to AKI. Low threshold to initiate if decompensates overnight Continue Toprol, ASA, statin, coumadin (pharmacy to dose) 01/14/2022 notes: Assessment and Plan Severe acute respiratory failure with hypoxia COVID19 PNA Immunosuppressed state -Currently O2 need increased from 6L-> HFNC @ 95% and 45L to maintain sats -is s/p vaccination and booster but immunosuppressed from transplant meds -procal normal -supra therapeutic INR makes suspicion for clot low -patient confirmed to be full code Plan: -decadron -> solumedrol 60mg BID with eventual slow taper if he improves -titrate O2 as able -warfarin for anticoagulation -repeat CXR 01/18/2022 notes: Severe acute respiratory failure with hypoxia COVID19 PNA Immunosuppressed state -Currently O2 need stable today at 80% FIO2 @ 50L/min -is s/p vaccination and booster but immunosuppressed from transplant meds -procal normal -supra therapeutic INR makes suspicion for clot low -patient confirmed to be full code Plan: -solumedrol 60mg BID for 7-14 days (day 5 today) with slow prednisone taper afterwards -titrate O2 as able -warfarin for anticoagulation -repeat CXR Disposition: DC timing unclear given severe hypoxia though hopefully DC in next week given lack of improvement over last few days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CAD in native artery Hypertension Dyslipidemia Liver disease Severe aortic stenosis Subclavian vein obstruction, right (HCC) Acquired cystic kidney disease Alcoholic cirrhosis (HCC) Anemia of chronic renal failure Obesity End stage renal failure on dialysis (HCC) Gout Hyperlipidemia Renal transplant recipient Monoclonal gammopathy of unknown significance (MGUS) Renal osteodystrophy Impaired fasting glucose GERD (gastroesophageal reflux disease) CKD (chronic kidney disease) AV block, Mobitz 1 Complete heart block (HCC) Chronic diastolic heart failure (HCC) Cardiac pacemaker in situ Long term (current) use of anticoagulants
Andere Medikamente: amLODIPine (NORVASC) 10 MG tablet aspirin 81 MG enteric coated tablet atorvastatin (LIPITOR) 40 MG tablet B Complex Vitamins (VITAMIN B COMPLEX) TABS cholecalciferol (CHOLECALCIFEROL) 25 MCG (1000 UT) tablet clindamycin (CLEOCIN) 300 MG cap
Allergien: Penicillins Clarithromycin Erythromycin Fluconazole Itraconazole Ketoconazole Minocycline Tetracycline Vancomycin
Vorherige Impfungen: -

VAERS 2028016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 24.10.2021
Beginn: 04.01.2022
Tage bis Beginn: 72,0
Dosis: 3
Route/Site: IM / -

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

Abdominal distension Abdominal pain Abdominal tenderness Acute kidney injury Acute respiratory failure Anticoagulant therapy Atrioventricular block first degree Bacterial test negative Blood creatinine increased Brain natriuretic peptide increased C-reactive protein increased COVID-19 COVID-19 pneumonia Cardiac failure Cardiac murmur Cardiac septal defect Chest X-ray abnormal Chest discomfort

Symptomtext

Hospitalized (1.4.22 - still admitted currently); COVID-19 positive (1.4.22 vs 12/31/21 positive home test -self reported); fully vaccinated PLUS Booster - pfizer x3 H&P: CHIEF COMPLAINT: COVID + Pneumonia AKI Pancytopenia ASSESSMENT / PLAN: Acute on chronic hypoxic respiratory failure COVID-19 Pneumonia - Onset of symptoms ~ 7 days ago, reports positive at home COVID test 5 days prior to admission - S/p mAb on 1/2/22 - COVID 19 PCR + on 1/4/22 - Influenza A/B and RSV negative - BNP elevated 13,582 - CXR 1/2 - slight interval worsening of bilateral airspace opacity/pneumonia - CXR 1/4 - stable persistent mild bronchopneumonia - On 2.5L O2 at night at baseline - increased needs at home -- > currently on 5L NC - S/p decadron in the ED, continue to complete 10 days - Not able to do Remdesivir 2/2 renal failure - Consult ID given high risk 2/2 pancytopenia - Nebs PRN - Continuous pulse ox AKI on CKD - Creat 1.79 on presentation, creat was 1.3 on 12/14/21 - S/p 1L IVF in the ED - Avoid nephrotoxins - Check UA - Monitor Multiple myeloma - Diagnosed in 2011 - S/p revlimid and dexa in 2011 - S/p 2 cycles CyBorD - stopped 2/2 toxicity - Changed to Velcade and dexa, possible addition of dara in near future - Referred to orthopedic surgery and Rad onc as outpt due to pathologic fracture seen in PET scan - Patient of Dr Pancytopenia - Monitor and transfuse for Hgb < 7, platelets <10 or <30 if bleeding Pulmonary arterial hypertension Right sided heart failure - NYHA functional class 1 - Last echo 10/28/21 with EF 63%, severe RV dilation and severe decreased function, flattened systolic septum, RVSP at least 95. Moderate tricuspid regurgitation - Follows with Dr as outpatient - will consult - BNP elevated 13,582 - Hold torsemide and aldactone - IV albumin followed by IV lasix x 1 now. Monitor daily diuresis needs - On Sildenafil 20mg TID, ambrisentan, selexipag - Was on midodrine - recently stopped - Daily weights, monitor I/Os Bilateral LE edema - Worsening over past 2 days - Likely 2/2 above - Diurese and monitor - Pt is on eliquis First degree AV block - EKG in ED: sinus bradycardia with heart rate 58, first-degree AV block. T-wave inversions in V1 through V5, inversions in V3 to V5 were present on prior EKG from October, but the 1 in V2 is new. Worsening ST depression in the lateral leads - Troponin flat 27 -- > 25 - Denies chest pain/pressure at time of visit - Curbeside with cards, overall EKGs appear similar to 2019, await Echo results and if changes then will place formal consult Atrial fibrillation - On amiodarone and eliquis HTN - Continue home meds - Monitor HLD - Not on statin OSA - Does not wear CPAP - On chronic 2.5L home O2 at night DVT prophy - On eliquis DNR/DNI SUBJECTIVE: Patient is a 75 year old female with PMH significant for multiple myeloma, pulmonary HTN, right sided heart failurem Atrial fibrillation, CKD,HLD, depression, who presented to the ER due to shortness of breath. On presentation to the ED pt was hypoxic to 83-86% on room air and was placed on 4L O2 improving to mid 90s. COVID PCR positive. Labs notable for pancytopenia, elevated BNP. EKG with sinus bradycardia with heart rate 58, first-degree AV block. T-wave inversions in V1 through V5, inversions in V3 to V5 were present on prior EKG from October, but the 1 in V2 is new. Worsening ST depression in the lateral leads. Troponin x 2 flat 27 -- > 25. Patient was given 1L IVF, albuterol and decadron. Patient is being admitted for further treatment. Patient seen in the ED, she reports onset of symptoms ~ 1 week ago, had a positive at home COVID test ~ 5 days ago. She has been experiencing worsening shortness of breath, chest tightness and increased oxygen needs. She wears 2.5L oxygen at night at baseline due to OSA (does not wear CPAP), over the last several days she has been needing to use her oxygen during the day. Reports O2 levels dropping to 70-80s on room air. Reports productive cough of yellow/gray phlegm. She was evaluated in the ED on Sunday, she received monoclonal antibodies and was instructed to increase O2 to 3L during the day/night. She was doing ok with that but needed to increase O2 more today due to low O2 sats. She feels that her breathing and chest tightness have improved after albuterol. Reports chills but has not been checking temperature. Reports nausea but no vomiting. She has chronic intermittent diarrhea but Sunday diarrhea seemed to worsen and she had several bouts of diarrhea, has not had a BM since yesterday. Reports mild abdominal pain. Denies urinary or bleeding concerns. Reports worsening of BLE swelling over the past couple of days. Appetite has been fair to poor. History was provided by the patient. Review of Systems Constitutional: Positive for appetite change, chills and fatigue. Negative for diaphoresis and fever. HENT: Positive for congestion and rhinorrhea. Negative for mouth sores, sore throat, trouble swallowing and voice change. Eyes: Negative for visual disturbance. Respiratory: Positive for chest tightness, cough, shortness of breath and wheezing. Negative for hemoptysis. Cardiovascular: Positive for chest pain and leg swelling. Negative for palpitations. Gastrointestinal: Positive for abdominal pain, diarrhea and nausea. Negative for abdominal distention, blood in stool, constipation and vomiting. Genitourinary: Negative for difficulty urinating, dysuria and hematuria. Musculoskeletal: Negative. Negative for extremity weakness. Skin: Negative for rash and wound. Neurological: Negative for dizziness, headaches, light-headedness, numbness, paresthesias and extremity weakness. Psychiatric/Behavioral: Negative. Objective OBJECTIVE: BP (!) 104/45 | Pulse 57 | Temp 37 ?C (Oral) | Resp 20 | Wt 91.8 kg | SpO2 93% | BMI 32.67 kg/m? Body surface area is 2.07 meters squared. Physical Exam Constitutional: General: She is not in acute distress. Appearance: Normal appearance. She is well-developed. She is ill-appearing. She is not toxic-appearing or diaphoretic. HENT: Head: Normocephalic and atraumatic. Mouth/Throat: Mouth: Mucous membranes are dry. Eyes: Extraocular Movements: Extraocular movements intact. Pupils: Pupils are equal, round, and reactive to light. Cardiovascular: Rate and Rhythm: Regular rhythm. Bradycardia present. Heart sounds: Murmur heard. Pulmonary: Effort: Pulmonary effort is normal. No respiratory distress. Breath sounds: Wheezing and rhonchi present. No rales. Comments: On 5L NC Diminished at bases Abdominal: General: Bowel sounds are normal. There is no distension. Palpations: Abdomen is soft. Tenderness: There is abdominal tenderness (mild LLQ). There is no guarding or rebound. Musculoskeletal: General: No tenderness. Normal range of motion. Cervical back: Normal range of motion and neck supple. Right lower leg: Edema present. Left lower leg: Edema present. Skin: General: Skin is warm and dry. Coloration: Skin is pale. Neurological: General: No focal deficit present. Mental Status: She is alert and oriented to person, place, and time. Cranial Nerves: No cranial nerve deficit. Psychiatric: Mood and Affect: Mood normal. Behavior: Behavior normal. Thought Content: Thought content normal. Judgment: Judgment normal. 1/10/22 Infectious Disease Progress Note: ASSESSMENT/PLAN: Diarrhea, unspecified Assessment & Plan o Has been a chronic problem for patient but had been worsening. 5x today o Enteric pathogens 1/5 and C difficile toxin 1/5 negative Multiple myeloma Assessment & Plan o Most recently treated with Velcade and dexamethasone o Places her at increased risk for complications and COVID-19 infection * Acute hypoxemic respiratory failure Assessment & Plan o Secondary to COVID-19 infection, PCR positive 1/4, remdesivir completed 1/9, mab 1/2 o Remains on O2 via HFNC o 1/5 chest CT with bilateral infiltrates with area of ground-glass opacities and some small areas of consolidation within the lower lobes, particularly left lower lobe, no areas of cavitation and no effusions; suspect all changes due to COVID-19 infection o 1/7 CXR-some increased infiltrate/consolidation in LLL o Sputum 1/7 gram stain polymicrobial, cult nl respiratory flora o Completed remdesivir 1/9 PLAN o PJP prophylaxis started by pulmonary team due to prolonged taper o Continue to monitor off additional antibiotics Following Please call with questions for Dr. Infectious Diseases 1/10/2022 Subjective: Interval events: sputum culture from 1/7 final with normal resp flora. Remains afebrile. Completed remdesivir 1/9. Remains on HFNC. ddimer up to 2080. CRP trend favorable. US extremities 1/10 unchanged nonocclusive right popliteal vein thrombus favored to be subacute/chronic. Feels more tired today. Denies change to work of breathing. 5 Bm thus far today. No abdominal pain Allergies: Amoxicillin-pot clavulanate, Asacol [mesalamine], Augmentin, Lisinopril, Penicillin g, Penicillins, and Verapamil Review of systems: SEE HPI Objective: Vitals: BP 126/51 | Pulse 69 | Temp 36.8 ?C (Oral) | Resp 20 | Ht 1.689 m | Wt 94.8 kg | SpO2 90% | BMI 33.23 kg/m? Gen: AOx3, NAD Respiratory: coarse, HFNC Cardiovascular: regular rate, edematous Abdomen: soft, mildly distended, nontender MSK: edematous Skin: not diaphoretic, no visible rash Psych: mood appropriate, cooperative, answers all questions

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 8,0
Labordaten: Labs, microbiology & imaging reviewed 1/10/2022 Serum creatinine: 1.37 mg/dL (H) 01/10/22 0804 Estimated creatinine clearance: 41.6 mL/min (A) White Blood Cell Date Value Ref Range Status 01/10/2022 1.23 (LP) 4.00 - 10.80 x10*3/uL Final 01/09/2022 0.86 (LP) 4.00 - 10.80 x10*3/uL Final 01/08/2022 1.06 (LP) 4.00 - 10.80 x10*3/uL Final Creatinine Date Value Ref Range Status 01/10/2022 1.37 (H) 0.50 - 1.10 mg/dL Final 01/09/2022 1.40 (H) 0.50 - 1.10 mg/dL Final 01/08/2022 1.54 (H) 0.50 - 1.10 mg/dL Final C-Reactive Protein Date Value Ref Range Status 01/09/2022 8.0 (H) <=5.0 mg/L Final 01/08/2022 8.5 (H) <=5.0 mg/L Final 01/07/2022 13.7 (H) <=5.0 mg/L Final Lab Results Component Value Date CULTSPUTUM 01/07/2022 Normal Upper Respiratory Flora, no MRSA or Pseudomonas aeruginosa isolated MRSASCREEN 02/22/2019 No methicillin resistant Staphylococcus aureus isolated. CXBLDPERIPH No bacteria or yeast isolated 10/27/2021 CXBLDPERIPH No bacteria or yeast isolated 10/27/2021 GRAMSTAIN Moderate WBCs 01/07/2022 GRAMSTAIN Moderate Yeast 01/07/2022 GRAMSTAIN Few Gram Positive Cocci 01/07/2022 GRAMSTAIN Few Gram Positive Rods 01/07/2022 GRAMSTAIN Few Gram Negative Rods 01/07/2022 CULTUREURI 10,000-50,000 CFU/mL Enterococcus faecalis (A) 09/28/2021 FNLRPT Bacteria Not Isolated 12/29/2011 FNLRPT Bacteria Not Isolated
Aktuelle Erkrankungen: ED visit 1/2/22-1/3/22 (7 hrs) -Dx: pneumonia d/t COVID 19, hypomagnesemia, diarrhea - received MAB
Vorgeschichte: Past Medical History: Diagnosis Date ? Acute respiratory failure ? Atrial fibrillation ? Chronic kidney disease ? Colon adenoma ? DVT (deep venous thrombosis), left 2011 ? Heart murmur 2011 ? Hypertension ? Multiple myeloma ? sleep apnea
Andere Medikamente: Acyclovir 400 mg Oral 2 times daily Albuterol Sulfate 108 (90 Base) MCG/ACT 2 puffs Inhalation Every 6 hours PRN Ambrisentan 10 mg Oral Daily Amiodarone HCl 200 mg Oral Daily, for heart rhythm Apixaban 2.5 mg Oral 2 times daily Calcium-Magn
Allergien: Amoxicillin-Pot Clavulanate Rash -Tolerated cephalosporins in past (cefpodoxime Jan2016, cefepime Feb2019) Asacol [Mesalamine] Affected kidney function Augmentin Rash Lisinopril Cough Penicillin G Tolerated CEFEPIME Nov 2021 Penicillins Rash Verapamil
Vorherige Impfungen: -

VAERS 2025906

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: WA
Alter: 73,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 30.09.2021
Beginn: 09.01.2022
Tage bis Beginn: 101,0
Dosis: 3
Route/Site: IM / -

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

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

Symptomtext

Patient received Pfizer COVID vaccine on 1/21/21 (lot # EL3247), 2/12/21 (lot # EM9810), and 9/30/21 (lot # FE3590). On 1/9/22, patient admitted to our hospital for acute hypoxic respiratory failure, COVID-19 infection with concern for bacterial super-infection. As of today (1/11/22), patient is still admitted in our med/surg unit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: COVID status positive 1/9/22.
Aktuelle Erkrankungen: -
Vorgeschichte: RA (rheumatoid arthritis) on rituximab (last infusion 11/3/21), ILD (initially thought to be sarcoid but biopsy was negative, felt to be possible RA-ILD), CLL (was on ibrutunib but on hold due to side effects), latent TB completed treatment 11/2021, h/o libman sacks endocarditis on AC, chronic pain
Andere Medikamente: acetaminophen PRN, albuterol inh PRN, atorvastatin, vitamin d3, diphenhydramine PRN, fluticasone/salmeterol (Airduo Respiclick), ibrutinib, oxycodone PRN, pantoprazole, vitamin b6, rivaroxaban, zolpidem PRN
Allergien: calcium fortified cookie
Vorherige Impfungen: -

VAERS 2024781

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: WI
Alter: 64,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 09.11.2021
Beginn: 05.01.2022
Tage bis Beginn: 57,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Death

Symptomtext

covid related death-vaccinated

Weitere VAERSDATA-Felder

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

VAERS 2005702

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: SC
Alter: 61,0
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 21.12.2021
Beginn: 02.01.2022
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: IM / RA

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

Myocardial infarction Stent placement

Symptomtext

Had a physical on nov 15th everytghing was fine sat o1 /2 had a massive heart attack

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 2,0
Labordaten: sat 2 2021 had to put a stent
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: dovato
Allergien: -
Vorherige Impfungen: -

VAERS 1999832

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: OK
Alter: 63,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 26.10.2021
Beginn: 02.11.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / AR

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

Death Myocardial infarction Resuscitation

Symptomtext

patient got pfizer (booster for Janssen) on 10/26, he also got Fluzone Quad, about a week later he had a heart attack at 7:15 AM 11/2/21. After some CPR he was taken by ambulance to a local Hospital ER. He was later transported to another Hospital. He passed away the same day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: trazodone 50 1-2 HS, promethazine 25 1q4-6h, crestor 10 1daily, gabapentin 300 3tid, pramipexole 0.25 1hs, methocarbamate 750 1tid, percocet 10/325 1tid, meloxicam 15 1qd, amlodipine 10 1daily
Allergien: none
Vorherige Impfungen: -

VAERS 1997827

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: FL
Alter: 31,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 19.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: SYR / UN

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

Caesarean section Cerebrovascular accident Exposure during pregnancy Intracranial aneurysm Vasospasm

Symptomtext

Massive brain aneurysm stroke vasospasms emergency cesarean on October 23rd baby's weight 5 lb regular birthdate December 7th

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 60,0
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Prenatals
Allergien: No
Vorherige Impfungen: -

VAERS 1952454

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: NV
Alter: 27,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 19.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Exposure during pregnancy Foetal death Foetal hypokinesia

Symptomtext

G1P0100 received vaccine at 31 3/7 EGA. Next day noted decreased fetal movement, which continued. Evaluated on 10/24/21, found to have intrauterine fetal demise.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Foetal death
Hospital-Tage: 2,0
Labordaten: Other possible contributing factors to fetal demise include bicornuate uterus, history of partial placental abruption.
Aktuelle Erkrankungen: preterm labor
Vorgeschichte: -
Andere Medikamente: prenatal vitamins, nifedipine 10mg every 8 hrs as needed for contractions, unisom 25mg, vitamin b6 50 mg
Allergien: nka
Vorherige Impfungen: -

VAERS 1948335

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: CO
Alter: 68,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 16.10.2021
Beginn: 13.11.2021
Tage bis Beginn: 28,0
Dosis: 3
Route/Site: IM / LA

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

Laparotomy Neoplasm malignant Paracentesis Septic shock Spontaneous bacterial peritonitis Uterine cancer

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA: one month after receiving immunization patient hospitalized for septic shock, spontaneous bacterial peritonitis, and pelvic mass found to be malignant (carcinosarcoma). Underwent paracentesis, laparotomy, and received antibiotics. Discharged medically stable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Septic shock
Hospital-Tage: 19,0
Labordaten: -
Aktuelle Erkrankungen: pelvic mass, ascites, tachycardia
Vorgeschichte: COVID-19, arthritis, GERD, hypertension, keloid, seasonal rhinitis
Andere Medikamente: albuterol, aspirin, B complex vitamins, calcium, evening primrose oil, flaxseed oil, fluticasone, glucosamine/chondriotin, lisinopril, multivitamin, Metamucil, tramadol, tumeric
Allergien: adhesive, bacitracin, doxycycline, tolectin, hydrocodone-guaifenesin, hydrocodone-acetaminophen
Vorherige Impfungen: -

VAERS 1919867

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: MI
Alter: 42,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 12.10.2021
Beginn: 29.11.2021
Tage bis Beginn: 48,0
Dosis: 3
Route/Site: UN / UN

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

Acute respiratory failure Alcohol withdrawal syndrome Angiogram normal Anxiety Atelectasis COVID-19 COVID-19 pneumonia Computerised tomogram head normal Condition aggravated Dyspnoea exertional Echocardiogram Echocardiogram normal Ejection fraction Fall Head injury Hepatic cirrhosis Myelopathy SARS-CoV-2 test positive

Symptomtext

Patient discharged after (2) inpatient admission. Patient is a 42-year-old female with past medical history of obesity and alcohol abuse and dependence who presented to the hospital with acute hypoxic respiratory failure secondary to COVID-19 pneumonia. Patient was admitted to the hospital on high-flow nasal cannula. Patient was able to be weaned to room air fairly quickly. Patient was treated with IV steroids. CT angiogram of the chest did not reveal any pulmonary embolism or significant respiratory disease. I believe the patient had a large component of anxiety, as well as alcohol withdrawal. Patient stated she drinks between 7-824 oz cans of beer every day and had stopped drinking the evening prior to admission. Patient was treated with Librium to avoid alcohol withdrawal which she responded to well. Patient was weaned to room air, she was not having any clinical signs of withdrawal. She was then considered stable for discharge home. Patient will finish 10 day course of Decadron for her COVID pneumonia. Patient will also be sent home on a Librium taper for a few days. Patient was in agreement this plan. Patient was counseled on cessation of alcohol use. Patient will follow-up with PCP. Patient discharged home in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: CV Echo Limited with Contrast [355507467] Collected: 11/29/21 1558 Order Status: Completed Updated: 11/29/21 1626 Narrative: Hospital LIMITED ECHOCARDIOGRAPHY REPORT Name: Patient Study Date: 11/29/2021 MRN: Patient Location: HOS DOB: Patient Class: Inpatient Gender: Female Ordering Physician: Age: 42 yrs Height: 167 cm Performed By: RDCS, RVT Weight: 110 kg Resting HR: 85 BSA: 2.2 m2 Resting BP: 161/88 mmHg Reason For Study: Dyspnea on exertion (DOE), DOE History/Symptoms: Covid 19 infection, Alcohol abuse, Hypertension, Obesity, Congestive heart failure, Dyslipidemia, Former tobacco abuse, Cerebrovascular accident Electronically signed by: MD on 11/29/2021 04:25 PM Interpretation Summary The left ventricular ejection fraction is 55%. The LV ejection fraction is normal. The right ventricular size, thickness, and function are normal. No pericardial effusion. Today's study was compared to one performed on 12/10/18. The LVEF was 74% on the prior report. STUDY PERFORMED/QUALITY: A two-dimensional transthoracic echocardiogram with color flow and spectral flow Doppler was performed in limited views only. The technical quality of the exam was limited due to suboptimal acoustic windows. Due to limited acoustic windows, Definity was administered. LEFT VENTRICLE: The left ventricular ejection fraction is 55%. The LV ejection fraction was determined utilizing visual estimation. The LV ejection fraction is normal. No regional wall motion abnormalities noted. RIGHT VENTRICLE: The right ventricular size, thickness, and function are normal. PERICARDIUM/PLEURAL: No pericardial effusion. INFERIOR VENA CAVA: The inferior vena cava was not visualized during the exam. Left Ventricle EDV(MOD-sp4): 169.9 ml ESV(MOD-sp4): 52.6 ml IVSd: 0.95 cm LVPWd: 1.2 cm LVIDd: 3.3 cm LVIDs: 2.2 cm Reference Table: Normal Mild ModerateSevere Men LVEF > 52% 41-51% 30-40% <30% Women LVEF > 54% 41-53% 30-40% <30% Men LVIDd 4.2-5.8 5.9-6.3 6.4-6.8 >6.8 Women LVIDd 3.8-5.2 5.3-5.6 5.7-6.1 >6.1 LA Volume (ml/m^2) < 34 35-41 42-48 >48 ______________________________________________________________________________ Electronically signed by: MD on 11/29/2021 04:25 PM All sources of data reside in the Cardiology PACS EJECTION FRACTION ECHO [355507471] Collected: 11/29/21 1558 Order Status: Completed Updated: 11/29/21 1626 EJECTION FRACTION ECHO 55 % CT HEAD WITHOUT IV CONTRAST [355378781] Resulted: 11/29/21 1055 Order Status: Completed Updated: 11/29/21 1057 Narrative: EXAMINATION: CT Head without Contrast EXAM DATE: 11/29/2021 9:56 AM TECHNIQUE: Multiple axial noncontrast images of the brain were obtained and reformatted according to the standard protocol. 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: Head trauma, mod-severe, fall, excessive alcohol use COMPARISON: None HAND DOMINANCE: Unknown ENCOUNTER: Not applicable ____________________ FINDINGS: No acute intracranial hemorrhage. No mass effect or midline shift. No hydrocephalus. The gray-white matter differentiation is maintained. No abnormal extra-axial fluid collection. The basal cisterns are patent. The orbits are unremarkable. The paranasal sinuses and left mastoid air cells are clear. Small amount of fluid in the right mastoid air cells. Calvarium is intact. Soft tissues are unremarkable. ____________________ Impression: 1. No acute intracranial abnormality. CT ANGIO THORAX WITH IV CONTRAST [355378783] Resulted: 11/29/21 1043 Order Status: Completed Updated: 11/29/21 1045 Narrative: EXAMINATION: CT Angiography of the Thorax EXAM DATE: 11/29/2021 9:56 AM 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: PE suspected, high prob, hypoxia, shortness of breath, hx of alcohol use. COMPARISON: CTA on 10/1/2021 ENCOUNTER: Not applicable ____________________ FINDINGS: Base of Neck & Axillae: There is no lymph node enlargement. Mediastinum & Hila: There is no mediastinal or hilar lymph node enlargement. Cardiovascular: The heart has a normal size. 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: Mild dependent atelectasis of both lungs. The lungs are otherwise clear. The previously seen opacification at the posterior aspect of the right lung has resolved. Pleural Space: There are no pleural effusions. There is no pneumothorax. Upper Abdomen: Again noted, there is a lobular contour of the liver, consistent with cirrhosis. There are postsurgical changes of a cholecystectomy and of the proximal stomach. Chest Wall & Musculoskeletal: Degenerative changes are noted at the spine. ____________________ Impression: 1. No evidence of pulmonary embolism. 2. Cirrhosis of the liver. COVID-19 PCR - Rapid [344444877] (Abnormal) Collected: 11/29/21 0855 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 11/29/21 0923 COVID-19 PCR Detected
Aktuelle Erkrankungen: 10/1/21- Pain and swelling of the right lower extremity; Pneumonia of right lower lobe due to infectious organism.
Vorgeschichte: Respiratory Seasonal allergic rhinitis Circulatory Essential hypertension Patent foramen ovale with atrial septal aneurysm Chronic congestive heart failure (HCC) Digestive Morbid obesity with BMI of 40.0-44.9, adult (HCC) Fatty liver NASH (nonalcoholic steatohepatitis) Infectious/Inflammatory COVID-19 Nervous Alcoholism (HCC) Peripheral neuropathic pain Fibromyalgia Alcohol abuse Genitourinary Primary ovarian insufficiency Premature ovarian failure Endocrine/Metabolic Mixed dyslipidemia Other History of CVA in adulthood Primary insomnia Depression Narcolepsy History of Roux-en-Y gastric bypass Anxiety Depression, major, recurrent (HCC) S/P hip replacement, right Closed supracondylar fracture of right humerus, initial encounter History of recent pneumonia
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet aspirin 81 MG enteric coated tablet benzonatate (TESSALON) 200 MG capsule buPROPion (WELLBUTRIN XL) 150 MG 24 hr tablet chlordiazePOXIDE (LIBRIUM) 25 MG capsule cyclobenzaprine (FLEXERIL) 10 MG tablet d
Allergien: NSAIDS- history of ulcers Dust, pollen, smoke, cats, and ragweed.
Vorherige Impfungen: -

VAERS 1897373

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: GA
Alter: 76,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 19.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Cerebrovascular accident Confusional state Hypotension Injection site pain Pyrexia

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Confusion-Severe, Systemic: Fever-Medium, Systemic: Hypotension-Medium, Systemic: Stroke-Medium

Weitere VAERSDATA-Felder

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

VAERS 1887766

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3590

kritisch

Staat: CA
Alter: 66,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Cerebrovascular accident Immunisation SARS-CoV-2 test Transient ischaemic attack

Symptomtext

woke up on 03Nov2021 with symptoms of a stroke went to the ER. It was a TIA stroke; woke up on 03Nov2021 with symptoms of a stroke went to the ER. It was a TIA stroke; Dose: 03; administration date: 18Oct2021; This is a spontaneous report from a contactable consumer (patient) reported for herself. A 66-year-old non pregnant female patient received third dose(BOOSTER), of BNT162B2 (BNT162B2, Solution for injection, PFIZER-BIONTECH COVID-19 VACCINE Lot Number: Fe3590), via an unspecified route of administration in arm left on 18Oct2021 as SINGLE for (at the age of 66) covid-19 immunization (Pharmacy or Drug Store). The patient medical history was not reported. Concomitant medications included influenza vaccine (INFLUENZA) taken for immunization on 08Oct2021; pneumococcal vaccine polysacch (PNEUMOCOCCAL POLYSACCHARIDE VACCINE) taken for immunization on 08Oct2021, estradiol, pantoprazole, multi vitamin, calcium all taken for an unspecified indication, start and stop date were not reported. Prior to vaccination, patient was not diagnosed with COVID-19, Since the vaccination, the patient has not been tested for COVID-19 (received within 2 weeks of vaccination). Patient was not pregnant at the time of vaccination. Historical vaccine included BNT162B2 (BNT162B2, Solution for injection, PFIZER-BIONTECH COVID-19 VACCINE Lot Number: EN6200) via an unspecified route of administration, administered in arm left on 18Feb20121 as dose 1, single and dose 2 of BNT162B2, PFIZER-BIONTECH Solution for injection, COVID-19 VACCINE Lot Number: EN6208) via an unspecified route of administration, administered in arm left on 11Mar2021 as dose 2, single (both at the age of 66) for COVID-19 immunization. The patient had dose: 03, administration date on 18oct2021, patient woke up on 03Nov21 with symptoms of a stroke went to the ER. It was a Transient ischaemic attack (TIA) stroke. The events resulted in Emergency room/department or urgent care, Hospitalization. Patient was hospitalized for one day from 03Nov2021 to 04Nov2021. Events was assessed as serious and seriousness criteria was reported as caused/prolonged hospitalization. The patient underwent lab tests and procedures which included nasal swab (covid 19,) test with negative result on 03Nov2021. Therapeutic measures were taken as a result of events (lots of medications). The outcome of evets was recovering. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 1,0
Labordaten: Test Date: 20211103; Test Name: Covid-19; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ESTRADIOL; PANTOPRAZOLE; CALCIUM
Allergien: -
Vorherige Impfungen: -

VAERS 1880626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: FL
Alter: 55,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 14.10.2021
Beginn: 14.11.2021
Tage bis Beginn: 31,0
Dosis: 2
Route/Site: IM / LA

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

Acute myocardial infarction Dyspnoea Fatigue

Symptomtext

Increased fatigue and SOB 1 week after receiving vaccine, Acute MI 4 weeks after vaccine administration

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: -
Labordaten: Hospital 11/14/21
Aktuelle Erkrankungen: HTN
Vorgeschichte: HTN
Andere Medikamente: HCTZ 25 mg daily
Allergien: NKA
Vorherige Impfungen: -

VAERS 1849731

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: FL
Alter: 90,0
Geschlecht: F
Eingang: 07.11.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Death

Symptomtext

Death approximately 6 hours after administration. Hospice patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: Parkinson's, HTN, Anemia, Dementia, CKD
Andere Medikamente: Clonidine patch, Prosource, hydralazine 25mg, nu-iron, losartan, Carbidopa-Levodopa, rasagline Mesylate, MVM, Levothyroxine, Nifedipine, sodium bicarb, senna,
Allergien: None known
Vorherige Impfungen: -

VAERS 1834246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: HI
Alter: 31,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 18.09.2021
Beginn: 27.10.2021
Tage bis Beginn: 39,0
Dosis: 2
Route/Site: IM / UN

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

Acute myocardial infarction Back pain Catheterisation cardiac abnormal Chest pain Coronary artery occlusion Coronary artery thrombosis Electrocardiogram ST segment elevation Pain Pain in extremity Thrombectomy Troponin I increased

Symptomtext

ST-elevation myocardial infarction secondary to coronary thrombus. Patient reported chest pain, midsternal w/ radiating to back and arm, onset 1130 on 10/27.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 4,0
Labordaten: EKG showed ST elevations in 2 3 and aVF, he has had ST elevations in leads V4, V5, V6. Taken to cardiac Cath Lab where he was found to have coronary thromboembolic disease he underwent mechanical thrombectomy to an occluded distal right coronary artery he also went a mechanical thrombectomy to the distal LAD. 10/28 Troponin I level of 43.3.
Aktuelle Erkrankungen: Had Covid prior to vaccination.
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1804831

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: HI
Alter: 45,0
Geschlecht: F
Eingang: 21.10.2021
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: ja Erholt: nein

Blood test Chest X-ray Chills Computerised tomogram Dizziness Dysmenorrhoea Dyspnoea Fatigue Headache Heavy menstrual bleeding Impaired work ability Intermenstrual bleeding Pain Pulmonary embolism Pyrexia Ultrasound scan

Symptomtext

The night of the vaccination, I had a headache, dizziness, fever, chills, fatigue, and body aches. It lasted for 36 hours. I called out sick from work because of those symptoms. Later I started having a headache daily along with the fatigue. On 10/09/2021, I woke up with heavy menstrual bleeding and cramping. This was odd because previously my periods would be normal and occur for 4 to 5 days. Around this time, I was bleeding through 3 or 4 pads an hour. On 10/12/2021, I went to my doctor. I was prescribed with hormone therapy Microgestin. Eventually, my period stopped being extremely heavy, but I was still experiencing spotting. This was strange to me because I had my fallopian tubes removed in June 2021. On 10/15/2021 early in the morning, I woke up with chest pains, cold sweat, and I was nauseated. I thought I was having a heart attack. I went to the ER at Medical Center. I took many tests. The doctor checked to see if I had a pulmonary embolism - and I tested positive for it. I was given four aspirins. They released me from the hospital. I have to follow-up with my physician soon. Currently, I wake up with a headache, light headedness, and I am still dealing with menstrual spotting. I've been dealing with shortness of breath as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: Ultrasound on 10/12/2021 On 10/15/2021 Blood test Chest X-ray CT scan CAT scan
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: None
Allergien: Codeine Peanuts Dust mites
Vorherige Impfungen: -

VAERS 1804494

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: WI
Alter: 34,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 15.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Chest discomfort Chills Computerised tomogram thorax Dyspnoea Fatigue Feeling abnormal Fibrin D dimer increased Flushing Full blood count Gait disturbance Hypoaesthesia Impaired work ability Pain Palpitations Paraesthesia Peripheral swelling Pulmonary embolism Pyrexia

Symptomtext

10/19/21 call to clinic stating tingling, numbness all over body, body aches, fatigue, fever, chest tightness and intermittent palpitations. 10/20/21 Office Visit Note below Friday got first dose of covid vaccine, states she is feeling off since then. Was fine for the first couple of hours but then 3 hours later started feeling drained, tired, arm was throbbing. As the days went on she has noticed more and more symptoms. Got chills, felt as though face was on fire. 101.5F, alternating tylenol and ibuprofen. This morning when she woke up this morning had a fever and took ibuprofen. Bilateral groin tenderness started Saturday/sunday. Gets weird numbness and tingling throughout body. Palpitations started Friday night. Every 2 hours, lasts 5-10 minutes. Slightly some shortness of breath and "slightly" some chest pain with it. Currently legs are sore, hard to walk because of the pain, elevates her legs because of the swelling. No noted redness. Swelling is new to her legs. No prior history of this. Notices sock line. This does improve once she elevates her legs but then as soon as she gets up again notices the swelling. Legs are bothering her the most with the leg swelling. Face feels hot but fingers and hands are freezing. Neck is also sore. Has been off of work due to her fevers and symptoms. No prior history of PEs. Has Mirena IUD in place. 10/21/21: Presents to ED, see notes below, still in ED at time of this form HPI The patient is a 35 year old female with a history of asthma who presents to the Emergency Department with a chief complaint of left leg pain. The patient received the first dose of the Pfizer COVID-19 vaccine on 10/15/2021 and states that she has been feeling "off" since. She was evaluated at the Respiratory Clinic yesterday for fatigue, fevers, chills, shortness of breath, chest tightness, and leg swelling and pain. A bilateral lower extremity ultrasound, CT angio of the chest, and labs were obtained. Findings were significant for a single subsegmental PE. Patient was contacted today with CT scan findings and was recommended to come into the Emergency Department for further evaluation of symptoms. The patient states that she woke up this morning with increased left anterior thigh pain and an acute onset of left sided abdominal pain. Notes that the pain work her up from her sleep this morning. Her left thigh pain is currently rated as a 7/10 in severity and described as aching with no radiation. No other associated symptoms noted. Symptoms are aggravated with palpation and movement of the left lower extremity and there are no alleviating factors. The patient denies nausea, vomiting, chest pain, back pain, head pain, dizziness, or lightheadedness. She denies taking any medications prior to arrival. No other reported symptoms at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: 10/20/21: Neg POCT Sars-COV, CBC, BMET, ESR, CRP wnl. D-Dimer abnormal 4,043 10/20/21: US venous duplex lower ext bilateral. No sonographic evidence of deep venous thrombosis in either lower extremity. 10/20/21 CT PE Chest Angio: Subsegmental pulmonary embolus along the posterior branch of the right upper lobe segmental artery. No heart right strain. 10/21/21: CT abd pelvis and labs ordered without results at time of this form.
Aktuelle Erkrankungen: 10/5/21 started with VIRAL URI symptoms, father COVID positive. Seen for OV 10/7/21, negative POCT COVID, negative Rapid Strep Test, negative Respiratory PCR panel
Vorgeschichte: Morbid obesity (*) Asthma Migraine without status migrainosus, not intractable Secondhand smoke exposure Left knee pain Sprain of MCL (medial collateral ligament) of knee Patellar tendinitis of left knee
Andere Medikamente: Albuterol HFA 90mcg inhaler, inhale 2 puffs q 6 hrs as needed -Mirena IUD -Multivitamin, 2 tablets daily -Maxalt-MLT, 1 tablet as needed may repeat second pill in 2 hours. -Topamax 50mg started 9/10/21 Sig: Take 0.5 tablets (25 mg total) by
Allergien: Penicillins
Vorherige Impfungen: -

VAERS 1804053

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: OH
Alter: 79,0
Geschlecht: M
Eingang: 21.10.2021
Impfdatum: 07.10.2021
Beginn: 10.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Death

Symptomtext

Patient passed away three days after receiving his third Pfizer COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None Known
Vorgeschichte: ASHD, COPD, Hypertension, Tongue Cancer in Remission
Andere Medikamente: Atorvastatin, Doxepin, Alprazolam, Famotidine, Trental
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 1801522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: OH
Alter: 81,0
Geschlecht: M
Eingang: 20.10.2021
Impfdatum: 18.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / -

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

Death

Symptomtext

Patient was a Hospice patient with no change in symptoms

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Hospice patient
Vorgeschichte: UNSPECIFIED DEMENTIA WITHOUT BEHAVIORAL DISTURBANCE HEART FAILURE, UNSPECIFIED TREMOR, UNSPECIFIED INSOMNIA, UNSPECIFIED ESSENTIAL (PRIMARY) HYPERTENSION DILATED CARDIOMYOPATHY LEFT VENTRICULAR FAILURE, BENIGN PROSTATIC HYPERPLASIA WITHOUT LOWER URINARY TRACT SYMPTOMS LACERATION WITHOUT FOREIGN BODY OF OTHER PART OF HEAD, CONTACT WITH AND (SUSPECTED) EXPOSURE TO COVID-19 NONTRAUMATIC INTRACRANIAL HEMORRHAGE,
Andere Medikamente: AzaSite Solution, hydrochlorothiazide, Lisinopril, Magnesium Oxide, Melatonin, Spironolactone, Toprol XL, Trazodone, Artificial Tears, Seroquel, Ativan, Tylenol
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1794807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: SD
Alter: 69,0
Geschlecht: F
Eingang: 18.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SC / LA

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

Asthenia Blood gases Cardiac arrest Chest X-ray Chest pain Coagulation test Death Electrocardiogram Full blood count Metabolic function test Resuscitation SARS-CoV-2 test Unresponsive to stimuli

Symptomtext

Patient received her booster dose from Pharmacy at an unknown time on 10/15/21. Her husband reports she had been well throughout the day. At some point, the patient began to complain of left sided chest pain and then became weak and had to lay down onto the floor. She then became unresponsive and upon arrival of EMS, she was asystole. She presented to our ED and we were able to get ROSC, but then the flight crew took off, the patient went into complete arrest again and was brought back to ED where resuscitation efforts continue, but the patient was pronounced dead at 2359.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: CXR, EKG, CMP, CBC, ABG, COVID-19 PCR, Coags
Aktuelle Erkrankungen: Unknown-- patient presented in full cardiac arrest. Husband reports the patient had been well that day.
Vorgeschichte: Unknown
Andere Medikamente: Loratadine 10mg daily, multivitamin, Aleve PRN
Allergien: NKA
Vorherige Impfungen: -

VAERS 1777314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

kritisch

Staat: MT
Alter: 74,0
Geschlecht: M
Eingang: 11.10.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Death No reaction on previous exposure to drug

Symptomtext

Patient did well with the first two doses, received the booster and two hours after he passed away. According to the wife, he was alright in the two hour time frame post vaccination. He went shopping and showed no signs of anaphylaxis or intolerance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: hypotension
Vorgeschichte: COPD, Congestive heart failure, Diabetes
Andere Medikamente: Novolog, pradaxa, pantoprazole, bumetanide, clopidogrel, sildenafil, calcitriol, brilinta, amlodepine, atorvastatin, potassium chloride, spironolactone, metoprolol, lantus
Allergien: Xarelto, Eliquis
Vorherige Impfungen: -

VAERS 2625740

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: AZ
Alter: 54,0
Geschlecht: F
Eingang: 03.05.2023
Impfdatum: 14.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / AR

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

Blood glucose normal Blood test normal Computerised tomogram normal Electrocardiogram normal Eye contusion Loss of consciousness Swelling face Vomiting

Symptomtext

Several hours after getting my initial dose of COVID-19 Vaccine I experienced a couple of brief periods of loss of consciousness, from 2:00 am to about 2:08 AM. I left bed to get a drink and wok up on my floor in the kitchen, then I woke up again on the floor in my bedroom. After catching COVID-19 and being hospitalized in February of 2021, I had bouts of vertigo. These were about 10 times a day for the first year, and they have diminished to multiple times a week currently. Participant is uncertain if these are related to the loss of consciousness episodes. in the middle of the night of 4/4/23 I had another episode of loss of consciousness, The length of time is unknown, Got out of bed in a hotel to get a drink and woke up on the floor. I checked into the ER after this incident as I had 2 black eyes and a large goose egg on my temporal lobe, right side. I vomited after I woke up, Inn the ER the doctor ordered a CAT scan. The Scan was normal. An ECG was also run. This ruled out a heart issue. Blood tests ruled out any other heart issue. Blood sugar was also normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: 4April2023 CAT scan, results normal. ECG, normal. Blood tests ruled out any other heart issue. Blood sugar was also normal.
Aktuelle Erkrankungen: NA
Vorgeschichte: Diabetes; thyroid cancer
Andere Medikamente: Synthroid; Lantus; Ozempic
Allergien: Adhesive; Aleve
Vorherige Impfungen: -

VAERS 2585805

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: FL
Alter: 59,0
Geschlecht: M
Eingang: 22.02.2023
Impfdatum: 20.10.2021
Beginn: 11.11.2021
Tage bis Beginn: 22,0
Dosis: 3
Route/Site: SYR / RA

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

Dizziness Electroencephalogram normal Generalised tonic-clonic seizure Magnetic resonance imaging normal Photophobia

Symptomtext

Two grand mail seizures 22 days after booster vaccine. Been on anti seizure meds since. Experiencing dizziness, bright light and strobe lights now make me dizzy and I have to wear sunglasses all the time now and remove myself whenever I see strobe lights.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Generalised tonic-clonic seizure
Hospital-Tage: 3,0
Labordaten: EEG and MRI. Nothing found. 11/11/2021.
Aktuelle Erkrankungen: None
Vorgeschichte: Cardiac patient 10 years
Andere Medikamente: Baby aspirin, flomax , Prozac, rosuvostatin, ezitimibe
Allergien: None
Vorherige Impfungen: -

VAERS 2579991

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: ND
Alter: 43,0
Geschlecht: F
Eingang: 11.02.2023
Impfdatum: 15.10.2021
Beginn: 01.01.2023
Tage bis Beginn: 443,0
Dosis: 3
Route/Site: IM / LA

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

Cerebral endovascular aneurysm repair Craniectomy Haematoma evacuation Haemorrhagic stroke Intensive care Intracranial aneurysm Ruptured cerebral aneurysm

Symptomtext

Hemorrhagic stroke from ruptured M1 MCA aneurysm resulting in emergent coiling followed by Craniectomy/hematoma evacuation. This followed by two weeks in intensive care. Now outpatient therapy (pt/ot/speech etc).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Haemorrhagic stroke
Hospital-Tage: 15,0
Labordaten: See operative reports 1/26 and 1/27
Aktuelle Erkrankungen: None
Vorgeschichte: HTN - controlled
Andere Medikamente: Lisinopril, nifedipine, valtrex, omeprazole, concerta
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2569877

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: TX
Alter: 59,0
Geschlecht: M
Eingang: 27.01.2023
Impfdatum: 07.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: SYR / LA

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

Arteriogram carotid Blood test Cerebellar stroke Computerised tomogram head normal Dizziness Echocardiogram Electrocardiogram Laboratory test Magnetic resonance imaging Musculoskeletal disorder Ultrasound Doppler Vertigo Vomiting

Symptomtext

BILATERAL CEREBELLAR STROKES I received the second shot of Pfizer MRNA on Nov 7, 2021. On Nov 29th, ,at the age of 59, I suffered the first of two strokes. Early that morning I woke up at approximately 1 am dizzy, throwing up and having some difficulty when moving my legs. My wife took me to a local emergency hospital. They did a CT scan of my head and said it was clear, no sign of a stroke. I was diagnosed with vertigo, given anti-nausea prescriptions and sent home that morning feeling ok. The following morning it happened again so we went back to the same emergency hospital and they wanted to transport me by ambulance (See continuation pg)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebellar stroke
Hospital-Tage: 78,0
Labordaten: November 30-Dec 1, 2021- Head Ct's, MRI, numerous blood tests, CTA Neck, US Doplr ART Carotid Bilat, EKG,Echocardiogram, bubble study. Too many tests to list see medical records
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Anastrozole, testosterone cypionate, (PRN: Zolipidem & Afrin)
Allergien: Sulfa, penicillins
Vorherige Impfungen: -

VAERS 2569483

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

schwer

Staat: OH
Alter: 73,0
Geschlecht: F
Eingang: 27.01.2023
Impfdatum: 13.10.2021
Beginn: 10.05.2022
Tage bis Beginn: 209,0
Dosis: 3
Route/Site: SYR / LA

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

Pericarditis

Symptomtext

Systemic: periocarditis-Medium, Additional Details: patient reports having instances of periocarditis starting in May of 2022. Per shot records - 3rd dose of Pfizer vaccine given 10-13-2021, and the most recent booster Pfizer Bivalent given 10-13-22

Weitere VAERSDATA-Felder

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

VAERS 2565234

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: TX
Alter: 72,0
Geschlecht: M
Eingang: 23.01.2023
Impfdatum: 04.03.2021
Beginn: 01.08.2022
Tage bis Beginn: 515,0
Dosis: 3
Route/Site: IM / RA

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

Electrocardiogram abnormal Myocarditis

Symptomtext

In January 2020, I retired and had a complete physical, head to toe. At 72 years old, I was 100% perfectly healthy. no chronic illnesses, no cancer, diabetes, NOTHING (except an enlarged prostrate). In 2020, I took the two Pfizer vaccinations, and then later had the Booster. Now (in August of 2022) at 74, after the 2 covid shots and a booster, I have been diagnosed with Myocarditis, which I NEVER had before.

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Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: EKG and completeCardiovascular workup
Aktuelle Erkrankungen: Enlarged Prostate, high PSA
Vorgeschichte: None before vaccination
Andere Medikamente: OTC Prostate med, Urinozinc
Allergien: N/A
Vorherige Impfungen: -

VAERS 2542102

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: -
Alter: 81,0
Geschlecht: M
Eingang: 23.12.2022
Impfdatum: 01.11.2021
Beginn: 23.11.2022
Tage bis Beginn: 387,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Anticoagulant therapy Atrial fibrillation Back pain Blood creatinine increased Blood culture Blood lactic acid Bundle branch block right CHA2DS2-VASc annual stroke risk high COVID-19 Chest X-ray abnormal Computerised tomogram thorax abnormal Dehydration Dyspnoea Electrocardiogram abnormal Full blood count abnormal Haemoglobin decreased Illness

Symptomtext

Assessment and Plan Patient is a 82 y.o. male patient of CNP with history of CAD s/p multiple stents, type 2 diabetes not on medications, hypertension, and hyperlipidemia who presented to the ED with a chief complaint of upper back pain and probably minimal shortness of breath. In the ED, the patient was in A. fib with RVR and heart rate 130-150. The patient was found to have AKI, leukocytosis, and x-ray of the chest showed pneumonia. He reports that he started to feel sick and tested positive for COVID and influenza A on 11/22/2022. The patient was started on oseltamivir on that day. Sepsis Present on admission: yes Etiology: Pneumonia SIRS criteria: Heart rate greater than 90, WBC greater than 12,000, less than 4,000, or greater than 10% bands Evidence of end organ damage: none Initial lactic acid: 1.9 Repeat lactic acid: N/A Current antibiotic regimen: Ceftriaxone and azithromycin Culture data: Blood and urine cultures ordered Vasopressors/steroids: none Initial sepsis checklist: ? Lactate ordered ??? ? Blood cultures obtained ??? ? Antibiotics initiated ??? ? IV fluids per sepsis protocol ??? Community-acquired pneumonia COVID-19 positive test (U07.1, COVID-19) with Acute Pneumonia (J12.89, Other viral pneumonia) Influenza pneumonia Leukocytosis CBC reviewed, shows leukocytosis XR chest reviewed, showed right mid and lower lobe pneumonia The patient reports positive COVID and influenza a test that were done on 11/22/2022. Repeat tests here showed positive COVID and negative influenza. The patient was started on Tamiflu once a day. Increase it to twice a day. Discontinue since influenza is negative Consult ID. Legionella and strept antigens negative CT chest showed consolidation that needs follow up for clearance. Also multiple pulmonary nodules that need follow up. Ceftriaxone and azithromycin Discharge on cefdinir Atrial fibrillation with RVR, resolved Hypertension CAD s/p multiple stents The patient presented with A. fib and RVR. EKG reviewed, shows A. fib and incomplete right bundle branch block. The patient was started on Cardizem drip in the ED and heart rate improved. The patient is on metoprolol tartrate 25 mg twice daily. Continue this medicine. Suspect the A. fib is due to acute illness and pneumonia. Consult cardiology for new onset A. Fib Heparin drip. The patient will need anticoagulation due to high CHA2DS2-VASc score (diabetic, CAD, hypertensive, age 82). Discharge the patient on Eliquis 5 mg twice daily Cardiology recommended increasing the dose of beta-blockers. We will switch him to long-acting metoprolol twice daily. Discontinued cardizem drip Outpatient echo as per cardiology recommendation Type 2 diabetes The patient is not on medications at home Sliding scale insulin while in the hospital AKI on CKD stage III, improving Creatinine was 1.2 about a month ago BMP reviewed, creatinine on presentation 1.63 The patient is clinically dehydrated. Started sepsis fluids protocol. Daily BMP Normocytic anemia No evident blood loss at this time. Hemoglobin drop after sepsis IV fluids. Possible dilutional. Continue to monitor If not resolved, outpatient evaluation and management Pulmonary nodules Outpatient evaluation Will need CT scan to confirm resolution of consolidation

Weitere VAERSDATA-Felder

Praegender Schweregrund: CHA2DS2-VASc annual stroke risk high
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2533447

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: IL
Alter: 70,0
Geschlecht: F
Eingang: 15.12.2022
Impfdatum: 12.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 16,0
Dosis: 3
Route/Site: IM / -

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

Dysarthria Fall Haemorrhagic stroke Lower limb fracture Magnetic resonance imaging head abnormal Mobility decreased Musculoskeletal disorder Paralysis

Symptomtext

about 3 weeks later, I noticed about the 28th of the month, I noticed that her speech started slurring, and it didnt get better, or worst. And that was the sign of a hemorrage (stroke) With in a few days later, the right one was totally paryalized and she couldnt make a fist. Her right leg started turning inward, she could not raise her leg. She took a fall a few days later, and ended up with a fracture in her leg. Her right side of the body was effected. The Neurologist showed the effects of the brain. A year later, shes making progress, but she still has effects from the stroke. MRI showed stroke as a 5 on a scale of 1 - 10. Her speech is not all the way back. She is a fall risk. I have had to spend 1000.00 out of pocket for someone to help with her. She has had falls due to this.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Haemorrhagic stroke
Hospital-Tage: -
Labordaten: Taken at outpatient and neurologist ordered mri
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Levothyroxine 25 mcg 1/day, Primidone 3/day 250 mg, Phenytoin 100mg 3/day.
Allergien: None
Vorherige Impfungen: -

VAERS 2528417

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: PA
Alter: 12,0
Geschlecht: F
Eingang: 10.12.2022
Impfdatum: 11.10.2021
Beginn: 04.01.2022
Tage bis Beginn: 85,0
Dosis: 2
Route/Site: IM / UN

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

Blood test normal Electrocardiogram normal Electroencephalogram normal Epilepsy Laboratory test normal Seizure Syncope

Symptomtext

Seizures/Epilepsy Fainting Spells

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Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: All normal Brain tests-EEG EKG?s Blood tests
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Smarty-pants vitamins
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2527353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: PA
Alter: 12,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 11.10.2021
Beginn: 04.01.2022
Tage bis Beginn: 85,0
Dosis: 2
Route/Site: - / -

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

Blood test Electrocardiogram Electroencephalogram Magnetic resonance imaging head Seizure

Symptomtext

Seizures; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). A 13-year-old female patient received BNT162b2 (BNT162B2), on 11Oct2021 as dose 2, single (Lot number: FE3590) at the age of 12 years for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (COVID-19 Vaccine: Dose 1, Manufacturer: Pfizer, Date: 20Sep2021, Time: 17:30 (Evening), LOT: FF2587, EXP: unknown, NDC: Unknown, Dose and Route: Unknown, Facility: (Hospital name)), administration date: 20Sep2021, when the patient was 12-year-old, for COVID-19 immunization. The following information was reported: SEIZURE (hospitalization, medically significant) with onset 04Jan2022, outcome "recovered" (16Jan2022), described as "Seizures". The patient was hospitalized for seizure (start date: 04Jan2022, discharge date: 05Jan2022, hospitalization duration: 2 day(s)). The event "seizures" required emergency room visit. The patient underwent the following laboratory tests and procedures: Blood test: Negative, notes: Everything has been negative; Electrocardiogram: Negative, notes: Everything has been negative; Electroencephalogram: Negative, notes: Everything has been negative; Magnetic resonance imaging head: Negative, notes: Everything has been negative. Therapeutic measures were taken as a result of seizure. Clinical information: Reported that, Reporter Wants to report that her daughter, the patient, had her vaccines, she had two doses. Ever since the last dose, patient has been getting seizures. Hasn't had time to report. Was going to do it on the computer, but it is hard to report on the computer. The Pediatrician did the thing to report it. Patient had second COVID-19 Vaccine around 14:00 to 15:00 on 11Oct2021. First seizure date was reported as 04Jan2022. Patient had two more seizures on 16Jan2022. Since then, patient has been seizure free. Has been on anti-seizure medication since 16Jan2022. Reporter did not provide product name of anti-seizure medication. Treatment included, for both seizure events patient was at the ER. Was admitted to the hospital after the first seizures on 04Jan2022. Patient had EEG of the head, everything was negative. Ever since then has had other outpatient EEGs as well. There's no recent activity of that. Patient never had seizures as a child. Asked if she needed to call and report to this other number, (Phone number). Advised reporter this number was not in this agent's resources. Advised reporter to use her own discretion to call that number and report. No Prior Vaccinations within 4 weeks. No other vaccines after 20Sep2021 besides second dose COVID-19 Vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: 2,0
Labordaten: Test Name: Bloodwork; Test Result: Negative ; Comments: Everything has been negative; Test Name: EKG of heart; Test Result: Negative ; Comments: Everything has been negative; Test Name: EEG of the head; Test Result: Negative ; Comments: Everything has been negative; Test Name: MRIs of the brain; Test Result: Negative ; Comments: Everything has been negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2428460

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: ND
Alter: 13,0
Geschlecht: F
Eingang: 03.09.2022
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Abdominal pain upper Ageusia Body temperature Catatonia Central nervous system inflammation Confusional state Fatigue Malaise Musculoskeletal disorder Nasopharyngeal swab Nausea Oropharyngeal pain Pyrexia SARS-CoV-2 antibody test Seizure Selective mutism Syncope Tic

Symptomtext

convulsions; fainting episodes/fainting spells; inflammation to her nervous system resulted from that massive immunological response; Tourette's; sore throat; stomach pain; confusion (wandering off and getting lost in a winter storm); loss of taste; lost use of her arm she got the shot in for a long time; tics; catatonic episodes; selective mutism; fatigue; mild fever; nausea; became so ill she couldn't leave bed; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 13-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 12Oct2021 as dose 2, single (Lot number: FE3590) at the age of 13 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Migraines" (unspecified if ongoing); "Insomnia" (unspecified if ongoing); "Asthma" (unspecified if ongoing); "Allergies" (unspecified if ongoing); "known allergies: Peanut" (unspecified if ongoing); "known allergies: egg" (unspecified if ongoing); "known allergies: other nuts" (unspecified if ongoing); "known allergies: latex" (unspecified if ongoing). The patient took concomitant medications. Past drug history included: Amoxicillin, reaction(s): "known allergies: Amoxicillin". Vaccination history included: BNT162b2 (Dose Number: 1, Single, Batch/Lot No: FF2587, Location of injection: Arm Left), administration date: 21Sep2021, when the patient was 13-year-old, for COVID-19 immunization. The following information was reported: TOURETTE'S DISORDER (disability, medically significant) with onset 12Oct2021, outcome "not recovered", described as "Tourette's"; MALAISE (disability) with onset 12Oct2021, outcome "not recovered", described as "became so ill she couldn't leave bed"; CATATONIA (disability) with onset 12Oct2021, outcome "not recovered", described as "catatonic episodes"; CONFUSIONAL STATE (disability) with onset 12Oct2021, outcome "not recovered", described as "confusion (wandering off and getting lost in a winter storm)"; SEIZURE (disability, medically significant) with onset 12Oct2021, outcome "not recovered", described as "convulsions"; SYNCOPE (disability, medically significant) with onset 12Oct2021, outcome "not recovered", described as "fainting episodes/fainting spells"; FATIGUE (disability) with onset 12Oct2021, outcome "not recovered"; CENTRAL NERVOUS SYSTEM INFLAMMATION (disability, medically significant) with onset 12Oct2021, outcome "not recovered", described as "inflammation to her nervous system resulted from that massive immunological response"; AGEUSIA (disability) with onset 12Oct2021, outcome "not recovered", described as "loss of taste"; MUSCULOSKELETAL DISORDER (disability) with onset 12Oct2021, outcome "not recovered", described as "lost use of her arm she got the shot in for a long time"; PYREXIA (disability) with onset 12Oct2021, outcome "not recovered", described as "mild fever"; NAUSEA (disability) with onset 12Oct2021, outcome "not recovered"; SELECTIVE MUTISM (disability) with onset 12Oct2021, outcome "not recovered"; OROPHARYNGEAL PAIN (disability) with onset 12Oct2021, outcome "not recovered", described as "sore throat"; ABDOMINAL PAIN UPPER (disability) with onset 12Oct2021, outcome "not recovered", described as "stomach pain"; TIC (disability) with onset 12Oct2021, outcome "not recovered", described as "tics". The events "convulsions", "fainting episodes/fainting spells", "inflammation to her nervous system resulted from that massive immunological response", "tourette's", "became so ill she couldn't leave bed", "sore throat", "stomach pain", "nausea", "confusion (wandering off and getting lost in a winter storm)", "fatigue", "mild fever", "loss of taste", "lost use of her arm she got the shot in for a long time", "tics", "catatonic episodes" and "selective mutism" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: Body temperature: (unspecified date) mild; Nasopharyngeal swab: (unspecified date) Negative; (15Oct2021) Negative; SARS-CoV-2 antibody test: (unspecified date) She has more Covid antibodies than anyone else. Therapeutic measures were taken as a result of seizure, syncope, central nervous system inflammation, tourette's disorder, malaise, oropharyngeal pain, abdominal pain upper, nausea, confusional state, fatigue, pyrexia, ageusia, musculoskeletal disorder, tic, catatonia, selective mutism. Clinical course: The patient did not receive any other vaccine in last four weeks at the time of report. The patient received unspecified multiviatamin in two weeks as of reporting. It was reported that first, hours after the vaccine she became so ill she could not leave bed (sore throat, stomach pain, nausea, confusion, fatigue, mild fever, loss of taste) but she tested negative twice for Covid. She lost use of her arm she got the shot in for a long time and had to do physical therapy for months. She had ER visits for tics and convulsions, confusion (wandering off and getting lost in a winter storm), and fainting episodes. Not too long after the vaccine injury, they sent her to a specialist who checked her blood for Covid antibodies. He literally said "She has more Covid antibodies than anyone else." The neurologist believes that inflammation to her nervous system resulted from that massive immunological response to the vaccine. The tics have now settled into a diagnosis of Tourette's, and she's also been diagnosed now with catatonic episodes/fainting spells and selective mutism. She's finally getting in to be seen by the experts at the Clinic in a month.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Test Name: Fever; Result Unstructured Data: Test Result:mild; Test Name: Nasal Swab; Test Result: Negative ; Test Date: 20211015; Test Name: Nasal Swab; Test Result: Negative ; Test Name: Covid antibodies; Result Unstructured Data: Test Result:She has more Covid antibodies than anyone else
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Allergy to nuts; Asthma; Egg allergy; Insomnia; Latex allergy; Migraine; Peanut allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2425089

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: OH
Alter: 47,0
Geschlecht: F
Eingang: 31.08.2022
Impfdatum: 23.09.1921
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / RA

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

Condition aggravated Seizure

Symptomtext

Patient has had seizures since 2009. Admitted to Epilelpsy Monitoring Unit for seizure characterization.

Weitere VAERSDATA-Felder

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

VAERS 2331768

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: GA
Alter: 18,0
Geschlecht: M
Eingang: 24.06.2022
Impfdatum: 15.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: IM / LA

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

Autopsy Congenital coronary artery malformation Histology abnormal Myocarditis SARS-CoV-2 test negative Syncope Toxicologic test normal

Symptomtext

Witnesses collapse

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: autopsy on 25 OCT 2021: Negative toxicology, negative COVID-19 testing by RT-PCR on FFPE tissue, myocarditis identified on histology of the heart. Anomalous left coronary artery from the right sinus of valsalva identified on gross exam of the heart, previously not diagnosed.
Aktuelle Erkrankungen: None
Vorgeschichte: Anomalous left coronary artery from the right sinus of Valsalva
Andere Medikamente: None
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2019934

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: IN
Alter: 42,0
Geschlecht: F
Eingang: 23.06.2022
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Antinuclear antibody negative Blood creatine phosphokinase normal Blood magnesium normal Blood test normal Blood thyroid stimulating hormone normal Autonomic nervous system imbalance Bone pain Burning sensation Cyanosis Electric shock sensation Brain natriuretic peptide normal C-reactive protein normal Chest pain Condition aggravated Fibrin D dimer normal Fluid retention Full blood count normal Gait disturbance

Symptomtext

Nerve/vein pain bottom of left foot; Nerve/vein pain bottom of left foot; unable to walk for 2 days; Burning backs of legs, like shards of glass in veins, sometimes like chemical acid feeling; hard rigid muscles; Burning around neck veins; Pulsating temple veins; Bulging veins in feet; Electrical shock zap sensations in left leg; Spasms leg muscles; Sternum pain and tenderness; Sensation backs of legs would explode from pressure; Hamstring area severe nerve pain; Swelling/edema legs; Swelling/edema legs; Sensation of pinching in and rubber band feeling around leg muscles; Buttock pain both sides; Tachycardia; Livedo reticularis on legs and cyanosis of feet; Livedo reticularis on legs and cyanosis of feet; diagnosis - suspected small fiber neuropathy and autonomic dysfunction; diagnosis - suspected small fiber neuropathy and autonomic dysfunction; dose 1, Drug Start date : 31Aug2021/dose 2, Drug Start date : 12Oct2021; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 12Oct2021 at 16:00 as dose 2, single (Lot number: FE3590) at the age of 42 years, in left arm for covid-19 immunization. The patient's relevant medical history included: "Known allergies: Sulfa" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (Dose Number: 1,SINGLE, Lot No: EW0173, Arm Left, 12:00 PM), administration date: 31Aug2021, when the patient was 42-year-old, for COVID-19 immunization, reaction(s): "Noticeable heart beat in stomach", "Deep pain in hamstring area", "Sciatic pain", "Pain/tender back of head"; BNT162b2 (Dose Number: 1,SINGLE, Lot No: EW0173, Arm Left, 12:00 PM), administration date: 31Aug2021, when the patient was 42--old, for COVID-19 immunization, reaction(s): "Chest rash". The following information was reported: INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious) with onset 12Oct2021, outcome "unknown", described as "dose 1, Drug Start date : 31Aug2021/dose 2, Drug Start date : 12Oct2021"; VEIN DISORDER (non-serious) with onset 13Oct2021, outcome "unknown", described as "Bulging veins in feet"; NECK PAIN (non-serious) with onset 13Oct2021, outcome "unknown", described as "Burning around neck veins"; BURNING SENSATION (non-serious) with onset 13Oct2021, outcome "unknown", described as "Burning backs of legs, like shards of glass in veins, sometimes like chemical acid feeling"; MUSCULOSKELETAL PAIN (non-serious) with onset 13Oct2021, outcome "unknown", described as "Buttock pain both sides"; ELECTRIC SHOCK SENSATION (non-serious) with onset 13Oct2021, outcome "unknown", described as "Electrical shock zap sensations in left leg"; NEURALGIA (non-serious) with onset 13Oct2021, outcome "unknown", described as "Hamstring area severe nerve pain"; LIVEDO RETICULARIS (non-serious), CYANOSIS (non-serious) all with onset 13Oct2021, outcome "unknown" and all described as "Livedo reticularis on legs and cyanosis of feet"; PAIN IN EXTREMITY (non-serious), NEURALGIA (non-serious) all with onset 13Oct2021, outcome "unknown" and all described as "Nerve/vein pain bottom of left foot"; SENSATION OF BLOOD FLOW (non-serious) with onset 13Oct2021, outcome "unknown", described as "Pulsating temple veins"; LIMB DISCOMFORT (non-serious) with onset 13Oct2021, outcome "unknown", described as "Sensation backs of legs would explode from pressure"; MUSCLE DISCOMFORT (non-serious) with onset 13Oct2021, outcome "unknown", described as "Sensation of pinching in and rubber band feeling around leg muscles"; MUSCLE SPASMS (non-serious) with onset 13Oct2021, outcome "unknown", described as "Spasms leg muscles"; BONE PAIN (non-serious) with onset 13Oct2021, outcome "unknown", described as "Sternum pain and tenderness"; PERIPHERAL SWELLING (non-serious), OEDEMA PERIPHERAL (non-serious) all with onset 13Oct2021, outcome "unknown" and all described as "Swelling/edema legs"; TACHYCARDIA (non-serious) with onset 13Oct2021, outcome "unknown"; SMALL FIBRE NEUROPATHY (non-serious), AUTONOMIC NERVOUS SYSTEM IMBALANCE (non-serious) all with onset 13Oct2021, outcome "unknown" and all described as "diagnosis - suspected small fiber neuropathy and autonomic dysfunction"; MUSCLE RIGIDITY (non-serious) with onset 13Oct2021, outcome "unknown", described as "hard rigid muscles"; GAIT INABILITY (non-serious) with onset 13Oct2021, outcome "recovered" (15Oct2021), described as "unable to walk for 2 days". Sender's Comments: Linked Report(s) : US-PFIZER INC-202200851441 same patient/ drug, different dose/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sulfonamide allergy.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2019934

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: IN
Alter: 42,0
Geschlecht: F
Eingang: 23.06.2022
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Antinuclear antibody negative Blood creatine phosphokinase normal Blood magnesium normal Blood test normal Blood thyroid stimulating hormone normal Autonomic nervous system imbalance Bone pain Burning sensation Cyanosis Electric shock sensation Brain natriuretic peptide normal C-reactive protein normal Chest pain Condition aggravated Fibrin D dimer normal Fluid retention Full blood count normal Gait disturbance

Symptomtext

Nerve/vein pain bottom of left foot; Nerve/vein pain bottom of left foot; unable to walk for 2 days; Burning backs of legs, like shards of glass in veins, sometimes like chemical acid feeling; hard rigid muscles; Burning around neck veins; Pulsating temple veins; Bulging veins in feet; Electrical shock zap sensations in left leg; Spasms leg muscles; Sternum pain and tenderness; Sensation backs of legs would explode from pressure; Hamstring area severe nerve pain; Swelling/edema legs; Swelling/edema legs; Sensation of pinching in and rubber band feeling around leg muscles; Buttock pain both sides; Tachycardia; Livedo reticularis on legs and cyanosis of feet; Livedo reticularis on legs and cyanosis of feet; diagnosis - suspected small fiber neuropathy and autonomic dysfunction; diagnosis - suspected small fiber neuropathy and autonomic dysfunction; dose 1, Drug Start date : 31Aug2021/dose 2, Drug Start date : 12Oct2021; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 12Oct2021 at 16:00 as dose 2, single (Lot number: FE3590) at the age of 42 years, in left arm for covid-19 immunization. The patient's relevant medical history included: "Known allergies: Sulfa" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (Dose Number: 1,SINGLE, Lot No: EW0173, Arm Left, 12:00 PM), administration date: 31Aug2021, when the patient was 42-year-old, for COVID-19 immunization, reaction(s): "Noticeable heart beat in stomach", "Deep pain in hamstring area", "Sciatic pain", "Pain/tender back of head"; BNT162b2 (Dose Number: 1,SINGLE, Lot No: EW0173, Arm Left, 12:00 PM), administration date: 31Aug2021, when the patient was 42--old, for COVID-19 immunization, reaction(s): "Chest rash". The following information was reported: INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious) with onset 12Oct2021, outcome "unknown", described as "dose 1, Drug Start date : 31Aug2021/dose 2, Drug Start date : 12Oct2021"; VEIN DISORDER (non-serious) with onset 13Oct2021, outcome "unknown", described as "Bulging veins in feet"; NECK PAIN (non-serious) with onset 13Oct2021, outcome "unknown", described as "Burning around neck veins"; BURNING SENSATION (non-serious) with onset 13Oct2021, outcome "unknown", described as "Burning backs of legs, like shards of glass in veins, sometimes like chemical acid feeling"; MUSCULOSKELETAL PAIN (non-serious) with onset 13Oct2021, outcome "unknown", described as "Buttock pain both sides"; ELECTRIC SHOCK SENSATION (non-serious) with onset 13Oct2021, outcome "unknown", described as "Electrical shock zap sensations in left leg"; NEURALGIA (non-serious) with onset 13Oct2021, outcome "unknown", described as "Hamstring area severe nerve pain"; LIVEDO RETICULARIS (non-serious), CYANOSIS (non-serious) all with onset 13Oct2021, outcome "unknown" and all described as "Livedo reticularis on legs and cyanosis of feet"; PAIN IN EXTREMITY (non-serious), NEURALGIA (non-serious) all with onset 13Oct2021, outcome "unknown" and all described as "Nerve/vein pain bottom of left foot"; SENSATION OF BLOOD FLOW (non-serious) with onset 13Oct2021, outcome "unknown", described as "Pulsating temple veins"; LIMB DISCOMFORT (non-serious) with onset 13Oct2021, outcome "unknown", described as "Sensation backs of legs would explode from pressure"; MUSCLE DISCOMFORT (non-serious) with onset 13Oct2021, outcome "unknown", described as "Sensation of pinching in and rubber band feeling around leg muscles"; MUSCLE SPASMS (non-serious) with onset 13Oct2021, outcome "unknown", described as "Spasms leg muscles"; BONE PAIN (non-serious) with onset 13Oct2021, outcome "unknown", described as "Sternum pain and tenderness"; PERIPHERAL SWELLING (non-serious), OEDEMA PERIPHERAL (non-serious) all with onset 13Oct2021, outcome "unknown" and all described as "Swelling/edema legs"; TACHYCARDIA (non-serious) with onset 13Oct2021, outcome "unknown"; SMALL FIBRE NEUROPATHY (non-serious), AUTONOMIC NERVOUS SYSTEM IMBALANCE (non-serious) all with onset 13Oct2021, outcome "unknown" and all described as "diagnosis - suspected small fiber neuropathy and autonomic dysfunction"; MUSCLE RIGIDITY (non-serious) with onset 13Oct2021, outcome "unknown", described as "hard rigid muscles"; GAIT INABILITY (non-serious) with onset 13Oct2021, outcome "recovered" (15Oct2021), described as "unable to walk for 2 days". Sender's Comments: Linked Report(s) : US-PFIZER INC-202200851441 same patient/ drug, different dose/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sulfonamide allergy.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2287516

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: CO
Alter: 68,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 08.10.2021
Beginn: 24.12.2021
Tage bis Beginn: 77,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy COVID-19 Dyspnoea Influenza Influenza A virus test positive Malaise Nausea Presyncope Productive cough SARS-CoV-2 test positive

Symptomtext

Pfizer COVID-19 Vaccine EUA: patient reported with malaise, presyncope, productive cough, dyspnea, and nausea. Found to have AHRF due to COVID-19 and influenza A. Received steroids, oxygen, and supportive measures. Discharged home medically stable with supplemental oxygen, steroids, and anticoagulation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: 2,0
Labordaten: SARS-COV-2: positive; Influenza A: positive
Aktuelle Erkrankungen: none reported
Vorgeschichte: sarcoidosis, Sjogrens syndrome, GERD
Andere Medikamente: albuterol, metformin, atorvastatin, diclofenac topical, duloxetine, econazole topical, fluticasone inhaler, gabapentin, guaifenesin, lidocaine patch, meloxicam, metformin, mirabegron, nitrofurantoin, nystatin powder, omeprazole, tacrolimus,
Allergien: penicillin, fish, nuts
Vorherige Impfungen: -

VAERS 2278376

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: MO
Alter: 88,0
Geschlecht: F
Eingang: 16.05.2022
Impfdatum: 24.02.2021
Beginn: 11.05.2022
Tage bis Beginn: 441,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Syncope

Symptomtext

Admitted to hospital with dizziness and fainting on 05/11/2022.

