VAERS Reports FJ6369

VAERS 2685840

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: FL
Alter: 94,0
Geschlecht: F
Eingang: 25.09.2023
Impfdatum: 20.05.2022
Beginn: 16.09.2023
Tage bis Beginn: 484,0
Dosis: 4
Route/Site: SYR / UN

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

Acute respiratory failure Atrial fibrillation COVID-19 pneumonia Hypertension Hypothyroidism Infectious pleural effusion

Symptomtext

Hospitalization for COVID-19 pneumonia with parapneumnoic effusions and acute hypoxemic respiratory failure, Afib, hypertension, hypothyroidism on dates 9/16/23- 9/22/23. Treated with dexamethasone, Remdesivir, and vitamin D 25 mcg PO daily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2678609

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: FL
Alter: 87,0
Geschlecht: M
Eingang: 01.09.2023
Impfdatum: 20.05.2022
Beginn: 24.08.2023
Tage bis Beginn: 461,0
Dosis: 4
Route/Site: SYR / UN

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

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

Symptomtext

Hospitalization for acute hypoxemic respiratory failure, sepsis, COVID-19 positive on dates 8/24/2023- 8/31/2023. Treated with dexamethasone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2667765

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: -
Alter: 75,0
Geschlecht: F
Eingang: 08.08.2023
Impfdatum: 26.01.2022
Beginn: 15.02.2023
Tage bis Beginn: 385,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure

Symptomtext

ACUTE HYPOXEMIC RESPIRATORY FAILURE

Weitere VAERSDATA-Felder

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

VAERS 2666955

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: -
Alter: 59,0
Geschlecht: M
Eingang: 07.08.2023
Impfdatum: 22.02.2022
Beginn: 22.02.2023
Tage bis Beginn: 365,0
Dosis: 3
Route/Site: - / -

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

Acute myocardial infarction

Symptomtext

ACUTE NON ST ELEVATION MI

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

VAERS 2644599

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: -
Alter: 39,0
Geschlecht: M
Eingang: 13.06.2023
Impfdatum: 01.02.2022
Beginn: 05.12.2022
Tage bis Beginn: 307,0
Dosis: 2
Route/Site: - / -

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

Acute respiratory failure Chronic respiratory failure Hypersomnia Hypoxia Neuropathy peripheral Obstructive sleep apnoea syndrome Respiratory failure Sleep apnoea syndrome Symptom recurrence

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE HYPERSOMNIA W SLEEP APNEA ADULT OBSTRUCTIVE SLEEP APNEA NEUROPATHY ACUTE HYPERCAPNIC RESPIRATORY FAILURE CHRONIC HYPERCAPNIC RESPIRATORY FAILURE ACUTE ON CHRONIC HYPERCAPNIC RESPIRATORY FAILURE RESPIRATORY FAILURE, UNSPECIFIED ACUITY HYPERCAPNIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY HYPOXIA 1/26/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2629920

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 10.05.2023
Impfdatum: 22.02.2022
Beginn: 06.06.2022
Tage bis Beginn: 104,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Agitation Encephalopathy

Symptomtext

JACUTE RESPIRATORY FAILURE 8/3/2022 AGITATION ACUTE RESPIRATORY FAILURE 8/3/2022 AGITATION ACUTE RESPIRATORY FAILURE 8/3/2022 ENCEPHALOPATHY

Weitere VAERSDATA-Felder

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

VAERS 2616362

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: -
Alter: 82,0
Geschlecht: M
Eingang: 17.04.2023
Impfdatum: 11.04.2022
Beginn: 15.03.2023
Tage bis Beginn: 338,0
Dosis: 4
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Blood creatinine increased Blood culture negative Blood thyroid stimulating hormone decreased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram head normal Cough Dehydration Diarrhoea Dysphonia Echocardiogram Ejection fraction normal Electrocardiogram Fibrin D dimer increased Functional gastrointestinal disorder

Symptomtext

This is an 83-year-old patient who presented with acute respiratory failure with hypoxia with concern for aspiration event patient is well was found to have COVID-19 pneumonia. Patient initially treated with antibiotic therapy had significant improvement was weaned down to room air. Patient is well found to have candidal esophagitis initiated on fluconazole with improvement in symptoms. Statin placed on hold while on focus on. Discussed plan of care at length with son at the bedside on the day of discharge including what to monitor for and when to seek medical attention. Acute hypoxic respiratory failure Aspiration pneumonia COVID 19 - concern for aspiration event - Initial CXR indicating tiny bilateral effusions but with no consolidation. - initially requiring 3L NC on admission, on 3/16 noted to de-sat to low 80s, and required 100% NRB and ICU transfer for heated high flow oxygen. -Treated with IV Unasyn for possible aspiration, stopped on 3/18 -Currently on room air. With significant improvement in symptoms. Hypotension -Had issues with hypotension overnight on 3/21. Unclear etiology. Treated with IV fluid boluses. Also received an extra dose of IV Solu-Cortef -Patient reports no symptoms -Levophed needed to be started completely and weaned off 3/22 -Received higher dose of steroids. That will be tapered down to his home dose today COVID-19, with Sepsis - Presented with: Nausea, vomiting, diarrhea, and cough - Symptom onset: 3/14 - Positive COVID-19: 3/15 at Facility - on admit noted to be febrile 102.9; blood cx negative -Initially started on Decadron, now stopped as do not think COVID-19 contributing much to his respiratory issues. Patient currently on room air -Can come out of isolation on 3/25 Ileus -KUB consistent with colonic ileus. NG placed. -Has return of bowel function, tolerating diet Oropharyngeal/laryngeal candidiasis -White spots were noted on the laryngeal vestibule on fees 3/17 -Started on 14 days of Diflucan by the ICU team on 3/20 -Hold statin while on Diflucan. -Reports hoarseness of voice but no difficulty swallowing. Oral exam without any evidence of oral candidiasis Acute metabolic toxic encephalopathy - multifactorial COVID-19, hypoxia, dehydration and AKI. - CT head negative for any acute process. - Delirium precautions in place. -Doing much better today. Awake and alert back to his baseline Nonoliguric AKI - Likely in the setting of intractable nausea and vomiting related to COVID. - Baseline creatinine about 1 year ago was 1.2, 2.20 on admission. -Resolved. Improved Elevated troponin -Likely demand ischemia from hypoxemia/respiratory failure - His EKG on admission showed a ventricularly paced rhythm with no signs of ischemia. - Trop 46/59 - TTE with EF 70%. Elevated D-Dimer - suspect in setting of infection - D-Dimer 1.32 - Doppler LE negative for DVT Adrenal insufficiency -This is a known diagnosis. Followed by Dr. No records in data. - Continue hydrocortisone IV. Home dosing 10 mg am and 5 mg pm. -Plan to transition to oral home dosing CAD status post CABG with chronic angina Had bypass surgery on 4/19/2019 by Dr. On aspirin and Lipitor - Continue home meds. He is on Ranexa and followed by Dr. -Holding statin while on Diflucan Complete heart block status post pacer Placed by Dr. in 2010, he continues to follow with him. Generator change was done in January 2021. Hypothyroidism On previous admissions this year, has had low TSH and high free T4, levothyroxine dose adjusted multiple times - Follows with Dr. -TSH continues to be low but on arrival in setting of acute illness. Will have patient repeat thyroid function test as outpatient with PCP

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2613230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: -
Alter: 85,0
Geschlecht: F
Eingang: 11.04.2023
Impfdatum: 19.01.2022
Beginn: 26.02.2023
Tage bis Beginn: 403,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Brain natriuretic peptide increased Bronchial secretion retention COVID-19 COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram thorax abnormal Dextrocardia Diuretic therapy Dyspnoea Echocardiogram abnormal Ejection fraction normal Hyponatraemia Hypophagia Hypovolaemia Hypoxia Lung disorder Lung opacity

Symptomtext

Patient is a 86 y.o. female patient of MD with history of multiple sclerosis with neurogenic bladder, who presented to the hospital from the resident facility with dyspnea on 2/26/2023/ Covid-19 Pneumonia Acute hypoxemic Respiratory Failure, POA Possible superimposed bacterial pneumonia Mucous plugging Date of onset of symptoms: 2/25/23 Symptoms present on admission: Hypoxia Date of covid positive test: 2/26/2023 Vaccination status: vaccinated Imaging: CT PE study on admission with bilateral left greater than right groundglass opacities on my interpretation. Repeat chest x-ray 3/2/2023 showing right hemithorax Oxygen requirements on admission: 2 L Current oxygen requirements: High flow, 90% FiO2 Medical therapy: Dexamethasone. Status post remdesivir Consultants following: ID following Continue cefepime and vancomycin for possible superimposed bacterial pneumonia Management of secretions/mucous plugging with Mucomyst, vibratory pep, and chest physiotherapy Diuresis as able Limited echo reviewed with normal EF, dextrocardia, small to moderate inferolateral pericardial effusion, indeterminate diastolic function. Goals of care discussions repeatedly addressed throughout hospitalization with patient and adult children (2 daughters and son). Ultimately CODE STATUS transition to DNR CC on 3/4/2023. Discussed with patient and daughters at bedside today, referred to hospice per patient and family wishes. Comfort medications ordered. Hospice meeting at 1 PM today. Hyponatremia, worsening Likely hypovolemic in the setting of decreased p.o. and diuresis Trend sodium Hold diuresis today Hold off on fluid resuscitation given her tenuous respiratory status Possible underlying heart failure with preserved ejection fraction On oral Lasix at home and BNP elevated on admission Unclear if has underlying heart failure. Chest x-ray not consistent with cardiogenic pulmonary edema and exam not consistent with decompensated heart failure. Chest x-ray 3/4 reviewed with near complete opacification of right hemithorax with minimal improvement from few days ago. Consistent with lung airspace disease possible pulm edema bilaterally. Diurese as able, on hold for now due to hyponatremia Echocardiogram with normal LV function

Weitere VAERSDATA-Felder

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

VAERS 2544600

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: MI
Alter: 80,0
Geschlecht: F
Eingang: 28.12.2022
Impfdatum: 18.08.2022
Beginn: 19.12.2022
Tage bis Beginn: 123,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Adrenal disorder Anticoagulant therapy Aspartate aminotransferase increased Blood alkaline phosphatase increased Blood gases normal Blood glucose increased Blood pH normal Blood potassium decreased Brain natriuretic peptide increased C-reactive protein increased COVID-19 COVID-19 pneumonia Cardiac failure acute Cardiac failure congestive Chest X-ray abnormal Chest discomfort Computerised tomogram abdomen abnormal

Symptomtext

Admission Date: 12/19/2022 Discharge Date: 12/24/2022 COVID positive date: 12/20/2022 Admitting Diagnoses: Acute respiratory failure with hypoxia PRESENTING PROBLEM: Hypoxia Warfarin anticoagulation Acute respiratory failure with hypoxia Acute on chronic congestive heart failure, unspecified heart failure type Pneumonia due to COVID-19 virus COVID-19 HOSPITAL COURSE: Per history of present illness "The patient is a 81 y.o. female with past medical history significant for nonischemic cardiomyopathy, stage 3 chronic kidney disease, acquired hypothyroidism, hyperlipidemia, DVT/PE on Coumadin, chronic combined systolic and diastolic heart failure, adrenal mass, hypertension, Crohn's disease, epilepsy, history of breast cancer, presented to the emergency department with chief complaint of difficulty breathing. Patient is currently BiPAP with difficulty answering questions, also information is obtained from neighbor was at bedside, emergency physician, and staff nurse. According to the neighbor, the patient took a home a COVID test 3 days ago that was positive. Today, patient woke up and was having breathing difficulties. Patient notified her neighbor. The patient apparently also had a visiting nurse that came and evaluated patient who subsequently requested EMS to transport patient to the emergency department for difficulty breathing. Patient was also complaining of some chest discomfort. In the emergency department, patient became progressively dyspneic and was transitioned from high-flow nasal cannula to BiPAP. With concern for pulmonary edema, patient received nitroglycerin paste. Chest x-ray with evidence of pneumonia versus interstitial pulmonary edema. BNP was elevated at 8827. EKG without acute ischemic changes. Troponins 28 and 34 respectively. Venous blood gas with evidence of normal pH with his pCO2 of 49.1. Other labs showed evidence of hypokalemia with potassium of 3.3, chronic kidney disease stage 3, stable, elevated alkaline phosphatase of 153, elevated glucose of 205, elevated AST of 37. Patient with evidence of elevated inflammatory markers with CRP of 20 and sed rate of 21. Procalcitonin 0.06. Thyroid studies within normal limits. Viral PCR positive for COVID-19. Urinalysis negative for infection. Given patient's increased oxygen demands with need for BiPAP, patient was empirically started on treatment for community-acquired pneumonia and remdesivir for COVID-19 along with Decadron. Patient was admitted to the intensive care unit for further management." Patient able to come off of BiPAP down to nasal cannula. She underwent treatment for COVID 19 pneumonia and acute on chronic systolic heart failure. TTE done 12/20 showed reduction of ejection fraction from 32 to 25%. Also showed global left ventricular hypokinesia, LV dilation. Patient had good response with IV Lasix, was able to wean down oxygen requirements. Patient did develop hypokalemia, needed to be started on daily potassium supplements. Patient was transitioned to oral Lasix 40 mg once daily. Her supplemental oxygen was weaned off 12/23. She did not display any other signs of superimposed bacterial infection. She was given treatment for community-acquired pneumonia empirically with Rocephin and azithromycin. Patient also received course of remdesivir. She has had 4 days of both antibiotics and remdesivir, on 5th day her IV went bad and patient declined to have further IV placed. Since she has had significant improvement, patient was not given antibiotics for the 5th day. PT/OT evaluated, recommended discharge home with home health. 12/24 patient underwent home oxygen evaluation, found to have normal oxygen saturations without need for supplemental oxygen on both rest and activity. Patient was instructed to continue using Lasix and potassium daily until she sees her cardiologist. Patient advised to follow-up with PCP regarding her incidental adrenal gland lesion detected on CT abdomen in November 2022. She will be sent home with 5 days of dexamethasone. Patient being discharged home today in stable condition with family.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic combined systolic and diastolic heart failure Dilated cardiomyopathy Cardiomyopathy, nonischemic ICD 2017 Essential hypertension Pulmonary embolism Acute deep vein thrombosis (DVT) of right peroneal vein VT (ventricular tachycardia) Gastro-esophageal reflux disease without esophagitis Epilepsy, unspecified, not intractable, without status epilepticus Acute midline thoracic back pain Stage 3b chronic kidney disease Postmenopausal bleeding Vaginal atrophy Goiter Acquired hypothyroidism Hyperlipidemia Crohn's disease, unspecified, without complications Adrenal mass History of breast cancer History of endometrial cancer Spinal stenosis of lumbar region without neurogenic claudication Gait instability History of nontraumatic rupture of cerebral aneurysm Closed fracture of right tibial plateau with routine healing, subsequent encounter Abnormal CT of thoracic spine Abnormal CT of the abdomen
Andere Medikamente: benzonatate (TESSALON) 100 MG capsule carvedilol (COREG) 25 MG tablet Cholecalciferol (VITAMIN D PO) cloNIDine (CATAPRES) 0.1 MG tablet dexamethasone (DECADRON) 6 MG tablet furosemide (LASIX) 20 MG tablet levothyroxine (SYNTHROID) 100 MCG t
Allergien: Penicillins
Vorherige Impfungen: -

VAERS 2542071

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 23.12.2022
Impfdatum: 08.04.2022
Beginn: 24.10.2022
Tage bis Beginn: 199,0
Dosis: 4
Route/Site: - / -

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

Acute respiratory failure COVID-19 Chronic respiratory disease Condition aggravated Death Endotracheal intubation Mechanical ventilation Respiratory failure

Symptomtext

Patient is a 74 y.o. male admitted to the hospital on 10/24/2022 for acute on chronic hypoxemic respiratory failure as well as COVID-19 infection. Patient was found to have acute exacerbation of his chronic lung disease. He suffered a complicated hospital course ultimately resulting in endotracheal intubation. Patient was unable to be weaned from the ventilator and the decision was made on hospital day 26 to pursue compassionate extubation. Patient passed away in the hospital on 11/19/2022. Please see previous notes for full detailed hospital course.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 26,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2542055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: -
Alter: 78,0
Geschlecht: M
Eingang: 23.12.2022
Impfdatum: 19.04.2022
Beginn: 17.11.2022
Tage bis Beginn: 212,0
Dosis: 4
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Blood creatinine increased COVID-19 Chest X-ray normal Cough Dyspnoea Erythema Hypoxia Lethargy Respiratory tract congestion Skin ulcer Skin warm Urinary retention

Symptomtext

Patient is a 78 y.o. male admitted to the hospital on 11/17/2022 for shortness of breath, lethargic and hypoxia after recent diagnosis of covid at his long term facility Discharge Diagnosis and Associated Hospital Course COVID-19 with acute hypoxic respiratory failure resolved -Suspect the main etiology shortness of breath and cough -currently 93% RA -Reported is not on any O2 at the rehab center -will stop decadron due to dm2 -Not a candidate for remdesivir due to elevated creatinine -ID recommended continue paxlovid to complete course -cxr with no consolidation -patient has cough and congestion, symptoms Type I IDDM w CKD 3 -Blood glucose is currently stable - continue his Lantus dose at 30 units -continue ssi -glucose elevated due to steroid Acute kidney injury on CKD 3 Acute urinary retention -Baseline creatinine 1.2 increased to 1.6 now down -Suspect combination from COVID and probably diuretic and if certain news -aki resolved, start flomax when off paxlovid for now will need straight cathed q8 hours Right heel ulcer -Chronic for him -warm to touch and erythematous will -We will continue wound care to see History of seizures -Continue Keppra Essential hypertension -Continue metoprolol Peripheral artery disease -Has had amputations of his toes in the past -Has had multiple interventions in the past -Continue aspirin Plavix and statin therapy Dementia without behavioral disturbance -Patient currently calm and collected -We will continue his Aricept for now

Weitere VAERSDATA-Felder

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

VAERS 2524129

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: MI
Alter: 89,0
Geschlecht: M
Eingang: 06.12.2022
Impfdatum: 12.06.2022
Beginn: 02.10.2022
Tage bis Beginn: 112,0
Dosis: 2
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Agitation Agonal respiration Aspiration Aspiration joint Aspiration pleural cavity Bacterial test positive Blood culture positive COVID-19 Chest pain Chondrocalcinosis Computerised tomogram thorax abnormal Condition aggravated Confusional state Corynebacterium test positive Death Echocardiogram abnormal

Symptomtext

Discharge Provider: * Primary Care Physician at Discharge: MD Admission Date: 10/28/2022 Date of Death: 12/3/2022 COVID Positive Date: 10/28/2022 PRESENTING PROBLEM: Acute respiratory failure with hypoxia [J96.01] Acute hypoxemic respiratory failure [J96.01] COVID-19 [U07.1] HOSPITAL COURSE: Pt is a 89 yr old M with PMHx of CAD s/p CABG and bioprosthetic AV replacement, chronic diastolic CHF, Atrial fib on warfarin, Hx of CVA, DM II, CKD IIIB, HTN, HPL, BPH, Hx of HSV and dementia (with activated DPOAs) admitted with acute respiratory failure with hypoxia and sepsis in the setting of acute COVID19 PNA and acute on chronic diastolic heart failure with right heart failure. He was started on diuretics and steroids; his son who is his activated DPOA declined use of remdesivir. Patient improved with rapid resolution of toxic/metabolic encephalopathy. Hypoxia slowly normalized. Echo showed preserved EF but with mod decreased RV function with TAPSE of 13mm, RVSP 58mm, and dilated IVC w/ poor collapse consistent w/ fluid overload. Patient's admission was complicated by a mild AKI secondary to cardiorenal which improved. Later in the hospital stay - he developed sudden acute on chronic hypoxic respiratory failure. Patient went from requiring room air to high-flow nasal cannula and subsequently weaned down to 3-4L NC. Blood cultures grew Corynebacterium - ID was consulted and recommended IV Vancomycin for 6 weeks (from 11/2/22 to 12/13/22). Workup noted left-sided pleural effusion - s/p thoracentesis by IR on 11/4 w/exudative pleural fluid. He was subsequent days IV Lasix. Pulmonary was consulted. CT thorax showed extensive consolidation and groundglass opacities in left lung, as well as pleural effusions. Follow up Chest X rays showed no improvements. Patient remained confused though able to answer basic orientation questions. Pt had intermittent agitation and refusal of care requiring restraints - discontinued on 11/7. Palliative care followed patient through 11/11 but given goals clear of aggressive care per DPOAs- they signed off. Patient had chest pain episode on 11/14 - refused labs. The patient had left knee effusion, aspirated earlier in November by Orthopedic service with crystals suggestive of pseudogout. Short court of oral steroids gave partial benefit (permission obtained from ID to give in setting of improving infection.) A course of oral NSAID and colchicine was not effective in removing pain. Intraarticular steroid and aspiration of effusion was performed on 11/21/22. Patient continued to worse despite being on vancomycin. Has noted to have increased oxygen requirements up to 4 L. Repeat chest x-ray showing worsening right lung base opacity. Sputum cultures positive for Gram-negative rods along with Gram-positive cocci. Cefepime was added. Repeat chest x-ray showed once again large pleural effusion and thoracentesis was repeated on 11/30/22 with 1L bloody fluid removed. Pulm was once again consulted, but the patient refused all treatment options that were suggested and they signed off. Due to patient refusing treatment options and continues to worsen extensive goals of care discussions were done with patient and his DPOA/son about the patient poor prognosis. Per DPOA if patient worsens does not wish for ICU transfer, intubation, or vasopressors. Would be OK with BiPAP/CPAP, but educated that in his current state he would not be a candidate as he would not be able to pull the mask off if needed, son expressed understanding. Patient now on 12/3/22 has become unresponsive with agonal breathing. DPOA again contacted that the patient appears to be actively passing away and stated to keep with the same plan and if he passes away to let him pass away peacefully, but continues to not want to change patient to comfort care. Patient passed away on 12/03/2022 at 1636. Pt.'s son was notified over the phone and all questions and concerns were addressed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 36,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Acute hypoxemic respiratory failure Pneumonia due to COVID-19 virus Pleural effusion, left Pneumonia of left lung due to infectious organism Hemoptysis Acute on chronic respiratory failure, unspecified whether with hypoxia or hypercapnia Permanent atrial fibrillation Essential hypertension, benign LVH (left ventricular hypertrophy) ASHD (arteriosclerotic heart disease) Chronic diastolic heart failure Acute on chronic diastolic heart failure Class 1 obesity in adult Zoster conjunctivakeratitis Candida rash of groin Onychomycosis Acute cystitis without hematuria Expressive aphasia syndrome Mixed cortical and subcortical vascular dementia without behavioral disturbance Other chronic pain BPH (benign prostatic hypertrophy) Stage 3a chronic kidney disease Type 2 diabetes mellitus without complication Mixed hyperlipidemia S/P AVR (aortic valve replacement) History of CVA (cerebrovascular accident) Family history of colon cancer Long term (current) use of insulin Functional quadriplegia Primary osteoarthritis of both hips Weakness Age-related physical debility Advanced care planning/counseling discussion Pseudogout Corynebacterium striatum Bacteremia likely secondary to pneumonia/complicated parapneumonic effusion Multiple comorbid conditions
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet acyclovir (ZOVIRAX) 800 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amlodipine (NORVASC) 2.5 MG tablet carboxymethylcellulose (REFRESH PLUS) 0.5 % SOL
Allergien: Beef-derived Products Flomax [Tamsulosin Hcl] Morphine Vardenafil
Vorherige Impfungen: -

VAERS 2491220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 06.08.2022
Beginn: 14.10.2022
Tage bis Beginn: 69,0
Dosis: 4
Route/Site: - / -

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

Abnormal behaviour Acute respiratory failure COVID-19 Cardiac failure congestive Chemotherapy Chest X-ray abnormal Chronic left ventricular failure Chronic obstructive pulmonary disease Condition aggravated Emphysema Hyperlipidaemia Hypertension Hypoxia Lymphopenia Myelosuppression Respiratory failure Restless legs syndrome SARS-CoV-2 test positive

Symptomtext

Discharge Provider: DO Primary Care Provider: DO Admission Date: 10/14/2022 Discharge Date: 10/16/2022 HOSPITAL COURSE 74-year-old presented to ER with four days of not acting right. She was more hypoxic than at baseline. See H&P for full details. Chest x-ray showed emphysema. COVID was positive. Clinically she had a COPD exacerbation 2? COVID. Admitted and treated with Solu-Medrol, Symbicort, Spiriva, albuterol MDI. Given three days Remdesivir. She did very well during the hospitalization. On the 2nd day of hospitalization she was stable on her home 2 L and did not desaturate with ambulation. We felt she would benefit from three days of Remdesivir and she agreed; this was completed. Today she is able to maintain saturations while ambulating up to 90 ft. She feels well and would like to go home. She is stable for this. DISCHARGE DIAGNOSES 1. COVID positive 2. Acute exacerbation of end-stage oxygen-dependent chronic obstructive pulmonary disease 3. Acute hypoxic respiratory failure on chronic hypoxic/hypercarbic respiratory failure 2? #1 and #2 4. Chronic diastolic CHF 5. HTN 6. SSS s/p pacemaker 7. History of PE and RLL arterial thrombosis 2? mass 8. RLS 9. HLD 10. History of genital HSV 11. Chronic pain syndrome 12. History of recurrent SCC lung 13. Left DCIS 14. Chronic thrombocytopenia/lymphopenia 2? bone marrow suppression from chemotherapy

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: Discharge Provider: MD Primary Care Provider at Discharge: DO Admission Date: 7/31/2022 Discharge Date: 8/6/2022 HOSPITAL Acute on chronic hypercarbic respiratory failure secondary to acute COPD exacerbation Possible undiagnosed OSA COPD on home O2 2L Anasarca, upper and lower extremities Hypoalbuminemia Hypercalcemia resolved A-fib - rate controlled Acute kidney injury- resolved Squamous cell lung cancer, in remission Discharge Provider: MD Primary Care Provider: DO Admission Date: 7/17/2022 Discharge Date: Jul 26, 2022 HOSPITAL PRESENTING PROBLEM: Pleural effusion [J90] Pulmonary vascular congestion [R09.89] Acute respiratory failure with hypoxia and hypercarbia [J96.01, J96.02] Acute on chronic respiratory failure with hypoxia and hypercapnia [J96.21, J96.22] Respiratory failure [J96.90] Atrial fibrillation with rapid ventricular response [I48.91] COPD (chronic obstructive pulmonary disease) [J44.9] A-fib [I48.91] Atrial fibrillation with RVR [I48.91]
Vorgeschichte: Trigger finger, acquired Sacroiliac pain Osteoarthritis of ankle and foot Osteoarthritis of shoulder Osteoarthritis of hand Osteoarthritis of right knee Osteoarthritis of left knee COPD, severe Osteoporosis, postmenopausal Benign essential hypertension Hyperlipidemia LDL goal < 100 Osteoarthritis of lumbar spine DDD (degenerative disc disease), lumbar Lung nodules Allergic rhinitis Genital HSV Vitamin D deficiency TIA (transient ischemic attack) Small cell carcinoma of lung, left Drug-induced coagulation inhibitor disorder SSS s/p pacemaker Hypoxemia requiring supplemental oxygen History of Pulmonary embolism 2016 Carcinoma in situ of breast Chronic pain syndrome Chronic prescription opiate use Chronic obstructive pulmonary disease with acute exacerbation Chloride-responsive metabolic alkalosis Acute on chronic respiratory failure with hypoxia and hypercapnia Moderate protein-calorie malnutrition Iron deficiency anemia due to chronic blood loss COVID
Andere Medikamente: acetaZOLAMIDE (DIAMOX) 250 MG tablet albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization amlodipine (NORVASC) 2.5 MG tablet atorvastatin (LIPITOR) 10 MG tablet AYR saline nasal GEL budesonide/formoterol (SYMBICORT) 160-4.5 MCG/ACT inhale
Allergien: Levaquin [Levofloxacin]Dizziness Bandaids Mirapex [Pramipexole]Nausea Only
Vorherige Impfungen: -

VAERS 2453786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: MO
Alter: 29,0
Geschlecht: F
Eingang: 21.09.2022
Impfdatum: 19.05.2022
Beginn: 06.06.2022
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: IM / -

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

Abdominal pain Anxiety Arthralgia Asthma COVID-19 Coccydynia Delivery Dysphagia Exposure during pregnancy Foetal death Foetal movement disorder Inappropriate schedule of product administration Pyrexia Skin texture abnormal Subchorionic haemorrhage Tongue disorder Ultrasound antenatal screen abnormal Uterine dilation and curettage

Symptomtext

5/16/2022 G1P000 "29 y.o. year old female @ 16+5 weeks gestation who presents for continued OB care. Patient does not feel fetal movements as of yet. + FHT's noted today. Patient denies any cramping/pain, bleeding, or LOF. Patient was having lower abdominal cramping sensation a few weeks ago, but no longer. Patient had an US today that showed normal cervical length. Patient denies having any UTI sx at this time. Patient having no complaints today. Covid and flu done; Recommended booster" RN MSN WHNP-BC 5/19/2022 3rd Pfizer (1st 12/14/20, 2nd 1/11/21) 6/6/2022 message from patient: "I?ve noticed the last few days that the skin on my belly appears slightly mottled and there is delayed cap refill. Is this normal? I am growing quite a bit and I am on the paler side. " "Delayed cap refill on your belly? How delayed?" RN "Its about 4-5 seconds, I had my coworker (another RN as well) look at it and confirm the timing. Not sure if im being overly worried but i just noticed it when I went to the bathroom at work and thought, hm, that's different. " Patient "Would you be able to send a picture of your belly for me to take a look at?" RN photos sent "Overall, this looks normal. This can happen from the quick growth during pregnancy, but nothing to be concerned with" RN 6/7/2022 Message to GI MD "My upper scope last fall looked good after reporting some difficulty with swallowing. This symptom has continued and now over the last month I have noticed that I am having some weird changes with my speech- difficult to explain fully but I feel like my tongue is not articulating the way it used to especially if I am having longer conversations and kind of like it flattens out and sticks to my teeth? Sounds goofy and again I am having a hard time explaining what I am feeling. At the time of my scope we had discussed possibly seeing a SLP for eval? I cannot remember but I feel like we decided against it since the scope was good. Is there something further you recommend for evaluation? I am also 20 weeks pregnant right now so I realize that may hinder some things. " "Congratulations on your pregnancy. Please try Pepcid 20 mg 2 times daily. You may buy these pills from over-the-counter. Please try this for a couple of weeks and kindly contact me if your symptoms do not improve with this. Thank you." MD 6/17/2022 prenatal visit: "Doing well. No complaints." 6/30/2022 ultrasound 7/1/2022 message :"Is there any concern regarding the last two ultrasounds not being able to visualize the heart? Also is there any concern regarding fetal growth?" patient "No, it's just suboptimal still. No concerns. As far as the growth, it's very early to determine if there is cause for concern or not. I plan to order the follow-up growth ultrasound as recommended after the follow-up cardiac one is completed." DO 7/13/2022 video visit; "Bad tailbone and left hip pain. Lots of anxiety related to new jobs both for her and for husband and now with home purchase. History of back surgery; Recommend OB Epidural consultation; Last imaging 2013 Pelvic girdle pain; Start belly binder Referral to Lumen for anxiety" DO 7/20/2022: "26w0d Called with ABSENT fetal movement all day Drank water, had dinner and still had no fetal movement Affirmed not just decreased but can't feel baby at all. No lof/vb/ctx. However did have SCB 1st trimester Advised to come to now" MD "26w0d, who presents with absent fetal movement today, she reports there had been more fetal movement than usual the previous 2 days. Today she had been busy at work today and after eating dinner this evening, she laid down and did not feel baby move. Contractions: none. Vaginal bleeding: None. Leakage of fluid: denies." "Her pregnancy has been complicated by: 1. Subchorionic hemorrhage - @ 7wks resolved 2. Asthma - albuterol inh 3. Covid in early pregnancy" 7/20 9:21 pm "I was called to confirm . Pt called exchanged with absent fetal movement and unfortunately the midwife and hospitalist did US confirming absent FHTs. With permission of patient, I also looked with US. Absent FHTs. No blood flow. Placenta observed w/o obvious abruption. No bleeding No abdominal pain. Appropriately grieving. Reviewed induction options today or return at later date. She is reviewing her choices now." MD 7/20/2022: note from MD "Principal and Secondary Diagnosis 1. 29 y.o. G1P0100 2. IUFD @ 26w 3. Retained placenta Principal and Secondary Procedures Induced vaginal delivery Suction D&C under US guidance Pertinent History & Physical See H&P. Hospital Course Patient was admitted. She underwent a vaginal delivery of IUFD @ 26w. Course complicated by maternal fever and retained placenta s/p D&C under US guidance. Concern for continued retained placenta, co-management for postop recommendations. She received IV antibiotics x 24 hrs. Please see delivery and op note for further details. Postop the patient was voiding spontaneously, tolerating a regular diet, ambulating, and analgesia controlled with oral pain medications. Bleeding remained minimal. She remained afebrile. She was discharged home in a stable condition." 7/20 11pm "Patient transferred safely from OB triage to L&D for MIL for IUFD. She presented for evaluation after not feeling any fetal movement for the past day. BSUS was performed by both OBH, which confirmed no fetal cardiac activity. No obvious placental abruption was noted. She reports some mild cramping pains that have started recently but denies any LOF or bleeding. She is appropriately grieving with her husband and parents. We reviewed the process of induction as well as pain control options and laboratory evaluation. Her questions were answered." Per record delivery/D and C of fetus with demise was on 7/21/22 - anesthetic epidural 9/14/2022 pt received D and C for retained products of conception for which I was involved with.

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Praegender Schweregrund: Foetal death
Hospital-Tage: -
Labordaten: 7/6/2022 24w 0d ultrasound follow up Cardiac activity present. FHR 144 bpm. Fetal movements: present. Presentation: cephalic Placenta: Fundal Umbilical cord: Cord vessels: 3 vessel cord. Insertion site: placental insertion: normal Amniotic fluid: Amount of AF: normal amount. MVP 5.6 cm
Aktuelle Erkrankungen: -
Vorgeschichte: asthma migraines Hemochromatosis carrier
Andere Medikamente: -
Allergien: Cephalexin
Vorherige Impfungen: -

VAERS 2447916

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: OH
Alter: 83,0
Geschlecht: M
Eingang: 16.09.2022
Impfdatum: 23.02.2022
Beginn: 11.08.2022
Tage bis Beginn: 169,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Asthenia Blood creatinine increased Blood glucose increased COVID-19 Chest X-ray abnormal Computerised tomogram thorax Cough Dyspnoea Fatigue Glycosylated haemoglobin increased Legionella test Lung opacity Oxygen saturation decreased Pneumonia SARS-CoV-2 test positive Sputum culture White blood cell count increased

Symptomtext

Patient is a 84 y.o. male patient of MD with history of CAD, CLL (Chronic Lymphocytic Leukemia), DM2, CKD, HTN and HLD presented with fatigue and shortness of breath. He was provided with oxygen therapy and started on antibiotics and his previously prescribed prednisone taper was continued. CXR was initially concerning for possible pneumonia. Testing for pneumonia was negative with sputum cultures pending at the time of discharge. CT Scan of the patient's chest was completed that was also pending at time of discharge. The patient's condition significantly improved. It was determined that his desaturation is likely due to post-covid changes to his lungs. He was evaluated for and discharged with home health services and supplemental oxygen in fair condition. He was discharged with 3 more days of antibiotics and a bowel regimen. He was advised to complete his previously prescribed prednisone taper as well. He was also discharged with Insulin Lantus as his blood sugar levels had been elevated while on steroids. He was instructed to follow-up closely with his PCP and Pulmonologist on discharge. Assessment and Plan Acute Hypoxemic Respiratory Failure Pt with worsening shortness of breath since having COVID ~1 month ago CXR with bilateral lower lobe opacities suspicious for pneumonia WBC is elevated in the setting of steroids 88% on RA, improved to 96% with 2L NC; currently 93% on RA Unlikely CAP; more likely Post-Covid ILD S. Pneumo and Legionella Urinary antigens negative Plan to continue steroid taper previously ordered by pulmonologist (prednisone 10mg daily for 5 more days) Sputum culture pending at time of discharge CT chest w/o contrast ordered; results pending Patient failed Home O2 Eval - requiring oxygen on discharge; Care Management consulted for home oxygen therapy; medical are setup Plan to discharge the patient with Cefdinir x 3 more days Encouraged patient to complete steroid taper as previously prescribed Covid-19 Virus Infection Date of onset of symptoms: ~7/17 Symptoms present on admission: shortness of breath, cough Date of covid positive test: 7/17 and again 8/11 Vaccination status: vaccinated Imaging: CXR with bibasilar pneumonia Oxygen requirements on admission: 2L NC Current oxygen requirements: RA Clinically I suspect this is not a repeat COVID infection, but rather post-covid ILD, likely incidental positive related to recent infection Weakness Likely secondary to CLL and lingering post-COVID SOB PT/OT consulted for further evaluation CM consulted for assistance with discharge; medical recommended on discharge Constipation Family reports no BM in 1 week Continue miralax daily + senna BID Start MoM Will discharge patient with a bowel regimen; encouraged PO intake of fluids and maintaining an adequate fiber diet upon discharge DM2 Hemoglobin A1c 10.9 on 06/21/22 Hold home dulaglutide and glimepiride Lantus and SSI while hospitalized Lantus 10 units nightly with SSI. Currently on steriods. Plan to discharge patient with 10 U Solostar (Lantus) Pen nightly with recommendations to follow-up closely with PCP CKD Baseline Cr 1.5-1.7 Creatinine today 1.59 Monitor HTN BP stable Continue carvedilol CLL On ibrutinib chronically Okay to hold while hospitalized

Weitere VAERSDATA-Felder

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

VAERS 2443224

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: OH
Alter: 87,0
Geschlecht: M
Eingang: 13.09.2022
Impfdatum: 07.01.2022
Beginn: 05.08.2022
Tage bis Beginn: 210,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure Asthenia Blood gases normal C-reactive protein increased COVID-19 Chest X-ray abnormal Encephalopathy Fibrin D dimer normal Liver function test normal Malaise Pyrexia SARS-CoV-2 test positive Sepsis

Symptomtext

Clinical Summary Patient is a 88 y.o. male with a history of HTN, HLD and TIAs who presented to RMH 8/5/2022 with generalized malaise/weakness and subjective fevers s/p positive COVID home test found to be septic and hypoxic. Discharged on 8/7/2022 1. Sepsis 2/2 COVID Infection: Confirmed PCR 8/5/22, unclear exact duration of symptoms but reported ~ 5 days. Admit CXR nonfocal. CRP 3.2. LFT WNL. Required 2-3L NC on admit. Initiated on decadron and remdesivir. Off O2 8/8/22. Plan to complete 10 day course of steroids. 2. Acute hypoxic respiratory failure: Secondary to above, CXR nonfocal. D-Dimer normal. Wean O2 as able. Intermittent lasix prn. Resolved. 3. Acute on chronic encephalopathy: baseline cognitive impairment with poor memory per wife. Suspect concurrent acute metabolic encephalopathy in setting of above. VBG WNL. Delirium precautions. Appears to be at baseline. 4. HTN: Known history, continued home meds with parameters 5. HLD: Known history, continued home statin 6. TIA: per hx, continued plavix Discharge Medications Medication List START taking these medications dexAMETHasone 6 MG tablet Commonly known as: DECADRON Take 1 (one) tablet (6 mg total) by mouth daily with breakfast for 6 days Start: 08/09/22. Start taking on: August 9, 2022

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: As above
Aktuelle Erkrankungen: none
Vorgeschichte: Gout HTN Hyperlipidemia Cerebrovascular disease Hearing loss
Andere Medikamente: acetaminophen 325mg 2tablets every 6 hours as needed for pain albuterol MDI 2 puffs QID prn SOB Vitamin C 1000mg daily atorvastatin 10mg daily clopidogrel 75mg daily coenzyme Q10 200mg daily cyanocobalamin 1000mcg daily Mucinex 600mg BID l
Allergien: NKA
Vorherige Impfungen: -

VAERS 2425117

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: MI
Alter: 79,0
Geschlecht: F
Eingang: 31.08.2022
Impfdatum: 02.02.2022
Beginn: 21.08.2022
Tage bis Beginn: 200,0
Dosis: 2
Route/Site: - / -

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

Acute respiratory failure Blood creatinine increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chills Culture negative Headache Hypoxia Lung infiltration Pain Pleural effusion Productive cough Rhinorrhoea SARS-CoV-2 test positive Sputum discoloured Tachycardia

Symptomtext

Discharge Provider: MD Primary Care Provider at Discharge: NP Admission Date: 8/21/2022 Discharge Date: 8/29/2022 PRESENTING PROBLEM: Acute and chronic respiratory failure with hypoxia (HCC) [J96.21] COVID-19 [U07.1] Pneumonia due to COVID-19 virus [U07.1, J12.82] HOSPITAL COURSE: HPI: 79-year-old lady with medical history of hypertension, CKD stage 4, Morbid Obesity (BMI> 70), GERD, gastric bypass, depression and dementia presenting to hospital on 08/21 with cough, headaches, rhinorrhea. Patient resides in a nursing home, states that she had headaches body aches and chills when she woke up in the morning. She started having cough which was dry but then started producing yellowish sputum. No fever reported. A home COVID test was done which was positive. She did not have any chest pain or tightness or discomfort. No lightheadedness or dizziness. She came to hospital where he was found to be tachycardic and hypoxic in mid 80's and was put on nasal cannula 2 L. CXR remarkable for Right lobe infiltrate/effusion. She does have some memory deficits and unable to provide complete history. She knows the children's name and where they are located. She would like her daughter be the DPOA. She would like to remain full code for resuscitation. HOSPITAL COURSE: Patient treated with dexamethasone x 10 days, She recieved 5 days of empiric abx for poss bacterial pna (Rocephin/Azithromycin). All cx were no growth to date. Pt has now been weaned off supplemental oxygen, we will reassess prior to discharge. Her vital signs have been stable. Her creatinine is 2.09. She will need close follow-up with this, of note her creatinine 1.7 in October 2001, 1.99 in February 2022. range in October 2021 Pt is stable for discharge. Patient will need assistance at home. I have discussed the case with her daughter. Patient has been working with therapy and showing gains

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Senile nuclear cataract, bilateral Chronic low back pain HTN (hypertension) Depression, major, recurrent Asthma, mild persistent History of intestinal bypass Microscopic hematuria GERD (gastroesophageal reflux disease) OA (osteoarthritis) of knee Restless legs syndrome (RLS) Chronic kidney disease (CKD), active medical management without dialysis, stage 4 (severe) (HCC) Pseudoexfoliation glaucoma, severe stage Glaucoma (increased eye pressure) Dyspareunia, female OSA (obstructive sleep apnea) Vocal cord dysfunction Edema Spinal stenosis of lumbar region, unspecified whether neurogenic claudication present Urinary incontinence, unspecified type Incarcerated ventral hernia s/p 7/24: ex-lap, LOA, Strattice mesh underlay Kidney stone Postlaminectomy syndrome Generalized anxiety disorder Postmenopausal bleeding Age-related osteoporosis without current pathological fracture Memory difficulty Vitamin D deficiency Pneumonia due to COVID-19 virus Dementia (HCC) Acute hypoxemic respiratory failure (HCC) Dry cough
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler atorvastatin (LIPITOR) 10 MG tablet budesonide/formoterol (SYMBICORT
Allergien: PenicillinsHives, Throat swelling Sulfa DrugsRash, Throat swelling, Hives CodeineNausea and Vomiting SulfadiazineHives, Throat swelling
Vorherige Impfungen: -

VAERS 2399163

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: WI
Alter: 75,0
Geschlecht: M
Eingang: 02.08.2022
Impfdatum: 18.04.2022
Beginn: 21.07.2022
Tage bis Beginn: 94,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Cardiac arrest Cardio-respiratory arrest Intensive care SARS-CoV-2 test positive

Symptomtext

Patient is a 75 y.o. year old male with complex medical history including bladder cancer receiving palliative chemo, and percutaneous nephrostomy tubes and urostomy, CKD, CAD with hx of CABG, GERD, admitted after cardiac arrest in the field, coded and ROSC, now in CCU, also found to be covid + on admission.

Weitere VAERSDATA-Felder

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

VAERS 2335253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: NJ
Alter: -
Geschlecht: M
Eingang: 25.06.2022
Impfdatum: -
Beginn: 05.02.2021
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

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

Abnormal behaviour Acute kidney injury Death Dementia Investigation Muscle twitching

Symptomtext

He died on the 11May; I would say may be a week or two later his dementia got a lot worse; Acute renal failure; He started developing twitches, big twitches; He started acting strange; This is a spontaneous report received from a contactable reporter(s) (Physician). A 62-year-old male patient received BNT162b2 (BNT162B2), as dose 4 (booster), single (Lot number: FJ6369), in arm for covid-19 immunisation. The patient's relevant medical history included: "He had an underlying neurologic disease that's called Cadasil" (unspecified if ongoing), notes: he had an underlying neurologic disease that's called Cadasil. The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose 1, single), for COVID-19 Immunization; Bnt162b2 (Dose 2, single), for COVID-19 Immunization; Bnt162b2 (Dose 3 (Booster), single), for COVID-19 Immunization. The following information was reported: ACUTE KIDNEY INJURY (medically significant) with onset 05Feb2021, outcome "unknown", described as "Acute renal failure"; ABNORMAL BEHAVIOUR (non-serious) with onset 05Feb2021, outcome "unknown", described as "He started acting strange"; MUSCLE TWITCHING (non-serious) with onset 05Feb2021, outcome "unknown", described as "He started developing twitches, big twitches"; DEMENTIA (medically significant) with onset 05Feb2021, outcome "unknown", described as "I would say may be a week or two later his dementia got a lot worse"; DEATH (death) with onset 11May2022, outcome "fatal", described as "He died on the 11May". The events "i would say may be a week or two later his dementia got a lot worse", "acute renal failure", "he started developing twitches, big twitches" and "he started acting strange" required emergency room visit. The patient underwent the following laboratory tests and procedures: Lab Work: Unknown results, notes: Doctor stated, He had a lot of it at the hospital. Therapeutic measures were not taken as a result of dementia, acute kidney injury, muscle twitching, abnormal behaviour. The patient date of death was 11May2022. The reported cause of death was unknown. No autopsy was performed. No follow-up attempts are needed. No further information is expected.; Sender's Comments: Based on the current available limited information in the case provided, the causal association between the events death, dementia, acute kidney injury and the use of suspect product BNT162B2 cannot be fully 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.; Reported Cause(s) of Death: He died on the 11May

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Test Name: Lab Work; Result Unstructured Data: Test Result:Unknown results; Comments: Doctor stated, He had a lot of it at the hospital
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: CADASIL (he had an underlying neurologic disease that's called Cadasil)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2324252

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: MI
Alter: 78,0
Geschlecht: M
Eingang: 20.06.2022
Impfdatum: 07.02.2022
Beginn: 12.06.2022
Tage bis Beginn: 125,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Chest discomfort Condition aggravated Electrocardiogram Hypoxia Laboratory test SARS-CoV-2 test positive

Symptomtext

Discharge Provider: MD Primary Care Provider at Discharge: DO Admission Date: 6/12/2022 Discharge Date: 06/13/2022 PRESENTING PROBLEM: Hypoxia [R09.02] Acute hypoxemic respiratory failure due to COVID-19 (HCC) [U07.1, J96.01] COVID-19 [U07.1] HOSPITAL COURSE: 78-year-old male with multiple medical problems including atrial fibrillation and history of chronic obstructive pulmonary disease. He presented actually with complaints of some left chest discomfort that resolved spontaneously. And no significant EKG or laboratories findings suggestive of ischemia. He was tested for COVID and found to be COVID positive and hypoxemic. He is admitted for further treatment of his hypoxia and presumed COVID pneumonia. The patient was started on remdesivir as well as dexamethasone. Surprisingly the patient had very dramatic and rapid improvement in oxygenation. By the day of discharge his oxygen levels return acceptable without supplemental oxygen. He was continued on dexamethasone post discharge. He was also encouraged to get a COVID booster in the future once he recovers from his current COVID infection. His other routine medications were left unchanged.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: 1/31/2022- Telephone Call to Triage-Poisoning Patient calling in today because accidentally took a double dose of his Laxis 20 mg. Pt reports he took one 20mg of Laxis this morning and another dose of 20mg of Laxis this evening. Pt is having no other symptoms currently, wife was able to check blood pressure which was 116/89, and heart rate was 66. Pt was transferred over to poison control for further evaluation. 1/27/2022- Urgent Care Visit for Pneumonia of Right Lower lobe 1/19/2022- Urgent Care Visit for COVID- 19; Diagnosed 1/12/2022 1/6/2022- Office Visit for Breathing Problems
Vorgeschichte: Erectile dysfunction Hyperlipidemia Essential hypertension, benign Seizure disorder Hypothyroidism History of CVA (cerebrovascular accident) Mild persistent asthma without complication Chronic rhinitis Cholelithiasis Nocturnal hypoxemia At risk for falls Persistent atrial fibrillation Dermatochalasis Tear film insufficiency History of head injury Disorder of optic nerve Posterior capsular opacification Peripheral vascular disease Pseudophakia Posterior vitreous detachment Vitiligo Visual field defect COPD with chronic bronchitis Class 3 severe obesity due to excess calories with serious comorbidity and body mass index (BMI) of 45.0 to 49.9 in adult History of DVT (deep vein thrombosis) Type 2 diabetes mellitus with diabetic peripheral angiopathy without gangrene, without long-term current use of insulin Anemia, unspecified type Proteinuria due to type 2 diabetes mellitus OSA (obstructive sleep apnea) Cough History of COVID-19 Abnormal EKG Pneumonia of right lower lobe due to infectious organism Recurrent major depressive disorder, in full remission Resolved condition, follow-up Advanced care planning/counseling discussion Gross hematuria Nocturnal enuresis Acute hypoxemic respiratory failure due to COVID-19 Chest pain Acute on chronic anemia Diabetes mellitus, type II
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler apixaban (ELIQUIS) 5 MG tablet Ascorbic Acid (VITAMIN C) 1000 MG tablet atorvastatin (LIPITOR) 40 MG tablet carvedilol (COREG) 6.25 MG tablet Cinnamo
Allergien: Cephalexin Clindamycin Pork Allergy
Vorherige Impfungen: -

VAERS 2322895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: NY
Alter: 82,0
Geschlecht: F
Eingang: 17.06.2022
Impfdatum: 01.06.2022
Beginn: 01.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Arthralgia Dizziness Erythema Fatigue Feeling abnormal Headache Myalgia Near death experience Pain in extremity Pyrexia Tremor

Symptomtext

was shaken all over and blanked out; Slight fever; lightheaded; Arm pain; left arm splotchy red; Tiredness; muscle and joint pain; muscle and joint pain; Headache; did not know what happened to her overnight; when she woke up, from elbows to fingertips, her hand was off the bed in a vertical position and her hands were shaken all over; nearly died/ Thought she was dying; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. An 82-year-old female patient received BNT162b2 (BNT162B2), in Jun2022 as dose 4 (booster), single (Lot number: FJ6369) at the age of 82 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "high blood pressure" (ongoing), notes: high blood pressure Diagnosed years ago. Was told her blood pressure was very good.; "cholesterol problems" (ongoing), notes: cholesterol problems Diagnosed years ago; "urinary tract infection" (unspecified if ongoing), notes: Had a urinary tract infection about a month ago; "ton of allergies" (unspecified if ongoing), notes: she was young, 5-7 years old; "COVID-19" (unspecified if ongoing), notes: a very mild case of it. Was prior to receiving any of her COVID-19 Vaccines. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose 1, LOT: EN6202, Dose and Route: Unknown dose; administered into left arm), administration date: 25Feb2021, when the patient was 81-year-old, for COVID-19 Immunization; BNT162b2 (Dose 2, LOT: EN6204, Dose and Route: Unknown dose; administered into left arm), administration date: 18Mar2021, when the patient was 81-year-old, for COVID-19 Immunization; BNT162b2 (Dose 3/first booster shot, LOT: FD7218, handwriting not sure, Dose and Route: Unknown dose; administered into left arm), administration date: 14Dec2021, when the patient was 82-year-old, for COVID-19 Immunization, reaction(s): "mild lightheadedness"; Pneumonia shot (pneumonia shot), administration date: 2022, for Immunization. The following information was reported: DIZZINESS (non-serious) with onset 10Jun2022, outcome "unknown", described as "lightheaded"; PYREXIA (non-serious) with onset 11Jun2022, outcome "recovered" (2022), described as "Slight fever"; TREMOR (non-serious) with onset 11Jun2022, 1 year 1 day after the suspect product(s) administration, outcome "recovered" (11Jun2022), described as "was shaken all over and blanked out"; PAIN IN EXTREMITY (non-serious) with onset Jun2022, outcome "recovering", described as "Arm pain"; HEADACHE (non-serious) with onset Jun2022, outcome "unknown"; FATIGUE (non-serious) with onset Jun2022, outcome "recovering", described as "Tiredness"; FEELING ABNORMAL (non-serious) with onset Jun2022, outcome "unknown", described as "did not know what happened to her overnight"; ERYTHEMA (non-serious) with onset Jun2022, outcome "recovering", described as "left arm splotchy red"; MYALGIA (non-serious), ARTHRALGIA (non-serious) all with onset Jun2022, outcome "recovering" and all described as "muscle and joint pain"; NEAR DEATH EXPERIENCE (medically significant) with onset Jun2022, outcome "unknown", described as "nearly died/ Thought she was dying"; TREMOR (non-serious) with onset Jun2022, outcome "unknown", described as "when she woke up, from elbows to fingertips, her hand was off the bed in a vertical position and her hands were shaken all over". Therapeutic measures were taken as a result of pyrexia. Clinical information: Caller states that she just spoke to a young lady and spent some time on the phone explaining the side effect. Caller was told she could take a survey at the end. At the end it asked her for a password and caller doesn't have a password. She wants to do the survey. Caller doesn't have the name and phone number for the person she was speaking with. caller had to put her glasses on to see straight and provide the reference of withheld. Product was the covid booster, the second one. Caller spent half an hour on the phone and provide all the information. Caller declined to provide lot number again. Caller confirmed that there is nothing new to report. She just had hung up with the other person. She reported on the side effect that she had that night with the booster. No further details provided. With her first booster shot, had mild lightheadedness. She was at hospital receiving the vaccine, stayed there for a while and then went home. Was at the hospital for an hour when everyone else left after 20-25min. It stopped on the same day. She was there at the hospital and was lightheaded. She stayed for a while, it seemed to be getting better. She went home. Her arm where she got the booster shot was her left arm, was extremely painful. When she went to sleep, couldn't sleep on left side. Couldn't press anything on that left arm Had tiredness, headache, muscle pain, muscle pain in the left arm, left arm was splotchy red, had joint pain. Something seemed wrong with muscles and joints. She lives in assisted living. When she came back was told she had a slight fever, she took Tylenol, stating this was in morning. In the afternoon, she took another Tylenol, and the slight fever went away. Then something happened that night. Went to sleep, in middle of night, her eyes opened, and she was shaking all over. Her arms instead of being flat on bed, from the elbows to fingertips were elevated and shaking really badly. Whole body was shaking. She was scared and terrified. This was not a side effect on the chart. Didn't know what was happening. Thought she was dying. She blanked out. She didn't know anything until 6am the following morning and couldn't believe she was alive. Spent the rest of the day in bed, didn't want to move. Was so scared of what was going on. Wants to make sure Pfizer knows this happened and this might happen to someone else. It should be listed as a side effect, so people know. Friday was the day she got the shot, Saturday stayed inside. Sunday took it easy. Today, feels a lot better. Would like to know what did the booster do to her? Her bother had two COVID-19 vaccines and two booster doses and had nothing, didn't feel a thing. he didn't have a problem with it. No further details provided. Caller did have COVID, a very mild case of it. Confirmed this was prior to caller receiving any of her COVID-19 Vaccines. Her left arm still hurts. Lightheadedness: When she got the shot, she sat down in chair and waited 15-20 minutes. Was still lightheaded and didn't leave until she felt better. left arm splotchy red: it's pink, splotchy when she touches it, hurts, but if not touching, doesn't hurt Muscle and joint pain This wasn't serious, it's minor It's hard for her to say which it is Slight fever: Nurse at her assisted living facility checked her temperature. It was slightly over what it should be Was told to take a Tylenol then and at 3pm took another. Then slight fever was gone. Shaking all over and blanked: Doesn't know the length of time it lasted for. Was sleeping, then blanked out, then that's it Woke up at 6AM on Saturday, 11Jun2022. First noticed it 2AM 11Jun2022, when she opened eyes, her hands were shaking. At her age it's difficult to tell what could happen next. Treatment: Tylenol for slight fever, but no other treatment After this experience, hopes she doesn't have to get a third booster. Doesn't want to go through this again. States nothing relevant to what's being reported. Takes 3-4 medications, been taking for years, things might have changed. No further details provided. Had a urinary tract infection about a month ago Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s): Pneumonia shot, has no information or NDC/LOT/EXP. Didn't have one previously in past ten years. Clarified that caller goes to withheld hospital for all of her doctor's appointments. She has not been admitted to the hospital. Maybe when she was young, 5-7 years old, she was told something. Does not provide a product name. States she has a ton of allergies. Patient's Medical History (including any illness at time of vaccination)? High blood pressure and cholesterol problems. Had both for years. What happened to her at night, is that part of the vaccine, is that a side effect or something different. Would like to know what happened to her. Should be put on a piece of paper that this is a side effect. Caller mentioned that she spoke with a representative and filled out a form for a side effect she had with the second booster dose of the Pfizer COVID-19 vaccine and was told to call Pfizer contact option 3 with reference withheld. Callback attempt #1 performed on 14Jun2022 at 02:34 as caller got disconnected. Able to reach caller. Recording disclaimer provided. Successfully provided response. Caller stated that she "spoke with a young lady for half an hour" regarding her side effects with the Pfizer COVID-19 vaccine. Caller wanted to know if her side effects had been reported for the second booster dose of the Pfizer COVID-19 vaccine. Caller mentioned that she "nearly died". Caller had "side effects at night" and mentioned she "was shaken all over and blanked out". When caller "woke up in the morning", she "couldn't believe she was still alive" as she "did not know what happened to her overnight". And this happened "the day she got her booster". Caller added, "when she woke up, from elbows to fingertips, her hand was off the bed in a vertical position and her hands were shaken all over". Caller stated that she "doesn't understand what happened" and what happened "between 3:30 or 2:30 in the morning until 06:00, that part was blank" for her. She "does not know if the shaking continued". Caller mentioned that she spoke with a representative and filled out a form for a side effect she had with the second booster dose of the Pfizer COVID-19 vaccine and was told to call Pfizer contact # option 3 with reference # withheld. Callback attempt #1 performed on 14Jun2022 at 02:34PM EST as caller got disconnected. Able to reach caller. Recording disclaimer provided. Successfully provided response. Caller mentioned that she already experienced 3 times of disconnection for her call for the Pfizer COVID-19 vaccine and that she spoke with a young lady for half an hour regarding reference # withheld. Caller also asked if she could be directly sent to the survey because when she was offered to take the survey yesterday, she had to enter a password, so this time she is requesting to be sent directly to the survey.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Near death experience
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Blood cholesterol abnormal (cholesterol problems Diagnosed years ago); Blood pressure high (high blood pressure Diagnosed years ago. Was told her blood pressure was very good.)
Vorgeschichte: Medical History/Concurrent Conditions: Allergy (she was young, 5-7 years old); COVID-19 (a very mild case of it. Was prior to receiving any of her COVID-19 Vaccines.); Urinary tract infection (Had a urinary tract infection about a month ago)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2314393

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: WI
Alter: 78,0
Geschlecht: M
Eingang: 09.06.2022
Impfdatum: 05.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / RA

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

Anticoagulant therapy Atrial fibrillation Blood glucose increased Blood test Cardiac telemetry abnormal Computerised tomogram thorax abnormal Condition aggravated Dizziness Dyspnoea Echocardiogram abnormal Electrocardiogram abnormal Feeling jittery Gait inability Hyperventilation Palpitations Pulmonary embolism Pulmonary thrombosis SARS-CoV-2 test negative

Symptomtext

4-8-22 Fri 2am-Can't breath bringing dog in, almost passed-out. Can't walk 5 feet w/o Hyperventilating. From 2:15am till 6am, I'm sitting in the kitchen using Diltiazem ER 120 mg, to stop A-Fib and catch my breath. 4:27am-1 Diltiazem. 5:17am Wheelchair to bedroom and back to kitchen, quite winded. 101 BPMin w/Oxg Meter at 92 %. Hyperventilating to get air. 5:25am-2nd Diltiazem. Feel alert but Jettery. 7:08am Morning Medications (Flecainide, Metoprol and Asprin 325mg) 93 BPMin / 92% Oxy. I feel things settling down and I go to bed at 7:10am. Getup at 10:35am. 87 BPMin / 89% Oxy. At home test for Covid is Negative. Blood Glucose is 255%. I'm out of breath with little movement. I'm at 90% Oxy but it's not getting to lungs. I decide to call my sister and have her take me to the Emergency Room. 2pm at the Emergency Room. They finally do a CT Scan of my chest and see Blood Clots in both my Lungs. Right side has Larger clots. They put and IV in my arm giving me Heparin (anti-coagulant) and decide to ship me to another hospital. 6:30pm I'm leaving Emergency Room. 7pm in Ambulance going to the other hospital. 8pm At the hospital and up to the 6th Floor. I was hospitalized from April 8th / Fri till April 11 / Mon - Discharged at 1pm. They did many blood test, Blood Sugar level test, EKG Scans, Heart Echo Scans, had me on a Telemetary Heart Monitor and had an IV in my arm for Heparin medication. I was discharged and told to take Xarelto 15mg / 2x/day and on May 1st take Xarelto 20mg 1x / day - this was for Bilateral Pulmonary Embolism. I was switched to Diltiazem 30mg (quick acting) for palpiations if and when Paroxysmal atrial fibrillation is present, for relief. I was given Insulin shots and now will start Lantus Insulin glargrin at 5 units at Bedtime. I was not told: How long this would last, What the outcome will be, What caused this, or how to prevent it, or if I should be concerned about future Covid vaccinations, so the outcome of this event is "Up in the Air". I was told to keep using my support shoe for my right foot and use Diclofenac Sodium Gel for Pain relief. Three other vaccines were listed as: Pfizer, Purple 12+Yrs. This 4th is listed as: Pfizer, TRI-SUCR (Grey-12+Yrs). I was concern at the listed difference. Are they the same ?.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: EKG, Blood Panel, CTScan of Chest, Covid Test(Neg) all done on April 8th 2022.
Aktuelle Erkrankungen: 03-25-2022 Closed fracture little toe, right foot, at Avulsion Junction.
Vorgeschichte: Diabetes-type 2, Atrial-fibrillation-occasionally.
Andere Medikamente: Metformin 1000 mg 2x/day. Flecainide 100 mg 2x/day. Metoprol 50 mg 1x/day. (Vitamin C 500 mg. Vitamin D-3 1000 units. Multi-Vitamin Tablet Nominal Levels. Glucosamine-Chondroitin 1500-600 mg. Omega-3 / Fish Oil 720 mg (EPA-DHA-Other 360-240
Allergien: Shingles (Shingrix) Vaccine.
Vorherige Impfungen: Shingles (Shingrix) 4-20-2021 and 6-21-2021 / Age - 78 Legs had a prickley feeling, it was hard to Walk, I Had to stretch the

VAERS 2289920

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: NV
Alter: 73,0
Geschlecht: F
Eingang: 22.05.2022
Impfdatum: 14.02.2022
Beginn: 01.03.2022
Tage bis Beginn: 15,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal neoplasm Blood uric acid increased Burkitt's lymphoma Computerised tomogram abdomen abnormal Death Decreased appetite Dyspnoea Gastrointestinal stromal tumour Laboratory test abnormal Malaise Metastases to liver Metastases to peritoneum Pulmonary embolism

Symptomtext

This report is from a hospital on March 29th an approximate one month history of decreased appetite and malaise and a new onset shortness of breath. Pulmonary embolism was suspected. 11 cm abdominal tumor was found. Pt was transferred to another hospital for care. A week later the tumor was 27 cm and 8 days after that the pt had reportedly died. The patient had been diagnosed with GIST vs Burkitt's lymphoma with mets to liver and peritoneum & PE of RLL

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 7,0
Labordaten: CT scan showed tumor, lab tests showed elevated uric acid levels.
Aktuelle Erkrankungen: allergic rhinitis, diabetes mellitus type 2, hyperlipidemia, benign essential hypertension, chronic lymphocytosis, morbid obesity, obstructive sleep apnea
Vorgeschichte: knee pain
Andere Medikamente: acetaminophen, allopurinol, aspirin, flax oil, lactobacillus, lidocaine patch, colchicine prn, albuterol inhalers, cholecalciferol vit D3, metformin,
Allergien: Unknown reaction to influenza vaccine.
Vorherige Impfungen: unknown reaction to influenza vaccine sometime in the past

VAERS 2271033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: MA
Alter: 59,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 05.01.2022
Beginn: 18.04.2022
Tage bis Beginn: 103,0
Dosis: 3
Route/Site: IM / RA

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

Axillary pain Echocardiogram normal Fatigue Lymph node pain Myocardial infarction Pyrexia Stent placement Thrombosis

Symptomtext

I experienced some pains in my lymph nodes in my armpit, a fever and fatigue after receiving my third dose. Everything except the lymph nodes subsided. The armpit and lymph nodes are still sensitive today. Three months later, I experienced a heart attack. The only thing that has changed in my life was receiving the booster. I had a stent installed while I was hospitalized, and I will probably need another one.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 3,0
Labordaten: I had an echocardiogram, but my PCP said everything looked good. There were a lot of collaterals to get around the blood clot. I have not heard the same thing from my cardiologist though.
Aktuelle Erkrankungen: I was not experiencing any illness.
Vorgeschichte: I have most of my colon removed. I have had Lupus since I was 12, but it's inactive and I'm not on medication for it.
Andere Medikamente: 2.5mg Amlodipine 2 Elderberry Gummies 2 Vitamin D Gummies 2 Multivitamins Fiber Powder Zyrtec Senna Tablets
Allergien: Lisinopril Penicillin Family Shellfish
Vorherige Impfungen: -

VAERS 2245944

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: CT
Alter: 84,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 20.04.2022
Beginn: 20.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Acidosis Ammonia increased Angiogram pulmonary abnormal Anticoagulant therapy Anuria Aortic dissection Blood gases Blood lactic acid increased Brain natriuretic peptide increased Bundle branch block right Computerised tomogram head normal Coronary artery thrombosis Cough Decorticate posture Dyskinesia Death Dyspnoea Hyperhidrosis

Symptomtext

Patient received a COVID 2nd booster and ~40 minutes later began to cough, became unresponsive, and was barely breathing in his cart. EMS was called and patient was transported to Medical Center ED where we was intubated. Prior to ED arrival, he was noted to be diaphoretic and having involuntary movements, suggestive of decorticate posturing. CTA did not show PE, CVA or significant dissection flap in the aortic arch, but did show renal infarct. Left leg below the knee was also found to be cold, dusky, pulseless and ultrasound showed intraluminal thrombus with associated near complete occlusion of the external iliac artery, extends through and includes posterior tibial, peroneal, anterior tibial arteries. Emergent embolectomy and fasciotomy was performed followed by heparin drip. Pt was transferred to the ICU, where he was acidotic and in shock, started on bicarb and vasopressors. Worsening labs noted along with anuria and no bowel sounds, right pupil fixed and dilated, EKG with later ST depressions and RBBB, increased troponins. CTA was repeated, showing type A dissection extending up to the carotids and down to renals ? not amenable to surgery and patient transitioned to CMO.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Imaging: o CTA chest for PE:Limited by poor timing bolus. No large pulmonary emboli are identified. Bilateral lung opacities are non-specific, likely infectious / inflammatory. o CT head w/o Contrast: negative for IC bleed o Bedside echo: Depressed LV function with mild pericardial effusion Labs: hyperammonemia (43), elevated troponin (99), elevated BNP (186), lactic acidosis (7.9), U tox negative, point-of-care COVID test negative, ABG pos-tintubation (7.18/47/66/80), ProCal 0.07
Aktuelle Erkrankungen: None noted
Vorgeschichte: left eye blindness due to ?stroke CAD s/p PCI (2 stents) HTN Hypothyroid L carotid stenosis Chronic cough with groundglass opacities in lungs
Andere Medikamente: amlodipine 5mg daily aspirin 81mg daily atorvastatin 20mg daily chlorthalidone 12.5mg every other day flonase 2 sprays daily labetalol 100mg twice daily levothyroxine 100mcg daily olmesartan 40mg daily
Allergien: NKA
Vorherige Impfungen: -

VAERS 2264499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: MA
Alter: 60,0
Geschlecht: U
Eingang: 02.05.2022
Impfdatum: 20.04.2022
Beginn: 26.04.2022
Tage bis Beginn: 6,0
Dosis: 4
Route/Site: IM / LA

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

Computerised tomogram thorax abnormal Deep vein thrombosis Fibrin D dimer Pulmonary embolism Troponin increased

Symptomtext

I suffered 2 (L) legt DVT and massive pulmonary embolism 1 week after my second Covid booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: LEN ++ D Dimer greater than 10,000 Trop greater than 160 pe-ct + massive PE improving
Aktuelle Erkrankungen: no
Vorgeschichte: none
Andere Medikamente: none
Allergien: No
Vorherige Impfungen: -

VAERS 2211356

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: -
Alter: 80,0
Geschlecht: F
Eingang: 01.04.2022
Impfdatum: 25.02.2022
Beginn: 04.03.2022
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / LA

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

Death Dyspnoea

Symptomtext

Patient presented to the ED and was subsequently hospitalized for chronic dyspnea and hospice care within 6 weeks of receiving covid vaccination. She died on 3/6/2022

Weitere VAERSDATA-Felder

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

VAERS 2206442

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 30.03.2022
Impfdatum: 19.02.2022
Beginn: 16.03.2022
Tage bis Beginn: 25,0
Dosis: 4
Route/Site: IM / LA

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

Anticoagulant therapy Buttock injury Central venous catheterisation Platelet count normal Sepsis Septic shock Tooth extraction

Symptomtext

Severe sepsis with septic shock. Oral surgery was consulted 03/14/2022 and recommended teeth extraction (#22 and #28). He went for extraction on 03/19/2022 when PLTs >50,000. Apixaban was resumed.Per recommendation, patient's PICC was replaced prior to discharging, unasyn IV and flagyl PO until 03/28/2022. He is scheduled to follow up as an outpatient. He developed wounds on his buttocks and Wound Care/Ostomy Service saw him weekly. Treated with saline, gauze and mepilex. He will follow up with doctors as an outpatient. Patient was stable and on oxygen (4L) at time of discharge to SNF. Hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Septic shock
Hospital-Tage: 15,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2201422

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: -
Alter: 75,0
Geschlecht: F
Eingang: 28.03.2022
Impfdatum: 09.03.2022
Beginn: 16.03.2022
Tage bis Beginn: 7,0
Dosis: 4
Route/Site: IM / LA

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

Anticoagulant therapy Cor pulmonale acute Pulmonary embolism Thrombectomy

Symptomtext

The patient was found to have Acute saddle pulmonary embolism with acute cor pulmonale (HCC).The patient was admitted to the hospital medical service for further care. The patient Underwent a thrombectomy and was put on IV heparin. The patient's initial symptoms have improved dramatically during the hospital stay. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2184744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: CA
Alter: 75,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 13.03.2022
Beginn: 14.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Angiogram pulmonary abnormal Arthralgia Atelectasis Blood electrolytes normal Blood gases abnormal Blood lactic acid normal Chest X-ray abnormal Hypoxia Lung consolidation Lung infiltration Pleural effusion Pulmonary embolism Pyrexia Respiratory alkalosis Tachycardia Tachypnoea Urine analysis abnormal White blood cell count normal

Symptomtext

Pt developed fever ~ 24h after vaccine on 3/14/2022. c/o L shoulder pain. On 3/14/22 at 2030 pt temp spiked at 102.6F and tachypnea/tachycardia noted. CT chest w contrast ordered as well as blood cx. WBC, lactate, electrolytes wnl; ABG showed resp alkalosis incompletely compensated with mild hypoxia; CXR showed atelectasis vs infiltrate bilaterally without much change to previous CXR. UA showed possible infection, CTA showed atalectasis/consolidation bilaterally, right segmental pulmonary emobli, bilateral moderate pleural effusions; Pt received acetaminophen, cefepime, fluconazole, and treatment dose enoxaparin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: WBC, lactate, electrolytes wnl; ABG showed resp alkalosis incompletely compensated with mild hypoxia; CXR showed atelectasis vs infiltrate bilaterally without much change to previous CXR. UA showed possible infection, CTA showed atalectasis/consolidation bilaterally, right segmental pulmonary emobli, bilateral moderate pleural effusions
Aktuelle Erkrankungen: Large Bowel Obstruction and Necrotic Cecum secondary to Stricture in the Rectum, s/p Exploratory Laparotomy with Small Bowel Resection and Right Colectomy with Reanastomosis, Sigmoid Resection with Mobilization of Splenic Flexure, Repair of Transverse Colotomy and Partial Proctectomy (2/9/22), septic shock, endometrial cancer, diabetes, acute normocytic anemia
Vorgeschichte: endometrial cancer
Andere Medikamente: Triad paste, humalog, lantus, Eucerin cream, TPN, Norco 5, fat emulsion, famotidine, enoxaparin
Allergien: amoxicillin, penicillin
Vorherige Impfungen: -

VAERS 2154823

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: MI
Alter: 59,0
Geschlecht: M
Eingang: 03.03.2022
Impfdatum: 10.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Cerebrovascular accident Haematemesis Loss of consciousness

Symptomtext

Patient reported that he was hospitalized for a stroke on the same day vaccination was given. He also reported "throwing up blood, and passing out".

Weitere VAERSDATA-Felder

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

VAERS 2149532

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: DE
Alter: 69,0
Geschlecht: M
Eingang: 28.02.2022
Impfdatum: 09.02.2022
Beginn: 16.02.2022
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Cerebrovascular accident Cognitive disorder Eye movement disorder Motor dysfunction Speech disorder Tremor

Symptomtext

CRNP Note: Stroke determined by clinical assessment Change in condition patient has a right field cut he has weakness which shakes he has delayed speech response he has delayed motor response his EOMI is not intact has no awareness of where he is sending to the hospital 911 The resident was transferred to a medical facility

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: The patient was not readmitted as of the date of this report.
Aktuelle Erkrankungen: -
Vorgeschichte: METHICILLIN-RESISTANT STAPHYLOCOCCUS AUREUS INFECTION AS THE CAUSE OF DISEASES CLASSIFIED ELSEWHERE 1/27/2022 PERSONAL HISTORY OF COVID-19 1/27/2022 ACUTE PANCREATITIS WITHOUT NECROSIS OR INFECTION, UNSPECIFIED UNSPECIFIED FRACTURE OF FIRST LUMBAR VERTEBRA, SUBSEQUENT ENCOUNTER FOR FRACTURE WITH ROUTINE HEALING ESSENTIAL (PRIMARY) HYPERTENSION KIDNEY TRANSPLANT STATUS PERSONAL HISTORY OF PULMONARY EMBOLISM
Andere Medikamente: -
Allergien: Bacitracin, Cephalexin, Sulfamethoxazole/Trimethoprim, Neosporin, NSAIDs, Penicillins, Coconut, Coconut Oil, Grapefruit, Orange Juice
Vorherige Impfungen: -

VAERS 2136987

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: TX
Alter: 78,0
Geschlecht: M
Eingang: 24.02.2022
Impfdatum: 17.01.2022
Beginn: 08.02.2022
Tage bis Beginn: 22,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Asthenia COVID-19 Chills Computerised tomogram head normal Cough Death Decreased activity Encephalopathy Fatigue Inappropriate schedule of product administration Lactic acidosis Mental status changes Pyrexia SARS-CoV-2 test positive Sepsis Septic shock

Symptomtext

Pfizer COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Received Pfizer Vaccines on 1/26/2021, 2/20/2021 and 1/17/2022. Presented to ED 2/8/2022 w/AMS, along with cough, fever, chills, fatigue and weakness. Diagnosed with COVID-19 on 1/31/2022 and since that time had decreased activity level. CTH in the ED was negative. Admitted for sepsis w/encephalopathy with septic shock, unspecified organism. Over the hospitalization patient required increasing supplemental oxygen, developed AKI, and lactic acidosis. Elected for comfort measures on 2/19/2022 and expired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 11,0
Labordaten: COVID-19 Positive on 1/31/2022 and 2/8/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Aneurysm, Atrial Fibrillation, ASCVD, BPH, Cardiomyopathy EF 20%, CNF, CKD, CAD, DM2, Diverticulitis, GERD, Gout,
Andere Medikamente: Acetaminophen, Allopurinol, Apixaban, Atorvastatin, Baclofen,
Allergien: Hydrocodone, Anesthesia, Penicillin, Iodinated Contrast, NSAID
Vorherige Impfungen: -

VAERS 2135216

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: ID
Alter: 66,0
Geschlecht: M
Eingang: 23.02.2022
Impfdatum: 31.01.2022
Beginn: 19.02.2022
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: IM / LA

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

Angiogram pulmonary abnormal Anticoagulant therapy Chest pain Echocardiogram Laboratory test Panic attack Pulmonary embolism Ultrasound Doppler

Symptomtext

Chest pain x2-4 days. Admitted 2/19 - 2/21/22 with acute right pulmonary embolism with large clot burden now on Eliquis. Hospitalized on oxygen, discharged home without oxygen. Returned to ED same day as discharge with a panic attack. Now home again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: CTPA, echo, BLE duplex, labs during hospitalization 2/19 - 2/21.
Aktuelle Erkrankungen: -
Vorgeschichte: Treated hepatitis C, IDDM2, COPD, CAD, CKD 3b, recovered alcoholic, IVDU in remission, current chew tobacco and marijuana user, chronic pain on Norco
Andere Medikamente: ? albuterol (PROVENTIL HFA;VENTOLIN HFA) 90 mcg/actuation inhaler INHALE 2 PUFFS INTO THE LUNGS EVERY 4 (FOUR) HOURS AS NEEDED FOR SHORTNESS OF BREATH OR WHEEZING. ? amitriptyline (ELAVIL) 25 MG tablet TAKE 1 OR 2 TABLETS BY MOUTH IN THE EV
Allergien: NKA
Vorherige Impfungen: -

VAERS 2132027

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: LA
Alter: 49,0
Geschlecht: M
Eingang: 22.02.2022
Impfdatum: 31.01.2022
Beginn: 19.02.2022
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: SYR / LA

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

Myocardial infarction Thrombosis

Symptomtext

Blood clot leading to heart attack

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: No
Vorherige Impfungen: -

VAERS 2130954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: CA
Alter: 49,0
Geschlecht: M
Eingang: 20.02.2022
Impfdatum: 28.01.2022
Beginn: 14.02.2022
Tage bis Beginn: 17,0
Dosis: UNK
Route/Site: IM / RA

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

Angiogram cerebral abnormal Carotid artery thrombosis Cerebral artery occlusion Cerebrovascular accident Death

Symptomtext

H received Pfizer booster 1/28/22 (first two Pfizer 7/14/21 and 8/4/2)/ Admitted to medical center of facility 2/14/22 with massive stroke. No clear risks for stroke he died 2/20/22. He had acute left mca occlusion and L ICA thrombus on CTA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Ankylosing Spondylitis Dyslipidemia
Andere Medikamente: Atorvastatin 40/d Humira Pen 40mg q 14 day
Allergien: None
Vorherige Impfungen: -

VAERS 2092532

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: CT
Alter: 56,0
Geschlecht: M
Eingang: 07.02.2022
Impfdatum: 26.01.2022
Beginn: 05.02.2022
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / LA

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

Cardiac arrest Chest pain Death Electrocardiogram Life support Myalgia Pericardial drainage Pericardial effusion Pulse absent Pulseless electrical activity Resuscitation Syncope Thrombosis Ultrasound scan abnormal

Symptomtext

Per ED note: Briefly, 56 y.o. male w/ hx of well-controlled HIV, recent Pfizer vaccination 1 wk ago who reports to ER as a cardiac arrest. For the past several days has been c/o CP + myalgias. This AM awoke w/ CP and after getting up to ambulate to the bathroom had a witnessed collapse and bystander CPR was initiated. Total down-time + ACLS by EMS 40 min prior to arrival. PEA during the entire time. On arrival, bedside US rapidly performed showing a large pericardial effusion with thick clot and no underlying cardiac activity. Once pericardiocentesis kit obtained paused compressions for pericardiocentesis under emergent conditions/consent. Accessed the pericardial sac under US and EKG guidance and aspirated a small amount of blood but unable to aspirate remainder of clot. Given lack of underlying cardiac activity, no pulses, TOD called at 0607.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 1,0
Labordaten: see above
Aktuelle Erkrankungen: none
Vorgeschichte: HIV
Andere Medikamente: Stribild, erogocalciferol
Allergien: none
Vorherige Impfungen: -

VAERS 2091866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: MA
Alter: 91,0
Geschlecht: F
Eingang: 06.02.2022
Impfdatum: 12.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / LA

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

Death

Symptomtext

Death on 1/19/2022 7 days after last booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: recent rib fractures
Vorgeschichte: hypertension
Andere Medikamente: Amlodipine
Allergien: none
Vorherige Impfungen: -

VAERS 2080308

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

kritisch

Staat: WA
Alter: 65,0
Geschlecht: M
Eingang: 01.02.2022
Impfdatum: 28.01.2022
Beginn: 29.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

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

Symptomtext

Patient received Pfizer COVID vaccine on 12/30/20 (lot # EL0140), 1/20/21 (lot # EL3302), and 1/28/22 (lot # FJ6369). Patient resides in (private) and was tested positive for COVID on 1/15/22 externally. On 1/29/22, patient admitted to our inpatient facility with acute respiratory failure with hypoxia s/p fall (COVID status negative on 1/29/22 upon admission). As of today (2/1/22), patient is still admitted in our med/surg unit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: COVID status positive 1/15/22 (external result) and negative 1/29/22.
Aktuelle Erkrankungen: -
Vorgeschichte: Private resident with history of type 2 diabetes, hypertension, post-polio syndrome, and hyperlipidemia
Andere Medikamente: acetaminophen PRN, amlodipine, atorvastatin, cetirizine, empagliflozin, famotidine, fluticasone nasal sp, guaifenesin, ibuprofen PRN, losartan, oxybutynin, tamsulosin
Allergien: aspirin, codeine
Vorherige Impfungen: -

VAERS 2685583

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: WA
Alter: 15,0
Geschlecht: M
Eingang: 23.09.2023
Impfdatum: 20.09.2023
Beginn: 21.09.2023
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / RA

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

Brain natriuretic peptide normal Echocardiogram abnormal Electrocardiogram ST segment elevation Left ventricular dysfunction Myocarditis Pericarditis Troponin increased

Symptomtext

Admitted for mild pericarditis/myocarditis 9/23

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: EKG 9/23 with diffuse ST segment elevation ECHO 9/23 with mild LV depression , normal anatomy BNP 9/23 nl TPN 3.22
Aktuelle Erkrankungen: none
Vorgeschichte: SIBO
Andere Medikamente: fluoxetine
Allergien: none
Vorherige Impfungen: -

VAERS 2667742

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: -
Alter: 25,0
Geschlecht: M
Eingang: 08.08.2023
Impfdatum: 28.01.2022
Beginn: 30.01.2023
Tage bis Beginn: 367,0
Dosis: 2
Route/Site: IM / LA

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

Acute coronary syndrome Myocarditis

Symptomtext

ACUTE CORONARY SYNDROME, UNSPECIFIED MYOCARDITIS

Weitere VAERSDATA-Felder

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

VAERS 2642856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: -
Alter: 77,0
Geschlecht: F
Eingang: 08.06.2023
Impfdatum: 01.04.2022
Beginn: 10.04.2023
Tage bis Beginn: 374,0
Dosis: 3
Route/Site: UN / UN

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

Asthenia Deep vein thrombosis Fatigue Malaise

Symptomtext

I82.401 ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN 4/29/2023 WEAKNESS I82.409 ACUTE DVT, UNSPECIFIED VEIN 4/14/2023 WEAKNESS I82.401 ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN 4/29/2023 WEAKNESS I82.409 ACUTE DVT, UNSPECIFIED VEIN 4/14/2023 WEAKNESS I82.401 ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN 4/29/2023 ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN I82.409 ACUTE DVT, UNSPECIFIED VEIN 4/14/2023 ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN I82.401 ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN 4/29/2023 MALAISE AND FATIGUE I82.409 ACUTE DVT, UNSPECIFIED VEIN 4/14/2023 MALAISE AND FATIGUE I82.401 ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN 4/29/2023 MALAISE AND FATIGUE I82.409 ACUTE DVT, UNSPECIFIED VEIN 4/14/2023 MALAISE AND FATIGUE

Weitere VAERSDATA-Felder

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

VAERS 2634786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 22.05.2023
Impfdatum: 08.02.2022
Beginn: 07.05.2022
Tage bis Beginn: 88,0
Dosis: 3
Route/Site: IM / RA

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

Ischaemic stroke

Symptomtext

ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY

Weitere VAERSDATA-Felder

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

VAERS 2629698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: -
Alter: 48,0
Geschlecht: M
Eingang: 10.05.2023
Impfdatum: 20.04.2022
Beginn: 27.04.2022
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: - / -

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

Cardiogenic shock Symptom recurrence

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE CARDIOGENIC SHOCK 5/16/2022 -- RECURRENCE OF SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2585654

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 22.02.2023
Impfdatum: 18.02.2022
Beginn: 18.02.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Cardiac imaging procedure Computerised tomogram Disorientation Gait inability Nervous system disorder Sleep disorder Syncope Wheelchair user

Symptomtext

I woke up at midnight after a half hour of laying down I woke up disoriented spatially, took a step and collapsed husband got me bathroom, could not remain on toilet, 911 was contacted transported to ER stayed for 8 hours. Discharged in wheelchair determined not having stroke, diagnosed as neuro vestibular disorder, non-ambulatory.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Ct Scan 19Feb2022, Heart Scan 19Feb2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Mild obesity; osteopenia
Andere Medikamente: Rosuvastatin; valsartan.
Allergien: N/A
Vorherige Impfungen: -

VAERS 2584312

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: WA
Alter: 52,0
Geschlecht: F
Eingang: 20.02.2023
Impfdatum: 02.02.2022
Beginn: 01.04.2022
Tage bis Beginn: 58,0
Dosis: 3
Route/Site: SYR / UN

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

Blood test abnormal Fall Fatigue Influenza like illness Internal haemorrhage Model for end stage liver disease score increased Muscular weakness Syncope

Symptomtext

I had vaccination 02/02/2022. About 04/2022 I had routine lab work done every 3 months to monitor my liver. My MELD Score kept going up after the vaccination. Since vaccination I have felt muscle weakness, fatigue, I trip and fall, and feel like I always have the flu. I am now on the list for a liver transplant. I was admitted to the hospital in 01/2023 due to syncope. I do have internal bleeding.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: 04/2022 and 08/2022 Blood panel MELD Score increased.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypothyroidism; Liver Disease 2006
Andere Medikamente: Levothyroxine; UROSTILL
Allergien: N/A
Vorherige Impfungen: Always feel like I have the flu after all vaccinations

VAERS 2582369

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: MO
Alter: 20,0
Geschlecht: U
Eingang: 15.02.2023
Impfdatum: 16.03.2022
Beginn: 01.04.2022
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: - / -

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

Acute disseminated encephalomyelitis Anaemia of chronic disease Angiogram cerebral abnormal Angiotensin converting enzyme decreased Anti-GAD antibody negative Anti-NMDA antibody negative Anti-ganglioside antibody negative Anti-thyroid antibody Antibody test negative Antineutrophil cytoplasmic antibody negative Antinuclear antibody negative Arteriogram carotid abnormal Autoantibody negative Autoimmune disorder Barium swallow Biopsy brain abnormal Blood copper Blood folate normal

Symptomtext

1 week after vaccine developed symptoms of headache, photophobia, phonophobia, meningisumus. Later was confused and irritable, worsened about 4 weeks after vaccine to witnessed, myoclonus, opsoclonus, dysarthria, decreased level of consciousness. LP with lymphocyte predominant pleocytosis. MRI with leptominengeal enhancement, later T2 hyperintensity upper cervical cord to thoracic cord. Diagnosis: meningoencephalomyelitis, no alternative cause identified and suspected related to COVID-19 vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: IVth nerve paralysis
Hospital-Tage: -
Labordaten: Numerous: - Ophthalmology notes reviewed: original notes indicated bilateral disc edema in low pressure headache (after LP), later bilateral disc edema grade I, R APD, left 6th and 4th nerve palsy. Improved by 5/10 assessment - MRI brain/MRV/pituitary 4/8/22 (report): 1. Findings of intracranial hypertension including prominent perioptic nerve CSF space and flattening at the level of optic disc suggestive papilledema. 2. Unchanged diffuse small caliber of the superior sagittal sinus, bilateral transverse and sigmoid sinuses is seen also likely represent changes due to intracranial hypertension. No evidence of filling defects within major dural venous sinuses to suggest dural venous sinus thrombosis. Apparent linear hypointense filling defect noted on postcontrast T1 weighted images is not seen on the postcontrast MR venogram and is artifactual. 3. Leptomeningeal enhancement and FLAIR sulcal hyperintensity scattered in both cerebral hemispheres and over the surface of the brainstem more prominent in the right frontal lobe. - MRI brain 4/10/22 (report): 1. Leptomeningeal enhancement and FLAIR sulcal hyperintensity in both cerebral hemispheres and over the surface of the brainstem shows interval worsening with increase in conspicuity and is now diffuse and present throughout the cerebral hemispheres. 2. Stable findings of intracranial hypertension including prominent perioptic nerve CSF space and flattening at the level of optic disc suggestive papilledema. 3. Unchanged diffuse small caliber of the superior sagittal sinus, bilateral transverse and sigmoid sinuses is seen also likely represent changes due to intracranial hypertension. No evidence of filling defects within major dural venous sinuses to suggest dural venous sinus thrombosis. 4. No acute infarct or intracranial hemorrhage. No evidence of effacement of the sulcal spaces and basal cisterns to suggest cerebral edema. No evidence of descending transtentorial herniation or tonsillar herniation. 5. Bulky pituitary gland is again noted measuring 8 mm in height. The appearance favors pituitary hyperplasia and less likely macroadenoma. There is no mass effect on the optic chiasm. - MRI spine w/wo 4/14/22 (report): Symmetric dorsal T2 hyperintensity within the spinal cord at the C1-C6 levels, continuing inferiorly into the bilateral medial spinal cord to level of T11 with postcontrast enhancement as well as leptomeningeal enhancement of the whole spinal cord. There is also diffuse enhancement of the cauda equina nerve roots and intramedullary enhancement. These findings are consistent with acute disseminated encephalomyelitis in this patient with aseptic meningitis. - MRI brain 4/18/22 (report): Interval decreased leptomeningeal enhancement is seen. There is subtle restricted diffusion within the splenium of the corpus callosum, which could be due to seizures. Similar bulky appearance of the pituitary gland, likely due to hyperplasia and age-appropriate. Stable appearance of the ventricles, and unable to assess optic nerve sheath CSF due to patient motion. - MRI brain 5/3/22 (report): 1. Interval visualization of T2/FLAIR hyperintensity involving the medulla with mild expansion, extending up to the cervicomedullary junction which continues with the T2 hyperintensity involving the upper cervical cord. Mild T2/FLAIR hyperintensities also seen surrounding the 4th ventricle. No associated postcontrast enhancement is seen. 2. Increased prominence of diffusion restriction in the splenium of the corpus callosum. This finding may represent cytotoxic lesion of the corpus callosum which is a reactionary phenomenon. Punctate foci of faint restricted diffusion seen in the corona radiata bilaterally and right basal ganglia, suspicious for recent microvascular infarcts. 3. Status post brain biopsy in the right posterior parietal temporal region with expected postprocedural changes. Interval decrease in diffuse sulcal FLAIR hyperintensity and leptomeningeal enhancement as compared to prior imaging. MRI SPINE 5/3/22 (report): 1. T2 hyperintensities in the upper cervical cord at C1-C2 levels which is more prominent as compared to prior imaging. There is decreased prominence of the previously seen T2 hyperintensities in the mid and lower cervical cord. There is no associated postcontrast enhancement. Considering brainstem imaging findings and upper cervical cord findings, differential considerations include NMO spectrum disorder with transverse myelitis along with the previously considered differentials of ADEM and atypical infectious process. 2. Decreased prominence of T2 hyperintensities in the thoracic cord. The current scan demonstrates faint, patchy thoracic cord involvement. Mild leptomeningeal enhancement of the distal thoracic cord is seen, improved as compared to prior imaging. 3. Mild, diffuse cauda equina thickening and faint postcontrast enhancement. - CT PE 4/29/22: Exam is severely limited due to respiratory motion. Within these limitations, no central or segmental pulmonary embolus. Small right-sided pneumothorax with right-sided chest tube in place. Small volume pneumomediastinum. Mucous plugging of the right lower lobe bronchus with associated right lower lobe collapse. - Echo 4/20/22: 1. Left ventricle: Normal LV wall thickness; normal LV internal dimensions; mild hypokinesis of the basal inferoseptal and basal anteroseptal wall. Mildly decreased LV systolic function, estimated LVEF 40-45%; normal diastolic function. Compared to study dated 4/13/22, there is mild improvement in the LVEF noted - CT chest/abdomen/pelvis 4/13/22: no adenopathy, no pulmonary sarcoidosis - PET report 4/15/22: diffuse intense cerebellar hypermetabolism, ddx cerebellitis, inflammatory, autoimmune, metastatic; mild hypermetabolic LL consolidation likely pneumonia. - CTP head 4/13/22: nondiagnostic related to motion artifact - CTA head/neck 4/13/22 interval improvement in cerebral edema; no LVO, aneurysm, significant stenosis - brain biopsy per notes: "brain dura matter larely unremarkable fibrous tissue with a few lymphocytes, brain with leptomeningeal and parenchymal lymphoid infiltrates consistent with reactive/inflammatory process. - VEEG: continuous generalized irregular delta activity, intermittent bifrontal predominant 1Hz generalized rhythmic delta activity, absent PDR. - CSF 5/1/22: R 129, W 93, L 91%, G 100, P 28, gram stain negative, crypto neg, cytology "Marked lymphocytes present. Correlate with flow if needed ATYPICAL CELLS PRESENT", ACE 1.7 (normal), autoimmune ENC2 panel reportedly negative, CSF Gq1b reportedly negative, GAD negative reportedly, - CSF 4/12/22: OP 26cm H2O, W 159, R 43, L 68%, N 16%, Ig G index 0.6, IgG synthesis 51.7 (H), OCB 0, xanthochromia, flow unavailable 8**, cytology negative, ACE 6.2 (H, 0-2.5), anaerobic gram stain gram positive cocci probable staphylococci, meningitis/encephalitis neg, arbovirus panel negative, LCMV igg igm negative, toxoplasma PCR negative, histoplasma abs neg, - CSF 4/11/22: R 65, W 299 L 82%, P 274 (H), G 43, cytology neg, flow normal cells with CD4:8 3:1, crypto ag neg, WNV abs neg, VDRL NR, ARB neg, fungus neg, cocciodioides ab neg, - CSF 4/6/22: R 0, W 251 L 96%, P 100, G 57, gram stain neg, EBV PCR neg, TB neg, - Labs: NMO reportedly negative, NMO/MOG (reportedly negative, ENS2 negative unknown, PAVAL reportedly negative, NMDA reportedly negative, ANA neg with cascade (SSA/b, etc), ACE 74 (H, 9-67), ANCAs neg, Gly unknown, Ma unknown, GM1 ab panel neg, Gq1b negative, vitamin B6 60.7, B12 348, RPR NR, B1 152, folate >22.3, COVID-19 IgM and IgG reactive (4/12/22), copper 66 (L, 80-155), ceruloplasmin 17, TPO ab 1.7, - Peripheral smear 4/26/22: RBC: Microcytic anemia seen in iron deficiency, anemia of chronic disease, thalassemia, hemoglobinopathy, hyperthyroidism and sideroblastic anemia. Serum iron studies are suggested to further evaluate. WBC: Granulocytic leukocytosis unremarkable leukocyte morphology is within normal limits. There are no blasts or dysplastic cells. PLT: Thrombocytopenia with unremarkable platelet distribution. Few large platelets noted; correlation with immature platelet fraction analysis is suggested. - Video swallow fluoroscopy 5/17/22: Shallow laryngeal penetration without tracheal aspiration was seen with thin barium consistency.
Aktuelle Erkrankungen: None
Vorgeschichte: Madelung wrist deformity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2560254

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: GA
Alter: 49,0
Geschlecht: F
Eingang: 15.01.2023
Impfdatum: 17.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / RA

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

Angiogram Arteriogram carotid Computerised tomogram Echocardiogram Facial paralysis Gait inability Hypoaesthesia oral Hypotonia Laboratory test Magnetic resonance imaging Scan with contrast Ultrasound Doppler Vision blurred

Symptomtext

On 1/21/22 approximately 6 PM, I noticed my left eye vision was blurry, my tongue was feeling numb and then my left cheek drooping. I asked my husband to look and then my whole left side of face was drooping. Within a minute or so, my left arm became limp and progressed down my left thigh and left leg. I was not able to ambulate. My husband carried me to the car and drove me immediately to the ER. Immediately was taken back and assessed by doctor (Via tele med) on computer. A CT with contrast was completed and a recommendation was to start on a ?migraine cocktail?. IV started and cocktail started. Then recommendation was for Stat MRI but no MRI facility nearby. They called multiple hospitals to locate a room (and stat MRI) and the nearest was at Medical Center I was transported via ambulance to (Med Ctr) around midnight/early AM of 1/22/22. Brought in by stretcher to ER, was given stat MRI and admitted to Neuro Science/Primary Stroke Center at Medical Center. Multiple tests were run throughout the next 1-2 days including Carotid arteriogram and ECHO cardiograms, IV fluids, medications. By Saturday evening I was able to talk and move both arms and legs. I was eager to leave the hospital and was discharged to home on Sunday 1/23/22. I was told to follow up with my PCP and with Neuro Dr., but no apt was made for me prior to my discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: 3,0
Labordaten: 1/21-1/23/2022: CT Scan MRI, Carotid Ultrasound, Echocardiogram, Angiogram, Labs, that is all I can remember
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Atorvastatin 10mg, Librax 10 mg, Topomax 25mg, Duloxetine 30mg
Allergien: NKA
Vorherige Impfungen: -

VAERS 2527411

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: NY
Alter: 47,0
Geschlecht: F
Eingang: 08.12.2022
Impfdatum: 08.02.2022
Beginn: 01.12.2022
Tage bis Beginn: 296,0
Dosis: 3
Route/Site: SYR / LA

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

Deep vein thrombosis Ultrasound Doppler abnormal

Symptomtext

I developed a DVT. I have never experienced blood clots until receiving the Covid vaccines. The first blood clot was 4/13/21 after receiving the second dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Ultrasound Duplex Right Lower extremity 12/8/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Pfizer 4/13/21. 2nd COVID vaccine. I had developed a superficial blood clot in my right leg.

VAERS 2483093

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: LA
Alter: 51,0
Geschlecht: F
Eingang: 19.10.2022
Impfdatum: 26.01.2022
Beginn: 29.01.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / -

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

Bell's palsy Burning sensation Crying Demyelination Discomfort Electric shock sensation Full blood count Gait disturbance Magnetic resonance imaging head Magnetic resonance imaging spinal Muscle spasms Neck pain Nerve conduction studies Neuropathy peripheral Pain Radiculotomy Scan Tremor

Symptomtext

This happened 3 days after the injection. I got Bells Palsy of my left eye. I have documents to concur from my eye doctor. It?s still current today. My muscles began spazzing across my neck and back and haven?t stopped. It?s 24/7 and sometimes extremely severe to the point I?m crying trying to figure out how to get comfortable. I had shocks and burning across my neck, back and upper legs. I had trouble walking, shaking in my left hand. The pain in my neck was so severe I literally couldn?t handle the pain. I did end up in the emergency room about 5 months into it with back and neck scans. They couldn?t find anything remarkable. At this point nobody can truly figure out where all the pain is coming from. I have been diagnosed with peripheral neuropathy now. I?ve had a brain scan and now diagnosed with dsymylenating disorder. I just want my life back. This vaccine has taken it away. I am walking better and it?s thanks to Ivermectin. God forbid I miss a dose. My body will be in a full body flare. I?ve also now had rhizotomy done on the top and lower half of my neck which has helped my pain there be more tolerable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: MRI?s, of all regions of the spine and brain, nerve test of the lower half of my body, full cbc blood test.
Aktuelle Erkrankungen: Just got over covid
Vorgeschichte: I had Lyme disease, Bartonella, and Babesia in 2014. I was in complete remission since 2018 after spending a fortune on stem cells.
Andere Medikamente: Cymbalta, Oxtellar Xr, topamax, tizanidine, sumatriptan, Ambien, potassium, levothyroxine, Lipitor, hctz,
Allergien: Azithromycin, erythromycin, flexeril, Aleve, and Keflex
Vorherige Impfungen: -

VAERS 2450103

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: GA
Alter: 45,0
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 17.05.2022
Beginn: 05.06.2022
Tage bis Beginn: 19,0
Dosis: 2
Route/Site: - / LA

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

Asthenia Bladder disorder Confusional state Cyanosis Dyspnoea Echocardiogram Electroencephalogram Generalised tonic-clonic seizure Loss of consciousness Partial seizures Petit mal epilepsy Somnolence Tonic clonic movements

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 45-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 17May2022 as dose 2, single (Lot number: FJ6369) at the age of 45 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Migraines" (unspecified if ongoing), notes: Migraines for 24 years; "Gilbert's liver disease" (unspecified if ongoing), notes: Gilbert's liver disease; "HTN" (unspecified if ongoing), notes: HTN; "Right AV block and left bundle branch block after COVID" (unspecified if ongoing), notes: Right AV block and left bundle branch block after COVID; "Right AV block and left bundle branch block after COVID" (unspecified if ongoing), notes: Right AV block and left bundle branch block after COVID; "COVID" (unspecified if ongoing), notes: If COVID prior vaccination: Yes. Concomitant medication(s) included: ATENOLOL; LOSARTAN; TOPAMAX. Vaccination history included: Pfizer (Dose Number: 1, Batch/Lot No: FJ6369, Location of injection: Arm Left), administration date: 12Apr2022, when the patient was 45-year-old, for COVID-19 immunization; flu (Dose Number: 1, Anatomical Location: Arm Right), administration date: 12Apr2022, when the patient was 45-year-old, for Immunization. The following information was reported: CONFUSIONAL STATE (non-serious) with onset 05Jun2022 at 11:00, outcome "recovered with sequelae" (2022), described as "Confusion"; GENERALISED TONIC-CLONIC SEIZURE (medically significant) with onset 05Jun2022 at 11:00, outcome "recovered with sequelae" (2022), described as "Grand mal seizure on 05Jun2022 less than 5 min long"; BLADDER DISORDER (non-serious) with onset 05Jun2022 at 11:00, outcome "recovered with sequelae" (2022), described as "Loss of bladder, consciousness"; SOMNOLENCE (non-serious) with onset 05Jun2022 at 11:00, outcome "recovered with sequelae" (2022), described as "Sleepiness"; DYSPNOEA (non-serious) with onset 05Jun2022 at 11:00, outcome "recovered with sequelae" (2022), described as "Stopped breathing for 1 minute, turned blue, clonic tonic right sided"; ASTHENIA (non-serious) with onset 05Jun2022 at 11:00, outcome "recovered with sequelae" (2022), described as "Weakness on right side after"; TONIC CLONIC MOVEMENTS (medically significant) with onset 05Jun2022 at 11:00, outcome "recovered with sequelae" (2022), described as "clonic tonic right sided"; LOSS OF CONSCIOUSNESS (medically significant) with onset 05Jun2022 at 11:00, outcome "recovered with sequelae" (2022), described as "consciousness"; PETIT MAL EPILEPSY (medically significant), PARTIAL SEIZURES (medically significant) all with onset 05Jun2022 at 11:00, outcome "recovered with sequelae" (2022) and all described as "focal and absent seizures"; CYANOSIS (non-serious) with onset 05Jun2022 at 11:00, outcome "recovered with sequelae" (2022), described as "turned blue". The events "grand mal seizure on 05jun2022 less than 5 min long", "consciousness", "clonic tonic right sided", "focal and absent seizures", "turned blue", "loss of bladder, consciousness", "stopped breathing for 1 minute, turned blue, clonic tonic right sided", "weakness on right side after", "confusion" and "sleepiness" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: Echocardiogram: Unknown results; Electroencephalogram: Unknown results. Therapeutic measures were taken as a result of generalised tonic-clonic seizure, loss of consciousness, tonic clonic movements, petit mal epilepsy, partial seizures, cyanosis, bladder disorder, dyspnoea, asthenia, confusional state, somnolence. Clinical information: Adverse event: loss of bladder, consciousness; stopped breathing for 1 minute, turned blue, clonic tonic right sided, used 2 smelling salts, to start breathing, called 911; post octal for 15+ min weakness on right side after, confusion and sleepiness after, focal and absent seizures since then daily, grand mal monthly, never had seizures before, only migraines. Hospitalization was not prolonged. AE treatment included EEG, echo, carotid Doppler, 1500mg keppra 2x/day. Patient was not tested for Covid post vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Generalised tonic-clonic seizure
Hospital-Tage: -
Labordaten: Test Name: Carotid Doppler; Result Unstructured Data: Test Result:Unknown results; Test Name: EEG; Result Unstructured Data: Test Result:Unknown results.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: AV block (Right AV block and left bundle branch block after COVID); COVID-19 (If COVID prior vaccination: Yes); Gilbert's syndrome (Gilbert's liver disease); Hypertension (HTN); Left bundle branch block (Right AV block and left bundle branch block after COVID); Migraine (Migraines for 24 years)
Andere Medikamente: ATENOLOL; LOSARTAN; TOPAMAX
Allergien: -
Vorherige Impfungen: -

VAERS 2444899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: MI
Alter: 16,0
Geschlecht: F
Eingang: 14.09.2022
Impfdatum: 29.04.2022
Beginn: 01.09.2022
Tage bis Beginn: 125,0
Dosis: 3
Route/Site: - / -

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

Atelectasis COVID-19 Chest X-ray abnormal Condition aggravated Exposure to SARS-CoV-2 Generalised tonic-clonic seizure Lung opacity Respiratory viral panel SARS-CoV-2 test positive Seizure White blood cell count increased

Symptomtext

Discharge Provider: DO Primary Care Physician at Discharge: MD Admission Date: 9/1/2022 Discharge Date: 09/02/2022 DETAILS OF HOSPITAL STAY: Seizure HOSPITAL COURSE: Patient is a 16 y.o. female Patient has a history of global developmental delay, ADHD, Autism, Epilepsy, Anxiety, mild OSA (without CPAP), and intermittent explosive disorder had been transferred from ER for increased frequency of seizure and COVID-19 positive. Patient had 8 episodes of grand mal seizures in a day prior to arrival to our hospital. Had COVID-19 sick contacts at home for the past 2 weeks, tested positive for Covid-19 on 8/31/22 at the outside hospital. Her labs were concerning for WBC of 15.9 and COVID 19, Respiratory panel otherwise negative. Outside hospital CXR on 8/31/22 with suboptimal inspiration, peripheral opacities in the left mid and lower lung may reflect combination of soft tissue chest wall opacity vs atelectasis. Patient had no other episodes of seizures during her admission here. Per neurology, she was started on Valium bridge on 9/1/22, 2.5 mg TID for 3 days, then 2.5 mg BID for 3 days, then 2.5 mg qD for 3 days. She was started on Remdesivir on 9/1/22 but disconnected her own IV. She was started Paxlovid on 9/1/22, given that her admission was not for COVID but instead for her seizures. She had no hypoxia during her stay. Her guanfacine dose was halved while on Paxlovid for the next 4 days. Otherwise patient had stable vital signs and did well during her admission

Weitere VAERSDATA-Felder

Praegender Schweregrund: Generalised tonic-clonic seizure
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: ADHD (attention deficit hyperactivity disorder) Complex partial epilepsy Anxiety state, unspecified Autism spectrum disorder History of neurological testing - DO NOT EDIT Eczema Sleep disorder Intermittent explosive disorder Pre-diabetes Severe obesity due to excess calories without serious comorbidity with body mass index (BMI) greater than 99th percentile for age in pediatric patient Hirsutism Irregular menses Abnormal genitalia Labial hypertrophy OSA (obstructive sleep apnea), mild Hallucinations Focal epilepsy Aggression Seizure Pneumonia due to COVID-19 virus
Andere Medikamente: amantadine (SYMMETREL) 100 MG capsule calcium carbonate (TUMS) 500 MG chewable tablet cholecalciferol (VITAMIN D3) 25 MCG (1000 UT) tablet cloBAZam (ONFI) 10 MG cloNIDine (CATAPRES) 0.2 MG tablet etonogestrel, 68 MG, (NEXPLANON) IMPL flutic
Allergien: Amoxicillin Dilantin [Phenytoin] Fosphenytoin Keppra Oxcarbazepine PhenobarbitalAgitation PineappleRash Zyprexa [Olanzapine
Vorherige Impfungen: -

VAERS 2431195

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: MI
Alter: 82,0
Geschlecht: F
Eingang: 07.09.2022
Impfdatum: 23.01.2022
Beginn: 28.08.2022
Tage bis Beginn: 217,0
Dosis: 3
Route/Site: - / -

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

Abdominal pain Angiogram cerebral abnormal Arteriogram carotid abnormal Blood sodium decreased COVID-19 Chills Colitis Computerised tomogram abdomen abnormal Computerised tomogram head normal Condition aggravated Dysuria Hyponatraemia Intensive care Malaise Mental status changes Perfusion brain scan normal Vertebrobasilar artery dissection

Symptomtext

Discharge Provider: MD Primary Care Provider: DO Admission Date: 8/28/2022 Discharge Date: Sep 4, 2022 PRESENTING PROBLEM: Acute hyponatremia [E87.1] Colitis [K52.9] Hyponatremia [E87.1] Vertebral artery dissection (HCC) [I77.74] COVID-19 [U07.1] HOSPITAL COURSE: 83 year old female with history of hypertension and hyperlipidemia. She was seen by her PCP 8/23 with complains of abdominal pain dysuria and was started on Bactrim. She thought she was allergic to bactrim and stopped taking it. She presented to the ED 8/27 and was discharged on Macrobid. She presented to the ED 8/28 with 2 days of chills, rigors and malaise which worsened 24 hours prior to admission and worsening mental status. On arrival to the ED a stroke code was called, CT head negative, CT angio head and neck showed concern for right cervical vertebral V2 segment dissection. CT perfusion brain negative. CT abdomen and pelvis showed left sided colitis. Labs significant for sodium of 103. She was given 100ml of 3% saline and admitted to the ICU for treatment of hyponatremia. She remained on room air and asymptomatic from COVID standpoint. Sodium continued to improve, but leveled off on 09/01/2022. Salt tablets were added 3 times a day with noted improvement. Sodium was 134 on day of discharge and sodium tabs were decreased to BID and she was recommended to follow-up with her PCP in 1 week for repeat sodium check and determine at that time if sodium tablets could be discontinued. Neurology was consulted in regards to her right cervical V2 segment dissection on CT and recommended ASA (81 mg daily) with outpatient follow-up with neurovascular clinic for repeat imaging in 3 months. PT/OT evaluated patient and recommended home on discharge. Patient was discharged in stable condition and discharge instructions provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: 12/23/2021- UTI
Vorgeschichte: Vertebral artery dissection (HCC) COVID-19 infection, incidental finding 8/2022 Osteoporosis Vitamin D deficiency Elevated serum protein level Dense breasts BMI less than 19,adult Lesion of pancreas Essential hypertension Atrophic vaginitis
Andere Medikamente: aspirin 81 MG chewable tablet estradiol (ESTRACE) 0.1 MG/GM vaginal cream sodium chloride 1 g tablet
Allergien: Bactrim [Sulfa Drugs]Other
Vorherige Impfungen: -

VAERS 2278522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: IN
Alter: 78,0
Geschlecht: M
Eingang: 30.08.2022
Impfdatum: 08.04.2022
Beginn: 25.04.2022
Tage bis Beginn: 17,0
Dosis: UNK
Route/Site: IM / LA

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

Altered state of consciousness Electroencephalogram Seizure Tongue biting Condition aggravated Magnetic resonance imaging

Symptomtext

Episode of altered consciousness went blank for several moments. Later episodes turned out to be seizures one with tongue biting. Now on levetiracetam

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: EEG labs Imaging. Neurology consultation
Aktuelle Erkrankungen: none
Vorgeschichte: CAD, htn, hyperlipidemia
Andere Medikamente: Metoprolol, Amlodipine, lisinopril, atorvastan, clopidogrel
Allergien: aspirin, nsaids
Vorherige Impfungen: -

VAERS 2422680

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: MO
Alter: 48,0
Geschlecht: M
Eingang: 29.08.2022
Impfdatum: 24.01.2022
Beginn: 01.04.2022
Tage bis Beginn: 67,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test Cardiac operation Echocardiogram Magnetic resonance imaging Pericardial drainage Pericardial excision Pericarditis Ultrasound scan X-ray

Symptomtext

Acute Pericarditis, heart surgery - pericardial liquid drain and permanent pericardial window. 6 month on colchicine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 10,0
Labordaten: x-rays, eco, MRI, ultrasounds, bloodwork
Aktuelle Erkrankungen: -
Vorgeschichte: elevated cholesterol
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: 47 y.o. 1 month after Pfizer C19 vaccine, acute pericarditis, April 2021 is the month of 2nd dose.

VAERS 2410802

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: TX
Alter: 32,0
Geschlecht: M
Eingang: 13.08.2022
Impfdatum: 02.03.2022
Beginn: 08.08.2022
Tage bis Beginn: 159,0
Dosis: 2
Route/Site: IM / LA

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

Bell's palsy Computerised tomogram Facial paralysis Tension headache

Symptomtext

Bell's palsy. Acute tension headache for two days prior, then physical symptoms of partial facial paralysis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: CT scan: 8/8/2022.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2407374

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: TX
Alter: 65,0
Geschlecht: F
Eingang: 10.08.2022
Impfdatum: 28.04.2022
Beginn: 25.07.2022
Tage bis Beginn: 88,0
Dosis: 4
Route/Site: IM / LA

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

Abdominal distension Arteriogram coronary abnormal Blood test abnormal Cardiac stress test Chest discomfort Chest pain Cholelithiasis Discomfort Electrocardiogram Myocardial necrosis marker increased Myocarditis Sleep disorder Troponin increased Ultrasound abdomen abnormal Vomiting

Symptomtext

On 07/25/2022, after I ate lunch, I had a feeling of fullness in my stomach and felt bloated. That night, I ate a really small dinner because I was still feeling uncomfortable but not in pain. Later that evening, probably around 10 or 10:30 at night, I was having gastrointestinal type chest pain. It wasn't sharp pain, but it was hugely uncomfortable. I tried using a heating pad, but that didn't help and I started throwing up. I thought I might have a virus. It didn't go away, and it kept me up all night. Early in the next morning, I drove myself to the emergency room because I was concerned about a heart attack. They did an EKG and I believe they took some blood. The doctor informed me that I did the right thing by coming in because I had a heart enzyme (troponin) that was showing up as high which typically indicates a heart attack or heart blockage. They said that I had to be admitted at that time due to these high levels, but I was unable to be admitted until later that day and at a different location. I was there until that Friday evening. while there, they did a stress test and an angiogram. They discovered some inflammation in my heart, but they don't know what it was caused from. They prescribed a few medications that I have been taking ever since and I am still being monitored by doctors. I have seen a cardiologist since being discharged and the numbers have gone down. The cardiologist put me on a daily regimin of baby aspirin and atorvastatin. They also discovered a gallstone during an abdominal ultrasound but they do not feel that it would cause the issues with my heart.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 4,0
Labordaten: 07/29/2022-Angiogram (inflammation of the heart found); Stress Test-07/28/2022; EKG; Blood Panel; Abdominal Ultrasound-gallstone found.
Aktuelle Erkrankungen: None.
Vorgeschichte: High Blood Pressure.
Andere Medikamente: Enalapril; Sertraline; Synthroid; Vitamin D2; Vitamin B12; Hydrochlorothiazide.
Allergien: Cipro.
Vorherige Impfungen: -

VAERS 2315512

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: IL
Alter: 30,0
Geschlecht: F
Eingang: 10.06.2022
Impfdatum: 25.05.2022
Beginn: 03.06.2022
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / RA

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

Abortion Endometrial hyperplasia Exposure during pregnancy Muscle spasms Ovarian cyst Pregnancy test positive Thrombosis Ultrasound uterus abnormal Vaginal haemorrhage

Symptomtext

Patient received 3rd Pfizer dose on 5/25/2022 at 7w5d gestation. She presented to the emergency department on 6/3/2022 for vaginal bleeding. She began having cramping on 5/31, then had mild spotting on 6/1, which progressed to more significant bleeding on 6/2, and heavy bleeding with clots on 6/3. She believes she may have passed fetal tissue on 6/3, which brought her to the ED. She is a G2P0020. She had a terminated abortion for her first pregnancy. This was her second pregnancy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: 5/25- positive urine pregnancy test in the office 6/3- bHCG 9433. Ultrasound with heterogenous thickened endometrium without IUP. Corpus luteum cyst seen 6/10- bHCG 917
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: prenatal vitamins
Allergien: none
Vorherige Impfungen: -

VAERS 2269019

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: WA
Alter: 62,0
Geschlecht: M
Eingang: 10.05.2022
Impfdatum: 18.02.2022
Beginn: 17.03.2022
Tage bis Beginn: 27,0
Dosis: 4
Route/Site: IM / LA

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

Angiogram cerebral normal Cerebral ischaemia Fall Limb injury Loss of consciousness Magnetic resonance imaging head abnormal Neck injury Seizure Sinus disorder Vascular calcification

Symptomtext

On 3/11/2022 approximately 3 weeks post Covid booster, I suffered a first ever seizure, losing consciousness and falling. I was taken to Hospital by ambulance with shoulder and neck injuries sustained during the fall. 1) During an MRI brain scan without contrast, there were findings related to extensive chronic paranasal sinus disease (not uncommon to a person with cystic fibrosis but unknown to me at the time). The scan also showed no evidence of an intracranial mass lesion, acute intracranial hemorrahage or infarct however, moderate chronic small vessel ischemic changes. Several small chronic ischemic foci involve the bilateral basal ganglia and bilateral cerebellar hemispheres. 2) A CT angiogram of the head showed unremarkable CTA of the head. No aneurysm. No significant stenosis. No large vessel occlusion. Moderate to marked circumferential vascular calcifications noted in cavernous and proximal supracavernous ICA. No significant stenosis. Mild to moderate vascular calcifications in proximal vertebral arteries. No significant stenosis. I was put on Keppra anti-seizure medication and will perform an EEG in the near future to discern future risk of another seizure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 7,0
Labordaten: 1. MRI brain scan without contrast. 2. CT angiogram of head.
Aktuelle Erkrankungen: none
Vorgeschichte: Bi-lateral lung translplant (Oct 1994) due to Cystic Fibrosis secondarily causing a history of skin cancer, gout, osteoporosis, immunosuppressed status, stage 3a chronic kidney disease.
Andere Medikamente: Tacrolimus, Mycophenolic Acid, Prednisone, Azithromycin, Valcyte, Bactrim, Quinipril, Allopurinol, Pantoprazole, Albuterol (inhailer), Folic Acid, Aspirin, Vitamin B6, B-Complex, Vitamin C, Vitamin D3, Vitamin E, Magnesium, Calcium with D
Allergien: Dapsone
Vorherige Impfungen: -

VAERS 2258296

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: OH
Alter: 55,0
Geschlecht: F
Eingang: 29.04.2022
Impfdatum: 23.02.2022
Beginn: 26.04.2022
Tage bis Beginn: 62,0
Dosis: 1
Route/Site: IM / LA

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

Dental discomfort Dizziness Electric shock sensation Tinnitus

Symptomtext

The symptom's beginning were subtle. Within the first week of receiving the vaccine, I began to experience a high pitched metalic "ringing" in my ears. I called my doctors office and was advised to try over the counter decongestant. Nothing I have tried has stopped the constant sound. There is also a metallic/electrical sensation in my back teeth. The ringing has been getting worse and there have been episodes of dizziness. My outcome is unknown at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: I had been transitioning between jobs and had a lapse in medical coverage so no tests have been done yet. Appointments are being set up today.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None -
Allergien: None
Vorherige Impfungen: -

VAERS 2214261

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: MN
Alter: 80,0
Geschlecht: F
Eingang: 14.04.2022
Impfdatum: 03.02.2022
Beginn: 04.03.2022
Tage bis Beginn: 29,0
Dosis: 3
Route/Site: - / -

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

Failure to thrive Gastrointestinal haemorrhage Hip arthroplasty Hip fracture Intensive care Transfusion

Symptomtext

Hospitalization within 6 weeks of COVID vaccination. Admitted 3/4/22 with diagnosis: Failure to thrive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 32,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2214261

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: MN
Alter: 80,0
Geschlecht: F
Eingang: 14.04.2022
Impfdatum: 03.02.2022
Beginn: 04.03.2022
Tage bis Beginn: 29,0
Dosis: 3
Route/Site: IM / RA

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

Failure to thrive Gastrointestinal haemorrhage Hip arthroplasty Hip fracture Intensive care Transfusion

Symptomtext

Hospitalization within 6 weeks of COVID vaccination. Admitted 3/4/22 with diagnosis: Failure to thrive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 32,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2200671

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

schwer

Staat: TX
Alter: 43,0
Geschlecht: F
Eingang: 26.03.2022
Impfdatum: 24.03.2022
Beginn: 24.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Headache Heart rate increased Myocarditis Nausea Pain Palpitations Pyrexia Vomiting

Symptomtext

Receives Covid 19 Booster vaccine of Pfizer at vaccine event on 03/24/2022, starts to have side effects on 03/24/2022 same day of Heart Palpitations (occurred with Primary Series Dose 1 and 2), Nausea, vomiting, and headache, She took Tylenol to help alleviate pain and assist with fever. Her HR gotten up to 140 and she went to ER, they ran test and ER provider Dx. with Myocarditis, advised her that she needs to see a Cardiologist and follow up. Continue to monitor for the next 48 hours and be advised by ER provider for future care .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Primary Series Dose 1 and 2 of Pfizer vaccine in right arm had heart palpitations

VAERS 2200444

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 26.03.2022
Impfdatum: 28.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Electric shock sensation SARS-CoV-2 test Therapeutic response unexpected

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program. The reporter is the patient. A 49 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 28Jan2022 (Lot number: FJ6369) at the age of 49 years as dose 3 (booster), single and administration date 21Dec2020 (Lot number: EJ1685) as dose 1, single for Covid-19 immunisation. Relevant medical history included: "an auto immune issue" (unspecified if ongoing). Concomitant medication(s) included: HYDROCODONE; CYMBALTA; NABUMETONE. Vaccination history included: Bnt162b2 (Dose: 2, Lot Number: EL1284, I know my last one was left), administration date: 19Jan2021, when the patient was 49 years old, for Covid-19 immunization. The following information was reported: THERAPEUTIC RESPONSE UNEXPECTED (non-serious), outcome "unknown", described as "believed to have an auto immune issue but felt significantly better after my first and third Pfizer vaccine."; ELECTRIC SHOCK SENSATION (non-serious), outcome "unknown", described as "I am getting electric shocks with my muscles". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Caller is calling about the Pfizer COVID-19 Vaccine just to let you know she gave a call back regarding previous interaction. She has sent online but her main concern is that she was wondering if there are any studies for people who felt better after receiving the vaccine, so she already provided the medical information for her, and she is believed to have an autoimmune issue, but she felt significantly better after the first and the third Pfizer vaccine. Patient stated she actually has some long-term issues for like 20 years, it helped and feel better after her first one and third one and she do not know why but everybody else use to get sick to it, but she tends to get better patient really good for like 2?3-week. Patient also experienced getting electric shocks with her muscles and all those stuff. Follow-up attempts completed. No further information is expected. The lot/batch number is not available despite the follow-up attempts made.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: Test Date: 20220125; Test Name: COVID test; Result Unstructured Data: Test Result: Unknown results.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Autoimmune disorder
Andere Medikamente: Hydrocodone; Cymbalta; Nabumetone
Allergien: -
Vorherige Impfungen: -

VAERS 2196003

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: SC
Alter: 13,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 23.03.2022
Beginn: 23.03.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Confusional state Dizziness Syncope Unresponsive to stimuli Visual impairment

Symptomtext

Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Visual Changes/Disturbances-Mild

Weitere VAERSDATA-Felder

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

VAERS 2189275

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: AR
Alter: 12,0
Geschlecht: M
Eingang: 20.03.2022
Impfdatum: 11.02.2022
Beginn: 01.03.2022
Tage bis Beginn: 18,0
Dosis: 2
Route/Site: IM / RA

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

Abdominal discomfort Blood test abnormal Cardiac disorder Chest X-ray normal Confusional state Dehydration Diarrhoea Echocardiogram abnormal Fatigue Hallucination Heart rate increased Hypotension Immunoglobulin therapy Inflammatory marker increased Influenza virus test negative Intensive care Laboratory test normal Multisystem inflammatory syndrome in children

Symptomtext

On 3/1/22 patient had stomach discomfort and muscle soreness/stiffness. On 3/2/22 muscle stiffness continued, especially in neck. Began feeling fatigued around midday, took a 2 hour nap and awoke with fever. On 3/3/22 symptoms continued and fever rose to 104. Took him to walk-in urgent care where he tested negative for flu and covid and was sent home. Vomited later that afternoon. Also woke around 1:00 am with vomit/diarrhea. Went back to sleep but when he awoke the morning of 3/4/22, rash was present on legs, buttocks, arms, and fever spiked to 106. Returned to the same clinic and they admitted him to the ER side where they gave him fluids and performed more tests, all of which were negative. Dr. decided to treat for strep and gave him antibiotics intravenously. Also prescribed antibiotics to continue at home (he was able to take 1 dose at home but wasn't able to keep subsequent dose down). He started feeling better that afternoon and was able to eat/drink a little, but had vomit/diarrhea again at bedtime. Woke around midnight with vomit/diarrhea and again on the morning of 3/5/22, so we took him to the ER at Hospital. Very dehydrated. Bloodwork showed high inflammation throughout entire body. High heart rate with low blood pressure. Chest x-ray and Echo looked normal. Doctor conversed throughout the day with the Infectious Disease Specialist at the Hospital, and they both felt like symptoms pointed to MIS-C. They helicoptered him that night to the PICU in where doctors ran tests to rule out infection from meningitis, tick-related illness, etc. By 3/6/22 another Echo showed trouble with heart. By that afternoon he was starting to show occasional mental confusion and mild hallucinations. Infection was ruled out, diagnosis of MIS-C confirmed, and they started IVIG treatment by 3/7/22 at which time symptoms began to slowly dissipate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: congestion/sinus
Vorgeschichte: OCD, anxiety, misophonia
Andere Medikamente: Sertraline 25mg, Children's multivitamin, Children's probiotic, Flonase
Allergien: doxycycline
Vorherige Impfungen: -

VAERS 1673347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: FL
Alter: 62,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 06.02.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Anaphylactic reaction Arthralgia Back pain Constipation Defaecation urgency Body temperature Craniocerebral injury Diarrhoea Fatigue Joint swelling Haematology test Heart rate increased Influenza like illness Myalgia Pain Pyrexia Vaccination site erythema Insomnia

Symptomtext

felt tired for days; swelling very painful joint; swelling very painful joint; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 62 year-old female patient received bnt162b2 (BNT162B2), administration date 06Feb2022 (Lot number: FJ6369) at the age of 62 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 (Vaccine: 1st dose COVID-19, Product name/Manufacture lot number: Pfizer FA7484), administration date: 10Aug2021, when the patient was 61 years old, for Covid-19 immunization; Bnt162b2 (Vaccine: 2nd dose COVID-19, Product name/Manufacture lot number: Pfizer FC3183), administration date: 31Aug2021, when the patient was 61 years old, for COVID-19 Immunization.The following information was reported: FATIGUE (non-serious), outcome "unknown", described as "felt tired for days"; JOINT SWELLING (non-serious), ARTHRALGIA (non-serious), outcome "not recovered" and all described as "swelling very painful joint". No follow-up attempts are possible. No further information is expected. Sender's Comments: Linked Report(s) : US-PFIZER INC-202101456485 Same patient, same product in different dose, partial same event.

Weitere VAERSDATA-Felder

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

VAERS 2182220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: NY
Alter: 28,0
Geschlecht: M
Eingang: 16.03.2022
Impfdatum: 09.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Pericarditis

Symptomtext

Pericarditis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Concerta (methylphenidate) 36 mg/day
Allergien: None
Vorherige Impfungen: -

VAERS 2179772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: AL
Alter: 17,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 19.02.2022
Beginn: 10.03.2022
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: IM / -

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

Facial paralysis

Symptomtext

Partial facial nerve palsy on left side of face.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Metabolic syndrome, High blood pressure, Hyperlipidemia, Overweight
Andere Medikamente: Metformin 500 mg tablet twice a day
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2177259

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: -
Alter: 47,0
Geschlecht: F
Eingang: 13.03.2022
Impfdatum: 27.01.2022
Beginn: 24.02.2022
Tage bis Beginn: 28,0
Dosis: 3
Route/Site: IM / -

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

Angiogram cerebral abnormal Cerebral infarction Computerised tomogram head normal Endotracheal intubation Headache Intensive care Lumbar puncture normal Magnetic resonance imaging head abnormal Mental status changes Nausea Pneumonia viral Vomiting

Symptomtext

Starting on 2/24 patient had altered mental status, headache and BP was in 200s. Patient went to hospital and was treated for viral pneumonia and discharged 3/1. On 3/5 patient began having severe headache, nausea, vomiting and altered mental status. She was then transferred to Neuro department. 2/25: LP (negative). 3/5: Head CT (negative) 3/11: MRI: Restricted diffusion in bilateral frontal, parietal, occipital and temporal lobes as well as Right Cerebellum. 3/12: CTA head: Moderate to large infarction in bilateral cerebral hemispheres with diminished venous flow. Patient was intubated upon admission to neuro critical care for protection of airway.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 14,0
Labordaten: See above.
Aktuelle Erkrankungen: GERD, HTN, Anxiety, Diabetes Type 2
Vorgeschichte: same as above
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2177134

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: IN
Alter: 23,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 12.03.2022
Beginn: 12.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Fall Head injury Loss of consciousness Syncope

Symptomtext

About 5 minutes after receiving her pfizer booster the patient fainted. She fell forward off of her chair onto the ground, she remained unconscious for about 60 seconds. Upon awakening she reported that she felt like she hit her head. She claimed that she was feeling fine, other than the small bump on her head. She was monitored for about 20 minutes before a friend picked her up to take her home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Took blood pressure immediately after, 126/82 mmHg
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: zafemy, escitalopram
Allergien: NKA
Vorherige Impfungen: -

VAERS 2176806

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 16.02.2022
Beginn: 24.02.2022
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: SYR / LA

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

Pericarditis

Symptomtext

Diagnosed with Pericarditis and having complications. Patient has been admitted into hospital 3 times. She has received colchicine during her visits. As of now colchicine has not worked, so MD added Lasix to her regimen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 2,0
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Lisinopril Losartan Januvia Pertussis Vaccine
Vorherige Impfungen: -

VAERS 2147677

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj6369

schwer

Staat: TX
Alter: 48,0
Geschlecht: M
Eingang: 09.03.2022
Impfdatum: 26.02.2022
Beginn: 26.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Back pain Dizziness Dysgeusia Electric shock sensation Feeling drunk Movement disorder Paraesthesia Peripheral swelling Swelling face Unevaluable event

Symptomtext

Onset 2/26/22: Lightheaded (Felt drunk), Incapacitated, Swollen Face & Hands, Extreme Lower Back Pain, Shocking Sensation to Left-side of Face, Metallic Taste in Mouth, Strange Tingling Sensation in Right Calf (H/O DVT to Calf 3 years ago and Factor 8 Leiden),

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2157439

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: OH
Alter: 16,0
Geschlecht: M
Eingang: 04.03.2022
Impfdatum: 03.03.2022
Beginn: 03.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Flushing Hyperhidrosis Hypotension Syncope

Symptomtext

Systemic: syncope-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Hypotension-Medium, Additional Details: syncope

Weitere VAERSDATA-Felder

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

VAERS 2148832

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: CA
Alter: 42,0
Geschlecht: F
Eingang: 28.02.2022
Impfdatum: 26.02.2022
Beginn: 26.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Bell's palsy Chills Fatigue Nausea Vision blurred

Symptomtext

within hours: nausea, blurry vision, chills, fatigue within 48 hours: bells palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: was seen in Urgent care morning of 2/28 and rxed prednisone 50mg x5 days for bells palsy. was seen in Primary care clinic afternoon of 2/28 and dx of bells palsy, most likely related to covid vaccination was made
Aktuelle Erkrankungen: contact dermatitis from poison oak
Vorgeschichte: migraines, hypothyroid, anxiety and depression
Andere Medikamente: effexor, sertraline, levothyroxine
Allergien: doxycycline
Vorherige Impfungen: 3 days of fever and malaise after dose 1 of pfizer covid vaccine

VAERS 2148533

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: NY
Alter: 27,0
Geschlecht: F
Eingang: 28.02.2022
Impfdatum: 10.02.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Axillary pain Chest pain Dyspnoea Echocardiogram Electrocardiogram Nausea Pain in extremity Pyrexia Syncope

Symptomtext

Severe chest pain, shortness of breath, nausea, fever, fainting (did not go unconscious), arm and armpit pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EKG & Echo
Aktuelle Erkrankungen: No; December 13th COVID
Vorgeschichte: No
Andere Medikamente: Vitamins - C, D, Biotin, Apple Cider Vinegar
Allergien: No
Vorherige Impfungen: Second dose, Pfizer

VAERS 2147637

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: RI
Alter: 12,0
Geschlecht: F
Eingang: 28.02.2022
Impfdatum: 13.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test normal Cardiac function test normal Epistaxis Injection site rash Injection site swelling Lip swelling Product administered to patient of inappropriate age Syncope Urine analysis normal

Symptomtext

Pt arrived at school vaccination clinic for second primary vaccination and requested Moderna. I corrected pt stating she was ineligible to receive Moderna due to her age. Her mother stated she received Moderna for her first vaccine, produced a vaccine card confirming, and her record also confirmed. I confirmed with DOH that the next steps were to administer the age-appropriate second vaccine to the patient (Pfizer 12+) and assure her pediatrician is made aware of the situation.

Weitere VAERSDATA-Felder

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

VAERS 2145389

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: AZ
Alter: 31,0
Geschlecht: M
Eingang: 26.02.2022
Impfdatum: 25.02.2022
Beginn: 25.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Injection site pruritus Syncope Tremor Unresponsive to stimuli

Symptomtext

Site: Itching at Injection Site-Mild, Systemic: Fainting/Unresponsive-Mild, Systemic: Shakiness-Mild, Additional Details: Patient reported to me he had issues with injections and blood draws before the vaccination. He said it is likely for him to feel clumsy and faint. He was monitored for 30 minutes. He was doing fine and left the building. He was not alone. He had someone with him during the whole process.

Weitere VAERSDATA-Felder

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

VAERS 2136995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: NY
Alter: 14,0
Geschlecht: M
Eingang: 24.02.2022
Impfdatum: 23.02.2022
Beginn: 23.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Electrocardiogram Loss of consciousness Vomiting

Symptomtext

Patient lost conciseness briefly, and vomited post COVID-19 booster

Weitere VAERSDATA-Felder

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

VAERS 2086400

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: CA
Alter: 17,0
Geschlecht: M
Eingang: 24.02.2022
Impfdatum: 24.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: - / LA

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

Blood test abnormal Chest X-ray Chest pain Chills Delirium Blood test Dyspnoea Bradycardia Capillary nail refill test Chest discomfort Echocardiogram normal Echocardiogram Electrocardiogram Lethargy Myalgia Myocarditis Neuralgia Pain

Symptomtext

17 Y 7 M generally healthy male who presents with acute onset of chest pain/pressure worsening Friday. He received COVID booster on 1/24/22, had intense fevers, myalgias, "nerve pain" all over body the 24-36hours after the booster. He was pretty much recovering by Wednesday and went to school since Thursday. However, on Friday, by 11:30am, he was feeling very tired and out-of-it. He started feeling chest pressure and pain. Denies tingling/numbness/radiation. Currently, he says he feels a little pressure at the chest right above the epigastric area--more like pressure rather than sharp. At one point, he did feel sharp pain but the general sensation of pressure was more bothering. He was seen this afternoon and referred for labs. His troponin came back elevated at 0.4 and so he was directed to the emergency room for further evaluation. In ED: repeat troponin 0.44, bedside echocardiogram showed good LV function and no effusion. Rest of labs reassuring. After discussion with cardiology, patient admitted for further management. on 1/31/22:17 y.o. M with post COVID vaccine-related myocarditis, admitted with intermittent chest pain and elevated troponin, awaiting troponin level <0.5. Overall down-trended from peak troponin of 3.55 but with mild uptrend in troponin to 1.16 from 0.95. Chest pain improved with q8h motrin, now with only intermittent chest pain (at decr level from prior) and no SOB. Plan: Trending troponin q12h until trop <0.5. 1/28 EKG: NSR, RSR' in V1/V2 prob normal variant per Cards. Also on nicotine patch 14mg/24h started 1/29/22 in s/o hx vaping and desire to quit. Dispo plan & recs per Cardiology: Plan for outpt cards f/u appt, no strenuous activities for 30 days after discharge and no competitive sports for 3 months until he can be cleared with a normal treadmill test. Recheck troponin 1 week after discharge. Will need nicotine patch wean - should be on (14 mg/day) for 2 weeks then step down to step 3 (7 mg/day) for 2 weeks. Exam notable for CV: mildly bradycardic rate, normal rhythm, normal S1/S2, no point tenderness of chest on palpation. Cap refill < 2 sec, normal pulse. Pulm: CTAB. Abd: soft, NT, ND.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 3,0
Labordaten: Results for patient as of 2/24/2022 13:58 1/28/2022 16:48 TROPONIN I: 0.40 (H) 1/28/2022 20:40 TROPONIN I: 0.44 (H) 1/29/2022 04:15 TROPONIN I: 0.84 (H) 1/29/2022 16:25 TROPONIN I: 1.75 (H) 1/30/2022 03:40 TROPONIN I: 3.55 (H) 1/30/2022 15:35 TROPONIN I: 0.95 (H) 1/31/2022 03:50 TROPONIN I: 1.16 (H) 1/31/2022 16:30 TROPONIN I: 0.32 (H) 2/7/2022 16:35 TROPONIN I: <0.02
Aktuelle Erkrankungen: -
Vorgeschichte: h/o Vaping
Andere Medikamente: -
Allergien: Sulfur (not Sulfonamides)
Vorherige Impfungen: -

VAERS 2086400

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: CA
Alter: 17,0
Geschlecht: M
Eingang: 24.02.2022
Impfdatum: 24.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Blood test abnormal Chest X-ray Chest pain Chills Delirium Blood test Dyspnoea Bradycardia Capillary nail refill test Chest discomfort Echocardiogram normal Echocardiogram Electrocardiogram Lethargy Myalgia Myocarditis Neuralgia Pain

Symptomtext

17 Y 7 M generally healthy male who presents with acute onset of chest pain/pressure worsening Friday. He received COVID booster on 1/24/22, had intense fevers, myalgias, "nerve pain" all over body the 24-36hours after the booster. He was pretty much recovering by Wednesday and went to school since Thursday. However, on Friday, by 11:30am, he was feeling very tired and out-of-it. He started feeling chest pressure and pain. Denies tingling/numbness/radiation. Currently, he says he feels a little pressure at the chest right above the epigastric area--more like pressure rather than sharp. At one point, he did feel sharp pain but the general sensation of pressure was more bothering. He was seen this afternoon and referred for labs. His troponin came back elevated at 0.4 and so he was directed to the emergency room for further evaluation. In ED: repeat troponin 0.44, bedside echocardiogram showed good LV function and no effusion. Rest of labs reassuring. After discussion with cardiology, patient admitted for further management. on 1/31/22:17 y.o. M with post COVID vaccine-related myocarditis, admitted with intermittent chest pain and elevated troponin, awaiting troponin level <0.5. Overall down-trended from peak troponin of 3.55 but with mild uptrend in troponin to 1.16 from 0.95. Chest pain improved with q8h motrin, now with only intermittent chest pain (at decr level from prior) and no SOB. Plan: Trending troponin q12h until trop <0.5. 1/28 EKG: NSR, RSR' in V1/V2 prob normal variant per Cards. Also on nicotine patch 14mg/24h started 1/29/22 in s/o hx vaping and desire to quit. Dispo plan & recs per Cardiology: Plan for outpt cards f/u appt, no strenuous activities for 30 days after discharge and no competitive sports for 3 months until he can be cleared with a normal treadmill test. Recheck troponin 1 week after discharge. Will need nicotine patch wean - should be on (14 mg/day) for 2 weeks then step down to step 3 (7 mg/day) for 2 weeks. Exam notable for CV: mildly bradycardic rate, normal rhythm, normal S1/S2, no point tenderness of chest on palpation. Cap refill < 2 sec, normal pulse. Pulm: CTAB. Abd: soft, NT, ND.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 3,0
Labordaten: Results for patient as of 2/24/2022 13:58 1/28/2022 16:48 TROPONIN I: 0.40 (H) 1/28/2022 20:40 TROPONIN I: 0.44 (H) 1/29/2022 04:15 TROPONIN I: 0.84 (H) 1/29/2022 16:25 TROPONIN I: 1.75 (H) 1/30/2022 03:40 TROPONIN I: 3.55 (H) 1/30/2022 15:35 TROPONIN I: 0.95 (H) 1/31/2022 03:50 TROPONIN I: 1.16 (H) 1/31/2022 16:30 TROPONIN I: 0.32 (H) 2/7/2022 16:35 TROPONIN I: <0.02
Aktuelle Erkrankungen: -
Vorgeschichte: h/o Vaping
Andere Medikamente: -
Allergien: Sulfur (not Sulfonamides)
Vorherige Impfungen: -

VAERS 2086400

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: CA
Alter: 17,0
Geschlecht: M
Eingang: 24.02.2022
Impfdatum: 24.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test abnormal Chest X-ray Chest pain Chills Delirium Blood test Dyspnoea Bradycardia Capillary nail refill test Chest discomfort Echocardiogram normal Echocardiogram Electrocardiogram Lethargy Myalgia Myocarditis Neuralgia Pain

Symptomtext

17 Y 7 M generally healthy male who presents with acute onset of chest pain/pressure worsening Friday. He received COVID booster on 1/24/22, had intense fevers, myalgias, "nerve pain" all over body the 24-36hours after the booster. He was pretty much recovering by Wednesday and went to school since Thursday. However, on Friday, by 11:30am, he was feeling very tired and out-of-it. He started feeling chest pressure and pain. Denies tingling/numbness/radiation. Currently, he says he feels a little pressure at the chest right above the epigastric area--more like pressure rather than sharp. At one point, he did feel sharp pain but the general sensation of pressure was more bothering. He was seen this afternoon and referred for labs. His troponin came back elevated at 0.4 and so he was directed to the emergency room for further evaluation. In ED: repeat troponin 0.44, bedside echocardiogram showed good LV function and no effusion. Rest of labs reassuring. After discussion with cardiology, patient admitted for further management. on 1/31/22:17 y.o. M with post COVID vaccine-related myocarditis, admitted with intermittent chest pain and elevated troponin, awaiting troponin level <0.5. Overall down-trended from peak troponin of 3.55 but with mild uptrend in troponin to 1.16 from 0.95. Chest pain improved with q8h motrin, now with only intermittent chest pain (at decr level from prior) and no SOB. Plan: Trending troponin q12h until trop <0.5. 1/28 EKG: NSR, RSR' in V1/V2 prob normal variant per Cards. Also on nicotine patch 14mg/24h started 1/29/22 in s/o hx vaping and desire to quit. Dispo plan & recs per Cardiology: Plan for outpt cards f/u appt, no strenuous activities for 30 days after discharge and no competitive sports for 3 months until he can be cleared with a normal treadmill test. Recheck troponin 1 week after discharge. Will need nicotine patch wean - should be on (14 mg/day) for 2 weeks then step down to step 3 (7 mg/day) for 2 weeks. Exam notable for CV: mildly bradycardic rate, normal rhythm, normal S1/S2, no point tenderness of chest on palpation. Cap refill < 2 sec, normal pulse. Pulm: CTAB. Abd: soft, NT, ND.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 3,0
Labordaten: Results for patient as of 2/24/2022 13:58 1/28/2022 16:48 TROPONIN I: 0.40 (H) 1/28/2022 20:40 TROPONIN I: 0.44 (H) 1/29/2022 04:15 TROPONIN I: 0.84 (H) 1/29/2022 16:25 TROPONIN I: 1.75 (H) 1/30/2022 03:40 TROPONIN I: 3.55 (H) 1/30/2022 15:35 TROPONIN I: 0.95 (H) 1/31/2022 03:50 TROPONIN I: 1.16 (H) 1/31/2022 16:30 TROPONIN I: 0.32 (H) 2/7/2022 16:35 TROPONIN I: <0.02
Aktuelle Erkrankungen: -
Vorgeschichte: h/o Vaping
Andere Medikamente: -
Allergien: Sulfur (not Sulfonamides)
Vorherige Impfungen: -

VAERS 2134298

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: GA
Alter: 17,0
Geschlecht: M
Eingang: 23.02.2022
Impfdatum: 16.02.2022
Beginn: 19.02.2022
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Alanine aminotransferase increased Aspartate aminotransferase increased Chest pain Magnetic resonance imaging heart Myocarditis Nausea SARS-CoV-2 antibody test positive Troponin increased

Symptomtext

developed chest pain and nausea, diagnosis of acute myocarditis, being treated with Naprosyn 250mg BID

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 2,0
Labordaten: 2/21/2022:Troponin 10.452, ALT 62, AST 67, 2/22/2022 COVID IGG positive. 2/22/2022 Cardiac MRI: IMPRESSION: 1. Normal right ventricular size, RVEDV = 63 cc/m2. Normal right ventricular systolic function, RV EF = 57%. 2. Normal left ventricular size, LVEDV = 60 cc/m2. Normal left ventricular systolic function, LV EF = 60%, with no regional wall motion abnormalities. 3. There is evidence of high signal intensity on T2 weighted imaging suggestive of edema and T1 early post-contrast imaging suggestive of hyperemia. There is also late gadolinium enhancement imaging within the basal and apical LV as described above. This patient does meet criteria for myocarditis.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2131761

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: LA
Alter: 33,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 18.02.2022
Beginn: 21.02.2022
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RA

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

Dyskinesia Electrocardiogram normal Electroencephalogram normal Metabolic function test Orthostatic hypotension Syncope

Symptomtext

Patient reported a vasovagal syncope episode that appeared to be psychogenic nonepileptic involuntary movements by bystanders, however the patient retained consciousness throughout the experience. It lasted roughly two minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Patient went to ER, found orthostatic hypotension. All other values were within limits, including BMP, EKG, and EEG.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2130082

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: IL
Alter: 23,0
Geschlecht: M
Eingang: 21.02.2022
Impfdatum: 21.02.2022
Beginn: 21.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Hyperhidrosis Malaise Nausea Syncope Tremor

Symptomtext

Patient's companion mentioned that the patient has fainted with vaccines before and that's why he wants to be in the room with the patient. After I administered the patient and observed the patient for a few minutes and he said he felt fine. I then asked them to sit in the imz waiting area for 30 minutes. I asked the companion to keep an eye on the patient while I went in the pharmacy to get a technician to observe the patient. As I was grabbing a technician. The technician was informed by another customer that the patient was not doing well. I rushed to the patient who was alert at this time. The companion stated that the patient fainted (had his held tilted and his eyes closed) and started to shake to which he nudged the patient who then regained consciousness. He stated that right before he nudged the patient he was shaking. I had my technician grab an ice pack and I applied it to his forehead. The patient appeared to be sweating and stated he was nauseous. He asked for something to drink or eat. I told him that since he's nauseous giving him food right now could cause problems. My technician paged code white and management arrived. At this point patient was feeling better and was alert. Since I did not like the fact that the patient was shaking, management called 911. I explained to the 911 operator what had happened. My technician stayed with management and they observed the patient till the paramedics arrived. The paramedics checked his vitals and the patient signed a consent form stating that he did not want to go with them. The patient later came to ask a question regarding his IMZ records and was feeling fine

Weitere VAERSDATA-Felder

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

VAERS 2115954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

schwer

Staat: CA
Alter: 30,0
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: 16.02.2022
Beginn: 16.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Loss of consciousness Seizure

Symptomtext

About 2 minutes after vaccine given pt began to pass out with possible seizure. another 3 or 4 minutes later the same thing happened, pass out/ seizure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: nka
Vorherige Impfungen: fainted

VAERS 2114527

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: OH
Alter: 27,0
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 21.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Cerebral endovascular aneurysm repair Computerised tomogram head abnormal Headache Hypoaesthesia Inappropriate schedule of product administration Intensive care Ruptured cerebral aneurysm SARS-CoV-2 test negative Scan with contrast abnormal Subarachnoid haemorrhage Vomiting

Symptomtext

Head pain, numbness and vomiting- brought to ER - dx with Subarachnoid Bleed-air flighted to hospital- aneurysm coil procedure, 4 days in ICU, 11 days in hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 11,0
Labordaten: 1/21/22 CT = subarachnoid bleed 1/21/22 Contrast CT = ruptured aneurysm of anterior communication artery - no family or known history of aneurysms Covid negative
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism Anxiety PCOS
Andere Medikamente: Synthroid Oral Contraceptive Adderal 10mg PRN Vit D
Allergien: Barley Peanuts
Vorherige Impfungen: -

VAERS 2113368

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: CT
Alter: 12,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 02.02.2022
Beginn: 02.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dehydration Syncope Unresponsive to stimuli

Symptomtext

Administered Pfizer vaccine in left deltoid, approximately 7-8 minutes later, while the patient was standing next to her mother, she had a syncopal episode. The mother grabbed her daughter and yelled for my help. The patient was non responsive. As I assisted her to the floor she became responsive. She was alert and oriented x 4. PT was able to stand, assisted her to a chair and assessed her vitals: BP 149/121; HR 69; SPO2 98. PT's mother contacted pt's pediatrician and brought pt in to office for exam. Pediatrician cleared pt, indicating pt may have been dehydrated. note: PT had indicated she had eaten a small meal(bread) about 3 hours prior to vaccination.