Weitere VAERSDATA-Felder

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

VAERS 2269050

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: AZ
Alter: 85,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 03.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain upper Asthenia Computerised tomogram thorax abnormal Dyspnoea Fatigue Hypotension Loss of consciousness Malaise Musculoskeletal disorder Nausea Pulmonary thrombosis Syncope Weight decreased

Symptomtext

Starting day 2 of receiving 2nd dose severe nausea, stomach pain, overall weakness, fatigue, shortness of breath, which carried on for months. PCP gave her ondansetron for nausea, then took her off ondansetron and replaced with famitodine. Nothing truly was helping things just continued. I, finally emailed her pcp and requested a referral for a Gastroenterologist due to all that's been going on and the weight loss. We finally had an appt. on April 4, 2022, He wanted to do a endoscopy. That afternoon after arriving home from the Dr. She was on the toilet and had a synchopy episode and was slumped over on the toilet, but was able to ring her medic alarm to alert me. We got her back to bed, blood pressure was low, she was alert and just kept saying I don't feel well, got her electrolite water and stayed by her side till her blood pressure raised to a normal level. Approx. a half hour later, her medic alert went off again, slumped on the toilet again but unconscious I checked her pulse and heartbeat, she was breathing, then she shook a moment with eyes wide open and could not hear me I had to yell, she came around when my son was on the phone with 911, they came and took her to the hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: CT Scan found blood clots in her lungs! no answers as to how or why they appeared
Aktuelle Erkrankungen: None
Vorgeschichte: have 1 stent 2009, Gurd, occipital neuropathy.
Andere Medikamente: Metaprolol 50 mg, Pravastatin, Oxycodone 5mg, vitamin D3, Horizant 600mg., famitodine 20mg
Allergien: sulfa, plavix
Vorherige Impfungen: -

VAERS 2254549

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 27.01.2021
Beginn: 25.04.2022
Tage bis Beginn: 453,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Hypoxia Intensive care Positive airway pressure therapy SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st vaccine received on 12/30/2020. 68 y/o female with PMHx of OSA, COPD, GERD, HTN, DM, Kidney stones, CHF, Dysphagia, complicated UTI with MDRO pseudomonas and ecoli presents from Inpatient rehab with Hypoxia requiring transfer to ICU on bipap at 80% FIO2. Pt treated with IV ABX, Remdesivir and steroids.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: SARS CoV2 PCR Covid19-Detected on 04/25/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Kidney stones, OSA, GERD, DM, HTN, COPD, Anemia, MDRO Pseudomonas UTI, CHF, Dysphagia
Andere Medikamente: -
Allergien: Clindamycin, Shellfish, Spinach
Vorherige Impfungen: -

VAERS 2228789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3590

schwer

Staat: GA
Alter: 39,0
Geschlecht: F
Eingang: 12.04.2022
Impfdatum: 28.10.2021
Beginn: 06.11.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Ataxia CSF cell count normal CSF protein increased Endotracheal intubation Guillain-Barre syndrome Headache Immunoglobulin therapy Intensive care Lumbar puncture Neurological symptom Pain Paraesthesia Plasmapheresis Polymerase chain reaction

Symptomtext

Patient reported to the emergency department on 11/10/2021 with multiple neurological symptoms including paresthesis, weakness, ataxic gait, pain, and headache with symptoms prior to admission starting 11/06/2021. Patient was admitted to the ICU with Acute Inflammatory Demylenating Polyradiculopathy (AIDP). Treatment included gabapentin and IVIG treatment 11/11/2021 - 11/16/2021. Patient intubated from 11/15/2021-11/19/2021. Additional treatment included PLEX (plasmapheresis) therapy 11/16/2021-11/23/2021 . Patient was discharged to an acute rehabilitation facility on 12/1/21. Noted doing well clinically with ongoing weakness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 21,0
Labordaten: LP on 11/11/2021 showed normal cells and high protein. Meningitis/encephalopathy PCR test on 11/11/2021 was negative.
Aktuelle Erkrankungen: Severe acute headache
Vorgeschichte: Breast Cancer s/p mastectomy
Andere Medikamente: Anastrazole, Vitamin D2, tramadol
Allergien: NKA
Vorherige Impfungen: -

VAERS 2206719

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: TN
Alter: 74,0
Geschlecht: M
Eingang: 30.03.2022
Impfdatum: 21.10.2021
Beginn: 09.01.2022
Tage bis Beginn: 80,0
Dosis: 3
Route/Site: SYR / -

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

Anticoagulant therapy COVID-19 Dyspnoea Gastrointestinal haemorrhage Leukocytosis Oedema peripheral Pelvic venous thrombosis Procalcitonin increased Red blood cell transfusion Ultrasound Doppler abnormal White blood cell count increased

Symptomtext

Diagnosed with covid and presented to ED with labored respirations, and edema of both lower extremities. Started on IV heparin by continuous infusion. Completed Remdesivir. GI bleed, and 1 unite of PRBC transfused. Family requested hospice care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pelvic venous thrombosis
Hospital-Tage: 14,0
Labordaten: USG of lower extremities revealed DVT of iliac veins bilaterally. WBC elevated at 20,400. Procalcitonin elavated and leukocytosis.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2074786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3590

schwer

Staat: ME
Alter: 32,0
Geschlecht: F
Eingang: 19.03.2022
Impfdatum: 08.10.2021
Beginn: 14.01.2022
Tage bis Beginn: 98,0
Dosis: 1
Route/Site: IM / LA

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

Blood fibrinogen Delivery Exposure during pregnancy Intensive care

Symptomtext

I was 7 months pregnant when I received the first dose of the vaccine. My son was born normal term with a VERY rare bleeding disorder with no family history and a heterzygous gene mutation (indicating disease was not inherited). He was diagnosed with Factor 1 deficiency. We were hospitalized Medical center in NICU for 29 days and currently are followed by Children's Cancer care and hematology clinic. We have all documentation and I'm just not sure who to reach out to notify CDC. I am currently a nurse practitioner at cancer care and hematology clinic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: fibrinogen assay? not sure what to write here.
Aktuelle Erkrankungen: none
Vorgeschichte: newborn born with rare bleeding disorder after I (mother) received covid vaccine while pregnant, no family history
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2074786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: ME
Alter: 32,0
Geschlecht: F
Eingang: 19.03.2022
Impfdatum: 08.10.2021
Beginn: 14.01.2022
Tage bis Beginn: 98,0
Dosis: 1
Route/Site: IM / RA

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

Blood fibrinogen Delivery Exposure during pregnancy Intensive care

Symptomtext

I was 7 months pregnant when I received the first dose of the vaccine. My son was born normal term with a VERY rare bleeding disorder with no family history and a heterzygous gene mutation (indicating disease was not inherited). He was diagnosed with Factor 1 deficiency. We were hospitalized Medical center in NICU for 29 days and currently are followed by Children's Cancer care and hematology clinic. We have all documentation and I'm just not sure who to reach out to notify CDC. I am currently a nurse practitioner at cancer care and hematology clinic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: fibrinogen assay? not sure what to write here.
Aktuelle Erkrankungen: none
Vorgeschichte: newborn born with rare bleeding disorder after I (mother) received covid vaccine while pregnant, no family history
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2162110

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: CO
Alter: 46,0
Geschlecht: F
Eingang: 06.03.2022
Impfdatum: 11.02.2021
Beginn: 01.08.2021
Tage bis Beginn: 171,0
Dosis: 4
Route/Site: IM / LA

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

Abdominal pain upper Blood creatine increased Blood gases Blood glucose increased Blood potassium decreased Blood sodium decreased Computerised tomogram head Confusional state Diabetic ketoacidosis Differential white blood cell count Full blood count Glycosylated haemoglobin increased Headache Intensive care Metabolic acidosis Metabolic function test Metamorphopsia Type 1 diabetes mellitus

Symptomtext

Abrupt onset DKA and new diagnosis of type 1 diabetes. Symptoms: confusion, headache, stomachache, blurry distorted vision. Went to ER, diagnosed with type 1 diabetes. No family history of type 1 only type 2. Admitted to ICU in severe metabolic acidosis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 3,0
Labordaten: 8/1/2021: CT scan head, VBG, CBC diff, Metabolic panel, POCT glucose = 455, A1C = 13.5, low potassium & sodium, elevated creatinine, urinalysis positive for ketones
Aktuelle Erkrankungen: Might have had covid in March 2000, but antibody tests were negative. I don?t know.
Vorgeschichte: Crohn?s disease, sleep apnea
Andere Medikamente: Stelara, norco, bupropion, fluoxetine, rhinocort, clonazepam
Allergien: Augmentin
Vorherige Impfungen: -

VAERS 2151095

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

schwer

Staat: OH
Alter: 32,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 18.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / AR

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

Asthma Facial paralysis Gait disturbance

Symptomtext

Systemic: difficulty walking, facial droop and worsening asthma-Moderate, Additional Details: Patient has experienced difficulty walking, facial droop, and worsening asthma. Symptoms presented 4 days after injection. Patient states she was admitted to hospital and has since been discharged. Unclear how many days the patient was in the hospital or diagnosis as patient is a poor historian, but she states she has follow up doctor appointments. Patient's symptoms are ongoing.

Weitere VAERSDATA-Felder

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

VAERS 2137260

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: WI
Alter: 72,0
Geschlecht: F
Eingang: 24.02.2022
Impfdatum: 25.10.2021
Beginn: 03.02.2022
Tage bis Beginn: 101,0
Dosis: 3
Route/Site: SYR / LA

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

Injury Mobility decreased Road traffic accident Thrombosis Vascular test X-ray

Symptomtext

I felt fine after the injection but months later I had a car accident & was banged up pretty bad & i couldn't move around much after the wreck and now i have blood clot in my left knee.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Xrays Vascular Test
Aktuelle Erkrankungen: None
Vorgeschichte: High Cholesterol Arthritis
Andere Medikamente: Rosuvastatin Vitamin D Baby Aspirin
Allergien: None
Vorherige Impfungen: -

VAERS 2102345

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: OK
Alter: 46,0
Geschlecht: M
Eingang: 10.02.2022
Impfdatum: 22.09.2021
Beginn: 22.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Chest pain Decreased appetite Dizziness Fatigue Hyperhidrosis Injection site pain Loss of consciousness Muscle spasms Nausea Pain Palpitations Pyrexia

Symptomtext

Extreme heart palpatations. Sweat, fever, dizziness, blackout (unconcious), chest pain, nausea, loss of appitite, burning in chest and injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None Visited alternative health professional and diagnosis was toxin still in my system causing continued fatigue and muscle cramping and soreness.
Aktuelle Erkrankungen: NA
Vorgeschichte: Chronic Sinusitus
Andere Medikamente: NA
Allergien: NA
Vorherige Impfungen: -

VAERS 2095702

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: CA
Alter: 41,0
Geschlecht: M
Eingang: 08.02.2022
Impfdatum: 18.11.2021
Beginn: 04.02.2022
Tage bis Beginn: 78,0
Dosis: 3
Route/Site: SYR / LA

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

Bell's palsy

Symptomtext

Diagnosis of Bell's palsy

Weitere VAERSDATA-Felder

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

VAERS 2091219

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: WA
Alter: 59,0
Geschlecht: U
Eingang: 05.02.2022
Impfdatum: 18.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / RA

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

Blood pressure fluctuation Blood pressure increased Blood pressure measurement Blood test Diarrhoea Disturbance in attention Epistaxis Guillain-Barre syndrome Headache Heart rate Heart rate increased Investigation Monocytosis Oropharyngeal pain Pain Restlessness Urine abnormality

Symptomtext

Guillain Barre syndrome; I had a blood pressure impulse, 212 and then it decrease but it's fluctuated there is no consistency to my diastolic and systolic impulse; I had a blood pressure impulse, 212 and then it decrease but it's fluctuated there is no consistency to my diastolic and systolic impulse; Headache; Elevated heart rate; Total restlessness; Nose bleeding; Everywhere I had surgery or injury, I was extremely sore; Foamy urine; Real problems with concentration; Sore throat; Constant diarrhea basically really soft stool; Monocytosis; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 59 year-old patient received bnt162b2 (BNT162B2), administered in arm right, administration date 18Oct2021 18:30 (Lot number: FE3590) at the age of 59 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "cranial hemorrhage" (unspecified if ongoing), notes: cranial hemorrhage; "constant headache" (unspecified if ongoing), notes: constant headache; "COVID", start date: Feb2021 (unspecified if ongoing), notes: recovered naturally; "flu" (unspecified if ongoing), notes: had the flu twice in life. There were no concomitant medications. Vaccination history included: Influenza (vaccinated with influenza twice in life); Tetanus shot; Polio vaccine (As a baby had the polio vaccine, that was the back in normal 1960s). The patient was concern about cranial hemorrhage because of the constant headache, prior to receiving the vaccination. In Feb2021 the patient got COVID (Intent History) and recovered naturally. It was rather mild and patient blood was type O+, went to doctor 14 months later and requested to blood draw to find If the patient had the T-cells for immunity it came up negative at that time with all the research that the patient have done and some of the question the patient has asked medical doctors about that, there is the time frame where the T-cell detect in the human body and at some point they go into your bone and your bone marrow is not detectable with that further test, the patient did not seek any test at that point based on the symptoms had on February 2021, had absolute positive had headache, don't get sick, have had the flu twice in life, only been vaccinated with influenza twice in life (Further not clarified) was much younger at teen, as teenager, had one other injection, aware that has to do with tetanus shot. As a baby the patient had the polio vaccine that was the back in normal 1960s. On 18Oct2021, the patient had first dose of Pfizer and since then started acquiring a headache that is really never gone away it's has been 90 days since have seen a doctor and along with that the patient had elevated heart rate, the first morning waking after receiving approximately 6:30 in the evening the day before, had a blood pressure impulse, 212 and since then it decrease but it's fluctuated there is no consistency to diastolic and systolic impulse, total restlessness, headache, nose bleeding. Everywhere had surgery or injury was extremely sore that eventually ran away. The patient also experienced really foamy urine and real problems with concentration, started having a sore throat and headaches, constant diarrhea basically really soft stool and diarrhea combination too that has not been subsided it's has been 90 days. The doctor possibly diagnosed me with Guillain Barre syndrome and have minor monocytosis. The following information was reported: GUILLAIN-BARRE SYNDROME (medically significant) with onset Oct2021, outcome "unknown", described as "Guillain Barre syndrome"; BLOOD PRESSURE INCREASED (medically significant), BLOOD PRESSURE FLUCTUATION (medically significant) all with onset Oct2021, outcome "unknown" and all described as "I had a blood pressure impulse, 212 and then it decrease but it's fluctuated there is no consistency to my diastolic and systolic impulse"; HEADACHE (non-serious) with onset Oct2021, outcome "not recovered", described as "Headache"; HEART RATE INCREASED (non-serious) with onset Oct2021, outcome "unknown", described as "Elevated heart rate"; RESTLESSNESS (non-serious) with onset Oct2021, outcome "unknown", described as "Total restlessness"; EPISTAXIS (non-serious) with onset Oct2021, outcome "unknown", described as "Nose bleeding"; PAIN (non-serious) with onset Oct2021, outcome "unknown", described as "Everywhere I had surgery or injury, I was extremely sore"; URINE ABNORMALITY (non-serious) with onset Oct2021, outcome "unknown", described as "Foamy urine"; DISTURBANCE IN ATTENTION (non-serious) with onset Oct2021, outcome "unknown", described as "Real problems with concentration"; OROPHARYNGEAL PAIN (non-serious) with onset Oct2021, outcome "not recovered", described as "Sore throat"; DIARRHOEA (non-serious) with onset Oct2021, outcome "not recovered", described as "Constant diarrhea basically really soft stool"; MONOCYTOSIS (non-serious) with onset 2021, outcome "unknown", described as "Monocytosis". The events "guillain barre syndrome" and "headache" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: blood test: unknown results; heart rate: elevated. Therapeutic measures were not taken as a result of guillain-barre syndrome, headache, heart rate increased, blood pressure increased, blood pressure fluctuation, restlessness, epistaxis, pain, urine abnormality, disturbance in attention, oropharyngeal pain, diarrhoea, monocytosis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: Test Name: blood pressure; Result Unstructured Data: Test Result:212; Comments: had a blood pressure impulse, 212 and since then it decrease but it's fluctuated there is no consistency to diastolic and systolic impulse; Test Name: blood pressure; Result Unstructured Data: Test Result:decreases; Comments: had a blood pressure impulse, 212 and since then it decrease but it's fluctuated there is no consistency to diastolic and systolic impulse; Test Name: blood pressure; Result Unstructured Data: Test Result:fluctuated; Comments: had a blood pressure impulse, 212 and since then it decrease but it's fluctuated there is no consistency to diastolic and systolic impulse; Test Name: blood draw; Result Unstructured Data: Test Result:unknown results; Test Name: Heart rate; Result Unstructured Data: Test Result:elevated; Test Name: T-cells; Test Result: Negative ; Comments: Ihad the T-cells for immunity it came up negative at that time with all the research that I have done and some of the question I have asked medical doctors about that, there is the time frame where the T-cell detect in the human body and at some point they go into your bone and your bone marrow is not detectable with that further test
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (recovered naturally); Flu (had the flu twice in life); Headache (constant headache); Hemorrhage (cranial hemorrhage)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2052239

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

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Staat: UT
Alter: 82,0
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: 30.01.2021
Beginn: 11.12.2021
Tage bis Beginn: 315,0
Dosis: 3
Route/Site: SYR / AR

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

Blindness Cerebellar stroke Cerebral thrombosis Colectomy Haemorrhagic disorder Intestinal ischaemia Laboratory test Stoma creation Thrombosis

Symptomtext

Hemorrhagic (blood clot) related brain stroke resulting in permanent loss of vision. Then patient experienced blood clots in intestines resulting in ischemic colon which had to be removed with stoma put in its place.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebellar stroke
Hospital-Tage: 21,0
Labordaten: Many tests were done but you'll have to ask the doctor for that information.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Rosuvastin, Furosemide, Sertraline, Doxazosin, Omeprazole, Diltiazen, Donepezil, Ferrous Sulfate, Lovenox
Allergien: -
Vorherige Impfungen: -

VAERS 2050959

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

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Staat: UT
Alter: 34,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 07.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 17,0
Dosis: 3
Route/Site: IM / LA

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

Chest X-ray Chest pain Computerised tomogram thorax Dyspnoea Echocardiogram Electrocardiogram Inflammation Laboratory test Loss of personal independence in daily activities Magnetic resonance imaging heart Pericarditis

Symptomtext

10/24/21- SOB, dyspnea and right sided chest pain began see item 19 for more details

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: 10/24/21- symptoms of SOB, right sided chest pain and dyspnea began 10/26/21 - Spoke with pulmonologist and he ordered a CXR which was completed this day 10/27/21- ER visit due to severe SOB, dyspnea (unable to say name, complete a sentence) and increased chest pain - in the ER I had EKG, labs, bedside Echo, pulmonary artery CT. Discharged home with no diagnosis/ treatment (diagnosis was missed at this time) 10/31/21- symptoms continue. Doctor prescribes prednisone for symptom management 11/1/21- follow up appointment from ER with PCP . Start Ibuprofen and continue prednisone - continue prednisone through 11/5. Some symptom improvement with prednisone 11/9/21- Symptoms reappear/worsen. Prednisone reordered by doctor x3 weeks Continue high dose ibuprofen 11/30/21- Last day of Prednisone- symptoms improved but not gone 12/13/21- Symptoms of severe SOB, dyspnea and bilateral chest pain return. Doctor places order for cardiology consult with specialist and orders a STAT Echocardiogram 12/15/21- Visit with specialist. Start high dose ASA, omeprazole. bilateral chest pain. Noted inflammation on CT done in ER that was missed. Diagnosis of Pericarditis likely caused by covid vaccine in october 12/16/21- echo 12/21/21- emailed doctor as symptoms continue to worsen. Start 0.6mg colchicine 12/23/21- Cardiac MRI 1/14/22- spoke with doctor again - worsening symptoms (no significant improvement since cardiology visit in december) but now worsening SOB, dyspnea and chest pain. Will attempt to contact insurance re: Rilonacept for pericarditis 1/18/22- Chest x ray, EKG completed 1/20/22- continuing symptoms with increased SOB, dyspnea and chest pain, awaiting cardiology recommendations I work as a Nurse and have to wear a N95 at all times because of the nature of the procedures that we do. I am having substantial difficulties completing my work. I have 2 small children and at times cant read books to them, play, give baths ect. This has had a dramatic effect on my daily living. I am unable to go up a flight of stairs or take my kids for a walk in their stroller.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Nuva Ring
Allergien: Bactrim, Reglan, Sucralfate, Neomycin, Cholorohexidine
Vorherige Impfungen: -

VAERS 2048579

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

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Staat: FL
Alter: 34,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 08.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / LA

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

Electric shock sensation Formication Inflammation Paraesthesia

Symptomtext

2 weeks after my 1st dose, I began to get shooting electrical pains in my nervous system, tingling, bug crawling like sensations, and general inflammation everywhere. It felt as if the spike protein was attacking me relentlessly. The symptoms started to stop for a few days or a week at a time and came back for a few days, then went away again. As of 1 week ago (3 months later)- I now have little to no symptoms. I did not seek any treatment "officially." I used energy, frequency, and vibrational medicine. I used bio-resonance machines, radionics, etc..I believe in holistic/natural treatments. I only got the vaccine out of employer coercion. Big mistake.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Suboxone, Gabapentin
Allergien: Ceclor
Vorherige Impfungen: -

VAERS 2037957

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

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Staat: OR
Alter: 15,0
Geschlecht: M
Eingang: 15.01.2022
Impfdatum: 15.01.2022
Beginn: 15.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Fall Syncope

Symptomtext

Patient experienced a syncope fall from sitting position and fell to his left side. Pt stated being scared of needles and stated he had fainted from getting blood drawn or getting injections in the past. Pt denied any medical history or taking any medications. Pt denied trouble breathing, dizziness or any allergic reactions.

Weitere VAERSDATA-Felder

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

VAERS 2036094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE 3590

schwer

Staat: WY
Alter: 62,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Loss of consciousness

Symptomtext

LEFT OUR FACILITY FEELING FINE, HOWEVER HUSBAND CALLED LATER AND STATED THAT SHE PASSED OUT WHILE AT LUNCH. SOMEONE CALLED THE AMBULANCE AND THEY CAME BY AND CHECKED HER VITALS. CHECKED WITH HER AFTER WE RECEIVED THE CALL, PATIENT STATED SHE WAS OKAY AND JUST RESTING.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: STATED SHE HAD ALLERGIES TO IODINE, SHELLFISH, INSECT BITES
Vorherige Impfungen: PATIENT STATED THAT SHE HAS HAD REACTIONS SUCH AS THIS IN THE PAST.

VAERS 2021590

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

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Staat: CA
Alter: 65,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 07.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 20,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Cognitive disorder Dyspnoea Fatigue Feeling abnormal Infection Laboratory test Loss of consciousness Mobility decreased Multi-organ disorder Multisystem inflammatory syndrome Pyrexia Unresponsive to stimuli

Symptomtext

Two weeks after booster, experienced weakness, extreme fatigue and cognitive difficulties/brain fog. Passed out on 11/11 and taken by ambulance while non responsive, to hospital where I stayed 8 days. Transferred by ambulance to hospital where I remained for 11 days and was diagnosed with MIS-A. I was treated with antibiotics and steroids for organ involvement/infection. High fever, breathing difficulty, immobile due to weakness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 19,0
Labordaten: Various, please get from Dr.
Aktuelle Erkrankungen: none
Vorgeschichte: occ asthma prediabetes
Andere Medikamente: Nifedipine, synthroid, edarbi, bystolic, mybetrec, jardiance
Allergien: levaquin, and all statins, sulfa, penicillin, gentamycin
Vorherige Impfungen: Pfizer second dose, 3 months of side effects March 2021

VAERS 2021215

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: ME
Alter: 58,0
Geschlecht: M
Eingang: 10.01.2022
Impfdatum: 11.11.2021
Beginn: 19.12.2021
Tage bis Beginn: 38,0
Dosis: 3
Route/Site: SYR / RA

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

Pain in extremity Thrombosis

Symptomtext

One month after booster shot I got a blood clot in my right leg

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: I went to the ER on December 20, 2021 with pain in my right leg. I have a blood clot in my right leg. I found out that the blood clot could be a side effect from the booster shot.
Aktuelle Erkrankungen: Darier Disease
Vorgeschichte: -
Andere Medikamente: 10 mg citalopram, multi vitamin, fish oil,
Allergien: -
Vorherige Impfungen: -

VAERS 2001827

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: CA
Alter: 54,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 01.04.2021
Beginn: 01.05.2021
Tage bis Beginn: 30,0
Dosis: 3
Route/Site: SYR / LA

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

Back pain Breast cancer Deep vein thrombosis

Symptomtext

Shot #1: 3/11/21 - symptom: mid back pain Shot #2: 4/2/21 - symptom: mid back pain; DVT symptoms early 05/21; DVT diagnosis 05/07/21 BRCA diagnosis 09/21 Shot #3: 11/18/21 - symptom: mid back pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: per above + factor v leiden mutation result 5/2021, post DVT diagnosis
Aktuelle Erkrankungen: None known at time. Breast cancer detected within 3-4 months.
Vorgeschichte: None known at time. Patient subsequently diagnosed with homozygous factor v leiden mutation.
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1999842

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

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Staat: CO
Alter: 49,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 29.10.2021
Beginn: 12.11.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / LA

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

Angiogram normal Chest discomfort Dyspnoea Echocardiogram normal Electrocardiogram normal Full blood count normal Metabolic function test normal Myocarditis Troponin normal

Symptomtext

NEW ONSET SHORTNESS OF BREATH AND CHEST DISCOMFORT CONSISTENT WITH POST-VACCINE MYOCARDITIS. 11/12/21 - ONSET; 11/26 URGENT CARE VISIT - EKG AND CBC NORMAL; 11/30 PCP VISIT - PRESUMED MYOCARDITIS DIAGNOSIS AND CARDIOLOGY FOLLOWUP ORDERED; 11/30 CTA CHEST R/O PE, EXAM UNREMARKABLE FOR DEFECTS; INITIATED INDOMETHACIN. 12/14 ECHOCARDIOGRAM, NORMAL; 11/20 CARDIOLOGY FOLLOW UP, LEXI SCAN ORDERED FOR JANUARY. 1/3/2022 CONFIRMATION FROM PCP OF DIAGNOSIS POST-VACCINE MYOCARDITIS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: CBC 11/26 WNL; EKG 11/26 WNL; BLOODWORK INCLUDING CBC, CMP, TROPONIN 11/30 - WNL; CTA CHEST R/O PE 11/30, UNREMARKABLE ECHOCARDIGRAM 12/14, UNREMARKABLE
Aktuelle Erkrankungen: NONE
Vorgeschichte: MIGRAINE WITHOUT AURA, ANXIETY/DEPRESSION, VIT D DEFICIENCY
Andere Medikamente: FLUOXETINE, TOPIRAMATE, VALACYCLOVIR, VITAMIN D USE OF APAP/IBUPROFEN/NAPROXEN PRN
Allergien: SULFA
Vorherige Impfungen: -

VAERS 1982454

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3590

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Staat: NV
Alter: 73,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 12.10.2021
Beginn: 04.11.2021
Tage bis Beginn: 23,0
Dosis: 3
Route/Site: IM / LA

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

Blood test Chest X-ray Deep vein thrombosis Electrocardiogram Hypertension Pain in extremity Thrombosis Ultrasound scan abnormal

Symptomtext

Pain in left arm, gradually lessening, but still active. Did not seem like a muscular pain. 12/22/2021 ultra sound revealed a non-occulusive blood clot in brachial vein. High blood pressure also present. Ongoing treatment with Losartan and Xarelto. Currently waiting to see results of ongoing treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: 12/2021 Ultra sound EKG Blood panel Chest X-ray
Aktuelle Erkrankungen: n/a
Vorgeschichte: High cholesterol, Overweight
Andere Medikamente: Atorvastatin, multi vitamin, Vit C, Vit D3, Fish oil, Calcium
Allergien: n/a
Vorherige Impfungen: age 73. Covid vaccine Pfizer 2nd dose, 3/18/2021 Adverse reactions started 3/29/2021 as follows: fever, dry noe and throat, fati

VAERS 1979234

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: NY
Alter: 40,0
Geschlecht: M
Eingang: 24.12.2021
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

SYNCOPE OBSERVED AFTER 2 -3 MIN OF VACCINE ADMINISTERED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: NOT APPLICABLE
Aktuelle Erkrankungen: NO ILLENESS REPORTED
Vorgeschichte: NO CHRONIC OR LONG STANDING HEALTH CONDITION
Andere Medikamente: NO MEDICATION WAS TAKEN BY PATIENTS AT TIME OF VACCINATION
Allergien: NO ALLERGIES TO MEDICATION OR FOOD OR OTHER PRODUCT
Vorherige Impfungen: -

VAERS 1974284

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: TN
Alter: 40,0
Geschlecht: M
Eingang: 23.12.2021
Impfdatum: 07.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

Chills Dizziness Fall Fatigue Foot fracture Head injury Immunisation Loss of consciousness X-ray

Symptomtext

third booster shot; he blacked out and fell and broke his foot; states he has a double fracture in his left foot; he blacked out and fell and broke his foot; hit his head on the door frame; extreme fatigue; some chills; Caller states he is still dizzy and lightheaded; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 40 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 07Dec2021 12:45 (Lot number: FE3590) at the age of 40 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Depression" (ongoing); "Panic attacks" (ongoing). Concomitant medication(s) included: BUPROPION taken for depression, start date: Sep2021 (ongoing); BUSPIRONE taken for panic attack, start date: Sep2021 (ongoing). Vaccination history included: Covid-19 vaccine (Dose 2, LOT-ER8737.), administration date: 08Apr2021, when the patient was 39 years old, for Covid-19 immunization; Covid-19 vaccine (Dose 1, LOT-ER8727), administration date: 18Mar2021, when the patient was 39 years old, for Covid-19 immunization, reaction(s): "chills", "fatigue". The following information was reported: IMMUNISATION (medically significant) with onset 07Dec2021 12:45, outcome "unknown", described as "third booster shot"; LOSS OF CONSCIOUSNESS (medically significant), FALL (non-serious) all with onset 07Dec2021, outcome "recovering" and all described as "he blacked out and fell and broke his foot"; FRACTURE (medically significant) with onset 07Dec2021, outcome "recovering", described as "states he has a double fracture in his left foot"; HEAD INJURY (non-serious) with onset 07Dec2021, outcome "recovering", described as "hit his head on the door frame"; FATIGUE (non-serious) with onset 07Dec2021, outcome "recovering", described as "extreme fatigue"; DIZZINESS (non-serious) with onset Dec2021, outcome "not recovered", described as "Caller states he is still dizzy and lightheaded"; CHILLS (non-serious) with onset 07Dec2021, outcome "recovering", described as "some chills". The events "he blacked out and fell and broke his foot", "he blacked out and fell and broke his foot", "hit his head on the door frame", "extreme fatigue", "caller states he is still dizzy and lightheaded" and "some chills" were evaluated at the emergency room visit. The event "states he has a double fracture in his left foot" was evaluated at the physician office visit and emergency room visit. Clinical course as follows: Caller states he is calling to report experience after the third booster shot, Pfizer Covid vaccine. Caller states they have the health division that sponsors the vaccine, got the third dose on Tuesday, 07Dec2021 at 12:45 PM, the booster, states he was okay until bedtime, woke up in the middle of the night with fatigue and some chills. Caller states he went to the bathroom and when he was on his way back to bed he blacked out and fell and broke his foot, states he has a double fracture in his left foot, hit his head on the door frame, went to the emergency room yesterday, spend the day there yesterday, did not see concerns about his head, x ray showed the double fracture in his foot, has a temporary support for now and going to an orthopedic specialist. Caller states he is still dizzy and lightheaded and that is not the case with his previous shots, states after the first vaccine he had chills and fatigue with the first shot but it was not as severe as this time. Exact dates not provided. Caller states his symptoms are improving but they are still there. The patient underwent the following laboratory tests and procedures: x-ray: (08Dec2021) double fracture in his foot.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101761145 same patient, different vaccine dose/AE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 20211208; Test Name: X-ray; Result Unstructured Data: Test Result:double fracture in his foot
Aktuelle Erkrankungen: Depression; Panic attacks
Vorgeschichte: -
Andere Medikamente: BUPROPION; BUSPIRONE
Allergien: -
Vorherige Impfungen: -

VAERS 1967529

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: WA
Alter: 42,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 20.10.2021
Beginn: 21.12.2021
Tage bis Beginn: 62,0
Dosis: 3
Route/Site: IM / UN

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

Blood test abnormal Deep vein thrombosis Factor V Leiden mutation Ultrasound Doppler abnormal

Symptomtext

Left leg deep vein thrombosis Patient has family history of Factor V Leiden. After the ultrasound showed DVT, the patient was subsequently tested positive for single R506Q mutation (heterozygote)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Ultrasound doppler Venous 11/2/21
Aktuelle Erkrankungen: -
Vorgeschichte: migraine headaches
Andere Medikamente: fremanezumab frovatriptan
Allergien: -
Vorherige Impfungen: -

VAERS 1963777

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: WI
Alter: 13,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 09.09.2021
Beginn: 10.10.2021
Tage bis Beginn: 31,0
Dosis: 2
Route/Site: SYR / LA

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

Dyspnoea Electrocardiogram abnormal Pain Painful respiration Pericarditis

Symptomtext

After my daughter received her second shot on 10/10/2021 she woke up around midnight and stated that it hurt to breathe. So we had her take a shower, take some Tylenol and take a nebulizer treatment to try help her lungs open up. After doing this it didn't help but she was able to fall back to sleep on and off. I did take her to the ER the next day because her pediatrician stated to go there. When we got the ER which after only 45 minutes then sent us home and said it was nothing to worry about. She wasn't getting any better so on 10/12/2021 I brought her to the walk in clinic for hospital for a second option. They stated that they couldn't read what ever ER wrote for the EKG so they were going back and forth with the ER's trying to figure out what we should do. After listening to her and trying to read the EKG they had thought that the wall of the heart was was swollen and said we could go home but they made an appointment for her to see a Cardiologist at Hospital. When we saw MD, he also stated that he couldn't read ER's EKG so he would have to do another one. After reading the EKG that he ran he did state that he did believe that the wall around he heart was swollen. He stated that it is a rare case that it happens in girls because they have been seeing it more in boys. He also said that it should heal on it's own but could take a few weeks to a month to heal. After about 3 weeks it did seem to go away but about once a week to every other week she will get some pains and says it is hard to breathe again. This will last a few minutes to a few hours and then goes away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: 2 EKG's done (in 2 different hospitals on different days)
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1962000

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: CT
Alter: 69,0
Geschlecht: M
Eingang: 18.12.2021
Impfdatum: 08.10.2021
Beginn: 12.12.2021
Tage bis Beginn: 65,0
Dosis: 3
Route/Site: IM / RA

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

Brain injury Computerised tomogram Endotracheal intubation Ischaemic stroke Magnetic resonance imaging Thrombectomy

Symptomtext

Ischemic stroke leading to hospitalization for 4 days. Needed thrombectomy and intubation. The stroke affected the area within right frontal lobe and area between right parietal-temporal lobe. No known residual deficits. There is some brain damage.

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Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: 4,0
Labordaten: 12/12 CT and MRI
Aktuelle Erkrankungen: -
Vorgeschichte: Mild dyslipidemia, osteoarthritis, history of prostate cancer post prostatectomy, allergies, asthma
Andere Medikamente: Lovastatin, nasonex, timolol eye drops, latanoprost eye drops
Allergien: Penicillins
Vorherige Impfungen: -

VAERS 1960958

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: UT
Alter: 22,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 15.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: IM / RA

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

Heavy menstrual bleeding Oligomenorrhoea Thrombosis

Symptomtext

Increase in heaviness of menstrual bleeding and passing blood clots the size of or larger than a golf ball, soaking through a super tampon within less than an hour. Days of period increased by 5 days.

Weitere VAERSDATA-Felder

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

VAERS 1947902

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

schwer

Staat: SD
Alter: 25,0
Geschlecht: M
Eingang: 14.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Feeling hot Loss of consciousness

Symptomtext

patient hadnt ate much (oatmeal) and stated he was nervous about getting the shot in general. We offered him some candy after the shot but he declined. Within 10 minutes he rose his hand...and then passed out. he was warm, and we offered him water, he decided to eat his treat. and then we used cold washcloth and ice pack to keep him cool. elevated legs and he recovered completely.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: 133/86 BP after recovery
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1944426

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: NE
Alter: 61,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 19.11.2021
Beginn: 10.12.2021
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: IM / RA

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

Blood test Pain in extremity Presyncope Thrombosis Ultrasound scan abnormal

Symptomtext

I got the third vaccine on 11/19, and I did not really have any huge side effects. No headache, fever or any other side effects. Just pain in my arm, which was normal, and I had that for the other two shots. Last Sunday when I woke up, I told my husband I must have slept wrong because my arm was hurting. And it continued to hurt on Monday and Tuesday while I was teaching. On Wednesday I decided to schedule an appointment for 12/13 for a doctor's appointment. On Thursday, I was teaching and Friday, while I was teaching, I almost blacked out. I had pain in my arm since then. I don't know why I almost blacked out. I made it to the principal's office where the school nurse took my blood pressure 147/84 - which was high for me. Principal called my husband to pick me up and he drove me to the ER, and they diagnosed the blood clot that day. They prescribed Eliquis blood thinner took one dose of on Friday and took the standard dose 2 in AM & 2 in PM on Saturday and Sunday and now we are here today, and I've taken my dose this morning. When I went to the doctor today for a follow up, he wanted me to follow up with a hematologist, Dr. and they want to do a procedure without contrast dye to see if there's any other clots or problems - waiting to schedule those appointments.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Ultrasound - determined the blood clot in the basilic vein; Blood tests - undetermined.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Omeprazole; Meloxicam; Levothyroxine; Pravastatin; Vitamin C; Vitamin D + Calcium; Daily Vitamin
Allergien: Contrast Dye; Antibiotics; Levaquin; Tequin
Vorherige Impfungen: Flu vaccine in 2001 - left arm - blood clot - went to the Clinic for that one, diagnosed Thoracic Outlet Syndrome - required sur

VAERS 1804458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3590

schwer

Staat: MI
Alter: 41,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 15.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: - / LA

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

C-reactive protein increased Chest pain Pericarditis

Symptomtext

Pericarditis; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 41 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 15Oct2021 16:00 (Lot number: Fe3590) at the age of 41 years as dose 3 (booster), single dose for COVID-19 immunisation. The patient's relevant medical history was not reported. ior to the vaccination, the patient was not diagnosed with COVID-19. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: Unknown. Unable to locate or read the details), for Covid-19 immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: Unknown. Unable to locate or read the details), for Covid-19 immunization. The following information was reported: PERICARDITIS (disability) with onset 19Oct2021 07:00, outcome "not recovered", described as "Pericarditis". The event "pericarditis" was evaluated at the physician office visit. Therapeutic measures were taken as a result of pericarditis which included ibuprofen and colchicine. Since the vaccination, the patient had not been tested for COVID-19.; Sender's Comments: Considering the plausible drug-event temporal association and known safety profile, there is a reasonable possibility that event of Pericarditis was related to suspect drug bnt162b2 (BNT162B2) administration.

Weitere VAERSDATA-Felder

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

VAERS 1804458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3590

schwer

Staat: MI
Alter: 41,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 15.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

C-reactive protein increased Chest pain Pericarditis

Symptomtext

Pericarditis; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 41 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 15Oct2021 16:00 (Lot number: Fe3590) at the age of 41 years as dose 3 (booster), single dose for COVID-19 immunisation. The patient's relevant medical history was not reported. ior to the vaccination, the patient was not diagnosed with COVID-19. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: Unknown. Unable to locate or read the details), for Covid-19 immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: Unknown. Unable to locate or read the details), for Covid-19 immunization. The following information was reported: PERICARDITIS (disability) with onset 19Oct2021 07:00, outcome "not recovered", described as "Pericarditis". The event "pericarditis" was evaluated at the physician office visit. Therapeutic measures were taken as a result of pericarditis which included ibuprofen and colchicine. Since the vaccination, the patient had not been tested for COVID-19.; Sender's Comments: Considering the plausible drug-event temporal association and known safety profile, there is a reasonable possibility that event of Pericarditis was related to suspect drug bnt162b2 (BNT162B2) administration.

Weitere VAERSDATA-Felder

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

VAERS 1925372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: OH
Alter: 57,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 22.10.2021
Beginn: 29.11.2021
Tage bis Beginn: 38,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Colon operation Colonoscopy abnormal Computerised tomogram Diarrhoea Faeces discoloured Fatigue Headache Large intestinal haemorrhage Pyrexia Rectal haemorrhage Thrombosis

Symptomtext

Last year in November I did have COVID. Each time I got the vaccine I would have a headache, a low grade fever, and chills. I would take Tylenol, and it would relieve those symptoms. I was tired as well. Last Monday night I started bleeding from my rectum. A few weeks before that I had loose stools and diarrhea. I had chronic bathroom issues. I started seeing the blood last night. My stools were totally black and loose. I went to bed. Then it did it again and it was getting worse. I went to a hospital. The doctor told me I was bleeding in my sigmoid colon. They placed a temporary clip where the bleeding was coming from. They told me if the bleeding started happening again to go back to the hospital so that they can stop it. I left the hospital on Wednesday. I will see my GI doctor tomorrow. They don't know why it happed and if it will happen again. I do still have loose stool but there is no blood. The whole time I was at hospital I was bleeding. I was prescribed Pepcid, but I have stopped taking it. The doctor also took me off of Spironolactone. I was released from the hospital on 12/3/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 4,0
Labordaten: CT (11/30/2021) Colonoscopy-found where a pocket had a blood clot and it had stopped (12/2/2021)
Aktuelle Erkrankungen: None
Vorgeschichte: Primary Biliary Cholangitis Lactose Intolerant Raynaud's Syndrome
Andere Medikamente: Ursodiol 250mg 3xday Vitamin D3 5000 units 1xday Calcium Baby Aspirin 81mg Claritin 10mg 1xday Spironolactone 25mg 1xday
Allergien: Shellfish Shellfish Oil Ceclor
Vorherige Impfungen: -

VAERS 1889097

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: WA
Alter: 40,0
Geschlecht: F
Eingang: 04.12.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Anaphylactic reaction Breast swelling Hypersensitivity Nausea Peripheral swelling Angioedema Breast enlargement Immunisation Pyrexia Swelling Urticaria

Symptomtext

angioedema from the neck up; a severe allergic reaction; urticarial covering entire body; nausea; a persistent high fever; significant swelling under the arm that the shot was administered; doubling size of the right breast; Booster; 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 right, administration date 19Nov2021 13:00 (Lot number: FE3590) at the age of 40 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0161, Location of injection: Arm Right, Vaccine Administration Time: 12:00 PM), administration date: 14Apr2021, when the patient was 40 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EP7534, Location of injection: Arm Right, Vaccine Administration Time: 12:00 PM), administration date: 23Mar2021, when the patient was 40 years old, for Covid-19 immunization. The patient had no relevant past drug history, reaction or allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient was tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive other medications within 2 weeks of vaccination. The following information was reported: IMMUNISATION (medically significant) with onset 19Nov2021 13:00, outcome "unknown", described as "Booster"; ANGIOEDEMA (medically significant) with onset 20Nov2021 19:00, outcome "not recovered", described as "angioedema from the neck up"; HYPERSENSITIVITY (medically significant) with onset 20Nov2021 19:00, outcome "not recovered", described as "a severe allergic reaction"; URTICARIA (medically significant) with onset 20Nov2021 19:00, outcome "not recovered", described as "urticarial covering entire body"; NAUSEA (medically significant) with onset 20Nov2021 19:00, outcome "not recovered", described as "nausea"; PYREXIA (medically significant) with onset 20Nov2021 19:00, outcome "not recovered", described as "a persistent high fever"; SWELLING (medically significant) with onset 20Nov2021 19:00, outcome "not recovered", described as "significant swelling under the arm that the shot was administered"; BREAST ENLARGEMENT (medically significant) with onset 20Nov2021 19:00, outcome "not recovered", described as "doubling size of the right breast". The events "booster", "angioedema from the neck up", "a severe allergic reaction", "urticarial covering entire body", "nausea", "a persistent high fever", "significant swelling under the arm that the shot was administered" and "doubling size of the right breast" were evaluated at the physician office visit. 30 hours after receiving the booster, patient experienced a severe allergic reaction. Sudden onset of angioedema from the neck up and urticarial covering entire body. Accompanied by nausea, a persistent high fever, and significant swelling under the arm that the shot was administered and doubling size of the right breast. Facility where the most recent COVID-19 vaccine was administered was reported as pharmacy or Drug Store. The patient was treated with enormous amounts of antihistamines. The adverse event resulted in doctor or other healthcare professional office/clinic visit. Therapeutic measures were taken as a result of angioedema, hypersensitivity, urticaria, nausea, pyrexia, swelling, breast enlargement. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
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 1889097

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: WA
Alter: 40,0
Geschlecht: F
Eingang: 04.12.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Anaphylactic reaction Breast swelling Hypersensitivity Nausea Peripheral swelling Angioedema Breast enlargement Immunisation Pyrexia Swelling Urticaria

Symptomtext

angioedema from the neck up; a severe allergic reaction; urticarial covering entire body; nausea; a persistent high fever; significant swelling under the arm that the shot was administered; doubling size of the right breast; Booster; 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 right, administration date 19Nov2021 13:00 (Lot number: FE3590) at the age of 40 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0161, Location of injection: Arm Right, Vaccine Administration Time: 12:00 PM), administration date: 14Apr2021, when the patient was 40 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EP7534, Location of injection: Arm Right, Vaccine Administration Time: 12:00 PM), administration date: 23Mar2021, when the patient was 40 years old, for Covid-19 immunization. The patient had no relevant past drug history, reaction or allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient was tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive other medications within 2 weeks of vaccination. The following information was reported: IMMUNISATION (medically significant) with onset 19Nov2021 13:00, outcome "unknown", described as "Booster"; ANGIOEDEMA (medically significant) with onset 20Nov2021 19:00, outcome "not recovered", described as "angioedema from the neck up"; HYPERSENSITIVITY (medically significant) with onset 20Nov2021 19:00, outcome "not recovered", described as "a severe allergic reaction"; URTICARIA (medically significant) with onset 20Nov2021 19:00, outcome "not recovered", described as "urticarial covering entire body"; NAUSEA (medically significant) with onset 20Nov2021 19:00, outcome "not recovered", described as "nausea"; PYREXIA (medically significant) with onset 20Nov2021 19:00, outcome "not recovered", described as "a persistent high fever"; SWELLING (medically significant) with onset 20Nov2021 19:00, outcome "not recovered", described as "significant swelling under the arm that the shot was administered"; BREAST ENLARGEMENT (medically significant) with onset 20Nov2021 19:00, outcome "not recovered", described as "doubling size of the right breast". The events "booster", "angioedema from the neck up", "a severe allergic reaction", "urticarial covering entire body", "nausea", "a persistent high fever", "significant swelling under the arm that the shot was administered" and "doubling size of the right breast" were evaluated at the physician office visit. 30 hours after receiving the booster, patient experienced a severe allergic reaction. Sudden onset of angioedema from the neck up and urticarial covering entire body. Accompanied by nausea, a persistent high fever, and significant swelling under the arm that the shot was administered and doubling size of the right breast. Facility where the most recent COVID-19 vaccine was administered was reported as pharmacy or Drug Store. The patient was treated with enormous amounts of antihistamines. The adverse event resulted in doctor or other healthcare professional office/clinic visit. Therapeutic measures were taken as a result of angioedema, hypersensitivity, urticaria, nausea, pyrexia, swelling, breast enlargement. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
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 1920560

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: IL
Alter: 54,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 28.10.2021
Beginn: 15.11.2021
Tage bis Beginn: 18,0
Dosis: 2
Route/Site: SYR / LA

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

Dizziness Presyncope

Symptomtext

I started having dizziness. It feels like I am on a ship, it comes and goes. It feels like I am going to pass out. These are new symptoms. I went to the doctor about this on November 29th. She was unsure what is causing it. If it gets worse then they are going to do more tests.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: N/a
Vorgeschichte: Depression
Andere Medikamente: Vitamin D, Hydrazine, Iodine, Meloxicam
Allergien: N/a
Vorherige Impfungen: -

VAERS 1886164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: AZ
Alter: 27,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 10.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Heavy menstrual bleeding Menstrual disorder Thrombosis

Symptomtext

day after, started my menstrual cycle even though i already had it a week prior. have now been bleeding for 8 days, extremely heavy. lots of blood clots, soaking through tampons within 30-40 minutes, and having to change my pads every time i stand up

Weitere VAERSDATA-Felder

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

VAERS 1878230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: WY
Alter: -
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Syncope

Symptomtext

Patient was seated in front of the pharmacy following the shot and fainted. This was 5 minutes after the shot.

Weitere VAERSDATA-Felder

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

VAERS 1877187

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: -
Alter: 17,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal pain lower Syncope

Symptomtext

Pt had a witnessed syncopal episode approx. four minutes after receiving her first dose of the Pfizer vaccine. Pt was assisted to the ground in a supine position. Pt regained consciousness approx. 20-30 seconds after fainting. After coming to, pt complained of abdominal pain to the RLQ. All vital signs stable and within normal limits. No signs of allergic reaction noted. Pt treated on site by paramedics. Pt transported to a local hospital ER for follow up.

Weitere VAERSDATA-Felder

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

VAERS 1876570

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: CA
Alter: 18,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / UN

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

Anaphylactic reaction Dyspnoea Pharyngeal swelling Swelling face Swollen tongue Urticaria

Symptomtext

Anaphylaxis. About 30 minutes after receiving the first dose of the Pfizer Covid vaccine, patient developed shortness of breath associated with hives throughout the entire body. Patient's tongue, face and throat started to swell. EMS gave 0.3 mg IM epinephrine and 50 mg Benadryl after which patient reported improvement of swelling in his throat and face. Upon arrival to ED, Pepcid and Solumedrol were administered and began LR IV fluid. Patient remained stable and felt much improved. ED provider discussed and counseled patient on condition. Prescriptions provided including Epi pen, and warned about possible delayed reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Unknown
Andere Medikamente: No medications reported.
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1867321

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: MI
Alter: 18,0
Geschlecht: M
Eingang: 13.11.2021
Impfdatum: 22.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: - / RA

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

Seizure

Symptomtext

Major Seizure; This is a spontaneous report from a contactable Consumer or other non-HCP (parent). An 18-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: FE3590, Expiration date: Unknown), via an unspecified route of administration in right arm on 22Oct2021 at 14:00 (at the age of 18-year-old), as DOSE 3 (BOOSTER), SINGLE for COVID-19 immunization. The patient medical history included allergy. There were no concomitant medications. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient was not tested for COVID-19. The patient did not receive any other vaccine within 4 weeks prior to the COVID-19 vaccine. The patient did not receive any other medications within 2 weeks of vaccination. The patient previously received the past drugs BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL3249, Expiration date: Unknown), via an unspecified route of administration in right arm on 15Jan2021, as dose 1, single and then BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EM9810, Expiration date: Unknown), via an unspecified route of administration in right arm on 05Feb2021, as dose 2, single for COVID-19 immunization. On 28Oct2021 at 07:00, the patient experienced major seizure. The adverse events resulted in doctor or other healthcare professional office, or clinic visit and emergency room or department or urgent care visit. Therapeutic measures were taken as a result of major seizure. The case was reported as non-serious and the event did not result death, Life threatening, Caused/prolonged hospitalization, Disabling/Incapacitating and Congenital anomaly/birth defect. The outcome of the event was unknown at the time of this report. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Drug allergy (Relevant past drug history: Name of Drug as Reported: No Reaction: Allergy)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1865757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: MA
Alter: 51,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 08.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Anaphylactic reaction Urticaria

Symptomtext

anaphylaxis reaction, received Prednisone and Benedryl through an IV drip, as well as an epipen at Hospital. Full body hives continued to appear for 2 days. Friday, November 12 was the first day that no additional hives appeared. I am still taking Prednisone, Pepcid, and Benedryl. I was also sent home with an epipen and need to see an allergist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: UTI
Vorgeschichte: -
Andere Medikamente: Macrobid
Allergien: None
Vorherige Impfungen: -

VAERS 1865717

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: ID
Alter: 90,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 25.10.2021
Beginn: 10.11.2021
Tage bis Beginn: 16,0
Dosis: 3
Route/Site: IM / RA

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

Aphasia Asthenia Blood cortisol Blood thyroid stimulating hormone C-reactive protein Computerised tomogram head Condition aggravated Echolalia Electrocardiogram Guillain-Barre syndrome Laboratory test Magnetic resonance imaging head Procalcitonin Red blood cell sedimentation rate SARS-CoV-2 test Troponin Urine analysis Vitamin B12

Symptomtext

Global profound weakness, receptive aphasia, echolalia. Currently admitted and being treated for guillain barre.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: brain MRI, non con head CT, RRP, Covid, UA, TSH, CRP, ESR, procalcitonin, alcohol, troponin, , B12, , AM cortisol, EKG .
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma-COPD overlap syndrome Stage 3b chronic kidney disease Hypertension Hypothyroidism Hoarseness Chronic pain of right knee Opiate dependence Weakness Chronic heart failure with preserved ejection fraction
Andere Medikamente: aspirin 81 MG EC tablet Take 1 tablet (81 mg total) by mouth Daily. cyanocobalamin, vitamin B-12, 1,000 mcg TbSR Take 1,000 mcg by mouth Daily. FLUoxetine (PROZAC) 20 MG capsule Take 1 capsule (20 mg total) by mouth Daily. FOLIC ACID/MV,
Allergien: ampicillin rash
Vorherige Impfungen: -

VAERS 1864861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: PA
Alter: 59,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Hypersensitivity Muscle spasms Pain in extremity Somnolence Syncope

Symptomtext

One hour following her first COVID19 vaccination the patient passed out in the car for a period of 1-2 minutes. Following that, she was weak and very groggy for ~ 1hr before starting to recover. Since then (past three weeks) she has exhibited muscle cramps and pain on her left side, primarily in her left arm and, to a lesser extent in her left leg. In addition, she has nerve sensitivity in her left arm and hand. These symptoms are very similar to those following her last previous vaccination which was for tetanus approximately 20 years ago.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: None
Allergien: some foods
Vorherige Impfungen: The patient was vaccinated for tetanus in ~2000 after having stepped on a nail. In that case, she passed out about 4-6 hours af

VAERS 1864831

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: NE
Alter: 49,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 01.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: SYR / RA

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

Aphasia Decreased appetite Drooling Ear pain Eyelid function disorder Facial paralysis Lacrimation increased Neurological symptom

Symptomtext

Work up in AM with stroke like or Beal?s Palsy symptoms. Left half of face could not be moved. Drooling, hard to talk or eat. Left eye waters constantly. Hard to blink. Pain about 3/4? inside left ear.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes
Andere Medikamente: Lithium 600mg Metformin 1000mg Adderall 30mg as needed Xanax 2-4 mg as needed
Allergien: None
Vorherige Impfungen: -

VAERS 1860365

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: FL
Alter: 62,0
Geschlecht: M
Eingang: 11.11.2021
Impfdatum: 30.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Asthenia Balance disorder Fall Fatigue Immunisation Loss of consciousness Syncope

Symptomtext

loss consciousness; fatigue; I felt like I lost my balance and started to faint; I lost balance and fell; I lost balance and fell; Booster; felt that the weakness was coming; This is a spontaneous report from a contactable consumer or other non-HCP (patient himself) via Medical Information Team. A 62-year-old male patient received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- FE3590) via an unspecified route of administration on 30Oct2021 as dose 3 (booster), single (at the age of 62-years-old) for COVID-19 immunization. Patient had no relevant medical history. The concomitant medications were reported as none. Historical vaccine included first dose of BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- EP7534) on 24Mar2021 as dose 1, single and received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- ER8737) on 16Apr2021 as dose 2, single for COVID-19 immunization. The patient had three shots of vaccine, the later was put on yesterday 31Oct2021. The patient lost balance and fall on 31Oct2021. The patient was now travelling and again the patient felt like the patient lost his balance and started to faint on 31Oct2021. The patient had not hit his head but the patient seated when the patient felt that the weakness was coming on an unspecified date in Oct2021. The patient may need her help to find out if this was a secondary effect of the Pfizer Vaccine. It happened before was manageable, now was very strong weakness. Syncope (fainting) may occur in association with administration of injectable vaccines, in particular in adolescents. Procedures should be in place to avoid injury from fainting. The patient experienced fatigue on an unspecified date. There had also been reports of fatigue. However, there was no information regarding reports of losing balance. Pfizer could not assess causality (cannot assess if what you described, are experiencing was associated with the Pfizer BioNTech COVID-19 vaccine. His doctor or healthcare provider was in the best position to assess and advise his as his doctor or healthcare provider was most familiar with his medical condition, clinical history, how his treatment had been conducted and any relevant information to their specific case. The patient was calling from withheld at this time due to traveling there on 31Oct2021, the patient will return. Caller received the Pfizer Covid 19 Booster on Sat 30Oct2021. The patient loss consciousness for a couple of seconds times 2 episodes falling to the floor on 31Oct2021. Today on 01Nov2021, the patient loss of consciousness for a few seconds and was seen in the hospital, but not admitted. He was asking if they symptom may be related to the vaccine. He stated the patient had his first two Pfizer Covid vaccines without any problem and the patient felt very protected and felt very happy. He stated that two days ago, clarified on 30Oct2021, that the patient got his booster shot. Stated the patient got the booster vaccine and then the next day he traveled. Stated that day the patient lost consciousness and fell to the floor once and then again the patient lost consciousness while walking, states this happened yesterday 31Oct2021. Stated when the patient lost consciousness, the patient completely blacked out for a few seconds each time. Stated today the patient lost consciousness again and went to the hospital there, he stated they discharged him and said him needs MRIs and a bunch of things that they did not had the equipment for in that country. The patient was waiting to go back to the states for testing. Stated the patient did not know if it was related to the vaccine or if the patient could be sick of something else. He confirmed the patient was not admitted to the hospital and wants to know if this could be related to the booster shot. The outcome of the events felt like lost his balance and started to faint, lost balance and fell, felt that the weakness was coming was not resolved while that of the events fatigue and loss of consciousness was unknown. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient History: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1857794

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: TX
Alter: 77,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Anticoagulant therapy Chest X-ray Pain in extremity Peripheral swelling Thrombosis Ultrasound Doppler Ultrasound scan X-ray

Symptomtext

The day after my 3rd COVID vaccine I had pain and swelling in my legs and feet. I went to the emergency room where the doctor admitted me overnight with blood clots in both legs. I am currently taking Eliquis, 5mg, twice daily, to try to dissolve the clots.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 2,0
Labordaten: Doppler, Ultrasound and x-rays of legs and chest, October 20th, 2021
Aktuelle Erkrankungen: None
Vorgeschichte: Two heart by passes, Diabetes, Blood Pressure.
Andere Medikamente: Fenofibrate, Atorvastatin, Ezetimibe, Losartan, Nifedipine, Levemir, Carvedilol, Aspirin, Tylenol, Trazadone, Vitamins: CQ10, Vitamin C, Vitamin D3, B12, Multi Vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1857423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: MA
Alter: 27,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Feeling hot Hypoaesthesia Loss of consciousness Paraesthesia Staring

Symptomtext

Approximately 7 minutes into observation, patient had a blank stare and became unconscious: sternal rub and awoke within a few seconds. Brought via wheelchair to a stretcher. Vitals taken. Patient C/O numbness and tingling in hands and feet and being hot. Ice packs to head and neck. Rested for a few minutes. Reported high anxiety around getting the vaccine and had been awake all night on call shift. Patient rested for about 20 minutes. Vitals signs taken. Was able to walk. Instructed to follow up with PCP if symptoms continued.

Weitere VAERSDATA-Felder

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

VAERS 1853271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: CA
Alter: 46,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 23.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Blood pressure increased Blood pressure measurement Chest discomfort Dizziness Feeling hot Palpitations Presyncope Tremor Visual impairment

Symptomtext

almost fainted; blood pressure elevation to 150/90; felt entire body was on fire; tremors; seeing black spots; dizziness; pressure on chest; palpitations; This is a spontaneous report from a contactable nurse (patient). A 46-year-old non-pregnant female patient received the first dose of bnt162b2 (COMIRNATY), via an unspecified route of administration, administered in Arm Left on 23Oct2021 09:00 (at the age of 46-year-old) (Lot Number: FE3590) as single dose for covid-19 immunisation. Medical history included Hypothyroidism, known allergies: Flagyl, Benadryl, Latex, Pork and kale. Concomitant medications included levothyroxine. The patient experienced almost fainted, blood pressure elevation to 150/90, felt entire body was on fire, tremors, seeing black spots, dizziness, pressure on chest, palpitations on 23Oct2021 09:30. Blood pressure elevation to 150/90 (baseline B/P is 110/60), she felt entire body was on fire, tremors, was seeing black spots, almost fainted, dizziness, pressure on chest and palpitations. AE resulted in Doctor or other healthcare professional office/clinic visit. Unknown if treatment received. The outcome of the events was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Test Date: 20211023; Test Name: blood pressure; Result Unstructured Data: Test Result:150/90; Comments: blood pressure elevation to 150/90 (baseline B/P is 110/60)
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism; Latex allergy; Meat allergy; Vegetable allergy
Andere Medikamente: LEVOTHYROXINE
Allergien: -
Vorherige Impfungen: -

VAERS 1850688

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: WI
Alter: 84,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 13.04.2021
Beginn: 26.10.2021
Tage bis Beginn: 196,0
Dosis: 3
Route/Site: IM / -

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

COVID-19 Intensive care SARS-CoV-2 test positive

Symptomtext

Pt completed initial Pfizer COVID 19 Vaccination (on 3/23/2021 and 4/13/2021 respectively), plus the Pfizer booster on 10/19/2021. COVID test was positive 10/26/2021 and he was transferred from a smaller hospital to this hospital for higher level of care. Pt eventually needed ICU level care here, but has since improved enough to be cared for in our ICU department.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 12,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: anemia, CAD, cardiomyopathy, CHF, chronic Afib, current use of long term anticoagulation, diverticulosis, enlarged prostate without urinary obstruction, HTN, gout, hyperlipidemia, hypothyroidism, asthma, MRSA, osteoarthrosis, peptic ulcer, pulmonary hypertension, rheumatic disorders of both mitral and aortic valves, OSA, venous stasis ulcers, vitamin D deficiency.
Andere Medikamente: allopurinol, budesonide-formoterol, bumetanide, carvedilol, celecoxib, ergocalciferol, fluticasone, levothyroxine, losartin, omega 3s, potassium chloride, rosuvastatin, spironolactone, warfarin.
Allergien: Lisinopril, niacin
Vorherige Impfungen: -

VAERS 1848993

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: -
Alter: 12,0
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Cold sweat Hyperhidrosis Pallor Syncope

Symptomtext

Attendee received second dose Pfizer vaccine at 09:40 am in the right arm. Lot# FE3590. Attendee was directed to observation area. At 09:50 pm the attendee fainted and was caught by the RN, who prevented him from falling to the floor. Attendee's skin was cool and clammy. Attendee immediately became alert Attendee's respirations were not tachypneic or dyspneic. Attendee assisted to the cot to lie down, legs elevated. HR: 45 BP: 126/65 RR: 16 O2Sat%: 96 09:56 - Attendee stated he felt better, no longer diaphoretic, or pale. Drinking water. HR: 59 BP: 124/68 RR: 18 O2Sat%: 100 10:04 -No voiced complaints- skin warm and dry. HR: 94 BP: 112/68 RR: 18 O2Sat%: 98 10:09 -No voiced complaints- skin warm and dry. HR: 82 BP: 112/58 RR: 18 O2Sat%: 98 10:20 -No voiced complaints- skin warm and dry. Had finished a 16.9 fluid ounce water. HR: 88 BP: 118/64 RR: 18 O2Sat%: 98 10:25 - Care Practitioner educated on home discharge/adverse reaction instructions and attendee was discharged to home with his mother. Attendee did not have any reported escalation of symptoms and was able to walk out of clinic independently. Attendee was retained for a longer observation time to make sure that it was safe for them to leave.

Weitere VAERSDATA-Felder

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

VAERS 1848829

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: ND
Alter: 37,0
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 31.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Blood glucose decreased Dizziness Hyperaesthesia Injection site pain Migraine Myalgia Ocular discomfort Presyncope

Symptomtext

Pain at injection site,muscle and joint pain,migraine,dizziness,blood sugar dropped almost to the point of synscope,pressure behind eyes and cutaneous hyperesthesia

Weitere VAERSDATA-Felder

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

VAERS 1843013

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE 3590

schwer

Staat: GA
Alter: 50,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Anosmia Blood test Chest discomfort Cold sweat Diarrhoea Electrocardiogram Fatigue Feeling hot Forced vital capacity Hypopnoea Pyrexia Stool analysis Syncope

Symptomtext

Fever, very tired, chest tightness, shallow breathing, Got really hot then cold sweat ,fainting and extreme diarrhea, Anosmia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: BP sitting standing laying, Vitals, Pulse, O2, FVC test, EKG, Blood/Labs Stool/Labs
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Carvedilol, multivitamin with omega 3, zinc, vitamin C, D3
Allergien: Celebrex
Vorherige Impfungen: Fever tired 1 full day

VAERS 1838056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

schwer

Staat: MI
Alter: 30,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Dizziness Loss of consciousness Skin laceration

Symptomtext

Pt sitting down after a shot. got light headed, woozy, and likely passed out. Patient wore glasses, and hit his face. Glasses caused a minor cut on his face. Pharmacist went to patient, stayed with G.I. until stable. Prior to shot... Pt expressed anxiety before requesting a shot. Was asked to sit for a period after the shot. Patient did not sit down, but wanted "fresh air" and went outside.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none known at thistime
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Unknown
Allergien: -
Vorherige Impfungen: -

VAERS 1836911

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

schwer

Staat: IL
Alter: 41,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Fall Flushing Head injury Hyperhidrosis Loss of consciousness Skin laceration Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Mild, Additional Details: Patient got both his COVID vaccine and flu shot and after getting up and putting on his coat he become lightheaded and fell to the floor. He hit his head on the floor and cut his face. He was going in and out of consciousness so we called an ambulance. he was taken via ambulance to make sure he did not have a concussion.

Weitere VAERSDATA-Felder

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

VAERS 1832337

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: CA
Alter: 29,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 31.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

Patient fainted for about 5 seconds and came back after the vaccine was administered.

Weitere VAERSDATA-Felder

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

VAERS 1832164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: PA
Alter: 15,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Confusional state Feeling abnormal Feeling hot Flushing Hyperhidrosis Loss of consciousness Malaise Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Confusion-Mild, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Mild, Systemic: Shakiness-Medium, Additional Details: Patient fainted 5 seconds after recieving 2nd dose vaccine. Patient was caught in her chair to prevent falling. Patient was unconscious for about 10 seconds. Patient appeared to start shaking slightly for 1 second right before she woke up to her mother calling her name. Patient felt like she woke up from sleeping and was confused as to what had happened. Patient complained of feeling hot/ unwell upon awakening. After drinking cold water patient felt better within minutes. Had not eaten that day

Weitere VAERSDATA-Felder

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

VAERS 1831861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

schwer

Staat: UT
Alter: 51,0
Geschlecht: M
Eingang: 30.10.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SC / LA

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

Electrocardiogram Loss of consciousness

Symptomtext

pt stated he had fear of needles prior to administration. after 5 mins of observation in a chair, patient shouted he was about to pass out. pt was braced for safety and remained unconscious in a chair for 2 minutes. EMS was called and was on scene within 4 minutes of incident. pt consulted EMS for medical assessment and was determined nothing else was wrong and he was good to leave if he felt better. pt refused to be transported for further assessment. pt drank apple juice and water and continued to recover in the pharmacy for 30 minutes prior to leaving.

Weitere VAERSDATA-Felder

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

VAERS 1829372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: -
Alter: 16,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 23.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Fatigue Syncope

Symptomtext

Patient's mother called the vaccine clinic hotline to report that the patient had a syncopal episode on 10/24 after receiving Dose 2 of Pfizer vaccine on 10/23. She reports that patient did not have any other symptoms except for fatigue and was kept in the ER for approximately 10 hours and was then discharged home and advised to follow up with cardiology. Patient is now home and is doing well. Patient's mother informed RN that her other child also received Dose 2 of Pfizer on 10/23 but did not experience any reactions except for fatigue. RN instructed patient's mom to call 911 or to go to their nearest ER if this recurs or if patient experiences any other reactions and is welcome to call the vaccine clinic hotline for any questions or concerns and she verbalized understanding.