Weitere VAERSDATA-Felder

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

VAERS 2109583

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: VA
Alter: 18,0
Geschlecht: F
Eingang: 13.02.2022
Impfdatum: 08.02.2022
Beginn: 08.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Injection site erythema Injection site pain Injection site swelling Pyrexia Syncope Unresponsive to stimuli Visual impairment

Symptomtext

Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Fainting / Unresponsive-Medium, Systemic: Fever-Medium, Systemic: Visual Changes/Disturbances-Medium

Weitere VAERSDATA-Felder

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

VAERS 2109414

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: ME
Alter: 24,0
Geschlecht: M
Eingang: 12.02.2022
Impfdatum: 12.02.2022
Beginn: 12.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Fall Pallor Syncope

Symptomtext

After administering vaccination the patient developed vasovagal syncope. Patient turned pale and started sliding off chair onto floor. I partially caught patient on the way down and he did not experience any injuries from the fall. I kept patient on the floor with legs elevated and applied a cold compress to back of neck. The patient regained consciousness after a couple seconds and was able to leave the pharmacy after a period of observation. Patient said he was feeling fine when leaving pharmacy.

Weitere VAERSDATA-Felder

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

VAERS 2105919

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: CA
Alter: 13,0
Geschlecht: M
Eingang: 11.02.2022
Impfdatum: 05.02.2022
Beginn: 06.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Blood electrolytes Blood glucose Blood thyroid stimulating hormone Dizziness Fall Full blood count Head injury Serum ferritin Syncope

Symptomtext

Patient has a fainting incident on 2/6/22 the morning after the 3rd covid vaccine shot. Mother found him on floor dizzy and bump in back of head. Shortly thereafter had another incident. Went to the lab to have blood drawn and had a 3rd incident of dizziness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: 2/6/22 Electrolytes/glucose, ferritin, cbc, tsh
Aktuelle Erkrankungen: -
Vorgeschichte: Atopic Dermatitis
Andere Medikamente: Triamcinolone .1% cream
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2104755

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: NY
Alter: 21,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 10.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Syncope

Symptomtext

Vasovagal syncope

Weitere VAERSDATA-Felder

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

VAERS 2104485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: AR
Alter: 15,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 10.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Injection site pain Syncope Unresponsive to stimuli

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Fainting / Unresponsive-Medium, Additional Details: PATIENT STOOD UP AND THEN SAID SHE FELT FAINT. THE IMMUNIZER TOLD HER TO SIT DOWN ON THE CHAIR AND BEFORE SHE COULD TO THIS SHE FAINTED.

Weitere VAERSDATA-Felder

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

VAERS 2091858

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

schwer

Staat: MN
Alter: 15,0
Geschlecht: M
Eingang: 11.02.2022
Impfdatum: 03.02.2022
Beginn: 05.02.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Adenovirus test C-reactive protein increased Chest pain Chlamydia test negative Cytomegalovirus test negative Electrocardiogram abnormal Pericarditis Troponin increased Echocardiogram normal Electrocardiogram ST segment abnormal Enterovirus test negative Epstein-Barr virus test negative HIV test negative Hepatitis B virus test Herpes simplex test negative Human metapneumovirus test Human rhinovirus test Influenza virus test negative

Symptomtext

Chest pain started 2/5/2022. The following morning (2/6/2022) he took antacids and the pain subsided. Admitted to the hospital on 2/6 for elevated troponin and ST changes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 1,0
Labordaten: 2/6: EKG with diffuse ST changes, troponin 13.47 ng/mL and repeated at our hospital (14,018 ng/L), CRP 44 2/7: echocardiogram normal, troponin down trending 8,720, CRP 46.5, extensive myopericarditis viral work-up negative (COVID, influenza, adenovirus, Chlamydia pneumoniae, HSV, HMPV, Hep B, HIV, HHV6, rhino/enterovirus, Mycoplasma pneumoniae, parainfluenza, RSV, EBV, CMV).
Aktuelle Erkrankungen: None noted
Vorgeschichte: asthma
Andere Medikamente: antacid, albuterol
Allergien: NKA
Vorherige Impfungen: -

VAERS 2091705

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: GA
Alter: 24,0
Geschlecht: F
Eingang: 06.02.2022
Impfdatum: 05.02.2022
Beginn: 05.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Confusional state Dizziness Fatigue Flushing Hyperhidrosis Lethargy Nausea Pallor Syncope Unresponsive to stimuli Vomiting

Symptomtext

Systemic: Confusion-Severe, Systemic: Dizziness/Lightheadedness-Severe, Systemic: Exhaustion/Lethargy-Severe, Systemic: Fainting/Unresponsive-Severe, Systemic: Flushed/Sweating-Medium, Systemic: Nausea-Severe, Systemic: Vomiting-Severe, Systemic: Weakness-Medium, Additional Details: Patient said she took a beta blocker (propranolol) for anxiety before coming to vaccine appointment, but subsequently fainted after administration. This was accompanied with sweating, pale face and severe nausea/vomiting.

Weitere VAERSDATA-Felder

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

VAERS 2091562

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: OH
Alter: 39,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 05.02.2022
Beginn: 05.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Balance disorder Heart rate decreased Loss of consciousness Pallor Unresponsive to stimuli

Symptomtext

The patient was sitting in observation area after getting the booster vaccine at 10:37. At 11:05, nurse noticed that the patient was pale and about to fall from her chair. A group of nurses (including men nurses) lifted patient on cart. The patient was unresponsive, pulse hard to feel- another nurse felt at carotid. Oxygen was started at 6 liters. EMS was called and arrived within 3-5 minutes. They assessed patient and patient was feeling better- but decided would keep her here an additional 30 minutes from episode. 11:05 Blood pressure 133/82 Pulse 88 and Pulse Ox was 100% 11:10 Blood pressure was 116/75 Pulse 89 pulse ox 98% 11:24 Blood pressure was 120/86 Pulse 71 Oxygen brought down to 4 liters- Puls eox 99% 11:30 oxygen brought down to 2 liters- Bp 120/78 74 Pulse ox 100% 11:35 Bp was 117/82 76 96 pulse ox 11:45 BP 116/70 76 pulse ox at 96% at room air. Patient did take Klopin at 10:00 am at home. At 11:45 patient's color look good, was able to communicate clearly and answer questions. Son and friend were present. Patient denies any chest pain or sob, Patient was placed in wheelchair and was escorted to car. Friend was driver. Patient stated that this has happened before with passing out (not with other 2 vaccines)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Anxiety, Depression (chronic)- sees psych and increased Lexapro in summer GERD Charot Marie
Andere Medikamente: Lexapro, Prilosec, Valtrex, Vit d ,Klonopin
Allergien: ASA, Cephalosporin, Demerol, Erythromycin, Morphine, Opiods, PCN, Sulfa
Vorherige Impfungen: -

VAERS 2091331

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: -
Alter: 44,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 28.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Asthenia Back pain Loss of consciousness Lymphadenopathy Malaise Musculoskeletal chest pain Neck pain Pain Paraesthesia Vision blurred

Symptomtext

Almost passed out; not feeling good; eyes start getting blurry and glassy; tingling sensation, in my chest; I was real slow; weak; hurting in my neck; could not move my neck, like my lymph nodes swell up in my neck; ribs hurt like when I cough; body hurt; my body felt like somebody beat the hell out of me and I was in so much pain; back is hurting; hurting in my neck; could not move my neck, like my lymph nodes swell up in my neck; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. Other Case identifier(s): -PFIZER INC-202200175283 (Pfizer). A 44 year-old female patient received bnt162b2 (COMIRNATY), administration date 28Jan2022 (Lot number: FJ6369, Expiration Date: 31May2022) at the age of 44 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: LOSS OF CONSCIOUSNESS (medically significant), outcome "unknown", described as "Almost passed out"; MALAISE (non-serious), outcome "unknown", described as "not feeling good"; VISION BLURRED (non-serious), outcome "unknown", described as "eyes start getting blurry and glassy"; PARAESTHESIA (non-serious), outcome "unknown", described as "tingling sensation, in my chest"; ASTHENIA (non-serious), outcome "unknown", described as "I was real slow; weak"; LYMPHADENOPATHY (non-serious), NECK PAIN (non-serious), outcome "unknown" and all described as "hurting in my neck; could not move my neck, like my lymph nodes swell up in my neck"; MUSCULOSKELETAL CHEST PAIN (non-serious), outcome "unknown", described as "ribs hurt like when I cough"; PAIN (non-serious), outcome "unknown", described as "body hurt; my body felt like somebody beat the hell out of me and I was in so much pain"; BACK PAIN (non-serious), outcome "unknown", described as "back is hurting".

Weitere VAERSDATA-Felder

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

VAERS 2091100

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: -
Alter: 33,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 26.01.2022
Beginn: 03.02.2022
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / -

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

Asthenia Exposure during pregnancy Fine motor skill dysfunction Guillain-Barre syndrome Hypoaesthesia Immunoglobulin therapy Muscle strength abnormal Neurological symptom Pulmonary function test abnormal

Symptomtext

Patient began having multiple neurological symptoms. Progressive extremity numbness with loss of muscle strength and fine motor skill. Patient is currently 14 weeks pregnant. NIF breathing tests indicate weakness. Diagnosed with GBS. First dose of IVIG given on 2/4.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: bipolar disorder, asthma, COPD, back pain, depression, hepatitis C
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2084906

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: GA
Alter: 24,0
Geschlecht: M
Eingang: 03.02.2022
Impfdatum: 02.02.2022
Beginn: 02.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Fatigue Flushing Hyperhidrosis Hypotension Lethargy Loss of consciousness

Symptomtext

Systemic: Dizziness / Lightheadness-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Flushed / Sweating-Mild, Systemic: Hypotension-Mild, Additional Details: Pt passed out approximately 2 minutes post-vaccination. EMS came to evaluate/ Pt declined transport. Stated mom would pick him up. Symptoms improved in approximately 15-20 minutes.

Weitere VAERSDATA-Felder

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

VAERS 2082734

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: FL
Alter: 16,0
Geschlecht: F
Eingang: 02.02.2022
Impfdatum: 02.02.2022
Beginn: 02.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cold sweat Pallor Syncope

Symptomtext

APPROXIMATELY 5 MINUTES AFTER VACCINATION PATIENT FAINTED. PT RECOVERED WITHIN 30 SECONDS. PT WAS CLAMMY AND PALE FOR ABOUT 10 MINUTES. PT RECOVERED AND FELT WELL AFTER ABOUT 30 MINUTES. HER FATHER REQUESTED PARAMEDICS TO BE CALLED. PARAMEDICS CAME AND CHECKED HER OUT. PARAMEDICS CLEARED HER TO LEAVE IN JUST A COUPLE OF MINUTES. PT WAS FEELING WELL WHEN SHE LEFT THE PHARMACY AREA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE KNOWN
Vorgeschichte: ECZEMA
Andere Medikamente: TRIAMCINOLONE 0.1% OINTMENT, CETIRIZINE 10MG TABLET
Allergien: NONE KNOWN
Vorherige Impfungen: -

VAERS 2079618

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: CA
Alter: 17,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 22.01.2022
Beginn: 22.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Syncope Unresponsive to stimuli

Symptomtext

Client presented to vaccine site with her mother on 1/22/2022 to receive the COVID Pfizer Booster dose. RN vaccinated client with the COVID Pfizer Booster dose (Lot# FJ6369) in the L arm while sitting upright at 1340. At approximately 1341 the client stated "i'm feeling dizzy" and RN called for help. RN stabilized the client in the chair as she fainted and Lead RN assisted in stimulating the client. Client had a strong pulse and patent airway. RN assessed client was unresponsive to stimuli for approximately 2 seconds. Client did not fall out of chair and did not sustain any injuries. When client became responsive to stimuli, RN assessed client was A&O x4 and reoriented client to the room. EMT provided client with water and took client's vitals. Vitals at 1342 were BP in R arm sitting upright 138/90, HR 93, and SPO2 99%. Client's mother reported "she starts to shake even talking about the vaccine" and stated that the client has a history of anxiety with needles. RN reported to Lead RN that the client did not disclose history of syncope with needles prior to vaccination. Client reported her last intake was carne asada fries at approximately 1230. Client denied SOB, pain, nausea, or changes in vision. Client reported mild dizziness. EMT and Lead RN assisted in transferring the client to lay down cot in observation area. EMT took vitals at 1355 with BP 132/94, HR 98, and SPO2 98%. At 1355 the client reported she was "not really dizzy anymore" and "a little lightheaded". Lead RN reviewed ER precautions and when to f/u with PCP with client and her mother. RN observed a steady and symmetrical gait as client walked around in observation. Client left the vaccine site with her mother who drove her at approximately 1410.

Weitere VAERSDATA-Felder

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

VAERS 2079163

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: CT
Alter: 15,0
Geschlecht: M
Eingang: 01.02.2022
Impfdatum: 20.01.2022
Beginn: 25.01.2022
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / AR

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

Asthenia Guillain-Barre syndrome Hypoaesthesia Immunoglobulin therapy Laboratory test Loss of proprioception Lumbar puncture normal Magnetic resonance imaging normal Paraesthesia Sensory loss

Symptomtext

Numbness, tingling, weakness, decreased sensation and proprioception in lower extremity. Diagnosed with variant of Gullain-Barre. Treated with IVIG.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 5,0
Labordaten: MRI--normal LP--normal Other labs pending
Aktuelle Erkrankungen: None
Vorgeschichte: ADHD
Andere Medikamente: Focalin
Allergien: None
Vorherige Impfungen: -

VAERS 2076970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: CA
Alter: 18,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 31.01.2022
Beginn: 31.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Eye movement disorder Syncope Tremor

Symptomtext

Patient is an 18 yo, F, who received her first series of Covid -19 vaccine today of Pfizer 0.3 mls Lot # FJ 6369 with Mfg date of 09/2021 on her left deltoid by MA at 18:15, tolerated the procedure well. She was asked to wait 15 minutes for observation, and was asymptomatic. At 18:30, she approached the Provider's table and complained of feeling dizzy, and passed out. She was laid in yoga mat and head was supported. VS checked. Pulses and breathing present throughout and were adequate. B/L hands cool to touch. She would sit up at times and pass out again. Appeared like eyes rolled but no seizure activity noted. HR between 48-54, Sats 87-99%. RR 12-14/min. BP=140/62 mmHg.At 18:32- In-house ED team activated by MA At 18:35-Epipen 0.15 mg given IM to right VL. 18:36-ED team arrived and updated. Patient awake, tried to call sister on cellphone, hands still shaking. Brought to ED with patient permission via WC accompanied by ED team.

Weitere VAERSDATA-Felder

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

VAERS 2074789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

schwer

Staat: NC
Alter: 60,0
Geschlecht: F
Eingang: 30.01.2022
Impfdatum: 28.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Dyspnoea Syncope Unresponsive to stimuli

Symptomtext

Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe

Weitere VAERSDATA-Felder

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

VAERS 2074456

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: MA
Alter: 43,0
Geschlecht: M
Eingang: 29.01.2022
Impfdatum: 28.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Flushing Head injury Hyperhidrosis Pallor Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Additional Details: Wife of patient had syncopal episode w/head strike to shelf. Denied LOCand none observed. Pt was alert and reponsive. info obtained w/help of person on phone to assist. Pt pale&diaphoretic. Placed in recovery position. Radial pulse steady/70's. no pmh, no medications. Patient was given cool, wet wash cloth for head. 911 called and upon eval states feeling better and agreed to hospital transfer.

Weitere VAERSDATA-Felder

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

VAERS 2073068

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: CA
Alter: 45,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 01.01.2022
Beginn: 25.01.2022
Tage bis Beginn: 24,0
Dosis: 3
Route/Site: SYR / LA

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

Amnesia Blood test Computerised tomogram Confusional state Dizziness Fatigue Feeling abnormal Syncope Urine analysis

Symptomtext

Brain fog, blacking out, memory loss, confusion, and lightheadedness. Doctor blamed fatigue, but it definitely seems like something way more serious, especially being that I get 8 + hours of sleep every night.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Bloodwork, urinalysis, CT scan.
Aktuelle Erkrankungen: Chest cold 2 weeks earlier
Vorgeschichte: Arthritis, fibromyalgia, depression, chronic pain
Andere Medikamente: None
Allergien: Sulfa
Vorherige Impfungen: Minor headaches.

VAERS 2069170

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: -
Alter: 25,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Syncope

Symptomtext

Pt was vaccinated in the supine postiion. Procedure tolerated well but then had a syncopal event Vitals: 113/63, 76, 10, 96.8. Pt recovered. Pt stable and released from the vaccination site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: syncope w/ vaccinations
Andere Medikamente: Unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 2068471

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

schwer

Staat: VA
Alter: 59,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 22.01.2022
Beginn: 23.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Injection site pain Muscle rigidity Nausea Seizure Syncope Unresponsive to stimuli Vomiting

Symptomtext

Site: Pain at Injection Site-Medium, Systemic: Fainting / Unresponsive-Severe, Systemic: Seizure-Severe, Additional Details: patient had 3 episodes. 1st: she had severe nausea that morning.2nd : nausea then vomited. 3rd. same say couple hours later, she fainted, unconscious and turned rigid. as she woke up she vomited. f/u with md awaits results

Weitere VAERSDATA-Felder

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

VAERS 2068457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

schwer

Staat: RI
Alter: 28,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 25.01.2022
Beginn: 25.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Flushing Hyperhidrosis Injection site pain Nausea Seizure Tremor Vomiting

Symptomtext

Site: Pain at Injection Site-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Nausea-Severe, Systemic: Seizure-Medium, Systemic: Shakiness-Medium, Systemic: Vomiting-Severe, Systemic: Weakness-Medium, Additional Details: Pharmacist monitored patient. Patient was give orange juice after experincing small seizure and vomiting twice. Color came back into skin shortly after. Patient came to pharmacy day after to report incident.

Weitere VAERSDATA-Felder

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

VAERS 2063086

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: AZ
Alter: 54,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: -
Beginn: 23.01.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Breast mass Confusional state Loss of consciousness Tenderness

Symptomtext

Per patient had vaccine done 1/21/22 and felt a lump next to her LT breast on 1/23/22. Patient then blacked out yesterday 1/24/22 at work at 1:00PM and when patient woke up, patient couldn't understand the words coming out of her mouth. This morning 1/25/22 patient didn't feel the lump anymore but it hurt to touch.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: 2 weeks prior patient states she was sick. SXS were lost of and coughing.
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 2062882

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: CA
Alter: 15,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 24.01.2022
Beginn: 24.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Nausea Staring Syncope

Symptomtext

Pt present for booster shot; Pt expressed nervousness about getting shot; Per pt's mother pt fainted when she received her initial series shots. Pt sat in vaccine chair, vaccine administered, pt c/o of nausea. Pt immediately experienced syncopal episode for 5 seconds. I sat pt upright in chair. I called her name pt responded by looking at me. I asked her questions. Pt responded to questions appropriately but still had distant stare. I continued to refocus her attention to me and to my questions. Pt closed eyes and shook head. Pt continued to answered appropriately and eventually engaged in conversation. We offered water and juice. Pt accepted and drank them. Pt indicated she was ok. I assessed for alertness. She continued to engage in conversation and wanted to stand. we assisted in standing and pt walked with steady gait under her own power.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: 5/14/21 -Pfizer dose 1 (Lot # Er8729) @ MCH , pt fainted 6/4/21 - Pfizer Dose 2 (Lot# EW0185) @ MCH, pt fainted

VAERS 2058855

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: CA
Alter: 12,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 20.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cold sweat Nausea Pallor Presyncope Vomiting

Symptomtext

During the 15min observation time, pt c/o feeling nauseated and started vomiting. Pt noted to be pale and skin was cool and clammy. RN provided pt with small sips of juice and proceeded to check vital signs. Initially, RN was not able to obtain BP and pulse was in 120s. RN laid pt down and elevated both legs in effort to improve cardiac perfusion. After a few minutes, BP was obtained and pulse was all within range. Paramedics arrived on scene to evaluate and pt's vitals were stable. RN and paramedic later determined that it was not an anaphylactic reaction but more of a vasovagal response to the injection. Mother declined to have pt be transported to nearby hospital for further evaluation. Pt stated he felt a lot better and was no longer experiencing symptoms.

Weitere VAERSDATA-Felder

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

VAERS 2058063

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: CA
Alter: 31,0
Geschlecht: M
Eingang: 23.01.2022
Impfdatum: 23.01.2022
Beginn: 23.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Nausea Paraesthesia Syncope Unresponsive to stimuli

Symptomtext

Patient received Pfizer booster at 2:16pm and went to go sit down to be observed for 15 minutes. Patient returned to vaccinator 5 minutes later saying that he felt faint and nauseous. Then vaccinator went to sit patient down and patient fainted. Staff caught patient and lowered him to the ground. Patient was verbally unresponsive for 4 seconds. Patient opened eyes, while he was resting on the floor. Had patient bend his knees with head resting on the floor. Took initial BP; 110/66 HR 63. Patient denies any pain and stated his arms felt tingly, which also occurred with previous covid19 vaccination. Patient stated he did not sleep well or eat before coming to be vaccinated. He also stated that he was anxious because he is scared of needles. Had patient sit up on the floor after 5 minutes, assessed patient to see if he was dizzy patient denied. After several minutes had patient sit on chair. Offered water and observed patient. Retook Vitals ; 126/84, HR 80, SpO2 98%, RR 16, Temp 98F. Patient stated tingling in arms resolved. Let patient rest in chair for additional 15 minutes to be observed. Patient appeared stable, advised him to let his doctor know what occurred today and with future vaccinations to let vaccinators know as well. Patient left with friend after appearing stable.

Weitere VAERSDATA-Felder

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

VAERS 2057723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: AR
Alter: 15,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 22.01.2022
Beginn: 22.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Loss of consciousness

Symptomtext

Within a minute of giving the patient her Pfizer booster 0.3ml dose, patient started to pass out. Patient's mother and immunization pharmacist quickly reacted to hold her up in her chair. Patient woke up shortly after passing out and her temperature was 97.6, blood pressure of 91/56, pulse was 63. Patient is 15 years old and her mother was with her in the room the entire time. Patient was given a bottle of water to drink and was kept in the immunization room for about 30 minutes. The immunization pharmacist offered to call the patient an ambulance, patient and her mother refuses. Various foods and drinks items were offered to help the patient feel better, but the patient refuse them all. The patient felt better and left the pharmacy with both of her parents. Immunization pharmacist called the patient's mother to check in with the patient at 5:48pm and the patient's mother reported what the patient is doing fine, with no problem.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: 1/22/2022 at 3:40pm patient temperature was 97.6, blood pressure of 91/56, pulse was 63
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 2057002

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: IL
Alter: 32,0
Geschlecht: M
Eingang: 22.01.2022
Impfdatum: 21.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Confusional state Dizziness Flushing Hyperhidrosis Loss of consciousness Nausea Pallor Syncope Unresponsive to stimuli

Symptomtext

Systemic: Confusion-Medium, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Medium, Systemic: Nausea-Medium, Additional Details: Approx. 5 min following vaccination, patient became nauseas, closed his eyes to help it pass and lost consciousness. Brought patient to lie on the floor, he immediately regained consciousness. Sweating, loss of color in face, nausea continued. EMS called for follow up. Normal BP and HR, no further concerns

Weitere VAERSDATA-Felder

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

VAERS 2043005

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

schwer

Staat: FL
Alter: 36,0
Geschlecht: M
Eingang: 21.01.2022
Impfdatum: 18.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Discomfort Malaise Syncope Hypotension Loss of consciousness

Symptomtext

On 01/18/2022 about 10 or 15 minutes after the vaccine, I just got my shot and fainted after my shot. I had never fainted before. I was sitting on the chair, mandatory waiting 10 or 15 minutes. I was not feeling good. I asked the pharmacist there was something wrong with my BP, they checked my BP it was 30/60 after that, I do not remember for 10 to 15 seconds, I woke up on the floor. The pharmacist did something, I do not remember the period of time. When I was in a horizontal position I was feeling a little bit better, I could see what was happening, in 5 or 10 minutes the EMT arrived, the raised my legs, and check my BP. I was almost okay after this manipulation. It was done by an emergency. The took me to the Hospital and they took one more measurement of my BP it was 120/80 in the car and pulse was around 67, it was around normal.. When I was in the hospital, they were checking my insurance, so for 2 or 3 hours nobody did anything. I left the hospital, I was feeling uncomfortable because of all the COVID cases, and it was uncomfortable for me. Today, 01/21/2022- I can still see my temperature 37.1 or 37.2 Celsius in the evening, and I could see my BP jumping sometimes, especially after I drink some coffee. and I am feeling some weakness, it is much better than it was on Tuesday. Note: I received my vaccination because it was mandatory by my employer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: middle of December, I was not feeling good, it was something minor like a rash for a couple of day, nothing serious
Vorgeschichte: no
Andere Medikamente: no
Allergien: no food allergies at age of 10, rash from penicillin, it was very minor
Vorherige Impfungen: -

VAERS 2043005

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: FL
Alter: 36,0
Geschlecht: M
Eingang: 21.01.2022
Impfdatum: 18.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Discomfort Malaise Syncope Hypotension Loss of consciousness

Symptomtext

On 01/18/2022 about 10 or 15 minutes after the vaccine, I just got my shot and fainted after my shot. I had never fainted before. I was sitting on the chair, mandatory waiting 10 or 15 minutes. I was not feeling good. I asked the pharmacist there was something wrong with my BP, they checked my BP it was 30/60 after that, I do not remember for 10 to 15 seconds, I woke up on the floor. The pharmacist did something, I do not remember the period of time. When I was in a horizontal position I was feeling a little bit better, I could see what was happening, in 5 or 10 minutes the EMT arrived, the raised my legs, and check my BP. I was almost okay after this manipulation. It was done by an emergency. The took me to the Hospital and they took one more measurement of my BP it was 120/80 in the car and pulse was around 67, it was around normal.. When I was in the hospital, they were checking my insurance, so for 2 or 3 hours nobody did anything. I left the hospital, I was feeling uncomfortable because of all the COVID cases, and it was uncomfortable for me. Today, 01/21/2022- I can still see my temperature 37.1 or 37.2 Celsius in the evening, and I could see my BP jumping sometimes, especially after I drink some coffee. and I am feeling some weakness, it is much better than it was on Tuesday. Note: I received my vaccination because it was mandatory by my employer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: middle of December, I was not feeling good, it was something minor like a rash for a couple of day, nothing serious
Vorgeschichte: no
Andere Medikamente: no
Allergien: no food allergies at age of 10, rash from penicillin, it was very minor
Vorherige Impfungen: -

VAERS 2051536

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

schwer

Staat: SC
Alter: 22,0
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: 20.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Hypotension Pallor Syncope

Symptomtext

patient fainted after getting first pfizer vaccine . patient was conscious all the time , he refused us to call 911, he stated he is feeling fine , he was a bit pale, he stated he didn't eat anything all day and it was 6pm when he got the shot. I checked his blood pressure which the bottom number was kind of low, patient had water and ate some snack and felt better after, his blood pressure was better after that and he got his color back.

Weitere VAERSDATA-Felder

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

VAERS 2047410

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: NM
Alter: 13,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 16.01.2022
Beginn: 16.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Immediate post-injection reaction Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Systemic: Shakiness-Mild, Additional Details: Patient fainted immediately after receiving vaccination. Patient was asked to lie down on floor with feet up for 10 minutes. Pt was monitored for signs of allergy or distress. Blood pressure and heart rate were normal. Mother declined any other medical intervention.

Weitere VAERSDATA-Felder

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

VAERS 2046277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

schwer

Staat: NC
Alter: 17,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LL

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

Disorientation Immediate post-injection reaction Loss of consciousness Nausea Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Additional Details: patient received covid vaccination and passed out immediately. patient revived in about 30 to 45 seconds and was disoriented and nauseated. ems was contacted. ems came on scene and evaluated patient. vital were normal patient seemed alright just disoriented and left with family and was not taken by ems to hospital or any were

Weitere VAERSDATA-Felder

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

VAERS 2043713

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: IL
Alter: 14,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Loss of consciousness

Symptomtext

Patient passed-out following receipt of the vaccination. Recovered consciousness within one minute of fainting.

Weitere VAERSDATA-Felder

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

VAERS 2036164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: TX
Alter: 20,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Dizziness Immediate post-injection reaction Loss of consciousness Syncope

Symptomtext

Immediately after administration, patient experience what we believe was vasovagal syncope. She said she felt dizzy and sat down on the ground, then loss consciousness from a seated position. The pharmacist was with her, she woke up and again lost consciousness. Her sister was with her and her mother was called. She left the pharmacy with her mother. Patient has a history of passing out after vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: Vyvanse 20 mg and Sertraline 25 mg
Allergien: NKDA
Vorherige Impfungen: unknown

VAERS 2036154

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: AZ
Alter: 47,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Consciousness fluctuating Syncope

Symptomtext

PT FAINTED AFTER RECIEVING VACCINE. SHE WAS IN AND OUT OF CONSCIOUSNESS FOR ABOUT 5 MINUTES. EMS WAS CALLED. ALL VITALS WERE NORMAL. PT REFUSED FURTHER CARE FROM EMS AND LEFT. PER HER ACOMPANYING FAMILY MEMEBER, THE PT HAS A HISTORY OF BEING ANXIOUS DURING VACCINATIONS AND FAINTING THAT SHE DID NOT DISCLOSE ON THE CHECK IN FORM. SHE REPORTED THAT HER LAST 2 DOSES OF THE COVID VACCINE DID NOT RESULT IN LOSS OF CONSCIOUSNESS.

Weitere VAERSDATA-Felder

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

VAERS 2032358

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: -
Alter: 58,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 12.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Hyperhidrosis Malaise Pallor Syncope

Symptomtext

Client arrived for Booster Dose COVID Vaccine. Client notified Vaccinator , that he felt a little lightheaded and nervous with needles. Vaccinator provided water prior to vaccination. Vaccinator had client sit in the zero gravity chair for vaccination. Client received the Booster Dose COVID vaccine (Pfizer, Lot # FJ369, expiration date 03/16/2022) at 1206PM. Client immediately following vaccination states he felt fine. At 1208 Client called over to Vaccinator stating that he was not feeling well. Client was pale, sweating, and feeling lightheaded. On arrival, Client fainted while in zero gravity chair for approximately 3 seconds. Vaccinator assessed Initial vitals (P 49, O2 87, A&O x4). At 1211 second assessment of vitals (P 60, 02 94, BP 92/59, and A&Ox4). Client has no pertinent medical history, NKA, and not taking any medications. Client color returning to normal, decreased sweating, and reports he is feeling better. Client provided juice and crackers. At 1219 Client tolerating juice and crackers. Vitals assessed (BP 124/73, P 63, O2 97, color within normal limits). Vaccinator had client sit up in zero gravity chair. At 1229 Vaccinator assessed vitals (BP 120/76, P 65, O2 97, color within normal limits). Client states he is feeling better. Client educated on signs and symptoms of when to seek medical care and to follow-up with primary care provider. At 1236 Client left with steady gait.

Weitere VAERSDATA-Felder

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

VAERS 2019276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

schwer

Staat: NY
Alter: 13,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 08.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Fall Head injury Headache Loss of consciousness Syncope

Symptomtext

Post vaccination got up, felt dizzy, lightheaded and had syncope. He fell down, hit his head in the back with the fall, woke up in a few seconds. Had headache and dizziness. Observed for 40 min. BP 106/68, P- 88. At the end of the observation he feels much better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin and vitamin C
Allergien: None
Vorherige Impfungen: -

VAERS 2711997

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MI
Alter: 60,0
Geschlecht: F
Eingang: 09.11.2023
Impfdatum: 25.01.2022
Beginn: 05.08.2023
Tage bis Beginn: 557,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Chest pain Coronary artery bypass Cough Culture urine positive Dyspnoea Echocardiogram normal Ejection fraction normal Hypertension Klebsiella test positive Prohormone brain natriuretic peptide increased Pyrexia SARS-CoV-2 test positive Tachypnoea Urine analysis abnormal White blood cell count normal

Symptomtext

BRIEF OVERVIEW: Admission Date: 8/5/2023 Discharge Date: Aug 7, 2023 Discharge Disposition: home or self care DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Shortness of breath [R06.02] Dyspnea [R06.00] Fever, unspecified fever cause [R50.9] Chest pain, unspecified type [R07.9] HOSPITAL COURSE: 62-year-old with past medical history of chronic diastolic congestive heart failure, type 1 diabetes, diabetic neuropathy, history of coronary artery disease with CABG in 2023, hypertension, blindness, depression, chronic short-term memory loss, OSA not on CPAP, who presented with dyspnea and cough. In ED febrile, mildly hypertensive, tachypneic to 30. ProBNP elevated to 7649 which is significantly elevated from her last few readings. White blood cell count within normal limits. COVID-19 positive. Discharge from the ED discussed with the patient, however she was not comfortable with this and so decision made to admit under observation status. On admission patient is placed on IV Lasix 40 mg 2 times a day. Noted last discharge weight 93.1 kg. Noted last echocardiogram 07/24/2023 ejection fraction 60% assessment for diastolic indeterminate. By 8/6 standing weight was 92.7 kg. Discussed with patient torsemide dose had been decreased from 60 mg daily to 20 mg 2 times a day. Patient felt she did not have significant urine output from the lower dose. On discharge patient will be given 40 mg once daily and advised to monitor daily weights and call physician if significant weight gain. Patient also noted positivity for COVID-19 on admission. Patient received 1 day of remdesivir given risk for progression with underlying multiple medical comorbidities. Patient was able to remain on room air including with ambulation. Fevers improved. Patient will be prescribed paxlovid at the reduced renal dosing on discharge. Urinalysis and urine culture obtained in emergency department grew Klebsiella however patient has absolutely no dysuria or abdominal discomfort and fevers can be attributed to the COVID-19 infection. Discussed with patient if she develops any urinary symptoms she will need to discuss with her PCP and start antibiotics however does not appear indicated at this time as patient asymptomatic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Type 1 diabetes mellitus with nephropathy, polyneuropathy Prurigo nodularis Hx MRSA infection Dyslipidemia due to type 1 diabetes mellitus OSA (obstructive sleep apnea) Coronary artery disease Legally Blind Cryptogenic organizing pneumonia Osteopenia of right hip History of cardiac arrest History of hyperkalemia Pancreatic insufficiency History of CVA in adulthood Major depression, recurrent, chronic Coronary artery disease of native artery of native heart with stable angina pectoris Chronic kidney disease due to type 1 diabetes mellitus Obesity AKI (acute kidney injury) Status post coronary artery stent placement Acquired hypothyroidism Hypertension associated with diabetes Diabetic autonomic neuropathy Edema Bilateral low back pain without sciatica, unspecified chronicity Ineffective esophageal motility Chronic diastolic congestive heart failure Iron deficiency Diabetic polyneuropathy associated with type 1 diabetes mellitus Primary insomnia Abnormal Pap smear of cervix Bilateral primary osteoarthritis of knee Stage 3b chronic kidney disease Family history of breast cancer Acute cystitis without hematuria Incomplete bladder emptying Dysphagia Constipation Lower obstructive uropathy Other fatigue GERD (gastroesophageal reflux disease) Cellulitis of left lower extremity Chronic nausea Abscess of left leg Eosinophilia Kidney stones Overactive bladder Urinary incontinence, unspecified type High-tone pelvic floor dysfunction Chronic pelvic pain in female Urinary urgency Urinary frequency Urge incontinence Pleural effusion Abnormal CT scan of lung Adhesive capsulitis of shoulder Anoxic encephalopathy Cardiac arrest Anxiety Chronic obstructive pulmonary disease Depressive disorder Glaucoma IBS (irritable bowel syndrome) Legal blindness Ischemic optic neuropathy Malignant neoplasm of uterus Memory impairment Migraine Pneumonia Steatorrhea Vitamin D deficiency Hyperlipidemia Restrictive lung disease Pulmonary hypertension Pathogenic Variant in BRCA2 (c.9253dup) Cat bite of index finger CHF (congestive heart failure) Chronic skin ulcer CVA (cerebral vascular accident) Hypoxic brain injury Osteoarthritis Pericarditis Port-A-Cath in place Anxiety and depression Osteopenia Elevated alkaline phosphatase level Venous insufficiency
Andere Medikamente: acetaminophen (TYLENOL) 500 mg tablet amLODIPine (NORVASC) 5 mg tablet aspirin 81 MG chewable tablet baclofen (LIORESAL) 5 MG tablet buPROPion (WELLBUTRIN XL) 150 mg 24 hr tablet busPIRone (BUSPAR) 30 MG tablet calcitriol (ROCALTROL) 0.25 M
Allergien: Ace InhibitorsUnknown, Other Contrast Media Ready-box Misc Diagnostic X-ray Materials ErythromycinRash ErythromycinUnknown Lipitor [Atorvastatin]Myalgia RosuvastatinMyalgia
Vorherige Impfungen: -

VAERS 2697078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: 86,0
Geschlecht: F
Eingang: 17.10.2023
Impfdatum: 11.01.2022
Beginn: 16.09.2023
Tage bis Beginn: 613,0
Dosis: 3
Route/Site: - / -

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

Abdominal pain upper Adult failure to thrive Angiogram pulmonary abnormal Asthenia Atelectasis COVID-19 Cast application Culture wound positive Dysphagia Electrocardiogram Fall Fatigue Forearm fracture Haemoglobin decreased Headache Impaired healing Infected dermal cyst Lung consolidation

Symptomtext

Patient is a 87 y.o. female patient of DO with history of left lower lobe squamous cell carcinoma, hypertension, hyperlipidemia presented to Hospital with covid and generalized weakness. Chronic respiratory failure Squamous cell lung cancer Baseline oxygen needs: Intermittently on 2 L NC- states sometimes she takes her O2 off and only requires it at night Currently: Requiring 2 L NC 100%, weaned down to 1L NC CTPA (9/16) no evidence of pulmonary embolism. Moderate and slightly decreased consolidation/atelectasis of left lower lobe. Filling defect in the distal aspect of the left mainstem bronchus measuring 1.5 cm could be due to mass or mucous plugging. Consolidation is up against left hilar region and additional central mass cannot be excluded. Stable 1.4 cm mass in the right medial lung base. Pulm consulted-continue remdesivir. Recommendation to hold off on steroids for now. We will give a week of antibiotics. Will need palliative radiation for the lesion. She is not a candidate for surgical resection. Doubt she will be a candidate for systemic therapy. Restrictive transfusion strategy for hemoglobin less than 7. Consider palliative care involvement. DDx COVID 19 infection +/- lung CA +/- postobstructive pneumonia Will initiate remdesivir Follow-up on procalcitonin- 0.1 Covid-19 Virus Infection Date of onset of symptoms: 9/15 Symptoms present on admission: headache and fatigue Date of covid positive test: 9/16/23 Vaccination status: vaccinated CTPA (9/16) no evidence of pulmonary embolism. Moderate and slightly decreased consolidation/atelectasis of left lower lobe. Filling defect in the distal aspect of the left mainstem bronchus measuring 1.5 cm could be due to mass or mucous plugging. Consolidation is up against left hilar region and additional central mass cannot be excluded. Stable 1.4 cm mass in the right medial lung base. Baseline oxygen needs: Intermittently on 2 L NC Currently: 2L NC Medical therapy: remdesivir Anticipated special isolation end date: TBD Epigastric pain EKG nonischemic Troponin flat at 14?15 Minimal improvement with Maalox. Denies any indigestion or nausea Describes as worsening with deep breath in. Toradol dose x1 and lidocaine patch ordered- improvement in sx Non-healing wound S/P infected sebaceous cyst Prior hx of wound: Seen by Dr. (surgery) on 7/31/23, recommended continued local wound care. Daughter reports continued drainage from the sebaceous chest area. Of note patient completed course of bactrim back in July for this She also completed course of doxycycline in august Wound care following Preliminary wound culture growing MRSA ID consulted-patient started on vanco, appreciate input Transitioned to p.o. doxycycline 9/3 Picture in H&P Consulted wound care-primary dressing Triad and secondary dressing with mepilex Recent Right Forearm Fracture after fall 7/11/23. Short cast exchanged with splint 8/22/23 per otho as Xrays with stable healing. Follow up with ortho Family concerned about wrist and requesting an ortho eval Repeat x-ray x-ray of the wrist on 9/02 ordered for an eval which showed interval placement of a stent at right wrist, no significant interval change in alignment/dorsal subluxation of the proximal carpals in relation to the distal radius Ortho was consulted and saw patient 9/3?she had a right distal radius fracture on 7/17 with no acute surgical intervention. Recommendation to maintain right wrist removable brace, WBAT right upper extremity and follow-up with Dr. as scheduled Adult failure to thrive Generalized weakness Decreased mobility secondary to multiple comorbidities Recently taking home by family from SNF Consult PT/OT/UM-PT and OT with AMPAC of 9. COVID SNF not able to accept will likely need to finish quarantine during hospitalization with SNF afterwards Dysphagia History of tonsillar cancer protein calorie malnutrition S/P radiation and chemotherapy 2017 Resuming as needed cellulitis. ? Follows with medical facility Patient was declining SLP eval last admission May need reassessment this admission- declined 9/18, Per patient she does not have her dentures with her and be amenable to trying a ground or pur?ed diet - doing well so far with ground diet Nutrition Anxiety and depression Resuming Cymbalta 30 mg daily Left renal lesion Noted on CTPA (8/2022) Daughter reports that this had been there a long time for her last discharge summary note Patient declined further evaluation per daughter

Weitere VAERSDATA-Felder

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

VAERS 2688906

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 29.09.2023
Impfdatum: 08.02.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Blood pressure measurement Brain fog Bronchospasm Condition aggravated Heart rate Heart rate irregular Increased need for sleep Magnetic resonance imaging Pulmonary function test Sleep apnoea syndrome

Symptomtext

her heart rate would go up and down from 160 to 140; sleep apnea since she would quit breathing; She could do things for 15 minutes and then would have to take a nap; diagnosed her with bronchospasms since she would wake up in the middle of the night not being able to breathe; Brain fog started with covid and became worse after she got the covid vaccines; Brain fog started with covid and became worse after she got the covid vaccines; This is a spontaneous report received from contactable reporter(s) (Nurse). The reporter is the patient. A 65-year-old female patient received bnt162b2 (BNT162B2), on 08Feb2022 as dose 3 (booster), single (Lot number: FJ6369) at the age of 64 years, in arm for covid-19 immunisation. The patient's relevant medical history included: "covid", start date: 03Nov2020 (unspecified if ongoing), notes: had a high fever at that time; "high blood pressure diagnosed a long time ago" (ongoing); "low thyroid diagnosed about ten years ago" (ongoing); "asthma" (unspecified if ongoing), notes: reports she had asthma in her twenties.; "brain fog" (ongoing). The patient took concomitant medications. Vaccination history included: bnt162b2 (DOSE 1, SINGLE, Lot: EL3248), administration date: 20Jan2021, when the patient was 63-year-old, for COVID-19 Immunization, reaction(s): "her heart rate would go up and down from 160 to 140", "sleep apnea since she would quit breathing", "She could do things for 15 minutes and then would have to take a nap", "Brain fog started with covid and became worse after she got the covid vaccines", "Brain fog started with covid and became worse after she got the covid vaccines", "diagnosed her with bronchospasms since she would wake up in the middle of the night not being able to breathe"; bnt162b2 (DOSE 2, SINGLE, Lot: EL3248), administration date: 10Feb2021, when the patient was 63-year-old, for COVID-19 Immunization, reaction(s): "her heart rate would go up and down from 160 to 140", "sleep apnea since she would quit breathing", "She could do things for 15 minutes and then would have to take a nap", "Brain fog started with covid and became worse after she got the covid vaccines", "Brain fog started with covid and became worse after she got the covid vaccines", "diagnosed her with bronchospasms since she would wake up in the middle of the night not being able to breathe". The following information was reported: The patient had the vaccine early on since she is a nurse. She had not got over the COVID infection she had (clarified to have occurred prior to COVID vaccines) since at that time they were not saying not to take the vaccine while sick, CDC was recommending now to not be sick with COVID before getting a COVID-19 vaccine. She has been sick for almost three years post-COVID. At the time of COVID infection, she had a high fever, she was bedridden and could not even get up to go to the bathroom, she did go to the bathroom but it was hard to get up, she has seen so many doctors. The patient reported that she really has bad brain fog. It started with COVID and became worse after she got the COVID vaccines and reports she became bedridden after the vaccines. When asked to clarify which dose she became bedridden after, states it got worse with each dose of the COVID vaccine. She was followed up by pulmonary, cardiology, sleep apnea since she would quit breathing, she cannot even think and she was put on hormones from gynecology hoping that it would help reset. Pulmonary doctor put her on steroid inhaler, rescue inhaler, and nebulizer. She was still experiencing brain fog and it was better. She also reported that she could do things for 15 minutes and then would have to take a nap. The patient mentioned that she had been on the same medications for a long time. The patient reported that cardiology changed her blood pressure medication and heart medication for a short period of time since her heart rate would go up and down from 160 to 140. Pulmonary did a lot of testing and diagnosed her with bronchospasms since she would wake up in the middle of the night not being able to breathe. Thinks most of the testing was hard to get to due to the COVID pandemic. She thinks that the MRI of her heart and pulmonary testing were done in Mar2021. Therapeutic measures were taken as a result of sleep apnoea syndrome. The outcome of event "brain fog started with COVID and became worse after she got the COVID vaccines" was recovering while the outcome of the remaining events was unknown.; Sender's Comments: Based on the available information in the case, an association between the reported events heart rate Irregular and The suspected drug cannot be ruled out. 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.,Linked Report(s) : US-PFIZER INC-202300312735 same patient/drug/event, different dose number;US-PFIZER INC-202300312483 same patient/drug/event, different dose number;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Name: blood pressure; Result Unstructured Data: Test Result:high; Comments: high blood pressure diagnosed a long time ago; Test Name: heart rate; Result Unstructured Data: Test Result:160; Test Name: heart rate; Result Unstructured Data: Test Result:140; Test Date: 202103; Test Name: MRI; Result Unstructured Data: Test Result:Unknown results; Comments: MRI of her heart and pulmonary testing was done she thinks in Mar2021; Test Date: 202103; Test Name: pulmonary testing; Result Unstructured Data: Test Result:diagnosed her with bronchospasms
Aktuelle Erkrankungen: Blood pressure high; Brain fog; Thyroid disorder
Vorgeschichte: Medical History/Concurrent Conditions: Asthma (reports she had asthma in her twenties.); COVID-19 (had a high fever at that time)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2667656

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: 46,0
Geschlecht: M
Eingang: 08.08.2023
Impfdatum: 09.02.2022
Beginn: 18.03.2022
Tage bis Beginn: 37,0
Dosis: 3
Route/Site: - / -

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

Hypotension

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE HYPOTENSION

Weitere VAERSDATA-Felder

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

VAERS 2659439

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: -
Geschlecht: M
Eingang: 21.07.2023
Impfdatum: 15.02.2022
Beginn: 15.05.2023
Tage bis Beginn: 454,0
Dosis: 3
Route/Site: - / -

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

Anticoagulant therapy Asthenia Atrial fibrillation Blood lactic acid COVID-19 Chemotherapy Chest X-ray normal Condition aggravated Dyspnoea Glycosylated haemoglobin normal Lactic acidosis Lymphoma SARS-CoV-2 test positive Sepsis Thrombocytopenia

Symptomtext

Patient is a 68 y.o. male patient of DO with history of afib, lymphoma presented to Medical Center with generalized weakness, found to have sepsis 2/2 COVID and afib with RVR. Sepsis - resolved Covid-19 Virus Infection Date of onset of symptoms: 5/13/23 Symptoms present on admission: weakness, dyspnea Date of covid positive test: 05/15/23 Vaccination status: vaccinated Imaging: CXR nonacute Oxygen requirements on admission: none Current oxygen requirements: 2LNC Pulm/CC consulted ID consulted, plan for 3 days of Remdesivir, cannot get paxlovid due to interactions with Xarelto. Afib with RVR - resolved HR 140s on presentation Transitioned off of Cardizem gtt Resume home Xarelt Resume home Xarelto, Toprol, ASA Cardiology consulted, have signed off Currently on oral metoprolol Rate controlled. DM2 Holding home metformin, glipizide A1c 6.4 in 3/2023, below goal for age Can likely DC glipizide on discharge and just continue metformin Afib with RVR - resolved HR 140s on presentation Transitioned off of Cardizem gtt Resume home Xarelto, Toprol, ASA Cardiology consulted, have signed off Currently on oral metoprolol Rate controlled. DM2 Holding home metformin, glipizide A1c 6.4 in 3/2023, below goal for age Can likely DC glipizide on discharge and just continue metformin Lymphoma Thrombocytopenia Next chemo due 5/16 Continue home Bactrim and acyclovir for infection ppx Consult oncology, follows with Dr - no further workup or therapy until after COVID. HTN Home lisinopril, metoprolol BP low normal May be able to DC lisinopril on discharge Lactic acidosis, POA. 3.6 on admission Trended down to 2.0

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2215841

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MI
Alter: 47,0
Geschlecht: F
Eingang: 08.05.2023
Impfdatum: 21.02.2022
Beginn: 27.02.2023
Tage bis Beginn: 371,0
Dosis: 1
Route/Site: - / -

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

Chills Nausea Pyrexia Vomiting COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

02/27/23 presents to ED for "shortness of breath". PMHx of "HIV, type 2 diabetes"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 02/27/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2215841

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MI
Alter: 47,0
Geschlecht: F
Eingang: 08.05.2023
Impfdatum: 21.02.2022
Beginn: 27.02.2023
Tage bis Beginn: 371,0
Dosis: 2
Route/Site: - / -

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

Chills Nausea Pyrexia Vomiting COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

02/27/23 presents to ED for "shortness of breath". PMHx of "HIV, type 2 diabetes"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 02/27/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2215841

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MI
Alter: 47,0
Geschlecht: F
Eingang: 08.05.2023
Impfdatum: 21.02.2022
Beginn: 27.02.2023
Tage bis Beginn: 371,0
Dosis: 2
Route/Site: UN / UN

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

Chills Nausea Pyrexia Vomiting COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

02/27/23 presents to ED for "shortness of breath". PMHx of "HIV, type 2 diabetes"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 02/27/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2615352

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NY
Alter: 82,0
Geschlecht: M
Eingang: 14.04.2023
Impfdatum: 05.04.2022
Beginn: 05.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Expired product administered Feeling abnormal Malaise Mobility decreased Oxygen saturation decreased SARS-CoV-2 test positive

Symptomtext

After receiving my fourth dose in April of 2022, I was contacted by my pharmacist to inform me that the vaccine was expired and had been stored at the improper temperature and may be less effective than it should have been. On 09/28/2022, I felt poorly. I drove to a neighboring town and was tested for COVID-19 and was positive. I had a temperature of just over 100 degrees. My symptoms were fairly conventional. I did not lose my sense of taste or smell but felt really quite sick for a few days. I measured my oxygen level, and it was down to around 90. I called my doctor who informed me to go to the emergency room if it went below 90. The next four or five days it ranged from 90-96. I was prescribed PAXLOVID, and I would say it was around 6 days before I was able to get up and around.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 28SEP2022 COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: Microscopic Colitis; BPH; Acid Reflux
Andere Medikamente: Lisinopril; omeprazole; tamsulosin; vitamin D; PEPTO BISMOL; DENTAGEL; PRESERVISION
Allergien: BACTRIM
Vorherige Impfungen: -

VAERS 2614589

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MI
Alter: 82,0
Geschlecht: F
Eingang: 13.04.2023
Impfdatum: 17.07.2022
Beginn: 04.04.2023
Tage bis Beginn: 261,0
Dosis: 2
Route/Site: - / -

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

COVID-19 pneumonia Chronic respiratory failure Condition aggravated Cystitis Interstitial lung disease Malaise Metabolic encephalopathy Renal impairment Respiratory failure SARS-CoV-2 test positive

Symptomtext

Discharge Provider: DO Primary Care Provider at Discharge: DO Admission Date: 4/4/2023 Discharge Date: 04/09/2023 Discharge disposition: SAR Condition on discharge: Stable ADMISSION AND DISCHARGE DIAGNOSES: HOSPITAL COURSE: COVID-19 pneumonia. Improving Chronic Respiratory Failure with Hypoxia and Hypercapnia due to ILD - Per facility, pt tested positive 3/29 and has had symptoms about 7 days - Treated with IV Decadron and IV abx for possible aspiration while inpatient - Switch to oral Augmenting and Decadron on DC - On 2L baseline - Supportive care - Eliquis for VTE prophylaxis Not a candidate for Remdesivir due to renal function Acute Cystitis without Hematuria/urinary incontinence/lethargy -Treated Acute Metabolic Encephalopathy due to above. Resolved Chronic Combined Congestive Heart Failure NICM CAD s/p CABG Hypertension Pulmonary Hypertension Persistent A-fib/A-flutter s/p MAZE History of DV/PE and LV thrombus -Pt has a CardioMEMS, follows with WM Cardiology -Continue Toprol XL, Aldactone, Demadex, Metolazone, Eliquis and Lipitor OAB -Can resume Ditropan Morbid obesity OSA -Pt does not wear a nightly Cpap -Chronically wears 2 L O2 per NC due to ILD (thought to be caused by Amiodarone use) DC to SAR

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: 7/5/2022 - 7/17/2022 (12 days) Hospital PRESENTING PROBLEM: Severe sepsis Typical atrial flutter Shock Cardiogenic shock
Vorgeschichte: Dysphagia CAD (coronary artery disease) Ischemic cardiomyopathy OSA (obstructive sleep apnea) Morbid obesity Chylothorax on left Essential hypertension Abnormal chest CT Chronic respiratory failure with hypoxia Pulmonary HTN CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min CHF (congestive heart failure) Acute on chronic combined systolic and diastolic heart failure Persistant a-fib/flutter with RVR Acute pulmonary embolism Acute deep vein thrombosis (DVT) of popliteal vein of left lower extremity Acute thrombus of left ventricle Acute on chronic combined systolic and diastolic CHF (congestive heart failure) Counseling regarding advance care planning and goals of care COVID-19 Pneumonia due to COVID-19 virus A-fib
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet aluminum, magnesium & simethicone (MAALOX EX) 400-400-40 MG/5ML apixaban (ELIQUIS) 2.5 MG tablet atorvastatin (LIPITOR) 20 MG tablet dexAMETHasone (DECADRON) 6 mg tablet diclofenac sodium 1 % gel docusa
Allergien: Cytotec [Misoprostol]Shortness of Breath, Swelling Shellfish AllergyHives Entresto [Sacubitril-valsartan]Dizziness
Vorherige Impfungen: -

VAERS 2593832

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: IL
Alter: 43,0
Geschlecht: F
Eingang: 09.03.2023
Impfdatum: 08.03.2022
Beginn: 02.03.2023
Tage bis Beginn: 359,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Chills Cough Dyspnoea Headache Lymphadenopathy Oropharyngeal pain Pain Respiratory tract congestion SARS-CoV-2 test positive Streptococcus test negative

Symptomtext

I had a sore throat with chills. I also had body aches as well as congestion and headache. I treated it with liquids and the diabetic Tussin. I completed a home COVID-19, and it was Positive. I contacted my doctor to get Paxlovid but was not given a prescription. I used Zinc, Vitamin D & C as well as probiotics to treat. I still have a cough and still get short of breath when speaking to much, but I began to feel better on Wednesday. On Tuesday I went to urgent care because my throat was still sore. I was tested for strep and it was negative. I also developed swollen lymph nodes under my left arm which lasted about a week. I did not see a doctor for this.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 March 02, 2023-Positive Strep Test-March 07, 2023-Negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; Diabetes
Andere Medikamente: Womens Probiotic; Zinc; Vitamin C; Diabetic Tussin
Allergien: N/A
Vorherige Impfungen: COVID-19 Dose 1 & 2 Moderna & Dose 3 Pfizer swollen lymph nodes-Age 42 with dose 1 and 2 and 43 with 3rd dose

VAERS 2583531

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FJ6369

moderat

Staat: MI
Alter: 70,0
Geschlecht: F
Eingang: 17.02.2023
Impfdatum: 21.07.2022
Beginn: 13.02.2023
Tage bis Beginn: 207,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Asthenia Blood creatinine increased Blood magnesium decreased Blood phosphorus decreased Blood potassium decreased Blood sodium decreased COVID-19 Cardiac function test normal Cardiomegaly Chest X-ray abnormal Chills Decreased appetite Dizziness Dyspnoea Fluid intake reduced Hypokalaemia Hypoxia

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 2/13/2023 Discharge Date: 02/14/2023 Admitting Diagnoses: Hypokalemia PRESENTING PROBLEM: Hypokalemia Hypoxia COVID HOSPITAL COURSE: 70-year-old lady with medical history of coronary artery disease status post CABG, chronic obstructive pulmonary disease, bipolar 1 disorder, ischemic cardiomyopathy, gastric ulcer, chronic opioid dependence, paroxysmal AFib on Xarelto presented to ER 2/13 with flu-like symptoms. According to patient, she started experiencing generalized body weakness/body aches, dizziness, dry heaves, shortness of breath, cough occasionally productive of yellowish-green sputum about 4 days prior to presentation. No fevers but she endorsed chills at home. Patient endorsed poor appetite, low water intake at home. Her symptoms worsened and she presented to ER 2/13. On presentation vital signs stable. Labs with sodium 132, potassium 2.5, creatinine 1.45. Cardiac workup negative, pro BNP normal and troponin 27> 22. Patient tested positive for COVID-19. Chest x-ray showed cardiomegaly but no acute cardiopulmonary process. No consolidation. Patient was given potassium supplements (30 mEq). She had slight desaturation with ambulation (88% on room air). Patient has home oxygen but uses it as needed. When she started noticing difficulty breathing, she will use 2.5 L. Due to COVID infection, AKI, severe hypokalemia she was admitted for further management. Started on dexamethasone 6 mg for COVID 19 infection. Patient was given potassium supplements, serum potassium improved. Was given 1 L IV fluid bolus, renal functions also improved. Serum magnesium low, replaced with IV magnesium sulfate. Patient also found to have low phosphate (1.5), started daily phosphate tablets. 2/14: Patient feeling significantly better. No body aches or chills. No nausea or vomiting. Normal appetite. No difficulty breathing. No phlegm, very minimal cough. No fevers. Supplemental oxygen weaned off. Patient would like to go home today. Labs showed resolution of AKI (serum creatinine 0.95), improvement in potassium (3.4). Patient informed to get magnesium, phosphorus, BMP checked next week. Will be discharged with dexamethasone course.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: 7/11/2022 - 7/22/2022 (11 days) Heart Failure
Vorgeschichte: COPD (chronic obstructive pulmonary disease) (HCC) DDD (degenerative disc disease), lumbar Bipolar 1 disorder (HCC) GERD (gastroesophageal reflux disease) S/P CABG x 3 TBI (traumatic brain injury) Osteoarthritis of hip Recurrent UTI Perforated gastric ulcer (HCC)- History of this, s/p repair Carotid disease, bilateral (HCC) PVD (peripheral vascular disease) (HCC) RLS (restless legs syndrome) Subarachnoid hemorrhage, traumatic S/P IVC filter Vertebral compression fracture (HCC) Aortic ectasia, abdominal (HCC) Colitis Oropharyngeal dysphagia Generalized abdominal pain Chronic pain disorder Neurogenic bladder Subclavian artery stenosis, left (HCC) Chronic occlusion of right subclavian vein (HCC) Alkaline phosphatase elevation Ischemic cardiomyopathy Primary insomnia Narcotic dependence (HCC) Age-related osteoporosis without current pathological fracture Coronary artery disease involving coronary bypass graft of native heart without angina pectoris Ventricular tachycardia Prolonged Q-T interval on ECG Dyslipidemia Paroxysmal atrial fibrillation (HCC) Chronic combined systolic and diastolic congestive heart failure (HCC) ICD (implantable cardioverter-defibrillator) in place History of stroke Presence of left atrial appendage closure device Thrombus of atrial appendage History of acetaminophen overdose Ulcerative esophagitis Closed fracture of right inferior pubic ramus with routine healing, subsequent encounter Shingles Retention of urine COVID-19
Andere Medikamente: albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amiodarone (PACERONE) 200 MG tablet apixaban (ELIQUIS) 5 MG tablet aspirin 81 MG enteric coated ta
Allergien: Bee VenomSwelling DoxycyclineHives, Itching Lyrica [Pregabalin]Hallucinations Adhesive Bandages MiscHives LatexRash NsaidsOther Sulfa DrugsHives Diflucan [Fluconazole] Zofran [Ondansetron] TapeOther
Vorherige Impfungen: -

VAERS 2580324

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj6369

moderat

Staat: IL
Alter: 37,0
Geschlecht: F
Eingang: 13.02.2023
Impfdatum: 01.01.2022
Beginn: 01.04.2022
Tage bis Beginn: 90,0
Dosis: 2
Route/Site: - / LA

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

Blood pressure increased Blood test Bone pain Exposure during pregnancy Induced labour Inflammation Magnetic resonance imaging Migraine Pain X-ray

Symptomtext

Received vaccination on last dose 01/29/2022, baby was born at 5lbs 5oz. My blood pressure rose after getting the vaccine, causing me to have to be induced. After the vaccine I have had sever migraines/headaches, and inflammation. I have no history of high blood pressure or migraines or inflammation. I am still experiencing high blood pressure, migraines, and inflammation(achy bones and organs) all of which I need medication for.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Multiple blood tests X rays 10/21/2022 Er visit 12/01/2022 Most recent blood test 01/12/2023 MRI 12/07/2022
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Prenatal vitamins
Allergien: -
Vorherige Impfungen: -

VAERS 2579967

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: DC
Alter: 42,0
Geschlecht: F
Eingang: 10.02.2023
Impfdatum: 12.02.2022
Beginn: 12.02.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

C-reactive protein increased Chest pain Decreased appetite Fatigue Headache Myalgia Nausea Pain

Symptomtext

Fatigue & Muscle Aches all over body developed later in day on 2/12/22. Bad headache, lots of body aches and pains (especially legs, neck, head, shoulders, and abdomen), nausea, loss of appetite throughout 2/13/22 Fatigue and body aches on 2/14/22 Continued fatigue, body aches, some chest pain on 2/15/22 In the six months following, I experienced increased chest pain that was undiagnosed. I had experienced chest discomfort prior as a Long Covid issue but it had simnifically lessened before this booster vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: HsCRP test: abnormally high in July 2022 (was normal in December 2021)
Aktuelle Erkrankungen: None.
Vorgeschichte: Presumed Long Covid since 2020, however, I was mostly doing better at time of vaccination.
Andere Medikamente: None
Allergien: None known.
Vorherige Impfungen: Covid-19 Johnson & Johnson Vaccine on 4/10/21

VAERS 2576388

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 04.03.2022
Beginn: 04.01.2023
Tage bis Beginn: 306,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

01/04/23 presents to ED for "shortness of breath". PMHx of "Sjogren's disease"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 01/04/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2566839

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MI
Alter: 60,0
Geschlecht: M
Eingang: 24.01.2023
Impfdatum: 03.03.2022
Beginn: 26.12.2022
Tage bis Beginn: 298,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

12/26/22 presents to ED for "SOB". PMHx of "invasive squamous cell carcinoma, ESRD on HD MWF, DVT, Hepatitis C, CAD s/p cath, lung nodules, depression/anxiety, hypothyroidism, paroxysmal Afib on amiodorone"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/26/22 SARS-CoV-2 (COVID-19) detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2562199

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: 78,0
Geschlecht: F
Eingang: 18.01.2023
Impfdatum: 19.03.2022
Beginn: 23.12.2022
Tage bis Beginn: 279,0
Dosis: 3
Route/Site: - / -

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

Blood creatinine normal COVID-19 Computerised tomogram abdomen abnormal Dehydration Diarrhoea Electrocardiogram QT prolonged Enteritis Glycosylated haemoglobin normal Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

Patient is a 79 y.o. female patient of PRIVATE MD with history of anemia, CAD S/P CABG, CHF, CKD, GERD, HLD, HTN, multiple myeloma, large B-cell lymphoma, renal cell carcinoma S/P right partial nephrectomy, mitral regurgitation S/P MVR, and thrombocytopenia presented with nausea vomiting Covid-19 Virus Infection Intractable nausea vomiting Date of onset of symptoms: 12/22/2022 Symptoms present on admission: Nausea vomiting and diarrhea Date of covid positive test: 12/23/2022 Vaccination status: vaccinated Imaging: CT abdomen and pelvis showed enteritis Oxygen requirements on admission: Room air Current oxygen requirements: Room air Medical therapy: not indicated Consultants following: None Anticipated special isolation end date: 12/27/2022 Antiemetics Gentle IV hydration Clear liquids advance as tolerated Nausea and vomiting 2/2 enteritis: Resolved CT scan abdomen showed patient having enteritis Patient nausea vomiting and diarrhea have resolved. Patient is doing well. Patient was to be discharged home and will be discharged with advised to follow-up with PCP. CAD Chronic congestive heart failure Continue home medications Type 2 diabetes on long-term insulin use Continue NPH 70/30, Continue insulin sliding scale Last A1c 8.5 Multiple myeloma History of RCC non-Hodgkin lymphoma Stable CKD-IIIb Creatinine at baseline Monitor renal function and electrolytes IVF to correct dehydration QT prolongation Avoid QT prolonging medications

Weitere VAERSDATA-Felder

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

VAERS 2546970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 77,0
Geschlecht: M
Eingang: 30.12.2022
Impfdatum: 03.02.2021
Beginn: 17.12.2022
Tage bis Beginn: 682,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Culture urine positive Enterococcus test positive Fall Mobility decreased Urinary tract infection White blood cell count abnormal

Symptomtext

Hospital Course and Significant Findings: Patient is a 79 year old male with a history of dementia, NPH who lives alone with part time caregiver who presented with fall and inability to get up. Daughter called emergency number. In the ER patient found to have UTI and COVID. For his UTI he was treated with cipro with improvement in WBC and no fever. Urine culture grew Enterococcus. In terms of his COVID, he was not hypoxic so received no decadron. He did receive Remdesivir while in the hospital. He will go home on COVID isolation through 12/26/22.

Weitere VAERSDATA-Felder

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

VAERS 2540568

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MI
Alter: 58,0
Geschlecht: F
Eingang: 22.12.2022
Impfdatum: 22.06.2022
Beginn: 16.12.2022
Tage bis Beginn: 177,0
Dosis: 3
Route/Site: IM / LA

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

Blood sodium decreased Bundle branch block right COVID-19 Chest X-ray Cough Dyspnoea Electrocardiogram abnormal Nausea Oral herpes SARS-CoV-2 test positive Sinus arrhythmia Suicidal ideation Tachypnoea Troponin normal Urine analysis normal

Symptomtext

PRESENTING PROBLEM: Pulmonary aspergillosis Anemia, unspecified type Chronic pulmonary aspergillosis COVID-19 HOSPITAL COURSE: 58 y.o. female with past medical history significant for severe chronic obstructive pulmonary disease, history of recurrent pneumothorax, history of pulmonary embolism, hypertension, chronic pulmonary aspergillosis, recent MRSA pneumonia, anemia who presented emergency department complaints of worsening shortness of breath and cough. Upon arrival to emergency department, patient was tachypneic other vitals were stable. Baseline blood work was obtained and independently reviewed. Blood work was remarkable for sodium 131, stable chronic thrombocytosis and chronic anemia. Troponin WNL. Viral PCR was positive for COVID-19. UA was negative for acute infection. EKG was obtained showing normal sinus rhythm with sinus arrhythmia and incomplete RBBB. CXR showing extensive chronic findings which are not substantially changes from 11/20. No new focal consolidations. Patient was given a dose of her antifungal and a dose of Zofran for nausea. Patient was then admitted for further evaluation and management. Patient stayed in hospital for approximately 3 days. During stay patient has been monitored and had remained to be in room air throughout stay. Infectious Disease consulted and evaluated patient during the 1st 24 hours of stay. Her voriconazole resumed with course to be determined. A prescription has been sent to her pharmacy. She is to follow-up with them in 3-4 weeks. Plan to have a repeat voriconazole level in 1 week. Patient was also given medication for her herpes labialis with valacyclovir. Also patient has been evaluated by LMSW for initially made suicidal comments on admission. Patient better main to be not at risk for suicide and that she was given resources for support in the community. Patient was discharged home stable on 12/19/2022 when medications are ensured available at her pharmacy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Respiratory COPD, severe History of recurrent pneumothorax Tracheomalacia Community acquired pneumonia, bilateral Cavitary pneumonia MRSA pneumonia Chronic pulmonary aspergillosis Circulatory Essential hypertension, benign Pulmonary embolus Digestive Unspecified severe protein-calorie malnutrition Infectious/Inflammatory COVID-19 Hematologic Leukocytosis Thrombocytosis Anemia Nervous Pain Endocrine/Metabolic Hypomagnesemia Other Tobacco abuse Alcohol use disorder, moderate, in early remission History of suicide attempt Multiple comorbid conditions Goals of care, counseling/discussion Anxiety and depression Insomnia Diarrhea History of pneumothorax
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler apixaban (ELIQUIS) 5 MG tablet benzonatate (TESSALON) 200 MG capsule budesonide/formoterol (SYMBICORT) 80-4.5 MCG/AC
Allergien: Penicillins Strawberries
Vorherige Impfungen: -

VAERS 2525193

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 23.02.2021
Beginn: 24.09.2022
Tage bis Beginn: 578,0
Dosis: 3
Route/Site: IM / -

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

Acute kidney injury Asthenia COVID-19 COVID-19 pneumonia Cough Dyspnoea Faeces discoloured SARS-CoV-2 test positive

Symptomtext

Narrative: Patient received three COVID 19 Vaccine in Feb/Mar 2021 and Feb 2022. The patient tested positive for COVID 19 on 24 Sep 2022. The patient presented to the ED with generalized weakness, cough, sob with any activity, and black stool. The patient was admitted to the hospital with covid pneumonia and acute kidney injury. The patient was treated with oxygen and antibiotics. The patient was discharged on a 27 Sep 2022 in stable condition. Reported per EUA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2499356

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CT
Alter: 47,0
Geschlecht: F
Eingang: 04.11.2022
Impfdatum: 18.08.2021
Beginn: 25.08.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / -

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

Ageusia Angiogram Anosmia COVID-19 Chest pain Dyspnoea Electrocardiogram Impaired quality of life Laboratory test Palpitations

Symptomtext

I am a registered nurse and I was mandated to take the covid vaccine. After i took the 1st dose, one week later i ended up in the ER at a local medical center for palpitations and chest pain and SOB. After the second dose i had similar symptoms and i was the in the hospital. After getting the booster, i had chest pain and palpitations and i was hospitalized. I was diagnosed with covid19 in December 2021, I loss my sense of smell and taste. It took me 6 months to get my taste buds back and it is going to be one year in December and i have not yet regained my sense of smell. I would like to know the rationale behind it. I am a professional and this has a negative impact in my life.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: EKG and angiogram were done among other things.
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: I take multiple vitamins
Allergien: NKA
Vorherige Impfungen: -

VAERS 2474215

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MI
Alter: 76,0
Geschlecht: F
Eingang: 10.10.2022
Impfdatum: 27.02.2022
Beginn: 27.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Lip swelling Oral discomfort Paraesthesia Paraesthesia oral

Symptomtext

Patient states that when she was on her way home from the store her lips started to tingle and when she got home they started burning and swelled up and the tingling went into her cheek. She said she was going to give herself her an Epipen that she keeps for allergic reactions to other medications but by the time she was going to give it to herself the swelling and tingling were completely gone. She told her doctor about it who told her not to get any more Covid vaccinations due to the reaction. She didn't alert the pharmacy of the reaction until 8 months later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: anxiety, allergies
Andere Medikamente: Xanax 1mg tab, Plavix 75mg tab, Epipen 0.3mg
Allergien: hydantoins, Valproic acid, aspirin, morphine, penicillin
Vorherige Impfungen: -

VAERS 2453674

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MI
Alter: 85,0
Geschlecht: F
Eingang: 21.09.2022
Impfdatum: 10.02.2022
Beginn: 19.09.2022
Tage bis Beginn: 221,0
Dosis: 3
Route/Site: - / -

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

Blood sodium decreased COVID-19 Chest X-ray normal Cough Diarrhoea Fatigue Fluid intake restriction Hyponatraemia Hypophagia Laboratory test abnormal Nausea Oropharyngeal pain Orthostatic hypotension SARS-CoV-2 test positive Vomiting

Symptomtext

Discharge Provider: MD Primary Care Provider at Discharge: MD Admission Date: 9/19/2022 Discharge Date: 9/21/2022 PRESENTING PROBLEM: Acute hyponatremia [E87.1] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 85-year-old female with a history paroxysmal atrial fibrillation, CKD stage 3, depression, who was admitted on 9/19 with significant fatigue, nausea, vomiting and diarrhea. Patient began to have symptoms of sore throat and cough beginning on Thursday 9/15. Patient was noted to be fully vaccinated, but over due for booster. In addition to sore throat and coughing, the patient began to have significant diarrhea, with decreased oral intake. At the time of presentation she was noted to be positive for COVID, but stable on room air. Chest x-ray was negative for acute cardiopulmonary process. Laboratory studies showed acute hyponatremia with sodium of 122. Patient was also noted to have orthostatic hypotension. Patient was admitted for further treatment of her acute hyponatremia, as well as COVID infection. The patient was stable on room air, and was not a candidate for remdesivir or dexamethasone. Patient was treated with supportive care. With regards to the patient's hyponatremia, she did receive 2 L saline in the emergency department, and was subsequently treated with fluid restriction, with her sodium rising to 131. The patient's orthostatic hypotension did resolve with hydration. Initially Cardizem was held, however this was restarted, with stable vital signs. With supportive care, and improvement in her hyponatremia the patient had significant improvement in her symptoms. As patient was clinically stable she was discharged to home on 09/21/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Orthostatic hypotension
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: B12 deficiency Hyperlipidemia Age-related osteoporosis without current pathological fracture Essential hypertension Paroxysmal atrial fibrillation (HCC
Andere Medikamente: apixaban (ELIQUIS) 5 MG tablet Ascorbic Acid (VITAMIN C) 1000 MG tablet benzonatate (TESSALON) 200 MG capsule Cholecalciferol (VITAMIN D3) 2000 UNITS TABS citalopram (CELEXA) 20 MG tablet dilTIAZem (CARDIZEM CD) 120 MG 24 hr capsule guaiFEN
Allergien: Ace Inhibitors Codeine Keflex [Cephalexin]Other Lipitor [Atorvastatin] Micardis Hct [Telmisartan-hctz] Morphine
Vorherige Impfungen: -

VAERS 2433867

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: GA
Alter: 73,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 09.03.2022
Beginn: 04.08.2022
Tage bis Beginn: 148,0
Dosis: 4
Route/Site: SYR / UN

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

COVID-19 Pneumonia bacterial Pyrexia

Symptomtext

Covid Mild Fever 101.0

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia bacterial
Hospital-Tage: -
Labordaten: Bacterial Lung infection Diagnosed 8-4-2022
Aktuelle Erkrankungen: -
Vorgeschichte: Bronchiectasis Osteoporosis Spinal Stenosis Rheumatoid Arthritis
Andere Medikamente: Methotrexate Prednisone Sulfasalazine Synthroid Omeprazole Plaqienil Folic Acid Sodium Chloride Solution Albuterol Sulfate Solution Metoprool ER Rosavastatin Estradiol Vitamin D Citracal Raw Zinc Vitamin C
Allergien: none
Vorherige Impfungen: -

VAERS 2420924

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: PA
Alter: 34,0
Geschlecht: F
Eingang: 26.08.2022
Impfdatum: 11.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Angiogram Electrocardiogram Heart rate increased Hypersensitivity Injection site erythema Injection site swelling Muscle spasms No reaction on previous exposure to drug Paraesthesia Rash Sinus tachycardia Swelling face Ultrasound Doppler

Symptomtext

REACTION TO BOOSTER no issues with first 2 vaccines. Had covid first week of december. 4 weeks later was told to get booster. Redness/swelling at injection site hours after vaccine Delayed allergic response 24 hours later ER visit for allergic response. Elevated HR, Rash face,chest, and arms, leg spasms, tingling in both left and right legs,face puffy, sinus tachcardyia Issues still not resolved coming out of ER ER Visit multiple times after For reaction not being resolved Eventually seen by allergist who starts anthistimaine medication round the clock

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Jan 12, 2022 at 5:45 pm Electrocardiogram Jan 15, 2022 at 6:17 pm Chest CTA Jan 15, 2022 at 4:15 pm Venous Duplex
Aktuelle Erkrankungen: post Covid had Covid first week of December
Vorgeschichte: None
Andere Medikamente: none
Allergien: bee sting*
Vorherige Impfungen: -

VAERS 2419337

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MI
Alter: 25,0
Geschlecht: M
Eingang: 24.08.2022
Impfdatum: 20.01.2022
Beginn: 15.08.2022
Tage bis Beginn: 207,0
Dosis: 3
Route/Site: - / -

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

Angiogram pulmonary normal Asthenia COVID-19 Cough Decreased appetite Dyspnoea Exercise tolerance decreased Exposure to SARS-CoV-2 Hypertension Loss of personal independence in daily activities Mobility decreased SARS-CoV-2 test positive Tachycardia Wheelchair user

Symptomtext

Admission Date: 8/15/2022 Discharge Date: Aug 24, 2022 PRESENTING PROBLEM: Weakness SOB (shortness of breath) COVID HOSPITAL COURSE: Patient is a 26 y.o. male with history of muscular dystrophy, hypertension and anxiety who presents to the ER with generalized weakness due to COVID 19 infection. Patient did not have any respiratory issues. He did not require any oxygen therapy. He was not started on remdesivir or Decadron. However, patient continued to have weakness during his stay related to this infection. Physical therapy recommended inpatient rehab. PMNR was consulted and he was accepted. Patient was discharged in medically stable condition. Patient is a 26 y.o. male, right handed, with past medical history of congenital myopathy (SMA/distal myopathy) followed by SH neurology and hypertension who presented initially to the ED with chief complaint of generalized weakness. Patient with positive home COVID test. Patient does have history of full vaccination booster with visor COVID vaccine. Patient apparently developed dry cough, shortness of breath, increased weakness with poor appetite. He had been exposed family members over the weekend that did test positive for COVID-19. Patient was noted to be tachycardic and hypertensive in the emergency department. O2 sats stable. CT angiogram thorax negative for pulmonary embolism. Was not given dexamethasone around the severe due to no hypoxia. Patient was evaluated by Rehabilitation deemed a good candidate for acute inpatient rehabilitation. Patient was admitted to in patient rehab unit on 08/20/2022 where following medical issues addressed as noted below: Patient seen on day of admission. Patient seen in no apparent stress sitting up in wheelchair. Denies any pain currently. Denies any fevers, chills, nausea, vomiting, headache, chest pain, shortness of breath, difficulty spelling, abdominal pain, dysuria, paresthesias, depression. Patient does report he is weaker than his at baseline. Last bowel was yesterday. Lives alone in a 1st floor apartment with 0 steps to enter. Uses a power wheelchair at baseline. Patient does not drive but had been modified independent to independent for ADLs. Functional and mobility deficits due to COVID 19, with hx of Spinal muscular atrophy This patient is noted with decreased independence with transfers, ambulation, ADLs, IADLs, decreased endurance. We will continue PT and OT to evaluate and treat regarding these deficits. They will continue 3 hours per day, 5 days per week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Spinal muscular atrophy (HCC) Neuromuscular scoliosis Seasonal allergies Essential hypertension Generalized anxiety disorder Insomnia, unspecified type Mild persistent asthma without complication Allergic rhinitis due to dust mite, tree pollen, grass pollen, weed pollen Moderate episode of recurrent major depressive disorder (HCC) Chronic nonintractable headache, unspecified headache type Atypical chest pain Renal colic COVID-19 virus infection
Andere Medikamente: albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization cetirizine (ZYRTEC) 10 MG tablet fluticasone (FLONASE) 50 MCG/ACT nasal spray guaiFENesin (MUCINEX) 600 MG 12 hr tablet guaiFENesin (MUCINEX) 600 MG 12 hr tablet losartan (COZAAR) 50 MG
Allergien: Keflet [Cephalexin]Other
Vorherige Impfungen: -

VAERS 2416974

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: KS
Alter: 50,0
Geschlecht: M
Eingang: 22.08.2022
Impfdatum: 18.03.2022
Beginn: 19.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Joint range of motion decreased Limb injury Muscle tightness Musculoskeletal stiffness Paraesthesia

Symptomtext

Systemic: Joint Pain-Mild, Error: Shoulder Joint Injury (prolonged pain, tingling, etc.). Additional details: Patient's wife reported his shoulder is stiff/muscles tight. Denied pain but unable to move above 90 degrees.

Weitere VAERSDATA-Felder

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

VAERS 2416346

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NY
Alter: 27,0
Geschlecht: F
Eingang: 19.08.2022
Impfdatum: 11.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: IM / RA

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

Abortion spontaneous Condition aggravated Dry skin Echocardiogram Electrocardiogram Exposure during pregnancy Eye swelling Human chorionic gonadotropin Lip swelling Pharyngeal swelling Skin exfoliation Supraventricular tachycardia Swelling face Ultrasound pelvis Uterine dilation and curettage

Symptomtext

The morning following my second vaccine, I woke up with my face, eyes, lips and throat completely swollen. One week later my heart condition (SVT) became uncontrollable/more severe. My skin on my face became extremely dry and peeling for weeks. I was pregnant and had a miscarriage one month later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: HCG quantitative & progesterone to confirm miscarriage: 2/15/2022; 2/17/2022; 2/21/2022; pelvic ultrasound: 3/1/2022; surgical D&C: 3/9/2022; echocardiogram and EKG: 3/15/2022.
Aktuelle Erkrankungen: Covid-19 2 weeks prior
Vorgeschichte: Asthma, SVTs
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397985

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: FL
Alter: 63,0
Geschlecht: M
Eingang: 01.08.2022
Impfdatum: 28.01.2022
Beginn: 01.05.2022
Tage bis Beginn: 93,0
Dosis: 4
Route/Site: IM / RA

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

Blood test normal Bundle branch block right Cardiac monitoring Electrocardiogram abnormal Palpitations

Symptomtext

In the mornings I have my protein shake and without physical activity I noticed I was having heart palpitations, like the butterflies and intermittent and fairly consistent. I went to Urgent Care and they took some reads and saw what was going on. I have Complete Right Branch Bundle Block that is benign. They didn't have enough/right equipment and sent me to ER. They observed me for 2-3 hours and they saw what was going on. They released me and recommended I follow up with cardiologist. I saw the cardiologist and he did another EKG. He put me on a monitor for one week and I turned it in this morning. I will get the results on the 31st.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Heart monitor; unknown; EKG, abnormal; Blood Panel, normal
Aktuelle Erkrankungen: N/A
Vorgeschichte: Kidney Transplant Patient
Andere Medikamente: Prograf; Levothyroxine; Zortress; Cialis; Magnesium Chloride; Multi Vitamin
Allergien: Iodine contrast dye
Vorherige Impfungen: -

VAERS 2397919

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

moderat

Staat: VA
Alter: 15,0
Geschlecht: M
Eingang: 01.08.2022
Impfdatum: 22.01.2022
Beginn: 07.02.2022
Tage bis Beginn: 16,0
Dosis: 3
Route/Site: SYR / LA

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

Blood glucose increased Blood test Dehydration Type 1 diabetes mellitus Urine analysis Vision blurred Weight decreased

Symptomtext

1 week after booster shot he began to look dehydrated and was complaining of blurred vision. We took him to Urgent care because he was loosing weight. Tests showed a blood sugar level over 700. He was hospitalized and diagnosed with Diabetes Type 1.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: 1,0
Labordaten: Blood and Urine tests Feb 7 Hospital tests
Aktuelle Erkrankungen: none
Vorgeschichte: History of asthma when young
Andere Medikamente: none
Allergien: nut allergy
Vorherige Impfungen: -

VAERS 2394892

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: OH
Alter: 44,0
Geschlecht: F
Eingang: 28.07.2022
Impfdatum: 27.01.2022
Beginn: 15.06.2022
Tage bis Beginn: 139,0
Dosis: 3
Route/Site: IM / AR

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

COVID-19 Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

I did not have an adverse reaction to the vaccine. On 06/17, I tested positive for COVID-19 with a home test and my doctor confirmed the diagnosis. I was given a prescription for benzonatate and it did not help. I was given a prescription for Z-PAK and a steroid but it didn't work either. I still have the cough and it is causing trouble with my breathing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Home test positive for COVID-19 on 06/17.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin
Allergien: Raspberries; PERCOCET
Vorherige Impfungen: -

VAERS 2388295

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NC
Alter: 60,0
Geschlecht: M
Eingang: 25.07.2022
Impfdatum: 22.04.2022
Beginn: 19.06.2022
Tage bis Beginn: 58,0
Dosis: 4
Route/Site: IM / LA

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

Ageusia Anosmia Asthenia COVID-19 Cough Dyspnoea Fatigue Influenza like illness Migraine Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I was having a cough on Sunday and it developed into congestion and runny nose. By the third day I was having flu like symptoms, a headache that was more like a migraine, and was tired and weak. I took a COVID-19 home test which was positive. I did lose my smell and taste on the fourth day. I tracked my blood oxygen levels and my heart rate and really did not have too bad of shortness of breath so I used cold medicine to cope with the symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 home test.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Cholesterol
Andere Medikamente: Rosuvastatin
Allergien: DEMEROL
Vorherige Impfungen: -

VAERS 2388280

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: IL
Alter: 52,0
Geschlecht: F
Eingang: 25.07.2022
Impfdatum: 22.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: SYR / RA

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

Ageusia Anosmia COVID-19 Computerised tomogram Dyspnoea Post-acute COVID-19 syndrome X-ray

Symptomtext

Covid 19- Long covid symptoms taste and smell hadn't fully come back trouble breathing with shortness of breath im now taking Asthma medication now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: X ray and Cat scan
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; COPD; Cervical spinal stanosis; GERD; Pituatary adenoma; high risk breast cancer; Vitamin D deficiency
Andere Medikamente: Multivitamin; Gabapentin 900mg; Tamoxifen 20mg; Venlafaxine ER 75MG; symbicort 160/4.5 MG; Omeprazole 40MG; Fenofibrate 48MG; Allegra 180MG; Albuterol inhaler 18Grams ; metamusal; Nystatin oral suspension
Allergien: N/A
Vorherige Impfungen: -

VAERS 2387492

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CT
Alter: 60,0
Geschlecht: F
Eingang: 24.07.2022
Impfdatum: 21.01.2022
Beginn: 20.02.2022
Tage bis Beginn: 30,0
Dosis: 3
Route/Site: - / -

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

Anal incontinence Atrophy Paraesthesia SARS-CoV-2 test Urinary incontinence

Symptomtext

Upper extremity forearm atrophy; bilateral lower extremity tingling and numbness. Felt from the feet to the front of the calf/thighs to abdomen/ Diagnosed by PCP on 25Feb2022 with paresthesia of both lower extremities.; Bed/chair bound with loss of urine and bowel control; Bed/chair bound with loss of urine and bowel control; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 21Jan2022 at 11:00 as dose 3 (booster), single (gray cap) (Lot number: FJ6369) at the age of 60 years for covid-19 immunisation. The patient's relevant medical history included: "OSA" (unspecified if ongoing), notes: OSA; "Hyperlipidemia" (unspecified if ongoing); "Known allergies: Penicillins" (unspecified if ongoing), notes: Known allergies: Penicillins; "Prior to vaccination, was the patient diagnosed with COVID-19?:Yes" (unspecified if ongoing), notes: Prior to vaccination, was the patient diagnosed with COVID-19?:Yes. The patient's concomitant medications were not reported. Vaccination history included: covid-19 mrna vaccine - pfizer 12+ (purple cap) (Dose Number: 1. Batch/Lot No: EW0158. Covid-19 MRNA Vaccine - Pfizer 12+ (Purple Cap)), administration date: 13Apr2021, when the patient was 60-year-old, for COVID-19 Immunization; covid-19 mrna vaccine - pfizer 12+ (purple cap) (Dose Number: 2. Batch/Lot No: EW0173. Covid-19 MRNA Vaccine - Pfizer 12+ (Purple Cap)), administration date: 04May2021, when the patient was 60-year-old, for COVID-19 Immunization. The following information was reported: ANAL INCONTINENCE (disability), URINARY INCONTINENCE (disability) all with onset 20Feb2022, outcome "not recovered" and all described as "Bed/chair bound with loss of urine and bowel control"; ATROPHY (hospitalization) with onset 20Feb2022, outcome "not recovered", described as "Upper extremity forearm atrophy"; PARAESTHESIA (disability) with onset 20Feb2022, outcome "not recovered", described as "bilateral lower extremity tingling and numbness. Felt from the feet to the front of the calf/thighs to abdomen/ Diagnosed by PCP on 25Feb2022 with paresthesia of both lower extremities.". The patient was hospitalized for atrophy (start date: 03Mar2022). The events "upper extremity forearm atrophy", "bilateral lower extremity tingling and numbness. felt from the feet to the front of the calf/thighs to abdomen/ diagnosed by pcp on 25feb2022 with paresthesia of both lower extremities." and "bed/chair bound with loss of urine and bowel control" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (03Mar2022) Negative, notes: covid test type post vaccination=Nasal Swab; (10Mar2022) Negative, notes: covid test type post vaccination=Nasal Swab; (17Mar2022) Negative, notes: covid test type post vaccination=Nasal Swab; (21Mar2022) Negative, notes: covid test type post vaccination=Nasal Swab; (11Apr2022) Negative, notes: covid test type post vaccination=Nasal Swab; (12Apr2022) Negative, notes: covid test type post vaccination=Nasal Swab; (23Apr2022) Negative, notes: covid test type post vaccination=Nasal Swab; (03May2022) Negative, notes: covid test type post vaccination=Nasal Swab. Therapeutic measures were taken as a result of atrophy, paraesthesia, anal incontinence, urinary incontinence. Clinical course: On 20Feb2022 the reporter was reported that had bilateral lower extremity tingling and numbness. Felt from the feet to the front of the calf/thighs to abdomen. Diagnosed by PCP on 25Feb2022 with paresthesia of both lower extremities. Hospitalized beginning 03Mar2022. During hospitalization, symptoms worsened and also diagnosed with bilateral upper extremity forearm atrophy. Now bed/chair bound with loss of urine and bowel control. Intensive rehabilitation at a long-term acute facility and short-term rehab facility with little improvement. Since the vaccination the patient had been tested for COVID-19. The adverse event result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. The patient received treatment for the adverse event Solu-Medrol and PLEX. Since the vaccination, has the patient been tested for COVID-19 was reported as Yes. Device Date: 18Jul2022. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20220303; Test Name: SARS CoV 2; Test Result: Negative ; Comments: covid test type post vaccination=Nasal Swab; Test Date: 20220310; Test Name: SARS CoV 2; Test Result: Negative ; Comments: covid test type post vaccination=Nasal Swab; Test Date: 20220317; Test Name: SARS CoV 2; Test Result: Negative ; Comments: covid test type post vaccination=Nasal Swab; Test Date: 20220321; Test Name: SARS CoV 2; Test Result: Negative ; Comments: covid test type post vaccination=Nasal Swab; Test Date: 20220411; Test Name: SARS CoV 2; Test Result: Negative ; Comments: covid test type post vaccination=Nasal Swab; Test Date: 20220412; Test Name: SARS CoV 2; Test Result: Negative ; Comments: covid test type post vaccination=Nasal Swab; Test Date: 20220423; Test Name: SARS CoV 2; Test Result: Negative ; Comments: covid test type post vaccination=Nasal Swab; Test Date: 20220503; Test Name: SARS CoV 2; Test Result: Negative ; Comments: covid test type post vaccination=Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19?:Yes); Hyperlipidemia; Obstructive sleep apnea syndrome (OSA); Penicillin allergy (Known allergies: Penicillins)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2147342

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: FL
Alter: 52,0
Geschlecht: F
Eingang: 24.07.2022
Impfdatum: 15.02.2022
Beginn: 18.07.2022
Tage bis Beginn: 153,0
Dosis: 3
Route/Site: - / -

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

Arthralgia Chest discomfort Dyspnoea Headache Heart rate COVID-19 SARS-CoV-2 test Vaccination failure Heart rate increased Lethargy Muscle tightness Musculoskeletal stiffness Nausea Pain in extremity Vaccination site pain

Symptomtext

breakthrough case of Covid after taking three doses of Pfizer BioNTech Covid vaccine; breakthrough case of Covid after taking three doses of Pfizer BioNTech Covid vaccine; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 52-year-old female patient received BNT162b2 (BNT162B2), on 04Aug2021 as dose 1, single (Lot number: EW0177), in arm, on 25Aug2021 as dose 2, single (Lot number: FC3184), in arm and on 15Feb2022 as dose 3 (booster), single (Lot number: FJ6369) at the age of 52 years, in arm for covid-19 immunisation. The patient's relevant medical history included: "thyroid" (unspecified if ongoing); "Allergy" (unspecified if ongoing). Concomitant medication(s) included: SYNTHROID taken for thyroid disorder; ALLEGRA-D 12 HOUR taken for hypersensitivity. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 18Jul2022 at 05:00, outcome "not recovered" and all described as "breakthrough case of Covid after taking three doses of Pfizer BioNTech Covid vaccine". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (18Jul2022) Positive; (18Jul2022) Positive, notes: She took two positive test today. Therapeutic measures were not taken as a result of vaccination failure, covid-19. Clinical course: She had breakthrough case of Covid after taking three doses of Pfizer BioNTech Covid vaccine. She filled a report because she worked for Pfizer and needed to report Covid when she had vaccines, so that was what she was doing. She can't find the protocol of what to do if she had Covid, how many days she should stay at home and what she found was outdated. She reported an adverse with vaccine and Pfizer should have all this information. Adverse event was from the booster dose. Pfizer had all the where and time and all that stuff. The initial report was filed end of Feb2022 for the AE on the booster dose. Patient took two at home covid tests on 18JUL2022, that were positive. Time the Vaccination was Given as they were all PM, in the afternoon or early evening. Vaccines were administered at pharmacy. No family medical history relevant to adverse events. No additional vaccines were administered on same date of the Pfizer suspect. Adverse event did not require a visit to emergency room or physician office. Time of onset of events was reported as 05:00 CT. The primary infection site was reported as unknown and did not cause any secondary site. No predisposing factors and no culture performed. No serotyping was done. Patient did not receive any treatment for events. Patient received antipyretic Use (around the date(s) of Vaccination) was possible she took Ibuprofen or Tylenol.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20220718; Test Name: Covid at home tests; Test Result: Positive ; Test Date: 20220718; Test Name: Covid at home tests; Test Result: Positive ; Comments: She took two positive test today.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Thyroid disorder
Andere Medikamente: SYNTHROID; ALLEGRA-D 12 HOUR
Allergien: -
Vorherige Impfungen: -

VAERS 2147342

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: FL
Alter: 52,0
Geschlecht: F
Eingang: 24.07.2022
Impfdatum: 15.02.2022
Beginn: 18.07.2022
Tage bis Beginn: 153,0
Dosis: 3
Route/Site: - / RA

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

Arthralgia Chest discomfort Dyspnoea Headache Heart rate COVID-19 SARS-CoV-2 test Vaccination failure Heart rate increased Lethargy Muscle tightness Musculoskeletal stiffness Nausea Pain in extremity Vaccination site pain

Symptomtext

breakthrough case of Covid after taking three doses of Pfizer BioNTech Covid vaccine; breakthrough case of Covid after taking three doses of Pfizer BioNTech Covid vaccine; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 52-year-old female patient received BNT162b2 (BNT162B2), on 04Aug2021 as dose 1, single (Lot number: EW0177), in arm, on 25Aug2021 as dose 2, single (Lot number: FC3184), in arm and on 15Feb2022 as dose 3 (booster), single (Lot number: FJ6369) at the age of 52 years, in arm for covid-19 immunisation. The patient's relevant medical history included: "thyroid" (unspecified if ongoing); "Allergy" (unspecified if ongoing). Concomitant medication(s) included: SYNTHROID taken for thyroid disorder; ALLEGRA-D 12 HOUR taken for hypersensitivity. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 18Jul2022 at 05:00, outcome "not recovered" and all described as "breakthrough case of Covid after taking three doses of Pfizer BioNTech Covid vaccine". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (18Jul2022) Positive; (18Jul2022) Positive, notes: She took two positive test today. Therapeutic measures were not taken as a result of vaccination failure, covid-19. Clinical course: She had breakthrough case of Covid after taking three doses of Pfizer BioNTech Covid vaccine. She filled a report because she worked for Pfizer and needed to report Covid when she had vaccines, so that was what she was doing. She can't find the protocol of what to do if she had Covid, how many days she should stay at home and what she found was outdated. She reported an adverse with vaccine and Pfizer should have all this information. Adverse event was from the booster dose. Pfizer had all the where and time and all that stuff. The initial report was filed end of Feb2022 for the AE on the booster dose. Patient took two at home covid tests on 18JUL2022, that were positive. Time the Vaccination was Given as they were all PM, in the afternoon or early evening. Vaccines were administered at pharmacy. No family medical history relevant to adverse events. No additional vaccines were administered on same date of the Pfizer suspect. Adverse event did not require a visit to emergency room or physician office. Time of onset of events was reported as 05:00 CT. The primary infection site was reported as unknown and did not cause any secondary site. No predisposing factors and no culture performed. No serotyping was done. Patient did not receive any treatment for events. Patient received antipyretic Use (around the date(s) of Vaccination) was possible she took Ibuprofen or Tylenol.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20220718; Test Name: Covid at home tests; Test Result: Positive ; Test Date: 20220718; Test Name: Covid at home tests; Test Result: Positive ; Comments: She took two positive test today.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Thyroid disorder
Andere Medikamente: SYNTHROID; ALLEGRA-D 12 HOUR
Allergien: -
Vorherige Impfungen: -

VAERS 2376779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: AZ
Alter: 79,0
Geschlecht: M
Eingang: 21.07.2022
Impfdatum: 20.04.2022
Beginn: 28.05.2022
Tage bis Beginn: 38,0
Dosis: 4
Route/Site: IM / RA

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

Cardiac function test Chest X-ray Chest X-ray abnormal Differential white blood cell count Dyspnoea Electrocardiogram Fibrin D dimer Full blood count Metabolic function test Pneumonia SARS-CoV-2 test

Symptomtext

Shortness of breath, admitted to Emergency Room, No Fever or Coughing, X-Ray taken, showed involvement of left lung, diagnosis: pheumonia of lower left lung, treatment Amoxycillin.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 05/28/2022 Cardia Injury Panel, SARS VOC 2, Complete Blood Count w/autodifferential, Comprehensive Metabolic Panel, ,D-Dimer | 12 lead EKG | Chest X-Ray
Aktuelle Erkrankungen: -
Vorgeschichte: Sleep Apnea
Andere Medikamente: Diltiazem, Allopurinol, Atorvastatin,
Allergien: Celiac (Gluten), Eggs
Vorherige Impfungen: -

VAERS 2373712

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: IL
Alter: 64,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 18.04.2022
Beginn: 28.06.2022
Tage bis Beginn: 71,0
Dosis: 4
Route/Site: SYR / AR

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

Ageusia Anosmia COVID-19 Cough Diarrhoea Dyspnoea exertional Headache Impaired work ability Oropharyngeal pain Pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Starting 06/28/2022, I had a sore throat, and developed a fever of 100.5, body aches, headache, cough, congestion and a little diarrhea. I tested myself that day with an at-home test which was positive. I called my physician that afternoon and the next day she called in Paxlovid which I started on 06/30/2022. After 4-5 days in, I no longer had a fever, but still congested and coughing. However, I felt better. I was still slightly short of breath if I walked fast. I didn't come back to work until 10 days out due to coughing quite a bit. At day 14, I felt perfectly fine. I lost my sense of taste and smell, and it returned about 72 hours after stopping Paxlovid,

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Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: At-home COVID-19 test (06/28/2022): Positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lipitor; Omeprazole; Vitamin D; Motrin
Allergien: Bactrim
Vorherige Impfungen: -

VAERS 2369007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: 50,0
Geschlecht: F
Eingang: 14.07.2022
Impfdatum: 08.02.2022
Beginn: 12.07.2022
Tage bis Beginn: 154,0
Dosis: 3
Route/Site: UN / UN

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

COVID-19 Chest pain Cough Dyspnoea Influenza virus test Respiratory syncytial virus test SARS-CoV-2 test positive

Symptomtext

cough, SOB, chest pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 7/12/2022 COVID, Flu, RSV by regulatory authority; SARS-CoV-2 (COVID-19) by NAA, Micro - detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2362721

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: OR
Alter: 12,0
Geschlecht: M
Eingang: 08.07.2022
Impfdatum: 31.01.2022
Beginn: 11.06.2022
Tage bis Beginn: 131,0
Dosis: 2
Route/Site: SYR / LA

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

COVID-19 Dizziness Dyspnoea Fatigue Feeling abnormal Headache Hypersomnia Myalgia Pyrexia SARS-CoV-2 test positive

Symptomtext

When he caught COVID-19 he had a fever of 101 to 102 degrees. He had a headache, muscle aches, and very tired. At one point he slept for 18 hours. He just didn't feel good. I gave him Tylenol and Advil. When he first got COVID-19 he was having a hard time breathing, and he felt dizzy. It seemed to pass with no further issues.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 6/13/2022- COVID-19 Test- Positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Amoxicillin
Vorherige Impfungen: bruises appeared all over his body. The doctors said it could've been from the Tdap or chickenpox vaccine, but they weren't for

VAERS 2357647

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CT
Alter: 45,0
Geschlecht: F
Eingang: 05.07.2022
Impfdatum: 11.01.2022
Beginn: 03.07.2022
Tage bis Beginn: 173,0
Dosis: 3
Route/Site: IM / -

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

Chest pain Cough Laboratory test

Symptomtext

Chest Pain, coughing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Rapid 7/3/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2341876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NY
Alter: 64,0
Geschlecht: F
Eingang: 29.06.2022
Impfdatum: 24.05.2022
Beginn: 24.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Bone pain Chest pain Cough Fatigue Feeling abnormal Gait disturbance Headache Impaired work ability Magnetic resonance imaging Memory impairment Pain Palpitations Visual impairment

Symptomtext

I have had on going foggy brain, very forgetful, extreme fatigue, issues with my vision, coughing, headaches, pain in my bones everyday and all over my body. I have had chest pains and palpitations and I was walking sideways like I was drunk. I have seen several Specialist for my ongoing health issues. My work productivity has decreased. I felt that I had COVID-19 in 2020 but never tested positive. I tested positive for COVID-19 in October 2021. I was prescribed antibiotic and coughing medicine . I had a headache for 17 months every single day.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Waiting for authorization to have another MRI and chest x-ray.
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure
Andere Medikamente: Blood pressure medicine (2); cholesterol, Tylenol
Allergien: Anything that ends with pril.
Vorherige Impfungen: -

VAERS 2338821

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: ME
Alter: 75,0
Geschlecht: F
Eingang: 28.06.2022
Impfdatum: 26.01.2022
Beginn: 22.02.2022
Tage bis Beginn: 27,0
Dosis: 3
Route/Site: SYR / RA

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

Breath sounds abnormal Dyspnoea Malaise Pulmonary function test Walking distance test

Symptomtext

I had my shot done on 01/26. On Feb 08, I left to go visit my daughter. My plan was to be there for 4 months. In Feb, probably around the 20-22, I started having problems with my breathing. I blamed it on possible the pollen or possibly the humidity. I did some extra breathing treatments and it didn't seem to be working. I did that until March. I called my pulmonologist and they prescribed prednisone. That was the middle of March. The prednisone worked. I came back home in May. I called them and they put me on another round of prednisone because I was still having trouble. As of June, yesterday, I went for my testing, and the lady that did my breathing test was worried because I wasn't sounding good. Today, they called and put me on another round of prednisone. I'm on a callback list to see my pulmonologists. I had testing in December when I was sick and none of this was going on then.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 06/27/2022: Pulmonary testing, breathing test, and walking test - results unknown as of yet.
Aktuelle Erkrankungen: None
Vorgeschichte: COPD
Andere Medikamente: Women's plus 50 multivitamin; DEXILANT; loratadine; amlodipine; atorvastatin; SPIRIVA; albuterol; clotrimazole
Allergien: Aspirin; penicillin; sulfa; BENADRYL
Vorherige Impfungen: At least 10 years ago - Pneumonia shot - rash and lump on my arm.

VAERS 2325578

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: IL
Alter: 49,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 21.06.2022
Beginn: 21.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Chest pain Dyspnoea Pruritus

Symptomtext

Chest pain, SOB, pruritis to chest/back/right arm, difficulty breathing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, allergic rhinitis
Andere Medikamente: Albuterol, fluticasone
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2321932

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 16.06.2022
Impfdatum: 18.05.2022
Beginn: 06.06.2022
Tage bis Beginn: 19,0
Dosis: 4
Route/Site: SYR / LA

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

Chest X-ray normal Dyspnoea Dyspnoea exertional Electrocardiogram normal Laboratory test normal Muscle spasms Palpitations

Symptomtext

About 3 weeks after vaccination on 6-6-2022, I started having shortness of breath with exertion and pounding heartbeat. I would rest if it started bothering me. On 6-10, I noticed the shortness of breath increased in intensity so I called my EP cardiologist and I spoke to the nurse practitioner who felt that something medically may be going on and suggested going to the ER. Within 90 minutes of talking to the nurse practitioner I was continuing to huff and puff with walking so I went to the local hospital ER. They ran labwork, 2 chest xrays and 2 ekgs. They said everything was fine but that I may have had an AFIB event that resolved before the ER visit. I was still short of breath when walking out of ER to go home. I have improved as far as shortness of breath but I am seeing a cardiologist for follow up. I did start taking my valium for muscle spasms that may have been instrumental in reducing the shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Labwork, 2 chest xrays, 2 ekgs at Medical Center on 6-10-2022
Aktuelle Erkrankungen: None
Vorgeschichte: Atrial Fibrillation, HTN, Hypothyroidism, GERD, Sleep Apnea, Osteoporosis
Andere Medikamente: Xarelto, Synthroid, Lisinopril, Gabapentin, Azelastine, Fluticasone, Cyclobenzaprine, Pantoprazole, B12, Vit C, Biotin, Vit D3, Probiotic, Tylenol, Multivitamin
Allergien: Adhesives, Polymyxin eye drops, Celestone
Vorherige Impfungen: Flu vaccine (high dose fluzone)- 09/2021 - large whelp, itchiness, redness and warmth at site Pfizer vacc dose 3 - 09/28/2021 l

VAERS 2318981

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NY
Alter: 61,0
Geschlecht: F
Eingang: 14.06.2022
Impfdatum: 03.06.2022
Beginn: 04.06.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Asthenia Chills Fatigue Malaise Nasal congestion Nausea Pain Pulmonary congestion Pyrexia Rhinorrhoea Tremor

Symptomtext

DAY 1:FEVER, NAUSEA , WEAKNESS, CHILLS, NASAL CONGESTION, CHEST CONGESTION, RUNNY NOSE, BODY ACHES DAY 10-- SHAKY, TIRED, WEAK, GENERAL FEELING OF NOT FEELING WELL.

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Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: uti
Vorgeschichte: HIGH BLOOD PRESSURE HIGH CHOLESTOROL
Andere Medikamente: SIMVASTATIN OMEPRAZOLE METROL PROZAC NUCYNTA
Allergien: NONE
Vorherige Impfungen: -

VAERS 2303664

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NC
Alter: 36,0
Geschlecht: F
Eingang: 31.05.2022
Impfdatum: 11.02.2022
Beginn: 16.02.2022
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / RA

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

Arthritis Burning sensation COVID-19 Hypoaesthesia Pain Pain in extremity Paraesthesia X-ray limb abnormal

Symptomtext

Within a week of the vaccine patient started having sharp pains in both feet and legs. It is not in a specific part of the foot, it is in the entire foot. Feet are much worse than legs. Pain in legs in localized to calf muscle and travels up the leg. Foot pain involves the arch of the foot, toes, padding off foot. Type of pain fluctuates between sharp and dull but is usually sharp. Foot numbness and tingling also present. Within the past two weeks patient is now getting burning, numbness and pain in her middle and pointer finger in the left hand. Patient is left handed. Patient recently sought care from a podiatrist who recommended a dose pack but is not sure anything will help with this pain. He recommended she start an over the counter supplement called NeuRX-TF which has made a very minor difference in symptoms. She is scheduled to see a neurologist this upcoming week. It is also important to note that the patient was covid positive in December. During this time she had sharp pains in her feet, legs and entire body aches. Pain in her feet did resolve as her condition improved from the virus during its normal course of recovery.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: X ray of the foot unremarkable minus a small amount of arthritis in the foot. The doctor said it was not enough to be concerned or cause the issues the patient is experiencing.
Aktuelle Erkrankungen: None that patient was aware of
Vorgeschichte: Migraines Anxiety Depression
Andere Medikamente: Trintellix Clonazepam
Allergien: Erythromycin
Vorherige Impfungen: -

VAERS 2295880

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: RI
Alter: 61,0
Geschlecht: F
Eingang: 26.05.2022
Impfdatum: 07.01.2022
Beginn: 01.01.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Blood test Fatigue Feeling abnormal General physical health deterioration Myalgia Pain in extremity Pneumocystis jirovecii pneumonia SARS-CoV-2 test

Symptomtext

muscle pain; fatigue; going downhill with her health; Her arm was sore with the covid vaccine; She's out of work and has been feeling so lousy/Feel horrible; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 61-year-old female patient received BNT162b2 (COMIRNATY), on 18Mar2021 as dose 1, single (Lot number: ER2613), on 08Apr2021 as dose 2, single (Lot number: EW0153) and on 07Jan2022 as dose 3 (booster), single (Lot number: FJ6369) at the age of 61 years for COVID-19 immunization. The patient's relevant medical history included: "Fibromyalgia" (unspecified if ongoing), notes: Comments: Fibromyalgia Diagnosed for 32 years; "Rheumatoid arthritis" (unspecified if ongoing), notes: Rheumatoid arthritis Diagnosed at least 3 years ago or longer.; "compromised immune system" (unspecified if ongoing), notes: she has a compromised immune system. The patient took concomitant medications. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset Jan2022, outcome "not recovered", described as "Her arm was sore with the covid vaccine"; FEELING ABNORMAL (non-serious) with onset Jan2022, outcome "not recovered", described as "She's out of work and has been feeling so lousy/Feel horrible"; FATIGUE (non-serious) with onset Jan2022, outcome "not recovered"; GENERAL PHYSICAL HEALTH DETERIORATION (non-serious) with onset Jan2022, outcome "not recovered", described as "going downhill with her health"; MYALGIA (non-serious) with onset Jan2022, outcome "not recovered", described as "muscle pain". The events "muscle pain", "fatigue" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Patient had not prior vaccinations (within 4 weeks) to the first administration date of the suspect vaccine. Patient family medical history relevant to AE(s) was none. Caller stated that she received her first booster dose of the Pfizer-Biontech COVID-19 vaccine on 07Jan2022. And ever since she has experienced muscle pain and fatigue. She wanted to know if these were common side effects due to the vaccine. Patient had the COVID booster shot; she has a compromised immune system. Ever since then, she has been going downhill with her health. She has been out of work for 3.5 weeks now. Symptoms were all in her muscles and she's fatigued. She felt like she can't function from the fatigue. She enquired that, this is a side effect, has this happened before? What should she do? Her muscles were in so much pain. She was out of work and has been feeling so lousy. She has not been doing much. Felt horrible.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumocystis jirovecii pneumonia
Hospital-Tage: -
Labordaten: Test Name: Blood work; Result Unstructured Data: Test Result:Normal; Comments: blood work was fine; Test Name: Blood work; Result Unstructured Data: Test Result:Unknown result; Comments: Had blood work in the last two months; Test Name: PCP blood test; Result Unstructured Data: Test Result:Normal; Test Name: SARS-CoV-2 test; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fibromyalgia (Comments: Fibromyalgia Diagnosed for 32 years); Immunodeficiency (she has a compromised immune system); Rheumatoid arthritis (Rheumatoid arthritis Diagnosed at least 3 years ago or longer.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2294615

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NJ
Alter: 40,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 22.01.2022
Beginn: 07.02.2022
Tage bis Beginn: 16,0
Dosis: 3
Route/Site: IM / LA

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

Headache Laboratory test Migraine Ophthalmic migraine

Symptomtext

I have been having monthly migraine attacks. Every month they come on and they are worse than they normally are- at first they were just headache but have developed into migraines. I saw the doctor on February 7th 2022 and discussed this and started to try over the counter meds for the headaches. They became worse and were full blown migraines so I saw another doctor on March 22nd. He gave me a medication to help me sleep and we also discussed how the migraines were keeping me from sleeping and coming on a monthly basis. I saw a different doctor on May 10th 2022 who gave me samples of a new migraine medicine and stated it may be Ocular Migraine and the sample he gave me to try which is Nurtec seems to help more than the other things I have tried.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Lab work
Aktuelle Erkrankungen: None
Vorgeschichte: Hashimoto's Disease
Andere Medikamente: Vitamin C and D, Zinc, Oregano Oil, Omega Oil, Elderberry
Allergien: Antibiotics; NYQUIL; THERAFLU; ROBITUSSIN; TYLENOL PM
Vorherige Impfungen: -

VAERS 2294581

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: TX
Alter: 53,0
Geschlecht: M
Eingang: 25.05.2022
Impfdatum: 12.04.2022
Beginn: 21.05.2022
Tage bis Beginn: 39,0
Dosis: 4
Route/Site: IM / RA

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

Blood pressure increased COVID-19 Condition aggravated Discharge Influenza like illness Insomnia Malaise Myalgia Oropharyngeal pain Pain SARS-CoV-2 test positive Upper respiratory tract congestion Vaccine breakthrough infection

Symptomtext

Breakthrough case of COVID 05/21/2022. On 05/21/2022, ate in the day I started with body aches, I had trouble sleeping with a sore throat and drainage. On 05/22/2022 I took a home COVID test which was positive. So, I started getting that malaise feeling kind of like the flu, I never got a fever it just felt like it on my body. I took Tylenol on that first day and then the drainage and sore throat went away. The malaise continued up to today. I was prescribed PAXLOVID yesterday and started taking it, today is the second day. I have never had a cough, the congestion has just been in my head, I am not coughing up anything and the congestion just appears to be in my head. I have never had a fever with the thermometer, my BP was slightly elevated from my normal baseline. PAXLOID is giving me a metallic taste in my mouth, I have not taken Tylenol since morning or midday on Sunday, that was the only thing I have been told to take. I have malaise with occasional muscle aches. The doctor thinks I have a mild case of COVID. Now I am at the point where I am getting side effects from the Paxlovid or if it is still the COVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Home test (Bi-Max Now) positive 05/21/2022.
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma; HBP; Seasonal allergies; High cholesterol
Andere Medikamente: Vytorin; Flonase nasal spray; metoprolol; losartan; Claritin; Qvar inhaler; HCTZ
Allergien: Cephalosporin
Vorherige Impfungen: Shingrix last year and I had normal effects of flu, achy and the chills, but they went away, I was told it was a different react

VAERS 2287920

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NY
Alter: 49,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 06.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: SYR / LA

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

Injected limb mobility decreased Injection site pain Pain in extremity Ultrasound scan

Symptomtext

MY LEFT ARM HAS A SHOCKING PAIN FROM WHERE I GOT THE VACCINE ALL THE WAY DOWN TO MY 5 FINGERS, I CAN'T RAISE MY LEFT ARM, I CAN'T STRETCH IT OUT BECAUSE THE PAIN IS UNBEARABLE. IT'S A PAIN WHEN YOU HIT YOUR ELBOW AND THE PAIN IS CONSTANT AND SHOCKING.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: SONOGRAM AND FUTURE MRI- MAY -16-2022
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: pollen, dust, peanuts, corn
Vorherige Impfungen: -

VAERS 2287525

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 30,0
Geschlecht: M
Eingang: 20.05.2022
Impfdatum: 26.04.2022
Beginn: 28.04.2022
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / RA

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

Cardiac disorder Chest pain Confusional state Cyanosis Dizziness Dyspnoea Heart rate increased Incoherent

Symptomtext

Symptoms: shortness of breath, chest pain, peripheral cyanosis, lightheadedness, dizziness, increased heart rate with very minor activities (conversations, very light walking), mental confusion Went to urgent care after my wife pointed out that I wasn't speaking coherently to her, which is when I noticed that I was short of breath and had chest pain. Urgent care believed I may have a cardiac issue from receiving the covid booster Still having the same issues three weeks after the adverse event

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma HSD/hEDS ADHD
Andere Medikamente: Vitamin B12 5000mcg Magnesium L-Threonate 200mg
Allergien: -
Vorherige Impfungen: J&J COVID-19 Vaccine

VAERS 2286739

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NY
Alter: 50,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 18.02.2022
Beginn: 10.05.2022
Tage bis Beginn: 81,0
Dosis: 3
Route/Site: - / LA

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

Candida infection Chest pain Ear pain Gastrooesophageal reflux disease Muscle spasms COVID-19 SARS-CoV-2 antibody test positive SARS-CoV-2 test Vaccination failure Neck pain Oropharyngeal pain Pain Pain in jaw

Symptomtext

She was positive for COVID; She was positive for COVID; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 50-year-old female patient received BNT162b2 (BNT162B2), on 15Apr2021 as dose 1, single (Lot number: EW0169), in left arm, on 14May2021 as dose 2, single (Lot number: EW0185), in left arm and on 18Feb2022 as dose 3 (booster), single (Lot number: FJ6369) at the age of 50 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 10May2022, outcome "unknown" and all described as "She was positive for COVID". The event "she was positive for covid" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 antibody test positive: (unspecified date) Positive; SARS-CoV-2 test: (10May2022) positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Two weeks ago she was diagnosed with thrush. She had throat and neck pain right after her COVID booster. It was a few days later after the COVID booster. She had chest pain. It radiated up to her neck, jaw, and ear. Every day she was going through it. She would take Tylenol for it, but it was not helping much. She doesn't have the NDC/lot/expiration for the Tylenol. She also tried Motrin. To try to figure out which would work best. She went to the Emergency room because she was nervous it could be her heart. They said she was having a muscle spasm and an acid reflux attack. She has a history of GERD and throat reflux. She just hasn't been on medication for it. Since she was boosted and everything. She took Tylenol and Pepcid AC. She just takes it here and there. It was necessary. She definitely took it when she was in pain. She is on medication for that thrush too now. The day she was diagnosed on a rapid was on Tuesday, and she saw her doctor then. She had to get a doctor's note saying she was positive for COVID so she could get COVID pay. prior Vaccinations (within 4 weeks): not provided. Patient's Medical History (including any illness at time of vaccination): Provide other relevant medical history including but not limited to these conditions: diagnosed allergies, compromised immune status, respiratory illness, genetic/chromosomal abnormalities, endocrine abnormalities (including diabetes) and obesity: no. Relevant Tests: List other relevant diagnostic and confirmatory test results for event(s), for example, from blood tests, cerebrospinal fluid culture, bacterial sero-type, diagnostic imaging, (e.g., chest X-ray, MRI): no. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Name: PCR; Test Result: Positive ; Test Date: 20220510; Test Name: rapid test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2280805

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 17.05.2022
Impfdatum: 21.01.2022
Beginn: 23.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Dyspnoea Fatigue Headache Laboratory test normal Memory impairment

Symptomtext

After the vaccine I got tired, more joint pain, headaches, I'm short of breath, and I forget things. I went to my doctor and they put up doses of joint medication and gave me an anxiety medication, but it has made me feel badly and I stopped it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Lab test were normal
Aktuelle Erkrankungen: none
Vorgeschichte: Arthritis Rheumatoid, lupus, Sj?gren, blood pressure.
Andere Medikamente: Plaquenil 200 mg daily, amlodipine 2.5 mg daily, leflunomide 10,000 gr daily, magnesium 200 mg daily, turmeric 1000 mg 1 daily, aspirin 81 mg daily
Allergien: ibuprofen, cortisonen
Vorherige Impfungen: -

VAERS 2269014

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: TX
Alter: 69,0
Geschlecht: M
Eingang: 10.05.2022
Impfdatum: 03.05.2022
Beginn: 05.05.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: - / -

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

Asthenia Chemotherapy Condition aggravated Deafness Fatigue Laboratory test abnormal Plasma cell myeloma

Symptomtext

The patient was admitted two days after the COVID vaccine with weakness, hearing loss, and fatigue. This was thought to be due to progression of his multiple myeloma on workup, and he was started on chemotherapy with Daratumumab, Carfilzomib, and dexamethasone. He was discharged on 5/10.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: Multiple myeloma, hearing loss
Vorgeschichte: GERD, hypertension, type 2 diabetes mellitus, hyperlipidemia
Andere Medikamente: Aspirin 81 mg daily, elotuzumab, dexamethasone, Lenalidomide 10 mg daily, losartan 50 mg daily, metformin ER 500 mg daily, pantoprazole 40 mg daily, valacyclovir 500 mg daily
Allergien: None
Vorherige Impfungen: -

VAERS 2268908

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: TX
Alter: 71,0
Geschlecht: M
Eingang: 10.05.2022
Impfdatum: 03.05.2022
Beginn: 04.05.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: - / -

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

Cardiac failure Condition aggravated Dyspnoea Orthopnoea Polyuria

Symptomtext

The patient was seen in the cardiology clinic on 5/4/22 and referred to follow up in the ED for further workup of dyspnea and orthopnea. He was evaluated by cardiology upon admission and was thought to be having a heart failure exacerbation, managed with diuretics while admitted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Multiple endocrine neoplasia type 2, Congestive heart failure, chronic low back pain, hypertension, anxiety, rheumatoid arthritis
Andere Medikamente: Vitamin C 1,000 mg daily, atorvastatin 40 mg daily, Breo Ellipta inhaler, carvedilol 25 mg twice daily, ferrous gluconate 324 mg daily, furosemide 20 mg daily, hydrochlorothizaide 25 mg daily, isosorbide mononitrate 30 mg daily, lisinopril
Allergien: Sulfa, iron analogues
Vorherige Impfungen: -

VAERS 2268764

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: 47,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 31.01.2022
Beginn: 03.04.2022
Tage bis Beginn: 62,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Chest pain Dyspnoea SARS-CoV-2 test positive

Symptomtext

04/03/22 presents to ED for "chest pain and shortness of breath". PMHx of "HIV, NIDDM"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 04/03/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2248391

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: 13,0
Geschlecht: M
Eingang: 06.05.2022
Impfdatum: 22.04.2022
Beginn: 22.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Erythema Feeling hot Flushing Hyperhidrosis Musculoskeletal chest pain Swelling face Skin warm

Symptomtext

Pt reported flushing/sweating. Pt had red/flushed face/cheeks and was warm to the touch. Pt complained of feeling warm all over, Vitals: 133/76, 98, 16, 99% RA. Pt was given benadryl 25mg PO x1 at 11:40AM Mother reported that his cheeks appeared slightly swollen to her. I confirmed that he had never had a reaction to his previous Pfizer vaccines or to any other medication in the past. She reports he has no PMH takes no daily medications and has no allergies. PE: Alert, oriented, no acute distress Heart RRR, no MRG no palpitations or irregular rhythm, 2+ pulse, brisk capillary refill Lungs CTAB without wheeze or rales, normal oxygen saturation Skin: Erythema of bilateral cheeks, no angioedema, no urticaria Exam consistent with allergic reaction to vaccine. Administered 25mg Benadryl PO. Re-checked patient 15-20 minutes later and he continued to do well with resolving facial erythema and no signs of anaphylaxis. He did not feel dizzy, faint, or short of breath. Repeat vitals were 125/73, 92bpm and oxygen 97%. He was observed to walk the hallway without any symptoms. Discussed diagnosis with mother. Recommended Benadryl PRN q6h and present to the ER if he develops any signs of anaphylaxis. Mother indicated that she understands diagnosis and treatment. She stated that she understands language and refused interpreter on two separate occasions. Will note allergy in chart and report to VAERS. Pt stable and released from the vaccination site with mom at 12:13PM. D/C instructions given. Recommended f/u w/ PCP, follow up instructions provided

Weitere VAERSDATA-Felder

Praegender Schweregrund: Musculoskeletal chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Recent Illness: Pt seen for left side rib pain lasting 30min-couple hours with similar pain resolving a couple months ago, here for clinic evaluation. Last pain was 2 days ago, comes and goes. Pain usually at bedtime. No limitations during activity, no falls, no history of trauma. Food diary - noticed soda make pain worse. Usually eating one large meal at the end of the day and going to bed. Taking no medications for pain. No abdominal pain, nausea or emesis. Suspected GERD association
Vorgeschichte: PMH: BMI 95-99% for age, Anxiety
Andere Medikamente: Medications: Albuterol PRN
Allergien: NKA
Vorherige Impfungen: -

VAERS 2264973

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NC
Alter: 65,0
Geschlecht: F
Eingang: 05.05.2022
Impfdatum: 23.03.2022
Beginn: 30.03.2022
Tage bis Beginn: 7,0
Dosis: 4
Route/Site: SYR / LA

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

Dehydration Dizziness Dizziness postural Vertigo

Symptomtext

48 hours after my vaccine I started to feel lightheaded upon standing up/ a head rush. Three weeks later I became really dizzy and the room was spinning, I went to the urgent care and everything came back clear. The doctors felt that I was dehydrated and just advised me to increase fluid and if it doesn't get better to come back in.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: High blood pressure Lupus
Vorgeschichte: N/A
Andere Medikamente: Potassium Emepozol Hydrocothzide Atenolol ValsaTrtin Aspren Apoxin Benadryl
Allergien: All pain relievers/Antibiotics Penicillin Solpha Codeine
Vorherige Impfungen: -

VAERS 2264724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: OR
Alter: 23,0
Geschlecht: F
Eingang: 05.05.2022
Impfdatum: 02.05.2022
Beginn: 02.05.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Blood pressure increased Dizziness Hyperhidrosis Pallor Tachycardia Throat tightness Tremor

Symptomtext

PT RECEIVED SECOND DOSE OF PFIZER VACCINE. 10 MINS S/P ADMINISTRATION PT REPORTED FEELING DIZZY, LIGHTHEADED. THIS RN ASSISTED PT TO SUPINE POSITION UNTIL DIZZINESS DISSIPATED. PT POSITION IN BED, HIGH FOWLERS AND ASSISTED DRINKING WATER, APPLE JUICE AND GRANOLA BAR. PT APPEARED MILDLY DIAPHORETIC, WITH PALLOR AND SHAKINESS. PT'S FIANCE REPORTED THIS HAS HAPPENED TO PATIENT SEVERAL TIMES IN THE RECENT PAST. THIS RN ADVISED PT TO ESTABLISH PCP AS SHE DOES NOT CURRENTLY HAVE A PROVIDER. PT SPO2 WNL. TACHYCARDIC BPM 120BPM, ABLE TO REDUCE WITH CALMING TECHNIQUES. NO SOB, CYANOSIS OR DYSPNEA. AIRWAY APPEARS PATENT. PT STATES "IT FEELS LIKE MY THROAT IS SWELLING SHUT BUT I THINK IT IS ANXIETY." PT DID NOT APPEAR TO HAVE ANGIOEDMA, HIVES, CONSTRICTING OF AIRWAYS. PT ABLE TO CONVERSE COHERENTLY AND IS AAOX4. BP ELEVATED TO 188/90, HAS HAPPENED SITUATIONALLY BEFORE. PT STAYED 45 MINS SP VAX AND WAS ABLE TO LEAVE WALKING, UNASSISTED. SHE WAS ADVISED TO RETURN TO ER IF BREATHING BECAME DIFFICULT, HIVES APPEARED OR LOC CHANGED. REFUSED BENADRYL R/T PRIOR ADVERSE REACTION. THIS RN ATTRIBUTES REACTION TO ANXIETY, LACK OF ADEQUATE CALORIC CONSUMPTION THIS DAY AS WELL AS FEAR OF NEEDLES.

Weitere VAERSDATA-Felder

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

VAERS 2264677

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: AZ
Alter: 15,0
Geschlecht: M
Eingang: 05.05.2022
Impfdatum: 07.01.2022
Beginn: 15.03.2022
Tage bis Beginn: 67,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test normal Colitis ulcerative Condition aggravated Culture stool negative Diarrhoea haemorrhagic

Symptomtext

Starting on March 15, 2022 he started with diarrhea. It was continuous. He said his diarrhea was bloody from the beginning. That continued until April 29, 2022 when he was put on Prednisone and Lialda because he was diagnosed with ulcerative colitis. He is better now. He didn't experience any fever or nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Stool Sample; Bloodwork- clear.
Aktuelle Erkrankungen: None
Vorgeschichte: Ulcerative colitis (now)
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2263474

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: TX
Alter: 72,0
Geschlecht: M
Eingang: 04.05.2022
Impfdatum: 28.04.2022
Beginn: 01.05.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / UN

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

Atrial fibrillation Bradycardia Chest pain Electrocardiogram ambulatory Myalgia

Symptomtext

He has been followed by cardiology for history of atrial fibrillation. He received his booster COVID vaccine on 4/28/22 on the same day he saw his cardiologist. At which time, his Multaq was changed to flecainide and metoprolol as he was having some episodes of break-through atrial fibrillation. He reported to the ED on 5/1, three days later, for episodes of bradycardia with heart rates in the 40s and chest pain. Cardiology evaluated the patient in the ED, and thought myalgias could possibly be secondary to the vaccine, though it did seem to resolve with holding the metoprolol and flecainide. He was discharged with a 48 hour Holter monitor and plans to follow-up with cardiology outpatient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Atrial fibrillation, hypertension, hyperlipidemia, sleep apnea, melanoma in remission
Andere Medikamente: apixaban 5 mg twice daily, atorvastatin 40 mg daily, levetiracetam 500 mg twice daily, pantoprazole 40 mg daily, senna-docsate PRN, tramadol 50 mg PRN, morphine IR 7.5 mg PRN,
Allergien: Pollen extracts
Vorherige Impfungen: -

VAERS 2250404

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: TX
Alter: 62,0
Geschlecht: F
Eingang: 25.04.2022
Impfdatum: 19.04.2022
Beginn: 20.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Arthralgia Arthritis Condition aggravated Exercise tolerance decreased Gait disturbance

Symptomtext

I was experiencing some arthritic pain before the injection that was gradually getting better. The day of the injection, it was getting harder to walk due to right hip pain. I went back to physical therapy but I wasn't able to do the exercises I was able to do before the shot. I saw my Dr on 4/18 and was told that there had been a rapid deterioration in w/ my arthritis since Jan 2022. I was was RX pain medication and I will have surgery.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, High cholesterol, Gout,
Andere Medikamente: Nifedipine, Lisinopril, Vitamin D, Atorvastatin, Alopurinol, Aspirin, Claritin, Synthroid, Voltarin, Gabapentin, Cyclobenzaprine
Allergien: Penicillin, Cipro, Latex
Vorherige Impfungen: -

VAERS 2249711

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 24.04.2022
Impfdatum: 09.03.2022
Beginn: 09.03.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Aphasia Arthralgia Back pain Chest X-ray abnormal Condition aggravated Cough Discomfort Dyspnoea Dysstasia Fall Feeling hot Gait disturbance Hyperhidrosis Joint lock Movement disorder Muscle spasms Pain Pain in extremity

Symptomtext

Vaccine recieved as new hire to hospital as a mandate to being hired, unless I appeal my signature and wait for approval to be exempt. Recieved injection and approximately an hour later while sitting, I preceeded to get up and felt sharp pains in my upper back and left leg and left foot making me fall back into my seat. I waited a few minutes and tried again and upon standing I could not lift my left leg or left foot . Nor did I have an gait to walk normally from that moment on. I went to restroom and sat on toilet and precedded to use bathroom, and became unable to breath, talk, or move while enduring spasmotic episodes of pain and discomfort accompanied with hot sweats and difficulty breathing. To date I am exp To date I am experiencing constant pain in my left foot that radiates/moves (feeling of something moving), from left foot to left knee and at times to the middle of my right knee in the back of it warranting me to take an aspirin. This is on going and a constant discomfort to me. I have felt spasmotic episodes in my left foot upon standing to the point where, I was thrusted back onto my bed due to the pain and unable to stretch my leg out, while my toes locked right infront of me. Leaving me to only try and apply some form of pressure against my dresser or the floor to alleviate the pains My right thumb has also since injection become locked and swollen to date. I had a complete physical on 3/8/22 with no complaints of left knee pain, only right knee pain from an accident in 2017 on a bus. I also had no pneumonia, which I was diagnosed with on 3/11/22. After the injection, I also started coughing profusely and had over flow of sinus drainage which prompted me to see medical doctor on 3/11/22, because it was unbearable. It is there where I took an xray complaining of back pain at Medicine in town was diagnosed with pneumonia and given antibiotics. I was prescribed 600 mg Motrin at Emergency Room of hospital on 3/10/22, went to employee health after ER visit and went back to work as tolerated.

Weitere VAERSDATA-Felder

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

VAERS 2248234

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MA
Alter: 62,0
Geschlecht: M
Eingang: 22.04.2022
Impfdatum: 22.04.2022
Beginn: 22.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Hypoaesthesia oral Lip erythema Lip swelling Paraesthesia oral Pharyngeal erythema

Symptomtext

Approx 10 min after receiving vaccine patient complained of lip tingling and numbness-on assessment, did appear to have some swelling/erythema to lower lip (was wearing mask on arrival so no baseline to compare); examined by clinic MD, was given first one dose of 25 mg Benadryl with no change/improvement, slight erythema noted in throat, second dose of 25mg Benadryl po given 10 min later--gradual / slow improvement. Held for observation for a full hour and 45min. VS remained stable/POX 99-100, lung/trach sounds remained cta. Released in improved state/stable--to f/u at facility if sx's return

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HLD, HTN DM-Type II
Andere Medikamente: Lipitor, Glypizide, Lisinopril
Allergien: NKA
Vorherige Impfungen: -

VAERS 2245721

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: IN
Alter: 49,0
Geschlecht: F
Eingang: 21.04.2022
Impfdatum: 19.04.2022
Beginn: 19.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Chills Ear inflammation Ear pain Gastric disorder Headache Impaired work ability Influenza like illness Initial insomnia Mobility decreased Nausea Pain Pain in extremity

Symptomtext

She got her vaccine, at first she started with a generalized headache within 2 hours of getting the vaccine. It then progressed to stomach issues, nausea, gurgling and then widespread joint pains to fingers and tops of her feet. Then had ear pain what feeling like inflammation in both ears. She has pretty much been off of work since then. She did not go to sleep until Tuesday morning at 5:00 AM. Said it feels like the flu on steroids. It is better now, still has joint pain and a dull headache, but no longer has the intense stomach issues that she did have. She has not taken anything for her reactions due to her intense reactions to medications. She wrapped herself in an electric blanket and opted for a liquid diet. She states that she had the same symptom body part with all vaccinations, body aches and headache, body chills but not fever and had the stomach issues with the last one, and also with the first one. She just waited out the course and she knew it was related to the vaccine. She feels better, able to get up off the couch today and will probably go back to work tomorrow.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: EBS, unspecified autoimmune condition, had thyroid removed at age 8.
Andere Medikamente: Levothyroxine, Estradiol, cromolyn sodium.
Allergien: Naproin, fennel and asparagus (carries Epipen for these).
Vorherige Impfungen: -

VAERS 2239071

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fJ6369

moderat

Staat: NY
Alter: 29,0
Geschlecht: F
Eingang: 18.04.2022
Impfdatum: 15.04.2022
Beginn: 17.04.2022
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: - / -

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

Gait disturbance Muscle spasms Paraesthesia

Symptomtext

tinging in fingers and arms muscle cramps in leg difficulty walking right side

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: n/a
Vorherige Impfungen: -

VAERS 2238821

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: TX
Alter: 39,0
Geschlecht: M
Eingang: 18.04.2022
Impfdatum: 29.03.2022
Beginn: 30.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Inflammation Palpitations Supraventricular extrasystoles Ventricular extrasystoles

Symptomtext

DIZZINESS, LIGHTHEADED, PALPITATION. PALPITATIONS STARTED OFF MILD AND SPORADIC AND OVER TIME BECAME MORE OFTEN AND MORE SEVERE. ON 4/15/2022 PALPITATIONS GOT SO BAD THAT SHE WENT HOME EARLY AND WENT TO HOSPITAL THE NEXT DAY 4/16/2022. THE HOSPITAL DIAGNOSED HER WITH PAC'S AND PVC'S SECONDARY TO INFLAMMATION FROM BOOSTER VACCINE. SHE WAS GIVEN FLUID BOLUS, MAGNESIUM, AND POTASSIUM IN HOSPITAL. SHE HAS APPOINTMENT WITH CARDIOLOGIST ON 4/20/2022.

Weitere VAERSDATA-Felder

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

VAERS 2238715

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: 15,0
Geschlecht: M
Eingang: 18.04.2022
Impfdatum: 13.04.2022
Beginn: 15.04.2022
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / -

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

Dyspnoea

Symptomtext

Pt presented 2 days later with SOB but was stable and discharged stable without oxygen requirement.

Weitere VAERSDATA-Felder

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

VAERS 2238712

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: PA
Alter: 78,0
Geschlecht: F
Eingang: 18.04.2022
Impfdatum: 13.04.2022
Beginn: 14.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Decreased appetite Inflammation Injected limb mobility decreased Injection site erythema Injection site induration Injection site pain Injection site swelling Injection site warmth Lethargy Nausea Pain Pain in extremity

Symptomtext

Red, hot, swollen, hard, painful, 2.5 inch raised area at injection site of the PPSV 13 vaccine. Arm difficult/sore to move, Nausea and loss of appetite, Lethargy started morning after vaccine given (approx. 18 hours). Swelling/inflammation beginning to subside on 4th day post vaccine. Nausea, loss of appetite, limb pain persist 5th day post vaccine. Patient denied warm compress to site in attempt to alleviate inflammation. Oral analgesics minimally effective in relief of pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2223593

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: KS
Alter: 54,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Dental paraesthesia Hypoaesthesia oral

Symptomtext

04/08/2022: client premedicated with 25 mg of Benadryl due to history of throat and tongue numbness and blood pressure drops. Clients provider is okay with her receiving 2nd booster. Vaccine administer in special care room @1500, client lying down. 1505: client reports mild numbness to the tip of her tongue and tingling to her teeth. Client also drinking water intermittently helpful. Blood pressure check, 122/82, pulse was 62, respirations were 14. Client administered her own 25mg Benadryl at that time. Client reports Benadryl relieved side effects. Client was observed for 30 minutes without any further incident.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dental paraesthesia
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: 10-1-2021: Patient reports that with her 2 previous vaccines, she had a reaction of tingling in throat & tongue (she felt like s

VAERS 2223115

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MA
Alter: 63,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 11.03.2022
Beginn: 11.03.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Abdominal pain Amnesia Arthralgia Blood culture Blood thyroid stimulating hormone C-reactive protein Chest pain Chills Diarrhoea Dizziness Dyspnoea Epstein-Barr virus antigen positive Epstein-Barr virus test Fatigue Headache Hypersomnia Myalgia Nasal congestion

Symptomtext

She has had a constellation of symptoms (now to date about 1 year of duration), with onset to a milder extent since prior to her COVID 19 in October 2021. The persistent, and most concerning symptoms: fatigue, non refreshing sleep and prolonged periods of sleeping, memory loss, dyspnea, always feeling as if she has a "cold" ( nasal and chest congestion), pains in her hands attributed to her arthritis Other concerning symptoms that are described as intermittent: subjective fever (has not recorded temperature), chills, sore throat, diarrhea, dizziness (imbalance; head doesn't "feel right"), finger tingling. She had COVID 19 in Oct 2021 treated with casirivimab/imdevimab (did not require hospitalization), citing feeling very ill initially. Shortly after the infusion, her symptoms markedly improved, citing resolution of hand pains though since this initial improvement the above symptoms had returned and never fully resolved. 3/11/22, she had her first PFIZER COVID 19 vaccine, and ever since then all the above symptoms have returned in a substantial, severe fashion. In addition, since the vaccination, she has had chest pain at a particular spot on her right chest worse with breathing and relieved by lying flat; her left arm over the muscle hurts. 4/7/22, she has had new abdominal pain as well. Headaches have become prominent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: TSH 4/1/22 2.849 Epstein Barr serology 4/1/22 EBV Nuclear antigen POSITIVE (early antigen, vca igg and vca igm all negative) CRP high sensitivity 4/1/22 3.14 Blood cultures and high sensitivity troponin ordered
Aktuelle Erkrankungen: Not known
Vorgeschichte: anxiety arthritis asthma cervical disc disorder depression HTN
Andere Medikamente: Albuterol Sulfate 108 (90 Base) MCG/ACT 1 puff Inhalation Every 4 hours PRN amLODIPine Besylate 5 mg Oral Daily Aspirin 81 MG TAKE 1 TABLET BY MOUTH EVERY DAY Atorvastatin Calcium 10 mg Oral Daily cycloSPORINE 0.05 % 1 drop Both Eyes 2
Allergien: Codeine (headaches) Vicodin (GI intolerance)
Vorherige Impfungen: -

VAERS 2204211

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: -
Geschlecht: U
Eingang: 07.04.2022
Impfdatum: 15.03.2022
Beginn: 01.03.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

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

Blood pressure measurement Hypertension Vomiting Blood test normal Chest X-ray normal Electrocardiogram normal Impaired work ability Malaise Neck pain Pain in extremity Skull X-ray

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A patient (no qualifiers provided) received bnt162b2 (BNT162B2), administered in arm, administration date 15Mar2022 (Batch/Lot number: unknown) as dose 2, single for covid-19 immunization. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE), administration date: 11Feb2022, for COVID-19 Immunization, reaction(s): "I did not feel any side effects". The following information was reported: VOMITING (hospitalization) with onset 15Mar2022, outcome "unknown", described as "puked"; HYPERTENSION (hospitalization) with onset Mar2022, outcome "unknown", described as "blood pressure went through the roof". The patient was hospitalized for vomiting, hypertension (start date: 17Mar2022). The patient underwent the following laboratory tests and procedures: blood pressure measurement: (Mar2022) went through the roof. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 202203; Test Name: blood pressure; Result Unstructured Data: Test Result:went through the roof
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2218235

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NV
Alter: 52,0
Geschlecht: F
Eingang: 06.04.2022
Impfdatum: 07.02.2022
Beginn: 07.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Balance disorder Dizziness Headache Hypoaesthesia Palpitations Tremor Vertigo

Symptomtext

Dose 2 02/07/2022, 02/08/2022, FJ6369 I was originally scheduled for 02/08/2021 but was able to received second dose early due to cancellation. Within 30 minutes after, right side of face is numb, and within the afternoon, I experience some heart palpitations. That evening a head ache presented around 09:28PM extreme head ace and took zinc, Vitamin C and Tylenol. 02/28/2022 experience shakiness, dizziness like equilibrium or vertigo issue and had has a pass history of this issue. End of March. Re-occurring face numbness right side below right nostril and spreads upward toward my eye, if you use your palm to face. With for March 16, 2022 and 04/05/2022. March 29, 2022, was doctors visit and he is scheduling blood on upcoming visit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: Cold but over before the vaccination
Vorgeschichte: Thyroid
Andere Medikamente: Effexor 150mg once daily, Levothyroxine 88mcg once daily, Liothyronine 5mcg once daily
Allergien: Generic for zoloft rash
Vorherige Impfungen: -

VAERS 2215998

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 05.04.2022
Impfdatum: 07.02.2022
Beginn: 12.02.2022
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: SYR / LA

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

Condition aggravated Jaw clicking

Symptomtext

Jaw (joint) popping. I believe I had COVID-19 back in February 2020. (my insurance / provider) refused to test given tests at that time were hard to come by and I did not have the 3 cardinal symptoms of that time. I am sure I had COVID-19 and for months after that I had the SAME problem I am now having with my jaw. Back in 2020 it resolved within 3-4 months. I am still having daily problems post my booster February 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Possible bout of diverticulitis
Vorgeschichte: Diverticulitis. Arthritis.
Andere Medikamente: none
Allergien: Sulfa - anaphylaxis
Vorherige Impfungen: -

VAERS 2212173

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 63,0
Geschlecht: F
Eingang: 01.04.2022
Impfdatum: 01.04.2022
Beginn: 01.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Chest pain Heart rate increased Paraesthesia

Symptomtext

Patient reported chest pain, elevated heart rate, some tingly feeling. Her O2 Stats were 96 on the pulse-oximeter. Patients BP was 194/94 HR 84. We called the fire department, they paramedics came and took her vitals and transported her to a local ER. She was there about an hour and a half, not admitted and sent home. Patient called to let us know. Then her caregiver also called to report that she was not admitted and was going home. No serious issues.