Weitere VAERSDATA-Felder

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

VAERS 1829267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: SC
Alter: 40,0
Geschlecht: M
Eingang: 29.10.2021
Impfdatum: 08.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / UN

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

Echocardiogram Ejection fraction normal Electrocardiogram Fatigue Full blood count Headache Laboratory test Metabolic function test Myocarditis Physical examination

Symptomtext

Approx 4 days post second COVID-19 vaccination dose patient with increase headaches and excessive fatigue. Pt was seen twice at treatment facility and determined on second visit concern for myocarditis was warranted. Currently member is being evaluated for diagnosis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: CMP and CBC 10 days post second dose obtained and were overall unremarkable. EKG obtained 28 Oct 2021 clinic visit showed 1st degree AV block, otherwise unremarkable. BP slightly elevated 130s/80s. Physical examination unremarkable. ECHO 29 Oct 2021 showed mildly dilated left ventricle, normal thickness, mild global hypokinesis, EF 40-45%. Grade 1 diastolic dysfunction. Mild mitral regurg. Normal pulmonary artery systolic pressure. Additional labs pending a time of report.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Aloe, Aspirin
Vorherige Impfungen: -

VAERS 1828709

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: GA
Alter: 41,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Abdominal pain Blood pressure increased Chest X-ray Chest pain Chills Electrocardiogram Epistaxis Heavy menstrual bleeding Pain Pain in extremity Pyrexia Specialist consultation Thrombosis

Symptomtext

Fever Body Aches Chills Abdominal Cramps Random Cycle Bleeding Heavy Large Blood Clots Out of Nose and from Cycle Sores on Arms Severe Chest Pains Blood Pressure Spikes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Blood Test EKG Chest X Ray
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin Cephalexin
Vorherige Impfungen: Flu shot causes sickness

VAERS 1825046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 08.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 17,0
Dosis: 2
Route/Site: IM / UN

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

Angiogram pulmonary abnormal Bladder catheterisation Blood culture negative Blood test normal Bronchial wall thickening Cough Deep vein thrombosis Dyspnoea Dyspnoea exertional Endotracheal intubation COVID-19 COVID-19 pneumonia Cardiomegaly Chest X-ray abnormal Chills Fatigue Gastrointestinal tube insertion Hypovolaemia

Symptomtext

a 74 y.o. female who has a pertinent medical history asthma, hypertension, hyperlipidemia, hypothyroid, anxiety, and diabetes mellitus that is diet controlled presented to the emergency department today for a week-long history fatigue, malaise, fever, and chill. The patient noticed that her roughly 1 week ago she was feeling more fatigued and having chills. It was not until this morning that her daughter decided to bring her to the ER to get checked out. The patient is a somewhat poor historian and is unable to describe her exact symptoms that have progressed over the week. While in the ER the patient was found to be febrile at 101.2 and hypoxic and was started on high-flow nasal cannula which improved her oxygen saturation to 92%. She subsequently tested positive for COVID-19 while in the ER however her remaining blood work was relatively unremarkable. Her chest x-ray demonstrated extensive multifocal bilateral airspace disease. The patient was vaccinated with the Pfizer COVID vaccine on 09/17 and 10/8. The patient was given 1 dose of dexamethasone and was subsequently admitted to the hospital with the hospitalist team. On exam the patient denies chest pain, fever, chills, nausea, vomiting, diarrhea, dizziness, lightheadedness. She does endorse shortness of breath especially with activity. She is a poor historian and cannot recall her specific symptoms and was progressed to lead her to the hospital. There is no other family member at bedside to confirm her story. I educated the patient on the plan of care to start steroids, remdesivir, and monitor her oxygen. She agrees with this plan of care and all questions and concerns were addressed with the patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 3,0
Labordaten: Results Procedure Component Value Ref Range Date/Time DR CHEST SINGLE VIEW [349436578] Resulted: 10/28/21 1134 Order Status: Completed Updated: 10/28/21 1136 Narrative: EXAMINATION: DR CHEST SINGLE VIEW EXAM DATE: 10/28/2021 10:45 AM TECHNIQUE: Single AP View INDICATION: Resp failure COMPARISON: 10/27/2021 ENCOUNTER: Not applicable _________________________ FINDINGS: Devices: Endotracheal tube is in proper position on the second image obtained, following reposition. Nasogastric tube extending into the stomach. Heart And Mediastinum: The heart is enlarged. Lung Fields And Pleura: bilateral patchy airspace disease Chest Wall: Degenerative changes of the thoracic spine. Additional Findings: Evaluation limited by rotation and low lung volumes. _________________________ Impression: Diffuse bilateral pneumonia appears similar to prior examination, given differences in positioning. DR CHEST SINGLE VIEW [349296940] Resulted: 10/27/21 1354 Order Status: Completed Updated: 10/27/21 1356 Narrative: EXAMINATION: Single View Chest EXAM DATE: 10/27/2021 1:29 PM TECHNIQUE: Single view chest INDICATION: Line placement COMPARISON: 10/27/2021 0816 hours ENCOUNTER: Not applicable _________________________ FINDINGS: Interval placement of Corpak tube likely having its tip curved in the distal stomach. The bowel gas pattern in the upper abdomen is nonspecific. Suspect some diffuse airspace disease distributed throughout both mid and lower lung fields becoming somewhat more confluent in the left lung base. Endotracheal tube in satisfactory position. No pneumothorax. The heart is borderline enlarged. Impression: 1. Corpak tube having its tip curved within the distal stomach. 2. Airspace disease as described above. USV Venous Upper Extremity Duplex Bilateral [349101474] Resulted: 10/27/21 1143 Order Status: Completed Updated: 10/27/21 1146 Narrative: EXAMINATION: Complete Bilateral Upper Extremity Venous Duplex Doppler Ultrasound EXAM DATE: 10/27/2021 11:25 AM 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: DVT 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 [349101473] Resulted: 10/27/21 1142 Order Status: Completed Updated: 10/27/21 1144 Narrative: EXAMINATION: Complete Right and Left Lower Extremity Venous Duplex Doppler Ultrasound EXAM DATE: 10/27/2021 11:25 AM 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: US COMPARISON: None _____________________ Right Lower Extremity Findings: Right Common Femoral Vein: Incompletely compressible with filling defect, suggesting acute deep vein thrombosis. This extends into the external iliac vein. 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: The common femoral vein waveforms are abnormally pulsatile. This finding may be seen with elevated central venous pressure from heart failure, tricuspid valve regurgitation, pulmonary hypertension, or right heart dysfunction. Additional Findings: None. _____________________ Impression: Nonocclusive acute appearing deep vein thrombosis within the right common femoral vein and extending into the right external iliac vein. DR CHEST SINGLE VIEW [349101457] Resulted: 10/27/21 0911 Order Status: Completed Updated: 10/27/21 0913 Narrative: EXAMINATION: Single View Chest EXAM DATE: 10/27/2021 8:28 AM TECHNIQUE: Portable semiupright AP radiograph of the chest INDICATION: Respiratory failure requiring intubation. Follow-up abnormal chest radiograph. COVID-19 positive 10/25/2000 COMPARISON: 10/26/2021 and 10/25/2021 chest single view ENCOUNTER: Initial FINDINGS: The ET tube tip is 4.5 cm above the carina. The NG tube extends off the base of the radiograph in the stomach. Allowing for differences in radiographic exposure the diffuse airspace disease is less confluent than seen on 10/26/2021, and definitely less dense and confluent in comparison to 10/25/2020. Impression: 1. Improving diffuse bilateral airspace disease. 2. Lines and tubes unchanged, as above. CT ANGIO THORAX WITH IV CONTRAST [348922561] Resulted: 10/26/21 1815 Order Status: Completed Updated: 10/26/21 1818 Narrative: EXAMINATION: CT Angiography of the Thorax EXAM DATE: 10/26/2021 5:21 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: 75 mL Isovue-370 QPP DOCUMENTATION: At least one of the following dose reduction techniques was utilized: Iterative reconstruction, and/or Automatic Exposure Control, and/or mA/kV adjustment based on body size. INDICATION: Pulmonary embolus suspected, high probability. Shortness of breath. Difficulty breathing. Color-19 pneumonia. COMPARISON: 10/26/2021 chest single view ENCOUNTER: Initial FINDINGS: Base of Neck & Axillae: There is no lymph node enlargement. Mediastinum & Hila: There is no mediastinal or hilar lymph node enlargement. There is an endotracheal tube in place with tip 2.5 cm above the carina. Nasogastric tube extends into the stomach. Cardiovascular: The heart has a normal size. 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: Diffuse patchy groundglass opacities throughout both lungs with additional consolidative airspace disease at the posterior lungs. Pleural Space: There are no pleural effusions. There is no pneumothorax. Upper Abdomen: Included portions of the upper abdomen are unremarkable. Chest Wall & Musculoskeletal: Moderate marginal osteophyte formation at the lower thoracic spine. Impression: 1. Negative for pulmonary embolism. 2. Extensive bilateral pneumonia. DR CHEST SINGLE VIEW [348922558] Resulted: 10/26/21 1434 Order Status: Completed Updated: 10/26/21 1436 Narrative: EXAMINATION: Single View Chest EXAM DATE: 10/26/2021 2:20 PM TECHNIQUE: Single view chest INDICATION: r/o pneumo COMPARISON: 10/25/2021 ENCOUNTER: Not applicable _________________________ FINDINGS: Endotracheal tube and nasogastric tubes appear to be in satisfactory position. The heart is enlarged. There is a similar burden of moderate to severe patchy and reticular opacities diffusely throughout both lungs representing airspace disease. No definite pneumothorax or pleural effusion. Osseous structures similar prior exam. _________________________ Impression: 1. Similar moderate to severe burden of airspace disease throughout both lungs. No pneumothorax. 2. Cardiomegaly and tubes and lines as described above. DR CHEST SINGLE VIEW [348892585] Resulted: 10/25/21 2020 Order Status: Completed Updated: 10/25/21 2022 Narrative: EXAMINATION: Single View Chest EXAM DATE: 10/25/2021 6:36 PM TECHNIQUE: Single view chest INDICATION: ET tube placement COMPARISON: 10/25/2021 at 1330 hours ENCOUNTER: Not applicable _________________________ FINDINGS: Endotracheal tube is been placed with its tip approximately 2.8 cm above the carina. The heart size is obscured. Monitor wires overlie the chest. There is a severe burden of patchy and poorly defined opacities distributed throughout all lung fields. No pneumothorax or pleural effusion. Osseous structures similar. Impression: 1. Severe burden of patchy and poorly defined opacities diffusely throughout both lungs. 2. Suspect cardiomegaly. 3. Endotracheal tube is been placed having its tip 2.8 cm above the carina. DR CHEST SINGLE VIEW [348823613] Resulted: 10/25/21 1354 Order Status: Completed Updated: 10/25/21 1356 Narrative: EXAMINATION: Single View Chest EXAM DATE: 10/25/2021 1:39 PM TECHNIQUE: Portable semiupright AP view. INDICATION: Cough. Shortness of breath. COMPARISON: None. ENCOUNTER: Not applicable _________________________ FINDINGS: Borderline/mild cardiomegaly. There is bilateral peribronchial cuffing. There is severe coarse linear/strandy and hazy/patchy bilateral airspace disease. The pulmonary vasculature is obscured. No effusion or pneumothorax is seen. _________________________ Impression: Extensive multifocal/bilateral airspace disease. Question COVID pneumonia, pulmonary edema or other. The former is more favored given the extent of the airspace disease and no pleural fluid. Procedure Component Value Ref Range Date/Time Peripheral Blood Culture [349101477] Collected: 10/27/21 1006 Order Status: Completed Specimen: Blood, Venous Updated: 10/28/21 1101 Cult Blood Peripheral No Growth 24 hours Peripheral Blood Culture [349101478] Collected: 10/27/21 1017 Order Status: Completed Specimen: Blood, Venous Updated: 10/28/21 1101 Cult Blood Peripheral No Growth 24 hours Legionella Antigen, Urine [349436571] Collected: 10/28/21 0949 Order Status: Sent Specimen: Urine, catheter Updated: 10/28/21 0954 Streptococcus Pneumoniae Antigen, Urine [349436570] Collected: 10/28/21 0949 Order Status: Sent Specimen: Urine, catheter Updated: 10/28/21 0953 Respiratory Pathogens by Film Array [349436572] Collected: 10/28/21 0945 Order Status: Sent Specimen: Swabbed Collection from Nasopharynx Updated: 10/28/21 0953 Peripheral Blood Culture [348823607] Collected: 10/25/21 1240 Order Status: Completed Specimen: Blood, Venous Updated: 10/27/21 1301 Cult Blood Peripheral No Growth 48 hours Narrative: Draw from a different site than draw one. COVID-19 PCR - Rapid BL and Regionals [348823611] (Abnormal) Collected: 10/25/21 1242 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 10/25/21 1305 COVID-19 PCR Detected Abnormal Not Detected Comment: COVID-19 (SARS-CoV-2) test is positive. Clinical correlation with patient history and other diagnostic information is necessary to determine infection status. This test has received Emergency Use Authorization (EUA) by the FDA, but performance has not been evaluated for asymptomatic patients. Testing was performed using a nucleic acid amplification method. The specimen source may have been changed from the original order per patient situation or symptoms. Covid 19 Result Comment See Comment Comment: COVID-19 results reported as "detected" means COVID-19 positive. Positive patients should self-isolate for 10 days or 24 hours after fever resolves and other symptoms are improving, whichever is longer: - Stay home except to get medical care and wear a facemask if you must leave - Separate yourself from other people in your home, known as home isolation - Cover your coughs and sneezes - Wash your hands often - Avoid sharing household items - Clean high-touch surfaces everyday - If you have a medical emergency and need to call 911, notify dispatch personnel that you may have COVID-19 and put on a facemask before emergency medical services arrive. If the result is "inconclusive" or "invalid" and you have not been contacted by a medical professional about your result or if you have questions about COVID-19, your symptoms, or need a return to work/school note, please contact your primary care provider (PCP).
Aktuelle Erkrankungen: -
Vorgeschichte: Non-Hospital Acute respiratory failure with hypoxia (HCC) Prediabetes
Andere Medikamente: Outpatient Medications cholecalciferol (VITAMIN D3) 50 MCG (2000 UT) capsule fluticasone-salmeterol (ADVAIR HFA) 230-21 MCG/ACT inhaler Lactobacillus (PROBIOTIC ACIDOPHILUS) CAPS levothyroxine (SYNTHROID) 25 MCG tablet lisinopril (PRINIVIL,
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 1821617

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

schwer

Staat: CA
Alter: 18,0
Geschlecht: M
Eingang: 27.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Syncope Tinnitus

Symptomtext

Patient received covid vaccine and fainted minutes after receiving the vaccination. Patient stated they felt lightheaded and head was "buzzing". After patient fainted stated that they felt better, ambulance arrived and took over patient care.

Weitere VAERSDATA-Felder

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

VAERS 1817594

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

schwer

Staat: TX
Alter: 36,0
Geschlecht: M
Eingang: 26.10.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Flushing Hyperhidrosis Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Medium, Additional Details: patient came back later in the afternoon in a cheerful mood to obtain COVID-19 card, say thank you, and that he was diagnosed with vasovagal syncope.

Weitere VAERSDATA-Felder

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

VAERS 1814061

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

schwer

Staat: OH
Alter: 16,0
Geschlecht: F
Eingang: 24.10.2021
Impfdatum: 24.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Blindness Feeling hot Loss of consciousness Thirst

Symptomtext

About 10 minutes after administering patient's second dose of the Pfizer COVID vaccine, patient's father called attention saying "she's not doing well." Patient passed in and out of consciousness for about 5-10 minutes. At that time EMS was call and patient regained consciousness. She reported loss of vision, thirst, and feeling hot. EMS arrived, checked vitals, and patient left on own accord with parent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Heart rate, respiration rate, and blood pressure.
Aktuelle Erkrankungen: Patient reports no other illness.
Vorgeschichte: Patient reports no health conditions.
Andere Medikamente: Patient reports no medications.
Allergien: Patient reports no allergies.
Vorherige Impfungen: -

VAERS 1793689

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: GA
Alter: 26,0
Geschlecht: M
Eingang: 24.10.2021
Impfdatum: 16.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Confusional state Dizziness Flushing Hyperhidrosis Injection site pain Syncope Unresponsive to stimuli

Symptomtext

Site: Pain at Injection Site-Medium, Systemic: Confusion-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Severe, Additional Details: Patient passed out within 2 minutes of being given the COVID-19 Pfizer vaccine on 10/16/2021. 911 was called and Epi-pen was administered as well. Please contact vaccination site if further information is needed.

Weitere VAERSDATA-Felder

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

VAERS 1813386

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: TX
Alter: 19,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 23.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Dizziness Hyperhidrosis Presyncope

Symptomtext

Patient was given Pfizer 2nd dose vaccine in left arm at 1324 and after that patient verbalized she was feeling dizzy. patient decided to lay back. At 1326 I examined the patient. Patient appeared sweaty, weak, and appeared to be having a vasovagal response. Patient was awake, alert and oriented x3 at all times. EMS examined vital signs: 81/47 pulse-63, O2-99%. Patient recommended to go to ER for further evaluation, but patient refused. Refusal form signed by patient. Patient refused for her fiance to drive in her stead. Patient left facility at 1409 in no acute distress.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: 106/63 @1355 hrs. pulse-63 O2-99%
Aktuelle Erkrankungen: Borderline personality disorder, anxiety, Bipolar disorder
Vorgeschichte: BPD, Anxiety
Andere Medikamente: Latuda, Duloxetin, Buspar, Ashwagandha, Marijuana
Allergien: None
Vorherige Impfungen: Vasovagal rxn with Pfizer 1st dose at 19 years, 9/30/21, Lot # FF8839

VAERS 1813336

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: CO
Alter: 22,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Flushing Head injury Hyperhidrosis Syncope Tremor

Symptomtext

Systemic: Dizziness / Lightheadness-Severe, Systemic: Flushed / Sweating-Mild, Systemic: Shakiness-Medium, Additional Details: Patient received the vaccine and waited the 15 minutes but after 10 minutes passed out, she hit her head on the floor, 911 was called and she was taken away for observation. Patient was alert and doing well.

Weitere VAERSDATA-Felder

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

VAERS 1967195

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: PA
Alter: 99,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 12.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / RA

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

Cough Dyspnoea Laboratory test Pneumonia Respiratory distress Respiratory tract congestion X-ray

Symptomtext

Pneumonia Chest Cong. Cough, SOB Resp. Distress.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory distress
Hospital-Tage: -
Labordaten: Res in hospital @ present time x-rays and labs
Aktuelle Erkrankungen: Anemia Leukocytosis Diastolic CHF HTN A-FIB Left spiral displaced fracture Humerus Glaucoma Severe Aortic Valve stenosis & regurg. H/O elevated troponin H/O Pneumonia 2012, 2018, 2019 Pulmonary Edema Cold Agglutinin Disease IgM Decreased Hg Resp Failure with hypoxia Non-Sustained V-Tach DVT HLD Moderate mitral valve regurg. Mild tricuspid valve regurg. Dry eye syndrome Macular degeneration (dry) S/P cataract surgery Ocular HTN (Bilat) Lumbar compression fracture Arterial left thigh stent 2009 Fall- 1 (2018) Anxiety/depression GI bleed-heme + stools 11/19 Squamous cell CA of face Basal cell CA of face Osteoarthritis
Vorgeschichte: Anemia Leukocytosis Diastolic CHF HTN A-FIB Left spiral displaced fracture Humerus Glaucoma Severe Aortic Valve stenosis & regurg. H/O elevated troponin H/O Pneumonia 2012, 2018, 2019 Pulmonary Edema Cold Agglutinin Disease IgM Decreased Hg Resp Failure with hypoxia Non-Sustained V-Tach DVT HLD Moderate mitral valve regurg. Mild tricuspid valve regurg. Dry eye syndrome Macular degeneration (dry) S/P cataract surgery Ocular HTN (Bilat) Lumbar compression fracture Arterial left thigh stent 2009 Fall- 1 (2018) Anxiety/depression GI bleed-heme + stools 11/19 Squamous cell CA of face Basal cell CA of face Osteoarthritis
Andere Medikamente: Prilosec Amlodipine/Valsartan Atenolol Calcium Carbonate with Vitamin D3 Multi-Vitamin Lasix Preservision Areds 2 Zoloft Lubricant Eye Drops O2 Tylenol Duoneb
Allergien: NKA
Vorherige Impfungen: -

VAERS 1804649

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: OH
Alter: 12,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Loss of consciousness

Symptomtext

Patient was given both vaccines and told to wait in waiting room. The patient felt dizzy and light headed, and may have slightly passed out. The patient told the pharmacist she had skipped breakfast and may have low blood sugar. The pharmacist gave her a bottle of water and a glucose tablet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: not known
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 1801125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: NJ
Alter: 39,0
Geschlecht: M
Eingang: 20.10.2021
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Decreased appetite Diarrhoea Fatigue Hyperhidrosis Loss of consciousness Nausea Nervousness Palpitations Pyrexia

Symptomtext

fever, profuse sweating, loss of consciousness, extreme heart racing, chest discomfort, nausea, nervousness, diarrhea, loss of appetite, fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: daily vitamins
Allergien: none
Vorherige Impfungen: -

VAERS 1798728

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

schwer

Staat: AZ
Alter: 35,0
Geschlecht: F
Eingang: 19.10.2021
Impfdatum: 19.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Syncope

Symptomtext

Syncope after receiving vaccine

Weitere VAERSDATA-Felder

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

VAERS 1798013

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: ID
Alter: 41,0
Geschlecht: M
Eingang: 19.10.2021
Impfdatum: 18.09.2021
Beginn: 12.10.2021
Tage bis Beginn: 24,0
Dosis: 2
Route/Site: IM / LA

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

Diabetic ketoacidosis Intensive care Malaise Nausea Pollakiuria Thirst Type 1 diabetes mellitus

Symptomtext

The patient began to feel ill and have episodes of frequent urination, increased thirst and nausea shortly after his 2nd dose of the Pfizer vaccine. On October 12th the patient presented to the Emergency Department and was admitted to the ICU for DKA and a new diagnosis of Type 1 diabetes.

Weitere VAERSDATA-Felder

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

VAERS 1795117

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: -
Alter: 32,0
Geschlecht: F
Eingang: 18.10.2021
Impfdatum: 17.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Nausea Syncope Vomiting

Symptomtext

the patient had a fainting spell after receiving the vaccination, she was also nauseous and vomiting

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: hypothyroid
Andere Medikamente: unknown
Allergien: codeine, shellfish, dairy
Vorherige Impfungen: Fainting

VAERS 1794748

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: TX
Alter: 68,0
Geschlecht: M
Eingang: 18.10.2021
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

Bell's palsy

Symptomtext

Bell's Palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Benicar, Bystolic
Allergien: N/A
Vorherige Impfungen: -

VAERS 1793751

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: PA
Alter: 38,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Malaise Seizure Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Medium, Systemic: Seizure-Mild, Systemic: Shakiness-Medium, Additional Details: She explained she has fainted in the past from vaccines. Received vaccine and shortly after said she wasn't feeling well. I went to grab her a wet paper towel. When I got back she had her head back and she was unresponsive, but breathing. she clenched the chair and had a sort of convulsion breifly. She came back to after about 2-3 minutes, shortly before the ambulance arrived and they looked at her. she decided not to go to the hospital.she drank some water & ate & said her husband would get her

Weitere VAERSDATA-Felder

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

VAERS 1793746

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

schwer

Staat: NJ
Alter: 23,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Flushing Head injury Headache Hyperhidrosis Injection site pain Seizure Syncope Unresponsive to stimuli

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Medium, Systemic: Headache-Medium, Systemic: Seizure-Severe, Additional Details: Patient stated that she had no issues with the first dose. About 2-3 minutes after receiving the second dose she began having convulsions and hitting her head on the wall. Her Father and I were able to get her to the floor then convulsions stopped. The paramedics arrived and took her to the ER for further evaluation.

Weitere VAERSDATA-Felder

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

VAERS 1793681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: OH
Alter: 30,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: 16.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Dizziness Hyperhidrosis Morning sickness Syncope Vomiting

Symptomtext

7 months pregnant patient, stated she has been having trouble eating breakfast due to morning sickness so she had not eaten anything. About 5 minutes after her vaccination she reports she felt sweaty and dizzy vomited a small amount and passed out for a short time. After 20-30 minutes she was feeling well enough to walk out of the store with her friend who was taking her to the hospital to be checked out on the advice of her obgyn.

Weitere VAERSDATA-Felder

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

VAERS 1793569

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: MA
Alter: 20,0
Geschlecht: F
Eingang: 16.10.2021
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

Anxiety Malaise Syncope

Symptomtext

Patient fainted approximately 10 minutes after receiving her vaccine. She stood up to throw away some trash and said she didn't feel well. She was caught by a nurse in the room so she had a controlled fall and didn't get hurt. She was treated by 2 nurses working at this clinic. They applied ice to her forehead, took her vitals and gave her a snack and some juice. After about 15 minutes she said she was feeling much better and left with her step mom. Her step mom said that she frequently faints when getting vaccines or other medical procedures. The patient, said it's anxiety related.

Weitere VAERSDATA-Felder

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

VAERS 1791059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: VA
Alter: 28,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: 01.10.2021
Beginn: 01.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Chest pain Chills Condition aggravated Fatigue Heart rate increased Palpitations Pyrexia Syncope Tachycardia

Symptomtext

tachycardia; heart rate of 140bpm (typically hover around 75); I had a fever of 101; chest pains; palpitations; fatigue; D-dimer was somewhat elevated; I felt much worse; faint; A few hours after vaccination I had chills but no fever.; This is a spontaneous report from a contactable other HCP (patient). A 28-year-old female patient received bnt162b2 (BNT162B2), dose 3 via an unspecified route of administration, administered in arm left on 01Oct2021 16:30 (at the age of 28-year-old) (Batch/Lot Number: FE3590) as dose 3 (booster), single for COVID-19 immunisation, administered at Pharmacy or Drug Store. Medical history was none. No known allergies. Concomitant medication(s) included omeprazole (OMPRAZOLE) 14 day series; ethinylestradiol, levonorgestrel (MARLISSA hormonal BC), both taken for an unspecified indication, start and stop date were not reported. The patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration, administered in arm left on 06Jan2021 (at the age of 28-year-old) (Batch/Lot Number: EL3246) as single dose, dose 2 via an unspecified route of administration, administered in arm left on 28Jan2021 (at the age of 28-year-old) (Batch/Lot Number: EN5318) as single dose for COVID-19 immunisation and experienced no side effects. Patient was not pregnant. No other vaccine in four weeks. Patient has not experienced COVID prior vaccination. COVID was not tested post vaccination. The patient experienced heart rate of 140bpm (typically hover around 75) (medically significant) on 02Oct2021 13:00 with outcome of recovering, tachycardia (medically significant) on 02Oct2021 21:00 with outcome of recovering, faint (medically significant) on 02Oct2021 with outcome of recovering, a few hours after vaccination she had chills but no fever (non-serious) on 01Oct2021 21:00 with outcome of recovering, fatigue (non-serious) on 01Oct2021 21:00 with outcome of recovering, she felt much worse (condition aggravated) (non-serious) on 02Oct2021 with outcome of recovering, she had a fever of 101 (non-serious) on 02Oct2021 13:00 with outcome of recovering, chest pains (non-serious) on 02Oct2021 with outcome of recovering, palpitations (non-serious) on 01Oct2021 21:00 with outcome of recovering, d-dimer was somewhat elevated (non-serious) on 02Oct2021 with outcome of recovering. Events resulted in Emergency room/department or urgent care. The clinical course of events was as follows: A few hours after vaccination on 01Oct2021 she had chills but no fever. The next day, on 02Oct2021 she felt much worse. Around 1pm she had a fever of 101 and a heart rate of 140bpm (typically hover around 75). She started getting chest pains, palpitations, and feeling feverish/faint. She did not have shortness of breath but decided to go to the ER just in case she had myocarditis/pericarditis. They did two EKGs while she was there and showed tachycardia and a few "benign palpitations" but no arrhythmias indicative of myocarditis/pericarditis according to her docs. Troponin was normal. D-dimer was somewhat elevated, so they did a CT scan. Scan didn't show anything in her lungs/heart. They put her on IV fluids which helped lower her heart rate and ultimately sent me home with a heart rate around 85-90 & a temperature of 100 to take Tylenol and fluids. After a night of sleep on 03Oct2021 her heart rate and temperature are normal, but still have lingering right-sided chest pain/fatigue. No follow-up attempts are needed. No further information is expected.; Sender's Comments: Based on a temporal association, a causal relationship between the reported events and BNT162B2 booster dose is considered possible. 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: Syncope
Hospital-Tage: -
Labordaten: Test Date: 20211002; Test Name: fever; Result Unstructured Data: Test Result:fever of 101; Comments: fever of 101; Test Date: 20211002; Test Name: fever; Result Unstructured Data: Test Result:100; Test Date: 20211003; Test Name: fever; Result Unstructured Data: Test Result:Normal; Test Date: 20211002; Test Name: CT scan; Result Unstructured Data: Test Result:didn't show anything in her lungs/heart; Test Date: 20211002; Test Name: EKG; Result Unstructured Data: Test Result:tachycardia and a few benign palpitations; Comments: no arrhythmias indicative of myocarditis/pericarditis according to my docs.; Test Date: 20211002; Test Name: D-dimer; Result Unstructured Data: Test Result:elevated; Test Date: 20211002; Test Name: heart rate; Result Unstructured Data: Test Result:140bpm (typically hover around 75); Test Date: 20211002; Test Name: heart rate; Result Unstructured Data: Test Result:rate around 85-90; Test Date: 20211003; Test Name: heart rate; Result Unstructured Data: Test Result:Normal; Test Date: 20211002; Test Name: Troponin; Result Unstructured Data: Test Result:Normal
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: OMPRAZOLE; MARLISSA
Allergien: -
Vorherige Impfungen: -

VAERS 1788946

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: OH
Alter: 12,0
Geschlecht: F
Eingang: 15.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Syncope

Symptomtext

Patient had a fainting episode after vaccination. Patient was observed sitting on the floor. Patient was given water and observed and blood pressure was taken and was adequate. After a few minutes patient felt better and the patient's mother took her home. I called the father later in the evening and he stated the patient was now fine, had eaten something and doing well.

Weitere VAERSDATA-Felder

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

VAERS 1788206

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: FL
Alter: 34,0
Geschlecht: M
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

Symptomtext

Patient passed out for about 30 seconds 2 minutes after getting the vaccine. Patient is coherent and back to normal after regaining consciousness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin - childhood allergy
Vorherige Impfungen: -

VAERS 1787884

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: IL
Alter: 21,0
Geschlecht: M
Eingang: 15.10.2021
Impfdatum: 14.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Seizure

Symptomtext

Seizure that lasted about 3-5 minutes , has history of Epilepsy with last seizure about 8 months ago

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Mild Asthma
Andere Medikamente: Levetiracetam 750mg Twice Daily D3 2000IU 1 tab daily Advil Cold&Sinus as needed
Allergien: Environmental allergies
Vorherige Impfungen: -

VAERS 1785692

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: ID
Alter: 18,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 05.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Syncope Unresponsive to stimuli

Symptomtext

Patient fainted shortly after 2nd pfizer dose and was unresponsive for a period of about 10-15 minutes, 911 was called, cold compress applied to back of neck, patient laid onto ground, BP was monitoring by vaccine administering nurse and reported as 98/58 and 98/52 for the 2 readings. EMTs arrived about 15mins later, by which time patient had just become responsive and was sitting upright, EMT performed their own evaluation/assessment of patient and was cleared by them, she sat in pharmacy waiting room for additional 15 minutes prior to leaving pharmacy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: N/A
Vorgeschichte: NONE KNOWN
Andere Medikamente: N/A
Allergien: nkda
Vorherige Impfungen: -

VAERS 1785499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: AZ
Alter: 46,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 10.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Extra dose administered Fall Head injury Loss of consciousness Pain Syncope

Symptomtext

Light-headed, dizzy, all over body aches started about 15-20 hours post-dose. Experienced a syncopal episode, which caused a fall and injury to the head. Lost of consciousness occurred prior to fall (syncope), which then caused the fall.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: ER visit to rule out other causes of syncope, and to asses severity of head injury.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: COVID-19 Pfizer vaccine Dose #2; Date: 01/09/2021; patient age: 45; adverse event: all over body aches, chills.

VAERS 1784853

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: OH
Alter: 22,0
Geschlecht: M
Eingang: 14.10.2021
Impfdatum: 13.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Loss of consciousness

Symptomtext

Patient stated fear of needles/shots prior to getting the shot. After getting the second Pfizer shot, patient was instructed to go sit in the waiting area for 15 minutes. During that time, the patient decided to go get a water bottle from a cooler by the front registers of the store. Shortly after, security camera shows patient sitting down on the ground, then falling back on elbows, and then passing out momentarily before regaining consciousness right after. Patient and patient's mother state that this has happened in the past though not in some time. Patient was assessed for injury however none was found so that patient was escorted back to the waiting area to wait out the remainder of his time under close watch. Several hours after the patient and his mother left, I called to check in on patient and the mother stated he was doing fine.

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 1784635

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: ME
Alter: 68,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 01.10.2021
Beginn: 02.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Fatigue Hyperhidrosis Loss of consciousness Nausea

Symptomtext

I was vaccinated at 4pm. At 2am I work up feeling nauseous. I walked into the bathroom and was standing at the sink when I suddenly passed out. When I came me to, I was sweating profusely and extremely chilled. I went back to bed. The next day I felt wiped out most of the day. I slept from noon till 4pm and then felt much better

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure
Andere Medikamente: Losartan 25 Mg Rosuvastatin 5 mg Ultimate Probiotic 14 Cranberry 4200 mg Magnesium 400mg AlgaeCal Plus
Allergien: None
Vorherige Impfungen: -

VAERS 1779393

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: TN
Alter: 82,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 11.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / AR

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

Blood glucose normal Presyncope Vertigo

Symptomtext

PATIENT'S HUSBAND CALLED CLINIC TODAY, 10/12/2021 AT 12:50 AND STATED THAT HIS WIFE CAME TO MEDICAL CENTER YESTERDAY FOR HER PFIZER COVID BOOSTER SHOT. HE STATES THAT HE JUST WENT INTO THE KITCHEN WHERE HIS WIFE "ABOUT PASSED OUT". HE STATES HE SAT HER IN A CHAIR. HE REPORTS HER BLOOD PRESSURE IS 140/86, PULSE IS 119, AND HER BLOOD GLUCOSE IS 110. INSTRUCTED PATIENT'S HUSBAND TO EITHER CALL PATIENT'S PCP OR CALL 911 FOR EVALUATION. I CALLED PATIENT TO CHECK ON HER AT 1:40 AND NO ANSER, I LEFT VOICEMAIL THAT I WAS CHECKING ON HER STATUS. AT 2:41 PATIENT'S SPOUSE CALLED BACK AND STATES HE CALLED 911 AND PATIENT WAS TRANSPORTED TO MEDICAL CENTER ER IN IN A NDIFFERENT CITY. HE STATES THE DOCTOR HAS SAID HE THINKS THE PATIENT LIKELY HAS VERTIGO. PATIENT'S HUSBAND STATES HAS HAD VERTIGO IN THE PAST.

Weitere VAERSDATA-Felder

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

VAERS 1779157

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: IA
Alter: 66,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 05.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Pneumonia Thrombosis

Symptomtext

Patients daughter called and said the patient was in the hospital with pneumonia that the doctor said was caused by the Covid booster. Daughter also mentioned that the patient had blood clots

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: not known
Vorgeschichte: new patient to us-not known
Andere Medikamente: not known
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1777572

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: NV
Alter: 70,0
Geschlecht: F
Eingang: 11.10.2021
Impfdatum: 05.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Pyrexia Syncope

Symptomtext

101 fever for most of 3 days and fainted on morning of day 2.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: hypertension, alopecia universalis, high cholesterol, hypothyroidism
Andere Medikamente: levothyroxine- 37 mcg; lovastatin 10 mg; losartan potassium 25 mg; calcium, vitamin D 1000, Estrace, Vitamin B12
Allergien: all nuts except almonds and macadamia, all fish except shellfish and some ahi tuna
Vorherige Impfungen: flu vaccine, 69, 10/2020

VAERS 1776602

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: -
Alter: 16,0
Geschlecht: F
Eingang: 11.10.2021
Impfdatum: 10.10.2021
Beginn: 10.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Flushing Posture abnormal Stress Syncope

Symptomtext

Following the Pfizer vaccination, patient experienced a vasovagal reaction with syncope lasting approximately 4 seconds. Patient appeared to be anxious prior to receiving the vaccine and exhibited stress related symptoms prior to becoming flush and "slumping." Medical personnel on staff attended to her monitoring blood pressure and pulse. Patient was laid down with legs elevated to help return blood flow. Patient was then monitored for 30 minutes and given some food and water. Upon leaving the facility, patient appeared to have regained normal function.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: -
Andere Medikamente: Unknown
Allergien: Not indicated in pre-health screening
Vorherige Impfungen: -

VAERS 1775860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

schwer

Staat: IL
Alter: 37,0
Geschlecht: F
Eingang: 10.10.2021
Impfdatum: 10.10.2021
Beginn: 10.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hyperventilation Loss of consciousness

Symptomtext

Patient was hyperventilating after shot. Passed out for about a minute and came to. EMS was called BP 120/72 and hr 110. Patient refused going to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: none reported
Vorherige Impfungen: seizure to flu shot five years ago.

VAERS 1775786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: ID
Alter: 30,0
Geschlecht: M
Eingang: 10.10.2021
Impfdatum: 10.10.2021
Beginn: 10.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Immediate post-injection reaction Seizure

Symptomtext

Patient had a seizure 10 seconds after giving dose. Paramedics came and patient made full recovery.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1775264

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: TX
Alter: 63,0
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: nein

Aphasia Cold sweat Fall Head injury Hyperhidrosis Loss of consciousness

Symptomtext

Patient was waiting for 15 minutes after vaccination outside of the pharmacy. He came up to the pharmacy looked like he was going to say something and then lost consciousness. He fell and landed on his head. He was bleeding from his head we put pressure on the wound and waited on EMT to get here. He was very sweaty and cold to the touch. He had trouble talking but was able to get across that he was diabetic and had not eaten anything today and that he had hypertension. EMS showed up and transported him to the hospital out of our care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Unknown, no tests were performed under our care.
Aktuelle Erkrankungen: None reported
Vorgeschichte: Diabetes, and Hypertension
Andere Medikamente: Unknown
Allergien: None reported
Vorherige Impfungen: -

VAERS 1775210

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: OH
Alter: 20,0
Geschlecht: M
Eingang: 09.10.2021
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

Dizziness Feeling hot Hyperhidrosis Nausea Presyncope

Symptomtext

While waiting 15 minutes after vaccine, patient became light headed and dizzy, and almost passed out. He then became very hot sweaty and nauseous. Had patient sit, wait, and use cold compress, water, and ate a granola bar. He stay 30 to an hour afterwards and then was feeling better

Weitere VAERSDATA-Felder

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

VAERS 1775127

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: AZ
Alter: 56,0
Geschlecht: F
Eingang: 09.10.2021
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

Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild

Weitere VAERSDATA-Felder

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

VAERS 1769505

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: -
Alter: 22,0
Geschlecht: F
Eingang: 07.10.2021
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: unbekannt

Condition aggravated Syncope

Symptomtext

22 yr old petite, slender built female with history of fainting after needles (told to staff AFTER the event), did just that. However her boyfriend caught her and placed on the floor without continued ALOC or hypotonia. Resolved with rest and leg elevation, ice on her face. Departed after education and without incident.

Weitere VAERSDATA-Felder

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

VAERS 1768991

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: NC
Alter: 53,0
Geschlecht: F
Eingang: 07.10.2021
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: ja Erholt: ja

Chills Hyperhidrosis Hypotension Paraesthesia Paraesthesia oral Presyncope

Symptomtext

Patient returned to clinic after approx 10minutes after leaving. Just prior to entering the building, she vasovagaled. She was immediately placed in a wheelchair and taken to a stretcher. BP was low 88/54 and diaphoretic. Stated she started to feel better once lay down. After approx 10min of stretcher, pt began to get the chills and stated she had tingling in her mouth and left side of face and neck. Transferred patient to ED for further evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Unknown
Allergien: -
Vorherige Impfungen: states she has "passed out" from flu vaccine in the 90's

VAERS 1768162

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: NY
Alter: 33,0
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

Eye movement disorder Hyperhidrosis Loss of consciousness Pallor Tremor

Symptomtext

Pt began to shake during administration. stated he has had reactions to blood work and other needles. he was stating his reaction and his eyes rolled back in his head and he went limp in his chair. He was unconscious for about 1-2 minutes and became pale and sweaty. He came to and tried to stand up and was calmed down and sat back in his chair. Pt stated had not eaten today and had not gotten much sleep in last few days. I offered him a soda. Pt chose to climbed down off chair and sat against wall drinking soda. EMS had been called and when they arrived they did their assessment and found 100s/60s bp, he reported normally 120/80 and that he was becoming more normal color. EMS felt he was stable, he signed off further treatment and had him stand up which we helped with. he was helped and moved to the waiting room for observation. he asked for some candy because he felt his blood sugar was still low. we advised against driving and he texted his mother to pick him up. he felt 70% at last discussion. his mother came and he left.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: na
Aktuelle Erkrankungen: None mentioned
Vorgeschichte: None mentioned
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1765394

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

schwer

Staat: CT
Alter: 23,0
Geschlecht: F
Eingang: 06.10.2021
Impfdatum: 05.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anaphylactic reaction Chest discomfort Discomfort Dizziness Dysphagia Dyspnoea Flushing Hyperhidrosis Hyperventilation Paraesthesia Throat tightness Tremor

Symptomtext

Systemic: Allergic: Anaphylaxis-Severe, Systemic: Allergic: Difficulty Breathing-Severe, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Severe, Systemic: Chest Tightness / Heaviness / Pain-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Flushed / Sweating-Medium, Systemic: Hyperventilation-Severe, Systemic: Shakiness-Severe, Systemic: Tingling (specify: facial area, extemities)-Severe, Additional Details: Patient get the 2nd dose of Pfizer shot at 7.40 pm after that around 10 mins she had felt uncomfortable. She was asked to lay down and had some sprite / water to drink. She said after laid down , did not feel like brething well. Bp was checked at 8 pm was 121/91 HR 104. At 8.10 pm BP 146/98 and HR 105 . At 8.18 pm Epipen was given ( 0.3 mg ) then at 8.22 mg Benadryl 50 mg was given. Paramedic took her to the hospital

Weitere VAERSDATA-Felder

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

VAERS 1764747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: AL
Alter: 44,0
Geschlecht: M
Eingang: 06.10.2021
Impfdatum: 01.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / RA

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

Bell's palsy

Symptomtext

Reported physician diagnosed patient with Bell's Palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1762743

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: OR
Alter: 23,0
Geschlecht: F
Eingang: 05.10.2021
Impfdatum: 05.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Fall Loss of consciousness Syncope

Symptomtext

Patient was seated, fainted and fell onto the floor. Recovered consciousness within about 30 seconds, was breathing normally and oriented x3

Weitere VAERSDATA-Felder

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

VAERS 1757449

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

schwer

Staat: DE
Alter: 17,0
Geschlecht: M
Eingang: 03.10.2021
Impfdatum: 03.10.2021
Beginn: 03.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Loss of consciousness Unresponsive to stimuli

Symptomtext

Patient states they "blacked out" soon after vaccination. Patient was unresponsive for approximately 3 minutes. Patient also states they felt "Dizzy" soon after vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1865515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

moderat

Staat: MA
Alter: 73,0
Geschlecht: F
Eingang: 20.12.2023
Impfdatum: 01.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: IM / RA

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

Balance disorder Biopsy ear Dizziness Erythema Fall Headache Vision blurred Gait inability Infection parasitic Migraine Nervous system disorder Otolithiasis Pathology test Vertigo Visual impairment

Symptomtext

eyes went black, then, kind of subsided a little bit, eyesight came back; mites on nose and ear; right leg, from ankle, all the way up calf, is always beet red; fell; dizzy; headaches; off balanced; could not walk; vertigo; possible crystals in her ear; migraines; could be something with central nervous system; This is a spontaneous report received from a Consumer or other non HCP. A 73-year-old female patient received BNT162b2 (COMIRNATY), in Oct2021 as dose 3 (booster), single (Lot number: FE5590) at the age of 73 years for covid-19 immunisation. The patient's relevant medical history included: "Diabetic" (unspecified if ongoing), notes: did not take any medication or anything; "high blood pressure" (unspecified if ongoing); "Acid reflux" (unspecified if ongoing); "compromised immune system" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: BNT162b2 (dose 1, administered in the left arm, Lot number EN6207), administration date: 13Mar2021, for COVID-19 immunisation; BNT162b2 (dose 2, administered in the left arm, Lot number: ER8731), administration date: 07Apr2021, for COVID-19 immunisation. The following information was reported: NERVOUS SYSTEM DISORDER (non-serious) with onset 19Oct2021, outcome "not recovered", described as "could be something with central nervous system"; GAIT INABILITY (non-serious) with onset 19Oct2021, outcome "not recovered", described as "could not walk"; DIZZINESS (non-serious) with onset 19Oct2021, outcome "not recovered", described as "dizzy"; HEADACHE (non-serious) with onset 19Oct2021, outcome "not recovered", described as "headaches"; MIGRAINE (non-serious) with onset 19Oct2021, outcome "not recovered", described as "migraines"; BALANCE DISORDER (non-serious) with onset 19Oct2021, outcome "not recovered", described as "off balanced"; OTOLITHIASIS (non-serious) with onset 19Oct2021, outcome "not recovered", described as "possible crystals in her ear"; VERTIGO (non-serious) with onset 19Oct2021, outcome "not recovered"; FALL (non-serious) with onset 2022, outcome "recovered", described as "fell"; VISUAL IMPAIRMENT (non-serious), outcome "recovered", described as "eyes went black, then, kind of subsided a little bit, eyesight came back"; INFECTION PARASITIC (non-serious), outcome "recovered", described as "mites on nose and ear"; ERYTHEMA (non-serious), outcome "unknown", described as "right leg, from ankle, all the way up calf, is always beet red". The events "dizzy", "headaches", "off balanced", "could not walk", "vertigo", "possible crystals in her ear", "migraines" and "could be something with central nervous system" required physician office visit. The events "mites on nose and ear" required emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of dizziness, headache, balance disorder, gait inability, vertigo, otolithiasis, migraine, nervous system disorder, infection parasitic, erythema. Additional information: Patient reported she has not been normal since the Pfizer shot, she had Oct2021. Patient reported date of booster dose as 21Oct2021; was not clarified, which date was correct date of receiving booster dose, 19Oct2021 or 21Oct2021. She was always dizzy, always got headaches, off balanced. Her life has been turned upside down, since that shot 19Oct2021 (as reported), at 11:00 AM, by 7:00 PM that night, was so dizzy, off balance, could not walk, was still suffering to this. Some days, it got worse, some days it was ok. First, they thought it was vertigo, they sent her from treatment, for possible crystals in her ear, went for that. Patient was waiting to see neurologist on 26Dec2023, it could be migraines, could be something with central nervous system, from shot, she did not know. When patient went to get up, eyes went black, then, kind of subsided a little bit, eyesight came back. From that point, she has not been the same. Patient just took paracetamol (TYLENOL), when headaches were bad. They thought she had crystals in her ear, was going to neurologist, that dealt with off balance, vertigo stuff. She was told it was because of the booster shot. Due to being off balance, she fell twice some time in 2022. Came in, fell, knocked over tv stuff, believed it was end of 2022 or beginning of 2023. She did call ambulance to come check her out, but did not go to the hospital. She had no other treatments. She had second fall, going to beauty parlor, there were 3 little steps, fell through plate glass window, that did not break. That was early spring time 2023. She had no treatment for that. Patient had other stuff after the booster. For some reason, had mites on nose and ear. That was 2022 or, before that. They sent her to see dermatologist, they didn't know what it was. They did biopsy son ear, did pathology, all this stuff. They gave her medication to try and get that out of her body. She did not remember the name. It all really started after this booster. She thought maybe it was because she was wearing a black mask. It had to be end of 2021, or early 2022. In right leg, from ankle, all the way up calf, was always beet red. They gave her medicine for that. She clarified this occurred during same time period this all took place, end 2021, early 2022. She had no other treatments or medication for mites or for right leg being red.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Test Name: biopsy son ear; Result Unstructured Data: Test Result:unknown results; Test Name: pathology; Result Unstructured Data: Test Result:unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Acid reflux (esophageal); Blood pressure high; Diabetic (did not take any medication or anything); Immune system disorder
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2724133

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge #FE3590

moderat

Staat: NY
Alter: 61,0
Geschlecht: M
Eingang: 14.12.2023
Impfdatum: 17.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Confusional state Dizziness Dyspnoea Fatigue Hypertension Loss of personal independence in daily activities Myalgia Palpitations Photopsia Tinnitus

Symptomtext

Muscle aches, dizziness, seeing stars, cognitive confusion, lassitude, severe tinnitus. The severe tinnitus remains now, two years later, as does the seeing of stars when I move my head. MOST IMPORTANTLY: I now have serious cardiovascular issues. I'm being medicated for extremely high blood pressure for the first time in my life, and have periodic racing heartbeat that impedes activity and makes breathing difficult.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: neurologist, consulted 7/25/2023. MRI currently recommended urgently, but being denied by insurance. Dr. Otolaryngologist, to be consulted 2/12/2024.
Aktuelle Erkrankungen: None
Vorgeschichte: Sleep apnea, Depression
Andere Medikamente: Sertraline, 100mg; Gabapentin, 600mg; Simvastatin, 20mg
Allergien: None
Vorherige Impfungen: -

VAERS 2723179

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MN
Alter: 74,0
Geschlecht: M
Eingang: 12.12.2023
Impfdatum: 06.10.2021
Beginn: 06.12.2023
Tage bis Beginn: 791,0
Dosis: 3
Route/Site: ID / RA

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

Asthenia Pneumonia

Symptomtext

ED NOTE 12/6/23: "Patient presented to the ER for further evaluation of pneumonia and increased weakness."

Weitere VAERSDATA-Felder

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

VAERS 2722767

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: WA
Alter: 30,0
Geschlecht: F
Eingang: 11.12.2023
Impfdatum: 12.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / -

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

Chest discomfort Echocardiogram normal Palpitations

Symptomtext

Palpitations (noticeable heart beating) and chest tightness. Started on the 14th. Palpitations more noticeable while lying down, and both tightness and palpitations were worse with walks around the neighborhood. The tightness was mostly like a pinching muscle pain between my 4th and 5th rib noticed on the 19th when attempting activities. I was taking 600mg ibuprofen around the clock, every 6 hours, suspecting myocarditis or pericarditis. At the time, I had tried to go to an urgent care, but it was going to be $150, and they would have still sent me to an ER because I was complaining of "chest pain." when I tried to make an office appointment, they did the same thing, and even called emergency services and connected me. I ended up just treating all of it at home because no one would professionally assess it as a side effect.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: I wasn't able to get any official testing because no one would evaluate it as a side effect instead of a heart attack. I did, however, tell my coworkers in my cardiac procedural unit, and they had a coworker come do an unofficial echo on me, which they said looked good on the 20th of October, 2021
Aktuelle Erkrankungen: n/a
Vorgeschichte: depression, tendonitis
Andere Medikamente: daily wellbutrin 150mg, occasional zinc, vit D, and fish oil
Allergien: nka
Vorherige Impfungen: -

VAERS 2707352

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MN
Alter: 59,0
Geschlecht: F
Eingang: 31.10.2023
Impfdatum: 19.10.2021
Beginn: 26.10.2023
Tage bis Beginn: 737,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

PT ARRIVED IN THE ED ON 10/26/23 COMPLAINING OF SHORTNESS OF BREATH STARTING 10/24. COVID TEST WAS POSITIVE. SHE ADMITTED TO THE HOSPTIAL AND WAS DISCHARGED HOME 10/28.

Weitere VAERSDATA-Felder

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

VAERS 2672419

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: AZ
Alter: -
Geschlecht: M
Eingang: 24.08.2023
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / AR

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

Ageusia Anosmia Asthenia Blood test normal Brain fog Blood test Computerised tomogram Computerised tomogram normal Disturbance in attention Fatigue Headache Migraine Distractibility Patient isolation Weight increased

Symptomtext

loss of sense of smell/taste; loss of sense of smell/taste; ongoing headaches; brain fog; feeling fatigued; difficulties focusing; 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 male patient received BNT162b2 (BNT162B2), on 02Nov2021 as dose 2, single (Lot number: FF2593) for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Batch/Lot No: FE3590), administration date: 12Oct2021, when the patient was 55-year-old, for COVID-19 immunization. The following information was reported: BRAIN FOG (non-serious) with onset 02Nov2021, outcome "not recovered"; DISTRACTIBILITY (non-serious) with onset 02Nov2021, outcome "not recovered", described as "difficulties focusing"; FATIGUE (non-serious) with onset 02Nov2021, outcome "not recovered", described as "feeling fatigued"; ANOSMIA (non-serious), AGEUSIA (non-serious) all with onset 02Nov2021, outcome "not recovered" and all described as "loss of sense of smell/taste"; HEADACHE (non-serious) with onset 02Nov2021, outcome "not recovered", described as "ongoing headaches". The events "loss of sense of smell/taste", "ongoing headaches", "brain fog", "feeling fatigued" and "difficulties focusing" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of anosmia, ageusia, headache, brain fog, fatigue, distractibility.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Test Name: Blood testing; Result Unstructured Data: Test Result:Unknown Results; Test Name: CT-SCAN; Result Unstructured Data: Test Result:Unknown Results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19; Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2673624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: AL
Alter: 31,0
Geschlecht: F
Eingang: 18.08.2023
Impfdatum: 14.10.2021
Beginn: 01.06.2023
Tage bis Beginn: 595,0
Dosis: 3
Route/Site: - / RA

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

Dizziness Fatigue Headache Hypoaesthesia Muscular weakness Musical ear syndrome Nausea Noninfective encephalitis Paraesthesia Tinnitus Vertigo

Symptomtext

inflammation of the brain; Severe headache; muscle weakness; vertigo; nausea; tingling and numbness of hands and legs; fatigue; dizziness; tingling and numbness of hands and legs; ringing in ears; hearing sounds of music or buzzing in my head; hearing sounds of music or buzzing in my head; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 32-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 14Oct2021 as dose 3 (booster), single (Lot number: FE3590) at the age of 31 years, in right arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose Number: 1, Batch/Lot No: El1284, Location of injection: Arm Right), administration date: 06Jan2021, when the patient was 30-year-old, for Covid-19 Immunization; BNT162b2 (Dose Number: 2, Batch/Lot No: EN5318, Location of injection: Arm Right), administration date: 27Jan2021, when the patient was 30-year-old, for Covid-19 Immunization. No other vaccine in four weeks. No Known allergies. No covid prior vaccination. The following information was reported: HEADACHE (non-serious) with onset 01Jun2023, outcome "not recovered", described as "Severe headache"; DIZZINESS (non-serious) with onset 01Jun2023, outcome "not recovered"; FATIGUE (non-serious) with onset 01Jun2023, outcome "not recovered"; MUSICAL EAR SYNDROME (non-serious) with onset 01Jun2023, outcome "not recovered", TINNITUS (non-serious) with onset 01Jun2023, outcome "not recovered" and all described as "hearing sounds of music or buzzing in my head"; NONINFECTIVE ENCEPHALITIS (medically significant) with onset 01Jun2023, outcome "not recovered", described as "inflammation of the brain"; MUSCULAR WEAKNESS (non-serious) with onset 01Jun2023, outcome "not recovered", described as "muscle weakness"; NAUSEA (non-serious) with onset 01Jun2023, outcome "not recovered"; TINNITUS (non-serious) with onset 01Jun2023, outcome "not recovered", described as "ringing in ears"; PARAESTHESIA (non-serious), HYPOAESTHESIA (non-serious) all with onset 01Jun2023, outcome "not recovered" and all described as "tingling and numbness of hands and legs"; VERTIGO (non-serious) with onset 01Jun2023, outcome "not recovered". The events "inflammation of the brain", "severe headache", "muscle weakness", "vertigo", "nausea", "tingling and numbness of hands and legs", "fatigue", "dizziness", "ringing in ears" and "hearing sounds of music or buzzing in my head" required physician office visit. Therapeutic measures were taken as a result of noninfective encephalitis, headache, muscular weakness, vertigo, nausea, paraesthesia, fatigue, dizziness, hypoaesthesia, tinnitus, musical ear syndrome, tinnitus. Severe headache and inflammation of the brain, muscle weakness, vertigo, fatigue, nausea, tingling and numbness of hands and legs, dizziness, ringing in ears, hearing sounds of music or buzzing in my head. There is covid tested post vaccination. AE treatment: Gabapentin, Indomethacin, Oxcarbazepine.; Sender's Comments: Based on the information provided, and a temporal association, a causal association between reported event noninfective encephalitis and suspect BNT162B2 cannot be excluded. This 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 to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

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

VAERS 2673522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: FL
Alter: 92,0
Geschlecht: F
Eingang: 18.08.2023
Impfdatum: 08.10.2022
Beginn: 09.06.2023
Tage bis Beginn: 244,0
Dosis: 3
Route/Site: IM / -

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

Asthenia Dyspnoea exertional

Symptomtext

2/10/2021 010M20A 3/10/2021 048A21A 10/27/2021 FE3590 5/5/2022 FK9894 10/8/2022 GH9702 Pfizer BiValent 6/9/2023 - 6/13/2023 (4 days) Presents hospital progressively worsening generalized weakness for last 1 week and dyspnea on exertion.

Weitere VAERSDATA-Felder

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

VAERS 2670898

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: FL
Alter: 75,0
Geschlecht: M
Eingang: 14.08.2023
Impfdatum: 13.07.2022
Beginn: 05.08.2023
Tage bis Beginn: 388,0
Dosis: 3
Route/Site: - / -

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

COVID-19 pneumonia Sepsis Superinfection bacterial

Symptomtext

Sepsis likely secondary to COVID-19 pneumonia with suspected bacterial superinfection

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: BPH (benign prostatic hyperplasia) Elevated brain natriuretic peptide (BNP) level Hypertension Hyperlipidemia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2659425

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 30,0
Geschlecht: F
Eingang: 21.07.2023
Impfdatum: 25.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Antiphospholipid antibodies Blood test abnormal Burning sensation C-reactive protein increased Cardiac monitoring Computerised tomogram Dyspnoea Electrocardiogram Inflammation Magnetic resonance imaging spinal abnormal Monoplegia Palpitations Paraesthesia

Symptomtext

First day I was fine I was the normal symptoms. The next day my legs paralyze from my hips to all the way down to my feet. I couldn't move them. They were burning and tingly like on fire. It's been 2 years and I am still going through the same thing. My hear sometimes it starts racing really fast making it hard for me to breathe.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: CT Scan MRI in the spine lower bottom inflamed Bloodwork a little high on the serum active protein Lupus panel heart monitor EKG
Aktuelle Erkrankungen: asthma obesity
Vorgeschichte: asthma
Andere Medikamente: inhaler
Allergien: no
Vorherige Impfungen: -

VAERS 2658230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: GU
Alter: 35,0
Geschlecht: F
Eingang: 19.07.2023
Impfdatum: 11.10.2021
Beginn: 17.11.2021
Tage bis Beginn: 37,0
Dosis: 2
Route/Site: SYR / LA

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

Chest discomfort Chest pain Electrocardiogram Electrocardiogram ambulatory Laboratory test Menstruation irregular Pulmonary function test X-ray

Symptomtext

chest pain, chest tightening, irregular menstruation (early and/or late)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 11/17/2021- labs and EKG; 01/17/2023- labs, x-ray, breathing test; 01/23/2023, 01/24/2023- holter monitor
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2653423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 06.07.2023
Impfdatum: 02.02.2021
Beginn: 06.11.2022
Tage bis Beginn: 642,0
Dosis: 3
Route/Site: IM / -

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

COVID-19 Confusional state Encephalopathy Tachycardia

Symptomtext

Reported Symptoms: 10010300:CONFUSION; 10014625:ENCEPHALOPATHY; 10043071:TACHYCARDIA; 10084268:COVID-19; Narrative: Patient received three doses of Pfizer and one dose of Moderna COVID 19 vaccine. The patient presented to the ED on 6 November 2022 with confusion and tachycardia. The patient was admitted with COVID 19. The patient was treated with diltiazem. The patient was discharged on 16 November 2022 in stable condition. Reported per EUA. Other Relevant HX: Other: covid encephalopathy

Weitere VAERSDATA-Felder

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

VAERS 2652962

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 06.07.2023
Impfdatum: 02.02.2021
Beginn: 06.11.2022
Tage bis Beginn: 642,0
Dosis: 3
Route/Site: IM / -

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

COVID-19 Confusional state Encephalopathy Tachycardia

Symptomtext

Reported Symptoms: Confusion; Encephalopathy; Tachycardia; Narrative: Patient received three doses of Pfizer and one dose of Moderna COVID 19 vaccine. The patient presented to the ED on 6 November 2022 with confusion and tachycardia. The patient was admitted with COVID 19. The patient was treated with diltiazem. The patient was discharged on 16 November 2022 in stable condition. Reported per EUA. Other Relevant Hx: Other: covid encephalopathy

Weitere VAERSDATA-Felder

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

VAERS 2614649

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 38,0
Geschlecht: F
Eingang: 13.04.2023
Impfdatum: 05.11.2021
Beginn: 01.08.2022
Tage bis Beginn: 269,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Blood test abnormal COVID-19 Contusion Cough Dyspnoea Platelet count decreased Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I tested positive for COVID-19 in August 2022. I had a very high fever with cough and congestion. It lasted about 5 days. I only slept and drank fluids for my treatment. My fever got up to about 104 before it broke. I did have trouble breathing but my pulse oxygen level remained normal. After this I was feeling so very fatigued and bruising very easy with overall weakness. I went to the doctor to find out what was causing this. The tests showed that my platelets were very low and was told to watch for 6 months. After 6 months we tested again, and I am now considered "chronic". The next for me is to have my blood drawn every two weeks to determine any other auto immune issues or deficiencies and blood cancers.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Blood Panels, abnormal, unknown
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Estrogen patch; ZYRTEC; multivitamin
Allergien: Seasonal
Vorherige Impfungen: -

VAERS 2583501

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MI
Alter: 65,0
Geschlecht: M
Eingang: 17.02.2023
Impfdatum: 26.10.2021
Beginn: 08.02.2023
Tage bis Beginn: 470,0
Dosis: 3
Route/Site: - / -

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

Abscess limb Acute kidney injury Anticoagulant therapy Aspiration pleural cavity Blood creatinine increased Blood potassium increased Blood urea increased COVID-19 Chest X-ray abnormal Chronic kidney disease Clostridium test Condition aggravated Diarrhoea Diuretic therapy Echocardiogram abnormal Ejection fraction Haemoglobin decreased Hyperkalaemia

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 2/8/2023 Discharge Date: Feb 12, 2023 PRESENTING PROBLEM: Acute renal failure, unspecified acute renal failure type [N17.9] Acute kidney injury superimposed on chronic kidney disease [N17.9, N18.9] HOSPITAL COURSE: Patient is a 66 y.o. male with past medical history significant for chronic combined systolic dysfunction and diastolic dysfunction CHF, severe RV dysfunction, valvular heart disease with repair for mitral valve, ASD repair, tricuspid valve annuloplasty 8/19, atrial fibrillation on Coumadin, CAD s/p CABG, type 2 diabetes, CKD III, malignant melanoma on left eye '19, iron deficiency anemia who was sent to ER by his cardiologist due to elevated creatinine, INR during routine check on the day of admission Patient recently had right thoracentesis on January 26 and pleural fluid study was suspicious for small B-cell lymphoma or CLL. In he ED; Vitals in ER showed blood pressure 97/53, pulse 58, temperature 5, respiration 18, O2 sat 98% on room air. Labs showed BUN 89, creatinine 3.84 which is elevated from his baseline, INR 2.7, potassium 5.2, hemoglobin 10.8, white count 7.3 platelet 172. BMP 1218. He was also positive for COVID-19. CXR showed pulmonary congestion and small to moderate right pleural effusion. Patient reported recently finishing a course of antibiotics for his abscess on his left buttock and has subsequently developed watery diarrhea after he finished antibiotics. Patient had a echocardiogram, which showed left ventricular ejection fraction 60% and small pericardial effusion. Patient stated that he has been taking home diuretics on time and has been making urine without decreased urine output noted. He also denies weight gain or weight loss or lower extremity edema. He was admitted to hospitalist service, and was started on fluid, and diuretics were held. His creatinine improved from 3.84 on admission to 1.68. The patient was also had hyperkalemia following improved after restricting his potassium intake as well as giving Kayexalate and coma. Chronic combined CHF was stable, he continued Coreg, but was advised to restart Torsemide in 2-3days as well as his Lisinopril and metolazone. He was instructed not to continue with spironolactone at this time due to hyperkalemia and was advised to follow-up with his primary care doctor or cardiologist in order to assess reassess restarting the medications. He was not interested in repeating thoracocentesis. Diarrhea resolved prior we were able to test for C. Diff. Chronic A. Fib with well controlled rate. He was discharged on warfarin He has known history of iron deficiency anemia and he received Ferrlecit 125 mg 5 infusion during this hospitalization. He will follow-up with hematologist as scheduled before for her this study to exclude small B-cell lymphoma CLL. The patient was discharged home in a stable condition. He was instructed to for 2 weeks. He was also given a prescription for repeating his BMP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Routine general medical examination at a health care facility Type II or unspecified type diabetes mellitus without mention of complication, not stated as uncontrolled Low-resistance pulmonary hypertension Diabetes mellitus type 2 in obese Exogenous obesity Current smoker Wheezing-associated respiratory infection (WARI) Persistent atrial fibrillation Rotator cuff tendinitis Endocarditis, acute OSA (obstructive sleep apnea) Left shoulder pain AC (acromioclavicular) arthritis LBP (low back pain) LVH (left ventricular hypertrophy) H/O endocarditis Family history of colon cancer heart Failure with Preserved LVEF (Advanced heart failure clinic) Valvular heart disease Status post childhood repair of ASD (atrial septal defect), sinus venosus defect with partial anomalous pulmonary venous return (PAPVR) CAD (coronary artery disease) Olecranon bursitis Tobacco use Influenza-like illness Anticoagulation monitoring, INR range 2.5-3.5 Pulmonary nodules, noted as far back as 2017. Chronic diastolic heart failure Chronic atrial fibrillation Choroidal nevus of right eye Malignant melanoma of choroid of left eye Chronic combined systolic and diastolic heart failure NICM (nonischemic cardiomyopathy) Venous stasis ulcer of left calf with fat layer exposed with varicose veins Acute on chronic combined systolic and diastolic heart failure Acute on chronic combined systolic (congestive) and diastolic (congestive) heart failure Obesity, morbid Symptomatic anemia Acute blood loss anemia Acute on chronic systolic heart failure Pleural effusion COVID-19 Iron deficiency anemia Acute kidney injury superimposed on chronic kidney disease
Andere Medikamente: aspirin 81 MG tablet atorvastatin (LIPITOR) 40 MG tablet carvedilol (COREG) 6.25 MG tablet Ferrous Sulfate (IRON) 325 (65 Fe) MG tablet lisinopril (PRINIVIL,ZESTRIL) 5 MG tablet metFORMIN (GLUCOPHAGE) 500 MG tablet metOLazone (ZAROXOLYN) 2.
Allergien: BactrimNausea and Vomiting, Dizziness
Vorherige Impfungen: -

VAERS 2576486

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NJ
Alter: 38,0
Geschlecht: M
Eingang: 06.02.2023
Impfdatum: 09.09.2021
Beginn: 20.10.2021
Tage bis Beginn: 41,0
Dosis: 2
Route/Site: SYR / AR

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

Chest pain Dyspnoea

Symptomtext

CHEST PAINS AND SHORTNESS OF BREATH MANIFESTED AFTER 2ND SERIES WAS GIVEN. IT WAS SEVER ENOUGH THAT MY PRIMARY CARE PROVIDER ISSUED A PHYSICAL TRAINING (PT) WAIVER DURING THIS PERIOD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 2545882

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 84,0
Geschlecht: F
Eingang: 29.12.2022
Impfdatum: 21.10.2021
Beginn: 29.11.2022
Tage bis Beginn: 404,0
Dosis: 1
Route/Site: - / -

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

Anticoagulant therapy Asthenia Blood creatinine increased Blood fibrinogen normal Blood lactate dehydrogenase increased Blood potassium decreased C-reactive protein increased COVID-19 Dyspnoea Ejection fraction normal Electrocardiogram normal Fibrin D dimer Glomerular filtration rate decreased Hypokalaemia Inflammatory marker test Malaise N-terminal prohormone brain natriuretic peptide increased SARS-CoV-2 test positive

Symptomtext

Patient is a 86 y.o. female patient of MD with history of HTN, DM, hypothyroidism, CKD presented to a local Hospital with weakness and sob. COVID-19 Infection Generalized weakness Vaccinated without booster Symptoms onset 11/25/22, positive test date 11/29/22 No current oxygen demand Trend inflammatory markers - CRP 3.4 LDH 386 Fibrinogen 385 D-dimer 1.85 MAB: Not indicated Steroids: Not indicated Anticoagulation: Heparin Consider discontinuation of isolation 12/8/22 Consult PT/OT - recommends skilled therapy Consult case management - discharge needs Stage 3b CKD Historical baseline: Cr 1.7 & GFR 32 Cr 1.78 Renally dose medications and avoid nephrotoxins DM2 Resume home medications Hypokalemia - resolved 2.8 on presentation Replace and recheck Hypothyroidism Continue supplement HTN SBP >200 in the ED Restart home medication - stopped meds several days ago due to not feeling well Prn hydralazine SBP 150s- change metoprolol to coreg 12.5mg BID to achieve better BP control Follow up with PCP Elevated trop in setting of COVID 19 Initial troponin 89 Repeat troponin 80 EKG NSR NT proBNP 4610 STT 2020 NLVFX EF 74% possible small mild area of ischemia the inferolateral segment. Medically managed

Weitere VAERSDATA-Felder

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

VAERS 2530042

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MI
Alter: 85,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 07.10.2021
Beginn: 03.12.2022
Tage bis Beginn: 422,0
Dosis: 3
Route/Site: - / -

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

Angiogram pulmonary abnormal Asthenia Bronchial obstruction Bronchostenosis COVID-19 Dyspnoea Dyspnoea exertional Fatigue Laboratory test Lung opacity Pneumonia Productive cough Sputum discoloured Tachycardia

Symptomtext

Admission Date: 12/3/2022 Discharge Date: 12/8/2022 COVID positive date: 12/3/2022 PRESENTING PROBLEM: Generalized weakness COVID-19 HOSPITAL COURSE: The patient is a 86 year old female with previous stage II lung adenocarcinoma and LU lobectomy in 2012 presents with worsening fatigue and shortness of breath. She was admitted with Covid and started on remdesivir and dexamethasone. She also had a history of pulmonary embolism, at that time she was treated with warfarin for several years and stopped. She also was found to have paroxysmal atrial fibrillation around the time of the pulmonary embolism. She has not been treated for either in several years and did have a Cardiology follow-up with negative workup for atrial fibrillation. During hospital course, due to shortness of breath, history of PE, history of lung Ca a CTA thorax was performed with significant findings. There is narrowing and obstruction of left bronchi which could be due to carcinoma, and has developed since the prior exam from 12/28/2021. Bronchoscopy is recommended. Soft tissue attenuation is seen along the posterior and posterolateral left heart border measuring 8.5 x 2.8 cm in the axial plane, and could represent postobstructive atelectasis and/or carcinoma. A moderate amount of groundglass opacity is seen in the left lower lobe compatible with pneumonia. Recommend to have repeat imaging in 4-6 weeks. She is scheduled to follow up with oncology in January. For the CAP, she received 5 days of ceftriaxone and azithromycin, will be discharged home with 2 additional days of azithromycin and ceftin for a 7 day course. She received five days of remdesivir and prednisone. On 12/7 multiple events of tachycardia (150s) Cardizem increased to 180 mg from 120 mg. Discuss to monitor blood pressure at home and to follow up with PCP. Physical therapy and occupational therapy recommend SAR and 4WW. Patient refused placement and will be returning home with the care of her daughter. Patient seen and examined- alert and oriented. She is not requiring any supplemental oxygen. Reports slight fatigue and shortness of breath. Denies fever, chills, chest pain, abdominal pain. Patient is discharged in stable condition- all labs and imaging reviewed. No concerns at this time. All questions were answered prior to discharge

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: Dyspnea, unspecified type; C/o 3 days of cough and shortness of breath. Cough is productive of yellow/green sputum. She denies fever but states that she is having difficulty breathing when ambulates a few steps. No nasal congestion. Using nebulizer at home every 4 hours with minimal relief. Due to patient's significant increased work of breathing with her history of lung cancer and LUL lobectomy (per her account) I did recommend that she go to the ER for further evaluation and treatment. She agreed. Spoke to the RN at hospital and gave report. She declined ambulance transfer
Vorgeschichte: COPD (chronic obstructive pulmonary disease) OSA (obstructive sleep apnea) SOB (shortness of breath) Lung nodules Essential hypertension Longstanding persistent atrial fibrillation Superficial phlebitis of leg, right Class 3 severe obesity due to excess calories without serious comorbidity with body mass index (BMI) of 40.0 to 44.9 in adult Chest pain History of pulmonary embolism History of lung cancer History of tachycardia Ventral hernia with bowel obstruction Generalized weakness
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler Ascorbic Acid (VITAMIN C PO) benzonatate (TESSALON) 100 MG capsule budesonide/formoterol (SYMBICORT) 160-4.5 MCG/ACT
Allergien: Aspirin Codeine Darvocet [Propoxyphene N-apap] Sulfamerazine Trimethoprim
Vorherige Impfungen: -

VAERS 2529057

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: PA
Alter: 45,0
Geschlecht: M
Eingang: 12.12.2022
Impfdatum: 29.10.2021
Beginn: 01.12.2021
Tage bis Beginn: 33,0
Dosis: 1
Route/Site: SYR / RA

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

Blood test Cardiac flutter Disturbance in attention Fatigue Malaise Migraine Tremor

Symptomtext

Severe Migraines, Extreme Fatigue, Heart fluttering, Loss of concentration, Tremors, overall extreme malaise

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Blood work
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: None
Allergien: Penicilin
Vorherige Impfungen: -

VAERS 2518833

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: LA
Alter: 86,0
Geschlecht: F
Eingang: 29.11.2022
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: ja Erholt: nein

Asthenia Cough Fatigue Oropharyngeal pain Pneumonia Rhinorrhoea SARS-CoV-2 test negative

Symptomtext

On 10/07/2021 in the morning I had a sore throat, runny nose, cough; fatigue, lack of energy. I went to urgent care where they diagnosed with pneumonia. The urgent care gave me a Z-PAK for 5 days. I took it on 12/30/2021-01/05/2022. I took it for 2 times a day. I still have runny nose. It can be from age but I still wanted to mention it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: 29NOV2022 COVID-19 test negative
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure; Thyroid
Andere Medikamente: Amlodipine; levothyroxine; metoprolol; estradiol; escitalopram; BENADRYL
Allergien: Seasonal allergies
Vorherige Impfungen: Sore arm dose 4.

VAERS 2503369

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: AZ
Alter: 34,0
Geschlecht: F
Eingang: 09.11.2022
Impfdatum: 22.01.2021
Beginn: 01.08.2021
Tage bis Beginn: 191,0
Dosis: 1
Route/Site: IM / LA

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

Axillary pain Chest pain Echocardiogram Electrocardiogram ambulatory Heart rate increased Hypertension Swelling Ventricular tachycardia

Symptomtext

After first 2 doses only had soreness and swelling under the arm in the armpit. This occurred in the first few days after vaccination and subsided after a week. Same happened after the booster. Received the first vaccination in January 2021. Was having chest pain off and on and went to primary doctor who referred me to a cardiologist in August 2021. I was diagnosed with ventricular tachycardia of unknown cause. Have been taking Propranlol due to this since then. Was recently in the ER for chest pain with high blood pressure and high pulse in October 2022. Still awaiting follow up with a cardiologist.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Echo, holter monitor. Both in September 2021.
Aktuelle Erkrankungen: None
Vorgeschichte: Diagnosed with tachycardia after vaccination
Andere Medikamente: Birth control patch
Allergien: None
Vorherige Impfungen: -

VAERS 2475297

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: AL
Alter: 41,0
Geschlecht: M
Eingang: 11.10.2022
Impfdatum: 08.10.2021
Beginn: 29.08.2022
Tage bis Beginn: 325,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal discomfort COVID-19 Chills Diarrhoea Fatigue Feeling hot Headache Oropharyngeal pain Pyrexia SARS-CoV-2 test positive Throat irritation Tremor

Symptomtext

After the 3rd dose I had tremendous chills and I was shaking. The next morning, some GI issues like diarrhea. 8/28/22 I felt a scratch throat and I woke up in the middle of the night and running a very low fever, it was 99.8 and I had the feeling of feeling very hot. At 4AM 8/29/22 I had a home test which was positive. I saw the doctor to get PAXLOVID. I did not have any worsening symptoms. From that Monday & Tuesday, I was very tired and I had a bad headache. Wednesday I developed the worst sore throat I ever had. Friday evening I felt better and Saturday I felt like nothing ever happened. I had no congestion.