Weitere VAERSDATA-Felder

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

VAERS 2211358

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 01.04.2022
Impfdatum: 28.03.2022
Beginn: 28.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Chills Condition aggravated Diarrhoea Fatigue Feeling abnormal Headache Pyrexia Tremor

Symptomtext

Severe shaking for several hours-started 11pm on 3/28/22. Chills. Fever 101.1. Diarrhea. Headache. Brain fog. Tired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: none.
Aktuelle Erkrankungen: RSD in hand/fingers. Chronic Back Pain. Osteoporosis. Asthma borderline. Acid Reflux. IBS.
Vorgeschichte: Chronic Pain-Back. RSD in left hand and fingers. Osteoporosis. Acid reflux. IBS. Borderline Asthma.
Andere Medikamente: Protonix. Miralax. Multiple vitamin. Calcium. Vitamin E, B, C.
Allergien: Aspirin. Antibiotics except penicillin. Motrin. Fentanyl.
Vorherige Impfungen: Age 69 Pfizer, fever, nausea, tired, headache, chills

VAERS 2209455

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: 29,0
Geschlecht: M
Eingang: 31.03.2022
Impfdatum: 07.03.2022
Beginn: 12.03.2022
Tage bis Beginn: 5,0
Dosis: 4
Route/Site: IM / LA

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

Condition aggravated Diabetic ketoacidosis Type 1 diabetes mellitus

Symptomtext

Diabetic ketoacidosis without coma associated with type 1 diabetes mellitus. He was treated appropriately with iv insulin, iv fluids with resolution of his DKA. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2187685

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: 34,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 18.03.2022
Beginn: 18.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Hypoaesthesia Impaired work ability Tremor Malaise

Symptomtext

3/31/2022 at 1643 Employee called the Employee Health COVID-19 Vaccine Nurse Support Line today to follow up on a reported COVID-19 booster vaccine reaction, in which she received treatment during the Observation period post vaccination via the Incident Management Team. Vaccine Name - Pfizer Vaccine Date - 3/18/2022 Booster Dose - Yes Location - Right Deltoid Date of Symptom Onset ? 3/18/2021 Symptoms ? Right Side of Body Went Numb and She Began to Shake (Occurred Within 5 minutes Post Vaccination and Employee Treated via Incident Management Team and Taken to Emergency Last Day of Work and Shift ? Schedule: 3 Shifts per Week (7p-7a) / Missed Work: Sunday, 3/20/22 Home Remedies ? N/A Any Improvement ? Yes

Weitere VAERSDATA-Felder

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

VAERS 2206595

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

moderat

Staat: -
Alter: 34,0
Geschlecht: F
Eingang: 30.03.2022
Impfdatum: 29.03.2022
Beginn: 29.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Breast swelling Breast tenderness Chills Dizziness Fatigue Injection site pruritus Lymphadenopathy Migraine Nausea Pain Pain in extremity Peripheral swelling Pyrexia Rash Respiratory tract congestion Visual impairment

Symptomtext

ARM IS SWOLLEN AND IN PAIN, RADIATING PAIN DOWN ARM TO WRIST, UNDER ARM LYMPH NODES SWOLLEN, BREAST TENDER AND SWOLLEN, FEVER (103, 101, 100.8), MIGRAINE, NAUSEA, CHILLS, LIGHT HEADED, BODY ACHES, DIZZY, FATIGUE, RASH ON SIDES OF FACE, INJECTION SITE ITCHY, CONGESTION, SEE'S SPOTS

Weitere VAERSDATA-Felder

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

VAERS 2206552

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

moderat

Staat: -
Alter: 37,0
Geschlecht: F
Eingang: 30.03.2022
Impfdatum: 29.03.2022
Beginn: 29.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Condition aggravated Headache Lymphadenopathy Oropharyngeal pain

Symptomtext

HEADACHE, CHEST PAIN, THROAT PAIN (SWOLLEN NODES IN BACK OF THROAT)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Throat pain (swollen nodes at back of throat)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2204335

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: 40,0
Geschlecht: F
Eingang: 29.03.2022
Impfdatum: 26.03.2022
Beginn: 27.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Anxiety Fatigue Hypoaesthesia Paraesthesia

Symptomtext

FATIGUE, NUMBNESS OF ARM AND LEG, PINS AND NEEDLES FEELING ON WHOLE LEFT SIDE OF BODY FROM JAW TO FEET, ANXIETY ATTACK FEELING

Weitere VAERSDATA-Felder

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

VAERS 2201417

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: TX
Alter: 36,0
Geschlecht: F
Eingang: 28.03.2022
Impfdatum: 17.03.2022
Beginn: 18.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Axillary mass Chest pain Dyspnoea Pain Palpitations

Symptomtext

KNOT IN RIGHT ARMPIT, BODY ACHES, CHEST PAIN, SHORTNESS OF BREATH, PALPITATIONS

Weitere VAERSDATA-Felder

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

VAERS 2196281

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: 26,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 23.03.2022
Beginn: 23.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Migraine Pain

Symptomtext

BODY ACHES, MIGRAINE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: AX: PENICILLIN
Vorherige Impfungen: -

VAERS 2195837

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: FL
Alter: -
Geschlecht: U
Eingang: 24.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Body temperature Fatigue Headache Paraesthesia Peripheral swelling Pyrexia Vaccination site pain

Symptomtext

Ached in all joints and site of shot; Ached in all joints and site of shot; Headache; Tired; Tingling on feet and under arms; Tingling on feet and under arms; Fever of 101; Swelling on arm I had jab; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program (005570). The reporter is the patient. A 60 year-old patient received bnt162b2 (BNT162B2), administered in arm left, administration date 17Feb2022 13:30 (Lot number: FJ6369) as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, Single, Date/Time: 26Mar2021, 11:30 AM, Left arm, Lot number: EL1283), administration date: 26Mar2021, for COVID-19 Immunization, reaction(s): "Little lethargic"; Bnt162b2 (DOSE 2, Single, Date/Time: 16Apr2021, 12:30 PM, Left arm, Lot number: EP7533), administration date: 16Apr2021, for COVID-19 Immunization. The following information was reported: ARTHRALGIA (non-serious), VACCINATION SITE PAIN (non-serious) all with onset 17Feb2022, outcome "recovering" and all described as "Ached in all joints and site of shot"; HEADACHE (non-serious) with onset 17Feb2022, outcome "recovering", described as "Headache"; FATIGUE (non-serious) with onset 17Feb2022, outcome "recovering", described as "Tired"; PARAESTHESIA (non-serious), PARAESTHESIA (non-serious) all with onset 17Feb2022, outcome "recovering" and all described as "Tingling on feet and under arms"; PYREXIA (non-serious) with onset 17Feb2022, outcome "recovering", described as "Fever of 101"; PERIPHERAL SWELLING (non-serious) with onset 17Feb2022, outcome "recovering", described as "Swelling on arm I had jab". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of arthralgia, vaccination site pain, headache, fatigue, paraesthesia, paraesthesia, pyrexia, peripheral swelling. Additional information: Reporter informed about side effects of COVID 19 booster. patient had first dose and second dose in Apr2021. And booster 5 days ago. after first shot patient was a little lethargic for 24 hours. patient booster was bad, the first night patient got ached in all joints and site of shot, headache, tired. Second day a little less joint pain with ibuprofen, tingling on feet and under arms. Third day super tired and fever of 101. Fourth & Fifth day better after ibuprofen but under arm swelling on arm. Day of vaccine just a little sore at shot sight. Woke up at 01:00 AM with pain at shot site and extreme ache in joints, headache, could not sleep, very uncomfortable. Next day extreme headache, joint aches, lethargic. took 200mg ibuprofen at 0830 AM and 0600PM. Next day a bit less Aches but fever of 101? and still tired. Took 200mg Ibuprofen at 800 AM and 0600PM. Next day less aches still fever of 101, Still lethargic. Next day no fever, no aches still lethargic with extreme swelling under left arm with pain into left breast. Day 12 - Still some swelling under left arm all other reaction subsided. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 202202; Test Name: Fever; Result Unstructured Data: Test Result:101
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2195007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 41,0
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 23.03.2022
Beginn: 23.03.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Fatigue Nausea Tremor

Symptomtext

Patient left clinic and returned approximately 30 min after vaccination with reports of nausea, shakiness, and fatigue. Vital signs report as following 156/95, 36.4 C, 88 HR, 99%, 18 RR. Patient monitored for an additional 15 minutes with resolution of symptoms. No rescue medications administered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Yes. Patient reported severe allergic reaction to something other than a vaccine in her appointment prescreen. Substance not listed.
Vorherige Impfungen: -

VAERS 2192674

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: 39,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 21.03.2022
Beginn: 22.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Crying Dyspnoea Pain Panic attack

Symptomtext

CRYING, CHILLS, BODY ACHES, WHOLE BODY PAIN, SHORTNESS OF BREATH, PANIC ATTACKS, PAIN WHEN MOVING ARM.

Weitere VAERSDATA-Felder

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

VAERS 2192393

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: WA
Alter: 56,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 17.03.2022
Beginn: 17.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Dizziness Feeling abnormal Interchange of vaccine products Joint stiffness Mental impairment Mobility decreased Nausea Nervousness Pain Respiratory tract congestion Rhinorrhoea

Symptomtext

Starting the evening of the shot, after physical therapy, I started feeling woozy and shaky. I got home and felt nauseous so I had to lie down. Also, my nose was runny and congested. Almost suddenly, I felt like I got hit by a truck. Most of my joints felt like they were on fire and I could not even make a fist. I couldn't think straight and couldn't get out of bed. I felt totally out of it and everything really hurt. I attempted to use my phone and couldn't function. It was not as bad as the 2nd dose and I was feeling better by Saturday evening.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Side effects still experienced from second dose and weird sensations all over my body that started before any dose (since having COVID)
Vorgeschichte: Spinal Fusion due to scoliosis
Andere Medikamente: Adderall (Generic) 20mg, Liquid Turmeric, Vitamin D, E and A, Omega 3, Glucosamine, B-complex and ibuprofen, Gabapentin and Cymbalta
Allergien: Iodine, Penicillin, Nitrofuron and Brazil nuts
Vorherige Impfungen: 1st (rash) and 2nd Moderna Shots - VAERS report

VAERS 2192234

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 24.02.2022
Beginn: 24.02.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Blood electrolytes Blood gases Blood glucose Blood pressure decreased Chest X-ray Cough Dyspnoea Electrocardiogram Full blood count Hepatitis C virus test Lung disorder Metabolic function test Pruritus Wheezing

Symptomtext

Generalized itching began about 30 min following vaccination, followed by acute airway issues (cough, shortness of breath, wheezing). At outset of symptoms, I took 1 chewable Zyrtec (10mg) and 1 hydroxyzine (25mg-allergy to benadryl. One dose of epinephrine was administered by clinic staff at about 45min or so after injection, followed by them calling EMS for ED transport. At ED, physician ordered 125 mg Solu-medrol and 3x dosing of Duo Neds. Duo nebs were repeated q. need or q.4h. My normal blood pressure (non-anaphylaxis) runs high, typically requiring repeat measurements to fall at or under 140/90. During ED management (approximately 25-25h of observation), my BP fell as low as 94/50 or low 100s/40s (examples). I was finally allowed to take my MCAS medications (Zyflo and ketotifen) (late evening on 2/24 and the morning of 2/25) that I routinely take prior to any vaccinations or medical procedures. For the week prior, this including Cromolyn, Zyflo, Ketotifen (dosing beginning 7d before the vaccine) and 4x Singulair dose (2x dose, 2x per day starting 2days prior). Along with my usual daily meds. When getting home from the hospital, my peak flows continued to be much lower that usual (after 2d on steroids - respiratory symptoms improved, my Peak Flows are still only 350, compared to now (3/20) when my PF is 460-470. My asthma was reasonably well controlled (no overt symptoms) the morning of my vaccine. My recent experience (since 2019) with Zyflo and ketotifen is that when I continue to to take these after a reaction, they help to reduce the number and severity of my rebound reactions. Technically, I was in the Emergency Department for my entire stay after the latest vaccine reaction, which was about 25-26h. I was moved from the main ED to their holding tank/observation unit across from the ED, and still staffed by ED people (mostly RN/NP). I opted to be discharged after 26h rather than waiting an additional 11h for a hospitalist consult because the NP did not want to consult with my usual care team - PCCM. I opted to get out and call pulmonary directly for advice post-discharge, which included using a step down dosing in prednisone on the following days of 40mg, 20mg, then 10mg. The advice was to followup with Internal Medicine at the beginning of the week and let them evaluate for need to continue with more prednisone, which I did on Monday afternoon. Her advice was to wait and see versus taking more prednisone, which I also followed. It took about 2 weeks for my airways to return to "normal"function and I did not add in any additional prednisone. However, I did continue with my MCAS meds at least through Monday of the following week instead of stopping soon after the vaccine. General comment: It is my understanding that Pfizer changed one ingredient (PSB-- > TRIS buffers) between doses 3 (booster #1) and 4 (booster #2). I am neither an anti-vaxxer nor someone reading social media to manufacture nonsense triggering vaccine concerns. However, because of my MCAS and multiple triggers, I DO look for possibly commonalities between reactions to different medications. Tris (tromethamine) is also in toradol and gadolinium. Toradol was my worst anaphylaxis ever. Since this is the only change in components, this seems to be a reasonable explanation for the reaction. Many of these reactions triggered by my MCAS are more likely to be anaphylactoid-mediate rather than classically-IgE mediated. Since the actual vaccine in the Pfizer Covid vaccine is RNA-based, I am defaulting to assume the change in buffer is the more likely culprit than IgE-mediated reaction to viral RNA (just making some basic molecular biologist/virologist assumptions here). Finally, while my personal medical history reads like its own horror story, I continue to be high functioning and still swim masters whenever the pandemic suggests my exposures at the pool are well managed, also considering when the threat of waning immunity and resurgence of Covid are taken into account.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: In ED: continuous monitoring - the usual: BP, O2 sats, HR, etc. Lab tests included: portable chest XR, ECG, electrolytes, venous blood gases, basic metabolic panel, HCV screen, CBC, POC glucose (multiple)
Aktuelle Erkrankungen: No acute illnesses - just the chronic ones listed in Item 12 -
Vorgeschichte: Severe asthmatic, MCAS, diabetic, hypertension, 3x cancer, multiple spinal surgeries/fusions, anaphylaxis to many meds Lynch Syndrome (MSH6 mutation). All are medically managed except the LS, which requires cancer surveillance. Prior cancer history includes melanoma, and primary (2009) &recurrent triple negative breast cancer (2019). I have undergone surgical resections, bi-lateral mastectomy, radiation treatment (breast, 2009), taxotere/cytoxin chemotherapy (2009), adriamycin/cytoxin (2019), and treatment for many medical complications (pseudomonas wound infections, DVT in the PICC line, pleurisy/pneumonia x3 during chemotherapy). While unrelated, this just highlights that my lungs/general body condition was pretty worn down heading into the Covid pandemic and I got the 2nd booster dose because of uncertainties about the robustness of the immune response to the first three, with acknowledgment that a primary infection would be pretty hard on my lungs, in the best of circumstances. Other health issues: Cancers: melanoma-scalp, TNBC - primary and recurrent, GERD, Multinodular thyroid, osteoporosis, bronchiectasis, osteoarthritis, BCC, and mixed hyperlipidemia.
Andere Medikamente: Cromolyn, Zyflo, Ketotifen, Levocertirizine, Combivent, montelucast,chewable Zyrtec (with reactions), hydroxyzine (with reactions, generalized itching-allergic to benadryl), duo nebs, prednisone, moxifloxacin (as needed - pulmonary infectio
Allergien: Doxycycline, EpiPen (preservative), Risedronate, Phenacaine hyrodrocodone-acetaminophen, alendronate, ketorolac tromethamine, levofloxacin, calcitonin, oxycodone-actaminophen, oxycodone -HCl, Hydromorphone Hcl, Lidocaine, Influenza Vacc, Tri (2003), IV magnesium, propoxyphene N-acetaminophen, promethazine, clarithromycin, tetanus vaccines and toxoid, gadolinium contrast agent, fentanyl, morphine sulfate, bupivacaine, lidocaine-epinephrine, tuberculin PPD, Sulfites, Insulin Lispro Protamin-Lispro, aspirin, diphenyramine, tramadol, mepeidine (Pf), propofol, Proparacaine, Buprenorphine, tape adhesive, cefuoxime, amoxicillin-Pot Clavulanate, Pneumococcal 13-valent conjugate to diptheria CRM, Denosumab, Aztreonam, tromethamine
Vorherige Impfungen: -

VAERS 2192189

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: 31,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 17.03.2022
Beginn: 17.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Condition aggravated Pyrexia Rash Vomiting

Symptomtext

Full body rash on palms of hands and soles of feet (same issue happened w/ 2nd dose), severe vomiting (10-12 times) for 24 hours and fever or 36hrs.

Weitere VAERSDATA-Felder

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

VAERS 2187402

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: PA
Alter: 28,0
Geschlecht: F
Eingang: 18.03.2022
Impfdatum: 17.03.2022
Beginn: 17.03.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Chest pain Hyperhidrosis

Symptomtext

Systemic: Chest Tightness / Heaviness / Pain-Mild, Systemic: Sweaty palms-Mild, Additional Details: Symptoms started approximately 10 minutes after Covid vaccine and lasted approximately 30 min. Declined

Weitere VAERSDATA-Felder

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

VAERS 2187354

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NY
Alter: 37,0
Geschlecht: M
Eingang: 18.03.2022
Impfdatum: 15.02.2022
Beginn: 13.03.2022
Tage bis Beginn: 26,0
Dosis: 3
Route/Site: OT / LA

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

COVID-19 Cough Dysphonia Fatigue Hot flush Nasal congestion Nasopharyngitis Pharyngeal paraesthesia SARS-CoV-2 test Vaccination failure

Symptomtext

Two covid home tests and he was positive/his employer (Name) performed a covid test and he is also positive; Two covid home tests and he was positive/his employer (Name) performed a covid test and he is also positive; hot and cold flashness; throat tingling; dry cough; nasal congestion; throat hoarseness; hot and cold flashness; feeling tired; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from product quality group. A 37 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 15Feb2022 (Lot number: FJ6369) at the age of 37 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: Pfizer biontech vaccine (Dose Number: 2, Batch/Lot No: EL9261, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 25Jan2021, when the patient was 36 old, for COVID-19 immunization; Pfizer biontech vaccine (Dose Number: 1, Batch/Lot No: EK9231, Location of injection: Arm Left), administration date: 06Jan2021, when the patient was 36 years old, for COVID-19 Immunization. The following information was reported: VACCINATION FAILURE (medically significant) with onset 13Mar2022, outcome "unknown", COVID-19 (medically significant) with onset 13Mar2022, outcome "not recovered" and all described as "Two covid home tests and he was positive/his employer (Name) performed a covid test and he is also positive"; NASOPHARYNGITIS (non-serious), HOT FLUSH (non-serious) all with onset 13Mar2022, outcome "not recovered" and all described as "hot and cold flashness"; PHARYNGEAL PARAESTHESIA (non-serious) with onset 13Mar2022, outcome "not recovered", described as "throat tingling"; COUGH (non-serious) with onset 13Mar2022, outcome "not recovered", described as "dry cough"; NASAL CONGESTION (non-serious) with onset 13Mar2022, outcome "not recovered", described as "nasal congestion"; DYSPHONIA (non-serious) with onset 13Mar2022, outcome "not recovered", described as "throat hoarseness"; FATIGUE (non-serious) with onset 13Mar2022, outcome "not recovered", described as "feeling tired". The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (13Mar2022) positive. Therapeutic measures were not taken as a result of covid-19, nasopharyngitis, pharyngeal paraesthesia, cough, nasal congestion, dysphonia, hot flush, fatigue. Reporter was Pfizer employee and registered nurse. Yesterday, on Sunday,13Mar2022 my husband woke up withthroat tingling, dry cough, nasal congestion, throat hoarseness, hot and cold flashness and feeling tired. I performed two covid home tests and he was positive. Today, Monday 14Mar2022, his employer [Withheld] performed a covid test and he is also positive.Patient did not receive any other vaccines in 4 weeks of vaccination and did not receive any other medications in 2 weeks of vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Patient did not have history of known allergies. The patient not visited emergency room or hospitalization due to events.; Sender's Comments: The efficacy of a drug varies from patient to patient and can be affected by different factors; however, a contributory role of the suspect product bnt162b2 to the reported vaccination failure / COVID-19 cannot be ruled out

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pharyngeal paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20220313; Test Name: covid; Result Unstructured Data: Test Result:Positive
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 2180615

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: LA
Alter: 14,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 14.03.2022
Beginn: 14.03.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea Oropharyngeal discomfort Swelling face Swelling of eyelid

Symptomtext

Pt reports onset of facial and eyelid swelling within hours of administration of COVID vaccine number one. She also reports some increased work of breathing and some discomfort in her throat. She did not have to administer an Epi-Pen but did take oral benadryl. The morning after the vaccine- facial swelling had increased- but was gradually improving as the hours progressed. No breathing difficulty or throat concerns reported by the next day at the clinic visit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Multiple food allergies
Andere Medikamente: Cetirizine 10 mg tablet by mouth one time daily
Allergien: Shrimp Penicillin Peanut dog Soy Walnut and Wheat
Vorherige Impfungen: -

VAERS 2176813

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: OH
Alter: 92,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 07.03.2022
Beginn: 07.03.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Dehydration Diarrhoea Electrocardiogram Faeces discoloured Pain Palpitations Pyrexia

Symptomtext

COVID booster 5 days ago. Felt achey later that night, associated with fever, diarrhea, had some black stool X 2. Normal today. Starting to eat today. Hydration was definitely down, 10 oz daily. Had some episodes of racing heart, never took her pulse. Has resolved in the past 24 hours. Does have known history of atrial fibrillation status post pacemaker placement for heart block.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: ECG: V-Paced, 77 BPM
Aktuelle Erkrankungen: N/A
Vorgeschichte: PAST MEDICAL HISTORY Diagnosis Date ? Arrhythmia ? B-cell lymphoproliferative disorder 2/20/2014 ? Chronic low back pain ? Esophageal reflux conrolled with Prilosec ? Femoral shaft fracture R leg; conservatively managed by doctor ? Neuropathy perpheral, idiopathic per pt ? Osteoporosis ? PMH - PAST MEDICAL HISTORY OF PAT controlled with Verapamil ? PMH - PAST MEDICAL HISTORY OF lumbago--cared for by doctor--has chronic back pain with spondylolithesis. ? Toxic diffuse goiter ? Unspecified hypothyroidism
Andere Medikamente: metoprolol, losartan, Eliquis, levothyroxine, simvastatin
Allergien: Amoxicillin Rash Not Specified Allergy 10/5/2020 skin test negative. developed generalized rash that lasted 1 week. Neurontin [Gabapentin] Not Specified Intolerance 5/7/2007 Leg swelling Skelaxin [Metaxalone] Rash Not Specified 3/16/2005 Sulfa [Other] Not Specified 10/24/1998 Sulfa is considered to be Sulfa-trimeth for the purpose of M Adverse Reactions/Drug Intolerances Kenalog [Triamcinolone Acetonide] Intolerance Not Specified Side Effect/Intolerance 5/31/2019 Muscle cramping
Vorherige Impfungen: -

VAERS 2173920

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MO
Alter: 51,0
Geschlecht: F
Eingang: 11.03.2022
Impfdatum: 04.03.2022
Beginn: 04.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Blood electrolytes normal Burning sensation Chest discomfort Dyspnoea Electrocardiogram normal Hypersensitivity

Symptomtext

The same day I got the vaccine, I was having trouble breathing I went to the doctor on 3/5/22 my whole body felt like it was on fire. The doctor gave me steroids' to help treat the allergic reaction I was having from the vaccine/shot. Today 3/11 /22 I woke up feeling better with slight chest tightening but feeling much better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG -Normal; Electrolytes - Normal.
Aktuelle Erkrankungen: Barter's syndrome; Hypocap PP; Thyroid
Vorgeschichte: N/A
Andere Medikamente: Metformin; Januvia; Potassium; Progestium; Styponel; Spironolactone; Claridian D; Zyrtec; Vitamin C; Zinc; Magnesium; B12; Phosphatidylserine; Ginger root; B3; Advil
Allergien: Antibiotic; Shrimp & Fish
Vorherige Impfungen: -

VAERS 2171630

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 10.03.2022
Impfdatum: 03.03.2022
Beginn: 03.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Erythema Fatigue Feeling abnormal Flushing Headache Influenza like illness Injection site pain Lymph node pain Lymphadenopathy Mobility decreased Myalgia Pain in extremity Pyrexia Sleep disorder

Symptomtext

3/3/22 5:30 pm Increasing soreness in left arm at injection site. 9:00pm Went to bed - just didn't "feel right" During the night woke up with fever and generalized muscle aches ( flu like symptoms) 3/4/22 6:00am Flushed, fever, red face, arm soreness, generalized muscle aches, swollen underarm glands on left side, massive headache. Slept off and on all day - did not get out of bed. 3/5/22 No fever, no flushed face. Swollen underarm lymph gland remains sore. Extremely tired. 3/6/22 Underarm lymph gland still enlarged, no fever, arm is not sore 3/7/22 Underarm lymph gland still sore but lessening 3/8/22 underarm lymph gland still enlarged but not sore

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Hashimoto's Disease Lichen Sclerosis
Andere Medikamente: Myrbetriq (50 mg) Levothyroxine (0.125mcg) Losartan HCTZ (50-12.5) Rosuvastatin (10mg)
Allergien: Bactrim
Vorherige Impfungen: 3/12/21 Second Pfizer Covid vaccine - 66 y/o- not as severe as this event. slight fever, headaches and swollen lymph gland

VAERS 2168105

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

moderat

Staat: TX
Alter: 29,0
Geschlecht: F
Eingang: 09.03.2022
Impfdatum: 21.01.2022
Beginn: 06.02.2022
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: SYR / RA

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

Blood iron decreased Cardiac monitoring Chest pain Electrocardiogram normal Haemoglobin decreased Headache Pain Pain in extremity Palpitations

Symptomtext

Day after vaccine- sore arm, body aches, headache 2/6/22- frequent heart palpitations, chest aches 2/17/22- was seen by NP, ran blood work and referred me to Cardiologist 2/24/22- Cardiologist recommended not to get booster, ran ecg- normal, placed on heart monitor and will have ultrasound completed. Unknown cause at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Heart monitor completed 3/5/22- pending results Ultrasound rescheduled (switching hospitals/same doctor) Bloodwork ran by NP 2/17/22- low hemoglobin/iron otherwise normal results
Aktuelle Erkrankungen: Covid positive 12/25/21
Vorgeschichte: Mitral Valve Prolapse
Andere Medikamente: n/a
Allergien: Shrimp, Scallops, sensitive to decongestants
Vorherige Impfungen: -

VAERS 2167974

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 09.03.2022
Impfdatum: 01.03.2022
Beginn: 02.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain upper Dyspnoea Hyperhidrosis Hypoaesthesia

Symptomtext

Difficulty breathing, Arm/hand numbness, sweating, stomach pain.

Weitere VAERSDATA-Felder

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

VAERS 2165751

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 16,0
Geschlecht: M
Eingang: 08.03.2022
Impfdatum: 02.03.2022
Beginn: 02.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Angina pectoris Blood test Chest X-ray Chest pain Dyspnoea Echocardiogram Electrocardiogram Palpitations

Symptomtext

As per mother, patient experienced chest and heart pain, shortness of breathe, and heart palpitations 3 hours after vaccination. Symptoms occurred immediately in conjunction to soccer practice.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 3/3/22 - EKG, chest X-ray, and ultrasound of the heart; 3/4/22 - EKG, chest X-ray, and full blood panel.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 2165534

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: DE
Alter: 56,0
Geschlecht: F
Eingang: 08.03.2022
Impfdatum: 08.02.2022
Beginn: 09.02.2022
Tage bis Beginn: 1,0
Dosis: N/A
Route/Site: IM / LA

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

Paraesthesia Pruritus

Symptomtext

Tingling and itching in both hands, same allergic reaction I have with Erythromycin and Sulfa

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Seasonal asthma
Andere Medikamente: Nuvigil, Prozac, Adderall, Biotin, Collegan
Allergien: Erythromycin, Sulfa
Vorherige Impfungen: -

VAERS 2165410

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: TX
Alter: 60,0
Geschlecht: M
Eingang: 08.03.2022
Impfdatum: 05.03.2022
Beginn: 07.03.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / -

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

Atrial fibrillation Condition aggravated Diarrhoea Dyspnoea Dyspnoea exertional Gastroenteritis viral Pain in extremity Pyrexia SARS-CoV-2 test negative Vomiting

Symptomtext

Pt had SOB for the past week. He recently had the stomach flu 2 weeks prior (he and family tested negative for COVID-19). He had fever, vomiting NBNB, diarrhea for several days which then improved. He however did not improve all the way to his baseline and started to feel short of breath with exertion moving around the house. He was unable to lie down flat and had to sleep semi-upright. He was seen by his PCP and prescribed prednisone and azithromycin on 3/1. He did not improve and came to town for his covid booster shot and decided to come in to the EC. He states noncompliant with lovenox because he left it at home and did not expect to stay in town for more than 24 hrs. Patient is on O2 at home and has been having increased need 4L-- >5L. Patient also states he feels his "afib is all over the place." Patient also states rue arm pain. In ED, went into Afrib with RVR.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: Possible worsening community-acquired pneumonia
Vorgeschichte: COPD, neuropathy, HTN, hyperlipidemia, bladder cancer, CHF, T2DM, paroxysmal afib
Andere Medikamente: Atorvastatin, amiodarone, Bacitracin ointment, carbamazepine, divalproex sodium, enoxaparin, esomeprazole, fluticasone/salmeterol, gabapentin, insulin glargine, isosorbide mononitrate, lisinopril, metoprolol succinate, polyethylene glycol,
Allergien: Allergies - codeine (shortness of breath), vancoymcin (itching/rash), iodanated contrast media (hives; gets premedication)
Vorherige Impfungen: Had SOB, tachycardia, elevated resp rate with initial Pfizer COVID-19 series in 5/1/2021

VAERS 2162669

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: PA
Alter: 69,0
Geschlecht: F
Eingang: 07.03.2022
Impfdatum: 02.03.2022
Beginn: 02.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Chest pain

Symptomtext

Patient started having chest pain and feeling weak 15 minutes after the dose was administered. 911 was called and she was transported to the ER for evaluation.

Weitere VAERSDATA-Felder

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

VAERS 2162072

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: OH
Alter: 15,0
Geschlecht: M
Eingang: 06.03.2022
Impfdatum: 05.03.2022
Beginn: 05.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Full blood count Pyrexia Tremor

Symptomtext

103.9 fever (11:00 pm); chills and uncontrollable shaking.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: CBC.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Ritalin LA 10mg
Allergien: -
Vorherige Impfungen: -

VAERS 2162035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CT
Alter: 45,0
Geschlecht: M
Eingang: 06.03.2022
Impfdatum: 11.02.2022
Beginn: 18.02.2022
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / RA

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

Magnetic resonance imaging head normal Paraesthesia

Symptomtext

Approximately 1 week after having the primary dose, I developed tingling/paresthesia in my left lower leg, which subsequently developed on my left forearm and left side of my face. I did not have any change in strength in upper or lower extremities. Symptoms have persistent for the past 2 weeks, seem to come and go, but still persistent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Obtained formal neurology input on 3/4/2022. MRI of the brain with and without contrast was normal. Formal neurology consultation scheduled for 3/98/2022.
Aktuelle Erkrankungen: None
Vorgeschichte: HTN, HLD, Depression, Seasonal Allergies, Eosinophilic Esophagitis, Barrett's Esophagus/GERD COVID-19 Primary Infection - Nov 2020.
Andere Medikamente: Carvedilol, Losartan, Atorvastatin, Fluoxetine, Loratadine, Montelukast, Nexium, Magnesium Oxide.
Allergien: Lisinopril - Dizziness. Green Peas - Anaphylaxis
Vorherige Impfungen: -

VAERS 2161993

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

moderat

Staat: TX
Alter: 17,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 11.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Back pain Dyspnoea Eye pain Hypoaesthesia Pain in extremity Pyrexia

Symptomtext

difficulty breathing, high fever, numb limbs, sore eyes, back ache, leg ache 1/12/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: A reaction to the booster shot 1/12/22
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2161965

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NY
Alter: 101,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 02.03.2022
Beginn: 03.03.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Cardiac failure congestive Chest X-ray abnormal Condition aggravated Dyspnoea Oedema peripheral

Symptomtext

dyspnea, and worsening lower extremity edema beginning next day, CHF on xray, admitted to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: CXR with CHF
Aktuelle Erkrankungen: -
Vorgeschichte: chronic copd, chf, afib, thyroid disease
Andere Medikamente: Albuterol, biotin, calcium, vit d, lasix, levothyroxine, b vitamins, mag oxide, trelegy, verapamil sr, vit a, vitc, zinc
Allergien: morphine
Vorherige Impfungen: -

VAERS 2161807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: 27,0
Geschlecht: M
Eingang: 05.03.2022
Impfdatum: 20.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Paraesthesia Sensory disturbance

Symptomtext

extreme sensation where when he touches his skin he feels pins and needles; has been experiencing a sharp sensation in his mouth when he eats something cold as well; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from medical information team. A 27 year-old male patient received bnt162b2 (BNT162B2), administration date 20Feb2021 (Lot number: FJ6369) at the age of 27 years as dose 3 (booster) (tris), single for covid-19 immunisation. Relevant medical history included: "Interchange of vaccine products" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Moderna (Dose number: 1, received his primary series of Moderna COVID-19 vaccine, starting in Dec2020), administration date: Dec2020, when the patient was 26 years old, for COVID-19 immunization; Moderna (Dose number: 2, received his primary series of Moderna COVID-19 vaccine, starting in Dec2020), for COVID-19 immunization. The following information was reported: PARAESTHESIA (non-serious), outcome "unknown", described as "extreme sensation where when he touches his skin he feels pins and needles"; SENSORY DISTURBANCE (non-serious), outcome "unknown", described as "has been experiencing a sharp sensation in his mouth when he eats something cold as well". Additional information: There was no PQC present. Call was transferred from the agency (Agent: (withheld), NT ID: #, Report number: #). Caller stated that he had a patient (Male, 27-years-old) who received his primary series of Moderna COVID-19 vaccine, starting in Dec2020 and who received his booster dose of the Pfizer-BioNTech COVID-19 vaccine on Sunday [20Feb2021]. Our patient has been experiencing some symptoms we has never seen before, an extreme sensation where when he touched his skin he feels pins and needles and he has been experiencing a sharp sensation in his mouth when he eats something cold as well". Caller asked that "Has an extreme sensation where after being touched, patients feel pins and needles on their skin being reported following administration of the Pfizer-BioNTech COVID-19 vaccine. Agency: E-transmitting as potential duplicate AE as caller declined warm-transfer to agency. Caller stated: "I will file a report online. I have to do so before". Information on previous reports was not requested. Callback was provided on 23Feb2022 at 11:37 am to provide additional information as per attached. Disclaimer was provided: "This call was being reported for training and quality assurance purposes". Caller asked "Has a sharp sensation the mouth when a patient eats something cold being reported following administration of the Pfizer-BioNTech COVID-19 vaccine". Patient was also not the reporter. Reporter stated, "Yes, and these side effects that I haven't seen with any other patient with Pfizer and I wasn't sure if you guys have had any similar cases." Reporter was informed about the role of Pfizer Drug Safety and also informed that Pfizer Medical Information is the concerned department to answer the question that reporter have regarding the vaccine and offered the number. Reporter was provided with the number of Pfizer Medical Information # # and was requested to select option 3, timings as and 8 am to 9 pm Monday to Fridays as per and also provided the website as (email withheld). When requested to probe to file a safety report, reporter asked can you transfer me to the department, so he can speak with that medical department. Call was placed on hold to transfer to Pfizer Medical Information, however reporter hung up the call abruptly before getting transferred, hence transfer unsuccessful. Further probing could not be done as the reporter was unwilling to share any further information. Hence limited information available over the call. QR Comment: Reporter type could not be probed as the reporter was unwilling to share any further information, hence captured by default as consumer or other non-health professional in tab. Report was not related to a study or program. Other Health professional was physician assistant. Caller did not wish to provide a mailing address and did not wish to complete report, stating she would do it online instead.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Interchange of vaccine products
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2161715

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NY
Alter: 49,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 14.02.2022
Beginn: 15.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / RA

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

Erythema Fatigue Hypoaesthesia Insomnia Lymphadenopathy Pain Paraesthesia Peripheral swelling

Symptomtext

severe pain; Right arm swelling; redness; hand numbness and tingling; hand numbness and tingling; right axillary lymph node enlargement; insomnia due to pain; insomnia due to pain; severe fatigue; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 49 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 14Feb2022 04:30 (Lot number: FJ6369) at the age of 49 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Arthritis" (unspecified if ongoing); "tachycardia" (unspecified if ongoing); "GERD" (unspecified if ongoing). No known allergies. Concomitant medication(s) included: PROTONIX [OMEPRAZOLE]; PROPRANOLOL; VITAMIN D [COLECALCIFEROL]. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: E43246, Location of injection: Arm Left), administration date: 13Jan2021, when the patient was 48 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EH9899, Location of injection: Arm Left), administration date: 23Dec2020, when the patient was 48 years old, for Covid-19 immunization. No other vaccine in four weeks. The following information was reported: PAIN (medically significant) with onset 15Feb2022 07:00, outcome "recovering", described as "severe pain"; PERIPHERAL SWELLING (non-serious) with onset 15Feb2022 07:00, outcome "recovering", described as "Right arm swelling"; ERYTHEMA (non-serious) with onset 15Feb2022 07:00, outcome "recovering", described as "redness"; HYPOAESTHESIA (non-serious), PARAESTHESIA (non-serious) all with onset 15Feb2022 07:00, outcome "recovering" and all described as "hand numbness and tingling"; LYMPHADENOPATHY (non-serious) with onset 15Feb2022 07:00, outcome "recovering", described as "right axillary lymph node enlargement"; INSOMNIA (non-serious), PAIN (non-serious) all with onset 15Feb2022 07:00, outcome "recovering" and all described as "insomnia due to pain"; FATIGUE (non-serious) with onset 15Feb2022 07:00, outcome "recovering", described as "severe fatigue". Due to the events the patient missed 2 days of work so far. No covid prior vaccination. No covid tested post vaccination. Therapeutic measures were taken as a result of pain, peripheral swelling, erythema, hypoaesthesia, paraesthesia, lymphadenopathy, insomnia, pain, fatigue included Tylenol , Ibuprofen, Benadryl ice packs. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on current available information, there is reasonable possibility of causal association between the event pain and the suspect drug BNT162B2

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis; GERD; Tachycardia
Andere Medikamente: PROTONIX [OMEPRAZOLE]; PROPRANOLOL; VITAMIN D [COLECALCIFEROL]
Allergien: -
Vorherige Impfungen: -

VAERS 2157630

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NC
Alter: 40,0
Geschlecht: F
Eingang: 04.03.2022
Impfdatum: 28.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Palpitations

Symptomtext

Patient experienced palpitations about 5 minutes after receiving second dose. Patient placed in recliner and vital signs monitored for 30 minutes. Vital signs within normal limits. Pulse Ox: 100%. No shortness of breath, rash or discoloration noted. After 30 minutes observation, patient stable and stated she felt much better.

Weitere VAERSDATA-Felder

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

VAERS 2109448

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: SC
Alter: 48,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 04.02.2022
Beginn: 14.02.2022
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / LA

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

Blood creatine phosphokinase C-reactive protein Chest X-ray Chest pain Dyspnoea Chills Fatigue Night sweats Palpitations Electrocardiogram Electrocardiogram ambulatory Full blood count Metabolic function test Red blood cell sedimentation rate Panic attack Thyroxine Troponin

Symptomtext

Chest pain/ Shortness of breath

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: CBC, CMP, Trop, ESR, CRP, CK, T4, ECG, Holter Monitor, Chest x-ray,
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes Mellitus type 2 Myasthenia Gravis Rheumatoid Arthritis Obstructive Sleep Apnea
Andere Medikamente: acetaminophen (generic for TYLENOL) 325mg tablet albuterol HFA (ProAir HFA) 108 (90 BASE)mcg/act inhaler 18 g Calcium Carb-Cholecalciferol 500-400 MG-UNIT chewable tablet cetirizine (generic for ZyrTEC) 10mg tablet clonazePAM (generic f
Allergien: Acetylcholine Aminoglycosides Apple Bacitracin Droperidol Echothiophate Emetine Erythromycin Ethosuximide Gallamine Gallium (radioactive Isotope) Haloperidol Hydromorphone Lidocaine Lincomycin Penicillins Phenytoin Sulfa Antibiotics
Vorherige Impfungen: -

VAERS 2147688

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: WA
Alter: 38,0
Geschlecht: F
Eingang: 27.02.2022
Impfdatum: 26.02.2022
Beginn: 26.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Chest pain Dizziness Dyspnoea Headache

Symptomtext

Severe headache, dissyness, chest pain and difficulty breathing, joint pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Aurovela 1.5/30
Allergien: None
Vorherige Impfungen: -

VAERS 2137666

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NM
Alter: 28,0
Geschlecht: F
Eingang: 24.02.2022
Impfdatum: 18.02.2022
Beginn: 18.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dysphagia Dyspnoea Neck pain Oedema peripheral Oropharyngeal pain Pain Sensory disturbance Skin discolouration Skin warm Vasodilatation

Symptomtext

Patient reported after getting booster pfizer had neck and throat pain and right arm pain and noticed veins protruding but this resolved. Pain has come down and now is 4/10. She had some swelling of arm pit area around quarter then these have reduced in size with of warm and ibuprofen. Today has shrunk even more and is the size of a penny. Noticed darker skin around the wrist but has cleared up. No fever no chills. Reported had some balls in the neck sensation and reported feeling difficult to swallow and breath but this has resolved this am.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Chronic foot pain
Vorgeschichte: Type A blood, Rh negative, Vitamin D deficiency
Andere Medikamente: None
Allergien: Cat dander, strawberry and latex
Vorherige Impfungen: -

VAERS 2134776

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: IL
Alter: 60,0
Geschlecht: F
Eingang: 23.02.2022
Impfdatum: 09.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Chills Decreased appetite Diarrhoea Dizziness Dyspnoea Fatigue Insomnia Malaise Myalgia Pain in extremity

Symptomtext

Arm pain, diarrhea, Insomnia, Decreased appetite, short of breath, Chills, Feeling unwell, dizziness, muscle soreness, Tiredness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Due to dose 1 Dizziness and sore muscles.
Vorgeschichte: Huntington's Disease and Thyroid
Andere Medikamente: Levothyroxine, B12 vitamin and Cinnamon herb
Allergien: Latex and penicillin
Vorherige Impfungen: -

VAERS 2134579

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: WY
Alter: 63,0
Geschlecht: F
Eingang: 23.02.2022
Impfdatum: 20.01.2022
Beginn: 27.01.2022
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: SYR / RA

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

Blood test Catheterisation cardiac abnormal Chest X-ray Chest pain Dyspnoea Nausea

Symptomtext

I had to have my heart check so they did a heart cath I started having a hard time breathing on the rt side of my chest i could barely breath it hurt so much & I was nauseous so I went to the Emergency Room & was given meds during night it got worse & i was admitted into hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 5,0
Labordaten: Bloodwork Chest xrays
Aktuelle Erkrankungen: None
Vorgeschichte: MCTD Constrictive Bronchitis Diabetes
Andere Medikamente: Tylenol Oxygen Carvedilol Raglen Torsemide Allopurinol Clopidogrel Escitalopram Levothyroxine Omeprazole Potassium Spironolactone Pramipexole Atorvastatin Magnesium lactate Novalen Vitamin d3
Allergien: -
Vorherige Impfungen: -

VAERS 2131089

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NY
Alter: 56,0
Geschlecht: M
Eingang: 22.02.2022
Impfdatum: 16.02.2022
Beginn: 16.02.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Dizziness Headache Hypertension Palpitations

Symptomtext

Started having Hypertension, intermittent palpitations 1 hour after Covid-19 booster today. Persistent occipital headache rates 5-7/10 and mild dizziness throughout today.

Weitere VAERSDATA-Felder

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

VAERS 2128397

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: FL
Alter: 14,0
Geschlecht: F
Eingang: 20.02.2022
Impfdatum: 19.02.2022
Beginn: 19.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Asthenia Dizziness Flushing Hyperhidrosis Hypotension Visual impairment

Symptomtext

Systemic: Abdominal Pain-Mild, Systemic: Dizziness/Lightheadedness-Mild, Systemic: Flushed/Sweating-Mild, Systemic: Hypotension-Mild, Systemic: Visual Changes/Disturbances-Mild, Systemic: Weakness-Mild, Additional Details: 14-year-old female arrived with parents. Discussed her nervousness; stated last shot was flu shot (painful). No history of "passing out." Had patient stay in seat for 2 to 3 minutes prior to moving to observation area. About 3 to 5 minutes later, she was weak and leaning with eyes closed over mom's shoulder. Called 911. She reported seeing spots; had her move from chair to floor. She was able to sit-up straight and keep eyes open. Vitals every 5 minutes, 92/49-100/72mmHg, 68-93bpm at 15:25-15:40. EMS arrived. Patient went home.

Weitere VAERSDATA-Felder

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

VAERS 2127959

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NY
Alter: 35,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 05.02.2022
Beginn: 06.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Condition aggravated Lymphadenopathy Migraine Pain

Symptomtext

Swollen lymph nodes in left armpit and neck that lasted a week and triggered multiple migraine attacks due to the soreness from the swelling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Chronic migraine
Andere Medikamente: norethindrone
Allergien: N/A
Vorherige Impfungen: -

VAERS 2124618

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: SC
Alter: 49,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 13.02.2022
Beginn: 13.02.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Chest pain

Symptomtext

Burning in chest

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: High blood pressure
Vorgeschichte: -
Andere Medikamente: -
Allergien: codeine
Vorherige Impfungen: -

VAERS 2123185

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: TX
Alter: 23,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 17.02.2022
Beginn: 18.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Hyperhidrosis Migraine Pain

Symptomtext

EE received COVID Booster on 2-17-22 around 1600pm. EE went home after shift. At 4am she awoke to chills, sweats, migraine, and body aches. EE missed work on 2-18-2022. EE received a Pfizer lot# FJ6369 in her Left arm.EE taking OTC medication Tylenol to relieve her migraine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: unknown
Allergien: N/A
Vorherige Impfungen: Pfizer Covid-19 Lot# UL3248 2/4/2021

VAERS 2119706

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NY
Alter: 15,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 09.02.2022
Beginn: 09.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test normal Dizziness Dyspnoea Electrocardiogram normal Eye movement disorder Headache Loss of personal independence in daily activities Pregnancy test negative Pyrexia Vomiting projectile

Symptomtext

She reacted to the first and 2nd vaccine the same. Bad headache, lightheaded. I gave her some Advil, she had a slight fever. Next morning she went to school but she called me to pick her up that she was really dizzy. She had a fever, headache, and dizzy spells that were stagnant and getting worse for the next couple of days. She began to projectile vomit and it was so strong I have never seen any of my kids vomit that way. She could not even breathe because it would not stop. Her eyes were rolling back, and it was just coming out. I took her to the ER room, and they took her right in. They claimed it was related to the vaccine. They gave her medication ondansetron, commonly known as Zofran. They were trying to get her to eat and she did not want to. Another doctor came in and did an EKG on her, they gave her an IV. They discharged her with Zofran and to remain on fluids.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG and blood work, nothing came out of it. Pregnancy test done that was negative.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Fructose intolerance; cadambine
Vorherige Impfungen: -

VAERS 2119294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: FL
Alter: 21,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / UN

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

Cyanosis Dyspnoea

Symptomtext

Patient received 1st dose Pfizer at 1245 on 12/17/2022. Five minutes into observation, patient began complaining of shortness of breath, difficulty breathing, and bluish discoloration was present around her lips. Interventions Performed: 1250 Vitals were taken ? 94% oxygen saturation and 108 heart rate, and Safety Specialist called emergency medical services (EMS). Patient was given Benadryl 50mg at 1259. Symptoms did not improve. Epinephrine was administered at 1304 ? NDC 4950210201, Lot number 0FM499, Exp 5/22. Immediately patient experienced relief of symptoms. Vitals taken again - 129/79 blood pressure, 99% oxygen saturation, 91 heart rate. Patient Outcome: Patient was transferred to care of EMS at 1315 ? patient headed to hospital ED. Concern/Issue Resolved?: Immediate danger resolved ? patient in care of EMS 911 Contacted?: Yes Patient Transported Via EMS?: Yes Did Patient Refuse EMS Transport Upon Arrival?: No

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none stated
Vorgeschichte: Asthma
Andere Medikamente: none stated
Allergien: egg whites,dairy,gluten,bacitracin, flu vaccine
Vorherige Impfungen: -

VAERS 2119094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MO
Alter: 45,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 01.02.2022
Beginn: 15.02.2022
Tage bis Beginn: 14,0
Dosis: 2
Route/Site: SYR / LA

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

Dyspnoea Fatigue Headache Muscle spasms Pain Respiratory tract congestion Streptococcus test Urine analysis Viral test

Symptomtext

About a week later, I have a severe fatigue, SOB, headaches, body aches, muscle cramping, and congestion. These lasted for about 8 days. I went to the doctor about this. They did a strep, pneumonia, sinus, and a UTI test.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Strep Pneumonia Sinus urine sample
Aktuelle Erkrankungen: N/a
Vorgeschichte: N/a
Andere Medikamente: N/a
Allergien: N/a
Vorherige Impfungen: -

VAERS 2113357

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NY
Alter: 34,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 10.02.2022
Beginn: 11.02.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Chest pain Dyspnoea Nausea Pain Pyrexia

Symptomtext

34 yo female, denies PMH, called to report chest pain which occurred Friday, 2/11/22 and she believes was a related to receiving the COVID19 booster shot. Pfizer mRNA covid10 vaccine at facility 2/10/22, she had mild fever, body aches and nausea that evening. At 3am on 2/12/22 she awoke with middle of the chest pain, sharp and severe, non-radiating and was associated with SOB. Resolved with a few sips of water while resting on bed after 10 min. Now she feels completely well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2112767

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: VA
Alter: 51,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 10.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Blood glucose normal Chest X-ray normal Chest discomfort Chest pain Chills Dizziness Fibrin D dimer Hypertension Limb discomfort Tachycardia Wheezing

Symptomtext

Patient experienced full body chills approximately 5 minutes following vaccine administration. Approximately 10-15 minutes are administration, patient began to experience weakness, "heaviness" in bilateral legs, hypertension (152/98), tachycardia (112 bpm), and lightheadedness. Approximately 30 minutes after vaccination, patient was evaluated by MD and noted to be wheezing. Patient given albuterol nebulizer and 25 mg of Diphenhydramine. Wheezing resolved. Patient was sent home by MD. 02/11/2022- Patient contacted MD regarding continued symptoms. She was prescribed Prednisone and given Albuterol inhaler. 02/14/2022- Patient returned to clinic and was evaluated by FNP. Patient reported chest pain/pressure, tachycardia, continued hypertension, and continued weakness. She had negative chest xray and negative d-dimer. Patient was sent home by FNP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 02/10/2022- Glucose 82 02/14/2022- d-dimer 107 02/14/2022- chest xray negative
Aktuelle Erkrankungen: none
Vorgeschichte: diastolic dysfunction, anxiety, eczema, anxiety, migraine, obstructive sleep apnea, obesity, insomnia
Andere Medikamente: Amitriptyline, Aspirin 81 mg, Breztri Aerosphere, hydroxyzine, lipitor, omeprazole, triamcinolone acetonide 0.1%, Xanax
Allergien: Biaxin, Flu shot, Metoprolol Tartrate, Phenergan, pseudophedrine, Tetanus vaccine, Zithromax
Vorherige Impfungen: Flu shot (rash, swelling), Tetanus vaccine (unknown reaction)

VAERS 2111082

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

moderat

Staat: FL
Alter: 54,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 14.02.2022
Beginn: 14.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chills Dizziness Dyspnoea Nausea Pharyngeal swelling Pyrexia Rash Tremor

Symptomtext

PATIENT CAME IN TO RECEIVE HER 2ND DOSE OF PFIZER VACCINE. SHE APPEARED PHYSICALLY AND EMOTIONALLY NORMAL. AFTER RECEIVING THE VACCINE WE ASKED HER TO SIT FOR 15 MINUTES. AFTER 5 MINUTES, HER HUSBAND NOTIFIED US SHE WAS FEELING NAUSEOUS. I CAME OVER TO CHECK AND SHE SHOWED ME A RASH SPOT ON HER NECK. SHE SAID SHE HASN'T HAD ANY OF THESE EFFECTS WITH THE FIRST SHOT. SHE STATED SHE DID EAT BEFORE COMING HERE. PATIENT'S BODY STARTED SHAKING AND SHE SAID SHE WAS DIZZY. HER HUSBAND SAID SHE IS PROBABLY VERY NERVOUS. WE MOVED HER INTO A ROOM AWAY FROM THE CROWD FOR HER TO CALM DOWN. I ASKED THE STORE MANAGER TO CALL 911. SHE LATER ON COMPLAINED OF CHILL AND FEVERISH AND I GAVE HER 2 TABLETS OF IBUPROFEN 200 MG (AS SHE USUALLY TAKES THESE FOR HER BACK PAIN EXCEPT TODAY DUE TO HAVING THE SHOT.) I GAVE HER 1 EPIPEN AFTER SHE SAID HER THROAT FELT SWOLLEN AND IT'S DIFFICULT FOR HER TO BREATH. SHE SAID SHE FELT BETTER BUT SHE WAS STILL SHAKING. HER HUSBAND SAID SHE HAS LUPUS AND HER IMMUNE SYSTEM IS NONEXISTENT. SHE IS AFRAID OF GOING TO THE HOSPITAL BUT EMS CONVINCED HER SHE NEEDS TO BE MONITORED. SHE WAS SHAKING TOO MUCH I COULDN'T GET HER BP AND PULSE. HER RESPIRATION PER MIN WAS NORMAL 15 BEATS PER MINUTE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Lupus
Andere Medikamente: Ibuprofen for back surgery
Allergien: None
Vorherige Impfungen: -

VAERS 2110392

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MO
Alter: 45,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Asthma Back pain Chest discomfort Chills Condition aggravated Fatigue Inflammation Laboratory test Lymphadenopathy Menstruation irregular Migraine Secretion discharge Sinusitis Urticaria Vertigo positional

Symptomtext

Fatigue, Migraine, Chills Hives on face 1 hour after 3rd dose Asthma inflammation - mucous, extreme chest tightness 24-36 hours after 3rd dose; asthma flare-up lasted 2 weeks, Neck lymph nodes swollen, Menstruation (cycle) changed, Inflammation chest cartilage, Constant back aches, Sinus infection with benign positional vertigo

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: February 5
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Advair 500/50, Spiriva Respimat Inhaler, Albuterol sulfate HFA, Progesterone Cream, Zyrtec, Azelastine nasal spray, Nasocort, Cordyceps (mushroom concentrate for breathing), 5 Defenders (mushroom concentrate for immunity), Magnesium, Berber
Allergien: Ibuprofen
Vorherige Impfungen: -

VAERS 2109748

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

moderat

Staat: NY
Alter: 33,0
Geschlecht: M
Eingang: 14.02.2022
Impfdatum: 07.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

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

Dizziness Dyspnoea Electrocardiogram normal Palpitations

Symptomtext

I developed palpitations, along with lightheadedness 3 days post my 3rd booster. Noted increased work of breathing with light exertion. No chest pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG within normal limits
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Vitamin D One a day mens
Allergien: -
Vorherige Impfungen: -

VAERS 2109615

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: IN
Alter: 49,0
Geschlecht: F
Eingang: 13.02.2022
Impfdatum: 21.01.2022
Beginn: 22.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal discomfort Diarrhoea Dyspnoea Gait disturbance Paraesthesia Swelling Swelling face Vomiting

Symptomtext

Full body swelling, gastrointestinal distress,diarrhea, vomiting, shortness of breath, swelled face and neck. Used diphenhydramine and an epi pen to stop swelling. Lost feeling in left arm and proceeded to Lose feeling in both hands and feet for 48 hours. Difficulty walking due to no feet for 48 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Epstein barr in remission
Vorgeschichte: Chronic fatigue and fibromyalgia both in remission
Andere Medikamente: Diphenhydramine and tylenol
Allergien: Latex, preservatives, steroids, floxins
Vorherige Impfungen: Flu vaccine

VAERS 2109508

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: IN
Alter: -
Geschlecht: U
Eingang: 13.02.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Body temperature increased Dyspnoea Nausea Pain Productive cough

Symptomtext

Temp 101.4, severe nausea, body aches. The most concerning is the amount of mucus i starting coughing up and significant SOB with walking at all, even just to the bathroom, I would would be struggling to breathe.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Influenza- severe reaction 44 yo ED tx steroids, multiple meds and was sick for weeks

VAERS 2109387

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: IL
Alter: 35,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 28.01.2022
Beginn: 03.02.2022
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: SYR / LA

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

Angina pectoris Blood test normal Chest pain Electrocardiogram normal Heavy menstrual bleeding Musculoskeletal chest pain Oligomenorrhoea

Symptomtext

I received both doses of the Pfizer-BioNTech COVID-19 Vaccine in January 2022. Since receiving the vaccination my menstrual cycle has been heavier and longer than normal. Also, I have also experienced what I would describe as frequent heart and or chest pain. I went to an Emergency Room (ER) for the chest pain on 02/03/2022. The staff performed an EKG and collected blood. I was told that the EKG and lab work results were all normal. My diagnosis was Chest Wall Pain. I still experience frequent chest wall pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: The staff performed an EKG and collected blood at the ER.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 2108785

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: -
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 10.01.2022
Beginn: 01.01.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Dizziness Dysgeusia Dyspnoea Loss of personal independence in daily activities Paraesthesia oral

Symptomtext

Unstable lightheaded/ severe Lightheadedness; Dizzy/ Woozy feeling; Little shortness of breath; Tingling sensation in my lip; Funny taste in my mouth; Cant drive the car; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A female patient received bnt162b2 (COMIRNATY), administration date 10Jan2022 (Lot number: FJ6369) as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Autoimmune disease" (unspecified if ongoing), notes: I have an autoimmune disease. The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Dose: 1, MANUFACTURER UNKNOWN), for COVID-19 Immunization, reaction(s): "light headedness"; Covid-19 vaccine (Dose: 1,MANUFACTURER UNKNOWN), for COVID-19 Immunization, reaction(s): "pain"; Covid-19 vaccine (Dose: 2, MANUFACTURER UNKNOWN), for COVID-19 Immunization, reaction(s): "light headedness", "pain". The following information was reported: LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious) with onset Jan2022, outcome "recovered" (Jan2022), described as "Cant drive the car"; DIZZINESS (non-serious) with onset 10Jan2022, outcome "not recovered", described as "Unstable lightheaded/ severe Lightheadedness"; DIZZINESS (non-serious) with onset Jan2022, outcome "unknown", described as "Dizzy/ Woozy feeling"; DYSPNOEA (non-serious) with onset Jan2022, outcome "unknown", described as "Little shortness of breath"; PARAESTHESIA ORAL (non-serious) with onset Jan2022, outcome "unknown", described as "Tingling sensation in my lip"; DYSGEUSIA (non-serious) with onset Jan2022, outcome "unknown", described as "Funny taste in my mouth". Additional information: The prior 2 shots patient felt some light headedness the 1st day or so, but had more pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Autoimmune disorder (I have an autoimmune disease)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2092084

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: IN
Alter: 38,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 01.02.2022
Beginn: 01.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Dyspnoea Hypersensitivity Pyrexia Rash Urticaria Migraine Pain in extremity Peripheral swelling SARS-CoV-2 test Vaccination site rash

Symptomtext

major allergic reaction; broke out in a rash, hives and whelps on arm where second dose Pfizer Adult Covid Vaccine was given; broke out in a rash, hives and whelps on arm where second dose Pfizer Adult Covid Vaccine was given; had a fever of 103 for 4 days; Had breathing problems two nights after receiving the second dose; Had a rash on arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 38 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 01Feb2022 13:00 (Lot number: FJ6369) at the age of 38 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Verbatim: Use to get migraines quite a bit." (unspecified if ongoing), notes: The caller use to get migraines quite a bit and received Botox for this. The last time the caller received Botox was in 2020.; "Shellfish" (ongoing), notes: Verbatim: Allergic to Iodine and Shellfish, caller had the reaction when was 14 or 15 years old. There were no concomitant medications. Past drug history included: Iodine for Known allergies: Iodine, notes: Known allergies: Iodine, caller had the reaction when was 14 or 15 years old. Vaccination history included: Bnt162b2 (First dose: 22DEC2021 , lot: 331308A, NDC: 59267-1000-03 , Expiration: 28FEB2022, Route of administration: left arm, .), administration date: 22Dec2021, when the patient was 37 years old, for COVID-19 Immunization, reaction(s): "Had a migraine for three days", "Headache". The following information was reported: HYPERSENSITIVITY (medically significant), outcome "unknown", described as "major allergic reaction"; PYREXIA (non-serious) with onset 06Feb2022, outcome "not recovered", described as "had a fever of 103 for 4 days"; VACCINATION SITE RASH (non-serious), URTICARIA (non-serious) all with onset 07Feb2022, outcome "unknown" and all described as "broke out in a rash, hives and whelps on arm where second dose Pfizer Adult Covid Vaccine was given"; DYSPNOEA (non-serious) with onset 02Feb2022, outcome "recovering", described as "Had breathing problems two nights after receiving the second dose"; RASH (non-serious) with onset 01Feb2022, outcome "recovering", described as "Had a rash on arm". Therapeutic measures were taken as a result of hypersensitivity, pyrexia, vaccination site rash, urticaria, rash. The caller had a major allergic reaction after receiving the second dose Adult Pfizer Covid Vaccine. The caller should have gone to the hospital but was a caregiver and did not want to leave 9 year old at home. The caller broke out in a rash, hives and whelps on arm where second dose Pfizer Adult Covid Vaccine was given, its like hard on the arm. The rash was going away today, 07Feb2022, but this was day 7 of the rash. The caller talked to the pharmacist. The caller had taken Benadryl pill, Benadryl cream and Tylenol. The patient called the family doctor on Saturday 05Feb2022, and the doctor made a note about the patient's reaction. Benadryl pill: lot: 1862T13; expiration: Feb2023. Benadryl cream: expiration: Jun2023. Tylenol: The caller just took some Tylenol last night, 06Feb2022. lot: AMA063; expiation Aug2023. No other vaccines administered on the same date with the Pfizer vaccine considered as suspect. AE(s) require a visit to: Emergency Room? Physician Office? No, caller spoke with doctor via phone. No other vaccinations within 4 weeks prior to the first administration of vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Shellfish allergy (Allergic to Iodine & Shellfish caller had reaction when was 14 or 15 years old)
Vorgeschichte: Medical History/Concurrent Conditions: Migraine (used to get migraines quite a bit & received Botox (last received in 2020))
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2104958

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: IL
Alter: 41,0
Geschlecht: M
Eingang: 11.02.2022
Impfdatum: 04.02.2022
Beginn: 04.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / AR

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

Chills Cough Decreased appetite Fatigue Feeling abnormal Feeling drunk Headache Hypersomnia Mobility decreased Musculoskeletal stiffness Pain Productive cough Pyrexia Rash pruritic SARS-CoV-2 test negative Sluggishness Vomiting

Symptomtext

Same day as vaccine I began to have an itchy rash develop. The next day I was feeling sluggish and not like myself, comparable to being inebriated. By 07:00PM day after vaccination, I was bedridden and pretty much slept for 3 days straight. Appetite was gone and if I did eat anything the food would come back out. Coughing and vomiting caused pain as well as headaches that came on. Fever of 101, body ache, chills, fatigue, muscle stiffness. Codeine cough syrup was prescribed to help with pain however cough is starting to improve however phlegm is still coming up. Achiness, fatigue, and loss of appetite comes and goes in comparison to when this all began. Headaches and fever have gone away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Covid Test: Negative
Aktuelle Erkrankungen: Wisdom Tooth being pulled
Vorgeschichte: Asthma, High blood pressure, Anxiety, PTSD
Andere Medikamente: Stopped taking prescriptions two days prior to vaccine. Clonidine , Duloxetine 3 times daily, Inhaler, Boosterone 1 tab twice daily, Losartan twice daily
Allergien: N/A
Vorherige Impfungen: -

VAERS 2101593

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NY
Alter: 40,0
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: 09.02.2022
Beginn: 09.02.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Interchange of vaccine products Paraesthesia Pruritus

Symptomtext

Pt. reported hives with previous doses of Moderna, as this was not a severe adverse event we proceeded with vaccination with Pfizer. We pre-administered 25mg of Benadryl orally, however pt. still had itching and tingling sensation in limbs a few minutes after receiving the vaccine. Approximately 15 minutes after injection, we orally administered 60mg of prednisolone, which decreased the itching. As itching was still present after about 45 min of observation after prednisolone administration, we gave pt. another oral dose of Benadryl 25mg. Pt. reported resolution of symptoms shortly thereafter, and we discharged pt. from clinic with prescriptions for oral cetirizine 10mg prn and oral prednisone 60mg prn.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Monitoring of vital signs, normal throughout visit.
Aktuelle Erkrankungen: Seasonal and perennial allergic rhino conjunctivitis, History of 2019 novel coronavirus disease (COVID-19), Grief reaction, Migraine with aura with intractable migraine, so stated, with status migrainosus, Moderate persistent asthma
Vorgeschichte: see above
Andere Medikamente: cetirizine (Zyrtec) 10 mg tablet, cyclobenzaprine (FLEXERIL) 10 mg tablet, mometasone 200 mcg/actuation HFAA, montelukast (SINGULAIR) 10 mg tablet, albuterol HFA (ProAir HFA) 90 mcg/actuation inhaler, acetaminophen prn, ibuprofen prn
Allergien: Hives when receiving Moderna Covid-19 vaccine
Vorherige Impfungen: Moderna Covid vaccines, hives, on 4/26/21, and 5/21/21.

VAERS 2101555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: OH
Alter: 52,0
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: 02.02.2022
Beginn: 03.02.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / -

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

Asthenia Chills Condition aggravated Fatigue Feeling abnormal Feeling cold Impaired work ability Pain Rectal haemorrhage

Symptomtext

2 nd. Pfizer shot. I woke up freezing, had shivers all day. I had pains all over my body in odd places. Never felt this way in my life. Late morning, early afternoon hours, I was out of it, not aware of my surroundings. Husband and son took care of me. Four days after the shot I bled from my rectum again. This also happened with the first Pfizer shot. I missed work for two days. No strength on second day. My body was worn out from the first day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: No tests. I did not go see my doctor. I have not visited him yet this year.
Aktuelle Erkrankungen: None.
Vorgeschichte: -
Andere Medikamente: Metformin, valsartan, Biotin, B-12
Allergien: latex, nickel, balsam, cobalt, various herbs, citrus
Vorherige Impfungen: -

VAERS 2098522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MN
Alter: 42,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 08.02.2022
Beginn: 08.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Cough Nausea Paraesthesia Rash erythematous Rash macular Throat tightness

Symptomtext

Patient received first pfizer covid vaccine at vaccine hub at 1:25 pm. 1:35 PM Patient developed a dry cough and tightness in the upper chest and throat. O2- 100%, HR-75. RN gave 25mg liquid bendryl and requested urgent care to send a nurse. 1:46 PM Dry cough and chest tightness improving. O2- 100%, HR-75. Patient reported feeling "tingly" in her hands and nauseous. Noted red blotchy rash on chest running down each arm. Triage RNs evaluated patient and advised she be taken to ED. Patient agreed and called her mother to pick her up and take her to ED. 2:30 PM Patient no longer coughing and states the chest tightness is improving. O2- 100%, HR-76, BP-153/101. Patient was driven to ED by her mom.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: OSA, Generalized Anxiety Disorder, Morbid Obesity
Andere Medikamente: -
Allergien: Penicillin (anaphylaxis), cymbalta, ciprofloxacin, gabapentin, contrast dye, hydrocodone, keflex, sulfa drugs
Vorherige Impfungen: -

VAERS 2201239

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

moderat

Staat: -
Alter: 63,0
Geschlecht: F
Eingang: 08.02.2022
Impfdatum: 27.01.2022
Beginn: 26.01.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Anxiety Feeling abnormal Headache Hypertension Injection site discomfort

Symptomtext

Headache, HYPERtension, anxiety, foggy Narrative: pt stated with 2nd pfizer vaccination, she had reaction and went to ER. so she wanted to be monitored closely after the booster dose. pt seemed very anxious. requested to check b/p frequently, sbp ranged from 181-207, dbp 84-100.pt started to c/o HA, fogginess and left arm injection site. denies of SOB or chest pain. called 911 for ER eval

Weitere VAERSDATA-Felder

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

VAERS 2096051

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: WA
Alter: 49,0
Geschlecht: F
Eingang: 08.02.2022
Impfdatum: 08.02.2022
Beginn: 08.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Dysarthria Dyspnoea Feeling abnormal Hypoaesthesia Muscular weakness

Symptomtext

Numbness, shortness breath, weakness in the extremities, fuzzy head, slurring words still having symptoms

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Vitamin D, Vitamin B12, Omega, Buproprion 450 mg 1xday, Modafinil 100mg 1xday, Seroquel 100 mg 1xday, Vraylar 1.5mg 1xday
Allergien: Milkfat Amoxicillian Percocet Percodan Hydrocodone
Vorherige Impfungen: -

VAERS 2095832

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MN
Alter: 20,0
Geschlecht: F
Eingang: 08.02.2022
Impfdatum: 25.01.2022
Beginn: 25.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anxiety Chest pain Condition aggravated Dyspnoea Paraesthesia Saliva altered Sensation of foreign body

Symptomtext

patient reported to pharmacist left chest pain, shortness of breath, ball in throat (sticky saliva), tingling in left arm down to fingertips and feelings of anxiety

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: blood pressure taken every five mintues, pulse monitored blood pressures were within normal limits as well as pulse, pt sat in pharmacy for 45 mintutes until self report able to go to work. patient color was good upon leaving pharmacy, called pt to make sure she got to work safe and f/u next afternoon. patient currently working on covid unit at a skilled nursing facility
Aktuelle Erkrankungen: patient reports no acute illness, patient reports untreated depression and anxiety and mood disorder
Vorgeschichte: depression, anxiety, mood disorder
Andere Medikamente: not taking prescribed medications at this time
Allergien: nkda
Vorherige Impfungen: -

VAERS 2095611

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 35,0
Geschlecht: F
Eingang: 08.02.2022
Impfdatum: 20.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / -

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

Chest pain Chills Condition aggravated Dizziness Electrocardiogram normal Eye pain Eyelid disorder Facial pain Feeling hot Flushing Headache Heart rate increased Hypoaesthesia Immediate post-injection reaction Insomnia Nausea Neck pain Neuralgia

Symptomtext

Immediately right after the dose in the left arm I felt a flush feeling in my body, dizzy, nausea, rapid heart beat, and felt really hot. Stayed at the clinic for about 1 hour. Had to laydown immediately after the injection. Sat with the EMT and the on Site Nurse came over to assist off and on. They did my blood pressure, oxygen level, and monitored my heart rate. They had Ice packs on my face and Neck. After 30 minutes I was able to sit up and they put me in a wheelchair for a little bit. Symptoms eased up and I went home to lay in bed. Still feeling the fast heartbeat off and on. At about 5:00Pm I was experiencing slight chest pain and random kidney pain. At this point my whole body ached and a headache started. Chills started a little later. Didn't sleep well and was up off and on through the night. Had a elevated temperature of 99.8. Woke up the next day and just the left side of my face was swollen and my left eye didn't want to open right away. Only the left side of my face was in alot of pain. Seemed like nerve pain. My face felt numb to touch but also in alot of pain. Like the worst face pain I have ever experienced. Tylenol was not helping. Called advice nurse and they said to ice my face which I did and it was the only thing that helped the pain. My heart rate that day was all over the place while sitting on the couch. Went from 85 to 128 back to 119 and up to 124 and back to 88 within seconds. I could fell the changes. Had a video doc appointment where he recommended I get seen in person on Saturday. Went in on Saturday January 22nd for a check up. Still random chest pain, heart palpitations but not as bad as the days prior. Face pain was still present just not as bad as on Friday with slight Swelling. They did an EKG and said it came back fine. On January 25th I started having noticeable kidney pain. On the 26th still kidney pain with on and off full head aches and random dizziness. Ever since, the facial pain is still present and off and on. Varies in intensity and it is only on the left side of my face. It can be behind my eye down my nose, in my jaw, temples, check and side of my head to the upper neck.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG done on Saturday Jan 22nd 2022.
Aktuelle Erkrankungen: My right foot was in pain and ended up getting x-rays and a boot.
Vorgeschichte: -
Andere Medikamente: None
Allergien: Novocaine
Vorherige Impfungen: The flu shot years ago but I don't have any other information.

VAERS 2092810

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj6369

moderat

Staat: NJ
Alter: 19,0
Geschlecht: M
Eingang: 07.02.2022
Impfdatum: 18.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / -

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

Headache Loss of personal independence in daily activities Migraine

Symptomtext

Very bead headaches and migraines. I have no history of headaches before vaccine. It started within couple hours of vaccine and continue to get since on daily basis. I am college student and it is interfering with my ability to study. This is definitely a reaction of the vaccine. I take Tylenol or advil when needed which I never had to do before vaccine. It's ruining my life

Weitere VAERSDATA-Felder

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

VAERS 2075898

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: IN
Alter: 49,0
Geschlecht: F
Eingang: 07.02.2022
Impfdatum: 16.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Headache Impaired driving ability Impaired work ability Mobility decreased

Symptomtext

PATIENT EXPERIENCED DIZZINESS ON 1/20/22 AND THEN HAD A HEADACHE ON 2/1/22. SHE TOOK TYLENOL TO TREAT IT. SHE WENT TO HER DOCTOR ON 2/7/22 AND HE RULED OUT EAR INFECTION OR FLUID IN THE EAR.

Weitere VAERSDATA-Felder

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

VAERS 2091531

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: -
Geschlecht: U
Eingang: 05.02.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: IM / RA

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

Arthralgia Asthenia Back pain Chills Cough Decreased appetite Dry mouth Heart rate increased Hyperhidrosis Migraine Nausea Vomiting

Symptomtext

Severe joint pain, low back pain, migraine, dry cough,shivers, sweat,nausea, vomiting, incresed heart rate( 111-126) Dry mouth, lost appetite, weakness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: 54, Pfizer Covid-19 vaccine, 01/15/2021

VAERS 2088665

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 25,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 03.02.2022
Beginn: 03.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Rash Throat irritation Tremor

Symptomtext

approx. 3 minutes after receiving the vaccine caregiver reported burning sensation on her throat. visible rash noted on her chest. caregiver was observed shaking. taken to the ED, provided care in the ED. D/C same day. Benadryl was given at the ED. Cleared to work that same night.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Taken to the Emergency Dept. of the hospital. Administered Benadryl, tolerated well. Symptoms resolved - cleared back to work that same night.
Aktuelle Erkrankungen: COVID positive in January but quarantine was completed and caregiver was cleared
Vorgeschichte: not known
Andere Medikamente: not known
Allergien: shellfish allergies as reported to the clinic
Vorherige Impfungen: -

VAERS 2085615

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MN
Alter: 64,0
Geschlecht: M
Eingang: 03.02.2022
Impfdatum: 19.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Echocardiogram abnormal Left ventricular dysfunction Troponin increased

Symptomtext

Chest pain, elevated troponin, LV wall motion abnormalities on ECHO.

Weitere VAERSDATA-Felder

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

VAERS 2082336

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj6369

moderat

Staat: NC
Alter: 33,0
Geschlecht: F
Eingang: 02.02.2022
Impfdatum: 20.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Chills Feeling abnormal Insomnia Pain Pyrexia Tremor

Symptomtext

830 pm felt all over very strange and started to get chills 930-10pm all over body chills and fever of 103 -ear thermometer Terrible shaking, body aches all over and chills throughout the night and fever stayed at 103-103.4 until 10 am and couldn?t sleep. then after 10 am Friday went down to 102 and fluctuating to 100 with medication (ibuprofen and Tylenol alternating) still having body aches and chills. Had fever/chills/body aches until Saturday afternoon 6pm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Covid-19 exposure no positive test Dec 25
Vorgeschichte: Chronic urticaria, dermographism, seasonal and animal allergies.
Andere Medikamente: Venlafaxine-Effexor, Zyrtec
Allergien: Penicillin- skin reaction hives
Vorherige Impfungen: Covid-19 first and second dose age 33 Pfizer 3/17/2021 ER8727 county public health 4/16/21 ER8731 local pharmacy

VAERS 2080333

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: IL
Alter: 62,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 26.01.2022
Beginn: 29.01.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Blood pressure increased Blood test abnormal Condition aggravated Headache Hypertension Migraine Myocardial necrosis marker increased

Symptomtext

3 DAYS AFTER VACCINE, PT PRESENTED TO THE EMERGENCY ROOM WITH A HEADACHE AND ELEVATED BLOOD PRESSURE ( 220/95) W/ NO PREVIOUS HISTORY OF HTN. PT WAS TREATED FOR MIGRAINE AND RELEASED SAME DAY. THE FOLLOING DAY, PT WENT TO THE ER AGAIN FOR UNCONTROLLED HIGH BLOOD PRESSURE, PT WAS ADMITTED 1/30/22 AND DISCHARGED ON 2/1/22 TO FOLLOW UP W/ CARDIOLOGIST. PT STATES THAT THE ER DOCTOR, NEUROLOGIST AND CARDIOLOGIST AT THE HOSPITAL SUGGESTED TO THE PATIENT THAT HER SUDDEN HTN COULD BE DUE TO THE VACCINE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 3,0
Labordaten: PT STATES THAT HER BLOOD WORK AT THE HOSPITAL INDICATED ELEVATED CARDIAC ENZYMES & HER BLOOD PRESSURE IS STILL ELEVATED.
Aktuelle Erkrankungen: -
Vorgeschichte: HISTORY OF MIGRAINE; HYPOTHYROIDISM
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2080063

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 23,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 01.02.2022
Beginn: 01.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Hypophagia Hypotension Interchange of vaccine products Nausea

Symptomtext

pt had received 2 doses of Sinopharm. Received pfizer booster today. Pt was having nausea. Had low bp. Did not have anything to eat today. Laid the pt down. Gave 2 glucose tablets and monitored for over 30 mins. Was feeling better when she left.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: felt tightening of throat (but not SOB) from first sinopharm vaccine. No reaction with the second.

VAERS 2079063

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NY
Alter: 30,0
Geschlecht: M
Eingang: 01.02.2022
Impfdatum: 31.01.2022
Beginn: 31.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Dizziness Electrocardiogram Hypotension Muscle spasms

Symptomtext

patient complained of feeling lightheaded and wanted to laydown after vaccine. Patient was hypotensive and had involuntary muscle spasms and had chest tightness. He was take to the ED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: Vital signs, oxygen saturation, EKG
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: melatonin
Allergien: phenylephrine
Vorherige Impfungen: -

VAERS 2074805

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: IN
Alter: 58,0
Geschlecht: F
Eingang: 30.01.2022
Impfdatum: 28.01.2022
Beginn: 29.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Headache Injected limb mobility decreased Nausea Pain Pain in extremity

Symptomtext

Severe chills 16 hours after injection which lasted 10 hours. Nausea, headache and horrible body ache. Left arm (injection site) could not be lifted, very sore.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Very healthy. No underlying health conditions
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2074617

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: WA
Alter: 63,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 01.01.2022
Beginn: 01.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / LA

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

Arthralgia Back pain Chest pain Joint swelling Pain Pain in jaw Peripheral swelling Swelling

Symptomtext

Shooting, aching pain on left-side where shot was given. Pain started at jawline, extended halfway down left-side of back and chest. Continued into badly swollen shoulder, down left arm to elbow. Pain intense in collarbone, shoulder bone and elbow. Pain medicine doesn't work.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes
Andere Medikamente: Metformin
Allergien: Haldol
Vorherige Impfungen: -

VAERS 2074499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 35,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 26.01.2022
Beginn: 27.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chest discomfort Chest pain Dyspnoea Electrocardiogram Hypoaesthesia Lymphadenopathy Pain Paraesthesia Peripheral swelling

Symptomtext

Day 1: Swollen Left Arm, Enlarged Lymph nodes left armpit, shortness of breath, numbness and tingling in left hand, chest pain/pressure in chest. EMR/AMR called to r/o heart attack. Followed up with MD. Day 2-3: swollen lymph nodes left arm, verbalized swelling in arm pit, swelling in fingers, pain on left side of body from jaw to left hand.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG
Aktuelle Erkrankungen: None
Vorgeschichte: Hashimotos
Andere Medikamente: Synthroid
Allergien: None
Vorherige Impfungen: -

VAERS 2074474

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: KY
Alter: 30,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 26.01.2022
Beginn: 27.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Body temperature increased Chest discomfort Chills Dizziness Dyspnoea Heart rate increased Hyperhidrosis Maternal exposure during breast feeding Nausea Palpitations Paraesthesia Tachycardia

Symptomtext

Went to ER- ER HPI below 30-year-old female with shortness of breath, tachycardia. She has a history of HTN, palpitations, anxiety, PCOS and is a non-smoker. She is currently breast-feeding. She states she had COVID in early January with similar symptoms. She received Pfizer COVID vaccines and had the booster yesterday around 1430. Before bed she had Temp 100.3, Chills. Took tylenol at 8pm and Motrin at 0200. She woke around 4 AM with tingling in her bilateral hands and feet, chest tightness with palpitations, feeling lightheaded, nauseous and sweaty. She checked her HR at home which was 160 bpm. No headache, sore throat, radiating or pleuritic CP, vomiting, stool changes or edema. No cough or hemoptysis. No IVDA. She started OCP 72 hours ago. With the first vaccine she tolerated well, the 2nd she had a fever Tmax 104 with antipyretics, no reported allergic reaction otherwise.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: 01/03/2022 covid positive, syncope- admitted to the hospital 12/4/2021 spontaneous vaginal delivery
Vorgeschichte: GERD, PCOS, Anxiety, HTN
Andere Medikamente: aspirin 81 mg, micronor, prenatal vitamin
Allergien: NKA
Vorherige Impfungen: -

VAERS 2074462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: NC
Alter: 50,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 25.01.2022
Beginn: 26.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Dizziness Headache Injection site bruising Injection site erythema Injection site pain Injection site swelling Limb injury Paraesthesia

Symptomtext

Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Headache-Medium, 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 2071971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: UT
Alter: 13,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 28.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Dyspnoea Injection site erythema Injection site swelling

Symptomtext

Patient presents with chest tightness/SOB. Arm at injection site is red and slightly swollen. Injection given at 10:10; reaction noted 10:15; oral diphenhydramine 25 mg administered @ 10:19. Patient reports improved symptoms at 10:35. At 10:40, pt reports additional tightness. Discussed options with patient and patient mom - can administer dose of epinephrine, call ambulance. Could also administer additional dose of benadryl and pt go to ED. Patient and patient mom elect for additional dose of benadryl and report immediately to ED (ambulance declined). Patient got additional dose of diphenhydramine 25 mg and departs with mom to emergency department.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: hyperthyroidism
Andere Medikamente: no known
Allergien: Reported allergy to mosquito bites and spider bites
Vorherige Impfungen: -

VAERS 2075279

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 13,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Cold sweat Dizziness Dyspnoea Hypoaesthesia Pallor Visual impairment

Symptomtext

Approx. 10 minutes after vaccination patient was pale, clammy, dizzy and said he was having trouble catching his breath. His breath, he said he had trouble seeing and that his arm felt numb. His mother requested Paramedics be called. While waiting for Paramedics, Pt's Blood Pressure was taken (94/63, 98) Pt was let to drink some water and color came back to his face. Paramedics came approx. 10-15 minutes after and reported normal vitals signs & O2 saturation. Pt left to home.

Weitere VAERSDATA-Felder

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

VAERS 2069235

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

moderat

Staat: CA
Alter: 61,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 24.01.2022
Beginn: 24.01.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / LA

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

Abdominal pain Blood test normal Cardiac function test normal Chest pain Chills Feeling cold X-ray normal

Symptomtext

temperature dropped to 95.5 at 7:28pm pm teeth chattering chest pain abdominal pain. went into emergency room . gotten extremely cold. body temp went back to 96 within 23min.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: blood work xray and did a test for heart attack . negative results
Aktuelle Erkrankungen: n/a
Vorgeschichte: diabetes. colitis . high blood pressure
Andere Medikamente: n/a
Allergien: avocados, glipizide, prednisone, amoxicillin
Vorherige Impfungen: -

VAERS 2068875

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 25,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 19.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Flushing Headache Interchange of vaccine products Paraesthesia

Symptomtext

pt here for booster dose, chose Pfizer, previously had Moderna Previous vaccine was from (Privacy) pt previously felt similar sx with 2nd Moderna shot and was sent to urgent care, discharged after 1549: flushed sensation, tingling, 4/10 generalized HA 1550: HR 103, BP 168/114, 98%, 97.9 F, RR 22 1555: HR 85, BP 177/110, 100%, RR 20 1605: HR 95, BP 167/107, 99%, RR 18 1620: HR 82, BP 166/100, 99%, 98.8 F, RR 22 1637: HR 75, BP 164/91, 99% 1657: BP 164/91, HR 75, 99% pt advised to go to the ER 1700: Pt brought to ER by wheelchair, in no acute distress, still feels 3/10 HA, all over tingling and flushed sensation 1710: in line for ED check in

Weitere VAERSDATA-Felder

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

VAERS 2068507

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MI
Alter: 21,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 18.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Arthralgia Chest pain Dyspnoea

Symptomtext

Reported fleeting pain right shoulder upper r chest. Also reported shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Gave snack and juice. Observed for 45-60 minutes. Advised to f/u with primary care. ER if symptoms return.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2065629

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MA
Alter: 21,0
Geschlecht: M
Eingang: 26.01.2022
Impfdatum: 12.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Chest pain Chills Dyspnoea Hyperhidrosis Myalgia Pyrexia

Symptomtext

Moderate to severe chest pain beginning within 24 hours of vaccine and lasting for approximately 10 days. Pain increased during strenuous activity and resulted in breathlessness and difficulty breathing due to pain. These symptoms were in addition to fever and chills lasting two days, excessive sweating for two days, and approximately 10 days of joint and muscle pain. Contacted a medical professional who advised the symptoms were similar to that of myocarditis and recommended I monitor the symptoms and self treat with ibuprofen and to seek emergency care if they worsened significantly. Symptoms resolved within 2 weeks with regular ibuprofen use.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Underweight BMI (16.5)
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2065554

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 18,0
Geschlecht: M
Eingang: 26.01.2022
Impfdatum: 22.01.2022
Beginn: 22.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Hyperhidrosis Pallor Tremor

Symptomtext

Patient felt dizzy 10 minutes after receiving his booster vaccine and experienced tremor, excessive sweating, and pale skin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Blood pressure was recorded to be 88/58 then improved to 94/60 10 minutes after drinking a can of apple juice.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2057666

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 22.01.2022
Beginn: 22.01.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Hypoaesthesia Injection site hypoaesthesia Injection site paraesthesia Paraesthesia

Symptomtext

While waiting immediately after the shot about 5 minutes later, tingling began at the shot area, pins and needles sensation, then moving down to the arm by the time 15 minutes were up. Then it moved down my left leg and left side of my neck and face and I went to talk to the nurse. It remained for about half an hour before disipating slowly. It seemed to mostly be gone in an hour, however, at nights it returns and I can feel pin and needle sensations in my fingers and my face and parts of my body. Seems mostly gone at night after I take a valerina or GABA to sleep.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site paraesthesia
Hospital-Tage: -
Labordaten: None yet, I can't see my doctor until Feb. 3rd so waiting for the doctor's visit.
Aktuelle Erkrankungen: lyme disease SIBO
Vorgeschichte: lyme disease
Andere Medikamente: cholysteramine amphotericin b ketotifen chromium sodium zyrtec claritin pepcid AC
Allergien: -
Vorherige Impfungen: -

VAERS 2062599

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: -
Geschlecht: U
Eingang: 25.01.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Hypoaesthesia Immediate post-injection reaction Muscle spasms Muscular weakness Myalgia Neuralgia Pain Paraesthesia Peripheral swelling Product administered at inappropriate site Vaccination site joint swelling

Symptomtext

Immediate pain after injection was giving. Injection placed too high, on top of shoulder. Per Emergency Room MD, Injection was placed in the Left Shoulder Joint. Symptoms include. Excruciating pain, radiating nerve pain, pulsating muscles pain, numbnessand tingly, swelling of left shoulder and arm. Weakness to left shoulder and arm, elbow and wrist, fingers . Muscle spasms to left arm, constant pain in the shoulder joint socket. Excruciating pain to left trapezius front &back of shoulder.

Weitere VAERSDATA-Felder

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

VAERS 2058419

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 34,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 20.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Limb injury Paraesthesia

Symptomtext

Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)

Weitere VAERSDATA-Felder

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

VAERS 2057711

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 19.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Chest pain Heart rate increased Malaise Pyrexia Sleep disorder

Symptomtext

In the evening of 1/19 I started to feel unwell but wasn't showing a fever. I felt my heart was beating fast and I couldn't fall asleep because of it. During the night I saw that I was starting to have a fever. I had taken some Tylenol to prevent having a high fever like I had when I took the Moderna vaccine. Both times my fever was around 101 and higher. I think my fever during this evening was around 99.9. I used an oximeter to try my pulse and it was high like near 100. The next day I felt sick and my temperature was around 100. I think the Tylenol kept it from going high. I'm not sure when this next symptom started but it was sometime near evening and it lasted awhile. I had pain in my chest. It seemed to have stopped then sometime later it started again. It continued to hurt for a while and I considered going to the hospital. I lay down to see if maybe it was stress related and eventually it did go away. I'm not sure what my pulse rate was at this time. By 1/21 I still was feeling a little sick but by around late afternoon I think (not sure) my temperature was back to normal at 98.6. What worried me the most was the fast heart rate and the pain in my chest. This may be the last vaccine I take because I'm afraid it's affecting my heart possibly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: As of today 1/22/22 I have not had any lab tests but I am planning to call my doctor.
Aktuelle Erkrankungen: Slight runny nose.
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Moderna 3/3/21 and 4/1/21 I had a fast heart rate and high fever.

VAERS 2055476

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 42,0
Geschlecht: M
Eingang: 21.01.2022
Impfdatum: 21.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Feeling hot Injection site paraesthesia Nausea Neck pain Paraesthesia Sensory loss

Symptomtext

Patient was vaccinated at Vaccine Center at 11:57am for his Pfizer booster. He sat for 15 minutes and then left. Returned to Vaccination Center at 12:25pm because he had concerns about his symptoms. He said that he had similar symptoms with his previous covid19 vaccines. Patient stated that he had a tingly feeling from the site (left deltoid) of his injection to his fingers, stated he felt warm and a little nauseous. Patient had stated that he had visited his doctor prior to being vaccinated and was told that his BP pressure needed to be rechecked, but patient did not return to see his doctor yet. Checked patient?s vital signs and saw that his BP was 210/106 using automatic blood pressure. Other vital signs: 97.8F, SpO2 99%, HR 84. Tried to retake blood pressure on his other arm, but cuff read error. Asked patient if he knew what his regular blood pressure is and if he took any medications. Patient denied taking any blood pressure medication and that he didn?t know what his usual blood pressure was. While patient was with staff, he mentioned that both of arms started feeling tingly and he felt like he was losing sensation in both his arms and he had pain in his neck. He stated that felt like this when he had a previous covid19 infection. Called 911 at 1246 and let patient know that staff wants him to be checked out. While waiting patient was pleasant, responsive and talkative. Paramedics arrived and took vital signs : BP 210/120 , SpO2 100% on room air, HR 84, RR 18. Patient decided to go with paramedics to the emergency room at 1310.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2050927

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CO
Alter: 42,0
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: 20.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Anxiety Dizziness Dyspnoea Paraesthesia Vision blurred Vomiting

Symptomtext

1000: APPREHENSION AND WORRY 1001: DIZZINESS : GAVE BENEDRYL 20 MG, GAVE THE PT WATER AND LOWERED PT TO GROUND, BP TAKEN: 120/86, 65 HR, 16 1005: PERIPHERAL EXTREMITY PARESTHESIA IN HANDS, SLOWED THE BREATHING WITH GUIDED COACHING 1006: VISUAL CHANGES "FEELING VISION IS DISTANT AND UNCLEAR", OBJECTS ARE FAR AND UNCLEAR. BP: 120/86, UNCHANGES RR: 20 1008: PT STARTED TO VOMIT CLEAR SPUTUM 1008: 911 CALLED, 1010: CONTINUED TO MONITOR AIRWAY AND COMFORT PT. 1014: PT SAT UP "I CANNOT BREATH". EPINEPHRINE 0.3 MG TO RIGHT THIGH 1020-1024: FIRE DEPARTMENT AND PARAMEDIC TRANSPORTED PT TO HOSPITAL 1011: CONTINUED TO ASSESS, PT REPORTED SOB AND DIFFICULTY GETTING BREATH

Weitere VAERSDATA-Felder

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

VAERS 2048371

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 25,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 19.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Paraesthesia Throat irritation Urticaria

Symptomtext

Hives to chest, tingling to hands, itchy to throat

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: na
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: PCN class medications
Vorherige Impfungen: -

VAERS 2048199

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: MI
Alter: 15,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 19.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal discomfort Disorientation Dizziness Flushing Hypotension Paraesthesia Vomiting

Symptomtext

Patient experienced abdominal discomfort. Patient had several episodes of vomiting. Facial coloration flushed. Tingling sensation in fingers. Patient was light headed/disoriented. Low blood pressure.

Weitere VAERSDATA-Felder

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

VAERS 2048122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: PA
Alter: 25,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 18.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Headache Injection site pain

Symptomtext

Chest pain, headache, and injection site pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 2043754

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: OH
Alter: 34,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 18.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Paraesthesia oral

Symptomtext

Patient said her lips started tingling 5 minutes after the vaccine. I gave the patient 25mg of diphenhydramine solution orally. She states she can take oral diphenhydramine. The patient stated she felt fine 15 minutes later and left the pharmacy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: IV Diphenhydramine Sumatriptan
Vorherige Impfungen: -

VAERS 2039572

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: CA
Alter: 51,0
Geschlecht: F
Eingang: 17.01.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / UN

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

Dizziness Dyspnoea Injection site hypoaesthesia

Symptomtext

Dizziness, SOB, injection site reaction numbness

Weitere VAERSDATA-Felder

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

VAERS 2031992

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

moderat

Staat: -
Alter: 20,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 12.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Condition aggravated Dizziness Hyperhidrosis Nausea

Symptomtext

Patient received a Pfizer booster dose (LOT# FJ6369). At 1344 reported feeling nauseous, sweaty, and slightly dizzy to vaccinator EMT. RN 1 and EMT assisted patient into anti-gravity chair. At 1345, RN 1 assessed patient: 120/80 blood pressure; pulse rate 103 beats/minute; and 98% SpO2. Patient denied itchiness, rashes, difficulty swallowing or difficulty breathing. Patient given juice. Patient drank juice. Patient reported history of similar reaction to second dose of Pfizer. Patient reported history of generalized anxiety disorder and feeling nervous before appointment. Patient takes Prozac and has no known allergies. At 1357, RN 1 reassessed patient: 122/88 blood pressure; pulse rate 95 beats/minute; and 98% SpO2. Patient denied feeling nauseous and dizzy. Patient reported history of reaction to his second dose of Pfizer. Patient reported indigestion and left sided chest pain radiating to shoulder and lower back. Patient reported seeking urgent care and no follow up with PCP. Patient reported he did not reported second dose reaction to vaccinator before vaccination. At 1410, RN 1 reassessed patient: 140/100 blood pressure; pulse rate 92 beats/min (irregular); and SpO2 97%. At 1414, RN 1 reassessed patient: 152/100 blood pressure; pulse rate 90 beats/minute (irregular); and SpO2 97%. RN 1 reported irregular pulse and patient history to RN 2. RN 1 offered EMS to patient. At 1430, RN 1 activated EMS. At approximately 1437, paramedics arrived on scene and assumed care. At 1443, paramedics left facility and transferred patient to another HCF.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Generalized anxiety disorder
Andere Medikamente: Prozac
Allergien: None reported
Vorherige Impfungen: Had nausea and dizziness after seconds dose of Pfizer.

VAERS 2728156

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: MN
Alter: 71,0
Geschlecht: F
Eingang: 28.12.2023
Impfdatum: 27.10.2022
Beginn: 27.12.2023
Tage bis Beginn: 426,0
Dosis: 4
Route/Site: IM / LA

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

Headache Nasopharyngitis Oropharyngeal pain SARS-CoV-2 test

Symptomtext

Sore throat, headache, cold symptoms

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: IDNOW
Aktuelle Erkrankungen: -
Vorgeschichte: Systemic lupus, Type 2 diabetes, osteoporosis, Barrett esophagus, GERD, diabetic neuropathy, osteoarthritis, depression
Andere Medikamente: Dulaglutide, aspirin, atenolol, duloxetine, glipizide, hydrochlorothiazide, hydroxychloroquine, Lisinopril, metformin, potassium chloride, januvia
Allergien: Hmg-coa-r inhibitors, amlodipine, dust mite extract, lactase, rofecoxib
Vorherige Impfungen: -

VAERS 2619559

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: CA
Alter: 27,0
Geschlecht: F
Eingang: 23.04.2023
Impfdatum: 08.03.2021
Beginn: 31.03.2021
Tage bis Beginn: 23,0
Dosis: 3
Route/Site: SYR / LA

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

Lip swelling Urticaria

Symptomtext

Random swollen lips, worse the first time, randomly every couple months. i also get hives on my eyelids randomly. only since the covid 19 vaccines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ortho tri cyclin lo 28 day birth control oral
Allergien: -
Vorherige Impfungen: -

VAERS 2613237

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: AZ
Alter: 72,0
Geschlecht: F
Eingang: 11.04.2023
Impfdatum: 01.04.2022
Beginn: 07.04.2022
Tage bis Beginn: 6,0
Dosis: 4
Route/Site: IM / RA

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

Discomfort Joint swelling Lymph node pain Lymphadenopathy Peripheral swelling Swelling

Symptomtext

The first time I had the adverse event was after the second vaccine, I started swelling at the base of my neck in the V of the collar bone and under my arm, behind my knees, and at my ankles. This lasted approximately one month but I did not see anybody for this. After the 4th vaccine, the symptoms were more pronounced with a the swelling about the size of a half of a tennis ball at the V in my neck/collar bone, and swelling under my arm, at my knees, and ankles. All of my lymph nodes were swollen. It was very painful and uncomfortable. This was only on the side of the body where I received the vaccine. The doctor told me to take Ibuprofen and gave a prescription for 7 day regiment of Prednisone to help bring down the swelling. This lasted approximately three months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Unstable Angina; Hyperthyroidism
Andere Medikamente: Verapamil; Zetia; PTU; Turmeric; Potassium; Vitamin C; Viviscal; Juicefestiv Multivitamin
Allergien: Adhesive; Penicillin; Erythromycin; Codeine; All Opioids
Vorherige Impfungen: -

VAERS 2581131

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: -
Geschlecht: U
Eingang: 14.02.2023
Impfdatum: 22.04.2022
Beginn: 23.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: - / -

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

Body temperature Fatigue Influenza like illness Myalgia Pyrexia

Symptomtext

muscle pain; low grade fever; flu like symptoms; tiredness; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A patient in their 60's received BNT162b2 (BNT162B2), on 22Apr2022 as dose 4 (booster), single (Lot number: FJ6369), in arm for covid-19 immunisation. The patient's relevant medical history included: "Crohns Disease" (unspecified if ongoing); "Hypothyroidism" (unspecified if ongoing). Concomitant medication(s) included: LIALDA oral taken for crohn's disease (ongoing); LEVOTHYROXINE oral taken for hypothyroidism (ongoing); LIOTHYRONINE oral taken for hypothyroidism (ongoing). Vaccination history included: BNT162b2 (Dose: 1st, Anatomical Site of injection: Arm, Route of administration: Intramuscular, Batch/Lot number: Lot: EN6201), administration date: 11Feb2021, for Covid-19 immunization, reaction(s): "Covid-19", "muscle pain", "low grade fever", "flu like symptoms", "tiredness"; BNT162b2 (Dose: 2nd, Anatomical Site of injection: Arm, Route of administration: Intramuscular, Batch/Lot number: Lot: EN6206), administration date: 04Mar2021, for Covid-19 Immunization, reaction(s): "Covid-19", "muscle pain", "low grade fever", "flu like symptoms", "tiredness"; BNT162b2 (Dose: 3rd, Date (dd-Mmm-yyyy): 24Sep2021, Anatomical Site of injection: Arm, Route of administration: Intramuscular, Batch/Lot number: FF2587), administration date: 24Sep2021, for COVID-19 Immunization, reaction(s): "Covid-19", "muscle pain", "low grade fever", "flu like symptoms", "tiredness". The following information was reported: INFLUENZA LIKE ILLNESS (non-serious) with onset 23Apr2022, outcome "recovered", described as "flu like symptoms"; PYREXIA (non-serious) with onset 23Apr2022, outcome "recovered", described as "low grade fever"; MYALGIA (non-serious) with onset 23Apr2022, outcome "recovered", described as "muscle pain"; FATIGUE (non-serious) with onset 23Apr2022, outcome "recovered", described as "tiredness". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of myalgia, pyrexia, influenza like illness, fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Name: fever; Result Unstructured Data: Test Result:low grade
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Crohn's disease; Hypothyroidism
Andere Medikamente: LIALDA; LEVOTHYROXINE; LIOTHYRONINE
Allergien: -
Vorherige Impfungen: -

VAERS 2579372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: TX
Alter: 68,0
Geschlecht: M
Eingang: 10.02.2023
Impfdatum: 03.03.2022
Beginn: 01.03.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

Arthralgia Dysstasia Immunisation Inflammation Joint stiffness Joint swelling Off label use Rheumatoid factor X-ray

Symptomtext

Inflammation; off label use; Booster; Both knees began to ache and turn stiff/Limited to knees, but it became very painful; Both knees began to ache and turn stiff; Can hardly stand up; His knees became puffy, pink, swollen, and warm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 68-year-old male patient received BNT162b2 (BNT162B2), on 03Mar2022 as dose 4 (booster), single (Lot number: FJ6369) at the age of 68 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "meniscus trim", start date: Jan2022 (unspecified if ongoing), notes: meniscus trim; "Blood pressure" (ongoing). Concomitant medication(s) included: TOPROL XL taken for blood pressure abnormal (ongoing); LIPITOR (ongoing); SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE. Vaccination history included: BNT162b2 (Dose: 1, Lot: EN5318), administration date: 24Jan2021, when the patient was 67-year-old, for COVID-19 immunization, reaction(s): "Both knees began to ache and turn stiff", "Both knees began to ache and turn stiff", "Can hardly stand up", "His knees became puffy, pink, swollen, and warm"; BNT162b2 (Dose: 2, Lot: EN6198), administration date: 22Feb2021, when the patient was 67-year-old, for COVID-19 immunization, reaction(s): "Both knees began to ache and turn stiff", "Both knees began to ache and turn stiff", "Can hardly stand up", "His knees became puffy, pink, swollen, and warm"; BNT162b2 (Dose: 3, Lot: ER8737), administration date: 27Sep2021, when the patient was 68-year-old, for COVID-19 immunization, reaction(s): "Both knees began to ache and turn stiff", "Both knees began to ache and turn stiff", "Can hardly stand up", "His knees became puffy, pink, swollen, and warm"; Flu shot (He gets a Flu shot every year). The following information was reported: IMMUNISATION (non-serious) with onset 03Mar2022, outcome "unknown", described as "Booster"; OFF LABEL USE (non-serious) with onset 03Mar2022, outcome "unknown"; JOINT STIFFNESS (non-serious) with onset Mar2022, outcome "not recovered", described as "Both knees began to ache and turn stiff"; ARTHRALGIA (non-serious) with onset Mar2022, outcome "not recovered", described as "Both knees began to ache and turn stiff/Limited to knees, but it became very painful"; DYSSTASIA (non-serious) with onset Mar2022, outcome "not recovered", described as "Can hardly stand up"; JOINT SWELLING (non-serious) with onset Mar2022, outcome "not recovered", described as "His knees became puffy, pink, swollen, and warm"; INFLAMMATION (non-serious), outcome "recovering". The events "both knees began to ache and turn stiff/limited to knees, but it became very painful", "both knees began to ache and turn stiff", "can hardly stand up", "his knees became puffy, pink, swollen, and warm" and "inflammation" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of arthralgia, joint stiffness, inflammation. Additional information: He wanted to report an adverse reaction to Pfizer COVID vaccine. where he got the vaccine. He went for an annual physical and asked for the second booster. It was his fourth shot. First 3 minimal if any reaction. The fourth shot, two days or three days after, both knees began to ache and turn stiff. It got hard from sitting to standing position. He can hardly stand up. It has continued since. Became puffy, pink, swollen, warm knees. No fever. Limited to knees, but it became very painful. He was a pickle ball player before, but he could hardly move around after. He went to his orthopedic doctor and primary. Nobody knows what to do. All they do is manage pain. Ortho doctor after 9 months did X rays and compared it to his x rays a year ago. The space between his knee has disintegrated on the inside edge. It is markedly worse to where it is now bone on bone on the inside edge. Seems to be inflammatory reaction. All they do is Pain meds or Diclofenac Gel (NSAID that he puts on knee joint) It seems to work to reduce pain. Atleast to the point where he can walk. The doctor basically told him they will manage pain until he can't, and then he will have to get his knees replaced. Outcome: in the last 3 weeks he heard things online from a doctor who put out a detox protocol, and to take ivermectin and NAC (amino acid) and something else. He changed what he eats to just salads. Trying to be non inflammatory. The last couple of weeks inflammation has seem to go down. until them has been the same. He gets a Flu shot every year. He did get his Flu shot in late Sep2022 and had a reaction to it. It was elevated heart rate and rapid breathing; it was the stronger dose. NDC/lot/expiration: Unknown. He considers himself fairly healthy. It didn't seem like osteoarthritis. He did have a meniscus trim in Jan2022. His Knees were in great shape with no arthritis or roughness then. There was a little reduction from spacing from inside to outside, but minimal. From Jan2022 and Jan2023, the space is now gone. They tested him for Rheumatoid arthritis factor it was negative. He has been on the same medications for a long time. No other vaccinations within four weeks prior to the first administration date of the suspect vaccine. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300053967 Same patient/vaccine/event, different dose;US-PFIZER INC-202300053968 Same patient/vaccine/event, different dose;US-PFIZER INC-202300053969 Same patient/vaccine/event, different dose;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Name: Rheumatoid arthritis factor; Test Result: Negative ; Test Name: X-Ray; Result Unstructured Data: Test Result:unknown result; Comments: X-ray a year ago; Test Name: X-Ray; Result Unstructured Data: Test Result:disintegrated on the inside edge; Comments: The space between his knee has disintegrated on the inside edge
Aktuelle Erkrankungen: Blood pressure abnormal
Vorgeschichte: Medical History/Concurrent Conditions: Meniscus operation (meniscus trim)
Andere Medikamente: TOPROL XL; LIPITOR; SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE
Allergien: -
Vorherige Impfungen: -

VAERS 2577326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: MI
Alter: 83,0
Geschlecht: F
Eingang: 07.02.2023
Impfdatum: 22.01.2022
Beginn: 06.02.2023
Tage bis Beginn: 380,0
Dosis: 3
Route/Site: - / -

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

Arthralgia Crying Fall Haemodialysis Hip fracture Pain

Symptomtext

Chief Complaint: Patient is an 84 y.o. with PMH Alzheimer, ESRD on HD MWF, HTN, hypothyroidism, and DM II presented to Hospital after a fall and sustained a right hip fracture. I was called for complaints of pain. Patient is fully awake, AOx1. She was able to verbalized right hip pain and crying. Patient is also currently on HD at bedside. No other complaints, VSS, NAD.

Weitere VAERSDATA-Felder

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

VAERS 2576533

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 43,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 04.02.2022
Beginn: 01.04.2022
Tage bis Beginn: 56,0
Dosis: 3
Route/Site: IM / LA

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

Anxiety COVID-19 Fatigue Heart rate increased SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

I experienced a breakthrough case of COVID-19 with fast heart rate, anxiety, tiredness and adrenaline rushes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Thyroids
Andere Medikamente: Levothyroxine
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2575052

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NH
Alter: 55,0
Geschlecht: F
Eingang: 03.02.2023
Impfdatum: 01.02.2022
Beginn: 25.10.2022
Tage bis Beginn: 266,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Exposure to SARS-CoV-2 Injection site pain SARS-CoV-2 test positive

Symptomtext

I had a little tenderness at the injection site after receiving the vaccine for a few days. I was exposed to COVID-19 while visiting a friend in the hospital. The hospital had about 42 positive cases. I tested positive for COVID-19 on 10/25/2022. This was my third time having COVID-19 so I took over the counter medication. I did contact my doctor, but I was doing what I needed to do to get better. I didn't have as much fear this time because I knew what to expect.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: 25OCT2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes; Hypothyroidism; Abnormal Kidney Function; Arthritis
Andere Medikamente: Levothyroxine; sertraline; metformin; pravastatin; hydroxychloroquine; JANUVIA; iron; JUICE PLUS; cinnamon; B complex; aspirin; vitamin D3; fish oil
Allergien: SYNTHROID; penicillin; sulfa; hydrocodone; epinephrine; levofloxacin
Vorherige Impfungen: -

VAERS 2567266

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: SC
Alter: 78,0
Geschlecht: F
Eingang: 25.01.2023
Impfdatum: 27.04.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: OT / RA

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

Magnetic resonance imaging Vaccination site pain

Symptomtext

sore at the injection site; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. A 78-year-old female patient received BNT162b2 (BNT162B2), on 27Apr2022 at 10:00 as dose 4 (booster), single (Lot number: FJ6369) at the age of 78 years intramuscular, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Had sciatica so bad" (unspecified if ongoing); "Had kidney removed last year", start date: Oct2021 (unspecified if ongoing), notes: Had kidney removed last year; "mass in her kidney" (unspecified if ongoing); "mass in her kidney and looks very cancerous" (unspecified if ongoing); "She had back surgery in the past" (unspecified if ongoing), notes: She had back surgery in the past. The patient's concomitant medications were not reported. Past drug history included: Oxycodeine, reaction(s): "nerve block". Vaccination history included: BNT162b2 (Dose 3 (Booster), Lot number: EW0185, EXP: Unknown, Route of administration: injected into right arm, Time: morning, exact time unknown), administration date: 11Oct2021, when the patient was 77-year-old, for COVID-19 immunization, reaction(s): "sore arm at the injection site"; BNT162b2 (Dose 2, single, Lot number: EN9581, Expiry date: May2021, Route of administration: injected into right arm, Time: 10AM), administration date: 08Feb2021, when the patient was 76-year-old, for COVID-19 immunization, reaction(s): "sore arm at the injection site"; BNT162b2 (Dose 1, Single, Lot number: EL3249, Expiry date: May2021, Route of administration: injected into right arm, Time: around 6-7pm Was a drive-thru vaccine facility), administration date: 18Jan2021, when the patient was 76-year-old, for COVID-19 immunization, reaction(s): "sore arm at the injection site"; Shingles (Caller and his wife had all vaccines, from shingles to whatever), for Immunization. The following information was reported: VACCINATION SITE PAIN (non-serious), outcome "unknown", described as "sore at the injection site". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: While she had the sciatica, one weekend she had to go to ER three times in four days. The last time she was there, they did an MRI on her back. Oxycodeine: NDC/LOT/EXP/Manufacturer: Unknown Unable to confirm spelling of product name as she does not have product at time of call. Strength: 5mg, but she did have some of the heavier dose before she could get the nerve block Oxycodeine did not take the pain away, only the nerve block did.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300032197 same patient/drug/event, different dose;US-PFIZER INC-202300032249 same patient/drug/event, different dose;US-PFIZER INC-202300032250 same patient/drug/event, different dose;US-PFIZER INC-202300030721 same patient/drug, different event/dose;US-PFIZER INC-202300030735 same patient/drug/event, different dose;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: Test Name: MRI; Result Unstructured Data: Test Result:Unknown results; Comments: nothing was wrong with the back, but she does have a mass in her kidney and looks very cancerous
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Back surgery (She had back surgery in the past); Kidney cancer; Nephrectomy (Had kidney removed last year); Renal mass; Sciatica
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2567240

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: SC
Alter: 80,0
Geschlecht: M
Eingang: 25.01.2023
Impfdatum: 27.04.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

Vaccination site pain

Symptomtext

They didn't have any side effects with the previous vaccines except maybe just a sore arm at the injection site.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. An 80-year-old male patient received BNT162b2 (BNT162B2), on 27Apr2022 at 10:00 as dose 4 (booster), single (Lot number: FJ6369) at the age of 80 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Pacemaker placement", start date: 2021 (unspecified if ongoing); "atrial fibrillation" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (Dose: 01 , Manufacturer: Pfizer, NDC: Unknown , LOT: EL3249 , EXP: May2021 , Dose and Route: injected into left arm; dose amount unknown , Time: 7PM), administration date: 18Jan2021, when the patient was 78-year-old, for COVID-19 immunization; BNT162b2 (Dose: 02, Manufacturer: Pfizer, NDC: Unknown , LOT: EN9581 , EXP: May2021 , Dose and Route: injected into left arm; dose amount unknown , Time: 10AM), administration date: 08Feb2021, when the patient was 78-year-old, for COVID-19 immunization; BNT162b2 (Dose: 03, Manufacturer: Pfizer, NDC: Unknown , LOT: EW0185 , EXP: Unknown , Dose and Route: injected into left arm; dose amount unknown , Time: 8AM-9AM), administration date: 11Oct2021, when the patient was 79-year-old, for COVID-19 immunization; Shingles (Had all vaccines, from shingles to whatever), for immunization. The following information was reported: VACCINATION SITE PAIN (non-serious), outcome "unknown", described as "They didn't have any side effects with the previous vaccines except maybe just a sore arm at the injection site". Additional Information: It was reported that He and his wife experienced the same situation. They have gotten two of the bivalent boosters for Pfizer COVID-19 vaccine. They had the first shot Jan2021 A second shot in Feb2021 A booster later in the year, 2021 Then a fourth dose in Apr2022. Both got a bivalent COVID-19 Vaccine on 09Sep2022 and a bivalent COVID-19 Vaccine again today 19Jan2023 They didn't have any side effects with the previous vaccines except maybe just a sore arm at the injection site. Clarifies there was only supposed to be just one bivalent dose given. All previous doses were manufactured by Pfizer, and they had no other negative reactions to any of them. Had all vaccines, from shingles to whatever. Took first bivalent COVID-19 Vaccine on 09Sep2022. Today when having their annual wellness, primary visit with primary doctor, their doctor said the new variant COVID-19 Vaccine was out and their doctor took it. Their doctor states that caller and his wife are always staying current that maybe they wanted to get the new variant COVID-19 Vaccine. Reporter and his wife took the variant COVID-19 Vaccines today, went home, looked at their cards, to find out it was the same bivalent COVID- 19 Vaccine. He has noticed references to heart issues, and he has a pacemaker. Pacemaker placed: sometime in the year of 2021, but he had issues before the COVID-19 vaccines More recently he had atrial fibrillation and was given two medications. The atrial fibrillation was light, so they didn't want to shock his heart. Appears the atrial fibrillation was gone. Atrial fibrillation: had symptoms of that at night before receiving the COVID-19 vaccines. Thought muscles were twitching before they discovered it was tied in with the heart. When he would lay on his left shoulder, it felt like a light vibration. He was given the pacemaker, then had Atrial fibrillation, then given the medicine to take care of it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Atrial fibrillation; Pacemaker insertion (cardiac)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2557517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: AR
Alter: 72,0
Geschlecht: M
Eingang: 11.01.2023
Impfdatum: 06.02.2022
Beginn: 10.01.2023
Tage bis Beginn: 338,0
Dosis: 3
Route/Site: IM / -

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

Abdominal pain Acute kidney injury Asthenia COVID-19

Symptomtext

Patient was seen at the R by Dr. for c/o weakness and abdominal pain. Patient was admitted with a Dx of weakness, acute kidney failure, abdominal pain, covid-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hx: small bowel obstruction, Colostomy, Anemia, Sepsis, Chronic hypotension, Atrial fibrillation, Feeding tube, Abdominal abscess, acute renal failure
Andere Medikamente: Calamine-lan-menth-Zn 0.44-20.6% apply topically prn Vitamin C 500 mg po daily Lexapro 20 mg po daily Seroquel 100 mg po BID Gabapentin 300 mg po TID Allopurinol 100 mg po daily Cyproheptadine 4 mg po BID Zofran 8 mg po prn Omeprazole 20 mg
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2545908

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: IL
Alter: 62,0
Geschlecht: F
Eingang: 29.12.2022
Impfdatum: 29.06.2022
Beginn: 17.08.2022
Tage bis Beginn: 49,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Cough Decreased appetite Fatigue Hypersomnia Myalgia Pain Pyrexia SARS-CoV-2 test Temperature regulation disorder Visual impairment

Symptomtext

On 08/17/22, I started feeling achy, the next day I was still achy and very tired, I tested with a home COVID-19 test but it came back negative. On 08/19/22, I had a fever of 104F but with TYLENOL it was 102F, I did not have an appetite but made myself eat. I had an unproductive cough that made my muscles hurt. I was very tired, slept a lot. I called my doctor, had a telehealth, he prescribed PAXLOVID, that I started immediately. I did start feeling within 48 hours after taking the PAXLOVID, but I did get rebound COVID-19. I do feel better, but I feel that COVID-19 left me some lingering effects, I cannot regulate my body temperature and my vision is off.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home COVID-19 test
Aktuelle Erkrankungen: No
Vorgeschichte: Heart Valve Replacement; Meniere's Disease
Andere Medikamente: Warfarin; atorvastatin; triamterene
Allergien: ADVIL; banana sensitivity
Vorherige Impfungen: Influenza, hives because I was taking a sulfa based medication

VAERS 2539105

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: MI
Alter: 99,0
Geschlecht: F
Eingang: 21.12.2022
Impfdatum: 29.01.2021
Beginn: 05.10.2022
Tage bis Beginn: 614,0
Dosis: 4
Route/Site: - / -

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

Atelectasis Blood creatinine increased COVID-19 Chest X-ray abnormal Cough Hypersomnia Lethargy Pyrexia SARS-CoV-2 test positive Skin laceration White blood cell count increased

Symptomtext

101y.o. year old female with history of mild asthma, hypertension and dementia. She lives at home with 24-hour day caregivers. She is fully vaccinated for COVID. She developed a nonproductive cough and appeared to be more lethargic, slept a lot on 10/3 10/4, she also had a low-grade fever on 10/4. Son, who is a retired pediatrician, did a home COVID test which was positive. They checked her pulse ox and at some point in time her saturation was 87%, however, the son is not sure if the pulse oximeter was functioning properly, plus the patient has painted nails which may have interfered with the pulse oximeter. They called her primary care physician and they were advised to come to the hospital. In the emergency department she did not have a fever, her white count was noted to be 14, repeated white count is 9.4. Initially her creatinine was elevated at 1.2, after hydration it is down to 1.08. COVID test was positive. Chest x-ray showed mild basilar atelectasis. Patient also suffered a skin tear on her left forearm, she has a visiting nurse who changes her dressings at home, the wound does not appear to be infected. ID is consulted in regards to COVID. History was obtained from the son at bedside, as the patient has dementia and is unable to provide meaningful information.

Weitere VAERSDATA-Felder

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

VAERS 2511983

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj6369

mild

Staat: FL
Alter: 31,0
Geschlecht: F
Eingang: 18.11.2022
Impfdatum: 28.02.2022
Beginn: 04.05.2022
Tage bis Beginn: 65,0
Dosis: 1
Route/Site: SYR / LA

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

Lip swelling Swelling of eyelid Urticaria chronic

Symptomtext

I have been having chronic hives starting may 5th 2022 all over my body, swollen eye lid, lips. I went to the emergency room at hospital and was told they were chronic hives and was given prednisone and when I left then gave me a prescription for prednisone for 5days with 1 refill. I still have these chronic hives till this day 11/18/2022 and I have tried other medications like Allegra, ibuprofen and Claritin and Zyrtec and the work and then started to not work as much

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria chronic
Hospital-Tage: -
Labordaten: I was at the hospital and they only looked at my body during out break
Aktuelle Erkrankungen: None
Vorgeschichte: No
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2504620

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: MI
Alter: 79,0
Geschlecht: M
Eingang: 10.11.2022
Impfdatum: 09.02.2021
Beginn: 14.09.2022
Tage bis Beginn: 582,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Fatigue Laboratory test abnormal SARS-CoV-2 test positive

Symptomtext

09/14/22 presents to ED for "fatigue, abnormal labs". PMHx of "BPH, glaucoma, essential hypertension, history of prostate cancer, prediabetes, osteoarthritis"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 09/15/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2499304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 04.11.2022
Impfdatum: 04.04.2022
Beginn: 04.10.2022
Tage bis Beginn: 183,0
Dosis: 2
Route/Site: UN / UN

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

Fatigue Feeling cold Myalgia Nausea Pyrexia Vomiting

Symptomtext

chills, fatigue, fever, nausea, vomiting, myalgias

Weitere VAERSDATA-Felder

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

VAERS 2486123

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: MI
Alter: 75,0
Geschlecht: F
Eingang: 22.10.2022
Impfdatum: 25.04.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

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

Pain in extremity

Symptomtext

sore arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 76-year-old female patient received BNT162b2 (BNT162B2), on 25Apr2022 as dose 4 (booster), single (Lot number: FJ6369) at the age of 75 years for covid-19 immunisation. The patient's relevant medical history included: "Seasonal allergies" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Lot number: EN6204), administration date: 11Mar2021, when the patient was 74-year-old, for Covid-19 immunization, reaction(s): "Sore arm"; BNT162b2 (DOSE 2, SINGLE; Lot number: ER8733), administration date: 31Mar2021, when the patient was 74-year-old, for Covid-19 immunization, reaction(s): "Sore arm"; BNT162b2 (DOSE 3 (BOOSTER), SINGLE; Lot number: EW0172), administration date: 15Nov2021, when the patient was 75-year-old, for Covid-19 immunization, reaction(s): "Sore arm"; flu shot (.), administration date: 26Oct2021, for Immunization, reaction(s): "Sore arm". Additional information: It was reported that she had no problems with the first 4 doses, there was a bit of sore arm. No additional vaccines administered on same date of the Pfizer suspect. The adverse events did not require a visit to emergency room and physician office. The patient did not receive other vaccines within four weeks prior to COVID vaccine . The following information was reported: PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "sore arm".; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201241797 same reporter/patient/AE, different dose;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Seasonal allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2484266

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: WI
Alter: 62,0
Geschlecht: F
Eingang: 20.10.2022
Impfdatum: 18.04.2022
Beginn: 18.09.2022
Tage bis Beginn: 153,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Cough Fatigue Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

COVID pos on 9/18/2022. Symptoms; body aches, cough; low grade fever and debilitating fatigue. I was prescribed a 5-day course of Paxlovid. However, I contracted COVID a second time on 10/04/2022. It was a very mild case so there are no symptoms to report. Tested COVID neg on 10/10/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Tacrolimus; Entyvio; Tylenol OTC; Vitamin D; Calcium; Boniva; Nasal Spray; Venlafaxine
Allergien: Pineapple; Walnuts; Kiwi
Vorherige Impfungen: Arm swelling, Pneumonia Vaccine

VAERS 2483941

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NJ
Alter: 58,0
Geschlecht: F
Eingang: 20.10.2022
Impfdatum: 20.04.2022
Beginn: 21.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Hypersomnia Malaise Pyrexia Rhinorrhoea SARS-CoV-2 test positive Sinus disorder

Symptomtext

On 4/21/2022, I woke up the next morning feeling very fatigue and it lasted most of the day. On 9/21/2022, I woke up feeling fatigue, and sinus symptoms. I thought maybe I was getting a sinus infection. I took a COVID-19 home test and it was negative. I took NYQUIL that night. On 9/22/2022, I woke up after sleeping for 12 hours and I was not feeling well and felt tired. I took a DAYQUIL at 1:00PM. I was going to work and I had to fill out a questionnaire about how I was feeling. I wrote I was having sinus problems. I took another COVID-19 home test at 4:00PM and it was positive. I went to the work and took a COVID-19 PCR test at the clinic at work, and it was positive. I came home and isolated. I called my doctor and asked for the PAXLOVID. On 9/24/2022, I got a fever of 102. I started taking the PAXLOVID on 9/24/2022. My symptoms were cough, runny nose, fatigue and my temperature. By the third dose of the PAXLOVID, I was feeling a little bit better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 9/22/2022 COVID-19 PCR test positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: CLARITIN; ZYRTEC
Allergien: N/A
Vorherige Impfungen: -

VAERS 2068889

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: MI
Alter: 74,0
Geschlecht: M
Eingang: 17.10.2022
Impfdatum: 15.01.2022
Beginn: 16.01.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Chills Cold sweat Constipation Injection site pain Insomnia Pyrexia

Symptomtext

pain in left shoulder at injection site, chills, clammy, constipated, trouble sleeping

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: urinary tract infection, epidemic vertigo, retention of urine
Vorgeschichte: transient cerebral ischemic attack, unspecified, post polio syndrome, osteoarthritis of both shoulders, ulcerative colitis, hypertension
Andere Medikamente: meclizine, mesalamine, Motrin, oxybutynin chloride, Tylenol extra strength
Allergien: none known
Vorherige Impfungen: -

VAERS 2469517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NJ
Alter: 63,0
Geschlecht: F
Eingang: 05.10.2022
Impfdatum: 28.02.2022
Beginn: 28.03.2022
Tage bis Beginn: 28,0
Dosis: 3
Route/Site: IM / RA

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

Alopecia Dizziness Immediate post-injection reaction Impaired work ability Iron binding capacity total normal Laboratory test normal Lethargy Liver function test normal Metabolic function test normal Pain Serum ferritin normal Tri-iodothyronine free normal Tri-iodothyronine normal

Symptomtext

IMMEDIATELY AFTER RECEIVING THE BOOSTER THAT WAS REQUIRED BY MY JOB TO GET I WAS DIZZY, LETHARGIC AND ACHY, SO MUCH SO THAT I HAD TO CALL OUT OF WORK FOR THE REST OF THE WEEK. I HAVE NEVER CALLED OUT OF WORK MORE THAN FIVE TIMES IN THE 35 YRS. I HAVE WORKED AS A NURSE. AT THE END OF MARCH BEGINNING OF APR. I NOTICED MORE HAIR IN MY BRUSH THAN USUAL. WHEN I WENT TO THE HAIRDRESSER FOR MY SUMMER CUT IN JUNE SHE NOTICED SEVERAL BALD PATCHES. AND BY THE MIDDLE OF JULY I WAS COMPLETELY BALD AND HAD NO BODY HAIR ANYWHERE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: 06/30/2022 TSH3, TEST FREE AND TOTAL, T3 FREE, FERRITIN, FE TIBC. 07/072022 QUANTIFERON, HEPATIC FUNC. B, BMP. EACH OF THESE TESTS CAME BACK NORMAL. I HAVE NO MEDICAL HISTORY OF AND KIND OF IMMUNE SUPRESSED DISEASES. THE IS NO HISTORY OF ANY IN MY FAMILY BORTH MATERNAL AND FATERNAL. I AM CURRENTLY TAKINF OLUMIANT 4MG. TO I HOPE HELP IN REGROWTH OF MY HAIR
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: MULT. VIT.
Allergien: NONE
Vorherige Impfungen: -

VAERS 2453750

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 15,0
Geschlecht: M
Eingang: 21.09.2022
Impfdatum: 25.01.2022
Beginn: 26.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Urticaria

Symptomtext

Patient sprouted dozens upon dozens of "hives" on his upper body - some 50-60 of them, Not one hive below the navel. Hives were increasing and "spreading" when we sought treatment. Reaction started within 18 hours of COVID "booster" shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: Physician prescribed Prednisone - and it was extremely effective. Hives gone 36 hours later.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Peanut and Shellfish food allergies
Vorherige Impfungen: -

VAERS 2450825

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NJ
Alter: 46,0
Geschlecht: F
Eingang: 19.09.2022
Impfdatum: 17.03.2022
Beginn: 17.03.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / AR

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

Asthenia Fatigue Influenza like illness Malaise Nasopharyngitis Respiration abnormal

Symptomtext

I experienced flu like symptoms but on a higher level. I felt more like I had a cold. I felt weak and fatigued. It affected my breathing and I felt like I had COVID. I would feel like this for about four days. I never had a temperature or felt like I had a fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Asthma Bronchitis
Vorgeschichte: Seasonal Allergies; Hypothyroidism; Type 2 Diabetes; Hypertension; Asthma
Andere Medikamente: Amathyroid 75mg 1x/day; Enalapril 20mg 1x/day; Folic Acid 1mg; Montelukast 10mg 1x/day; Metformin 500mg 2x/day;
Allergien: None
Vorherige Impfungen: Flu Vaccine - Over the age of 18.

VAERS 2447845

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 16.09.2022
Impfdatum: 12.01.2022
Beginn: 23.08.2022
Tage bis Beginn: 223,0
Dosis: 3
Route/Site: - / -

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

Angiogram cerebral normal Arteriogram carotid normal COVID-19 Computerised tomogram head normal Dizziness Headache Hemiparesis Hypoaesthesia Intervertebral disc protrusion Magnetic resonance imaging head abnormal Magnetic resonance imaging spinal abnormal Perfusion brain scan normal SARS-CoV-2 test positive

Symptomtext

Admission Date: 8/23/2022 Discharge Date: 9/5/2022 PRESENTING PROBLEM: Left-sided weakness [R53.1] Acute left-sided weakness [R53.1] Acute nonintractable headache, unspecified headache type [R51.9] HOSPITAL COURSE: The patient is a 66 yo woman with a history of T2DM on trulicity, HTN, fibromyalgia, who presented to hospital on 8/23/22 with headache, dizziness, and L sided numbness. On presentation she was afebrile with stable vital signs. Stroke code was activated and she underwent evaluation with CT head, CTA head/neck and CT perfusion without evidence of acute infaction. MRI brain and cspine was negative for infarct but did show previous ACDF at c5/c6 and new disc bulge at C7-T1 but no high grade stenosis. Neurology was consulted and recommended starting the patient on an asa 81mg daily due to her stroke risk factors, zio patch at discharge, and followup in stroke clinic. The patient was also noted to be covid +, which was felt to be the cause of her headache and likely her symptoms of dizziness as well. She otherwise remained on room air without SOB or hypoxia. PT/OT were consulted and recommended SAR. She was recommended to followup with her previous spine surgeon after discharge for her cervical disc disease. Her stay in the hospital was prolonged with covid isolation precautions at the SAR facility. Discharged in a stable condition to SAR on 9/4/22 with recommendations to follow up with PCP, Neurology and her spinal surgeon.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: 13,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Fibromyalgia Irritable bowel syndrome with constipation Hypertension Migraine headache GERD (gastroesophageal reflux disease) Disc disorder of lumbar region Disc disorder of cervical region Depressive disorder Chronic rhinitis Type 2 diabetes mellitus (HCC) Hyperlipidemia Left-sided weakness Dizziness COVID-19 virus infection, +09/23/2022 Anemia
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler aspirin 81 MG chewable tablet atorvastatin (LIPITOR) 40 MG tablet benzonatate (TESSALON) 200 MG capsule Blood Glucos
Allergien: GatifloxacinRash, Hives, Itching MorphineHives, Unknown Sulfa Drugs LisinoprilCough MetforminRash SemaglutideOther Tramadol-acetaminophenNausea and Vomiting, Nausea Only, Other, Rash AzithromycinOther DiazepamFatigue Duloxetine ErythromycinOther Gabapentin Jardiance [Empagliflozin] LatexRash LevaquinSkin Rashes/Hives Penicillin G BenzathineSkin Rashes/Hives PregabalinSwelling RofecoxibCough, Unknown Topamax [Topiramate]Nausea Only, Other NitrofurantoinRash
Vorherige Impfungen: -

VAERS 2442893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 65,0
Geschlecht: F
Eingang: 13.09.2022
Impfdatum: 22.02.2022
Beginn: 05.09.2022
Tage bis Beginn: 195,0
Dosis: 3
Route/Site: UN / UN

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

Dizziness

Symptomtext

dizziness

Weitere VAERSDATA-Felder

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

VAERS 2431027

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: MI
Alter: 62,0
Geschlecht: M
Eingang: 07.09.2022
Impfdatum: 20.04.2021
Beginn: 07.08.2022
Tage bis Beginn: 474,0
Dosis: 3
Route/Site: - / -

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

Agitation COVID-19 Device issue Ear pain Homicidal ideation Pain Pulmonary mass SARS-CoV-2 test positive Suicidal ideation

Symptomtext

This 63-year-old gentleman was admitted on 08/07/2022. He has been noted to have a left upper lobe lung mass which is suspicious for carcinoma. Evaluation is ongoing. The patient describes a 2-week history of otalgia. Initially, this involved the left ear, but later involved the right ear as well. Pain is intermittent, moderate intensity, and may be triggered by opening his mouth wide. He denies any habit of clenching of teeth, but he has a lower denture which fits poorly. He has had no otorrhea. He was kept on Ativan, Haldol and Thorazine for agitation. He was certified by the psychiatrist. Currently awaiting placement. Incidentally, patient was noted to have swabbed positive for COVID-19. He is currently admitted as psych facility will not take him till he is off COVID precautions. He does not have any upper respiratory symptoms at this time. No fevers or chills. No chest pain or shortness of breath. He mentions to have received 2 doses of the vaccine in 2021. When I examined the patient, he did not want to go into details of why he was having homicidal and suicidal ideations. Pt medically cleared for discharged to Inpt Psych with Behavioral Center, with EMS transportation. Coordinated and arranged by Inpt psych. No other needs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: 8/8 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --not detected 8/26 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2417580

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 66,0
Geschlecht: F
Eingang: 22.08.2022
Impfdatum: 18.02.2022
Beginn: 10.08.2022
Tage bis Beginn: 173,0
Dosis: 4
Route/Site: SYR / LA

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

Asthenia COVID-19 Fatigue Hyperhidrosis Loss of personal independence in daily activities SARS-CoV-2 test positive Throat irritation Vaccine breakthrough infection

Symptomtext

On 8-8-2022 I began having a scratchy throat and I tested using a home COVID-19 test with negative results. On 8-9-2022, I felt fatigued. I again tested negative with home COVID-19 test. On 8-10, I was having a hard time functioning due to weakness so I retested with a home COVID-19 test and this time it was positive. I called my doctor and I spoke with the on call doctor who sent in a prescription of Paxlovid. I started taking it on 8-11 after speaking with my cardiologist. During the night of 8-11, I woke up sweating and it is questionable if I had a fever due to it not being over 99.0. I started feeling better on 8-14 or 8-15. I am reporting a breakthrough case of COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 8-8-2022 home COVID-19 test -negative result; 8-9-2022 home COVID-19 test -negative result; 8-10-2022 home COVID-19 test - positive result
Aktuelle Erkrankungen: None
Vorgeschichte: Left Bundle Branch Block; Invasive Breast Cancer; Hypothyroidism; Peripheral Neuropathy in both feet and legs
Andere Medikamente: Liothyronine; Omeprazole; Synthroid; Crestor; Carvedilol; Eplerenone; Losartan Potassium; Letrozole; Tylenol; Aleve; Refresh eye drops; Vitamin B100 Complex; Vitamin B12; Calcium Citrate; CoQ10; Probiotic; Glucosamine and Chondroitin; React
Allergien: None
Vorherige Impfungen: Shingrix vaccine - year unknown about 6 years ago. Age 60- symptoms similar to a shingles outbreak at site of injection with red

VAERS 2405767

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: AR
Alter: 75,0
Geschlecht: F
Eingang: 09.08.2022
Impfdatum: 06.05.2022
Beginn: 01.08.2022
Tage bis Beginn: 87,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Fatigue SARS-CoV-2 test positive

Symptomtext

I did not have an adverse reaction to the vaccine. I tested positive for COVID-19 with a home test on 08/02/2022. I contacted my doctor via the patient portal for the PAXLOVID vaccine due to my age. I started to fill better after taking the PAXLOVID. As of today, I'm feeling tired but I do feel better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home test for COVID-19 on 08/02/2022 was positive.
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure, environmental allergies; high cholesterol
Andere Medikamente: Losartan; rosuvastatin; montelukast; gabapentin; ADVAIR inhaler; VENTOLIN; fluticasone; azelastine; allergy nose spray; vitamin D
Allergien: Avocado; penicillin; codeine
Vorherige Impfungen: -

VAERS 2396439

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: FL
Alter: 71,0
Geschlecht: F
Eingang: 29.07.2022
Impfdatum: 27.01.2022
Beginn: 16.07.2022
Tage bis Beginn: 170,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Chills Cough Fatigue Malaise Nausea Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19 on 07/16/2022 with symptoms of fever of 103.8 at highest point, sore throat, congestion, cough, chills, mild nausea, and fatigue. I was prescribed Paxlovid Renal Dose on 07/19/2022, and I experiencing a bitter metallic taste, and diarrhea while taking it. I was ill for 7 days before my symptoms began to resolve. I am fully recovered with no lingering symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 rapid nasal swab home test was positive on 07/17/2022.
Aktuelle Erkrankungen: N/A
Vorgeschichte: 3A Kidney Disease; Osteoarthritis; Irritable Bowel Syndrome Diarrhea; Cardiac Arrhythmia
Andere Medikamente: Multivitamin; Vitamin D3; Biotin; Atenolol; Triamterene; Baclofen; Gabapentin; Letrozole; Pepcid; Calcium
Allergien: Levaquin
Vorherige Impfungen: -

VAERS 2395185

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 68,0
Geschlecht: M
Eingang: 28.07.2022
Impfdatum: 18.05.2022
Beginn: 18.07.2022
Tage bis Beginn: 61,0
Dosis: 4
Route/Site: IM / AR

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

COVID-19 Cough Fatigue Headache Nasal congestion Pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Sneezing

Symptomtext

Sneezing, cough, body aches, fever of 100.6, nasal and chest congestion, headache, fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Tested positive for COVID-19 on 07/20/2022 at 4:16 PM Pacific Daylight Time via On/Go self-administered at home COVID-19 test
Aktuelle Erkrankungen: None
Vorgeschichte: HIV+ since 03/1985; Elite Controller of HIV; Antiretroviral Na?ve Hyperlipidemia Essential Hypertension IBS Arthritis Depression Insomnia IBS Hypothyroidism Anxiety Essential Hypertension Essential Hypertension Migraine 7.5 mg Dry mouth GERD Kidney stones Migraine Migraine HSV
Andere Medikamente: Amoxicillin 500 mg; Atorvastatin 40 mg; Chlorthalidone 50 mg; Celebrex 200 mg; Colestipol1 GM IBS desvenlafaxine er 50 mg; Eszopiclone 3 mg; Hyoscyamine ER .375 mg; Levothyroxine 75 mcg; Lorazapam 1 mg; Losartan 100 mg; Metoprolol 50
Allergien: Lactose intolerance Amlodipine allergy
Vorherige Impfungen: -

VAERS 2394970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 49,0
Geschlecht: F
Eingang: 28.07.2022
Impfdatum: 16.02.2022
Beginn: 21.07.2022
Tage bis Beginn: 155,0
Dosis: 2
Route/Site: UN / UN

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

Chills Cough Fatigue Myalgia Oropharyngeal pain Respiratory tract congestion Upper-airway cough syndrome

Symptomtext

chills, fatigue, congestion, postnasal drip, sore throat, cough, myalgias

Weitere VAERSDATA-Felder

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

VAERS 2376831

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NJ
Alter: 70,0
Geschlecht: F
Eingang: 21.07.2022
Impfdatum: 20.04.2022
Beginn: 17.07.2022
Tage bis Beginn: 88,0
Dosis: 4
Route/Site: IM / RA

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

Abdominal pain upper COVID-19 Cough Fatigue Headache Heart rate increased Hypopnoea Nasal congestion Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had an intense sore throat, and I felt fatigued. I also noticed my breathing was more shallow, and my pulse may have been faster. I normally have a cough but it had gotten worse. I took a COVID-19 test the next day and it was positive. Two days later I started to get a stomach ache, nasal congestion, runny nose, and in intermittent headache. Yesterday I had a virtual appointment with my doctor and they prescribed me Paxlovid. I am still experiencing symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: COVID-19 Test- Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2374783

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: TX
Alter: 52,0
Geschlecht: F
Eingang: 20.07.2022
Impfdatum: 18.04.2022
Beginn: 10.07.2022
Tage bis Beginn: 83,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Chills Cough Diarrhoea Ear discomfort Exposure to SARS-CoV-2 Headache Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive Sinus congestion Vomiting

Symptomtext

On 07/04/2022 my mother flew and she tested positive for COVID-19 on 07/07/2022. She lives with me and I was caring for her. On 07/10 I began having symptoms such as headache, sore throat, body aches, fever, vomiting, diarrhea, chills, coughing, sinus congestion, and ear pressure. I tested positive for COVID-19 on 07/11/2022. On 07/13/2022 I received a Monoclonal antibody infusion. By 07/14 my symptoms were starting to improve and I no longer had a fever. I tested negative with an at home test on 07/19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: At home COVID-19-positive-07/11/2022.
Aktuelle Erkrankungen: None.
Vorgeschichte: Celiac's Disease
Andere Medikamente: Women's Multivitamin; Allegra; Pepcid AC; Zysol.
Allergien: Wheat
Vorherige Impfungen: 1st dose of Pfizer/COVID-19. 12/18/2020. Age-51. Elevated heart rate.

VAERS 2372557

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: PA
Alter: 71,0
Geschlecht: F
Eingang: 18.07.2022
Impfdatum: 16.04.2022
Beginn: 27.05.2022
Tage bis Beginn: 41,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

I developed a sore throat and cough and tested positive. I called my doctor the same day and received an anti-viral

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism; Lupus;
Andere Medikamente: Mustinon; Kegratol; Atenolol; Zofran; Singulair; Prednisone; Zoloft; Xanax; Synthroid; Calcium; Melatonin
Allergien: None
Vorherige Impfungen: Flu vaccine

VAERS 2368822

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: IL
Alter: 49,0
Geschlecht: F
Eingang: 14.07.2022
Impfdatum: 08.07.2022
Beginn: 11.07.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: SYR / LA

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

Blood test COVID-19 Chills Fatigue Nasal congestion Nasopharyngitis Pain in extremity Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Sore arm: chills: fatigue: nasal drainage: cold symptoms: stuffy nose: fever: tested positive for Covid19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Blood
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Multivitamin; vitamin C; calcium; vitamin B complex
Allergien: None
Vorherige Impfungen: -

VAERS 2366230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: WA
Alter: 60,0
Geschlecht: M
Eingang: 12.07.2022
Impfdatum: 07.04.2022
Beginn: 25.06.2022
Tage bis Beginn: 79,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Malaise Pain Productive cough SARS-CoV-2 test positive

Symptomtext

I received my second Pfizer booster for COVID-19 on 4/7/2022. On 6/25/2022, I developed very slight body aches. I also had a slight cough with a little bit of phlegm. That day, I took a home test for COVID-19 and got a positive result. The mild symptoms lasted for 3 days. On 6/28/2022, I took two more home tests to confirm that I had COVID-19, and they both yielded a positive result. On about 6/29/2022, my doctor gave me a 5-day course of Paxlovid. All of my symptoms went away and I felt fine. On 7/6/2022, I took two home tests and got a negative result with both of them.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: Home tests with positive result: 6/25/2022, 6/28/2022. Home tests with negative result: 7/6/2022.
Aktuelle Erkrankungen: None.
Vorgeschichte: COPD.
Andere Medikamente: Atorvastatin; Stiolto; Vitamin C; Vitamin D; Fiber Capsules.
Allergien: None.
Vorherige Impfungen: -

VAERS 2366154

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: MN
Alter: 67,0
Geschlecht: F
Eingang: 12.07.2022
Impfdatum: 11.04.2022
Beginn: 09.07.2022
Tage bis Beginn: 89,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Cough Fatigue Headache Myalgia Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I have had a runny nose, cough, muscle aches, very sore throat, a slight headache. I have had no fever. I also experienced fatigue. My doctor prescribed me PAXLOVID, and I am on my third dose today. I am also taking ADVIL. My doctor had me stop taking my cholesterol medication while I am taking PAXLOVID. Also my NORVASC dosage is now cut in half while I am taking PAXLOVID for this 5 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: At home test- positive.
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood pressure
Andere Medikamente: Lisinopril; NORVASC; women's multivitamin; calcium; vitamin D; vitamin E; green tea capsule
Allergien: Cats; squash
Vorherige Impfungen: -

VAERS 2359580

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: WA
Alter: 68,0
Geschlecht: F
Eingang: 06.07.2022
Impfdatum: 01.04.2022
Beginn: 27.06.2022
Tage bis Beginn: 87,0
Dosis: 4
Route/Site: IM / RA

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

Back pain COVID-19 Chills Cough Depression Discomfort Ear pain Feeling abnormal Headache Musculoskeletal stiffness Pain Productive cough SARS-CoV-2 test positive Temperature intolerance

Symptomtext

6/27/2022 Woke up with back hurting and neck stiff. That night I felt bad, whole body aches. 6/28 at home COVID 19 test positive. Ear soreness; headache; shivering/chills; Increased sensitivity temperature and pressure; Deep depression feelings. Tele visit with doctor on 6/28. Doctor prescribed PAXLOVID. Got a PCR COVID 19 test, also positive. 6/29 symptoms got worse, and coughing increased. Sputum from coughing still clear. 7/5 symptoms improved noticeably, but not fully recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: At home COVID 19 test and PCR test, both positive.
Aktuelle Erkrankungen: No
Vorgeschichte: Bronchiectasis; MAC
Andere Medikamente: Amoxicillin; duloxetine; valaciclovir; lorazepam
Allergien: Ofloxacin
Vorherige Impfungen: -

VAERS 2357925

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: WA
Alter: 64,0
Geschlecht: M
Eingang: 05.07.2022
Impfdatum: 30.03.2022
Beginn: 09.06.2022
Tage bis Beginn: 71,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Cough Headache Impaired work ability Lethargy Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I started getting symptoms of fever, headache, lethargic, and sore throat. I took an at home COVID-19 test that was positive. My coughing progressed and was severe. I contacted my doctor after 10 days. It took me over 3 weeks to recover. I was off of work for 3 weeks as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 test - positive.
Aktuelle Erkrankungen: None
Vorgeschichte: N/A
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2356310

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: MA
Alter: 27,0
Geschlecht: F
Eingang: 03.07.2022
Impfdatum: 10.05.2022
Beginn: 12.05.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / LA

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

Abortion spontaneous Chills Dysmenorrhoea Haemorrhage Intermenstrual bleeding Maternal exposure during pregnancy Pyrexia

Symptomtext

I started having spotting and slowly bleeding and cramping every day which lead to miscarriage; started having spotting and slowly bleeding and cramping every day which lead to miscarriage; My PCP told I was 9weeks pregnant according to my last menstural period so she told me to get Pfizer vaccine so I got it; started having spotting and slowly bleeding and cramping every day which lead to miscarriage; started having spotting and slowly bleeding and cramping every day which lead to miscarriage; chills; fever; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 27-year-old female patient (pregnant) received BNT162b2 (BNT162B2), on 10May2022 as dose 3 (booster), single (Lot number: FJ6369) at the age of 27 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. Date of last menstrual period: 04Mar2022. The patient was 9 weeks pregnant at the time of exposure to BNT162b2. The patient was 10 weeks pregnant at the event onset. The patient is expected to deliver a baby(s) on 09Dec2022. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete but unknown manufacturer, Lot number: FJ6369, Administration date and time: 10May2022 04:45 PM, Dose number: 1, location: Left arm), for COVID-19 immunization. The following information was reported: CHILLS (non-serious) with onset 12May2022, outcome "unknown"; PYREXIA (non-serious) with onset 12May2022, outcome "unknown", described as "fever"; ABORTION SPONTANEOUS (medically significant), outcome "unknown", described as "I started having spotting and slowly bleeding and cramping every day which lead to miscarriage"; HAEMORRHAGE (medically significant), INTERMENSTRUAL BLEEDING (non-serious), DYSMENORRHOEA (non-serious), outcome "unknown" and all described as "started having spotting and slowly bleeding and cramping every day which lead to miscarriage"; MATERNAL EXPOSURE DURING PREGNANCY (non-serious), outcome "unknown", described as "My PCP told I was 9weeks pregnant according to my last menstural period so she told me to get Pfizer vaccine so I got it". The events "i started having spotting and slowly bleeding and cramping every day which lead to miscarriage", "started having spotting and slowly bleeding and cramping every day which lead to miscarriage", "my pcp told i was 9weeks pregnant according to my last menstural period so she told me to get pfizer vaccine so i got it", "chills" and "fever" required emergency room visit. Therapeutic measures were taken as a result of abortion spontaneous, maternal exposure during pregnancy, chills, pyrexia. Clinical Course: patients Last menstrual date was on 04Mar2022. patient had Gestational period: 9. Patient received other Pfizer vaccine same date product with lot# FJ6369, Facility type vaccine at Hospital. patient did not had other vaccine in four weeks and other medications in two weeks patient reported On 11May My PCP told she was 9weeks pregnant according to her last mensural period so she told her to get Pfizer vaccine so she got it and 12May she had chills fever and had to call out. she was healthy fit and fine before vaccine. she started having spotting and slowly bleeding and cramping every day which lead to miscarriage. Adverse Event start date: 11May2022. Adverse event start time: 11:45 PM. Patient did not had COVID prior vaccination and not COVID tested post vaccination. Patient did not had known allergies and other medical history. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2347416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: WI
Alter: 58,0
Geschlecht: M
Eingang: 01.07.2022
Impfdatum: 30.03.2020
Beginn: 09.06.2020
Tage bis Beginn: 71,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Chest X-ray normal Electrocardiogram normal Fatigue Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

It started with a sore throat as I flew home sore throat got worse and I became more and more congested a rapid test showed an immediate positive I went the next day to urgent care an EKG and chest xray showed no results I was prescribed Paxlovid and within twenty-four my symptoms subsided although I was still wiped and tire within five to seven days I was symptom free with congestion in about TEN days I felt OR better or well

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: EKG Chest X-ray no results or nothing showed
Aktuelle Erkrankungen: Seasonal Allergies
Vorgeschichte: Chrons disease Osteoporosis
Andere Medikamente: Amlodipine Protonic Claritin D Calcium Vitamin D Multivitamin Humira B twelve shots
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2344727

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: VA
Alter: 65,0
Geschlecht: M
Eingang: 30.06.2022
Impfdatum: 30.03.2022
Beginn: 26.06.2022
Tage bis Beginn: 88,0
Dosis: 4
Route/Site: IM / LA

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

Asthenia COVID-19 Cough Fatigue Headache Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I started getting symptoms of sore throat that I thought was allergies. That evening, I started getting a cough that was deep and painful. I had a headache and was tired and achy. I went to bed early and got up that morning feeling worse. I took an at home COVID-19 test that was positive. I went to a clinic due to my symptoms getting worse. I was taking ADVIL and TYLENOL combined. I felt feverish with a low grade fever. I was prescribed ritonavir and nirmatrelvir. My symptoms went until 6/28/2022. Then the next day, I still felt fatigued. I almost feel normal now except for low energy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Mild HTN (Controlled)
Andere Medikamente: Levothyroxine; ezetimibe; losartan; supplements
Allergien: Statins
Vorherige Impfungen: 1975 Swine flu vaccine, bad case of the flu, nausea, vomiting, headache.