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Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: 8/29/22 at home COVID-19 positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multivitamin; CLARITIN
Allergien: N/A
Vorherige Impfungen: -

VAERS 2473499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 10.10.2022
Impfdatum: 04.11.2021
Beginn: 29.09.2022
Tage bis Beginn: 329,0
Dosis: 3
Route/Site: - / -

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

Aortic valve incompetence Brain natriuretic peptide increased COVID-19 Cardiac failure acute Cardiac failure congestive Chest X-ray abnormal Condition aggravated Cough Dyspnoea Echocardiogram abnormal Hypoxia Left ventricular failure Lung infiltration Mitral valve incompetence Polyuria SARS-CoV-2 test positive

Symptomtext

Discharge Provider: Primary Care Provider: Admission Date: 9/29/2022 Discharge Date: Oct 1, 2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Acute on chronic combined systolic and diastolic CHF (congestive heart failure) (HCC) [I50.43] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 75 year old female with PMHx of chronic systolic CHF, HTN, CKD3, CAD, A-fib who presented to the hospital with shortness of breath and cough. She was found to be COVID-19 positive in the ER and had hypoxia. Patient had a CXR showing bilateral infiltrates. However the patient also had a significantly elevated BNP and was given IV lasix along with remdesivir and decadron. Patient improved quickly and was able to be weaned to room air off her O2. Patient diuresed well. She was afebrile after admission. Given her quick improvement (and symptoms only a few days) decadron was stopped as COVID-19 pneumonia was unlikely. Patient was kept and given 3 days of IV remdesivir. Patient was feeling much better at the time of discharge, she was breathing well on room air with no shortness of breath or cough, no fever. Patient was then considered stable for discharge home. Patient was instructed on signs and symptoms of when to return to the ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: HTN (hypertension), benign Edema extremities Hypothyroidism due to acquired atrophy of thyroid Glaucoma Sensorineural hearing loss Macular degeneration, wet (HCC) Breast mass, right At risk for injury from chemotherapy History of radiation exposure Non-ischemic cardiomyopathy, EF 35% s/p CRT-D (chemo vs other) Atrial fibrillation (HCC) Acute on chronic combined systolic and diastolic heart failure (HCC) History of breast cancer GERD (gastroesophageal reflux disease) Enlarged lymph node, subcarinal seen on CT, 14 mm Pulmonary nodules Nausea Mood insomnia (HCC) Advance care planning Atrial flutter (HCC) Atrial flutter/AF with rapid ventricular response (HCC) Complete heart block (HCC) MR (mitral regurgitation), mild/mod Echo 6/2022 Nonrheumatic aortic valve insufficiency, mild/mod Echo 6/2022 Coronary artery disease involving native coronary artery of native heart without angina pectoris Biventricular implantable cardioverter-defibrillator (ICD) in situ Chronic combined systolic and diastolic heart failure (HCC) Pneumonia due to COVID-19 virus Acute respiratory failure with hypoxia (HCC)
Andere Medikamente: amiodarone (PACERONE) 200 MG tablet apixaban (ELIQUIS) 5 MG tablet aspirin 81 MG chewable tablet atorvastatin (LIPITOR) 40 MG tablet calcium-vitamin D (CALCIUM 600+D) 600-200 MG-UNIT TABS per tablet dapagliflozin (FARXIGA) 10 MG TABS tablet
Allergien: ThimerosalSwelling Ceclor [Cefaclor]Hives Arimidex [Anastrozole]Other Brinzolamide Dye-contrastHives Netarsudil Shellfish Allergy
Vorherige Impfungen: -

VAERS 2467735

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 58,0
Geschlecht: M
Eingang: 03.10.2022
Impfdatum: 01.10.2021
Beginn: 01.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Cardiomegaly Colitis Computerised tomogram abnormal Constipation Diarrhoea Dyspnoea Echocardiogram Fatigue Laboratory test

Symptomtext

I started having symptoms after dose 1 but after dose 2, my symptoms seem to have gotten worse. I started having diarrhea and constipation. I also continued having shortness of breath and now I have been having fatigue. I had a CAT Scan of my internal organs after the first vaccine and they found enlarged heart, enlarged liver and enlarged colon. They do not know what has caused this. I have not been prescribed any medications at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Multiple labwork visits - results unknown (doctor said everything was normal) Echocardiogram - 9/2021 - results unknown
Aktuelle Erkrankungen: Unknown
Vorgeschichte: None
Andere Medikamente: Multivitamin
Allergien: Hay Fever; Shrimp; No known Drug Allergies
Vorherige Impfungen: Pfizer Covid-19 - 7-9-2021 - i just didn't feel well - 58 years old

VAERS 2454588

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MI
Alter: 75,0
Geschlecht: F
Eingang: 22.09.2022
Impfdatum: 11.10.2021
Beginn: 14.09.2022
Tage bis Beginn: 338,0
Dosis: 3
Route/Site: - / -

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

Brain natriuretic peptide increased COVID-19 COVID-19 pneumonia Cardiomegaly Chest X-ray abnormal Cough Dyspnoea Echocardiogram Ejection fraction normal End stage renal disease Hypoxia Lung carcinoma cell type unspecified stage 0 Oropharyngeal pain Pulmonary congestion Wall motion score index abnormal

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 9/14/2022 Discharge Date: Sep 20, 2022 PRESENTING PROBLEM: ESRD (end stage renal disease) (HCC) Pulmonary vascular congestion Malignant neoplasm of lung, unspecified laterality, unspecified part of lung (HCC) COVID-19 virus infection HOSPITAL COURSE: Patient 76-year-old female with her significant past medical history for stage IV lung cancer, history of breast cancer, chronic diastolic heart failure, CKD stage 4 with planning for fistula in future, presented to the hospital with multiple days of cough, dyspnea, sore throat since 9/12 found to have hypoxia with acute COVID-19 pneumonia. CXR with Mild cardiomegaly and vascular congestion without overt pulmonary edema. BNP elevated and TTE with small new WMA but LVEF normal and no signs of acute new CHF. Patient was not in any acute respiratory distress but needed 2 L of oxygen and was high risk so was admitted. Patient started on both dexamethasone and remedesivir along with supportive care. Improved to room air and remained stable. Plan discharge home with close follow up with both Oncology and Nephrology as well as PCP to consider repeat echo after resolution of covid infection. The patient was educated on need for close followup with PCP and nephrology with repeat labs in 1-2 weeks as her torsemide dose was decreased from BID to daily due to her renal function while inpatient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: 10/4/2021 Urgent Care Leg Swelling Change of Skin Color
Vorgeschichte: Calculus of kidney Chronic gastric ulcer without hemorrhage or perforation Arthropathy Stage IV squamous cell carcinoma of lung (HCC) Major depressive disorder with single episode, in partial remission (HCC) Premature atrial complexes Bilateral lower extremity edema Stage IV squamous cell carcinoma of lung Essential hypertension Coronary artery calcification seen on CT scan Stage 4 chronic kidney disease Obesity (BMI 30-39.9) Acute renal failure (ARF) (HCC) History of left breast cancer Colitis At risk for adverse drug interaction Edema, unspecified type New daily persistent headache Laceration of left lower extremity, subsequent encounter Acute bronchitis due to other specified organisms Epigastric pain and heartburn Encounter for antineoplastic immunotherapy Drug-induced thyroiditis Balance problems Closed displaced fracture of medial condyle of right femur with routine healing Adjustment disorder with mixed emotional features Chronic anemia Other and unspecified coagulation defects Frequent UTI Esophageal reflux History of nephrolithiasis Hyperparathyroidism (HCC) Hypothyroidism Malignant neoplasm of upper lobe, bronchus, or lung Other abnormal glucose Secondary malignant neoplasm of liver (HCC) Other malaise and fatigue Shortness of breath Urinary tract infection Benign essential tremor Restless leg syndrome Chronic bilateral low back pain with sciatica Primary insomnia Pruritus Chronic pain Lymphedema Cellulitis Cat bite of forearm, right, initial encounter Hypoxia Breast cancer (HCC) COVID-19 virus infection
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet aluminum, magnesium & simethicone (MAALOX EX) 400-400-40 MG/5ML budesonide (ENTOCORT EC) 3 MG delayed release capsule calcitriol (ROCALTROL) 0.25 MCG capsule cyclobenzaprine (FLEXERIL) 5 MG tablet diphe
Allergien: Iv ContrastHives ClonidineRash Penicillins Sulfa DrugsRash
Vorherige Impfungen: -

VAERS 2453417

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MI
Alter: 86,0
Geschlecht: F
Eingang: 21.09.2022
Impfdatum: 08.10.2021
Beginn: 06.09.2022
Tage bis Beginn: 333,0
Dosis: 3
Route/Site: - / -

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

Asthenia COVID-19 Chest discomfort Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

Discharge Provider: MD Primary Care Provider: DO Admission Date: 9/6/2022 Discharge Date: Sep 7, 2022 PRESENTING PROBLEM: Weakness COVID-19 virus infection COVID-19 HOSPITAL COURSE: Patient is a 87 y.o. female with atrial fibrillation, coronary artery disease status post CABG, hypertension, iron deficiency anemia, diastolic CHF, pulmonary hypertension, type 2 diabetes, hyperlipidemia, history of GI bleeding, CKD 3 and asthma who presented with chest discomfort associated with shortness of breath and slight cough starting four days prior to arrival. Significant workup in the ED included COVID 19 positive test. She was not requiring any supplemental oxygen in the ED. Family expressed concerns about increased care for her at this time so she was admitted for therapy evaluation and possible placement in deemed necessary. PT/OT recommended home with assist and patient was discharged home in stable condition under the care of her daughter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min (HCC) GERD (gastroesophageal reflux disease) Diabetic neuropathy (HCC) Asthma Atrial fibrillation (HCC) Mitral valve insufficiency Chest pain Coronary artery disease involving native coronary artery of native heart with angina pectoris (HCC) Essential hypertension S/P tricuspid valve repair Fe deficiency anemia DJD (degenerative joint disease) of knee Myopia of both eyes Diverticular disease Lumbar compression fracture (HCC) History of upper gastrointestinal hemorrhage Microalbuminuria Opiate dependence, continuous (HCC) Dyslipidemia Hyperkalemia Hyponatremia Type 2 diabetes mellitus with stage 3a chronic kidney disease, with long-term current use of insulin (HCC) Abnormal urinalysis Acute on chronic diastolic congestive heart failure (HCC) Chronic diastolic CHF (congestive heart failure) (HCC) Pleural effusion Unspecified severe protein-calorie malnutrition (HCC) COVID-19 virus infection
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler ALPRAZolam (XANAX) 0.25 MG tablet amLODIPine (NORVASC) 5 MG t
Allergien: None
Vorherige Impfungen: -

VAERS 2404642

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

moderat

Staat: OH
Alter: 76,0
Geschlecht: F
Eingang: 19.09.2022
Impfdatum: 28.10.2021
Beginn: 16.07.2022
Tage bis Beginn: 261,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

Patient is a 76 y.o. female with history of stage IV metastatic adenocarcinoma of the lung (s/p resection, radiation, chemotherapy), T2DM, CAD, prior PE (March 2022) on Eliquis, and asthma admitted to the hospital on 7/16/2022 for worsening SOB s/p COVID+ diagnosis on 7/12. Patient was placed on heated high flow, pulmonology and infectious disease consulted. She was started on Decadron 6 mg for total of 10 days, continue on home Symbicort, Spiriva, albuterol. Infectious disease recommended monoclonal antibodies, however patient declined at that time. Patient continually improved throughout the clinical course, and was eventually weaned down to 4L supplemental oxygen via nasal cannula. Patient was discharged w/ steroid taper per pulmonology

Weitere VAERSDATA-Felder

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

VAERS 2436254

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FE3590

moderat

Staat: MN
Alter: 78,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 23.02.2021
Beginn: 23.08.2022
Tage bis Beginn: 546,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Cough Dyspnoea Headache Hypoxia Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

HYPOXIA, FEVER, HEADACHE, BODY ACHE, COUGH, SOB

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: POSITIVE COVID TEST 8/26/22
Aktuelle Erkrankungen: -
Vorgeschichte: Angina pectoris Atherosclerosis of coronary artery Atrial fibrillation Cardiomyopathy CHF (congestive heart failure) Chronic pain Coronary artery disease Degenerative joint disease of ankle and foot Depressive disorder Dislocated finger Elevated cholesterol Fen-phen history GERD (gastroesophageal reflux disease) HTN (hypertension) Hyperlipidemia Hypothyroidism Incontinence, bladder Major depressive disorder MI (myocardial infarction) Osteoarthritis PMR (polymyalgia rheumatica) Pneumonia Takotsubo syndrome Venous (peripheral) insufficiency
Andere Medikamente: amiodarone (CORDARONE) 200 mg oral tablet amLODIPine (NORVASC) 5 mg oral tablet Cholecalciferol, Vitamin D3, 50 mcg (2,000 unit) oral tablet clindamycin hcl (CLEOCIN) 300 mg oral capsule DULoxetine (CYMBALTA) 60 mg oral delayed release ca
Allergien: -
Vorherige Impfungen: -

VAERS 2431103

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MN
Alter: 67,0
Geschlecht: M
Eingang: 07.09.2022
Impfdatum: 21.01.2021
Beginn: 21.07.2022
Tage bis Beginn: 546,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

SOB

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 6,0
Labordaten: POSITIVE COVID TEST 7/28/22
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension Malignant neoplasm of right lung
Andere Medikamente: amLODIPine (NORVASC) 5 mg tablet clobetasoL (TEMOVATE) 0.05 % cream Dupixent Syringe 300 mg/2 mL injection ibuprofen (ADVIL,MOTRIN) 600 mg tablet lisinopriL (PRINIVIL,ZESTRIL) 40 mg tablet metoprolol succinate (TOPROL-XL) 100 mg 24 hr
Allergien: Cat Dander
Vorherige Impfungen: -

VAERS 2430985

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MN
Alter: 60,0
Geschlecht: M
Eingang: 07.09.2022
Impfdatum: 03.03.2021
Beginn: 21.07.2022
Tage bis Beginn: 505,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

SOB

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: POSITIVE COVID TEST 7/22/2022
Aktuelle Erkrankungen: -
Vorgeschichte: ? A-fib (HCC) ? High cholesterol ? HTN (hypertension) ? Morbid obesity (HCC) ? OSA (obstructive sleep apnea) ? Gastroesophageal reflux disease K21.9 ? Tobacco use disorder F17.200 ? Hyperlipidemia E78.5 ? Unspecified sleep apnea G47.30 ? Obesity, unspecified E66.9 ? Dyslipidemia E78.5 ? OSA (obstructive sleep apnea) G47.33 ? A-fib (HCC) I48.91 ? Tachycardia R00.0 ? LBP (low back pain) M54.50 ? GERD (gastroesophageal reflux disease) K21.9 ? Dyspnea R06.00 ? Acute exacerbation of chronic obstructive pulmonary disease (COPD) (HCC) J44.1 ? Acute bronchitis J20.9 ? Upper respiratory infection J06.9 ? BPH (benign prostatic hyperplasia) N40.0
Andere Medikamente: albuterol HFA 90mcg/puff (PROVENTIL;VENTOLIN HFA) 90 mcg/actuation Inhl inhaler albuterol HFA 90mcg/puff (PROVENTIL;VENTOLIN HFA) 90 mcg/actuation Inhl inhaler atenolol-chlorthalidone (TENORETIC) 100-25 mg Oral Tab dilTIAzem (DILTIA XT;DILA
Allergien: Contrast [Xray Dyes (Nic)] Iodinated Contrast Media
Vorherige Impfungen: -

VAERS 2429777

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MN
Alter: 61,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 21.10.2021
Beginn: 30.08.2022
Tage bis Beginn: 313,0
Dosis: 2
Route/Site: IM / LA

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

Dyspnoea Oxygen saturation decreased

Symptomtext

Increasing SOB and low O2 sats. Treatment includes oxygen, IV steroids and an antibiotic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CHF, Diabetes, HTN, COPD, Obesity
Andere Medikamente: -
Allergien: Lisinopril, Seasonal
Vorherige Impfungen: -

VAERS 2425243

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MI
Alter: 81,0
Geschlecht: M
Eingang: 31.08.2022
Impfdatum: 29.01.2021
Beginn: 29.08.2022
Tage bis Beginn: 577,0
Dosis: 3
Route/Site: - / -

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

Asthenia COVID-19 pneumonia Cough Dyspnoea Haemodialysis Hypoxia

Symptomtext

Pt arrives with shortness of breath, cough, and generalized weakness for 3 days. Pt is on hemodialysis. Pt has COVID-19 pneumonia with hypoxia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2048405

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MI
Alter: 58,0
Geschlecht: M
Eingang: 27.08.2022
Impfdatum: 10.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: UN / UN

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

Atelectasis COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Chest X-ray Laboratory test Oxygen saturation Polymerase chain reaction Dyspnoea Hyponatraemia Hypoxia Influenza A virus test negative Influenza B virus test Laboratory test abnormal Oxygen saturation decreased Pulmonary fibrosis Respiratory syncytial virus test negative

Symptomtext

Recent COVID infection/COVID pneumonia; This spontaneous case was retrieved on 15-Aug-2022 from Vaccine Adverse Event Reporting System (VAERS) (reference number: 2048405-1), reported by other healthcare professional and concerned a 58-year-old, male patient. The patient's concurrent conditions included respiratory: COPD, moderate (chronic obstructive pulmonary disease), circulatory: internal hemorrhoids, benign hypertension, infectious/inflammatory: tinea pedis, hematologic: iron deficiency, anemia, nervous: tobacco abuse in remission, alcohol abuse, tension-type headache, intractable, diabetic polyneuropathy, endocrine/metabolic: type two diabetes mellitus and other: environmental allergies and anxiety. The patient's historical condition included malignant melanoma of right neck. The patient's concomitant medications included albuterol HFA inhaler (brand names used: Proventil HFA, Ventolin HFA, Proair HFA), Lipitor (atorvastatin), Decadron (dexamethasone) and lisinopril-hydrochlorothiazide (brand names used: Prinzide, Zestoretic), all used for unreported indications. On 10-Oct-2021, the patient was vaccinated with Flucelvax Quadrivalent (influenza vaccine inact sag 4v; dose: reported as 'one'; route of administration: injection (reported as 'SYR'); anatomical location and indication: not reported). The batch number reported was 308451. On the same date, the patient was vaccinated with a booster dose of non-company co-suspect Pfizer-BioNTech COVID-19 vaccine (tozinameran; dose: reported as '3'; route of administration: injection (reported as 'SYR'), anatomical location and indication: not reported). The batch number reported was FE3590. On unspecified date, an unknown amount of time after receiving Flucelvax Quadrivalent and non-company co-suspect Pfizer-BioNTech COVID-19 vaccine, the patient experienced COVID-19 infection, reported as 'recent COVID infection' and was placed on prednisone in the outpatient setting. On 07-Jan-2022, two months and 28 days after receiving Flucelvax Quadrivalent and non-company co-suspect Pfizer-BioNTech COVID-19 vaccine, the patient presented to the emergency department with worsening symptoms of shortness of breath, cough and congestion. In the emergency department, the patient was hemodynamically stable, with desaturations noted 87% with ambulation and was placed on 2 L nasal cannula. On the same date chest X-ray was performed due to acute cough/dyspnoea and hypoxia, frontal and lateral. The heart size and pulmonary vascularity appeared normal. There appeared to be mild left basilar atelectasis or scar. There was focal eventration of the right hemidiaphragm. The remainder of the thorax was without significant change. On the same date, a nasopharyngeal swab specimen was collected for the PCR (polymerase chain reaction) detection of COVID-19, Influenza A and B, and RSV (Respiratory syncytial virus). All test results came back negative. Labs were with mild hyponatremia, otherwise unremarkable. The patient was admitted to the hospital for COVID pneumonia, with steroids increased, dexamethasone at a dose of 6 mg. The patient did well and remained stable on 2 L nasal cannula. On 09-Jan-2022, after two days, the patient was discharged home on home oxygen. At time of discharge, the patient had vital signs within normal limits, and was comfortable with discharge plan home. The outcome of the event was unknown. The reporter did not provide a causality assessment. The events of 'COVID-19 pneumonia' was considered to be serious due to seriousness criteria of hospitalization and was considered to be medically significant by a Physician within Seqirus' Pharmacovigilance and Risk Management Department. Company comment: A 58-year-old, male patient was vaccinated with Flucelvax Quadrivalent and non-company co-suspect Pfizer-BioNTech COVID-19 vaccines. An unknown amount of time following vaccination, the patient experienced COVID-19 infection. In addition, two months and 28 days after vaccination, the patient presented to the emergency department with worsening symptoms of shortness of breath, cough and congestion. In the emergency department, the patient was hemodynamically stable, with desaturations noted 87% with ambulation and was placed on 2 L nasal cannula. A nasopharyngeal swab specimen was collected for the PCR (polymerase chain reaction) detection of COVID-19, Influenza A and B, and RSV (Respiratory syncytial virus). All test results came back negative. The patient was admitted to the hospital for COVID pneumonia. Causal role of the suspect vaccine is assessed as not related due to biological implausibility.; Sender's Comments: Company comment: A 58-year-old, male patient was vaccinated with Flucelvax Quadrivalent and non-company co-suspect Pfizer-BioNTech COVID-19 vaccines. An unknown amount of time following vaccination, the patient experienced COVID-19 infection. In addition, two months and 28 days after vaccination, the patient presented to the emergency department with worsening symptoms of shortness of breath, cough and congestion. In the emergency department, the patient was hemodynamically stable, with desaturations noted 87% with ambulation and was placed on 2 L nasal cannula. A nasopharyngeal swab specimen was collected for the PCR (polymerase chain reaction) detection of COVID-19, Influenza A and B, and RSV (Respiratory syncytial virus). All test results came back negative. The patient was admitted to the hospital for COVID pneumonia. Causal role of the suspect vaccine is assessed as not related due to biological implausibility.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 2,0
Labordaten: Test Date: 20220107; Test Name: Chest x-ray; Result Unstructured Data: The heart size and pulmonary vascularity appears normal. There appears to be mild left basilar atelectasis or scar. There is focal eventration of the right hemidiaphragm. The remainder of the thorax is without significant change.; Test Date: 20220107; Test Name: Labs; Result Unstructured Data: Mild hyponatremia, otherwise unremarkable.; Test Date: 20220107; Test Name: Saturation; Result Unstructured Data: 87 % with ambulation; Test Date: 20220107; Test Name: PCR; Result Unstructured Data: COVID-19 detected, Influenza A not detected, Influenza B not detected, RSV not detected
Aktuelle Erkrankungen: Alcohol abuse; Anxiety; Benign essential hypertension; COPD; Diabetic polyneuropathy; Environmental allergy; Internal hemorrhoids; Iron deficiency anemia; Tension headache; Tinea pedis; Tobacco abuse; Type 2 diabetes mellitus
Vorgeschichte: Medical History/Concurrent Conditions: Malignant melanoma
Andere Medikamente: Albuterol Hfa; Lipitor; Decadron; Hydrochlorothiazide;Lisinopril dihydrate
Allergien: -
Vorherige Impfungen: -

VAERS 2048405

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MI
Alter: 58,0
Geschlecht: M
Eingang: 27.08.2022
Impfdatum: 10.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: OT / -

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

Atelectasis COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Chest X-ray Laboratory test Oxygen saturation Polymerase chain reaction Dyspnoea Hyponatraemia Hypoxia Influenza A virus test negative Influenza B virus test Laboratory test abnormal Oxygen saturation decreased Pulmonary fibrosis Respiratory syncytial virus test negative

Symptomtext

Recent COVID infection/COVID pneumonia; This spontaneous case was retrieved on 15-Aug-2022 from Vaccine Adverse Event Reporting System (VAERS) (reference number: 2048405-1), reported by other healthcare professional and concerned a 58-year-old, male patient. The patient's concurrent conditions included respiratory: COPD, moderate (chronic obstructive pulmonary disease), circulatory: internal hemorrhoids, benign hypertension, infectious/inflammatory: tinea pedis, hematologic: iron deficiency, anemia, nervous: tobacco abuse in remission, alcohol abuse, tension-type headache, intractable, diabetic polyneuropathy, endocrine/metabolic: type two diabetes mellitus and other: environmental allergies and anxiety. The patient's historical condition included malignant melanoma of right neck. The patient's concomitant medications included albuterol HFA inhaler (brand names used: Proventil HFA, Ventolin HFA, Proair HFA), Lipitor (atorvastatin), Decadron (dexamethasone) and lisinopril-hydrochlorothiazide (brand names used: Prinzide, Zestoretic), all used for unreported indications. On 10-Oct-2021, the patient was vaccinated with Flucelvax Quadrivalent (influenza vaccine inact sag 4v; dose: reported as 'one'; route of administration: injection (reported as 'SYR'); anatomical location and indication: not reported). The batch number reported was 308451. On the same date, the patient was vaccinated with a booster dose of non-company co-suspect Pfizer-BioNTech COVID-19 vaccine (tozinameran; dose: reported as '3'; route of administration: injection (reported as 'SYR'), anatomical location and indication: not reported). The batch number reported was FE3590. On unspecified date, an unknown amount of time after receiving Flucelvax Quadrivalent and non-company co-suspect Pfizer-BioNTech COVID-19 vaccine, the patient experienced COVID-19 infection, reported as 'recent COVID infection' and was placed on prednisone in the outpatient setting. On 07-Jan-2022, two months and 28 days after receiving Flucelvax Quadrivalent and non-company co-suspect Pfizer-BioNTech COVID-19 vaccine, the patient presented to the emergency department with worsening symptoms of shortness of breath, cough and congestion. In the emergency department, the patient was hemodynamically stable, with desaturations noted 87% with ambulation and was placed on 2 L nasal cannula. On the same date chest X-ray was performed due to acute cough/dyspnoea and hypoxia, frontal and lateral. The heart size and pulmonary vascularity appeared normal. There appeared to be mild left basilar atelectasis or scar. There was focal eventration of the right hemidiaphragm. The remainder of the thorax was without significant change. On the same date, a nasopharyngeal swab specimen was collected for the PCR (polymerase chain reaction) detection of COVID-19, Influenza A and B, and RSV (Respiratory syncytial virus). All test results came back negative. Labs were with mild hyponatremia, otherwise unremarkable. The patient was admitted to the hospital for COVID pneumonia, with steroids increased, dexamethasone at a dose of 6 mg. The patient did well and remained stable on 2 L nasal cannula. On 09-Jan-2022, after two days, the patient was discharged home on home oxygen. At time of discharge, the patient had vital signs within normal limits, and was comfortable with discharge plan home. The outcome of the event was unknown. The reporter did not provide a causality assessment. The events of 'COVID-19 pneumonia' was considered to be serious due to seriousness criteria of hospitalization and was considered to be medically significant by a Physician within Seqirus' Pharmacovigilance and Risk Management Department. Company comment: A 58-year-old, male patient was vaccinated with Flucelvax Quadrivalent and non-company co-suspect Pfizer-BioNTech COVID-19 vaccines. An unknown amount of time following vaccination, the patient experienced COVID-19 infection. In addition, two months and 28 days after vaccination, the patient presented to the emergency department with worsening symptoms of shortness of breath, cough and congestion. In the emergency department, the patient was hemodynamically stable, with desaturations noted 87% with ambulation and was placed on 2 L nasal cannula. A nasopharyngeal swab specimen was collected for the PCR (polymerase chain reaction) detection of COVID-19, Influenza A and B, and RSV (Respiratory syncytial virus). All test results came back negative. The patient was admitted to the hospital for COVID pneumonia. Causal role of the suspect vaccine is assessed as not related due to biological implausibility.; Sender's Comments: Company comment: A 58-year-old, male patient was vaccinated with Flucelvax Quadrivalent and non-company co-suspect Pfizer-BioNTech COVID-19 vaccines. An unknown amount of time following vaccination, the patient experienced COVID-19 infection. In addition, two months and 28 days after vaccination, the patient presented to the emergency department with worsening symptoms of shortness of breath, cough and congestion. In the emergency department, the patient was hemodynamically stable, with desaturations noted 87% with ambulation and was placed on 2 L nasal cannula. A nasopharyngeal swab specimen was collected for the PCR (polymerase chain reaction) detection of COVID-19, Influenza A and B, and RSV (Respiratory syncytial virus). All test results came back negative. The patient was admitted to the hospital for COVID pneumonia. Causal role of the suspect vaccine is assessed as not related due to biological implausibility.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 2,0
Labordaten: Test Date: 20220107; Test Name: Chest x-ray; Result Unstructured Data: The heart size and pulmonary vascularity appears normal. There appears to be mild left basilar atelectasis or scar. There is focal eventration of the right hemidiaphragm. The remainder of the thorax is without significant change.; Test Date: 20220107; Test Name: Labs; Result Unstructured Data: Mild hyponatremia, otherwise unremarkable.; Test Date: 20220107; Test Name: Saturation; Result Unstructured Data: 87 % with ambulation; Test Date: 20220107; Test Name: PCR; Result Unstructured Data: COVID-19 detected, Influenza A not detected, Influenza B not detected, RSV not detected
Aktuelle Erkrankungen: Alcohol abuse; Anxiety; Benign essential hypertension; COPD; Diabetic polyneuropathy; Environmental allergy; Internal hemorrhoids; Iron deficiency anemia; Tension headache; Tinea pedis; Tobacco abuse; Type 2 diabetes mellitus
Vorgeschichte: Medical History/Concurrent Conditions: Malignant melanoma
Andere Medikamente: Albuterol Hfa; Lipitor; Decadron; Hydrochlorothiazide;Lisinopril dihydrate
Allergien: -
Vorherige Impfungen: -

VAERS 2400285

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: KY
Alter: 61,0
Geschlecht: F
Eingang: 03.08.2022
Impfdatum: 02.09.2021
Beginn: 24.06.2022
Tage bis Beginn: 295,0
Dosis: 2
Route/Site: IM / LA

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

Acute kidney injury COVID-19 Diarrhoea Dyspnoea Dysuria Full blood count SARS-CoV-2 test positive Urine output decreased

Symptomtext

Patient presents with worsening shortness of breath and issues urinating. She said her breathing "is just not doing well" but was unable to elaborate further. She usually uses 3L of O2 at home and is on baseline oxygen here in the hospital. She says she that for the past few days she hasn't been making much urine and has been going a lot less frequently. It has hurt a little bit when urinating but denies any hematuria. Denies any abdominal pain, fevers/chills, nausea, vomiting, flank pain. She has been having some diarrhea but when questioned further this is a chronic problem and is at baseline. Hospitalization course: - Patient oxygenating well on close to baseline O2 requirement - Started dexamethasone 6mg for 10 days, not a candidate for remdesivir with AKI - Completed with azithromycin 500mg for 3 days. She may benefit from chronic Azithromycin use, defer to outpatient follow up - Goal O2 >88% - Incentive spirometry Q4, Duonebs Q4 PRN, home dulera, singulair - Continue monitoring CBC with improvement prior discharge, will recheck in a week. Discharge Disposition/Condition Disposition: Home Condition: Stable (s/sx potential problems absent or manageable)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: COVID-19 PCR confirmed positive on 6/24/22
Aktuelle Erkrankungen: N/A
Vorgeschichte: T2DM substance use disorder, alcohol, tobacco
Andere Medikamente: Albuterol Sulfate Aspirin atorvastatin azithromycin fluoxetine ferrous sulfate fluticasone-salmeterol insulin glargine ipratropium-albuterol lisinopril metoprolol succinate montelukast oxybutynin pantoprazole sitagliptin sulfamethoxazole
Allergien: tomato
Vorherige Impfungen: -

VAERS 2395213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: IN
Alter: 71,0
Geschlecht: F
Eingang: 28.07.2022
Impfdatum: 06.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: IM / LA

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

Atrial fibrillation Cardiac monitoring normal Condition aggravated Pain in extremity Tachycardia

Symptomtext

I noticed that a while after the Pfizer booster 1, there was an increase in frequency of tachycardia AND I seemed to notice a-fib occuring daily one to two times. This continued well into January. I notified Dr in November and a cardiac monitor which, of course, showed none of what I had experienced. I did NOT have any adverse arrthymias with the first two doses of the Pfizer Vaccine. It only occurred with the booster. I hesitated to have the second booster and finally after considering the benefits and the risks, I decided to have the 2nd booster but to have the Moderna. I had consulted Dr via his nurse and there was no verbal objection. I advised my primary doctor. My thinking was as there were no issues with the first 2 Pfizers, perhaps I developed some sensitivity with the 3rd one. Additionally, my left arm remains sore at times. This also did not occur with the first two doses of the vaccine. The first two doses were given at a vaccination clinic. My memory may be faulty with the dates but I do know that my arm still hurts and I did have an increase in the frequency of tach and had more a-fib episodes than I've had since I had the ablation. Most of the interaction between cardiology was via the portal and phone. I did not present at the office.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: NONE
Vorgeschichte: Obesity, arrthymias (tachycardia mainly but still rare a-fib after oblation), depression
Andere Medikamente: Sotalol, Warfarin, Lexapro, Prilosec, Tums, Vit D3, Multivitamin
Allergien: Flecainide, Avelox
Vorherige Impfungen: -

VAERS 2374676

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: PR
Alter: 47,0
Geschlecht: F
Eingang: 20.07.2022
Impfdatum: 15.01.2022
Beginn: 01.01.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Electroencephalogram normal Fatigue Headache Memory impairment Mental impairment Somnolence Tooth fracture Tremor Vomiting

Symptomtext

In January of 2022, I felt really exhausted, I wanted to sleep all day and I started to have really bad headaches, I use to have hair down to my waist and now my hair is up to my shoulders. The headaches are so bad that I throw up. I am also having mental blocks, when I am driving I can forget things. I got my first appointment in June with my neurologist. I was having trimmers and the medicine they gave me, made me feel sick. My neurologist ran an EEG test. The EEG results came back normal. I am waiting on approval from my insurance for a MRO with or with contract. My teeth are also chipping off.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: June I had an EEG test ran and results came back normal.
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure
Andere Medikamente: BENICAR
Allergien: Aminophylline
Vorherige Impfungen: Smallpox vaccine.

VAERS 2370744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NY
Alter: 51,0
Geschlecht: M
Eingang: 15.07.2022
Impfdatum: 11.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: IM / RA

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

Blood cholesterol normal Laboratory test normal Libido decreased Mobility decreased Thyroid function test normal Weight increased

Symptomtext

3 weeks after 3rd dose I noticed a decrease in sexual drive and maintaining it, and desire to not do anything as far as social events. I also had weight gain, and it all started after the 3rd dose. I called my Doctor and my Doctor scheduled me with another professional which was a therapist, and it wasn't depression or anything and they ruled that out but kept it on the tables just incase. My diet is pretty good and I have no problems with my health so I don't know why or how the weight gain started. I have another appointment with him in 3 months to prescribe something that can help with this situation. The Doctor did labs and everything was in normal range.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Multiple Labs, Thyroid, Cholesterol (all normal) 11/2021
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Metoprolol; Atorvastatin; Clopidogrel; B12; Iron; Calcium; Vitamin D3
Allergien: None
Vorherige Impfungen: -

VAERS 2361140

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: KY
Alter: 70,0
Geschlecht: F
Eingang: 07.07.2022
Impfdatum: 30.09.2021
Beginn: 06.07.2022
Tage bis Beginn: 279,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Dyspnoea

Symptomtext

Presented to Health clinic complaining of cough and shortness of breath which started on 6/29/22. She is found to have COVID-19 and had room air oxygen saturations as low as 87% in the ER. She had been doing well on 2L NC and does not use supplemental oxygen at home.

Weitere VAERSDATA-Felder

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

VAERS 2339443

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

moderat

Staat: -
Alter: 59,0
Geschlecht: U
Eingang: 28.06.2022
Impfdatum: 12.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / -

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

Condition aggravated Emphysema

Symptomtext

patient reports worsening of emphysema with each additional vaccination

Weitere VAERSDATA-Felder

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

VAERS 2320507

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MN
Alter: 83,0
Geschlecht: M
Eingang: 15.06.2022
Impfdatum: 19.10.2021
Beginn: 12.06.2022
Tage bis Beginn: 236,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Cough Dyspnoea Fatigue Pyrexia

Symptomtext

6/12/22- began feeling fatigued and weak. Cough, SOB, and fever began after. Treatment includes: Dexamethasone, Remdesivir, oxygen, and IV fluids.

Weitere VAERSDATA-Felder

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

VAERS 2311630

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: KY
Alter: -
Geschlecht: U
Eingang: 07.06.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: ID / RA

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

Aphonia Arthralgia Bone pain Computerised tomogram Cyst Deafness Dysphagia Electrocardiogram Electromyogram Headache Hypoaesthesia Hysterectomy Infection Laboratory test Magnetic resonance imaging Pain in extremity Paraesthesia Sinus disorder

Symptomtext

Cyst, open wound spots every on body, bones and joint hurt, hand an feet hurt, swelling. Numbing. Tingling, severe headaches, sinus issues, being testes for possible blood disorder/cancer, calcification in spine, bleeding from vaginal over 2 months, active infection in body, each day a new symptom shows up, swallowing issues. Lost voice, loss of hearing, being tested for Rhamatoid arthritis and lupus, see mutiple specialist for all this. Have not worked since 11/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: 1,0
Labordaten: Four sinus surgeries and more to come 2/2022, hysterectomy due to cyst 3/2022, labs, emg, ekg, CT, mri, urine samples. X rays, us, more to come.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2310103

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: KY
Alter: 71,0
Geschlecht: M
Eingang: 06.06.2022
Impfdatum: 09.10.2021
Beginn: 04.06.2022
Tage bis Beginn: 238,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Cough Dyspnoea Exposure to SARS-CoV-2 Oropharyngeal pain Peripheral swelling Pyrexia SARS-CoV-2 test positive

Symptomtext

72 year old gentleman who presented to the emergency room with shortness of breath, cough and fever which started 6/3/22 (1 day prior to admission); he also had a sore throat; his wife had similar symptoms and was admitted with covid earlier on 6/4/22; he denies chest pain; he went to urgent care where he tested positive for covid and ems was called he has had swelling of his legs; he is not on home oxygen Patient admitted to hospital. Is currently receiving remdesivir 200 mg IV x1 dose followed 24 hours later by 100 mg IV q24h x4 days

Weitere VAERSDATA-Felder

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

VAERS 2306993

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MT
Alter: 69,0
Geschlecht: M
Eingang: 02.06.2022
Impfdatum: 27.10.2021
Beginn: 12.05.2022
Tage bis Beginn: 197,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Dyspnoea Hypoxia Lung opacity Pyrexia SARS-CoV-2 test positive

Symptomtext

Case completed primary Covid vaccine and one booster as of October2021, then was hospitalized for Covid in May 2022. Hospitalized at: Hospital. Pneumonia due to COVID-19 virus Presented with 7-10 days of cough, one day of fever and shortness of breath. Chest x-ray revealed bilateral ground glass opacities. Tested positive for Covid-19. Vaccinated x 3. Hypoxic to 80s at time of admission, corrected with 2 lpm to low 90s. He was out of window for dexamethasone based on reported onset of cough more than a week prior to admission (and there is little evidence this provides significant benefit for hospitalized patients) and so was treated with dexamethasone 6 mg daily. Asked to finish course at home. He is back on room air at time of discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 4,0
Labordaten: Ordered Test: No Information Given Accession Number: Specimen Source: Nose (nasal passage) Specimen Site: Bilateral Nares Specimen Collection Date/Time: 05/12/2022 Patient Status at Specimen Collection: outpatient * Resulted Test: SARS-CoV-2 Ag Resp Ql IA.rapid Coded Result: detected Numeric Result: Units: Text Result: Reference Range From: Reference Range To: Status: Final
Aktuelle Erkrankungen: ? Coronary artery disease ? Hyperlipidemia ? Hypertension ? Prostatism ? Malignant neoplasm of base of tongue ? Hypothyroid ? Neuralgia ? Carotid atherosclerosis ? Malignant neoplasm metastatic to left lung ? S/P lobectomy of lung (left upper) ? GERD (gastroesophageal reflux disease) ? Hematuria ? Acute respiratory failure with hypoxia ? Anemia ? Protein deficiency ? Left-sided chest wall pain ? Dyspnea on exertion ? Radiculopathy of cervical spine
Vorgeschichte: ? Coronary artery disease ? Hyperlipidemia ? Hypertension ? Prostatism ? Malignant neoplasm of base of tongue ? Hypothyroid ? Neuralgia ? Carotid atherosclerosis ? Malignant neoplasm metastatic to left lung ? S/P lobectomy of lung (left upper) ? GERD (gastroesophageal reflux disease) ? Hematuria ? Acute respiratory failure with hypoxia ? Anemia ? Protein deficiency ? Left-sided chest wall pain ? Dyspnea on exertion ? Radiculopathy of cervical spine
Andere Medikamente: ? amLODIPine (NORVASC) 5 mg tablet Take 1 tablet by mouth twice daily. ? aspirin 81 mg EC tablet Take 81 mg by mouth Daily Ran out and doesn't always take. ? atorvaSTATin (LIPITOR) 40 mg tablet TAKE ONE TABLET BY MOUTH NIGHTLY ? DUL
Allergien: Promethazine
Vorherige Impfungen: -

VAERS 2301005

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NJ
Alter: 43,0
Geschlecht: M
Eingang: 28.05.2022
Impfdatum: 06.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

Autonomic nervous system imbalance Bradycardia Chest pain Condition aggravated Dizziness COVID-19 SARS-CoV-2 test Vaccination failure Flushing Palpitations Small fibre neuropathy Tachycardia Vertigo

Symptomtext

COVID-19 Nasal Swab Positive; COVID-19 Nasal Swab Positive; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 43-year-old male patient received BNT162b2 (BNT162B2), on 20Jan2021 as dose 1, single (Lot number: EL9262), in right arm, on 10Feb2021 as dose 2, single (Lot number: EN6201), in right arm and on 06Oct2021 as dose 3 (booster), single (Lot number: FE3590) at the age of 43 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Hypothyroidism" (unspecified if ongoing). Concomitant medication(s) included: SYNTHROID; AFLURIA QUAD, start date: 27Oct2021, stop date: 27Oct2021. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID-19 Nasal Swab Positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (22Nov2021) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19 included steroids. Clinical course: At Pharmacy or Drug Store patient received the BNT162b2 vaccine. Patient was not diagnosed with Covid prior vaccination. Patient tested Covid post vaccination on 22Nov2021. On 01Mar2021, patient began developing autonomic dysfunction that progressively worsened over the course of 6 months. Symptoms and signs included flushing, heart palpitations, bradycardia, tachycardia, chest pain, dizziness, vertigo. Patient was diagnosed with small fibre neuropathy in Jan2022. Patient was hospitalised for 7 days and was recovered with lasting effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20211122; Test Name: Nasal Swab; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism
Andere Medikamente: SYNTHROID; AFLURIA QUAD
Allergien: -
Vorherige Impfungen: -

VAERS 2284738

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: PA
Alter: 52,0
Geschlecht: M
Eingang: 19.05.2022
Impfdatum: 17.05.2022
Beginn: 18.05.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Atrial fibrillation Condition aggravated

Symptomtext

I have a pre-existing condition, atrial fibrilation, controlled through daily dose of Metoprolol 25 mg with no symptoms. After each does of the COVID19 vaccine I experienced the onset of atrial fibrilation within 1-2 days that would last for more than one week and eventually subside.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: -
Vorgeschichte: Prostate cancer
Andere Medikamente: Metoprolol 25 mg Ajovy 225 mg
Allergien: Skin allergies - latex, adhesive
Vorherige Impfungen: Atrial fibrilation, 51 years old at previous three COVID19 vaccinations

VAERS 2277770

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

moderat

Staat: NY
Alter: 67,0
Geschlecht: F
Eingang: 15.05.2022
Impfdatum: 05.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Joint injury Limb injury Pain 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 2277708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: RI
Alter: 41,0
Geschlecht: F
Eingang: 14.05.2022
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arteriogram coronary normal Chest X-ray abnormal Chest pain Dyspnoea Electrocardiogram normal Fibrin D dimer increased Full blood count Hypertension Lymphadenopathy Mammogram normal Metabolic function test Palpitations Stress Tachycardia Troponin normal Ultrasound abdomen normal

Symptomtext

Severe left axillary lymphadenopathy approximately 3 weeks duration developed after the booster. However, since the first vaccine in February 2021. I have had a sudden onset of high blood pressure, palpitations, tachycardia, chest pains and SOB of varying degrees and duration that has resulted in ER and PCP visits throughout the year without an exact cause found. Most recent ER visit I had in April 2022 chest pains, SOB, Palpitations, very high blood pressure and a D-Dimer of 1,165. Chest x-ray, EKG, CTA Chest normal. All labs/testing negative for heart disease. Recent mammogram & Abdominal US done 5/2022 normal. Drs decided ?stress? even though I was under no stress this latest episode.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 4/2023 EKG, Chest XR, CTA Chest, D-Dimer, troponin, CMP, CBC
Aktuelle Erkrankungen: Right Shoulder Pain
Vorgeschichte: ADHD, Seasonal depression, Asthma (mild)
Andere Medikamente: Adderall XR 25mg, Bupropion XR 150mg, Larissa, Albuterol prn, Ibuprofen prn, multivitamin, biotin/collagen supplement
Allergien: Avelox, Latex, Nifedipine
Vorherige Impfungen: -

VAERS 2328594

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 59,0
Geschlecht: M
Eingang: 10.05.2022
Impfdatum: 27.02.2021
Beginn: 06.10.2021
Tage bis Beginn: 221,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Chest pain Cough Dyspnoea Ischaemic cardiomyopathy SARS-CoV-2 test positive

Symptomtext

Narrative: The patient was admitted to the hospital on 6 Oct 2021 with chest pain. The patient was discharged on 8 Oct 2021. The patient was readmitted on 16 Oct 21 with chest pain and coughing. The patient was discharged on 19 Oct 21. The patient presented to the ED with worsening shortness of breath and coughing on 20 Nov 2021 and was admitted to the hospital on 21 Nov 21. The patient was discharged in stable condition on 24 Nov 21. The patient presented to the ED with chest pain and shortness of breath on 1 Jan 2022 and was admitted. The patient was discharged on 6 Jan 2022. The patient was readmitted on 10 Jan 2022 with chest pain and tested positive for COVID 19. The patient was discharged on 11 Jan 2022 in stable condition. The patient was readmitted to the hospital on 23 Feb 2022 with chest pain and shortness of breath. The patient is diagnosed with ischemic cardiomyopathy. Reported per EUA.

Weitere VAERSDATA-Felder

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

VAERS 2260394

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: IL
Alter: 36,0
Geschlecht: M
Eingang: 02.05.2022
Impfdatum: 10.10.2021
Beginn: 10.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Diarrhoea Dizziness Dyspnoea Feeling of body temperature change Impaired work ability Lethargy Mobility decreased Pain in extremity Somnolence

Symptomtext

Starting a few hours after receiving the vaccine, I was going from hot to cold spells. I was having a hard time breathing and I was very lethargic. I had some diarrhea, and a sore arm, which I expected, and dizziness. I missed several days of work. Getting out of bed was difficult and I was having trouble staying awake and felt extremely drained. This went on for a couple of days. Then, when I got the 2nd dose, I had the same thing happen: same symptoms and same duration. I was told by the clinic doctors that "this is just what happens when people get the shots".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Bronchitis; Asthma
Andere Medikamente: Symbicort, Albuterol and Singulair
Allergien: Shellfish
Vorherige Impfungen: -

VAERS 2260346

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 27,0
Geschlecht: F
Eingang: 02.05.2022
Impfdatum: 29.10.2021
Beginn: 23.04.2022
Tage bis Beginn: 176,0
Dosis: 2
Route/Site: SYR / LA

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

Asthenia COVID-19 Cough Feeling abnormal Impaired work ability Migraine Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Starting 04/23/2022, I started getting a runny nose and mild cough. I thought it was just allergies because they act up around this time of the year. On 04/24/2022, I had no energy, a bad migraine, my cough was bad and I just felt very off. It rolled over into the early week and by 04/26/2022 the dry patch cough would be intermittent. On 04/27/2022, my cough was so bad that I ended up calling out of work that day. I was coughing so hard that I thought I would cough up blood. So, I made an appointment for Urgent care for 04/28/2022. On 04/28/2022, I was tested for COVID-19 which was positive. My whole family then tested positive for COVID-19. For the rest of the family, they had intermittent cough but that's it. To this day, the cough is lingering on for me but varies in intensity. My husband tested again today, and he is still positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: COVID-19 test on 04/28/2022: Positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Tylenol PRN (unsure if took day of vaccine)
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2256760

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CO
Alter: 66,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 26.10.2021
Beginn: 07.01.2022
Tage bis Beginn: 73,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal X-ray Abdominal infection Abdominal pain lower Condition aggravated Diverticulitis Dysuria Fatigue Intestinal obstruction Ostomy bag placement Pyrexia Surgery White blood cell count increased

Symptomtext

I started running a fever, and I had pain in my lower left abdomen. It was hard to go to the bathroom. This was caused by the diverticulitis. I had an event with it about 25 years ago. It just came back which caused this event. My doctor gave me 2 weeks of antibiotics to get my white count down. The doctor said I had a blockage. The doctor wanted to do a colonoscopy on me but couldn't so they tried to do a barium x-ray but that didn't work either. I saw a surgeon on a Tuesday and had surgery on that Thursday. I was in the hospital for 5 days. Now I have an ostomy bag. I didn't have any pain after surgery. I was prescribed an antibiotic and a hydrocodone. I am very tired, but my doctor said that is what happens when someone has an abdominal infection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 5,0
Labordaten: Barium x ray- no results, didn't work; colonoscopy- no results, didn't work
Aktuelle Erkrankungen: None
Vorgeschichte: Diverticulitis (don't have it anymore);Asthma
Andere Medikamente: Losartan 50mg Protandim 1xday Vitamin B Super Complex
Allergien: Nickel; Iodine; any medication that ends in -pril
Vorherige Impfungen: -

VAERS 2255200

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CO
Alter: 45,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 02.10.2021
Beginn: 06.01.2022
Tage bis Beginn: 96,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Dyspnoea Fatigue Feeling abnormal Headache Post-acute COVID-19 syndrome Pulmonary function test Pyrexia SARS-CoV-2 test positive Sleep disorder Vaccine breakthrough infection

Symptomtext

I had a breakthrough Covid-19 infection beginning January 6, 2022. I had a crazy bad headache for an entire day. Sometime overnight I had a fever that lasted two or three days and my breathing was difficult. I went to doctor on January 10, 2022 and was monitored for oxygen level. I went back to the doctor the following week because of more difficulty breathing. Due to my allergies, I was unable to take the prescribed meds. I now experience long Covid-19 symptoms; extreme fatigue, brain fog and I cannot breathe cold air, sleep inconstancies.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Blood pressure; O2; Covid panel; breathing test
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Alclometasone; Dipropionate USP Ointment; Vitamin D3; Multi Vitamin; acetaminophen; ibuprofen; gas X
Allergien: Fish; penicillin; clarithromycin; CLINDAMYCIN; fluconazole; narcotic
Vorherige Impfungen: -

VAERS 2254884

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CO
Alter: 22,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 22.10.2021
Beginn: 03.01.2022
Tage bis Beginn: 73,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain Blood test normal COVID-19 Cardiac monitoring normal Chest pain Cough Dizziness Dyspnoea Fatigue Feeling abnormal Heart rate increased Migraine Myalgia Oropharyngeal pain Postural orthostatic tachycardia syndrome Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Breakthrough case of COVID-19. I had a sore throat, congestion, cough and a migraine. I had some abdominal and muscle pain. About 6 days in I started having chest pain, brain fog, trouble breathing and some dizziness. I think that was it, I never had a significant fever. I had an elevated heart rate at 14 days in and that is when I went to see my doctor. I was given 7 days of a a steroid pack because I was still having elevated heat rate, trouble breath, dizziness and fatigue. I was still feeling pretty bad after that, and she gave me another 7 days of steroids and that seemed to help with the fatigue. I was probably not back to 100% until about 4 weeks later, I still had had trouble breathing and fatigue. My doctor ended up diagnosing me with post COVID-19 postural orthostatic tachycardia. My heart rate is elevated whenever I stand up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 01/03/2022 PCR test, positive results. Blood work normal. Heart monitor patch for 2 weeks to rule out any long term damage to my heart, test was normal.
Aktuelle Erkrankungen: None
Vorgeschichte: Endometriosis; IBS; Asthma
Andere Medikamente: Claritin 2 tab BID; Pepcid QD
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2246043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: AZ
Alter: 73,0
Geschlecht: M
Eingang: 21.04.2022
Impfdatum: 09.03.2021
Beginn: 15.12.2021
Tage bis Beginn: 281,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Hypertension

Symptomtext

Appears that Covid May have caused my high blood pressure in December 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Dr office visit showed high blood pressure as did several at home blood pressure readings. Prescribed additional high blood pressure medicine and it appears to be working.
Aktuelle Erkrankungen: None.
Vorgeschichte: Sleep apnea since 2000. Other issues noted on med comments.
Andere Medikamente: - Ceturizine, 10 mg daily, usually with dinner. Allergies. - Losartan, 50 mg daily, usually with dinner. High blood pressure. - Paroxetine, 20 mg daily, usually with dinner. Anxiety. - Atorvastatin, 10 mg daily, usually with dinner. High
Allergien: None.
Vorherige Impfungen: -

VAERS 2245865

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MN
Alter: 72,0
Geschlecht: F
Eingang: 21.04.2022
Impfdatum: 03.11.2021
Beginn: 09.04.2022
Tage bis Beginn: 157,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Cardiac monitoring Dyspnoea Hypoxia

Symptomtext

Began with symptoms on 4/9/22- SOB with increasing weakness and hypoxia noted on admit to hospital. Treatment includes: admission, O2, cardiac monitoring, dexamethasone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, Diabetes, CKD
Andere Medikamente: -
Allergien: Statins
Vorherige Impfungen: -

VAERS 2245674

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: FL
Alter: 88,0
Geschlecht: F
Eingang: 21.04.2022
Impfdatum: 10.02.2021
Beginn: 20.04.2022
Tage bis Beginn: 434,0
Dosis: UNK
Route/Site: - / -

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

Angiogram pulmonary normal COVID-19 Chest X-ray normal Chest pain Decreased appetite Dyspnoea Fibrin D dimer increased Headache Nausea Productive cough SARS-CoV-2 test positive Vaccine breakthrough infection Vomiting

Symptomtext

Covid19 breakthrough. 1st vaccince on 01/20/2021. 89 y/o female with PMHx CAD with stents, Afib, Pacemaker, HTN, HLD, Anxiety presents with c/o 3 day history of worsening SOB, productive cough, poor appetite, chest pain, nausea, vomiting and headache. CXR with no acute process, Room air sat 98% and afebrile. D-Dimer elevated but CTA chest with no pulmonary emboli. Covid severity score=0 per MD. No treatment presently.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19- detected on 04/20/2022
Aktuelle Erkrankungen: -
Vorgeschichte: CAD with stents, AFIB, HTN, HLD, Anxiety, Pacemaker, lung nodules
Andere Medikamente: -
Allergien: Beta Blockers
Vorherige Impfungen: -

VAERS 2244076

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 45,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 19.10.2021
Beginn: 25.01.2022
Tage bis Beginn: 98,0
Dosis: 3
Route/Site: IM / LA

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

Asthma COVID-19 Condition aggravated Dyspnoea Ear infection Oxygen saturation decreased Pyrexia Respiratory tract infection

Symptomtext

Three months after I received my booster I developed COVID-19. I was immediately put on a breathing machine, using Mucinex, Tylenol/Ibuprofen regime for my fever, by day 17 I was put on prednisone for an ear and respiratory infection. Breathing and asthma are worse my oxygen levels are in the low 90's, my doctor is trying to work on getting that back up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Various Asthma Medications
Allergien: Aloe; Wool
Vorherige Impfungen: -

VAERS 2243047

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CT
Alter: 69,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 25.10.2021
Beginn: 25.12.2021
Tage bis Beginn: 61,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Blood test Erythema Investigation Pain Paraesthesia Peripheral swelling Pruritus Rheumatoid arthritis Skin discomfort X-ray

Symptomtext

rheumatoid arthritis; Very swollen upper arm; Wrist are swollen and they look very deformed; redness and my upper arm was swollen; itching; bilateral hand swelling.; fingers were swollen; pain; Her skin was so tight back to the finger till the fingertip; My skin was tightening from the back of the finger to the fingertip; I started developing joint pain in my shoulder, elbow, wrist and everywhere else / The pain is in my neck, shoulder, wrist and everywhere; This is a spontaneous report received from a contactable reporter(s) (Nurse) from medical information team. The reporter is the patient. A 70-year-old female patient received BNT162b2 (BNT162B2), on 25Oct2021 as dose 3 (booster), single (Lot number: FE3590) at the age of 69 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Aortic stenosis" (unspecified if ongoing); "Type 2 diabetes" (unspecified if ongoing); "Blood pressure high" (unspecified if ongoing); "Hypothyroidism" (unspecified if ongoing); "High cholesterol" (unspecified if ongoing); "I had a previous ganglion on the wrist" (unspecified if ongoing). Concomitant medication(s) included: METFORMIN taken for type 2 diabetes mellitus; LISINOPRIL taken for hypertension; LEVOTHYROXINE taken for hypothyroidism; ZETIA taken for blood cholesterol increased; QUNOL LIQUID COQ10 taken for supplementation therapy. Vaccination history included: BNT162b2 (Dose 1), administration date: 19Mar2021, when the patient was 69-year-old, for COVID-19 Immunization; BNT162b2 (Dose 2), administration date: 16Apr2021, when the patient was 69-year-old, for COVID-19 immunization. The following information was reported: SKIN DISCOMFORT (non-serious) with onset 25Dec2021, outcome "unknown", described as "Her skin was so tight back to the finger till the fingertip"; ARTHRALGIA (non-serious) with onset 25Dec2021, outcome "unknown", described as "I started developing joint pain in my shoulder, elbow, wrist and everywhere else / The pain is in my neck, shoulder, wrist and everywhere"; PARAESTHESIA (non-serious) with onset 25Dec2021, outcome "unknown", described as "My skin was tightening from the back of the finger to the fingertip"; PERIPHERAL SWELLING (non-serious) with onset 25Dec2021, outcome "unknown", described as "Very swollen upper arm; Wrist are swollen and they look very deformed"; PERIPHERAL SWELLING (non-serious) with onset 25Dec2021, outcome "unknown", described as "bilateral hand swelling."; PERIPHERAL SWELLING (non-serious) with onset 25Dec2021, outcome "unknown", described as "fingers were swollen"; PRURITUS (non-serious) with onset 25Dec2021, outcome "unknown", described as "itching"; PAIN (non-serious) with onset 25Dec2021, outcome "unknown"; ERYTHEMA (non-serious) with onset 25Dec2021, outcome "unknown", described as "redness and my upper arm was swollen"; RHEUMATOID ARTHRITIS (medically significant) with onset 25Dec2021, outcome "unknown". The events "rheumatoid arthritis", "very swollen upper arm; wrist are swollen and they look very deformed", "redness and my upper arm was swollen", "itching", "bilateral hand swelling.", "fingers were swollen", "pain", "her skin was so tight back to the finger till the fingertip", "my skin was tightening from the back of the finger to the fingertip" and "i started developing joint pain in my shoulder, elbow, wrist and everywhere else / the pain is in my neck, shoulder, wrist and everywhere" required physician office visit. The patient underwent the following laboratory tests and procedures: Blood test: Positive, notes: rheumatoid arthritis panel blood tests which came back positive; lupus disease: Negative; Negative; X-ray: arthritis in my left wrist, notes: x-ray only on one hand and he noticed in the x-ray that there was arthritis in my left wrist. Therapeutic measures were taken as a result of rheumatoid arthritis, peripheral swelling, erythema, pruritus, peripheral swelling, peripheral swelling, pain, skin discomfort, paraesthesia, arthralgia. Additional information: Pt liked to report an adverse event following the Pfizer COVID-19 vaccine. Pt had first dose of Pfizer COVID-19 vaccine on 19Mar2021 and the second one on 16Apr2021. Pt received my booster dose of Pfizer COVID-19 vaccine on 25Oct2021. Eight weeks after receiving the booster dose pt started developing side effects. After receiving the two primary vaccination series pt had no symptoms. However, pt went to do some antibody tests and there were no antibodies detected. Pt had a local reaction after receiving the booster dose, such as itching, a lot of redness and upper arm was swollen. It was very itchy for a few days. On holiday, pt developed a bilateral hand swelling. Pt fingers were swollen. Pt was in such a pain. Pt thought pt had carpal tunnel syndrome. When the doctor analyzed and assessed he did not see signs of carpal tunnel syndrome. Pt skin was tightening from the back of the finger to the fingertip. Pt had a previous ganglion on the wrist which was reassessed by the doctor. Upon reassessing the doctor found that pt had an arthritis on left wrist. Pt proposed warm heat and ibuprofen. Two weeks later, Pt started developing joint pain in shoulder, elbow, wrist and everywhere else. The doctor performed rheumatoid arthritis panel blood tests which came back positive. However, Lyme disease and lupus disease came back negative. Pt wanted to see specialist on the 09May but the pain was unbelievable pt also had to see a cardiologist in the month of Feb due to an aortic stenosis. He did not want me to take ibuprofen for some reason but when pt do not take it pt was in a lot of pain. The pain was in neck, shoulder, wrist and everywhere. Pt also had to take Prednisone for a five day regimen. Pt wrist was so swollen and looked very deformed. When the doctor looked at it, pt was surprised on how swollen and deformed it looked. Caller also tried to report online but it was very confusing for her. Caller stated and though it was a good thing that it was triggering my immune system. Pt believe pt had developed this symptom from the COVID-19 vaccine. Pt know it was gonna clean out on its own. Caller wants to know if these symptoms are associated with Pfizer COVID-19 vaccine. Caller was a female turning 71 years old soon. Follow-up (14Apr2022): This is a spontaneous follow-up report from a contactable Nurse. This 70-Year-old female nurse (Patient) reported that: Updated Information Included: Reporter Information (Address in Slider 01) update. Patient Details (DOB, Age, Height, weight and Ethnicity) updated. RMH updated. Historical Vaccine updated. Lab data updated. Dosage regimen updated. New events updated. Concomitant drugs added. Additional Information: Adverse Event: Transferring agent stated, So the caller had received the first dose on 19Mar2021 and second one on 16Apr2021, and the booster dose on 25Oct2021. There was couple of side effect, pt will go ahead and list them all if you like or if you want to speak to caller directly. Pt was going to be turning 71, she mentioned that there was no antibody detected after she received the two primary vaccination series (hence PC Filed Conservatively), after receiving the booster dose she had local reaction such as itching, a lot of redness, very swollen upper arm, very itchy for a few days. On Christmas day pt had bilateral hand swelling, finger was swollen, there was so much pain she thought she had Carpal tunnel syndrome, but the doctor said she does not. Her skin was so tight back to the finger till the fingertip, she had an accidental ganglion on her wrist which was evaluated by the Physician. The doctor found out that she has left arthritis in her wrist, they prescribed her warm heat Ibuprofen. 2 weeks later the joint pain went from the elbow, shoulder, and wrist and everywhere else, pt did some tests, and her rheumatoid arthritis came as positive. Pt had to see a specialist on the 9th of May. The pain was unbelievable she said, when she does not take the Ibuprofen, the pain was a lot worst and her wrist are swollen and they look very deformed. Nurse was informed about role of Pfizer Drug Safety and requested to probe. Anatomical site and Route of administration: Nurse Stated, The administration site was left upper arm and the symptoms occurred bilaterally in pt hands, progressed into my wrist and shoulder and neck. Nurse Stated, was treating with 800 mg of Ibuprofen not knowing what it was, thinking that it was just, pt had no idea that it was in hand, so pt was treating it with Ibuprofen. When pt went to see a doctor and pt had, pt went to an orthopedic because been working with the computers pt thought perhaps before retiring perhaps pt thought pt had Carpal tunnel, so pt went to an orthopedic and he said it definitely was not Carpal tunnel and he took an x-ray only on one hand and he noticed in the x-ray that there was arthritis in my left wrist. And he made that as after (voice not clear) by the way your x-ray showed you have arthritis in that wrist. So, he said to continue with the Ibuprofen for the pain and again that was only when it was in hand, but then it started progressing into the different areas, nothing (Unspecified Medications) was working. Concomitant medication: Nurse Stated, Zetia 10 mg Once a day for high cholesterol, and it was the generic form Ezetimibe (further not clarified if nurse was using the brand or generic, hence not captured in tab). Pt took CoQ10 product over the counter Qunol and it was a 100 mg and pt take that just for heart health, it was an over the counter product as supplement. Lab Test: Nurse stated, within last 2 weeks no, but pt did had rheumatoid arthritis panel performed in Feb or Mar. Nurse was informed about PDS. When confirmed if Nurse consumed Ibuprofen and experienced pain, Nurse Stated, Treated with 800 mg of Ibuprofen not knowing what it was. Pt thought pt had Carpal tunnel, orthopedic said it definitely was not Carpal tunnel. And he said that x-ray showed you have arthritis in that wrist. So, he said to continue with the Ibuprofen for the pain and again that was only when it was in my hand, but then it started progressing into the different areas, nothing (Unspecified Medications) was working.; Sender's Comments: Based on the available information a causal relationship between the reported events and suspected 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: Paraesthesia
Hospital-Tage: -
Labordaten: Test Name: rheumatoid arthritis panel blood tests; Test Result: Positive ; Comments: rheumatoid arthritis panel blood tests which came back positive; Test Name: lupus disease; Test Result: Negative ; Test Name: Lyme disease; Test Result: Negative ; Test Name: x-ray; Result Unstructured Data: Test Result:arthritis in my left wrist; Comments: x-ray only on one hand and he noticed in the x-ray that there was arthritis in my left wrist.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Aortic stenosis; Blood pressure high; Ganglion; High cholesterol; Hypothyroidism; Type 2 diabetes mellitus
Andere Medikamente: METFORMIN; LISINOPRIL; LEVOTHYROXINE; ZETIA; QUNOL LIQUID COQ10
Allergien: -
Vorherige Impfungen: -

VAERS 2241694

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: AL
Alter: 45,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 05.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / RA

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

Arthralgia Back pain Blood test normal Dyspnoea Faeces discoloured Gastrointestinal disorder Haematochezia Magnetic resonance imaging normal Migraine Nerve compression Pain in extremity Respiratory disorder Respiratory tract congestion Sinus disorder Stool analysis normal Thyroid cyst X-ray normal

Symptomtext

Week 1: was a migraine that lasted for 4 days. Nothing that took at the time was working. Usually Excedrin works for me but it didn't this time. There was no warning, it just came and did not go away for 4 days, week of 11/07/2021. Week 2: respiratory sinus problems, no allergy medication was working. I was completely congested. I am used to having congestion that goes away 1 or 2 days, never a full week. Going into week 3 and 4: Left shoulder, upper back, arm was all hurting. Lasted about 4 days. During week 2 to week 4 it was harder to breathe then usual and my bowels were not normal. There were streaks of blood on the toilet paper, the stool looked like fish tank algae. I went to do the doctor and she made sure I didn't have type of cancer or COVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Full stool testing, full blood work. MRI and x-ray. Everything came back fine. Nothing abnormal. They found pinch nerves on my thyroid and a small benign cyst.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Ambien
Allergien: Promethazine
Vorherige Impfungen: -

VAERS 2240869

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MN
Alter: 77,0
Geschlecht: M
Eingang: 19.04.2022
Impfdatum: 11.04.2022
Beginn: 15.04.2022
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea

Symptomtext

SOB

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, ASTHMA, CHF, HTN
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2238151

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: FL
Alter: 90,0
Geschlecht: F
Eingang: 17.04.2022
Impfdatum: 26.03.2021
Beginn: 14.04.2022
Tage bis Beginn: 384,0
Dosis: UNK
Route/Site: - / -

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

Asthenia COVID-19 Chest X-ray abnormal Cough Dyspnoea Fatigue Pneumonia Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st vaccine received on 03/05/2021. 91 y/o female with PMHX of HTN, HLD, Iliac stent on Eliquis, Chronic kidney disease presents to ED with 2 day history of generalized weakness, fatigue, cough, SOB, and fever. Room air sat 91%, placed on O2 at 2L NC. CXR with multifocal pneumonia. Treated with ABX, Steroids and Remdesivir.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19- detected on 04/14/2022
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, HLD, Iliac stent on Eliquis, Chronic Kidney disease
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2225559

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: IL
Alter: 32,0
Geschlecht: F
Eingang: 10.04.2022
Impfdatum: 13.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Antinuclear antibody C-reactive protein increased C-reactive protein normal DNA antibody positive Dizziness Double stranded DNA antibody positive Echocardiogram Electrocardiogram Inappropriate schedule of product administration Laboratory test Nausea Palpitations Sensory disturbance Sleep disorder Tachycardia

Symptomtext

After first dose- within 2 days, significant increase in nausea and dizziness, tachycardia waking me up from sleep feeling my heart pounding. Doctor prescribed a medrol pack which seemed to calm my symptoms down a bit. I waited almost 4 weeks to get second vaccine, fearing complications. Second dose- within 2 days, debilitating nausea, dizziness, vibrating/buzzing sensations. On 10/19/21, 6 days after second dose, I went to doctor and had a full lab work up, which revealed my CRP, C Reactive protein was 147.8, I had a positive DNA panel and Anti Ds DNA was positive. Urgent rheumatology referral was placed. Rheumatologist re-ran the labs and CRP was back normal by 10/28/21. Doctor said ?Of note the CRP is now normal. Thus this makes me suspect that the initial CRP elevation could have been due to the Covid vaccine?.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: EKG, Echocardiogram, full rheumatologic laboratory work up including ANA panel, CRP.
Aktuelle Erkrankungen: Long term effects from Covid illness in May 2021.
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2225430

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NC
Alter: 61,0
Geschlecht: M
Eingang: 10.04.2022
Impfdatum: 22.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 7,0
Dosis: UNK
Route/Site: SYR / RA

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

Asthenia Dizziness Heart rate increased Hypertension Laboratory test Palpitations

Symptomtext

High Blood Pressure, Rapid and Pounding Heart first few days after knee surgery and first week after Pfizer shot. Blood pressure check showed heart rate of 147 to 167 bpm with palpitations sitting at rest during next few weeks of recovery. Palpitations continued until Cardiologist prescribed Metoprolol 25mg the following month.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: All test completed at a Cardiovascular Center
Aktuelle Erkrankungen: none
Vorgeschichte: Chronic Pain. Weaned off Oxycodone/Ace 7.5/325 same year as Pfizer shot. Nurse noticed High Blood pressure right before knee surgery. 10/29/2021. Note: Never identified with High Blood Pressure before. Morning of 10/30/2021, rapid and pounding heartbeat with weakness and feeling of faint. That happened as I stepped into the shower. Next day, same event. The palpitations continued until my Cardiologist prescribed Metoprolol 25mg twice a day.
Andere Medikamente: Levothyroxine 137mg, Zolpidem Tartrate 10 mg
Allergien: none
Vorherige Impfungen: -

VAERS 2189947

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: SC
Alter: 42,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 21.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Breast pain Chest discomfort Electrocardiogram normal Mobility decreased Muscular weakness Injection site muscle weakness Myalgia Vaccination site movement impairment Vaccination site pain

Symptomtext

Not able to use left arm fully as I once did, losing strength in arm, upper left side aches, vaccine location=left arm; Not able to use left arm fully as I once did, losing strength in arm, /vaccine location=left arm; Ongoing sore muscle; Not able to use left arm fully as I once did, losing strength in arm, /vaccine location=left arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 21Nov2021 (Lot number: 320308D) at the age of 42 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Known allergies: Sulfur" (unspecified if ongoing); "Known allergies: Shellfish" (unspecified if ongoing). Concomitant medication(s) included: IRON; WELLBUTRIN. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: FE3590, Location of injection: Arm Left), administration date: 27Oct2021, when the patient was 42 years old, for Covid-19 immunization. The following information was reported: VACCINATION SITE PAIN (disability) with onset 21Nov2021, outcome "not recovered", described as "Not able to use left arm fully as I once did, losing strength in arm, upper left side aches, vaccine location=left arm"; VACCINATION SITE MOVEMENT IMPAIRMENT (disability), INJECTION SITE MUSCLE WEAKNESS (disability) all with onset 21Nov2021, outcome "not recovered" and all described as "Not able to use left arm fully as I once did, losing strength in arm, /vaccine location=left arm"; MYALGIA (disability) with onset 21Nov2021, outcome "not recovered", described as "Ongoing sore muscle". The events "not able to use left arm fully as i once did, losing strength in arm, upper left side aches, vaccine location=left arm", "not able to use left arm fully as i once did, losing strength in arm, /vaccine location=left arm", "ongoing sore muscle" and "not able to use left arm fully as i once did, losing strength in arm, /vaccine location=left arm" were evaluated at the physician office visit. Therapeutic measures were taken as a result of vaccination site pain, vaccination site movement impairment, myalgia, injection site muscle weakness. Treatment includes Upcoming physical therapy. No covid prior vaccination. Not covid tested post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Shellfish allergy; Sulfonamide allergy
Andere Medikamente: IRON; WELLBUTRIN
Allergien: -
Vorherige Impfungen: -

VAERS 2209460

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: AR
Alter: 37,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 10.11.2021
Beginn: 07.01.2022
Tage bis Beginn: 58,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal discomfort COVID-19 Diarrhoea Disturbance in attention Feeling abnormal Impaired work ability Neurological symptom Pain Palpitations SARS-CoV-2 test positive

Symptomtext

I had mild symptoms after three days experienced racing heart beats, diarrhea, body pain, brain fog lasted for three weeks. The Gastro issues have lingered ever since COVID. In February 2022 contacted my doctor spoke with the nurse have an upcoming appointment at the end of April 2022 for Gastro and Neurological issues. I'm still having trouble concentrating this is effecting my work.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: COVID test (results positive).
Aktuelle Erkrankungen: No
Vorgeschichte: Borderline Type II Diabetes; Eczema
Andere Medikamente: Lopressor 40mg twice daily; Magnesium Oxide 400mg once daily; Mirena birth control
Allergien: Bactrim; Zofran
Vorherige Impfungen: -

VAERS 2201506

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NY
Alter: 65,0
Geschlecht: F
Eingang: 28.03.2022
Impfdatum: 15.11.2021
Beginn: 04.12.2021
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: IM / RA

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

Electrocardiogram Heart rate increased Palpitations Troponin

Symptomtext

I woke up early in the morning to use the restroom and my heart rate was very high and I had heart palpitations- I could feel it in my chest, hear it in my ears and it remained high even after sitting down to try and get it be lower.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: EKG, a blood test- not sure the name but it checks the chemicals your heart produced in the last few hours to see if you had a heart attack.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Hydrochlorothiazide, Nisoldipine, Vitamin D3 and C, Zinc
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2194887

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MI
Alter: 54,0
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 15.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: SYR / LA

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

Blood thyroid stimulating hormone normal Discomfort Dizziness Dyspnoea Echocardiogram abnormal Electrocardiogram ambulatory abnormal Extrasystoles Headache Malaise Mitral valve prolapse Palpitations Thyroxine normal

Symptomtext

Five days after the third dose of the Pfizer COVID shot I had an episode of my heart skipping several beats in a row for about 5 seconds total, making me short of breath and light-headed. All I was doing was sitting down. After that I had continual skipping (or premature) heart beats, pounding, etc. Not rapid, not slow, but almost continual skipped/premature/pounding beats. Some days were better, some days were worse. My doctor prescribed a 48 hour heart monitor that showed the premature/skipping beats but nothing serious. I also had an echocardiogram which showed mild to moderate mitral valve prolapse. I then came down with COVID two months later. When I was sick my heart pounded a lot, was very uncomfortable, sometimes making me short of breath. The only other COVID symptoms I had was a headache. My doctor prescribed a 14 day heart monitor, which showed the activity of skipped and premature heart beats, but did not show my heart going into afib. I have not taken my doctor's offer to take medication to control the heart irregularities because he said it would only be for my own comfort and wasn't medically necessary, and I feel I'm on enough meds already. I didn't report right away because I figured that it would go away eventually, but it still bothers me almost every day and I just think it should be reported. I didn't notice any side effects from the 1st and 2nd doses of the Pfizer vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/6/21 - T4 Free (normal) 12/6/21 - TSH (normal) 12/10/21 - Holter monitor 12/10/21 - Echo 2/4/21 - 14 day heart monitor
Aktuelle Erkrankungen: none
Vorgeschichte: Ulcerative Colitis, Crohn's Disease
Andere Medikamente: Humira, Singulair, Vitamin D
Allergien: none
Vorherige Impfungen: -

VAERS 2194591

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: UT
Alter: 66,0
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 11.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 15,0
Dosis: 3
Route/Site: SYR / AR

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

Blood pressure decreased Computerised tomogram head Computerised tomogram neck Dizziness Exercise tolerance decreased Neuralgia Oxygen saturation decreased Paraesthesia Paraesthesia oral Scan with contrast normal

Symptomtext

10/26/2021 Tingling on face and lips that caused me to go to the doctors. It was only on the right side of face and I did not want to get an MRI right away. It has progressed to both side of my face and fingers. Exercise tolerance has become terrible and have been needing to use my oxygen more. I did have a CT of head and neck that showed no issues. I am having dizziness accompanying everything else. Respiratory therapist was doing well however my blood pressure was too low and drops while I exercise and was told to meet with the cardiologist. I have been taking Gabapentin for nerve pain and had stopped due to vertigo I was experiencing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: CT with contrast of head and neck which did not show anything abnormal.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Type 2 Diabetes, Hypertension, Obstructive Pulmonary Disease, Arthritis
Andere Medikamente: Provigil, Spironolactone, Jardiance, Metformin, Lisinopril, Montelukast, Claritin, Airduo Rest Click Inhaler, Albuterol as needed, Turmeric, Sudafed, Omega 3 oil, Multivitamin
Allergien: Narcotics due to blood pressure crashing
Vorherige Impfungen: -

VAERS 2194495

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: AL
Alter: 65,0
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 03.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Blood test normal Condition aggravated Eczema Pain Pain in extremity Rheumatoid factor negative

Symptomtext

I experienced severe eczema on my right hand especially on my fingertips. I tolerated it for a few weeks using previously prescribed medication that did not help. My doctor put me on Celebrex and added a new cream for my hands. It took a few weeks for it to get better. They have also put me on Dupixent because it did not resolve and began spreading to my feet. I will have my 2nd Dupixent injection today. My hands are much improved and look almost normal. There is no more throbbing in the hands.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: blood panel including rheumatology screening-all were negative
Aktuelle Erkrankungen: None.
Vorgeschichte: Fibromyalgia; Acid Reflux; Eczema.
Andere Medikamente: Lexapro; Wellbutrin XL; Montelukast; Xyzal; Omeprazole; Aspirin 81 mg.
Allergien: Codeine; Outdoor allergies.
Vorherige Impfungen: -

VAERS 2187232

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: FL
Alter: 72,0
Geschlecht: F
Eingang: 18.03.2022
Impfdatum: 04.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 25,0
Dosis: 1
Route/Site: - / RA

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

Migraine SARS-CoV-2 test

Symptomtext

Three migraines with Aura in less than a year.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP and Physician). The reporter is the patient. A 72 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 04Jan2021 (Lot number: FE3590) at the age of 72 years as dose 1, single and administered in arm right, administration date 04Feb2021 (Lot number: En5318) as dose 2, single for covid-19 immunisation. Relevant medical history included: "Hypertension" (unspecified if ongoing); "Arthritis" (unspecified if ongoing); "type 2 diabetes" (unspecified if ongoing). The patient took concomitant medications. The following information was reported: MIGRAINE (non-serious) with onset 29Jan2021, outcome "unknown", described as "Three migraines with Aura in less than a year.". The patient underwent the following laboratory tests and procedures: sars-cov-2 test: negative. Therapeutic measures were taken as a result of migraine. No follow-up attempts are possible. No further information is expected. Additional Information: Three migraines with Aura in less than a year. Excedrin immediately at onset of aura. Patient did not provide information regarding the reported adverse event(s) with the use of the product. Administration date was 14Jan2021 of Dose number 3,Vaccine location was Right arm.If other vaccine in four weeks was Unknown. Other medications in two weeks were taken. Adverse event treatment was Excedrin immediately at onset of aura.covid prior vaccination was no.covid tested post vaccination was yes.Covid test type post vaccination was Nasal Swab. Patient had no Known allergies.Other medical history: Hypertension, arthritis, type 2 diabetes.Updated information included: Reporter slider unchecked. The patient did not provide information regarding the reported adverse event(s) with the use of the product. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis; Hypertension; Type 2 diabetes mellitus
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2182213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MA
Alter: 64,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 08.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Mobility decreased Pain Pain in extremity X-ray

Symptomtext

Within 12 hours of receiving vaccine, there was extreme pain in left arm which radiated down to my hand. Since the vaccine, I have limited mobility in that arm and pain when with motion. I waited to seek treatment as I hoped it was getting better but seemed to plateau and increase in pain level. I went to my primary care who referred me to a physiatrist. His treatment plan is pending an EMG.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: X-ray 2/10/2022, EMG pending 4/18/2022, PT in progress 3/14, 3/28, 4/4, 4/12, 4/19- follow up with Dr. pending.
Aktuelle Erkrankungen: no
Vorgeschichte: hypothyroidism, cervical syrinx, osteoarthritis
Andere Medikamente: levothyroxine. daily multivitamin, ibuprofen - as needed - do not recall if I had take any, cyclobenzaprine take as needed - don't think I took any then
Allergien: gabapentin, amitriptyline, venlafaxine
Vorherige Impfungen: -

VAERS 1858504

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3590

moderat

Staat: NC
Alter: 72,0
Geschlecht: U
Eingang: 12.03.2022
Impfdatum: 01.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / LA

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

Abdominal pain upper Axillary pain Dizziness Fatigue Headache Abdominal pain Back pain Nausea Neck pain Paraesthesia Rash

Symptomtext

Severe headache; very severe nausea; dizziness; rash on arms; tingling arms, upper back, & neck; pain in armpits & stomach; pain in armpits & stomach; extreme fatigue; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 72 year-old patient received bnt162b2 (BNT162B2), administered in arm left, administration date 01Nov2021 (Lot number: Fe3590) at the age of 72 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Penicillin allergies" (unspecified if ongoing); "Suphanomides allergies" (unspecified if ongoing); "Asthma" (unspecified if ongoing); "chronic lyme disease" (unspecified if ongoing); "HBp" (unspecified if ongoing); "Hypothyroidism" (unspecified if ongoing). Concomitant medication(s) included: PRISTIQ; VYVANSE; LOSARTAN; CARVEDILOL; SYNTHROID. Past drug history included: Codein, reaction(s): "Allergy". Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: GNG200, Location of injection: Arm Left), administration date: 23Feb2021, when the patient was 71 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN5318, Location of injection: Arm Left), for Covid-19 immunization. The following information was reported: HEADACHE (non-serious) with onset 03Nov2021, outcome "recovered" (Nov2021), described as "Severe headache"; NAUSEA (non-serious) with onset 03Nov2021, outcome "recovered" (Nov2021), described as "very severe nausea"; DIZZINESS (non-serious) with onset 03Nov2021, outcome "recovered" (Nov2021), described as "dizziness"; RASH (non-serious) with onset 03Nov2021, outcome "recovered" (Nov2021), described as "rash on arms"; PARAESTHESIA (non-serious) with onset 03Nov2021, outcome "recovered" (Nov2021), described as "tingling arms, upper back, & neck"; AXILLARY PAIN (non-serious), ABDOMINAL PAIN UPPER (non-serious) all with onset 03Nov2021, outcome "recovered" (08Nov2021) and all described as "pain in armpits & stomach"; FATIGUE (non-serious) with onset 03Nov2021, outcome "recovered" (Nov2021), described as "extreme fatigue". Therapeutic measures were not taken as a result of headache, nausea, dizziness, rash, paraesthesia, axillary pain, abdominal pain upper, fatigue. Additional information: It was unknown if prior to vaccination, the was patient diagnosed with COVID-19 and since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Blood pressure high; Chronic disease; Hypothyroidism; Penicillin allergy; Sulfonamide allergy
Andere Medikamente: PRISTIQ; VYVANSE; LOSARTAN; CARVEDILOL; SYNTHROID
Allergien: -
Vorherige Impfungen: -

VAERS 1858504

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3590

moderat

Staat: NC
Alter: 72,0
Geschlecht: U
Eingang: 12.03.2022
Impfdatum: 01.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal pain upper Axillary pain Dizziness Fatigue Headache Abdominal pain Back pain Nausea Neck pain Paraesthesia Rash

Symptomtext

Severe headache; very severe nausea; dizziness; rash on arms; tingling arms, upper back, & neck; pain in armpits & stomach; pain in armpits & stomach; extreme fatigue; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 72 year-old patient received bnt162b2 (BNT162B2), administered in arm left, administration date 01Nov2021 (Lot number: Fe3590) at the age of 72 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Penicillin allergies" (unspecified if ongoing); "Suphanomides allergies" (unspecified if ongoing); "Asthma" (unspecified if ongoing); "chronic lyme disease" (unspecified if ongoing); "HBp" (unspecified if ongoing); "Hypothyroidism" (unspecified if ongoing). Concomitant medication(s) included: PRISTIQ; VYVANSE; LOSARTAN; CARVEDILOL; SYNTHROID. Past drug history included: Codein, reaction(s): "Allergy". Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: GNG200, Location of injection: Arm Left), administration date: 23Feb2021, when the patient was 71 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN5318, Location of injection: Arm Left), for Covid-19 immunization. The following information was reported: HEADACHE (non-serious) with onset 03Nov2021, outcome "recovered" (Nov2021), described as "Severe headache"; NAUSEA (non-serious) with onset 03Nov2021, outcome "recovered" (Nov2021), described as "very severe nausea"; DIZZINESS (non-serious) with onset 03Nov2021, outcome "recovered" (Nov2021), described as "dizziness"; RASH (non-serious) with onset 03Nov2021, outcome "recovered" (Nov2021), described as "rash on arms"; PARAESTHESIA (non-serious) with onset 03Nov2021, outcome "recovered" (Nov2021), described as "tingling arms, upper back, & neck"; AXILLARY PAIN (non-serious), ABDOMINAL PAIN UPPER (non-serious) all with onset 03Nov2021, outcome "recovered" (08Nov2021) and all described as "pain in armpits & stomach"; FATIGUE (non-serious) with onset 03Nov2021, outcome "recovered" (Nov2021), described as "extreme fatigue". Therapeutic measures were not taken as a result of headache, nausea, dizziness, rash, paraesthesia, axillary pain, abdominal pain upper, fatigue. Additional information: It was unknown if prior to vaccination, the was patient diagnosed with COVID-19 and since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Blood pressure high; Chronic disease; Hypothyroidism; Penicillin allergy; Sulfonamide allergy
Andere Medikamente: PRISTIQ; VYVANSE; LOSARTAN; CARVEDILOL; SYNTHROID
Allergien: -
Vorherige Impfungen: -

VAERS 2173642

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: WA
Alter: 75,0
Geschlecht: F
Eingang: 11.03.2022
Impfdatum: 09.10.2021
Beginn: 12.11.2021
Tage bis Beginn: 34,0
Dosis: 3
Route/Site: IM / LA

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

Dry skin Ear pain Herpes zoster Pain Paraesthesia

Symptomtext

On 11/12/2021, my right ear began to ache, and it would continue to ache for the next 3 or 4 days. I went to my PCP, on 11/17/2021, and he thought I possibly had a cold. On 11/19/2021, a rough area about the size of a quarter appeared in front of my right ear. I took a picture of it and sent it to my PCP. I then got a prompt response from him telling me that I had Shingles. On 11/22/2021, I saw another doctor in doctor practice, as the doctor was out of town. I was prescribed Gabapentin for the pain and an antiviral. They weren't effective, so I had to ride out the Shingles. In January 2022, I went to my annual dermatologist's appointment, and she observed that I had residual Shingles activity on my right ear lobe and the right side of my scalp. At the time of this writing, the symptoms have mostly vanished, though I still occasionally experience a tingling sensation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: Coronary arterial disease, osteoarthritis, occasional muscular pain in both legs.
Andere Medikamente: Lisinopril, Hydrochlorothiazide, Carvedilol, Atorvastatin, half an Aspirin daily, PreserVision AREDS 2, CoQ10, Cetirizine, Vitamin D.
Allergien: Isoniazid, Meloxicam.
Vorherige Impfungen: In 2016 or 2018, I got shingles about 2 weeks after getting a Shingrix vaccination.

VAERS 2165987

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: WI
Alter: 84,0
Geschlecht: M
Eingang: 08.03.2022
Impfdatum: 22.10.2021
Beginn: 01.01.2022
Tage bis Beginn: 71,0
Dosis: 3
Route/Site: UN / UN

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

Asthenia COVID-19 Chest X-ray abnormal Hypoxia Influenza virus test negative Pericardial effusion Pneumonia Productive cough SARS-CoV-2 antibody test SARS-CoV-2 test positive Sputum discoloured

Symptomtext

Pt presented to the ED on 1/1/2022 with weakness, hypoxia, afebrile, sats in the mid 80s, productive cough - white sputum. CXR showed L lower lobe pneumonia, pericardial effusion. Tested negative for influenza and positive for Covid. Started on cefepime and dexamethasone, O2 at 2L and was admitted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: 1/1/2022: Covid positive by PCR, Influenza negative 1/3/2022: SARS CoV-2 Nucleocapsid Protein IgG: negative Pt received covid vaccines as follows: 1st dose: Pfizer EN6200 2/26/2021 2nd dose: Pfizer ER2613 3/19/2021 Booster: Pfizer FE3590 10/22/2021
Aktuelle Erkrankungen: unknown
Vorgeschichte: HTN, Dementia, hx CVA, anemia, arthritis
Andere Medikamente: unknown
Allergien: lisinopril - cough
Vorherige Impfungen: -

VAERS 2165446

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NC
Alter: 76,0
Geschlecht: M
Eingang: 08.03.2022
Impfdatum: 16.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: SYR / LA

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

Paraesthesia Rash Rash papular Rash pruritic Vaccination site pruritus

Symptomtext

About 2 weeks after 3rd dose, I began to get itchy, near vaccination site first. Noticed near my watch band bumps below the skin. Seems like they follow blood vessels up my left arm to shoulder. Always there, sometime itchier than other times, sometimes they are very itchy.. Sometimes arm feels tingley, like my arm falls asleep. Bumps on upper arm are above skin, resemble small mosquito bites.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Prescribed Triamcinolone Acetonide cream USP 0.5%
Aktuelle Erkrankungen: None
Vorgeschichte: Leukemia in 2015, in remission since 08/20. 08/18 open-heart surgery
Andere Medikamente: Baciglar 14u, Metformin, Symbystatin 20mg, Adenyl 25mg, Aspirin 81mg, Glipizide 2.5mg
Allergien: Morphine
Vorherige Impfungen: -

VAERS 2161702

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 81,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 08.11.2021
Beginn: 01.01.2022
Tage bis Beginn: 54,0
Dosis: 3
Route/Site: - / LA

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

Back pain Blood pressure increased Blood pressure measurement Breast pain Herpes zoster Illness Insomnia Pain in extremity Paraesthesia Rash Skin burning sensation

Symptomtext

I have been so sick; cannot sleep; skin burns and everything; like somebody is burning you with a lit cigarette and stabbing you with needles that never goes away; severe case of a rash/got rash on breast, under and along left breast-arm-to back rash on back/rash worse; My arm, my back, my breast horrible painful/Sharp, stabbing pains in left breast, arm length inside & onto back; My arm, my back, my breast horrible painful/Sharp, stabbing pains in left breast, arm length inside & onto back; My arm, my back, my breast horrible painful/Sharp, stabbing pains in left breast, arm length inside & onto back; Blood pressure increased; I get shingles; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 81 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 08Nov2021 16:10 (Lot number: FE3590) at the age of 81 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "High Blood Pressure" (unspecified if ongoing); "acid reflux" (unspecified if ongoing); "Cholesterol" (unspecified if ongoing), notes: I take 'Roboc' something that is one for Cholesterol, that is the generic for 'Crestor'. Concomitant medication(s) included: VALSARTAN taken for hypertension; MAXZIDE taken for hypertension; OMEPRAZOLE taken for gastrooesophageal reflux disease; ROSUVASTATIN taken for blood cholesterol abnormal. Vaccination history included: Bnt162b2 (1st dose, Lot# EL9264, Administration time: 02:00 PM, Anatomical site of Injection: left arm), administration date: 05Feb2021, when the patient was 80 years old, for COVID-19 immunization; Bnt162b2 (2nd dose, Lot# EN6203), administration date: 26Feb2021, when the patient was 80 years old, for COVID-19 immunization. The following information was reported: RASH (disability, medically significant) with onset 09Jan2022, outcome "not recovered", described as "severe case of a rash/got rash on breast, under and along left breast-arm-to back rash on back/rash worse"; PAIN IN EXTREMITY (disability, medically significant), BACK PAIN (disability, medically significant), BREAST PAIN (disability, medically significant) all with onset Jan2022, outcome "not recovered" and all described as "My arm, my back, my breast horrible painful/Sharp, stabbing pains in left breast, arm length inside & onto back"; BLOOD PRESSURE INCREASED (disability, medically significant) with onset Jan2022, outcome "not recovered", described as "Blood pressure increased"; HERPES ZOSTER (non-serious) with onset Jan2022, outcome "unknown", described as "I get shingles"; ILLNESS (non-serious), outcome "unknown", described as "I have been so sick"; INSOMNIA (non-serious), outcome "unknown", described as "cannot sleep"; SKIN BURNING SENSATION (non-serious), outcome "unknown", described as "skin burns and everything"; PARAESTHESIA (non-serious), outcome "not recovered", described as "like somebody is burning you with a lit cigarette and stabbing you with needles that never goes away". The events "severe case of a rash/got rash on breast, under and along left breast-arm-to back rash on back/rash worse", "my arm, my back, my breast horrible painful/sharp, stabbing pains in left breast, arm length inside & onto back", "my arm, my back, my breast horrible painful/sharp, stabbing pains in left breast, arm length inside & onto back", "my arm, my back, my breast horrible painful/sharp, stabbing pains in left breast, arm length inside & onto back", "blood pressure increased" and "i get shingles" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: blood pressure measurement: (Jan2022) going so high. Therapeutic measures were taken as a result of rash, pain in extremity, back pain, breast pain, blood pressure increased, herpes zoster. Patient got the booster shot on 08Nov2021 went to (state name withheld) to buy timeshare and 10Jan, she came down with severe case of a rash and she sent pictures to her dermatologist. Patient arm, her back, her breast horrible painful and they said it is shingles. So, how in the hell did she get shingles. Then come to find out she talked to her manager at the real state office, and she said her son in law took the booster and he came down with shingles (Further clarification unknown). She knows three other people that the same thing has happened to (Further clarification unknown). So, that is why she was calling you. When probed if patient has any query reporter stated, well, she thinks you should know that people getting shingles (Further clarification unknown) and this is the worst thing she have ever had in my entire life. She has been so sick; you cannot sleep, and your skin burns and everything. So, she thinks you should make people aware that get a booster you, got a good chance of getting horrible shingles (Further not clarified). Reporter stated, (email withheld) but do not send me anything that you want me to print because she cannot do that (Further not appropriately clarified hence not captured in tab). Expiration date reporter stated, no, but she thinks they sent me an email about congratulations on being vaccinated or something. It says anything let me see they gave me four pages about (Incomplete Sentence). Anatomical Site of administration reporter stated, she got, she thought every time they used the same arm, my left (arm) one. Consumer stated, well, she has high blood pressure so, she takes a blood pressure medicine. she takes a cholesterol reducing medicine (Further not clarified). she takes a diuretic (Further not clarified) for my part of my high blood pressure. I take acid reflux medicine (Further not clarified). Reporter stated, what she takes, she takes normally Valsartan (Further not clarified) and Maxide (Further not clarified) and the acid reflux is called, she has to go look up that up better, it is generic for Prilosec whatever that is, and she take Roboc something that is one for Cholesterol, that is the generic for 'Crestor' (Further clarification unknown). Reporter stated, since this happened you mean or before no, not yet because all of these medicines the doctor gave me. He is gonna do my blood work like in a week or two to see what it is is doing to my kidneys and bladder and all of this to 'motion' with all of these pills I have to take now (Further clarification unknown hence not captured). Reporter stated, Yes, she took pictures of my breast and sent them to the skin doctor because like she said, she was in (state name withheld) and she did not know if she came in contact with something or spider bit me or something (Further clarification unknown hence event captured as per verbatim) so she sent the pictures of my breast, my arm and my back to the skin doctor and he wanted me to go to the emergency room, a doctor or clinic (Further clarification unknown) and she said, no she was coming home in a few days and she do not wanna go to a hospital and get COVID from people (Further clarification unknown) you know what she mean. So, he sent me medicine and he sent me prescriptions for me to go pick up at the drug store, but she had to send somebody and pay them to go get it because she cannot go 'like that' to a drug store (Further clarification unknown). Reporter stated, she started in (state name withheld) because she was there for my timeshare time and then she came home, and it is not better, and the pain is like she said before it is the worst thing she have ever got in her life. It is like somebody is burning you with a lit cigarette and stabbing you with needles that never goes away (Further clarification unknown hence event captured as per verbatim) and it is just absolutely horrible your skin burns, and your clothing burns your skin to touch it (Further clarification unknown hence event captured as per verbatim), it is just horrible. It was right before it was getting dark. So, she would say it was like 4 something, 4:30 (Further clarification unknown) say but she could ask my daughter if you need it to be more accurate because we went at the same time, and she drove. No Prior Vaccination (4 weeks prior). She just put it in my arm in normal way, my left arm. reporter stated, no, but she just thinks people should be aware of the possibility of getting this horrible case and the doctor told me that this pain can last for years (Further clarification unknown), and I mean, it is absolutely terrible. She sent that doctor pictures, it was like sending them pornography. It is so terrible, it is my whole left breast, under my arm all the way down my left arm onto my back and it is as big as a saucer in my back. She still has the pictures in my phone. She just wants to help the people you know everybody should report if something is wrong. Vaccination facility type was pharmacy or drug store. Vaccination facility type was pharmacy or drug store. Booster dose due to high risk of frequent institutional or occupational exposure to coronavirus. Event date reported as 09Jan2022 with onset 15hours, Seriousness criteria was persistent/significant disability/incapacity, important medical event. 09Jan2022 on vaccination got rash on breast, under and along left breast-arm-to back rash on back saucer size sent photos to Dr. (Name) in (withheld). To see he prescribes 3 per. MEDS. Returned home 17Jan rash worse, Shingles was diagnosed, went to Dr. office more medicines worst pain was experienced still ongoing today is 10Feb over 1 month as of today. Sharp, stabbing pains in left breast, arm length inside & onto back. Blood pressure going so high do recommend another pill. Never have been sick like this so horrible, hard to take care of herself. The initial safety information received was reporting only non-serious adverse drug reaction(s), upon receipt of follow-up information on [18Feb2022], this case now contains serious adverse reaction(s). Information processed together. Follow-up (18Feb2022): New information received from a contactable consumer. This consumer reported in response to Non-HCP letter sent in cross referenced case which included that:Updated information included: General Tab: (Reporter middle name), Patient tab: (Patient middle name, Historical vaccine, Lab test), Product tab (Dose administration date and time), Events Tab: New SAE events (Blood pressure increased), (Outcome, Treatment received). Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 202201; Test Name: Blood pressure; Result Unstructured Data: Test Result:going so high
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Acid reflux (oesophageal); Blood cholesterol abnormal (I take 'Roboc' something that is one for Cholesterol, that is the generic for 'Crestor'); Blood pressure high
Andere Medikamente: VALSARTAN; MAXZIDE; OMEPRAZOLE; ROSUVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2151101

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NV
Alter: 52,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Abnormal faeces Arthralgia Gallbladder disorder Hemiplegic migraine Nausea Pain

Symptomtext

Systemic: Joint Pain-Mild, Systemic: Nausea-Mild, Systemic: Headache-Mild, Systemic: Gallbladder flare-Mild, Additional Details: gallbladder flare with associated nausea, pain, changes in stool; new onset join pain in R ankle and shoulder; 1 episode of hemiplegic migraine

Weitere VAERSDATA-Felder

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

VAERS 2148657

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: DE
Alter: 70,0
Geschlecht: M
Eingang: 28.02.2022
Impfdatum: 14.10.2021
Beginn: 24.12.2021
Tage bis Beginn: 71,0
Dosis: 2
Route/Site: SYR / LA

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

COVID-19 Chest pain Chills Cough Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had chest pain in the center. It still going but not as bad. I had running nose, cough, fever, and chills. These lasted for about a week. On Dec. 24th, I was tested positive for Covid-19. I went to my doctor about it. I tested positive there also at the doctor offices.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Covid-19 test
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure Arthritis
Andere Medikamente: N/A
Allergien: Sofia
Vorherige Impfungen: -

VAERS 2148646

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 51,0
Geschlecht: F
Eingang: 28.02.2022
Impfdatum: 12.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Dizziness Drop attacks Headache Hypoaesthesia Muscle spasms Muscular weakness Pain in extremity Palpitations Paraesthesia Photophobia

Symptomtext

After the first dose, patient had pain, tingling and numbness in the right arm extending to the fore arm happened after the first dose. She also experienced headaches associated with photophobia with no known h/o migraines. After the second dose, she experienced sudden onset of weakness in the right arm, suddenly drops the objects in her right hand. Feels right side weaker than left, and paresthesia on the right leg- this has now improved. . Also started experiencing pain in both the knees and the legs associated with cramping, for the past 4 months since the 2nd dose of vaccine. she also reports that she is having episodes of palpitations, dizziness, and headache. .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: calcium supplements, vitamin C, Vit D 1000 units, ferrous sulfate
Allergien: No known drug allergies
Vorherige Impfungen: -

VAERS 2147284

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: OH
Alter: 68,0
Geschlecht: F
Eingang: 27.02.2022
Impfdatum: 13.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Asthenia Chest pain Fatigue Gait disturbance Musculoskeletal discomfort Oral discomfort Pain in extremity Pain in jaw

Symptomtext

Severe chest pain; jaw pain; could barely open my mouth; felt like someone sitting on my shoulders; I could barely walk; extreme fatigue; My arm was very sore; I had no energy and I was just dragging; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 13Oct2021 13:15 (Lot number: FE3590) at the age of 68 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 2, SINGLE, Batch/Lot No: EN6201, Location of injection: Arm Left, Vaccine Administration Time: 10:15 AM), administration date: 02Mar2021, when the patient was 69 years old, for Covid-19 immunization; Bnt162b2 (DOSE 1, SINGLE, Batch/Lot No: EL9265, Location of injection: Arm Left, Vaccine Administration Time: 10:00 AM), administration date: 09Feb2021, when the patient was 69 years old, for COVID-19 Immunization. The following information was reported: CHEST PAIN (medically significant) with onset 13Oct2021 20:30, outcome "recovered" (2021), described as "Severe chest pain"; PAIN IN JAW (non-serious) with onset 13Oct2021 20:30, outcome "recovered" (2021), described as "jaw pain"; ORAL DISCOMFORT (non-serious) with onset 13Oct2021 20:30, outcome "recovered" (2021), described as "could barely open my mouth"; MUSCULOSKELETAL DISCOMFORT (non-serious) with onset 13Oct2021 20:30, outcome "recovered" (2021), described as "felt like someone sitting on my shoulders"; GAIT DISTURBANCE (non-serious) with onset 13Oct2021 20:30, outcome "recovered" (2021), described as "I could barely walk"; FATIGUE (non-serious) with onset 13Oct2021 20:30, outcome "recovered" (2021), described as "extreme fatigue"; PAIN IN EXTREMITY (non-serious) with onset 13Oct2021 20:30, outcome "recovered" (2021), described as "My arm was very sore"; ASTHENIA (non-serious) with onset 13Oct2021 20:30, outcome "recovered" (2021), described as "I had no energy and I was just dragging". The events "severe chest pain", "jaw pain", "could barely open my mouth", "felt like someone sitting on my shoulders", "i could barely walk", "extreme fatigue", "my arm was very sore" and "i had no energy and i was just dragging" were evaluated at the physician office visit. Therapeutic measures were not taken as a result of chest pain, pain in jaw, oral discomfort, musculoskeletal discomfort, gait disturbance, fatigue, pain in extremity, asthenia. Additional Information: Patient did not received any treatment for AE. Patient did not tested Covid post vaccination. There was no Known allergies. Other medical history was N/A. Patient had Covid prior vaccination. Device timestamp was 14Feb2022.

Weitere VAERSDATA-Felder

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

VAERS 2138054

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3590

moderat

Staat: MA
Alter: 50,0
Geschlecht: F
Eingang: 24.02.2022
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Alanine aminotransferase increased Alopecia Arthralgia Asthma Back pain Bone pain C-reactive protein increased Chest pain Condition aggravated Discomfort Eye pain Fatigue Feeling abnormal Inflammatory marker increased Limb discomfort Muscular weakness Ocular discomfort Pain in extremity

Symptomtext

Hair loss Chest and jaw pain Persistent Eyeball pressure/pain Throat pressure/fullness Severe debilitating generalized joint pain followed by bone pain Debilitating hand joint pain in bilateral hands , worsening and more sever pain in thumb joints Severe low back pain Fatigue and brain fog for months Severe leg fatigue-feeling as if weights are on my legs holding them down especially when attempting to walk upstairs High abnormal Inflammatory lab tesults Severe asthma flare up requiring me to use my rescue inhaler more than I've used in the last 10 years combined

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: ESR-53 C reactive protein 11.1 Alt-41
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma Allergies Occasional neck/left shoulder blade discomfort from history of cervical disc herniating Right side si joint injury
Andere Medikamente: Flovent, Vit D, Omega 3 vitamins
Allergien: Sudafed Environmental allergies
Vorherige Impfungen: -

VAERS 2134505

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MT
Alter: 98,0
Geschlecht: F
Eingang: 23.02.2022
Impfdatum: 21.10.2021
Beginn: 30.12.2021
Tage bis Beginn: 70,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Dyspnoea Hypoxia Influenza A virus test Influenza B virus test Respiratory syncytial virus test Rib fracture SARS-CoV-2 test positive

Symptomtext

Case was vaccinated and boosted by 10/21/21, then was hospitalized for Covid 21/30/21. Admitted for rib fracture and found to be Covid positive. Required up to 20 litres of oxygen during hospitalization for shortness of breath and hypoxia. Discharged after 12 day in hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 12,0
Labordaten: Ordered Test: FLUABV+SARS-CoV-2+RSV RNA Pnl Resp NAA+p (SARS CoV2-Flu-RSV PCR) Ordered Test Codes: 95941-1 (LN LOINC)/7917436711 (L LOCAL) Status: Final Accession Number: 2021364001558001 Specimen Source: Nasopharynx Specimen Site: Specimen Collection Date/Time: 2021-12-30 09:40:00.0 Results: * Resulted Test: SARS-CoV-2 RNA Resp Ql NAA+probe (SARS CoV-2 PCR (COVID-19)) Coded Result: Positive (LOCAL) Numeric Result: Units: Text Result: Reference Range From: Negative Reference Range To: Performing Facility Details: Date/Time: 2021-12-30 10:31:41.0 Performing Facility: Med Cntr Facility ID: Interpretation: Abnormal Result Method: SARS-Co Status: Final Test Code: 94500-6 (LN LOINC)/7140701041 (L LOCAL) Result Code: 10828004 (SCT/Positive (L LOCAL)
Aktuelle Erkrankungen: Biventricular pacemaker, compression fractures, cataracts
Vorgeschichte: Biventricular pacemaker, compression fractures, cataracts
Andere Medikamente: ASA, Calcium, Ferrous sulfate, Fosamax, furosemide, ICaps AREDS, Levothyroxine, Loratadine, losartan, Metoprolol, Mirilax, Multivitamin, Nitroglycerine PRN, Plavix, Vitamin C, Voltarin gel prn.
Allergien: Oxycodone, Oysters
Vorherige Impfungen: -

VAERS 2131332

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 86,0
Geschlecht: M
Eingang: 22.02.2022
Impfdatum: 07.10.2021
Beginn: 12.11.2021
Tage bis Beginn: 36,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Diabetic ketoacidosis Hypoxia Lung infiltration Pneumonia bacterial

Symptomtext

Patient presented with diabetic ketoacidosis and acute kidney injury. During his swing bed stay, he developed mild hypoxia and further work-up revealed multifocal bilateral pulmonary infiltrates. He was treated for bacterial pneumonia (hospital-acquired) with Zosyn and clinically improved. Hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2128267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE 3590

moderat

Staat: AL
Alter: 32,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 14.02.2022
Beginn: 16.02.2022
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Chills Injection site pain Injection site pruritus Injection site reaction Injection site warmth Lethargy Migraine Nausea Pain Pain in extremity Pyrexia Rash erythematous

Symptomtext

15 hrs post vax/Wednesday AM: woke with notable chills, migraine, fever, severe body aches, extreme lethargy, nausea, painful vax arm Last until 28 hours post vax with migraine lingering but treatable with Tylenol. 39 hrs post vax/Thurs AM : woke with extremely itchy upper arm at site of vax. Skin was hot to touch and red rash starting around vax sit spread up over shoulder and down towards elbow quickly after itchiness began. Had to treat with benAdryl and cold compress. Rash was visibly shocking to see. Shot site was still sore and painful. Rash/severe itchiness resolved on it own over next 24 hours. fri and Sat (18th-19th) arm mildly sore, rash clear but still has random itching at vax site.

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Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Covid (likely Omicron) 1/20/22 to 1/26/22 Rotavirus type 24 hour Illness 2/7/22 Vaginal Yeast infection 2/13/22
Vorgeschichte: Genetic: mitral valve prolapse(heart), carry Factor II promthrombin, carry homozygous Factor V Leiden w R2 positive Skin: eczema, sebhorreic dermatitis, folliculitis prone Mental: anxiety disorder, situational depression Physical: 2 cesarean section surgeries, 1 elected breast augmentation, 3 term pregnancies, 2 early miscarriages Complications during one birth-induction of labor with breech baby resulted in severe cervical laceration needing repair at time of cesarean section. HPV positive, pre-cancerous and semi-cancerous cells found on cervix, biopsy and removal needed
Andere Medikamente: Buprenorphine 8 mg tablet SId Dextroamphetamine 20mg SID Vitacraves women gummy multivitamin
Allergien: Sulfa Allergy-Bactrim antibiotic results in systemic reaction of flu like symptoms, body rash, leukopenia-drop in white blood cell Sensitive Skin reactions to harsh chemicals, mold/fungus, and various soaps/hygiene products
Vorherige Impfungen: -

VAERS 2128055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 34,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 16.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Chest pain Palpitations SARS-CoV-2 test Urticaria

Symptomtext

Chest pain; Palpitations; Intense hives; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 34 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 16Oct2021 13:45 (Lot number: FE3590) at the age of 34 years as dose 3 (booster), single, administered in arm left, administration date 08Apr2021 (Lot number: EW0158) as dose 2, single and administered in arm left, administration date 18Mar2021 (Lot number: EQ7534) as dose 1, single for covid-19 immunisation. Relevant medical history included: "I've had cocci meningitis" (unspecified if ongoing), notes: Other medical history: I've had cocci meningitis. The patient's concomitant medications were not reported. The following information was reported: CHEST PAIN (medically significant) with onset 2021, outcome "not recovered", described as "Chest pain"; PALPITATIONS (medically significant) with onset 2021, outcome "not recovered", described as "Palpitations"; URTICARIA (medically significant) with onset 2021, outcome "not recovered", described as "Intense hives". The events "chest pain", "palpitations" and "intense hives" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (01Feb2022) negative, notes: covid test type post vaccination: Nasal Swab. Therapeutic measures were taken as a result of chest pain, palpitations, urticaria. Additional information: The patient was a reporter and Received 3 Doses with covid-19 vaccine of Pfizer. The patient had Previous doses . The patient did not other vaccine in four weeks. The patient had adverse event First chest pain and palpitations. Went to ER and cardiologist for over a month. Intense hives also started and hasn't stopped since the booster shot. Then patient was consulted Doctor or other healthcare professional office/clinic visit, Emergency room/ department or urgent care. The patient was AE treatment with Trying to get a referral for allergist. The patient was prior covid tested post vaccination and known allergies Was not before but now she got hives often. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20220201; Test Name: Nasal Swab; Test Result: Negative ; Comments: covid test type post vaccination: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Coccidioidal meningitis (Other medical history: I've had cocci meningitis)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2102103

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NY
Alter: 46,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Asthma Chest X-ray Chest discomfort Cough Dizziness Chest pain Dyspnoea Fatigue Electrocardiogram Flatulence Investigation Paraesthesia SARS-CoV-2 test Wheezing

Symptomtext

had tingling in the right hand but got the shot in the left arm; dizziness; tightness in chest; bronchial asthmatic coughing; trouble breathing; tiredness/she was exhausted; wheezing; feeling winded; she had a bronchial asthmatic cough and trouble breathing; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. Other Case identifier(s): US-PFIZER INC-202200223003 (Pfizer). A 47 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 20Oct2021 10:40 (Lot number: FE3590) at the age of 46 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: Moderna (1st dose of moderna vaccine, Lot: 040B21A), administration date: 10Apr2021, when the patient was 46 years old, for COVID-19 Immunization, reaction(s): "had a life threating reaction", "had numbness in arm", "dizziness", "bronchial asthmatic coughing", "coughing", "tiredness", "chest tightness", "tinging and numbness in her lower arm, hands and fingers and it kept getting worse and worse/bronchial asthmatic coughing was worse", "states her left arms, hands, and fingers were completely swollen", "she had no feeling", "her hands and fingers were turning blue", "Caller states two nurses came rushing out and she never got up on her own", "she woke up with full blown flu like side effects all from that Moderna shot", "she did not have a Second Dose of the Moderna Covid Vaccine"; Bnt162b2 (1st dose of Pfizer vaccine Lot: FE3592), administration date: 28Sep2021, when the patient was 46 years old, for COVID-19 Immunization, reaction(s): "her first and only dose of the Moderna Covid Vaccine on 10Apr2021", "administered slowly over 4 hours", "tired", "fell asleep for 2 of the 4 hours during the special dosing"; Flu shot (Caller states other than the Covid Vaccines, no reactions in the past, caller she she had all her childhood vaccines in the past and she gets her flu shot every year with no issues and both pneumonia vaccines), for Immunization; Pneumonia vaccines (Caller states other than the Covid Vaccines, no reactions in the past, caller she she had all her childhood vaccines in the past and she gets her flu shot every year with no issues and both pneumonia vaccines). The following information was reported: PARAESTHESIA (non-serious) with onset 20Oct2021 11:00, outcome "recovered" (31Oct2021), described as "had tingling in the right hand but got the shot in the left arm"; DIZZINESS (non-serious) with onset 20Oct2021 11:00, outcome "recovered" (31Oct2021), described as "dizziness"; CHEST DISCOMFORT (non-serious) with onset 20Oct2021 11:00, outcome "recovered" (31Oct2021), described as "tightness in chest"; COUGH (non-serious) with onset 20Oct2021 11:00, outcome "recovered" (31Oct2021), described as "bronchial asthmatic coughing"; DYSPNOEA (non-serious) with onset 20Oct2021 11:00, outcome "recovered", described as "trouble breathing"; FATIGUE (non-serious) with onset 20Oct2021 11:00, outcome "recovered" (31Oct2021), described as "tiredness/she was exhausted"; WHEEZING (non-serious) with onset 20Oct2021 11:00, outcome "recovered" (31Oct2021), described as "wheezing"; FLATULENCE (non-serious) with onset 20Oct2021 11:00, outcome "recovered" (31Oct2021), described as "feeling winded"; ASTHMA (non-serious) with onset 20Oct2021 11:00, outcome "recovered" (31Oct2021), described as "she had a bronchial asthmatic cough and trouble breathing". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of paraesthesia, dizziness, chest discomfort, cough, dyspnoea, fatigue, wheezing, flatulence, asthma. Additional information: PFIZER COVID VACCINE SECOND DOSE AE: Caller states her second dose was also administered in Dr. withheld Covid Vaccine Clinic, but it was administered normally, all at once in a shot. Caller states shortly after she got it, she had a reaction in the waiting area. Caller states she got the vaccine in her left arm, she never felt anything in the left arm, not even the shot going in, but after 15 minutes she had tingling in her right hand. Caller states she was laying down in the waiting area because she was very tired. Caller states she also was dizzy and had tightness in her chest. Caller states she had a bronchial asthmatic cough and trouble breathing, so she got her albuterol out of her purse. Caller states the person from the vaccine area told the nurses she was not feeling good and got the nurses to come. Caller states while waiting, she gave herself 2 puffs of Albuterol and the nurses came to vaccine area and called Dr. withheld out, he came and spoke to her in the waiting area and assisted her in to a wheelchair and they gave her an exam and took her vitals. Dr. withheld ordered a nebulizer treatment and she spent 4-5 hours in his office under medical monitoring before she was discharged from that reaction. Caller states she fully recovered on 31Oct2021. Caller states she had a residual cough and took Albuterol 2 puffs twice a day. Caller states when she was wheezing and feeling winded, it was like when she would get out of bed and go to the bedroom door she was winded and needing albuterol. Caller states she knows tiredness is normal but she was exhausted. Treatment: Albuterol and Nebulizer Treatment. Caller states other than the Covid Vaccines, no reactions in the past, caller she she had all her childhood vaccines in the past and she gets her flu shot every year with no issues and both pneumonia vaccines. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 202104; Test Name: Chest X-ray; Test Result: Negative ; Test Date: 202104; Test Name: EKG; Test Result: Negative ; Test Date: 202104; Test Name: her vitals; Result Unstructured Data: Test Result:Unknown result; Test Date: 202110; Test Name: her vitals; Result Unstructured Data: Test Result:Unknown result; Test Date: 202104; Test Name: rapid Covid test; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2102103

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

moderat

Staat: NY
Alter: 46,0
Geschlecht: F
Eingang: 19.02.2022
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

Asthma Chest X-ray Chest discomfort Cough Dizziness Chest pain Dyspnoea Fatigue Electrocardiogram Flatulence Investigation Paraesthesia SARS-CoV-2 test Wheezing

Symptomtext

had tingling in the right hand but got the shot in the left arm; dizziness; tightness in chest; bronchial asthmatic coughing; trouble breathing; tiredness/she was exhausted; wheezing; feeling winded; she had a bronchial asthmatic cough and trouble breathing; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. Other Case identifier(s): US-PFIZER INC-202200223003 (Pfizer). A 47 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 20Oct2021 10:40 (Lot number: FE3590) at the age of 46 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: Moderna (1st dose of moderna vaccine, Lot: 040B21A), administration date: 10Apr2021, when the patient was 46 years old, for COVID-19 Immunization, reaction(s): "had a life threating reaction", "had numbness in arm", "dizziness", "bronchial asthmatic coughing", "coughing", "tiredness", "chest tightness", "tinging and numbness in her lower arm, hands and fingers and it kept getting worse and worse/bronchial asthmatic coughing was worse", "states her left arms, hands, and fingers were completely swollen", "she had no feeling", "her hands and fingers were turning blue", "Caller states two nurses came rushing out and she never got up on her own", "she woke up with full blown flu like side effects all from that Moderna shot", "she did not have a Second Dose of the Moderna Covid Vaccine"; Bnt162b2 (1st dose of Pfizer vaccine Lot: FE3592), administration date: 28Sep2021, when the patient was 46 years old, for COVID-19 Immunization, reaction(s): "her first and only dose of the Moderna Covid Vaccine on 10Apr2021", "administered slowly over 4 hours", "tired", "fell asleep for 2 of the 4 hours during the special dosing"; Flu shot (Caller states other than the Covid Vaccines, no reactions in the past, caller she she had all her childhood vaccines in the past and she gets her flu shot every year with no issues and both pneumonia vaccines), for Immunization; Pneumonia vaccines (Caller states other than the Covid Vaccines, no reactions in the past, caller she she had all her childhood vaccines in the past and she gets her flu shot every year with no issues and both pneumonia vaccines). The following information was reported: PARAESTHESIA (non-serious) with onset 20Oct2021 11:00, outcome "recovered" (31Oct2021), described as "had tingling in the right hand but got the shot in the left arm"; DIZZINESS (non-serious) with onset 20Oct2021 11:00, outcome "recovered" (31Oct2021), described as "dizziness"; CHEST DISCOMFORT (non-serious) with onset 20Oct2021 11:00, outcome "recovered" (31Oct2021), described as "tightness in chest"; COUGH (non-serious) with onset 20Oct2021 11:00, outcome "recovered" (31Oct2021), described as "bronchial asthmatic coughing"; DYSPNOEA (non-serious) with onset 20Oct2021 11:00, outcome "recovered", described as "trouble breathing"; FATIGUE (non-serious) with onset 20Oct2021 11:00, outcome "recovered" (31Oct2021), described as "tiredness/she was exhausted"; WHEEZING (non-serious) with onset 20Oct2021 11:00, outcome "recovered" (31Oct2021), described as "wheezing"; FLATULENCE (non-serious) with onset 20Oct2021 11:00, outcome "recovered" (31Oct2021), described as "feeling winded"; ASTHMA (non-serious) with onset 20Oct2021 11:00, outcome "recovered" (31Oct2021), described as "she had a bronchial asthmatic cough and trouble breathing". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of paraesthesia, dizziness, chest discomfort, cough, dyspnoea, fatigue, wheezing, flatulence, asthma. Additional information: PFIZER COVID VACCINE SECOND DOSE AE: Caller states her second dose was also administered in Dr. withheld Covid Vaccine Clinic, but it was administered normally, all at once in a shot. Caller states shortly after she got it, she had a reaction in the waiting area. Caller states she got the vaccine in her left arm, she never felt anything in the left arm, not even the shot going in, but after 15 minutes she had tingling in her right hand. Caller states she was laying down in the waiting area because she was very tired. Caller states she also was dizzy and had tightness in her chest. Caller states she had a bronchial asthmatic cough and trouble breathing, so she got her albuterol out of her purse. Caller states the person from the vaccine area told the nurses she was not feeling good and got the nurses to come. Caller states while waiting, she gave herself 2 puffs of Albuterol and the nurses came to vaccine area and called Dr. withheld out, he came and spoke to her in the waiting area and assisted her in to a wheelchair and they gave her an exam and took her vitals. Dr. withheld ordered a nebulizer treatment and she spent 4-5 hours in his office under medical monitoring before she was discharged from that reaction. Caller states she fully recovered on 31Oct2021. Caller states she had a residual cough and took Albuterol 2 puffs twice a day. Caller states when she was wheezing and feeling winded, it was like when she would get out of bed and go to the bedroom door she was winded and needing albuterol. Caller states she knows tiredness is normal but she was exhausted. Treatment: Albuterol and Nebulizer Treatment. Caller states other than the Covid Vaccines, no reactions in the past, caller she she had all her childhood vaccines in the past and she gets her flu shot every year with no issues and both pneumonia vaccines. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 202104; Test Name: Chest X-ray; Test Result: Negative ; Test Date: 202104; Test Name: EKG; Test Result: Negative ; Test Date: 202104; Test Name: her vitals; Result Unstructured Data: Test Result:Unknown result; Test Date: 202110; Test Name: her vitals; Result Unstructured Data: Test Result:Unknown result; Test Date: 202104; Test Name: rapid Covid test; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2122787

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: KY
Alter: 83,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 08.03.2021
Beginn: 17.02.2022
Tage bis Beginn: 346,0
Dosis: 2
Route/Site: IM / LA

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

Dyspnoea Pyrexia

Symptomtext

developed fever and become short of breath, admitted to hospital on 2/17. placed on O2, started on decadron and remdesivir

Weitere VAERSDATA-Felder

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

VAERS 2122593

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NC
Alter: 85,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 20.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / -

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

Arthralgia Condition aggravated Gait disturbance Groin pain Investigation Osteoarthritis Pain in extremity Pyrexia SARS-CoV-2 test

Symptomtext

fever; pain in right hip; pain in right hip area and right groin and thigh; pain in right hip area and right groin and thigh; could not lift my right leg; aggregation to my hip and groin basically; flare up to my s ostoarthritus; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 85 year-old male patient received bnt162b2 (BNT162B2), administration date 20Oct2021 14:00 (Lot number: FE3590) at the age of 85 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "COPD" (unspecified if ongoing), notes: Other medical history: COPD, MDS on chemo for MDS, Smoldering myeloma; "MDS on chemo for MDS" (unspecified if ongoing), notes: Other medical history: COPD, MDS on chemo for MDS, Smoldering myeloma; "Smoldering myeloma" (unspecified if ongoing), notes: Other medical history: COPD, MDS on chemo for MDS, Smoldering myeloma; "Known Allergy: sulfa drugs" (unspecified if ongoing), notes: Known Allergy: sulfa drugs; "MDS on chemo for" (unspecified if ongoing), notes: Other medical history: COPD, MDS on chemo for MDS, Smoldering myeloma. Concomitant medication(s) included: ASPRIN; POLYETHYLENE GLYCOL [MACROGOL]; SIM. Vaccination history included: Bnt162b2 (Dose Number: 1, Prev dose product=COVID 19, Prev dose brand=Pfizer EL3247, Prev dose brand unknown=False, Prev dose lot number= EL3247, Prev dose lot unknown=False, Prev dose administration date=23Jan2021, Prev dose dose number=1, Prev dose vaccine location=Left arm), administration date: 23Jan2021, when the patient was 85 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 2, Prev dose product=COVID 19, Prev dose brand=Pfizer Em9810, Prev dose brand unknown=False, Prev dose lot number=Em9810, Prev dose lot unknown=False, Prev dose administration date=15Feb2021, Prev dose dose number=2, Prev dose vaccine location=Left arm), administration date: 15Feb2021, when the patient was 85 years old, for Covid-19 immunization. The following information was reported: PYREXIA (non-serious) with onset 21Oct2021 12:00, outcome "unknown", described as "fever"; ARTHRALGIA (non-serious) with onset 21Oct2021 12:00, outcome "unknown", described as "pain in right hip"; GROIN PAIN (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 21Oct2021 12:00, outcome "unknown" and all described as "pain in right hip area and right groin and thigh"; GAIT DISTURBANCE (non-serious) with onset 21Oct2021 12:00, outcome "unknown", described as "could not lift my right leg"; CONDITION AGGRAVATED (non-serious) with onset 21Oct2021 12:00, outcome "unknown", described as "aggregation to my hip and groin basically"; OSTEOARTHRITIS (non-serious) with onset 21Oct2021 12:00, outcome "unknown", described as "flare up to my s ostoarthritus". The events "fever", "pain in right hip area and right groin and thigh", "could not lift my right leg", "aggregation to my hip and groin basically" and "flare up to my s ostoarthritus" were evaluated at the emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pyrexia, arthralgia, groin pain, pain in extremity, gait disturbance, condition aggravated, osteoarthritis. Additional information: No other vaccine in four weeks. The last shot taken last Wednesday, made him run a fever of 100.2 for three to four nights, horrible pain in right hip area and right groin and thigh so bad he could not lift his right leg and could barely walk. His doctor sent him to emergency room for a test to see if he had blood clot in leg or groin, did not, they did say he had and they and his doctor concluded the covid shot caused aggregation to his hip and groin basically a flare up to his osteoarthritis. No covid prior vaccination. Covid tested post vaccination, covid test type post vaccination was nasal swab on 25Oct2021, covid test result was negative. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 20211021; Test Name: test to see; Result Unstructured Data: Test Result:i did not; Comments: test to see if I had blood clot in leg or groin i did not; Test Date: 20211021; Test Name: fever; Result Unstructured Data: Test Result:100.2; Test Date: 20211025; Test Name: Nasal Swab; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Chemotherapy (Other medical history: COPD, MDS on chemo for MDS, Smoldering myeloma); COPD (Other medical history: COPD, MDS on chemo for MDS, Smoldering myeloma); MDS (Other medical history: COPD, MDS on chemo for MDS, Smoldering myeloma); Smoldering myeloma (Other medical history: COPD, MDS on chemo for MDS, Smoldering myeloma); Sulfonamide allergy (Known Allergy: sulfa drugs)
Andere Medikamente: ASPRIN; POLYETHYLENE GLYCOL [MACROGOL]; SIM
Allergien: -
Vorherige Impfungen: -

VAERS 2118711

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: IL
Alter: 65,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 09.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Condition aggravated Rash

Symptomtext

had a rash on the right side of her face; rash on left side of face was reported as worsened; 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 65-year-old female patient received bnt162b2 (COMIRNATY), administration date 09Oct2021 (Lot number: FE3590) at the age of 65 years as dose 3 (booster), single for covid-19 immunization. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (dose 1, single, Batch number: EP7334, Anatomical location: left arm), administration date: 19Mar2021, when the patient was 64 years old, for Covid-19 immunization; Bnt162b2 (dose 2, single, Batch number: EN0158, Anatomical location: left arm), administration date: 09Apr2021, when the patient was 64 years old, for Covid-19 immunization. The following information was reported: RASH (non-serious) with onset 16Oct2021, outcome "not recovered", described as "had a rash on the right side of her face"; CONDITION AGGRAVATED (non-serious) with onset Oct2021, outcome "not recovered", described as "rash on left side of face was reported as worsened". Additional information: Caller wanted to know if this was a reported side effect from the Pfizer Covid-19 vaccine. Caller received the Pfizer booster shot on 09Oct2021, she stated that she was out on vacations this week and about 4 days ago, clarified on the 16Oct2021 she noticed a rash on the right side of her face only, it was not the left side, she wanted to know if this was a side effect of the booster shot. Caller sated that it progressively got worse and in the last three days it has stayed the same and was not going away. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2118710

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: IN
Alter: 61,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 08.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Feeling abnormal Headache Heart rate Heart rate increased Heart rate irregular Supraventricular extrasystoles Tachycardia Ventricular extrasystoles

Symptomtext

headache; she has not felt great/she hadn't felt good; an increased heart rate; PVC; PAC; tachycardia; I had an irregular, fast heart beat after my first dose; This is a spontaneous report received from contactable reporter(s) (Other HCP) from medical information team. The reporter is the patient. Other Case identifier(s): US-PFIZER INC-202101417521 (Pfizer). A 61 year-old female patient received bnt162b2 (COMIRNATY), administered in arm left, administration date 08Oct2021 (Lot number: FE3590) at the age of 61 years as dose 1,single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: HEADACHE (non-serious), outcome "not recovered", described as "headache"; HEART RATE INCREASED (non-serious) with onset 08Oct2021, outcome "recovering", described as "an increased heart rate"; VENTRICULAR EXTRASYSTOLES (non-serious) with onset 08Oct2021, outcome "recovering", described as "PVC"; SUPRAVENTRICULAR EXTRASYSTOLES (non-serious) with onset 08Oct2021, outcome "recovering", described as "PAC"; FEELING ABNORMAL (non-serious), outcome "unknown", described as "she has not felt great/she hadn't felt good"; TACHYCARDIA (non-serious) with onset Oct2021, outcome "unknown", described as "tachycardia"; HEART RATE IRREGULAR (non-serious) with onset 2021, outcome "unknown", described as "I had an irregular, fast heart beat after my first dose". Relevant laboratory tests and procedures are available in the appropriate section. Caller was a consumer (61 years old, female) inquiring about side effect information for the Pfizer Covid-19 vaccine. Caller reports the patient received her first dose of on 08Oct. Caller states " she had a headache for 2 days now, her main concern was the patient had a headache and cannot get rid of. She was in bed and be honest the patient did not had a headache since yesterday and got it when she got her vaccine, pretty severe, no concerns for anything, but the Johnson and Johnson had problems with headaches, wanted to make sure there was nothing to be concerned about." Caller states "it had been 10 or 11 days since she got the shot and did not get a headache at the beginning. They said her heart arrhythmia and tachycardia was an allergic reaction not just side effect, the patient supposed to get second dose on 29Oct. Caller states the patient got her first dose of the BioNtech covid vaccine on the 8th. 7 minutes after the dose she had an increased heart rate, PVC, PAC and they resolved in 15 minutes and she calmed down. Today was Day 12 and she had a headache. States her daughter is 41 years old and was fully vaccinated as on 12 April. In June she started having episodes of severe vomiting to where she could not hold potassium. She had crazy numbers of GFR, BUN, and Creatinine and had a port placed yesterday. She was currently in the emergency room via ambulance today and it was a mix between CHF and kidney failure. There were no other changes besides her getting the vaccine. Says she had not felt great since she got the shot, she had not felt good. Her head does not stop hurting, it was so much. Did take Tylenol for her to get rid of the headache, just bought it today. Unable to provide any product details for the Tylenol. States the headaches started yesterday and today they are non stop. Unable to provide the NDC, expiry, or dose for the first vaccine. No other vaccines given the same day and none 4 weeks prior. Not sure, but may had problems with Tetanus shot in past, but unable to provide NDC, Lot, or expiry for Tetanus shot. They asked her if she wanted to go to the emergency room and she said she did not know if she needed to or not. She decided to wait a few minutes and they had 4 people stationed with her and a pulse ox on her watching. It finally was coming down and she said she was okay. She had sat for about an hour and then went home. Asks if she should get the second vaccine or not. She did not imagine that she should. They told her it was an allergic reaction she had, but she does not know about the headaches. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: Test Name: heart beat; Result Unstructured Data: Test Result:fast
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2118657

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: PA
Alter: 67,0
Geschlecht: M
Eingang: 17.02.2022
Impfdatum: 13.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Decreased appetite Lethargy Pollakiuria Pyrexia Tremor

Symptomtext

Lethargic; Low grade fever on at least three occasions; Tremors; Loss of appetite; frequent urination; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 67-year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 13Oct2021 11:00 (Lot number: FE3590) at the age of 67 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Gastritis" (unspecified if ongoing). Concomitant medication(s) included: FLU, administration date 15Sep2021. Past drug history included: Nsaids, reaction(s): "known allergies: NSAIDS". Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EN6204, Location of injection: Arm Left, Vaccine Administration Time: 04:00 PM), administration date: 18Mar2021, when the patient was 67 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6204, Location of injection: Arm Left, Vaccine Administration Time: 03:00 PM), administration date: 25Feb2021, when the patient was 67 years old, for Covid-19 immunization. The following information was reported: LETHARGY (non-serious) with onset 13Oct2021 23:00, outcome "recovering", described as "Lethargic"; PYREXIA (non-serious) with onset 13Oct2021 23:00, outcome "recovering", described as "Low grade fever on at least three occasions"; TREMOR (non-serious) with onset 13Oct2021 23:00, outcome "recovering", described as "Tremors"; DECREASED APPETITE (non-serious) with onset 13Oct2021 23:00, outcome "recovering", described as "Loss of appetite"; POLLAKIURIA (non-serious) with onset 13Oct2021 23:00, outcome "recovering", described as "frequent urination". Therapeutic measures were not taken as a result of lethargy, pyrexia, tremor, decreased appetite, pollakiuria. Additional information: Covid prior vaccination and covid tested post vaccination was reported as NO. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Gastritis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1848799

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: FL
Alter: 50,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 21.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Dysmenorrhoea Gastritis Gastrooesophageal reflux disease Heavy menstrual bleeding Nervous system disorder Dysphagia Pharyngeal swelling Paraesthesia

Symptomtext

Trouble swallowing; right side of throat feels swollen; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 50-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 21Oct2021 10:15 (Lot number: FE3590) at the age of 50 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Rheumatoid arthritis" (unspecified if ongoing). Concomitant medication(s) included: BARICITINIB; DROSPIRENONE AND ETHINYL ESTRADIOL. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0151, Location of injection: Arm Right, Vaccine Administration Time: 10:15 AM), administration date: 08Apr2021, when the patient was 50 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EP6955, Location of injection: Arm Right, Vaccine Administration Time: 10:15 AM), administration date: 18Mar2021, when the patient was 50 years old, for COVID-19 Immunization. The following information was reported: DYSPHAGIA (non-serious) with onset 22Oct2021 03:45, outcome "not recovered", described as "Trouble swallowing"; PHARYNGEAL SWELLING (non-serious) with onset 22Oct2021 03:45, outcome "not recovered", described as "right side of throat feels swollen". Therapeutic measures were not taken as a result of dysphagia, pharyngeal swelling. Additional information The patient did not receive any other vaccine in last four weeks. Other medications in two weeks were Rinvoq and Loryna bcp. 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 did not have any Known allergies 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: Rheumatoid arthritis.
Andere Medikamente: BARICITINIB; DROSPIRENONE AND ETHINYL ESTRADIOL.
Allergien: -
Vorherige Impfungen: -

VAERS 1848799

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: FL
Alter: 50,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 21.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Dysmenorrhoea Gastritis Gastrooesophageal reflux disease Heavy menstrual bleeding Nervous system disorder Dysphagia Pharyngeal swelling Paraesthesia

Symptomtext

Trouble swallowing; right side of throat feels swollen; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 50-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 21Oct2021 10:15 (Lot number: FE3590) at the age of 50 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Rheumatoid arthritis" (unspecified if ongoing). Concomitant medication(s) included: BARICITINIB; DROSPIRENONE AND ETHINYL ESTRADIOL. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0151, Location of injection: Arm Right, Vaccine Administration Time: 10:15 AM), administration date: 08Apr2021, when the patient was 50 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EP6955, Location of injection: Arm Right, Vaccine Administration Time: 10:15 AM), administration date: 18Mar2021, when the patient was 50 years old, for COVID-19 Immunization. The following information was reported: DYSPHAGIA (non-serious) with onset 22Oct2021 03:45, outcome "not recovered", described as "Trouble swallowing"; PHARYNGEAL SWELLING (non-serious) with onset 22Oct2021 03:45, outcome "not recovered", described as "right side of throat feels swollen". Therapeutic measures were not taken as a result of dysphagia, pharyngeal swelling. Additional information The patient did not receive any other vaccine in last four weeks. Other medications in two weeks were Rinvoq and Loryna bcp. 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 did not have any Known allergies 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: Rheumatoid arthritis.
Andere Medikamente: BARICITINIB; DROSPIRENONE AND ETHINYL ESTRADIOL.
Allergien: -
Vorherige Impfungen: -

VAERS 2116383

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: FL
Alter: 93,0
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: 01.02.2021
Beginn: 12.02.2022
Tage bis Beginn: 376,0
Dosis: UNK
Route/Site: - / -

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

Asthenia COVID-19 Chest X-ray abnormal Dyspnoea SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st vaccine received on 01/11/2021. 94 y/o with PMHx of DM type 2, HTN, HLD, CAD s/p CABGx4, GERD, BPH with LUTS presents to ED via EMS for c/o SOB and generalized weakness. EMS found pt with O2 sats in the 80's, placed on 4L NC. CXR with possible atypical viral PNA. Afebrile. Pt started on Steroids and then Remdesivir added.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19- Detected on 02/12/2022
Aktuelle Erkrankungen: -
Vorgeschichte: DM2,HLD, HTN, CAD/CABG, GERD,BPH,OA
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2114231

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: KY
Alter: 64,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 04.11.2021
Beginn: 30.01.2022
Tage bis Beginn: 87,0
Dosis: 3
Route/Site: SYR / RA

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

Electrocardiogram Electrocardiogram ambulatory Heart rate irregular Tachycardia

Symptomtext

Irregular heart rate, tachycardia for about 4 hours (I really don?t think this is related to the vaccine but I guess we don?t know!)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: 1/31/22: EKG 2/15/22: Holter monitor in process
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism, depression, hypertension, hyper -cholesterolemia
Andere Medikamente: Bupropion SR, levothyroxin, atorvastatin, Amlodipine, HCTZ, Claritin, Osteo-Biflex
Allergien: None
Vorherige Impfungen: -

VAERS 2113332

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 54,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 15.02.2022
Beginn: 15.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Hypoaesthesia Paraesthesia Swelling face

Symptomtext

Pt complained of swelling in her jaw after receiving Pfizer booster vaccine. Experienced tingling and numbness in jaw. Vitals were taken BP 149/87, HR 106, temp 98.3, O2 98%. Pt was alert and oriented; Benadryl was given 50mg po 1 dose. Vitals were rechecked at 13:40; BP 150/89, HR 101, temp 98.4, O2 98%. Patient refused ambulance transportation to ER facility, went home with family members.

Weitere VAERSDATA-Felder

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

VAERS 2113086

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: KY
Alter: 60,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 07.10.2021
Beginn: 21.01.2022
Tage bis Beginn: 106,0
Dosis: 3
Route/Site: IM / RA

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

Albumin globulin ratio Anaemia Anion gap Blood creatinine increased Blood glucose normal Blood lactic acid Blood magnesium normal Blood phosphorus Blood potassium decreased Blood urea increased Brain natriuretic peptide increased COVID-19 COVID-19 pneumonia Cardiac flutter Chest X-ray abnormal Chest pain Differential white blood cell count abnormal Dyspnoea

Symptomtext

1/21/22 61 yr/o female who presents with right sided pleuritic chest pain. Symptoms have been present for the past 2 days. The patient has history of asthma, acute on chronic respiratory failure, is on 3 L/min oxygen via nasal cannula at baseline. States she has increased her oxygen use to 4 L/min when active but has maintained her baseline oxygen rate while at rest. Reports productive cough since onset of symptoms.. No fevers or chills. Patient has been compliant with her dialysis schedule. Patient arrives via EMS. Vital stable during transport per EMS. Patient reports sharp pain in her right lower chest which is worse with deep breaths. Reports associated dyspnea. Denies any abdominal pain Review of Systems Constitutional: Negative for chills and fever. Respiratory: Positive for shortness of breath. Negative for cough. Cardiovascular: Positive for chest pain. Negative for leg swelling. Gastrointestinal: Negative for abdominal pain, nausea and vomiting. Skin: Negative for rash. Neurological: Negative for dizziness and headaches. All other systems reviewed and are negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 8,0
Labordaten: 1/21/22 COVID-19 Result Detected Abnormal CBC W/DIFF - Abnormal; Notable for the following components: Result Value White Blood Count 15.25 Red Blood Count 3.04 Hemoglobin 8.6 (*) Hematocrit 28.9 (*) Mean Corpuscular HGB Conc 29.8 (*) Neutrophils % 89.0 (*) Lymphocyte % 1.9 (*) Neutrophil Abs 13.58 (*) Lymphocyte-Absolute 0.29 (*) Immature Granulocyte Abs 0.11 (*) All other components within normal limits COMPREHENSIVE METABOLIC PANEL (CMP) - Abnormal; Notable for the following components: Potassium 3.4 (*) Anion Gap 16 (*) Glucose 182 (*) Blood Urea Nitrogen (BUN) 22 (*) Creatinine-Blood 3.81 (*) Estimated GFR 12 (*) Estimated GFR if race 15 (*) Albumin/Globulin Ratio 0.9 (*) All other components within normal limits PROCALCITONIN - Abnormal; Notable for the following components: Procalcitonin 7.14 (*) All other components within normal limits B-TYPE NATRIURETIC PEPTIDE - Abnormal; Notable for the following components: B-Type Natriuretic Peptide 343.6 (*) All other components within normal limits COVID-19, NOVEL CORONAVIRUS + FLU A/B PCR TROPONIN MAGNESIUM PHOSPHORUS LACTIC ACID 1/21/22 XR Chest 2Vw: IMPRESSION: 1.Acute right midlung and left infrahilar pulmonary infiltrates concerning for pneumonia superimposed on chronic interstitial lung disease with associated moderately severe cylindrical and cystic bronchiectasis 61 yr/o with PMH PAF, ESRD, DM, chronic respiratory failure, CHF, COPD, anemia who presented with dyspnea and was found to have PNA due to COVIVD19. She was treated for following: COVID-19 pneumonia: Scheduled + as needed albuterol. Vitamin C. Symbicort. Delsym. Mucinex. Remdesivir x5d. ZnSO4. Incentive spirometry. Flutter. Supplemental oxygen as needed. Daily inflammatory markers.flutter, IS, mucinex, delsym, ZnSO4, vit C - on 3L NC (her home O2) Acute on chronic anemia: Hemoglobin 6.8 1/28 and got PRBC. Gradual decrease noted over the last few days, suspect iatrogenic etiology. Stable after transfusion N/V: continue zofran, compazine, scopolamine patch ESRD: nephrology following. Outpatient arrangements are made. COPD: continue inhaled medications Hypoglycemia: Resolved -Remains off lantus, actos, tradjenta, starlix. Continue SSI (if needed at discharge Hypotension: midodrine Discharge Diagnoses:Principal Problem: Multifocal pneumonia (6/11/2019) Active Problems: Diabetes mellitus (3/31/2015) End-stage renal disease on hemodialysis (9/23/2018) Chronic anticoagulation (8/17/2020) Chronic respiratory failure with hypoxia (12/2/2020) Chronic diastolic (congestive) heart failure (12/24/2020) COPD (chronic obstructive pulmonary disease) (12/24/2020) PAF (paroxysmal atrial fibrillation) (1/11/2021) Intractable vomiting with nausea (5/26/2021) Hypotension (6/18/2021) Pneumonia due to COVID-19 virus (1/24/2022)
Aktuelle Erkrankungen: -
Vorgeschichte: Acute and chronic respiratory failure with hypoxia 08/2020 requiring intubation and mechanical ventilatio Acute and chronic respiratory failure with hypoxia 08/2020 requiring intubation and mechanical ventilation o Anxiety o Asthma o Atrial fibrillation o Atrial flutter o Bacteremia due to Staphylococcus 8/18/2015 o Breast cancer, left Dx 12/2014 had lumpectomy and chemo and radiation o CAP (community acquired pneumonia) 1/1/2017 o Cardiomegaly o CHF (congestive heart failure) o COPD (chronic obstructive pulmonary disease) chronic resp failure with hypoxia o DDD (degenerative disc disease), lumbar o Depression o Diabetes mellitus, type II o Dialysis (juvenile) of retina (with detachment) o ESRD on hemodialysis o Fe deficiency anemia o Fibromyalgia o GERD (gastroesophageal reflux disease) o Healthcare associated bacterial pneumonia 11/4/2017 o Hypercholesterolemia o Hyperlipidemia o Hypertension o Intracranial hypertension o Necrotizing fasciitis 08/2020 of left groin o Neuropathy o NSVT (nonsustained ventricular tachycardia) o Obesity o On home oxygen therapy 02/02/2018 o Pancytopenia due to chemotherapy 7/15/15 o Pneumonia of both lower lobes due to infectious organism 6/11/2019 o Pulmonary HTN 02 dependent o Restless leg syndrome o Sarcoidosis of lung o Sleep apnea wears bipap o Syncope and collapse o V-tach o Vision abnormalities
Andere Medikamente: albuterol-ipratropium (DUO-NEB) 0.5-2.5 mg/3 mL nebulizer Take 1 ampule by nebulization every 4 (four) hours as needed for Wheezing for up to 30 days. o amikacin sulfate (AMIKIN) 500 MG/2ML SOLN injection Take 1 mL by nebulization Twice a
Allergien: Adhesive
Vorherige Impfungen: -

VAERS 2101606

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: FL
Alter: 76,0
Geschlecht: M
Eingang: 10.02.2022
Impfdatum: 16.04.2021
Beginn: 04.02.2022
Tage bis Beginn: 294,0
Dosis: UNK
Route/Site: - / -

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

Aortic valve replacement COVID-19 Chest pain Computerised tomogram thorax abnormal Dyspnoea Lung consolidation Pneumonia Productive cough Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st vaccine received on 03/26/2021. 77 y/o with PMHx of CVA, COPD, HLD, HTN, Pacemaker, CAD/CABG, Valvular heart dz/TAVR, back surgery presents to ED with c/o CP, productive cough, SOB and fevers x1 week. Room air sat 92%, placed on 2L NC, febrile and Ct with dense consolidation PNA. Pt started on IV Abx, Steroids and Remdesivir.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19- Detected on 02/04/2022
Aktuelle Erkrankungen: -
Vorgeschichte: CVA, COPD, Valvular heart dz/TAVR, CAD/CABG, HLD, HTN, Pacemaker
Andere Medikamente: -
Allergien: Aminosyn 11 Sulfite-free, Sulfites
Vorherige Impfungen: -

VAERS 2095758

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 80,0
Geschlecht: M
Eingang: 08.02.2022
Impfdatum: 07.10.2021
Beginn: 06.02.2022
Tage bis Beginn: 122,0
Dosis: 3
Route/Site: - / -

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

COVID-19 pneumonia

Symptomtext

Admitted to hospital, Covid-19 PNA

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2092565

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: VA
Alter: 29,0
Geschlecht: F
Eingang: 07.02.2022
Impfdatum: 03.11.2021
Beginn: 28.12.2021
Tage bis Beginn: 55,0
Dosis: 3
Route/Site: SYR / LA

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

Back pain Drug hypersensitivity Gait disturbance Hypoaesthesia oral Mobility decreased Pain Sciatica Sleep disorder

Symptomtext

Became allergic to Advil and Aleve (numbness in entire mouth, couldn't tell if throat was closing). Previously, I would take Advil once a month over the course of a week. Developed sciatica. Woke up with intense pain 12/28/2021 in lower back. Couldn't bend over, sitting was very uncomfortable. Continued until 1/15/2022, at which point the pain became severe with no relief. Loss of mobility due to pain. Pain started to become less severe on 1/19/2022. Still have pain and mobility issues related to the pain to this day (can't walk for very long or sit/lie down in one position, bend, move certain ways), but it seems to be getting better. I was prescribed muscle relaxers for treatment but only took it once. Have been stretching and walking to treat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Was seen by a doctor on 1/19/2022. She did review my symptoms and analyze mobility and pain. No lab tests were performed.
Aktuelle Erkrankungen: Hemorrhoids month before booster. Started for the first time after second vaccination. Fine now.
Vorgeschichte: N/A
Andere Medikamente: B12
Allergien: Mango. Also developed a reaction to Advil and Aleve around November 2021.
Vorherige Impfungen: -

VAERS 2206297

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 81,0
Geschlecht: M
Eingang: 04.02.2022
Impfdatum: 01.10.2021
Beginn: 23.12.2021
Tage bis Beginn: 83,0
Dosis: 3
Route/Site: IM / RA

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

Blood bicarbonate increased Blood pH normal Brain natriuretic peptide normal COVID-19 Cough Dyspnoea Fatigue Headache Inappropriate schedule of product administration Myalgia Oropharyngeal pain PCO2 increased PO2 decreased Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection following COVID vaccine series 02/24, Pfizer, dose #1 003/19, Pfizer, dose #2 10/01,Pfizer, dose #3 12/24 SARS-COV-2 Variant Sequencing: pending 12/24 COVID swab, result: detected 12/23 pt cc: cough, fatigue, headache, myalgias, rhinorrhea, sore throat exposure: unknown 12/28 abg: i-pH: 7.44 i-PC02: 46.5, i-P02: 70, i-HC03: 31.7 12/28 BNP: 45 12/28 pt admit ED, cc: shortness of breath and worsening cough, dx: COVID Viral Syndrome LOS: 1 dav 01/03/22 clinically resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/24 SARS-COV-2 Variant Sequencing: pending 12/24 COVID swab, result: detected 12/28 abg: i-pH: 7.44 i-PC02: 46.5, i-P02: 70, i-HC03: 31.7 12/28 BNP: 45
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2087730

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MI
Alter: 39,0
Geschlecht: M
Eingang: 04.02.2022
Impfdatum: 13.10.2021
Beginn: 02.01.2022
Tage bis Beginn: 81,0
Dosis: 3
Route/Site: IM / LA

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

Chills Cough Dyspnoea Fatigue Influenza A virus test negative Influenza B virus test Oropharyngeal pain Pain Respiratory syncytial virus test negative Rhinorrhoea SARS-CoV-2 test negative

Symptomtext

On January 2nd 2022, developed a sore throat which developed to severe body ache, headache and further into chills and severe chills on January 3rd. Chills subsided on January 4th, cough began developing, mucus discharge from nose, general fatigue and exhaustion set in. The January 4th symptoms progressed until January 9th, when mucus discharge abated. Cough intensity had reduced by this time, but persisted. Attempts to resume normal activities increased cough intensity and caused difficulty breathing. Cough continued to gradually abate until Week of January 23rd.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Saw NP on January 5th. She reviewed my symptoms and ordered COVID testing which was available no earlier than January 8th. Test was take on January 8th. Results received on January 9th. Results are pasted below. Influenza A Not detected by Alinity Influenza B Not detected by Alinity Respiratory Syncytial Virus by PCR Not detected by Alinity SARS-CoV-2 (COVID-19) by PCR Not detected by Alinity Device: Abbott Alinity SARS-CoV-2 assay
Aktuelle Erkrankungen: No diagnosed illnesses
Vorgeschichte: Treated for blood clots in May 2020, discontinued treatment in September 2021
Andere Medikamente: Trintellix - 5mg daily Vitamin D3 - 5000 IU daily L-Methylfolate - 15mg daily
Allergien: -
Vorherige Impfungen: -

VAERS 2086169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: KY
Alter: 13,0
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: 04.12.2021
Beginn: 08.01.2022
Tage bis Beginn: 35,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal pain Abdominal pain upper Abdominal tenderness Acidosis Acidosis hyperchloraemic Activated partial thromboplastin time shortened Alanine aminotransferase increased Amylase normal Anticoagulant therapy Anticoagulation drug level Antithrombin III Aspartate aminotransferase increased Bacterial test positive Blood albumin decreased Blood alkaline phosphatase normal Blood bicarbonate decreased Blood bilirubin normal Blood calcium normal

Symptomtext

ICC visit 1/8/22 patient has been sick since yesterday, with vomiting,diarrhoea , chills ( no fever ) headache, sore throat.ea ache bodyaches, clear runny nose, dry cough, SOB, has asthma Mom states she is exposed to COVID-19 and patient wants to get tested for COVID -19 1/14/22 ED note:Presented due to tender nodules on bilateral arms. Patient developed COVID symptoms 1/7 and tested positive the next day. She received sotrovimav 1/9 with improvement in symptoms two days later; however, two days ago, she developed a sharp pain in the right AC and realized there was a nodule there. She also developed nausea, vomiting, decreased PO intake, abdominal pain, and orange urine. She has been treating with zofran, tylenol, and motrin at home. She then developed a second nodule on her L forearm yesterday and a third nodule on her L AC this AM. ID and pharmacy were contacted yesterday but have not heard of nodules occurring with sotrovimav infusions. Of note, IV for infusion was in the right hand. No hx of blood clots but patient on birth control. On exam, nodules are tender to palpation (clinical photography in chart). She complains of right sided abdominal pain but abdomen soft. No lymphadenopathy. No fever since initial COVID symptoms began prior to infusion. Acetaminophen (TYLENOL PO) Take by mouth. albuterol HFA 108 (90 Base) MCG/ACT inhaler Inhale 4 puffs into the lungs every 4 (four) hours as needed for Wheezing or Shortness of Air cetirizine (ZYRTEC) 10 MG tablet Take 40 mg by mouth 20 mg AM 20 MG PM. Cholecalciferol 250 MCG (10000 UT) CAPS Take 250 mcg by mouth daily. clindamycin (CLINDAGEL) 1 % gel APPLY TO AFFECTED AREA TWICE DAILY cyclobenzaprine (FLEXERIL) 5 MG tablet Take 1 tablet by mouth 2 (two) times daily as needed for Muscle spasms. EPINEPHrine (EPIPEN) 0.3 MG/0.3ML SOL A-IJ use as directed by prescriber for ALLERGIC REACTION famotidine (PEPCID) 20 MG tablet Take 20 mg by mouth 2 (two) times daily. ferrous gluconate (FERGON) 324 MG tablet Take 1 tablet by mouth 2 (two) times daily. levonorgestrel-ethinyl estradiol (SEASONALE) 0.15-0.03 MG Take 1 tablet by mouth daily Take in a continuous manner, skipping placebo week and moving directly to next new pack meloxicam (MOBIC) 7.5 MG tablet Take 1 tablet by mouth daily. midodrine (PROAMATINE) 5 MG tablet Take 1 tablet by mouth Twice a Day for 7 days, THEN 2 tablets Twice a Day. Afternoon dose no later than 4 :00 pm. (Patient taking differently: THEN 2 tablets Twice a Day. Afternoon dose no later than 4 :00 pm.) montelukast (SINGULAIR) 5 MG chewable tablet Chew 5 mg by mouth nightly . polyethylene glycol (GLYCOLAX) powder Take 17 g by mouth as needed for Constipation : Mix in 4 oz of water/juice/milk. rizatriptan (MAXALT) 10 MG tablet Take 1 tablet by mouth as needed for Migraine, may repeat once in 2 hrs - max 30 mg/24 hrs. Spacer/Aero-Holding Chambers DEVICE Use 1 each as needed (For use with albuterol inhaler) tiotropium (SPIRIVA RESPIMAT) 1.25 MCG/ACT AERS inhalation Inhale 1 puff into the lungs nightly . topiramate (TOPAMAX) 25 MG tablet Take 1 tablet by mouth 2 (two) times daily for 7 days, THEN 2 tablets 2 (two) times daily. traZODone (DESYREL) 50 MG tablet Take 1 tablet by mouth nightly triamcinolone (KENALOG) 0.1 % ointment Apply topically 2 (two) times daily to affected area(s) of bilateral axilla twice a day for up to 2 weeks as needed. triamcinolone (NASACORT ALLERGY 24HR) 55 MCG/ACT nasal inhaler Instill 2 sprays into nose 2 (two) times daily 2 spray every day and she can use 4 spray PRN. WIXELA INHUB 250-50 MCG/DOSE AEPB inhaler INL 1 PUFF PO Q 12 HOURS. RM AFTER U 1/17/22-dischaHospital Course (by problem): Thrombophlebitis On admission, she had a exquisitely tender nodules without overlying erythema or rash in the superior aspect of the right antecubital fossa, left antecubital fossa, and anterior aspect of left forearm. The left forearm nodule had a hyperpigmented streak starting at the nodule and extending toward the hand. Her differential included nodular lymphangitis felt less likely due to lack of exposures and BL findings, new viral infection such as EBV, CMV, complications of the COVID itself or a reaction to her Sotrovimab. A Hepatitis panel was negative and EBV and CMV titers were sent and serial CMPs were ordered. She was initially just admitted on motrin prn with her home medications, PO ad lib and MIVFs. Infectious Disease and Heme Onc were consulted. By the next morning, her physical exam was notable for an "L" shaped hyperpigmented, painful lesion on the left forearm and this and her other lesions seemed more hard and cord like more so than mobile nodules or lymph nodes. Given this and the fact that she had multiple risk factors for increase risk of clotting (lupus anticoagulant, obesity, birth control, acute COVID-19 infection, and venous stasis), physical exam findings were felt to be most consistent with superficial thrombophlebitis. Pediatric ID and Heme/Onc agreed. A hypercoagulable work-up was initiated and she was started on Lovenox 40mg BID (prophylactic dose) for at least 2 weeks, stopping her estrogen-containing birth control during this time. She did develop some posterior calf and BL foot pain with a cord over her R foot and BL foot hyperpigmented streaking but these rapidly resolved and her UE lesions greatly improved. She'd also remained afebrile in house and repeat BL LE doppler was also again negative. By the day of discharge she had only some improving L forearm pain with improved TTP and discoloration and only mild BL AC TTP with minimal remaining masses with superficial changes. Heme Onc thus did not feel she needed increased to therapeutic dosing or Anti-Xa levels. Her mother, pharmacy, ID and Heme Onc were all okay with discharge to home. Her mother, already familiar with giving her sister injections for eczema, was easily able to take over her Lovenox injection in house and voiced comfort with doing so at home. She was then sent home in good condition. Her d-dimer was only mildly elevated at 612 and her homocyteine and ATIII had resulted as nml with Prothrombin, Factor V Leiden, Lipoprotein A, Pro C and Pro S as well as her EBV and CMV titers all still pending at the time of discharge. She will be followed up in 2 weeks at Hematology and ID. The length of her Lovenox and hold on OCPs will be readdressed at that time. Transaminitis with hyperbili and mild hypoalbuminemia on RUQ Pain, N/V, poor PO On admission, Hepatitis panel was normal and EBV/CMV testing were still in process at the time of discharge. Transaminitis was felt to be secondary to viral infection versus regular tylenol use during her COVID-19 infection versus COVID-19 itself. Throughout admission, CMP were trended. Her bili normlized, her alb dipped to 3.3 but was back up to 3.7 and AST and ALT downtrended to 82 and 526 respectively. Her RUQ tenderness improved some and then stabilized, her N/V resolved and her oral intake improved. She will continue to avoid tylenol (and motrin given her Lovenox) and needs another repeat CMP on 1/19/22 to continue to follow. Mild Hyperchloremic Acidosis on Dehydration Her Cl- bumped to 115 likely from her IVFs with a likely related mild acidosis to 19. Ketosis and her dehydration may have played roles as well. Her UOP normalized and her PO intake improved as above. She was off IVFs by HD#2. Her Cl and HCO3 improved to stable at 110 and 18 on last checks. Abnormal urine Her nurse noted some possible urine sediment on the night prior to d/c. Her UA was abnormal with moderate LE, 4 WBCs and trace bacteria but as she was not having any symptoms of a UTI this was not cultured. Repeat UA by her PMD is recommended. Of note her urobili was negative and her orange urine color change had resolved however as expect as her her hyperbili resolved and with hydration. Significant Hospital Labs: 1/14/2022 09:31 1/15/2022 04:49 1/15/2022 16:19 1/16/2022 05:37 1/17/2022 04:44 C-Reactive Protein <0.1 <0.1 Sodium 142 143 143 140 142 Potassium 3.6 3.7 4.2 4.1 4.0 Chloride 109 (H) 113 (H) 115 (H) 112 (H) 110 (H) CO2 22 22 19 (L) 22 18 (L) Glucose 111 (H) 88 101 (H) 103 (H) 107 (H) BUN 7 6 (L) 7 11 10 Creatinine 0.59 0.57 0.60 0.57 0.58 Total Protein 7.0 6.1 (L) 6.1 (L) 6.7 (L) Albumin 3.9 (L) 3.3 (L) 3.5 (L) 3.3 (L) 3.7 (L) Globulin 3.1 2.8 2.8 3.0 Calcium 9.8 8.8 8.8 9.0 9.5 Bilirubin-Total 0.9 (H) 0.8 (H) 0.4 0.4 ALT/SGPT 1,020 (H) 967 (H) 723 (H) 526 (H) AST/SGOT 442 (H) 431 (H) 173 (H) 82 (H) Alkaline Phosphatase 89 76 73 77 Phosphorus 3.5 Homocysteine 7.0 Amylase 24 (L) Lipase 15 1/14/2022 11:00 1/15/2022 17:34 1/16/2022 11:16 PT 11.9 INR 1.0 PTT 31.7 D-Dimer Quantitative 612 (H) AntiThromb III Func 114 Heparin LMW 0.29 1/15/2022 04:49 Hepatitis A IgM Ab Nonreactive Hepatitis B Surface Ag Nonreactive Hepatitis B Core Ab(IgM) Nonreactive Hepatitis C Ab Nonreactive 1/14/2022 09:31 WBC 5.00 RBC 4.88 HGB 13.1 HCT 39.4 MCV 80.7 MCH 26.8 MCHC 33.2 Platelet Count 403 Significant Hospital Imaging/Diagnostic Tests: Duplex US Venous Bilateral LE (1/14) Impression: No evidence of deep veinous thrombosis involving either lower extremity. Duplex US Venous Bilateral UE (1/14) IMPRESSION: No evidence of upper extremity deep venous thrombosis. Duplex US Venous Bilateral LE (1/16) IMPRESSION: No obvious evidence of thrombosis noted in the imaged part of bilateral lower extremities veins as described above. Abdominal US (1/14) FINDINGS: The liver demonstrates normal echotexture without focal defect or mass evident. Common duct is normal measuring 2 mm. Gallbladder is within normal limits for appearance. Visualized pancreas is unremarkable. Tail of pancreas is obscured by bowel gas. Kidneys are normal size measuring 9.6 cm on the right and 10.6 cm in length on the left. No renal mass lesion is visible. No hydronephrosis seen. Spleen demonstrate normal echotexture measuring 9.6 cm . Doppler evaluation demonstrates that the hepatic veins are patent. The portal vein is also patent and demonstrates normal direction of flow. Normal resistive index and waveform of the hepatic artery. IVC and aorta are grossly patent. Bladder demonstrates normal contour. IMPRESSION: No significant abnormality is identified.