VAERS 2335842

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: FL
Alter: 76,0
Geschlecht: M
Eingang: 27.06.2022
Impfdatum: 29.04.2022
Beginn: 17.06.2022
Tage bis Beginn: 49,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Headache Malaise Respiration abnormal SARS-CoV-2 test positive Sneezing Vaccine breakthrough infection

Symptomtext

COVID breakthrough case, tested positive on 06/18/2022. I received my 2nd booster shot on 04/29/2022 and my COVID symptoms started on 06/17/2022 breathing, sneezing, headache, no fever. I am going to the doctor tomorrow 06/27/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID test clinic.
Aktuelle Erkrankungen: None
Vorgeschichte: Artificial valve 1998 since
Andere Medikamente: Warfarin; proprinal; tropic protonic; aspirin
Allergien: None
Vorherige Impfungen: -

VAERS 2325646

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NC
Alter: 64,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 16.05.2022
Beginn: 16.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Arthralgia Extra dose administered Gastrooesophageal reflux disease Oesophagitis Pyrexia

Symptomtext

The same day as the vaccine I developed a low grade fever and joint pain. A few hours I developed severe esophagitis. I do suffer from acid reflux. I spoke to my dr who recommended acid reflux medication. Symptoms ceased completely later that evening.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Osteo-arthritis
Andere Medikamente: HRT, Vit D3, fish oil
Allergien: Sulfa, hohoba oil, ecanasia pills
Vorherige Impfungen: Experienced similar symptoms from 2nd and 3rd covid vaccine

VAERS 2322764

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: SC
Alter: -
Geschlecht: U
Eingang: 17.06.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / LA

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

Protein albumin ratio Pruritus Swollen tongue Troponin

Symptomtext

Facial Itching; My tongue has been swollen; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 26-year-old patient received BNT162b2 (BNT162B2), as dose number unknown, single (Batch/Lot number: FJ6369), in left arm for COVID-19 immunization; influenza vaccine (INFLUENZA VACCINE), as dose number unknown, single (Batch/Lot number: unknown). The patient's relevant medical history and concomitant medications were not reported. The following information was reported: PRURITUS (non-serious), outcome "unknown", described as "Facial Itching"; SWOLLEN TONGUE (non-serious), outcome "unknown", described as "My tongue has been swollen". The patient underwent the following laboratory tests and procedures: Protein albumin ratio: Normal, notes: I did have a lab test to look at my blood protein values to test for allergic reaction and that all back normal; Troponin: Unknown Results.Therapeutic measures were taken as a result of pruritus, swollen tongue. Additional information: Patient reported of taking Pfizer COVID vaccine on January 18. The side effect that patient had were facial itching which started immediately after reporter got the vaccine and also had tongue swelling ever since got the vaccine. Patient got it on January 18 and tongue has been swollen a couple of time a week ever since then. Expiration date was not written on patient's card. Patient did not have any other medical conditions and medications. Whenever the tongue swelling started doctor prescribed hydroxyzine hcl to help with the swelling (Later clarified as treatment). Patient saw an allergist as well but they did not find anything in the test. Patient never did see an allergist as well but they did not find anything in the test. Patient never had any other side effect from any other vaccine. Had Flu vaccine(confirmed later as Influenza vaccine, Unknown manufacturer and captured) a few days before I got the Pfizer vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Test Name: Blood protein; Result Unstructured Data: Test Result:Normal; Comments: I did have a lab test to look at my blood protein values to test for allergic reaction and that all back normal; Test Name: Troponin; Result Unstructured Data: Test Result:Unknown Results
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2318959

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: TX
Alter: 77,0
Geschlecht: F
Eingang: 14.06.2022
Impfdatum: 12.04.2022
Beginn: 18.05.2022
Tage bis Beginn: 36,0
Dosis: 4
Route/Site: IM / AR

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

COVID-19 Cough Decreased appetite Fatigue Feeling abnormal Influenza virus test negative Laryngitis Oropharyngeal pain SARS-CoV-2 test positive Streptococcus test negative

Symptomtext

It started with a sore throat and a cough. I tend to cough a lot but it worsened. I developed fatigue and loss of appetite. I also developed brain fog. I also had laryngitis. On that Thursday when I was not any better, I called the doctors office and they scheduled a telemedicine appointment and the doctor told me she wanted me to go and get tested. I was tested that for Flu, Strep and COVID-19 on May 19. The COVID-19 test was positive. I had an antibody infusion on Wednesday May 25, 2022 and was prescribed the albuterol on May 24, 2022. I am definitely better. The cough is not gone but I am over the sore throat. I tested negative on Saturday the 21st of May. I have not completely recovered as the cough is still a nuisance but I don't feel bad nor do I have the fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Strep-May 19,2022-Negative COVID-19-May 19, 2022-Positive Flu Test-Negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypothyroidism Overactive Bladder Seasonal Allergies Hypertension Acid Reflux Coronary Artery Disease
Andere Medikamente: Levothyroxine, Oxybutynin Chloride, Loratadine, Losartan, Co Q 10, Align, I-caps, Omega 3, Tylenol Arthritis, Aspirin, Famotidine, Atorvastatin, Atenolol, Vitamin D3, Gabapentin, Prolia Infusion
Allergien: N/A
Vorherige Impfungen: -

VAERS 2318888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: PA
Alter: 56,0
Geschlecht: F
Eingang: 14.06.2022
Impfdatum: 16.05.2022
Beginn: 06.06.2022
Tage bis Beginn: 21,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Feeling abnormal Headache Malaise Parosmia Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Sneezing Taste disorder Vaccine breakthrough infection

Symptomtext

Breakthrough case of Covid sx began 06/06/2022. Positive test 6/07/2022. Sx began later in the day of 6/06/2022 with sneezing a lot. By the next morning, 06/07/2022 I woke up feeling terrible. Over the course of the night, I had a fever (without use of thermometer as I did not have one handy) but I know my body. I had coughing and congestion, I also had a terrible headache. I booked a PCR test which came back positive, and a rapid home test was also positive. My PCP. Things got worse before they got better, I am fatigued, I was still had a fever of 102.5 - 102.9. I was taking TYLENOL and MOTRIN alternating and did not go down. My SpO2 was getting into the 80s and I was feeling over all crappy. My PCP prescribed PAXLOVID. I improved by 06/10/2022, my sense of smell and taste have been altered slightly but are starting to comeback. I am grateful for the vaccine, I feel it could have been worse.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home rapid test, positive. PCR, positive.
Aktuelle Erkrankungen: No
Vorgeschichte: Slightly elevated HBP
Andere Medikamente: NORVASC
Allergien: Penicillin; seasonal allergies; bee stings
Vorherige Impfungen: -

VAERS 2315427

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CT
Alter: 52,0
Geschlecht: F
Eingang: 10.06.2022
Impfdatum: 28.04.2022
Beginn: 28.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Decreased appetite Diarrhoea Feeling cold Headache Impaired work ability Joint lock Nausea Pain Vomiting

Symptomtext

The evening of the third dose I began to have a headache and body aches. As the night progressed it got worse I felt like my joints were locking and I got very cold. I had loss of appetites, nausea, vomiting and diarrhea. I felt the same the next day and was unable to work. I called my doctor to see what I needed to do and she stated it would run its course. Saturday and Sunday it slowly got better. I remained home from work Monday but was able to return on Tuesday.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin chewable; venlafaxine
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2311578

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: VA
Alter: 13,0
Geschlecht: F
Eingang: 07.06.2022
Impfdatum: 22.01.2022
Beginn: 02.06.2022
Tage bis Beginn: 131,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Hypogeusia Hyposmia Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

My child had gotten a fever last Thursday and I gave them an at home Covid-19 test and it was negative. The next day they started having congestion and a sore throat along with a slight cough. We did the test again and it was positive. Up until today they have experienced diminished taste and smell, so not fully lost them but they are less than normal. Today I will be contacting their PCP and following up with them as my child is still testing positive but symptoms have not changed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: Covid-19 home test.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2305122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 58,0
Geschlecht: M
Eingang: 01.06.2022
Impfdatum: 17.04.2022
Beginn: 23.05.2022
Tage bis Beginn: 36,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Cough Exposure to SARS-CoV-2 Fatigue Malaise Myalgia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19 on 05/23/2022 with symptoms of fatigue, runny nose, cough, congestion, and myalgia. I thought it was allergies initially until I did a COVID-19 rapid nasal swab home test was positive on 05/28/2022. I went to a conference 05/20 to 05/22 and received an exposure notification via email, and when I tested initially it was negative. I was ill for 7 to 8 days until my symptoms began to resolve, but I still have a slight lingering cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 rapid nasal swab home test was positive on 05/28/2022
Aktuelle Erkrankungen: No
Vorgeschichte: PTSD
Andere Medikamente: Vitamin B12; Duloxetine; Gabapentin; Amlodipine; Vitamin B1
Allergien: No
Vorherige Impfungen: -

VAERS 2295833

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NY
Alter: 33,0
Geschlecht: F
Eingang: 26.05.2022
Impfdatum: 16.05.2022
Beginn: 16.05.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Angina pectoris Burning sensation Investigation Oropharyngeal pain Swelling

Symptomtext

Angina; Burning swollen pain in tonsils 1 minute after injection; Burning swollen pain in tonsils 1 minute after injection; cystic-like sore near tonsil; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 33-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 16May2022 at 12:00 as dose 2, single (Lot number: FJ6369) at the age of 33 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: fruits" (unspecified if ongoing); "known allergies: Penicillin" (unspecified if ongoing); "Recent diagnoses on HTN" (unspecified if ongoing), notes: Recent diagnoses on HTN. Concomitant medication(s) included: AMLODIPINE. Vaccination history included: BNT162b2 (previous dose details , previous dose product: COVID 19, previous dose brand: Pfizer, previous dose brand unknown: False, previous dose lot number: FJ6369, previous dose lot unknown: False, previous dose administration date: 28Jan2022, previous dose administration time: 08:00AM, previous dose dose number: 1, previous dose vaccine location: Left arm), administration date: 28Jan2022, when the patient was 33-year-old, for COVID-19 Immunization. The following information was reported: ANGINA PECTORIS (medically significant) with onset 16May2022 at 12:00, outcome "not recovered", described as "Angina"; BURNING SENSATION (non-serious), SWELLING (non-serious) all with onset 16May2022 at 12:00, outcome "not recovered" and all described as "Burning swollen pain in tonsils 1 minute after injection"; OROPHARYNGEAL PAIN (non-serious) with onset 16May2022 at 12:00, outcome "not recovered", described as "cystic-like sore near tonsil". The patient underwent the following laboratory tests and procedures: HTN: Unknown results, notes: Recent diagnoses on HTN. Therapeutic measures were not taken as a result of angina pectoris, burning sensation, swelling, oropharyngeal pain. Additional information: report about covid vaccine was yes. If other vaccine in four weeks reported as No. other medications in two weeks reported as amlodipine 2.5 mg once a day. If covid prior vaccination reported as No. If covid tested post vaccination reported as No. Adverse event reported Burning swollen pain in tonsils 1 minute after injection, followed by cystic-like sore near tonsil. Angina. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: Test Name: HTN; Result Unstructured Data: Test Result:Unknown results; Comments: Recent diagnoses on HTN
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fruit allergy; Hypertension (Recent diagnoses on HTN); Penicillin allergy
Andere Medikamente: AMLODIPINE
Allergien: -
Vorherige Impfungen: -

VAERS 2294593

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: GA
Alter: 52,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 12.04.2022
Beginn: 21.05.2022
Tage bis Beginn: 39,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Chest discomfort Cough Exposure to SARS-CoV-2 Fatigue Hypersomnia Neck pain SARS-CoV-2 test negative

Symptomtext

My husband tested positive for Covid on 5/19. My daughter and I went for a PCR on 5/18 due to a known exposure but that was negative. My symptoms began on 5/21 with cough and fatigue. I went to urgent care on 5/22 for another PCR and that was negative. Through that day, my symptoms got worse with chest tightness, pain in neck and shoulders, worsening cough and fatigue. I slept all day that day and Monday, 5/23. Since 5/23 my symptoms have gotten progressively better and today I am feeling basically normal. I received another PCR test yesterday on 5/24 and am still waiting on the results.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Multiple Covid tests negative results.
Aktuelle Erkrankungen: None.
Vorgeschichte: High Blood Pressure
Andere Medikamente: Amlodipine 5mg; lisinopril 20mg; multivitamin; Zyrtec
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2294423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: MA
Alter: 73,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 22.02.2022
Beginn: 21.05.2022
Tage bis Beginn: 88,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Chills Diarrhoea Dysgeusia Ear congestion Fatigue Nasal congestion Pain Pyrexia SARS-CoV-2 test positive Throat irritation Vaccine breakthrough infection

Symptomtext

Breakthrough Case of COVID Sx started on 05/21/2022, with a scratchy throat and progressed to nasal and ear congestion, chills, body aches, fevers up and down between 100.2 and 100.4. I tested positive on a home test on 05/22/2022. I spoke to the doctor on 05/22/2022, she called in a RX for Paxlovid. I did not start taking the med until the evening of 05/23/2022. I am still taking the Paxlovid, sx have improved and I have no fever and body aches, but I still nasal congestion and fatigue as of 05/225/2022. Paxlovid has left a terrible metallic taste in my mouth and I have had some diarrhea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Home test on 05/22/2022 - positive
Aktuelle Erkrankungen: no
Vorgeschichte: breast cancer survivor
Andere Medikamente: Letrozole 2.5mg QD, Levothyroxine 100mcg, QD, Pravastatin 20mg QD, metoprolol 25mg QD, Colace 100mg QD, Tylenol PRN, multivitamin
Allergien: codeine, shellfish, malarone, kiwi
Vorherige Impfungen: -

VAERS 2287433

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 81,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 21.04.2022
Beginn: 13.05.2022
Tage bis Beginn: 22,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Cough Fatigue Headache Oropharyngeal pain SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough COVID Case: The case started last Friday, the 13th of May. Symptoms: headache, sore throat, dry cough, general fatigue. That's it for that day. Treatment: Called my primary doctor. I told her I had a positive test at home. She prescribed Paxlovid, Tessalon for the cough, Doxycycline 100mg 2xday for 10 days, Prednisone 20mg 1 tab per day for 5 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: FOUR At Home Tests - Positive
Aktuelle Erkrankungen: none
Vorgeschichte: Type 2 Diabetes, Asthma
Andere Medikamente: Advair 100/50 2xday, Micardis 80mg 1xday, Diltiazem 180mg 1xday, Myrbitriq 25mg 1xday, Crestor 10mg daily, Januvia 100mg 1xday, Jardiance 10mg 1xday, Glimepiride 1mg 2xday, Areds 2 2capsules daily, Vitamin 3D 50000iu 1xmonth, Ultra Balance
Allergien: Penicillin, Levaquin, Myrbetric, specific tape that dermatologists use
Vorherige Impfungen: 02/11/2021 - 2nd dose Pfizer - Lot #EN6201 - Age 800 - Arm was sore. Fatigue was overwhelming. Horrible headache. A whole genera

VAERS 2286957

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CT
Alter: 66,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 14.04.2022
Beginn: 11.05.2022
Tage bis Beginn: 27,0
Dosis: 4
Route/Site: SYR / RA

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

COVID-19 Dizziness Dysphonia Head discomfort Interchange of vaccine products Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Sinus congestion

Symptomtext

My first 3 doses were Moderna and my 4th dose was Pfizer. Starting 05/11/2022, I had a sore throat, hoarseness, sinus congestion, chest congestion and fever. The fever went away and then I was tested and it was positive for COVID. So, I did a telehealth visit with my doctor and she prescribed Paxlovid. I felt really good for 2 days and now I am having head congestion again and some slight dizziness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Positive PCR COVID Test
Aktuelle Erkrankungen: None
Vorgeschichte: ITP and High Blood Pressure
Andere Medikamente: Synthroid, Losartan, Azelastine, Hydrochlorothiazide, Amlodipine Besylate, Multivitamin and Calcium
Allergien: Sulfa drugs and Codeine
Vorherige Impfungen: -

VAERS 2284977

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 27,0
Geschlecht: M
Eingang: 19.05.2022
Impfdatum: 07.02.2022
Beginn: 08.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Axillary pain Lymphadenopathy Muscle twitching Oedema peripheral Pain

Symptomtext

Significant swelling (and some pain) under left armpit for 7-10 days. Swollen lymph node as per my individual assessment. Also, muscle twitching at several places in body for few days. Severe body pain for around 2 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: High cholesterol, fatty liver
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2280903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: FL
Alter: 62,0
Geschlecht: M
Eingang: 17.05.2022
Impfdatum: 16.05.2022
Beginn: 16.05.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Pain Sinus congestion

Symptomtext

Soreness & Sinus congestion

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergies
Vorgeschichte: None
Andere Medikamente: -
Allergien: Iodine& Pencillin
Vorherige Impfungen: -

VAERS 2278555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 57,0
Geschlecht: M
Eingang: 16.05.2022
Impfdatum: 12.05.2022
Beginn: 15.05.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: - / -

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

Back pain

Symptomtext

Patient received the COVID vaccine booster on 5/12/22 and presented to the ED on 5/16/22 with back pain (likely unrelated to vaccine).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Type 2 diabetes mellitus, neuropathic pain, malignant carcinoid of unknown primary, Secondary carcinoid tumor of bone, Neuroendocrine tumor
Andere Medikamente: Acetaminophen-codeine (Tylenol-Codeine #4) 300-60 mg per tablet every 4 hours PRN for pain, albuterol inhaler PRN, ascorbic acid 250 mg daily, carvedilol 12.5 mg twice daily, celecoxib 200 mg daily, cyclobenzaprine 10 mg daily, empagliflozi
Allergien: NSAIDs, Aspirin
Vorherige Impfungen: -

VAERS 2277865

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: OR
Alter: 58,0
Geschlecht: F
Eingang: 15.05.2022
Impfdatum: 04.04.2022
Beginn: 24.04.2022
Tage bis Beginn: 20,0
Dosis: 4
Route/Site: IM / LA

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

Balance disorder Dizziness Vertigo

Symptomtext

Vertigo, dizziness, imbalance lasting now over 3 weeks. Constant light-headedness, and dizziness upon lifting head.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: ENT examination, 5/10/2022. Scheduled for a VNG. No ear infection.
Aktuelle Erkrankungen: None
Vorgeschichte: Degenerative osteoporosis-arthritis lumbar and feet due to 1986 car accident and multiple corrective surgeries.
Andere Medikamente: Magnesium, D3, ginko biloba, B6 complex
Allergien: Penicillin, bactrum, morphine
Vorherige Impfungen: Vertigo with nausea, 57, 03/17/21, Covid, Pfizer

VAERS 2275665

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NJ
Alter: 59,0
Geschlecht: F
Eingang: 13.05.2022
Impfdatum: 07.05.2022
Beginn: 07.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / LA

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

Headache Heart rate increased Pain Sleep disorder

Symptomtext

Body Aches started around 5pm and through to the next morning Headache started around 5pm and through to the next morning Banging sound of my Rapid Heartbeat woke me up just after midnight; Fitbit showed heart beat around around 107 bpm. Next day when I read my Fitbit information, I found out my heart beach had been up to 127 around midnight

Weitere VAERSDATA-Felder

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

VAERS 2273262

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 66,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 27.01.2022
Beginn: 09.01.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Delirium Impaired healing Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

Narrative: Fully vaccinated found COVID positive during admission. Patient presented with delirium, nausea/vomiting, and nonhealing sacral wound. Patient found to be COVID positive upon day 3 of admission due to patient not get testing initially. No hx of prior infection.

Weitere VAERSDATA-Felder

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

VAERS 2264761

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 37,0
Geschlecht: F
Eingang: 05.05.2022
Impfdatum: 05.05.2022
Beginn: 05.05.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Cough Dizziness Dry throat Nasal congestion Stridor Throat tightness

Symptomtext

Patient developed symptoms of dryness/tightness in throat, cough, mild dizziness, and nasal congestion approximately 15-20 minutes after vaccine administration. Patients vitals remained within normal range (BP/HR), breathing non-labored, lungs clear to auscultation, denied SOB, or worsening of symptoms. Patient given 25mg Diphenhydramine by mouth and observed for 50 minutes. Symptoms did not worsen. Given symptoms and audible upper airway expiratory stridor on auscultation, I recommended she be evaluated further in ED or UC, though she declined. Worsening symptoms/precautions for seeking additional care were discussed at length. Patient has a past history of anaphylaxis to unknown allergen necessitation ICU admission. No reaction to 1st dose of COVID vaccine (Pfizer).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Ongoing allergic symptoms, unknown etiology.
Vorgeschichte: N/A
Andere Medikamente: Cetirizine, Diphenhydramine, Famotidine
Allergien: Patient has a history of anaphylaxis to unknown allergen. Allergy testing not completed after ICU stay. No reaction to 1st Pfizer vaccine.
Vorherige Impfungen: -

VAERS 2264415

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 61,0
Geschlecht: F
Eingang: 05.05.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

Body height Diarrhoea Malaise Vomiting Weight

Symptomtext

My aunt very sick from it; She had a diarrhea all day; She throw up the Pepto-Bismol that I gave her earlier/ She throw up everything.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 61-year-old female patient received BNT162b2 (BNT162B2), as dose 4 (booster), single (Lot number: FJ6369) at the age of 61 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "doesn't stand up" (unspecified if ongoing); "multiple sclerosis" (unspecified if ongoing), notes: she has multiple sclerosis(intent: history); "paralyzed from waist down" (unspecified if ongoing), notes: She is paralyzed from waist down(intent: history); "bedridden" (unspecified if ongoing), notes: she bedridden(intent: history); "colostomy bag" (unspecified if ongoing), notes: she has a colostomy bag; "catheter" (unspecified if ongoing). Concomitant medication(s) included: HYDROCORTISONE. Vaccination history included: johnson and johnson (he got it 25Jun2021, the lot number. I guess it's the number underneath is 1808978, First Dose), administration date: 25Jun2021, when the patient was 60-year-old, for COVID-19 immunization; Covid-19 vaccine (Third Dose (first booster)), for COVID-19 immunization. The following information was reported: MALAISE (non-serious), outcome "unknown", described as "My aunt very sick from it"; DIARRHOEA (non-serious), outcome "recovering", described as "She had a diarrhea all day"; VOMITING (non-serious), outcome "unknown", described as "She throw up the Pepto-Bismol that I gave her earlier/ She throw up everything.". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of diarrhoea. Additional information: Reporter stated, "Me and my aunt both have Pfizer the booster (Pfizer covid vaccine) second booster vaccine my aunt very sick from it she has multiple sclerosis (intent: history), and she bedridden (intent: history) she has a colostomy bag, a catheter, she had a diarrhea all day I change her 4 times today, she throw up everything and I suppose to report it that is what the paper says. she doesn't stand up, she has multiple sclerosis. She is paralyzed from waist down (intent: history) and she probably weigh probably 180 to 190 pound may be, you know they are heavy when they are paralyses so, but normally she weigh around 160 something like that if she was normal (Reporter was not sure about the height and weight of the patient hence not captured in tab). she takes medication for her she take hydrocortisone (not confirmed over the call hence not captured in tab). Reporter stated she gave her Imodium A-D for diarrhea and it stop, it slow down now, and she throw up the Pepto-Bismol that the reporter gave her earlier. Reporter stated that its been longer than 4 weeks the last vaccine was given, like 15Dec2021, Dec2021 somewhere around there the booster, no she got Johnson and Johnson the first time. No, that's the one she got in Jun2021. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Test Name: height; Result Unstructured Data: Test Result:5,10; Comments: her height is probably 5,10; Test Name: weight; Result Unstructured Data: Test Result:180 to 190 lbs; Comments: she probably weigh probably 180 to 190 pound may be; Test Name: weight; Result Unstructured Data: Test Result:160 lbs; Comments: normally she weigh around 160
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bedridden (she bedridden(intent: history)); Catheter placement; Colostomy (she has a colostomy bag); Difficulty in standing; Multiple sclerosis (she has multiple sclerosis(intent: history)); Paralyzed (She is paralyzed from waist down(intent: history))
Andere Medikamente: HYDROCORTISONE
Allergien: -
Vorherige Impfungen: -

VAERS 2263347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: KS
Alter: 69,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 02.04.2021
Beginn: 02.04.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Urticaria

Symptomtext

Patient said she got hives 2 weeks after J&J. Discussed with doctor and told to get Moderna.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: Unknown.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Codeine, PCN
Vorherige Impfungen: -

VAERS 2258418

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: TX
Alter: 12,0
Geschlecht: F
Eingang: 29.04.2022
Impfdatum: 27.04.2022
Beginn: 28.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Extra dose administered Pyrexia

Symptomtext

Fever

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Ewing sarcoma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Patient reported fever with prior COVID vaccine doses

VAERS 2251828

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: AZ
Alter: 43,0
Geschlecht: F
Eingang: 26.04.2022
Impfdatum: 18.04.2022
Beginn: 01.04.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Blood test Crying Gait disturbance Illness Influenza like illness Mammogram Pain

Symptomtext

Flu like symptoms; I can't go for a walk; extremely ill; Iam in Pain; it hurt so much, I cried; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 43-year-old female patient received BNT162b2 (BNT162B2), on 18Apr2022 as dose 2, single (Lot number: FJ6369) at the age of 43 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Depression" (unspecified if ongoing); "Anxiety" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 1, Lot No.- FJ6369), administration date: 28Mar2022, when the patient was 43-year-old, for Covid-19 Immunization. The following information was reported: INFLUENZA LIKE ILLNESS (non-serious) with onset Apr2022, outcome "unknown", described as "Flu like symptoms"; GAIT DISTURBANCE (non-serious) with onset Apr2022, outcome "unknown", described as "I can't go for a walk"; PAIN (non-serious) with onset Apr2022, outcome "unknown", described as "Iam in Pain"; ILLNESS (non-serious) with onset Apr2022, outcome "unknown", described as "extremely ill"; CRYING (non-serious) with onset Apr2022, outcome "unknown", described as "it hurt so much, I cried". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of influenza like illness, gait disturbance, illness, pain. Additional information: Consumer stated, "Patient had a Additional information: Consumer stated, "Patient had a complaint about the Pfizer shot, it made me extremely sick. he got it 2 days ago, he got it on Monday, and having bad reactions to it, later Flu like symptoms, he can't go for a walk, and missing him classes." When paraphrased the concern: Consumer stated, "Yes, extremely ill." both of them? The first one was administered on 28Mar2022, FJ6369 and the second one was administered on 18Apr2022" Other medical condition: Consumer stated, " 'Spider bite'(not clarified further hence not captured in tab), felt this way the first time got the shot and the same time, first time tonight I got severe flu like symptom, it hurt so much, cried." Lab test: Consumer stated, "he had a mammogram and a Blood test." Result: Consumer stated, " don't know the result, he had to get another test, the tissue is too thin" Treatment for adverse events: Consumer stated, "Ibuprofen but he missed 2 of him classes, it doesn't work, Ibuprofen was temporarily." LOT# for Ibuprofen: Consumer stated, "oh man, he don't know the lot number, he can't do that." Consumer hung up the call abruptly. Thus, further probing could not be done. Hence, limited information available over the call. Description of Product Complaint: Consumer stated, "I have a complaint about the Pfizer shot, it made me extremely sick. he got it 2 days ago, he got it on Monday, having bad reactions to it, later Flu like symptoms, he cant go for a walk, and missing him classes." Name of the vaccine: Pfizer COVID-19 vaccine. Consumer hung up the call abruptly. Thus, further probing could not be done. Hence, limited information available over the call.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Test Date: 202204; Test Name: Blood test; Result Unstructured Data: Test Result:Unknown result; Test Date: 202204; Test Name: mammogram; Result Unstructured Data: Test Result:Unknown result
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Depression
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2248246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NJ
Alter: 51,0
Geschlecht: M
Eingang: 22.04.2022
Impfdatum: 22.04.2022
Beginn: 22.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Haemorrhage Immediate post-injection reaction Injection site nodule

Symptomtext

Customer started to bleed immediately after being injected. A bump formed at injection site. It looked like blood was trapped under his skin at injection site. Patient waited in pharmacy with no other reaction except for bump at injection site.

Weitere VAERSDATA-Felder

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

VAERS 2248191

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 56,0
Geschlecht: F
Eingang: 22.04.2022
Impfdatum: 19.04.2022
Beginn: 19.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Pruritus

Symptomtext

Pt states that she is "ichy" at 30min observation mark. MAR called. MD at bedside @11:12 to evaluate pt. Vitals: 139/82, 82, 16. Pt stable and released from the vaccination site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: Hypothyroidism, OA, Trochanteric burstis, female stress incontinence, Pre-DM
Andere Medikamente: Medications: Ketoconazole 2% shampoo for use twice weekly levothyroxine 75mcg PO Daily
Allergien: Allergies: allegra [fexofenadine], aspirin, codeine, cyclobenzaprine hcl, gabapentin, hydrocodone, lidoderm [lidocaine], lidopro patch [lidocaine-methyl sal-menthol], meperidine, morphine sulfate, naproxen, zofran (as hydrochloride) [ondansetron hcl], lidopro [lidocain-me.salicyl-caps-menth], mobic [meloxicam], nubain [nalbuphine], oxycodone, phenergan [promethazine], skelaxin [metaxalone], soma [carisoprodol], talwin [pentazocine lactate], and ultram [tramadol].
Vorherige Impfungen: -

VAERS 2245713

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 57,0
Geschlecht: M
Eingang: 21.04.2022
Impfdatum: 20.04.2022
Beginn: 21.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Back pain Chills Headache Hyperhidrosis Malaise Pyrexia

Symptomtext

Chills, Fever, Sweaty, Lower back pain, headache, general malaise

Weitere VAERSDATA-Felder

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

VAERS 2243595

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NJ
Alter: 29,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 28.02.2022
Beginn: 01.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Erythema Injection site pain Injection site reaction Injection site swelling Muscle spasms Muscle twitching Skin discolouration Urticaria

Symptomtext

I received my Covid booster (3rd shot) on 2/28/22 and the next day I had a huge red welt on my arm which lasted for 5 days. After the redness went away, the welt turned into a black and blue (bruise-like) color and that lasted another 2 days. Since then, I have had a bump in the same spot that I received my shot. My muscle occasionally twitches in that spot and causes spasms that hurt for at least an hour long for each episode. I had no reaction to the first 2 doses. The RN who administered my vaccine did a great job and I didn't feel it. However, since then I have been in pain in the same spot I got my vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2238772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 66,0
Geschlecht: F
Eingang: 18.04.2022
Impfdatum: 01.04.2022
Beginn: 14.04.2022
Tage bis Beginn: 13,0
Dosis: 4
Route/Site: IM / LA

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

Chills Headache Pain Pyrexia

Symptomtext

Three days of high fever (102, 103 and 103.9) with severe body aches, headaches and chills lasted 30 minutes, relieved after taking naproxen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes type 2, asthma, hypothyroid, hypertension
Andere Medikamente: Acarbose, Metformin, Glipizide, Lisinopril, Lipitor, Synthroid, Centrum, Hair and Nail vitamin, Vitamin E
Allergien: Peanuts
Vorherige Impfungen: High fever of 102, headaches and body aches lasting one day; age 65; vaccine on 02/01/2021 in left arm, intramuscular injection.

VAERS 2238125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: MN
Alter: 72,0
Geschlecht: F
Eingang: 16.04.2022
Impfdatum: 15.04.2022
Beginn: 16.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Chills Myalgia

Symptomtext

severe chills and muscle aches lasting one hour

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: cardiac disease (MI 2009), arthritis, gastroenteritis
Andere Medikamente: losartan, simvastatin, D3, B12, baby aspirin, acetominophen
Allergien: lobster, bromine, ibuprofen, norfloxin, streptomycin
Vorherige Impfungen: -

VAERS 2238069

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NY
Alter: 58,0
Geschlecht: F
Eingang: 16.04.2022
Impfdatum: 13.04.2022
Beginn: 14.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / RA

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

Hypersensitivity Rash Rash pruritic Skin warm

Symptomtext

Received vaccine at medical 4/13/2022 @ 845 am At 4:50 pm on 4/13/2022 broke out with rash over over most of my body. Itchy and very warm to touch. Took 50 mg of Benadryl. Continued Benadryl every 4 hours and rash just did get better. Drive to Hospital ER was seen in ER and diagnosed with Allergic reaction to COVID 19 Vaccine. Was prescribed Prednisone, ZyrTec and Pepcid. Was discharged and not admitted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Nine
Vorgeschichte: High blood pressure but is controlled with medication Thyroid nodules controlled with medication
Andere Medikamente: Losartan50mg OD HCTZ 25 2tabs OD Levothyroxine 25 mg OD
Allergien: Tobradex eye drops
Vorherige Impfungen: -

VAERS 2235846

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: PA
Alter: 55,0
Geschlecht: M
Eingang: 15.04.2022
Impfdatum: 05.02.2022
Beginn: 05.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Injection site induration Injection site mass Injection site pain Muscle spasms Musculoskeletal stiffness Pain in extremity Sleep disorder Trigger finger

Symptomtext

I recently had a checkup and was discussing my reaction to my booster shot and was told I should report it. On 02/05/2022 11:am at my local Pharmacy, I received my third Pfizer FJ6369 booster shot. As the day progressed (over 12 hours), the shot site was extra sore and developed a quarter sized hard bump. Then I went to bed at approximately 11:pm. Around 5:am on 02/06/2022 I awoke to extreme pain in both my hands, The middle fingers of both hands curled and cramped. As the morning progressed, I was able to finally move them. However, it left me with trigger fingers in both hands. Oddly, about 5 to 7 days later, the trigger finger in my right hand (none shot side) completely went away. And while it is improving (I sleep with a finger splint on left hand) But, the left hand middle finger still has the trigger finger.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site induration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Aged Garlic and Multi-vitamin
Allergien: Seasonal allergies
Vorherige Impfungen: -

VAERS 2231183

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: LA
Alter: 53,0
Geschlecht: F
Eingang: 13.04.2022
Impfdatum: 07.03.2022
Beginn: 07.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Dizziness Malaise

Symptomtext

Spoke to employee on telephone on 03/11/22 and she reported to me that approximately 2 hours after vaccine administration she began feeling weak, dizzy & general malaise. She reported that she was taken to ATU (Assessment & Triage Unit @ a facility), seen by MD, then transferred to outside facility for further testing & treatment.

Weitere VAERSDATA-Felder

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

VAERS 2225729

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 11.04.2022
Impfdatum: 05.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / RA

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

Rash

Symptomtext

Rash

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Seasonal allergies/sinusitis/rhinitis
Vorgeschichte: Hypertension, diabetes, fibromyalgia, seasonal allergies/asthma
Andere Medikamente: Various for hypertension, diabetes, seasonal allergies
Allergien: Bactrim, Levaquin, Voltaren, Omnicef
Vorherige Impfungen: -

VAERS 2225336

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 58,0
Geschlecht: M
Eingang: 09.04.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Headache

Symptomtext

At 7 hours after injection, mild headache on Day 1. Slightly worse headache on afternoon of Day 2. This is not unusual. On Day 3, severe intermittent throbbing headache, especially on exertion or standing, left temple. Pain was 8.5 out of 10. 1000 mg Tylenol did not help. Lasted about 6 - 10 hours. Consulted with health insurance nurse on call and was advised could go to nearest hospital if desired. Day 4 (today) I feel fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Decline
Vorgeschichte: Decline
Andere Medikamente: Decline
Allergien: Decline
Vorherige Impfungen: Mild symptoms after previous COVID shots, such as headache. I have never had a reaction to any other vaccine, and I receive t

VAERS 2220372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: IL
Alter: 27,0
Geschlecht: M
Eingang: 07.04.2022
Impfdatum: 27.02.2022
Beginn: 27.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Adverse reaction Arthralgia Bursitis Injection site pain Injection site swelling Joint range of motion decreased

Symptomtext

Site: Pain at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Lack of Range of Motion-Severe, Systemic: Joint Pain-Severe, Additional Details: Patient had his Pfizer booster on 2/27/22. He reported his vaccine adverse reaction on 4/3/22. Patient stated his shoulder was "messed up" after receiving his vaccine at pharmacy. His shoulder is in a lot of pain and he has a lack of range of motion for the shoulder. Patient went to his PCP and was told by the PCP that this pain was due to the vaccine administration. His PCP diagnosed it as Bursitis and referred him to an orthopedic surgeon. Patient would like a call back from someone at corporate.

Weitere VAERSDATA-Felder

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

VAERS 2218417

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 27,0
Geschlecht: F
Eingang: 06.04.2022
Impfdatum: 31.03.2022
Beginn: 01.04.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Fatigue Headache Pyrexia

Symptomtext

FATIGUE, HEADACHE, LOW GRADE FEVER

Weitere VAERSDATA-Felder

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

VAERS 2211438

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: -
Alter: 46,0
Geschlecht: F
Eingang: 01.04.2022
Impfdatum: 22.03.2022
Beginn: 23.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Chills Fatigue Musculoskeletal stiffness Pain Pyrexia

Symptomtext

BODY ACHE, STIFFNESS, CHILLS, FEVER, FATIGUE

Weitere VAERSDATA-Felder

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

VAERS 2211435

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: -
Alter: 40,0
Geschlecht: F
Eingang: 01.04.2022
Impfdatum: 31.03.2022
Beginn: 31.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Headache Pain Pyrexia

Symptomtext

HEADACHE, BODY ACHE, JOINT PAIN, FEVER

Weitere VAERSDATA-Felder

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

VAERS 2211432

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: -
Alter: 42,0
Geschlecht: F
Eingang: 01.04.2022
Impfdatum: 31.03.2022
Beginn: 31.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Dizziness Fatigue Headache Nausea Pain

Symptomtext

RIGHT SIDE OF BODY HURTS, DIZZY, NAUSEA, FEELS WEAK, BODY ACHES, FATIGUE, HEADACHE

Weitere VAERSDATA-Felder

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

VAERS 2211425

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 42,0
Geschlecht: F
Eingang: 01.04.2022
Impfdatum: 31.03.2022
Beginn: 31.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Chills Headache Musculoskeletal stiffness Nausea Neck pain Oropharyngeal pain

Symptomtext

RIGHT NECK IS STIFF AND PAINFUL, THROAT PAIN, HEADACHE, NAUSEA, CHILLS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: AX: NEOMYACIN
Vorherige Impfungen: -

VAERS 2211049

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CO
Alter: 12,0
Geschlecht: F
Eingang: 01.04.2022
Impfdatum: 28.01.2022
Beginn: 19.03.2022
Tage bis Beginn: 50,0
Dosis: 3
Route/Site: IM / LA

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

Angiotensin converting enzyme Antinuclear antibody Eye pain Full blood count Lysozyme Metabolic function test Ocular hyperaemia Periorbital cellulitis Red blood cell sedimentation rate Rheumatoid factor Treponema test Urine analysis Uveitis

Symptomtext

3-19-22 - Pain + redness to Left eye - Augmentin, tobrex 3-24-22 - dx c periorbital cellulitis 3-28. 22 - refer to ophtho - ED Uveitis of left eye - steroids & atropine drops

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: UA, CBC, CMP, rheumatoid factor, angiotensin,conv,Enzyme s. Lysozyme muramidase sed Red , ANA , Rapid plasma Reagin
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: NA
Allergien: -
Vorherige Impfungen: NA~ ()~~0.00~Patient

VAERS 2209377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 38,0
Geschlecht: M
Eingang: 31.03.2022
Impfdatum: 22.03.2022
Beginn: 22.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Fatigue Pain Pain in extremity

Symptomtext

SORE ARM, FATIGUE, BODY ACHES, PAIN IN RIGHT ARM DOWN TO HAND

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: ALLERGIC TO VINEGAR AND WOOL
Vorherige Impfungen: -

VAERS 2209338

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 48,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 30.03.2022
Beginn: 30.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Headache Pain

Symptomtext

HEADACHE, BODY ACHES, CHILLS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Asthma flare up, congestion, coughing, runny nose
Vorgeschichte: Asthma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2207134

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: FL
Alter: 57,0
Geschlecht: F
Eingang: 30.03.2022
Impfdatum: 21.02.2022
Beginn: 23.02.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Biopsy Extra dose administered Feeling abnormal Feeling jittery Hyperventilation Pruritus Urine analysis

Symptomtext

I went to Pharmacy and had 4th Shot. I waited my 15 minutes and went home after that. Once I got home I started feeling bad I felt I had to much caffeine. The next day at dinner time and I was eating I started itching and I started hyperventilating and went to Urgent care and was not able to be treated they sent me to ER where they gave me medication and I was there for about 20mins where the Itchy subside. I am still taking medication and will follow up with my doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Urinalysis Test, Biopsy
Aktuelle Erkrankungen: -
Vorgeschichte: Ehlers-Danlos Syndrome
Andere Medikamente: Calcium
Allergien: Garlic, Sulfa Drugs
Vorherige Impfungen: -

VAERS 2206677

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: -
Alter: 37,0
Geschlecht: F
Eingang: 30.03.2022
Impfdatum: 29.03.2022
Beginn: 29.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Fatigue Flushing Headache

Symptomtext

HEADACHE, FLUSHING OF FACE, FATIGUE, DIZZINESS

Weitere VAERSDATA-Felder

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

VAERS 2206179

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj6369

mild

Staat: AZ
Alter: 31,0
Geschlecht: M
Eingang: 30.03.2022
Impfdatum: 07.02.2022
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Fatigue Feeling abnormal

Symptomtext

The first shot I was tired and I felt like I was in a fishbowl.; The first shot I was tired and I felt like I was in a fishbowl.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 31 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 07Feb2022 (Lot number: Fj6369) at the age of 31 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Gerd" (unspecified if ongoing); "IBS" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: FATIGUE (non-serious), FEELING ABNORMAL (non-serious), outcome "unknown" and all described as "The first shot I was tired and I felt like I was in a fishbowl.". Additional Information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine, prior to vaccination and since the vaccination the patient did not tested for Covid-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: GERD; Irritable bowel syndrome
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2206139

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: AL
Alter: 64,0
Geschlecht: F
Eingang: 30.03.2022
Impfdatum: 21.03.2022
Beginn: 21.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Arthralgia Gait disturbance Muscle spasms Pain Pain in extremity

Symptomtext

she started aching in her joints / caller states her thighs are hurting so bad and her legs and ankles; she started aching in her joints and saw that one listed but has throbbing muscle cramps; Caller states her thighs are hurting so bad and her legs and ankles and she can barely walk; Caller states her thighs are hurting so bad and her legs and ankles and she can barely walk; Caller experienced muscle cramps on her legs, feet, and thighs every hour or every other hour.; 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 64 year-old female patient received bnt162b2 (COMIRNATY), administered in arm right, administration date 21Mar2022 09:00 (Lot number: FJ6369) at the age of 64 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: POTASSIUM (ongoing); POTASSIUM (ongoing); MAGNESIUM OXIDE (ongoing). Vaccination history included: Bnt162b2 (Dose: 1, Lot: EW0172 , Expiry date: Aug2021), administration date: 02Aug2021, when the patient was 63 years old, for Covid-19 immunization; Bnt162b2 (Dose: 2, Lot: EW0172 , Expiry date: Aug2021), administration date: 23Aug2021, when the patient was 63 years old, for Covid-19 Immunization; Dupixent (Dupixent 300mg administered to her thigh), administration date: 14Mar2022, when the patient was 64 years old. The following information was reported: MUSCLE SPASMS (non-serious) with onset 21Mar2022, outcome "recovering", described as "Caller experienced muscle cramps on her legs, feet, and thighs every hour or every other hour."; ARTHRALGIA (non-serious), outcome "unknown", described as "she started aching in her joints / caller states her thighs are hurting so bad and her legs and ankles"; PAIN (non-serious), outcome "unknown", described as "she started aching in her joints and saw that one listed but has throbbing muscle cramps"; PAIN IN EXTREMITY (non-serious), GAIT DISTURBANCE (non-serious), outcome "unknown" and all described as "Caller states her thighs are hurting so bad and her legs and ankles and she can barely walk". Therapeutic measures were taken as a result of muscle spasms, arthralgia, pain, pain in extremity. Additional information: Female patient called in about receiving the Pfizer COVID-19 Vaccine booster dose yesterday, 21Mar2022. Caller experienced muscle cramps on her legs, feet, and thighs every hour or every other hour. Caller has already been better. Caller wants to know if there is information on cramping after getting the booster dose. Unable to obtain caller's age. Caller states her 1st dose of the Pfizer Covid vaccine was on 02Aug2021 with lot EW0172 and expiry date Aug2021, the 2nd dose was on 23Aug2021 with lot EW0172 and expiry date on Aug2021 and the booster dose was yesterday 21Mar2022 with lot FJ6369 and states her patient card has no NDC numbers or expiry date for her booster dose written on the card. Prior Vaccinations (within 4 weeks): Yes, states she was administered Dupixent 300mg administered to her thigh and is not sure which thigh as she rotates thighs every month to rotate the site; states she has no lot, expiry date or manufacturer to provide and her last Dupixent was administered on 14Mar2022. Caller states she takes her normal medications and does those every day. States she has the Potassium bottle and it is an orange pharmacy bottle with lot 3127179 and has no manufacturer on the bottle or expiry date and NDC 00378456177 and the dose is she takes 10meq ER and now sees it is manufactured by Mylan; states she takes the Potassium two of the tablets once a day with food and began taking it 15-20 years ago. Caller states for the magnesium it has lot 21D001, expiry date Mar2024, NDC 5793 and then states that is not it but the NDC is 5796310212 and it is a white manufacturer bottle of Mag Oxide 400mg and she began taking it 15-20 years ago and it is a generic pharmaceutical company. Caller states she has to take another Ibuprofen and they are tablets that are 200mg coated tablets and it is the Equate brand of Ibuprofen with lot P126071, expiry date Jul2024, and for the UPC has to get closer to the light to see it and it is #. Caller states she takes blood pressure medicine and stuff during the day but did not start any of her other medications within 2 weeks prior to the reported event. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: POTASSIUM; POTASSIUM; MAGNESIUM OXIDE
Allergien: -
Vorherige Impfungen: -

VAERS 2206081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: TX
Alter: 37,0
Geschlecht: F
Eingang: 30.03.2022
Impfdatum: 03.02.2022
Beginn: 01.02.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / RA

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

Maternal exposure during pregnancy Poor quality product administered Product temperature excursion issue Vaccination site pain

Symptomtext

The patient receive the vaccine on 03Feb2022 at 2:13 pm, 26 hours after the vial had been punctured. The pre filled vaccine was stored in the refrigerator at 40 degrees during the entire time after; a 37 year old pregnant female that received a Pfizer Covid 19 vaccine; The patient receive the vaccine on 03Feb2022 at 2:13 pm, 26 hours after the vial had been punctured. The pre filled vaccine was stored in the refrigerator at 40 degrees during the entire time after; mild soreness at injection site; This is a spontaneous report received from contactable reporter(s) (Other HCP) from medical information team. A 37 year-old female patient (pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in deltoid right, administration date 03Feb2022 14:13 (Lot number: FJ6369, Expiration Date: 30Jun2022) at the age of 37 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Low grade squamous ASCUS" (ongoing); "Over weight" (ongoing). Date of last menstrual period: 24Jun2021. The patient was 32 weeks pregnant at the time of exposure to bnt162b2; 30 weeks pregnant to influenza vaccine. The patient was 32 weeks pregnant at the event onset. The patient is expected to deliver a baby(s) on 31Mar2022. Concomitant medication(s) included: INFLUENZA VACCINE, start date: 20Jan2022. The following information was reported: PRODUCT TEMPERATURE EXCURSION ISSUE (non-serious) with onset 03Feb2022, outcome "unknown", POOR QUALITY PRODUCT ADMINISTERED (non-serious) with onset 03Feb2022 14:13, outcome "unknown" and all described as "The patient receive the vaccine on 03Feb2022 at 2:13 pm, 26 hours after the vial had been punctured. The pre filled vaccine was stored in the refrigerator at 40 degrees during the entire time after"; MATERNAL EXPOSURE DURING PREGNANCY (non-serious) with onset 03Feb2022, outcome "unknown", described as "a 37 year old pregnant female that received a Pfizer Covid 19 vaccine"; VACCINATION SITE PAIN (non-serious) with onset Feb2022, outcome "recovered" (Feb2022), described as "mild soreness at injection site". Additional information: Patient received a Pfizer Covid 19 vaccine LOT FJ6369 expiration date 30Jun2022 that had been drawn up on 02Feb2022 at 11:44am. The patient received the vaccine on 03Feb2022 at 2:13 pm, 26 hours after the vial had been punctured. The pre filled vaccine was stored in the refrigerator at 40 degrees during the entire time after it was drawn up. The reporter wanted to have some guidance in regards to re-vaccination for the patient or any other guidance in regards to this incidence. Other products, patient history and investigation assessment was reported as no. Anatomical location of vaccine administration was unknown. History of all previous immunization with the Pfizer vaccine considered as suspect and additional vaccines administered on same date of the Pfizer suspect was reported as no. Did not require Emergency Room or physician office visit. History of all previous immunization with the Pfizer vaccine considered as suspect and Additional Vaccines Administered on Same Date of the Pfizer Suspect was reported as no. No prior Vaccinations (within 4 weeks). Medical History (including any illness at time of vaccination) was reported as no. No Relevant Tests done. Patient Medical History (including any illness at time of vaccination) was reported as none. Specific relevant test for thromboembolic events with thrombocytopenia was reported as none. Follow-up (08Feb2022): This is a follow-up spontaneous report from a contactable other-HCP. This other-HCP reported for a 37-year-old female patient that: Updated information included: Vaccine facility information, Other Products, Patient History, Vaccination Details. Follow up (21Mar2022): This is a follow-up spontaneous report from a same contactable nurse. This nurse reported for the patient in response to the HCP letter sent via follow-up letter which included that: New information included: New event added ''mild soreness at injection site''. For suspect product route of administration added. Facility name and phone number added.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Low grade squamous intraepithelial lesion; Weight increased
Vorgeschichte: -
Andere Medikamente: INFLUENZA VACCINE
Allergien: -
Vorherige Impfungen: -

VAERS 2204338

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 54,0
Geschlecht: F
Eingang: 29.03.2022
Impfdatum: 28.03.2022
Beginn: 29.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Fatigue Headache Pain

Symptomtext

HEADACHE, FATIGUE, WEAKNESS, BODY ACHES

Weitere VAERSDATA-Felder

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

VAERS 2204106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 42,0
Geschlecht: F
Eingang: 29.03.2022
Impfdatum: 28.03.2022
Beginn: 28.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Fatigue Headache Pain

Symptomtext

HEADACHE, FATIGUE, BODY ACHE, JOINT PAINS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: AX: LEVOQUIN
Vorherige Impfungen: -

VAERS 2201640

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: WY
Alter: 26,0
Geschlecht: F
Eingang: 28.03.2022
Impfdatum: 16.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Fatigue Fungal infection Lymphadenopathy Pain Pyrexia

Symptomtext

Swollen lymph nodes under my left arm causing fungal infection. Fever and body aches for a day and a half. Severe fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Cervix infection; a UTI a month prior to vaccination
Vorgeschichte: IGG deficiency; Endometriosis; Neck Injury; GERD; Asthma; Mental Health Diagnosis
Andere Medikamente: Lithium 1500mg; Lamictal 200mg; Propranolol 20mg; Gabapentin 1200 mg; Levothyroxine 50mg; Singulair 10mg; Birth control; Methylphenidate 10mg; Methocarbamol 500mg; Omeprazole 40mg; Vitamin D
Allergien: Penicillin
Vorherige Impfungen: Measles Vaccine

VAERS 2201558

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CT
Alter: 13,0
Geschlecht: M
Eingang: 28.03.2022
Impfdatum: 14.01.2022
Beginn: 17.03.2022
Tage bis Beginn: 62,0
Dosis: 3
Route/Site: IM / LA

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

Anaemia Blood iron decreased Blood test abnormal Erythema Haemoglobin decreased Malaise Peripheral swelling Skin warm

Symptomtext

24 hours after this vaccine Pt developed a red arm. It was puffy and hot to the touch. It went from his neck to his wrist, the entire arm that received the vaccine was red. After 3 days it went away and we thought it was going to be ok because he had never had a reaction before. Approximately 45 days later Pt began feeling unwell. He went to his nephrologist who ran routine blood tests and was shocked to see that Pt was now extremely anemic. His hemoglobin was 8.8. Pt had routine blood work done in December 2021 and his hemoglobin was 12.5. From December 2021 to March 2022 Pt became severely anemic, and this required hospitalization to try and correct the low iron. Nothing has changed from December when Pt was normal except that he got the COVID shot. The vaccine made him anemic and he now requires IV infusions of iron.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: 2,0
Labordaten: December 1, 2021 hemoglobin was 12.5 March 17th, 2022 hemoglobin was 8.8 The vaccine occurred on January 16
Aktuelle Erkrankungen: None
Vorgeschichte: Short bowel
Andere Medikamente: Potassium chloride, Nitrofurantoin, children's chewable multivitamin with iron
Allergien: None
Vorherige Impfungen: -

VAERS 2200810

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: MA
Alter: 18,0
Geschlecht: F
Eingang: 27.03.2022
Impfdatum: 18.01.2022
Beginn: 11.02.2022
Tage bis Beginn: 24,0
Dosis: 2
Route/Site: - / LA

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

Antinuclear antibody Arthralgia Blood immunoglobulin G Blood immunoglobulin M Blood test C-reactive protein Chills Epstein-Barr virus test Fatigue Full blood count Headache Influenza A virus test Influenza B virus test Influenza virus test Liver function test Lymphadenopathy Metabolic function test Mononucleosis heterophile test

Symptomtext

Extreme body aches, pain in muscles and joints Headache Sore throat Swollen throat/lymph nodes Fever 102-103 Chills Fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: FEBRUARY 13, 2022: EBV viral capsid Ag (vca) Ab (IgM) EBV viral capsid Ag (vca) Ab (IgG) EBV nuclear Ag (EBNA) Ab (IgG) Rapid strep group A, throat Rapid SARS CoV 2 Ag Rapid flu (A+B) Mononucleosis, heterophile Ab, blood FEBRUARY 24, 2022: ANA Rheumatoid Factor ANA pattern CBC with differential Basic metabolic panel LFT panel CRP ESR RSV PCR SARS-CoV 2 PCR Influenza A PCR Influenza B PCR Lyme screen
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2200779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj6369

mild

Staat: OH
Alter: 39,0
Geschlecht: M
Eingang: 27.03.2022
Impfdatum: 18.02.2022
Beginn: 06.03.2022
Tage bis Beginn: 16,0
Dosis: UNK
Route/Site: SYR / -

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

Ear discomfort Ear pain Headache Hyperacusis Laboratory test Tinnitus

Symptomtext

Severe ringing in ears, hypersensitivity to sounds, ear pain, feeling of fullnesss, headache. Still ongoing 3/27/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: Radiology with ct fhc twin (i-stat) on 3/24/2022
Aktuelle Erkrankungen: Tested positive for Covid sars-cov-2 on 1/3/2022
Vorgeschichte: -
Andere Medikamente: Meloxocam Omeprazole
Allergien: -
Vorherige Impfungen: -

VAERS 2200689

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: TX
Alter: 50,0
Geschlecht: F
Eingang: 26.03.2022
Impfdatum: 25.03.2022
Beginn: 26.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Chills Headache Pain Pyrexia

Symptomtext

Perosn Receives Covid 19 Booster vaccine of Pfizer at Facility vaccine event on 03/25/2022, starts to have side effects 03/26/2022 the next morning of Fever (100.6), headache, chills, and body aches. Taken Tylenol to help alleviate pain and assist with fever. Will Continue to monitor for the next 48 hours.

Weitere VAERSDATA-Felder

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

VAERS 2200534

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: OH
Alter: 68,0
Geschlecht: F
Eingang: 26.03.2022
Impfdatum: 23.02.2022
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / RA

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

Herpes zoster Pruritus Rash

Symptomtext

Shingles-like rash on the torso; Like a mild case of shingles; Started to itch; 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 68 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 23Feb2022 (Lot number: FJ6369) at the age of 68 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Shingles" (unspecified if ongoing), notes: I had it 17 years ago, but now it's on the opposite side".; "Blood pressure" (ongoing); "COVID", start date: 18Dec2021 (unspecified if ongoing), notes: like a whole month. She reports fatigue leftover from COVID. Family history included: "Borderline diabetes" (unspecified if ongoing), notes: The borderline diabetes has been on her record because it runs in her family. Concomitant medication(s) included: METOPROLOL SUCCINATE taken for blood pressure measurement (ongoing); OLMESARTAN MEDOXOMILO + HIDROCLOROTIAZIDA taken for blood pressure measurement (ongoing). The following information was reported: RASH (non-serious) with onset 2022, outcome "recovered", described as "Shingles-like rash on the torso"; HERPES ZOSTER (non-serious) with onset 2022, outcome "recovered", described as "Like a mild case of shingles"; PRURITUS (non-serious) with onset 2022, outcome "recovered", described as "Started to itch". Therapeutic measures were taken as a result of rash, herpes zoster, pruritus. Additional information: As treatment she self administered tea tree oil, washing or keeping the area clean with alcohol. She received the Pfizer COVID-19 vaccine on 23Feb2022 and is due to get the second COVID-19 vaccine on 23Mar2022. Caller states it is a week away. She reports that days after she received the COVID-19 vaccine she developed a rash resembling shingles, like a mild case of shingles, on her right side trunk area. She states the rash is still going on and she still has a small patch of the rash, like it is going away, its healing. She is due to get the COVID-19 vaccine again on 23Mar2022 and she wants to know is it safe to get second dose with this reaction from the first dose. Clarifies a week after Wednesday, 23Feb2022 when she received the COVID-19 vaccine it was not the next day or Friday but like the Thursday of the following week after the shot, when she noticed itching. She states the rash was on her right torso below her right breast down to not even the pubic area. Caller clarified to the navel not the pubic area. She had her first shot she had a rash that resembled shingles on the right side of her torso but milder than shingles, like a mild case that lasted like 2 or 2.5 weeks. Time the Vaccination between 2:30pm and 3:00 pm on 23Feb2022. She reports she has been taking concomitant drugs for years. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s): No. AE(s) following prior vaccinations: None No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Blood pressure
Vorgeschichte: Medical History/Concurrent Conditions: Borderline diabetes (The borderline diabetes has been on her record because it runs in her family.); COVID-19 (like a whole month. She reports fatigue leftover from COVID.); Shingles (I had it 17 years ago, but now it's on the opposite side".)
Andere Medikamente: METOPROLOL SUCCINATE; OLMESARTAN MEDOXOMILO + HIDROCLOROTIAZIDA
Allergien: -
Vorherige Impfungen: -

VAERS 2198780

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: -
Alter: 49,0
Geschlecht: F
Eingang: 25.03.2022
Impfdatum: 24.03.2022
Beginn: 24.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Headache Malaise Pain Pyrexia

Symptomtext

FEVER, HEADACHE, BODY ACHES, FEELS WEAK, FEELS ILL

Weitere VAERSDATA-Felder

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

VAERS 2198775

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 25.03.2022
Impfdatum: 23.03.2022
Beginn: 24.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Headache Pain Pyrexia Respiratory tract congestion

Symptomtext

FEVER, HEADACHE, CONGESTION, BODY ACHES, CHILLS

Weitere VAERSDATA-Felder

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

VAERS 2198653

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CT
Alter: 27,0
Geschlecht: M
Eingang: 25.03.2022
Impfdatum: 25.03.2022
Beginn: 25.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chest discomfort Dizziness Electrocardiogram Interchange of vaccine products Nausea

Symptomtext

Here at booster clinic, first vaccine was J&J over 8 months ago. Today requested Pfizer for his booster. Within 10 minutes of the vaccination he developed nausea, lightheadedness, and chest tightness. Wheeled down to the ED from the vaccination clinic that was running.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: EKG, Refused Blood Work that MD ordered in the ED.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: unknown
Allergien: almonds, penicillin
Vorherige Impfungen: -

VAERS 2196267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: -
Alter: 30,0
Geschlecht: F
Eingang: 25.03.2022
Impfdatum: 23.03.2022
Beginn: 24.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Headache Oedema peripheral Pain Pyrexia

Symptomtext

FEVER, HEADACHE, BODY ACHES, CHILLS, SWOLLEN ARMPIT

Weitere VAERSDATA-Felder

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

VAERS 2196627

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 33,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 21.03.2022
Beginn: 23.03.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Headache

Symptomtext

SEVERE HEADACHE, FATIGUE

Weitere VAERSDATA-Felder

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

VAERS 2196345

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 45,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 21.03.2022
Beginn: 23.03.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Abdominal pain upper Asthenia Headache Pain in extremity Vomiting

Symptomtext

WEAK, VOMITING, HEADACHE, SORE ARM, AND STOMACH PAIN

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2196317

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: TX
Alter: 61,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 22.03.2022
Beginn: 23.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Chills Fatigue Headache Pain

Symptomtext

Receives Covid 19 Booster vaccine of Pfizer at vaccine event on 03/22/2022, starts to have side effects 03/23/2022 the next morning of headache, chills, and body aches, fatigue. Taken Tylenol to help alleviate pain and assist with fever. Continue to monitor for the next 48 hours. Did recover from side effects

Weitere VAERSDATA-Felder

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

VAERS 2196214

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: TX
Alter: 45,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 23.03.2022
Beginn: 24.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Adverse drug reaction Chills Feeling of body temperature change Headache Pain Pyrexia

Symptomtext

Person received Covid 19 Booster vaccine of Pfizer at vaccine event on 03/23/2022. Started to have side effects on 03/24/2022, which states Headache, Fever (temp unknown) just keep getting cold and hot episodes, chills, and Body aches, Took Advil to help alleviate some pain and help with fever. Will Continue to monitor her side effects for the next 48 hours

Weitere VAERSDATA-Felder

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

VAERS 2195844

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NJ
Alter: 64,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 03.02.2022
Beginn: 03.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Eye pruritus Pruritus

Symptomtext

Within 20 minutes after receiving the first dose of Pfizer vaccine until today, I feel itchiness on my face, my ears, my neck, my whole body and my eyes.; Within 20 minutes after receiving the first dose of Pfizer vaccine until today, I feel itchiness on my face, my ears, my neck, my whole body and my eyes.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program (005570). The reporter is the patient. A 64 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 03Feb2022 15:45 (Lot number: FJ6369) at the age of 64 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Known allergies: Yes" (unspecified if ongoing); "If COVID prior vaccination: Yes" (unspecified if ongoing). Concomitant medication(s) included: VITAMIN D3. The following information was reported: EYE PRURITUS (non-serious), PRURITUS (non-serious) all with onset 03Feb2022 16:00, outcome "not recovered" and all described as "Within 20 minutes after receiving the first dose of Pfizer vaccine until today, I feel itchiness on my face, my ears, my neck, my whole body and my eyes.". Therapeutic measures were not taken as a result of eye pruritus, pruritus. Additional information: No other vaccine received by the patient in four weeks. Patient has not been tested Covid post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; COVID-19
Andere Medikamente: VITAMIN D3
Allergien: -
Vorherige Impfungen: -

VAERS 2194430

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: WI
Alter: 47,0
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 23.03.2022
Beginn: 23.03.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Urticaria

Symptomtext

REPORTED HIVES AFTER 15 MINUTES RECIEVING THE MEDICATION. CLIENT HAD BENADRYL ON HAND AND TOOK IT IMMEDIATELY UPONE SEEING THE HIVES. CLIENT WAS A RN EHRSELF AND DENIED TREATMENT AND STAYING LONGER THAN 15 MINUTES. CLIENT HAD A FRIEND THAT WAS AN RN WITH HER AND LEFT THE FACILITY TOGETHER. CLIENT HAD EPI-PEN WITH HER AND WAS AWARE OF THE NEED TO SEEK ADDITIONAL MEDICAL ATTENTION IF SYMPTOMS WORSEN.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: REPORTED COVID HX IN DECEMBER 2021
Vorgeschichte: BLOOD CLOTING DISORDER (HIT)
Andere Medikamente: BLOOD THINNERS, UNKOWN ADDITIONAL MEDS
Allergien: REPORTED HAVING AN EPI-PEN DUE TO MEDICATION REACTIONS (ANTIBIOTICS). REPORTED HAVING A SKIN/RASH REACTION AFTER FIRST PFIZER DOSE.
Vorherige Impfungen: SPECIFIC FLU VACCINE WHICH AHD AN ANTIBIOTIC USED WHILE MAKING IT. ALSO REPORTED REACTION WITH FIRST PFIZER VACCINE.

VAERS 2194309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: -
Alter: 52,0
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 21.03.2022
Beginn: 21.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Chest discomfort Dysgeusia Pain Rash Tinnitus

Symptomtext

METALLIC TASTE IN MOUTH, RINGING IN THE EARS, RASH ON FACE, BODY ACHES, BODY HURTS, FEELS LIKE RIB CAGE IS TIGHT

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: ax: vicodin
Vorherige Impfungen: -

VAERS 2194301

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 36,0
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 22.03.2022
Beginn: 23.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Chills Dizziness Nausea Pain Pyrexia

Symptomtext

FEVER, BODY ACHES, CHILLS, LIGHTHEADED AND NAUSEA

Weitere VAERSDATA-Felder

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

VAERS 2192292

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 36,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 09.03.2022
Beginn: 09.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Dizziness Headache Pyrexia

Symptomtext

DIZZINESS, HEADACHE, CHILLS, FEVER

Weitere VAERSDATA-Felder

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

VAERS 2192070

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: TX
Alter: 33,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 18.03.2022
Beginn: 20.03.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Headache Malaise Oropharyngeal pain Pain SARS-CoV-2 test negative

Symptomtext

Received Covid 19 Pfizer vaccine booster on 03/18/2022. States she started to have side effects on 03/20/2022 of Sore throat body aches no fever bad headache, she took Tylenol and ibuprofen to help alleviate some of the pain but wasn't able to maintain to have it assist. Went to ER due to not still feeling well and having this sore throat, and thought she might have contracted Covid. She went and got a test done but came back negative for Covid and still is having sore throat and feeling sick. She states she had a reaction to the 2nd dose she took last year of respiratory issues and seen a provider . States that she will get another Covid test done because it might have been to early

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Pfizer vaccine 10/2021

VAERS 2191545

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NY
Alter: 53,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 17.02.2022
Beginn: 18.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / RA

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

Axillary pain Fatigue Headache Infection Lymphadenopathy Myalgia Pain in extremity

Symptomtext

Tiredness; Headache; Muscle ache at the infection area -right upper arm; Pain in the right armpit; Muscle ache at the infection area -right upper arm; sore arm; Lymph node in the right armpit; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53 year-old female patient (not pregnant) received bnt162b2 (COMIRNATY), administered in arm right, administration date 17Feb2022 17:45 (Lot number: FJ6369) at the age of 53 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Comirnaty (Dose 2, Lot number: EL3247, Administration time: 10:00 AM , Dose vaccine location: Left arm), administration date: 22Mar2021, when the patient was 52 years old, for Covid-19 immunization; Comirnaty (Dose 1, Lot number: EL3247, Administration time: 09:30 AM , Dose vaccine location: Left arm), administration date: 01Mar2021, when the patient was 52 years old, for Covid-19 immunization. The following information was reported: FATIGUE (non-serious) with onset 18Feb2022 06:00, outcome "not recovered", described as "Tiredness"; HEADACHE (non-serious) with onset 18Feb2022 06:00, outcome "not recovered", described as "Headache"; MYALGIA (non-serious), INFECTION (non-serious) all with onset 18Feb2022 06:00, outcome "not recovered" and all described as "Muscle ache at the infection area -right upper arm"; AXILLARY PAIN (non-serious) with onset 18Feb2022 06:00, outcome "not recovered", described as "Pain in the right armpit"; LYMPHADENOPATHY (non-serious) with onset 18Feb2022, outcome "not recovered", described as "Lymph node in the right armpit"; PAIN IN EXTREMITY (non-serious) with onset 18Feb2022 06:00, outcome "unknown", described as "sore arm". Therapeutic measures were not taken as a result of fatigue, headache, myalgia, axillary pain, lymphadenopathy, infection. Additional information: The patient had not received any other vaccine in 4 weeks. The patient had not other medications in 2 weeks. Patient had not covid prior vaccination and had not covid tested post vaccination. Patient had received the booster on (thursday) 17Feb around 17:45, and and events occurred was (friday) 18Feb. In early morning, around 6:00AM patient was experienced headache, sore arm etc. The lymph nodes part was a bit later during the day. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2062850

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: OH
Alter: 59,0
Geschlecht: M
Eingang: 22.03.2022
Impfdatum: 24.01.2022
Beginn: 24.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Fatigue Pain in extremity Poor quality product administered Product storage error Product temperature excursion issue No adverse event

Symptomtext

soreness at the injection site that permeated to his other arm; fatigue; They didn't realize over the weekend the temperature wasn't kept properly of the product; Then that product was administered to the patient; They didn't realize over the weekend the temperature wasn't kept properly of the product; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. Other Case identifier(s): US-PFIZER INC-202200150334 (Pfizer). A 59 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 24Jan2022 (Lot number: FJ6369) at the age of 59 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Dose 1, Manufacturer unknown, which he also experienced during his first and second shot (side effects he mentioned were: soreness at the injection site that permeated to his other arm, fatigue),), for COVID-19 immunization, reaction(s): "fatigue", "soreness at the injection site that permeated to his other arm"; Covid-19 vaccine (Dose 2, Manufacturer unknown, which he also experienced during his first and second shot (side effects he mentioned were: soreness at the injection site that permeated to his other arm, fatigue),), for COVID-19 immunization, reaction(s): "fatigue", "soreness at the injection site that permeated to his other arm". The following information was reported: PRODUCT STORAGE ERROR (non-serious), PRODUCT TEMPERATURE EXCURSION ISSUE (non-serious) all with onset 24Jan2022 and all described as "They didn't realize over the weekend the temperature wasn't kept properly of the product"; POOR QUALITY PRODUCT ADMINISTERED (non-serious) with onset 24Jan2022, described as "Then that product was administered to the patient"; PAIN IN EXTREMITY (non-serious), described as "soreness at the injection site that permeated to his other arm"; FATIGUE (non-serious), described as "fatigue". No follow-up attempts are possible. No further information is expected. Additional information: The vaccine was not studied in that manner and at this time we do not have information on that topic. Third dose of Covid-19 vaccine Pfizer was booster shot and manufacturer was unknown. The patient did not realize over the weekend the temperature was not kept properly of the product. Then that product was administered to the patient. They were advised that this may not be effective and to get another dose.Description of complaint: Caller following up on a previously filed report and mentioned that he received his Pfizer COVID vaccine booster dose on 24Jan2022, he was informed by the pharmacist that the vaccine was improperly handled over the weekend, the temperature in their storage got too low. The pharmacist called to notify him that it might not be effective because of the lower temperature and advised him to have a 4th shot. Probed for NDC, lot number and expiry date and caller does not see the NDC or expiry date on the COVID vaccination record card. Follow-up (26Jan2021): This is a spontaneous follow-up report received from the same contactable Consumer. Updated information included: Other relevant History (historical vaccine: reaction), New event (side effects he mentioned were: soreness at the injection site that permeated to his other arm, fatigue). Additional information updated. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2062850

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: OH
Alter: 59,0
Geschlecht: M
Eingang: 22.03.2022
Impfdatum: 24.01.2022
Beginn: 24.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Pain in extremity Poor quality product administered Product storage error Product temperature excursion issue No adverse event

Symptomtext

soreness at the injection site that permeated to his other arm; fatigue; They didn't realize over the weekend the temperature wasn't kept properly of the product; Then that product was administered to the patient; They didn't realize over the weekend the temperature wasn't kept properly of the product; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. Other Case identifier(s): US-PFIZER INC-202200150334 (Pfizer). A 59 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 24Jan2022 (Lot number: FJ6369) at the age of 59 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Dose 1, Manufacturer unknown, which he also experienced during his first and second shot (side effects he mentioned were: soreness at the injection site that permeated to his other arm, fatigue),), for COVID-19 immunization, reaction(s): "fatigue", "soreness at the injection site that permeated to his other arm"; Covid-19 vaccine (Dose 2, Manufacturer unknown, which he also experienced during his first and second shot (side effects he mentioned were: soreness at the injection site that permeated to his other arm, fatigue),), for COVID-19 immunization, reaction(s): "fatigue", "soreness at the injection site that permeated to his other arm". The following information was reported: PRODUCT STORAGE ERROR (non-serious), PRODUCT TEMPERATURE EXCURSION ISSUE (non-serious) all with onset 24Jan2022 and all described as "They didn't realize over the weekend the temperature wasn't kept properly of the product"; POOR QUALITY PRODUCT ADMINISTERED (non-serious) with onset 24Jan2022, described as "Then that product was administered to the patient"; PAIN IN EXTREMITY (non-serious), described as "soreness at the injection site that permeated to his other arm"; FATIGUE (non-serious), described as "fatigue". No follow-up attempts are possible. No further information is expected. Additional information: The vaccine was not studied in that manner and at this time we do not have information on that topic. Third dose of Covid-19 vaccine Pfizer was booster shot and manufacturer was unknown. The patient did not realize over the weekend the temperature was not kept properly of the product. Then that product was administered to the patient. They were advised that this may not be effective and to get another dose.Description of complaint: Caller following up on a previously filed report and mentioned that he received his Pfizer COVID vaccine booster dose on 24Jan2022, he was informed by the pharmacist that the vaccine was improperly handled over the weekend, the temperature in their storage got too low. The pharmacist called to notify him that it might not be effective because of the lower temperature and advised him to have a 4th shot. Probed for NDC, lot number and expiry date and caller does not see the NDC or expiry date on the COVID vaccination record card. Follow-up (26Jan2021): This is a spontaneous follow-up report received from the same contactable Consumer. Updated information included: Other relevant History (historical vaccine: reaction), New event (side effects he mentioned were: soreness at the injection site that permeated to his other arm, fatigue). Additional information updated. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2191875

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 36,0
Geschlecht: F
Eingang: 21.03.2022
Impfdatum: 14.04.2021
Beginn: 12.03.2022
Tage bis Beginn: 332,0
Dosis: 3
Route/Site: IM / LA

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

Decreased appetite Dizziness Fatigue Headache Myalgia

Symptomtext

Narrative: Pt received booster COVID-19 vaccine dose (Pfizer) on 03/11/2022. After the vaccine (exact date/time of sx not reported by pt), pt started to feel headache, dizziness, exhaustion, lack of appetite, and muscle soreness. No treatment given.