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Praegender Schweregrund: Dehydration
Hospital-Tage: 3,0
Labordaten: 1/8/22 COVID Result IPOC PCR Not Detected Detected Abnormal
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, Fibromyalgia, complex regional pain syndrome, potts disease
Andere Medikamente: Acetaminophen (TYLENOL PO) Take by mouth. o albuterol HFA
Allergien: Seasonal, Lyrica
Vorherige Impfungen: -

VAERS 2085467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: KY
Alter: 89,0
Geschlecht: M
Eingang: 03.02.2022
Impfdatum: 09.02.2021
Beginn: 31.01.2022
Tage bis Beginn: 356,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 COVID-19 pneumonia Mental status changes SARS-CoV-2 test positive

Symptomtext

Pt admitted for COVID pna, altered mental status and requiring o2. pt tx w/ dexamethasone and remdesivir

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: 1/31 COVID positive
Aktuelle Erkrankungen: has a past medical history of Anemia, Chronic kidney disease (CKD), COPD (chronic obstructive pulmonary disease) (HCC), Diabetes mellitus (HCC), Hyperlipidemia, and Hypertension.
Vorgeschichte: has a past medical history of Anemia, Chronic kidney disease (CKD), COPD (chronic obstructive pulmonary disease) (HCC), Diabetes mellitus (HCC), Hyperlipidemia, and Hypertension.
Andere Medikamente: amLODIPine, aspirin, budesonide, furosemide, glipizide, insulin lispro protamine-insulin lispro, ipratropium-albuterol, meclizine, metoprolol tartrate, and pravastatin
Allergien: -
Vorherige Impfungen: -

VAERS 2080346

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: IL
Alter: 90,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 15.01.2021
Beginn: 27.01.2022
Tage bis Beginn: 377,0
Dosis: 3
Route/Site: IM / RA

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

Acute kidney injury Blood creatinine increased Brain natriuretic peptide increased COVID-19 Cardiomegaly Chest X-ray abnormal Chronic kidney disease Condition aggravated Dyspnoea Dyspnoea exertional Echocardiogram abnormal Ejection fraction decreased Interchange of vaccine products Oedema peripheral Pleural effusion SARS-CoV-2 test positive Weight increased

Symptomtext

Patient received Moderna vaccine 1/15/21, 2/12/21, and Pfizer on 11/3/21. Presented to ER on 1/27/22 and found to be COVID positive. was admitted on 1/27/2022 presented with shortness of breath, weight gain dyspnea on exertion, leg edema. Known combined CHF, was on outpatient diuresis.Chest x-ray left pleural effusion marked cardiomegaly. BNP 815. Echo EF 30-40%. Cardiology consulted. AKI on CKD, Creatinine 1.8, baseline 1.5-1.6. Found to have COVID-19 positive, clinically asymptomatic. Vital stable on room air. No new concerns. Patient is medically stable to be discharged Home on 2/1/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 5,0
Labordaten: 1/27/22 COVID19: positive 1/27/22 chest xray: Small left pleural effusion, new from the prior study.
Aktuelle Erkrankungen: -
Vorgeschichte: Adverse effect of amiodarone (induced pulmonary toxicity) 11/30/2015 ? Anemia 1/25/2017 ? Asymptomatic COVID-19 virus infection 01/2022 1/27/2022 ? Atrial fibrillation s/p WACA 11/30/2015 ? CAD (coronary artery disease) ? Chronic combined systolic and diastolic CHF (congestive heart failure) 11/30/2015 ? Chronic kidney disease, stage 3 (moderate) 11/30/2015 ? Colon cancer ? Dilated cardiomyopathy (Moderate LV dysfunction) 8/6/2018 ? Encounter for therapeutic drug level monitoring 11/30/2015 ? Hypercholesterolemia 11/30/2015 ? Hypertensive heart and kidney disease with chronic combined systolic and diastolic congestive heart failure and stage 4 chronic kidney disease 11/30/2015 ? Hypoalbuminemia 1/27/2022 ? Nonrheumatic aortic valve stenosis (Moderate- Severe AS with Mild AR) Low ouput-Low Gradient AS 6/14/2018 ? OSA on CPAP ? Pulmonary edema, acute, hx 09/2011, 03/2012 ? s/p permanent pacemaker 11/30/2015
Andere Medikamente: metoprolol Succinate 25 MG Tab-sr-24hr Commonly known as: TOPROL-XL 75 mg, Oral, 2 TIMES DAILY allopurinol 100 MG Tabs Commonly known as: ZYLOPRIM 100 mg, Oral, DAILY citalopram 10 MG Tabs Commonly known as: CeleXA 10 mg, Oral, EVERY MOR
Allergien: Amiodarone, donnatal, cephalexin, librium, novocain, horse serum, penicillins, sulfacetamide,
Vorherige Impfungen: -

VAERS 2079262

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MN
Alter: 62,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 28.10.2021
Beginn: 31.01.2022
Tage bis Beginn: 95,0
Dosis: 3
Route/Site: SYR / LA

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

Asthenia COVID-19 Pneumonia SARS-CoV-2 test positive

Symptomtext

Received Pfizer vaccines on 4/1, 4/22, 10/28/21 COVID-19 positive by PCR on 1/31/22 admitted to hospital on 1/31/22 d/t COVID infection, weakness, suspect pneumonia underlying MS

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

VAERS 2074832

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NJ
Alter: 66,0
Geschlecht: F
Eingang: 30.01.2022
Impfdatum: 01.10.2021
Beginn: 01.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Migraine

Symptomtext

I began having very intense migraines from that day of the Booster shot, lasting for 52 continuous days. Some days were worse than others. This is unprecedented in my life. The only reason it ended was because I began treatment with Aimovig, an injection which prevents migraines. I had tried Aimovig once before but stopped because of dangerous side effects. Now I am living with those side effects. I stopped the Aimovig 2 months later, and the daily migraines returned. The side effect I am experiencing from the drug is narcolepsy type 2.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: I am awaiting to have tests done. The doctor wanted to check up on me in February.
Aktuelle Erkrankungen: None.
Vorgeschichte: Chronic Migraine
Andere Medikamente: Magnesium Citrate, Calcium Citrate, Vitamin C, B-complex, Chromate.
Allergien: Allergies to Caffeine products, Wheat, Deadly Nightshade Family (Tomatoes, Eggplant, Peppers) Sensitivities to foods containing Tyramine, such as aged cheese and alcohol.
Vorherige Impfungen: -

VAERS 2074494

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NY
Alter: 45,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 21.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SC / LA

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

Migraine

Symptomtext

8-day migraine resolved within 24 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Rhinovirus 2 weeks prior
Vorgeschichte: migraines
Andere Medikamente: duloxetine, nurtec, imitrex, magnesium
Allergien: NKA
Vorherige Impfungen: -

VAERS 2068841

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 84,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 18.02.2021
Beginn: 26.01.2022
Tage bis Beginn: 342,0
Dosis: 1
Route/Site: - / -

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

Asthenia Dyspnoea Fatigue

Symptomtext

hospitalized for weakness/fatigue/shortness of breath

Weitere VAERSDATA-Felder

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

VAERS 2059272

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NY
Alter: 56,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 23.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: SYR / RA

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

Chills Condition aggravated Fatigue Herpes zoster Pain Psoriasis Rash Rash erythematous Rash pruritic Skin exfoliation Urticaria

Symptomtext

A few hours after the booster I started feeling very tired, achy, and had some chills. About a week later, I started to develop a rash around my eyes and my psoriasis flared. The rash was red, itchy had hived and caused my eyelids to peel. This lasted for a few months and I had to seek medical treatment from MD (Dermatologist) and various ophthalmologists for my eyes.. On January 1, 2022, I developed shingles and my psoriasis flared again.. My immune system has not been the same since the booster. I am currently receiving treatment for the shingles from Dr.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Psoriasis
Andere Medikamente: None
Allergien: Sulfa and ragweed
Vorherige Impfungen: -

VAERS 2055455

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NM
Alter: 64,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 25.03.2021
Beginn: 08.04.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: SYR / LA

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

Contusion Lethargy Musculoskeletal chest pain Petechiae Purpura Rash erythematous Rash macular

Symptomtext

04/08/21- Sporadically distributed petechial and purpuric rash with recent areas of large macular erythemic confluence on both legs.2nd dose-Pfizer on O4/15/21; Pronounced purpura on 4-23-21 on both lower legs. 3rd dose-Pfizer 1O/14/21, marked increase of rash about 11/03/21. Rash with purpuric confluent patches on both inner thighs with petechiae on both legs, thigh to ankles. On 12/6/21. through 12/31/21; most recent development, left leg extensive macular rash (bright red) on left inner thigh 3'x 8" varigated, also left popliteal area with macular rash. Additional: 1) 2 month period of intermittant pain under left rib area, lasting 30 minutes to 1 hour. 2) Bruise easily 3)lethargy 01/6/22- large confluent patch

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Praegender Schweregrund: Musculoskeletal chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NON
Allergien: NONE
Vorherige Impfungen: -

VAERS 2053852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: IN
Alter: 32,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 19.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / LA

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

Arthralgia Neck pain Pain in extremity Paraesthesia

Symptomtext

Arm is graduating getting worse with pains and is tingling. Moving to shoulder and neck.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/a
Vorgeschichte: Heart murmur
Andere Medikamente: Probiotics, Xanax. Adderall
Allergien: N/a
Vorherige Impfungen: -

VAERS 2052238

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

moderat

Staat: IA
Alter: 37,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 06.04.2021
Beginn: 07.04.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Injected limb mobility decreased Injection site joint pain Insomnia Mononucleosis heterophile test negative Oropharyngeal pain Pharyngeal ulceration SARS-CoV-2 test negative Streptococcus test negative

Symptomtext

Day after vaccine 2: Sore throat strep like symptoms and throat ulcer (size: tip of a pencil eraser), sought treatment at urgent care Clinic, strep test negative, negative for covid, negative for walking pneumonia, negative for mono, got antibiotic Rx. Began to feel better with antibiotics within a day, fully resolved within 4-5 days. After vaccine 3: Nurse at the Pharmacy injected my 3rd dose directly into my right shoulder joint. I could not use my arm for 3 days due to joint pain, couldn't sleep, gradually got range of motion back starting on day 4 but still in pain for about 1 week as a result of poorly placed injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: On 4/7/21 (day after vaccine 2): Sore throat strep like symptoms and throat ulcer (size: tip of a pencil eraser) began 4/10/21: Sought treatment at urgent care Clinic, strep test negative, negative for covid, negative for walking pneumonia, negative for mono, got antibiotic Rx. Began to feel better with antibiotics within a day, fully resolved within 4-5 days. On 10/8/21 (onset with administration of vaccine 3): Nurse at the Pharmacy injected my 3rd dose directly into my right shoulder joint. I could not use my arm for 3 days due to joint pain, couldn't sleep, gradually got range of motion back starting on day 4 but still in pain for about 1 week as a result of poorly placed injection. Was planning to see physician if symptoms didn't improve within 3 days.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Overweight/obese, pain with menses each month
Andere Medikamente: Norethindrone tablets USP, 0.35 mg, 28 day, at bedtime (currently off of this one) Montelukast sodium 10 mg - 1 tablet at bedtime Olopatadine HCI nasal spray 665 mcg/spray, 2 sprays/nostril 2x/day Calcium citrate + D3 maximum (vitamin as ch
Allergien: No known allergies to medications. Other: Wheat/gluten (celiac), cat dander, seasonal (pollen, grasses, trees), dust mites, molds in the environment
Vorherige Impfungen: -

VAERS 2046229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: GA
Alter: 45,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 02.11.2021
Beginn: 29.12.2021
Tage bis Beginn: 57,0
Dosis: 1
Route/Site: IM / LA

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

Blood pressure increased Blood test COVID-19 Chest X-ray normal Chest pain Ear pain Heart rate increased Peripheral swelling SARS-CoV-2 test positive Vaccination complication

Symptomtext

I was sent to the ER on 10/22/21 for chest pains. My blood pressure and heart rate were elevated- and still remain elevated for my body. I'm on aspirin therapy and I was checked for heart attack and pericarditis. Both were negative. I had lower leg swelling. I continue to have Covid eye and sharp pains in my ears.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Chest xray, blood tests on 10/22/21. I was fully vaccinated and received a positive covid test on 12/29/21. I retested with my husband on 12/30/21 at the Medical center Pavilion. We were both positive.
Aktuelle Erkrankungen: Chronic fatigue syndrome, anxiety
Vorgeschichte: Chronic fatigue syndrome, anxiety disorder
Andere Medikamente: Adderall, xanax, methyl folate, bioton, DIM, effexor
Allergien: Sulfa, monistat, Reglan, trazadone
Vorherige Impfungen: -

VAERS 2039364

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 19.10.2021
Beginn: 16.01.2022
Tage bis Beginn: 89,0
Dosis: 3
Route/Site: - / -

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

Anxiety COVID-19 Cough Dyspnoea Nervousness SARS-CoV-2 test positive

Symptomtext

Cough, SOB, nervous/anvious

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: COVID-19 PCR test positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2037783

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: UT
Alter: 37,0
Geschlecht: M
Eingang: 15.01.2022
Impfdatum: 01.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 20,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia Chest discomfort Exercise tolerance decreased Fatigue Headache New daily persistent headache Painful respiration Paraesthesia Pulmonary pain

Symptomtext

Severe headaches and fatigue for 36 hours. It?s been 3 months since and I get headaches almost daily. Onset is usually when I?m working out but not always. My normal was 7:15 minute miles for a sustained 4 miles. I am having a hard time getting to that without suffering debilitating pain in my lungs. I have experienced a multitude of what I can only describe as pin needles in my lungs where it hurts to breath.

Weitere VAERSDATA-Felder

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

VAERS 2035872

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MN
Alter: 79,0
Geschlecht: M
Eingang: 14.01.2022
Impfdatum: 17.10.2021
Beginn: 05.01.2022
Tage bis Beginn: 80,0
Dosis: 3
Route/Site: IM / RA

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

Accelerated idioventricular rhythm Asthenia Blood glucose increased COVID-19 Cardiac telemetry abnormal Condition aggravated Cough Dyspnoea Echocardiogram abnormal Ejection fraction normal Electrocardiogram abnormal Fatigue Headache Heart rate decreased Hypoxia Left ventricular dysfunction Malaise Mitral valve incompetence

Symptomtext

Patient is a 79 y.o. male with a history of mixed hyperlipidemia, diabetes, hypertension, and myocardial infarction who presents to the emergency department for evaluation of COVID-19 exacerbation. The patient presents to triage for shortness of breath, and his oxygen saturation was 77%, so he was brought back to stabilization room 2. The patient tested positive for COVID-19 on Saturday (1/1). The patient states that he started to feel sick with symptoms of fatigue, cough, and weakness 3 to 4 days prior to testing positive. The patient is currently nauseous. The patient is not on oxygen at baseline. The patient does not have a history of asthma, COPD, or emphysema. The patient does not use an inhaler. The patient states that he had a heart attack in June 2021, which he was treated for at hospital. The patient is fully COVID-19 vaccinated including his booster, which he received on 10/17/21. The patient denies fevers, lightheadedness, dizziness, headache, or chest pain. Patient is a very pleasant 79 y.o. male with a history of CAD s/p PCI 6/2021 (follows at Mercy), diabetes, HTN, hyperlipidemia (declines statins), PVCs who was admitted 1/5/2022 for dyspnea, fatigue, headache, positive COVID test 1/1/2022, found to be hypoxic to 71% at admit. Cardiology called due to PVCs and short runs of NSVT (4-8 beats) and accelerated idioventricular rhythm on telemetry, no chest pain, palpitations, on-going dyspnea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 10,0
Labordaten: Telemetry reporting accelerated idioventricular run at 1449 hrs - had incr metoprolol XL to 25mg this am since -Troponin remains low/WNL -Echo reviewed-normal EF, mild Mitral prolapse/MR. No WMA -EKG without acute ischemia -During visit noted to have runs of non conducted bigeminal PVCs resulting in pulse rate around 40s, lasting for a few seconds, then increases back to 100s.. Pt asx during - BG high today -Echo reviewed-normal EF, mild Mitral prolapse/MR. No WMA -EKG without acute ischemia -During visit noted to have runs of non conducted bigeminal PVCs resulting in pulse rate around 40s, lasting for a few seconds, then increases back to 100s.. Pt asx during - BG high today Most Recent Echocardiogram: 1/13/2022 * The left ventricular systolic function is normal, estimated LVEF 60-65%. * Left ventricular wall motion is grossly normal however, endocardial definition is limited. * Normal right ventricular systolic function. * There is mild mitral regurgitation. * Due to inadequate tricuspid regurgitant velocity, unable to calculate right ventricular systolic pressure. * The proximal ascending aorta is normal in size measuring 3.4 cm. * Compared to prior study on 12/29/2020, no significant change in left ventricular systolic function with side by side comparison; the mitral valve leaflets are not well visualized on today's study; in the parasternal view there appears to be mild prolapse with at least mild mitral regurgitation.
Aktuelle Erkrankungen: -
Vorgeschichte: Allergic rhinitis, cause unspecified 11/30/2009 ? Diabetes mellitus ? Edema of both lower extremities ? Heartburn ? HTN (hypertension) ? Minimal change disease 3/3/2021 Formatting of this note might be different from the original. 2/17/2021 Kidney Bx. Incidental mild IgA nephropathy (Oxford score MO EO SO TO CO). TUBULES AND INTERSTITIUM: Interstitial fibrosis and tubular atrophy involves approximately 20% of the cortex sampled. There is mild interstitial inflammation mainly composed of mononuclear cells and localized in the areas of scarring but without tubuliti ? Non-ST elevated myocardial infarction 6/29/2021 ? Renal disease
Andere Medikamente: -
Allergien: Atorvastatin and Rosuvastatin
Vorherige Impfungen: -

VAERS 2035678

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: RI
Alter: 40,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 18.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Chest pain Heart rate increased Palpitations Physical examination

Symptomtext

I received my covid booster vaccine the evening of Thursday, 11/18/21. The following day on Friday, I experienced a rapid heart rate of 120's-130's at rest and 140's-150's with normal activity. (My normal resting heart rate is 70's-80's and 80's-90's with normal activity). I also experienced constant heart palpitations, and chest pain/ache. This continued through the next day as well, Saturday. On Sunday, heart rate was better, 100's-110's, palpitations subsided, but chest pain/ache was still present though not as intense. I considered going to the ER for evaluation but ER's in my area were so full the wait times were hours and hours long. I called a few urgent cares and I was told that with my heart rate being that fast they would send me to the ER anyway. I made an appointment with my pcp on Monday, 11/22/21. He performed a physical exam and told me that everything sounded fine. I did take ibuprofen sometime on Saturday pm for the chest pain/ache which helped a bit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: physical exam by pcp
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: drosperinone/ethinyl estradiol birth control pills, vitamin C supplement, elderberry supplement, vitamin D supplement
Allergien: none
Vorherige Impfungen: -

VAERS 2035357

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: PA
Alter: 70,0
Geschlecht: M
Eingang: 14.01.2022
Impfdatum: 02.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 17,0
Dosis: UNK
Route/Site: IM / UN

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

Back pain Cardiomyopathy acute Catheterisation cardiac normal Chest pain Echocardiogram abnormal Ejection fraction normal Electrocardiogram T wave abnormal Electrocardiogram abnormal Left ventricular dysfunction Stress cardiomyopathy Troponin increased

Symptomtext

ED on 11/19/2021: CArdiology follow up on 12/8/2021 I saw patient today for cardiac evaluation post hospital discharge. He was hunting and while resting in the cabin developed severe chest and back pain. His symptom waxed and waned in the following morning there were no better. He went to the local ER and underwent a cardiac catheterization which revealed normal coronary arteries. His serum troponin levels were in the 2500 range according to the patient. His echo revealed anterolateral wall motion abnormalities with an EF 45%. His symptoms occurred 2 weeks post COVID-19 booster injection. Since discharge he has been asymptomatic and has resume normal activities avoiding strenuous activities. His 12 lead EKG today revealed a sinus rhythm with marked T-wave abnormalities in the anterior lateral precordial leads. These are similar to his hospital tracings. There were no old tracings for comparison. Active medical problems Takotsubo Cardiomyopathy ( possibly Covid Booster related ) COPD HLD PLAN 1. Acute cardiomyopathy, coronary arteries normal. Possible acute takotsubo cardiomyopathy possibly related to COVID-19 booster injection. Continue with current meds and re-evaluate in 4 weeks with a limited echo and repeat EKG. If no improvement will schedule for cardiac MRI. In the meantime begin cardiac rehab. 2. Hyperlipidemia on Crestor 10 mg daily 3. History of COPD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: cardiology OV on 1/13/22 PLAN 1. Takotsubo cardiomyopathy with recovery of LV function, recent echo revealing EF 60-65%. Repeat ECG normalizing. Low blood pressures on metoprolol and Diovan. For now will not resume meds and continue to monitor heart rate blood pressures during cardiac rehab and will adjust treatment as needed. 2. Hyperlipidemia on Crestor 10 mg daily HPI I saw patient today for cardiac follow-up regarding takotsubo cardiomyopathy which occurred 2 weeks following his COVID-19 booster. He presented with severe chest pain ECG changes and was helicoptered to the nearest hospital. He underwent a cardiac catheterization which revealed normal coronary arteries. His echo revealed moderate LV dysfunction with wall motion abnormalities. His 12 lead EKG revealed marked T-wave abnormalities across the precordial leads. He has been on metoprolol and Diovan which recently have caused significant drop in his heart rate blood pressure. He started cardiac rehab and is doing well. He had a limited echo prior to today's visit and his EF is normal at 60-65%. Active medical problems Takotsubo Cardiomyopathy ( possibly Covid Booster related ) Cath 12/8/21 Nl Cs COPD HLD second cardiology follow up on 1/13/2022
Aktuelle Erkrankungen: 10/18/2021 cough, negative for covid-19, prescribed augmentin 875-125 BID X 10 DAYS.
Vorgeschichte: Osteoarthritis of shoulder, hyperlipidemia
Andere Medikamente: famotidine 20mg twice daily, rosuvastatin 5mg every other day.
Allergien: NKA
Vorherige Impfungen: -

VAERS 2034542

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 05.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Condition aggravated Feeling abnormal Gait inability Immunisation Joint injury Pain Sciatica

Symptomtext

booster; I CAN BARELY WALK MOST DAYS.; Pain not diminishing at all; Serious brain fog never had before; Old sacroiliac hip injury and sciatica flared up immediately after each injection; Old sacroiliac hip injury and sciatica flared up immediately after each injection; Old sacroiliac hip injury and sciatica flared up immediately after each injection; This is a spontaneous report received from a contactable reporter (Consumer or other non-HCP). The reporter is the patient. A 68-year-old female patient (not pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), administered in arm left, administration date 05Oct2021 (Lot number: FE3590) at the age of 68 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "hypothyroid" (unspecified if ongoing); "sacroiliitis" (unspecified if ongoing), notes: for 3 years; "sciatica" (unspecified if ongoing), notes: for 11 years; "old sacroiliac hip injury" (unspecified if ongoing). There were no concomitant medications. Past drug history included: Statins, reaction: "drug allergy". Vaccination history included: BNT162B2 (Dose 1, single), administration date: 05Mar2021, for COVID-19 immunization, reaction(s): "Old sacroiliac hip injury and sciatica flared up immediately after each injection"; BNT162B2 (Dose 2, single), administration date: 01Apr2021, when the patient was 68 years old, for COVID-19 immunization, reaction(s): "Old sacroiliac hip injury and sciatica flared up immediately after each injection". The following information was reported: IMMUNISATION (disability) with onset 05Oct2021, outcome "unknown", described as "booster"; GAIT INABILITY (disability) with onset 05Oct2021, outcome "not recovered", described as "I CAN BARELY WALK MOST DAYS."; PAIN (disability) with onset 05Oct2021, outcome "not recovered", described as "Pain not diminishing at all"; FEELING ABNORMAL (disability) with onset 05Oct2021, outcome "not recovered", described as "Serious brain fog never had before"; JOINT INJURY (disability), SCIATICA (disability), CONDITION AGGRAVATED (disability) all with onset 05Oct2021, outcome "not recovered" and all described as "Old sacroiliac hip injury and sciatica flared up immediately after each injection". Therapeutic measures were not taken as a result of gait inability, pain, feeling abnormal, joint injury, sciatica, condition aggravated. Clinical course details: Patient had no COVID prior to vaccination and had not tested positive post vaccination. Patient reported old sacroiliac hip injury and sciatica flared up immediately after each injection-inflammation. This faded after first vaccination after a couple of days then after second vaccination in a week, with third vaccine, patient can barely walk most days. Serious brain fog never had before. Almost 3 months of pain and brain fog after third vaccine. Pain not diminishing at all as of 01Jan2022. Cannot function in my life. Definitely related to vaccine. Patient did not have flare ups in these areas for years. Pain started the day of each injection. Serious side effects. Exercises and diet that helped in the past did not work. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hip injury; Hypothyroidism; Sacroiliitis (for 3 years); Sciatica (for 11 years)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2029555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NY
Alter: 30,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 14.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Abdominal distension Asthenia Computerised tomogram Gait inability Inflammation Joint dislocation Mobility decreased Pain Peripheral swelling X-ray limb

Symptomtext

My body became inflamed terribly, especially my foot and then my neck and shoulders. I went to the hospital and had an emergency rheumatology appointment. I was given steroids, which made the swelling go down after a few days in my foot so I could sleep. After about a month, I was able to walk again, but my shoulders, neck and spine were still weak. Since then, I have dislocated my shoulder, just by standing up. I can no longer perform normal daily functions with my left arm. My feet and knees are still recovering, but I have seen a lot of progress in the past few days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: I don't have the exact dates, but I had an X-ray on my foot, a CT scan on my foot, and then a duel energy CT scan on my foot to check for gout. They could not find the cause for the swelling and pain.
Aktuelle Erkrankungen: -
Vorgeschichte: Possible arthritis
Andere Medikamente: -
Allergien: Amoxycillin
Vorherige Impfungen: -

VAERS 2028805

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 11,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
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

11 year old female c/o SOB x 3 days

Weitere VAERSDATA-Felder

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

VAERS 2028282

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: TX
Alter: 42,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Headache Injected limb mobility decreased Lymphadenopathy Pain

Symptomtext

After the shot, that night it hurt to lay down. The next couple of days, I couldn't extend my arm 90 degrees moving out away from my body. This lasted for the two days. Also had a headache and lymph nodes swelling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; Iron deficiency Anemia
Andere Medikamente: Flintstone Vitamin with Iron
Allergien: Dairy-Lactose; Seasonal Allergies; Sulfa drugs
Vorherige Impfungen: 1st Covid Pfizer Vaccine, 04/01/2021. About 15-30 mins after the first vaccine, my arm started hurting and pulsing. That lasted

VAERS 2463040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 40,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 07.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Chest pain Dyspnoea Paraesthesia Paraesthesia oral Pruritus Urticaria

Symptomtext

UrticariaPruritus TINGLING HANDS AND LIPS, SHORT OF BREATH, CHEST PAIN; ITCHING Narrative: EMPLOYEE STATES- ITCHING IS INTENSE AND SOMETHING SHE DID NOT EXPERIENCE FROM THE FIRST INJECTION

Weitere VAERSDATA-Felder

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

VAERS 2463032

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 63,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 18.10.2021
Beginn: 13.10.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

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

Dizziness Hypotension Palpitations Vision blurred

Symptomtext

BlurredVision, Dizziness, Palpitations & HYPOtension Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: yes-same symptoms with the second vaccine

VAERS 2024719

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: TX
Alter: 58,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 19.10.2021
Beginn: 24.11.2021
Tage bis Beginn: 36,0
Dosis: UNK
Route/Site: IM / RA

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

Anxiety Intention tremor Metabolic function test normal Tremor

Symptomtext

Severe unrelenting anxiety with uncontrollable mostly hand and arm intention tremors, The anxiety and intention tremor still exist today but reduced from date of presentation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intention tremor
Hospital-Tage: -
Labordaten: 12-3-21 full physical and normal metabolic lab work
Aktuelle Erkrankungen: Left Shoulder Replacement
Vorgeschichte: NONE
Andere Medikamente: Simvistatin, Citalopram, Advil,
Allergien: NONE
Vorherige Impfungen: Pfizer Covid 19 Lot EK5730 and EL3248 same symptoms increasing with each progressive dose of the vaccine, Dat of administration

VAERS 2555570

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 52,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Anxiety Hypertension Peripheral swelling

Symptomtext

HYPERtension SWOLLEN ARM, HAND AND FINGERS Narrative: AT TIME OF VACCINATION- PATIENT APPEARS TO HAVE HAD AN ANXIETY REACTION AND WAS OBSERVED FOR ONE HOUR ICE WAS APPLIED TO THE ARM SWELLING AND PATIENT RELEASED

Weitere VAERSDATA-Felder

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

VAERS 2010585

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MI
Alter: 79,0
Geschlecht: M
Eingang: 06.01.2022
Impfdatum: 11.10.2021
Beginn: 01.01.2022
Tage bis Beginn: 82,0
Dosis: 3
Route/Site: IM / AR

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

Angiogram Angiogram pulmonary normal Arteriosclerosis Atelectasis Atrial flutter Brain natriuretic peptide increased COVID-19 COVID-19 pneumonia Cardiac ablation Chest X-ray abnormal Condition aggravated Dyspnoea Echocardiogram abnormal Ejection fraction decreased Femoral artery aneurysm Fibrin D dimer increased Heart rate increased Hypoxia

Symptomtext

Hospitalized 1/1/2022; COVID-19 positive 1/1/2022; fully vaccinated plus booster BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider at Discharge: NP Admission Date: 1/1/2022 Discharge Date: 1/4/2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Typical atrial flutter COVID-19 virus infection Pneumonia due to COVID-19 virus HOSPITAL COURSE: PATIENT is a 79-year-old male who presented for evaluation of shortness of breath. The patient has a history of afib/aflutter on eliquis s/p multiple cardioversions and ablations. His last ablation was in October 2021. He was scheduled for a cardioversion about 2 weeks ago but he converted on his own. This did not last long and on 12/29 he was seen in the cardiology office and started on amiodarone. Later that day he developed worsening symptoms and fever. He came to the ER on 1/1 with significant shortness of breath. In the ER the patient was found to be COVID positive. His labs showed an elevated BNP, indeterminate but down trending troponin, no leukocytosis. His heart rates were elevated in the 110-120s. The ER provider spoke with EP who recommended the addition of cardizem which was administered in ER. The patient had a CXR which showed left perihilar infiltrate and streaky atelectasis or infiltrate in the right lung base. He was not hypoxic and therefore was not started on dexamethasone. Due to his significant symptoms he was felt to be high risk and the hospitalist team was contacted to admit the patient for further observation. The patient did end up requiring some supplemental oxygen during his stay but was able to be weaned to room air before discharge. Due to his hypoxia he was started on dexamethasone and remdesivir. His D dimer was elevated and he underwent CTA thorax which was negative for PE but showed possible fluid overload. He was started on IV laisx for diuresis with improvement in his symptoms. He had an echo which showed a reduced ejection fraction at 28%. He was evaluated by cardiology who felt that this was likely due to his acute illness as well as due to rapid rates and a flutter. The patient was started on cardizem as well as coreg with improvement in his heart rates. Cardiology recommended that the patient have a repeat EKG next week in the office to determine if cardioversion should happen next week. The patient was instructed to monitor his BP and heart rates at home and call the cardiology office for worsening symptoms or elevated heart rates for a more expedited cardioversion. He will also need a follow up limited echo in 2-3 months to evaluate his EF. Due to the patient's elevated D dimer he underwent bilateral upper and lower extremity dopplers which were negative for DVT however there was a finding of bilateral aneurysmal dilation of the distal femoral and popliteal arteries with significant atherosclerotic disease. A CT angiogram was completed for better evaluation and the patient was advised to follow up with his PCP for referral to vascular as an outpatient. At discharge the patient was given prescriptions for coreg, cardizem and decadron. He was feeling well and had no further shortness of breath. He verbalized understanding of follow up instructions and discharged home with his wife in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Pneumonia due to COVID-19 virus SVT (supraventricular tachycardia) Typical atrial flutter Cardiomyopathy, nonischemic Atypical atrial flutter Paroxysmal atrial fibrillation Primary hypertension Colon polyp Cataract Glaucoma SNHL (sensorineural hearing loss) Subjective tinnitus, bilateral Otosclerosis, left - suspcious Mixed hearing loss, unilateral BPH (benign prostatic hypertrophy) Dyslipidemia Mixed hyperlipidemia Hypothyroid
Andere Medikamente: amiodarone (PACERONE) 200 MG tablet amiodarone (PACERONE) 200 MG tablet apixaban (ELIQUIS) 5 MG TABS carvedilol (COREG) 3.125 MG tablet dexamethasone (DECADRON) 6 MG tablet dilTIAZem (CARDIZEM CD) 120 MG 24 hr capsule fluticasone (FLONASE)
Allergien: NKA
Vorherige Impfungen: -

VAERS 2010267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MI
Alter: 34,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 25.10.2021
Beginn: 05.01.2022
Tage bis Beginn: 72,0
Dosis: 3
Route/Site: - / -

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

Cough Dizziness Dyspnoea Headache Nausea Vomiting

Symptomtext

admitted to ED with symptoms of cought SOB n/v dizziness and headache

Weitere VAERSDATA-Felder

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

VAERS 2531890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 61,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 04.10.2021
Beginn: 20.12.2021
Tage bis Beginn: 77,0
Dosis: 3
Route/Site: IM / LA

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

Burning sensation COVID-19 Cough Dyspnoea Fatigue Headache Hyperhidrosis Myalgia Oropharyngeal pain Pharyngeal erythema Pyrexia Rhinorrhoea SARS-CoV-2 test positive Wheezing

Symptomtext

Narrative: COVID infection after COVID vaccine series 02/23 COVID vaccine dose #1 03/16 COVID vaccine dose #3 12/20 pt present w/ c/o cough, fatigue, rhinorrhea, sore throat, red throat; COVID POSITIVE 12/21 pt with continued SOB, reports burning up and sweating like crazy, c/o cough, fever, headache, myalgia, rhinorrhea, dyspnea, wheezing; seen in ED; treated with dexamethasone 6mg IV x 1, duoneb; r/o PE, discharged from ED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/20/2021@13:26 COVID-19 DIAG DETECTED 08/03/2021@00:11:02 COVID-19 NOTDETECTED 02/05/2021@15:00 COVID-19 SCR NotDetected 07/27/2020@01:42 COVID-19 NotDetected 06/07/2020@17:40 COVID-19 NotDetected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1999357

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MI
Alter: 58,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 12.10.2021
Beginn: 25.12.2021
Tage bis Beginn: 74,0
Dosis: 3
Route/Site: UN / UN

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

Angiogram pulmonary abnormal Anion gap Asthenia Blood bicarbonate increased Blood chloride normal Blood creatinine normal Blood glucose normal Blood potassium normal Blood sodium normal Blood urea increased COVID-19 Cardiomegaly Chest X-ray abnormal Cholelithiasis Cough Dyspnoea Glomerular filtration rate normal Haematocrit normal

Symptomtext

Patient currently hospitalized (9) days. HOSPITAL COURSE: Patient is a 58-year-old female with a history of primary progressive MS who presented with increasing generalized weakness, worse from her baseline (at baseline, right lower extremity worse than left lower extremity) and dyspnea/cough. In ER she was noted to have COVID-19 along with chest x-ray showing patchy bilateral airspace disease. She has received her COVID vaccination and her booster in October. She was admitted and started on decadron. She was seen by neurology who recommended MRI brain to rule out acute demyelinating lesions. MRI brain without acute changes compared to prior. Neurology felt weakness represented a pseudo flare in the setting of acute COVID infection. Oxygen needs began to increase. CT angio thorax showing no PE. The patient was transitioned to IV solumedrol, started on IV lasix and ppx antibiotics for CAP. The patient slowly started to show improvement and oxygen was weaned down to 2L at and rest and 4L with activity. Pulm rehab evaluated the patient for home oxygen. PT/OT evaluated the patient and recommended IRC, but did not get insurance authorization and SAR was recommended instead. After further discussion with the patient she is declining SAR and prefers to discharge home. She will be sent home with a prednisone taper and HHC will be arranged.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 9,0
Labordaten: Lab Results Component Value Date GLUCOSE 97 01/01/2022 SODIUM 143 01/01/2022 POTASSIUM 3.9 01/01/2022 CHLORIDE 101 01/01/2022 HCO3 30 (H) 01/01/2022 ANIONGAP 12 01/01/2022 BUN 30 (H) 01/01/2022 CREATININE 0.53 01/01/2022 EGFR >60 01/01/2022 Lab Results Component Value Date WBC 7.14 01/01/2022 RBC 5.02 01/01/2022 HGB 13.1 01/01/2022 HCT 41.9 01/01/2022 MCV 83.5 01/01/2022 PLATELET 233 01/01/2022 NEUTABSOLU 5.11 12/31/2021 MRI Brain w/wo contrast 12/26/2021 Impression: No acute intracranial abnormality. Specifically, no evidence of active demyelination or new lesion with respect to the 3/23/2021 examination. CTA Thorax 12/27/2021 Impression: 1. No evidence of acute pulmonary embolus. 2. Mild cardiomegaly. 3. Pulmonary trunk appears distended measuring up to 35 mm. This is nonspecific but can be seen in the setting of pulmonary hypertension. 4. Patchy bilateral groundglass opacities as can be seen in the setting of Covid infection. 5. Cholelithiasis. CXR 12/28/2021 Impression: 1. There is diffuse patchy opacification of both lungs. This is not significantly changed from prior imaging. 2. No pneumothorax or sizable pleural effusion is seen. 3. The mediastinal contour and the cardiac silhouette are stable. 4. No suspicious osseous lesion is seen.
Aktuelle Erkrankungen: -
Vorgeschichte: Hospital Multiple sclerosis Acute respiratory failure with hypoxia Non-Hospital SVT (supraventricular tachycardia) Acute pain of right shoulder Allergic rhinitis Ataxia Bilateral optic neuritis Chronic low back pain Foot-drop Hyperlipidemia Hypotension Impacted cerumen of both ears Internuclear ophthalmoplegia Sacroiliac joint pain Secondary progressive multiple sclerosis Urinary incontinence Vitamin D deficiency
Andere Medikamente: cholecalciferol (VITAMIN D3) 25 MCG (1000 UT) capsule escitalopram (LEXAPRO) 20 MG tablet montelukast (SINGULAIR) 10 MG tablet pantoprazole (PROTONIX) 40 MG tablet pravastatin (PRAVACHOL) 40 MG tablet predniSONE (DELTASONE) 20 MG tablet tiZ
Allergien: Dimethyl Fumarate- Rash Seasonal Allergies, Unspecified- Sneezing Teriflunomide - Diarrhea
Vorherige Impfungen: -

VAERS 1998506

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: IA
Alter: 81,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 22.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 COVID-19 pneumonia Chills Cough Diarrhoea Nausea Pneumonia bacterial Pyrexia SARS-CoV-2 test positive

Symptomtext

Developed a Fever, Chills, Cough and nausea on 11/28. Went to ER on 12/01/21 and tested positive for Covid 19. Sent her home with no medications or oxygen. Developed severe nausea and bad diarrhea from 12/02/21 to 12/05/21. Went back to ER and was admitted for Covid Pneumonia on 12/05/21. Also developed bacterial pneumonia. Patient is currently still in the Hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 29,0
Labordaten: Tested Positive for Covid 19 on 12/01/21 Tested Positive for Covid pneumonia on 12/05/21
Aktuelle Erkrankungen: None
Vorgeschichte: Heart Disease A-fib Obesity
Andere Medikamente: Famotidine Potassium Chloride Furosemide Levothyroxine Metoprolol Atorvastatin Lisinopril Warfarin Fluticason nasal spray Vitamin D3
Allergien: Tylenol 3 Cipro Oxycodone Cephalexin
Vorherige Impfungen: -

VAERS 1997269

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 01.01.2022
Impfdatum: 05.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Condition aggravated Feeling abnormal Gait disturbance Immediate post-injection reaction Inflammation Joint injury Loss of personal independence in daily activities Pain Sciatica

Symptomtext

OLD SACROILIAC HIP INJURY AND SCIATICA FLARED UP IMMEDIATELY AFTER EACH INJECTION?INFLAMMATION. THIS FADED AFTER FIRST VACCINE AFTER A COUPLE OF DAYS, AFTER SECOND IN A WEEK, WITH THIRD VACCINE I CAN BARELY WALK MOST DAYS. SERIOUS BRAIN FOG NEVER HAD BEFORE. ALMOST 3 MONTHS OF PAIN AND BRAIN FOG AFTER 3RD VACCINE. PAIN NOT DIMINISHING AT ALL AS OF 1-1-22. CANNOT FUNCTION IN MY LIFE. DEFINITELY RELATED TO VACCINE. HAVE NOT HAD FLARE UPS IN THESE AREAS FOR YEARS -- SCIATICA FOR 11 YRS, AND SACROILIACITIS FOR 3 YRS. PAIN STARTED DAY OF EACH INJECTION! SERIOUS SIDE EFFECTS. EXERCISES AND DIET THAT HELPED IN THE PAST DO NOT WORK. PLEASE NOTE I WAS 100% PRO-VACCINE PRIOR TO THIS EXPERIENCE.

Weitere VAERSDATA-Felder

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

VAERS 1992858

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 60,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Mobility decreased Pain Pain in extremity Sleep disorder

Symptomtext

Both arms are sore with intermittent pain. Can not use full range of motion, IE - can not reach behind to put on a shirt or jacket. Wake up at night with pain while sleeping. Need to adjust position.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Seeing Dr. in 2 days
Aktuelle Erkrankungen: pneumothorax
Vorgeschichte: -
Andere Medikamente: Vitamins
Allergien: no
Vorherige Impfungen: -

VAERS 1992858

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 60,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Mobility decreased Pain Pain in extremity Sleep disorder

Symptomtext

Both arms are sore with intermittent pain. Can not use full range of motion, IE - can not reach behind to put on a shirt or jacket. Wake up at night with pain while sleeping. Need to adjust position.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Seeing Dr. in 2 days
Aktuelle Erkrankungen: pneumothorax
Vorgeschichte: -
Andere Medikamente: Vitamins
Allergien: no
Vorherige Impfungen: -

VAERS 1992653

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MA
Alter: 13,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 01.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: IM / LA

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

Angina pectoris Chest pain Dyspnoea exertional Electrocardiogram

Symptomtext

1st dose of Pfizer was given on 12/12/21. On 12/13/21 patient came back from school and asked 'is it normal that my heart feels that someone is stabbing it all the time?' Increased pain during 'walking between classrooms at school' and 'when I was at recess'. PCP was called and next day appointment was scheduled. 10 days later, still c/o sharp pain and SOB with increased activity.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Physical exam on 12/14 by patients PCP. EKG on 12/15.
Aktuelle Erkrankungen: none
Vorgeschichte: autism, adhd
Andere Medikamente: none
Allergien: environmental, pollen, carrots
Vorherige Impfungen: -

VAERS 1989558

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

moderat

Staat: CA
Alter: 63,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Decreased appetite Fatigue Headache Mobility decreased Nasopharyngitis Pain in extremity Sleep disorder

Symptomtext

The evening of 11/12/2021, I was very tried and did not have an appetite. I had cold like symptoms and woke up in the middle of the night with chills but I did not have a temperature. for three to four days I had a severe headache and my arm was very sore I could not lift it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: I had a bone marrow transplant (12/15/2020)
Vorgeschichte: Diabetes
Andere Medikamente: Lantus, Novolog, Amlodipine, Glipizide, Synthroid, Lisinopril, Voltaren, Accuview, Prenatal Vitamin, Multivitamin, Calcium with Vitamin D
Allergien: Sulfa, Amoxicillin
Vorherige Impfungen: -

VAERS 1985945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: WI
Alter: 68,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Mobility decreased Pain Pain in extremity

Symptomtext

It hurts to raise my left arm and I cannot cross my arms to take off a shirt over my head. It aches during most of the day and I really notice it at night when I try to roll over.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None I was hoping it would go away.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Sertraline 25mg 1 a day Atorvastatin 10mg 1 a day D3 5000iu 1 a day
Allergien: None just seasonal
Vorherige Impfungen: -

VAERS 1974664

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: PA
Alter: 26,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 06.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Angiopathy Headache Magnetic resonance imaging Migraine

Symptomtext

Day one after first dose, started with a slight headache which later developed into a 3 day migraine type with zero relief despite medication and hydration attempts. Then resolved. Second dose then gave me a constant headache with no relief from medication and hydration attempts. At times i feel a pulse in my head when bending over. some days i cannot get out of bed due to the pounding feeling and how heavy my head feels. Went to PCP, they ordered MRI/MRA and referral to neurology.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Pending result of MRI/MRA, scheduled for 01/03/2022 Pending referral to Neurology, scheduled for 12/23/2021
Aktuelle Erkrankungen: no illnesses noted
Vorgeschichte: anxiety and depression
Andere Medikamente: Atarax 25mg, PRN Prenatal Vitamin daily Valtrex, PRN with outbreaks(none currently)
Allergien: Doxyclicline, rash.
Vorherige Impfungen: -

VAERS 1971136

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MI
Alter: 50,0
Geschlecht: M
Eingang: 22.12.2021
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: ja

Dizziness Feeling abnormal Heart rate increased Pyrexia Tremor

Symptomtext

High fever: 102.5 Uncontrollable tremors Dramatically increased heart rate: Supine - 150 bpm, standing or sitting 170 bpm Dizzy spells I eventually took Motrin to help with the above symptoms. It dropped the fever down to 101. My heart rate decreased to between 120-130 bpm. The above mentioned symptoms persisted from Friday evening until Sunday evening of the same weekend. Monday morning 12/20, the fever was gone, my heart rate was within my normal range and overall I felt fairly normal.

Weitere VAERSDATA-Felder

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

VAERS 1968181

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: TN
Alter: 49,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 19.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Abdominal pain lower Chills Computerised tomogram abnormal Condition aggravated Fatigue Headache Hepatic enzyme increased Influenza virus test negative Liver disorder Lymphadenopathy Mononucleosis heterophile test negative Pain Pruritus Pyrexia SARS-CoV-2 test negative Ultrasound scan vagina

Symptomtext

The day of the 1st dose, I felt achy, chills and headache. The day of the 2nd dose (within an hour after receiving), I had itching all over my body for roughly 5 hours. Within 2 days of receiving 2nd dose, lymph nodes on left-side of body were all swollen. I noticed I was much more tired than usual. Roughly 3 ? weeks after the 2nd dose, I started getting a low-grade fever every day at some point. Aches, chills and headaches every day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 11/22/2021, I went to urgent care. I tested for COVID-19 and flu (both came back negative). 11/24/2021, I went to the ER for severe pain in lower right abdomen (CT scan and transvaginal ultrasound completed). CT scan showed spot on liver and lymph node next to liver swollen. 12/09/2021, I tested for mono: negative result. 12/16/2021, bloodwork taken at PCP office. 12/21/2021 results of bloodwork show elevated liver enzymes. Future appointments made for another CT scan of chest and abdomen and liver specialist to determine further steps needed.
Aktuelle Erkrankungen: None
Vorgeschichte: Headaches (3-4/week)
Andere Medikamente: Vitamin C, D and B-Complex, Multivitamin
Allergien: N/A
Vorherige Impfungen: -

VAERS 1968145

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: TN
Alter: 44,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 09.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Chest X-ray normal Chills Cough Dyspnoea Feeling cold Impaired work ability Malaise Respiratory tract congestion Sneezing Throat irritation

Symptomtext

I started off sneezing like crazy, uncontrollable. Saturday, throat was itchy. By later that night into Sunday morning, I was in full blown chills, cough, freezing cold. I didn't want to get out of bed, and I just did not feel good. Monday, I got up and went to work, I still wasn't feeling well and went to the doctor's office. By this time, I had mucus and everything else. I couldn't breathe. I had to sleep sitting up because if I laid down, I would cough and felt like I was being suffocated. So I went to the doctor that Monday and was prescribed Promethazine. So, I got up on Tuesday, I felt at my worst so I couldn't go to work. I worked from home, and I just had really bad congestion and cough. Cough was worse than what it originally was. Called the doctor and asked maybe they need to do a chest x-ray. The x-ray was clear, and it was within normal limits. I stayed home on Wednesday and went to work Thursday, still had the congestion and cough even with the medication. Every day I went to Starbucks to get a medicine ball to help with the symptoms, but cough is still consistent every hour. Even with taking the medication. In the hour, I cough every 10 - 15 minutes and it's like a strangling feeling. I do feel a little better but still ongoing coughing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Chest x-ray - normal
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertrophic Cardiomyopathy
Andere Medikamente: Aspirin 81mg; Atenolol 25mg; Research study medication - Mavacamten
Allergien: Codeine; Robaxin; Methocarbamol - Causes brain tumors
Vorherige Impfungen: -

VAERS 1968130

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: OH
Alter: 50,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 29.10.2021
Beginn: 24.11.2021
Tage bis Beginn: 26,0
Dosis: UNK
Route/Site: IM / LA

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

Blood pressure increased Chest pain

Symptomtext

I started having chest pain. It would come and go. I check my blood pressure it was 180/92 on Dec 3rd. I show my doctor on that following Tuesday. She prescribed me medicine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Obesity; Anxiety
Andere Medikamente: Affixer; Matrix
Allergien: N/A
Vorherige Impfungen: -

VAERS 1966913

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: -
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: -
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Arthralgia Burning sensation Cough Dyspnoea SARS-CoV-2 test Swollen tongue

Symptomtext

burning in mouth; joint pains; cough; SOB; tongue swelling; This is a spontaneous report received from a contactable reporter(s) (Other HCP). A 59-year-old female patient (not pregnant) received bnt162b2 (BNT162B2) (Lot number: FE3590) as dose 1, single for Covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: LOSARTAN; LIPITOR. Past drug history included: Iodine, reaction(s): "known allergies: Iodine", notes: known allergies: Iodine. The following information was reported: BURNING SENSATION (medically significant) with onset Oct2021, outcome "recovered with sequelae", described as "burning in mouth"; ARTHRALGIA (medically significant) with onset Oct2021, outcome "recovered with sequelae", described as "joint pains"; COUGH (medically significant) with onset Oct2021, outcome "recovered with sequelae", described as "cough"; DYSPNOEA (medically significant) with onset Oct2021, outcome "recovered with sequelae", described as "SOB"; SWOLLEN TONGUE (medically significant) with onset Oct2021, outcome "recovered with sequelae", described as "tongue swelling". The events "burning in mouth", "joint pains", "cough", "sob" and "tongue swelling" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (Nov2021) negative, notes: Nasal Swab. Therapeutic measures were taken as a result of burning sensation, arthralgia, cough, dyspnoea, swollen tongue. No other vaccine in four weeks. No Covid prior vaccination. No follow-up attempts are possible. No further information is expected.; Sender's Comments: As there is limited information in the case provided, the causal association between the reported events and the suspect drug BNT162B2 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 product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 202111; Test Name: Nasal Swab; Test Result: Negative; Comments: Nasal Swab.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: LOSARTAN; LIPITOR
Allergien: -
Vorherige Impfungen: -

VAERS 1959943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: WA
Alter: 65,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 22.10.2021
Beginn: 11.12.2021
Tage bis Beginn: 50,0
Dosis: 3
Route/Site: IM / RA

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

Acute kidney injury Asymptomatic COVID-19 Chronic kidney disease Condition aggravated Encephalopathy Haemodialysis Metabolic acidosis SARS-CoV-2 test positive

Symptomtext

Patient received Pfizer COVID vaccine on 3/26/21, 4/12/21, and 10/22/21. On 12/11/21, patient came to our ED with acute encephalopathy and was found to be on acute on chronic renal failure with metabolic acidosis and positive COVID status. Patient was admitted to CCU from 12/11/21 to 12/14/21 (with nephrology and pulmonary consulted), then transferred to med/surgical unit on 12/14/21, and discharged home with family on 12/16/21. Throughout the hospitalization, patient's AKI on CKD3 and acute metabolic encephalopathy resolved (completed HD on 12/11 and 12/12). In-addition during hospitalization, patient was never hypoxic (asymptomatic from respiratory standpoint) regardless of the positive COVID status.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 5,0
Labordaten: COVID status positive 12/11/21.
Aktuelle Erkrankungen: -
Vorgeschichte: Morbidly obese, diabetes type 2, complicated by CKD stage III, previous CVA x2 with mild right-sided deficits now ambulating with use of a cane, asthma/COPD, and concern for undiagnosed/untreated OSA/OHS.
Andere Medikamente: Acetaminophen PRN, albuterol inhaler, amlodipine, atorvastatin, clopidogrel, fluticasone furoate disk inhaler, gabapentin, hydrochlorothiazide, insulin aspart, insulin glargine, lisinopril, metformin.
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1947160

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MO
Alter: 84,0
Geschlecht: M
Eingang: 14.12.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Blood pressure diastolic Blood pressure measurement Blood test Chest X-ray Fatigue Hypotension Immunisation Myalgia Pain assessment Somnolence

Symptomtext

extreme upper body muscle pain; terrible fatigue; low blood pressure/The diastolic is what was low, it was like 52; booster; sleeping "14 hours a day; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP) from medical information team. An 84-year-old male patient received bnt162b2 (COMIRNATY), administered in arm left, administration date 01Nov2021 13:55 (Lot number: FE3590) at the age of 84 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "heart disease" (unspecified if ongoing), notes: Verbatim: Heart disease, Additional Information for Other Conditions: This is the main concern. His heart is doing fine now; "Age" (unspecified if ongoing), notes: Verbatim: Age; "Cholesterol" (unspecified if ongoing); "Blood pressure" (unspecified if ongoing); "Leg cramps" (unspecified if ongoing). Concomitant medication(s) included: COREG taken for cardiac disorder (ongoing); SIMVASTATIN taken for hypercholesterolaemia (ongoing); LISINOPRIL taken for hypertension (ongoing); ASPIRIN [ACETYLSALICYLIC ACID] (ongoing); POTASSIUM taken for muscle spasms (ongoing). Vaccination history included: Bnt162b2 (second dose, Card is so messed up can hardly read it to provide product details. , Exact dates of first and second dose of Pfizer Covid Vaccine unknown to caller. , Second Dose Lot- EN5318 , Exp Unknown, thinks given in Apr, but not sure), administration date: Apr2021, when the patient was 84 years old, for COVID-19 immunization; Bnt162b2 (first dose, Card is so messed up can hardly read it to provide product details. , Exact dates of first and second dose of Pfizer Covid Vaccine unknown to caller. , First Dose Lot-EL3248 , Exp, Unknown), for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 01Nov2021 13:55, outcome "unknown", described as "booster"; MYALGIA (non-serious) with onset 02Nov2021 07:00, outcome "recovering", described as "extreme upper body muscle pain"; FATIGUE (non-serious) with onset 02Nov2021 07:00, outcome "recovering", described as "terrible fatigue"; HYPOTENSION (non-serious) with onset 02Nov2021, outcome "not recovered", described as "low blood pressure/The diastolic is what was low, it was like 52"; SOMNOLENCE (non-serious) with onset Nov2021, outcome "unknown", described as "sleeping "14 hours a day". The events "extreme upper body muscle pain" and "terrible fatigue" were 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 myalgia. Additional information: Patient did not get a Covid test. He was just told to drink plenty of water for the muscle pain and take Extra Strength Tylenol for muscle pain- 500mg, one prn. The events resulted in visit to Emergency Room. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: Test Date: 202111; Test Name: Diastolic blood pressure; Result Unstructured Data: Test Result:52; Comments: The diastolic is what was low, it was like 52.; Test Date: 202111; Test Name: Blood pressure; Result Unstructured Data: Test Result:Low; Comments: It has jumped back and forth for the past two weeks.; Test Date: 20211111; Test Name: Blood work; Result Unstructured Data: Test Result:Normal; Test Date: 20211111; Test Name: Chest X-ray; Result Unstructured Data: Test Result:Normal; Test Date: 202111; Test Name: Muscle pain; Result Unstructured Data: Test Result:11; Comments: In the beginning it on the scale it was an 11, but now it's a 5; Test Date: 20211201; Test Name: Muscle pain; Result Unstructured Data: Test Result:5; Comments: In the beginning it on the scale it was an 11, but now it's a 5
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Cholesterol blood excessive; Elderly (Verbatim: Age); Heart disease, unspecified (Verbatim: Heart disease This is the main concern. His heart is doing fine now); Leg cramps
Andere Medikamente: COREG; SIMVASTATIN; LISINOPRIL; ASPIRIN [ACETYLSALICYLIC ACID]; POTASSIUM
Allergien: -
Vorherige Impfungen: -

VAERS 1945319

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: OH
Alter: 50,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Chest pain Headache Lymphadenopathy Musculoskeletal stiffness Pain in extremity Swelling X-ray

Symptomtext

Arm pain, headaches, swelling, lymph nodes swelled, and stiff neck. On December 7 I had chest pain?s.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: X-ray done, waiting on ultrasound.
Aktuelle Erkrankungen: None at the time one month prior I had Vertigo.
Vorgeschichte: None
Andere Medikamente: None
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1944508

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MO
Alter: 52,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 13.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Blood pressure increased Dizziness Hypoaesthesia Injection site irritation Paraesthesia

Symptomtext

On 12-13-2021 at approximately 1010 am, HCP administered a COVID-19 vaccine in the left arm of a female patient. Within 3 minutes after receiving the vaccine the patient stated she was dizzy. Pt was seated and the time. Upon checking her blood pressure, pt asked that I use her right arm as she had had cancer in her left arm. Her blood pressure was elevated. She had not eaten nor had anything to drink all day and has a history of high blood pressure. She was given water, food and took her blood pressure meds. She then stated her left arm was feeling numb and tingling. Upon inspection of her left arm injection site I noted the band aid to be placed approximately 1 inch below the deltoid muscle. I removed the band aid and visualized a small red dot injections site. The site was not swollen nor tender to touch. I explained that the injection could have irritated some nerves and that I would keep a close eye on her. Pt was able to move her arm, hand and fingers on the left without limitation or pain. Within in 20 minutes patient stated she no longer felt the numbness in her left arm. I re checked her blood pressure and it was with in normal limits. Pt was released from the clinic by 1100 am.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown.
Vorgeschichte: Hypertension as reported by patient.
Andere Medikamente: None listed. Pt did state she was on a blood pressure medication, but did not state the name.
Allergien: None stated on consent form.
Vorherige Impfungen: -

VAERS 1944242

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: TX
Alter: 54,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 13.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Condition aggravated Dizziness Immediate post-injection reaction

Symptomtext

Patient stated pre-vaccination that she feels lightheaded after any injection or blood draw Immediately upon vaccination, pt c/o lightheadedness, states " I feel like I'm about to faint". Cold compress placed on back of neck, pt sitting forward with head close to knees. Encouraged to take deep breaths. Within 3 minutes, symptoms diminished. Vitals 128/84, R14 even and unlabored, P87 strong and regular, O2 Stat 98%. Released from site at 1454 with no remaining c/o of symptoms. Encouraged to seek medical care if symptoms worsened.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Seizure disorder, depression
Andere Medikamente: Lamictal, Prestiq
Allergien: NKDA
Vorherige Impfungen: Feels lightheaded following every injection, blood draw, experience w/ needles

VAERS 1935106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MA
Alter: 64,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Blood pressure measurement Fatigue Heart rate Heart rate increased Hypotension Immunisation Sleep disorder

Symptomtext

one low reading blood pressure 93/70; fatigue; trouble with sleep night; Rapid heart rate for about 48 hours after vaccine (around 100) (resting heart rate usually 67-70); Booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 64 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 19Nov2021 09:00 (Lot number: FE3590) at the age of 64 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "high blood pressure" (unspecified if ongoing); "covid" (unspecified if ongoing), notes: if covid prior vaccination Yes; "osteoporosis" (unspecified if ongoing); "food poisoning" (unspecified if ongoing); "low sodium level", start date: 27Oct2021, stop date: 2021, notes: 27Oct2021 hospitalized for low sodium level (recovered) after food poisoning. Concomitant medication(s) included: ALENDRONATE; LISINOPRIL. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0151, Location of injection: Arm Left, Vaccine Administration Time: 01:00 PM), administration date: 19Apr2021, when the patient was 64 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8733, Location of injection: Arm Left, Vaccine Administration Time: 11:00 AM), administration date: 29Mar2021, when the patient was 64 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 19Nov2021 09:00, outcome "unknown", described as "Booster"; HEART RATE INCREASED (non-serious) with onset 19Nov2021 19:30, outcome "recovered" (Nov2021), described as "Rapid heart rate for about 48 hours after vaccine (around 100) (resting heart rate usually 67-70)"; HYPOTENSION (non-serious) with onset 20Nov2021 09:00, outcome "recovered" (Nov2021), described as "one low reading blood pressure 93/70"; FATIGUE (non-serious) with onset 19Nov2021 19:30, outcome "recovered" (Nov2021), described as "fatigue"; SLEEP DISORDER (non-serious) with onset 19Nov2021 19:30, outcome "recovered" (Nov2021), described as "trouble with sleep night". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of heart rate increased, hypotension, fatigue, sleep disorder. 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: multivitamin. Since the vaccination, has the patient been tested for COVID-19: No. No known allergies. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: Test Date: 20211120; Test Name: blood pressure; Result Unstructured Data: Test Result:93/70; Comments: one low reading blood pressure; Test Name: heart rate; Result Unstructured Data: Test Result:67-70; Comments: resting heart rate; Test Date: 20211121; Test Name: heart rate; Result Unstructured Data: Test Result:around 100; Comments: Rapid heart rate
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; COVID-19 (if covid prior vaccination Yes); Food poisoning; Osteoporosis; Sodium low (27Oct2021 hospitalized for low sodium level (recovered) after food poisoning)
Andere Medikamente: ALENDRONATE; LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 1935091

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: UT
Alter: 39,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Contusion Hypoaesthesia Immunisation Oropharyngeal pain Paraesthesia Tenderness

Symptomtext

fingertips and the both hands of tips of index finger, the middle finger and the thumb they started to feel little tingly, a little numb, not numb; but it felt like its a little tender; could say that kind like needle kind of thing like I didn't understand and that's start happening Saturday; little bit of like internal bruising on my fingers like red bruises inside my finger and at the top it covers about the finger tip along it covers like ten fifteen percent just like red bruisy areas; I had a sore throat and I still have a minor sore throat; After the booster shot I had minor problems; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 39 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 12Nov2021 16:00 (Lot number: FE3590) at the age of 39 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose: 2nd), when the patient was 39 years old, for Covid-19 immunization; Bnt162b2 (Dose: 1st), when the patient was 39 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 12Nov2021, outcome "unknown", described as "After the booster shot I had minor problems"; HYPOAESTHESIA (non-serious), outcome "unknown", described as "fingertips and the both hands of tips of index finger, the middle finger and the thumb they started to feel little tingly, a little numb, not numb"; TENDERNESS (non-serious), outcome "unknown", described as "but it felt like its a little tender"; PARAESTHESIA (non-serious), outcome "unknown", described as "could say that kind like needle kind of thing like I didn't understand and that's start happening Saturday"; CONTUSION (non-serious), outcome "unknown", described as "little bit of like internal bruising on my fingers like red bruises inside my finger and at the top it covers about the finger tip along it covers like ten fifteen percent just like red bruisy areas"; OROPHARYNGEAL PAIN (non-serious), outcome "unknown", described as "I had a sore throat and I still have a minor sore throat". Additional information: Patient stated, So patient was calling because he got a booster shot recently, it was on Friday last Friday so the exact date here 12Nov and after getting the booster shot after about a day, a day and a half his fingertips and the both hands of tips of index finger, the middle finger and the thumb they started to feel little tingly, a little numb, not numb but it felt like its a little tender could say that kind like needle kind of thing like he didn't understand and that's start happening Saturday, Saturday night something like that Sunday morning it persisted and then it moved down. It kept on going to the other the ring finger after that and then also his heel on his left foot started to do the same thing and now its been like 6 days, 5 days since the vaccine like there was like little bit of like internal bruising on his fingers there was just like red bruises inside his finger and at the top it covers about the finger tip along it covers may be like ten fifteen percent just like red bruisy areas. Prior vaccinations (within 4 weeks): Consumer stated, "Not within the four weeks I have taken the first two doses of the vaccine. I mean the first two in April of this year and then this will be booster. Other medications were reported as Patient do not, he had been taking Ibuprofen (Intent Treatment) when he took the booster shot. After the booster shot he had minor problems. Consumer stated, Yes like he said when he went to go tested they offered him the booster shot but he wasn't feeling that well meaning when he went to get the test he had some kind of virus and it wasn't COVID but it was like they only lasted like 24 hours, he got heavy fever and after 24 hours that was gone and then it was replaced by the(Incomplete sentence). Consumer stated, well you know the main reason why he was calling was because he was wondering if this was a regular thing. If it was correlated with him taking the booster shot you know the first time patient have taken the booster shot not the booster but the vaccine the first two then he didn't have this kind of reaction but it was a normal thing its gonna go away, don't need to go you know if you think he should go to doctors. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1931520

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: -
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Allergy test Blood pressure measurement Diarrhoea Dizziness Erythema Facial pain Headache Heart rate Hypersensitivity Hypertension Nausea Pallor Palpitations Sensation of foreign body Throat irritation Throat tightness

Symptomtext

feeling dizzy; face turned cherry red; throat started shutting; Heart was pounding fast/My heart was beating really fast; BP was extremely high/Blood pressure was extremely high; I was really pale; Throat was like something was getting stuck in my throat; Nauseated; Diarrhea; possible allergic reaction to Pfizer; face turned cherry red, it was 'throbbing'; throat was like 'scratchy'; Headache; it hasn't gone away; This is a spontaneous report received from a contactable reporter (consumer or other non HCP) from medical information team. The reporter is the patient. A 40 year-old female patient received bnt162b2 (COMIRNATY), administration date 01Nov2021 09:30 (Lot number: FE3590) at the age of 40 as dose 1, single for covid-19 immunization. Relevant medical history included: "allergic to iodine" (unspecified if ongoing); "allergic to seafood" (unspecified if ongoing); "allergic to shellfish" (unspecified if ongoing); and "allergic to salt" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: prednisone, reaction(s): "allergic to prednisone"; and steroid, reaction(s): "allergic to steroid". The following information was reported: DIZZINESS (medically significant) with onset 01Nov2021, outcome "unknown", described as "feeling dizzy"; ERYTHEMA (medically significant) with onset 01Nov2021, outcome "recovering", described as "face turned cherry red"; THROAT TIGHTNESS (medically significant) with onset 01Nov2021, outcome "unknown", described as "throat started shutting"; PALPITATIONS (medically significant) with onset 01Nov2021, outcome "unknown", described as "Heart was pounding fast/My heart was beating really fast"; HYPERTENSION (medically significant) with onset 01Nov2021, outcome "unknown", described as "BP was extremely high/Blood pressure was extremely high"; PALLOR (medically significant) with onset 01Nov2021, outcome "unknown", described as "I was really pale"; SENSATION OF FOREIGN BODY (medically significant) with onset 01Nov2021, outcome "unknown", described as "Throat was like something was getting stuck in my throat"; NAUSEA (medically significant) with onset 01Nov2021, outcome "unknown", described as "Nauseated"; DIARRHOEA (medically significant) with onset 01Nov2021, outcome "unknown", described as "Diarrhea"; HEADACHE (medically significant) with onset Nov2021, outcome "not recovered", described as "Headache; it hasn't gone away"; HYPERSENSITIVITY (medically significant) with onset 01Nov2021, outcome "not recovered", described as "possible allergic reaction to Pfizer"; FACIAL PAIN (medically significant) with onset 01Nov2021, outcome "recovering", described as "face turned cherry red, it was 'throbbing'"; THROAT IRRITATION (medically significant) with onset 01Nov2021, outcome "unknown", described as "throat was like 'scratchy'". Clinical course: Patient received the first dose of the Pfizer COVID-19 vaccine 01Nov2021. Patient was afraid and concerned to get the second dose because patient had a severe reaction to the first one. After receiving the vaccine at 9:30 AM, three hours later patient started feeling dizzy, face turned cherry red and throat started shutting. She also expressed she had to clear her throat. Heart was pounding fast. She did take Benadryl before arriving to the ER. Face was puffy cherry red, and BP was extremely high and the people in the ER didn't know what to do. They gave me IV fluids and Tramadol. After the treatment, she started feeling better and face wasn't as cherry red. The redness calmed down. The next day, she was really pale (also reported as occurring on 01Nov2021). She wanted to know Pfizer can provide her an exemption letter for the second dose of the Pfizer COVID-19 vaccine. She went to see her doctor who referred her to the allergist. The allergist explained the reaction she had was not a severe allergic reaction. She was not able to obtain the exemption letter from her doctor. She has all the notes that were taken in the ER department but unfortunately on the notes it did not state she had an allergic reaction but a possible allergic reaction to Pfizer medical information (01Nov2021). She explained she took Benadryl before getting to the emergency room this may have masked her allergic reaction. She was allergic to many medications. She was allergic to iodine, seafood, shellfish, prednisone, steroid and salt. She mentioned the vaccine Pfizer COVID-19 vaccine, Moderna and Johnson do contain salt. This may have caused her to react. She believed she had an allergic reaction. She did not want to get the second dose. She was afraid she would be dead or have to return back to the ER after receiving the second dose. She also asked if a reduced second dose can be administered which was a suggestion made by her doctor. Patient was advised that it is not recommended to administer the vaccine in any other way then described in the prescribing information. A reduced dose has not the been authorized as per the fact sheet. Patient was concerned about the Pfizer COVID Shot. She took it on 01Nov2021 of this year that was the 1st dose, it was not booster, it was the first shot. She did not get no reactions into let's say (incomplete sentence). 3 hours later (01Nov2021), she got like, face turned cherry red, it was 'throbbing' and my heart was beating really fast and throat was like 'scratchy' like it was like something was getting stuck in throat. So she decided to go to the ER because she thought it was allergic reaction or something (consumer was unsure, hence not captured as event), she didn't know, she was confused like they don't know what to do, they only gave fluids, IV fluids (treatment) and they gave me 'Tramadol' (consumer was unsure). Blood pressure was extremely high when she went there (Further clarification unknown if consumer had high blood pressure prior taking the vaccine or after hence captured as event). She did not know and so once they gave her that (Not clarified over the call), her body calm down and stuff you know and the redness did not go right away. The redness on face went away the next day like slowly. The first day after she got the shot, she started feeling nauseated, the normal symptoms that as mentioned of side effects right like nauseated, diarrhea and stuff like that right. So what patient was asking though was my next shot it on 22nd, it was yesterday right, she went there, they were going to give it to her they seen that she went to the ER because of the COVID Shot that she had on the first, they didn't give it to her they said they need to do more research to give them a copy of the 'exemption' form, something from the CDC or something so that the doctor can fill it out but they are saying this is a rare allergic reaction because it didn't happened after 30 minutes, it happened like 3 hours later, still she wanted to research on it and on this CDC website and so it mentioned something about 'hypertension' hyper something to hypertension or something (consumer was unsure) like that "your body goes through when we get that and that's indicating like an allergic reaction your heartbeat pounding, you are flushing like really red, like cherry red and you are having blood pressure like extremely high or something (Further clarification unknown)". Patient just trying to figure out because she was just talking to her doctor, they do not know what to do like they are confused like they are saying that's not an allergic reaction. They are expecting her not to believe which she thought as an allergic reaction because she have a lot of allergies to a lot of medication (Unspecified Medication), a lot and her chart has a lot of allergies medications Prednisone, shellfish: allergic to Iodine, allergic to 'Gadavist' (Not clarified over the call), allergic to steroids (Unspecified Medication), allergic to all this kind of stuff and the ingredients that patient saw in Johnson and Johnson, Moderna and Pfizer, they all containing 'salt' on them but they were telling her that's all involved with the (incomprehensible voice) that they put in her and she did not agree on that. She was scared to take the second dose because they think everything was going to be worse. Once they gave her the first one, they told her the second one is going to be worse, "you are going to feel more symptoms and you are going to feel this and that". So if the first one gave her that reaction rapidly within 3 hours, the second one is going to do the same thing too. She was going to go straight to the ER and that is not her thing to do at all. She did not want heartbeat to be raising high, she did not want to get into this stressful moment so she was trying to get into the bottom line what can she do. The events "feeling dizzy", "face turned cherry red", "throat started shutting", "heart was pounding fast/my heart was beating really fast", "bp was extremely high/blood pressure was extremely high", "i was really pale", "throat was like something was getting stuck in my throat", "nauseated", "diarrhea", "headache; it hasn't gone away", "possible allergic reaction to pfizer", "face turned cherry red, it was 'throbbing'" and "throat was like 'scratchy'" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: allergy test: (Nov2021) unknown result, notes: I did have some allergy testing for blood; blood pressure measurement: (01Nov2021) extremely high; heart rate: (01Nov2021) really fast. Therapeutic measures were taken as a result of dizziness, erythema, throat tightness, palpitations, hypertension, pallor, sensation of foreign body, nausea, diarrhoea, headache, hypersensitivity, facial pain, throat irritation. Follow-up attempts are completed. No further information is expected.

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Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 202111; Test Name: allergy testing for blood; Result Unstructured Data: Test Result:Unknown result; Comments: I did have some allergy testing for blood; Test Date: 20211101; Test Name: blood pressure; Result Unstructured Data: Test Result:extremely high; Test Date: 20211101; Test Name: heart beat; Result Unstructured Data: Test Result:really fast
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to chemicals; Iodine allergy; Seafood allergy; Shellfish allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1929339

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: FL
Alter: 85,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 23.10.2021
Beginn: 07.11.2021
Tage bis Beginn: 15,0
Dosis: UNK
Route/Site: - / LA

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

Arteriosclerosis coronary artery Blood pressure increased Condition aggravated Electrocardiogram

Symptomtext

Approximately two weeks after the vaccine had been given, began increase in blood pressure. Still elevated, ARPN prescribed Lisinoprol 2.5 mg, on December 1, 2021, to help lower the BP. Partially worked but still in the range of 140s, compared to mainly `120 with Terazosin. Now Terazosin and Lisinoprol 2.5 mg taken at night. Today a lowering of the BP appears to have started. At 12.30pm it had dropped to 125/63, pulse 68, taken again while filling out form, slightly higher at 3;40 pm, 131/71 pulse 51. It was recommended I see a cariologist, appointment made, but not available until Februay 2, 2022. Hopefully the Lisinoprol 2.5 mg will help keep the BP at acceptable levels for my age of 85.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: EKG December 1, 2021 partial blockage of artery from the heart
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure, under control with medication, acne rosacea, arthritis
Andere Medikamente: Terazosin 10mg, Famotidine 20 mg, Pantoprazole 40 mg, Bactrim, Citalpram 10 mg, ethromycin, Voltaren
Allergien: None known
Vorherige Impfungen: -

VAERS 1928672

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE 3590

moderat

Staat: NH
Alter: 55,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Condition aggravated Tinnitus

Symptomtext

Tinnitus. I had preexisting Tinnitus that was not bothersome but after the 1st shot is has increased in volume and has not subsided. I am waiting for my appointment with an ENT that is scheduled for Jan 10

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

VAERS 1925610

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 54,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 15.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Central nervous system lesion Condition aggravated Headache Magnetic resonance imaging head abnormal Migraine

Symptomtext

Patient admitted 10/18/21, three days after covid booster shot. Female with a history of migraine/hypothyroidism/hypertension/anxiety and depression/mild asthma/obesity who presents with headache. Over the last several months patient has had difficulty with recurring migraines. Patient with possible TIA v complicated Migraine in August 2021. Patient is followed by neurology, she had MRI of the brain done 10/14/2021 that showed nonspecific signal abnormalities at the junction of the right frontal and right parietal lobe. Patient was referred for admission to work-up abnormal MRI. There is concern that perhaps lesions noted on MRI represent a demyelinating process. Also, cannot exclude mass as previous MRI was done without contrast. Patient with features concerning for SUNCT (Short-lasting neuralgiform headache with conjunctival injection and tearing). Abnormal MRI- noted low grade glial or glioneuroal lesion is favored. Recommend yearly MRIs for surveillance.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1917815

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NY
Alter: 37,0
Geschlecht: M
Eingang: 02.12.2021
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Abdominal distension Abdominal pain upper Appendicectomy Appendicitis Arthritis Computerised tomogram abdomen abnormal Condition aggravated Scan with contrast abnormal

Symptomtext

I am a healthy, fit, 37 year old male, previously infected with COVID in 2020 and mandated to receive the COVID vaccine by my employers. I received my first dose of Pfizer COVID19 vaccine (LOT 30135BA) on October 26th, 2021. Hours after receiving the vaccine I developed facial numbness. It started in my neck, beneath my chin and all around my chin. Later it would move into my cheeks, around my jaw, and near my eyes. It would only go away for short periods of time and remained pretty constant. This lasted until about November 9th (15 days). Two days after the numbness subsided, I began to have sharp abdominal pains and felt very bloated. The pain and discomfort was constant and would not go away, even days after it began. I received my second dose on November 19th (LOT FE3590). The day after the second dose I began having joint inflammation in my knees and ankles. By November 22rd my stomach pain had become more concerning. I could no longer button my pants due to abdominal swelling. I went to the ER locally where I was given CT scans and was diagnosed with acute appendicitis. The surgeons wanted to perform surgery immediately, but I was hesitant and declined. On November 23rd, after doing research and making an informed decision, I proceeded to the ER of a second hospital. I was again given a CT scan and diagnosed with acute appendicitis. I stayed overnight in the ER and on November 24th I had an appendectomy performed.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: CT Scan with contrast : ACUTE APPENDICITIS
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1916742

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: TX
Alter: 24,0
Geschlecht: F
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

Chest discomfort Hypoaesthesia Tremor

Symptomtext

At 10:37AM PT complain of shakiness, chest tightness, numbness, RN assessed PT vital sign taken. Ice pack was applied.PT was stable in 32mins and left.

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Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: BP 130/100 , HR 90, RESP 6 unable to obtain 02sat. BP 126/83 , HR 89 ,
Aktuelle Erkrankungen: NO
Vorgeschichte: NO
Andere Medikamente: Acetminophen
Allergien: NKA
Vorherige Impfungen: -

VAERS 1916517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MN
Alter: 49,0
Geschlecht: M
Eingang: 02.12.2021
Impfdatum: 04.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 7,0
Dosis: UNK
Route/Site: IM / -

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

Balance disorder Chills Constipation Fatigue Feeling cold Pain Pain in extremity Paraesthesia Peripheral coldness Pruritus Pyrexia Somnolence Vertigo

Symptomtext

Taken from a clinical note in neurology. 11/04/2021 he had the Pfizer COVID-19 booster. He had side effects including fever, chills, generalized achy, fatigue, and sleepiness for about 24 hours followed by improvement. He had arm soreness on the side of the vaccination that has persisted to some degree. He has had some reaction to all of the vaccinations. 11/11/2021 he developed itching in his hands and feet that intensified as the day went on. By the following day he had a sensation of coldness with tingling from the knees and elbows on down. He was mildly unsteady. He does not feel he was weak. He was still able to walk. Symptoms persisted for days and then gradually began to resolve. Over the weekend began to feel much better. Today he has some mild residual feeling of coldness in his feet. Yesterday was the best he has felt since 11/11/2021. He has never had anything like this happen to him before. During this time he developed constipation. He did not develop dry eyes, dry mouth, orthostatic intolerance, tachycardia, abdominal symptoms, or other systemic constitutional symptoms. Overall his baseline vertigo symptoms remained about the same. The paresthesias may have been somewhat positional. When he was standing and walking in busy he could be distracted from them during the day. They tended to be more noticeable when he was sitting with a flexed spinal posture. He felt better laying flat in bed verses curled up on his side. He did not have a classic Lhermitte's. Emergency department presentation 11/16/2021 documented normal reflexes gait and Romberg. CLARIFICATION OF QUESTION BELOW: He has largely recovered with minimal persistent tingling symptoms limited to hands and feet at per 12/2/2021

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: 11/19/2021 EMG demonstrated some very mild changes in insertional activity in proximal muscles but was otherwise normal.
Aktuelle Erkrankungen: chronic likely benign vestibular symptoms
Vorgeschichte: psoriasis
Andere Medikamente: None at the time per patient
Allergien: PCN, Lexapro
Vorherige Impfungen: -

VAERS 1916428

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 21,0
Geschlecht: M
Eingang: 02.12.2021
Impfdatum: 29.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Electrocardiogram ST segment elevation Electrocardiogram abnormal Ischaemia

Symptomtext

Acute chest pain onset 2.5 days after 2nd COVID vaccination. Chest pain radiated to neck and down left arm. ST elevation present on inferior ECG leads revealing ischemia. Transferred to emergency department.

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

VAERS 1915880

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 38,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Abdominal discomfort Asthenia Back pain Blood pressure measurement Blood test Body temperature Burning sensation Chest pain Contusion Decreased appetite Diarrhoea Dizziness Dyspnoea Fatigue Feeding disorder Feeling abnormal Gait inability Gastrooesophageal reflux disease

Symptomtext

I don't have any appetite at all; not able to walk around or anything; tremors\shakes / especially from the tremors makes your body go either way and you can't control it; can't eat; nausea; upper torso all on fire; tingling sensation as well; acid reflux really bad; whole left side is weak / weak overall; constantly in pain / because your whole body is shaking, and going different ways, and it causes lots of pain; makes my neck pain worse; back hurts really bad; short winded/short of breath; fatigued; dizzy / Lightheadedness; brain fog; she has bruises all over her hands, arms and her abdomen; heartrate was steadily rising; head was pounding / headache / headache that does not go away; whole left side of her chest was hurting; stands and sits up she doesn't feel like she is going to pass out anymore; issues with her pancreas; stomach has gone to crap; non-stop throwing up; diarrhea; my left arm is weaker, but it is not as bad as my leg and weak. My hands grip on both hands even though my left side is weaker, when I try to hold on my right hand it is harder; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP, patient) from medical information team. The reporter is the patient. A 38 year-old female patient received bnt162b2 (COMIRNATY), administration date 04Nov2021 (Lot number: FE3590) 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: DECREASED APPETITE (hospitalization, disability) with onset 04Nov2021, outcome "not recovered", described as "I don't have any appetite at all"; GAIT INABILITY (hospitalization, disability) with onset 04Nov2021, outcome "not recovered", described as "not able to walk around or anything"; TREMOR (hospitalization, disability) with onset 04Nov2021, outcome "not recovered", described as "tremors\shakes / especially from the tremors makes your body go either way and you can't control it"; FEEDING DISORDER (hospitalization, disability) with onset 04Nov2021, outcome "unknown", described as "can't eat"; NAUSEA (hospitalization, disability) with onset 04Nov2021, outcome "not recovered", described as "nausea"; BURNING SENSATION (hospitalization, disability) with onset 04Nov2021, outcome "not recovered", described as "upper torso all on fire"; PARAESTHESIA (hospitalization, disability) with onset 04Nov2021, outcome "not recovered", described as "tingling sensation as well"; GASTROOESOPHAGEAL REFLUX DISEASE (hospitalization, disability) with onset 04Nov2021, outcome "unknown", described as "acid reflux really bad"; ASTHENIA (hospitalization, disability) with onset 04Nov2021, outcome "not recovered", described as "whole left side is weak / weak overall"; PAIN (hospitalization, disability) with onset 04Nov2021, outcome "not recovered", described as "constantly in pain / because your whole body is shaking, and going different ways, and it causes lots of pain"; NECK PAIN (hospitalization, disability) with onset 04Nov2021, outcome "unknown", described as "makes my neck pain worse"; BACK PAIN (hospitalization, disability) with onset 04Nov2021, outcome "unknown", described as "back hurts really bad"; DYSPNOEA (hospitalization, disability) with onset 04Nov2021, outcome "not recovered", described as "short winded/short of breath"; FATIGUE (hospitalization, disability) with onset 04Nov2021, outcome "not recovered", described as "fatigued"; DIZZINESS (hospitalization, disability) with onset 04Nov2021, outcome "unknown", described as "dizzy / Lightheadedness"; FEELING ABNORMAL (hospitalization, disability) with onset 04Nov2021, outcome "not recovered", described as "brain fog"; CONTUSION (hospitalization, disability) with onset 04Nov2021, outcome "unknown", described as "she has bruises all over her hands, arms and her abdomen"; HEART RATE INCREASED (hospitalization, disability) with onset 04Nov2021, outcome "unknown", described as "heartrate was steadily rising"; HEADACHE (hospitalization, disability) with onset 04Nov2021, outcome "unknown", described as "head was pounding / headache / headache that does not go away"; CHEST PAIN (hospitalization, disability) with onset 04Nov2021, outcome "unknown", described as "whole left side of her chest was hurting"; FEELING ABNORMAL (hospitalization, disability) with onset 04Nov2021, outcome "recovered" (2021), described as "stands and sits up she doesn't feel like she is going to pass out anymore"; PANCREATIC DISORDER (hospitalization, disability) with onset 04Nov2021, outcome "recovered" (2021), described as "issues with her pancreas"; ABDOMINAL DISCOMFORT (hospitalization, disability) with onset 04Nov2021, outcome "not recovered", described as "stomach has gone to crap"; VOMITING (hospitalization) with onset 04Nov2021, outcome "recovering", described as "non-stop throwing up"; DIARRHOEA (hospitalization, disability) with onset 04Nov2021, outcome "unknown", described as "diarrhea"; MUSCULAR WEAKNESS (hospitalization, disability) with onset 04Nov2021, outcome "unknown", described as "my left arm is weaker, but it is not as bad as my leg and weak. My hands grip on both hands even though my left side is weaker, when I try to hold on my right hand it is harder". The patient was hospitalized for decreased appetite, gait inability, tremor, feeding disorder, nausea, burning sensation, paraesthesia, gastrooesophageal reflux disease, asthenia, pain, neck pain, back pain, dyspnoea, fatigue, dizziness, feeling abnormal, contusion, heart rate increased, headache, chest pain, feeling abnormal, pancreatic disorder, abdominal discomfort, vomiting, diarrhoea, muscular weakness (start date: 04Nov2021, discharge date: 10Nov2021, hospitalization duration: 6 day(s)). The events "i don't have any appetite at all", "not able to walk around or anything", "tremors\shakes / especially from the tremors makes your body go either way and you can't control it", "can't eat", "nausea", "upper torso all on fire", "tingling sensation as well", "acid reflux really bad", "whole left side is weak / weak overall", "constantly in pain / because your whole body is shaking, and going different ways, and it causes lots of pain", "makes my neck pain worse", "back hurts really bad", "short winded/short of breath", "fatigued", "dizzy / lightheadedness", "brain fog", "she has bruises all over her hands, arms and her abdomen", "heartrate was steadily rising", "head was pounding / headache / headache that does not go away", "whole left side of her chest was hurting", "stands and sits up she doesn't feel like she is going to pass out anymore", "issues with her pancreas", "stomach has gone to crap", "non-stop throwing up", "diarrhea" and "my left arm is weaker, but it is not as bad as my leg and weak. my hands grip on both hands even though my left side is weaker, when i try to hold on my right hand it is harder" were evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: blood pressure measurement: (Nov2021) unknown results; blood test: (Nov2021) unknown results; body temperature: (Nov2021) unknown results; heart rate: (Nov2021) steadily rising, notes: it was to the point where it was so high; investigation: (Nov2021) unknown results; scan: (Nov2021) unknown results; ultrasound abdomen: (Nov2021) unknown results. Therapeutic measures were taken as a result of feeding disorder, nausea, gastrooesophageal reflux disease, vomiting. Addition information: 10 minutes after receiving the vaccine he started to have a reaction and was in an ambulance within 20 minutes to the hospital. On protonix twice a day, and nausea medicine every 6-8 hours, Zofran, and phenergan at night to help sleep and relax. The patient stated:" whenever I try to hold something for awhile the tremors and the shaking something harder left side of the body is way weaker than the right. The events had pretty much left her disabled. My doctors point blank have told I am having the same reaction that children are having to your shot I am, so you can tell me that it is not being reported having a ramp put in in order for me to get around. She wants to see what Pfizer's plan is and get all the information from Pfizer. She was a healthy personal trainer and then within 10 minutes her whole life was screwed, she is screwed essentially. She wants to walk through the steps and she has called everyone who has been recommended for her to call and is trying to figure out everything that she can do for this. Event Details: She wanted to get the vaccine and she was perfectly fine at first. She got the shot and it wasn't a big deal, it didn't hurt, just a little poke. Then she was hit like a brick wall. All of a sudden she got lightheaded, dizzy and she felt like she was going to throw up. She told her husband that she needed to sit down and she told him how she was feeling. She sat down and then the lady who gave her the shot was coming to check on her. While the caller was sitting there she was calm but her heartrate was steadily rising and it was to the point where it was so high that it was not funny, it was pounding. The whole left side of her chest was hurting, she had pain in her left arm, her chest was killing her, she was short winded, her head was pounding and she felt like she was going to pass out at any second. She was more calm than the lady that gave her the shot was. The lady said that she didn't know how the caller was so calm but the caller said that there was no point in freaking out, that won't help. She was sitting there and they had the blood pressure cuff hooked up, they were taking her temperature, talking to her and they were getting an ambulance for her. That is kind of how it all started and then the symptoms became more and then more symptoms came on and pretty much she left there and went to the hospital in an ambulance. The only symptoms that have calmed down are when she stands and sits up she doesn't feel like she is going to pass out anymore, that one is good. She was having issues with her pancreas but that all went back to normal before she was released from the hospital. She cannot walk by herself at all, her whole body shakes and her left leg is harder to control and move now. She didn't have a stroke or a heart attack, the doctor said that she has one of the strongest hearts that he has ever seen. She didn't have any blood clots, she brain was functioning properly, her lungs were never filled with liquid. She does still get short winded and her body is completely exhausted all the time. She has to have a wheelchair and a walker when she is trying to walk. Doing physical things makes her shakes worse. She has a harder time speaking when her body is shaking. Her stomach has gone to crap, literally. Her whole upper torso gets on fire and tingles, that comes and goes when it wants to. She has to take Protonix and nausea medications around the clock. She is pretty much on all liquids. Yesterday and today she tried eating fruit because she is physically hungry. Her body isn't tolerating food and going to the bathroom just hurts and when she has to go she has diarrhea the whole time. She can drink and everything but if she doesn't have the nausea medicine she is non-stop throwing up and dry heaving. Her headache doesn't give and she has all over fatigue. When she is grabbing things with her hands to grip, it is hard and she starts shaking even when grabbing a cup. She uses a cup with a lid because when she is trying to grab it she shakes when she tries to drink. She could be relaxed and her whole body shakes. She gets brain fog, not all the time but she does sometimes. It's hard and it's hard to talk about, it is heart breaking. In the hospital it was hard, coming home it was hard. To realize you can't just get up and go fix it and help your kids and you have to have someone help you to get up or have to have someone pick you up and take you into another room. Caller confirms that she was admitted inpatient. She was taken into the emergency room and had all kinds of different doctors and they asked questions and monitored her and then by the evening they had told her that they were waiting on a room for her because they were admitting her. By the end of that night, between 8:00 and 11:00 she was put into a room and was admitted to the hospital. She was there with lots of doctors and she has bruises all over her hands, arms and her abdomen. She had lots of scans, ultrasounds and lots of tests and blood work. She had all kinds of different things performed for her and pretty much the only thing that they could definitely tell her is that she had a severe reaction to the shot. Caller states that these side effects began on 04Nov2021, she was admitted that same night 04Nov2021, and she believes that she was discharged 10Nov2021. Inquired for outcome and she says that the only thing that has gotten better is not wanting to pass out and the headache is not as severe as it was the first few days, but everything else is the same. She is thankful that she hasn't gotten any new symptoms but everything has been the same instead of it getting worse or having any new symptoms. No organs are affected but it's a lot going on. Her husband had the Pfizer vaccine too and he had no reactions. This is the first time that she has ever had a reaction to any vaccine. The patient wonder what information can give me about what Pfizer is doing about people like me who are not able to work or provide, what answers do you have and I'm I permanently going to be like this. They couldn't tell her how long her symptoms would last, they couldn't tell her if this was going to be permanent or not permanent, they said it was just a learning thing and everyone is trying to figure it out. She has to just go day by day and have doctors appointments, physical therapy and everything else and fully work through it is essentially what it all rounded up to be. She has never had anything like this. She had walked in perfectly healthy before this, she was perfectly fine. She was training multiple people daily and she never had any issues other than the obvious of getting sore and tired but that was it. She is fully active, she goes on mission trips, she kayaks more than 30 miles, she bikes, she skate, she runs, well she did before this. Reviewed side effects that have been recorded during the clinical trials and after the release to the public.Also informed caller that unexpected and serious side effects may occur, in addition:COVID-19 vaccination will help protect you from getting COVID-19. You may have some side effects, which are normal signs that your body is building protection. These side effects may affect your ability to do daily activities, but they should go away in a few days. Some people have no side effects. Serious side effects that could cause a long-term health problem are extremely unlikely following any vaccination, including COVID-19 vaccination. Vaccine monitoring has historically shown that side effects generally happen within six weeks of receiving a vaccine dose. For this reason, the FDA required each of the authorized COVID-19 vaccines to be studied for at least two months (eight weeks) after the final dose." A review of the Prescribing Information for <Pfizer-Biontech Covid Vaccine> did not find information regarding tremors, or inability to walk. As the Prescribing Information does not include all adverse reactions that have been reported or that may occur, please consult with your doctor/healthcare provider about what you have experienced/are experiencing. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 6,0
Labordaten: Test Date: 202111; Test Name: blood pressure; Result Unstructured Data: Test Result:unknown results; Test Date: 202111; Test Name: Blood work; Result Unstructured Data: Test Result:unknown results; Test Date: 202111; Test Name: temperature; Result Unstructured Data: Test Result:unknown results; Test Date: 202111; Test Name: heartrate; Result Unstructured Data: Test Result:steadily rising; Comments: it was to the point where it was so high; Test Date: 202111; Test Name: tests; Result Unstructured Data: Test Result:unknown results; Test Date: 202111; Test Name: scans; Result Unstructured Data: Test Result:unknown results; Test Date: 202111; Test Name: ultrasounds; Result Unstructured Data: Test Result:unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1912858

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: WA
Alter: 36,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 30.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Conjunctivitis Dizziness Flushing Nausea Paraesthesia Throat tightness

Symptomtext

Light headed, facial tingling, flushing, nausea, conjunctivitis, sensation of throat tightening

Weitere VAERSDATA-Felder

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

VAERS 1909751

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: OK
Alter: 55,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Extra dose administered Hallucination Headache Magnetic resonance imaging Migraine

Symptomtext

patient forgot she had received her booster already and came in for her another one. It was not caught until after the patient had went home. migraine headache, hallucinations

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: awaiting MRI
Aktuelle Erkrankungen: fell at 0615 the morning of the vaccine, lost balance while carrying cupcakes
Vorgeschichte: pseudotumor cerebri, Thyroid, anxiety, depression
Andere Medikamente: Multivitamin, Sodium Chloride 1gm, Vitamin D3; Citracal D3; Biotin
Allergien: Tetracycline
Vorherige Impfungen: -

VAERS 1907172

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: TX
Alter: 67,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Decreased appetite Dyspepsia Malaise Mobility decreased Muscle spasms Myalgia Pain

Symptomtext

General body pain beginning at about 6 hours. Lower body bilateral muscle cramping & pain beginning at about 10 hours, lasting 3 days, interfering with mobility. Dyspepsia at about 12 hours last 4-5 days. Continuing lower body cramping with less frequency continuing thru day 7. Malaise and decrease in appetite day 2 thru today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic Osteoarthritis and DJD
Andere Medikamente: Armour Thyroid q daily Levothyroxine q daily Lomitil prn Flexeril prn Tramadol prn
Allergien: Rocephin Vancomycin Clindomycin Coxx2 NSAIDS Valium Fentanyl
Vorherige Impfungen: -

VAERS 1906221

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: ID
Alter: 39,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / RA

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

Dyspnoea Impaired work ability Lymph node pain Lymphadenopathy Pain in extremity Peripheral swelling Product storage error

Symptomtext

Vaccine kept in freezer in 3 weeks vs 2 weeks as recommended. Spoke to patient today to come in to have dose repeated per guidelines. Patient stated after she received the dose, the following day she had SOB. She had to go home from work and get her inhaler. Patient was very close to going to the ER. Also the following day, her right arm and axillary were swollen and had pain. Took Ibuprofen. Today she is 70% better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, insulin resistance, pre-diabetes
Andere Medikamente: Losartan; Metformin ER
Allergien: Penicillin, Erythromycin-base
Vorherige Impfungen: -

VAERS 1906182

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: WI
Alter: 46,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Blood glucose Dizziness Peripheral coldness Tremor

Symptomtext

Within 15 minutes got cold hands & feet, tremors throughout body, lightheaded/dizzy, all over weakness. Stayed at location of vaccine for 2.5 hours and laid down and they monitored my BP, HR, Pulse Oximetry & then went to Urgent Care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Went to Urgent Care and they just checked my vitals, blood sugar and Basic Chemisrty Panel. I am still waiting to be seen by my PCP on 12/8/21.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Prozac, Claritin, Vit D/K2, Vit C, Biotin, Digestive enzymes, Curcumin, Fish Oil, Magnesium, Cranberry Concentrate, Iron
Allergien: Sulfa, Macrobid, Amoxicillin, Cipro, Benzoyl Peroxide
Vorherige Impfungen: -

VAERS 1906038

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 46,0
Geschlecht: M
Eingang: 29.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Flushing Paraesthesia oral Throat tightness

Symptomtext

flushing, tongue tingling, sensation of throat closing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: hearing loss, vertigo, GERD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1905993

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MO
Alter: 55,0
Geschlecht: U
Eingang: 29.11.2021
Impfdatum: 25.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Asthenia Chest discomfort Chest pain Chills Dizziness Headache Injection site pain Joint swelling Lymphadenopathy Musculoskeletal stiffness Myalgia Pain Ultrasound scan normal

Symptomtext

10/26/21 - temp, body aches, chills, stiff neck, HA muscle aches. 10/27/21 - chest heaviness with fluttering feeling, dizziness. 10/28/21 - continuous pain in right arm, swelling in right axilla. 11/1/21 - weakness, continuing symptoms that began 10/26/21. 11/16/21 - temp, chills, achy, HA, dizziness. 11/26/21 - episodes of chest pain/fluttering with dizziness several times a week, fatigue and body aches daily, joint swelling of right wrist, right shoulder, left ankle, left knee and left hip.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Only testing disclosed was a ultrasound to detect a blood clot on 11/12/21 which was negative.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: TDAP
Vorherige Impfungen: -

VAERS 1905993

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MO
Alter: 55,0
Geschlecht: U
Eingang: 29.11.2021
Impfdatum: 25.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia Chest discomfort Chest pain Chills Dizziness Headache Injection site pain Joint swelling Lymphadenopathy Musculoskeletal stiffness Myalgia Pain Ultrasound scan normal

Symptomtext

10/26/21 - temp, body aches, chills, stiff neck, HA muscle aches. 10/27/21 - chest heaviness with fluttering feeling, dizziness. 10/28/21 - continuous pain in right arm, swelling in right axilla. 11/1/21 - weakness, continuing symptoms that began 10/26/21. 11/16/21 - temp, chills, achy, HA, dizziness. 11/26/21 - episodes of chest pain/fluttering with dizziness several times a week, fatigue and body aches daily, joint swelling of right wrist, right shoulder, left ankle, left knee and left hip.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Only testing disclosed was a ultrasound to detect a blood clot on 11/12/21 which was negative.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: TDAP
Vorherige Impfungen: -

VAERS 1904693

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: HI
Alter: 48,0
Geschlecht: F
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: nein

Abdominal distension Asthenia Back pain Bowel movement irregularity Burning sensation Cough Discomfort Dyspnoea Eating disorder Feeling of body temperature change Insomnia Mobility decreased Pain Pelvic pain Pollakiuria Pyrexia Respiratory tract congestion Throat irritation

Symptomtext

At 22:00 hrs on the 24th (my shot was at 11:30 am that day), I started having a fever, my entire body was in great pain, it felt like fire ants or acid running through my veins, and cement in my lymphatic system. Completely unable to sleep, weak as a kitten. Maximum recorded temperature: 103 F. Freezing cold, boiling hot, swollen abdomen, out of breath, very frequent urination & inconsistent bowel movements. Fever persisted until later in the morning of the 28th. However, the evening of the 25th a tremendous pain in my lower back & pelvis became overwhelming - as of writing this still persists. I have only been able to lie down on my back for most of the time. My whole abdomen has been swollen out of proportion & I've had difficulty eating - as of writing this still persists. Congestion, a chesty cough, & tickly throat. Normally, I am very athletic swimming 3 km a day, cycling to commute, and diving. I've been 90% bed-ridden since the evening of the 24th & am very concerned for my welfare, particularly my abdomen and lower back pain, which is uncompromising. I do not earn enough money for health insurance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None - I do not have the finances for health insurance or health treatment.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Dairy, Alcohol, do not take any medications.
Vorherige Impfungen: When I was a child. My last vaccination was at age 12, where I was hospitalised. I'm from another country & the medical records

VAERS 1894439

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NY
Alter: 47,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Hyperhidrosis Hypoaesthesia Nausea Paraesthesia Tremor Vomiting

Symptomtext

Patient developed body wide tremor, lightheaded, dizzy, diaphoretic, nausea, vomiting, numbness and tingling bilateral hands and feet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: unknown transferred to ED
Aktuelle Erkrankungen: Leiomyosarcoma stage 3
Vorgeschichte: Leiomyosarcoma stage 3
Andere Medikamente: yes prescription
Allergien: yes medication and seasonal
Vorherige Impfungen: -

VAERS 1893872

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: PA
Alter: 49,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 02.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Chills Dizziness Headache Heart rate increased Hyperhidrosis Hypertension Hypoaesthesia Muscle spasms Nausea Oropharyngeal pain Pain Palpitations Pyrexia

Symptomtext

WEDNESDAY -NOVEMBER 3RD-HEADACHE,SORE THROAT,BODY ACHES,MUSCLE SPASM,CHILLS, FEVER,FEEL NAUSEOUS THURSDAY- NOVEMBER 4TH TO NOVEMBER 6TH-HEART PALPITATIONS, ,SWEATING IN UNDERARMS, FEET AND HANDS SUNDAY - NOVEMBER- 7TH- NUMBNESSIN LEFT THUMB DIZZINESS HIGH BLOOD PRESSURE AND HEART RATE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: HOSPITAL EMERGENCY
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: AIRBORNE VITAMIN C ,D3 ,ZINC ,
Allergien: PENICILLINS
Vorherige Impfungen: -

VAERS 1893250

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NJ
Alter: 65,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 10.10.2021
Beginn: 10.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Body temperature COVID-19 Dehydration Drug ineffective Electrocardiogram Immunisation Pain in extremity Polyuria SARS-CoV-2 test Sinus pain X-ray

Symptomtext

Since the vaccination, has the patient been tested for COVID-19?:Yes/Positive; Since the vaccination, has the patient been tested for COVID-19?:Yes/Positive; sore arm; sinus pain; sinus pain; dehydration; Booster; This is a spontaneous report from a contactable consumer (patient). A 66-year-old male patient received bnt162b2 (COMIRNATY), via an unspecified route of administration, administered in Arm Left on 10Oct2021 12:00 (Batch/Lot Number: FE3590) at the age of 66-year-old as dose 3 (booster), single; via an unspecified route of administration administered in Arm Left on 06Mar2021 17:00 PM (Batch/Lot Number: EN6205) at the age of 65-year-old as dose 2, single, via an unspecified route of administration administered in Arm Left on 17Feb2021 17:00PM at the age of 65-year-old (Batch/Lot Number: EM9809) as dose 1, single for covid-19 immunisation. Medical history included enlarged prostate, kidney stones from an unknown date and unknown if ongoing. Concomitant medications included influenza vaccine (FLU) taken for immunisation on 24Sep2021 in Left arm; rosuvastatin calcium (CRESTOR, 10 miligrans) taken for an unspecified indication, start and stop date were not reported. The patient experienced since the vaccination, has the patient been tested for covid-19:yes/positive on 19Oct2021, The events was reported as serious per medically significant. The patient also experienced headache, sore arm, 100 fever, scratchy throat, excessive cough, sneezing, heavy phlegm, sinus pain, excessive urination, dehydration on 12Oct2021 07:00. Therapeutic measures were taken as a result of these events, outpatient clinic visit, outpatient hospital visit for IV fluids, Xray, EKG (Electrocardiogram). The events resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care. The patient underwent lab test which included fever: 100 on 12Oct2021, EKG: unknown results on 12Oct2021, Sars Cov 2, NAA: positive on 19Oct2021 (Nasal Swab, NAA; Positive CoronavirusOC43), x-ray: unknown results on 12Oct2021. The outcome of events since the vaccination, has the patient been tested for covid-19:yes/positive was unknown, for other events was resolving. Facility where the most recent COVID-19 vaccine was administered was Pharmacy or Drug Store. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient hasn't been tested for COVID-19. Not known allergies. Investigation results of BNT162B2 for lot EN6205: BNT162 covid-19 vaccine suspension for intramuscular 2ml multiple dose vial x 1. Lot number: EN6205. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZERBIONTECH COVID-19 VACCINE lot EN6205 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot and product type. The final scope included the reported finished goods lot EN6205, fill lot EN5337, and the formulated drug product lot EN5326. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. Investigation results of BNT162B2 for lot EM9809: Compound BNT162 covid-19 vaccine suspension for intramuscular 2ml multiple dose vial x 1; Lot number: EM9809. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZERBIONTECH COVID-19 VACCINE lot EM9809 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot EM9809, fill lot EM9807, and the formulated drug product lot EM9805.A complaint sample was not returned, and photographs were not received. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: Test Date: 20211012; Test Name: fever; Result Unstructured Data: Test Result:100; Test Date: 20211012; Test Name: EKG; Result Unstructured Data: Test Result:unknown results; Test Date: 20211019; Test Name: Sars Cov 2, NAA; Test Result: Positive ; Comments: Nasal Swab NAA; Positive CoronavirusOC43; Test Date: 20211012; Test Name: Xray; Result Unstructured Data: Test Result:unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Enlarged prostate; Kidney stones
Andere Medikamente: CRESTOR
Allergien: -
Vorherige Impfungen: -

VAERS 1890042

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: IL
Alter: 56,0
Geschlecht: M
Eingang: 22.11.2021
Impfdatum: 18.02.2021
Beginn: 20.11.2021
Tage bis Beginn: 275,0
Dosis: 2
Route/Site: IM / -

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

Mental status changes Pneumonia

Symptomtext

Altered mental status changes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: Pneumonia
Aktuelle Erkrankungen: -
Vorgeschichte: PMHx of hypertension, Bell's palsy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1888789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3590

moderat

Staat: OK
Alter: 27,0
Geschlecht: F
Eingang: 21.11.2021
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Dyspnoea Throat tightness

Symptomtext

Chest pain Shortness of breath/ tightening of airway

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Aneurysm Autoimmune
Andere Medikamente: None
Allergien: codeine
Vorherige Impfungen: -

VAERS 1887793

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: KY
Alter: 29,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 06.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Arthritis reactive Immunisation Palpitations SARS-CoV-2 test

Symptomtext

reactive arthritis in both hands; heart palpitations; booster; This is a spontaneous report from a contactable other HCP (patient). A 29-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 3 via an unspecified route of administration, administered in Arm Right at the age of 29-year-old on 06Oct2021 (Lot Number: FE3590) as DOSE 3 (BOOSTER), SINGLE for COVID-19 immunisation. Facility where the most recent COVID-19 vaccine was administered was Pharmacy or Drug Store. Medical history included none (other medical history: No). Prior to vaccination, the patient was not diagnosed with COVID-19. No Known Allergies. Patient was not pregnant. The patient's concomitant medications were not reported. The patient previously took first dose BNT162B2 (Batch/Lot No: Ez0140, Location of injection: Arm Right) at the age of 28-year-old on 28Dec2020 for COVID-19 immunization, second dose BNT162B2 (Batch/Lot No: EL3248, Location of injection: Arm Right) at the age of 28-year-old on 18Jan2021 for COVID-19 immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient had experienced reactive arthritis in both hands since the day after receiving patient's booster. Patient also had heart palpitations that were occurring consistently post vaccine, but now only happen intermittently. The reactive arthritis has not lessen in intensity or frequency. Adverse event start date 07Oct2021. AE resulted in: [Disability or permanent damage]. The patient underwent lab tests and procedures which included sars-cov-2 test: negative on 11Oct2021 (Nasal Swab). No treatment received for events reactive arthritis in both hands and heart palpitations. The outcome of events reactive arthritis in both hands and heart palpitations was not recovered. The outcome of event booster was unknown.; Sender's Comments: Based on available information and the close drug event temporal association, a possible contributory role of suspect product BNT162B2 to the development of event Immunisation, Arthritis reactive, Palpitations cannot be totally 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: Palpitations
Hospital-Tage: -
Labordaten: Test Date: 20211011; Test Name: PCR and Rapid; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: other medical history: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1808317

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3590

moderat

Staat: TX
Alter: 35,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 18.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: - / LA

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

Dyspnoea Fibrin D dimer Fibrin D dimer increased Respiratory tract congestion Fatigue Injection site pruritus Injection site urticaria Pain Pain in extremity

Symptomtext

Chest congestion; Difficulty breathing; Positive d-dine test; This is a spontaneous report from a contactable consumer (patient). A 35-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: Fe3590), via an unspecified route of administration, administered in arm left on 18Oct2021 at 16:45 (at the age of 35-years-old) as DOSE 1, SINGLE for COVID-19 immunisation. Medical history included known allergies: penicillin, wheat and almonds, grass, dust and trees. The patient's concomitant medications were not reported. The patient experienced chest congestion, difficulty breathing and positive d-dine test on 22Oct2021 at 21:30. The events resulted in emergency room/department or urgent care. The patient underwent lab tests and procedures which included fibrin d dimer: positive on an unspecified date. The event chest congestion was assessed as serious and medically significant by the regulatory authority. The outcome of the events was not recovered. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: d-dine test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to grains (Known allergies: Penicillin, wheat and almonds, grass, dust and trees); Allergy to nuts (Known allergies: Penicillin, wheat and almonds, grass, dust and trees); Allergy to plants (Known allergies: Penicillin, wheat and almonds, grass, dust and trees); Dust allergy (Known allergies: Penicillin, wheat and almonds, grass, dust and trees); Grass allergy (Known allergies: Penicillin, wheat and almonds, grass, dust and trees); Penicillin allergy (Known allergies: Penicillin, wheat and almonds, grass, dust and trees)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1886127

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: TX
Alter: 28,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 11.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Electrocardiogram Myalgia

Symptomtext

Muscle soreness at site and chest pain lasting for a few hours and resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: ekg
Aktuelle Erkrankungen: no
Vorgeschichte: HTN
Andere Medikamente: HCTZ, sodium fluoride dentall paste
Allergien: -
Vorherige Impfungen: -

VAERS 1881168

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MS
Alter: 29,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest pain Electrocardiogram Laboratory test

Symptomtext

Patient c/o chest pain after receiving her 1st dose of the Pfizer vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG, cardiac workup
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported
Andere Medikamente: None reported
Allergien: Answered no to the questions
Vorherige Impfungen: -

VAERS 1880463

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: VA
Alter: 66,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / UN

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

Dyspepsia Hypertension Joint stiffness Muscle tightness Neck pain

Symptomtext

3rd Dose Pfizer ? @ 1918 PT reported to Adult Daughter (Translating) tightness in jaw. ? No complaint of airway compromise, no difficulty breathing. ? Safety notified. Escorted to Special Obs., Requested water. ? @1920 PT reported sensation of heartburn, onset of headache, sore neck in back, stiffness in jaw. ? PT HX Diabetes & High BP. ? @ 1926 BP 200/96, PR 76. ? @ 1926 Safety notified Site Director; SD initiated 911 call. ? @ 1934 BP 209/103 PR 82. ? @ 1940 EMS on scene. ? @ 1942 BP 210/98. ? @ 1945 EMS transport to Hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes, Hypertension
Andere Medikamente: Unknown
Allergien: unknown
Vorherige Impfungen: Pfizer COVID19 Vaccination

VAERS 1879649

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: PA
Alter: 32,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 13.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: - / LA

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

Condition aggravated Dysgeusia Parosmia

Symptomtext

It made my improving parosmia and dysgeusia worse; It made my improving parosmia and dysgeusia worse; Condition aggravated; This is a spontaneous report from a contactable consumer, the patient. A 32-year-old male patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FE3590) via an unspecified route of administration in the left arm on 13Oct2021 (at the age of 32-years-old) as a single dose for COVID-19 immunisation. Medical history included COVID-19. The patient had known unspecified allergies. Prior to the vaccination, the patient was diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications were not reported. On 18Oct2021, it was reported that the vaccination made his improving parosmia and dysgeusia worse. 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 it made his improving parosmia and dysgeusia worse was not resolved at the time of this report. The patient also received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: 32030BD) via an unspecified route of administration in the left arm on 03Nov2021 (at the age of 32-years-old) as a single dose for COVID-19 immunisation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Dysgeusia (It made my improving parosmia and dysgeusia worse); Parosmia (It made my improving parosmia and dysgeusia worse)
Vorgeschichte: Medical History/Concurrent Conditions: Allergy (Known allergies: Yes); COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19?: Yes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1879587

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MS
Alter: 38,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Asthenia Blood pressure measurement Dizziness Feeling hot Heart rate Hypertension Nausea Tachycardia

Symptomtext

Blood pressure 155/95/ her blood pressure was going up; tachycardic; hot; dizzy; weak/ weakness; nauseated; This is a spontaneous report from a contactable nurse practitioner. A 38-year-old female patient (Weight: 68.04, Height: 165) received bnt162b2 (COMIRNATY Batch/Lot Number: FE3590; Expiration Date: 30Nov2021, NDC number: 59267100002) via an unspecified route of administration, administered in Arm on 04Nov2021 (at 38-year-old) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included Allergy, had allergies to soy and wheat. Concomitant medication included diphenhydramine. The patient previously took folic acid, Calamine, and calamine;zinc oxide (CALADRY) and experienced allergies. Caller clarifies that she is reporting on a patient, and she was the vaccinator of the patient, but is not a primary care provider for the patient. The patient was sent to the hospital in an ambulance, though it is not known if she was admitted to the hospital. The patient's reaction was that she was tachycardia, her blood pressure was going up, she was hot, dizzy, and weak. The patient was nauseated after two mins after she gave the injection, which was when she started having symptoms. At 4 minutes after injection she gave the patient 50mg of Benadryl PO, and maintained her vitals every few minutes until the ambulance arrived. The patient's blood pressure did come down some, but as far as the patient's dizziness and weakness, that was still the same before she left. Other Medical Conditions: Caller says the only difference for the two medications that patient is allergic to is that one is clear and one is not. On patient's questionnaire she did not report anything abnormal. The nurse considered the events as serious with Seriousness criteria-Other medically important condition. Results of tests and procedures for investigation of the patient included: the highest Blood pressure: 155/95 and Pulse rate: got up to 125 beats per minute, both on 04Nov2021 at 1444. Outcome of reaction/event at the time of last observation: Unknown.; Sender's Comments: As there is limited information in the case provided, the causal association between the events and the suspect drug BNT162B2 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 product and on the conduct of the study 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: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 20211104; Test Name: Blood Pressure; Result Unstructured Data: Test Result:155/95; Comments: at 1444; Test Date: 20211104; Test Name: Pulse rate; Result Unstructured Data: Test Result:got up to 125 beats per minute; Comments: at 1444
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Food allergy
Andere Medikamente: DIPHENHYDRAMINE
Allergien: -
Vorherige Impfungen: -

VAERS 1878348

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: FL
Alter: 38,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 11.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Asthenia Chills Fatigue Migraine Pain Pyrexia

Symptomtext

Severe migraine, chills, body aches, low grade fever, low to no energy for about 24hrs and then for about 3-5days low energy/ fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Heart murmur
Andere Medikamente: Vitamin C, Vitamin D, Zinc, Probiotics, Turmeric, fish oil
Allergien: Cefuroxime
Vorherige Impfungen: Severe migraine

VAERS 1877583

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: IN
Alter: 52,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 12.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / RA

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

Arrhythmia Cardiac monitoring abnormal Electrocardiogram normal Heart rate increased Laboratory test normal Metabolic function test Palpitations Sinus tachycardia Urine analysis

Symptomtext

11/15/21 1804-2030:Irregular heart rhythm and high heart rate 150?s noted on iPhone with palpitations while at home. 911 called to evaluate, cardiac monitor showed sinus tachycardia. BP 170/96 at home.12 lead ekg in ED appeared to be sinus, labs WNL. Discharged home to be evaluated by cardiologist within the next few days. 11/16/21: cardiac monitor placed for 2 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: 11/15/21:12 lead ekg, BMP, urine sample done in the ED. 11/16/21:Currently being monitored on a cardiac monitor for 2 weeks( Body Guardian mini plus).
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, murmur
Andere Medikamente: Multi-vitamin, fish oil and Metamucil
Allergien: None
Vorherige Impfungen: -

VAERS 1876884

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3590

moderat

Staat: NC
Alter: 39,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Computerised tomogram head normal Computerised tomogram thorax abnormal Dyspnoea Endotracheal intubation Gastric ulcer Gastrointestinal examination abnormal Immediate post-injection reaction Lung infiltration Melaena Mental status changes Nausea Oesophagitis Pain in extremity Vomiting

Symptomtext

Immediate mild shortness of breath and arm soreness, worsening overnight. In addition, nausea and vomiting, melena Called EMS next day. Required intubation en route to hospital. Brief IV antibiotics. Discharged on omeprazole with plans for GI following, B12 and iron supplements

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: GI workup revealed esophagitis and gastic ulcer without active bleeding. CT showed infiltrates but no embolism. CT head for altered mental status, negative.
Aktuelle Erkrankungen: possible viral stomach illness
Vorgeschichte: none
Andere Medikamente: none
Allergien: shellfish
Vorherige Impfungen: -

VAERS 1876863

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: IN
Alter: 72,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Asthenia Chills Extra dose administered Headache Muscle spasms Nausea Pain Tremor

Symptomtext

See below

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Starting hours after injection I developed a severe headache and a wave of nausea. Took ibuprofen and headache got better. At 1:42 awoke with headache again hard chills and severe aching and cramps in legs, arms, joints, fingers shoulder and just all over. Took more ibuprofen and a HOT bath and put heating blanket on bed to help with the shaking. Took another hot back but still had weakness in legs arms and body. This lasted allday Tuesday and am still having issues Wednesday but not quite as bad. if there is a 4th booster I will tell you right now I WILL NOT TAKE OT PERIOD
Aktuelle Erkrankungen: -
Vorgeschichte: Breast cancer osteoporosis
Andere Medikamente: Lexapro. Maxcide (water pill).
Allergien: Sulfa.Hydrocodone
Vorherige Impfungen: -

VAERS 1873645

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: OH
Alter: 35,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test normal Chest X-ray normal Chest discomfort Chest pain Dyspnoea exertional Electrocardiogram normal Lymphadenopathy

Symptomtext

Began feeling pain/tightness in chest within 24 hours. Pain was generally more mild in the morning, but progressively got worse over the day. During exercise, pain was very noticeable along with shortness of breath that was not normal to the exercise being performed. Symptoms have persisted for over two weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG, blood tests, and chest X-ray were all normal; no signs of myocarditis, pericarditis, or blood clots. ER doctor diagnosed with chest wall discomfort and lymphadenopathy in the tissues as an immunologic response to the COVID vaccine.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1873343

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: TX
Alter: 69,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Injected limb mobility decreased Injection site bruising Injection site rash Injection site swelling Pain in extremity

Symptomtext

Patient developed a swollen rash at injection site with bruising. Within a couple of days the patients arm became very sore and has been sore for the last month with times she is unable to raise it without assistance. She has been taking Aleve and using Biofreeze on injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1872975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: FL
Alter: 20,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Insomnia Migraine Mobility decreased Myalgia Pain in extremity

Symptomtext

Quick-developing extreme arm and shoulder pain, extreme migraine through the night, sleeplessness, aching muscles that developed around 7PM, inability to lift arm with injection due to pain, migraine through the day following vaccine, continuing muscle and joint pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Anxiety disorder
Andere Medikamente: Venlafaxine
Allergien: Sulfa drugs, nickel, seasonal allergies
Vorherige Impfungen: -

VAERS 1872790

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MO
Alter: 27,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 19.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Axillary pain Lymph node pain Lymphadenopathy Mobility decreased Oedema peripheral

Symptomtext

10/21/21 reported lymph node swelling in neck and right armpit. Stated very sore. 11/10/21 - Per Dr note: Continued pain and swelling since vaccination of right armpit. Steroids prescribed which caused increased blood sugar issues. He noted "softball size lymphadenopathy" that resulted in pain and reduced use of right arm. Continues to be treated by her PCP with next appt on 11/17/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1872247

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 23.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Dyspnoea Hypersensitivity Palatal swelling SARS-CoV-2 test Swollen tongue

Symptomtext

Allergic reaction; Swelling of tongue, roof of mouth; Swelling of tongue, roof of mouth; Shortness of breath; This is a spontaneous report from a contactable consumer (patient). A 59-year-old (age at vaccination) non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in Arm Left on 23Oct2021 13:00 (Batch/Lot Number: FE3590) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included known allergies: Shellfish, Iodine. Concomitant medications included losartan and atorvastatin calcium (LIPITOR) taken for an unspecified indication, start and stop date were not reported. On 23Oct2021 13:30, the patient experienced allergic reaction-swelling of tongue, roof of mouth and shortness of breath. The patient underwent lab tests and procedures which included sars-cov-2 test: negative on 27Oct2021 Nasal Swab. Therapeutic measures were taken as a result of the events which included treatment with EPIPEN. The patient did not recover from the events. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20211027; Test Name: PR SARSCOV2 AMP PRB; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Iodine allergy (known allergies: Iodine); Shellfish allergy (known allergies: Shellfish)
Andere Medikamente: LOSARTAN; LIPITOR
Allergien: -
Vorherige Impfungen: -

VAERS 1871122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: SD
Alter: 38,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 27.10.2021
Beginn: 03.11.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: SYR / RA

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

Feeling hot Mobility decreased Pain in extremity Pyrexia

Symptomtext

Bad soreness in the right arm after injection that lasted for about 2 days; the soreness after 24 hours was really bad in particular, I could barely lift my arm (the best way to describe it is as if someone took a brick and punched me with it). Arm soreness is a common side effect though after this shot, but I thought I would still mention it. On Nov. 3rd, 2021, one week after the first shot, for no longer than up to 2 hours in the evening starting at about 6:15 pm and lasting until approximately 8pm, I felt a slight tinge of a fever. Warm forehead and cheeks. It was very, very mild. No other symptoms were present. Treatment: Rest and Sleep; Arm soreness eventually went away on its own Outcome: No further complications

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: None
Vorgeschichte: Anxiety Depression
Andere Medikamente: Clonazepam
Allergien: Cephalexin, Cephalexin Penicillin
Vorherige Impfungen: -

VAERS 1869016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

moderat

Staat: IN
Alter: 58,0
Geschlecht: M
Eingang: 15.11.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Paraesthesia

Symptomtext

Systemic: Tingling (specify: facial area, extemities)-Medium, Additional Details: Tingling in upper arm and forearm of injection arm. Advised patient to call doctor

Weitere VAERSDATA-Felder

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

VAERS 1868455

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NY
Alter: 51,0
Geschlecht: M
Eingang: 14.11.2021
Impfdatum: 20.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / RA

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

Blood pressure increased Condition aggravated Diarrhoea Electrocardiogram normal Extra dose administered Neck pain Tachycardia

Symptomtext

I received a booster dose of Pfizer COVID 19 vaccine on 10/20/2021. I had the following adverse effects: 1. Tachycardia, started 1 day after vaccination. 2. Worsening of my chronic neck pain, started 4 days after vaccination. 3. Elevated blood pressure, started 6 days after vaccination. 4. Diarrhea, two episodes within one week of the vaccination. I did not have these adverse effects after the first two doses of the vaccine. I took Aleve a few times within the first two weeks to control neck pain. Then, starting two weeks from the vaccination, I started taking Aleve on a regular basis, 220 mg two times a day. Tachycardia improved several days after onset and went away on week 3. Elevated blood pressure improved several days after onset but I was advised by my doctors that I have chronic hypertension anyway and may need to start blood pressure medications. Neck pain improved on week 3.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 1. Heart rate 110 one day after vaccination, 90-100 on days 2-4. 2. Blood pressure around 135/100 on day 6 after vaccination. 3. EKG - I was told that my EKG was normal. 4. Echocardiogram - I was told it was normal except for signs that may be related to chronic hypertension.
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic neck pain Chronic rhinitis Meniscus tear
Andere Medikamente: Vitamin D 2000 units/day Rhinocort nasal spray
Allergien: -
Vorherige Impfungen: -

VAERS 1865963

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE 3590

moderat

Staat: CT
Alter: 50,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 04.10.2021
Beginn: 11.11.2021
Tage bis Beginn: 38,0
Dosis: 3
Route/Site: IM / LA

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

Chest X-ray normal Condition aggravated Cough Full blood count normal Productive cough

Symptomtext

Progressively Worsening cough and productive sputum

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Pulmonology visit, CXR (normal), CBC (normal), AFB pending, CT Chest pending, Sweat test pending, possible bronchoscopy is contemplated.
Aktuelle Erkrankungen: None
Vorgeschichte: Intermittent Bronchorrhea, Intermittent cough, Question Asthma/COPD
Andere Medikamente: Vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 1865310

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: KY
Alter: 61,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 26.10.2021
Beginn: 10.11.2021
Tage bis Beginn: 15,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Dyspnoea SARS-CoV-2 test negative SARS-CoV-2 test positive

Symptomtext

Presented w/ c/o shortness of breath. Pt diagnosed w/ COVID on 10/29. Tested negative for COVID on Wednesday (11/10). Symptoms initially developed 1-2 weeks prior to admission. Repeat COVID test (+) on 11/10 at our facility. Initial room air saturation 78%; on 3L oxygen at admission.

Weitere VAERSDATA-Felder

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

VAERS 1861866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 77,0
Geschlecht: M
Eingang: 11.11.2021
Impfdatum: 28.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Chills Dyspnoea Pain Productive cough Pyrexia Rales Sputum discoloured

Symptomtext

PRN visit for complaint of SOB, productive cough, body aches and chills. Febrile (101.9). Temporal crackles in all lobes. Spouse reported productive cough with brown sputum x2 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Orders obtained for azithromycin with probiotic added for support. Acetaminophen suppository given.
Aktuelle Erkrankungen: -
Vorgeschichte: Acute combined systolic (congestive) and diastolic (congestive) heart failure
Andere Medikamente: Atorvastatin, Carbamazepine, Colchicine, Senna-S, Allopurinol, Furosemide, Floranex, Famotidine, Clonazepam, Diltiazem, Aspirin, Potassium chloride, Metropolis, Calcium
Allergien: NKA
Vorherige Impfungen: -

VAERS 1861020

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 45,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Paraesthesia Pruritus

Symptomtext

Approximately 3 minutes after vaccination patient felt tingling all over and itchiness. No raised red areas noted to body. Pt also felt dizziness. Denied any chest pain, shortness of breath or other respiratory issues. 11:14 pt was given benedryl 25mg. Vials 138/72 99% room air HR 100. 11:18 Pt states she is feeling better. PT denied need for EMS transport.

Weitere VAERSDATA-Felder

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

VAERS 1860853

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: FL
Alter: 59,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea Feeling hot Flushing Heart rate increased Palpitations

Symptomtext

Shortness of breath Palpitations, heart rate over 100 Flush warm feeling All lasted a few hours approx 12-3pm on 10/30/2021 , the day after the vaccination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Foot ankle surgery , 10/12/2021
Vorgeschichte: High BP , high cholesterol
Andere Medikamente: Lisinopril,lovastatin , fish oil , vit d , fenofibric acid, baby asa
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1857739

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MI
Alter: 23,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 09.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Cough Dyspnoea Muscle spasms Musculoskeletal pain Swollen tongue

Symptomtext

patient slept fine through the night, but woke up experiencing cough and trouble breathing as well as a muscle spasm/soreness between her shoulder blades. She also thought her tongue felt as though it might be swollen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: No Known Drug Allergies
Vorherige Impfungen: -

VAERS 1857153

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 25,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: UN / LA

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

Chest discomfort Chest pain Dyspnoea

Symptomtext

Chest pain, shortness of breath, chest tightness

Weitere VAERSDATA-Felder

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

VAERS 1854532

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 27.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Interchange of vaccine products Oral herpes

Symptomtext

I got a cold sore inside the right nostril of my nose. The same thing happened after the second dose of the Moderna vaccine. Although I get cold sores, they are always on my top lip, never inside my nostril. I noticed it after the Moderna vaccine as well. When it happened again with the Pfizer vaccine, I decided to report it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Herpes Simplex - I get a cold sore on my lips once every two-three years
Andere Medikamente: Prolensa eye drops for dry eye
Allergien: Food sensitivities to dairy and wheat
Vorherige Impfungen: Moderna, second dose 02/16/21 same reaction

VAERS 1854504

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 30,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 09.10.2021
Beginn: 10.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Back pain Dizziness Exposure during pregnancy Fatigue Haemorrhage Injection site hypoaesthesia Injection site paraesthesia Loss of personal independence in daily activities Migraine Nausea Pain Sleep disorder

Symptomtext

It started around 2 am the next day. I woke up in the middle of night, feeling dizzy and nauseous and body aches all over. My left arm was numb and tingly. I overall felt like I had the flu, but as if I was having an allergic reaction. It felt similar to the past reaction to a medicine I'm allergic to. I felt fatigue, and unable to do anything. I had a migraine and lower back pain. This lasted about 2 to 4 days. It was very similar to the Sectrum medicine I mentioned under my allergies. I had a couple of doctor appointments. No lab test just the doctors thought I had nerve damage. They put me in a vitamin called alphalypoticacid. This has been helping me. I'm still experiencing the numbness in my arm but most of the symptoms have gone away. This was my first pregnancy, I found out on October 30th that I was pregnant. I was about six weeks pregnant. I had cramping on Nov 1st. My htg levels were going down and being monitored by my doctor and with bleeding on Nov 5th

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site paraesthesia
Hospital-Tage: -
Labordaten: No lab test done.
Aktuelle Erkrankungen: None
Vorgeschichte: I have chronic Migraines Upper back pain.
Andere Medikamente: Folic acid once day its a tablet calcium supplements once day It's a gummy chew Hair skin & nail vitamins once day its a tablet I had a routine injection given to me 1 week before the vaccine It's an allergy injection (its for cats, dogs
Allergien: I'm allergic to two medication Sectrum Sofascore I'm allergic to Plantains Coffee Trees Grass Dogs Cat Dust
Vorherige Impfungen: The flu vaccine has given me very similar effects to how I reacted to the pfizer vaccine.

VAERS 1853918

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: WI
Alter: 42,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest pain Dyspnoea Musculoskeletal pain Urticaria

Symptomtext

Hives, trouble breathing, pain between shoulder blades/ chest pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin, morphine, apples, strawberries, melons
Vorherige Impfungen: -

VAERS 1853861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: IL
Alter: 31,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Extra dose administered Fall Fatigue Hyperhidrosis Migraine Nausea Neuralgia Photophobia Pyrexia Vomiting

Symptomtext

At 11:00 PM, 12 hours after the booster,, l became very nauseous and dizzy. I stood up to go to the restroom to vomit, and immediately collapsed and almost lost consciousness. Stuck on the floor, I began to feel intense shooting nerve pain in both of my arms, and broke out into an extremely intense sweat. I became hypersensitive to light, and felt like I was going to faint if I moved. I dialed emergency number. At the ER, I was treated with an anti-inflammatory injection, and with an injection of a migraine medication. I slowly began to feel better, and the next day had just a fever and fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Sleep apnea
Andere Medikamente: Vyvanse, sertraline
Allergien: Avocado, pecans, macadamia nuts
Vorherige Impfungen: -

VAERS 1851142

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: PA
Alter: 34,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Arthralgia Chills Diarrhoea Dizziness Erythema Fatigue Feeling hot Gait disturbance Impaired work ability Influenza virus test negative Mobility decreased Myalgia Nausea Pain Pain in extremity Peripheral swelling Pruritus Pyrexia

Symptomtext

About 2 hours after receiving the vaccine, my arm became very sore and red. I started feeling dizzy and light headed so I went to bed. I woke up around 1am and I could not move my arm. It was hot to the touch, red swollen and itchy. I had fever of 101 and could barely walk to the bathroom. For the next week I experienced, nausea, vomiting, diarrhea, fatigue, dizziness, fevers ranging from 99-101.9, chills, muscle and joint pain. body aches. I could barely move my arm or even get around my house. I could not work. I eventually called my doctor and made an appt, she said that there was not much she could do besides test me for flu and covid, and give me nausea medicine. As her and I both knew I was going to react to the vaccine but I did not have a choice in getting in it. She was not allowed to write me an exemption either.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Flu and covid- both negative
Aktuelle Erkrankungen: Acute Cholecystitis
Vorgeschichte: Reflux disease, PTSD, Anxiety, Migraine with Aura, Depression, Iron deficiency, Acute Cholecystitis,
Andere Medikamente: Escitalopram 20mg daily, lamoTRIgine 100mg daily, Topiramate 50mg 2x daily, SUMAtriptan 100mg prn x2, ferrous gluconate daily magnesium oxide daily, lansoprazole 30mg daily , dicyclomine 10mg 2x daily, Yaz,
Allergien: Azithromycin, Citalopram, Hydrocodone-Acetaminphen, Phentermine, Flu Vaccines, Gluten, Eggs, Seasonal allergies
Vorherige Impfungen: Flu vaccine- very allergic to it

VAERS 1850912

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NY
Alter: 75,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 23.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

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

Arthralgia Blindness Chest pain Chills Headache Pain in extremity Pyrexia

Symptomtext

Pt. states that after receiving the 3rd Booster of Phizer 10/23/2021, started experiencing symptoms that evening of loss of vision (both), chest pain, pain in the hips and feet, fever (101.0), headache, and chills. Self-treating with (Advil, Aleve, Tylenol) no relief, still continuing to experience symptoms. No noted Primary visit/communications.

Weitere VAERSDATA-Felder

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

VAERS 1850868

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MS
Alter: 38,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain Asthenia Blood pressure increased Chest discomfort Chest pain Confusional state Dizziness Hypertension Nausea Tachycardia

Symptomtext

Systemic: Abdominal Pain-Mild, Systemic: Chest Tightness / Heaviness / Pain-Mild, Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Hypertension-Medium, Systemic: Nausea-Medium, Systemic: Tachycardia-Medium, Systemic: Weakness-Medium, Additional Details: Pt reported symptoms within 2 minutes of injection. Benadry 50 mg po given. vitals obtained. BP increased to 165/95 and p118. consulted with pharmacist. 911 called. pt chose to go to the hospital injection given at 1429, reported symptoms at 1431, 1433 benadryl given, 1440 911 called, 1453 ems arrives, 1501 pt leaves via ambulance.

Weitere VAERSDATA-Felder

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

VAERS 1850486

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CO
Alter: 37,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 09.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Nausea Pneumonia Pyelonephritis Vomiting

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA: patient hospitalized for pyelonephritis, pneumonia, and recurrent nausea and vomiting after receiving vaccination. Received antiemetics, antimicrobials, and supportive care. Discharged to home medically stable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: two hospitalizations for nausea/vomiting, hematuria, elevated creatinine, pyelonephritis, gastroparesis, pneumonia, sepsis, abdominal pain, hypoxia
Vorgeschichte: hyperlipidemia, SVT, prolonged QT, lower extremity venous thromboembolism, hyperparathyroidism, copper deficiency, hiatal hernia, vomiting, abdominal pain, kidney transplant, CKD, iron deficiency anemia, chronic back pain, seizure disorder, asthma, OSA, head trauma
Andere Medikamente: apixaban, azathioprine, Symbicort, calcitriol, calcium acetate, cyclosporine, diclofenac, duloxetine, vitamin D2, famotidine, iron, Flonase nasal, fosfomycin, gabapentin, levalbuterol, lidocaine patch, loratadine, memantine, metazalone, met
Allergien: adhesive, buppropion, phenytoin, levetircetam, tacrolimus, mycophenolate
Vorherige Impfungen: -

VAERS 1849627

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: FL
Alter: 32,0
Geschlecht: F
Eingang: 07.11.2021
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

Dyspnoea Palpitations Pharyngeal swelling Throat tightness

Symptomtext

1 minute after vaccine injection throat closed, feeling difficulty breathing and swollen throat for a few hours. Palpitations for 3 hours after injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: vitamin D, ferrous sulfate
Allergien: caffeine, dust mites, polen
Vorherige Impfungen: -

VAERS 1848878

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 63,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Arrhythmia Chest discomfort

Symptomtext

About 1 hour after dose, I started having severe arrhythmia which lasted over 2 hours. (no pain in my chest). It seemed to be much stronger when I laid down. I was getting ready to go to ER, when as fast as they came on...they went away. After that, I had discomfort in my chest and slight arrhythmia's for a few weeks. My 2nd dose of Pfizer didn't cause this but it did give me a temp of 103.8 so am I allergic to Pfizer? It is important that you know that I was never nervous to get the booster as I believe this is the answer to getting us out of this mess.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: kidney disease, Hashimotos, Ulcerative Colitis
Andere Medikamente: Levothyroid, Wellbutrin, Vit D, Fish Oil
Allergien: none
Vorherige Impfungen: fever of 103.8

VAERS 1848698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3590

moderat

Staat: OH
Alter: 17,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 13.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Condition aggravated Fatigue Gallbladder disorder Lymph node pain Lymphadenopathy

Symptomtext

Gall Bladder attack starting at about 8pm. Normally attacks are gradual and start over a course of days, increasing in intensity. No symptoms of attack in morning, had vaccine, attack starting around 8pm. Attack was about a 7 out of 10, so not the worst. Also, lymph nodes started to swell under armpit day after, very painful. Stayed swollen for about 7 days. She is also very very tired, even weeks after.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None taken.
Aktuelle Erkrankungen: None
Vorgeschichte: Gall bladder Anxiety
Andere Medikamente: Buspar Birth control Fluexotine
Allergien: None
Vorherige Impfungen: -

VAERS 1846532

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: TX
Alter: 34,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Hypoaesthesia Paraesthesia

Symptomtext

Pt experienced Dizziness, light haded, numbness and tingling. Nurse attended cleared.

Weitere VAERSDATA-Felder

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

VAERS 1845954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: VA
Alter: 17,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Blood test normal Cardiac disorder Cardiac function test abnormal Chest X-ray normal Chest discomfort Crying Dyspnoea Electrocardiogram normal Muscle disorder

Symptomtext

When she woke up that morning after, she came to me crying of chest discomfort and difficulty breathing. I took her to the Emergency Room, they did a chest x-ray and EKG. They came back normal, they said it was a vaccine reaction. They gave her Tylenol and Ibuprofen, she took it alternating, but the pain did not go away. It came back a couple of days later. I called her pediatrician, they said to take her to the emergency room. I took her to the Emergency Room. They did bloodwork EKG to check the functioning of her heart to check for damages. They said the vaccine has caused some issues to the muscles around and behind and behind her heart also the center of her chest behind her ribs. They said to keep using the previous medications but the pain she has was not relieved. She was Still having difficulty breathing. The doctor just gave her Naproxen because the other medications were not helping. She went to school today but is still having discomfort in her chest. Second doctor seen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Chest X-Ray EKG Bloodwork
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: Bananas Coconut Cantaloupe
Vorherige Impfungen: -

VAERS 1845751

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

moderat

Staat: MO
Alter: 33,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 12.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / AR

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

Alopecia Palpitations

Symptomtext

Systemic: hair loss. palpitations-Medium

Weitere VAERSDATA-Felder

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

VAERS 2576977

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 38,0
Geschlecht: M
Eingang: 04.11.2021
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: nein

Headache Myalgia Pain Palpitations

Symptomtext

Myalgia Occasional p[alpitations; body aches and headaches at night and conitnued for two days Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: yes, similar with dose #1

VAERS 1843526

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

moderat

Staat: IN
Alter: 37,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Arrhythmia Blood thyroid stimulating hormone Cardiac stress test Chest X-ray Computerised tomogram thorax Echocardiogram Electrocardiogram ambulatory Full blood count Metabolic function test Palpitations Troponin

Symptomtext

Heart palpitations, heart arrhythmia (Non-sustained Ventricular Tachycardia)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: CTA of chest, chest x ray, tsh, troponin, cbc, bmp, magniesum, holter monitor, Echocardiogram, stress test
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Vyvanse
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1843285

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: PA
Alter: 44,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 15.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: IM / LA

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

Adenovirus test Angiogram cerebral normal Arteriogram carotid normal Bordetella test negative COVID-19 Chest X-ray normal Chlamydia test negative Computerised tomogram head normal Condition aggravated Coronavirus test negative Diffusion-weighted brain MRI normal Echocardiogram Echocardiogram abnormal Ejection fraction normal Enterovirus test negative Hemiparesis Human metapneumovirus test Human rhinovirus test

Symptomtext

ED to Hosp-Admission Discharged 10/28/2021 - 10/30/2021 (2 days) Hospital MD Left-sided weakness Hospital Diagnosis Left-sided weakness Hospital Course 44-year-old female with hypertension, Crohn's disease, admitted on 10/28/2021 for left arm and leg weakness. Patient had recently received the Covid vaccine on 10/15/21. Noted onset of Covid symptoms including sore throat around 10/25/21. On 10/28/2021, patient noted left arm and leg weakness. Came to the hospital for further evaluation. Symptoms were concerning for stroke and she received TPA. CT angiogram head/neck without stenosis. Follow-up MRI luckily without stroke. Echocardiogram with EF 60 to 65%. No significant wall motion abnormalities. Neurology was consulted. Recommend continuing aspirin 81 mg and atorvastatin 40 mg nightly. Follow-up with neurology as outpatient. Patient does report a prior history of migraines more than 20 years ago. Denied any headache or migraine symptoms with this episode. Does report that she is under some stress, but this would be a diagnosis of exclusion. PT/OT cleared for discharge to home. Does still have some minimal left arm and leg weakness. Have ordered outpatient physical therapy. On discharge, patient is satting well on room air, feels well to go home. Given instructions on COVID care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: 10/28/2021 1216 Respiratory virus detection panel Collected: 10/28/21 1216 | Final result | Specimen: Swab from Nasopharynx Adenovirus Not Detected Mycoplasma pneumoniae Not Detected Chlamydophila pneumoniae Not Detected Parainfluenza Not Detected COVID-19 SARS-CoV-2 Overall Result Detected Critical Enterovirus/Rhinovirus Not Detected Coronavirus Not Detected Respiratory Syncytial Virus Not Detected Influenza A Not Detected Bordetella pertussis Not Detected Influenza B Not Detected Bordetella parapertussis Not Detected Metapneumovirus Not Detected Transthoracic echo (TTE) limited Resulted: 10/29/21 1406 Order Status: Completed Updated: 10/29/21 1409 LVIDd 4.00 3.7 - 5.6 cm LVIDs 2.80 2 - 3.8 cm IVSd 1.00 0.6 - 1.1 cm LVPWd 1.10 0.6 - 1.1 cm LADs 2.10 1.9 - 4 cm LVOT diameter 2.00 cm Aortic Root (2.0-3.7) 2.70 cm TR max PG 17.30 mmHg TR max vel 207.70 cm/sec Narrative: FINALIZED REPORT TWO-DIMENSIONAL ECHOCARDIOGRAPHIC FINDINGS LEFT VENTRICLE: Normal LV size and function. EF is estimated at 60 to 65%. No regional wall motion abnormality. RIGHT VENTRICLE: RV function is normal AORTIC VALVE: Opens well MITRAL VALVE: Grossly normal TRICUSPID VALVE: Grossly normal PULMONIC VALVE: Grossly normal LEFT ATRIUM: Normal size RIGHT ATRIUM: Normal size AORTIC ROOT: Normal size PERICARDIUM: No effusion INTERATRIAL SEPTUM: No shunt by color Doppler. Saline contrast bubble study was negative for interatrial shunt IVC: Not well seen AORTIC ARCH: Not seen COLOR AND SPECTRAL DOPPLER: No aortic stenosis. No aortic insufficiency. Mild tricuspid regurgitation. Trace mitral regurgitation. Indeterminate diastolic function. RV systolic pressure estimate is 25 mmHg which is within the range of normal FINAL IMPRESSIONS: Normal LV size and function. EF is estimated at 60 to 65%. No regional wall motion abnormality. RV function is normal. No significant valvular abnormalities. Normal right ventricular systolic pressure estimate. No pericardial effusion. Saline contrast bubble study was negative for interatrial shunt. CT head without contrast - Tomorrow Resulted: 10/29/21 1319 Order Status: Completed Updated: 10/29/21 1320 Narrative: CT HEAD WO CONTRAST IMPRESSION: No acute intracranial abnormality. END OF IMPRESSION: INDICATION: Suspected stroke, COVID-19. TECHNIQUE: Helical CT scanning of the head is performed without IV contrast. Multiplanar reformations created and submitted for review. Dose limiting techniques utilized when possible. COMPARISON: Noncontrast head CT yesterday 10/20/2021 FINDINGS: No acute intracranial hemorrhage. No measurable mass or mass effect. Normal gray-white distinction and CSF spaces. No acute or aggressive osseous abnormality; no acute fluid. This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient. MRI brain without contrast Resulted: 10/29/21 1247 Order Status: Completed Updated: 10/29/21 1247 Narrative: MRI BRAIN WO CONTRAST IMPRESSION: There is no acute infarct in the brain. END OF IMPRESSION: INDICATION: Stroke, Covid positive. TECHNIQUE: Axial T1, T2, FLAIR sequence, diffusion-weighted imaging, axial gradient echo sequence, sagittal T1-weighted sequences were obtained. FIELD STRENGTH: 1.5 Tesla COMPARISON: CT 10/29/2021 FINDINGS: There is no acute infarct in the brain. No restricted diffusion on the diffusion-weighted imaging. No intracerebral or subdural hemorrhage. No focal dark signal intensity with blooming effect in the brain on the gradient echo sequences. No mass effect or midline shift. No cerebral edema identified. The ventricular system and basal cisterns are normal. Normal flow-voids of the intracranial vascular structures are well preserved. No focal T2 bright white matter signal abnormality both hemispheres, posterior fossa and brainstem. The craniovertebral junction is normal. The sella and corpus callosum are unremarkable. The paranasal sinuses and mastoid air cells show normal aeration. Both orbits and the optic nerves are unremarkable. This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient. X-ray chest 1 view Resulted: 10/28/21 1547 Order Status: Completed Updated: 10/28/21 1547 Narrative: XR CHEST 1 VW PORT IMPRESSION: No acute cardiopulmonary disease. END OF IMPRESSION: INDICATION: shortness of breath COVID+. TECHNIQUE: Single view of the chest COMPARISON: Chest x-ray 9/5/2017 FINDINGS: No evidence for focal consolidation, pleural effusion, or pneumothorax. The cardiomediastinal silhouette is stable in appearance. The thoracic skeleton appears intact. This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient. CT head without contrast Resulted: 10/28/21 1329 Order Status: Completed Updated: 10/28/21 1329 Narrative: CT HEAD WO CONTRAST IMPRESSION: No acute intracranial abnormality. END OF IMPRESSION: INDICATION: Change in symptoms status post TPA TECHNIQUE: Spiral CT scan through the head from the skull base through the vertex was performed with 5 mm axial reconstructions. Images obtained without contrast. CONTRAST: No contrast was administered. COMPARISON: Same day. FINDINGS: Contrast is identified within the intracranial vasculature. No acute hemorrhage. No acute territorial infarction. Ventricles remain within normal limits and basal cisterns are patent. No extra-axial fluid collections are identified. Paranasal sinuses and mastoid air cells are clear This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient. CT angiogram neck with and without contrast Resulted: 10/28/21 1147 Order Status: Completed Updated: 10/28/21 1147 Narrative: CT ANGIOGRAM NECK W WO CONTRAST IMPRESSION: Unremarkable CT angiography neck. No evidence of internal carotid artery stenosis using the NASCET criteria. END OF IMPRESSION: INDICATION: stroke. TECHNIQUE: Enhanced helical CTA scan of the neck was performed with sequential transaxial images before and after iodinated contrast administration. Coronal and sagittal reconstructions were performed. 3D postprocessing images were obtained and stored. CONTRAST: 130mL of IOHEXOL 350 MG IODINE/ML INTRAVENOUS SOLUTION administered INTRAVENOUS. COMPARISON: None available. FINDINGS: The partially visualized lung apices are unremarkable. The origins of the great vessels and visualized upper thoracic aortic arch are unremarkable. The common carotid arteries are patent bilaterally. The carotid bulb regions are unremarkable. The internal and external carotid artery origins are patent. The cervical internal carotid arteries are patent. Bilateral cervical segments of the vertebral arteries are patent. The basilar artery is well perfused. The source images show no evidence of dissections. The cervical spine is in anatomic alignment. Note: Any estimation of ICA stenosis is based on data which utilizes the distal internal carotid diameter as the denominator for stenosis measurement. This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient. CT brain perfusion with and without contrast Resulted: 10/28/21 1144 Order Status: Completed Updated: 10/28/21 1144 Narrative: CT BRAIN PERFUSION W WO CONTRAST IMPRESSION: Unremarkable cerebral perfusion map imaging. END OF IMPRESSION: INDICATION: stroke. TECHNIQUE: Dynamic CT of the brain is performed after administration of iodinated contrast at 4 mL/sec with perfusion map imaging software for determination of cerebral blood flow, blood volume and mean transit time. CONTRAST: 130mL of IOHEXOL 350 MG IODINE/ML INTRAVENOUS SOLUTION administered INTRAVENOUS. COMPARISON: None available. FINDINGS: The initial noncontrast enhanced images of the head show no areas of abnormal high or low attenuation throughout the brain parenchyma. The perfusion map images show normal cerebral perfusion in the supra and infratentorial regions. There are no areas of hypoperfusion to suggest ischemia or penumbral area. Blood Flow: Normal Blood Volume: Normal Mean Transit Time: Normal This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient. CT angiogram head with and without contrast Resulted: 10/28/21 1144 Order Status: Completed Updated: 10/28/21 1144 Narrative: CT ANGIOGRAM HEAD W WO CONTRAST IMPRESSION: Unremarkable CT angiography of the circle of Willis. END OF IMPRESSION: INDICATION: stroke. TECHNIQUE: Enhanced helical CTA scan of head was performed with sequential transaxial images after iodinated contrast administration including noncontrast images, if performed. Coronal and sagittal reconstructions were performed. 3D postprocessing images were obtained and stored. CONTRAST: 130mL of IOHEXOL 350 MG IODINE/ML INTRAVENOUS SOLUTION administered INTRAVENOUS. COMPARISON: None available. FINDINGS: There is no mass-effect or midline shift. There are no intra or extra-axial fluid collections, intraventricular or intraparenchymal hemorrhages. The ventricles and cisterns are normal. The contrast-enhanced images of the head show no abnormal post contrast enhancement. Bilateral intracranial vertebral arteries, basilar artery, and superior cerebellar arteries are unremarkable. The supraclinoid internal carotid arteries, petrous, cavernous and distal intracranial segments of the internal carotid arteries are unremarkable. The A1 and A2 segments of the anterior cerebral arteries are patent. The anterior communicating artery is unremarkable. The middle cerebral arteries and branches are patent distally. The posterior cerebral arteries are unremarkable. There are no aneurysms or significant atherosclerotic disease noted. There are no arteriovenous malformations seen. This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient. CT head stroke without contrast Resulted: 10/28/21 1140 Order Status: Completed Updated: 10/28/21 1140 Narrative: CT HEAD STROKE WO CONTRAST IMPRESSION: 1. Normal noncontrast brain CT scan. 2. No evidence of acute intracranial hemorrhage or acute cortical-based infarct at this time. END OF IMPRESSION: INDICATION: Stroke TECHNIQUE: Axial images from skull base to vertex of head were obtained. COMPARISON: None available. CONTRAST: No IV contrast was administered. FINDINGS: Ventricles: Normal. Brain parenchyma: Normal. No areas of abnormal high or low attenuation. Midline shift: None. Mass effect: None. Extra-axial collection: None. Calvarium and skull base: Intact. Soft tissues: Normal.
Aktuelle Erkrankungen: -
Vorgeschichte: Nervous Left-sided weakness Aphasia Respiratory Chronic seasonal allergic rhinitis due to pollen OSA (obstructive sleep apnea) Circulatory Benign essential hypertension Hot flash, menopausal PAC (premature atrial contraction) PVC (premature ventricular contraction) Incomplete right bundle branch block (RBBB) Digestive Indeterminate colitis Vitamin D deficiency Regional enterocolitis Ileostomy in place Intestinal malabsorption, unspecified type Genitourinary Postmenopausal atrophic vaginitis Recurrent UTI Vaginal atrophy Kidney cyst, acquired Vaginal discharge Bacterial vaginosis Vulvar abscess Musculoskeletal Kyphosis, acquired Hidradenitis Endocrine/Metabolic Dyslipidemia Hyperglycemia Hypokalemia Hypomagnesemia Hypophosphatemia Hematologic Anemia, unspecified type Other Alkaline phosphatase raised Anxiety Attention-deficit/hyperactivity disorder Insomnia Overweight S/P colectomy Insomnia, unspecified type
Andere Medikamente: aspirin 81 mg chewable tablet atorvastatin (LIPITOR) 40 mg tablet busPIRone (BUSPAR) 15 mg tablet chlorthalidone (HYGROTON) 25 mg tablet cholecalciferol, vitamin D3, 400 unit capsule DULoxetine (CYMBALTA) 60 mg capsule metoprolol tart
Allergien: InfliximabHives / Urticaria, Shortness of breath / Dyspnea, Swelling Oxycodone-acetaminophenHives / Urticaria, Swelling
Vorherige Impfungen: -

VAERS 2597351

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 38,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 12.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Headache Myalgia Tachycardia

Symptomtext

Headache, Myalgia & Tachycardia Narrative: Continues to have prolonged Tachycardia.

Weitere VAERSDATA-Felder

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

VAERS 1840978

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Chest pain Hypersensitivity Nausea Palpitations

Symptomtext

Patient is a 33 year old female who has completed a 45-minute observation period with the following signs and symptoms of an adverse reaction: other - c/o sharp stabbing and pressure chest pain, palpitations, nausea. Pfizer-BioNTech COVID-19 vaccine #1 in series administered. o Action(s) taken: Other - vital signs, monitoring, MD consult o Allergy to COVID-19 vaccine documented in Allergies activity: yes o Patient advised to discuss second dose considerations with a clinician 1249: Pt was observed sitting on chair past her 30 minute observation period which ended at 1248. When asked if she felt well, pt reported sharp chest pain and palpitations. Pt reported feeling symptoms for the last 5 minutes. Pt had reported feeling anxious about receiving vaccine. Stated it was mandated by her employer and that was the only reason she received it. Pt was reassured and instructed on deep breathing and relaxation, however, after a couple minutes she continued to c/o chest pain and palpitations. 1255: Pt taken to HR. Vitals taken. BP 121/74, HR 62 SpO2 100% RA. Pt continues to c/o stabbing CP and now pressure, palpitations and nausea. Pt did report hx of panic attacks during her pregnancy. 1300: Continued reassuring patient. No c/o pruritis, no rash noted, no angioedema, clear breath sounds bilaterally. No c/o SOB, pt able to speak in full sentences without pausing, skin pink and warm. 1304: I have attempted to reach Dr. and no answer. I called reception on 6th floor and they also attempted to reach Dr. No answer. 1305: While I was on the phone pt stated she wanted to leave. Pt declined to wait for provider, declined further monitoring. Stated she just needed to go home and lay down. . Pt was instructed to keep paperwork (EUA and What to Expect After Your Covid 19 Vaccination) in a safe place and to refer to it if she developed any sxs of severe allergic reaction such as swelling of the tongue, throat, face, difficulty breathing, SOB, generalized rash, abdominal pain, vomiting, dizziness and / or palpitations. In which case she should seek immediate medical attention. Pt verbalized understanding. Left ambulatory in no distress. - RN

Weitere VAERSDATA-Felder

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

VAERS 1840610

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 52,0
Geschlecht: M
Eingang: 03.11.2021
Impfdatum: 26.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Diarrhoea Dyspnoea Fatigue Injection site pain Pyrexia Rash Urticaria

Symptomtext

WITH IN 24 HRS: SLIGHT FEVER (REOCCURRING OFF AND ON), FATIGUE, DIARRHEA, SORENESS AT SHOT AREA, HIVES/RASH ON BOTH ARMS, LEGS AND PARTS OF BACK. SHORTNESS OF BREATH. ALL SIDE EFFECTS HAVE BEEING GOING ON SINCE 10/27 - 11/3/2021, MOST HAVE STOPPED OR HAVE GONE DOWN IN LEVEL OF PAIN.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CHF COPD OBESITY
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: PFIZER - SECOND DOSE ONLY (NOT FIRST)

VAERS 1840179

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: PA
Alter: 46,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 19.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Angiogram Computerised tomogram neck Dizziness Feeling of body temperature change Hypoaesthesia Muscular weakness Paraesthesia Scan normal Spinal X-ray Spinal X-ray normal X-ray normal

Symptomtext

After the shot I started to feel dizzy and a hot feeling on my neck. My legs felt weak. The next day I had the normal vaccine side effects. 6 days later I developed numbness and tingling on my left side. My whole left side felt cold. I went to the ER. They did a CT and CTA of my neck and head. Everything was negative. I still have those symptoms on and off. I also went to my PCP and had x-rays done on my back, lumbar and cervical, which did not show anything wrong. Something I found weird is that the nurse that gave me the shot started to rub it very vigorously and she said it was to get it into the muscle faster, which I have never seen before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: CT and CTA of my neck and head, normal. X-rays done on my back, lumbar and cervical, normal
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism GERD
Andere Medikamente: Vitamin D Vitamin C Probiotic Elder berry Zinc Levothyroxine Prilosec
Allergien: Atropine
Vorherige Impfungen: -

VAERS 1839250

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: SD
Alter: 61,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 27.10.2021
Beginn: 02.11.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / UN

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

Bronchoscopy Chest X-ray Mechanical ventilation Pneumonia Respiratory failure Swallow study abnormal

Symptomtext

Six days after receiving vaccine, she developed worsening hypoxemic respiratory failure and pneumonia requiring non-invasive vent support and bronchoscopy for pulmonary toilet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: CXR Bronchoscopy She did have a swallow study that she failed on 11-1-21
Aktuelle Erkrankungen: Acute hospitalization for West Nile encephalitis with respiratory failure
Vorgeschichte: ITP Immunosuppression Recent diffuse NM weakness due to West Nile encephalitis
Andere Medikamente: -
Allergien: PCN, metals
Vorherige Impfungen: -

VAERS 2596747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 30.09.2021
Beginn: 02.09.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Chest X-ray normal Chest discomfort Cough Dyspnoea Dyspnoea exertional Fibrin D dimer Procalcitonin SARS-CoV-2 test SARS-CoV-2 test positive Troponin I normal

Symptomtext

Narrative: COVID infection following COVID vaccine series 02/16, Pfizer, dose #1 0/09, Pfizer, dose #2 09/30, Pfizer, dose #3 09/03 COVID swab, result: detected 09/03 DDIMER result: <0.22 09/03 PROCALCITONI result: <0.05 09/03 SARS-COV-2 Variant Sequencing result: pending 09/03 TROPONIN I result: <0.016 09/03 pt cc: cough, chest tightness, and shortness of breath on exertion. exposure: unknown 09/17 COVID swab, result; detected 09/20 TROPONIN I result: <0.016 09/20 DDIMER result: 0.33 09/20 pt admit to ED cc: chest tightness and shortness of breath dx: COVID-19 LOS: 1 09/20 CXR impression: No lobar pneumonia. 09/23 clinically resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 09/03 COVID swab, result: detected 09/03 DDIMER result: <0.22 09/03 PROCALCITONIN result: <0.05 09/03 SARS-COV-2 Variant Sequencing result: pending 09/03 TROPONIN I result: <0.016 09/17 COVID swab, result: detected 09/0 TROPONIN I result: <0.016 09/20 DDIMER result: 0.33 09/20 CXR impression: No lobar pneumonia.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1837032

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

moderat

Staat: NY
Alter: 37,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 18.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / AR

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

Asthenia Hypertension Injection site pain Nausea Vomiting

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Hypertension-Medium, Systemic: Nausea-Medium, Systemic: Vomiting-Medium, Systemic: Weakness-Medium

Weitere VAERSDATA-Felder

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

VAERS 1833955

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: OH
Alter: 83,0
Geschlecht: M
Eingang: 01.11.2021
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: unbekannt Erholt: ja

Chest pain Dyspnoea Electrocardiogram normal

Symptomtext

About 5 hours after receiving the vaccine, the patient reported shortness of breath and extreme chest pain. He saw his cardiologist the next day who said everything was normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG a few days after was normal
Aktuelle Erkrankungen: unknown
Vorgeschichte: heart disease, hypertension
Andere Medikamente: unknown
Allergien: sulfa
Vorherige Impfungen: -

VAERS 1833910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MT
Alter: 68,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Catheterisation cardiac normal Chest pain Electrocardiogram normal

Symptomtext

The morning of the 28th awoke with chest pain, Felt like an elephant sitting on her chest. She sat on her bed for 45 min and then awoke her son to take her to the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG, Cardiac cath done on 28th and they found no blockage (according to pt).
Aktuelle Erkrankungen: -
Vorgeschichte: COPD- 3 L Oxygen, Rheumatoid arthritis, Fibromyalgia, Ostoperosis
Andere Medikamente: Hydrocodone x 3 daily, trelegy inhaler, Gabipentinx 4 daily, N
Allergien: Beta blockers, Dilantin, inderal, Codeine, Sulpher drugs, Suda
Vorherige Impfungen: -

VAERS 1833054

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: WA
Alter: 34,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 28.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / RA

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

Fatigue Headache Heavy menstrual bleeding Migraine Pain Pyrexia

Symptomtext

Fever less than 8 hours after injection, severe fatigue with body aches. 3 days after each injection, I started a menstrual cycle which was very heavy. I have not had a menstrual cycle in 8 years due to having the IUD. Since covid and the vaccinations, I have endured headaches daily which turn into migraines at least once a week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: None at this time
Aktuelle Erkrankungen: Confirmed Covid infection
Vorgeschichte: None
Andere Medikamente: Vitamin B ; Vitamin D; Adult MultiVitamin; Vitamin C Excederin, and Ibeuprophen
Allergien: Penicillin, Bees
Vorherige Impfungen: -

VAERS 1832916

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 04.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / RA

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

Immunodeficiency Palpitations

Symptomtext

Per doctor's office visit note by physician: 57-year-old patient with palpitations, which have since resolved entirely. These may have been attributable to her vaccine, or may have been incidental. She is otherwise feeling at her baseline. If her symptoms recur or become more bothersome to her, we could consider obtaining baseline labs and/or placing a Holter monitor. Her rhythm is normal and her physical exam is reassuring, so I do not feel any further work-up is necessary at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: No known drug allergies
Vorherige Impfungen: -

VAERS 1831777

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: FL
Alter: 60,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 22.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / LA

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

Chills Diarrhoea Dyspnoea Renal failure Injection site reaction Livedo reticularis Oedema Pyrexia

Symptomtext

Chills, shortness of breath, kidney failure, diarrhea

Weitere VAERSDATA-Felder

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

VAERS 1832243

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: IL
Alter: 32,0
Geschlecht: M
Eingang: 31.10.2021
Impfdatum: 19.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Blood test normal Chest X-ray normal Chest discomfort Electrocardiogram normal Heart rate increased Palpitations

Symptomtext

Patient called the pharmacy on 10/29/2021 and stated that about 45 minutes after his 2nd COVID vaccine was administered he experienced an increase in heart rate and palpitations. He has continued to have palpitations and an increase heart rate. Patient states that his chest also continues to "weird" but could not elaborate. Patient was advised to go to urgent care or ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: At urgent care patient had an EKG and which was inconclusive. Patient was sent to the ER where he had an EKG, blood work and a chest x-ray. All were normal.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Noone
Vorherige Impfungen: -

VAERS 1832216

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: ME
Alter: 31,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 05.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Blood pressure increased Headache Immediate post-injection reaction Paraesthesia Urticaria Vaccine positive rechallenge

Symptomtext

Bp became elevated. ?High normal? hives tingly arm terrible headache. Happened with both vaccines. Treatment tylonal and benedryl. Happened immediately after shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Bp checks often.
Aktuelle Erkrankungen: None
Vorgeschichte: Factor V Leiden, protein s deficiency, DVTs
Andere Medikamente: Eliquis, gabapentin
Allergien: Erythromycin, penicillin, sulfites, wool
Vorherige Impfungen: -

VAERS 1831711

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CO
Alter: 50,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Back pain Chest discomfort Chest pain Dizziness Dyspnoea Electrocardiogram normal Fatigue Headache Hot flush Insomnia Nausea Palpitations

Symptomtext

10/22/21-Within first 5 mintues expriences hot flash, dizziness, Shortness of breath, nausea. 10/24/21-Headache, joint pain all over body, back pain, chest discomfort and chest burning (severe), short of breath (especially when laying down), insomina, acitivty intolerance, fatigue, palpitations, 10/27/21- Doctor visit- EKG- normal, assessment consistent with COVID 19 vaccine side effects, RX sleep aide. 10/30/21- Still have symptoms from 10/24.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG - normal
Aktuelle Erkrankungen: none
Vorgeschichte: Long Hauler COVID 19 from July, 2021.
Andere Medikamente: Vit D, zinc, vitamin C, fish oil
Allergien: none
Vorherige Impfungen: symptoms lasted 6 months with first COVID vaccine. Flu shot usually makes me ill for a week.

VAERS 1831087

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: IL
Alter: 54,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 16.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Burning sensation Fatigue Hypersensitivity Hypoaesthesia oral Paraesthesia oral Rash Rash erythematous Skin discolouration Weight

Symptomtext

lips started tingling; lips felt still numb; allergic reaction; my arms felt like they are burning; rash/really red; She got the rash/she felt little bluish; tired; rash; This is a spontaneous report from a contactable consumer (patient). A 54-year-old female patient received the third dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: FE3590), intramuscularly in the left arm on 16Oct2021 at 09:30 (at the age of 54-years-old) at dose 3 (booster), single for COVID-19 immunisation. Medical history included rash before from certain drug or stuff, like she could not take Sulphur drug and was allergic to calamari, symptoms in her thumbs in Sep2021. Concomitant medications included acyclovir, influenza vaccine (FLU) in Oct2021 at single dose for flu immunization, vitamins nos, steroid shot in her thumb for those symptoms in her thumbs. The patient received first and second dose of BNT162b2 on unspecified dates for COVID-19 immunization. Patient had the booster shot, the Pfizer booster shot on 16Oct2021 like 9:30 in the morning and she thought may be 4 hours later, she had a rash. She had that rash before from certain drug or stuff, like she could not take Sulphur drug and was allergic to calamari. Patient went to the hospital cause it was really red, and they prescribed her to take 3 pills of 60 mg of prednisone. Patient did not take it yet, so she was feeling well. Then the day before the report, on 17Oct2021, she ended up feeling a little better and the red color disappearing. On 18Oct2021, she was sitting outside and her arms were covered but her arms felt like they were burning and the rash felt like it was on her arm and a little on her chest and stuff and then her lips started tingling, like allergic reaction and so she went to the pharmacist and she was breathing and everything ok so obviously she was going to be ok but she went to the pharmacist and got BENADRYL cause it helped with that and she did fill the prescription for the prednisone but she did not know whether she had to take it or not, the day after. About her weight, patient stated it was 140 pound, well 130 pounds 140 yes; she thought it was like 130, she thought 138, 137; she did not know. Patient stated that she got the rash on 16Oct2021, she felt little bluish or whatever nothing too bad at all just tired, she was just tired, the first one or second one was little more bluish (unspecified). About concomitant medications, patient reported that she was taking just vitamins and acyclovir but she did not take it on that Saturday and was given a steroid shot in her thumb for those symptoms in her thumbs for like 3 to 4 weeks prior the report so it did not spread it out, she got a flu shot a couple weeks prior the report, in Oct2021. Patient stated that at the time of the report it felt a little warm, it seemed like it disappeared a little bit, but it was her lips felt tingly that was why she took BENADRYL, but she did not know if she had to take this prednisone or not, if it went against the vaccine or what. Rash seemed like it was subsided a little bit, she had a little on the neck and it was not burning as much but her lips felt still numb but like tingling; they said at the pharmacy it was like anything it was going to happen like you were not breathing or anything like that, that would happen right away, you did not get it 2-3 days later. About treatment, she said that instead of taking prednisone they wanted to give her, she took BENADRYL and then she got the script for the prednisone; pharmacist recommended her to take it, she said you just could have a reaction to it and to get the reaction out of your body just take the steroid for 5 days. The patient was recovering from rash/really red, had not recovered from lips started tingling, lips felt still numb, the outcome of the other events was unknown. Follow-up (22Oct2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: Test Name: Weight; Result Unstructured Data: Test Result:140 pound; Comments: ell 130 pounds 140 yes; she thought it was like 130, she thought 138, 137
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Musculoskeletal disorder; Rash (from certain drug or stuff); Seafood allergy
Andere Medikamente: ACYCLOVIR [ACICLOVIR]; VITAMINS NOS
Allergien: -
Vorherige Impfungen: -

VAERS 1794913

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: OH
Alter: 33,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / RA

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

Asthenia Body temperature Chills Dizziness Fatigue Dizziness postural Extrasystoles Fear Flushing Gait disturbance Headache Heart rate increased Heart rate irregular Hyperhidrosis Insomnia Immediate post-injection reaction Injection site pain Muscular weakness

Symptomtext

Irregular hearbeat; I was flushed; Fever of 102 Fahrenheit; Was sweating and shaking uncontrollably with chills and constant teeth chattering; Was sweating and shaking uncontrollably with chills and constant teeth chattering; Was sweating and shaking uncontrollably with chills and constant teeth chattering; Had extreme dizziness when sitting up; Weakness in arms and hands and legs; I could not take myself to toilet, needed assistance with transferring, toileting and drinking a glass of water; My neck and temples were throbbing in the veins causing a tremendous headache.; My neck and temples were throbbing in the veins causing a tremendous headache.; I could not sleep; Still feel very fatigued; This is a spontaneous report received from a contactable other healthcare professional (Patient). A 33-years-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: FE3590), via intramuscular route of administration, administered in Arm right on 14Oct2021 10:00 (at the age of 33-years-old) as dose 2, single for COVID-19 immunisation. Medical history included lactose intolerance, sensitivities to animal products and gluten from an unknown date and unknown if ongoing. Concomitant medications included vitamin c [ascorbic acid] (VITAMIN C [ASCORBIC ACID]) and flaxseed oil [linum usitatissimum seed oil] (FLAXSEED OIL [LINUM USITATISSIMUM SEED OIL]) taken for an unspecified indication, start and stop date were not reported. Prior to vaccination, was the patient did not diagnosed with COVID-19. Since the vaccination, did not patient been tested for COVID-19. Patient received vaccine facility in Pharmacy or Drug Store. The patient previously received first dose of bnt162b2(PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: 301308A), via intramuscular route of administration, administered in Arm right on 23Sep2021 10:00 (at the age of 33-years-old) as dose 1, single for COVID-19 immunisation. The patient had no COVID prior to vaccination and was not tested to COVID prior to vaccination. The patient got into bed on 14Oct2021 at 10:15 PM and by 10:30 PM and began a full onslaught of symptoms. The patient stated I was flushed, fever of 102 fahrenheit and was sweating and shaking uncontrollably with chills and constant teeth chattering. The patient reported she sweat through 2 frozen ice packs, had extreme dizziness when sitting up, weakness in arms and hands and legs. The patient stated, I could not take herself to toilet, needed assistance with transferring, toileting and drinking a glass of water. My neck and temples were throbbing in the veins causing a tremendous headache. The patient stated, i could not sleep but was afraid to take any medication for how it might react. The patient's husband assisted her in getting water every 30 mins or so. The chills/shaking lasted until about 4 am. On 15Oct2021 at 6:30 AM the patient had to get up for work, so she took 600 mg OTC ibuprofen which did help her headache. Her fever dropped down to 99 Fahrenheit as well by mid-day on 15Oct2021. Over the last three days she continued to be 1 degree above regular body temperature and still feel very fatigued with a headache and cycles of irregular heartbeat. The patient underwent lab tests and procedures which included body temperature: 102 fahrenheit on 14Oct2021, body temperature: 99 fahrenheit (Fever dropped down to 99) on 15Oct2021. The outcome of the events tremor, chills was reported as recovered on an unknown date in 2021 and while all other events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Date: 20211014; Test Name: Fever of 102; Result Unstructured Data: Test Result:102 Fahrenheit; Test Date: 20211015; Test Name: Fever of 102; Result Unstructured Data: Test Result:99 Fahrenheit; Comments: Fever dropped down to 99
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Food allergy; Gluten sensitivity; Lactose intolerance
Andere Medikamente: VITAMIN C [ASCORBIC ACID]; FLAXSEED OIL [LINUM USITATISSIMUM SEED OIL]
Allergien: -
Vorherige Impfungen: -

VAERS 1794913

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: OH
Alter: 33,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Asthenia Body temperature Chills Dizziness Fatigue Dizziness postural Extrasystoles Fear Flushing Gait disturbance Headache Heart rate increased Heart rate irregular Hyperhidrosis Insomnia Immediate post-injection reaction Injection site pain Muscular weakness

Symptomtext

Irregular hearbeat; I was flushed; Fever of 102 Fahrenheit; Was sweating and shaking uncontrollably with chills and constant teeth chattering; Was sweating and shaking uncontrollably with chills and constant teeth chattering; Was sweating and shaking uncontrollably with chills and constant teeth chattering; Had extreme dizziness when sitting up; Weakness in arms and hands and legs; I could not take myself to toilet, needed assistance with transferring, toileting and drinking a glass of water; My neck and temples were throbbing in the veins causing a tremendous headache.; My neck and temples were throbbing in the veins causing a tremendous headache.; I could not sleep; Still feel very fatigued; This is a spontaneous report received from a contactable other healthcare professional (Patient). A 33-years-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: FE3590), via intramuscular route of administration, administered in Arm right on 14Oct2021 10:00 (at the age of 33-years-old) as dose 2, single for COVID-19 immunisation. Medical history included lactose intolerance, sensitivities to animal products and gluten from an unknown date and unknown if ongoing. Concomitant medications included vitamin c [ascorbic acid] (VITAMIN C [ASCORBIC ACID]) and flaxseed oil [linum usitatissimum seed oil] (FLAXSEED OIL [LINUM USITATISSIMUM SEED OIL]) taken for an unspecified indication, start and stop date were not reported. Prior to vaccination, was the patient did not diagnosed with COVID-19. Since the vaccination, did not patient been tested for COVID-19. Patient received vaccine facility in Pharmacy or Drug Store. The patient previously received first dose of bnt162b2(PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: 301308A), via intramuscular route of administration, administered in Arm right on 23Sep2021 10:00 (at the age of 33-years-old) as dose 1, single for COVID-19 immunisation. The patient had no COVID prior to vaccination and was not tested to COVID prior to vaccination. The patient got into bed on 14Oct2021 at 10:15 PM and by 10:30 PM and began a full onslaught of symptoms. The patient stated I was flushed, fever of 102 fahrenheit and was sweating and shaking uncontrollably with chills and constant teeth chattering. The patient reported she sweat through 2 frozen ice packs, had extreme dizziness when sitting up, weakness in arms and hands and legs. The patient stated, I could not take herself to toilet, needed assistance with transferring, toileting and drinking a glass of water. My neck and temples were throbbing in the veins causing a tremendous headache. The patient stated, i could not sleep but was afraid to take any medication for how it might react. The patient's husband assisted her in getting water every 30 mins or so. The chills/shaking lasted until about 4 am. On 15Oct2021 at 6:30 AM the patient had to get up for work, so she took 600 mg OTC ibuprofen which did help her headache. Her fever dropped down to 99 Fahrenheit as well by mid-day on 15Oct2021. Over the last three days she continued to be 1 degree above regular body temperature and still feel very fatigued with a headache and cycles of irregular heartbeat. The patient underwent lab tests and procedures which included body temperature: 102 fahrenheit on 14Oct2021, body temperature: 99 fahrenheit (Fever dropped down to 99) on 15Oct2021. The outcome of the events tremor, chills was reported as recovered on an unknown date in 2021 and while all other events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Date: 20211014; Test Name: Fever of 102; Result Unstructured Data: Test Result:102 Fahrenheit; Test Date: 20211015; Test Name: Fever of 102; Result Unstructured Data: Test Result:99 Fahrenheit; Comments: Fever dropped down to 99
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Food allergy; Gluten sensitivity; Lactose intolerance
Andere Medikamente: VITAMIN C [ASCORBIC ACID]; FLAXSEED OIL [LINUM USITATISSIMUM SEED OIL]
Allergien: -
Vorherige Impfungen: -

VAERS 1829889

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe 3590

moderat

Staat: WI
Alter: 70,0
Geschlecht: M
Eingang: 29.10.2021
Impfdatum: 07.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / RA

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

Anxiety Blood glucose decreased Condition aggravated Hyperphagia Mobility decreased

Symptomtext

I have been a diabetic for 52 years. I got the second shot of the Pfizer COVID vaccine in February 2021 and shortly after that I started noticing the my blood sugar levels would stay low for long periods of time even though my food intake was way over my normal amounts. This went on for 2 or 3 weeks, Then the low blood sugar levels would become sporadic. After I got the 3rd shot ( Booster ) on 10/07/2021, the low blood sugars started up again. For the last three weeks I can't get my blood sugar levels to stay high enough for me to do any activities, even though I have reduced my insulin intake a lot . This is causing severe anxiety. I have no way to prove this is the cause. Two other notes; I got the flu shot on 09/24/2021 and started experiencing diariah . My doctor gave me a prescription for Ciprofloxacin 500mg to b e taken twice a day for 5 days 0n 10/11/2021. The next day my blood sugar levels went low. Can you look into this? I don't know if there is any and effect.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: 52 years as a diabetic.
Vorgeschichte: Diabetic.
Andere Medikamente: Aspirin; Cetirizine; Fish Oil; B12; Isosorbide Mononitrate; Lactaid tablets Losartan; Metamucil; Simvastatin;Multi vitamin Men 50+; Novolog Insulin under 30 units.
Allergien: Shellfish; Milk
Vorherige Impfungen: Possibly on the second COVID vaccine after February 2021.

VAERS 1828728

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: PA
Alter: 34,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Areflexia Blood test normal Computerised tomogram head normal Computerised tomogram spine Discomfort Hypersensitivity Hypoaesthesia Lumbar puncture normal Magnetic resonance imaging head normal Magnetic resonance imaging spinal normal Muscular weakness Musculoskeletal stiffness Paraesthesia Paranasal sinus discomfort Pharyngeal swelling

Symptomtext

Throat swelling after 10mins of shot - heavy steroids to assist in allergic reaction right foot tingling 1 day after shot. Left and right foot tingling day 2 after shot partial numbness in left leg from foot to knee day 3 after shot - still occuring partial numbness in right leg from foot to groin day 3 after shot, loss of reflexes i ankle and knee, severe muscle weakness - still occuring numbness and pressure and stiffness in neck and lower part of back of the head, pressure in sinuses - 30mins after eating since day 4 after shot - still occuring. muscle weakness in right arm day 4 after shot - still occuring

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: 6,0
Labordaten: MRI of skull to base of lumbar - no findings CT scan head and lower lumbar - no finding spinal tap - no findings blood work - no findings follow up with neurology to see if perm. .damage to nerves
Aktuelle Erkrankungen: n/a
Vorgeschichte: sarcoidosis - pulmonary
Andere Medikamente: prednisone 7mg daily Famotidine 20mg daily naltrexone 4.5mg daily
Allergien: latex - rash reglan - anaphylaxis ketorolac - anaphylaxis PNC penicillin - nausea/vomiting
Vorherige Impfungen: -

VAERS 1825797

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: WI
Alter: 42,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood test Computerised tomogram Dyspnoea Ear discomfort Ear pain Eye pain Headache Migraine Ocular discomfort Pain in extremity

Symptomtext

I had severe headache on Thursday. Turned into severe migraine, pain in left calf, shortness of breath, and pain and pressure in my left ear and eye. I went to the doctor and was prescribed migraine prescription.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Blood Test CT scan
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vyvanse Vitamin C Vitamin D3
Allergien: None
Vorherige Impfungen: Flu Vaccine- Extreme illness, couldn't keep food down.

VAERS 1825381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: WV
Alter: 45,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 08.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / RA

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

Burning sensation Dizziness Fatigue Hypoaesthesia Muscular weakness Pain in extremity Palpitations Paraesthesia

Symptomtext

The morning of the 14th woke up with numbness/tingling in feet with pain in legs, 15th tingling started in lower legs with same pain in legs, 16th tingling all the way up thighs and in hands, had palpitations numerous times through the day, felt like I was going to pass out several times, even while sitting, legs felt very fatigued 17th palpitations went away, but all other symptoms remained the same for several days. When walking up stairs, legs felt very fatigued and I would get burning in the muscles to the point I could only climb 1 flight of stairs before having to rest my legs. Tingling in my hands went away around the 25th. Tingling in upper legs went away around the same time, but the tingling in the feet and lower legs is still present today. Fatigue/weakness in legs improving. Now able to climb 2 flights of stairs with only minimal fatigue, no more burning in the muscles.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: No tests, went to PCP and he referred me to Neurology. Unfortunately long waiting list to get it. Appointment isn't until January 6th.
Aktuelle Erkrankungen: none
Vorgeschichte: osteopenia, melanoma (resected with clear margins)
Andere Medikamente: Calcium, Vitamin D, Vitamin A, B complex, Collagen, zinc
Allergien: prior reaction to flu and tetanus vaccine (similar symptoms) , otherwise no allergies
Vorherige Impfungen: Flu and Tetanus given same time in September 2020

VAERS 1825228

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: GA
Alter: 40,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Breast pain Injection site swelling Lymphadenopathy Mobility decreased Oedema peripheral Pain Pain in extremity

Symptomtext

Site: Swelling at Injection Site-Medium, Systemic: Body Aches Generalized-Medium, Systemic: pt stated pain on first day and 2nd day very painful 3rd could not lift arm and swollen under the arm pits and painful on left side of breast-Medium, Systemic: Lymph Node Swelling-Medium, Additional Details: patient stated her left arm was painful on first day and 2 nd day the left side of arm hurt on the third she was unable to lift her arm and under the armpit it was swollen and left side of her breast hurts

Weitere VAERSDATA-Felder

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

VAERS 1825082

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NY
Alter: 39,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 23.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / -

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

Diarrhoea Dyspnoea Headache Pruritus Pyrexia Swollen tongue

Symptomtext

Horrible itching clawing my face and body, trouble breathing, fever, headache, diarrhea, tongue felt swollen

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Factor v liededn
Andere Medikamente: None
Allergien: Morphine
Vorherige Impfungen: TDAP 05/21

VAERS 1824853

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 69,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Joint injury 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 1822408

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: DC
Alter: 24,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 14.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Migraine Nausea Vomiting

Symptomtext

I developed a severe migraine that lasted approximately six days. This was accompanied by nausea and vomiting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Oral contraceptive pill (Junel Fe 1.5/30), Zyrtec, Singulair, multivitamin
Allergien: N/A
Vorherige Impfungen: -

VAERS 1821854

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: KS
Alter: 26,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 23.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Dizziness Headache Injected limb mobility decreased Injection site erythema Injection site pain Injection site rash Injection site swelling Injection site warmth Nausea Pain Paraesthesia Pruritus Skin texture abnormal

Symptomtext

Approximately an hour and a half after receiving the vaccine I removed the band aid that was applied to the injection site. When I removed the band aid I noticed that there was a small area of skin around the injection site that was red, swollen, and hot to the touch. This area was approximately the size of my fingertip, and hurt when touched. It also hurt to raise my arm. Over the next 48 hours this rash began to worsen. By 24 hours post-vaccination it had grown to approximately 4-5 centimeters, was swollen, red, painful, hot to the touch and radiating heat, hurt when touched, and hurt when I moved my arm. It had also developed a goosebump-like texture. The pain was burning and tingling in sensation, and radiated outward from the injection site to approximately my elbow. I had a headache, and was dizzy, lightheaded, and nauseous. These systemic symptoms began approximately an hour and a half post vaccination and continued to worsen along with the rash. I iced my arm and treated with Tylenol and Zyrtec. The next day (48 hours post-vaccination) the rash continued to worsen, with the same symptoms (pain, heat, swelling, restricted movement of my arm), and my systemic symptoms persisted. I reached out to my primary care provider and was instructed to treat with Advil in addition to Tylenol, and to call in the morning if the rash continued to worsen overnight. The next morning when I woke up, the rash had grown in size, and the pain, heat, swelling, and restricted movement of my arm persisted, along with the systemic symptoms. I called my doctor and was instructed to come into the clinic for evaluation. By the time I was seen at the clinic it had been approximately 68-69 hours since the vaccine was administered. The size of my rash was measured, and it measured at approximately 5-6 cm. I was instructed to begin taking famotidine and Benadryl along with the Zyrtec, to take Advil and Tylenol round the clock, and to ice my arm. I was instructed to return if the rash worsened, if my systemic symptoms worsened, or if new symptoms began. I began treatment immediately with 40 mg of Benadryl 1x/day, 10 mg of Zyrtec 1x/day, and 20 mg of Famotidine 1x/day, as well as 400 mg of Advil and 500 mg of Tylenol every 4-6 hours, and icing the area when possible. By 96 hours post-vaccine administration the swelling had gone down, and the area was no longer as hot to the touch (though still warmer than the surrounding skin). The red coloring and goosebump-like texture persisted, but the burning pain had been reduced to an itching sensation, and the pain that restricted movement of the arm had lessened.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: No.
Aktuelle Erkrankungen: No illnesses at the time of the vaccine. From approximately 10/7/2021 through 10/14/2021 I had a cold. My primary symptoms were sinus congestion, headaches, and fatigue. I did not have a fever, and I did not have any rashes or other skin irritation.
Vorgeschichte: Chronic Kidney Disease, stage 3
Andere Medikamente: Buproprion XL 300 mg daily Sertraline 10 mg daily Adderall IR 20 mg 2x/day
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1821701

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MA
Alter: 42,0
Geschlecht: M
Eingang: 27.10.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Dizziness Dysphagia Pharyngeal swelling Throat irritation

Symptomtext

Patient received his second Pfizer dose under observation in our office on 10/21/21. Pt premedicated with Prednisone 50mg at hour 13, 7 and 1 before he received the Pfizer vaccine in our office. He also took Zyrtec 10mg about 20 minutes before receiving his vaccine. He required epinephrine in our office shortly after receiving the vaccine. See below for timeline of events: Baseline vitals: P 111, SpO2 98%, RR 20, T 99.1 F 1. 10:17a - Pfizer dose given. 2. 10:20a - Within 3 minutes of receiving the Pfizer vaccine he noticed the same sensation in his throat (swelling & difficulty swallowing) that he experienced with his first dose of Pfizer. Dr. notified. 3. 10:26a ? Dr. gave epinephrine 0.3mg IM and listened to his lungs (clear to auscultation). SpO2 = 97%, Pulse 115, RR 22. 4. 10:30a ? SpO2 = 97%, Pulse 118, RR 22. Pt felt a sensation in his throat now in the clavicle area. He took a sip of water and had some more difficulty swallowing it. 5. 10:35a - SpO2 = 97%, Pulse 115, RR 22. Sensation in clavicle area now improved, water slightly easier to swallow. 6. 10:40a ? BP 158/84, SpO2 = 97%, Pulse 118, RR 22. Sensation in his clavicle area/throat now feels worse. He had some more difficulty swallowing water. 7. 10:50a - BP 142/80, SpO2 = 97%, Pulse 122, RR 22. Sensation in clavicle area/throat and difficulty swallowing water are all the same as previously stated. Gave liquid Zyrtec 10mg. 8. 11:10a - BP 142/70, SpO2 = 98%, Pulse 114, RR 20. Sensation in throat slightly improved. 9. 11:30a - BP 134/78, SpO2 = 98%, Pulse 110, RR 20, T 98.4 F. Sensation in throat slightly improved. 10. 11:54a - BP 122/86, SpO2 = 98%, Pulse 105, RR 20. No changes. 11. 12:15p ? BP 126/84, SpO2 = 98%, Pulse 107, RR 20. Pt walked to the bathroom, a little lightheaded, but it improved after standing and walking around. Throat sensation mostly improved and Dr. OK?d him to leave. He had two epi pens with him and instructed to use it if throat symptoms worsen, then call 911.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Swelling of lymph nodes, colon polyps
Vorgeschichte: Unknown
Andere Medikamente: Prednisone, Zyrtec, Amlodipine, famotidine
Allergien: Amoxicillin, penicillin
Vorherige Impfungen: His first Pfizer dose given at a local pharmacy. History of reactions to flu vaccines resulting in him feeling "Sick as a dog"

VAERS 1821114

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MI
Alter: 39,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 21.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Blood pressure decreased Cardiac discomfort Cardiac disorder Dizziness Fear Feeling cold Tremor

Symptomtext

I was completely fine the first day after the shot and then about 34 hours later my heart started to feel like it was a baby turning about in a mother's womb, after about 20-30 minutes I became very cold and light headed and called 911 when I was very close to passing out. My heart stabilized by the time the paramedics arrived and my blood pressure slowly came back up, I then shook uncontrollably for about 45 minutes. My heart felt a little tired the following day but I was otherwise totally fine outside of that rather scary hour or so.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: multivitamin
Allergien: unfermented soy and sea sponge
Vorherige Impfungen: -

VAERS 1802415

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

moderat

Staat: TN
Alter: 17,0
Geschlecht: M
Eingang: 27.10.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Heart rate increased Hypoaesthesia Musculoskeletal stiffness Paraesthesia Vision blurred Hypersensitivity Muscle tightness Pallor Palpitations Throat tightness Tremor

Symptomtext

3:14 Blurred vision, 126/80 high pulse 90.tightness in neck 3:23 , 3:24 called 911, legs felt numb and tingle, 3:31 EPI pen, 3:32 breathing easier.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: decadron, steriods
Aktuelle Erkrankungen: none
Vorgeschichte: pain, IBS, headaches
Andere Medikamente: none
Allergien: severe grass allergys,
Vorherige Impfungen: -

VAERS 1802415

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: TN
Alter: 17,0
Geschlecht: M
Eingang: 27.10.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Heart rate increased Hypoaesthesia Musculoskeletal stiffness Paraesthesia Vision blurred Hypersensitivity Muscle tightness Pallor Palpitations Throat tightness Tremor

Symptomtext

3:14 Blurred vision, 126/80 high pulse 90.tightness in neck 3:23 , 3:24 called 911, legs felt numb and tingle, 3:31 EPI pen, 3:32 breathing easier.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: decadron, steriods
Aktuelle Erkrankungen: none
Vorgeschichte: pain, IBS, headaches
Andere Medikamente: none
Allergien: severe grass allergys,
Vorherige Impfungen: -

VAERS 1818661

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: OH
Alter: 37,0
Geschlecht: M
Eingang: 26.10.2021
Impfdatum: 15.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Iridocyclitis

Symptomtext

Developed anterior uveitis after months of no flare-ups within 7 Days of receiving my second Pfizer covid-19 vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Physician (opthamologist) diagnosis upon examination was anterior uveitis.
Aktuelle Erkrankungen: -
Vorgeschichte: Uveitis flare-ups
Andere Medikamente: CBD OIL
Allergien: -
Vorherige Impfungen: -

VAERS 1818258

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 16.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Chest discomfort Chest pain Condition aggravated Dysphagia Electrocardiogram Head discomfort

Symptomtext

Patient started with symptoms approximately 11 minutes after vaccination. She reports feelings of difficulty swallowing as well as some chest discomfort with radiation up into her head. She has had similar reactions in the past vaccinations. Reports no associated rashes at this time. Has not had any nausea or vomiting. Does have slight burning sensation in her chest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: ECG: normal blood presure: 192/79
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, enviromental allergies, fibromyalgia, hashimotos disease, IBS
Andere Medikamente: Pepcid, Fioricet, albuterol, levothyroxine
Allergien: Aspirin, Bactrim, Ciprofloxacin, gabapentin, IV contrast, Morphine, Levaquin, Metronidazole, Bee stings, oxycodone, penicillins, sulfa abx, toradol, vancomycin, questran
Vorherige Impfungen: -

VAERS 1818073

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: UT
Alter: 77,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Condition aggravated Epistaxis Nausea Neck pain Pain Product preparation issue

Symptomtext

Patient was given an undiluted dose of vaccine. As a result patient has experience nausea, chills, body aches, had blood on tissue when blowing nose, and worsening neck pain. Symptoms are resolving.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Neck Pain
Vorgeschichte: Menopausal and perimenopausal disorder Essential hypertension Coagulation defect; Hyperlipidemia; Insomnia; Arthritis; Adjustment disorder with physical complaints Diverticulitis BMI 31.0-31.9
Andere Medikamente: colestipol 1 g tablet, Sig: 2 tab(s) orally 2 times a day melatonin 10 mg capsule, Sig: 1 cap(s) orally once a day (at bedtime) Lisinopril 40 mg tablet, Sig: 1 tab orally daily Start Date: 10/13/2020 Tylenol Arthritis Extended Release
Allergien: penicillin Cephlasporins Sulfa Metronidazole.
Vorherige Impfungen: -

VAERS 1817610

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NC
Alter: 50,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 21.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / AR

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

Dyspnoea Extra dose administered Hypersensitivity Injection site erythema Injection site pruritus Injection site swelling Pruritus Rash Urticaria

Symptomtext

Site: Itching at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Allergic: Rash (specify: facial area, extremeties)-Severe, Additional Details: Pt recieved 3rd dose of Pfizer vaccine. Had no reaction with first 2 doses in Dec/Jan. When got 3rd dose pt broke out in hives ALL OVER body taking Benadryl around the clock and prednisone dose pak. Itchy and welps all over body started night after got vaccine. Still experiencing allergic reaction.

Weitere VAERSDATA-Felder

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

VAERS 1817591

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

moderat

Staat: NC
Alter: 72,0
Geschlecht: F
Eingang: 26.10.2021
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: nein

Constipation Dizziness Dyspnoea Erythema Flushing Gait disturbance Headache Hyperhidrosis Injection site pain Lymphadenopathy Muscle rigidity Skin swelling Tremor

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: constipation (severe)-Severe, Systemic: Flushed / Sweating-Mild, Systemic: Headache-Mild, Systemic: Lymph Node Swelling-Mild, Systemic: Shakiness-Mild, Additional Details: patient presented with complaints of constipation that per patient increased in severitiy post vaccine and warrented an er trip. patient also stated she experienced shaking, muscle rigidity, headache, sob red raised skin areas and gait changes, patient went through vaers form which will be physically faxed to vaers.

Weitere VAERSDATA-Felder

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

VAERS 1815931

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: TX
Alter: 57,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Hyperhidrosis Migraine Muscle spasms Rash Urticaria

Symptomtext

Muscle spasms in legs & feet; hives & rash around neck; migraine with heavy sweating.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: High blood pressure, high cholesterol
Andere Medikamente: Losartan, Carvedilol, allergy tablets
Allergien: Gentamicin, Iodine Contrast
Vorherige Impfungen: -

VAERS 1815434

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: TX
Alter: 51,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain Chest pain

Symptomtext

Patient return to vaccination site 2 hours and 20 minutes after getting their third dose. Patient presented with cheif compaint of severe abdominal pain. Roughly 20 minutes later chest pain developed with the abdominal pain. The medic onsite administered the patient 25mg Benadryl PO with no relief. The facility nurse then administered the patient's prescribed nitro and evacted the patient to the ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: -
Allergien: Coconut and bees
Vorherige Impfungen: -

VAERS 1815111

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 14.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / UN

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

Pain in extremity Paraesthesia Peripheral swelling

Symptomtext

patient got booster shot on 10/14/21. started complaining of arm pain (tingling feeling) on 10/24/21 when she lifts her arm.patient also states she feels her arm has started to swell. called the pharmacy 10/25/21 to report it.

Weitere VAERSDATA-Felder

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

VAERS 1814617

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

moderat

Staat: AZ
Alter: 59,0
Geschlecht: M
Eingang: 25.10.2021
Impfdatum: 23.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / UN

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

Chest discomfort Chest pain Chills Fatigue Lethargy Nausea Pain Paraesthesia Pyrexia Tremor

Symptomtext

Systemic: Body Aches Generalized-Severe, Systemic: Chest Tightness / Heaviness / Pain-Medium, Systemic: Chills-Severe, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fever-Medium, Systemic: Nausea-Medium, Systemic: Shakiness-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium

Weitere VAERSDATA-Felder

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

VAERS 1813818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: WA
Alter: 39,0
Geschlecht: M
Eingang: 24.10.2021
Impfdatum: 23.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Dyspnoea Hyperhidrosis Pallor

Symptomtext

Couldn't breathe, nurse said i looked gray and i was sweating. Felt like i was going to throw up. They moved me to an area to monitor me longer., gave me food and water. . I still didn't feel good and they were holding down a 12- year-old girl who didn't want it. So they were busy with her so i went and sat in my car for a while and went home some 4:15.pm. My wife has a medical background and has a pulse and oxygen thing and stuff still. When i came home i immediately laid down. I don't know how long after but i woke to my wife shaking me. Mr pulse was 44 and blood oxygen was 88. She wanted to call 911. I refused. This morning my oxygen is 92. Still monitoring for rashes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Was sick but tested negative .
Vorgeschichte: Non alcoholic fatty liver disease, central sleep apnea , migraines, GI issues, pituitary gland low functioning.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1809006

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: -
Alter: 34,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Dysphagia Dyspnoea Hypoaesthesia oral Throat irritation Throat tightness

Symptomtext

Pt c/o tongue numbness, throat itching, throat tightening, difficulty breathing, difficulty swallowing, lightheadedness. Epi IM 0.3 mg right lateral thigh X1 given at 1628. V/S taken 134/72, 102, 20, 100% O2 Sat. Called 911 per protocol. Ambulance arrived arrived at 1645.

Weitere VAERSDATA-Felder

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

VAERS 1808262

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: TX
Alter: 46,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia Feeling cold Peripheral coldness Tremor

Symptomtext

Coldness on legs and upper body, shakiness and weakness. Nurse assessed and cleared patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamins, birth control, Unknown
Allergien: None
Vorherige Impfungen: pfizer, weakness, coldness and trembling, Lot# EN6204, 46 years old, 3/17/2021

VAERS 1967197

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: PA
Alter: 92,0
Geschlecht: M
Eingang: 21.10.2021
Impfdatum: 12.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Cough Dyspnoea Oxygen saturation decreased Pneumonia viral Respiratory tract congestion

Symptomtext

Chest congestion, cough, O2 Sat desaturation, weakness, SOB. Hospice doctor felt it was viral pneumonia COVID-19 booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Wet macular degeneration; Legally blind; Hard of hearing; Diagnosed with prostate cancer; BPH; Rotator cuff; HTN; HLD; CAD S/P Bypass; Carotid Stenosis; Degenerative changes of spine; Cholelithiasis; Diverticular Disease of Sigmoid Colon; MVA 5/17; COPD; Pleural effusion; Cataract surgery 3/2017; Insomnia; Ocular HTN; Dry eyes' Amyloidosis of heart; Metastatic prostate cancer to b/l ribs, spine, pelvis, femur; Constipation; Basal cell cancer of left elbow; Joint support; Edema; Depression; Pain; SOB
Andere Medikamente: Proscar; Aspirin; Lasix; Miralax; Ativan; Melatonin; Zoloft; Tylenol; Cosopt, Lubricant Eye Drop; Tylenol; Acetaminophen; Haloperidol; Atropine; Lorazepam; Prochlorperazine; Morphine Sulfate
Allergien: -
Vorherige Impfungen: -

VAERS 1967188

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: PA
Alter: 59,0
Geschlecht: F
Eingang: 21.10.2021
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: unbekannt Erholt: nein

Headache Hypertension Local reaction

Symptomtext

Severe local reaction of left arm Severe headache HTN BP 180/102 and never had high BP

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroidism/ Gastroparesis
Andere Medikamente: Synthroid and Omeprazole
Allergien: -
Vorherige Impfungen: -

VAERS 1806178

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: AZ
Alter: 25,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Hypoaesthesia Paraesthesia

Symptomtext

Patient experienced severe lightheadedness. Patient was given candy and it did not help. Patient started to tense up with their hands and could not relax them. Patient was able to feel touch but not able to unclench hands Patient said their hands went numb and had a tingling sensation in both hands. Patient could breathe and did not have any swelling from the neck up. Paramedics were called and patient was evaluated. Patient was alert and able to walk after evaluation.

Weitere VAERSDATA-Felder

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

VAERS 1804864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 26,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Dizziness Dyspnoea Fatigue Hypoaesthesia Muscular weakness Nausea Paraesthesia

Symptomtext

Patient started feeling faint 5 to 10 minutes after getting the shot. Upon seeing the patient she felt nauseous and short of breath. Breathing rate became more rapid we moved her to a supine position on a cot. She complained of shortness of breath and tingling in extremities. We took her blood pressure at 2:05 PM which gave an initial reading of 119/51. After that patient began to shiver and complained of numbness in the arm where we did the blood pressure. Her O2 sats were at 100 with a HR of 81. 10 minutes later we took a follow up blood pressure at 2:19 PM which gave a reading of 118/88. After she began experiencing muscle weakness and fatigue we called EMS and they took her at 2:35 PM

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: No known
Aktuelle Erkrankungen: No known
Vorgeschichte: Fibro myalgia, PTSD, Anxiety
Andere Medikamente: CBD, Nucynta, Advil, Norco,
Allergien: Nitrates, amoxicillin, capsaicin
Vorherige Impfungen: Similar Event shakiness and difficultly breathing, 25, 04/05/21

VAERS 1801693

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: TX
Alter: 48,0
Geschlecht: F
Eingang: 20.10.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Migraine Paraesthesia Vein disorder Vision blurred

Symptomtext

As I was walking home after the shot I got blurry vision. And then about 3 pm I noticed my veins in my left hand were getting really big and shrinking and the veins were pulsating. I now have a migraine and my left leg is tingling and I am having to talk out of the right side of my mouth.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: environment allergies
Vorgeschichte: yes
Andere Medikamente: I do take prescriptions and a multivitamin
Allergien: Proponolol, hydrocodon. amatrix, cefalexin, pollen, mold, mildew, ceder
Vorherige Impfungen: -

VAERS 1801356

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge fe3590

moderat

Staat: AZ
Alter: 73,0
Geschlecht: F
Eingang: 20.10.2021
Impfdatum: 14.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Hypoaesthesia Injection site erythema Injection site pain Injection site swelling Insomnia Paraesthesia

Symptomtext

Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Numbness (specify: facial area, extremities)-Severe, Systemic: Tingling (specify: facial area, extemities)-Severe, Systemic: Unable to Sleep-Medium, Systemic: Weakness-Severe

Weitere VAERSDATA-Felder

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

VAERS 1801268

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 20.10.2021
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: ja Erholt: ja

Fatigue Gait disturbance Lethargy Tachycardia

Symptomtext

Systemic: Exhaustion / Lethargy-Medium, Systemic: Tachycardia-Medium, Additional Details: patient stated she had trouble walking home and ended up needing to go to emergency room

Weitere VAERSDATA-Felder

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

VAERS 1801244

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

moderat

Staat: FL
Alter: 43,0
Geschlecht: F
Eingang: 20.10.2021
Impfdatum: 19.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chest discomfort Dizziness Headache Hypertension Hypoaesthesia Nausea Tachycardia

Symptomtext

Systemic: Chest Tightness / Heaviness / Pain-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Headache-Medium, Systemic: Hypertension-Medium, Systemic: Nausea-Mild, Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Tachycardia-Medium, Additional Details: numbness on left side of face and neck

Weitere VAERSDATA-Felder

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

VAERS 1799332

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: IL
Alter: 16,0
Geschlecht: M
Eingang: 19.10.2021
Impfdatum: 19.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Hypoaesthesia Paraesthesia

Symptomtext

After 10 minutes patient stated arm felt numb and tingles radiating down to hand

Weitere VAERSDATA-Felder

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

VAERS 1798523

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NJ
Alter: 38,0
Geschlecht: M
Eingang: 19.10.2021
Impfdatum: 08.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Extrasystoles Palpitations

Symptomtext

Heart Palpitations. When checking pulse feels like skips a beat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: -
Vorgeschichte: Type I diabetic
Andere Medikamente: Insulin
Allergien: N/A
Vorherige Impfungen: -

VAERS 1798322

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MD
Alter: 41,0
Geschlecht: F
Eingang: 19.10.2021
Impfdatum: 08.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test Chest discomfort Chest pain Dizziness Electrocardiogram Injection site paraesthesia Paraesthesia

Symptomtext

Left side chest pain and pressure started Monday October 11, 2021 around 3 am. Tingling down left arm into hand and fingers started October 13th in the evening. I was also having dizzy spells which started on October 11, 2021. I went to the emergency department. I was examined and given blood tests and received an EKG. I was given sodium chloride and ketorolac. I was given a prescription for ibuprofen for the chest pain. I was also given a prescription for amoxicillin for a sinus infection that is unrelated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Blood tests 10/14/2021 EKG 10/14/2021
Aktuelle Erkrankungen: Possibly a sinus infection at the time of vaccination
Vorgeschichte: I had a total thyroidectomy in 2005, so I am a thyroid patient ( hypothyroidism)
Andere Medikamente: Levothyroxine Sertraline Zyrtec
Allergien: Lactose intolerant
Vorherige Impfungen: -

VAERS 1798099

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: TX
Alter: 57,0
Geschlecht: F
Eingang: 19.10.2021
Impfdatum: 19.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Chest discomfort Chest pain Dyspnoea

Symptomtext

11:29AM - NP notified of pt C/O SOB, chest pain. NP at car assessed pt noted with chest pain that she described as heaviness and SOB denies these symptoms prior to vaccine @ 11:35am. PT given 0'3 of epi to left thigh. EMS on scene PT BP 135/71, HR 78 , EKG NSR on monitor. PT reports history of blood clots, ulcers, strokes, z ta, seizure. TIA (2016 & 2018) taking Keppra, Eliquis daily 7 days. PT reports after 5mins 11:40am of chest pain & SOB subsiding. PT educated about the side affects of epi injection and the importance of being evaluated by the hospital.PT agreed and transported to Hospital by EMS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: BP 135/71, HR 78 , EKG
Aktuelle Erkrankungen: Blood clots,
Vorgeschichte: Seizures
Andere Medikamente: Keppra 3000mg Eliquis 10mg
Allergien: N/A
Vorherige Impfungen: -

VAERS 1797818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NC
Alter: 44,0
Geschlecht: F
Eingang: 19.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Feeling hot General physical condition abnormal Hypertension Pharyngeal paraesthesia Swollen tongue Throat irritation

Symptomtext

A few minutes after receiving her vaccination and while I was about to administer the vaccination to her husband, the patient (while sitting in a chair next to her husband) stopped her conversation to say that her throat was itching/tingling. She said that she felt her throat might be closing up as well and immediately wanted benadryl. Patient was able to chew two tabs (50mg total) of benadryl and swallow. She continued to sit there for a moment and talk. Then, she went silent and limp over the chair. We immediately got her to wake up and she still said that she felt that her tongue was swelling. I informed her that we would have to give Epinephrine and call EMT if she continues on this route. She did not want to be given Epinephrine at that time and was very hot. We fanned her to cool her down and continued to assess her. We finally came to the decision to call the EMTs for assistance. EMTs arrived and took blood pressure, which was high but did eventually go down. EMTs said it was more than likely high due to the anxiety. She did not want to go with the EMTs to the hospital and agreed to go home with her husband as she was sleepy at this point due to the benadryl. Patient returned three days letter in a better state describing her recovery as joint pain, not feeling too good, yet feeling better the day she came back in to the pharmacy that day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: Unknown
Allergien: Sulfa, TB ppd, Iodine, Vitamin D
Vorherige Impfungen: Yes, but details not provided. She just said that she did not experience an ADR to the COVID Pfizer vaccine with her first dose.

VAERS 1797747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: ID
Alter: 75,0
Geschlecht: M
Eingang: 19.10.2021
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: unbekannt Erholt: nein

Ageusia Condition aggravated Cough Fatigue Feeling abnormal Headache Influenza like illness Oropharyngeal pain Pain Pain in extremity Pyrexia SARS-CoV-2 test negative

Symptomtext

For clarity I am going to lists the reactions to all three Covid-19 shots that I received: Dose 1: No reactions Dose 2: Reactions similar to a mild full blown case of Covid-19. Symptoms lasting up to 28 days. Dose 3: REactions more similar to the flu with the addition of brain fog and fatigue. The duration of each symptom. First Vaccination Second Vaccination Booster Vaccination 2/28/21 3/21/21 10/08/21 N/A 2 Days - Sore arm 4 Days - Sore Arm N/A 4 Days - Low grade fever 3 Days - Low grade fever - 100.5 for one day N/A 4 Days - Body aches 2 Days - Body Aches N/A 10 Days - Brain fog 8 Days - Brain fog N/A 14 Days - Head Ache 9 Days - Head Ache N/A 14 Days - Loss of Taste N/A N/A 21 Days - Fatigue 9 Days - Fatigue N/A 28 Days- Minor loss of taste N/A N/A N/A 1 Day - On day three a minor cough N/A N/A 5 Days - Minor sore throat starting on day 5. N/A 1st Symptom in 15 hours 1st Symptoms in 9 Hours N/A N/A The remaining symptoms are minor: Head ache, fatigue, and minor sore throat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: April 2, 2021 Negative Covid-19 test October 11, 2021 Negative Covid-19 test
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lovostatin, Levothyroxin, Aspirin, Vitamin C, Vitamine D
Allergien: None
Vorherige Impfungen: Covid-19 Pfizer on March 21, 2021. Age 74 years. See item 18 for adverse events.

VAERS 1795996

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: WA
Alter: 88,0
Geschlecht: F
Eingang: 18.10.2021
Impfdatum: 16.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Decreased appetite Dizziness Extra dose administered Feeling abnormal Headache Heart rate increased Tremor

Symptomtext

Had the booster on Sat. morn. at 3am next morning went to bathroom and it hit me like ton of bricks and could hardly make it back to bed. I was shaking and fast heartbeat and very weak. Next morning was very weak an shaky, had to just rest all day, no appetite. Very bad headache. Next day somewhat better, but almost passed out at one point. Still weak and shaky on the 3rd day of the shot. The first two shots that I had last Jan. and Feb. there were no reactions at all. Why would this booster be so different. I thought it was supposed to be a weaker dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: type II diabetes - no medication
Andere Medikamente: Zocor, Avapro, multi vitamins
Allergien: N/A
Vorherige Impfungen: -

VAERS 1795759

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NY
Alter: 43,0
Geschlecht: F
Eingang: 18.10.2021
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Feeling abnormal Heart rate increased Hot flush Hypoaesthesia oral Paraesthesia oral

Symptomtext

About 5 minutes after the vaccine I felt really hot all over and my tongue started tingling. This lasted about 2 minutes. After this, for the next hour and a half, my tongue felt numb and I had intermittent hot flashes and increased heart rate until I took 25mg of Benadryl at home. The symptoms then resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Cold 2 weeks prior
Vorgeschichte: None
Andere Medikamente: Zoloft, vitamin b12, vitamin D
Allergien: Codeine, sulfa
Vorherige Impfungen: -

VAERS 1795027

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MD
Alter: 49,0
Geschlecht: M
Eingang: 18.10.2021
Impfdatum: 13.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / -

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

Fatigue Headache Injection site paraesthesia

Symptomtext

Severe headaches, tingle feeling on the left side of the body (injection site) , fatigued.

Weitere VAERSDATA-Felder

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

VAERS 1794967

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: WA
Alter: 29,0
Geschlecht: F
Eingang: 18.10.2021
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Chest discomfort Chills Cough Dyspnoea Fatigue Pyrexia SARS-CoV-2 test negative Sneezing

Symptomtext

9 hours after injection, all-over body exhaustion 10 hours after injection, convulsion-like chills & fever of 103.9 24 hours after injection, pressure on chest (like someone firmly pressing a hand into the center of my chest, affecting my breathing) and a cough develop 48 hours after injection, non-stop sneezing develops

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Negative covid test, administered 10/16
Aktuelle Erkrankungen: -
Vorgeschichte: depression, pmdd, endometriosis
Andere Medikamente: lamictal, oral birth control
Allergien: latex
Vorherige Impfungen: -

VAERS 1794865

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: MO
Alter: 48,0
Geschlecht: U
Eingang: 18.10.2021
Impfdatum: 12.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Blood electrolytes normal Blood glucose normal Chest X-ray normal Chest pain Chills Dyspnoea exertional Electrocardiogram normal Full blood count normal Pain Renal function test normal Troponin normal Urine analysis normal

Symptomtext

Patient reported to the ED on 10/13/21 stating symptoms of weakness, chest pain, shortness of air with exertion, body aches and chills began that morning. No issues were reported on 10/12/21. EKG was normal. Chest x-ray was normal. Lab testing CBC, Troponin, electrolytes, renal values, urine specimen and glucose were all within normal limits. She was instructed to take OTC medication for symptoms and was dismissed from the ED that same day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: See above: EKG, Chest x-ray and lab tests all completed on 10/13/21
Aktuelle Erkrankungen: None known
Vorgeschichte: None Known
Andere Medikamente: Zrytec; Flonase; Zaditor; Multi-vitamin; Junel Fe
Allergien: None Known
Vorherige Impfungen: -

VAERS 1794851

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: TX
Alter: 51,0
Geschlecht: F
Eingang: 18.10.2021
Impfdatum: 16.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Dizziness Dyspnoea

Symptomtext

Pt c/o dizzy and difficulty breathing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Uterine fibroids
Andere Medikamente: BP medications, premarin, pregabalin
Allergien: IV contrast, Lisinopril
Vorherige Impfungen: -

VAERS 1794769

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: IL
Alter: 55,0
Geschlecht: M
Eingang: 18.10.2021
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: ja Erholt: nein

Asthma Blood test normal Chest X-ray normal Chest discomfort Condition aggravated Cough Dyspnoea Electrocardiogram normal Gastrooesophageal reflux disease Heart rate increased Hypertension Rash Rash pruritic

Symptomtext

Chest tightness and shortness of breath within 20-30 mins of receiving shot on evening of 10/13/21. Itchy rash on arms, legs and chest within 2 hours, which got better after took benedryl. However, chest tightness, shortness of breath didn't get much better even though took albuterol. Bad gerd that night. When tightness and shortness of breath and gerd didn't improve by Saturday morning 10/15/21 and started coughing , I went to urgent care. They sent me in ambulance to the Hospital ER. There I received EKG, chest xray, blood tests, which were normal, and treatment for asthma and gerd. When my symptoms improved I was discharged. I still have some chest tightness, shortness of breath, gerd and cough today 10/18/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: EKG, chest xray, blood tests, all normal. BP and heart rate were a little high when initally came to ER.
Aktuelle Erkrankungen: none
Vorgeschichte: asthma, gerd, prostatitis, hemorrhoids
Andere Medikamente: albuterol inhaler as needed
Allergien: sulfites, aspirin, ciproflaxacin, bactrim
Vorherige Impfungen: -

VAERS 1794099

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: WI
Alter: 54,0
Geschlecht: F
Eingang: 17.10.2021
Impfdatum: 16.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Condition aggravated Extra dose administered Hot flush Sleep disorder Supraventricular tachycardia

Symptomtext

At 5:00 a.m., about 20 hours after receiving my vaccines, I was awakened from sleep by a strong hot flash and a very fast supraventricular tachycardia. Note that I am prone to SVT due to mitral valve prolapse, but I do not normally have hot flashes in general, and do not nor do I normally have hot flashes when I have SVT. The SVT was also faster than what I normally have. For about 15 minutes I attempted vagal maneuvers (coughing), slow breathing and relaxation, and splashing cold water on my face, to no avail. At that point I took 50 mg Atenolol and returned to slow breathing and relaxation, and within about another 15 minutes the SVT had stopped and the hot flash had lessened significantly (but did not completely go away). Today I feel fine other than being tired (from interrupted sleep) and still having slight hot flash. I took my temperature and it is very slightly elevated (98.8 F) from my normal (around 98.2 F). I have not previously had any side effects from a seasonal flu vaccine, which I have been receiving for many years. I did not previously have any side effects from either of my two doses of Covid19 vaccine. While an unpleasant episode, even if I had known beforehand that it would happen, it would not have stopped me from getting my vaccines. Thank you.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism, hypertension, mitral valve prolapse (symptomatic with PVCs and SVT)
Andere Medikamente: Synthroid, Losartan, Hailey (oral contraceptive), Co-Q10
Allergien: Antibiotic ointments (Neosporin, Bacitracin, etc.)
Vorherige Impfungen: -

VAERS 1793983

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: NV
Alter: 21,0
Geschlecht: M
Eingang: 17.10.2021
Impfdatum: 16.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Dizziness Paraesthesia

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium, Additional Details: Patient asked to call 911 -cannot speak English (Mom translated)..seemed the longer he waited he got more anxious after the shot

Weitere VAERSDATA-Felder

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

VAERS 1793980

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3590

moderat

Staat: NJ
Alter: 34,0
Geschlecht: M
Eingang: 17.10.2021
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Injected limb mobility decreased Injection site pain Paraesthesia

Symptomtext

Site: Pain at Injection Site-Severe, Systemic: Tingling (specify: facial area, extemities)-Mild, Additional Details: pain of the arem received the injection, couldn't lift the arm well, no mobility of the affected arm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1793764

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: TX
Alter: 40,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: 16.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Dizziness Paraesthesia

Symptomtext

Tingling on vaccinated arm and dizziness. EMS attended and cleared patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: Left valve leak on heart
Andere Medikamente: Levothyroxine, Furosemide, Xarelto, Vitamin D3
Allergien: None
Vorherige Impfungen: -

VAERS 1793758

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: TX
Alter: 36,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: 16.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Chills Palpitations

Symptomtext

10 mins of getting the pfizer vaccine patient stated she was having heart palpation, chills, pain in the left shoulder. Blood pressure 130/74 at 1:10 patient walked to restoom after being observed.

Weitere VAERSDATA-Felder

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

VAERS 1788468

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3590

moderat

Staat: TX
Alter: 27,0
Geschlecht: F
Eingang: 15.10.2021
Impfdatum: 09.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Immediate post-injection reaction Incorrect route of product administration Pain in extremity Paraesthesia

Symptomtext

Vaccine injected too high, into the shoulder joint. Immediate pain and tingling down my arm. Continued pain down to the elbow for the rest of the day. Seemed to resolve by the following morning

Weitere VAERSDATA-Felder

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

VAERS 1788396

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3590

moderat

Staat: CT
Alter: 70,0
Geschlecht: F
Eingang: 15.10.2021
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: ja Erholt: nein

Bronchitis Chest discomfort Cough Dyspnoea Headache Immune system disorder Lung disorder Pain SARS-CoV-2 test negative Wheezing

Symptomtext

Body aches, headaches. Followed by bronchitis. No fever and oxygen levels @95. Terrible non-stop coughing. Lungs very ?junky?, wheezing, whistling, heaviness, trouble breathing. After one week, went to Urgent Care At the time I got the vaccine, a family member had been sick for 2 weeks with bronchitis. I believe I caught his ?bug? due to lowered immunity after getting the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Covid test Oct 10, results on Oct 12: negative. Covid rapid test at Urgent Care Oct 13: negative Prescribed: Azithromycin 250 mg once a day for 5 days Albuterol sulfate 90 mcg every 4 hours Prednisone 20 mg 2 daily for 5 days
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma until 1997. No asthma since then until now.
Andere Medikamente: Prevastatin 40 mg, multi vitamin, calcium, CoQ10
Allergien: Bees
Vorherige Impfungen: -