Weitere VAERSDATA-Felder

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

VAERS 2190252

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: TX
Alter: 22,0
Geschlecht: F
Eingang: 21.03.2022
Impfdatum: 02.04.2021
Beginn: 14.04.2021
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: SYR / LA

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

Rash macular

Symptomtext

Areas on the left side of my body look like birthmarks. There are no bumps or actual bruises. They occurred after my vaccinations

Weitere VAERSDATA-Felder

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

VAERS 2189772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: TX
Alter: 49,0
Geschlecht: F
Eingang: 21.03.2022
Impfdatum: 18.03.2022
Beginn: 19.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Headache Lymph node pain Nausea Oedema peripheral Pain Pain in extremity Pyrexia Vaccine positive rechallenge Vomiting

Symptomtext

Person Took Pfizer Covid 19 vaccine Booster on 03/18/2022 at Vaccine event, this the the 2nd time she has had a reaction to vaccine which previous was Moderna her 2nd Covid 19 vaccine, had the same side effect and reaction as this vaccine. She has Fever of 101, headache, nausea vomiting, body aches, left arm pain away from injection site swelling under both arm as in lymph nodes pain. She took Tylenol/ibuprofen to help with assisting in side effects helped with fever but still pain and swelling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Covid 19 vaccine reaction to moderna vaccine in late 2021

VAERS 2189742

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 52,0
Geschlecht: F
Eingang: 21.03.2022
Impfdatum: 17.03.2022
Beginn: 17.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Fatigue Pain Pain in extremity Pyrexia

Symptomtext

FEVER, BODY ACHES, FATIGUE, SORE ARM

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: SULFA, CODEINE
Vorherige Impfungen: -

VAERS 2189714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 46,0
Geschlecht: F
Eingang: 21.03.2022
Impfdatum: 17.03.2022
Beginn: 18.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Fatigue Nausea Pyrexia

Symptomtext

FEVER, FATIGUE, CHILLS, NAUSEA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: PENICILLIN, EGGS
Vorherige Impfungen: -

VAERS 2189688

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 27,0
Geschlecht: F
Eingang: 21.03.2022
Impfdatum: 17.03.2022
Beginn: 17.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Erythema Fatigue Headache Lymphadenopathy Pain Peripheral swelling Urticaria

Symptomtext

HIVES ON LEFT ARM (RED AND SWOLLEN), SWOLLEN LYMPH NODES, HEADACHE, BODYACHES, FATIGUE

Weitere VAERSDATA-Felder

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

VAERS 2189328

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: IN
Alter: 53,0
Geschlecht: F
Eingang: 21.03.2022
Impfdatum: 18.03.2022
Beginn: 19.03.2022
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 Headache Influenza Injection site pain Malaise Oedema peripheral Pain Pyrexia

Symptomtext

Flu symptoms including chills, fever, body aches, sore at injection site, swelling under left arm pit area started and lasted the following day. Headache lasted 2 days. Extremely tired lasted 2 days. Took shot Friday at 1:00pm, Didn?t feel better til Monday 4:00am after taking 1 dose of Tylenol on Sunday at 7pm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Ditalizem, hydrocholethizide, citalopram, Zyrtec, multivitamin centrum
Allergien: Latex, mango, penicillin
Vorherige Impfungen: Headache only after 1st vaccination

VAERS 2187587

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 35,0
Geschlecht: F
Eingang: 18.03.2022
Impfdatum: 16.03.2022
Beginn: 16.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Headache Pain Pyrexia

Symptomtext

HEADACHE, FEVER, BODYACHES

Weitere VAERSDATA-Felder

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

VAERS 2187571

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: ME
Alter: 16,0
Geschlecht: F
Eingang: 18.03.2022
Impfdatum: 15.03.2022
Beginn: 16.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Injection site erythema Injection site pain Injection site swelling Vaccination error

Symptomtext

Vaccine was given too low, caused site redness, pain and some swelling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: ulcerative colitis in pediatric patient, low bone density, crohns disease of ileum without complication, IBD, hypvitaminosis D, raynaud disease
Vorgeschichte: -
Andere Medikamente: Sumatriptan, budesonide, ondansetron, vitamin C, methotrexate, calcium, vitamin D, folic acid
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2184436

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 27,0
Geschlecht: M
Eingang: 17.03.2022
Impfdatum: 16.03.2022
Beginn: 16.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Headache Pain

Symptomtext

Headache; body aches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 2184244

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 43,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 16.03.2022
Beginn: 16.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Headache Pain Pain in extremity

Symptomtext

HEADACHE, BODY ACHES, CHILLS, SORE ARM

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NO
Vorgeschichte: NO
Andere Medikamente: NO
Allergien: NO
Vorherige Impfungen: -

VAERS 2184174

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NJ
Alter: 27,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 16.03.2022
Beginn: 17.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Myalgia

Symptomtext

Muscle soreness

Weitere VAERSDATA-Felder

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

VAERS 2182545

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge FJ6369

mild

Staat: CA
Alter: 43,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 11.03.2022
Beginn: 13.03.2022
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Hypersensitivity Injection site pain Periorbital swelling Pruritus Rash papular Urticaria

Symptomtext

c/o itchiness and papular rash around the body, primarily on her stomach and back that started on Sunday (03/13/2022) s/p covid vaccine 2nd dose (03/11). Pt also noticed of wheals (2x1cm) on her both feet and right elbow. States feeling soreness on the injection site. This morning (3/16) she also noticed that her eyes alittle bit puffy. Patient also states that she applied lotrimine cream for her stomach and notice of mild improvement on her itchiness. Denies tongue swelling, fever, or SOB at the moment she was at the clinic. Prescribed kenalog 0.1% bid for affected skin, and benadryl p.o 25 mg q4h PRN for 2 days for the allergy reaction. Request to be off work today for possible adverse effect of covid 19 vaccine. Request to follow up with herPCP by the end of today or tomorrow, or visit ER if the symptoms worsen. F/U call is scheduled today as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Dx: bacterial vaginosis 03/05/2022
Vorgeschichte: patient denies having significant chronic conditions but she mentioned that one of her doctors told her that she has a rheumatic arthritis on her back. Patient never seen her PCP for the specific issue.
Andere Medikamente: pt denies
Allergien: pt denies
Vorherige Impfungen: -

VAERS 2182419

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: TX
Alter: 38,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 10.03.2022
Beginn: 11.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / UN

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

Headache Pain

Symptomtext

Person received Covid-19 vaccine booster 03/10/22 and started having side effects of headache along with body aches, dis take tylenol and ibuprofen regimens to help, side effects have subsided.

Weitere VAERSDATA-Felder

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

VAERS 2182399

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: TX
Alter: 45,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 15.03.2022
Beginn: 16.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Chills Headache Pain

Symptomtext

Patient took booster vaccine on 3/15/22 and started have side effects of headache shill and body aches on next day 3/16/22. Patient took Tylenol, outcome symptoms expected to last 1-2 days.

Weitere VAERSDATA-Felder

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

VAERS 2179733

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: -
Alter: 38,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 12.03.2022
Beginn: 13.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Headache Injection site pain Injection site pruritus Injection site rash Pain Pyrexia Rash Vaccine positive rechallenge

Symptomtext

Received pfizer booster in left arm on 3/12/2022. The next day had symptoms of headache, dizziness, pain at injection site, rash at injection site that itches and is painful, fever, and pain when moving left arm. Tylenol is what is being taken to help improve symptoms as well as a rash cream that was prescribed by physician. Symptoms have remained the same since they started.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: Vitamins
Allergien: Sunflower seeds, flu vaccine
Vorherige Impfungen: Same reaction to pfizer 1st and 2nd doses

VAERS 2177375

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NC
Alter: 20,0
Geschlecht: M
Eingang: 13.03.2022
Impfdatum: 13.03.2022
Beginn: 13.03.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Throat tightness Urticaria

Symptomtext

Hives throughout upper body beginning within a few hours of receiving vaccine, as well as a constriction sensation in the throat. Vaccine was administered around 2:15 pm on 03/13/22, symptoms began to emerge around 4:30 pm the same day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Gluten, Dairy, Mammalian meat
Vorherige Impfungen: -

VAERS 2174046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: MI
Alter: 42,0
Geschlecht: F
Eingang: 11.03.2022
Impfdatum: 09.03.2022
Beginn: 09.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect route of product administration Injection site bruising Pain in extremity

Symptomtext

pharmacist gave vaccine too low, patient complain today 3/11 of severe pain in arm, she had a bruise where the shot was given. recommended drinking plenty of water and ice pack

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site bruising
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: n/a
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2173719

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 26,0
Geschlecht: F
Eingang: 11.03.2022
Impfdatum: 10.03.2022
Beginn: 10.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Chills Exposure during pregnancy Headache Hyperhidrosis Pain Pyrexia

Symptomtext

Currently Pregnant. Symptoms include headache, fever, chills, body aches, and sweats.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: OTC Prenatal Vitamins
Allergien: none
Vorherige Impfungen: -

VAERS 2163267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 12,0
Geschlecht: M
Eingang: 11.03.2022
Impfdatum: 26.01.2022
Beginn: 09.02.2022
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: - / LA

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

Blood blister Injection site bruising Incorrect route of product administration Injection site granuloma Injection site haemorrhage Pyogenic granuloma Skin lesion

Symptomtext

Site: Bruising at Injection Site-Medium, Additional Details: Mom reports pt having blood bolus develop 2 weeks after receiving COVID vaccine booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site granuloma
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2163267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: CA
Alter: 12,0
Geschlecht: M
Eingang: 11.03.2022
Impfdatum: 26.01.2022
Beginn: 09.02.2022
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / LA

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

Blood blister Injection site bruising Incorrect route of product administration Injection site granuloma Injection site haemorrhage Pyogenic granuloma Skin lesion

Symptomtext

Site: Bruising at Injection Site-Medium, Additional Details: Mom reports pt having blood bolus develop 2 weeks after receiving COVID vaccine booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site granuloma
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2168216

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: TX
Alter: 56,0
Geschlecht: F
Eingang: 09.03.2022
Impfdatum: 02.03.2022
Beginn: 02.03.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chills Diarrhoea Headache Nausea Pain Pyrexia Vomiting

Symptomtext

Nausea, fever, diarrhea, chills, vomiting, body aches, head aches that lasted for a week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Omeprazole, Cranberry supplements
Allergien: N/A
Vorherige Impfungen: -

VAERS 2168169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: AL
Alter: 39,0
Geschlecht: F
Eingang: 09.03.2022
Impfdatum: 27.01.2022
Beginn: 27.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenopia COVID-19 Fatigue SARS-CoV-2 test positive Vomiting

Symptomtext

Really tired. I could not open eyes at all and was throwing up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Went to clinic & got tested positive for COVID-19
Aktuelle Erkrankungen: None
Vorgeschichte: Obese
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2165968

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: MI
Alter: 16,0
Geschlecht: F
Eingang: 08.03.2022
Impfdatum: 22.02.2022
Beginn: 23.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

C-reactive protein increased Culture urine negative Diarrhoea Differential white blood cell count abnormal Full blood count abnormal Laboratory test Metabolic function test abnormal Pancreatitis acute Ultrasound abdomen normal Urine analysis normal Vomiting

Symptomtext

Acute pancreatitis with Vomiting/diarrhea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Labs: CBC w/diff abnormal- Metabolic Panel abnormal- CRP 3.2/1.8- UA/UCX: normal- ESD: 19- Abdominal Ultrasound - neg.
Aktuelle Erkrankungen: Covid-19 disease January 2022
Vorgeschichte: Low Ferritin
Andere Medikamente: Fluoxetine HCI 20mg, Junel FE 24 1-20MG-MCG(24) per tablet PO QD, Omeprazole 40mg, Vitamin D, Zofran, Fluticasone 50 MCG/ACT
Allergien: none
Vorherige Impfungen: -

VAERS 2162879

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: FL
Alter: 61,0
Geschlecht: F
Eingang: 07.03.2022
Impfdatum: 02.02.2022
Beginn: 20.02.2022
Tage bis Beginn: 18,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal discomfort Heart rate increased Neck pain Pyrexia

Symptomtext

fever, upsetstomah, high pulse rate, neck pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Neck pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: metformin, lisinopril
Allergien: -
Vorherige Impfungen: -

VAERS 2162848

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 12,0
Geschlecht: M
Eingang: 07.03.2022
Impfdatum: 03.03.2022
Beginn: 03.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Cough Dizziness Ear pain Fatigue Hallucination, auditory Hallucination, visual Influenza A virus test negative Influenza virus test negative Nasal congestion SARS-CoV-2 test negative Tinnitus Visual impairment

Symptomtext

Was seen in office 3/3/22 for sudden onset left leg pain with standing up from seated position. Around 2:49 pm received covid booster shot (3rd dose Pfizer vaccine). Returned to clinic on 3/4/22 due to perceived side effects from vaccine. Around 8:30 pm on 3/3 started to cough. Woke up in the morning late, slept in, felt fatigued. Dizziness started in the AM at school, no LOC. Rested head and felt better. Was walking at lunch and saw "a black figure" in right eye and started to "hear little talking noises." The noises lasted for about 15 minutes, the black blob in the vision for about 10 minutes. Rapid antigen test at home negative. Cough started around 8:30 pm. Had stuffy nose at lunch time. Also reported ear pain and ringing resolved by time of the visit on 3/4.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: COVID-19 and Flu A & B PCR negative on 3/4/22
Aktuelle Erkrankungen: On day of vaccination was seen for sudden onset R leg pain with standing from a seated position. No symptoms of illness at that time.
Vorgeschichte: Obesity, otherwise healthy child.
Andere Medikamente: ibuprofen
Allergien: none
Vorherige Impfungen: -

VAERS 2162689

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NY
Alter: 58,0
Geschlecht: F
Eingang: 07.03.2022
Impfdatum: 28.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Eye pain Laboratory test abnormal Magnetic resonance imaging head abnormal Magnetic resonance imaging spinal Neurological symptom Optic neuritis Pyrexia

Symptomtext

2 hours after vaccination my eyeballs begun to hurt. Fever, chills. I went to eye clinic to get my eyes checked and was referred to go to an eye specialist. I was admitted upon arrival as, the doctor found out from an MRI and other test run that, my optic nerves were inflamed. I was admitted in the hospital for 5 days. The doctor then stated I am having symptoms of Multiple sclerosis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: 5,0
Labordaten: MRI of my brains and spinal cord
Aktuelle Erkrankungen: COVID 3weeks before the vaccination
Vorgeschichte: High Cholesterol
Andere Medikamente: Protonix 20mg/daily Crestol 20mg/daily
Allergien: None
Vorherige Impfungen: Flu shot

VAERS 2162648

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 52,0
Geschlecht: F
Eingang: 07.03.2022
Impfdatum: 04.03.2022
Beginn: 05.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Cough Fatigue Pain Pyrexia Respiratory tract congestion SARS-CoV-2 test

Symptomtext

Symptoms - cough, congestion, fatigue, fever, and body aches on 3/5/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Received COVID PCR test on 3/5/22 by PCP. Awaiting results
Aktuelle Erkrankungen: Allergies causing cough and congestion at the same time of vaccination
Vorgeschichte: High BP and Cholesterol
Andere Medikamente: Blood pressure and cholesterol medication , over the counter cough medication
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2162484

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: VA
Alter: 61,0
Geschlecht: F
Eingang: 07.03.2022
Impfdatum: 01.03.2022
Beginn: 04.03.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

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

Rash

Symptomtext

Rash...started on back of neck, them stomach, arms, behind ears, scalp, legs

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypersensitivity to the sun
Andere Medikamente: B6, omeprazole Dr 40, pristiq 100mg, wellbrutrin 300, levothyroxine 7.5
Allergien: None known
Vorherige Impfungen: -

VAERS 2162170

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: FL
Alter: 42,0
Geschlecht: F
Eingang: 06.03.2022
Impfdatum: 29.01.2022
Beginn: 30.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Erythema Joint swelling Pain in extremity Peripheral swelling Vasculitis

Symptomtext

Patient is experiencing pain, swelling, and redness on inner elbow of left arm. The pain and swelling can extend up into the upper medial side of arm. She states that at times her blood vessel specifically seems swollen and stands out. This is continuing to this day. I advised her to seek medical attention to confirm or exclude a blood clot.

Weitere VAERSDATA-Felder

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

VAERS 2162053

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: WA
Alter: 69,0
Geschlecht: F
Eingang: 06.03.2022
Impfdatum: 11.02.2022
Beginn: 12.02.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Blood test Headache

Symptomtext

Headache for three weeks and still present. Stronger headache the first week but still difficult to use the computer for more than a few minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Blood test 3/4/2022. CT scan 3/8/2022.
Aktuelle Erkrankungen: None
Vorgeschichte: Only one kidney
Andere Medikamente: Levothyroxine, Buspirone, Bupropion, Multivitamin, B-complex, Fish oil
Allergien: None
Vorherige Impfungen: -

VAERS 2157744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: WA
Alter: 46,0
Geschlecht: F
Eingang: 04.03.2022
Impfdatum: 20.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Eye pain Headache Joint swelling Ophthalmological examination Rash Vision blurred

Symptomtext

Eye pain in my left eye; Joints in my thumbs are swollen. Joints in my right knee is swollen and pain full. Reoccurring rash from my forehead to my eyes. Blurry/foggy vision. Reoccurring headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Eye test, whole in my eye; Laser surgery on my eye.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Adderall 10mg
Allergien: Latex; Citrus fruits; Environment allergies; Nuts
Vorherige Impfungen: -

VAERS 2157724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 30,0
Geschlecht: F
Eingang: 04.03.2022
Impfdatum: 28.02.2022
Beginn: 03.03.2022
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Gingival pain Lip swelling Oral herpes Pain

Symptomtext

Patient's grandmother asked about side-effects of fever blisters on top lip and swollen, throbbing gums. 4 blisters on patient's top lip with some swelling. No swelling of face or tongue. No difficulty breathing. Patient has history of fever blisters, but not for a long time. Grandmother told to inform patient's physician, take antihistamines and acetaminophen.

Weitere VAERSDATA-Felder

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

VAERS 2157440

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: PA
Alter: 60,0
Geschlecht: M
Eingang: 04.03.2022
Impfdatum: 20.01.2022
Beginn: 06.02.2022
Tage bis Beginn: 17,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Genital atrophy Lethargy

Symptomtext

Systemic: Exhaustion / Lethargy-Mild, Systemic: 20% decrease (shrinkage) of male genitalia-Severe

Weitere VAERSDATA-Felder

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

VAERS 2154899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: OH
Alter: 25,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 01.03.2022
Beginn: 02.03.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Maternal exposure during pregnancy Uterine contractions during pregnancy Uterine pain

Symptomtext

Due date June 3rd currently 26 weeks 6 days. History of low progesterone in pregnancy and a SCH in the first and second trimester. Over the last two days a significant increase in contractions. Pain in the uterus not associated with contractions as well starting 3/3.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Uterine pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Covid in January 2022 food poisoning February 2022
Vorgeschichte: Hypothyroid
Andere Medikamente: Aspirin Lovenox Progesterone Vitamin E Vitamin D Acidophilus Prenatal
Allergien: Sesame oil
Vorherige Impfungen: -

VAERS 2154878

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: NC
Alter: 60,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 10.02.2022
Beginn: 11.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Headache Nausea

Symptomtext

Dizziness, severe headache, nausea

Weitere VAERSDATA-Felder

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

VAERS 2152163

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NJ
Alter: 53,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 01.03.2022
Beginn: 01.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal discomfort Arthralgia Headache Nausea Rash

Symptomtext

Patient reported generalized rash to upper body, Nausea, Headache, achy joints and upset stomach

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Patient reported history of COVID -19
Vorgeschichte: Not reported in the form
Andere Medikamente: None
Allergien: Pfizer COVID - 19 vaccine - reported mild symptoms at second dose
Vorherige Impfungen: -

VAERS 2151792

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 34,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 01.03.2022
Beginn: 02.03.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Fatigue Headache Myalgia Nausea

Symptomtext

Headache, chills, muscle aches, fatigue, nausea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None.
Allergien: Pears, apples, plumbs, peaches
Vorherige Impfungen: TDAP

VAERS 2151357

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 70,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 25.01.2022
Beginn: 26.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: OT / RA

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

Headache Hypoaesthesia Neuralgia Oral pain Piriformis syndrome

Symptomtext

experienced nerve pain on past injuries from a torn rotor cuff from 3 yrs. ago; a very sharp intense sciatic pain from piriformis syndrome; tenderness in my mouth from cementifying fibromas dx'd in the 1970's; numbness on my left thumb at tip; tenderness on my left temple area from a concussion in the 1970's; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 70 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 25Jan2022 12:00 (Lot number: FJ6369) at the age of 70 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Known allergies: sulfa" (unspecified if ongoing), notes: Verbatim:Known allergies: sulfa; "past injuries" (unspecified if ongoing), notes: Verbatim: Past injuries from a torn rotor cuff from 3 yrs; "cementifying fibromas", start date: 1970 (unspecified if ongoing), notes: tenderness in my mouth from cementifying fibromas dx'd in the 1970's; "concussion", start date: 1970 (unspecified if ongoing), notes: Verbatim:Tenderness on my left, temple area from a concussion in the, 1970's. The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose 2, Single, 09:00 AM; Intramuscular; Batch/Lot No: FA7484, Location of injection: Arm Right), administration date: 20Aug2021, when the patient was 70 years old, for Covid-19 Immunization; Bnt162b2 (Dose 1, Single, 09:00 AM; Intramuscular; Batch/Lot No: FA7484, Location of injection: Arm Right), administration date: 30Jul2021, when the patient was 70 years old, for Covid-19 Immunization. The following information was reported: NEURALGIA (non-serious) with onset 26Jan2022 06:00, outcome "not recovered", described as "experienced nerve pain on past injuries from a torn rotor cuff from 3 yrs. ago"; PIRIFORMIS SYNDROME (non-serious) with onset 26Jan2022 06:00, outcome "not recovered", described as "a very sharp intense sciatic pain from piriformis syndrome"; ORAL PAIN (non-serious) with onset 26Jan2022 06:00, outcome "not recovered", described as "tenderness in my mouth from cementifying fibromas dx'd in the 1970's"; HYPOAESTHESIA (non-serious) with onset 26Jan2022 06:00, outcome "not recovered", described as "numbness on my left thumb at tip"; HEADACHE (non-serious) with onset 26Jan2022 06:00, outcome "not recovered", described as "tenderness on my left temple area from a concussion in the 1970's". Therapeutic measures were not taken as a result of neuralgia, piriformis syndrome, oral pain, hypoaesthesia, headache. Additional information: Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with Covid-19 prior to vaccination. The patient has not been tested for Covid-19 since the vaccination. Patient received other medications within 2 weeks of vaccination. Facility where the most recent COVID-19 vaccine was administered was reported as Pharmacy. Patient did not experience covid-19 prior to vaccination. Patient did not tested post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Concussion (Verbatim:Tenderness on my left temple area from a concussion in the 1970's); Fibroma (tenderness in my mouth from cementifying fibromas dx'd in the 1970's); Injury (Verbatim: Past injuries from a torn rotor cuff from 3 yrs); Sulfonamide allergy (Verbatim:Known allergies: sulfa)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2151094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 32,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 24.02.2022
Beginn: 24.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Inappropriate schedule of product administration Pain in extremity

Symptomtext

She received her booster shot two months early. I followed up with her days after her shot and she reports that she is completely fine. Aside from a sore arm, she had no other symptoms or issues. She was confused by the vaccine mandate the the hospital has for everyone to get their booster shot by 3/1/22. She didn't understand that it didn't apply to her.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2151078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CO
Alter: 56,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 04.02.2022
Beginn: 05.02.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Ear disorder Ear pain Eczema Fatigue Illness Influenza like illness Injection site reaction Nausea Pain Pyrexia Quarantine Rash SARS-CoV-2 test positive Sinus disorder Vomiting

Symptomtext

I started feeling like I had the flu. I felt very achy with an earache. It felt like I got COVID. As it progressed, I was sore and tired with nausea and an earache. It was intense allergies that went on for 2 weeks. On the 15th day, I woke up with a fever and was vomiting. Fever was 102.4. I was so sick, I felt like I had the flu. My family told me to get tested for COVID so I went on Monday and I was diagnosed with COVID. I have been quarantined since then but I have not gotten any better. Its all in my head, my ears, throat and sinuses. I was supposed to be off quarantine today but I am still highly symptomatic. I no longer have fever, intense body aches or throwing up but I am still feeling the symptoms with my head. I also got a rash on my hand like eczema and a ring appeared around the area where I got the shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: COVID 19 Test.
Aktuelle Erkrankungen: Seasonal allergies
Vorgeschichte: None
Andere Medikamente: Emergen C Gingko biloba Milk thistle
Allergien: Gabapentin Buspirone Mucinex Claritin most man made medications cause an allergic reaction.
Vorherige Impfungen: -

VAERS 2151033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 29,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 26.01.2022
Beginn: 26.01.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Interchange of vaccine products Rash erythematous Rash papular Rash pruritic

Symptomtext

Received Pfizer booster vaccination at approx. 1200. At 8pm began to have red, raised rash to both anterior thighs with itching. Rash and itching lasted approx. 5 days, spreading to slightly larger area on ant. things. Slowly resolving since then. Used over-the-counter creams on rash. Denies shortness of breath, difficulty breathing, facial swelling, generalized rash or any other symptoms. Janssen vaccination give on 6/13/21

Weitere VAERSDATA-Felder

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

VAERS 2150869

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: FL
Alter: 43,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 25.02.2022
Beginn: 26.02.2022
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 Back pain Breast pain Chills Fatigue Pain Pain in extremity Pyrexia Swelling Tenderness

Symptomtext

Patient initially had typical post vaccination symptoms of chills, fever, and fatigue. The following day post vaccination began having tenderness to her right axilla area the day after vaccination on 02/26/2022. She then additionally noticed swelling, tenderness, and radiating pain since that time. Her pain is currently a 8/10. Pain is located to her right axilla area with tenderness and pain to surrounding region. the pain radiates to the top of her right breast, to her upper right back, and occasionally down her arm.

Weitere VAERSDATA-Felder

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

VAERS 2148483

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 28.02.2022
Impfdatum: 11.02.2021
Beginn: 11.02.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Pruritus

Symptomtext

Itchiness on face. Capsule benadryl 50mg given. BP: 144/96 HR: 74 O2: 98% -Patient had anaphylactic reaction from shingles vaccine(october2021). No any adverse reations from pfizer covid 1st and 2nd shot. -Patient feels itchiness on face after booster shot, no any difficulty in breathing. -Cap. Benadryl 50mg given, seems effective. -Adviced patient to go to ER for further education. Patient refused to go with clinics protocol, stated she will go by herself to ER accompanied with son.

Weitere VAERSDATA-Felder

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

VAERS 2148292

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: TX
Alter: 27,0
Geschlecht: F
Eingang: 28.02.2022
Impfdatum: 26.02.2022
Beginn: 26.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Headache Injection site pain Pain Pyrexia

Symptomtext

EE had a fever, HA, Chills, body aches, soreness at injection site. EE treated with Tylenol at home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: asthma
Andere Medikamente: Tylenol
Allergien: n/a
Vorherige Impfungen: Covid Moderna 1&2 1/15/21 & 3/5/21

VAERS 2147606

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: FL
Alter: 35,0
Geschlecht: F
Eingang: 27.02.2022
Impfdatum: 27.02.2022
Beginn: 27.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Blood pressure increased Dizziness Dry mouth Heart rate increased

Symptomtext

Patient felt lightheaded, had a elevated heart rate, had elevated blood pressure, and dry mouth. These symptoms started approximately 5 minutes after administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Blood pressure was taken at the pharmacy. EMS came and performed other tests.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2147591

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: MA
Alter: 36,0
Geschlecht: M
Eingang: 27.02.2022
Impfdatum: 23.02.2022
Beginn: 24.02.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Chills Muscular weakness Pain in extremity Pyrexia

Symptomtext

Chills, Fever, and Leg weakness/pain, mild posterior right knee pain after taking the booster shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: I will see my primary care physician for my annual physical in less than 35 day and will discuss these symptoms if they still persist by then.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: Itchiness after second shot of pfizer covid 19 vaccine

VAERS 2147399

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NC
Alter: 20,0
Geschlecht: F
Eingang: 27.02.2022
Impfdatum: 21.02.2022
Beginn: 21.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Dizziness Pain in extremity

Symptomtext

Dizzy/ Lightheaded; Sore arm; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 20-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 21Feb2022 at 17:00 (Lot number: FJ6369) at the age of 20 years as dose 1, single for COVID-19 immunisation. The patient's relevant medical history was not reported. Concomitant medications included: PROZAC; HYDROXYZINE and GLYCOPYRROLATE. The following information was reported: DIZZINESS (non-serious) with onset 21Feb2022 at 17:15, outcome "not recovered", described as "Dizzy/ Lightheaded"; PAIN IN EXTREMITY (non-serious) with onset 21Feb2022 at 17:15, outcome "not recovered", described as "Sore arm". Therapeutic measures were taken as a result of the pain in extremity. Additional Information: The patient had no known allergies. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Treatment included tylenol for pain in extremity. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: PROZAC; HYDROXYZINE; GLYCOPYRROLATE
Allergien: -
Vorherige Impfungen: -

VAERS 2147257

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 27.02.2022
Impfdatum: 07.02.2022
Beginn: 07.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Blood pressure measurement Body temperature Chills Dizziness Feeling abnormal Feeling cold Headache Leukopenia Mean cell haemoglobin concentration Nausea Neutrophil count Pain in extremity Peripheral swelling White blood cell count

Symptomtext

white blood cell count is low/ on 13Oct2022 it was 4.1 and on some current blood it was 3.3; sore arm; I felt like I was fainting/ a feel-like-fainting sensation (extreme light-headedness); a terrible headache; extreme cold (icy cold sensation); nauseous/ nausea; felt so horrible like something just came over me/ felt awful; chilled and had to sleep in different garments because she was shivering; arm was swollen; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 69 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 07Feb2022 (Lot number: FJ6369, Expiration Date: 07Feb2022) at the age of 69 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Pre-diabetic" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose 1, single, lot FA7485, unknown, expiration date 31Oct2021.), administration date: 04Aug2021, when the patient was 68 years old, for Covid-19 immunization; Bnt162b2 (Dose 2, single, lot FC3184, expiration date 31Oct2021, unknown.), administration date: 27Aug2021, when the patient was 68 years old, for Covid-19 immunization, reaction(s): "The caller had the second dose and she had a reaction", "White blood cell count low". The following information was reported: LEUKOPENIA (medically significant) with onset 11Feb2022, outcome "recovering", described as "white blood cell count is low/ on 13Oct2022 it was 4.1 and on some current blood it was 3.3"; DIZZINESS (non-serious) with onset 07Feb2022, outcome "recovering", described as "I felt like I was fainting/ a feel-like-fainting sensation (extreme light-headedness)"; HEADACHE (non-serious) with onset 07Feb2022, outcome "recovering", described as "a terrible headache"; FEELING COLD (non-serious) with onset 07Feb2022, outcome "recovering", described as "extreme cold (icy cold sensation)"; NAUSEA (non-serious) with onset 07Feb2022, outcome "recovering", described as "nauseous/ nausea"; FEELING ABNORMAL (non-serious) with onset 07Feb2022, outcome "recovering", described as "felt so horrible like something just came over me/ felt awful"; CHILLS (non-serious) with onset 07Feb2022, outcome "recovering", described as "chilled and had to sleep in different garments because she was shivering"; PERIPHERAL SWELLING (non-serious) with onset 07Feb2022, outcome "recovering", described as "arm was swollen"; PAIN IN EXTREMITY (non-serious) with onset 08Feb2022, outcome "recovering", described as "sore arm". The patient underwent the following laboratory tests and procedures: blood pressure measurement: (11Feb2022) 99/65, notes: which is normal, but it usually runs on the low end; body temperature: (11Feb2022) 97 or 97.5, notes: which is normal for her; mean cell haemoglobin concentration: (13Oct2020) 32; neutrophil count: (13Oct2020) 1.5, notes: 1.5 instead of 1.2; neutrophil count (40-68): (13Oct2020) 33.6, notes: when it should be 40-68; white blood cell count (4.5-11): (13Oct2020) 4.1, notes: instead of 4.5-11; (11Feb2022) 3.3, notes: The caller's WBC is usually low but not this low. Clinical course: The patient took her usual vitamins (unspecified). The patient received dose 3 in the shoulder, number was unknown and had an extreme cold (icy cold sensation) reported as a side effect following administration of the Pfizer-BioNTech COVID-19 vaccine for 12 years and older formulation (purple cap). Patient declined to be provided with additional information. A review of the Prescribing Information for the Pfizer-BioNTech COVID-19 vaccine did not found information regarding an extreme cold (icy cold sensation). As the Prescribing Information did not include all adverse reactions that had been reported or that may occur, please consult with your doctor/healthcare provider about what you have experienced/are experiencing. Because your doctor/healthcare provider is most familiar with your medical condition, clinical history, how your treatment had been conducted and any relevant information to your specific case, your doctor/healthcare provider is in the best position to advise you about the appropriate action to take. Patient believed she was given an almost expired dose of the Pfizer-BioNTech COVID-19 vaccine for 12 years and older formulation (purple cap) as previously they used to put in her vaccination card the date the vaccine of expiry and it was the same dame she was administered the vaccine. Patient asked, could you please verify the expiration date on lot number FJ6369. Patient had received her primary vaccination series of the Pfizer-BioNTech COVID-19 vaccine. And had no adverse reactions to her first two doses. On Monday [07Feb2022], patient had received booster dose of the Pfizer-BioNTech COVID-19 vaccine for 12 years and older formulation (purple cap), lot number FJ6369 and within minutes patient experienced some side effects: felt icy cold, nauseous and had a terrible headache. Felt like she was fainting and was extremely light-headed but that could've been because patient got up too fast, she felt so horrible like something just came over her. Patient sat on the car as it was a very strong reaction. She was feeling better on those events, however her white blood cell count was low, on 13Oct2020 it was 4.1 and on some current blood it was 3.3. Patient asked, has lower white blood cell count been reported as a side effect of the Pfizer-BioNTech COVID-19 vaccine? Some of her friends had experienced adverse events as well. Patient asked, has nausea been reported as a side effect following administration of the Pfizer-BioNTech COVID-19 vaccine for 12 years and older formulation (purple cap)? Patient asked, has a feel-like-fainting sensation (extreme light-headedness) been reported as a side effect following administration of the Pfizer-BioNTech COVID-19 vaccine for 12 years and older formulation (purple cap)? Patient declined to be provided with additional information. Responded as per attached pfizer-biontech covid-19 vaccine for 12 years and older formulation (purple cap) vaccine information fact sheet for recipients and caregivers about comirnaty (covid-19 vaccine, mrna) and the pfizer-biontech covid-19 vaccine to prevent coronavirus disease 2019 (covid-19) (lab-1451-17.0, revised: 31jan2022). Informed to patient, Side effects that had been reported with the vaccine include fainting in association with injection of the vaccine. A review of the Prescribing Information for the Pfizer-BioNTech COVID-19 vaccine did not find information regarding feel-like-fainting sensation (extreme light-headedness). As the Prescribing Information did not include all adverse reactions that had been reported or that may occur, please consult with your doctor/healthcare provider about what you have experienced/are experiencing. Because your doctor/healthcare provider was most familiar with your medical condition, clinical history, how your treatment had been conducted and any relevant information to your specific case, your doctor/healthcare provider is in the best position to advise you about the appropriate action to take. Patient asked, "Has headache been reported as a side effect following administration of the Pfizer-BioNTech COVID-19 vaccine for 12 years and older formulation (purple cap)?". The patient will be traveling and she will be at 5 months and got the booster. No other products received. The patient was calling about the Pfizer Biontech vaccine. The patient had the first shot which was no issue. The patient had the second dose and she had a reaction. The patient was glad to had a reaction because she typically has a low WBC. The patient had the booster dose, the third dose, on Monday and was dizzy and felt horrible and they said to wait at the office. The patient got up from the room and felt awful and sat in the car for a while and in fear of blacking out. The patient arm was swollen and so she exercised it and its less swollen today. The patient had her annual blood count today and her white blood cell count was lower than last year. Is this normal? The patient would have thought it would have been at least where it was last year. The patient got over the side effects although she isn't 100%, her arm isn't swollen and its normalizing. The patient was shocked her count went so low. The patient got the booster dose on Monday. The patient was feeling better she was chilled and had to sleep in different garments because she was shivering. The patient arm was improved but still slightly sore. The patient exercised her arm and it dissipated. She took her usual vitamins. The patient blood pressure today was 99/65 which is normal, but it usually runs on the low end. The patient temperature today was 97 or 97.5 which is normal for her. The patient WBC was usually low but not this low. The patient has been having headaches, but she has been stressed. The patient was working on herself so she should have seen an improvement. The patient clarified and confirmed that her previous labs were drawn in 2020 not 2021 as previously reported. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20220211; Test Name: blood pressure; Result Unstructured Data: Test Result:99/65; Comments: which is normal, but it usually runs on the low end; Test Date: 20220211; Test Name: temperature; Result Unstructured Data: Test Result:97 or 97.5; Comments: which is normal for her.; Test Date: 20201013; Test Name: MCHC; Result Unstructured Data: Test Result:32; Test Date: 20201013; Test Name: Neutro ABS; Result Unstructured Data: Test Result:1.5; Comments: 1.5 instead of 1.2; Test Date: 20201013; Test Name: Neutrophils; Result Unstructured Data: Test Result:33.6; Comments: when it should be 40-68; Test Date: 20201013; Test Name: WBC; Result Unstructured Data: Test Result:4.1; Comments: instead of 4.5-11; Test Date: 20220211; Test Name: WBC; Result Unstructured Data: Test Result:3.3; Comments: The caller's WBC is usually low but not this low.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pre-diabetic
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2129035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: TX
Alter: 53,0
Geschlecht: F
Eingang: 27.02.2022
Impfdatum: 09.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Contusion Injection site erythema Injection site nodule Injection site pain Injection site reaction Injection site swelling Musculoskeletal stiffness Pain Pain in extremity Vaccination site pain

Symptomtext

Pain from injection site to the neck and through the shoulder; Pain from injection site to the neck and through the shoulder; This is a spontaneous report received from a contactable reporter (other healthcare professional). The reporter is the patient. A 53-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 09Feb2022 at 15:15 (Lot number: FJ6369) at the age of 53 years as dose 3 (tris booster), single for COVID-19 immunisation. Relevant medical history included: "COVID-19" (unspecified if ongoing), notes: Prior to vaccination, was the patient diagnosed with COVID-19?: Yes. The patient did not receive any concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: EJ1685; Anatomical Location: Left arm; Administration time: 06:00), administration date: 18Dec2020, when the patient was 52 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot Number: EJ1686; Anatomical Location: Right arm; Administration time: 06:00), administration date: 08Jan2021, when the patient was 52 years old, for COVID-19 immunisation. The following information was reported: VACCINATION SITE PAIN (non-serious); PAIN (non-serious); all with onset 10Feb2022, outcome "not recovered", and all described as "Pain from injection site to the neck and through the shoulder". Therapeutic measures were not taken as a result of vaccination site pain and pain. Additional information: It was unknown if the patient had any known 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 COVID vaccine. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19?: Yes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2129035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: TX
Alter: 53,0
Geschlecht: F
Eingang: 27.02.2022
Impfdatum: 09.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Contusion Injection site erythema Injection site nodule Injection site pain Injection site reaction Injection site swelling Musculoskeletal stiffness Pain Pain in extremity Vaccination site pain

Symptomtext

Pain from injection site to the neck and through the shoulder; Pain from injection site to the neck and through the shoulder; This is a spontaneous report received from a contactable reporter (other healthcare professional). The reporter is the patient. A 53-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 09Feb2022 at 15:15 (Lot number: FJ6369) at the age of 53 years as dose 3 (tris booster), single for COVID-19 immunisation. Relevant medical history included: "COVID-19" (unspecified if ongoing), notes: Prior to vaccination, was the patient diagnosed with COVID-19?: Yes. The patient did not receive any concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: EJ1685; Anatomical Location: Left arm; Administration time: 06:00), administration date: 18Dec2020, when the patient was 52 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot Number: EJ1686; Anatomical Location: Right arm; Administration time: 06:00), administration date: 08Jan2021, when the patient was 52 years old, for COVID-19 immunisation. The following information was reported: VACCINATION SITE PAIN (non-serious); PAIN (non-serious); all with onset 10Feb2022, outcome "not recovered", and all described as "Pain from injection site to the neck and through the shoulder". Therapeutic measures were not taken as a result of vaccination site pain and pain. Additional information: It was unknown if the patient had any known 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 COVID vaccine. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19?: Yes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2146349

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: WA
Alter: 55,0
Geschlecht: F
Eingang: 26.02.2022
Impfdatum: 23.02.2022
Beginn: 23.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Pain in extremity Rash Rash pruritic Skin warm

Symptomtext

Patient had soreness, warmth, and an itchy rash on right upper arm after receiving the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Adjustment disorder with anxiety, vitamin D deficiency, tension headache
Vorgeschichte: Asthma, HTN, hyperlipidemia, fatty liver, allergic rhinitis, atopic dermatitis, chronic LBP w/ left sciatica, overweight, stress incontinence, prediabetes
Andere Medikamente: Hydroxyzine Pamoate 25 mg, Vitamin B Complex with C, Cholecalciferol 5000 IU, Cetirizine 10 mg, Acetaminophen 500 mg, Amlodipine 5 mg, Atorvastatin 40 mg, Docusate 100 mg, Albuterol HFA, and Mometasone Furo-Formoterol Fum 100-5 MCG/ACT
Allergien: wool blankets
Vorherige Impfungen: -

VAERS 2140498

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj6369

mild

Staat: FL
Alter: 44,0
Geschlecht: F
Eingang: 25.02.2022
Impfdatum: 18.02.2022
Beginn: 18.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Rash

Symptomtext

Rash all around neck and face and shoulder.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Seen and Sent to ER 2/25/22
Aktuelle Erkrankungen: No
Vorgeschichte: -
Andere Medikamente: -
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2140176

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 43,0
Geschlecht: F
Eingang: 25.02.2022
Impfdatum: 08.01.2022
Beginn: 09.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Headache Loss of personal independence in daily activities Pain Pyrexia Sleep disorder

Symptomtext

About 12-14 hours I woke up with fever, ache all over my body and a very bad headache, I took Tylenol. I drank soup to feel better but still didn't help. I can't sleep my head hurts all the time. But it goes and goes . It's hurting all the time. I went to the doctor on Feb. 15 she gave me medication to sleep but I took it for long but still didn't help much. I can't do anything because of the headache. I don't want to take medication for rest of my life because of the headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Endometriosis
Andere Medikamente: Birth control seminar, daily multi vitamins
Allergien: Morin, coding, allergy to pineapple, any kind of peppers
Vorherige Impfungen: -

VAERS 2139993

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NY
Alter: 65,0
Geschlecht: F
Eingang: 25.02.2022
Impfdatum: 18.02.2022
Beginn: 18.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Chest discomfort Chills Myalgia Peripheral swelling Sleep disorder

Symptomtext

I received my booster 2/18/2022 as mandated. That night I awoke at 11 pm out of a sound sleep. I suffered terribly: severe rigor, severe arthralgia and myalgia for hours. My fingers swelled. I was able to remove one ring but not another. I had some tightness in my chest. I had to take a prescription strength NSAID (recently prescribed by my MD for persistent headaches post COVID-19 infection 12/24/2021). The worst of the symptoms subsided after 48 hours. I can only hope the now milder arthralgia, myalgia and headaches resolve.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Myalgia; arthralgia; persistent headaches.

VAERS 2139941

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj6369

mild

Staat: AR
Alter: 31,0
Geschlecht: F
Eingang: 25.02.2022
Impfdatum: 15.02.2022
Beginn: 16.02.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Blood test normal Computerised tomogram normal Headache Oversensing Photophobia

Symptomtext

Headache sensitivity to light and noise nausea, started 2/16/2022 doesn?t respond to over the counter medication. Did not respond to toradol Im or fioricet

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Md orders ct scan and blood work- 2/22 all WNL
Aktuelle Erkrankungen: None
Vorgeschichte: Depression Adhd Anxiety
Andere Medikamente: Effexor
Allergien: Pineapples
Vorherige Impfungen: -

VAERS 2137179

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: GA
Alter: 15,0
Geschlecht: F
Eingang: 24.02.2022
Impfdatum: 17.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Asthenia Dizziness Echocardiogram normal Electrocardiogram normal Heart rate increased

Symptomtext

The day after receiving her booster shot, she felt light-headed a lot the day after; they didn't have school that day due to a holiday. She has been taking high blood pressure for some years due to diagnosis of high blood pressure some years ago. Every time she tried getting up just to be active in the day, she didn't have much energy to stand up so I decided to take her blood pressure to check just in case. When we checked her blood pressure, it read 120/59 and 99bpm. We tried to get her hydrated and eat; later that evening, we checked her BP again and it stayed the same but her heart rate increased. The next morning, 97/43 was her blood pressure and 89bpm heart rate; she insisted on going to school so we allowed her. When she got to school, I called the nurse to check her measures again, and they read 115/58 and 117bpm heart rate. I picked her from school and checked it and it read the same so we called her cardiologist and they advised for her to stop taking her blood pressure medication. The next morning, we checked her blood pressure again and it read 97/52 but steadily increased during the day. We went to the cardiologist 01/27/2022 for an appointment out of concern. They performed an echocardiogram and EKG, but the results came back normal. They put her back on her on BP medication (only Lisinopril), and had a follow-up appointment 2 weeks later. They increased the dosage of the Lisinopril and currently she's still being monitored with a follow-up appointment beginning of March. Last night (02/23/2022) we checked her measures and it read 143/84 and 78bpm heart rate, so we're just constantly watching her activities and checking her measures until then.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Echocardiogram & EKG: 01/27/2022
Aktuelle Erkrankungen: COVID-19 PCR test: 12/25/2021
Vorgeschichte: High blood pressure
Andere Medikamente: Amlodipine; lisinopril; chlorophyll drops; multivitamin supplement
Allergien: Penicillin; lactose intolerant
Vorherige Impfungen: -

VAERS 2135011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 31,0
Geschlecht: F
Eingang: 23.02.2022
Impfdatum: 23.02.2022
Beginn: 23.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Heart rate increased

Symptomtext

PATIENT RECEIVED BOOSTER DOSE OF PFIZER VACCINE, AFTER HER WAITING PERIOD PATIENT LEFT, SHE RETURNED BACK A FEW MINUTES LATER AND COMPLAINED OF INCREASED HEART RATE AND SHE FELT LIKE SHE WAS GOING TO PASS OUT. PARAMEDICS CAME TO EVALUATE AND DISCHARGED HER

Weitere VAERSDATA-Felder

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

VAERS 2132266

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: OH
Alter: 43,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 11.02.2022
Beginn: 21.02.2022
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered Neck pain

Symptomtext

Patient received expired vaccine. Clinic and Pfizer recommend revaccination. Patient was contacted to schedule an appointment. She rescheduled for 2/24/2022. States she has experienced Right neck pain since injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Neck pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: celiac
Andere Medikamente: -
Allergien: aspirin
Vorherige Impfungen: -

VAERS 2131423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NY
Alter: 67,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 15.02.2022
Beginn: 16.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Back pain Chills Fatigue Feeling cold Headache Hypersomnia Myalgia Night sweats Pain Pain in extremity

Symptomtext

Fatigue within 2 hours. next morning, headache, body and muscle aches, terrible lower back and leg pain. As day continued chills and cold bones, nightsweats. Sleeping for 10 hours at a time. These symptoms lasted 48 hours. I still have residual back aches. I had the same symptoms in Dec- January when I was diagnosed positive with Covid. I felt like I was sick all over except in January I was sick for 10 days to 2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Covid positive 12/30/2021 through 1-9-2022 at home
Vorgeschichte: diabetes-adult onset, hypothroidism, hypercholestrolemia, hypertriglyceridemia, sleep apnea
Andere Medikamente: janumet, zetia, prandin, tricor, synthroid, lexapro, multivitamin, vit d, biotin, claritin
Allergien: statins, ultram, tramadol, Morphine?
Vorherige Impfungen: terrible muscle aches, fatigue, but was not incapacitated

VAERS 2131412

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: KY
Alter: 44,0
Geschlecht: M
Eingang: 22.02.2022
Impfdatum: 31.01.2022
Beginn: 02.02.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / -

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

Asthenia Chills Constipation Dizziness Eye irritation Headache Illness Malaise Pain Pain in extremity Pain of skin Rash Sleep disorder Tenderness Vaccination complication

Symptomtext

Received vaccine 1/31/22 at 12:45PM. Became ill starting Tuesday evening around 5PM. Awakened by extreme cold chills around 1:30AM Wednesday morning. Dealt with extreme chills, headaches, crippling body pain, skin/nerves on right leg sensitive to touch, rash like sores in middle of chest, back, shoulders and forehead, loss of strength, unable to pass bowel during duration of feeling ill, left arm soreness but right arm used for shot and eye irritation when looking left to right. Symptoms started to subside Thursday evening but still felt lightheaded with headaches in left temple area. Unable to sustain energy for short periods of time. Scheduled appointment with PCP on 2/18/22 - unable to be seen sooner. After discussing incident with provider, he recommended that I send a report to VAERS and to suspend 2nd shot until we review labs to try and determine why I had a strong adverse reaction to vaccine. Also explained that I have continued to have mild headaches (currently speaking) but have been taking headache medicine since the onset of events.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: After discussing incident with provider, he recommended that I send a report to VAERS and to suspend 2nd shot until we review labs to try and determine why I had a strong adverse reaction to vaccine. Also explained that I have continued to have mild headaches (currently speaking) but have been taking headache medicine since the onset of events. Answer to Item 20, Still having mild headaches.
Aktuelle Erkrankungen: -
Vorgeschichte: High blood pressure
Andere Medikamente: Amlodipine, indapamide
Allergien: -
Vorherige Impfungen: -

VAERS 2130596

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: AZ
Alter: 23,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 05.02.2022
Beginn: 06.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / RA

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

Fatigue Lymph node pain Lymphadenopathy Vaccination site pain

Symptomtext

My lymph node in my right armpit has swelled immensely and is severely painful; My lymph node in my right armpit has swelled immensely and is severely painful; fatigue is moderate; the muscle of the injection site is moderately sore; This is a spontaneous report received from a contactable reporter. The reporter is the patient. A 23-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 05Feb2022 (Lot number: FJ6369) at the age of 23 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "COVID-19" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8735, Location of injection: Arm Right), administration date: 26Apr2021, when the patient was 23 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8733, Location of injection: Arm Right), administration date: 06Apr2021, when the patient was 23 years old, for COVID-19 Immunization. The following information was reported: LYMPHADENOPATHY (non-serious), LYMPH NODE PAIN (non-serious) all with onset 06Feb2022, outcome "recovering" and all described as "My lymph node in my right armpit has swelled immensely and is severely painful"; FATIGUE (non-serious) with onset 06Feb2022, outcome "recovering", described as "fatigue is moderate"; VACCINATION SITE PAIN (non-serious) with onset 06Feb2022, outcome "recovering", described as "the muscle of the injection site is moderately sore". Therapeutic measures were not taken as a result of lymphadenopathy, lymph node pain, fatigue, vaccination site pain. Additional information included a covid tested post vaccination was not performed and since the vaccination, the patient has been tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2130302

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: OH
Alter: 78,0
Geschlecht: M
Eingang: 22.02.2022
Impfdatum: 07.02.2022
Beginn: 14.02.2022
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered Laboratory test Malaise

Symptomtext

Patient received expired vaccine. DH and Pfizer recommended revaccination. Upon calling patient to reschedule, the patient stated he was ill post vaccination and was seen by his doctor. The doctor ran tests. The patient states he is fine now. He stated he was unsure if the reaction was caused by the vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2128483

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: WV
Alter: 70,0
Geschlecht: F
Eingang: 20.02.2022
Impfdatum: 14.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Contusion Erythema Pain Pain in extremity

Symptomtext

Patient received Pfizer booster on 2/14/2021. On 2/17/2021 she reported redness/pain of her left big toe. She believed it was related to getting the booster, especially after hearing from her sister about "COVID-19 toe." She said it was bruised in appearance and only hurt when she walked. The pain was mild. Patient is going to follow-up with her doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: None as of yet.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: -
Andere Medikamente: Unknown
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2128438

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: FL
Alter: 65,0
Geschlecht: F
Eingang: 20.02.2022
Impfdatum: 10.02.2022
Beginn: 12.02.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Periorbital swelling Pruritus Rash macular Swelling face Urticaria

Symptomtext

Pt presents to the Pharmacy with a swollen face, similar to allergic rxn. Eyes were puffy. spots and hives as well on skin on arms. Occurred roughly 2 days after receiving her Pfizer 1st dose vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: pt went to er got rx on 2/12 got rx for Pepcid 20 mg 1qd prednisone 20 mg 1 bid hydrocortisone cream 2.5% on 2/20 we gave here hydrocortisone 1 % otc bc pt said still itching
Aktuelle Erkrankungen: not known
Vorgeschichte: -
Andere Medikamente: oxycodone/apap klor con labeatol lipitor pregablin hctz hydralyzine elavil
Allergien: Aspin latex morphine nitroglygine
Vorherige Impfungen: -

VAERS 2079315

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: TX
Alter: -
Geschlecht: U
Eingang: 19.02.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Blood glucose increased Nasopharyngitis Blood glucose Eye pain Hyperglycaemia Rhinorrhoea

Symptomtext

high blood sugars are 600 for a week; cold like symptoms; runny nose; my eyes are stinging; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program. The reporter is the patient. A patient (no qualifiers provided) received bnt162b2 (BNT162B2) (Batch/Lot number: unknown) as dose number unknown (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Dose number unknown, Manufacturer unknown), for Covid-19 immunization. The following information was reported: HYPERGLYCAEMIA (medically significant), outcome "unknown", described as "high blood sugars are 600 for a week"; NASOPHARYNGITIS (non-serious), outcome "unknown", described as "cold like symptoms"; RHINORRHOEA (non-serious), outcome "unknown", described as "runny nose"; EYE PAIN (non-serious), outcome "unknown", described as "my eyes are stinging". The patient underwent the following laboratory tests and procedures: blood glucose: 600, notes: high blood sugars are 600 for a week. The clinical course of events was as follows: Patient got the booster Pfizer on the 23rd (month and year not indicated) and had high blood sugars are 600 for a week, patient had also since then had cold like symptoms caused a runny nose, eyes were stinging since the 23rd. Patient still was having all these symptoms. The lot number for bnt162b2 was not provided and will be requested during follo up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: Test Name: blood sugars; Result Unstructured Data: Test Result:600; Comments: high blood sugars are 600 for a week
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123964

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: FL
Alter: 19,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 21.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Headache Rash Vision blurred

Symptomtext

Blurred vision in right eye, headaches, and rash after injection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Head cold once or twice before the first shot.
Vorgeschichte: No.
Andere Medikamente: No.
Allergien: Not that patient know of.
Vorherige Impfungen: -

VAERS 2123665

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 40,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 28.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Lymph node pain Lymphadenitis Lymphadenopathy

Symptomtext

Significant swelling and pain in left armpit and breast lymph nodes after Pfizer full dose booster. The doctor recommended heat packing area, ibuprofen for inflammation, Tylenol for pain, and antihistamines. Swelling in the left armpit went down over two weeks, but still, some swelling in the lower outside of the left breast now at three weeks continues. The swollen area becomes painful with exercise.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Under the watch of a Rheumatologist for Autoimmune issues.
Andere Medikamente: Vitamin D 2,000MG
Allergien: -
Vorherige Impfungen: -

VAERS 2123296

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NH
Alter: 7,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Incorrect dose administered No adverse event Pain in extremity Pyrexia

Symptomtext

7-year-old pediatric male patient received full dose of Pfizer .3mL instead of receiving the pediatric dose .2mL. Patient's mother informed immediately. Patient observed for 30 minutes after vaccination with no adverse reactions. The following day, patient saw pediatrician for follow-up. Patient had a low-grade fever despite taking Motrin. His arm was very sore, but no swelling. Pediatrician instructed mother to monitor son and watch for any signs of reaction or myocarditis. Patient's mother will be contacted again in 4 days to follow-up on son's well-being.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: -
Allergien: No
Vorherige Impfungen: -

VAERS 2121117

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NM
Alter: 66,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 16.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SC / LA

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

Bone pain Dysstasia Heart rate irregular Pelvic pain Spinal pain

Symptomtext

I awoke with extreme bone pain pain in the marrow of the bones all long bones entire pelvis and spine?.. My heart rate would go up and down the bone pain was unbearable I was actually screaming for a couple of hours until my husband got a hold of my pulmonologist who had me take prednisone 40 mg I have been a registered nurse for 46 years and extremely aware of my body and of the human body After my second Pfizer shot which was on 4/22/2021 I had bone pain and have continued to have bone pain in my pelvis and difficulty at some time standing I am physically very fit I work 40+ hours a week and I?m not a crybaby?. The pain was excruciating reminded me of when I worked and took care of sickle cell anemia patients it was the same type of pain that those people were described to me over and over again

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bone pain
Hospital-Tage: -
Labordaten: The soonest I can get into see my pulmonologist is Monday which is 21st of February?.. The pain is so severe I had to me calling in sick to work tomorrow leaving the other nurses short staffed
Aktuelle Erkrankungen: None
Vorgeschichte: Pulmonary hypertension Asthma
Andere Medikamente: Adderall 30 mg Amlodpine 10 mg Propanolol 20 mg Losartan 100 mg Ativan PRN Estradiol 0.1 mg/day
Allergien: NKA
Vorherige Impfungen: -

VAERS 2119174

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: OH
Alter: 12,0
Geschlecht: M
Eingang: 17.02.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Hypersensitivity Pruritus

Symptomtext

Called to room by patients father approximately 22 minutes after vaccine was given dad reported patient may be having an allergic reaction, he's c/o itching on neck and arms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Vital signs obtained98.1, 106/60, 98%, pulse 100, patient was alert and able to describe the itching on neck and arms and Dr. notified and came to evaluate patient, 10mg of cetrizine given per doctors order and patient waited an additional 15 minutes and stated he felt somewhat better.
Aktuelle Erkrankungen: None.
Vorgeschichte: ADHD; insomnia; Anorexia.
Andere Medikamente: Methylphenidate; Clonidine; Intuniv; Melatonin; Concerta; Ritalin.
Allergien: Amoxicillin.
Vorherige Impfungen: -

VAERS 2119115

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NY
Alter: 33,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 11.02.2022
Beginn: 12.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Abdominal pain Arthralgia Asthenia Diplopia Dizziness Eating disorder Gait disturbance Headache Helplessness Injection site pain Loss of personal independence in daily activities Malaise Musculoskeletal stiffness Nausea Pain Sleep disorder

Symptomtext

1. Stabbing abdominal pain lasting 60 hours (2.5 days). It started about 13 hours after vaccine administration at 2 am 12 Feb 2022. The pain woke me up. Nausea is still present today but is intermittent. It became intermittent on 16th February. 2. Double vision, headaches and dizziness. Double vision and headaches lasted 24 hrs. Lasting dizziness stayed until 16 February. It became came intermittent since then. 12 February symptoms were the worst. I was unable to walk straight, move more that 5 steps with out needing to sit/laydown. I felt completely helpless and sick. In addition to the above symptoms there were body aches that were 8/10 in severity and neck stiffness. I also experiences the normal injection site pain at 6hrs post vaccination administration and mild headache. 17 February (today) I experienced onset of joint pain in knees that was aching (new symptom ). I still have mild body aches and mild intermittent dizziness. I was unable to complete daily life activities from 12 February until 17 February. The symptoms were debilitating. The worst one was the abdominal pain, which felt like knives were going into my stomach for close to 3 days. It was hard to eat with that pain. OTC pain medication did not help it. Current symptoms as of 17 February 2022 are; Intermittent nausea & dizziness, body aches and joint pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: Was told to rest at home. I will follow up with medical professional.
Aktuelle Erkrankungen: No acute illness.
Vorgeschichte: Rheumatoid arthritis w/chronic pain, neuropathy in feet, & finger joint deformity, History of mTBI w/change in memory lead to acquired ADHD, C-PTSD, Asthma, cervical and lumbar radiculopathy w/decreased sensation of left lower extremity L4-L5 dermatome distribution, Migraines, Supraventricular Tachycardia (SVT), Thalassemia Minor Beta Trait (shows in blood work) - asymptomatic iron deficiency anemia (not treatabe with iron supplements), Cachexic appearance (asymptomatic) /low BMI 16.6-17.
Andere Medikamente: Medications were held at the time of vaccination to prevent interactions or AEs.
Allergien: Sulfa antibiotics, Sulfate medications, Sulfur medications, mushrooms, lemongrass.
Vorherige Impfungen: Flu Vaccine

VAERS 2113893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 47,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 04.02.2022
Beginn: 04.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness

Symptomtext

Vaccinated: 17:30; Reaction: 17:47; Pt reported that she felt dizzy. Vitals: 161/100, 98, 18, 100% -- > 144/87, 87, 20, 100%. Pt stable and released from the vaccination site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: Obesity; GERD; Migraines.
Andere Medikamente: Famotidine; Omeprazole; Ketoconazole; Premarin.
Allergien: Allergies: Morphine (rash), seafood (rash).
Vorherige Impfungen: -

VAERS 2113030

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: IN
Alter: 17,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 18.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Discomfort Inflammation Injection site reaction Pain X-ray limb

Symptomtext

Patient experienced pain in her left shoulder on January 21 (3 days after her shot). It was just an annoying uncomfortable feeling at first, but then quickly became severe (within 4 additional days). She began physical therapy (not knowing the cause) a week after the pain occurred. Physical therapy seemed to intensify the pain. She was then told by her PT to get an x-ray to see if something else is wrong. At that time, the PT asked about having an injection recently. We then took patient to the ortho specialist on February 14 where he confirmed that the pain she is experiencing must have been a reaction to the administration of the injection. She was given a steroid pack to see if that would help the inflammation that occurred from the shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: x-ray taken on Feb 7.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: sertraline 50 mg tablet
Allergien: none
Vorherige Impfungen: -

VAERS 2110373

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj6369

mild

Staat: OH
Alter: 58,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 14.02.2022
Beginn: 14.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Pruritus Rash Rash erythematous Urticaria

Symptomtext

Approximately 20 minutes after dose was given, patient started complaining of red rash and hives on chest as well as itchy. Patient given 60 mg of Claritin. Patient observed for additional 15 minutes without any other complaints.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/a
Vorgeschichte: Hx of DVT/PE
Andere Medikamente: Cetirizine, Warfarin, Tylenol
Allergien: Cat scan Iodine and latex
Vorherige Impfungen: -

VAERS 2110349

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: MO
Alter: 52,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 08.02.2022
Beginn: 08.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Chills Headache Pyrexia

Symptomtext

Fever, headache, and chills.

Weitere VAERSDATA-Felder

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

VAERS 2109934

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: OK
Alter: 37,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 09.02.2022
Beginn: 09.02.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Erythema Feeling hot Hyperhidrosis Immediate post-injection reaction Pruritus Vaccine positive rechallenge

Symptomtext

Patient immediately felt "itchy" and warm after injection, we had her sitting in a chair and she expressed feeling warm and showed us redness in her upper chest area. Patient wanted to scratch her chest and neck area from the feeling, she stated it was very warm in the room and didn't like the sweating. She was given two Diphenhydramine HCL 25 mg capsules, and water. She used a wet paper towel to cool her neck and face she sat in chair until 2:15 pm then left on her own.

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Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: her vitals were taken, 135/85 in left arm, T 98.4 F, P 88, R 24 on 2/9/22 at 2:00pm.
Aktuelle Erkrankungen: none
Vorgeschichte: systemic scleroderma, rheumatoid arthritis, glasses x 30 years
Andere Medikamente: Merina IUD, Dicyclomine, omeprazole, methotrexate, folic acid, respi-quick inhaler
Allergien: none
Vorherige Impfungen: same type of episodes with previous Pfizer injections

VAERS 2109923

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NC
Alter: 27,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 08.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Axillary pain Limb discomfort Lymphadenopathy Musculoskeletal discomfort Pain Pain in extremity

Symptomtext

Sharp pain in armpit with lymph node swelling for the first 2-3 days (2/9/22 through 2/12/22) following Pfizer COVID 3rd dose on 2/8/22, with onset of severe ache in left shoulder that began around 2/12/22 with radiating 8/10 pain down left arm that does not seem to be eased with OTC anti-inflammatory medications. Comfort not found with positioning of arm/shoulder nor heat/cold compresses.

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: I, the patient, have not yet sought out medical assistance. No tests performed to date.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, otherwise none.
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2109753

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj6369

mild

Staat: AZ
Alter: 51,0
Geschlecht: M
Eingang: 14.02.2022
Impfdatum: 17.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Dizziness Injection site swelling Peripheral swelling

Symptomtext

Site: Swelling at Injection Site-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: severe swelling of right arm and hand-Severe

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

VAERS 2109396

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: MI
Alter: 70,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 21.01.2022
Beginn: 22.01.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Chills Decreased appetite Diarrhoea Fatigue Headache Hepatic enzyme Myalgia Nausea Vomiting

Symptomtext

Chills, nausea, vomiting, diarrhea, headache, muscle aches, fatigue, loss of appetite for approx 36 hrs.

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Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Hepatic screen drawn on 1/24/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Autoimmune hepatitis, GERD
Andere Medikamente: Prednisone, Prilosec, Lipitor, Azathioprine, LoDose ASA. Melatonin
Allergien: Toradol, Tolectin
Vorherige Impfungen: 01/16/2021, 02/06/2021, 08/14/2021

VAERS 2108953

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: -
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: -
Beginn: 05.01.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

COVID-19 Chills Drug ineffective Fatigue Headache Interchange of vaccine products Myalgia Off label use Pain in extremity SARS-CoV-2 test

Symptomtext

Off label use; Dose_number=3, brand=Pfizer, prev_dose_brand=Moderna; Chills; Headache; Muscle pain; Arm pain; Fatigue; Covid test result=Positive; Covid test result=Positive; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 47 year-old female patient received bnt162b2 (BNT162B2) (Lot number: FJ6369) as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. It was reported that prior to vaccination the patient was not diagnosed with COVID-19. Vaccination history included: Moderna (Dose Number: 1, Batch/Lot No: 038A21A), for COVID-19 immunization; Moderna (Dose Number: 2, Batch/Lot No: 037B21A), for COVID-19 immunization. The following information was reported: OFF LABEL USE (medically significant), outcome "unknown", described as "Off label use"; INTERCHANGE OF VACCINE PRODUCTS (medically significant), outcome "unknown", described as "Dose_number=3, brand=Pfizer, prev_dose_brand=Moderna"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 05Jan2022, outcome "unknown" and all described as "Covid test result=Positive"; CHILLS (non-serious), outcome "unknown", described as "Chills"; HEADACHE (non-serious), outcome "unknown", described as "Headache"; MYALGIA (non-serious), outcome "unknown", described as "Muscle pain"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "Arm pain"; FATIGUE (non-serious), outcome "unknown", described as "Fatigue". The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (05Jan2022) positive. It was reported that patient has been tested for COVID-19 since the vaccination. Clinical course: It was reported that seriousness criteria was not resulted in death, life threatening, caused/prolonged hospitalization, disabling/incapacitating and congenital anomaly/birth defect. Device date was provided as 26Jan2022. No follow-up attempts are possible. No further information is expected.

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Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20220105; Test Name: Nasal Swab; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2108885

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NC
Alter: 68,0
Geschlecht: M
Eingang: 12.02.2022
Impfdatum: 11.02.2022
Beginn: 11.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Feeling cold Nausea

Symptomtext

Feeling extremely cold, shivering, fever of 99.3, feeling nauseas time 11:30 p.m. Fever of 99.9 at 12:15 a.m.. One tablet Tylenol, 500 mg at 12:20 a.m. Temperature at 1:45a.m. 98.4

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Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: High blood pressure, AFib,, Thyroid ,clogged arteries
Andere Medikamente: Aspirin, Famotidine, Amiodarone
Allergien: -
Vorherige Impfungen: -

VAERS 2108826

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: -
Alter: 64,0
Geschlecht: M
Eingang: 12.02.2022
Impfdatum: 20.01.2022
Beginn: 01.01.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Axillary pain Lymphadenopathy

Symptomtext

again experiencing swelling in his armpits, however "not as bad" and glands are not currently painful this time; again experiencing swelling in his armpits, however "not as bad" and glands are not currently painful this time; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 64 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 20Jan2022 (Lot number: FJ6369) at the age of 64 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Diabetic", start date: 1994 (ongoing), notes: Verbatim: Diabetic; "immune deficient" (unspecified if ongoing), notes: Caller states he is diabetic, immune deficient. There were no concomitant medications. Vaccination history included: Bnt162b2 (First shot was on 17Mar2021. He didn't experience the swelling so much. Lot number: ER2613.), administration date: 17Mar2021, for COVID-19 Immunization, reaction(s): "First shot was on 17Mar2021. He didn't experience the swelling so much"; Bnt162b2 (He got the second one on 07Apr2021. Lot number looks like EB8729), administration date: 07Apr2021, for COVID-19 Immunization, reaction(s): "experienced painful swollen glands in his neck and armpits that resolved after 3-4 months", "swollen glands in arm and neck". The following information was reported: LYMPHADENOPATHY (non-serious) with onset Jan2022, outcome "unknown", AXILLARY PAIN (non-serious), outcome "unknown" and all described as "again experiencing swelling in his armpits, however "not as bad" and glands are not currently painful this time".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Diabetic (Verbatim: Diabetic)
Vorgeschichte: Medical History/Concurrent Conditions: Immune imbalance (Caller states he is diabetic, immune deficient.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2108792

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: NY
Alter: 53,0
Geschlecht: M
Eingang: 12.02.2022
Impfdatum: 18.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / RA

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

Arthralgia Body temperature Chills Pyrexia Vaccination site pain

Symptomtext

Fever; Chills; Arm was sore at site of the shot; Joint pain/joint aches; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). Other Case identifier(s): US-PFIZER INC-202200112656 (Pfizer). A 53 year-old male patient received bnt162b2 (COMIRNATY), administered in deltoid right, administration date 18Jan2022 (Lot number: FJ6369) at the age of 53 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Hypertension" (ongoing). The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose 1, single, Lot number: EP6955, Expiry date: 30Jun2021, Anatomical location: right deltoid), administration date: 19Mar2021, when the patient was 52 years old, for COVID-19 immunization; Bnt162b2 (Dose 2, single, Lot number: EP6955, Expiry date 30Jun2021, Anatomical location: right deltoid), administration date: 07Apr2021, when the patient was 52 years old, for COVID-19 immunization. The following information was reported: PYREXIA (non-serious) with onset 19Jan2022, outcome "recovered" (Jan2022), described as "Fever"; CHILLS (non-serious) with onset 19Jan2022, outcome "recovered" (Jan2022), described as "Chills"; VACCINATION SITE PAIN (non-serious) with onset 19Jan2022, outcome "recovered" (Jan2022), described as "Arm was sore at site of the shot"; ARTHRALGIA (non-serious) with onset 19Jan2022, outcome "not recovered", described as "Joint pain/joint aches". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The concomitant medication included unspecified hypertension medication. Caller clarified the typical reaction to be last evening her husband started to have a fever, the highest was 102.3, chills, joint aches, arm was sore at site of the shot. Caller confirmed all these events have resolved, but he still had joint pain; no additional details provided. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Date: 20220119; Test Name: Body temperature; Result Unstructured Data: Test Result:102.3; Comments: highest was 102.3
Aktuelle Erkrankungen: Hypertension
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2108767

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: -
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: -
Beginn: 16.01.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Axillary pain Pain Pain in extremity Peripheral swelling

Symptomtext

armpits start hurting; body ache; swollen right arm and it is tender; I do not know if it is my lymph node; swollen right arm and it is tender; I do not know if it is my lymph node; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 34 year-old female patient received bnt162b2 (BNT162B2), administered in arm left (Lot number: FJ6369) as dose 3 (booster) , single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (1ST DOSE, Lot number: EW0176 (first shot).), for covid-19 immunization; Bnt162b2 (2ND DOSE), for Covid-19 Immunization. The following information was reported: AXILLARY PAIN (non-serious) with onset 16Jan2022, outcome "unknown", described as "armpits start hurting"; PAIN (non-serious) with onset 16Jan2022, outcome "unknown", described as "body ache"; PERIPHERAL SWELLING (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 16Jan2022, outcome "unknown" and all described as "swollen right arm and it is tender; I do not know if it is my lymph node". Therapeutic measures were taken as a result of axillary pain, pain, peripheral swelling, pain in extremity. Additional information: Drug Code number, Product Code number and expiry date of COVID-19 vaccine was unknown. No any other product. Patient had no history. She got the booster pfizer shot on Saturday morning (not clarified further hence, not captured in tab) morning. She felt fine and then the next day Sunday, she felt okay, she did not had you know not a lot of body ache but last night she mean yeah, last night Sunday she noticed, actually afternoon, she noticed that her armpits start hurting. she looked at it and it is swollen right arm and it is tender. So, she was thinking, she don't know if it is her lymph nodes. So, she want to know if that is like a side effect of that but it is like it is tender and then it is swollen. She dont know lot number of second shot. No nay other medical conditions. Lab tests reported as no. The birth control reported as no. Treatment received for event she just took Ibuprofen and Tylenol. Sunday she took 650 milligrams twice and then Ibuprofen she did not take Ibuprofen until like Monday morning or night, fell like it, sick, really swollen arm, Ibuprofen 600 milligrams. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
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 2105494

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ6369

mild

Staat: CA
Alter: 51,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 25.01.2022
Beginn: 25.01.2022
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 Blood creatinine Blood electrolytes Blood urea Bundle branch block Cardiac monitoring abnormal Dizziness Ear discomfort Electrocardiogram Fatigue Feeding disorder Feeling abnormal Full blood count Headache Heart rate irregular Myalgia Nausea Paranasal sinus discomfort

Symptomtext

about 3 hours after vaccine felt foggy and fuzzy-headed, started with headache, then by the end of the day had severe muscle body aches all over, each day after vaccine above symptoms got worse and additionally had sinus pressure, ear pressure, severe heachache, feeling abnormally tired, abdominal cramps and nausea, was unable to eat and then started to feel my heart beat irregulary (3 days after vaccine), tried to alleviate body aches with ibuprofen and Tylenol, but neither touched the pain, on day 4 all listed symptoms were still present, especially my heart rate felt more irregular and it was "beating in my throat", I felt light headed and "off", I went to a colleague who attached a heart monitor to my chest and saw the irregularity of my heart (very frequent PAC's, PVC's and every now and then a bundle branch block), my BP was borderline low, too, I checked myself into the ER and Dr. checked me through

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: In the ER: EKG Vital signs including orthostatic BPs Lab work (electrolytes, CBC dif, troponin, thyroid, BUN, Creat, etc) IV was started to my L forearm just in case
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -