VAERS Reports EW0179

VAERS 2682055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: FL
Alter: 44,0
Geschlecht: F
Eingang: 14.09.2023
Impfdatum: 19.06.2021
Beginn: 27.06.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: SYR / LA

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

Angiogram pulmonary abnormal Fibrin D dimer Pulmonary embolism

Symptomtext

Blood clot in lower right lobe resulting in acute pulmonary embolism

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 1,0
Labordaten: CT A, D-Dimer. Etc.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2679575

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: TX
Alter: 67,0
Geschlecht: M
Eingang: 06.09.2023
Impfdatum: 15.06.2021
Beginn: 26.01.2022
Tage bis Beginn: 225,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 Chest X-ray normal

Symptomtext

Presented with Acute hypoxemic respiratory failure secondary to COVID-19 /possible viral sepsis Tx with remdesivir, decadron, antibiotics, lovenox, singulairzinc; Chest x-ray no evidence of pneumonia. On room air at D/C

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2641621

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: FL
Alter: 74,0
Geschlecht: M
Eingang: 06.06.2023
Impfdatum: 22.04.2021
Beginn: 29.08.2022
Tage bis Beginn: 494,0
Dosis: 2
Route/Site: - / -

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

Angiogram pulmonary abnormal COVID-19 Chest pain Coronary artery disease Dyspnoea Laboratory test normal Peripheral artery stenosis Pulmonary embolism Pulmonary mass SARS-CoV-2 test positive Scan with contrast abnormal Vaccine breakthrough infection

Symptomtext

BREAKTHROUGH COVID: FULLY VACCINATED WITH BOOSTER, COVID POSITIVE. PATIENT WAS ADMITTED D/T COVID+ PT C/O CHEST PAIN AND SHORTNESS OF BREATH, AND PRE PROCEDURE TEST WORK UP WAS NEGATIVE FOR ACUTE PROCESS. PAXLOVID FOR OUTPATIENT TREATMENT FOR HIGH RISK COVID PERSON.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: CT Angio Chest Pulmonary Embolism W IV ContrastNo evidence of pulmonary embolus. 2. Stable right upper lobe thin-walled cavitary nodule. 3. Coronary artery disease. 4. No evidence of acute chest pathology. 5. Severe stenosis of greater than 70% in the right upper brachial artery.
Aktuelle Erkrankungen: UNKNONWN
Vorgeschichte: Chronic hepatitis, Coronary artery disease involving native heart,DM2 (diabetes mellitus, type 2), Iron deficiency Obstructive sleep apnea syndrome,
Andere Medikamente: UNKNOWN
Allergien: Cyclobenzaprine
Vorherige Impfungen: -

VAERS 2634792

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: -
Alter: 63,0
Geschlecht: M
Eingang: 22.05.2023
Impfdatum: 02.02.2022
Beginn: 29.03.2022
Tage bis Beginn: 55,0
Dosis: 3
Route/Site: - / -

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

Acute myocardial infarction

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE NON ST ELEVATION MI ACUTE MI

Weitere VAERSDATA-Felder

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

VAERS 2628413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 08.05.2023
Impfdatum: 29.11.2021
Beginn: 21.12.2021
Tage bis Beginn: 22,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Angina unstable Cerebral artery occlusion Cerebrovascular accident

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE UNSTABLE ANGINA ACUTE STROKE DUE TO OCCLUSION OF LEFT MIDDLE CEREBRAL ARTERY ACUTE RESPIRATORY FAILURE

Weitere VAERSDATA-Felder

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

VAERS 2626574

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: -
Alter: 49,0
Geschlecht: M
Eingang: 04.05.2023
Impfdatum: 08.06.2022
Beginn: 19.06.2022
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / LA

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

Acute myocardial infarction Coronary artery disease Symptom recurrence

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE ST ELEVATION MI, LEFT ANTERIOR DESCENDING CORONARY ARTERY ACUTE ST ELEVATION MI, ANTERIOR WALL ACUTE ST ELEVATION MI, UNSPECIFIED 6/20/2022 -- RECURRENCE OF SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2623276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: -
Alter: 58,0
Geschlecht: M
Eingang: 28.04.2023
Impfdatum: 14.12.2021
Beginn: 12.07.2022
Tage bis Beginn: 210,0
Dosis: 3
Route/Site: IM / LA

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

Acute myocardial infarction

Symptomtext

ACUTE ST ELEVATION MI, INFEROLATERAL WALL ACUTE ST ELEVATION MI, UNSPECIFIED

Weitere VAERSDATA-Felder

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

VAERS 2573206

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 01.02.2023
Impfdatum: 04.05.2021
Beginn: 10.12.2022
Tage bis Beginn: 585,0
Dosis: 2
Route/Site: - / -

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

Actinomyces test positive Acute respiratory failure Anaemia Blood culture positive Bone marrow disorder COVID-19 pneumonia Coagulation test normal Debridement Deep vein thrombosis Endotracheal intubation Fournier's gangrene Heparin-induced thrombocytopenia test Hyperglycaemic hyperosmolar nonketotic syndrome Infection Intensive care Mechanical ventilation Necrotising soft tissue infection Sepsis

Symptomtext

This is a 61 yo female with pmh dm2 presented to the hospital 12/10/22 and was admitted to the ICU with necrotizing fasciitis of the labia and groin, HHS, sepsis and acute respiratory failure. She was treated with ivf and iv insulin. She has required 4 operations for debridement of necrotizing infection thus far. She has been treated for covid-19 pneumonia and has completed remdesvir and dexamethasone. She required mechanical ventilation and has been extubated. Hospital course complicated by acute bilateral upper and lower DVT, hematology consulted due to concern for HIT/DIC and further evaluation. Negative HIT/DIC workup. Negative inpatient hypercoagulability workup. Anemia is most probably reactive/hypoproliferative bone marrow response with acute significant infection inflammation. Negative hemolysis, negative iron deficiency. ID on board and recommend for MRSA, B frag, continue vancomycin through tomorrow, meropenem through 1/31/23. Continue empiric fluconazole. Actinomyces on blood culture. Continue wound care. Patient accepted to go to LTAC. We will discharge in stable condition. Continue with meropenem until January 31.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 24,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2556283

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: -
Alter: 57,0
Geschlecht: M
Eingang: 10.01.2023
Impfdatum: 18.05.2021
Beginn: 23.12.2022
Tage bis Beginn: 584,0
Dosis: 2
Route/Site: - / -

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

Acute respiratory failure Angiogram pulmonary abnormal COVID-19 Cardiac failure Cardiac failure acute Cardiac failure congestive Chest X-ray abnormal Chest pain Condition aggravated Coronary artery bypass Coronary artery disease Cox-Maze procedure Diuretic therapy Dyspnoea Echocardiogram abnormal Ejection fraction decreased Glycosylated haemoglobin increased Hypoxia

Symptomtext

Clinical Summary Patient is a 58 y.o. male with a history of CAD with multiple PCIs, recent hospitalization at hospital 12/7/22-12/17/22 for multivessel CAD s/p CABG with Dr. 12/9/22, IDDM2 who presented to hospital 12/23/22 with sudden onset shortness of breath, episode of chest pain and hypoxia. Found to have suspected CHF exacerbation with CXR showing pulmonary edema and NT Pro BNP up to 5,579 in the ED and subsequently found to have COVID. 1. Acute hypoxic respiratory failure: Hypoxia noted by medics, briefly required BiPAP in ED transitioned back to O2 by NC therafter. Suspected due to pulmonary edema. CTPA - neg for PE. Covid-19 + on 12/23/22. Treatment as below for pulm edema. Resolved and on RA. 2. Covid - 19: Tested + on 12/23/22 same day as Symptoms onset. Given hypoxemia and presentation, Case discussed with Dr. and Dr. (on Call ID) and pt started on IV Remdezivir x 5 days which ended on 12/28/22. Symptoms resolved. 3. Acute on chronic HFrEF with acute pulmonary edema/pleural effusion: CXR noted interstitial edema in ED. NT Pro BNP 5,579 (increased from 2,775 two weeks prior). Preop EF 35-40%, repeat TTE done 12/23/22 in ED noted slightly improved EF of 46% with regional WMA consistent with ischemic cardiomyopathy. No pericardial effusion. Left pleural effusion noted on TTE and CXR and CTPA on admission. IV diuresis initiated and switched to lasix oral as an outpatient per recs with BID for 3 days with daily after for a week. 4. Acute chest pain: Episode occurred en route to hospital at rest and self-abated. Troponin elevated as below but down significantly from recent admission. EKG in ED without acute ischemic changes. CTPA neg. CTS followed 5. CAD with recent CABG: CABG x4 12/9/22 with Dr. (CTS). Continued home aspirin, statin, BB and amiodarone. CTS followed 6. Paroxysmal atrial fibrillation: Occurred in the setting of CAD/CABG. S/p LA maze and clipping of left atrial appendage 12/9/22. Home BB continued. Not on AC. Rate controlled. 7. IDDM2: Last A1c - 9.1% BG 142 on admission. Home meds include Levemir + Lispro + Metformin. Will need to follow with pcp for glucose control.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2518860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0179

kritisch

Staat: CO
Alter: 75,0
Geschlecht: F
Eingang: 29.11.2022
Impfdatum: 11.06.2021
Beginn: 25.11.2022
Tage bis Beginn: 532,0
Dosis: 1
Route/Site: IM / RA

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

Acute respiratory failure Anticoagulant therapy Blood culture Blood magnesium Blood phosphorus COVID-19 Chest X-ray Coagulation test Dialysis Diarrhoea Dyspnoea Full blood count Illness Influenza like illness Insulin therapy Metabolic function test Nausea Respiratory disorder

Symptomtext

This 76 year-old female presented to the Emergency Department complaining of flu-like symptoms that had persisted for several days. Recently, this was accompanied by nausea, vomiting, diarrhea, and difficulty breathing with increasing supplemental oxygen requirements. Relevant medical history included chronic obstructive pulmonary disease and type 2 diabetes associated with end-stage kidney disease requiring chronic hemodialysis. Because of the acute respiratory illness, she had been unable to attend her last two scheduled dialysis sessions. She tested PCR positive for SARS-CoV-2. Accordingly, her admitting diagnosis was acute hypoxemic respiratory failure associated with COVID-19 infection. She was initiated on treatment with IV dexamethasone and remdesivir along with heparin thromboprophylaxis, adjusted insulin therapy, and daily dialysis targeting 2 L of fluid removal. Clinical improvement ensued and she is medically stable with follow-up healthcare plans in place including discharge to her home and rearrangements for chronic hemodialysis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: Comprehensive Metabolic Panel Complete Blood Count Magnesium Phosphorus Urinalysis Routine Coagulation Respiratory Virus Panel Blood Culture Chest X-ray
Aktuelle Erkrankungen: -
Vorgeschichte: Congestive heart failure Kidney failure Right total knee arthroplasty Gastroesophageal reflux Diabetic retinopathy
Andere Medikamente: Albuterol Tiotropium Levothyroxine
Allergien: Linagliptin Sitagliptin Penicillin Sertraline Nephro-vite Atorvastatin Amlodipine Aspirin Sevelamer Insulin glargine
Vorherige Impfungen: -

VAERS 2512421

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: -
Alter: 64,0
Geschlecht: M
Eingang: 19.11.2022
Impfdatum: 14.05.2021
Beginn: 27.10.2022
Tage bis Beginn: 531,0
Dosis: 2
Route/Site: IM / LA

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

Blood culture negative Blood glucose normal Bradycardia COVID-19 Cardiac failure congestive Chest X-ray abnormal Chronic obstructive pulmonary disease Computerised tomogram head normal Computerised tomogram thorax abnormal Condition aggravated Confusional state Death Delirium Echocardiogram Ejection fraction Endotracheal intubation Glycosylated haemoglobin increased Haemophilus test positive

Symptomtext

Patient is a 65 y.o. male patient of local MD with history of COPD with chronic hypoxic respiratory failure (on 3-4L NC), DM2, chronic venous stasis with chronic BLE wounds, OSA noncompliant with CPAP who presents with AMS and hypoxia, COVID positive Acute on chronic hypoxic hypercapneic respiratory failure COVID-19 Acute COPD exacerbation H/O left upper lobectomy Found to be confused at his PCP office, hypoxic on RA (wasn't wearing his baseline O2 of 4L), bradycardic to 30s, and hypotensive to 70s. Semi-emergently intubated in ER due to worsening responsiveness. Pulmonology consult appreciated Intubated Completed 10 day course of IV Decadron Hold IV Lasix due to hypotension DuoNebs VAP Chest x-ray-retrocardiac consolidations noted, sputum cultures MSSA and haemophilus influenza MRSA probe is positive, blood cultures negative Due to worsening hypoxia, antibiotics broadened to vancomycin and ceftriaxone on 11/4 Sputum culture positive for MRSA and Haemophilus Influenzae MRSA DNA probe positive Abx stopped on 11/09/22 due to palliative extubation and changing to DNRCC Blood cultures negative Pulmonary consulted. Bilateral chronic venous stasis Noted right lower extremity purplish discoloration and cold Bilateral ABI-mild peripheral artery disease noted Monitor Shock Unlikely Cardiogenic as per Cardio ECHO- preserved LVEF, with right ventricular systolic dysfunction CTPE- no p.e, probable Pulmonary HTN Likely due to hypovolemia and sedatives Initially required pressors but weaned off Hypotension on 11/8/22 and not responsive to fluid boluses Family wanted to hold off on additional IVF boluses and/or pressor Covid-19 Virus Infection Date of onset of symptoms: 10/25/22 Symptoms present on admission: lethargy Date of covid positive test: 10/27/22 Vaccination status: unvaccinated (according to brother POA) Imaging: CXR with left whiteout, CHF Oxygen requirements on admission: up to 15L NRB, intubated 10/27/22 Medical therapy: Finished course of steroids. CRP <75 Consultants following: pulm critical care Anticipated special isolation end date: TBD Metabolic Encephalopathy Delirium Due to polypharmacy, recent start of Marijuana, on Flexeril and Gabapentin CT head on admission- normal On delirium protocol, up titrated Seroquel to 25 mg 3 times daily T2DM Home RX: lantus 20 units at bedtime, SSI. Recent A1C 7.8% in June 2022. On decreased dose of lantus to 10 units given relative normoglycemia, continue SSI Blood sugar stable Nutrition Received TF Add free water 300 every 6 hours Bowel regimen Goals of Care Palliative Care consulted. Palliative extubated on 11/09/22 and pronounced deceased at 1310 DNRCC

Weitere VAERSDATA-Felder

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

VAERS 2489933

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: TX
Alter: 62,0
Geschlecht: M
Eingang: 26.10.2022
Impfdatum: 10.02.2022
Beginn: 21.10.2022
Tage bis Beginn: 253,0
Dosis: 2
Route/Site: IM / AR

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

Atelectasis Blood creatinine Brain natriuretic peptide increased COVID-19 Computerised tomogram abdomen Computerised tomogram thorax abnormal Cough Death Dyspnoea Haematocrit Haemoglobin Lung consolidation Pleural effusion SARS-CoV-2 test positive Tachycardia Troponin normal White blood cell count

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization/Death. Rec'd Pfizer BioNTech vaccine on 9/8/2021, 5/18/2021 and 2/10/2022. Presented to ED with c/o SOB and coughing. Pt was dx'ed w/covid-19 and admitted. Upon admission pt was tachycardic in 130s, sats 96% on 4L O2.BNP elevated 1700+, trops neg, creatinine, h/h, and wbc near baseline. CT ab pelv and chest: findings included large bilateral lower lung consolidations, atelectasis and small pleural effusions. Pt continued to decline despite treatment. Transitioned to comfort care and changed to DNAR/AND. Admitted to inpatient hospice service, expired 10/21/22. Tx'd w/decadron and rifaximin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 3,0
Labordaten: Covid-19 + 10/19/22 - This sample was analyzed using the Roche LIAT SARS assay platform using PCR or equivalent Nucleic Acid Amplification(NAA)technology.
Aktuelle Erkrankungen: -
Vorgeschichte: EtOH cirrhosis, diastolic CHF, CKD4, obesity, anemia, BPH, Cancer, DM, HLD, CAD, HTN, Hypothyroidism, Cancer
Andere Medikamente: cephalexin, albuterol sulfate, calcium citrate/vitamin D3,
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2436402

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: KY
Alter: 56,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 03.06.2021
Beginn: 19.01.2022
Tage bis Beginn: 230,0
Dosis: 2
Route/Site: IM / LA

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

Death Vaccine breakthrough infection

Symptomtext

Patient had a breakthrough infection and expired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Positive COVID test on 1/25/2022.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2431224

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: TX
Alter: 83,0
Geschlecht: M
Eingang: 07.09.2022
Impfdatum: 31.08.2021
Beginn: 31.08.2022
Tage bis Beginn: 365,0
Dosis: 1
Route/Site: IM / RA

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

Asthenia Atrial fibrillation COVID-19 Chest X-ray abnormal Death General physical health deterioration Hypotension Intensive care Pneumonia Respiratory failure SARS-CoV-2 test positive Tremor White blood cell count increased

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization/Death. Rec'd Pfizer-BioNTech on 8/12/21, and 8/31/21. Presented to ED from hospice care 8/27/22 w/weakness and increased hand tremors. In ED noted to be in afib with RVR c/b elevated WBC, hypotensive and CXR showed PNA. Admitted to ICU. Initially Covid+ on 8/11/22 and remained + on 8/28/22. Cont'd to decline, w/worsening resp failure. Transitioned to comfort care/hospice care. Expired on 8/31/22. Tx'd w/zosyn and vancomycin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 4,0
Labordaten: covid + 8/28/22 - This sample was analyzed using the Roche LIAT SARS assay platform using PCR or equivalent Nucleic Acid Amplification (NAA) technology.
Aktuelle Erkrankungen: -
Vorgeschichte: MM, MDS, bladder cancer, CHF, anemia, BPH, GERD, cardiomyopathy, HTN
Andere Medikamente: allopurinol, ascorbic acid, aspirin, budeoside, cetirizine, vitamin d3, colchicine, ferrous sulfate, finasteride, furosemide, gabapentin, glimepiride, levothyroxine, metoprolol, multivitamin, omeprazole, sacubitril/valsartan, spironolactone
Allergien: Lisinopril
Vorherige Impfungen: -

VAERS 2431224

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: TX
Alter: 83,0
Geschlecht: M
Eingang: 07.09.2022
Impfdatum: 31.08.2021
Beginn: 31.08.2022
Tage bis Beginn: 365,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia Atrial fibrillation COVID-19 Chest X-ray abnormal Death General physical health deterioration Hypotension Intensive care Pneumonia Respiratory failure SARS-CoV-2 test positive Tremor White blood cell count increased

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization/Death. Rec'd Pfizer-BioNTech on 8/12/21, and 8/31/21. Presented to ED from hospice care 8/27/22 w/weakness and increased hand tremors. In ED noted to be in afib with RVR c/b elevated WBC, hypotensive and CXR showed PNA. Admitted to ICU. Initially Covid+ on 8/11/22 and remained + on 8/28/22. Cont'd to decline, w/worsening resp failure. Transitioned to comfort care/hospice care. Expired on 8/31/22. Tx'd w/zosyn and vancomycin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 4,0
Labordaten: covid + 8/28/22 - This sample was analyzed using the Roche LIAT SARS assay platform using PCR or equivalent Nucleic Acid Amplification (NAA) technology.
Aktuelle Erkrankungen: -
Vorgeschichte: MM, MDS, bladder cancer, CHF, anemia, BPH, GERD, cardiomyopathy, HTN
Andere Medikamente: allopurinol, ascorbic acid, aspirin, budeoside, cetirizine, vitamin d3, colchicine, ferrous sulfate, finasteride, furosemide, gabapentin, glimepiride, levothyroxine, metoprolol, multivitamin, omeprazole, sacubitril/valsartan, spironolactone
Allergien: Lisinopril
Vorherige Impfungen: -

VAERS 2431011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: MI
Alter: 56,0
Geschlecht: M
Eingang: 07.09.2022
Impfdatum: 20.04.2021
Beginn: 04.08.2022
Tage bis Beginn: 471,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Cardiac arrest Dyspnoea Dyspnoea exertional Goitre Intensive care Liver function test SARS-CoV-2 test positive Stridor Tracheal compression Tracheostomy Tracheostomy tube removal

Symptomtext

58-year-old man with past medical history of cardiac arrest in 2/2022, HFrEF, bilateral LE DVTs obesity, OSA, anoxic brain injury, HTN, thyroid mass, and diabetes who came to the emergency department on 5/4 due to shortness of breath and stridor. Patient is accompanied by wife at bedside who helps with a history. He has been having shortness of breath on minimal exertion, and abnormal stridor sound for the past few days before presentation. Patient is status post tracheostomy in March 2022 that was eventually decannulated but he required repeat urgent tracheostomy in May 2022, and was eventually decannulated. Patient was found to have asymmetric enlargement of the left lobule of the thyroid gland measuring up to 8 cm in size compressing the left lateral subglottic trachea which was scheduled for thyroidectomy in the middle of August 2022. But due to worsening of symptoms patient presented on 8/4. He was found to be COVID-19 positive, he is vaccinated with 2 doses of Pfizer and received a booster dose too. He was evaluated by endocrine surgery, ENT, and ICU during this admission. He received 1 dose of Solu-Medrol and racemic epinephrine, did not have desaturations, evaluated by ID with recommendations for treatment with remdesivir, received 3 doses by 8/7. LFTs and heart rate were monitored were on remdesivir. Discharged on room air with plan for follow-up with endocrine surgery for thyroidectomy with ENT recommendations for lower tracheal placement of the endotracheal tube and using extended length 6.5 Mm tube, Dr. performed balloon dilatation of the site if necessary following thyroid surgery.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 3,0
Labordaten: 8/4 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2424211

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: SC
Alter: 59,0
Geschlecht: F
Eingang: 30.08.2022
Impfdatum: 27.08.2021
Beginn: 01.12.2021
Tage bis Beginn: 96,0
Dosis: 3
Route/Site: SYR / AR

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

Aphasia Blood test normal Cerebrovascular accident Cognitive disorder Computerised tomogram head normal Dysgraphia Gait disturbance Headache Hypertension Hypoaesthesia Insomnia Magnetic resonance imaging head normal Malaise Slow speech Visual impairment

Symptomtext

About 3 1/2 months after vaccination of dose 3, I started having a pretty intense headache and generally did not feel well. I was having insomnia. I went to the doctor in December 2021 and I was noted to have high blood pressure. They gave me an aspirin due to blood pressure being in stroke range. I was put on blood pressure medication and it did not lower my blood pressure. After 10 days, I was switched to a different blood pressure medication as well as a diuretic and these did not work well either. In January 2022, I was switched to a 3rd blood pressure medication (BYSTOLIC). Later in the month of January 2022, I had a spiking headache that was over my left eye. I lost my ability to speak and write. My cognitive ability was also affected and I was having difficulty texting and I knew I was having a stroke. I went to the doctors office but by that time I could speak but it was slow. I was also having problems walking. My blood pressure was really high. My doctors office complex is very large and so we did a CAT scan of my head which showed normal. I also had an MRI a few days later at the hospital and it showed I had no active bleeding but could not rule a stroke out. My doctor added a 2nd blood pressure medication (losartan). He told me my symptoms went on longer than a TIA. I started monitoring my blood pressure at home. In July 2022, I had another episode of a spiking headache over my left eye again but I could talk. I did have numbness down my left arm. I was aware of what was happening. I did see a lot of pretty colors in both eyes. I went back to my primary care doctors office and I saw a different doctor in my doctors practice and I had another CT scan of my head but it returned as normal results. I had another MRI a few days later and it showed that I did not have an active bleed. I was given a prescription for a diuretic as needed for elevated blood pressure but I do not like the way it makes me feel and is not really effective. I have subsequently had a lot of blood work done but this was not related to my symptoms. All came back normal. My headache has lessened in severity but has never gone away. I am still having problems controlling my blood pressure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: January 2022 CT of the head and MRI of the head - both normal results; July 2022 CT of the head and MRI of the head - both normal results; August 2022 blood work - normal results.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroid
Andere Medikamente: Np thyroid; levothyroxine; IODORAL; vitamin D3; vitamin B complex; multivitamin; vitamin C; alfalfa
Allergien: Penicillin; sensitive to codeine; morphine
Vorherige Impfungen: -

VAERS 2402974

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: MI
Alter: 83,0
Geschlecht: F
Eingang: 05.08.2022
Impfdatum: 13.04.2021
Beginn: 20.07.2022
Tage bis Beginn: 463,0
Dosis: 2
Route/Site: - / -

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

Abdominal pain Angiogram abnormal Angiogram pulmonary abnormal Anticoagulant therapy Asthenia Bladder catheterisation Blood pressure decreased COVID-19 COVID-19 pneumonia Chest X-ray Diarrhoea Dyspnoea Echocardiogram abnormal Ejection fraction decreased Electrocardiogram ST-T segment depression Gait inability Haemoglobin decreased Inflammatory marker increased

Symptomtext

7/20--currently admitted 84y.o. female with a PMH significant for atrial fibrillation, metastatic ovarian cancer on chemotherapy, pulmonary hypertension, HFpEF, who was recently hospitalized for COVID pneumonia 7/20, who presents with shortness of breath, weakness. During previous admission, patient was treated with loading dose of remdesivir, her oxygen saturations remained appropriate, and she was discharged. Patient's respiratory status began to deteriorate and she became progressively more weak with watery diarrhea and fever at home. Given her worsening respiratory status, her daughter-in-law and son felt as if they could no longer care for her appropriately, and brought her to the hospital to be evaluated. In the ED, lab work was notable for elevated troponin, elevated inflammatory markers, and pancytopenia. CXR was obtained. EKG with normal sinus rhythm with some ST-T wave depressions in leads II, III, to aVF. She was then admitted to the Medicine team for further evaluation and management of shortness of breath and weakness. Remdesivir and antibiotics 5 day courses were completed. CTA confirmed subsegmental pulmonary embolism in the right posterior lower lobe. Patient was transfused 1 unit of platelets followed by IV heparin initiation. 2D echo was notable for EF 40%, mild mitral and tricuspid regurgitation, multiple wall motion abnormalities, and left pleural effusion. Coreg 3.125 mg BID was started. Sotalol was switched to amiodarone given reduced EF. On 07/27, patient had new onset left sided abdominal pain with significant decrease in Hgb and BP secondary to retroperitoneal bleed confirmed by CTA. IV heparin was immediately discontinued. 1 L bolus and 500 mL bolus were given as well as 2 units PRBCs. Interventional radiology embolized bilateral lumbar arteries. Hemoglobin stabilized around 7.5. Patient was initiated on Lovenox. Hematology is recommending that she be maintained on subcutaneous Lovenox 40 mg upon discharge for prophylaxis. Patient with persistent urinary retention while admitted and was thought to be associated with her mirabegron which was discontinued. She continued to have urinary retention and a foley was placed on 8/1 and urology was consulted for their recommendations. A bilateral lower extremity doppler was ordered to determine if patient needs an IVC filter. PT/OT recommend patient be discharged to SAR when medically stable. Patient has been non ambulatory while admitted secondary to deconditioning after being diagnosed with COVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: 7/20 -- SARS-CoV-2 detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2361138

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: MI
Alter: 71,0
Geschlecht: M
Eingang: 07.07.2022
Impfdatum: 17.05.2021
Beginn: 01.08.2021
Tage bis Beginn: 76,0
Dosis: 2
Route/Site: - / -

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

Cognitive disorder Creutzfeldt-Jakob disease Death Feeding disorder Gait inability Impaired driving ability Impaired self-care Laboratory test Lumbar puncture abnormal Memory impairment

Symptomtext

My Dad started experiencing symptoms of CJD Creutfeldt Jakob Disease within months of the 2nd vaccine dose. He was unable to sleep, he also had coordination issues and double vision. After receiving his booster on 12/16/21, he went drastically downhill within one week, He became unable to walk unassisted, had memory and cognitive issues, had trouble feeding and caring for himself, He could no longer drive. or be left alone for long periods of time. After seeing multiple specialists through January 2022, he was hospitalized and a Lumbar punch was performed. Three weeks later on Feb 28th, 2022 his test results returned positive for CJD. My Dad came home from the hospital on hospice and passed on 4/21/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 22,0
Labordaten: A multitude of tests were run between Dec 2021 & Feb 2022. Dad's Lumbar punch was performed 2/8/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Iodine & Shellfish
Vorherige Impfungen: -

VAERS 2344740

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: IA
Alter: 36,0
Geschlecht: F
Eingang: 30.06.2022
Impfdatum: 16.08.2021
Beginn: 02.04.2022
Tage bis Beginn: 229,0
Dosis: 1
Route/Site: IM / -

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

Anxiety Asthenia Blood culture positive Blood lactic acid COVID-19 Cellulitis Chest X-ray abnormal Chills Culture throat Drug abuser Endocarditis Erythema Headache Hyperhidrosis Hypotension Inflammatory marker increased Influenza virus test negative Intensive care

Symptomtext

Pfizer Dose 1 8/16/21 (EW0179) COVID Positive 4/1/22 4/1/22: Patient is a 36-year-old female with past medical history of untreated hepatitis-C and polysubstance abuse (marijuana, heroin, methamphetamine, cigarettes). She was admitted to the hospital yesterday for sepsis secondary to community-acquired pneumonia verses possible left upper extremity cellulitis in the location that she was injecting heroin verses possible endocarditis given her history of daily IV drug use. Despite antibiotics and aggressive hydration, the patient continued to have worsening hypotension and eventually developed septic shock and was transferred to the ICU for pressor administration. She then signed out AMA because she felt anxious and wanted to smoke a cigarette. She came back within a few hours because she felt very weak. She denies any changes that occurred in the few hours that she was outside of the hospital. Her biggest complaints at this time arm weakness and headache. She denies using any drugs while she left the hospital. Please see yesterday's history attached below as it is unchanged per patient report. Patient is a 36-year-old female with past medical history of untreated hepatitis-C, daily heroin use, and daily methamphetamine use. She states that her daughter was taken away from her about 9 months ago and she has been on a downward spiral ever since. She is using injection drugs daily. She is not being treated for her hepatitis-C. She would like to get sober, but this has been a challenge for her. She presented on 03/31/2022 with chief complaint of fever, sore throat, sweating, chills, and diffuse muscle aches. She also notes that she has swelling and redness in her left upper extremity where she has been shooting up. She denies any chest pain or shortness of breath. She did admit to neck pain, but states that she basically has pain everywhere. Her symptoms began on 03/26/2022. In the emergency department, patient's temperature was as high as 104.7? F. She was also tachycardic with a rate as high as 122. She was otherwise maintaining adequate saturations on room air and had normal and stable blood pressures. Chest x-ray was notable for possible pneumonia in the left lung base. Blood cultures and throat culture were obtained. Her lab work was otherwise notable for lactic acid of 2.4. No leukocytosis was noted. Influenza and group A strep testing was negative. COVID-19 testing, pregnancy test, and UA were pending at time of admission. Patient was administered vancomycin, Rocephin, Tylenol, ibuprofen, Zofran, and normal saline for management of her sepsis. She denied alcohol use. She does smoke cigarettes. Family history was reviewed and is noncontributory. 4/3/22: Patient was admitted with very high spiking fevers, left upper extremity cellulitis and endocarditis with very elevated inflammatory markers. Blood cultures were positive, patient was continued on IV Vancomycin. Plan was to have the pateint evaluated by Infectious Disease and possibly have a TEE. Second set of blood cultures was also starting to turn positive. The source is likely the IV drug use that the patient continues to struggle with. Patient was found in the ICU is be using/snorting a brown power substance that was felt by all parties to be heroin, which the patient eventually did admit to. The entire team/staff did our best to help ease the patients worries about being in the hospital but she continue to be adamant that she wanted to leave the hospital. Patient left AMA the afternoon of 4-3-22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Septic shock
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hep C Polysubstance abuse hepatomegaly sleep apnea smoker oligohydramnios
Andere Medikamente: None
Allergien: NKA
Vorherige Impfungen: -

VAERS 2324183

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: MI
Alter: 75,0
Geschlecht: F
Eingang: 20.06.2022
Impfdatum: 01.10.2021
Beginn: 09.06.2022
Tage bis Beginn: 251,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Angiogram pulmonary abnormal Blood phosphorus decreased Blood potassium decreased Bronchial secretion retention Bronchitis COVID-19 Chest X-ray abnormal Chest discomfort Chest pain Dyspnoea Hypertension Hypoxia Lung opacity Pleural effusion SARS-CoV-2 test positive

Symptomtext

Discharge Provider: "Private" DO Primary Care Provider: "Private" DNP, A-GNP Admission Date: 6/9/2022 Discharge Date: Jun 13, 2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Nonspecific chest pain [R07.9] Acute hypoxemic respiratory failure due to COVID-19 (HCC) [U07.1, J96.01] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 75y.o. female with a HX of COPD, as well as loss of sense of taste and smell d/t sinus surgery, and NSCLC on left with resection of middle lobe, who presented to the local ER on 6/9/2022 with worsening shortness of breath and left sided chest discomfort. Work-up in the ER r/o cardiac etiology for her chest discomfort but she was found to be COVID-19 positive. In addition she was found to be hypoxic with mild exertion and hypertensive w/o prior HX of HTN. Chest imaging was not consistent with presence of pneumonia. She was admitted for TX of COVID-19 associated acute on chronic bronchitis. She required 4 liters of O2 supplement via NC. She was started on Dexamethasone 6 g q day per protocol. A repeat X-ray revealed what appeared to be worsening air space opacity and pleural fluid on the left. As a result CT angio chest was performed revealing a mucus plug in the left main bronchus. There was no evidence of pneumothorax or PE. Given the proximity of the mucus plug, we contacted the vICU team for input re: the possibility for transfer to higher echelon of care to undergo bronchoscopy. The recommendation was to encourage use of flutter valve device as well as huff coughing and increasing ambulation as tolerated. By 6/12 in the AM the patient's O2 requirement had improved to 2 and subsequently in the evening was weaned off O2 supplement except at bedtime. For reference, her home O2 requirements are 2L via NC at bedtime. Serum potassium and Phos was noted to be low thus PO supplement was initiated. On 6/13 with labs and vitals in stable condition and the patient feeling back to baseline she was discharged to home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Sepsis (HCC) Low serum cortisol level (HCC) COPD (chronic obstructive pulmonary disease) (HCC) Non-small cell lung cancer s/p surgery 2015 Kidney stone Pulmonary fibrosis (HCC) Allergic rhinitis Alopecia Hyperlipidemia Bruxism Depression Acute bronchitis with chronic obstructive pulmonary disease (COPD) (HCC) Mucus plugging of bronchi Asthma Gastroesophageal reflux disease Osteopenia History of smoking Scoliosis, unspecified scoliosis type, unspecified spinal region Age-related osteoporosis without current pathological fracture Respiratory failure with hypoxia (HCC) Prolonged Q-T interval on ECG COVID-19 with Acute Hypoxic Respiratory Failure Acute hypokalemia
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler Biotin 10 MG TABS budesonide/formoterol (SYMBICORT) 160-4.5 MCG/ACT inhaler cholecalciferol (VITAMIN D3) 25 MCG (1000 UT) tablet citalopram (CELEXA) 2
Allergien: Levaquin [Levofloxacin]Hives Cats Ceftin [Cefuroxime]Other DoxycyclineHives Environmental Seasonal Allergies, UnspecifiedItching
Vorherige Impfungen: -

VAERS 2294444

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: -
Alter: 69,0
Geschlecht: M
Eingang: 25.05.2022
Impfdatum: 21.05.2021
Beginn: 01.08.2021
Tage bis Beginn: 72,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

pt had a positive COVID test on 8/16/21; post-mortem testing from Medical Education Research Institute; pt died at Hospital.

Weitere VAERSDATA-Felder

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

VAERS 2289295

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: MI
Alter: 77,0
Geschlecht: F
Eingang: 21.05.2022
Impfdatum: 01.10.2021
Beginn: 01.05.2022
Tage bis Beginn: 212,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Death

Symptomtext

Patient died of COVID infection in May 2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2277774

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

kritisch

Staat: TX
Alter: 71,0
Geschlecht: F
Eingang: 15.05.2022
Impfdatum: 25.09.2021
Beginn: 25.10.2021
Tage bis Beginn: 30,0
Dosis: 3
Route/Site: IM / LA

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

Autoimmune disorder Cardiac disorder Confusional state Death Fatigue Hypercoagulation Injection site pain Injection site swelling Intracardiac thrombus Lethargy Multisystem inflammatory syndrome Myocardial infarction

Symptomtext

Site: Pain at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Autoimmune Disease (diagnosed by MD)-Medium, Systemic: Cardiac Disorder (diagnosed by MD)-Medium, Systemic: Confusion-Medium, Systemic: Exhaustion / Lethargy-Severe, Systemic: Heart Attack-Severe, Systemic: MIS (Multisystem Inflammatory Syndrome)(diagnosed by MD)-Severe, Additional Details: Death cetificate stated that patient had a hyperactive immune response which led to hyper coagulation which resulted in cardioac thrombosis

Weitere VAERSDATA-Felder

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

VAERS 2267609

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

kritisch

Staat: IA
Alter: 68,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 01.07.2021
Beginn: 26.11.2021
Tage bis Beginn: 148,0
Dosis: 2
Route/Site: IM / -

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

Asthenia Blood culture positive Body temperature decreased COVID-19 Chest X-ray normal Hypervolaemia Hyponatraemia Hypotension Inappropriate schedule of product administration Lactic acidosis Mental status changes Musculoskeletal disorder Paracentesis Peritoneal fluid analysis abnormal Polyuria SARS-CoV-2 test positive Sepsis Septic shock

Symptomtext

COVID Vaccine Breakthrough Case Pfizer Dose 1 4/1/21 (EN6198) Pfizer Dose 2 7/31/21 (ew0179) COVID Positive 11/29/21 11/29/21: Patient is a 69-year-old male with past medical history of alcoholic cirrhosis with recurrent ascites, chronic atrial fibrillation, HFrEF, hypothyroidism, and chronic hyponatremia. He also had a recent hospitalization from 11/15/21-11/19/21 with 1/2 blood cultures positive for MSSA. He also had peritoneal fluid grow Staph epi. He was prescribed a 14 day course of Keflex in regards to this. This is scheduled to finish 12/01/2021. The patient presented to the emergency department on 11/28/2021 with chief complaint of altered mental status and weakness. His wife stated that he was fairly altered for the last 2 days and was slumped over in his chair today. She was concerned about a stroke and therefore had him transferred to the emergency department. The patient was diagnosed with septic shock on arrival as his rectal temperature was low and his blood pressures were low as well. He was administered appropriate fluids and was still hypotensive. He therefore received Levophed in the ED overnight. He was also administered midodrine, Zosyn, vancomycin. A chest x-ray was negative. A UA is pending. Blood cultures were drawn. Patient came back positive for COVID-19. It was later felt that his hypotension may in fact be chronic in nature as he struggled with this during his last hospitalization and was discharged on midodrine and fludrocortisone. He was nonetheless admitted for rule out sepsis/septic shock/weakness secondary to COVID-19 infection. The patient confirms the above story. He believes that he is currently back to his baseline health. He has no acute complaints. Review of systems is negative. He denies any recent alcohol use and states that he quit drinking several years ago. Family history is noncontributory. 12/9/21: Patient is a 69-year-old male with past medical history of alcoholic cirrhosis with recurrent ascites, chronic atrial fibrillation, HFrEF, hypothyroidism, and chronic hyponatremia. He also had a recent hospitalization from 11/15/21-11/19/21 with 1/2 blood cultures positive for MSSA. He also had peritoneal fluid grow Staph epi. He was prescribed a 14 day course of Keflex in regards to this. This is scheduled to finish 12/01/2021. The patient presented to the emergency department on 11/28/2021 with chief complaint of altered mental status and weakness. Patient was then admitted with Septic shock verses chronic hypotension with acute COVID-19 infection Chronic hyponatremia Lactic acidosis Recent MSSA bacteremia, finishing course of antibiotics Peritoneal fluid culture positive for MSSA Chronic Alcoholic cirrhosis with recurrent ascites Chronic Atrial fibrillation Chronic HFrEF Chronic Hypothyroidism Patient was then started with started with IV antibiotics. Ascites has been evaluated and there is increase WBC suggesting a possible SBP. IV antibiotics have been started. The patient is on both midodrine and Florinef for his hypotension, but diuretic for his fluid overload have been discontinued. He unexpectedly tested positive for COVID-19 infection but has no hypoxemia or respiratory symptoms. Patient had repeated paracentesis and did not show any sign of infection and was discharged to SNF to follow-up as outpatient

Weitere VAERSDATA-Felder

Praegender Schweregrund: Septic shock
Hospital-Tage: 21,0
Labordaten: -
Aktuelle Erkrankungen: alcoholic cirrhosis recurrent ascites a fib HFrEF hypothyroidism chronic hyponatremia
Vorgeschichte: alcoholic cirrhosis recurrent ascites a fib HFrEF hypothyroidism chronic hyponatremia
Andere Medikamente: allopurionl 100 mg PO QD aspirin 325 mg PO QD baclofen 10 mgPO TID PRN calcium-vitamin D 1 tab PO QD vitamin D 500 units PO QD digoxin 125 mcg PO QD duloxetine 30 mg PO QD ferrous sulfate 325 mg PO QD fludrocortisone 0.1 mg PO QD folic acid
Allergien: NKA
Vorherige Impfungen: -

VAERS 2226134

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: SD
Alter: 47,0
Geschlecht: M
Eingang: 11.04.2022
Impfdatum: 24.08.2021
Beginn: 03.02.2022
Tage bis Beginn: 163,0
Dosis: 1
Route/Site: SYR / LA

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

COVID-19 Death Diabetes mellitus inadequate control Inappropriate schedule of product administration Malaise SARS-CoV-2 test positive Vaccine breakthrough infection Vomiting

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred, also administration error in interval between doses. The individual was vaccinated with the Pfizer product on 05/12/2021 and 08/24/2021. Please note the sub-optimal time interval between doses. The individual became symptomatic for COVID-19 disease on 01/31/2022. The individual was on a trip out of state at the time. The individual was admitted to hospital due to vomiting, thought to be associated with poor control of blood sugar; the individual had Type I Diabetes. The individual died on 02/06/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 7,0
Labordaten: Positive COVID-19 test despite being vaccinated (albeit, on a non-optimal schedule)
Aktuelle Erkrankungen: -
Vorgeschichte: Type I Diabetes, Hypothyroidism,
Andere Medikamente: -
Allergien: Sulfamethoxazole W-Trimethoprim (reaction: hives); Shellfish-Derived Products (Reactions: Hives, Edema); Clindamycin (Reactions: "stomach pain, "esophagus burns")
Vorherige Impfungen: -

VAERS 2173393

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: MI
Alter: 58,0
Geschlecht: M
Eingang: 11.03.2022
Impfdatum: 27.04.2021
Beginn: 09.03.2022
Tage bis Beginn: 316,0
Dosis: 2
Route/Site: - / -

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

Arthritis bacterial Ascites Bilirubin urine present Blood bilirubin increased Blood lactic acid increased AST/ALT ratio Acidosis Acinetobacter infection Acute kidney injury Anaemia macrocytic Blood potassium decreased C-reactive protein increased COVID-19 Central venous catheterisation Chest X-ray normal Computerised tomogram abdomen abnormal Condition aggravated Death

Symptomtext

Patient with 2 Pfizer COVID vaccinations, last dose 04/27/21, who admitted to the hospital for wound complications and incidentally tested detected for COVID during admission testing. Patient died of septic shock from complications of MRSA infection. Provider d/c note below: "59 year-old male with past medical history of HFrEF with EF 40-45% by TEE (09/2021), CAD s/p stents (x3, most recent 2019), hypertension, hyperlipidemia and osteomyelitis s/p R 4th toe amputation (10/29/2021). Notably, during his hospitalization for amputation of R 4th digit he had MRSA, Acinetobacter, and E faecalis bacteremia treated with 2 weeks of Cefepime and Vancomycin. ED course was remarkable for hypotension with SBP ranging from 67- 98 mmHg despite 3.0L IVF. Central line was placed and he was started on NE. He was also noted to be tachycardic with HR: 118 bpm. CBC demonstrated macrocytic anemia of 6.8; he was given 1U PRBC. He was noted to be hypokalemic with K: 2.6; he received KCl with IVF resuscitation. Hypomagnesemia was repleted with 2g IV MgSO4 (x2). LFTs were notable for AST:ALT >2, elevated TBili of 3.7. ESR and CRP were elevated. Lactate was elevated. CXR was unremarkable. R foot XR demonstrated soft tissue swelling with osteomyelitis of L great toe. CT A/P demonstrated R inguinal hernia. UTI demonstrated positive nitrite, moderate leukocyte, moderate bili, 40 WBC; he was started on Zosyn and Vancomycin. ID was consulted and he was subsequently admitted to CCU for treatment and evaluation of septic shock. Left great toe amputation was completed on 2/15 without complications. He was transferred to the floor on 2/16. Hospitalization was complicated by septic arthritis, s/p I&D of right wrist on 2/19. Additional complications included acute kidney injury with associated acidosis and hyperkalemia. He was started on lasix and bicarb with minimal improvement. Vancomycin was changed to Daptomycin for continued coverage of MRSA bacteremia. On 2/22 he was noted to have multiple melanotic stools. GI was consulted and he was subsequently started on twice daily IV PPI. EGD was completed on 2/25 and demonstrated gastric ulcer without signs or symptoms of bleeding noted. However, he developed stigmata of bleeding overnight. Hgb was noted to be 6.6 and he was subsequently transfused. He was re-admitted to the ICU. Pressors were re-started due to hemorrhagic shock. Nephrology was consulted for worsening renal failure and the patient was started on CRRT, which continued until discharge. NM blood scan on 2/26 demonstrated suspected GI Bleed from mid to upper abdominal small bowel. IR was consulted and completed embolization of the gastroduodenal artery on 2/27. His clinical status deteriorated with up-trending lactic acid and increased pressor needs. CTA A/P was completed and was negative for infarcted bowel. EGD was repeated on 2/28 and demonstrated stigmata of recent bleeding. Surgery was consulted for possible surgical intervention. However, due to his clinical status surgery was held at that time. Patient had stabilization of his Hgb following EGD on 2/28 for approximately 48 hrs, able to wean down from four pressors to one. However, on 3/5 he again developed stigmata of bleeding. GI repeated EGD, which demonstrated large peptic and duodenal ulcers with large amount of blood in the gastric body. Repeat NM blood scan was non-contributory. He required additional blood products. Surgery completed ex-lap with duodenal ulcer oversew, gastroduodenostomy, and pylorplasty with truncal vagotomy of anterior branch overnight. He had initial improvement in clinical status following surgery. Of note, during surgery cirrhotic liver with ascites was noted. Imaging prior to surgery indicated hepatic steatosis. TBili was elevated and continued to up-trend during his hospitalization. Multiple RUQ U/S were negative for biliary obstruction. Ursodiol was started on 03/05, however discontinued following surgery due for bowel rest. Patient again required additional pressor support. In the setting of multiple organ failure and worsening clinical status, family transitioned to comfort care. He was terminally extubated and placed on comfort care. Patient expired on 3/9 at 1943 with family by his side. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: COVID detected PCR on 02/14/22.
Aktuelle Erkrankungen: -
Vorgeschichte: Coronary artery disease involving native coronary artery of native heart Essential hypertension Gastroesophageal reflux disease without esophagitis Current smoker HFrEF (heart failure with reduced ejection fraction) (*) Alcohol abuse Macrocytic anemia Neuropathic ulcer with fat layer exposed (*) Hyperlipidemia Gout Ulcer of left foot Bilateral direct inguinal hernia Peripheral vascular disease (*) Alcoholic hepatitis without ascites Folate deficiency Hyponatremia Hypomagnesemia Hypokalemia Hepatic steatosis Staphylococcal arthritis of right wrist (*) UGIB (upper gastrointestinal bleed) Severe protein-calorie malnutrition (*) Bleeding duodenal ulcer
Andere Medikamente: Aspirin Atenolol Plavix Colcry Lisinopril
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2134430

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: TX
Alter: 81,0
Geschlecht: F
Eingang: 23.02.2022
Impfdatum: 31.08.2021
Beginn: 09.02.2022
Tage bis Beginn: 162,0
Dosis: 3
Route/Site: IM / LA

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

Biopsy lung normal Bronchoscopy COVID-19 Computerised tomogram thorax abnormal Condition aggravated Cough Death Dehydration Fatigue Fungal test negative General physical health deterioration Inappropriate schedule of product administration Leukopenia Lung consolidation Lung opacity Malaise Malnutrition Neutropenia

Symptomtext

Pfizer COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Received Pfizer Vaccine on 2/09/21, 3/09/21, and 8/31/21. Covid + 1/09/22. Previously admitted for covid19 (10/2021 tx remdesivir and dexamethasone), leukopenia, presented 12/26-12/30/21 with fevers, cough and mass like left upper lobe consolidation found. New right lower lobe nodules 1.6 cm, multiple ground glass opacities present. Underwent bronchoscopy on 12/30/21, fungitel negative. Tx'd w/cefepime and vancomcyin. D/C'd 01/03/2022. Presented with fevers, tx'd x10 days of abx, completed 1/16/22. Presented to ED 1/26/22 with fatigue, fever, and malaise, admitted for PNA, UTI, thrombocytopenia, mild neutropenia, dehydration and malnutrition. CT chest showed increased left upper lobe mass, new left sided effusions, increased nodules, all worrisome for metastatic disease. CT guided bx of lung mass via IR 1/27/22, negative for malignancy. Continued to deteriorate, transitioned to comfort care. Tx'd w/Vancomycin, Cefepime, flagyl, Zosyn, and isavuconazonium. Expired on 2/9/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 14,0
Labordaten: 1/09/22 - This sample was analyzed using the LIAT SARS assay platform using PCR or equivalent Nucleic Acid Amplification (NAA) technology.
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, HLD, RA, left lung mass
Andere Medikamente: ascorbic acid, carboxymethylcellulose, vitamin D2, ezetimibe/simvastatin, lisinopril, loratidine, PEG 3350, senna.docusate, vitamin E
Allergien: Adhesive, Latex, Morphine, Acetazolamide
Vorherige Impfungen: -

VAERS 2129341

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: TX
Alter: 60,0
Geschlecht: M
Eingang: 21.02.2022
Impfdatum: 01.09.2021
Beginn: 09.02.2022
Tage bis Beginn: 161,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 Compartment syndrome Death Deep vein thrombosis Fasciotomy Hypoxia Pneumonia bacterial Respiratory acidosis SARS-CoV-2 test positive Superinfection

Symptomtext

Pfizer COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccine on 1/30/21, 2/20/21, 9/1/21. Covid + 1/25/22. Admitted 1/21 for acute hypoxemic resp failure 2/2 Covid19 and superimposed bacterial PNA. Per wife sxs onset 1/10, Covid + 1/12. Recived monoclonal antibiodies prior to this admission. Course c/b L arm DVT > compartment syndrome > fasicotomy. Intermittently proned for low P/F, paralyzed, and started on inhaled Velitri. Respiratory acidosis and hypoxia cont to worsen despite interventions required 2 vasopressors. Transitioned to comfort care. Treated with molnupiravir, ambisome, cefepime,vancomycin, and cresemba. Pt expired on 2/9/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 16,0
Labordaten: 1/25/22 - The sample was analyzed using one or a combination of Real-Time PCR based methods and multiplex reagents including that utilize primer/probe sets specific for the detecti
Aktuelle Erkrankungen: -
Vorgeschichte: NASH cirrhosis (prior transplant), CAD s/p PCI, DM, HTN, HLD, s/p kidney and liver transplant
Andere Medikamente: cacitriol, carvedilol, dexamethasone, enoxaparin, ezetimibe, famotidine, HC/APAP, insulin glargine, insulin lispro, montelukast, mycophenolate, nifedipine, omega 3, omeprazole, prednisone, rosuvastatin, sertraline, sirolimus, sodium bicarb
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2129276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: KY
Alter: 69,0
Geschlecht: F
Eingang: 21.02.2022
Impfdatum: 13.09.2021
Beginn: 12.02.2022
Tage bis Beginn: 152,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Anticoagulant therapy Blood pressure decreased Bradycardia COVID-19 Cardiac arrest Cardiac pacemaker insertion Death Endotracheal intubation Malaise Positive airway pressure therapy Respiratory distress Resuscitation Shock Syncope Ventilation/perfusion scan Vomiting

Symptomtext

admitted for syncope. She was found to have covid and was treated for 5 days with remdesivir. She was on heparin drip for intermediate VQ scan. She had several episodes of bradycardia in the hospital. She had a subsequent short cardiac arrest that she was quickly resuscitated from and Started on a dopamine drip. She was taken for PPM and tolerated well. The last 2 days dopamine was titrated off however her blood pressure began to drop. This morning she began to feel very ill and developed abdominal pain. Workup was in process and she developed profound respiratory distress, bipap was placed and she subsequently vomited. She was intubated and suctioned and cardiac arrested. Cardiac resuscitation were attempted however despite all treatments, we were unable to obtain cardiac rythm. TOD was 1157 Cause of death was not clear, suspect circulatory shock

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CAD, HTN, Type 2 DM,
Andere Medikamente: plavix, imdur, multivitamins, crestor, ASA, norvasc, Triglide, novolog, robaxin
Allergien: nka
Vorherige Impfungen: -

VAERS 2125283

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: CO
Alter: 70,0
Geschlecht: M
Eingang: 19.02.2022
Impfdatum: 20.05.2021
Beginn: 03.01.2022
Tage bis Beginn: 228,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure Angiogram pulmonary abnormal Aortic arteriosclerosis Arteriosclerosis coronary artery Blood lactic acid decreased Chronic respiratory failure Condition aggravated Cor pulmonale Cough Dyspnoea COVID-19 COVID-19 pneumonia Cardiac failure Chest pain Chronic obstructive pulmonary disease Fatigue Headache Hypoxia

Symptomtext

"Admit Date: 1/7/2022 Discharge Date: 1/22/22 This is a 71 yo male w/ extensive PMhx pertinent for severe COPD on 4L and Prednisone 20mg daily W/ recurrent admissions, HFpEF, cor pulmonale, OSA noncompliant w/ CPAP, morbid obesity, and recurrent DVT that presented to ED for evaluation of shortness of breath. Patient known to me from prior admission, 10/27-11/1/21 w/ severe COPD exacerbation. Required up to 10L. COVID negative. D/c home on his usual therapies. Has had 4 days of increasing SOB/severe dyspnea, nonproductive cough w/ mild sputum changes, myalgia, fatigue, headache. Denies fevers, chills, rigors. Received COVID vaccine, but is overdue for booster. Baseline of 3-4L but on EMS arrival was 64% on 5L. In ED, is afebrile and normotensive. HR 110s, sinus. Labs w/ WBC 12.8 w/ shift, lactic 2.3, nml ProBNP and troponin. Was transitioned to HHFNC on arrival, initially required 60lpm now down to 45lpm. Procal back at 0.6, was given cefepime and solumedrol. COVID returned positive after call to me for admission. On exam, speaking in short sentences w/ pursed lips. Toxic appearing. Hospital Course by Problem List: 71yo male with chronic respiratory failure due to COPD and HFpEF/cor pulmonale admitted to hospital with acutely worse hypoxia due to COVID 19 pneumonia and AECOPD. He had slow recovery but is near prehospitalization condition at time of discharge, he is able to ambulate in room and feels well. #Acute on chronic hypoxemic respiratory failure (Baseline 4L NC) #Severe COPD with acute exacerbation #COVID19 pneumonia COVID+ on 1/7/22; day 1 of symptoms 1/3/22. Overdue for pfizer vaccine #3 Pulmonologist: Dr. On chronic prednisone 20mg daily and PJP prophylaxis CTA PE: no PE, bilateral parenchymal opacities c/w acute pneumonia - s/p remdesivir x5 days; briefly on baricitinib - Dexamethasone tapered - Resume home Prednisone 20mg daily 1/19 - RT protocol, nebs - oxygen to baseline 4LNC and stable - continue home PJP prophy - pulm consult greatly appreciated-d/w Dr who fill continue to follow post discharge -COVID isolation completed #Atypical chest pain - troponins negative - given covid positive and resolution/atypical pain will defer further ischemic workup at this time - if recurrent issues would check d-dimer and consult cardiology #Sepsis, POA-resolved Possibly due to viral illness, possible bacterial pneumonia on top of COVID19. PCL 0.32 1/9. MRSA PCR negative. Completed course of IV Cefepime #Chronic HFpEF #Cor pulmonale - continue home lasix & spironolactone - strict I&Os - heart healthy diet with 2L fluid restriction #T2DM with neuropathy #Steroid induced hyperglycemia (SIHG) - uncontrolled at baseline-A1C 9.1 - hold metformin - continue glargine at discharge, patient's family taught how to do injections, f/up with PCP, as he gets farther from high dose steroids may be able to wean back to oral therapy, if uncontrolled may need dose titration vs resume achs correction factor, patient instructed to monitor glucose qam and document for review with PCP - titrate PRN #Non-obstructive CAD LHC 2018: 30% LAD, 50% LCx, 30% RCA - continue coreg, aspirin, statin #OSA: intolerant of CPAP #Obesity: Body mass index is 37.45 kg/m?. #h/o recurrent DVT w/ IVC filter in place. Not on anticoagulation due to hx of GI bleed "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 15,0
Labordaten: "Result Impression IMPRESSION: No evidence of pulmonary emboli. There are bilateral parenchymal opacities, compatible with acute pneumonia. Report E-Signed By: MD at 1/8/2022 3:34 AM Result Narrative CT angiogram of the chest: Indication: Hypoxia. History of COVID-19. Technique: Helical CT was performed through the chest following IV contrast enhancement with 80 cc of Isovue 370. Multiplanar reconstructions and MIP images are reviewed. One of the following dose optimization techniques was utilized in the performance of this exam: Automated exposure control; adjustment of the mA and/or kV according to the patient's size; or use of an iterative reconstruction technique. Specific details can be referenced in the facility's radiology CT exam operational policy. Comparison: 12/28/2019 Pulmonary arteries: There is uniform contrast enhancement. There are no signs of acute or chronic pulmonary emboli. Aorta and great vessels: There is chronic atherosclerotic calcification in the aortic arch and descending thoracic aorta. There are no signs of dissection, aneurysm, or focal luminal narrowing. Heart and pericardial soft tissues: There is chronic calcification in the coronary arteries. The heart is upper limits of normal in size. No pericardial effusion or soft tissue abnormality is identified. Mediastinal soft tissues: Unremarkable and unchanged. Lung fields: There are multiple small areas of ill-defined opacity in the periphery of both lungs, compatible with acute pneumonia. There is evidence of underlying chronic emphysema in the upper lung fields. Pleural spaces: There are no signs of effusion, focal pleural abnormality, or pneumothorax. Skeletal structures: There are chronic degenerative changes in the spine. No acute skeletal deformity is clearly identified. Upper abdomen: Unremarkable, as visualized. The superior tip of an IVC filter is visualized below the renal veins "
Aktuelle Erkrankungen: None
Vorgeschichte: ? Arthritis ? BPH (benign prostatic hyperplasia) ? CAD (coronary artery disease) LHC 2019 - 50% LCx lesion, no intervention ? Chronic low back pain ? COPD (chronic obstructive pulmonary disease) (CODE) severe. On prednisone 20mg daily and 4L baseline O2 ? Cor pulmonale (code) ? COVID-19 01/07/2022 Admitted to ICU on HHFNC 60lpm/FiO2 70%. ? DDD (degenerative disc disease), cervical ? Diabetes mellitus (CODE) Type 2. w/ polyneuropathy ? DVT (deep venous thrombosis) (CODE) recurent. Xarelto stopped 2019 due to GI bleeing. IVC filter was placed. ? GERD (gastroesophageal reflux disease) w/ erosive gastritis. GI bleed 2019 ? GI bleed 2019 EGD w/ erosive gastritis ? Gout ? HTN (hypertension) ? Hyperlipidemia ? Moderate episode of recurrent major depressive disorder (CODE) 7/20/2021 ? Neuropathy ? Obesity morbid obesity, BMI >40 ? OSA on CPAP refusing CPAP ? Pulmonary hypertension (code) ? SOB (shortness of breath) 08/13/2018 chronic and severe ? Syncope
Andere Medikamente: acetaminophen (TYLENOL) 500 mg tablet albuterol HFA (PROAIR HFA) 90 mcg/actuation inhaler allopurinoL (ZYLOPRIM) 300 mg tablet aspirin 81 mg EC tablet atorvaSTATin (LIPITOR) 20 mg tablet budesonide-glycopyr-formoterol (BREZTRI AEROSPHERE) 1
Allergien: None
Vorherige Impfungen: -

VAERS 2116399

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: MI
Alter: 62,0
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: 12.05.2021
Beginn: 24.01.2022
Tage bis Beginn: 257,0
Dosis: 2
Route/Site: UN / UN

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

Acute respiratory failure Blood culture negative COVID-19 Chest X-ray abnormal Cough Dyspnoea Echocardiogram normal Influenza A virus test negative Influenza B virus test Lung disorder Oxygen saturation decreased Procalcitonin increased Pyrexia Respiratory syncytial virus test negative SARS-CoV-2 test positive

Symptomtext

Respiratory Acute respiratory failure (CMS/HCC) Assessment & Plan Acute respiratory failure 1/23, etiology unclear. Note radiographic findings. In conjunction with fever and elevated procalcitonin, the possibility of pneumonia is a concern, with onset of shortness of breath and non-productive cough on 1/23 per chart review, with accompanying drop in 02 sat (which appears to have actually begun the evening prior). Initial findings on CXR appeared to primarily involve the right lung, with subsequent rapid progression throughout 1/23 to involve the bilat lung fields. His coverage has been broadened to include cefepime and azithromycin with continuation of vancomycin. The possibility of aspiration has also been raised, although he doesn't appear to have any obvious risk factors of aspiration, and none was witnessed. Could the radiographic findings be due to non-cardiogenic pulm edema? But if so, why? Could there be a relationship to the MRSA bacteremia? Endovascular infection? Possible, although initial TTE on 1/4 was negative for vegetation (recognizing limited sensitivity of this test), and repeat BC 12/30 were negative. For now, will continue empiric antibiotic coverage and monitor his clinical course. Obtain resp culture, and repeat NAA for SARS CoV2 (specimen collected personally). Await blood cultures. Await results of repeat TTE - if non-diagnostic, TEE? Will discuss. Discussed at bedside with his wife, and questions addressed. She thanked us for our care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: (Privacy) HEALTH SYSTEM (Privacy) LABORATORY Chart Review Copy (Privacy) HAR: (Privacy) DOB: (Privacy) (63 yrs) PT CLASS: Inpatient CSN: (Privacy) DEPT: (Privacy) PATIENT STATUS: Admission GENDER: male BED: (Privacy) ORD DR: (Privacy) AUTH DR: (Privacy) Results Covid-19, Flu, RSV by NAA Contains abnormal data Covid-19, Flu, RSV by NAA Order: (Privacy) Status: Final result Visible to patient: No (inaccessible in patient portal) Next appt: None Specimen Information: Nasopharyngeal; Swab 0 Result Notes Component Ref Range & Units Influenza A Not Detected Not Detected Influenza B Not Detected Not Detected RSV Not Detected Not Detected SARS-CoV-2 (COVID-19) by NAA, Micro Not Detected Detected Abnormal Narrative Methodology: Nucleic Acid Amplification(NAA)/Polymerase Chain Reaction(PCR) The SARS-CoV-2 (COVID-19) test is for in vitro diagnostic use under the Emergency Use Authorization (EUA) for (Privacy) laboratories certified under (Privacy) to perform high complexity testing. This test has not been cleared or approved. Specimen Collected: 01/24/22 3:01 PM Last Resulted: 01/24/22 4:16 PM
Aktuelle Erkrankungen: ? Anemia ? Diabetes mellitus (CMS/HCC) ? Gastroesophageal reflux disease ? Osteomyelitis (CMS/HCC) Left foot ? Wears partial dentures upper
Vorgeschichte: ? Anemia ? Diabetes mellitus (CMS/HCC) ? Gastroesophageal reflux disease ? Osteomyelitis (CMS/HCC) Left foot ? Wears partial dentures upper
Andere Medikamente: acetaminophen (TYLENOL) 325 MG PO Tab take 650 mg by mouth every 6 hours as needed for FOR MILD PAIN, FOR FEVER or FOR HEADACHE. ARIPiprazole (ABILIFY) 10 MG PO Tab take 10 mg by mouth once daily. Med Note (Mon Dec 27, 2021 1:58
Allergien: No Known Drug Allergy
Vorherige Impfungen: -

VAERS 2116024

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: WI
Alter: 74,0
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 02.06.2021
Beginn: 15.02.2022
Tage bis Beginn: 258,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Death

Symptomtext

DEATH RELATED TO COVID-19 INFECTION

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Other significant conditions: Alzheimer?s dementia, Asthma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2113338

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: KY
Alter: 52,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 15.07.2021
Beginn: 07.02.2022
Tage bis Beginn: 207,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

Pt admitted to hospital where she died on Feb 7, 2022. No other information available.

Weitere VAERSDATA-Felder

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

VAERS 2113338

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: KY
Alter: 52,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 15.07.2021
Beginn: 07.02.2022
Tage bis Beginn: 207,0
Dosis: 2
Route/Site: IM / RA

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

Death

Symptomtext

Pt admitted to hospital where she died on Feb 7, 2022. No other information available.

Weitere VAERSDATA-Felder

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

VAERS 2101672

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: WI
Alter: 72,0
Geschlecht: M
Eingang: 10.02.2022
Impfdatum: 25.05.2021
Beginn: 06.06.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: IM / AR

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

Angiogram pulmonary abnormal Echocardiogram Pulmonary embolism

Symptomtext

Pulmonary Embolism on 6/6/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 6,0
Labordaten: CTPA, tPA, echocardiogram
Aktuelle Erkrankungen: None
Vorgeschichte: Smoking
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2203721

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: -
Alter: 69,0
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 12.05.2021
Beginn: 08.11.2020
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Cerebrovascular accident SARS-CoV-2 test positive

Symptomtext

Narrative: PT WAS IMMUNIZED IN A TIMELY MANNER WITH PFIZER MRNA VACCINE 4/21/21 AND 5/12 RESPECTIVELY. PT WAS INPATIENT ON 4J FOR STROKE REHAB WHEN HE CONTRACTED COVID. HE DECLINED MOST COVID TREATMENTS AND DID NOT QUALIFY FOR MONOCLONAL ABS. HE RECIEVED 02 SUPPORT UP TO 3L NC. WITH TIME, HE IMPROVED AND WAS TRANSFERRED BACK FOR FURTHER REHABLITATION

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: POSITIVE BIOFIRE 11/08/21
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2071977

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: CA
Alter: 58,0
Geschlecht: U
Eingang: 28.01.2022
Impfdatum: 06.05.2021
Beginn: 05.01.2022
Tage bis Beginn: 244,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure Alanine aminotransferase normal Anion gap Aspartate aminotransferase normal Basophil percentage increased Blood albumin decreased Blood alkaline phosphatase normal Blood bilirubin normal Blood chloride decreased Blood creatinine increased Blood glucose increased Blood magnesium normal Blood potassium normal Blood sodium decreased Blood urea increased Brain natriuretic peptide increased C-reactive protein increased COVID-19

Symptomtext

58 y/o man with severe obesity with BMI of 50, OSA on CPAP, history of T2DM ( a1c of 9.7 as of 12/29/21), diabetic CKD3 (baseline creatinine 1.3-1.6) , AFib (single episode, not on AC), who presents with fatigue, shortness of breath and diarrhea was found to have covid pneumonia with hypoxemic respiratory failure. His symptoms started on 1/3 or 1/4. Lives at home with his mother, who has no symptoms. Completed 2nd Pfizer vaccine in May. No known sick contacts but regularly visits a local Bingo hall. Hospital course: COVID-19 Disease with acute hypoxemic respiratory failure: Pt s/p 2 Pfizer vaccine in May 2021. Symptoms started 1/3/22. COVID + 1/5/22. Hypoxic to high 80s with ambulation/exertion. Mild lung involvement on CXR and mildly elevated inflammatory markers. Risks for severe disease include obesity, poorly controlled DM2. He has completed 5 days of remdesivir on 1/10. He is on D5 of decadron, will prescribe on discharge to complete a 10 day course. Albuterol MDI PRN. Isolation 20 days from start of symptoms per ID, until 1/25. He requires 1L NC on ambulation to keep O2 sat above 88%. Referral sent to oxygen clinic. Poorly controlled T2DM: A1c >9% recently. On insulin 70/30 at 62 units BID. Gabapentin for peripheral neuropathy. He required NPH 30-35 units here on steroids. Discharged on lower doses of insulin. Close follow up. History of hypertension/HLP: on PTA lisinopril 20 mg daily, lasix 20 mg daily and Atorvastatin 40 mg daily. He was hypertensive so increased lisinopril to 20 mg bid. Please monitor blood pressure. Diabetic CKD 3 ( creatinine 1.3-1.6): creatinine at baseline Chronic papular/scaly rash neck/back: photos (HC) appear to be psoriasis per Dr. She review the photos and feels most likely psoriasis and chronic. Most likely does not need treatment but since patient has itchiness she recommended triamcinolone 0.1% bid for 2 weeks then bid only Sat/Sun chronically. I talked to patient, he wants the prescription. Primary Procedures: none Secondary Procedures: None Reason for Hospital Admission (Admitting Diagnosis): Covid pneumonia and hypoxemic respiratory failure

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: Results for patient (MRN 110007799461) as of 1/28/2022 10:45 1/5/2022 22:55 NA: 134 (L) K: 3.7 CL: 97 (L) CO2: 28 BUN: 13 CREAT: 1.58 (H) ANION GAP4 SERPL: 9 GLUC: 317 (H) TROPONIN I: <0.02 BNP: 50 ALT: 9 AST: 11 GFR-AFRAM: 55 (L) GFR NONAFR AMER: 48 (L) CRP, SER QL: 1.4 (H) WBC: 8.2 RBC'S: 5.48 HGB: 14.5 HCT: 47.4 MCV: 86 RDW, RBC: 15.9 PLT: 236 IMMAT GRANULO % AUTO: 3 (H) NRBC: 0 NEUTROPHILS % AUTO: 70 ANC: 5.8 LYMPHS % AUTO: 14 (L) MONOS % AUTO: 9 EOS % AUTO: 3 BASO'S % AUTO: 1 PT: 13.3 INR: 1.1 D-DIMER: 0.77 (H) 1/6/2022 15:09 NA: 136 K: 3.9 CL: 97 (L) CO2: 25 BUN: 16 CREAT: 1.58 (H) ANION GAP4 SERPL: 14 MG: 1.6 (L) GLUC: 301 (H) ALT: 9 AST: 12 ALKP: 128 (H) TBILI: 0.6 WBC: 8.0 RBC'S: 5.41 HGB: 13.9 HCT: 46.5 MCV: 86 RDW, RBC: 15.9 PLT: 271 IMMAT GRANULO % AUTO: 2 (H) NRBC: 0 NEUTROPHILS % AUTO: 84 (H) ANC: 6.7 LYMPHS % AUTO: 9 (L) MONOS % AUTO: 4 (L) EOS % AUTO: 0 BASO'S % AUTO: 0 1/7/2022 07:09 NA: 141 K: 3.6 CL: 103 CO2: 29 BUN: 18 CREAT: 1.51 (H) ANION GAP4 SERPL: 9 MG: 1.9 GLUC: 116 ALT: 10 AST: 13 ALKP: 110 TBILI: 0.6 CRP, SER QL: 0.7 WBC: 9.2 RBC'S: 5.02 HGB: 13.1 HCT: 42.3 MCV: 84 RDW, RBC: 15.9 PLT: 271 IMMAT GRANULO % AUTO: 1 NRBC: 0 NEUTROPHILS % AUTO: 69 ANC: 6.3 LYMPHS % AUTO: 20 MONOS % AUTO: 8 EOS % AUTO: 1 BASO'S % AUTO: 0 1/8/2022 07:03 NA: 140 K: 4.0 CL: 103 CO2: 29 BUN: 21 CREAT: 1.51 (H) ANION GAP4 SERPL: 8 MG: 1.9 GLUC: 97 ALT: 9 AST: 12 ALKP: 102 TBILI: 0.6 WBC: 8.0 RBC'S: 4.97 HGB: 12.9 (L) HCT: 42.1 MCV: 85 RDW, RBC: 16.2 PLT: 266 IMMAT GRANULO % AUTO: 1 NRBC: 0 NEUTROPHILS % AUTO: 73 ANC: 5.8 LYMPHS % AUTO: 18 MONOS % AUTO: 7 EOS % AUTO: 0 BASO'S % AUTO: 0 1/9/2022 07:03 NA: 142 K: 4.0 CL: 103 CO2: 32 BUN: 22 CREAT: 1.51 (H) ANION GAP4 SERPL: 7 MG: 1.9 GLUC: 60 ALT: 9 AST: 12 ALKP: 98 TBILI: 0.6 ALB: 3.2 (L) WBC: 9.1 RBC'S: 4.95 HGB: 13.0 HCT: 43.1 MCV: 87 RDW, RBC: 16.0 PLT: 250 IMMAT GRANULO % AUTO: 1 NRBC: 0 NEUTROPHILS % AUTO: 74 ANC: 6.8 LYMPHS % AUTO: 16 MONOS % AUTO: 8 EOS % AUTO: 0 BASO'S % AUTO: 0
Aktuelle Erkrankungen: -
Vorgeschichte: severe obesity with BMI of 50, OSA on CPAP, history of T2DM ( a1c of 9.7 as of 12/29/21), diabetic CKD3 (baseline creatinine 1.3-1.6) , AFib (single episode, not on AC),
Andere Medikamente: Acetaminophen (TYLENOL) 325 mg Oral Tab Stopped Taking Sig: Take 2 tablets by mouth every 4 hours as needed for mild pain . Do not exceed 10 tablets in 24 hours. Do not exceed 4,000 mg of acetaminophen per day from all sources Patient not t
Allergien: nkda
Vorherige Impfungen: -

VAERS 2065378

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: MI
Alter: 75,0
Geschlecht: M
Eingang: 26.01.2022
Impfdatum: 15.10.2021
Beginn: 16.01.2022
Tage bis Beginn: 93,0
Dosis: 3
Route/Site: IM / AR

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

Acute left ventricular failure Acute myocardial infarction Acute pulmonary oedema Acute respiratory failure Akinesia Anticoagulant therapy Arterial catheterisation Blood culture negative Brain natriuretic peptide increased Bronchoalveolar lavage Bronchoscopy COVID-19 COVID-19 pneumonia Cardiac failure Chest pain Condition aggravated Coronary artery disease Dysphagia

Symptomtext

Hospitalized 01/16/2022-still currently admitted; COVID-19 positive 01/16/2022; fully vaccinated plus booster Admitting Diagnosis: Acute hypoxemic respiratory failure due to COVID-19 Admitted: 1/16/2022 1:35 PM ASSESSMENT / PLAN: Patient is a 75 y.o. male with past medical history of type 2 diabetes, hypertension, hyperlipidemia, chronic obstructive pulmonary disease, PVD status post fem-pop bypass who is admitted to the intensive care unit for further management of acute hypoxic respiratory failure and NSTEMI. New was hypoxic requiring BiPAP with 100% FiO2. His EKG showed ST depressions and elevated troponins he had further chest pain in the ER. Case was discussed with interventional cardiology from ER no recommendation for emergent catheterization recommended heparin and transfer to Hospital. Given patient's tenuous respiratory status and requiring BiPAP recommended intubation prior to transfer patient was intubated. Upon arrival to medical intensive care unit patient was requiring pressors. And had cool lower extremities. We ordered stat echocardiogram and placed arterial line. # Acute hypoxic respiratory failure with bilateral pulmonary infiltrates Pulmonary edema secondary to HF COVID 19 Hx of COPD Possible etiologies include COVID pneumonia, superimposed bacterial pneumonia, pulmonary edema secondary to heart failure. Some of these, most likely is heart failure due to elevated BNP to 19000, reduced ejection fraction noted on echocardiogram. Heart failure likely secondary to ischemic event. Plan: o Empiric coverage with Unasyn o Blood cultures, sputum culture, bronchoscopy with BAL and associated labs, antigens and cultures o Dexamethasone 6 mg for 10 days o Finish course of remdesivir started at outside hospital o Titrate oxygen to maintain saturation greater than 90% o Albuterol PRN 01/20/22 notes: 1. Acute hypoxic respiratory failure - resolved Possible etiologies include COVID pneumonia, superimposed bacterial pneumonia, pulmonary edema secondary to heart failure. Some of these, most likely is heart failure due to elevated BNP to 19000, reduced ejection fraction noted on echocardiogram. Heart failure likely secondary to ischemic event. Patient does have a history of COPD. Patient was successfully extubated to room air on 1/20/22 with no immediate issues. Plan: - COVID 19 - Continue Decadron 6mg qd for 10 d (1/26) - Continue to monitor respiratory status overnight post-extubation - titrate to maintain >90%SpO2 - albuterol PRN - Possible bacterial PNA - unlikely given overall clinical picture showing greater cardiogenic component with little signs of bacterial infection - Cultures NGTD - Unasyn 5 days, last day tomorrow (1/21)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 10,0
Labordaten: Continued notes from ITEM 18 01/26/2022 notes: Acute hypoxic respiratory failure: Likely multifactorial from flash pulmonary edema 2/2 HFrEF 25%, COVID pneumonia, and possible aspiration pneumonia. Patient was treated with 5 days of Unasyn for possible aspiration pneumonia. COVID pneumonia Possible aspiration pneumonia Dysphagia o Intermittent BiPAP as needed for continued dyspnea o Continue Lasix 40 IV TID and spironolactone, he appears to be nearing euvolemia, but will defer management of diuretics to Cardiology o Continue Decadron for 10 days, last day 1/26 o SLP following, continue dysphagia diet Shock, resolved: possibly mixed cardiogenic > septic. Was on pressors in the intensive care unit Acute systolic heart failure: EF of 25% CAD Elevated troponin, type 1 vs type 2: akinesis of mid distal, anterior/anteroseptal/inferior septal, apical, and distal ill inferior segments. Patient status post 48 hours heparin drip. o Cardiology followup planning possible left heart catheterization 1/25 pending their re-evaluation, continuing Lasix 40 mg IV 3 times a day o Cardiology repeating TTE today
Aktuelle Erkrankungen: -
Vorgeschichte: Acute hypoxemic respiratory failure due to COVID-19 Essential hypertension COPD (chronic obstructive pulmonary disease) Anxiety state RLE PAD s/p bypass Insomnia Rosacea Type 2 diabetes mellitus without complication, without long-term current use of insulin Hypokalemia Prostate troubles Pneumonia due to COVID-19 virus AKI (acute kidney injury) NSTEMI (non-ST elevated myocardial infarction) Acute respiratory failure
Andere Medikamente: amLODIPine (NORVASC) 5 MG tablet ascorbic acid (VITAMIN C) 1000 MG tablet aspirin 81 MG tablet citalopram (CELEXA) 40 MG tablet clopidogrel (PLAVIX) 75 MG tablet cyanocobalamin 500 MCG tablet hydroCHLOROthiazide (HYDRODIURIL) 25 MG tablet i
Allergien: Bee Venom Statin (Atorvastatin) Zolpidem
Vorherige Impfungen: -

VAERS 2062442

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: SD
Alter: 69,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 21.09.2021
Beginn: 08.12.2021
Tage bis Beginn: 78,0
Dosis: 1
Route/Site: SYR / LA

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

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

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. The individual was vaccinated with the Pfizer product on 08/31/2021 and 09/21/2021. The individual had a symptom onset of 12/04/2021 and tested positive for COVID-19 via PCR test on 12/08/2021. The individual was admitted to hospital on 12/08/2021, was transferred to a different hospital on 12/11/2021. They remained hospitalized until their death on 12/16/2021. The individual had complications of a large acute stroke.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 8,0
Labordaten: Positive COVID-19 test despite being vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: History of COPD, obstructive sleep apnea, morbid obesity,
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2046435

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: MI
Alter: 77,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 15.10.2021
Beginn: 09.01.2022
Tage bis Beginn: 86,0
Dosis: 3
Route/Site: IM / AR

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

Acute respiratory failure Anticoagulant therapy Asthenia Atrial flutter C-reactive protein increased COVID-19 COVID-19 pneumonia Cardiac failure congestive Chest X-ray abnormal Fibrin D dimer Lung consolidation Lung opacity SARS-CoV-2 test positive

Symptomtext

Hospitalized 01/10/2022-still currently admitted; COVID-19 positive 01/09/2022; fully vaccinated plus booster CHIEF COMPLAINT: COVID Assessment/Plan ASSESSMENT / PLAN: Acute hypoxemic resp failure secondary to COVID-19 pneumonia -positive PCR 1/9/2022 -decadron 6mg qdaily -dvt px: SQ lovenox as below -current o2 req: wean as able Atrial flutter with RVR Reported history of paroxysmal atrial fibrillation, (remote, post-op) -CHADS-vasc score: at least 6 -Echo ordered -rate control: received IV and PO diltiazem at OHS. Start toprol XL, titrate prn -TSH ordered ordered -anticoagulation: high risk of falls, will defer systemic therapeutic anticoagulation after discussion with wife, discussed risks/benefits of oac and stroke risk. Continue lovenox at prophylactic doses Generalized weakness -primary reason for presentation to hospital per wife -monitor oral intake -PT/OT to see 01/13/2022 notes: ASSESSMENT / PLAN: Acute hypoxemic resp failure secondary to COVID-19 pneumonia/ CHF -CXR 1/12: Slightly worsened chest. Follow-up recommended. -positive PCR 1/9/2022 -decadron 1/10-12, Solumedrol 40 mg bid 1/12- -Lovenox 40 mg sq daily -currently HFNC FiO2 95-- >85% -- > 50-- >40 l/min -CRP 72-- >150.9 -D-dimer 440-- > 560 01/19/2022 notes: ASSESSMENT / PLAN: Acute hypoxemic resp failure secondary to COVID-19 pneumonia/ CHF -CXR 1/17: No significant interval change in diffuse bilateral interstitial opacities and patchy left basilar airspace consolidation. -positive PCR 1/9/2022 -decadron 1/10-12, Solumedrol 40 mg bid 1/12- -Lovenox 40 mg sq daily -still on HFNC FiO2 95-- >90%, 55 l/min -CRP 72-- >150.9-- >73.9 -D-dimer 440-- > 560-- >490 -Cefepim/Dox day # 3/5

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Mixed hyperlipidemia Smoker Major neurocognitive disorder (HCC) Essential hypertension History of small bowel obstruction History of CVA (cerebrovascular accident) History of falling Colon cancer screening declined Skin lesion Weight loss Other urinary incontinence
Andere Medikamente: amLODIPine (NORVASC) 10 MG tablet aspirin 81 MG tablet clopidogrel (PLAVIX) 75 MG tablet simvastatin (ZOCOR) 40 MG tablet
Allergien: Bee Codeine Iodine Penicillins
Vorherige Impfungen: -

VAERS 2039479

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: WI
Alter: 64,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 14.05.2021
Beginn: 11.01.2022
Tage bis Beginn: 242,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Death

Symptomtext

Death related to COVID 19

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Other significant conditions: COPD, Venous insufficiency, Hyperlipidemia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2031118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: NJ
Alter: 54,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 08.06.2021
Beginn: 13.06.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: - / LA

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

Anxiety Chest discomfort Myocardial infarction Palpitations SARS-CoV-2 test

Symptomtext

Heart attack; Very high anxiety; Heart racing; uncomfortable chest; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 54-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 08Jun2021 14:00 (Lot number: EW0179) at the age of 54 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Covid-19" (unspecified if ongoing, notes: Was covid prior vaccination) Concomitant medication(s) included: LUNESTA. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0170, Location of injection: Arm Left, Vaccine Administration Time: 02:00 PM), administration date: 28Apr2021, when the patient was 54 years old, for COVID-19 immunization. The following information was reported: MYOCARDIAL INFARCTION (medically significant) with onset 13Jun2021, outcome "recovered with sequelae" (2021), described as "Heart attack"; ANXIETY (non-serious) with onset 13Jun2021, outcome "recovered with sequelae" (2021), described as "Very high anxiety"; PALPITATIONS (non-serious) with onset 13Jun2021, outcome "recovered with sequelae" (2021), described as "Heart racing"; CHEST DISCOMFORT (non-serious) with onset 13Jun2021, outcome "recovered with sequelae" (2021), described as "uncomfortable chest". The events "heart attack", "very high anxiety", "heart racing" and "uncomfortable chest" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (22Jun2021) negative, notes: Nasal Swab; (03Jul2021) negative, notes: Nasal Swab. Therapeutic measures were not taken as a result of myocardial infarction, anxiety, palpitations, chest discomfort. The events were not life threatening, did not caused/prolonged hospitalization, did not result in death, did not result in disabling/incapacitating nor a congenital anomaly/birth defect. The patient did not receive any other vaccine in four weeks. The events were not life threatening, did not caused/prolonged hospitalization, did not result in death, did not result in disabling/incapacitating nor a congenital anomaly/birth defect. The patient was covid prior vaccination and tested covid post vaccination. The patient had no known allergies. After the second source, patient became very anxious. Very high anxiety (which the patient never had). The patient actually thought had a heart attack while on vacation.It was significant anxiety for about 5-6 hours - heart racing, uncomfortable chest. The patient was checking while on vacation before but this started before vacation, continued on vacation and then continues after vacation for about 3-4 months. At the time of report now just have light anxiety but it had not gone away. The patient saw a heart doctor. No follow-up attempts are possible. No further information is expected. Follow-Up (03Jan2022): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: Test Date: 20210622; Test Name: Antigen; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20210703; Test Name: Antigen; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (if_covid_prior_vaccination Yes)
Andere Medikamente: LUNESTA
Allergien: -
Vorherige Impfungen: -

VAERS 1998925

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: OH
Alter: 55,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 07.07.2021
Beginn: 01.08.2021
Tage bis Beginn: 25,0
Dosis: 2
Route/Site: SYR / LA

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

Back pain Blood test Burning sensation Cerebrovascular accident Computerised tomogram Electromyogram Facial paralysis Hemiparesis Hypoaesthesia Intensive care Magnetic resonance imaging Musculoskeletal stiffness Neuropathy peripheral Paraesthesia Swelling Ultrasound scan

Symptomtext

1st dose of Pfizer was administered 06/16/2021 and 2nd on 07/07/2021. My right thigh became totally numb in mid-August of 2021. In September, my neck became stiff and left side was very swollen. This lasted 3-4 days. October 3, 2021, I was resting in my camper when I felt a sharp pain on the right side of my middle back. This was followed by weakness, numbing, pins and needles on the entire right side of my body. I also had a slight droop to the right side of my face. I contacted my doctor's office, who then transferred me to the nurses' line with my insurance company. They instructed me to call 911. I was admitted to intensive care stroke center and diagnosed with Acute CVA. I was discharged on day 3 and instructed to follow up with my primary doctor and a neurologist. Approximately 3 days after discharge I was then affected by full body neuropathy. I have pins, needles, weakness and burning throughout my entire body which last 24/7. It does not go away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: 10/04/2021 Bloodwork, CT Scans. MRI's, UltraSounds, 10/20/2021 EMG, 10/29/2021 MRI, 11/05/2021 Bloodwork, 11/27/2021 MRI.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroid, Neurocardiogenic Syncope, Optic Nerve Atrophy, Chronic Migraines.
Andere Medikamente: Synthroid 75mcg
Allergien: Penicillin, Sulfa, Vancomycin, Sumatriptan, Cephalexin
Vorherige Impfungen: -

VAERS 1985201

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: WI
Alter: 74,0
Geschlecht: M
Eingang: 28.12.2021
Impfdatum: 26.06.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Death

Symptomtext

fully vaccinated-covid related death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, A-Fib, CAD, DM2, CKD4, Obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1971658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: WI
Alter: 76,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 26.06.2021
Beginn: 21.12.2021
Tage bis Beginn: 178,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Death

Symptomtext

Fully vaccinated-Covid-19 related death.

Weitere VAERSDATA-Felder

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

VAERS 1971658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: WI
Alter: 76,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 26.06.2021
Beginn: 21.12.2021
Tage bis Beginn: 178,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Death

Symptomtext

Fully vaccinated-Covid-19 related death.

Weitere VAERSDATA-Felder

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

VAERS 1936984

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 09.08.2021
Beginn: 07.12.2021
Tage bis Beginn: 120,0
Dosis: 2
Route/Site: UN / UN

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

Accidental overdose Acute respiratory failure Angiopathy Anticoagulant therapy Asthenia Autoimmune thyroiditis Blood sodium decreased COVID-19 COVID-19 pneumonia Cardiomegaly Chest X-ray abnormal Cognitive disorder Condition aggravated Cough Deep vein thrombosis Dementia Diarrhoea Dry skin

Symptomtext

Patient currently admitted fo inpatient stay at (2) days. H & P: Patient is a 65 y.o. female with history of DVT in 9/2021, HTN, hashimotos who presented with COVID and shortness of breath with hypoxia. Patient has neurocognitive deficits/dementia and is a very poor historian. Lives with her daughter but daughter is UNvaccinated and was unable to come back to provide history. ED called daughter several times with no call back and other daughter was called but patient does not live with her and there appears to be some sort of odd family dynamics so also unhelpful. Apparently per daughter who spoke with nurse at triage prior to leaving, patient tested positive 12/1 and on Saturday unintentionally took 20-22 tabs of tylenol (unconfirmed). Symptoms have included cough, weakness, shortness of breath and diarrhea. She was hypoxic at home in the mid 80s which prompted daughter to bring her in. She was very weak in the ED and hypoxic to 88 on room air sitting at the edge of the bed. She was admitted for further management. Decadron given. Patient says she thinks she started having symptoms last week. Initially doesn't recall getting vaccinated against covid, doesn't understand many questions. Says she doesn't know if she's been taking eliquis. Doesn't knwo when she started or when she stopped. Doesn't recall taking so much tylenol. Very poor historian. ED labs revealed hyponatremia at 127 patient appeared dry received 1 L IVF. Assessment and plan:Acute respiratory failure with hypoxia COVID-19 pneumonia -supplemental O2 as needed -positive 12/1/21 -vaccinated July/august 2021, no booster yet -currently on 2L O2 -daughter with whom she lives is not vaccinated, did not come back with her and unable to be reached via telephone. Will hold off on remdesivir until she can be reached. -continue decadron x 10 days Hyponatremia -likely hypovolemic + HCTZ use -repeat BMP at midnight -s/p 1L in ED. Cautious fluid resuscitation given COVID. Unintentional tylenol overdose -apparently per daughter took 22 tabs of tylenol (unclear exact amount) -LFTs normal -tylenol level <5 -monitor CMP daily -avoid acetaminophen DVT 9/2021 -was on eliquis. Per patietn she doesn't recall when she started or stopped it. -await pharmacy review of meds and if not on it any longer, will start lovenox. If still taking it will continue. HTN -hold HCTZ -continue lisinopril Dementia/neurocognitive deficits -sees neuropsych outpatient -unclear if she has DPOA paperwork, but will likely need it. Hashimotos -continue synthroid Diet: general DVT ppx: Lovenox Code Status: FULL CODE BY DEFAULT GIVEN DEMENTIA AND INABILITY TO REACH DAUGHTER Dispo: Admit to IM

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: DR CHEST SINGLE VIEW Resulted: 12/07/21 1754 Order Status: Completed Updated: 12/07/21 1756 Narrative: EXAMINATION: Single View Chest EXAM DATE: 12/7/2021 5:17 PM TECHNIQUE: Single view chest INDICATION: Cough. Covid positive. COMPARISON: 10/2/2021. ENCOUNTER: Not applicable _________________________ FINDINGS: Low lung volumes with hypoventilatory changes including vascular crowding. Possible pulmonary vascular congestion. There are bilateral peripheral predominant pulmonary opacities. There is no pleural effusion or pneumothorax. There is mild cardiomegaly. _________________________ Impression: 1. Bilateral nonspecific linear opacities most compatible with Covid 19 pneumonia given the patient's history. 2. Mild cardiomegaly and possible pulmonary vascular congestion.
Aktuelle Erkrankungen: 7/29/21- dysphagia ; EGD (ESOPHAGOGASTRODUODENOSCOPY) 7/22/21- globus sensation 7/20/21- acute exacerbation of lower back pain
Vorgeschichte: Colon polyp H/O hysterectomy for benign disease Spondylosis of thoracic region without myelopathy or radiculopathy History of total left hip arthroplasty Back muscle spasm Hypothyroidism, unspecified type Cellulitis of hip Adenoma of large intestine Environmental allergies Hypertension Chronic midline low back pain without sciatica Hashimoto's thyroiditis Adenoma of large intestine Environmental allergies Unspecified vitamin D deficiency Heart murmur Primary osteoarthritis of right hip
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet busPIRone (BUSPAR) 10 MG tablet DULoxetine (CYMBALTA) 60 MG delayed release capsule gabapentin (NEURONTIN) 300 MG capsule levothyroxine (SYNTHROID) 100 MCG tablet Lidocaine (LIDODERM) 4 % patch lisinopr
Allergien: PenicillinsHives Phenergan [Benzyl Alc-promethazine]Itching Sulfa DrugsHives Latex MethylprednisoloneHeadache CodeineConfusion
Vorherige Impfungen: -

VAERS 1932469

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: -
Alter: 88,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 29.04.2021
Beginn: 21.11.2021
Tage bis Beginn: 206,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Cardiac arrest Fall SARS-CoV-2 test positive

Symptomtext

11/21/21 presented to ED by EMS for "cardiac arrest and fall". PMHx of "carotid stenosis, insulin dependent DM, HTN, legal blindness, seizure disorder"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: 11/21/21 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1932390

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: -
Alter: 44,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 17.05.2021
Beginn: 18.11.2021
Tage bis Beginn: 185,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Cerebral haemorrhage Cerebrovascular accident SARS-CoV-2 test positive

Symptomtext

11/18/21 presents to EC ED as transfer with "hemorrhagic CVA". PMHx "left PCA CVA on 81mg ASA, DM2, HTN, hypothyroidism".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: -
Labordaten: 11/19/21 SARS-CoV-2 (COVID-19) detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1929265

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: TX
Alter: 58,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 31.08.2021
Beginn: 08.11.2021
Tage bis Beginn: 69,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Chronic kidney disease Condition aggravated Death Hypoxia Immunoglobulin therapy Mechanical ventilation SARS-CoV-2 test positive

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 1/29/2021, 2/21/2021, and 8/31/2021. Pt. w/PMHx of unifocal langerhands cell histiocytosis, pulmonary fibrosis and emphysema s/p bilateral lung transplantation 1/2019. Hx Covid-19, dx'd on 11/4/21 tx'd w/monoclonal antibodies on 11/6. Admitted on 11/08 tx'd with remdesivir, decadron and IVIG, d/c'd home on 11/14. Admitted 11/20 for acute on chronic respiratory failure with hypoxia secondary to Covid pneumonia and CKD. Tx'd w/azithromcin, meropenem, and methylprednisolone. Underwent prolonged mechanical ventilation x13 days. Expired 12/06/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 16,0
Labordaten: Positive COVID-19 tests on 11/6/2021, 11/9/2021, 11/22/2021, 11/30/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Anemia, CKD, GERD, Unifocal Langerhans Cell Histiocytosis s/p lung transplant in 2019, Chronic hypoxemic respiratory failure
Andere Medikamente: Acetaminophen PRN, Azithromycin 250 mg MWF, Oscal BID, Clonazepam 0.5 mg QHS prn Anxiety, Dapsone 100 mg QD, Multivitamin QD, Gabapentin 200 mg BID, Itraconazole 100 mg BID, Lisinopril 20 mg QD, Magnesium oxide 400 mg BID, Metoprolol 75 mg
Allergien: Rivaroxaban, Amlodipine
Vorherige Impfungen: -

VAERS 1870007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: IL
Alter: 71,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 26.05.2021
Beginn: 08.09.2021
Tage bis Beginn: 105,0
Dosis: 1
Route/Site: IM / -

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

Acute kidney injury Anal incontinence Angiogram Angiogram pulmonary normal Atrial fibrillation Biopsy lung Bladder catheterisation Blood potassium decreased COVID-19 COVID-19 pneumonia Candida test positive Chest X-ray abnormal Chest discomfort Chest tube insertion Computerised tomogram head abnormal Computerised tomogram thorax abnormal Culture positive Culture urine positive

Symptomtext

On 9/8/21 patient presented to ER, and was admitted to the hospital. For the last couple days she felt slight uneasy feeling or a pressure in the chest. When she came to the ER, she was found to have problem with AFib with rapid ventricular rate at times going up to 150-200. She had no specific symptoms related to that of palpitations, syncope or near syncope. Case was discussed with cardiologist. She is started on Cardizem drip. She has a previous history of peptic ulcer disease. Not too long ago she also had significant nosebleed. She had a recent hip surgery done due to infected hip and has a spacer and ongoing antibiotics. The patient's potassium was also low. She also has been having problem with this watery diarrhea, not foul smelling for last 4 or 5 days. Frequent BM. Every time she eats she has to go and sometimes it starts before she can even control it. When she came to the ER, her potassium was low also. Due to that, she is being admitted for further management. On 9/18/21, was positive for COVID. She was incidentally found ot have RLL nodule on admission concerning for low grade adenocarcinoma . Fine needle aspiration 09/10/21 was complicated by pleural bleed which caused hemorrhagic shock s/p multiple units of PRBC and platelets , septic shock was also suspected , required pressor support , s/p chest tube that was removed 09/17/21 , s/p IR angiography selective right intercostal artery T 6 - T11 but no active bleeding or aneurysm noted . The pathology from the aspiration was negative for malignancy . Diagnosed with COVID 19 pneumonia positive 09/18/21 , though vaccinated with Pfizer 06/16/21 . This is likely due to immunocompromised status . Completed Remdesivir , Required mechanical ventilation due to COVID 19 pneumonia , initially extubated 09/11/21, but subsequently re intubated 09/19/21. She is s/p trach and PEG 10/06/21. Respiratory culture 10/30/21 did grow serratia marcecens. Respiratory culture prior to this was positive for candida albicans 10/07/21.Patient was managed with Ertapenem. Foley catheter associated UTI - Klebsiella oxytoca. Urine culture positive 10/29/21. GI bleed also reported , but remained unstable for invasive GI interventions. She had AKI requiring CCRT . Also CT head 10/10/21 noted intracranial bleed , neurosurgery evaluated , conservative treatment for now. IVC filter was placed 09/24/21 for non occlusive DVT right common femoral vein Non occlusive thrombus right proximal superficial femoral vein. Discharged on 11/10/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Septic shock
Hospital-Tage: 63,0
Labordaten: 9/18/21 COVID19: positive 9/8/21 Chest xray: negative 9/8/21 CTA chest: negative for PE 9/10/21 chest xray: pulmonary hemorrhage 9/18/21 CT chest: Diffuse bilateral lung ground-glass changes highly consistent with COVID pneumonia
Aktuelle Erkrankungen: -
Vorgeschichte: past medical history of Arthritis, Avascular necrosis of bone of ankle (HCC), Avascular necrosis of bones of both hips (HCC), Basal cell carcinoma of skin of ear, Cholecystitis (Cholelithesis ), Compression fracture (T4 level ), Fatty liver, Fusion of spine of thoracic region (2-04-12, T2-T6 levels ), Hypertension, Liver transplant recipient (HCC), Melanoma in situ (HCC) (removed from bottom of foot ), Osteoarthritis, Osteoporosis, and Thyroid disease.
Andere Medikamente: Levothyroxine, vitamin D, norco PRN, levetiracetam, Magnesium oxide, metaxalone, metoprolol tartrate, pantoprazole, sertraline, tacrolimus, alendronate, allopurinol, amlodipine, aspirin, colestipol, IBgard, mycophenolate, oxycontin, multiv
Allergien: IV dye, nubain, calcitrol, iodine, lisinopril
Vorherige Impfungen: -

VAERS 1865152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: VA
Alter: 33,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 21.05.2021
Beginn: 01.06.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: IM / AR

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

Angiogram pulmonary abnormal Dyspnoea exertional Echocardiogram Pulmonary embolism Scan with contrast abnormal

Symptomtext

Patient was given Pfizer Covid 19 vaccine initially 21 May 2021 and second dose 10 Jun 2021 - both with LOT EW0179. he says sometime in JUN 2021 , he started having dyspnea on exertion, which worsened during a fitness test 1 NOV 2021 - at which time he was diagnosed with pulmonary embolism

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 5,0
Labordaten: CTA chest 1 NOV 2021: IMPRESSION: Question of very subtle central filling defect in one or two segmental/subsegmental arteries to the right lower lobe. Reflux of contrast into the posthepatic IVC and hepatic veins. This is relatively unusual in a patient of this age and can represent right heart dysfunction. Recommend correlation with cardiac exam/evaluation. Patient had normal transthoracic echocardiogram 2 NOV 2021
Aktuelle Erkrankungen: denies
Vorgeschichte: denies
Andere Medikamente: -
Allergien: denies
Vorherige Impfungen: -

VAERS 1784945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: SC
Alter: 12,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 11.07.2021
Beginn: 02.08.2021
Tage bis Beginn: 22,0
Dosis: 1
Route/Site: SYR / UN

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

Death Respiratory tract haemorrhage

Symptomtext

Blood in airway, Death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Trisomy 18, Scoliosis, Closed Ventricular Septal Defect, Ectopic Kidney, Gastrostomy Tube dependent, GERD, and Obstructive Sleep Apnea
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1779074

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: WI
Alter: 40,0
Geschlecht: M
Eingang: 12.10.2021
Impfdatum: 28.04.2021
Beginn: 07.10.2021
Tage bis Beginn: 162,0
Dosis: 2
Route/Site: IM / LA

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

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

Symptomtext

Patient admitted as inpatient on 10/7 due to acute hypoxemic respiratory failure due to COVID-19. Patient was tested for COVID-19 and was positive on 10/7. Patient required high-flow oxygen 25 L at 70%.

Weitere VAERSDATA-Felder

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

VAERS 2657514

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: NM
Alter: 86,0
Geschlecht: F
Eingang: 11.10.2021
Impfdatum: 03.06.2021
Beginn: 15.06.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: IM / -

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

Agitation Anxiety Constipation Death Decreased activity Delirium Dementia Dyspnoea Haemoptysis Hallucination Ischaemic cardiomyopathy Oedema Pain Psychomotor hyperactivity

Symptomtext

This patient was medically fragile and on hospice care at the time of the event. We are reporting this because the EUA at the time stated to report all deaths. However, it is unlikely this was related to the vaccine. The patient received her first Pfizer vaccine on 6/3/2021 and expired on 6/15/2021. Per Death Summary: Cause of Death: ischemic cardiomyopathy Patient was admitted to Hospice on 6/14/2021 for the diagnosis of Ischemic cardiomyopathy. Her symptoms of pain, dyspnea, delirium, respiratory secretions and aspiration were managed with both medications and behavioral interventions. The Hospice interdisciplinary team was involved in care of patient and family. She died peacefully at 1425 on 6/15/2021 with her family at the bedside. The hospice bereavement team will follow up with the family. History and Physical note: #1 new hemoptysis: The etiology of this is unclear. There is not a simple answer such as secondary to epistaxis or dental problems. The patient is not fully anticoagulated and takes only 81 mg of aspirin a day. She is about 1 week status post first Covid vaccination. We will check a CBC and platelet count. This could represent pneumonia in the right lung with secondary hemoptysis or it could represent primary hemoptysis in the airways leading to aspiration of blood within the lung. Her oxygen saturation and respiration rate are okay with 2 L of supplemental oxygen. However, it is very early in the course and she could progress with further respiratory distress. #2 delirium and dementia: The family clearly describes several days of distinct delirium with hallucinations and mixed hyper and hypoactivity. Her baseline dementia is primarily forget fullness and lack of self-care. #3 ischemic cardiomyopathy: The patient does not have symptoms that are unstable regarding this baseline disease. She does not have signs of decompensated heart failure or volume overload. Prior to Admission Medications LORazepam (ATIVAN) 0.5 mg tablet Sig: Take 0.5 mg by mouth every 6 hours as needed for anxiety. indications: anxious acetaminophen (TYLENOL) 325 mg Tablet Sig: Take 650 mg by mouth every 6 hours as needed for Fever or Pain. Acetaminophen (TYLENOL) 650 mg Suppository Sig: place 650 mg rectally every 6 hours as needed (mild pain or fever). Indications: mild pain or fever aspirin (ECOTRIN) 81 mg EC tablet Sig: Take 81 mg by mouth nightly. bisacodyL (BISCOLAX) 10 mg suppository Sig: Place 10 mg rectally as needed (constipation). Indications: constipation donepezil (ARICEPT) 5 mg tablet Sig: Take 5 mg by mouth nightly. famotidine (PEPCID) 20 mg tablet Sig: Take 20 mg by mouth 2 times daily. furosemide (LASIX) 40 mg tablet Sig: Take 40 mg by mouth daily as needed (edema). haloperidol (HALDOL) 2mg/mL solution Sig: Take 1 mg by mouth every 6 hours as needed (agitation). Indications: agitation hyoscyamine (ANASPAZ,LEVSIN) 0.125 mg tablet Sig: Take 0.125 mg by mouth every 4 hours as needed (terminal secretions). Indications: terminal secretions ibuprofen (ADVIL LIQUI-GEL ORAL) Sig: Take 200 mg by mouth 3 times daily. magnesium hydroxide (MILK OF MAGNESIA) 400 mg/5 mL suspension Sig: Take 30 mLs by mouth 2 times daily as needed for Constipations. magnesium hydroxide (MILK OF MAGNESIA) 400 mg/5 mL suspension Sig: Take 10 mLs by mouth daily. memantine (NAMENDA) 10 mg tablet Sig: Take 10 mg by mouth at bedtime: mirtazapine (REMERON) 7.5 mg tablet Sig: Take 7.5 mg by mouth nightly. morphine (ROXANOL) 20 mg/1 mL concentrated solution Sig: Take 5-10 mg by mouth every 3 hours as needed (secere pain or dyspnea). Indications: secere pain or dyspnea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: This is a 86 year old lady with ischemic cardiopathy myopathy and LVEF of 25%, and also with advanced dementia, who is on home hospice with primary hospice diagnosis chronic systolic congestive heart failure secondary to ischemic cardiomyopathy.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1765265

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: MI
Alter: 65,0
Geschlecht: M
Eingang: 06.10.2021
Impfdatum: 03.05.2021
Beginn: 16.09.2021
Tage bis Beginn: 136,0
Dosis: 2
Route/Site: IM / AR

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

Acute kidney injury Acute respiratory distress syndrome Acute respiratory failure Adrenal insufficiency Ageusia Anosmia Asthenia Blood culture COVID-19 COVID-19 pneumonia Cardiogenic shock Chest X-ray abnormal Cough Diarrhoea Dyspnoea Echocardiogram normal Endotracheal intubation Fatigue

Symptomtext

Hospitalized (9.25.21 - present; now in ICU intubated); COVID-19 positive (9.16.21); Fully Vaccinated HPI from admission: HISTORY OF PRESENT ILLNESS: Patient is a 66 y.o. male who presents today with SOB. He has a known history of coronary artery disease, hypertension, hyperlipidemia, atrial fibrillation on Xarelto. He is fully vaccinated against COVID-19. He presents the emergency department complaining of shortness breath that started 12 days ago. He eventually got tested + for COVID-19 09/16/2021. He has been monitoring his oxygen level at home when it was noted that he has been dropping below 80s. He then proceeded to be evaluated emergency department. He has been having generalized weakness and fatigue with mild cough. He denies chest pain nor hemoptysis. He has had intermittent fevers. He reports diarrhea, no abdominal pain. He states he initially lost his sense of taste and smell but slowly regaining it back. On admission his blood pressure is 153/79 heart rate 89 respiratory rate 25 94% NRB Chest x-ray showing bibasilar airspace opacities likely due to pneumonia. ASSESSMENT / PLAN: Acute respiratory failure COVID 19 pneumonia Received Pfizer COVID 19 vaccine 5/2021 Symptom onset 9/14/21 Positive test 09/16/2021 Chest x-ray showing bilateral airspace opacities Decadron 6 mg daily Out of the window for remdesivir Monitor CRP D-dimer Check procalcitonin Elevated procalcitonin at 0.27 Blood culture and sputum cultures Rocephin and azithromycin x5 days Progress note from 10.6.21: (intubated in ICU; declining status) ASSESSMENT / PLAN: 66 y.o. vaccinated patient with morbid obesity (BMI 34), aflutter on Xarelto, CAD (STEMI 12/4/2008 s/p D1 DES), HTN, hyperlipidemia, GERD presented with COVID-19 pneumonia on 9/25. AKI improving. Mild hepatitis. Symptom onset 9/14, positive test 9/16. Prior to this had newly identified well differentiated neuroendocrine tumors in his duodenum and was planning to undergo surgical resection 10/14/21. Otherwise does not appear to be immunosuppressed. Transferred to ICU 10/1 with progressive hypoxia as cc2; supported w/ HHFNC and prn NRBM. Assessment and Plan Acute respiratory failure with hypoxia Assessment & Plan Due to COVID-19 Pneumonia 9/26: On 100% HFNC and NRB 10/2: Intubated FIO2 (%): 60 % Type of Mechanical Vent: Avea Mechanical Rate: 34 breaths/min Set/Target Tidal Volume: 510 PEEP (cm H2O): 14 cm H2O Plan: - Lung protective ventilation - adjust Vt/Peep for pplat < 30 and driving pressure < 15 as able - daily assessment for prone position 16/8 for p/f < 150 (until p/f > 150 on Peep 10 or less and fio2 60% or less) Serial ABG - collect sputum culture - continue steroids * Pneumonia due to COVID-19 virus Overview Vaccinated: Pfizer 4/5/21, 5/3/21 Symptom onset 9/14 Positive test 9/16 Admission 9/25 Intubated 10/2 Treatment: Remdesivir: out of window Tocilizumab: none due to shortage Steroids: Dexamethasone 9/25 - 9/26 Methylprednisolone 60 mg iv q 12 9/26 - Assessment & Plan Patient has confirmedSARS-CoV-2/COVID-19 infection Vaccinated Isolation: Severe respiratory isolation Risk stratification (High if 1 from each or >1 clinical criteria): History - Age >/= 60 years old, History of cardiovascular disease, Diabetes (A1C >/= 7.6), BMI >/= 30 Labs: - Daily labs qAM: CMP, CBC with diff, - Every other day: CRP, ferritin, Fibrinogen, LDH, D-dimer, triglycerides. Therapy: - Dexamethasone 6mg daily transitioned to methylprednisolone - Unable to provide remdesivir or tocilizumab Respiratory failure and hemodynamics: Lung protective ventilation with 4-6 ml/kg and appropriate PEEP escalation. Initiate neuromuscular blockade and proning as appropriate. Concern for arrhythmia/hemodynamic worsening. Consider EKG and bedside cardiac US, evaluate for need for TTE. Pneumomediastinum Assessment & Plan - extensive, related to COVID-19, ARDS Plan: - okay to continue to monitor as there is no evidence of pneumothorax - monitor for changes in peak and plateau airway pressures. Shock Assessment & Plan - unclear etiology: Cardiogenic versus hemorrhagic versus adrenal insufficiency. - echocardiogram with no valvular dysfunction and normal LVEF. - troponins unremarkable Plan: - resolved at this time - continue antibiotics - stress dose steroids not continued

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 12,0
Labordaten: -
Aktuelle Erkrankungen: 9.15.21 - called office reporting cough, chest congestion; bronchitis symptoms 9.16.21 - COVID-19 positive 9.21.21 - ED visit for shortness of breath / COVID-19; prescribed benzonatate and albuterol
Vorgeschichte: Mixed hyperlipidemia Essential hypertension Coronary artery disease without angina pectoris IFG (impaired fasting glucose) Gastroesophageal reflux disease History of ST elevation myocardial infarction (STEMI) Presence of drug coated stent in LAD coronary artery Tussive syncope Bifascicular block Snoring Preop cardiovascular exam Sensorineural hearing loss (SNHL) of both ears History of basal cell carcinoma (BCC) of skin
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amoxicillin (AMOXIL) 500 MG capsule Ascorbic Acid (VITAMIN C PO) aspirin 81 MG tablet atorvastatin (LIPITOR) 40 MG tablet CALCIUM CITRATE-VITAMIN D3 PO es
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1765233

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: MI
Alter: 72,0
Geschlecht: F
Eingang: 06.10.2021
Impfdatum: 03.05.2021
Beginn: 16.09.2021
Tage bis Beginn: 136,0
Dosis: 2
Route/Site: IM / AR

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Cough Dyspnoea Emotional disorder Fatigue Hypoxia SARS-CoV-2 test positive

Symptomtext

Hospitalized (9.25.21 - present); COVID-19 positive (9.16.21); fully vaccinated From Admission note: HISTORY OF PRESENT ILLNESS: Patient is a 73 y.o. female who presents today with CC of dyspnea. Patient states that she and her husband tested positive foir COVID on 9/16. Both are fully vaccinated. Patients husband was very SOB today and EMS was called. EMS found both the husband and the patient were hypoxic and both were transported to hospital. Other than dyspnea, patient only complaint is fatigue and cough.. PROGRESS NOTE FROM 10/5/21: Date of admission: 9/25/2021 Date of encounter: 10/05/2021 COVID 19 Pneumonia Acute hypoxic respiratory failure secondary Patient is vaccinated Continue dexamethasone to complete 10 days Completed 5 days of Remdesivir Encourage acapella, IS and Proning Monitor CMP, CRP, D-dimer Continue to wean oxygen as tolerated PT/OT Disposition Pending improvement of respiratory status Anticipating pulmonary rehab evaluation or home oxygen need Possible DC in the next 24-48 hours SUBJECTIVE: Patient improving slowly however she is very emotional as her husband is now intubated in intensive care unit due to COVID-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 12,0
Labordaten: -
Aktuelle Erkrankungen: 9.15.21: reported COVID symptoms starting 9.14.21
Vorgeschichte: Pure hypercholesterolemia Essential hypertension, benign Generalized anxiety disorder Gastroesophageal reflux disease without esophagitis BMI 40.0-44.9, adult OSA (obstructive sleep apnea) Primary osteoarthritis involving multiple joints Hx of renal cell carcinoma Choroidal nevus of right eye Hyperopia, bilateral Vision loss, left eye History of thyroid cancer Postoperative hypothyroidism Controlled type 2 diabetes mellitus without complication, without long-term current use of insulin History of basal cell carcinoma (BCC) of skin NASH (nonalcoholic steatohepatitis) Thrombocytosis after splenectomy
Andere Medikamente: acetaminophen (TYLENOL) 650 MG tablet alprazolam (XANAX XR) 0.5 MG tablet amLODIPine (NORVASC) 10 MG tablet atorvastatin (LIPITOR) 40 MG tablet Cholecalciferol 2000 units CAPS esomeprazole (NEXIUM) 20 MG delayed release capsule fexofenadine
Allergien: TramadolNausea and Vomiting, Headache Clonazepam Dilaudid [Hydromorphone]Nausea and Vomiting GabapentinNausea Only Hydrocodone-acetaminophenNausea and Vomiting Klonopin [Benzodiazepines] Vicodin [Hydrocodone-acetaminophen]Nausea and Vomiting, Headache
Vorherige Impfungen: -

VAERS 1736748

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: TX
Alter: 74,0
Geschlecht: F
Eingang: 27.09.2021
Impfdatum: 19.05.2021
Beginn: 02.09.2021
Tage bis Beginn: 106,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Chills Death Diarrhoea Dyspnoea Exposure to SARS-CoV-2 Illness Nausea Oxygen saturation decreased Pyrexia SARS-CoV-2 test positive Vomiting

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 4/28/2021 and 5/19/2021. Presentes to ED on 9/2/2021 with complaints of illness for 5 days with symptoms of nausea, vomiting, diarrhea, chills and subjective fever. Also reports COVID-19 exposure. Patient admitted. At time of admission no respiratory symptoms, SpO2 of 98%. Patient reports dyspnea on 9/6, with need for O2 via nasal cannula. Patient experiences desturation on 9/11 requiring 7 L/min (SpO2 = 93%). On 9/12 requiring 60L FiO2 70%. On 9/13 60L FiO2 86% with an SpO2 of 100%. On 9/14, while receiving HFNC at 50L 80% patient desats to 80%. Patient transitioned to comfort care. Patient expired on 9/16/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 15,0
Labordaten: COVID-19 Positive on 9/2/2021 using PCR or other technology.
Aktuelle Erkrankungen: -
Vorgeschichte: CLL, Acute cystitis without hematuria, Acute kidney injury, Chemotherapy induced neutropenia, Anemia, Sepsis, UTI, DM
Andere Medikamente: Amlodipine, Aspirin, Carvedilol, Furosemide, Ibrutinib, insulin glargine, metoprolol.
Allergien: Adhesive, Codeine, Penicillin, Promethazine, Sulfa, Novacare, Tetracycline
Vorherige Impfungen: -

VAERS 1727253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: KY
Alter: 27,0
Geschlecht: M
Eingang: 23.09.2021
Impfdatum: 14.09.2021
Beginn: 14.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / UN

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

Death Vomiting

Symptomtext

Patient's grandmother found him dead in the bathroom 4 to 4:30 hours after his vaccine. She was not aware of him having complaints. He had vomited in the commode -that was the only comment that she had.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: none.
Aktuelle Erkrankungen: HIV and Opioid DO,Tricuspid Prosthetic valve endocarditis. His grandmother found him dead on 9/14 8 to 8:30 pm. She said it looked like he had vomited in the commode. She did not use Narcan on him and denied that she saw evidence of drug use. She called 911 and EMS /coroner did not think an autopsy was appropriate and said "he had heart disease ".
Vorgeschichte: HIV, Hep C - status treatment, Prosthetic TV endocarditis, Treated with IV cefazolin and then linezolid, He received sublacade previously for his Opioid use DO, ( last dose of sublacade 7/30/21).
Andere Medikamente: Biktarvy, Albuterol, Advair, Lopressor, Sublocade - (last dose 7/30/21).
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1628284

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: TX
Alter: 42,0
Geschlecht: F
Eingang: 24.08.2021
Impfdatum: 02.06.2021
Beginn: 20.06.2021
Tage bis Beginn: 18,0
Dosis: 1
Route/Site: IM / LA

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

Blood glucose increased Blood test abnormal Cardiac arrest Hyperkalaemia Hypotension Unresponsive to stimuli

Symptomtext

Cardiac arrest. Presented via EMS after niece found her unresponsive at home. Per EMS patient was hypotensive with blood glucose of 450 in the field. She was then given 1 L of IV fluids with improvement in her blood pressure. On Arrival to the ED patient was noted to be in a wide complex rhythm with initial blood work showing hyperkalemia. Patient subsequently had a cardiac arrest and was treated with epinephrine, bicarbonate therapy, calcium, insulin with ROSC 6 minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Congestive heart failure, hypertension, end stage renal disease on hemodialysis, diabetes mellitus type 2.
Andere Medikamente: Amlodipine 10mg daily, Insulin Glargine, Warfarin, Atorvastatin 40mg daily, Calcium Acetate 667mg capsule 3 caps 3 times a day, carvedilol 25mg tablet twice a day, Sodium Bicarbonate 650mg tablet 2 tablets twice a day.
Allergien: None listed
Vorherige Impfungen: -

VAERS 1583033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: IL
Alter: 79,0
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 15.07.2021
Beginn: 09.08.2021
Tage bis Beginn: 25,0
Dosis: 2
Route/Site: IM / RA

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

Angiogram cerebral normal Anticoagulant therapy Arteriogram carotid normal Bradycardia Cerebral infarction Cerebrovascular accident Computerised tomogram head abnormal Condition aggravated Echocardiogram abnormal Ejection fraction normal Grip strength decreased Magnetic resonance imaging head abnormal Muscular weakness Tricuspid valve incompetence

Symptomtext

Patient with CVA on 8/9/2021 and would like reported for monitoring. "HPI per admitting physician with additions: "Pt is a 79-year-old female With past medical history significant for CVA, HTN, GERD, presents to be evaluated for arm weakness. Pt states that yesterday evening she began experiencing right arm weakness and was unable to hold utensils or a pen. Pt denies other weakness, numbness, tingling, fever, chills, cp, sob, emesis, diarrhea etc. SHe does not take blood thinners. She had expecting the symptoms to improve but they did not so she came to the emergency room for further evaluation and treatment. In the ER CT revealed an old MCA territory infarct and a left frontoparietal hypodensity suspicious for subacute infarction. Telemetry neurology was consulted and did not recommend any aspirin or Plavix. Patient was also bradycardic down to the 50s at times in the emergency room." CVA Patient presented with right arm weakness, inability to hold utensils or pen on presentation CT showed subacute left frontoparietal infarct, old right temporal lobe infarct also seen. Telemetry Neurochecks Fall precautions MRI of the brain showed acute watershed infarct at the left subcortical central sulcus, no hemorrhagic transformation. MRA of the head and neck showed no evidence of significant stenosis, dissection or aneurysm Echocardiogram showed LVEF of 65 to 70%, no evidence of shunting, mild tricuspid regurgitation. Neurology was consulted: Recommended aspirin 81 mg and Plavix for at least 3 months, discontinued Crestor and start atorvastatin 81 mg for 6 months. Neurology also recommended event monitor and cardiology follow-up as outpatient. Cardiology was consulted and plan to send event monitor to patient's home. Patient was recommended to follow-up with neurology in 2 to 3 weeks. 8/11 patient was evaluated by PT/OT and speech, and found not to have further skilled needs at this time. Patient's hand grip and arm weakness have improved. She was discharged with follow-up plan as above. Recommended medications were sent to her pharmacy"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 2,0
Labordaten: see above
Aktuelle Erkrankungen: none
Vorgeschichte: Anxiety, chronic pain, HTN, HLP, hx of CVA, CLL, GERD, RBBB, hx of DVT, LBP
Andere Medikamente: Xanax 1 mg, ASA 81, crestor 20, lasix 20, mobic 15, metformin 500, tramadol 50
Allergien: tylenol, PCN, morphine, codeine, fent, meperidine
Vorherige Impfungen: -

VAERS 1522915

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: NJ
Alter: 48,0
Geschlecht: F
Eingang: 04.08.2021
Impfdatum: 02.06.2021
Beginn: 10.07.2021
Tage bis Beginn: 38,0
Dosis: 2
Route/Site: - / LA

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

Cerebrovascular accident Computerised tomogram abnormal Impaired work ability Loss of personal independence in daily activities Magnetic resonance imaging abnormal Mobility decreased

Symptomtext

I had a stroke 5 weeks after my Pfizer second dose.; This is a spontaneous report from a contactable consumer (patient). A 48-year-old female (non-pregnant) patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EW0179), via an unspecified route of administration at the age of 48-year-old administered in arm left on 02Jun2021 09:00 at single dose for covid-19 immunisation. Medical history and concomitant medications were reported as none. There was no Covid prior vaccination. There was no other vaccine in four weeks. There was no Covid tested post vaccination. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EW0165) at the age of 48-year-old at left arm on 11May2021 09:00 AM for COVID-19 immunisation. The patient had a stroke 5 weeks after my Pfizer second dose on 10Jul2021. She was a healthy 48 years old active person and a stroke was highly unusual at her age. Her family and she were devastated. she went from having no medical conditions to now being on maintenance medication and needing follow up care with a neurologist, cardiologist, haematologist, and vascular surgeon, all in the blink of an eye. She want you to investigate the lot that she received and to study how your Pfizer vaccine led to her stroke during the prime of her life. The patient was hospitalized for 2 days. Adverse event resulted in doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, hospitalization, Life threatening illness (immediate risk of death from the event), disability or permanent damage. Facility type vaccine was reported as other. The patient received treatment for event. The outcome of events was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1522915

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: NJ
Alter: 48,0
Geschlecht: F
Eingang: 04.08.2021
Impfdatum: 02.06.2021
Beginn: 10.07.2021
Tage bis Beginn: 38,0
Dosis: 2
Route/Site: SYR / LA

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

Cerebrovascular accident Computerised tomogram abnormal Impaired work ability Loss of personal independence in daily activities Magnetic resonance imaging abnormal Mobility decreased

Symptomtext

I had a stroke 5 weeks after my Pfizer second dose.; This is a spontaneous report from a contactable consumer (patient). A 48-year-old female (non-pregnant) patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EW0179), via an unspecified route of administration at the age of 48-year-old administered in arm left on 02Jun2021 09:00 at single dose for covid-19 immunisation. Medical history and concomitant medications were reported as none. There was no Covid prior vaccination. There was no other vaccine in four weeks. There was no Covid tested post vaccination. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EW0165) at the age of 48-year-old at left arm on 11May2021 09:00 AM for COVID-19 immunisation. The patient had a stroke 5 weeks after my Pfizer second dose on 10Jul2021. She was a healthy 48 years old active person and a stroke was highly unusual at her age. Her family and she were devastated. she went from having no medical conditions to now being on maintenance medication and needing follow up care with a neurologist, cardiologist, haematologist, and vascular surgeon, all in the blink of an eye. She want you to investigate the lot that she received and to study how your Pfizer vaccine led to her stroke during the prime of her life. The patient was hospitalized for 2 days. Adverse event resulted in doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, hospitalization, Life threatening illness (immediate risk of death from the event), disability or permanent damage. Facility type vaccine was reported as other. The patient received treatment for event. The outcome of events was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1474379

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: KY
Alter: 54,0
Geschlecht: M
Eingang: 30.07.2021
Impfdatum: 05.05.2021
Beginn: 11.06.2021
Tage bis Beginn: 37,0
Dosis: UNK
Route/Site: - / LA

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

Abdominal pain Aspiration pleural cavity Autopsy Biopsy bone marrow Blood test abnormal Catheterisation cardiac Computerised tomogram Death Decreased appetite Eosinophil count increased Inflammation Myocarditis Nausea Night sweats Paraesthesia Pericardial effusion Pleural effusion Pyrexia

Symptomtext

See Attachments

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: See Attachments
Aktuelle Erkrankungen: None resulted into heart issues
Vorgeschichte: Asthma; Leukocytosis
Andere Medikamente: See Attachment
Allergien: KNDA
Vorherige Impfungen: -

VAERS 1478465

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: FL
Alter: 69,0
Geschlecht: F
Eingang: 16.07.2021
Impfdatum: 07.05.2021
Beginn: 11.07.2021
Tage bis Beginn: 65,0
Dosis: 2
Route/Site: IM / -

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

Acute respiratory failure COVID-19 Dyspnoea SARS-CoV-2 test positive Viral sepsis

Symptomtext

7.11.21: Patient presents to ER with shortness of breath. Has history of receiving Pfizer COVID-19 vaccine on 4/16/21. Found to be hypoxic and COVID-19 positive. diagnosed with acute hypoxic respiratory failure and viral sepsis due to COVID. Started Remdesivir. 7.15.21: completed 5 day course of remdesivir. discharged home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: SARS CoV 2 PCR Detected 7/11/2021
Aktuelle Erkrankungen: -
Vorgeschichte: diabetes, asthma, and hypertension
Andere Medikamente: gabapentin,atorvastatin,bumex,coreg,humalog,glipizide,levothyr
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1463311

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: IL
Alter: 54,0
Geschlecht: F
Eingang: 11.07.2021
Impfdatum: 14.05.2021
Beginn: 01.05.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Arthritis Asthenia Bladder disorder C-reactive protein Cardiac arrest Claustrophobia Computerised tomogram Condition aggravated Contusion Deafness Dehydration Fear Gait disturbance Immobile Investigation Magnetic resonance imaging Nerve injury Pain

Symptomtext

bruises on her ribcage; heart stopped; weakness; uncontrollable urine; dehydrated; couldn't get up off the floor/having trouble walking; they weren't sure what was going on with her, her bladder; downhill from there; couldn't get out of car; can't hold the phone very long, and can't sit up for very long either; hearing loss and can't hear the consonants; superficial blood clot in left leg; L5 compression fracture; claustrophobic; had a hard time pronouncing the letters; affected all of her nerves/all the nerve damage; arthritis everywhere; scaring her; very painful/physical in pain; This is a spontaneous report from a contactable consumer (patient). A 54-year-old female patient received the second dose of BNT162B2 (PFIZER COVID-19 VACCINE, lot number: EW0179), at the age of 54 years old, in left arm on 14May2021 at single dose for COVID-19 immunisation. Medical history included post-traumatic stress disorder (PTSD) (diagnosed in 1995, 1996, 2000, been for years, unsure of exact year), bipolar disorder (a mental disorder; a cross between bipolar disorder and PTSD; last hospitalization for this was in Jan2019), carpal tunnel in right and left hand (being treated for this prior to the shot), lower back injury (took paracetamol (TYLENOL) for a lower back injury from about 30 years ago, she fell down a flight down of stairs with her daughter, when she was first born, states her daughter will be 34 at the end of this month. Caller stated she saw an orthopedic doctor, who said not to do anything about it, just keep taking what she's taking), blood pressure abnormal (diagnosed about 5-7 years ago), diabetic non-insulin dependent from 2015 (also provided hypoglycemia as a medical condition), sleep apnea (diagnosed about 15 years ago), history of blood clots, allergies to two muscle relaxers (unknown drug name), fall in Apr2021 (Sunday, being treated). Concomitant medications included lorazepam (ATIVAN) taken for PTSD and mental disorder at 0.25 mg three times a day as needed, paracetamol taken for carpal tunnel, general pain and back injury at 1000 mg every day in the morning, and furosemide for blood pressure abnormal at 40 mg daily as needed; usually takes half, 20 mg. The patient previously received the first dose of BNT162B2 (lot number: EW0169), at the age of 54 years old, in left arm on 23Apr2021 at single dose for COVID-19 immunisation and experienced some events. Caller stated she took the first shot on 23Apr2021, and didn't have too bad of reaction, just like a little bit of the flu. Caller stated in between first shot and just before the second shot, she had some reactions, and in and out of the hospital quite a few times, trying to figure out what was going on. Caller stated she was at hospital on 13Apr2021, 14Apr2021, and then 15Apr2021. Caller stated they had to code her, she'd been unable to work, it had set off arthritis from the top of her head to the bottom of her feet, it's pretty much crippled her to point to where they'd figured out that it was the covid shot that the side effects. Caller stated she just saw her family doctor yesterday, finally able to go in and see her physically, and she had piles of paperwork she'd having to go through, and that was why she started back with paperwork from hospital, dated 15Apr2021. Caller stated she had the shot on 23Apr2021. Caller confirmed first shot was 23Apr2021. Caller stated there was more, it was just started a bunch of things, she was got stacks of papers, and she was sicker than a dog right now, because she got an infection just after, not sure if it was tied into this. Caller stated she was having trouble thinking at times, had caused nerve damage, where she could barely hold the phone. Caller stated she was pretty much grounded; this was the first time she'd been able to get into her apartment, because she couldn't get up the stairs, so she had all the time in the world right now. Caller stated she was a home health aide, clarifies not a nurse. But she'd recently been working, and was emailed papers for the type of leave for COVID-19, and extended leave of absence from work. Caller stated the last time she worked was 05Apr2021, seventh, ninth, tenth, something like that. Caller stated she could't think right now; she'd in and out of it due to medications. Caller provided a health department as healthcare professional site. Caller added on 15Apr2021, she had family and her boyfriend, someone tested positive, so from 13Apr until 27Apr, she quarantined herself in a hotel, close to her work. Caller initially provided date of second dose as three weeks after first dose on 15May2021, but then clarified correct date as 14May2021. Caller stated she was just taking her normal medications, and stated she did not want to go through those at this minute. Caller stated she had an appointment to get first shot, but they spelled her name wrong, and a VIP thing had to be done. Before she went to get the shot she was trying to ask the medical doctor some questions because she had concerns, but before she could tell them any part of her history, the doctor just said to go ahead and gave her the shot. Caller stated the reason she got the number for Pfizer was from when, on 15Apr2021, they tested her for covid, and gave her instructions, she was off of work. Caller clarified she never got a phone call, when agent asked for test results of the test. Caller confirmed this test was done before her shot. Caller stated she got first shot and a couple days later, it was the normal flu-like body aches; she was told to got to store and get stuff for allergies, and for the flu, but she already had paracetamol and diphenhydramine hydrochloride (BENADRYL) for allergies. Caller clarified she was told this by the site which gave the shot, had them sit down and wait 15-20 minutes, then let them go, and told them what to do. Caller stated these symptoms only lasted a couple of days. Caller stated that she didn't remember if she actually took the paracetamol and diphenhydramine hydrochloride as treatment for the flu-like body aches. Caller stated that she had all this paperwork that was going back to 15Apr2021, and she did not remember at the moment what she took for treatment of symptoms. Caller states she had everything journaled written down, stated in between the first and second shot, she was in and out of emergency rooms, trying to figure out what was going on. States she had to go back she was having reactions, she was in the emergency room for weakness, and other things, and had to be checked for blood clots, so she had to go back. She was there on 13May2021, 14May2021, they did a venous doppler on everything because she was having all kinds of pain in legs. Then on 15May2021, she had to go back to be checked for something, right after she got out of emergency room, and after she had the test, she was medically transferred to get the second shot (corrected on 14May2021), and after she got the second shot, it's been downhill from there. Caller stated she was admitted into a hospital and was in and out of the hospital. Caller stated she coded, they had to do CPR on her, and this had affected all of her nerves. Caller stated they gave both shots in her left arm and it had set off everything and all the nerve damage. Caller stated this was scaring her because she was the only family member who had the Pfizer shot. Everybody else was out of the state, and had the Johnson and Johnson or all the other vaccines, and she was the only one who'd this shot, and the one who had the most damage. Call handler made multiple attempts to clarify information provided and get further details but asked to move on because all the questions were setting her off. Caller stated maybe she should have had the case worker call. Caller clarified she did not have arthritis prior to this. Caller stated 31May2021, she was rushed to a hospital because she couldn't get up off the floor, they weren't sure what was going on with her, her bladder, so they put her on prednisone for a week. Caller did not finish statement regarding her bladder. Caller stated all hospitals she had been in, with exception of one. Caller provided a hospital when agent asked for spelling or clarification. Caller stated she could't hold the phone very long, and she can't sit up for very long either. Caller stated she had a hard time pronouncing the letters, when agent asked her to spell the hospital name. Caller stated the problem was agent was on a headset and her phone was set up for handicap for an ear that could't hear properly, so she stated the agent being on a headset was why agent could't hear her. Caller stated she had hearing loss and could't hear the consonants. Caller stated she was due to take medicine and could't take it while on the phone. Caller asked if there a fax number to fax the rest of this to. Caller stated all of the hospitals were all under a health, it was a whole medical group with all different hospitals in different towns. Caller stated prior to emergency room visit, she was in a hospital because she couldn't walk, was having trouble walking. She coded while they were admitting her; her heart stopped and they had to code her. Caller added she had not had a paycheck since 09Apr2021 or tenth, stated landlord hadn't thrown her out but she'd close to being evicted because she hadn't worked, it was been determined the side effects have caused more damage. Caller stated 15Apr2021 she got Pfizer's phone number when she was tested for covid. Caller stated that was when they did the test, but she never heard anything back regarding the results of the test. She quarantined at a hotel and had to be away from work. Caller stated it was been a hospital where it started. Caller stated maybe agent needed to call back and finish report because she had all of hospital papers dissected with dates. Caller stated she was given a huge packet on 15Apr2021, when she was tested for covid. Went to the only local medical facility, and she went there on 15Apr2021 because her boyfriend's sons' girlfriend tested positive, and they gave her a note for her work with instructions. Caller clarified they gave her a huge packet so that was where she got all the paperwork in Apr2021 before she got the shot. Caller stated after the first shot she had 48 hours of hot flashes, the chills, typical flu-like symptoms; only lasted 48 hours, and then from the twenty third she had different symptoms, and had been in an out of hospitals, trying to figure out what was going on with her. Caller stated she was healthy and working until 07Apr2021, 08Apr2021, or 09Apr2021, was the last time she worked. Then she quarantined from 13Apr2021 until 27Apr2021, and then they had to get vaccinated, so she registered, and when she went there, they spelled her name wrong, she started asking questions trying to give medical history before the shot. She had not given any of her history and doctor said to just give it. They gave the shot in her left arm and from then on, the damage hit and it has been one thing after another. Caller stated she previously had a test done in 2017, electrical shock from toes to head, and acupuncture same day, and only thing showed up was carpal tunnel in right and left hand. She was being treated with 1000 mg paracetamol, and she was fine working since 2018. Caller stated she was physically fine and is 54 years old, the oldest one working there and now she'd been back and forth from hospitals. Caller stated she was in the hospital with weakness 10Jun2021 or 07Jun2021. Caller stated this had been a continuous thing going to hospitals for weakness, bladder is just letting go like just having uncontrollable urine, she got dehydrated. She only had to be inpatient at hospital. Caller stated right after admitted there, primary doctors found a superficial blood clot in left leg and started her on rivaroxaban (XARELTO), and they discharged her and transferred her by med car from main hospital to the emergency room satellite. She was there to do an MRI and had to sedate her because she was claustrophobic. They found an L5 compression fracture, which caller clarified was new since the shot. Caller stated the back specialist said not going to do anything it, it will heal on it was own. Caller stated she was sent to get her car and had a major allergic reaction to a drug given while in hospital but the nurse didn't listen, they let her drive her car, which is satellite for hospital. Caller stated she stopped, paid for diphenhydramine hydrochloride and had to park the car while she took two diphenhydramine hydrochloride for having major symptoms. Caller stated when she felt she was ok, she drove back to hotel, but when she got there, she couldn't get out of car so the manager called 911, and withheld came and assessed her. Her cognitive level was fine, but she was sitting in urine and couldn't get out of car, so they rushed her to a hospital and she was admitted on an orthopedic floor, this was 20May2021 or 21May2021, and she went unresponsive while they were admitting her, so they coded her. Caller stated that she still had bruises on her ribcage. A cardiologist came and actually he listened to her. They did three different cat scans and determined that she now has arthritis everywhere. It's very painful. States that she is sitting with 5 piles of paperwork from 15Apr to her most current one which would have been at hospital just a couple of days ago. She has been diagnosed with so many different things because the doctor's couldn't figure out what was going on. Call handler attempted to query the name of the medication that caused her allergic reaction. Caller stated that there are 4 medications that she reacts to, two are muscle relaxers that she was allergic to, and one of them was given to her at a hospital. Caller stated that the problem was that people looked at your mental disabilities first, they did't look at your other history, and nurses were over worked, so even though she told the nurse to call her doctor because she was having a major reaction and she knew what it was, they were still discharging her. Call handler again asked for the name of the product. Caller became upset and stated that she was physically in pain. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: Test Name: CAT scan; Result Unstructured Data: Test Result:Arthritis everywhere; Test Name: CPR; Result Unstructured Data: Test Result:affected all of her nerves; Test Date: 2017; Test Name: Test; Result Unstructured Data: Test Result:carpal tunnel in right and left hand; Comments: electrical shock from toes to head, and acupuncture same day, and only thing showed up was carpal tunnel in right and left hand; Test Date: 20210515; Test Name: Test; Result Unstructured Data: Test Result:unknown; Test Name: MRI; Result Unstructured Data: Test Result:L5 compression fracture; Test Date: 20210415; Test Name: Covid-19; Test Result: Positive ; Comments: Caller adds on 15Apr, she had family and her boyfriend, someone tested positive.; Test Date: 202105; Test Name: venous doppler; Result Unstructured Data: Test Result:unknown; Comments: on everything because she was having all kinds of pain in legs
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Back injury (from about 30 years ago, she fell down a flight down of stairs with her daughter, took Tylenol); Bipolar disorder (a mental disorder; a cross between bipolar disorder and PTSD; hospitalized in Jan2019); Blood pressure abnormal (diagnosed about 5-7 years ago); Carpal tunnel syndrome (being treated for this prior to the shot); Clot blood; Diabetes mellitus non-insulin-dependent (Also provided hypoglycemia as a medical condition); Drug allergy (unknown drug name); Fall (being treated); Hypoglycemia; Post-traumatic stress disorder (diagnosed in 1995, 1996, 2000, been for years, unsure of exact year); Sleep apnea (diagnosed about 15 years ago)
Andere Medikamente: ATIVAN; TYLENOL; FUROSEMIDE
Allergien: -
Vorherige Impfungen: -

VAERS 1460062

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: NY
Alter: 42,0
Geschlecht: F
Eingang: 09.07.2021
Impfdatum: 01.06.2021
Beginn: 01.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Anaphylactic shock Electrocardiogram abnormal Full blood count Pericarditis Swelling face Urticaria

Symptomtext

Hives swollen face and got anaphylactic shock bith both 1 and 2 series of pfizer vaccine Also got pericarditis was treated with predisone and benadryl also with an ansthma inhaler and got referred to see a cardiologist to check my heart because EKG showed possible LEft Atrial Enlargement but tests showed no LAE it is pericarditis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic shock
Hospital-Tage: -
Labordaten: Date of medical tests 6/1/21 and 6/22/21 Ekg 6-1-21 Cbc 6-1-21 EKG 6-22-21 Results showed LEft atrial enlargement Anaphylactic shock 6-1-21 and 6-22-21 Cbc 6-22-21
Aktuelle Erkrankungen: No illnesses
Vorgeschichte: Diabetic
Andere Medikamente: None
Allergien: Shell fish allergies
Vorherige Impfungen: -

VAERS 1443199

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: WI
Alter: 33,0
Geschlecht: F
Eingang: 02.07.2021
Impfdatum: 25.05.2021
Beginn: 30.06.2021
Tage bis Beginn: 36,0
Dosis: 1
Route/Site: IM / LA

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

Exposure during pregnancy Foetal death Foetal hypokinesia Headache Induced labour

Symptomtext

Subjective: 33-year-old G4 P3 @36w5d presents for admission due to fetal demise diagnosed in clinic earlier today. Her pregnancy is complicated by hypothyroid, obesity, h/o LTCS with subsequent VBAC x 2, h/o GDM with normal screen this pregnancy, h/o preeclampsia in prior prgnancy, COVID this pregnancy. PNC with doctor. Patient called the office this morning noting lack of fetal movement. She believes she felt baby last night but is unsure. Possibly the last time was this weekend. She denies contractions, vaginal bleeding, LOF, fever, chills. Has mild HA now but that just started since being admitted. BP in office 160/94. Now normal.

Weitere VAERSDATA-Felder

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

VAERS 1413517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: NY
Alter: 60,0
Geschlecht: M
Eingang: 20.06.2021
Impfdatum: 08.05.2021
Beginn: 16.05.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: IM / RA

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

Angiogram cerebral normal Chest pain Cognitive disorder Computerised tomogram head normal Electroencephalogram Gait disturbance Loss of consciousness Lumbar puncture normal Magnetic resonance imaging head normal Neurological symptom Neuromyopathy Pulse absent Respiratory arrest Resuscitation Unresponsive to stimuli Walking aid user

Symptomtext

Started to have chest pains a few days after vaccine. I passed out and was unresponsive with no pulse and breathing. Received cpr from my partner who found me on the floor at approximately 2:00am on 5/16/21. I was taken to the emergency room of the hospital and underwent extensive tests of the brain: CT scan, MRI, Angiogram, and Spinal Puncture. All tests negative. I cannot walk without a walker and have other cognitive neurological symptoms. I was discharged from hospital on 6/2/21 to sub-acute rehabilitation facility. I was discharged from rehab on 6/12/21. Neurological and neuromuscular symptoms are still present.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory arrest
Hospital-Tage: 18,0
Labordaten: CT scan, MRI, Angiogram, EEG, Lumbar Puncture
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D3, Vitamin B12
Allergien: None
Vorherige Impfungen: -

VAERS 1354936

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: NJ
Alter: 35,0
Geschlecht: M
Eingang: 08.06.2021
Impfdatum: 29.04.2021
Beginn: 12.05.2021
Tage bis Beginn: 13,0
Dosis: 2
Route/Site: - / LA

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

Cardiac failure Catheterisation cardiac abnormal Chest discomfort Coronary artery occlusion Electrocardiogram abnormal Heart rate increased Myocardial infarction Stent placement SARS-CoV-2 test negative

Symptomtext

About 2 weeks after second dose, experienced heart attack with complete blockage of LAD artery, requiring cardiac catheterization with two stents.; This is a spontaneous report from a contactable consumer (patient). A 35-year-old male patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration, administered in arm left on 29Apr2021 12:45 (Batch/Lot Number: EW0179) as single dose at the age of 35-year-old for COVID-19 immunisation, administered at School. Medical history included pre-diabetic. Patient had not COVID prior vaccination. Concomitant medication(s) included budesonide, formoterol fumarate (SYMBICORT, Inhaler) taken for an unspecified indication, start and stop date were not reported. The patient previously took garlic [allium sativum] and experienced drug hypersensitivity. Vaccine history included bnt162b2 (BNT162B2), dose 1 in right arm on 08Apr2021 02:30 PM (Batch/Lot Number EW0158) for COVID-19 immunisation. No other vaccine in four weeks. About 2 weeks after second dose, on 12May2021 the patient experienced heart attack with complete blockage of LAD artery, requiring cardiac catheterization with two stents. The event resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Hospitalization, Life threatening illness. The event resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care, hospitalization, life threatening illness. The event outcome was recovered with sequelae. The patient was hospitalized for the events for 4 days. The patient underwent lab tests and procedures which included: Sars-cov-2 test (nasal swab): negative on 14May2021. Therapeutic measures were taken as a result of the event, which required cardiac catheterization with two stents.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 4,0
Labordaten: Test Date: 20210514; Test Name: Nasal Swab; Test Result: Negative ; Comments: nasal swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pre-diabetic
Andere Medikamente: SYMBICORT
Allergien: -
Vorherige Impfungen: -

VAERS 1354936

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: NJ
Alter: 35,0
Geschlecht: M
Eingang: 08.06.2021
Impfdatum: 29.04.2021
Beginn: 12.05.2021
Tage bis Beginn: 13,0
Dosis: 2
Route/Site: SYR / LA

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

Cardiac failure Catheterisation cardiac abnormal Chest discomfort Coronary artery occlusion Electrocardiogram abnormal Heart rate increased Myocardial infarction Stent placement SARS-CoV-2 test negative

Symptomtext

About 2 weeks after second dose, experienced heart attack with complete blockage of LAD artery, requiring cardiac catheterization with two stents.; This is a spontaneous report from a contactable consumer (patient). A 35-year-old male patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration, administered in arm left on 29Apr2021 12:45 (Batch/Lot Number: EW0179) as single dose at the age of 35-year-old for COVID-19 immunisation, administered at School. Medical history included pre-diabetic. Patient had not COVID prior vaccination. Concomitant medication(s) included budesonide, formoterol fumarate (SYMBICORT, Inhaler) taken for an unspecified indication, start and stop date were not reported. The patient previously took garlic [allium sativum] and experienced drug hypersensitivity. Vaccine history included bnt162b2 (BNT162B2), dose 1 in right arm on 08Apr2021 02:30 PM (Batch/Lot Number EW0158) for COVID-19 immunisation. No other vaccine in four weeks. About 2 weeks after second dose, on 12May2021 the patient experienced heart attack with complete blockage of LAD artery, requiring cardiac catheterization with two stents. The event resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Hospitalization, Life threatening illness. The event resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care, hospitalization, life threatening illness. The event outcome was recovered with sequelae. The patient was hospitalized for the events for 4 days. The patient underwent lab tests and procedures which included: Sars-cov-2 test (nasal swab): negative on 14May2021. Therapeutic measures were taken as a result of the event, which required cardiac catheterization with two stents.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 4,0
Labordaten: Test Date: 20210514; Test Name: Nasal Swab; Test Result: Negative ; Comments: nasal swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pre-diabetic
Andere Medikamente: SYMBICORT
Allergien: -
Vorherige Impfungen: -

VAERS 1371183

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 03.06.2021
Impfdatum: 04.05.2021
Beginn: 22.05.2021
Tage bis Beginn: 18,0
Dosis: 2
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure Blood creatinine increased COVID-19 Convalescent plasma transfusion Endotracheal intubation Fibrin D dimer increased Intensive care SARS-CoV-2 antibody test SARS-CoV-2 test positive

Symptomtext

57 YO female pt presented to outside institution on 5/22 with acute respiratory failure, found to be COVID positive, also w AKI on admission (Cr 4.9). Denies cough, sputum production or fevers at home prior to presentation. She was intubated on arrival to outside institution 5/22 and admitted to ICU. She has been treated with dexamethasone 6mg IV and Remdesivir x1, convalescent plasma. Treated with empiric vanc/zosyn since admission for possible superimposed bacterial PNA. Also were empirically treating for PE due to elevated D-dimer though no CTPE. Transferred to this institution on 5/28. Pt is s/p mRNA vaccination on 4/13 and 5/4, but on immunosuppression with mycophenolate + sirolimus + prednisone...

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: COVID-19 IGG - SARS-COV-2 Spike (S) Protein Antibody NOT detected (5/28/2021) Novel Coronavirus PCR - SARS-COV-2 detected (5/28/2021)
Aktuelle Erkrankungen: -
Vorgeschichte: ESRD 2/2 diabetes s/p renal transplant (2014) now with CKD IV of transplant kidney, DM, HLD, HTN, and GERD
Andere Medikamente: Mycophenolate + sirolimus + prednisone + cyclosporine
Allergien: Lisinopril, losartan, tuberculin purified protein derivative
Vorherige Impfungen: -

VAERS 1368544

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: -
Alter: 77,0
Geschlecht: F
Eingang: 02.06.2021
Impfdatum: 07.05.2021
Beginn: 13.05.2021
Tage bis Beginn: 6,0
Dosis: UNK
Route/Site: IM / LA

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

Sepsis Septic shock

Symptomtext

Patient presented to the ED and was subsequently hospitalized for Severe sepsis with septic shock within 6 weeks of receiving COVID vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Septic shock
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1361858

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: MI
Alter: 42,0
Geschlecht: F
Eingang: 30.05.2021
Impfdatum: 01.05.2021
Beginn: 10.05.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: IM / RA

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

Blood test Computerised tomogram Coronary artery dissection Echocardiogram Electrocardiogram Magnetic resonance imaging Myocardial infarction

Symptomtext

Admitted to the hospital for 5 days after ER visit. Had a heart attack. Was diagnosed with spontaneous coronary artery dissection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 5,0
Labordaten: From 5/10-5/15 was at the hospital. Had CT, Echos, MRI, EKGs, numerous blood tests.
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: NA
Allergien: NA
Vorherige Impfungen: -

VAERS 1360838

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: -
Alter: 57,0
Geschlecht: M
Eingang: 29.05.2021
Impfdatum: 17.05.2021
Beginn: 20.05.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RA

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

Anticoagulant therapy Chest pain Cough Deep vein thrombosis Dyspnoea Echocardiogram abnormal Full blood count Haemoptysis Leukocytosis Murphy's sign test Pneumonia Pulmonary embolism SARS-CoV-2 test negative Sepsis Supraventricular tachycardia Tachypnoea Ultrasound abdomen normal

Symptomtext

Presented to ED with complaint of chest pain onset 0800 this morning. He endorse shortness of breath and a cough that has been ongoing for three weeks.Patient even at rest has significant tachypnea usually in the 40s and sometimes even into the 50s breaths per minute. Sepsis present on admission. COVID-19 infection was diagnosed on the eighth of this month, now is negative. Has been on a ceftriaxone and azithromycin. Could be due to multifocal pneumonia and PE. Changed to cefuroxime,7-day course. Leukocytosis could be due to steroids, recommend to repeat CBC in about a week. Multifocal pneumonia: With underlying COVID-19 diagnosed on the eighth, now is negative. Completed azithromycin for 3 days and was on a ceftriaxone, changed to p.o. cefuroxime on antibiotic for suspicion for secondary bacterial infection, will complete the course. Acute bilateral pulmonary emboli: on Xarelto. Echo reviewed. Mild hemoptysis: Could be due to pulmonary emboli, infarcts, remains on anticoagulation. No recurrence. Left lower extremity DVT/SVT: Anticoagulation as above. Transaminitis: Denies use of alcohol, he has some nonspecific complaint on the right sided abdomen but negative Murphy and ultrasound shows normal gallbladder, normal liver, stable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1350702

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: CA
Alter: 31,0
Geschlecht: F
Eingang: 26.05.2021
Impfdatum: 11.05.2021
Beginn: 20.05.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: IM / RA

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

Blood homocysteine normal Cardiolipin antibody Chest pain Coagulation factor V level normal Computerised tomogram thorax abnormal Dyspnoea Fibrin D dimer increased Liver function test normal Platelet count normal Protein C Protein S normal Prothrombin level normal Prothrombin time prolonged Pulmonary embolism Renal function test normal SARS-CoV-2 test negative Ultrasound Doppler normal

Symptomtext

A 31=year-old female received the first dose of mRNA Covid-19 vaccine (EW0179, Pfizer) IM on May 11th, 2021, without any reported clinical problem. Patient has no known medical illness and no previous history of DVT or PE. Patient had negative COVID-19 PCR on April 16th, 2021. She had 3 healthy pregnancies and no miscarriages. She did not have any long flights or car rides for the last several months, except for over 2 months ago. Patient denies any allergic problems, smoking tobacco or use any oral contraceptives. However, patient stated patient's father has a history of unprovoked DVT. On May 20th, 2021 patient experienced worsening of left-sided chest pain and shortness and visit ED on May 22nd, 2021. At the ED, physical examination was unremarkable. Blood tests (renal, hepatic function) were normal and labs resulted in D-dimer 0.86 mcg (FEU)/mL and platelet count 288k (Baseline of 200-250k). CT showed suspected very subtle segmental and subsegmental PE involving the left lower lobe. Duplex did not show evidence of DVT in either lower extremity. Given the family history of DVT, hypercoaguable workup was done with the following results: homocysteine level 5.5, thrombin time 14.9, negative factor II and V mutations, cardiolipin Ab IgG < 1.6 GPL (normal range < 20 GPL), lupus anticoagulant with reflex indeterminate, protein C activity 92 (normal range 70-130%) and protein S activity 67 (normal range 65-140%). Patient was admitted to the hospital. At the ED, enoxaparin 60 mg x 1 and morphine 4 mg x 1 were given. Later, it was switched to apixaban 10 mg BID on the floor and patient was discharged with apixaban 5 mg BID x 7 days and once daily BID. Patient is scheduled to follow up with her PCP in regards to the duration of therapy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: At the ED (5/22/2021), physical examination was unremarkable. Blood tests (renal, hepatic function) were normal and labs resulted in D-dimer 0.86 mcg (FEU)/mL and platelet count 288k (Baseline of 200-250k). CT showed suspected very subtle segmental and subsegmental PE involving the left lower lobe. Duplex did not show evidence of DVT in either lower extremity. Given the family history of DVT, hypercoaguable workup was done with the following results: homocysteine level 5.5, thrombin time 14.9, negative factor II and V mutations, cardiolipin Ab IgG < 1.6 GPL (normal range < 20 GPL), lupus anticoagulant with reflex indeterminate, protein C activity 92 (normal range 70-130%) and protein S activity 67 (normal range 65-140%).
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1342247

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: CO
Alter: 41,0
Geschlecht: M
Eingang: 23.05.2021
Impfdatum: 09.04.2021
Beginn: 10.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Acute myocardial infarction Catheterisation cardiac abnormal Chest pain Coronary arterial stent insertion Coronary artery occlusion Electrocardiogram abnormal

Symptomtext

Acute myocardial infarction in the LAD. Chest pain migrating to left arm down through elbow. Cardiac catheterization s/p DES-pLAD. Chest pain started roughly 19 hours after the first dose of the Pfizer vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 3,0
Labordaten: EKG was performed in the ER to confirm MI was occurring and I was immediately taken to the catheterization operating room to have a stent put in the LAD artery on April 30th. The first chest pain occurred the day after the first shot, then went away. Then it came back a week and a half later, then went away, then it came back again on the morning of 04/29/2021 at about 2:45 am and we went straight to the ER. I was due for my second dose on 04/30/2021 but was postponed until 05/14/2021.
Aktuelle Erkrankungen: None
Vorgeschichte: Slightly elevated cholesterol
Andere Medikamente: 10mg Ezetimibe (cholesterol) 125mcg Vitamin D supplement
Allergien: None
Vorherige Impfungen: -

VAERS 1337723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: WI
Alter: 36,0
Geschlecht: M
Eingang: 21.05.2021
Impfdatum: 13.05.2021
Beginn: 18.05.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: IM / RA

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

Death

Symptomtext

PATIENT WAS IMMUNIZED 5/13. PATIENT WAS FOUND DECEASED IN THEIR APARTMENT ON 5/18. FAMILY LAST SAW HIM ON 5/16 WHEN THEY DROPPED HIM OFF AT HIS APARTMENT. MEDICAL EXAMINER HAS NOT YET DETERMINED CAUSE OF DEATH OR EXACT DATE OF DEATH.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: UNKNOWN
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: 05/13-DISCUSSED WITH PHARMACIST A TOPICAL ALLERGIC REACTION HE HAD BEEN HAVING FROM A NEW BODY SOAP. PHARMACIST RECOMMENDED TOPICAL HYDROCORTISONE CREAM AND ORAL BENADRYL TO HELP MANAGE SYMPTOMS.
Andere Medikamente: UNKNOWN
Allergien: UNKNOWN
Vorherige Impfungen: -

VAERS 1331836

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: NJ
Alter: 59,0
Geschlecht: M
Eingang: 19.05.2021
Impfdatum: 13.05.2021
Beginn: 14.05.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / LA

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

Chest discomfort Coronary artery occlusion Myocardial infarction Stent placement

Symptomtext

Received first vaccine 4/21/21. Within two days started having tightness in chest, but no other adverse reactions, happened a couple times a day. 5/13/21 received second vaccine....had tightness two more times, then 5/14:22 evening had a heart attack....ambulance to Hospital. 99% blockage in LAD. Hospital inserted stent. Spoke with all of the Cardiologists about my concerns as Heart problems ?Do not? run in my family. I have always had excellent blood pressure and low cholesterol....my father is 86 and was a smoker, and never been on blood pressure medication, same with my late Grandfather. I?ve ?never? had any type of chest pains in my life. Also, I am retired and have had numerous vaccines, with no issues. The hospital cardiologists said that I could report this, but they believe the Heart attack is due to the fact that I smoke....I just don?t believe that....the Heart Attack occurred 36 hours after my second vaccine!!!

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 4,0
Labordaten: I will release all medical records for this event if needed...I may be one of a very small percentage of this type of adverse effect....and the plaque in my artery may have already been there, but I believe it ruptured due to the vaccine, and at a minimum should Be evaluated! Happy
Aktuelle Erkrankungen: None
Vorgeschichte: Smoker
Andere Medikamente: Multi-Vitamin
Allergien: Some shellfish alergies
Vorherige Impfungen: -

VAERS 1314971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

kritisch

Staat: MN
Alter: 62,0
Geschlecht: M
Eingang: 13.05.2021
Impfdatum: 07.05.2021
Beginn: 12.05.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: IM / -

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

Arterial catheterisation Arteriogram coronary abnormal Blood gases Cardiac arrest Cardioversion Catheter placement Catheterisation cardiac abnormal Coronary artery disease Coronary artery occlusion Coronary artery stenosis Intra-aortic balloon placement Lung assist device therapy Percutaneous coronary intervention Resuscitation Ventricular fibrillation

Symptomtext

Unclear if event is related to vaccination but occurred 5 days after the 2nd dose of vaccine Pt admitted on 5/12/2021 with refractory cardiac arrest. (PMH unknown). Patient reportedly went for a walk with his wife. Upon returning home, he went to take the garbage out. The patient was found down approximately 15 minutes later in his garage. The patient's wife called 911 immediately?it is unclear if bystander CPR was initiated. EMS was on scene within several minutes and initiated CPR. The patient 3 shocks, and epinephrine. ROSC was achieved at approximately 14:41. At approximately 14:50, the patient again went into VF. He received an additional 5 shocks, 1 mg of epinephrine, and 300 mg of amiodarone. He went into asystole at approximately 1510. ACLS was continued and the patient was given an additional 1 mg of epinephrine. Upon arrival to the University of Minnesota cardiac Cath Lab, the patient remained in asystole with Lucas on. He was cannulated on VA ECMO. In the cardiac cath lab, he was found to have OM disease and diffuse CAD involving LAD Received intervention to his OM. Initial LA was 14.3. ABG 6.94/54/44/12.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: ECMO cannulation: - Successful insertion of 17Fr and 25Fr ECMO cannulae and initiation of VA ECMO. - 8Fr antegrade perfusion catheter in the R SFA. - Right radial arterial line placement. Coronary angiogram: left-dominant circulation. Left main: angiographically normal. LAD: long 70% in the proximal-to-mid LAD; diffuse disease otherwise. Cx: 100% occlusion of OM1; 80% left PDA stenosis. RCA: 80% diffuse disease in a non-dominant vessel. Percutaneous coronary intervention: - Successful PCI of the first OM with two overlapping DES (2.5x12mm and 2.25x38mm DES). Intra-aortic balloon pump insertion: - 50cc IABP via the LCFA - 1:1 augmentation.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2700705

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: TX
Alter: 71,0
Geschlecht: M
Eingang: 24.10.2023
Impfdatum: 29.04.2021
Beginn: 23.01.2022
Tage bis Beginn: 269,0
Dosis: 2
Route/Site: IM / UN

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

Anticoagulant therapy Arteriovenous fistula Arteriovenous fistula operation COVID-19 pneumonia Jugular vein thrombosis Renal impairment

Symptomtext

admitted on 01/23/2022 with severe COVID-pneumonia. Tx: antibiotics, steroids, no remdesivir due to kidney function; zinc, singulair, 2 LPM O2; During his clinical course found to have right internal jugular vein thrombosis and was instituted on anticoagulation therapy. Also found to have nonfunctioning arteriovenous fistula and underwent ligation of right arm AV fistula on 04/28/2022. The patient had a prolonged hospital stay awaiting placement however was refused by multiple facilities and eventually is being planned for discharge home with home health. He also was unable to be enrolled in outpatient HD facility and has been advised for return to ER MWF every week for HD ; back to baseline at d/c

Weitere VAERSDATA-Felder

Praegender Schweregrund: Jugular vein thrombosis
Hospital-Tage: 135,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2651811

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MI
Alter: 61,0
Geschlecht: F
Eingang: 01.07.2023
Impfdatum: 20.04.2020
Beginn: 20.04.2020
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / AR

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

Ageusia Angina pectoris Asthenia Atrial fibrillation Balance disorder Computerised tomogram Electrocardiogram Electromyogram Epistaxis Eye pain Fall Gait disturbance Guillain-Barre syndrome Haemoptysis Headache Hypoaesthesia Insomnia Joint range of motion decreased

Symptomtext

Arm swollen pain, arm motion range couldn't lift arm, heart palpation nosebleed, spit up blood clotes fallen neuropathy, cane, thrombocytopenia, nerves attacted (AFib) heart pain musle loss Gullain Bar Syndrome Patient given Pfizer shot 4/2020. Patient began 1 1/2 hour later arm swollen legs num/needle pins in feet and legs. Coughing up bloot clots, lost muscle mas, weakness lost balance to walk, headaches, nauseous at stomach couldn't sleep heart paltation! Nosebleeds, arm range motion lost! Nerves attacted. Muscle mass lost, weight gain Brain to go blood clots in legs. Long Covid. Taste gone. Shots 4/16/21 Eye Sight low Pfizer Lot ER8732 5/07/21 Pfizer Lot EW0179 01/18/22 Pfizer Lot FD7218 7/04/22 PFR-BNT 30mcg/0.3mL Lot FM0173 11/15/22 Pfizer Bivalent 30mcg/0.3mL Lot GJ3277 Uptic Neuritis-Pain in eyes. I have Thrombocytopenia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: MRI 04/20/2023 EKG EMG, Ct
Aktuelle Erkrankungen: none
Vorgeschichte: Long Covid reaction to vaccine
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2642934

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: FL
Alter: 78,0
Geschlecht: M
Eingang: 08.06.2023
Impfdatum: 19.05.2021
Beginn: 30.08.2022
Tage bis Beginn: 468,0
Dosis: 2
Route/Site: - / -

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

Atrial fibrillation Bacteraemia COVID-19 Cystoscopy Embolism venous Febrile neutropenia Gastritis Lithotripsy Malnutrition Oesophagogastroduodenoscopy abnormal Pancytopenia Proteus infection SARS-CoV-2 test positive Sepsis Ureteral stent insertion Ureterolithiasis Ureteroscopy abnormal Urinary tract infection

Symptomtext

BREAKTHROUGH COVID: FULLY VACCINATED COVID POSITIVE, INCEDENTAL FINDING. PATIENT WAS ADMITTED D/T NEUTROPENIC FEVER D/T PROTEUS BACTEREMIA IN THE SETTING OF COMPLICATED UTI WITH OBSTRUCTIVE UROPATHY UNCOMPLICATED CYSTOSCOPY, UTEROSCOPY, LASER LITHO, AND STENT PLACEMENT COMPLETED ABX PER ID TEAM, UPPER EGD WITH REACTIVE GASTRITIS Atrial fibrillation with RVR (HCC),PROGRESSED TO SEPSIS. Venous thromboemblism, Neutropenic fever, Severe protein-calorie malnutrition, Pancytopenia, Ureteral calculus, Urinary tract infection due to Proteus. COVID 19 was not treated during admission.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Embolism venous
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: UNKNONWN
Vorgeschichte: Angioimmunoblastic lymphoma , CAD (coronary artery disease)
Andere Medikamente: UNKNOWN
Allergien: Tylenol
Vorherige Impfungen: -

VAERS 2507388

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MO
Alter: 67,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 15.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / LA

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

Metabolic function test normal Syncope

Symptomtext

Fainted the next morning after my first Pfizer covid booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Metabolic panel on 10/16/2021 & 10/17/2021 performed in hospital with overnight stay. Excellent results!
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2490427

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: SC
Alter: 45,0
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 22.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Blood test Dizziness Dyspnoea Electrocardiogram Immunisation reaction Loss of consciousness Lymphadenopathy Presyncope SARS-CoV-2 test negative

Symptomtext

10/23/2022 I woke up in the morning with a swollen lymph node under my right arm for about 8 days. After 14 weeks I've noticed I was having some kind of reaction where I passed out 2 times on February. On September It happened again when I went camping I had short of breath and I felt like I was going to pass out. On March 2022 I went to my doctor who did Blood Panel and EKG. She then diagnosed me with Vasovagal reaction. She also referred me to a cardiologist. He prescribed me beta blockers but I said will try to avoid the medication for now and will try other option.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: 26 OCT2022-COVID-19-Test- Negative; Blood Panel; EKG
Aktuelle Erkrankungen: None
Vorgeschichte: Migraines
Andere Medikamente: Magnesium; Multivitamin; Co Q10
Allergien: Bactrim
Vorherige Impfungen: -

VAERS 2465682

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: OR
Alter: 31,0
Geschlecht: M
Eingang: 30.09.2022
Impfdatum: 13.09.2022
Beginn: 25.09.2022
Tage bis Beginn: 12,0
Dosis: 2
Route/Site: IM / AR

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

Arrhythmia Arteriogram coronary normal Atrial tachycardia Blood magnesium decreased Blood potassium decreased Blood test Cardiac ablation Cardiac electrophysiologic study abnormal Cardioversion Dyspnoea Echocardiogram abnormal Ejection fraction Heart rate increased Loss of consciousness Prosthetic cardiac valve regurgitation

Symptomtext

On 9/25/22 Experienced loss of consciousness while out on a hike, and upon regaining consciousness I realized my heart rate was extremely fast and I was struggling to breathe. Called 911, was found to have a resting heart rate of ~300bpm. Was air lifted to hospital. Received cardioversion which successfully restored normal sinus rhythm. Received an angiogram with clear results. Received echocardiogram showing moderate paravalvular leak and EF of ~30% (EF thought to be a result of cardioversion) Received electrophysiology study which was able to reproduce atrial tachycardia, then received cardiac ablation, reported to be successful in preventing reporduction of atrial tachycardia. Was released on 9/28/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 4,0
Labordaten: 9/25-9/28/22 Various blood tests - was found to be slightly low in magnesium and potassium post tachycardia episode. 9/26/22 - Angiogram - found to be clear of blockages 9/27/22 - Cardiac Electrophysiology study - was able to reproduce arrhythmia, received successful cardiac ablation.
Aktuelle Erkrankungen: Post roux-en-y bariatric surgery on 8/18/22
Vorgeschichte: Heart Failure Bicuspid Aortic valve (was replaced in 2018 and again in 2020) Aortic Valve Replacement x2 Mitral Valve Repair Cardiac Fistula Repair Ascending Aortic Aneurysm High Blood Pressure Obesity ADHD
Andere Medikamente: Entresto 49/51mg x2 daily Metoprolol Succinate 25mg x2 daily Eplerenone 25mg x1 daily Penicillin 500mg x2 daily Usodiol 250mg x2 daily Melatonin 5mg x1 daily Bariatric Advantage All-in-one multivitamin x4 daily Chamomile Tea x1
Allergien: Nickel (metal) - causes skin rash
Vorherige Impfungen: -

VAERS 2433398

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MI
Alter: 32,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 13.04.2021
Beginn: 09.08.2022
Tage bis Beginn: 483,0
Dosis: 2
Route/Site: - / -

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

Asymptomatic COVID-19 Bell's palsy Caesarean section Foetal growth restriction Maternal exposure before pregnancy Postpartum haemorrhage Pre-eclampsia Pyogenic granuloma SARS-CoV-2 test positive Thrombocytopenia Twin pregnancy

Symptomtext

Pt was admitted to Antepartum Unit on 8/9/122 for DCDA twins, Newly Dx IUGR both twins, Pre Eclampsia w/o SF, Thrombocytopenia. Pt also had Dx of Bell's Palsy, Pyogenic granuloma, Dx with Asy positive Covid on admission Pt developed Pre Eclampsia with SF on 8/13/22. Primary LT C-Section done. S/P Postpartum Hemorrhage S/P Magnesium Sulfate 24 hour postpartum. Started on Labetalol 200mg BID Discharge from hospital on 8/17/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: 8,0
Labordaten: 8/9 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2418335

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NY
Alter: 62,0
Geschlecht: F
Eingang: 23.08.2022
Impfdatum: 08.11.2021
Beginn: 15.04.2022
Tage bis Beginn: 158,0
Dosis: 2
Route/Site: IM / -

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

Asymptomatic COVID-19 Computerised tomogram thorax abnormal Dizziness Glomerular filtration rate decreased Heart rate increased Hypoglycaemia Hypotension Intensive care Limb injury Lung infiltration Peritoneal dialysis SARS-CoV-2 test positive

Symptomtext

4/15/2022-Presents to ED via EMS, Lightheadedness and Hypoglycemic episode. Chest ct : pleural-based airspace infiltrate in the right lower lobe. Covid + on admission. Admit hypoglycemia. Vitals stable maintaining spo2 on RA. Start Levofloxacin x1. 4/17/2022-Am: B/P 58/43 Midodrine and Levophed given. HR increased to 100-200's. Transfer to ICU. Started vancomycin and ceftraixone. Also has significant wound on R foot. B/P now 95/52. Hr down to 93. 4/20/2022-Levophed d/c and SBP's WNL. 4/22/2022-eGFR up to 13 from 9. Covis asymptomatic. Continue Midodrine. 4/24/2022-Continues on RA, B/P maintaining around 100/50-60's. 4/26/2022- Downgraded to MS from ICU.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 12,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: ESRD, Type 1 Dm, HTN, CAD and hyperkalemia
Andere Medikamente: -
Allergien: Iodine contrast media, PCN and Loversol
Vorherige Impfungen: -

VAERS 2402965

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MI
Alter: 59,0
Geschlecht: M
Eingang: 05.08.2022
Impfdatum: 08.04.2021
Beginn: 30.07.2022
Tage bis Beginn: 478,0
Dosis: 2
Route/Site: - / -

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

Acute kidney injury Arthralgia COVID-19 Drug use disorder Fall Fatigue Leukocytosis Malaise Metabolic acidosis Presyncope Procalcitonin decreased Pyrexia SARS-CoV-2 test positive Syncope

Symptomtext

7/30--8/3 61 yo gentleman known to me from 2014 admission with history of hemorrhagic CVA , admitted with syncopal episode/ presyncopal episodes and falls in outpatient setting. Pain in left hip after previous fall- no obvious deformity, prior THA reported. Rule out fracture. COVID 19 - with fever, leukocytosis. Fatigue and malaise present. On room air. Low procalcitonin lever. AKI with metabolic acidosis- likely prerenal. Recent rehab stay for cocaine use. Completing day 3 of 3 remdesivir.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: 7/30 -- SARS-CoV-2 detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2379336

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MI
Alter: 78,0
Geschlecht: F
Eingang: 22.07.2022
Impfdatum: 09.10.2021
Beginn: 15.07.2022
Tage bis Beginn: 279,0
Dosis: 3
Route/Site: - / -

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

Anaemia Angiogram pulmonary normal Blood loss anaemia COVID-19 Colonoscopy normal Echocardiogram normal Electrocardiogram abnormal Gastrointestinal haemorrhage Haemoglobin normal Hypophagia Hypovolaemia Malaise Melaena Oesophagogastroduodenoscopy normal SARS-CoV-2 test positive Syncope

Symptomtext

Discharge Provider: Private Primary Care Provider at Discharge: Private Admission Date: 7/15/2022 Discharge Date: 07/18/2022 Discharge disposition: Home Condition on discharge: Stable. GI bleed [K92.2] ADMISSION AND DISCHARGE DIAGNOSES: HOSPITAL COURSE: Acute blood loss anemia -No acute bleeding on EGD and colonoscopy. GI will see outpatient for possible endoscopic ultrasound versus video capsule study. Continue on PPI. -Discussed with GI prior to DC, no further workup planned inpatient. -Hemoglobin stabilized and improving prior to discharge. Symptomatically much improved. Syncope secondary to hypovolemia in setting of profound anemia - secondary to decreased oral intake and GIB - CTA negative for PE - ECHO normal - No arrhythmia detected on tele COVID positive - vaccinated and boosted - symptom onset 7/9, COVID + 7/13 - CTA negative for PE or infiltrates - received 2 doses of Paxlovid - no indication for further therapy at this time Abnormal EKG. New problem. accelerated junctional rhythm that overrides her sinus node. Benign in etiology per EP

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes mellitus, type II (HCC) Hyperlipidemia Depressive disorder Irritable bowel syndrome Symptomatic menopausal or female climacteric states Essential hypertension Mild cognitive impairment TIA (transient ischemic attack) Pelvic floor weakness Dyslipidemia GI bleed
Andere Medikamente: amoxicillin (AMOXIL) 500 MG capsule B Complex Vitamins (VITAMIN B COMPLEX) tablet cholecalciferol (VITAMIN D3) 25 MCG (1000 UT) tablet ezetimibe (ZETIA) 10 MG tablet glycerin-hypromellose-PEG 400 (ARTIFICIAL TEARS) 0.2-0.2-1 % SOLN lis
Allergien: None
Vorherige Impfungen: -

VAERS 2374736

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MI
Alter: 73,0
Geschlecht: M
Eingang: 20.07.2022
Impfdatum: 28.10.2021
Beginn: 06.07.2022
Tage bis Beginn: 251,0
Dosis: 2
Route/Site: - / -

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

Anticoagulant therapy COVID-19 Dyspnoea Hypoxia Positive airway pressure therapy Productive cough Respiratory distress SARS-CoV-2 test positive Sputum discoloured Wheezing

Symptomtext

Patient with 3 Pfizer COVID vaccinations who admitted to hospital with complications of COVID and positive COVID PCR. Provider d/c note below: "74-year-old male with a history of chronic obstructive pulmonary disease on chronic home oxygen (2L), hypertrophic cardiomyopathy with EF 55%, type 2 diabetes, hypertension, BPH, gout who presented to the emergency department with shortness of breath for the previous 3 days associated with worsening cough and white sputum production. In the emergency department, patient appeared to be in respiratory distress, wheezing was noted on physical exam, he was not noted to be hypoxic at that time. He was placed on CPAP with improvement of symptomatology, he was transferred to Hospital for further evaluation. COVID test was ordered, and he was positive. He was started on remdesivir, Decadron, and Lovenox, his home inhalers were otherwise continued. During hospitalization, patient's symptoms continue to improve with steroids and remdesivir. Apart from intermittent CPAP at night, patient was otherwise on no more than 3 L of oxygen during his stay. He was restarted on his azithromycin, as this appears to have been a home medication longer-term. On day of discharge, patient was walking around comfortably on his home oxygen. Patient felt comfortable going home. Physical therapy recommended home with assist. He will be discharged home in stable medical condition"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory distress
Hospital-Tage: 4,0
Labordaten: COVID detected PCR on 07/06/22
Aktuelle Erkrankungen: -
Vorgeschichte: BPH with retention Gout Hypertension Smoker Dependence on continuous supplemental oxygen Bladder cancer (HCC) Hyperlipemia Atrial fibrillation (*) Chronic respiratory failure with hypoxia (*) Type 2 diabetes mellitus without complication, without long-term current use of insulin (*) Umbilical hernia without obstruction and without gangrene Anemia Stage 3 severe COPD by GOLD classification (*)
Andere Medikamente: Albuterol Zyloprim Eliquis Breo-Ellipta Lotrimin cream Proscar Feosol Bifera Toprol XL O2 at 2L Spiriva Respimat Hytrin
Allergien: -
Vorherige Impfungen: -

VAERS 2325618

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: OR
Alter: 42,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 04.05.2021
Beginn: 04.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chest X-ray normal Cough Dyspnoea Dyspnoea exertional Electric shock sensation Feeling abnormal Gait inability Laboratory test normal Pain in extremity Pulmonary function test normal SARS-CoV-2 test negative

Symptomtext

05/04/2021 I felt poorly that evening. I had shortness of breath and a mild cough, but I wasn?t sure if anything was happening. I also had sort of an electric shock pain down my left arm into my finger. On 5/7/2022 there was no doubt. I had a worsening with my breathing, I would get short of breath walking from the couch to the bathroom. I had tried to go for my normal walk, and I was unable to breathe, I could not walk. That started a series of events that lasted weeks with trouble breathing. I had an appointment with my doctor on May 12, virtual, then an in person visit on May 13. I had a chest x ray, a COVID test and was checked for shingles. I had a mark on my finger that corresponded with the pain I had after my vaccination. A sample was taken even though it had been a while and it had started to resolve. It was negative for shingles, but since it had mostly cleared up, she was unable to get a good sample. I had pulmonary function testing in September of 2021, because I had a history of multiple respiratory viruses. The test indicated I did not have asthma. I ended up not getting answers and was not diagnosed. I am not at 100% recovered now, but am not like I have been. I plan to see an allergist next.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: Chest x-ray, normal. COVID test, negative; Shingles test, negative. Pulmonary function test, normal
Aktuelle Erkrankungen: None
Vorgeschichte: Endometriosis, Ehlers-Danlos Syndrome, migraines
Andere Medikamente: Zyrtec, extra strength Tylenol, Vegetarian Omega supplement, Vitamin D, Magnesium, B Complex
Allergien: Ibuprofen , food cooked on wood plank, Contrast dye with MRI or CT
Vorherige Impfungen: Flu, made me so sick

VAERS 2317481

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: FL
Alter: 65,0
Geschlecht: M
Eingang: 13.06.2022
Impfdatum: 09.06.2021
Beginn: 15.06.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: - / LA

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

Acute motor-sensory axonal neuropathy Albumin CSF increased Anal incontinence Anti-GAD antibody negative Anti-ganglioside antibody negative Antiacetylcholine receptor antibody Antibody test negative Anticoagulant therapy Autonomic nervous system imbalance Bacterial test Bacterial test negative Blood albumin normal Blood creatine phosphokinase normal Blood folate normal Blood immunoglobulin E normal Blood immunoglobulin G normal Blood magnesium normal Blood phosphorus normal

Symptomtext

Symptoms started after 2nd dose of vaccine more markedly. He started to complain of fatigue, weight loss and appetite loss. Was seen by primary care physician by end of June, and malignancy was ruled out, negative endoscopy, colonoscopy, PET/CT, CT chest/abd/pelvis. started having more fatigue, and dizziness. By the end of July 2021 started using a cane and then a wheelchair for . In September 2021, the patient started complaining of orthotic dizziness, urinary urgency, incontinence, bowel incontinence and paraosmia . On September 17, 2021, EMG and nerve conduction study showed neuropathy and dysautonomia. On September 30, 2021, the patient underwent extensive workup to rule out paraneoplastic disorder, malignancy including lumbar puncture and all of them were unremarkable. lost about 50-60 lbs during this time and also developed temporal wasting. Also developed a right popliteal clot managed with oral anticoagulant. Dysautonomia neuropathy Difficulty in gait and ambulating Cognitive decline

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: EMG performed September 27, 2021, autonomic nervous system dysfunction affecting sympathetic and parasympathetic system with no heart rate variability on absent SSR at the level of the feet. Sensory, motor, axonal neuropathy with mild-to-moderate axonal loss. Laboratory workup, September 14, 2021, myasthenia gravis antibody negative, acetylcholine receptor antibody negative for blocking, modulating, and binding, anti striational antibody negative, anti musk pending, anti rheumatoid factor negative, B12 at 1528, elevated, CK 177, normal. Laboratory workup, October 2, 2021, CMP negative, magnesium 2.1, phosphorus 3.2, uric acid 4.3, normal, anti GAD negative. Continuous EEG 5 hours, normal. EKG, sinus tachycardia, right axis. CSF cell count is white blood cells 0, red blood cell 0, glucose 88, protein 57, elevated. CSF bacterial culture negative. Cytology negative, VDRL negative, myelin basic protein normal, enterovirus PCR negative, CMV PCR negative, Epstein-Barr virus PCR negative, varicella zoster PCR negative, encephalitis panel negative. CSF IgG 5.6, elevated, IgG serum the 1258 normal, IgG ratio 0.16, normal. Albumin CSF 34.1, elevated, albumin serum 41, normal, IgE index 0.54 normal. Oligoclonal bands negative. Ultrasound testicles, multiple right epididymal calcifications. Paraneoplastic antibodies negative. Anti GAD antibody negative. B12 normal. Folate normal. Vitamin E normal, TSH 1.03, normal. CT chest, abdomen, pelvis negative. C-reactive protein negative. MRI of the brain with and without gadolinium showed scattered white matter changes consistent with small-vessel disease. Anti ganglioside antibody negative. Antigen 1 and 2 negative, anti GDA and B negative, anti-GQ1b negative. MRI of the brain, September 28, 2021, mild vermian atrophy. EMG, September 14, 2021, sensory motor peripheral neuropathy axonal, small fiber autonomic neuropathy with absent sympathetic skin response.
Aktuelle Erkrankungen: Diabetes mellitus type 2
Vorgeschichte: Diabetes mellitus type 2
Andere Medikamente: Metformin
Allergien: none
Vorherige Impfungen: -

VAERS 2283047

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: -
Alter: 63,0
Geschlecht: M
Eingang: 18.05.2022
Impfdatum: 21.04.2021
Beginn: 02.05.2022
Tage bis Beginn: 376,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Dizziness Haemorrhage Head injury Loss of consciousness SARS-CoV-2 test positive Syncope

Symptomtext

5/2 64y.o. male with PMH of CAD/stents x 3, HTN/dyslipidemia, and allergic rhinitis presented with episode of lightheadedness and collapse and LOC. Found down at work with back of head bleeding. Patient discharged home post Remdesivir course.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 2,0
Labordaten: 5/2 SARS-CoV-2 (COVID-19) by NAA Detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2261676

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: FL
Alter: 56,0
Geschlecht: M
Eingang: 03.05.2022
Impfdatum: 24.08.2021
Beginn: 02.05.2022
Tage bis Beginn: 251,0
Dosis: 2
Route/Site: - / -

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

Asthenia COVID-19 Facial paralysis Gait disturbance Pain in extremity Patient elopement SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st vaccine received on 08/02/2021. 2nd vaccine on 08/24/2021. 56 y/o male presents to ED after being found wandering around with Left facial droop and c/o left leg pain, trouble ambulating and weakness. Pt lives at group home and has a PMHx of Autism, Bell's palsy, depression, anxiety, Hypothyroidism, AVF for renal dialysis and schozophrenia. No specific treatment for Covid19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19- Detected on 05/02/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Autism, Bell's Palsy with Left facial droop, Depression, Anxiety, hypothyroidism, schizophrenia, AVF/renal dialysis
Andere Medikamente: -
Allergien: PCN, Tegretol
Vorherige Impfungen: -

VAERS 2243615

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NC
Alter: 36,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 13.11.2021
Beginn: 21.02.2022
Tage bis Beginn: 100,0
Dosis: 3
Route/Site: SYR / RA

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

Blood test Chest X-ray Computerised tomogram thorax Dizziness Dyspnoea Dysstasia Echocardiogram Electrocardiogram Muscle spasms Pneumonia Pulmonary thrombosis Ultrasound chest

Symptomtext

I starting feeling SOB, light-headiness, and dizziness. I starting having leg cramp that would not stop. It move from my legs to my hips. I could not stand without getting SOB. I went to the ER on Feb. 21st. They did chest x-rays, EKG, CT scan, blood work, lung and heart ultra sound, it show that I had blood clots in both lungs. My heart was okay. I also got pneumonia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 3,0
Labordaten: Chest x-rays, EKG, CT scan, Bloodwork, lung and heart ultrasound
Aktuelle Erkrankungen: N/A
Vorgeschichte: High blood pressure
Andere Medikamente: Hydrochloride, Low thyroid, Silicas, Motorize, Levocetirizine
Allergien: Lisinopril, Niludipine
Vorherige Impfungen: -

VAERS 2237641

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NC
Alter: 76,0
Geschlecht: F
Eingang: 16.04.2022
Impfdatum: 04.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 28,0
Dosis: 3
Route/Site: - / -

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

Deep vein thrombosis Peripheral swelling Ultrasound Doppler

Symptomtext

lower extremity swelling of her leg; DVT; 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 77-year-old female patient received BNT162b2 (BNT162B2), on 04Oct2021 as dose 3 (booster), single (Lot number: EW0179) at the age of 76 years for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 1, single, Lot Number: EL3248, Expiry Date: unknown, Route, Anatomical Location: left arm), administration date: 16Jan2021, when the patient was 76-year-old, for Covid-19 Immunization; BNT162b2 (Dose 2, single, Lot Number: EN9581, Expiry Date: unknown, Route, Anatomical Location: left arm), administration date: 06Feb2021, when the patient was 76-year-old, for COVID-19 immunization; Flu vaccine (Manufacturer and lot number: unknown, Route of anatomical location: unknown, No. of Previous Doses: NA, Date: Caller states sometime in Oct2021), administration date: Oct2021. The following information was reported: DEEP VEIN THROMBOSIS (medically significant) with onset Nov2021, outcome "recovered" (Feb2022), described as "DVT"; PERIPHERAL SWELLING (non-serious) with onset Feb2022, outcome "not recovered", described as "lower extremity swelling of her leg". The events "dvt" and "lower extremity swelling of her leg" required physician office visit. The patient underwent the following laboratory tests and procedures: Ultrasound Doppler: (Nov2021) Positive, notes: DVT Unit: Not provided; (Feb2022) Negative, notes: Unit: Not provided. Therapeutic measures were taken as a result of deep vein thrombosis. She had received prior vaccination within 4 weeks. She had no Adverse event occurred prior to vaccination. Pt received first booster dose of the Pfizer Covid-19 vaccine back in the middle of Oct2021 and in the middle of Nov2021 was diagnosed with a DVT. Her HCP has ran tests to determine the cause of her DVT but so far no reason has been found. Patient denies a medical history of DVT. Patient asked if the second booster dose of the Pfizer Covid-19 vaccine related to DVT and if it is safe to get a second booster dose of the Pfizer Covid-19 vaccine. She was diagnosed with a DVT, and that she had never had one before. She had not been in emergency room with respect to events however she had visited physician office with respect to events. She was still having lower extremity swelling of her leg, but her DVT resolved completely. She was not admitted to the hospital. She was on a blood thinner for 3 months, and the medication helped the clot absorb. She had a follow up venous ultrasound and it was negative for DVT. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Test Date: 202111; Test Name: Venous Doppler; Test Result: Positive ; Comments: DVT Unit: Not provided.; Test Date: 202202; Test Name: Venous Doppler; Test Result: Negative ; Comments: Unit: Not provided.
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2235973

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MI
Alter: 85,0
Geschlecht: M
Eingang: 15.04.2022
Impfdatum: 01.10.2021
Beginn: 07.04.2022
Tage bis Beginn: 188,0
Dosis: 3
Route/Site: IM / -

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

Angiogram Anion gap Appetite disorder Asthenia Atelectasis Basophil count decreased Basophil percentage decreased Blood bicarbonate decreased Blood calcium decreased Blood chloride decreased Blood creatinine decreased Blood creatinine normal Blood glucose normal Blood potassium normal Blood sodium decreased Blood urea increased Breath sounds normal C-reactive protein increased

Symptomtext

Hospitalized (4.7.22 - 4.9.2022); COVID-19 positive (4.7.22); fully vaccinated PLUS Booster - pfizer x3 D/c Summary:Discharge Summary BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider at Discharge: MD Admission Date: 4/7/2022 Discharge Date: 4/8/2022 Active Hospital Problems Diagnosis Date Noted POA ? COVID-19 04/08/2022 Yes ? Osteoarthritis 09/02/2015 Yes Resolved Hospital Problems Diagnosis Date Noted Date Resolved POA ? Toxic encephalopathy 04/08/2022 04/09/2022 Unknown ? Generalized weakness 04/07/2022 04/09/2022 Yes ? AMS (altered mental status) 04/08/2022 DISCHARGE DISPOSITION: Home with services - Nursing Appointments Needing to be Scheduled 1) COVID 19 patient instructed to get home pulse ox and notify primary care physician or return to ER if below 90%. Patient is to finish his course of paxlovid. 2) toxic encephalopathy Resolved. Was evaluated for stroke and tele Stroke not showing any acute infarct but history of infarct and neurology recommended 81 mg of aspirin and 20 mg of Lipitor as secondary stroke prevention. 3) placed on aspirin and Lipitor Writer had a long discussion with patient regarding aspirin and Lipitor. Patient states that he is not allergic to aspirin. Writer reviewed risk and benefits of aspirin including bleeding bruising risk and if he noticed any bright red blood or dark stools is to call DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Weakness [R53.1] Generalized weakness [R53.1] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 86 y.o. male who presented to the emergency department with complaints of generalized weakness. . Patient presents to emergency department in the morning of 04/07/2022 with complaints of unable to perform ADLs independently. After workup, patient was found to be positive for COVID-19. CT of the head showed no acute intracranial abnormalities. Chest x-ray did show bibasilar subsegmental atelectasis. Patient was discharged with a prescription for Paxlovid and instructions to return with worsening symptoms. He returned in the evening with complaints of increased weakness and inability to ambulate independently. In the emergency department, patient was hypertensive, however, other vital signs are stable. He did not require supplemental oxygen. Complete blood count and BMP were unremarkable. Suspect increased weakness secondary to COVID-19. A stroke code was called as patient was leaning to the right with PT OT. And H was 3. CT CTA as an MRI did not show any acute process. Patient did well and the following day was at baseline. NIH was 0. The patient was sitting in his chair eating breakfast. He was able to walk independently. His weakness had resolved and his altered mental status the day before was thought to be secondary to toxic encephalopathy secondary to COVID-19. Questions and concerns addressed. Patient was counseled to come back to the ER if he had any new or worsening symptoms. Patient was comfortable with this plan. Active Issues Requiring Follow-up 1) COVID-19 --patient advised to get home pulse ox and monitor oxygen saturation and notify primary care physician return to ER if below 90%. Patient is to finish plaxlovid. 2) secondary stroke prevention Neurology did recommend aspirin and 20 mg of Lipitor. Patient states that he was not allergic to aspirin. Patient counseled on the risks and benefits of taking aspirin and Lipitor. Patient was agreeable. CONSULTS / RECOMMENDATION: IP CONSULT TO CARE MANAGEMENT IP TELEMEDICINE CONSULT INPATIENT PROCEDURES: Surgery and Procedures None OBJECTIVE: BP 143/66 | Pulse 51 | Temp 36.2 ?C (Oral) | Resp 18 | Ht 1.753 m | Wt 91.8 kg | SpO2 95% | BMI 29.87 kg/m? Physical Exam Vitals and nursing note reviewed. Constitutional: Appearance: Normal appearance. HENT: Head: Normocephalic. Nose: Nose normal. Mouth/Throat: Mouth: Mucous membranes are moist. Eyes: Pupils: Pupils are equal, round, and reactive to light. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Pulses: Normal pulses. Heart sounds: Normal heart sounds. Pulmonary: Effort: Pulmonary effort is normal. Breath sounds: Normal breath sounds. Abdominal: General: Bowel sounds are normal. Palpations: Abdomen is soft. Musculoskeletal: General: Normal range of motion. Cervical back: Normal range of motion. Skin: General: Skin is warm and dry. Neurological: General: No focal deficit present. Mental Status: He is alert. Psychiatric: Mood and Affect: Mood normal. Behavior: Behavior normal. H&P: CHIEF COMPLAINT: Generalized weakness ASSESSMENT / PLAN: COVID-19 Assessment & Plan Patient presents to emergency department in the morning of 04/07/2022 with complaints of unable to perform ADLs independently. After workup, patient was found to be positive for COVID-19. CT of the head showed no acute intracranial abnormalities. Chest x-ray did show bibasilar subsegmental atelectasis. Patient was discharged with a prescription for Paxlovid and instructions to return with worsening symptoms. He returned in the evening with complaints of increased weakness and inability to ambulate independently. In the emergency department, patient was hypertensive, however, other vital signs are stable. He did not require supplemental oxygen. Complete blood count and BMP were unremarkable. Suspect increased weakness secondary to COVID-19. -routine vital signs -titrate oxygen to maintain saturation greater than 90% -not a candidate for dexamethasone at this time -not a candidate for IV remdesivir this time -continue Paxlovid -incentive spirometry and cough and deep breathe -prone positioning while asleep -a.m. labs complete blood count, CMP, CRP D-dimer Generalized weakness Assessment & Plan Patient states that he has been unable to rise or get out of bed without significant assistance. At baseline, patient is able to walk with a cane. Currently unable to ambulate independently. Generalized weakness likely secondary to COVID-19. -PT and OT to evaluate patient and make recommendation -care management consulted for discharge planning Osteoarthritis Assessment & Plan Analgesics available for pain p.r.n. Subjective HISTORY OF PRESENT ILLNESS: Patient is a 86 y.o. male who presented to the emergency department with complaints of generalized weakness. Patient has a past medical history of Boca hernia, bilateral hearing loss, CVA, BPH, and arthritis. Patient presents to emergency department in the morning of 04/07/2022 with complaints of unable to perform ADLs independently. After workup, patient was found to be positive for COVID-19. CT of the head showed no acute intracranial abnormalities. Chest x-ray did show bibasilar subsegmental atelectasis. Patient was discharged with a prescription for Paxlovid and instructions to return with worsening symptoms. He returned in the evening with complaints of increased weakness and inability to ambulate independently. In the emergency department, patient was hypertensive, however, other vital signs are stable. He did not require supplemental oxygen. Complete blood count and BMP were unremarkable. Suspect increased weakness secondary to COVID-19. Patient has been admitted for further evaluation and management of generalized weakness secondary to COVID-19. Review of Systems Constitutional: Positive for appetite change and fatigue. Negative for chills and fever. HENT: Positive for rhinorrhea and sore throat. Negative for sneezing. Eyes: Negative. Negative for light sensitivity. Respiratory: Positive for cough. Negative for shortness of breath. Cardiovascular: Negative. Negative for chest pain. Gastrointestinal: Negative for nausea, vomiting, abdominal pain and diarrhea. Genitourinary: Negative. Negative for difficulty urinating, urinary incontinence and flank pain. Musculoskeletal: Negative for neck pain, back pain and joint pain. Neurological: Positive for headaches, dizziness and weakness. Psychiatric/Behavioral: Negative. Skin: Negative. Negative for itching, changed spots and rash. OBJECTIVE: BP 137/68 | Pulse 65 | Temp 37 ?C (Oral) | Resp 21 | Wt 94 kg | SpO2 95% | BMI 30.60 kg/m? Physical Exam Vitals reviewed. Constitutional: General: He is not in acute distress. Appearance: Normal appearance. He is not ill-appearing or diaphoretic. HENT: Head: Normocephalic. Nose: Nose normal. No congestion or rhinorrhea. Mouth/Throat: Mouth: Mucous membranes are moist. Pharynx: Oropharynx is clear. Eyes: Conjunctiva/sclera: Conjunctivae normal. Pupils: Pupils are equal, round, and reactive to light. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Pulses: Normal pulses. Heart sounds: Normal heart sounds. No murmur heard. No gallop. Pulmonary: Effort: Tachypnea present. No respiratory distress. Breath sounds: No wheezing or rales. Abdominal: General: Bowel sounds are normal. There is no distension. Palpations: Abdomen is soft. Tenderness: There is no abdominal tenderness. There is no guarding. Musculoskeletal: General: No tenderness or signs of injury. Normal range of motion. Cervical back: Normal range of motion. Skin: General: Skin is warm and dry. Capillary Refill: Capillary refill takes less than 2 seconds. Findings: No erythema or rash. Neurological: General: No focal deficit present. Mental Status: He is alert and oriented to person, place, and time. Psychiatric: Attention and Perception: Attention normal. Mood and Affect: Mood normal. Speech: Speech normal. Behavior: Behavior normal. Behavior is cooperative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: NIH stroke scale
Hospital-Tage: 2,0
Labordaten: Complete Blood Count w/Differential (Abnormal) Collected: 04/09/22 0711 Order Status: Completed Specimen: Blood, Venous Updated: 04/09/22 0900 White Blood Cell 7.03 4.00 - 10.80 x10*3/uL Red Blood Cell 5.75 4.60 - 6.00 x10*6/uL Hemoglobin 16.2 14.0 - 18.0 g/dL Hematocrit 49.5 42.0 - 52.0 % Mean Cell Volume 86.1 80.0 - 100.0 fL Mean Cell Hemoglobin 28.2 27.0 - 33.0 pg Mean Cell Hemoglobin Concentration 32.7 32.0 - 37.0 g/dL Red Cell Diameter Width 15.0 11.0 - 16.0 % NRBC Absolute Count 0.00 0.00 - 0.01 x10*3/uL NRBC Automated 0.0 0.0 - 0.1 %WBC Platelet 220 140 - 400 x10*3/uL Mean Platelet Volume 9.4 7.4 - 11 fL Neutrophil Automated 44.3 35.0 - 80.0 % Immature Granulocyte Automated 1.6 High 0.0 - 0.6 % Lymphocyte Automated 29.2 20.0 - 50.0 % Monocytes Automated 24.6 High 2.0 - 12.0 % Eosinophil Automated 0.0 0.0 - 6.0 % Basophil Automated 0.3 0.0 - 2.0 % Neutrophil Absolute Count 3.12 1.80 - 7.80 x10*3/uL Immature Granulocyte Absolute Count 0.11 High 0.00 - 0.05 x10*3/uL Lymphocyte Absolute Count 2.05 1.00 - 4.00 x10*3/uL Monocyte Absolute Count 1.73 High 0.00 - 0.90 x10*3/uL Eosinophil Absolute Count 0.00 0.00 - 0.50 x10*3/uL Basophil Absolute Count 0.02 0.00 - 0.20 x10*3/uL D-Dimer (Abnormal) Collected: 04/09/22 0711 Order Status: Completed Specimen: Blood, Venous Updated: 04/09/22 0806 D-Dimer Quant 530 High 0 - 500 ng/mL FEU Med.2015;163:701-711 Blood Adv 2018;2:3226 Basic Metabolic Panel (BMP) (Abnormal) Collected: 04/09/22 0711 Order Status: Completed Specimen: Blood, Venous Updated: 04/09/22 0803 Sodium Level 130 Low 134 - 146 mmol/L Potassium Level 3.5 3.4 - 5.0 mmol/L Chloride 96 Low 98 - 112 mmol/L HCO3 22 21 - 29 mmol/L Anion Gap 12 9 - 18 mmol/L Glucose Level 94 70 - 99 mg/dL Blood Urea Nitrogen 27 High 8 - 20 mg/dL Creatinine 0.92 0.60 - 1.30 mg/dL MDRD eGFR >60 >=60 mL/min CG eCrCl 58 mL/min/1.73 m2 Calcium Level Total 8.9 8.6 - 10.4 mg/dL C Reactive Protein (CRP), Blood Level (Abnormal) Collected: 04/09/22 0711 Order Status: Completed Specimen: Blood, Venous Updated: 04/09/22 0803 C-Reactive Protein 75.8 High <=5.0 mg/L
Aktuelle Erkrankungen: -
Vorgeschichte: Past Medical History: Diagnosis Date ? Arthritis Lumbar spine for 30 years ? BPH (benign prostatic hyperplasia) ? Cataracts, bilateral Last eye exam fall 2014 ? CVA (cerebral vascular accident) ? Erectile dysfunction Used viagra and it was ineffective ? Gastric ulcer 2013 w/ rectal bleeding ? Hearing loss Left>Right; Has hearing aids but doesn't use them ? Insomnia ? Pneumonia 1958 ? Umbilical hernia ~15 years ago
Andere Medikamente: diphenhydrAMINE-APAP (sleep) 25-500 MG 1 tablet Oral Nightly PRN Lactobacillus 1 each Oral Daily Meloxicam 7.5 mg Oral Daily PRN
Allergien: Aspirin - GI bleeding penicillin - unsure
Vorherige Impfungen: -

VAERS 2225956

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: IL
Alter: 46,0
Geschlecht: M
Eingang: 11.04.2022
Impfdatum: 17.12.2021
Beginn: 10.04.2022
Tage bis Beginn: 114,0
Dosis: 2
Route/Site: SYR / -

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

Chest pain Deep vein thrombosis Dyspnoea

Symptomtext

Patient admitted with sternal chest pain and SOB. Previously diagnosed with DVT on 4/5/2022.

Weitere VAERSDATA-Felder

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

VAERS 2201779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: -
Alter: 33,0
Geschlecht: F
Eingang: 28.03.2022
Impfdatum: 01.03.2022
Beginn: 03.03.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Diabetic ketoacidosis Dyspnoea Endotracheal intubation Respiratory distress Tracheostomy

Symptomtext

Patient fully vaccinated and boosted with Pfizer on 4/20/21, 5/11/21, and 3/1/22. Patient has a history of type 1 diabetes and ESRD. Presented to ED on 3/3/22 with complaints of shortness of breath. Previously hospitalized for over one month in January for acute respiratory distress requiring intubation and trach. Patient was admitted for DKA on 3/4/22 and discharged on 3/12/22.

Weitere VAERSDATA-Felder

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

VAERS 2180152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: OH
Alter: 70,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 27.10.2021
Beginn: 05.01.2022
Tage bis Beginn: 70,0
Dosis: 3
Route/Site: SYR / LA

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

Anti-GAD antibody Autoimmune pancreatitis Blood glucose increased Blood immunoglobulin G Dry mouth Fatigue Headache Hydronephrosis Intensive care Nasal dryness Pollakiuria SARS-CoV-2 antibody test Type 1 diabetes mellitus Ultrasound kidney abnormal Unresponsive to stimuli

Symptomtext

January 5th began excessive urinating, dry mouth, nose, headache & fatigue. January 13, 2022, EMTs transported unresponsive patient yo the Hospital ER. Ended up in ICU for 5 days. Autoimmune attack on pancreas causing Type 1 diabetes in previously healthy/fit 70 yr old woman. Extreme blood sugar numbers: 1332. Now on insulin injections 5x per day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 5,0
Labordaten: 1/13/22 Renal-hydronephrosis 1/24/22 GAD 1/24/22 Covid-19 IGG 1/24/22 Generic order 1- 200279 HLA Dr genotyping 2- 2014079 HLA DQ genotyping
Aktuelle Erkrankungen: None
Vorgeschichte: Skin allergies/ excema
Andere Medikamente: Multi vitamin, Vitamin D , Gemtesa
Allergien: Environmental allergies to grasses & walnut trees
Vorherige Impfungen: -

VAERS 2132218

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CO
Alter: 64,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 15.05.2021
Beginn: 30.10.2021
Tage bis Beginn: 168,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Hypoxia Syncope

Symptomtext

Patient presented to hospital on 10/30/21 for monoclonal antibody treatment however she had a syncopal episode and was hypoxic. Patient was transferred and admitted to hospital for treatment of hypoxia due to COVID. Previously fully vaccinated with Pfizer on 4/24/21 and 5/15/21. Patient was discharged on 11/3/21.

Weitere VAERSDATA-Felder

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

VAERS 2131542

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MI
Alter: 53,0
Geschlecht: M
Eingang: 22.02.2022
Impfdatum: 27.04.2021
Beginn: 24.08.2021
Tage bis Beginn: 119,0
Dosis: 2
Route/Site: IM / AR

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

Blood test Cerebral thrombosis Electrocardiogram Inappropriate schedule of product administration Ischaemic stroke Magnetic resonance imaging

Symptomtext

Pt. states that after receiving the 2nd dose of Phizer 04/27/2021, started experiencing symptoms 08/24/2021 of a Ischemic Stroke (blood clot in the brain). 6 weeks Rehabilitation, at a local Medical Center.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral thrombosis
Hospital-Tage: 5,0
Labordaten: EKG 08/24/2021 MRI 08/24/2021 Blood Panel 08/24/2021
Aktuelle Erkrankungen: N/A
Vorgeschichte: HBP
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2127995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: SC
Alter: 45,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 11.06.2021
Beginn: 27.06.2021
Tage bis Beginn: 16,0
Dosis: 2
Route/Site: - / LA

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

Chest X-ray Colonoscopy Echocardiogram Endoscopy Pericardial effusion Pericarditis Thyroid function test X-ray

Symptomtext

pericarditis; pericardial effusions; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 45 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 11Jun2021 (Lot number: EW0179) at the age of 45 years as dose 2, single for covid-19 immunisation. There was no other vaccine in the 4 weeks prior. Relevant medical history included: "Asthma" (unspecified if ongoing); "shellfish allergy" (unspecified if ongoing). She had not had COVID prior to vaccination. Concomitant medication(s) included: NASACORT and daily multivitamin. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0179, Location of injection: Arm Left), administration date: 21May2021, for Covid-19 Immunization. The following information was reported: PERICARDITIS (medically significant) with onset 27Jun2021 13:15, outcome "recovering", described as "pericarditis"; PERICARDIAL EFFUSION (medically significant) with onset 27Jun2021 13:15, outcome "recovering", described as "pericardial effusions". On 27Jun2021 experienced chest pain, radiated to neck and jaw. Then had persistent neck pressure afterwards. The events "pericarditis" and "pericardial effusions" were evaluated at the physician office visit; patient saw PCP (primary care physician), and was referred to GI and ENT, urgent care at one point. The patient underwent the following laboratory tests and procedures: chest x-ray: normal; colonoscopy: unknown result; echocardiogram: pericardial effusions; endoscopy: unknown result; thyroid function test: normal; x-ray (soft tissue neck): normal. Multiple meds to treat GERD. Finally has echo and had pericardial effusions. She saw cardiologist "last week" (as of 07Feb2022) who confirmed pericarditis. She was still having intermittent chest pain. She had not been Covid tested post-vaccination.; Sender's Comments: Considering the temporal association, a causal association between administration of bnt162b2 and the onset of "pericarditis" and "pericardial effusions" cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Test Name: chest x-ray; Result Unstructured Data: Test Result:Normal; Test Name: colonoscopy; Result Unstructured Data: Test Result:Unknown result; Test Name: Echo; Result Unstructured Data: Test Result:pericardial effusions; Test Name: upper endoscopy; Result Unstructured Data: Test Result:Unknown result; Test Name: Thyroid; Result Unstructured Data: Test Result:Normal; Test Name: soft tissue neck xray; Result Unstructured Data: Test Result:Normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Shellfish allergy
Andere Medikamente: NASACORT
Allergien: -
Vorherige Impfungen: -

VAERS 2119326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: MO
Alter: 63,0
Geschlecht: M
Eingang: 17.02.2022
Impfdatum: 14.05.2021
Beginn: 15.02.2022
Tage bis Beginn: 277,0
Dosis: 2
Route/Site: IM / RA

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

Condition aggravated Seizure

Symptomtext

was having seizures and went to hospital

Weitere VAERSDATA-Felder

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

VAERS 1662458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MI
Alter: 50,0
Geschlecht: M
Eingang: 15.02.2022
Impfdatum: 18.08.2021
Beginn: 11.09.2021
Tage bis Beginn: 24,0
Dosis: 3
Route/Site: IM / LA

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

Abstains from alcohol Ageusia Areflexia Blood glucose normal Bordetella test negative Angiogram cerebral normal Antineutrophil cytoplasmic antibody negative Biopsy artery normal Blood HIV RNA below assay limit Blood culture negative Facial paresis Guillain-Barre syndrome Immunoglobulin therapy Magnetic resonance imaging head Blood folate normal C-reactive protein increased Chest X-ray normal Complement factor C3

Symptomtext

Onset of multiple neurological symptoms 5 days after receiving the 3rd dose of Pfizer's COVID-19 vaccine. Patient was hospitalized, underwent extensive workup and diagnosed with vaccine-induced Acute Inflammatory Demyelinating Polyneuropathy (AIDP - Guillain-Barre Syndrome) with bilateral facial nerve palsy, which is detailed in VAERS Event Report 1759017-1. The patient experienced a second post-vaccination autoimmune inflammatory syndrome, beginning 24 days after the 3rd COVID-19 vaccine (5 days post-hospitalization for AIDP). It presented with a daily low-grade fever 99.5-100.4, fatigue, malaise, generalized pressure headache; phono-phobia; infrequent nausea with dry heaving; and episodic dizziness with motion. Normal CBC and negative blood cultures x2. Infection and tumor surveys were unremarkable. HIV remained stable and undetectable. Treatment with a 6-day Medrol steroid pack without effect. Continued daily low-grade fever <100.4 with subsequent start of Ibuprofen and then with alternating dosages of Acetaminophen. Elevated temperature breakthrough with prominent constitutional symptoms persisting for 70 days despite Ibuprofen/ Acetaminophen. AIDP neurological symptoms never relapsed and progressively improved over this time period. No patient or family history of autoimmune diseases. Headache characteristics changed with temporal/frontal aching and point tenderness over temporal artery/branch vessels. No respiratory, gastrointestinal, skin or urinary symptoms. Elevated ESR rate of 58 mm/Hr and C-reactive protein of 17.8 mg/L. Rheumatology suspected Giant Cell Arteritis and initiated Prednisone 60mg QD. All symptoms and low-grade fever resolved within 3-5 days. MRI Head Angiogram without evidence of aneurysm or stenosis. No eye abnormalities noted on a dilated fundoscopic examination by Ophthalmology. Pulmonary radiography and computed tomography demonstrated no active disease. Temporal Artery Biopsy after 17 days on high-dose steroids demonstrated no evidence of acute or chronic inflammatory vasculitis. Positive titer for Serine Protease 3 Antibody with 34 AU/ mL. Diagnosis of COVID-19 Vaccine-Related ANCA Positive Vasculitis. Prednisone taper x3 months, currently at 10mg QD with continued remission of symptoms/elevated temperature.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: CBC/Chemistry Panel - unremarkable. Vitamin B12 & Folate levels - Normal. C-Reactive Protein - 17.8 mg/L; Sed Rate (ESR) - 58 mm/Hr. Negative blood cultures x2. Positive titer for Serine Protease 3 Antibody with 34 AU/ mL, MPO antibody negative; Non-reactive Hepatitis B & C panel, negative TB panel, normal protein electrophoresis, normal Complement C3 & C4, mildly elevated urinary protein creatinine ratio of 0.257 g/day and otherwise unremarkable urinalysis. HIV viral load - undetectable. CT of Head/Thorax/Abdomen/Pelvis with contrast - no evidence of malignancy; mildly enlarged bilateral axillary and cervical lymph nodes; a few solid calcified lung nodules < 4mm with non-specificity. MRI Head Angiogram without evidence of aneurysm or stenosis of major proximal intracranial arteries. Temporal Artery Biopsy with adequate 2.5 cm artery segment demonstrated no evidence of acute or chronic inflammatory vasculitis.
Aktuelle Erkrankungen: None
Vorgeschichte: Obstructive Sleep Apnea, Obesity, Major Depressive Disorder, Non- Insulin Dependent Diabetes Type II, Hypertension, HIV (long-term non-detectable), and Gastro-esophageal Reflux Disease
Andere Medikamente: Escitalopram, Bupropion, Omeprazole, Losartan, Amlodipine, Dolutegravir, Emtricitabine & Tenofovir Alafenamide, Glimepiride, Centrum Multi-Vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2110143

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: IL
Alter: 15,0
Geschlecht: M
Eingang: 14.02.2022
Impfdatum: 25.05.2021
Beginn: 27.07.2021
Tage bis Beginn: 63,0
Dosis: 2
Route/Site: IM / LA

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

Aphonia Cognitive disorder Conversion disorder Dyskinesia Fine motor skill dysfunction Hyperventilation Laboratory test normal Memory impairment Neurological examination abnormal Paralysis Syncope

Symptomtext

He collapsed and was hyperventilating. When he came around, he had all over paralysis. When his voice and upper body returned, his legs remained paralyzed. He was released from ER

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paralysis
Hospital-Tage: 14,0
Labordaten: He was at hospital initially. After all tests, there was nothing significant. After Neuro evaluated him, they thought he may have FND (Functional Neurological Disorder). He did rehab. He is now enrolled in Pain Clinic. He has some function in the right leg but the left leg continues to have paralysis. He has been removed from school because he is experiencing memory and cognitive issues. As well as other FND related things such as fine motor skill issues and uncontrolled movement of the fingers and eyelids.
Aktuelle Erkrankungen: He has been sick with flu-like symptoms days prior.
Vorgeschichte: ADHD. Post Concussion Syndrome.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 2075531

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NM
Alter: 15,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 28.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Presyncope

Symptomtext

Pt. experienced vasovagal response 10 minutes post vaccine administration. Recovered and had 2nd episode approximately 15 minute later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: none reported
Andere Medikamente: not known
Allergien: none reported
Vorherige Impfungen: Pt. states post HPV vaccine vasovagal episode

VAERS 2054353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MI
Alter: 66,0
Geschlecht: M
Eingang: 21.01.2022
Impfdatum: 28.04.2021
Beginn: 30.12.2021
Tage bis Beginn: 246,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 Chest X-ray normal Computerised tomogram head normal Cough Dizziness Loss of consciousness Malaise Nausea Palpitations SARS-CoV-2 test positive Syncope Vomiting

Symptomtext

This is a 67y.o. male with significant past medical history of HTN, DM, ESRD on hemodialysis, BPH, nonischemic cardiomyopathy, MI, TIA, S/P AICD that presented to the hospital with chief complaint of syncope. Patient reportedly completed his HD session at his dialysis center when he suddenly loss consciousness. EMS was called and upon their arrival he was awake and conversing. Upon ED evaluation he reports feeling unwell. He states the past couple of days he has had intermittent dizziness, palpitations, non productive cough, nausea, and vomiting. He denies any fever, chills, chest pain, abdominal pain, constipation, or diarrhea. In the ED, patient normotensive, afebrile, stable SPO2 on room air. COVID positive. CT head negative for acute process. CXR negative for acute process. He has been admitted for further evaluation and management with consultation in place to nephrology and cardiology. Patient seen and examined only by the attending physician; NP only responsible for chart review in an effort to limit exposure given the patient's COVID positive status.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 8,0
Labordaten: This is a 67y.o. male with significant past medical history of HTN, DM, ESRD on hemodialysis, BPH, nonischemic cardiomyopathy, MI, TIA, S/P AICD that presented to the hospital with chief complaint of syncope. Patient reportedly completed his HD session at his dialysis center when he suddenly loss consciousness. EMS was called and upon their arrival he was awake and conversing. Upon ED evaluation he reports feeling unwell. He states the past couple of days he has had intermittent dizziness, palpitations, non productive cough, nausea, and vomiting. He denies any fever, chills, chest pain, abdominal pain, constipation, or diarrhea. In the ED, patient normotensive, afebrile, stable SPO2 on room air. COVID positive. CT head negative for acute process. CXR negative for acute process. He has been admitted for further evaluation and management with consultation in place to nephrology and cardiology. Patient seen and examined only by the attending physician; NP only responsible for chart review in an effort to limit exposure given the patient's COVID positive status.
Aktuelle Erkrankungen: ? BPH (benign prostatic hyperplasia) ? Diabetes mellitus (CMS/HCC) ? Diabetic neuropathy (CMS/HCC) ? ESRD on dialysis 09/15/2019 M,W,F ? Essential hypertension 11/30/2015 ? Hyperlipidemia ? Medical non-compliance 11/30/2015 ? MI (myocardial infarction) (CMS/HCC) ? Nonischemic Cardiomyopathy 6/22/2017 Last ejection fraction 40% ? Reported loss of consciousness. Chronic 4/16/2016 ? Sinus bradycardia 12/27/2015 ? TIA (transient ischemic attack)
Vorgeschichte: ? BPH (benign prostatic hyperplasia) ? Diabetes mellitus (CMS/HCC) ? Diabetic neuropathy (CMS/HCC) ? ESRD on dialysis 09/15/2019 M,W,F ? Essential hypertension 11/30/2015 ? Hyperlipidemia ? Medical non-compliance 11/30/2015 ? MI (myocardial infarction) (CMS/HCC) ? Nonischemic Cardiomyopathy 6/22/2017 Last ejection fraction 40% ? Reported loss of consciousness. Chronic 4/16/2016 ? Sinus bradycardia 12/27/2015 ? TIA (transient ischemic attack)
Andere Medikamente: acetaminophen (TYLENOL) 325 MG PO Tab take 650 mg by mouth every 4 hours as needed. aspirin EC (HALFPRIN) 81 MG PO Tablet Delayed Response take 1 Tab by mouth once daily. atorvastatin (LIPITOR) 40 MG PO Tab take 1 Tab by mouth once ever
Allergien: Allergen Reactions ? Iodine Swelling, lips/throat/tongue ? Metformin Swelling, lips/throat/tongue ? Penicillins Swelling, lips/throat/tongue ? Shellfish Allergy Swelling, lips/throat/tongue ? Sulfa Antibiotics
Vorherige Impfungen: -

VAERS 1944275

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: -
Alter: 71,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 17.05.2021
Beginn: 15.12.2021
Tage bis Beginn: 212,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Condition aggravated Decreased appetite Diarrhoea Productive cough Pyrexia SARS-CoV-2 test positive Seizure

Symptomtext

12/15/21 presents to ED for "fever". PMHx of "seizures on Keppra, Covid positive, CAD, and CVAs with aphasia"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: 12/01/21 SARS-CoV-2 (COVID-19) detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2019740

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NJ
Alter: 56,0
Geschlecht: F
Eingang: 09.01.2022
Impfdatum: 31.08.2021
Beginn: 01.09.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Abdominal pain upper Burning sensation Diarrhoea Electrocardiogram normal Eosinophil count increased Faeces discoloured Fatigue Hypoaesthesia Hypotension Mean platelet volume decreased Nausea Neck pain Neutrophil count Rash Skin laceration Syncope Vertigo

Symptomtext

Syncope, low blood pressure (2 weeks), nausea (1 month), diarrhea (2 weeks), stool color change (2 weeks), severe lacerations due to rash, neck pain (2 months), stomach pain (1 month), extreme exhaustion (2 weeks), exhaustion (2 months), numbing/burning in hands (2 weeks), vertigo (3 months) IV fluid 9/10/21. Physical Therapy for vertigo October/November 2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: 9/10/2021 EKG-normal 02Sat normal Temperature-Normal Blood work: Low MPV Low Eosinophils High Neutrophil, Absolute
Aktuelle Erkrankungen: none
Vorgeschichte: Hashimoto's disease
Andere Medikamente: Synthroid, multi vitamin
Allergien: shellfish, sulfa drug, anchovy
Vorherige Impfungen: -

VAERS 2018583

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: GA
Alter: 56,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 09.08.2021
Beginn: 01.08.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Abdominal pain Asthenia COVID-19 Dizziness Drug ineffective Job dissatisfaction Loss of consciousness Pyrexia SARS-CoV-2 test Ultrasound scan Vomiting

Symptomtext

she was going to pass out; positive COVID-19 test with symptoms; positive COVID-19 test with symptoms; Weakness; Dizziness; Throwing up; Fever; abdominal pain; she didn't go back to work until 24Sep2021; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56 year-old female patient received bnt162b2 (BNT162B2), administration date 09Aug2021 (Lot number: EW0179) at the age of 56 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: LOSS OF CONSCIOUSNESS (medically significant) with onset 27Aug2021, outcome "recovered" (24Sep2021), described as "she was going to pass out"; COVID-19 (medically significant), DRUG INEFFECTIVE (medically significant) all with onset 27Aug2021, outcome "unknown" and all described as "positive COVID-19 test with symptoms"; ASTHENIA (non-serious) with onset 27Aug2021, outcome "recovered" (24Sep2021), described as "Weakness"; DIZZINESS (non-serious) with onset 27Aug2021, outcome "recovered" (24Sep2021), described as "Dizziness"; VOMITING (non-serious) with onset 27Aug2021, outcome "recovered" (24Sep2021), described as "Throwing up"; ABDOMINAL PAIN (non-serious) with onset Aug2021, outcome "not recovered", described as "abdominal pain"; JOB DISSATISFACTION (non-serious) with onset Aug2021, outcome "recovered" (24Sep2021), described as "she didn't go back to work until 24Sep2021"; PYREXIA (non-serious) with onset 27Aug2021, outcome "recovered" (24Sep2021), described as "Fever". The events "she was going to pass out", "positive covid-19 test with symptoms", "positive covid-19 test with symptoms", "weakness", "dizziness", "throwing up", "abdominal pain", "she didn't go back to work until 24sep2021" and "fever" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: pyrexia: (27Aug2021) 102; sars-cov-2 test: (27Aug2021) positive; ultrasound scan: (unspecified date) unknown results. Therapeutic measures were taken as a result of loss of consciousness, covid-19, asthenia, vomiting, abdominal pain, job dissatisfaction, pyrexia. Therapeutic measures were not taken as a result of dizziness.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101851769 same patient/product, different dose/events.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 20210827; Test Name: Fever; Result Unstructured Data: Test Result:102; Test Date: 20210827; Test Name: Covid; Test Result: Positive ; Test Name: Ultrasound; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2010121

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MO
Alter: 32,0
Geschlecht: M
Eingang: 06.01.2022
Impfdatum: 04.05.2021
Beginn: 05.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Chest pain Laboratory test Myocarditis

Symptomtext

Symptoms presented as debilitating chest pain daily for approximately one week. Blood pressure and pulse were normal. Took aspirin for pain. Follow up visit with Primary Care Provider after several days of pain provided probable Myocarditis diagnosis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: PCP referred to cardiologist for heart monitor and calcium score. Both tests were not conducted until long after symptoms had subsided, found to be normal.
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure, ADHD
Andere Medikamente: Adderall, Lisinopril
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1997996

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MO
Alter: 60,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 03.05.2021
Beginn: 24.12.2021
Tage bis Beginn: 235,0
Dosis: 2
Route/Site: SYR / -

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

Fatigue Intensive care Polymerase chain reaction positive Pyrexia Somnolence

Symptomtext

12/24 persistent fever, extreme fatigue/drowsiness, SPO2 <80; hospitalized on 12/26, ICU 2 days; still in hospital at time of interview on 12/30, current status not known.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 7,0
Labordaten: 12/24 Real-Time Reverse Transcriptase PCR, NP swab, Positive
Aktuelle Erkrankungen: None known
Vorgeschichte: Chronic kidney disease (severity/stage not known); diabetes
Andere Medikamente: Diabetes managed w/Rx (could not say which), no other reported
Allergien: NKA
Vorherige Impfungen: -

VAERS 1968109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: IL
Alter: 43,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 10.05.2021
Beginn: 11.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / AR

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

Arthralgia Blood glucose increased Blood test normal Diarrhoea Electrocardiogram normal Gait disturbance Heavy menstrual bleeding Insomnia Joint swelling Memory impairment Menstruation irregular Pain in extremity Peripheral swelling Thrombosis Vaccine positive rechallenge

Symptomtext

Shortly after the vaccine, I started having extremely bad hip pain where I couldn't sleep. My legs and hips were swelling, and I would have to stop walking because of the swelling and pain. Those symptoms have subsided, but I can't walk the way I used to. I got 2 blood clots underneath my toenails when we were walking 20,000 steps. I've never had blood clots before. I had periods every 2 weeks and eventually they stabilized but they are sometimes light sometimes heavy and they're no longer 28 days consistently anymore. Right after the shot, I had intense diarrhea that seemed uncontrollable and that happened twice after the vaccine. That also subsided as well. Haven't been the same in regard to memory since the vaccine as well. My blood sugars also were elevated after the vaccine, and they're currently bouncing, but I did just switch insulins so that maybe it as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: EKG - normal; Blood work - normal
Aktuelle Erkrankungen: None
Vorgeschichte: Type 1 Diabetes
Andere Medikamente: Humalog Insulin, Vitamins, Airborne, Tylenol, Aleve
Allergien: Statins
Vorherige Impfungen: 1st Pfizer COVID-19 vaccine - same symptoms, worsened after the 2nd vaccine

VAERS 1967527

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: WI
Alter: 40,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 24.05.2021
Beginn: 16.12.2021
Tage bis Beginn: 206,0
Dosis: 1
Route/Site: IM / RA

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

Agitation Alcohol poisoning COVID-19 Craniocerebral injury Endotracheal intubation Facial bones fracture Intensive care Intraventricular haemorrhage Laboratory test abnormal Mental status changes Multiple injuries Road traffic accident SARS-CoV-2 test positive Subarachnoid haemorrhage Subdural haematoma Toxicity to various agents Unresponsive to stimuli

Symptomtext

Pt. is a 41 y.o. male who presented on 12/16/21 for injuries sustained in a pedestrian injured in a traffic accident involving a motor vehicle. Labs showed alcohol and methamphetamine intoxication. Per report, patient was crossing the street and the mirror of a motor vehicle hit his head while traveling at 45mph. He had altered mental status and was unresponsive. on scene was E1, V1, M4 (6). upon arrival in ED, required intubation and extubated on 12/18/21. Patient tested positive for COVID-19. Patient sustained TBI/SAH/SDH/IVH and multiple facial fractures. Patient was transferred back to CCU on 12/19/21 due to increased agitation and need for a Precedex. Tested positive for COVID-19 upon admission on 12/16/21. Patient is homeless.

Weitere VAERSDATA-Felder

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

VAERS 1951235

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW 0179

schwer

Staat: MO
Alter: 53,0
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: 21.05.2021
Beginn: 04.12.2021
Tage bis Beginn: 197,0
Dosis: 1
Route/Site: IM / AR

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

Ageusia Anosmia Aortic dissection Aortic surgery Chest pain Fatigue Intensive care

Symptomtext

developed loss of taste and loss of smell and fatigue on 12/04. THen developed chest pain and admitted to Hospital on 12/05. Then transferred to Hospital on 12/05 with an aortic dissection. Underwent surgery. Moved from ICU on 12/13 to a COVID floor. Currently on 1-2 liters of oxygen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 9,0
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: hypertension, migraines
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 1948004

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MN
Alter: 70,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 14.05.2021
Beginn: 06.12.2021
Tage bis Beginn: 206,0
Dosis: 2
Route/Site: IM / RA

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

Arthralgia Aspiration joint Asthenia COVID-19 Facial paralysis Gout Pain in extremity SARS-CoV-2 test positive Synovial fluid crystal present

Symptomtext

Patient is a 70 YOF with PMH of DM2, CKD4, cardiorenal syndrome, anemia of CKD, HTN, mitral regurgitation, STEMI in 2020, and CHF who presents with 3 days of generalized weakness and pain in her feet, knees and wrists as well as a left-sided facial droop. Arthrocentesis of right knee shows monosodium urate crystals consistent with diagnosis of acute gout flare. Covid PCR positive. Admitted on 12/06/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Penicillins, Latex, Ergocalciferol (Vitamin D2)
Vorherige Impfungen: -

VAERS 1921094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MN
Alter: 43,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 12.05.2021
Beginn: 16.09.2021
Tage bis Beginn: 127,0
Dosis: UNK
Route/Site: SYR / AR

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

C-reactive protein abnormal Chest X-ray Echocardiogram Electrocardiogram Full blood count Inflammation Metabolic function test Pericardial effusion Pericarditis Red blood cell sedimentation rate Stress echocardiogram Troponin I

Symptomtext

pericardial effusion, pericarditis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: CBC with auto differential 9/16/2021 basic metabolic panel 9/16/2021 EKG 12 lead 9/16/2021 Chest x-ray PA and Lateral 9/16/2021 Troponin I 9/16/2021 Troponin I (again) 9/16/2021 Echo Stress Echocardiogram 9/30/2021 ESR 10/12/2021 CRP Inflammation 10/12/2021 EKG 12 lead 10/15/2021 Troponin I 10/15/2021 Echocardiogram, 11/12/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Sjogren's syndrome, depression
Andere Medikamente: trintellix, meloxicam, cyclobenzaprine, multivitamin
Allergien: -
Vorherige Impfungen: -

VAERS 1897787

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: LA
Alter: 34,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 04.05.2021
Beginn: 06.08.2021
Tage bis Beginn: 94,0
Dosis: 1
Route/Site: SYR / RA

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

Abortion spontaneous Deep vein thrombosis Gait disturbance Maternal exposure before pregnancy Pain in extremity Ultrasound scan

Symptomtext

Pregnancy was discovered shortly rafter first vaccine. Was advised to safely continue, so I did. My date date was January 16, 2022. Late June I started feeling stabbing pain in my leg occasionally. At 16 weeks pregnant, I suffered a miscarriage and had to deliver the fetus on August 6, 2021. After delivery the pain in my leg was so bad I couldn?t walk. There was no swelling, nor color or temperature change- just stabbing and burning pain. An ultrasound found a DVT, and I have been on blood thinners ever since. I have had two perfectly healthy pregnancy prior to this. And have no history of blood clots; and no family history of blood clots.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Ultrasound done at 16 weeks checkup showed no heartbeat, August 4, 2021. Confirmation of fetal demise, August 4, 2021. Ultrasound on leg done August 17, 2021- results, DVT.
Aktuelle Erkrankungen: N/a
Vorgeschichte: N/a
Andere Medikamente: Prenatal vitamins
Allergien: None
Vorherige Impfungen: -

VAERS 1889487

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NY
Alter: 36,0
Geschlecht: M
Eingang: 22.11.2021
Impfdatum: 24.05.2021
Beginn: 28.05.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: - / LA

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

Brain natriuretic peptide normal Cardiac imaging procedure Chills Dizziness Electrocardiogram repolarisation abnormality Fatigue Hypertrophy Loss of consciousness Pain Palpitations Sinus bradycardia Syncope Troponin normal Ultrasound scan abnormal Visual impairment

Symptomtext

Patient is a 36 y.o. male w/ no PMH p/w 3d of palpitations and one episode of concomitant syncope. Patient in perfect health until 5d PTA when he got COVID vax - had usual side effects (body aches, chills) for 1-2d. Then 2d PTA started getting palpitations which happen predominantly when he is laying down to go to bed. 1d PTA patient woke up, got up from bed then started feeling palpitations and light headed with dimming of vision - layed down on ground and raised legs, however still LOC for a few minutes. No prodromal flushing or dizziness, no tongue biting or incontinence, no post-ictal state. However felt fatigued when he woke up - still able to walk to bathroom. Notably patient is athletic and rides a bike >200miles/week and never has had presyncope or syncopal symptoms, and has baseline sinus bradycardia in 50s. In ED patient AFHDS. Not currently feeling episodic symptoms described above. ROS positive for chills and body aches post vaccine but otherwise no fever, headache, uri sx, cough, shortness of breath, chest pain/tightness/pressure, Nausea and vomiting, diarrhea, constipation, melena/hematochezia, dysuria, brusing, rashes, weight gain/loss. Tele showing sinus bradycardia, ekg w/ right bundeloid pattern and LVH w/ repolarization abnormalities (no STE, I.e. no brugada). BNP neg, trop neg, POCUS w/ hypertrophy, IVS 1.4cm, however did not seem asymmetric.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 4,0
Labordaten: - Hospitalization from 5/28 to 6/1 - Cardiology consultation/imagery on 6/1
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1888443

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0179

schwer

Staat: TX
Alter: 28,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 01.06.2021
Beginn: 21.07.2021
Tage bis Beginn: 50,0
Dosis: 1
Route/Site: SYR / RA

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

Computerised tomogram Electroencephalogram Magnetic resonance imaging Memory impairment Seizure

Symptomtext

Seizures for unknown reason while at school.limited memory. Advised at urgent care to go to er. Went to er and was admitted for monitoring and neurology consult

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: 3,0
Labordaten: Mri, Ct scan, eeg
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Linsinopril
Allergien: Gentamicin
Vorherige Impfungen: -

VAERS 1876578

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: KY
Alter: 14,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 12.08.2021
Beginn: 13.08.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Computerised tomogram Electrocardiogram Electrocardiogram ambulatory Electroencephalogram Magnetic resonance imaging Seizure

Symptomtext

Had seizure next day after vaccine on 8/12/2021 at school and transported by ambulance to Medical Center with kepra and follow up with Neurologist Dr. Dr. added Zimpat to Kepra for treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Neurologist did EEG, EKG, Heart Monitor, MRI, CT
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: reported yesterday 11/16/2021 he had First seizure 3 hours after first Pfizer vaccine, then another siezure 3 days after that

VAERS 1869244

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge EW0179

schwer

Staat: IL
Alter: 56,0
Geschlecht: M
Eingang: 15.11.2021
Impfdatum: 03.05.2021
Beginn: 04.11.2021
Tage bis Beginn: 185,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Chest X-ray Intensive care SARS-CoV-2 test positive

Symptomtext

Pt. Tested positive for COVID on 11/4

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: CXR, ICU stay
Aktuelle Erkrankungen: Diabetic, Diastolic Heart Failure, HTN, Pulmonary Fibrosis ,Pulmonary, HTN CKD
Vorgeschichte: DM
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1861070

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NY
Alter: 49,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 20.05.2021
Beginn: 28.06.2021
Tage bis Beginn: 39,0
Dosis: 2
Route/Site: - / RA

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

Asthenia Electric shock sensation Feeling abnormal Inflammation Injection site pain Magnetic resonance imaging Migraine Muscular weakness Neuralgia Pain Pain in extremity Paraesthesia Periarthritis X-ray

Symptomtext

Following vaccine debilitating migraine that lasted 4 days, felt like head would explode and foggy for about two weeks-this was the short term side effect. Initially, felt pain by injection sight. Eventually it spread and felt shocks in both right and left shoulder joints when reaching for items and sudden movements. The right shoulder is frozen, and the left is a little frozen, can move it up more than the right hand. Extreme constant radiating pain, tingling and muscle weakness in both arms and shoulders and sometimes radiating to upper back and neck when exerting shoulder muscles. Pain is worse at night, need constant hand movement or extremely sore, inflammation and possible nerve damage. Orthopedics took X-rays and MRI, currently on Meloxicam and Cyclobezaprine for several months. Also, saw a Neurologist who recommended Cymbalta for the nerve pain. Will see a Rheumtologist on 11/19 . Did not have any pain previous ta vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: Xray 8/9/21 MRI 10/13/21
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Apri-Birth Control, Biotin, Vitamin D3, Vitamin C, 1/2 of a centrum multivitamin, elderberry, low dose 81 mg aspirin
Allergien: peniciilin
Vorherige Impfungen: -

VAERS 1854482

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: KS
Alter: 22,0
Geschlecht: M
Eingang: 09.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Confusional state Delirium Eye movement disorder Malaise Seizure

Symptomtext

Patient received vaccine and went to go sit down. He asked for water and said he didn't feel well. He then slumped in his chair and started convulsing in his chair. His eyes rolled back and he was delirious when he came to and didn't know where he was. EMS was called.

Weitere VAERSDATA-Felder

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

VAERS 1839648

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: WI
Alter: 16,0
Geschlecht: M
Eingang: 03.11.2021
Impfdatum: 30.04.2021
Beginn: 17.10.2021
Tage bis Beginn: 170,0
Dosis: 2
Route/Site: IM / RA

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

Acute kidney injury Alanine aminotransferase increased Aspartate aminotransferase increased Blood creatinine increased Breath sounds abnormal Capillary disorder Chapped lips Chest X-ray abnormal Conjunctival hyperaemia Conjunctivitis Coronary artery disease Diarrhoea Disseminated intravascular coagulation Dyspnoea Echocardiogram abnormal Ejection fraction normal Erythema Exposure to SARS-CoV-2

Symptomtext

Provider history and physical 10/20/21: "PT is a 16 y.o. male patient without a significant past medical history who presents with shock in the setting of fevers, vomiting, and diarrhea. Symptoms began on 10/17 with fever, body aches and headaches. Fevers have continued daily since that time, T 100-103F and managed at home with Advil. Vomiting and diarrhea onset on 10/18, with 2 episodes of vomiting per day over the past 3 days and "continuous" watery, non-bloody diarrhea. PO intake has been minimal due to the vomiting. He has not had any abdominal pain despite his symptoms. Headaches onset on 10/18 and are described as generalized and worse with movement. No neck stiffness or altered mental status. Mom noticed bilateral conjunctival injection on 10/18, which she attributed to dry heaving. He has not had any rashes. Denies any nasal congestion or rhinorrhea, however, does note preceding symptoms of nasal congestion on 10/4 that resolved by the 11th. Patient has had intermittent fatigue and general feeling of unwellness over the past several weeks but no other symptoms until 10/17. Patient was seen by PCP on 10/18 because of lethargy and intermittent fever, report of negative COVID-19 test on 10/18, recommended symptomatic management. He attends school and wears a mask (although no other classmates do) - known COVID-19+ contact on 10/15. No known COVID-19+ contacts 1-3 months prior to presentation. Patient was vaccinated against COVID-19 in 4/2021. Most recent travel includes various states all over summer 2021. Pt has not had any hematuria, dysuria, respiratory distress, peripheral edema, or known sick contacts with the exception of the aforementioned close COVID contact. On the day of presentation mom noticed that PT had cracked lips and tacky mucous membranes, which prompted presentation to an OSH ED. In the ED, vital signs included BP 90/52, HR 112, RR 20, SpO2 99% in RA, T 37.9C. Exam notable for cool distal extremities with delayed capillary refill and conjunctival injection. He was given a total of 3L of NS for fluid resuscitation and given cefepime and vancomycin for empiric antibiotic coverage. Due to persistent hypotension (as low as 80s/60s) despite fluids CHW was consulted and he was transported to the CHW PICU for further management. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 7,0
Labordaten: Hospital Course-unable to inlcude results from entire hospitalization "CNS: Remained at baseline through admission, no issues with pain. Patient noticed blurry vision after given IV steroids that improved throughout his stay. Discussed with ophthalmology and given improvement, it was thought to be 2/2 to the steroids. He does not wear glasses. No further work up needed and recommended follow up with an optometrist. Cardiovascular: Arrived on norepi 0.1mcg/kg/hr, initially tolerated weans and eventual discontinuation of norepi. However, Pt had an increase in his vasodilatory state with subsequent hypotension, tachycardia, and decreased perfusion and was briefly placed on both norepi and epi. He tolerated weans and has been off of inotropic support since 10/23. HRs overall downtrending and age-appropriate and BPs/MAPs overall improved and age-appropriate with resolution of shock. Initial troponin 0.560, proBNP 4600. Troponin peaked at 2.430 and downtrended x2 (most recently 0.217 on 10/24). Initial echocardiogram with mildly diminished LV systolic function and mild mitral valve insufficiency with normal coronaries. ECHO on discharged showed and EF of 58% and mildly ectatic L anterior descending coronary artery. Patient will require an echocardiogram again prior to discharge and follow-up in the cardiology COVID clinic at 2 weeks, 6 weeks, and 6 months post-MISC. No sports until cleared by cardiology. Respiratory: Placed on supplemental O2 on arrival to optimize saturations per septic shock protocol. On day 2 of hospitalization Patient was noted to have increased WOB with diminished lung sounds, and CXR identified pulmonary edema and L>R pleural effusions. He received a total of 6 spot doses of lasix to address the edema. Placed on HFNC (max 40L) and tolerated weans to 2 L low flow oxygen by 10/24 for desats to high 80s when lying flat. Pulmonary edema/pleural effusions improved both on imaging and clinically with decreased O2 needs and more comfortable WOB. Off oxygen for >24 hours prior do discharge. FEN/GI: Stool hemoccult positive on presentation, enteric pathogens neg. On 70% maintenance IV fluids and tolerated a general diet through admission. AST/ALT mildly elevated and downtrended prior to discharge. PPI while on steroids. Hematology: Started on lovenox prophylaxis on arrival given increased risk of VTE in the setting of MISC. LMWH level checked after 3rd dose d/t initial AKI - lovenox was prophylactic range and no dose adjustments were made. No other hematologic concerns throughout PICU stay. DIC panels reassuring. Lovenox discontinued on discharge. Infectious Disease: On Ceftriaxone and Clindamycin (did not want to start Vanc due to AKI) for 48 hours until cultures negative, d/c'd on 10/24. IVIG on 10/21 for MIS-C, persistently febrile with conjunctivitis and rash after infusion, prompting initiation of pulse dose steroids from 10/23-10/25, with plans to continue daily steroids at 60 mg after completion of pulse dosing. By day of transfer 10/24, rash and conjunctivitis resolved and afebrile for > 24 hours. Enteric pathogen panel, respiratory viral panel negative. COVID NAAT negative, IgG positive (however difficult to interpret because he is vaccinated). Rheumatology: Discussed with Rheumatology. HLH workup negative. Renal: Acute kidney injury with Cr peaking at 1.67 on admission, downtrended to normal (0.88) on discharge. Discharge Exam BP 90/52 (Vitals Position: Sitting, NIBP Cuff Size: Maroon) | Pulse 96 | Temp 36.7 ?C (98.1 ?F) (Oral) | Resp 22 | Ht 170.4 cm (67.09") | Wt (!) 109.9 kg (242 lb 4.6 oz) | SpO2 94% | BMI 37.84 kg/m? General: Comfortable in NAD HEENT: No congestion, no nasal discharge, lips not chapped, no drainage from eyes. Slight erythema on sclera. Respiratory: no retractions, no nasal flaring and clear breath sounds bilaterally. CV: regular rate, regular rhythm, normal S1, S2, no murmur noted and distal pulses 2+ Abdomen: soft, non-distended, non-tender and no rebound tenderness or guarding Extremities: warm, no edema MSK: no joint swelling Neuro: no focal abnormalities Skin: no rashes visible on exposed skin Discharge Plan -Aspirin, prednisone taper, and omeprazole while on steroids -Cardiology f/u as below -No sports until cleared by cardiology Discharge Medication List: Medication List START taking these medications ? aspirin 81 MG chewable tablet; Chew 1 tablet (81 mg total) by mouth daily.; Start taking on: October 27, 2021 ? melatonin 3 mg Tab tablet; Take 1 tablet (3 mg total) by mouth At bedtime. ? omeprazole 40 MG capsule; Commonly known as: PRILOSEC; Take 1 capsule (40 mg total) by mouth every morning before breakfast.; Start taking on: October 27, 2021 ? predniSONE 10 MG tablet; Commonly known as: DELTASONE; Take 6 tablets (60 mg total) by mouth daily for 3 days, THEN 5 tablets (50 mg total) daily for 3 days, THEN 4 tablets (40 mg total) daily for 3 days, THEN 3 tablets (30 mg total) daily for 3 days, THEN 2 tablets (20 mg total) daily for 3 days, THEN 1 tablet (10 mg total) daily for 3 days.; Start taking on: October 27, 2021 CONTINUE taking these medications ? acetaminophen 500 mg tablet; Commonly known as: TYLENOL ? ibuprofen 200 mg tablet; Commonly known as: MOTRIN STOP taking these medications ? ondansetron 8 MG disintegrating tablet; Commonly known as: ZOFRAN-ODT
Aktuelle Erkrankungen: None documented
Vorgeschichte: None
Andere Medikamente: None
Allergien: Dust mites Pollen
Vorherige Impfungen: -

VAERS 1327289

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 02.05.2021
Beginn: 02.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Anaphylactic reaction Dysphagia Palpitations Rash

Symptomtext

Rash on forearms; Difficulty swallowing; Palpitations; This is a spontaneous report from a contactable healthcare professional (patient). This non-pregnant 51-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; lot number EW0179) via an unspecified route of administration in the left arm on 02May2021 at 08:15 (at 51-years-old) as a single dose for COVID-19 immunisation. Medical history included COVID-19 from an unknown date and unknown if ongoing; and known allergies to latex, sap, and birch fruits from unknown dates. Concomitant medications included venlafaxine hydrochloride (EFFEXOR) and valsartan, both from unknown dates for unknown indications. The patient previously received the first dose of BNT162B2 (lot number EW0158) on 11Apr2021 at 08:15 (At 51-years-old) in the left arm for COVID-19 immunisation; and prochlorperazine (COMPAZINE) from an unknown date for an unknown indication and experienced allergy. The patient had not received any other vaccines in four weeks. On 02May2021 at 09:15 the patient experienced rash on forearms, difficulty swallowing and palpitations. The events resulted in an emergency department or urgent care visit. The patient was treated with a shot of prednisone and diphenhydramine hydrochloride (BENADRYL). The clinical outcome of the events was recovering. Since vaccination, the patient had not been tested for COVID-19.; Sender's Comments: Based on the information provided, the contributory role of the suspect product BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; lot number EW0179), to reported events rash, dysphagia and palpitations is possible. Case will be reassessed upon receipt of follow-up information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to plants (known allergies: sap); COVID-19 (If covid prior vaccination: yes); Fruit allergy (known allergies birch fruits); Latex allergy (known allergies: latex)
Andere Medikamente: EFFEXOR; VALSARTAN
Allergien: -
Vorherige Impfungen: -

VAERS 1327289

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 02.05.2021
Beginn: 02.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anaphylactic reaction Dysphagia Palpitations Rash

Symptomtext

Rash on forearms; Difficulty swallowing; Palpitations; This is a spontaneous report from a contactable healthcare professional (patient). This non-pregnant 51-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; lot number EW0179) via an unspecified route of administration in the left arm on 02May2021 at 08:15 (at 51-years-old) as a single dose for COVID-19 immunisation. Medical history included COVID-19 from an unknown date and unknown if ongoing; and known allergies to latex, sap, and birch fruits from unknown dates. Concomitant medications included venlafaxine hydrochloride (EFFEXOR) and valsartan, both from unknown dates for unknown indications. The patient previously received the first dose of BNT162B2 (lot number EW0158) on 11Apr2021 at 08:15 (At 51-years-old) in the left arm for COVID-19 immunisation; and prochlorperazine (COMPAZINE) from an unknown date for an unknown indication and experienced allergy. The patient had not received any other vaccines in four weeks. On 02May2021 at 09:15 the patient experienced rash on forearms, difficulty swallowing and palpitations. The events resulted in an emergency department or urgent care visit. The patient was treated with a shot of prednisone and diphenhydramine hydrochloride (BENADRYL). The clinical outcome of the events was recovering. Since vaccination, the patient had not been tested for COVID-19.; Sender's Comments: Based on the information provided, the contributory role of the suspect product BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; lot number EW0179), to reported events rash, dysphagia and palpitations is possible. Case will be reassessed upon receipt of follow-up information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to plants (known allergies: sap); COVID-19 (If covid prior vaccination: yes); Fruit allergy (known allergies birch fruits); Latex allergy (known allergies: latex)
Andere Medikamente: EFFEXOR; VALSARTAN
Allergien: -
Vorherige Impfungen: -

VAERS 1329464

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 30.04.2021
Beginn: 30.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Condition aggravated Headache Pain in extremity Peripheral swelling Rash Contusion Swelling face Thrombosis

Symptomtext

My legs started swelling; the first shot I got I had like a fever and chills, very bad like pain in my arm, in my neck from the first shot. But the 2nd shot is worst.; felt like my head was going to explode and the pain was sudden and instant; My arms started getting sore; I was starting to feel kind of rash or a bruise or rash just started appeared out of no were; This is a spontaneous report from a contactable consumer (patient) A 57-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EW0179; Expiration Date: 31Aug2021) via an unspecified route of administration, in arm left on 30Apr2021 11:15 (Age at vaccination: 57 years) as Dose 2, Single for covid-19 immunization. The patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: ER8737 and Expiration Date: 31Jul2021) via an unspecified route of administration, in arm left on 07Apr2021 (at the age of 57-year-old) as dose 1, Single for covid-19 immunization and experienced very bad like pain in my arm, in my neck, chills and fever. The patient's concomitant medications were not reported. The patient stated that she received her Pfizer second shot on 30Apr2021. So, on Friday 30Apr2021 it was administered at 11:15 AM and towards the end of the day, her arms started getting sore and then she was starting to feel kind of rash or a bruise or rash just started appeared out of no were. Then at 21:30 that night, because she was talking to her friend on the phone, the same night she felt like her head was going to explode and the pain was sudden and instant. So, it was not progressive but all of the sudden she had this unusual headache, and she never had that severe headache before in her life. She stated that duration of her severe head pain for 2nd shot was like 9 hours straight. Without any change it was severe, the severity stayed at the same level the entire time. Yes and it was at the same level pain which was at 10. It was actually more because she thought her head was going to explode. It was really bad. There are more side effects though. When that was happening, her legs started swelling, she can feel them swelling which she never felt that before. She was really worried because she had the instant, sudden excruciating pain in her head. Then she had the swelling rash like the rash came out suddenly and then her legs were swelling, so all of these things were happening at the same time. Patient took ibuprofen as treatment. She wanted to report it but she was also concerned about how bad reaction. The 2nd shot was worst. So she wanted to see now, she still feel a little bit like she was having effects of the shot even for today. Patient queried for whether she need to get follow up care on this because the symptoms she experience seems to fall in prescription of something like a blood clot possibly so she need to check if she need to get follow up care. Outcome of all events was recovered/resolved with sequel on unspecified date in 2021. Information on Lot/Batch number was available. Additional information has been requested. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

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

VAERS 1753715

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: SC
Alter: 75,0
Geschlecht: F
Eingang: 01.10.2021
Impfdatum: 30.08.2021
Beginn: 31.08.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Fatigue Loss of consciousness

Symptomtext

Extreme fatigue and passed out in the shower. Spent entire day in bed. Felt fine the next day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Atorvastatin Amlodipine Vitamin D3 Calcium Aspirin (81 mg) Turmeric Aller-fex Elderberry
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1746180

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: SD
Alter: 73,0
Geschlecht: M
Eingang: 29.09.2021
Impfdatum: 06.08.2021
Beginn: 11.08.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Anaemia Blood test Colonoscopy Endoscopy upper gastrointestinal tract Full blood count Gastrointestinal haemorrhage Haematochezia Haemoglobin decreased Intensive care Laboratory test Transfusion

Symptomtext

Patient developed bloody stools on the evening of August 11. After several bloody stools pt presented to the ER and was admitted for GI bleed. He underwent serial blood work testing and was treated with several blood transfusions for his anemia. He had 2 colonoscopies, and upper endoscopy and the pill swallow test. None of these test showed the source of his GI bleed. He continued to bleed but lessened over several days. He was discharged after 6 nights in the hospital, 3 of which in the ICU. He was monitered after his dismissal with CBC and his Hgb slowly went up to normal over several weeks time. Pt was advised to have a longer colonoscopy to reach sections of the small bowel and large intestine that their scopes couldn't reach. That is only done as larger facilities. Since pt hasn't had a rebleed since his discharge he hasn't scheduled this test as of yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, obesity, arthritis, enlarged prostate
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1741637

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NC
Alter: 19,0
Geschlecht: F
Eingang: 28.09.2021
Impfdatum: 24.08.2021
Beginn: 24.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hyperhidrosis Slow response to stimuli Syncope

Symptomtext

Hx of ADD and past vaccine injection, vasovagal events. Pt was administered vaccine and was observed by sister to be faint, slow to respond to questions. pt was diaphoretic, dazed, slow to respond, faint, Unable to obtain BP. EMS notified, EMS on scene at 9:53. A&O x4, After EMS evaluation pt declined transport to hospital for further evaluation. Pt given snack and water and pt walked without assistance with sister out of the building.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: ADD
Vorgeschichte: ADD
Andere Medikamente: Focalin, Junel-21
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1396660

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: GA
Alter: 14,0
Geschlecht: M
Eingang: 23.09.2021
Impfdatum: 10.06.2021
Beginn: 17.06.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / UN

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

Blood albumin Blood calcium Blood glucose Blood pressure measurement Body height Body mass index Body surface area Body temperature Breath sounds Cardiac murmur Chest pain Electrocardiogram T wave abnormal Electrocardiogram T wave amplitude decreased Electrocardiogram T wave inversion Magnetic resonance imaging heart Coronary artery aneurysm Echocardiogram Ejection fraction

Symptomtext

myocarditis; Elevated troponin; first his L arm was sore; a Slight increase in heart rate; This is a spontaneous report from a contactable consumer. A 14-year-old male patient (consumer son) received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot# not provided), via an unspecified route of administration on 10Jun2021 (at the age of 14-year-old ) at single dose for COVID-19 immunization. Medical history included asthma, Raynaud disease and torn meniscus. The patient has not had COVID-19. Not on daily controller med cannot remember the last time he required albuterol. Early on 12Jun2021, the patient was experiencing left sided chest pain so he came to ER for evaluation. The patient presenting with 2 days of chest pain. He first noticed the pain 2 days before, first his L arm was sore after receiving Pfizer COVID vaccines on 10Jun2021, he then noticed L sided chest pain. Describes pain as left sided, burning pain that is worse with inspiration and when laying down, pain does not radiate. No nausea, no diaphoresis, Denies reproducible pain with palpation. Due to mildly elevated troponin. Mildly abnormal ECG, he had echo which was normal; however, he was admitted to trend troponins and monitor for arrhythmia. ED course: Troponin mildly elevated at 0.088, normal echo. Admit to cardiology service for observation of rhythm, repeat troponins. Admission on 12Jun2021 Troponin on12Jun2021 Value: 0.088, on 13Jun2021Value: 2.000, on 14Jun2021 Value: 0.519. On 13Jun2021, has further elevation of troponin to 2 in setting of continuing, intermitted chest pain (improved with Motrin), though still no fever. Given timing of chest pain, abnormalities on ECG as well as rising troponin, he did appear to have possible post-covid-vaccine myocarditis, so obtained cardiac MRI on 14Jun2021. The patient was hospitalized from 12Jun2021 to 14Jun2021. Patient physical findings: Pulse 82, Resp 16, BP RUE 110/74 (adult cuff) , BP LLE 114/0, BMI 19.32 kg/m2, 49%ile (Z= -0.02) based on CDC (Boys, 2-20 Years) BMI-for-age based on BMI available as of 28Jun2021, BSA 1.46 sq meters pulse Ox: 97 % (finger) Oxygen Supplementation: Room Air. Review of Systems: Constitutional: no symptoms, Eyes: no symptoms, Ears: no symptoms, Nose: no symptoms, Throat: no symptoms, Cardiovascular: (myocarditis), Respiratory: (asthma). Gastrointestinal: no symptoms, Genitourinary: no symptoms, Musculoskeletal: no symptoms, Skin: no symptoms, Neurological: no symptoms, Psychiatric no symptoms, Hematologic/lymphatic: no symptoms, Endocrine: no symptoms, Hematologic/lymphatic: no symptoms, Endocrine: no symptoms. Constitutional: appropriate for age, non-distressed , Head: normocephalic, atraumatic , Eyes: normal sclera, conjunctiva and lids , ENT: inspection of nares, oral mucosa, and external ears appear normal, Neck: supple without masses , Chest and lungs: symmetric, clear to auscultation, normal air movement, no retractions o or deformity and no tenderness to palpation Cardiac: normally active precordium, regular rhythm, normal S1, physiologically split S2, no murmurs, clicks, rubs, or gallops, or normal distal perfusion with brisk capillary refill, no jugular venous distention, no clubbing, cyanosis, or edema and brachial and lower extremity (DP/DT) pulses are 2+ and symmetric without delay , Abdomen: soft and non-tender, active bowel sounds, no masses, no hepatomegaly and no splenomegaly , Musculoskeletal: grossly normal muscle mass. Strength and tone , Extremities: no joint swelling or tenderness, no obvious deformities , Skin: clear, no rashes, no lesions, Neurological: grossly intact, normal behavior for age. Laboratory tests: EKG: In order to assess the heart, a 12 lead electrocardiogram was performed. This showed: Normal Sinus rhythm at 89 bpm. ORS axis +63 degree, normal intervals, normal voltages, and inverted T-waves in lead III, only. Echocardiogram: an echocardiogram was performed to heart function due to the post vaccine myocarditis. It demonstrated: 1. Normal intra-cardiac and aortic arch anatomy. 2. Physiologic tricuspid regurgitation and pulmonary insufficiency. 3. Normal cardiac dimensions and biventricular function, including normal tissue Doppler ,4. NO pericardial effusion. Impression: Acute myocarditis following 2nd Pfizer vaccine for 2019 novel coronavirus disease. Elevated troponin. T-wave abnormalities on electrocardiograms. Normal cardiac function by echocardiography (including today's) and heart MRI , Normal heart MRI-does not meet imaging criteria for myocarditis. Meets case definition of post-Covid vaccine myocarditis. Chest pain; presumably secondary to Acute myocarditis. Physical Exam at discharge on 14Jun2021: Vital signs at discharge: BP 108/67 | Pulse 83 | Temp 36.3 degree Celsius (Tympanic) | Resp. 18 |Ht 161cm | Wt 48.3kg | Sp02 99% | BMI 18.63kg/m2 Room Air Result Date: 14Jun2021 Impression: Normal right ventricular size, RVEDV 64 cc/m2, Normal right ventricular systolic function, RV EF = 55%. Normal left ventricular size, LVEDV = 58 cc/m2. Normal left ventricular systolic function. LV EF = 59%. With no regional wall motion abnormalities No evidence of high signal intensity on T2 weighted imaging to suggest edema, T1 early post-contrast imaging to suggest hyperemia, or late gadolinium enhancement imaging to suggest myocardial fibrosis. The patient does not meet CMR criteria for myocarditis. Normal origins of the left and right coronary arteries, without evidence of dilation or aneurysm. Rhythm data: ECG on: 13Jun2021, Heart rate 90 , RR 668 , P-R Interval 165 , P Axis 31 , QRS Duration 74 , QT Interval 367 , Q 449 , QRS Axis 71 , T wave Axis 33 Impression Normal ECG Pediatric ECG interpretation Sinus rhythm normal p axis, V-rate 60-119 , Normal axes and intervals Flattened T waves In lll, V5, V6 Compared to ECG from 12Jun2021 , now see normal T wave axis, Still see flattened T waves in VS, V6 and now in Ill. Somewhat slower rate on current recording; otherwise, no significant change Discharge Medications. Amoxicillin 875mg 1 Tablet (875mg) by mouth 2 times a day for 1 dose Last dose is tonight Ibuprofen (MOTRIN) 400mg 1 Tablet (400mg) by mouth every 6 hours as needed for mild chest pain or moderate pain and ALBUTEROL IN, Inhale into lungs as needed. Oxygen-l supplementation: RA , Feeding regimen for home: Regular diet Recommended no strenuosu exercise for the next 2 weeks until his follow up cardiology visit on 28Jun2021. Discharge date: 14Jun2021 4:05 PM Since his Discharge from on 14Jun2021, the Patient has continued to have episodic chest pain. He describes a sharp pain that is worse with breathing occurring over a moderate-sized region of the mid-upper left anterior chest without radiation. The last episode occurred on 17Jun2021 when he was walking and running outside playing a "water gun" game with friends. He ran about 10 minutes and developed chest pain for several minutes that then lasted for a total of an hour. He felt a Slight increase in heart rate with the chest pain. He has no history of chest pain prior to the second dose of the Pfizer COVID-19 vaccine. His asthma episodes are triggered by upper respiratory tract infections. He has had no lightheadedness, syncope, dyspnea or exercise intolerance. The recent records were reviewed, Including the discharge summary, electrocardiograms, labs, heart MRI report, and echocardiogram reports. The electrocardiograms used T wave abnormalities and elevated troponin, but a structurally and functionally normal heart by echocardiogram and heart MRI. Diaqnosis of, post, Covid Vaccine myocarditis was made. An echocardiogram was performedto assess heart function due to the post vaccine myocarditis. It demonstrated: Normal intra-cardiac and aortic arch anatomy. Physiologic tricuspid regurgitation and pulmonary insufficiency. Normal cardiac dimensions and biventricular function, including normal tissue Doppler NO pericardial effusion. The patient who was previously healthy, developed chest pain with electrocardiographic abnormalities and elevated troponin after his second Pfizer COVID-19 vaccine, consistent with post-Covid vaccine myocarditis. He has had 1 other episode of chest pain since discharge from the hospital. I recommended restricting from significant physical activity or competitive sports, pending a repeat troponin level. At the time of this writing (30Jun2021 at 11 PM), I have not received a copy of the troponin level. If the troponin level is normal or significantly trending down, I would refer him for a cardiopulmonary exercise test in the near future prior to allowing return to normal physical activities. Cardiac: normally active precordium, regular rhythm, normal S1, physiologically split S2, no murmurs, clicks, rubs, or gallops, or normal distal perfusion with brisk capillary refill, no jugular venous distention, no clubbing, cyanosis, or edema and brachial and lower extremity (DP/DT) pulses are 2+ and symmetric without delay . Laboratory tests: EKG: In order to assess the heart, a 12 lead electrocardiogram was performed. This showed: Normal Sinus rhythm at 89 bpm. ORS axis +63 degree, normal intervals, normal voltages, and inverted T-waves in lead III, only. Follow-up will be determined on results of these tests. Pending Tests: Blood tests (Troponin level). Disposition: Ibuprofen (Motrin) 400mg tablet, Take 1 Tablet (400mg) by mouth every 6 hours as needed for mild pain moderate pain , ALBUTEROL IN, Inhale into lungs as needed. The outcome of the events was unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 2,0
Labordaten: Test Name: Albumin; Result Unstructured Data: Test Result:No value display; Test Name: Calcium; Result Unstructured Data: Test Result:No value display; Test Name: Glucose; Result Unstructured Data: Test Result:No value display; Test Name: BP; Result Unstructured Data: Test Result:108/67; Comments: BP RUE 110/74 (adult cuff) I BP LLE 114/0; Test Name: Height; Result Unstructured Data: Test Result:158.5 cm; Test Name: Height; Result Unstructured Data: Test Result:161cm; Test Name: BMI; Result Unstructured Data: Test Result:18.63; Comments: BMI 18.63kg/m2 Room Air; Test Date: 20210628; Test Name: BMI; Result Unstructured Data: Test Result:19.32 kg/m2; Comments: 9%ile (Z= -0.02) based on CDC (Boys, 2-20 Years); Test Name: BSA; Result Unstructured Data: Test Result:1.46 sq meters; Test Name: Temperature; Result Unstructured Data: Test Result:36.3; Comments: Temperature 36.3 degree Celsious; Test Name: breath sounds; Result Unstructured Data: Test Result:clear breath sounds; Comments: Comfortable respiratory effort with clear breath sounds; Test Name: murmur; Result Unstructured Data: Test Result:No murmur in systole or diastole; Test Date: 20210614; Test Name: aneurysm; Result Unstructured Data: Test Result:without evidence of dilation or aneurysm; Comments: Normal origins of the left and right coronary arteries, without evidence of dilation or aneurysm; Test Name: Doppler; Result Unstructured Data: Test Result:normal tissue Doppler; Test Date: 20210612; Test Name: Echocardiogram; Result Unstructured Data: Test Result:Structurally normal heart.; Comments: Normal LV size and systolic function, Normal RV size and systolic function. Normal coronary arteries. No pericardial effusion.; Test Date: 20210614; Test Name: LV EF; Result Unstructured Data: Test Result:59%; Comments: LV EF = 59%. With no regional wall motion abnormalities; Test Date: 20210614; Test Name: RV EF; Result Unstructured Data: Test Result:55%; Comments: RV EF = 55%.; Test Date: 20210612; Test Name: Electrocardiogram; Result Unstructured Data: Test Result:Normal Sinus rhythm, inverted T-waves; Comments: Normal Sinus rhythm at 89 bpm. ORS axis +63 degree, normal intervals, normal voltages, and inverted T-waves in lead III, only.; Test Date: 20210613; Test Name: Electrocardiogram; Result Unstructured Data: Test Result:now see normal T wave axis; Comments: Still see flattened T waves in VS, V6 and now in Ill Somewhat slower rate on current recording; otherwise, no significant change; Test Date: 20210614; Test Name: P-R Interval; Result Unstructured Data: Test Result:165; Test Date: 20210614; Test Name: Q; Result Unstructured Data: Test Result:449; Test Date: 20210614; Test Name: QRS Duration; Result Unstructured Data: Test Result:74; Test Date: 20210614; Test Name: QT Interval; Result Unstructured Data: Test Result:367; Test Date: 20210614; Test Name: RR; Result Unstructured Data: Test Result:668; Test Date: 20210612; Test Name: inverted T-waves; Result Unstructured Data: Test Result:inverted T-waves in lead III, only; Test Date: 20210614; Test Name: inverted T-waves; Result Unstructured Data: Test Result:Flattened T waves In lll, V5, V6; Comments: Compared to ECG from 12Jun2021 , now see normal T wave axis; Test Date: 20210614; Test Name: T wave Axis; Result Unstructured Data: Test Result:33; Test Name: Heart rate; Result Unstructured Data: Test Result:increase; Test Date: 20210614; Test Name: Heart rate; Result Unstructured Data: Test Result:90; Test Name: Pulse; Result Unstructured Data: Test Result:82; Test Name: Pulse; Result Unstructured Data: Test Result:83; Test Name: biventricular function; Result Unstructured Data: Test Result:Normal; Test Name: cardiac dimensions; Result Unstructured Data: Test Result:Normal; Test Date: 20210612; Test Name: intervals; Result Unstructured Data: Test Result:normal; Test Date: 20210612; Test Name: ORS axis; Result Unstructured Data: Test Result:+63 degree; Test Date: 20210614; Test Name: P Axis; Result Unstructured Data: Test Result:31; Comments: normal p axis; Test Date: 20210612; Test Name: voltages; Result Unstructured Data: Test Result:normal; Test Date: 20210614; Test Name: MRI; Result Unstructured Data: Test Result:normal; Comments: did not show evidence of myocarditis No evidence of high signal intensity on T2 weighted imaging to suggest edema, T1 early post-contrast imaging to suggest hyperemia, or late gadolinium enhancement imaging to suggest myocardial fibrosis. The patient does not meet CMR criteria for myocarditis.; Test Name: SpO2; Result Unstructured Data: Test Result:97 %; Comments: 97 % (finger); Test Name: SpO2; Result Unstructured Data: Test Result:99%; Test Name: Pain; Result Unstructured Data: Test Result:at best as 2/10, at worst as 4/10; Comments: pain at best as 2/10 and at worst as 4/10 (currently); Test Name: pericardial effusion; Result Unstructured Data: Test Result:NO pericardial effusion; Test Name: pulmonary insufficiency; Result Unstructured Data: Test Result:Physiologic tricuspid regurgitation and pulmonary; Test Date: 20210614; Test Name: QRS Axis; Result Unstructured Data: Test Result:71; Test Name: Resp; Result Unstructured Data: Test Result:18; Test Name: Resp; Result Unstructured Data: Test Result:16; Test Date: 20210614; Test Name: right ventricular systolic function; Result Unstructured Data: Test Result:Normal; Comments: Normal right ventricular size, RVEDV 64 cc/m2,; Test Date: 20210612; Test Name: Sinus rhythm; Result Unstructured Data: Test Result:Normal; Comments: Normal Sinus rhythm at 89 bpm; Test Name: tricuspid regurgitation; Result Unstructured Data: Test Result:Physiologic tricuspid regurgitation; Test Date: 20210612; Test Name: Troponin; Result Unstructured Data: Test Result:0.088; Test Date: 20210613; Test Name: Troponin; Result Unstructured Data: Test Result:2.000; Comments: Elevated troponin; Test Date: 20210614; Test Name: Troponin; Result Unstructured Data: Test Result:0.519; Test Date: 20210614; Test Name: V-rate; Result Unstructured Data: Test Result:60-119; Test Name: Weight; Result Unstructured Data: Test Result:48.5 kg kg; Test Date: 20131124; Test Name: Weight; Result Unstructured Data: Test Result:21.9 kg kg; Comments: (43%, Z- -0.17); Test Date: 20210602; Test Name: Weight; Result Unstructured Data: Test Result:49 kg kg; Comments: (36 %, Oh, Z- -0.37); Test Date: 20210613; Test Name: Weight; Result Unstructured Data: Test Result:48.3 kg kg; Comments: 48.3 kg (32%, Z: -0.47)
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Meniscus tear; Raynaud's disease
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1724102

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: TN
Alter: 48,0
Geschlecht: M
Eingang: 22.09.2021
Impfdatum: 03.05.2021
Beginn: 21.06.2021
Tage bis Beginn: 49,0
Dosis: 2
Route/Site: IM / LA

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

Atonic seizures Blood test Computerised tomogram Electroencephalogram Magnetic resonance imaging Seizure

Symptomtext

Seizures began 6/21/2021; no history of seizures; no family history of seizures. Doctors unable to find any other cause of adult onset atonic seizures.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Atonic seizures
Hospital-Tage: -
Labordaten: Two hour EEG 8/31/2021; multiple MRIs, CT Scans, and numerous blood tests run.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes
Andere Medikamente: Martoporol
Allergien: None
Vorherige Impfungen: -

VAERS 1700554

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NJ
Alter: 14,0
Geschlecht: F
Eingang: 15.09.2021
Impfdatum: 07.06.2021
Beginn: 15.06.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test normal Echocardiogram normal Electrocardiogram normal Fatigue Feeling abnormal Intensive care Lethargy Palpitations Pyrexia

Symptomtext

8Jun2021 she didn't feel right , tired then 15Jun was extremely tired and 16 Jun on virtual school , she fell asleep and heart was racing and she had a low grade fever of 101. she was very lethargic and not herself because she was an athletics. On 16Jun2021 Pediatrician and sent to ER was evaluated - ibuprofen, went to ICU over night. discharged following day. No other treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 1,0
Labordaten: Bloodwork - normal EKG - normal, elevated heart rate Echocardiogram - normal Heartrate -132-135 sitting still
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: Daily Vitamin Kirkland daily Vitamin
Allergien: all tree nuts
Vorherige Impfungen: -

VAERS 1693146

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: -
Alter: 19,0
Geschlecht: F
Eingang: 11.09.2021
Impfdatum: 10.09.2021
Beginn: 10.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / AR

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

Cold sweat Fall Pallor Syncope

Symptomtext

Attendee received second dose Pfizer vaccine at 12:35. Lot# EW0179. Attendee was directed to observation area. At 12:50 attendee attempted to stand and started to fall, patient was able to catch her and assist her back to the seated position. Attendee's skin was cool and clammy. Attendee's respirations were not tachypneic or dyspneic. Attendee was then assisted to the cot to lie down, with her legs elevated. HR: 83 BP: 106/80 RR: 16 O2Sat%: 97 12:55 - Attendee stated she felt better, no longer clammy or pale. Sat up in the cot. 13:10 -No voiced complaints- skin warm and dry. Took another set of vital signs before discharge without documentation. Care Practitioner educated on home discharge/adverse reaction instructions and attendee was discharged to home with her friend. Attendee did not have any reported escalation of symptoms and was able to walk out of clinic independently.

Weitere VAERSDATA-Felder

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

VAERS 1693122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: -
Alter: 19,0
Geschlecht: F
Eingang: 11.09.2021
Impfdatum: 10.09.2021
Beginn: 10.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / AR

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

Cold sweat Pallor Presyncope

Symptomtext

Attendee received second dose Pfizer vaccine at 12:35. Lot# EW0179. Attendee was directed to observation area. At 12:50 attendee attempted to stand and started to fall, someone was able to catch her and assist her back to the seated position. Attendee's skin was cool and clammy. Attendee's respirations were not tachypneic or dyspneic. Attendee was then assisted to the cot to lie down, with her legs elevated. HR: 83 BP: 106/80 RR: 16 O2Sat%: 97 12:55 - Attendee stated she felt better, no longer clammy or pale. Sat up in the cot. 13:10 -No voiced complaints- skin warm and dry. Took another set of vital signs before discharge without documentation. Care Practitioner educated on home discharge/adverse reaction instructions and attendee was discharged to home with her friend. Attendee did not have any reported escalation of symptoms and was able to walk out of clinic independently.

Weitere VAERSDATA-Felder

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

VAERS 1536500

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: -
Geschlecht: U
Eingang: 08.09.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: SYR / LA

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

Arthralgia Asthenia Blood iron decreased Blood phosphorus decreased Blood test Bladder disorder Gait disturbance Gait inability Electric shock sensation Fatigue Hypoaesthesia Mobility decreased Loss of control of legs Muscle spasms Ultrasound scan Movement disorder Nerve conduction studies normal Pain

Symptomtext

loss of control of legs; trouble walking; numbness in my abdomen and legs; muscle spasms in legs; knee and ankle pain; loss of bladder control; cannot walk up steps/stairs or on uneven ground/grass; This is a spontaneous report from a contactable consumer or other non hcp. A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number/expiration date unknown), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as DOSE NUMBER UNKNOWN, SINGLE for covid-19 immunisation. Relevant medical history and concomitant medications were not reported. On an unspecified date the patient experienced trouble walking, numbness in abdomen and legs, muscle spasms in legs, knee and ankle pain, loss of bladder control, cannot walk up steps/stairs or on uneven ground/grass, loss of control of legs. Patient also informed that MDs ordered a lot of lab test, including ultrasound, nerve induction study, blood work, but nothing was abnormal. At the time of the reporting events outcome was unknown. The lot number for the vaccine, [BNT162B2], was not provided and will be requested during follow up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: Test Name: Blood work; Result Unstructured Data: Test Result:Normal; Test Name: ultrasound; Result Unstructured Data: Test Result:Normal
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1679127

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: KY
Alter: 53,0
Geschlecht: F
Eingang: 07.09.2021
Impfdatum: 02.09.2021
Beginn: 03.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy

Symptomtext

Bell's Palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: hx htn, lyme disease, hx Bell's Palsy
Vorgeschichte: htn
Andere Medikamente: blood pressure med
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1678800

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NM
Alter: 19,0
Geschlecht: F
Eingang: 07.09.2021
Impfdatum: 06.09.2021
Beginn: 06.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Loss of consciousness

Symptomtext

19-year-old female passed out after receiving her first Pfizer vaccination she was in 15 min observation area. She was responsive an attended to by medical staff on team. EMS was called individuals vital checked, blood pressure, VGL and oxygen all normal. Mother was present and patient declined to go to hospital for further evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Fainted when blood was drawn in the past

VAERS 1670275

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: KY
Alter: 26,0
Geschlecht: F
Eingang: 03.09.2021
Impfdatum: 02.09.2021
Beginn: 03.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Loss of consciousness Nausea Paraesthesia

Symptomtext

She said she woke up 09/03/2021 0100 with severe nausea, dizziness. she stood up to go to the bathroom and passed out. She said her arms felt like pins and needles were in them

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Dexilant, birth control, Sertraline, nortriptyline, mvi, B, D E
Allergien: Maybe Bactrim
Vorherige Impfungen: -

VAERS 1646331

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: TX
Alter: 48,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 11.06.2021
Beginn: 01.06.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Arthralgia Asthenia Back pain Gastrooesophageal reflux disease Myalgia Oropharyngeal discomfort Presyncope

Symptomtext

Severe center upper back pain; joint pain; muscle aches; fainting episodes; throat discomfort; weakness; diagnosed with acid reflux; This is a spontaneous report from a contactable consumer (patient). A non-pregnant 48-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in left arm on 11Jun2021 at 10:15 am (Lot Number: EW0179, unknown expiration; at the age of 48 years old) as dose 2, single for COVID-19 immunization. Medical history reported as none. No known allergies. No past drug history. Concomitant medication included unspecified vitamins. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: ER8736) on 21May2021 at 10:15 am in the left arm at the age of 48 years old for COVID-19 immunisation. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On the date of the 2nd shot (on 11Jun2021 at 22:00), the patient experienced joint pain and muscle aches that lasted 1.5 days. Then the patient experienced severe center upper back pain the next day on 12Jun2021 that lasted for a few hours. Two weeks later (in Jun2021), the patient visited emergency room due to near fainting episodes, throat discomfort, and weakness. The patient had followed up with doctor one week later and diagnosed with acid reflux. The patient is taking pantoprazole as treatment for acid reflux. The patient was not diagnosed with COVID-19 prior to vaccination and has not been tested for COVID-19 since the vaccination. The patient recovered from events joint pain, muscle aches, and back pain in Jun2021, while recovering from the remaining events. The events were assessed as non-serious. No follow-up attempts are possible; information about batch number was already obtained.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1645812

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: FL
Alter: 61,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 14.06.2021
Beginn: 01.06.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

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

Activated partial thromboplastin time Blood pressure abnormal Contusion Full blood count Haematocrit Haematocrit increased Haemoglobin Haemoglobin increased Haemorrhage Headache Oropharyngeal pain Prothrombin time Pyrexia Swelling Thrombosis

Symptomtext

insane bleeding; bruising down to her breast/bruised from her chin to her breast; Miserable headache/ splitting headache; Fever; Sore throat; bad about not checking her blood pressure and thinks the headache could be related to her blood pressure; The Hemoglobin and Hematocrit were on the higher side; The Hemoglobin and Hematocrit were on the higher side; hard blood not dissolved on the right side of her face; swelling in her neck; This is a spontaneous report from a contactable nurse (patient). A 61-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in arm right on 14Jun2021 14:15 (Lot Number: EW0179) as DOSE 2, SINGLE for COVID-19 immunization. Medical history included melanoma with 100 plus stitches and gallbladder surgery. Her uncle years ago when she was 12 years old, did have ITP and it was not hereditary. There were no concomitant medications. Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EW0179), dose 1 on 24May2021 at 14:15 (at the age of 61 years), in the arm right for Covid-19 immunization and it was fine. The patient was not diagnosed with COVID-19 prior to vaccination. The patient had the second dose last 14Jun2021 and experienced miserable headache/ splitting headache, fever, and sore throat. The splitting headache and sore throat were persistent. The headache was reported as medically significant. She mentioned that she has been bad about not checking her blood pressure and thinks the headache could be related to her blood pressure, stating there is a vein sticking out on her forehead (Jun2021). In Jun2021, she stated that her hemoglobin and hematocrit were on the higher side. One was 16 but she doesn't remember which one. On 29Jun2021, two weeks after the vaccine, the patient underwent blepharoplasty, which is a cosmetic surgery, on the upper, lower and both sides and during the surgery, she had insane bleeding. States that the bleeding was terrible; they aspirated 100cc of blood. It was a day surgery and she was discharged but because of this, she had to go back to her surgeon everyday to have the blood aspirated from her face. She was also bruising down to her breast, bruised from her chin to her breast on 29Jun2021. Finally the bleeding improved after three weeks, but the doctor talked about going back to surgery to place drains as there is still some hard blood not dissolved on the right side of her face and has swelling in her neck that looks like ITP (Idiopathic thrombocytopenic purpura) but the doctor said she didn't have it (in 2021). The patient underwent lab tests in Jun2021 which included PTT, CBC, PT, all fine while hematocrit and hemoglobin were on the higher side. With regards to causality the patient states all of her events were related to the Pfizer COVID 19 vaccine, she can't think of anything else. Outcome of insane bleeding was recovering; fever recovered on 14Jun2021; headache and sore throat were not recovered; while the other events was unknown.; Sender's Comments: based on the available information the causal relationship between the adverse events splitting headache, fever, and sore throat, thrombosis , haematocrit increased ,blood pressure abnormal .haemoglobin increased ,contusion ,Bleeding ( haemorrhage )and the suspect vaccine comirnaty cannot be completely ruled out

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Date: 202106; Test Name: PTT; Result Unstructured Data: Test Result:Fine; Test Date: 202106; Test Name: CBC; Result Unstructured Data: Test Result:Fine; Test Date: 202106; Test Name: Hematocrit; Result Unstructured Data: Test Result:Higher side; Test Date: 202106; Test Name: Hemoglobin; Result Unstructured Data: Test Result:Higher side; Test Date: 202106; Test Name: PT; Result Unstructured Data: Test Result:Fine
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cholecystectomy; Melanoma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1582840

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: SC
Alter: 27,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 02.08.2021
Beginn: 02.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Cataplexy Disease recurrence Hallucination Intermenstrual bleeding Menstrual disorder Condition aggravated Fatigue Heavy menstrual bleeding Narcolepsy Sleep paralysis Sleep terror Somnolence

Symptomtext

Extreme worsening of Narcolepsy; Extreme worsening of Narcolepsy; very frequent cataplexy; very frequent cataplexy; Hallucinations; Breakthrough blood clots between menstrual cycle; Excessive daytime sleepiness; night terrors; sleep paralysis; Breakthrough blood clots between menstrual cycle; This is a spontaneous report from a contactable consumer. This 27-year-old non-pregnant female consumer (patient) reported for herself that she received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EW0179, Expiry Date: Unknown), via an unspecified route of administration, administered in left arm on 02Aug2021 as dose 1, single for covid-19 immunisation. Patient's known allergies were allergic to Macrobid, Morphine, Thiuram Mix, Gold, Gluten, Dairy, Eggs. Other medical history: Narcolepsy (Type 1 with Cataplexy), Endometriosis. Other medications in two weeks: Armodafinil 250mg, Bupropion XL 150mg, Zyrtec. No other vaccine in four weeks. No Covid prior vaccination and post vaccination. On 02Aug2021 at 17:00, the patient experienced extreme worsening of Narcolepsy (Type 1, with Cataplexy), with symptoms: excessive daytime sleepiness, very frequent cataplexy, night terrors, hallucinations, sleep paralysis. She also experienced breakthrough blood clots between menstrual cycle. Adverse events resulted in doctor or other healthcare professional office/clinic visit. She did not receive any treatment. The outcome of all events was not recovered. Information on Lot/Batch number was available. Additional information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Sleep paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to allopathic drugs (Known allergies: Macrobid, Morphine, Thiuram Mix, Gold, Gluten, Dairy, Eggs); Allergy to gold; Cataplexy (Narcolepsy (Type 1 with Cataplexy)); Dairy intolerance; Egg allergy; Endometriosis (Other medical history: Narcolepsy (Type 1 with Cataplexy), Endometriosis); Gluten sensitivity; Narcolepsy (Narcolepsy (Type 1 with Cataplexy))
Andere Medikamente: ARMODAFINIL; ACT BUPROPION XL; ZYRTEC [CETIRIZINE HYDROCHLORIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 1582840

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: SC
Alter: 27,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 02.08.2021
Beginn: 02.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Cataplexy Disease recurrence Hallucination Intermenstrual bleeding Menstrual disorder Condition aggravated Fatigue Heavy menstrual bleeding Narcolepsy Sleep paralysis Sleep terror Somnolence

Symptomtext

Extreme worsening of Narcolepsy; Extreme worsening of Narcolepsy; very frequent cataplexy; very frequent cataplexy; Hallucinations; Breakthrough blood clots between menstrual cycle; Excessive daytime sleepiness; night terrors; sleep paralysis; Breakthrough blood clots between menstrual cycle; This is a spontaneous report from a contactable consumer. This 27-year-old non-pregnant female consumer (patient) reported for herself that she received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EW0179, Expiry Date: Unknown), via an unspecified route of administration, administered in left arm on 02Aug2021 as dose 1, single for covid-19 immunisation. Patient's known allergies were allergic to Macrobid, Morphine, Thiuram Mix, Gold, Gluten, Dairy, Eggs. Other medical history: Narcolepsy (Type 1 with Cataplexy), Endometriosis. Other medications in two weeks: Armodafinil 250mg, Bupropion XL 150mg, Zyrtec. No other vaccine in four weeks. No Covid prior vaccination and post vaccination. On 02Aug2021 at 17:00, the patient experienced extreme worsening of Narcolepsy (Type 1, with Cataplexy), with symptoms: excessive daytime sleepiness, very frequent cataplexy, night terrors, hallucinations, sleep paralysis. She also experienced breakthrough blood clots between menstrual cycle. Adverse events resulted in doctor or other healthcare professional office/clinic visit. She did not receive any treatment. The outcome of all events was not recovered. Information on Lot/Batch number was available. Additional information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Sleep paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to allopathic drugs (Known allergies: Macrobid, Morphine, Thiuram Mix, Gold, Gluten, Dairy, Eggs); Allergy to gold; Cataplexy (Narcolepsy (Type 1 with Cataplexy)); Dairy intolerance; Egg allergy; Endometriosis (Other medical history: Narcolepsy (Type 1 with Cataplexy), Endometriosis); Gluten sensitivity; Narcolepsy (Narcolepsy (Type 1 with Cataplexy))
Andere Medikamente: ARMODAFINIL; ACT BUPROPION XL; ZYRTEC [CETIRIZINE HYDROCHLORIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 1326979

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MI
Alter: 54,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 07.05.2021
Beginn: 08.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Atrial fibrillation Atrial septal defect Back pain Blood test Cardiac stress test Chest discomfort Dyspnoea Dyspnoea exertional Magnetic resonance imaging heart Chest X-ray Echocardiogram Electrocardiogram Metabolic function test Paraesthesia SARS-CoV-2 test negative Spinal pain Musculoskeletal discomfort Myocardial fibrosis

Symptomtext

extreme scarring on heart; myocarditis; Atrial Fibrillation; severe SOB; intense chest and entire back pressure; could not walk past neighbor's house w/out stopping for breath.; intense chest and entire back pressure; This is a spontaneous report from a contactable consumer (patient). A 54-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), 2nd dose via an unspecified route of administration on 07May2021 09:00 (Lot Number: EWO179, expiration date unknown) at age of 54 years old as a single dose for covid-19 immunisation. The patient was not pregnancy at time of vaccination. Medical history included seasonal allergies. Concomitant medication included oxymetazoline hydrochloride (CLARITIN) taken for seasonal allergies. The patient previously took monistat and experienced allergies, 1st dose of BNT162B2 for covid-19 immunisation on 16Apr2021 08:30 at age of 54 years old (lot number=ERB732). The patient experienced severe sob, intense chest and entire back pressure, could not walk past neighbor's house w/out stopping for breath, atrial fibrillation, all on 08May2021 13:00, myocarditis, extreme scarring on heart, both on 27Jul2021. The patient was hospitalized for severe sob, intense chest and entire back pressure, could not walk past neighbor's house w/out stopping for breath, atrial fibrillation for 5 days. The patient was prolonged hospitalization for myocarditis, extreme scarring on heart. The patient underwent lab tests and procedures which included Cardiac MRI: myocarditis, extreme scarring on heart on 27Jul2021, PET Scan: unknown results on an unknown date, PCR: negative on 07Jun2021 Nasal Swab, negative on 07Jul2021 Nasal Swab, negative on 12Jul2021, negative on 22Jul2021 Nasal Swab, Rapid PCR: negative on 22Jul2021 Nasal Swab. Therapeutic measures were taken as a result of severe sob all events. The outcome of the events was not recovered. Clinical course: Day after 2nd shot the patient experienced severe SOB, intense chest and entire back pressure - could not walk past neighbor house w/out stopping for breath. Could not walk 1 block, nor 1 flight of stairs w/out being extremely winded with chest and back pressure. Went to ER twice/admitted twice for cardiac within 10 days of 2nd shot. Referred to Congenital Heart Specialist at #. Many tests /medications/ consults since 07May2021. Cardioversion and then Cardiac Ablation performed to treat Atrial Fibrillation in Jul2021. 27Jul2021 Cardiac MRI results show myocarditis, extreme scarring on heart - Dr. (Name) confirmed direct result from COVID vaccine. Currently wearing a Life Vest/portable defibrillator since 1Aug, waiting on a PET Scan (24Sep) for sarcoidosis and an EP Study (1Oct) to determine if a lethal arrhythmia can be induced under a safe environment - result would lead to permanent defibrillator, steroid treatment and potential biopsy. All events were resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Hospitalization, Life threatening. The treatment included Tests/treatment/medication/cardiac referral to U-M. No covid prior vaccination. Covid tested post vaccination. No other vaccine in four weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Test Date: 20210727; Test Name: Cardiac MRI; Result Unstructured Data: Test Result:myocarditis, extreme scarring on heart; Test Name: PET Scan; Result Unstructured Data: Test Result:Unknown results; Test Date: 20210607; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20210707; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20210712; Test Name: PCR; Test Result: Negative ; Test Date: 20210722; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20210722; Test Name: Rapid PCR; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Seasonal allergy
Andere Medikamente: CLARITIN ALLERGIC
Allergien: -
Vorherige Impfungen: -

VAERS 1632826

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: IL
Alter: 51,0
Geschlecht: F
Eingang: 25.08.2021
Impfdatum: 20.08.2021
Beginn: 24.08.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / RA

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

Cardioversion Catheterisation cardiac abnormal Chest pain Intensive care Pericardial effusion

Symptomtext

At 7:10 AM on 8/24/21 Patient reported that her ICD was firing and that she would be going to the ED for evaluation. After arriving at the ED Patient's husband reported that the Patient would be having a cardiac catheterization completed due to chest pain . Around 11:10am on 08/24/21. Husband reported following the cardiac catheterization that there was no new blockage identified, with fluid build up surrounding heart, the treatment was to provide diuretics with plan for the patient to remain in the hospital for at least 24 hours. On 8/25/21 husband reported that the patient remained in the ICU for monitoring of output. Cardiac defibrillator did not deliver any further shock (defibrillation).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Insulin Dependent Diabetic
Vorgeschichte: History of cardiac stents, MI and internal cardiac defibrillator
Andere Medikamente: -
Allergien: Erythromycin
Vorherige Impfungen: -

VAERS 1628473

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: OH
Alter: 12,0
Geschlecht: M
Eingang: 24.08.2021
Impfdatum: 06.08.2021
Beginn: 06.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Loss of consciousness

Symptomtext

Patient passed out post injection. Patient was seated in chair and regained consciousness in a few seconds. He sat for a few minutes and drank cold water. The pharmacy intern took him outside for fresh air with his mother where they remained for about 30 minutes to make sure he felt better. Upon follow up around 4pm the mother stated he was resting and felt fine.

Weitere VAERSDATA-Felder

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

VAERS 1583018

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 16,0
Geschlecht: M
Eingang: 18.08.2021
Impfdatum: 06.08.2021
Beginn: 09.08.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Back pain Brain natriuretic peptide increased Chest discomfort Chest pain Dyspnoea exertional Echocardiogram normal Electrocardiogram ST segment elevation Intensive care Malaise Myocarditis Pain Pericarditis Troponin I increased

Symptomtext

16 Y 8 M male who presents with chest pain and found to have elevated Troponin I. Pt previously healthy male who received his second Pfizer COVID-19 vaccine dose on 8/6. He began having some intermittent chest pain/pressure yesterday, sometimes radiating to the back. The pain continued and progressed to include shortness of breath with exertion, particularly with stairs (after 2 steps). He was able to go to school but looked unwell so his mom brought him into the ED for evaluation. There he had an elevated troponin of 30 and EKG changes (diffuse ST elevation) consistent with pericarditis. During the time that he was waiting to be evaluated, his pain resolved. Pt with Pfizer COVID-19 vaccine induced myopericarditis. He was monitored for a few days in the ICU given risk for decompensation. Subsequently transferred to the floor given asymptomatic and troponin downtrending. Echo and EKG both unremarkable. Treated with ibuprofen and pepcid and plan to continue for 2 weeks. On discharge patient is hemodynamically stable, tolerating PO, saturating well on room air, without cardiopulmonary symptoms. Troponin down trended and is <1. Follow up with cardiology outpatient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 3,0
Labordaten: Results for patient as of 8/18/2021 10:53 1/4/2014 17:51 7/20/2017 15:59 3/21/2019 16:54 8/9/2021 16:47 8/9/2021 16:56 8/9/2021 17:36 8/9/2021 17:49 TROPONIN I: 30.08 (H) BNP: 119 (H) 8/9/2021 21:30 8/10/2021 00:05 8/10/2021 00:10 TROPONIN I: 32.32 (H) 8/10/2021 06:05 TROPONIN I: 19.73 (H) BNP: 194 (H) 8/10/2021 11:38 8/10/2021 12:30 TROPONIN I: 14.38 (H) 8/10/2021 15:53 8/11/2021 06:00 8/11/2021 06:10 TROPONIN I: 10.89 (H) BNP: 190 (H) 8/11/2021 18:05 TROPONIN I: 5.14 (H) 8/12/2021 07:00 TROPONIN I: 2.60 (H) BNP: 110 (H) 8/12/2021 18:25 TROPONIN I: 1.07 (H) BNP: 118 (H)
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Selenium Sulfide 2.5% Top Lotion
Allergien: Amoxicillin-hives
Vorherige Impfungen: -

VAERS 1582631

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: OK
Alter: 47,0
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 10.08.2021
Beginn: 11.08.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / RA

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

Blood test Gynaecological examination Heavy menstrual bleeding Muscle spasms Pelvic pain Thrombosis Urine analysis Uterine haemorrhage

Symptomtext

Extreme sudden onset of clotted uterine bleeding. Clots were fist size and coming every fifteen minutes along with pelvic cramping. Pads/tampons were useless and overflowing. Bleeding continued from 3:30am until about 10pm when the Tranexamic Acid finally helped slow it. abnormal heavy bleeding persisted for three days after the extreme bout.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Pelvic exam, catheter urine sample, blood work,
Aktuelle Erkrankungen: n/A
Vorgeschichte: Rheumatoid Arthritis, anxiety, depression
Andere Medikamente: Leflunomide, Diclofenac, Losartan, Atorvastatin, Escitlopram, Buspiroine, Turbafine, daily vitamin
Allergien: Lisinopril
Vorherige Impfungen: -

VAERS 1550165

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: UT
Alter: 17,0
Geschlecht: M
Eingang: 12.08.2021
Impfdatum: 09.08.2021
Beginn: 09.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dyskinesia Loss of consciousness

Symptomtext

Nurse administered Vaccine and client passed out and started to slide off chair to the left. This nurse caught client by right arm and pulled him upright in chair. Client was slumped over in chair until nurse popped ammonia Ampule and placed by nostrils to smell. Client had minimal involuntary contractions during incident. v/s at 16:27: B/P: 82/40 HR: 64% R:16 O2:98%. Client came to and was responsive to Verbal stimuli. Gave water, snacks, v/s at 16:40 B/P: 90/70 HR: 63 O2: 95% R:16. Client states that this happens a lot after any medical procedure or shot. Client alert and verbally responsive; eating snacks. V/s at 16:55 B/P 98/68 HR: 98/68, R: 17, O2:97%. Client alert and oriented x3, Verbally responsive. states that he is feeling well, and a lot better, and has notified mom of his incident.

Weitere VAERSDATA-Felder

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

VAERS 1549840

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: KY
Alter: 54,0
Geschlecht: F
Eingang: 12.08.2021
Impfdatum: 22.07.2021
Beginn: 12.08.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: SYR / LA

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

Anticoagulant therapy Arthralgia Back pain Chest pain Cold sweat Computerised tomogram normal Dizziness Echocardiogram Electrocardiogram Fatigue Pain Pain in extremity Peripheral swelling Spinal pain Surgery Thrombosis Ultrasound Doppler

Symptomtext

Received the vaccine 7/22/21 at 1:00pm had a sore left arm, felt a bit dizzy & clammy but symptoms went away by Saturday 7/24/21. Monday night 7/26/21 felt really tired & a bit achy. 7/27/21 I woke up with a stabbing knife feeling under my right shoulder blade up my spine & it ran thru front of chest & left leg started swelling a bit. Self medicated with tylenol, advil, ice & heat. 7/28/21 I went to store & bought ladocaine patches, creams to try to relieve the symptoms along with the other things I was doing. 7/29/21 I went to get a massage but I couldn't take my shirt off & it just hurt too much so it was short & sweet. Friday 7/30/21 my leg was huge! I couldn't take it any longer & went to the ER at 3:30, I was admitted at 5:00 with blood clots in my stomach & down my left leg. Still not answers on back but it didn't show any clots with they did the CT's. I was put on heporon blood thinner & had surgery on 8/2/21. I got to go home on 8/3/21 but started having chest pains & the back pain really bad so went back to ER on 8/6. They did another CT to see if any clots were in back but there wasn't. Sent home with oxy & fentanyl patches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 4,0
Labordaten: When I went to the ER they did EKG, 4 CT's, echocardiogram, ultrasound on leg.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Immune Gummy Vitamin, Zinc Gummy, protonix, D3, iron
Allergien: N/A
Vorherige Impfungen: -

VAERS 1540534

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NC
Alter: 14,0
Geschlecht: M
Eingang: 10.08.2021
Impfdatum: 10.08.2021
Beginn: 10.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Fall Seizure

Symptomtext

Pt received vaccine and 13 minutes after began having seizure and fell to floor. Vitals were taken and ambulance called for transport to hospital

Weitere VAERSDATA-Felder

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

VAERS 1536262

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: GA
Alter: 15,0
Geschlecht: F
Eingang: 09.08.2021
Impfdatum: 06.08.2021
Beginn: 06.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Retching Seizure

Symptomtext

Dry Heaving, Full Seizure activity for approximately 1 minute or less. Patient has no History of Seizure's.

Weitere VAERSDATA-Felder

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

VAERS 1528399

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: FL
Alter: 15,0
Geschlecht: M
Eingang: 09.08.2021
Impfdatum: 04.08.2021
Beginn: 04.08.2021
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 Chest discomfort Chest pain Chills Flushing Echocardiogram Electrocardiogram Electroencephalogram Full blood count Loss of consciousness Hyperhidrosis Hypotension Nausea Syncope Tremor Metabolic function test Seizure like phenomena Unresponsive to stimuli

Symptomtext

Passed out x 2 and had seizure like activity

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: 8/4 cbc, bmp, eeg ekg 8/5 echo
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multi vitamin Fish oil
Allergien: None
Vorherige Impfungen: -

VAERS 1531694

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: FL
Alter: 17,0
Geschlecht: M
Eingang: 06.08.2021
Impfdatum: 04.08.2021
Beginn: 04.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blindness Blood glucose normal Dizziness Electrocardiogram Hyperhidrosis Loss of consciousness

Symptomtext

While waiting 30 mins after vaccine administration, 10 mins into waiting period, patient was in waiting room felt dizzy & started sweating. While Walking him to an examine room, pt stated that he lost vision, everything went black, within a few seconds, the vision returned he said. When we walked into the exam room, he felt like he was going to pass out, and started to fall. He was caught before falling by myself & his mother and sat on the floor. BP at that time was 90/52, HR 52, O2 100%. 911 called, rechecked, normal Blood sugar per paramedic, sitting BP around the same, after standing him up, BP drops to 65/32, pt began to feel dizzy & loss of vision again. Pt transported to ER via EMS, mom with him

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: BP, O2, Blood sugar checked, EKG checked in office before transferred to ER
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin, nuts
Vorherige Impfungen: -

VAERS 1531572

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: UT
Alter: 31,0
Geschlecht: F
Eingang: 06.08.2021
Impfdatum: 14.05.2021
Beginn: 30.05.2021
Tage bis Beginn: 16,0
Dosis: 2
Route/Site: IM / RA

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

Arthralgia Chest X-ray abnormal Chest pain Dyspnoea Electrocardiogram abnormal Fatigue Magnetic resonance imaging heart Pain in extremity Pericarditis

Symptomtext

Developed Pericarditis. Severe chest pain, trouble breathing, shoulder and arm pain, extreme fatigue. Went to a 24-hour medical clinic and they thought it was muscular and prescribed Prednisone. The chest pain continued to be severe and I began to have trouble breathing. At this point I went to the Emergency Room, where I was diagnosed with Pericarditis. **My first Covid Vaccine's LOT # was changed: someone crossed out the last number on the lot number (that was stamped on my card) and hand wrote a different number on top of it. The original lot number was: EW0169, but when I received the card, a 2 was hand-written over the 9. This was my first Covid vaccine, given on 04/17/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: EKG, MRI, chest xray: 8/2/2021 - Diagnosed with Pericarditis, prescribed Colchicine and after a follow up visit the next day with my Doctor, gabapentin.
Aktuelle Erkrankungen: None
Vorgeschichte: Borderline High Blood Pressure
Andere Medikamente: Norethindrone, Labetalol, Ibuprofen
Allergien: Penecillan
Vorherige Impfungen: -

VAERS 1528397

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: FL
Alter: 35,0
Geschlecht: M
Eingang: 05.08.2021
Impfdatum: 02.08.2021
Beginn: 02.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Flushing Hyperhidrosis Hypotension Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Mild, Systemic: Hypotension-Mild

Weitere VAERSDATA-Felder

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

VAERS 1526151

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: IA
Alter: 15,0
Geschlecht: F
Eingang: 04.08.2021
Impfdatum: 04.08.2021
Beginn: 04.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Eye movement disorder Loss of consciousness Pallor Posture abnormal Tremor

Symptomtext

Patient blacked out 30 -60 seconds after injection. Head slumped back and eyes rolled back. Head was shaking. Patient came back to consciousness within 30 seconds. Patient was aware of what happened. Face was extremely pale. About 3 minutes after incident her blood pressure was taken and it was normal 120/70. We had patient and her mother sit for 30 minutes after vaccination/incident. Reported the incident to patient's pediatrician who requested a follow-up visit in-person today.

Weitere VAERSDATA-Felder

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

VAERS 1523658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: ND
Alter: 45,0
Geschlecht: F
Eingang: 03.08.2021
Impfdatum: 03.08.2021
Beginn: 03.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hyperhidrosis Loss of consciousness Seizure

Symptomtext

She became diaphoretic, passed out and seemed to have a seizure. She was given some water and vitals were taken and stable. She left with her husband and was advised to take it easy today and drink lots of fluids

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NOne
Vorgeschichte: None
Andere Medikamente: Unknown
Allergien: NOne
Vorherige Impfungen: -

VAERS 1519911

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NM
Alter: 14,0
Geschlecht: F
Eingang: 02.08.2021
Impfdatum: 02.08.2021
Beginn: 02.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Asthenia Dizziness Loss of consciousness Photopsia

Symptomtext

Patient was given Pfizer vaccine and then asked to walk down the hall way to get vitals. While walking down the hallway patient reports that she felt "light headed" and like she was "seeing stars" but did not alert nursing staff. Once patient sat in chair and the MA put blood-pressure cuff on patient's arm, she started to feel even more faint and she slumped over and briefly lost consciousness. Another MA put ammonia under patient's nose and she instantly regained consciousness. Patient reported feeling a little weak. Patient drank water and returned to room. Patient was observed for 40 minutes afterwards, no additional syncopal events. Patient left feeling well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None reported
Vorgeschichte: Dysmenorrhea
Andere Medikamente: None reported
Allergien: None reported
Vorherige Impfungen: -

VAERS 1519614

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: KY
Alter: 43,0
Geschlecht: F
Eingang: 02.08.2021
Impfdatum: 06.05.2021
Beginn: 01.08.2021
Tage bis Beginn: 87,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test abnormal Heavy menstrual bleeding Menstrual disorder Menstruation irregular Platelet count decreased Polymenorrhoea Thrombosis

Symptomtext

After my se one dose I began having abnormal blood clotting during my period beginning on 5/8/2021. Each cycle has gotten progressively worse- cycles shorter and irregular, and very heavy menstrual flow with significant clotting. Culminated with event on Aug 1. Began my period on Sunday 25th, light bleeding, then stopped, and period began again on July 31st with heavy bleeding on August 1st I was bleeding through super tampons and pads every time I would stand. Went through tampons every 30min. Contacted my physician and she called in prescription and advised I go to ER if bleeding continued, it continued with very large clots and so went to ER on 8/1 at 15:56 PM. Indicated possible fibroid and have never had issues with fibroids. Follow up appointment in process of being scheduled with my OB/GYN for further testing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Blood tests, Ultrasound. Blood tests low platelet levels but not low enough for transfusion. Ultrasound not completed at hospital facility and will be done by OBGYN.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Fluoxetine, Propranolol
Allergien: Some sulfa medications
Vorherige Impfungen: -

VAERS 1510486

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NY
Alter: 41,0
Geschlecht: F
Eingang: 31.07.2021
Impfdatum: 23.07.2021
Beginn: 23.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Asthenia Dizziness Feeling abnormal Hypoacusis Loss of consciousness Dysstasia Immediate post-injection reaction Mobility decreased Nausea

Symptomtext

I began to feel that I was losing consciousness.; I almost stopped hearing people around me; But I felt pretty bad that night.; I felt a little dizzy/my dizziness and nausea were getting worse.; felt that my legs and arms, and my body began to lose strength; my dizziness and nausea were getting worse.; This is a spontaneous report from a contactable consumer (Patient). This 41-year-old non-pregnant female patient reported that received BNT62B2 (FIZER-BIONTECH COVID-19 VACCINE, Formulation : Solution for injection, Lot Number EW0179), via intramuscular route of administration in left arm on 23Jul2021 04:30, as dose 1, single for COVID-19 immunization (age at time of vaccination 41 years). The patient medical history known allergies to Pollen. Concomitant medication were not reported. The patient was not pregnant, and she did not receive any other medications within 2 weeks of vaccination. The patient had not received any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed COVID-19 Prior to vaccination, Since the vaccination, has the patient been tested for COVID-19 as no. On 23Jul2021 04:30 PM, a few seconds after the vaccination, she felt a little dizzy. She felt that her dizziness and nausea were getting worse. after about 4 or 5 minutes, she began to feel that she was losing consciousness. She took a few steps and felt that her legs and arms, and her body began to lose strength. She almost stopped hearing people around her. they picked her up and sat down on a chair. The patient received treatment A lot of water and citrus juice. She drank 3 bottles of water and a juice. It helped to feel better she stayed there for half an hour. She felt better and went home. But she felt pretty bad that night. Next morning she was OK. The outcome of all events was recovered on 24Jul2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pollen allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1510486

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NY
Alter: 41,0
Geschlecht: F
Eingang: 31.07.2021
Impfdatum: 23.07.2021
Beginn: 23.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Dizziness Feeling abnormal Hypoacusis Loss of consciousness Dysstasia Immediate post-injection reaction Mobility decreased Nausea

Symptomtext

I began to feel that I was losing consciousness.; I almost stopped hearing people around me; But I felt pretty bad that night.; I felt a little dizzy/my dizziness and nausea were getting worse.; felt that my legs and arms, and my body began to lose strength; my dizziness and nausea were getting worse.; This is a spontaneous report from a contactable consumer (Patient). This 41-year-old non-pregnant female patient reported that received BNT62B2 (FIZER-BIONTECH COVID-19 VACCINE, Formulation : Solution for injection, Lot Number EW0179), via intramuscular route of administration in left arm on 23Jul2021 04:30, as dose 1, single for COVID-19 immunization (age at time of vaccination 41 years). The patient medical history known allergies to Pollen. Concomitant medication were not reported. The patient was not pregnant, and she did not receive any other medications within 2 weeks of vaccination. The patient had not received any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed COVID-19 Prior to vaccination, Since the vaccination, has the patient been tested for COVID-19 as no. On 23Jul2021 04:30 PM, a few seconds after the vaccination, she felt a little dizzy. She felt that her dizziness and nausea were getting worse. after about 4 or 5 minutes, she began to feel that she was losing consciousness. She took a few steps and felt that her legs and arms, and her body began to lose strength. She almost stopped hearing people around her. they picked her up and sat down on a chair. The patient received treatment A lot of water and citrus juice. She drank 3 bottles of water and a juice. It helped to feel better she stayed there for half an hour. She felt better and went home. But she felt pretty bad that night. Next morning she was OK. The outcome of all events was recovered on 24Jul2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pollen allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1505443

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: WI
Alter: 57,0
Geschlecht: M
Eingang: 27.07.2021
Impfdatum: 21.07.2021
Beginn: 22.07.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / RA

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

Bell's palsy

Symptomtext

Right Bells Palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: No labs or tests done Sorry I entered Hep B in wrong place. Hep B was given on July 19 and COVID vaccine on July 21. Bells palsy diagnosed on July 22.
Aktuelle Erkrankungen: Received Hepatitis B vaccine on July 19 2021 and the COVID 19 vaccine on July 21 2021
Vorgeschichte: obesity Type 2 DM Gout Sarcoidosis Obstructive sleep apnea Hypercalcemia hypercholesterolemia Asthma
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1502190

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: KY
Alter: 13,0
Geschlecht: M
Eingang: 26.07.2021
Impfdatum: 26.07.2021
Beginn: 26.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Loss of consciousness Pallor

Symptomtext

Patient lost consciousness for a few seconds, turned pale, and was put in a wheel chair. Patient offered ambulance. Moved to private room and laid down on crash pad. (13:25)HR - 86 / R-14 / BP - 118/74. (13:26) more alert talking, oriented, pale, color improved. (13:29) - HR-94 Psox - 98% - BP-115/75. (13:43) - patient sat up and vital signs measured - HR - 92 / BP - 127/86. (13:53) vitals BP -128/82 - HR-90 / Psox- 98% (14:01) Standing BP - 109/86 - HR-92 / O2 Sat- 99%. Dad went to pick up car. Patient standing and walking without problem . Parents declined EMS, stating patient had had similar episode in the past.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: No labs ordered
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown - has passed out in the past
Andere Medikamente: Concerta - medicines for ADD and ADHD Probably Behavioral issues
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1501012

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NJ
Alter: 24,0
Geschlecht: M
Eingang: 24.07.2021
Impfdatum: 14.07.2021
Beginn: 16.07.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / AR

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

Antibody test negative Antinuclear antibody positive Asthenia Blood creatine phosphokinase normal Blood thyroid stimulating hormone normal Borrelia test negative Computerised tomogram head normal Dysstasia Gait inability Guillain-Barre syndrome Immunoglobulin therapy Magnetic resonance imaging head normal Magnetic resonance imaging spinal normal Muscular weakness Red blood cell sedimentation rate normal Vitamin B12 normal

Symptomtext

Patient experienced diffuse muscle weakness in all 4 extremities, beginning 2 days after the 2nd dose of the Pfizer COVID-19 Vaccine. It progressed equally in upper and lower extremities. 4 days after vaccination, he was unable to walk and couldn't stand from a seated position. Presented to the ER and had a 5 day hospital stay. His upper extremities graded 4/5 strength, his lower extremities graded 3/5. Initially throught to be Guillan-Barre Syndrome, he received 5 doses of IV IG over 3 days. Reflexes preserved throughout his stay. He was treated by physical therapy and occupational therapy throughout his hopsital stay. He improved dramatically over the last two days of his stay and was discharged home with home PT.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: CT head negative, MRI brain and C/T/L spine normal. CPK, ESR, TSH, B12 all normal. Lyme negative, ANA +, reflex AB's all negative.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1500741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: TX
Alter: 22,0
Geschlecht: M
Eingang: 24.07.2021
Impfdatum: 23.07.2021
Beginn: 23.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Severe

Weitere VAERSDATA-Felder

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

VAERS 1498627

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: -
Alter: 16,0
Geschlecht: M
Eingang: 23.07.2021
Impfdatum: 21.07.2021
Beginn: 21.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hyperhidrosis Hypotension Pallor Syncope

Symptomtext

Fainting (few seconds), pale, sweating, shallow breathing, low blood pressure. Patient was awake and responding to questions. By the time ambulance arrived, patient was able to walk. Patient contacted last night and he was completely fine.

Weitere VAERSDATA-Felder

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

VAERS 1497550

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: OH
Alter: 14,0
Geschlecht: M
Eingang: 23.07.2021
Impfdatum: 15.05.2021
Beginn: 16.06.2021
Tage bis Beginn: 32,0
Dosis: 1
Route/Site: OT / LA

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

Blood test Guillain-Barre syndrome Lumbar puncture Magnetic resonance imaging

Symptomtext

typical Guillain-Barre syndrome; he could not walk; he cannot play any sport because he cant run/ no control from his waist down; he needed a catheter ,he was not able to pee or poop; he needed a catheter ,he was not able to pee or poop; This is a spontaneous report from a contactable consumer (parent). A 14-years-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/Lot Number: EW0179; Expiration Date: 31Aug2021; NDC number and UPC number: unknown) via intramuscular on 15May2021 (at the age of 14-years-old) in left arm (shoulder) as a DOSE 1, SINGLE for covid-19 immunization and second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/Lot Number: EW0182; Expiration Date: 31Aug2021; NDC number and UPC number: unknown) via intramuscular on 05Jun2021 (at the age of 14-years-old) in left arm (shoulder) as DOSE 2, SINGLE for covid-19 immunization. Medical history included papilloma viral infection from 06May2021 to 06May2021 and bowel movement irregularity from an unknown date and unknown if ongoing. The report was not related to a study or programme. Prior vaccinations (within 4 weeks) included HPV (human papilloma virus) vaccine on 06May2021. Concomitant medication included macrogol 3350 (MIRALAX) as he had trouble going to the bathroom because he didn't had control and had trouble with bowel movement, he started when he left the hospital, so he can get back to his bowel, but he stopped using it couple of days ago as he started to go to the bathroom on his own again. The patient received both doses of Pfizer covid vaccine. He had a serious reaction to the vaccine, he couldn't go to the bathroom on his own, he had no control from his waist down, he needed a catheter as he was not able to pee or poop. He was admitted to the emergency room on 16Jun2021 and spent 3 days in the ICU because he could not walk and move, spent 3 days in out the down rated version, total 6 days in the hospital. He was diagnosed with Guillain-Barre syndrome and he was in the hospital on his birthday in Jun2021 and was doing physical therapy to walk and run again. His mother was trying to deal with the covid compensation because they had work. She and her husband were alone in the hospital. She reported that their medical bills were going to be crazy because they had to go by ambulance from one hospital to other because they were afraid of Guillain-Barre syndrome. The patient didn't have any movement in his legs all the way up to his heart. He was not able to play any sport because he can't run. The patient was discharged from the hospital and was on physical therapy (water therapy). The patient underwent lab tests and procedures which included two MRI, spinal test, and blood work with unknown results in the emergency room as they weren't sure what was going on with him. The patient was treated with IVIG and blood thinner everyday two times a day. The outcome of all the events were unknown. Information on Lot/Batch number was available. Additional information has been requested. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 6,0
Labordaten: Test Date: 2021; Test Name: Blood work; Result Unstructured Data: Test Result:Unknown; Test Date: 2021; Test Name: Spinal tap; Result Unstructured Data: Test Result:Unknown; Test Date: 2021; Test Name: MRI; Result Unstructured Data: Test Result:Unknown; Test Date: 2021; Test Name: MRI; Result Unstructured Data: Test Result:Unknown
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bowel movement irregularity; Human papilloma virus infection
Andere Medikamente: MIRALAX
Allergien: -
Vorherige Impfungen: -

VAERS 1490807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: -
Alter: 21,0
Geschlecht: F
Eingang: 21.07.2021
Impfdatum: 23.06.2021
Beginn: 26.06.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Anticoagulant therapy Hypoaesthesia Pain in extremity Therapy change Thrombosis

Symptomtext

Patient's arm was sore after receiving the vaccine, 3 days later she woke up with numbness. She went to the hospital and was diagnosed with a blood clot in her arm. She was placed on warfarin and the clot dissolved. Her OBGYN lowered her dose of birth control. Her PCP advised her to still get her second dose.

Weitere VAERSDATA-Felder

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

VAERS 1486847

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: OH
Alter: 50,0
Geschlecht: F
Eingang: 20.07.2021
Impfdatum: 01.07.2021
Beginn: 01.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Chest pain Dyspnoea Electrocardiogram Pain Pericarditis

Symptomtext

Diagnosed with pericarditis. Chest pain/pressure that did not resolve itself after a week, shortness of breath, pain in left

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: ekg - 7/19/2021
Aktuelle Erkrankungen: bronchitis
Vorgeschichte: afib complicated by svt
Andere Medikamente: verapamil 120 mg melatonin 5mg
Allergien: codeine bandage adhesive
Vorherige Impfungen: -

VAERS 1485837

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 38,0
Geschlecht: F
Eingang: 19.07.2021
Impfdatum: 04.05.2021
Beginn: 06.05.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / AR

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

Anaphylactic reaction Anxiety Autonomic nervous system imbalance Chronic fatigue syndrome Cognitive disorder Confusional state Feeling abnormal Inflammation Mast cell activation syndrome Neuropathy peripheral Palpitations Panic attack Pharyngeal swelling Post viral fatigue syndrome Swollen tongue

Symptomtext

Symptoms consistent with MCAS, ME/CFS, neuropathy, anxiety, panic attacks, anaphylaxis, swelling of throat and tongue, dysautonomia, heart palpitations, widespread inflammation and neuropathy especially at sites of old or previous injury. Cognitive issues consistent with brain fog and extreme confusion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: No tests, I don?t have coverage.
Aktuelle Erkrankungen: None diagnosed.
Vorgeschichte: None diagnosed.
Andere Medikamente: None
Allergien: Pepper and foods containing capsaicin.
Vorherige Impfungen: -

VAERS 1483480

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NC
Alter: 71,0
Geschlecht: M
Eingang: 18.07.2021
Impfdatum: 30.06.2021
Beginn: 30.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Cheilitis Fatigue Loss of consciousness Syncope Tooth injury

Symptomtext

unconscious for 15 minutes.; two teeth knocked out; lips busted; laid up for 3 days; fainted; This is a spontaneous report from a contactable consumer (Patient). A 71-years-old male patient received bnt162b2 (Pfizer-Biontech Covid-19 Vaccine, Formulation: solution for injection, Lot Number EW0179, expiration date not reported), via an unspecified route of administration on 30Jun2021 as dose 2, single for covid-19 immunization (71 years when vaccinated). Historical vaccine included bnt162b2 (Pfizer-Biontech Covid-19 Vaccine, Formulation: solution for injection, Lot Number EWO170, expiration date not reported), via an unspecified route of administration on 30Jun2021 as dose 1, single for covid-19 immunization (71 year when vaccinated) and had no adverse effect. The patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. The patient was not diagnosed with COVID-19 prior to the vaccination. Since the vaccination, the patient had not been tested for COVID-19. Medical history included multiple sclerosis from an unknown date in Jan2002 to an unknown date (he has been okay for the past 7 years, as reported). The patient's concomitant medications were not reported. The patient previously took Avonex for central nervous system lesion and experienced adverse drug reaction (very bad). On 30Jun2021, the patient received his second dose and after 10mins the patient headed for home and the patient drove for about 400 yards from the country health department, walked in the kitchen and as soon as he got inside the patient fainted. The patient was unconscious for 15min. The fainting resulted in lips busted, two teeth knocked out and was laid up for 3days. The patient was not hospitalized for the events. The patient did not visit any emergency room or physician due to the events. The outcome of the events was reported as unknown at the time of report. Information about lot/batch number has been requested. Follow-Up (07Jul2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Multiple sclerosis (Verbatim: Multiple sclerosis he has been okay for the past 7 years)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1474053

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: FL
Alter: 24,0
Geschlecht: F
Eingang: 15.07.2021
Impfdatum: 14.07.2021
Beginn: 14.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Chest discomfort Chest pain Dysphagia Dyspnoea Paraesthesia Pruritus Throat tightness

Symptomtext

Systemic: Allergic: Anaphylaxis-Severe, Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Medium, Systemic: Allergic: Itch (specify: facial area, extremeties)-Severe, Systemic: Chest Tightness / Heaviness / Pain-Medium, Systemic: Tingling (specify: facial area, extemities)-Severe

Weitere VAERSDATA-Felder

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

VAERS 1470526

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: WI
Alter: 18,0
Geschlecht: M
Eingang: 14.07.2021
Impfdatum: 29.06.2021
Beginn: 04.07.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / RA

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

Loss of consciousness Syncope Vomiting

Symptomtext

Five days post vaccination the patient was participating in a cross country meet. While running, the patient lost consciousness and needed to be rushed via ambulance to the emergency department. Patient stated he had no abnormal feelings leading up the the syncopal event. Patient's mother stated he was unconscious for 20 minutes, but she was unable to confirm. Also, stated patient vomited multiple times en route to the hospital. Treatment was performed in the emergency department, so I am unaware of exact therapies.

Weitere VAERSDATA-Felder

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

VAERS 1466962

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MO
Alter: 26,0
Geschlecht: M
Eingang: 13.07.2021
Impfdatum: 12.07.2021
Beginn: 12.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Loss of consciousness Seizure Syncope Tremor Unresponsive to stimuli Vomiting

Symptomtext

Systemic: Fainting / Unresponsive-Severe, Systemic: Seizure-Severe, Systemic: Vomiting-Mild, Additional Details: shortly after receiving vaccination, the patient became unconscious, fell out of his chair and to the floor, and began to seize. Body shaking lasted around 15-20 seconds. Patient then immediately became alert and concscious. Stated after this episode that he has a history of fainting and having seizures after he receives vaccinations. Patient vomited ~15-20 minutes after this episode.

Weitere VAERSDATA-Felder

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

VAERS 1459451

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: IL
Alter: 31,0
Geschlecht: F
Eingang: 09.07.2021
Impfdatum: 08.07.2021
Beginn: 08.07.2021
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 Seizure Syncope Unresponsive to stimuli Vomiting

Symptomtext

Site: Redness at Injection Site-Mild, Systemic: Fainting / Unresponsive-Severe, Systemic: Seizure-Medium, Systemic: Vomiting-Mild, Additional Details: Patient got the vaccine and was fine sat down and after 5 minutes fainted. Then got back consciousness then had seizure and lost consciousness. Then was ok but went to hospital to be evaluated.

Weitere VAERSDATA-Felder

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

VAERS 1402451

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: FL
Alter: 13,0
Geschlecht: M
Eingang: 09.07.2021
Impfdatum: 04.06.2021
Beginn: 06.06.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

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

Anxiety Atrial enlargement Body temperature increased C-reactive protein increased Chest pain Blood test Echocardiogram Electrocardiogram Immunoglobulin therapy Myocardial necrosis marker Myocardial necrosis marker increased Myocarditis SARS-CoV-2 test Echocardiogram normal Electrocardiogram T wave abnormal Fatigue Headache Influenza like illness

Symptomtext

6/5: midsternal Chest pain with respiratory effort evening of 6/5; 6/6: constant chest pain 04:45 on 6/6. Tmax 103' ILI, headache, muscle ache, fatigue. Presented to ED. Troponin 0.35, CRP 29.9, neutrophils 70.8. Transferred to cardiac ICU r/o myocarditis post COVID 19 vaccine (2nd dose.) COVID-19 negative test. 6/7: continues with chest pain, troponin increased to 0.62. 6/8: troponin trending down now to 0.56. given IVIG. patient unable to tolerate MRI without sedation, refuses. 6/9: troponin trending down to 0.36. No complaints of chest pain. continues to refuse cardiac MRI. patient discharged home with cardiology follow-up 1 week later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 4,0
Labordaten: EKG T wave abnormalities and atrial enlargement. ECHO cardiogram within normal limits. Both on 6/6/21. Unable to complete cardiac MRI due to anxiety.
Aktuelle Erkrankungen: Immunology work up for IGM deficiency
Vorgeschichte: Eczema
Andere Medikamente: One ibuprofen and turmeric powder
Allergien: NKA
Vorherige Impfungen: -

VAERS 1450355

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: OR
Alter: 34,0
Geschlecht: M
Eingang: 06.07.2021
Impfdatum: 28.04.2021
Beginn: 18.05.2021
Tage bis Beginn: 20,0
Dosis: 1
Route/Site: IM / RA

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

Blood glucose Electromyogram Guillain-Barre syndrome HIV test negative Hepatic enzyme increased Hepatitis viral test negative Muscular weakness Nerve conduction studies Nonalcoholic fatty liver disease Paraesthesia Red blood cell sedimentation rate increased Treponema test negative Vitamin B12 decreased

Symptomtext

Symptoms of generalized ascending paresthesias with right hand weakness since May 18, 2021, first right foot then left, then ascending to the trunk and upper extremities. As of June 21 left with residual right hand weakness and paresthesias. second Covid Pfizer vaccine given May 19, 2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: low B12 levels, now on supplements. Neurology consult has ordered an MRI C spine to check for transverse myelitis. Working diagnosis is Guillain Barre syndrome. High ESR. elevated liver enzymes from NAFLD, pre diabetes. HIV, syphilis, and acute hepatitis serology negative. EMG/NCVS still pending along with second neurology visit.
Aktuelle Erkrankungen: morbid obesity
Vorgeschichte: morbid obesity
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1408230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: WA
Alter: 22,0
Geschlecht: M
Eingang: 06.07.2021
Impfdatum: 10.06.2021
Beginn: 11.06.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Aspartate aminotransferase increased Chest X-ray normal Chest discomfort Echocardiogram normal Laboratory test normal Body temperature Brain natriuretic peptide Chest X-ray Echocardiogram Electrocardiogram Electrocardiogram ST segment elevation Pericarditis Troponin Vital signs measurement

Symptomtext

Pericarditis; Initial EKG does show some diffuse ST segment elevation; This is a spontaneous report from a contactable Physician. A 22-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EW0167), intramuscular, administered in Arm Left on 10Jun2021 11:15 (at age of 22 years old) as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. No COVID prior vaccination. No COVID tested post vaccination. This is a 22-year-old active duty male without significant past medical history presenting with several days of chest pressure after coronavirus vaccination. His vital signs are stable and he was afebrile upon arrival to the ED with a benign and reassuring physical examination. His initial EKG does show some diffuse ST segment elevation/PR depression that was not as impressive on a repeat EKG. Bedside point-of-care echocardiogram shows grossly normal function without obvious pericardial effusion or other acute abnormalities. Chest x-ray unremarkable. Laboratory work-up with undetectable troponin and normal BNP, all on 11Jun2021. Ultimately diagnosed with pericarditis at emergency department. Adverse event start date was 11Jun2021 11:15 AM. Ae resulted in: [Doctor or other healthcare professional office/clinic visit/Emergency room/department or urgent care]. Treatment (Ibuprophen 800 mg TID x 3 weeks) received. The outcome of the events was Recovering.; Sender's Comments: Considering a plausible temporal relationship and a known product safety profile, a possible contributory role of suspect product BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EW0167) to the reported "Pericarditis" and " EKG ST segment elevation" cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees, and Investigators, as appropriate

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Test Date: 20210611; Test Name: body temperature; Result Unstructured Data: Test Result:afebrile; Test Date: 20210611; Test Name: BNP; Result Unstructured Data: Test Result:Normal; Test Date: 20210611; Test Name: Chest X-Ray; Result Unstructured Data: Test Result:Unremarkable; Test Date: 20210611; Test Name: Echocardiogram; Result Unstructured Data: Test Result:Normal function; Comments: Bedside point-of-care echocardiogram shows grossly normal function without obvious pericardial effusion or other acute abnormalities; Test Date: 20210611; Test Name: EKG; Result Unstructured Data: Test Result:diffuse ST segment elevation/PR depression; Comments: show some diffuse ST segment elevation/PR depression that was not as impressive on a repeat EKG; Test Date: 20210611; Test Name: Troponin; Result Unstructured Data: Test Result:Undetectable; Test Date: 20210611; Test Name: vital signs; Result Unstructured Data: Test Result:stable
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1446083

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: AZ
Alter: 38,0
Geschlecht: M
Eingang: 03.07.2021
Impfdatum: 02.07.2021
Beginn: 02.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Loss of consciousness Syncope

Symptomtext

Systemic: Fainting / Unresponsive-Medium, Additional Details: Patient who bloodwork done before receiving vaccine came to get dose 1 of pfizer vaccine. The patient received the vaccine and seemed fine. During the 15 minute observation, the patient briefly passed out and the paramedics was called. Patient was laid down flat on back and started to talk and wake up fully. The paramedics checked him out and he was deemed ok. The patient stayed a extra 15 minutes and rested on covid waiting bench with girlfriend and the was able to go home fine.

Weitere VAERSDATA-Felder

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

VAERS 1440691

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: -
Alter: 61,0
Geschlecht: M
Eingang: 01.07.2021
Impfdatum: 13.05.2021
Beginn: 14.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Deep vein thrombosis Ultrasound Doppler abnormal

Symptomtext

Presented to ED on 6/21 w/ left knee pain. Doppler demonstrated DVT in left gastrocnemius veins. Discharged from ED on apixaban and to f/u with PCP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Doppler
Aktuelle Erkrankungen: N/A
Vorgeschichte: CKD, Hypertension, lumbar disc displacement/lumbar spinal stenosis
Andere Medikamente: Amlodipine, ibuprofen, lisinopril/hydrochlorothiazide, metoprolol succinate, potassium chloride, spironolactone
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1433435

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: MI
Alter: 15,0
Geschlecht: M
Eingang: 29.06.2021
Impfdatum: 14.06.2021
Beginn: 21.06.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / AR

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

Electrocardiogram ST segment elevation Myocarditis Troponin increased

Symptomtext

myopericarditis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 5,0
Labordaten: elevated troponin, st elevation on ekg
Aktuelle Erkrankungen: diabetes melilites 1
Vorgeschichte: diabetes
Andere Medikamente: methylphenidate, sertraline, glargine, lispro
Allergien: none
Vorherige Impfungen: -

VAERS 1431024

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: IL
Alter: 18,0
Geschlecht: F
Eingang: 28.06.2021
Impfdatum: 14.05.2021
Beginn: 28.05.2021
Tage bis Beginn: 14,0
Dosis: UNK
Route/Site: IM / -

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

Cardiac stress test Chest pain Dyspnoea exertional Echocardiogram Myocarditis

Symptomtext

Myocarditis, Chest pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Transthoracic Echocardiogram , Stress Test
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKA
Vorherige Impfungen: -

VAERS 1430286

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CO
Alter: 48,0
Geschlecht: M
Eingang: 27.06.2021
Impfdatum: 30.04.2021
Beginn: 14.05.2021
Tage bis Beginn: 14,0
Dosis: 2
Route/Site: SYR / RA

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

Blood test Catheterisation cardiac Pericarditis X-ray

Symptomtext

Pericarditis: Onset on May 14th

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 1,0
Labordaten: cardiac catheterization, x-ray, blood work
Aktuelle Erkrankungen: Mild ear infection, treated with amoxicillin beginning of April
Vorgeschichte: hyperlipidemia
Andere Medikamente: Atorvastatin
Allergien: none
Vorherige Impfungen: -

VAERS 1429632

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: IL
Alter: 14,0
Geschlecht: M
Eingang: 26.06.2021
Impfdatum: 24.06.2021
Beginn: 24.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Disorientation Electrocardiogram abnormal Fall Hyperhidrosis Pallor Seizure

Symptomtext

The patient received the vaccine and 4-5 minutes later he fell out of his chair, facedown. He appeared to be convulsing. He was pale, diaphoretic, and disoriented. His blood pressure was 76/36 and his pulse was 84. Radial pulse was 2+. EMT was called. His EKG appeared to have a slight elevation in his inferior leads. He and his guardian deny any significant history. Upon discharge with EMT, the patient was alert and tolerating liquids well. The patient's guardian states that he has had a similar reaction prior when he was the age of 6. She states that he also felt slightly lightheaded from the first Pfizer vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: EKG at the site.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: Unknown

VAERS 1428428

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: IL
Alter: 12,0
Geschlecht: M
Eingang: 25.06.2021
Impfdatum: 25.06.2021
Beginn: 25.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Eye movement disorder Immediate post-injection reaction Loss of consciousness

Symptomtext

Patient passed out about 3 minutes after receiving the vaccine. Patient was seated and rolled forward then his whole body stiffened backwards. The eyes rolled back then he started to slowly come to.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Same thing happened after receiving the HPV (Gardasil) vaccine.

VAERS 1400416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: DE
Alter: 22,0
Geschlecht: M
Eingang: 25.06.2021
Impfdatum: 13.05.2021
Beginn: 16.05.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: - / LA

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

Abdominal pain Blood test Chest X-ray Chest discomfort Chest pain Chills Computerised tomogram Electrocardiogram abnormal Feeling of body temperature change Influenza like illness Migraine Myocarditis Pain Troponin increased Vomiting

Symptomtext

myocarditis

Weitere VAERSDATA-Felder

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

VAERS 1400416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: DE
Alter: 22,0
Geschlecht: M
Eingang: 25.06.2021
Impfdatum: 13.05.2021
Beginn: 16.05.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain Blood test Chest X-ray Chest discomfort Chest pain Chills Computerised tomogram Electrocardiogram abnormal Feeling of body temperature change Influenza like illness Migraine Myocarditis Pain Troponin increased Vomiting

Symptomtext

myocarditis

Weitere VAERSDATA-Felder

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

VAERS 1424839

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: FL
Alter: 41,0
Geschlecht: M
Eingang: 24.06.2021
Impfdatum: 22.06.2021
Beginn: 22.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Hypotension Loss of consciousness

Symptomtext

PT REPORTED THAT APPROXIMATELY 6 HOURS AFTER GETTING THE SHOT HE LOST CONCIOUSNESS AND EMERGENCY SERCIVES HAD TO BE CALLED. HE WAS FOUND TOP HAVE LOW PRESSURE. PT IS DOING OK NOW

Weitere VAERSDATA-Felder

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

VAERS 1424430

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: KY
Alter: 15,0
Geschlecht: F
Eingang: 24.06.2021
Impfdatum: 01.06.2021
Beginn: 24.06.2021
Tage bis Beginn: 23,0
Dosis: 2
Route/Site: IM / RA

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

Dizziness Hyperhidrosis Loss of consciousness Visual impairment

Symptomtext

Complaints of seeing stars and feeling faint. Wheel chair and stretcher pad with legs up. Mom states she passed out with needle sticks or the sight of blood. 94/62, pulse 92, resp 14. Passed out a for few seconds. Mom declined EM. Pretty sweaty. 97/65, 92/14 states she feels better. Given water and cool cloth. 10:45 am 91/63, 97/14. Patient states no longer feels faint. Setting up . 11:00 Patient states she feels normal. Skin warm, dry and pink. Standing vital signs 116/86, 16. Mom and patient comfortable and walks without problems. Instructed to notify staff prior to vaccine so she can lay done before administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None ordered
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: Patient often passes out with vaccine.

VAERS 1424040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: IL
Alter: 14,0
Geschlecht: M
Eingang: 24.06.2021
Impfdatum: 10.06.2021
Beginn: 12.06.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / RA

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

Blood creatine Chest X-ray Chest pain Computerised tomogram thorax Differential white blood cell count Dyspnoea Electrocardiogram Full blood count Metabolic function test Pericarditis SARS-CoV-2 test Scan with contrast Troponin

Symptomtext

Woke with chest pain and trouble breathing at 6:00am on 6/12/21 (two days after seconod shot). Doctor in emergency room diagnosed acute pericarditis. Need to follow up with Pediatrician and recommended Cardiology. Tests were blood work, x-ray and CT scan. CT Angiogram Chest for PE with IV Contrast 6/12/21 ECG performed 2x 6/12/21 X Ray Chest 2 views PA/Lat 6/12/21 will be seeing Pediatrician on 6/28/21 - 773-522-6100

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: CBC with Differential 6/12/21, D Dimer Fibrin Derivatives 6/12/21, ED Troponin 2 times 6/12/21 Comprehensive Metabolic Panel 6/12/21, POC COVID-19 6/12/21, POC Creatinine 6/12/21,
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1423618

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: IL
Alter: 12,0
Geschlecht: F
Eingang: 24.06.2021
Impfdatum: 26.05.2021
Beginn: 26.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Syncope

Symptomtext

FAINTING AMMONIA INHALANT ADMINISTERED AND PT FEELING FINE

Weitere VAERSDATA-Felder

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

VAERS 1423528

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: IL
Alter: 13,0
Geschlecht: F
Eingang: 24.06.2021
Impfdatum: 20.05.2021
Beginn: 20.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Fall Syncope

Symptomtext

PT STARTED FALLING OF A CHAIR , FAINTING. AMMONIA INHALANT ADMINISTERED AND PT FEELING FINE.

Weitere VAERSDATA-Felder

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

VAERS 1420388

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 18,0
Geschlecht: F
Eingang: 23.06.2021
Impfdatum: 25.05.2021
Beginn: 26.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / AR

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

Angiogram cerebral Brain operation Computerised tomogram head Haemorrhagic stroke Headache Intensive care Therapeutic embolisation Visual impairment

Symptomtext

At midnight that night she experienced a hemorrhagic stroke which led us to the ER and subsequently her being admitted to the stroke ICU for 19 days - where she had a brain surgery via angiogram to embolize the hemorrhage. It was successful with lingering vision problems and headaches

Weitere VAERSDATA-Felder

Praegender Schweregrund: Haemorrhagic stroke
Hospital-Tage: 19,0
Labordaten: ER visit to Hospital and subsequent admission to ICU at Hospital Medical Center on 5/26/21 with multiple CT scans and angiogram on that day. Another CT performed on 5/28/21 and again on 6/7/21 Angiogram performed on 6/9/21 Discharge on 6/13/21
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1382265

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: KY
Alter: 42,0
Geschlecht: F
Eingang: 23.06.2021
Impfdatum: 03.06.2021
Beginn: 03.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Abdominal pain Colitis Computerised tomogram abnormal Dizziness Gastrointestinal haemorrhage Dehydration Diarrhoea Fatigue Loss of consciousness Nausea Pain Pyrexia Haematochezia Thrombosis Vomiting

Symptomtext

Nearly passed out twice; Passing blood clots; GI bleed; Severe body aches; Fatigue; Abdominal pain; Nausea; Vomiting; Fever; Diarrhea; Dehydration; Colitis; This is a spontaneous report from a contactable Nurse (patient) reported for herself. A 42-year-old female patient (not Pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) at 42-year-old, dose 2 via an unspecified route of administration, administered in Arm Left on 03Jun2021 06:30 PM (Lot Number: EW0179) as dose 2, single for covid-19 immunisation in Clinic. Medical history included hypertension, anxiety, seasonal allergy, asthma, Known allergies to Cephalosporin. Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Concomitant medications received within 2 weeks included spironolactone; irbesartan; buspirone hydrochloride (BUSPAR); silybum marianum (MILK THISTLE), all taken for an unspecified indication, start and stop date were not reported. the patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously took miralax and experienced Allergy, lisinopril and experienced Allergy, venlafaxine and experienced Allergy, patient previously took first dose of BNT162B2 (Brand: Pfizer, Lot number: EW0177) into left arm on 13May2021 06:30 PM at 42 years old for COVID-19 immunization. Patient experienced Severe body aches, fatigue, abdominal pain, nausea/vomiting, fever, nearly passed out twice, diarrhea followed by passing blood clots, dehydration, treated in ER twice. Once for dehydration, second for colitis with GI bleed. Event Start Date was 03Jun2021 09:00 PM. the adverse event result in Emergency room/department or urgent care. treatment received for the adverse event included IV fluids, antibiotics, and antiemetic. Outcome of the events was recovering. Information on Lot/Batch number was available. Additional information has been requested.; Sender's Comments: The limited information provided in this report does not allow a full assessment of the case, however, a possible contributory role of the suspect drug to the reported events "Nearly passed out twice, Passing blood clots and GI bleed" cannot be completely excluded based on temporal association. This case will be re-assessed when additional information becomes available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identifies as part of this review, as well as any appropriate action in response, will be promptly notifies to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to antibiotic; Anxiety; Asthma; COVID-19; Hypertension; Seasonal allergy
Andere Medikamente: SPIRONOLACTONE; IRBESARTAN; BUSPAR; MILK THISTLE
Allergien: -
Vorherige Impfungen: -

VAERS 1382265

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: KY
Alter: 42,0
Geschlecht: F
Eingang: 23.06.2021
Impfdatum: 03.06.2021
Beginn: 03.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain Colitis Computerised tomogram abnormal Dizziness Gastrointestinal haemorrhage Dehydration Diarrhoea Fatigue Loss of consciousness Nausea Pain Pyrexia Haematochezia Thrombosis Vomiting

Symptomtext

Nearly passed out twice; Passing blood clots; GI bleed; Severe body aches; Fatigue; Abdominal pain; Nausea; Vomiting; Fever; Diarrhea; Dehydration; Colitis; This is a spontaneous report from a contactable Nurse (patient) reported for herself. A 42-year-old female patient (not Pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) at 42-year-old, dose 2 via an unspecified route of administration, administered in Arm Left on 03Jun2021 06:30 PM (Lot Number: EW0179) as dose 2, single for covid-19 immunisation in Clinic. Medical history included hypertension, anxiety, seasonal allergy, asthma, Known allergies to Cephalosporin. Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Concomitant medications received within 2 weeks included spironolactone; irbesartan; buspirone hydrochloride (BUSPAR); silybum marianum (MILK THISTLE), all taken for an unspecified indication, start and stop date were not reported. the patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously took miralax and experienced Allergy, lisinopril and experienced Allergy, venlafaxine and experienced Allergy, patient previously took first dose of BNT162B2 (Brand: Pfizer, Lot number: EW0177) into left arm on 13May2021 06:30 PM at 42 years old for COVID-19 immunization. Patient experienced Severe body aches, fatigue, abdominal pain, nausea/vomiting, fever, nearly passed out twice, diarrhea followed by passing blood clots, dehydration, treated in ER twice. Once for dehydration, second for colitis with GI bleed. Event Start Date was 03Jun2021 09:00 PM. the adverse event result in Emergency room/department or urgent care. treatment received for the adverse event included IV fluids, antibiotics, and antiemetic. Outcome of the events was recovering. Information on Lot/Batch number was available. Additional information has been requested.; Sender's Comments: The limited information provided in this report does not allow a full assessment of the case, however, a possible contributory role of the suspect drug to the reported events "Nearly passed out twice, Passing blood clots and GI bleed" cannot be completely excluded based on temporal association. This case will be re-assessed when additional information becomes available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identifies as part of this review, as well as any appropriate action in response, will be promptly notifies to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to antibiotic; Anxiety; Asthma; COVID-19; Hypertension; Seasonal allergy
Andere Medikamente: SPIRONOLACTONE; IRBESARTAN; BUSPAR; MILK THISTLE
Allergien: -
Vorherige Impfungen: -

VAERS 1417199

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CO
Alter: 44,0
Geschlecht: F
Eingang: 22.06.2021
Impfdatum: 21.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test Chills Gait disturbance Pain Peripheral swelling Pyrexia Skin discolouration Thrombosis Ultrasound scan Vaccination site reaction

Symptomtext

On the eve of the vaccine, I felt a lot of pans shooting from vaccination sight down arm, felt feverish, chills, fever was 101.0, The morning of the 22nd, I felt fine, but around 6 in the evening I got another fever, closer to 102.0, injection site still very sore, a week later I got another fever and it was around 101.5, a few days after that I started to get leg pain but the arm pain had subsided. Because I had had a surgery 5 weeks before the thought of blood clots was on my mind, I began stretches and walking but it seemed to make it worse. That leg swelled and started to change color, it was my left leg, I went to ER they prescribed Xarelto, I was told I had clotting from my side to my ankle and circulation restriction. Bloodwork showed positive results for blood clots. I still have some pain and swelling. I did walk with a limp for a couple weeks. Treatments with Xarelto will continue for 3 more months. I had a follow up at trilakes primary on 06/08/2021. She confirmed it was blood clots and said she believes it was vaccine related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Blood work Ultrasound
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Tylenol Supplement
Allergien: Nsaids Cefalexin Paralytic-Suxanthoniun Shellfish
Vorherige Impfungen: -

VAERS 1417194

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MI
Alter: 15,0
Geschlecht: F
Eingang: 22.06.2021
Impfdatum: 17.06.2021
Beginn: 18.06.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / UN

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

Aphasia Bacterial infection Borrelia test CSF glucose normal CSF protein increased CSF red blood cell count positive CSF white blood cell count increased Computerised tomogram head normal Cytomegalovirus test Cytotoxic oedema Depressed level of consciousness Drug screen negative Dysarthria Electroencephalogram abnormal Encephalopathy Enterovirus test Epstein-Barr virus test Headache

Symptomtext

Patient had Pfizer COVID-19 vaccines on 5/27/2021 and 6/17/2021. On the evening of 06/18/2021 she started having headache with nausea and vomiting. Over that weekend she progressively got worse with slurred speech and then aphasia although she could still follow commands. She was then seen in the emergency department where she was then transferred to emergency department. There she was noted to have deterioration in her neurologic exam with inability to follow commands. She was then transferred to Hospital where she became more obtunded and encephalopathic and was transferred to the.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 3,0
Labordaten: On 6/20/2021 she had a normal CT of the head, negative comprehensive drug screen, LP with elevated opening pressure of 34, CSF protein elevated at 270, CSF RBC 700, CSF glucose 51 and CSF WBC 910 (84 segmented neutrophils, 6 lymphocytes and 10 monocytes). The CSF was sent for several studies including HSV PCR (negative), Enterovirus PCR (uninterpretable due to interfering substance), CMV PCR, EBV PCR, HHV-6 PCR, Lyme antibody, West Nile antibodies, Arbovirus panel, and Jamestown Canyon Virus. She had a partial MRI on 06/20/2021 because of patient motion but it showed "Nonspecific restricted diffusion in the centrum semiovale and corpus callosum. These findings at the corpus callosum in have been described with cytotoxic edema secondary to multiple etiologies. Differential considerations include, but not limited to, bacterial and viral infectious processes and toxic/metabolic etiologies." An MRI done on 6/21/2021 showed " Interval decrease in the extent of the cytotoxic lesion of the corpus callosum posteriorly. There is been resolution of involvement in the deep white matter. Differential remains unchanged. There are no other interval changes." The MRA/MRV was normal. The EEG on 06/20/2021 showed "This routine awake and sleep EEG is abnormal due to following: - Poor or lack of common background organization, diffuse background slowing, poorly sustained posterior dominant rhythm and/or sleep architecture, suggestive of diffuse cerebral dysfunction, or encephalopathy, nonspecific to etiology. - Focal slowing noted in bilateral frontal areas, suggestive of underlying focal cerebral dysfunction in the above head region(s). No seizures were recorded during the study."
Aktuelle Erkrankungen: Tick bite about 1.5 months prior.
Vorgeschichte: Anxiety and depression
Andere Medikamente: Loritadine, Zoloft and Trazadone
Allergien: Azithromycin
Vorherige Impfungen: -

VAERS 1414953

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: OK
Alter: 15,0
Geschlecht: M
Eingang: 21.06.2021
Impfdatum: 11.06.2021
Beginn: 11.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hyperhidrosis Nausea Pallor Syncope

Symptomtext

Approximately 11 minutes post COVID19 injection, client experienced syncopal episode per family member. Patient conscious and A+O x 4 at time of nurse response, client was noted to be pale and diaphoretic with c/o nausea, vital signs stable, lungs clear to auscultation bilaterally, no visible or verbal complaint of shortness of breath, edema to face/mouth, hoarseness/throat tightness, vital signs remained stable: 1351-HR 89, BP-92/64, SpO2-99%, R-18, 1353-HR 79, BP-102/74, SpO2-99%, R-18, 1400-HR 79, BP-108/78, SpO2-100%, R-18. Client waited an additional 15 minutes in clinic for observations, at time of discharge patient reported resolved nausea, skin color within normal limits for race, no visible or verbalized distress from patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None
Allergien: No known allergies.
Vorherige Impfungen: Lightheaded feeling with previous vaccines at age 11.

VAERS 1413565

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: TX
Alter: 13,0
Geschlecht: F
Eingang: 20.06.2021
Impfdatum: 01.06.2021
Beginn: 01.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Blood test Chest pain Dyspnoea Electrocardiogram Feeding disorder Insomnia Myocarditis Troponin I increased X-ray

Symptomtext

Shortness of breath on the day of the shot. Then symptoms went away. About a week after she had chest pains for 1 day. On Sunday, June 13, she had chest pains and she couldn't eat or sleep. Symptoms continued for 2 days. Took her to the doctor who ordered blood tests, EKG and x-rays.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: June 18, Triponon I level were extremely high. Rushed her to ER. Diagnosis was myocarditis likely cause by the vaccine shot. She was sent home and ordered to do more bloodwork on June 21 and follow up with a cardiologist in 1 week.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Multi-vitamins, fiber gummies, miralax
Allergien: No
Vorherige Impfungen: -

VAERS 1413224

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: AZ
Alter: 34,0
Geschlecht: F
Eingang: 20.06.2021
Impfdatum: 19.06.2021
Beginn: 19.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Blood glucose normal Dizziness Flushing Hyperhidrosis Injection site pain Syncope Unresponsive to stimuli

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Felt light-headed, and fell unresponsive for less then 1 minute-Mild, Systemic: Flushed / Sweating-Mild, Additional Details: called 911, EMT/paramedics came, checked vitals (all were fine), Blood glucose 100.

Weitere VAERSDATA-Felder

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

VAERS 1412732

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: PA
Alter: 24,0
Geschlecht: M
Eingang: 19.06.2021
Impfdatum: 18.06.2021
Beginn: 18.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Fall Fatigue Flushing Hyperhidrosis Lethargy Syncope Unresponsive to stimuli Vision blurred Visual impairment

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Exhaustion / Lethargy-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Mild, Systemic: Visual Changes/Disturbances-Mild, Additional Details: PATIENT CAME IN TO GET 2ND COVID VACCINE AT 12 PM. AFTER VACCINE PATIENT SAT IN OBSERVATION AREA. AFTER ABOUT 6 MINS, PATIENT STATES BLURRED VISION, HE TRIED TO GET UP BUT THEN FELL TO THE GROUND. PATIENT WAS HELPED UP AND GIVEN WATER. AMBULANCE WAS CALLED IMMEDIATELY. PATIENT STATED HE DID NOT EAT ANYTHING WHICH COULD BE THE CAUSE OF THIS. EMT ARRIVED CHECKED PULSE AND BP. PATIENT WAS NORMAL. PATIENT REFUSED TO GO TO ER. PATIENTS DAD ARRIVED 20 MINS LATER TO DRIVE PATIENT HOME.

Weitere VAERSDATA-Felder

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

VAERS 1409947

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MO
Alter: 31,0
Geschlecht: F
Eingang: 18.06.2021
Impfdatum: 17.06.2021
Beginn: 17.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Dizziness Loss of consciousness Muscle twitching Posture abnormal Respiratory rate increased Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Shakiness-Mild, Additional Details: Within 10 seconds of vaccine, pt sat back on bench and started going limp, breathing rapidly, and shortly after lost consciousness for about 10-20 seconds. After fainting the patient was shaking/twitching in her extremities which she could not control for about 1 minute. Her blood pressure was 115/71, 10 minutes later 115/73, 10 minutes later 121/73. She was given ice water. She felt fine within 10 minutes and left pharmacy after about 30 minutes.

Weitere VAERSDATA-Felder

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

VAERS 1409739

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: PA
Alter: 37,0
Geschlecht: F
Eingang: 18.06.2021
Impfdatum: 26.05.2021
Beginn: 07.06.2021
Tage bis Beginn: 12,0
Dosis: 2
Route/Site: - / -

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

Eye disorder Facial paralysis Hypoaesthesia Hypoaesthesia oral

Symptomtext

left side facial paralysis/left half of her face became paralyzed; numbness on the left side part of her face; her tongue is still numb; cannot blink her left eye; This is a spontaneous report received from a contactable consumer (patient). A 37-years-old female patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EW0179), via an unspecified route on 26May2021 (at the age of 37-years) at left shoulder as single dose for Covid-19 immunization. Medical history and concomitant medications were not reported. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EW0179), via an unspecified route on 05May2021 as single dose in the left arm for covid-19 immunization. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient did not took any other products. On 07Jun2021, the patient experienced left side facial paralysis/ left half of her face became paralyzed which was facial paralyzed. It started to have numbness on the left side part of her face and it already went out since yesterday, but her tongue was still numb. She has been experiencing numbness but not painful. She also cannot blink her left eye. Patient stated that numbness went away but the look got worse and sometimes feels numbness but not all the time. Patient stated that she started drinking B complex vitamins yesterday. She wanted to know if this was a recorded side effect of the vaccine and if she needs to see a doctor for treatment. Patient stated that she just searching online probable connection to Pfizer and facial paralyzed and saw there were some studies that connected the two. The patient did not went to Emergency Room. Patient stated she just had a phone consultation from her country it was just a virtual consultation to a doctor, but she did not go to a doctor here. Patient stated she decided to get it to be protected since she has never been infected with COVID and when it was available, she got it to feel safe. The outcome of events was left side facial paralysis and her tongue was still numb, cannot blink her left eye was not recovered, numbness on the left side part of her face was recovering. Information on Lot/Batch number was available. Additional information has been requested.

Weitere VAERSDATA-Felder

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

VAERS 1400885

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: FL
Alter: 31,0
Geschlecht: F
Eingang: 15.06.2021
Impfdatum: 01.06.2021
Beginn: 01.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Aphasia Bell's palsy Hypoaesthesia Musculoskeletal stiffness Paraesthesia

Symptomtext

Vaccine received 6/1/2021 at 12:20pm. Tingles on right side of my face was occurring within an hour of injection. Tingles occurred for 24 hours then progressed to tingles, stiffness and somewhat "numb" like sensation all along the side of my cheek up to my right eye. I was straining to talk and noticed I had to move my mouth differently to talk Thursday 6/3/2021 afternoon + evening. Went to my primary care doctor on the morning of 6/4/2021 and was diagnosed with Bells Palsy. I then began a prescription for steroids - Prednisone (60 mg for six days with tapering down over 10 days). The Bells did not get worse but now that I have completed the steroids the the tingle, stiff, and numb sensations remain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Went to primary care doctor on Friday 6/4/2021 and was diagnosed with Bells Palsy
Aktuelle Erkrankungen: None
Vorgeschichte: Migraine headaches with aura - 2 to 4 per year
Andere Medikamente: Zoloft - 25mg, kyleena
Allergien: None
Vorherige Impfungen: -

VAERS 1400874

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NJ
Alter: 68,0
Geschlecht: F
Eingang: 15.06.2021
Impfdatum: 02.06.2021
Beginn: 03.06.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Intensive care Ruptured cerebral aneurysm Surgery

Symptomtext

1 Ruptured brain aneurysm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 12,0
Labordaten: Surgery and in ICU for 12 days
Aktuelle Erkrankungen: -
Vorgeschichte: High blood pressure
Andere Medikamente: olmsrtn-amlepn hctz 40 -5-25 mg clonieine hcl 0.1 mg
Allergien: -
Vorherige Impfungen: -

VAERS 1400653

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: DC
Alter: 38,0
Geschlecht: F
Eingang: 15.06.2021
Impfdatum: 19.04.2021
Beginn: 10.06.1921
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

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

Anticoagulant therapy Arteriosclerosis coronary artery Coagulation test normal Muscular weakness Pain in extremity Peripheral artery thrombosis

Symptomtext

6/10/21, began experience LUE pain/weakness. Found to have left brachial artery thrombus and aortic arch atheroma. Placed on Heparin drip initially, transitioned to Bivalrudin gtt, then now on Eliquis. Hypercoagulable work-up overall unremarkable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Peripheral artery thrombosis
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: migraines, hiatal hernia, pre-DM
Andere Medikamente: Wellbutrin 150mg BID, omeprazole 40mg BID, metformin 500mg QD, phentermine 37.5 QD, NP Thyroid 30 mg QD, nuvaring qMonth
Allergien: Demerol and sulfa drugs
Vorherige Impfungen: -

VAERS 1398557

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MO
Alter: 13,0
Geschlecht: M
Eingang: 15.06.2021
Impfdatum: 20.05.2021
Beginn: 23.05.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: - / LA

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

Chest pain Dyspnoea Electrocardiogram Loss of consciousness

Symptomtext

My son had sharp chest pain, difficulty breathing & lost consciousness briefly.; My son had sharp chest pain, difficulty breathing & lost consciousness briefly.; My son had sharp chest pain, difficulty breathing & lost consciousness briefly.; This is a spontaneous report from contactable consumer (parent). A 13-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in Arm Left on 20May2021 13:30 (Lot Number: EW0179, at age of 13 years old) as single dose for COVID-19 immunisation. Medical history included asthma. Concomitant medications included cetirizine hydrochloride (ZYRTEC ALLERGY); montelukast sodium (SINGULAIR). The patient previously took azithromycin and experienced allergy. The patient experienced had sharp chest pain, difficulty breathing & lost consciousness briefly on 23May2021 11:30. The event result in Doctor or other healthcare professional office/clinic visit. Events were reported as non-serious. The patient received treatment for events and visit pediatrician & EKG. Had been referred to a cardiologist. The outcome of events was recovered in May2021. Further information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Name: EKG; Result Unstructured Data: Test Result:Unknown results; Comments: Visit to pediatrician & EKG. Has been referred to a cardiologist.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma
Andere Medikamente: ZYRTEC ALLERGY; SINGULAIR
Allergien: -
Vorherige Impfungen: -

VAERS 1391895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: IL
Alter: 55,0
Geschlecht: F
Eingang: 11.06.2021
Impfdatum: 16.05.2021
Beginn: 10.06.2021
Tage bis Beginn: 25,0
Dosis: 2
Route/Site: - / -

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

Alanine aminotransferase normal Amylase Angiogram cerebral normal Aortic arteriosclerosis Aphasia Arteriogram carotid normal Aspartate aminotransferase normal Asthenia Blood albumin decreased Blood alkaline phosphatase normal Blood bilirubin decreased Blood calcium normal Blood chloride decreased Blood creatinine increased Blood glucose increased Blood magnesium normal Blood potassium decreased Blood sodium decreased

Symptomtext

55 y.o. female with a lifetime history of insulin-dependent diabetes that presented to the emergency room just a few hours after she started having a left-sided neurologic deficit. The patient reports that she had a stroke several years ago but for some reason was told to not take aspirin and was not started on Plavix. Irregardless, the patient came in with a very significant left-sided neurologic deficit. She states that she could not speak, she had left facial droop, left arm weakness, and left leg weakness. She initially had an NIH stroke scale in the emergency room of 11. Initial CT of the head showed nothing acute. Consultation with neurology was obtained and the patient was sent for a CTA of the head and neck. No large vessel occlusion was identified and shortly after this the patient's NIH stroke scale reduced to 2 and shortly after this the neurologic deficit completely resolved and stroke scale return to 0. At that point, the patient was diagnosed with a TIA and admitted to the hospital for observation. This morning she states she feels fine. She has no neurologic deficit whatsoever. She denies any sensory or strength deficits this morning at all. The patient sugars have been a little bit high, but otherwise she had an uneventful evening

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: 2,0
Labordaten: CBC Recent Labs Lab 06/11/21 0532 06/10/21 1320 WBC 8.5 11.5* HGB 9.6* 10.8* HCT 32.0* 36.0 PLT 332 380 MCV 81.8* 81.1* RBC 3.91* 4.44 CHEMISTRY Recent Labs Lab 06/11/21 0532 06/10/21 1320 04/20/21 1408 04/20/21 1408 07/08/20 1450 07/08/20 1450 GLU 434* 165* < > 234* < > 55* BUN 24* 22* < > 16 < > 15 CREATININE 1.0 1.0 < > 1.2* < > 0.9 NA 135* 136 < > 137 < > 139 K 3.4* 2.4* < > 2.8* < > 2.3* CL 96* 94* < > 97* < > 97* CO2 31 38* < > 33* < > 37* CALCIUM 9.1 9.9 < > 9.3 < > 9.9 MG -- -- -- 1.8 -- 2.1 LABALBU -- 3.4 -- 3.4 < > 3.4 ALT -- 24 -- 32 < > 30 AST -- 19 -- 23 < > 24 ALKPHOS -- 101 -- 89 < > 90 LABBILI -- 0.3 -- 0.2 < > 0.2 < > = values in this interval not displayed. GI No results for input(s): AMYLASE, LIPASE in the last 70080 hours. COAGS Recent Labs Lab 06/10/21 1320 PROTIME 13.2* INR 1.1 CARDIAC No results for input(s): TROPONINI, TROPONIN2, TROPONIN3, TROPONIN4, BNP in the last 70080 hours. URINE Recent Labs Lab 06/10/21 1458 LEUKOCYTESUR NEGATIVE NITRITE NEGATIVE BLOODU NEGATIVE WBCU 0 to 5 SPECGRAV 1.010 KETONESU NEGATIVE PROTEINUA NEGATIVE PHUR 7.0 Imaging Review XR CHEST PORTABLE Result Date: 6/10/2021 EXAM: XR CHEST 1 VIEW CLINICAL INDICATION: Weakness COMPARISON: None TECHNIQUE: A portable upright AP view of the chest was clear for interpretation. FINDINGS: The lungs are clear. The heart size is at the upper limits of normal. The hilar and mediastinal structures are unremarkable. There is no pneumothorax or pleural effusion. IMPRESSION: No radiographic evidence for acute cardiopulmonary disease. Electronically signed by: MD 6/10/2021 1:40 PM CDT CT HEAD WO CONTRAST Addendum Date: 6/10/2021 ADDENDUM #1 I discussed the above findings with Dr. at 1322 hours CST on 6/10/2021. Electronically signed by: MD 6/10/2021 1:25 PM CDT Result Date: 6/10/2021 EXAMINATION: CT Head without Contrast, Axial Imaging with 2-D Coronal and Sagittal Reconstruction. INDICATION: Weakness. Clinical concern for acute stroke. COMPARISON: 7/5/2014. FINDINGS: No mass, midline shift, intracranial hemorrhage, areas of acute macrovascular ischemia, or acute osseous abnormality. No extra-axial fluid collections. Ventricles and sulci are normal for age. Chronic calcific densities along the inner table of the left frontotemporal calvarium are likely benign osteomas, with densely calcified meningiomas much less likely. No surrounding edema or mass effect on the adjacent brain parenchyma. Brain parenchyma is within normal limits for age with no significant cortical or significant white matter lesions identified; minimal chronic white matter microvascular disease is not excluded. Atherosclerotic calcifications in the carotid siphons and in the right vertebral artery near the skull base. No significant disease in the partially visualized paranasal sinuses or mastoid air cells. IMPRESSION: 1. No acute intracranial abnormality. Please see above report for the chronic findings. This CT exam was performed using one or more of the following dose reduction techniques: automated exposure control, adjustment of the mA and/or kV according to patient size, and/or use of iterative reconstruction technique. Radiation Dose: 1085.7 mGy*cm total DLP Electronically signed by: MD 6/10/2021 1:17 PM CDT CTA HEAD AND NECK W CONTRAST Result Date: 6/10/2021 EXAMINATION: CTA Head and Neck with Contrast. Axial imaging, with 2-D Coronal and Sagittal Reconstructions and 3-D MIP and 3-D Volume Rendered Reconstructions. 100 mL Omnipaque 300 was administered intravenously for the post-contrast images. INDICATION: Left-sided numbness. COMPARISON: CT head without contrast 6/10/2021. CTA NECK WITH CONTRAST FINDINGS: Classic 3 vessel aortic arch anatomy. Atherosclerotic calcifications in the aortic arch and proximal left subclavian artery. No hemodynamically significant stenosis or aneurysm of the great vessels, common carotids, or the cervical internal carotid and vertebral arteries. The right vertebral artery is dominant. Moderate calcifications in the left carotid bulb with slightly less than 50% stenosis using NASCET criteria. Minimal calcifications in the right carotid bulb and proximal left external carotid artery with no significant stenosis. Diffuse bilateral pulmonary edema. Mildly enlarged mediastinal lymph nodes with a right paratracheal lymph node measuring approximately 1 x 1.4 cm on series 2, axial image 8. Benign-appearing lymph nodes with fatty hila bilaterally in the neck, most prominent in the submandibular chain posterior to the submandibular glands, measuring up to 1.2 cm in short axis diameter. No suspicious neck mass or abnormal enhancement./Degenerative changes in the cervical and included upper thoracic spine including the atlantodental joint. No acute osseous abnormality. CT ARTERIOGRAM CIRCLE OF WILLIS: Mild calcifications in the right vertebral artery at the skull base medial to the right occipital condyle with less than 50% diameter stenosis. Calcified plaques in bilateral cavernous carotid arteries with up to moderate slightly less than 50% narrowing. No hemodynamically significant stenosis or aneurysm in the intracranial internal carotid, major segments of the anterior and middle cerebral arteries, intracranial vertebral and basilar arteries, or in the posterior cerebral or superior cerebellar arteries. A tiny anterior communicating artery is seen. Posterior communicating arteries are not well seen. No abnormal intracranial enhancement. Please see the CT head without contrast exam earlier today regarding the other chronic intracranial findings. IMPRESSION: 1. Moderate calcified plaque in the left carotid bulb with slightly less than 50% stenosis using method criteria. Mild plaque in the right carotid bulb with no significant stenosis. 2. Calcified plaque in the right vertebral artery medial to the right occipital condyle with less than 50% diameter stenosis. Right vertebral artery is dominant. 3. Moderate calcified plaques in bilateral carotid siphons with likely slightly less than 50% stenosis, with limited measurement of the stenosis due to the extensive calcifications. 4. No other significant stenosis or aneurysm in the cervical carotid or vertebral arteries. 5. No aneurysms or other significant stenosis in the major arteries of the Circle of Willis. 6. No abnormal intracranial enhancement. Please see the earlier CT head without contrast exam regarding the chronic intracranial findings. This CT exam was performed using one or more of the following dose reduction techniques: automated exposure control, adjustment of the mA and/or kV according to patient size, and/or use of iterative reconstruction technique
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Current Outpatient Medications: ? buPROPion (WELLBUTRIN) 75 MG tablet, Take 1 tablet (75 mg) by mouth 2 times daily, Disp: 60 tablet, Rfl: 5 ? furosemide (LASIX) 40 MG tablet, TAKE 1 & 1/2 (ONE & ONE-HALF) TABLETS BY MOUTH TWICE DAILY AS
Allergien: Allergen Reactions ? Codeine ? Lisinopril Cough ? Losartan Cough ? Lovenox [Enoxaparin] ? Nsaids ? Penicillins
Vorherige Impfungen: -

VAERS 1391825

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: OH
Alter: 34,0
Geschlecht: F
Eingang: 11.06.2021
Impfdatum: 12.05.2021
Beginn: 07.06.2021
Tage bis Beginn: 26,0
Dosis: 2
Route/Site: IM / UN

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

Anticoagulant therapy Antinuclear antibody positive Antiphospholipid antibodies positive Cardiolipin antibody Coagulopathy Embolic stroke

Symptomtext

Stroke, thromboembolic source. Suspected due to autoimmune coagulopathy . Symptom onset was ~3 weeks after last vaccine. Anticoagulation initiated with enoxaparin and warfarin for destination therapy of warfarin x 3 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Embolic stroke
Hospital-Tage: 4,0
Labordaten: Lupus anticoagulant positive, ANA pattern speckled, cardiolipin IgG >80
Aktuelle Erkrankungen: 1.) Positive ANA possible RA 2.) History of VTE following C-section 3.) Heart palpitations
Vorgeschichte: See above
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1391792

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: OH
Alter: 45,0
Geschlecht: F
Eingang: 11.06.2021
Impfdatum: 19.04.2021
Beginn: 23.04.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: - / LA

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

Balance disorder Dizziness Loss of consciousness Nausea

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA Experienced dizziness, nausea and extreme imbalance since the first dose that has not resolved and led to me passing out and needing two separate trips to the ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: All tests negative
Aktuelle Erkrankungen: none
Vorgeschichte: Asthma, migraines, 2-TIA's
Andere Medikamente: Aspirin 81mg, B2, D3, multivitamin, melatonin 3mg, nortriptyline 75mg, biotin
Allergien: Imitrex, Maxalt, Lisinopril
Vorherige Impfungen: -

VAERS 1390997

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CO
Alter: 31,0
Geschlecht: F
Eingang: 11.06.2021
Impfdatum: 03.05.2021
Beginn: 14.05.2021
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: - / LA

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

Bell's palsy

Symptomtext

Diagnosed with Bells Palsy; This is a spontaneous report from a contactable consumer (patient). A 31-year-old non-pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection, Lot number: EW0179, Expiration Date: unknown), via an unspecified route of administration, administered in left arm on 03May2021 at 10:15 (at the age of 31-year-old) as single dose for covid-19 immunization. The patient's medical history and known allergies were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Concomitant medications included escitalopram oxalate (LEXAPRO); vitamin D NOS [VITAMIN D] and vitamin B complex (VITAMIN B). The patient previously received first dose of BNT162B2 (Lot number: ER8731) via an unspecified route of administration, administered in left arm on 12Apr2021 at 10:15 for COVID-19 immunization. Prior to the vaccination the patient was not diagnosed with COVID-19. The patient was not pregnant at the time of vaccination. On 14May2021 at 20:00, the patient was diagnosed with Bell's Palsy. Treatment received for the adverse event included Steroid pills and antibiotics for 1 week. The event resulted in emergency room/department or urgent care. Therapeutic measures were taken as a result of event. Since the vaccination the patient had not been tested for COVID-19. The outcome of the event was resolving. Device Date: 01Jun2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: LEXAPRO; VITAMIN D [VITAMIN D NOS]; VITAMIN B
Allergien: -
Vorherige Impfungen: -

VAERS 1389515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0179

schwer

Staat: NY
Alter: 32,0
Geschlecht: M
Eingang: 10.06.2021
Impfdatum: 10.06.2021
Beginn: 10.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Fall Feeling hot Heart rate increased Loss of consciousness Nausea Unresponsive to stimuli

Symptomtext

After receiving the vaccine the patient was instructed to sit at the designated post vaccination area. As he was sitting in the chair, a few minutes after receiving the vaccine the patient lost consciousness and fell from the chair onto the floor. The patient was unresponsive for a few seconds. When I positioned him in an upward position he regained consciousness and did not remember what happened. The patient had a fast heart rate and was feeling hot, dizzy, and nauseated. He showed no signs of anaphylactic/allergic reaction. Patient admitted he was nervous and anxious about the vaccine and does not like needles. I instructed the patient to remain seated on the floor and gave him an ice pack, water, and told him to take deep breathes. Patient stated he felt better. The store manager and I called 911 to get paramedics to check his vitals. Patient denied to go to emergency room, said he was feeling better. Patient confirmed he lived only a few blocks away and he had someone to drive him. Paramedics cleared the patient and stated all vitals were in normal range. Patient stayed at the pharmacy for 10 more minutes after that with instructions if he felt any symptoms to call his doctor or 911.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Paramedics took vitals; all in normal ranges as stated by the paramedic.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1388946

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: UT
Alter: 15,0
Geschlecht: M
Eingang: 10.06.2021
Impfdatum: 05.06.2021
Beginn: 05.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Brain natriuretic peptide increased Chest pain Echocardiogram Electrocardiogram ST segment elevation Myocarditis Pericarditis Troponin I increased

Symptomtext

Presented with chest pain and diagnosed with my and pericarditis as evidenced by elevated troponin, , elevated BNP and diffuse ST changes on EKG

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 5,0
Labordaten: Chemistry Troponin-I: 1.59 ng/mL High (06/09/21 17:29:00) Troponin-I: 1.55 ng/mL High (06/09/21 06:14:00) Troponin-I: 1.72 ng/mL High (06/09/21 00:11:00) Echo TransTHORacic TTE Ltd 06/08/21 16:29:31 Summary 1. Normal coronary dimensions, see above for measurements. 2. Aortic root and ascending aorta dimensions are within normal limits. 3. Normal right ventricular size and qualitatively normal systolic function. 4. Normal left ventricular size and qualitatively normal systolic function. 5. Global peak systolic LV strain is -18.7 %. 6. No pericardial effusion. EKG 6/8/21 with diffuse ST elevation
Aktuelle Erkrankungen: 4 weeks prior his family was symptomatic and tested positive for covid 19 but he was tested and negative, He did not have symptoms.
Vorgeschichte: none
Andere Medikamente: Imitrex prn migraine Trazadone for sleep
Allergien: none
Vorherige Impfungen: -

VAERS 1386168

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: DE
Alter: 16,0
Geschlecht: M
Eingang: 09.06.2021
Impfdatum: 09.06.2021
Beginn: 09.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Eye movement disorder Feeling abnormal Pallor Syncope Visual impairment

Symptomtext

2 MINUTES APPROXIMATELY AFTER RECEIVING DOSE SAID I DON'T FEEL RIGHT, THE INJECTION SITE DOESN'T FEEL RIGHT, I FEEL DIFFERENTLY, I FEEL LIKE I'M GOING TO PASS OUT" STATES HIS PUPILS DILATED, EYES ROLLED BACK, COLOR IN THE FACE CHANGED (PALOR) AND THEN HE FAINTED AND PRVENTED HIM FROM FALLING. HE DESCRIBES FEELING THAT THE VISION HAD CHANGED, LOOKED BLACK AND SPOTTY, AND THE HUMIDITY, THE GROUND LOOKED SPOTTY TO HIM. IN LESS THAN A MINUTE HE CAME TO CONSCIOUSNESS BEFORE WE COULD ADMINISTER AMMONIUM SALTS. PULSE RATE WAS STEADY AND POUNDING, FELT NORMAL. TOOK VITAL SIGNS, PULSE OX 98%, WITH PULSE OF 55 ON THAT DEVICE AND THEN WITH WRIST B/P READ B/P OF 174/75 AND HR UP TO 66BPM, PATIENT KEPT FOR ADDITIONAL 25 MINUTES FOR OBSERVATION AND DOING JUST FINE NOW.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: JUST VITAL SIGNS ABOVE AND OBSERVATION, NO SIGN OF ANAPHYLAXIS
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1384810

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NJ
Alter: 56,0
Geschlecht: F
Eingang: 09.06.2021
Impfdatum: 24.05.2021
Beginn: 02.06.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: SYR / LA

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

Bell's palsy Blood test normal Muscle twitching Musculoskeletal stiffness

Symptomtext

Bell's Palsy. Prednisone, Antiviral medication and artificial tear eye drops. Left Ear Pain on 6/1/2021 in the evening. Twitching on the left side of my mouth. Woke up on 6/2/2021 with the left side of my face very stiff. Went to ER. They said it was the early stages of Bell's Palsy. Followed up with my Primary Care Physician on 6/8/2021 and confirmed Bell's Palsy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Lyme's Disease Test which came out negative. Going within the next day or so for an MRI of the Brain to rule out anything else.
Aktuelle Erkrankungen: None
Vorgeschichte: Colitis, Hashimoto Thyroiditis
Andere Medikamente: Citalopram, Delzicol, Mercaptopurine, Multi Vitamin, Calcium, Vitamin D
Allergien: N/A
Vorherige Impfungen: -

VAERS 1343229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: SC
Alter: 13,0
Geschlecht: F
Eingang: 09.06.2021
Impfdatum: 21.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Anaphylactic reaction Arthralgia Asthenia Back pain Chest discomfort Diplegia Dizziness Dyspnoea Gait disturbance Hypoaesthesia Pain in extremity Muscular weakness Paraesthesia Paralysis Pharyngeal swelling Pruritus Spinal pain SARS-CoV-2 test negative

Symptomtext

Anaphylactic reaction; left cheek started swelling; looking woozy; throat and tongue started swelling; throat and tongue started swelling; having a hard time breathing; from the neck down, she had a temporary paralysis and she could not move./she could not feel anything from the waist down.; whole body was shaking; numbness and tingling all over.; numbness and tingling all over.; extreme pain in her back; When they would touch her hips, toes, spine, ankles, and knees she would complain of extreme pain, like joint pain.; When they would touch her hips, toes, spine, ankles, and knees she would complain of extreme pain, like joint pain.; When they would touch her hips, toes, spine, ankles, and knees she would complain of extreme pain, like joint pain.; very weak; chest was tight.; cannot walk without assistance; itching all over and in her throat; itching all over and in her throat; This is a spontaneous report from a contactable consumer (parent). A 13-years-old female patient received first dose of bnt162b2 (Pfizer-BioNTech COVID-19 Vaccine, 0.3 ML), at the age of 13-years-old , via an unspecified route of administration, administered in Arm Right on 21May2021 11:55 (Lot Number: EW0179; Expiration Date: Aug2021) as 0.3 ML SINGLE for covid-19 immunisation. Medical history included ongoing asthma, Diagnosed as a toddler. Had RSV as a baby. ongoing seasonal allergy, To like grass and pollen. ongoing constipation, Diagnosed about a year ago. allergic to shellfish because she gets sick. She said that it happened when her daughter was 4-5 years old. Whenever she has contrast for a MRI she throws it up. The patient's concomitant medications were not reported. The patient previously took Azithromycin and Amoxicillin and were allergic. The patient experienced anaphylactic reaction on 21May2021 with outcome of recovering, left cheek started swelling on 21May2021 with outcome of unknown, looking woozy on 21May2021 with outcome of unknown, throat and tongue started swelling on 21May2021 with outcome of unknown, having a hard time breathing on 21May2021 with outcome of unknown, from the neck down, she had a temporary paralysis and she could not move./she could not feel anything from the waist down on 21May2021 with outcome of unknown, whole body was shaking on 21May2021 with outcome of unknown, numbness and tingling all over on 21May2021 with outcome of unknown, extreme pain in her back on 21May2021 with outcome of unknown , when they would touch her hips, toes, spine, ankles, and knees she would complain of extreme pain, like joint pain on 21May2021 with outcome of unknown, very weak on 21May2021 with outcome of unknown , chest was tight on 21May2021 with outcome of unknown , cannot walk without assistance on 21May2021 with outcome of unknown , itching all over and in her throat on 21May2021 with outcome of unknown. Patient was in hospital from 21May2021 to 23May2021. AE(s) require a visit to Emergency Room. No AE(s) following prior vaccinations. No Family Medical History Relevant to AE(s). No Relevant Tests. Clinical courses as follows: It was reported they wanted her to wait for 30 minutes after her daughter received the vaccine. She said that after about 20 minutes, her daughter said that it felt like someone punched her in the face and her left cheek started swelling. She said that her husband said that their daughter started looking woozy and her eyes were closing. The staff laid her down on a mat on the floor. Then her daughter's throat and tongue started swelling and she was having a hard time breathing. Then her daughter complained that from the neck down, she had a temporary paralysis and she could not move. Her daughter asked if she asked if she was going to die. The nurse gave her an EpiPen and called a ambulance. Her whole body was shaking, probably from the EpiPen, like almost convulsing. She said that they got her onto the ambulance and her daughter was having trouble breathing. They gave her another dose of an EpiPen in the ambulance. They also gave her daughter a steroid and some Benadryl through an IV. Her daughter was rushed to the ER, having a hard time breathing and complaining she could not feel anything from the waist down. Caller said that her daughter was also complaining of numbness and tingling all over. She also started to complain about extreme pain in her back. When they would touch her hips, toes, spine, ankles, and knees she would complain of extreme pain, like joint pain. Her daughter had numbness from waist down. If they touched her foot she could not feel it. Her daughter was admitted to the hospital and got released yesterday 23May2021. She is still experiencing pain and numbness. The numbness is from the waist down and the tingling was up and down her arms. She said that her daughter was very weak and could not feed herself. They had to give her several albuterol breathing treatments in the hospital because her chest was tight. She was not wheezing, but they could tell it was constricted and treated her with Albuterol. She said that her daughter still cannot walk without assistance this morning. She was treated with Motrin, Benadryl and Atarax, and Prednisone in the hospital. The caller said that her daughter also complained about itching all over and in her throat. The caller said that her daughter did not have a rash though.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: Asthma (Diagnosed as a toddler. Had RSV as a baby); Constipation chronic (Diagnosed about a year ago.); Seasonal allergy
Vorgeschichte: Medical History/Concurrent Conditions: Grass allergy; Pollen allergy; Shellfish allergy (4-5 years old); Sickness (4-5 years old); Vomiting
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1382905

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0179

schwer

Staat: MN
Alter: 41,0
Geschlecht: F
Eingang: 08.06.2021
Impfdatum: 13.05.2021
Beginn: 07.06.2021
Tage bis Beginn: 25,0
Dosis: 2
Route/Site: SYR / AR

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

Bell's palsy Computerised tomogram normal Electrocardiogram normal

Symptomtext

Bell?s Palsy on right side of face

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Urgent care visit June 7, 2021. Normal EKG and clear CT scans. Diagnosis of Bell?s Palsy concluded.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroid
Andere Medikamente: Fluexotine, levothyroxine
Allergien: Succinylcholine
Vorherige Impfungen: -

VAERS 1382055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NC
Alter: 14,0
Geschlecht: F
Eingang: 08.06.2021
Impfdatum: 05.06.2021
Beginn: 06.06.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Blood calcium decreased Dizziness Electrocardiogram normal Hyperhidrosis Loss of consciousness Lymphocyte count decreased Lymphocyte percentage decreased Neutrophil percentage decreased Protein urine present Syncope

Symptomtext

Fainting 24 hours after receiving 2nd dose of Pfizer vaccine. Started feeling lightheaded, dizzy, broke out into a sweat and passed out for approximately 15 seconds. EMT called and observed at scene; transported to ER for additional observation. Received IV fluid and monitoring at ER and discharged later the same day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: EKG by EMS CBC, BMP, urinalysis, EKG at ER on same day as fainting 6/6/2021 Neutrophils - 82 high Lymphocytes - 10 low Lymphocytes Absolute - 0.6 low Calcium, Total - 8.5 low Urine Protein - +1 high All other test results, including ECG - normal
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: AUROVELA FE 1-20, 28, 1 mg-20 mcg
Allergien: None
Vorherige Impfungen: -

VAERS 1381754

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: IL
Alter: 14,0
Geschlecht: M
Eingang: 08.06.2021
Impfdatum: 01.06.2021
Beginn: 03.06.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

C-reactive protein increased Chest pain Echocardiogram normal Electrocardiogram repolarisation abnormality Feeling abnormal Myocarditis Troponin I increased

Symptomtext

Patient developed sudden onset of chest pain which was diagnosed as myocarditis. Feeling a little bad on 6/2/2021 with some mild chest pain on that date. Took ibuprofen. Woke up suddenly on 6/3/2021 with severe chest pain. Called pediatrician and was going to wait for them to open; however, it was so severe that they took him to the Emergency Department.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 1,0
Labordaten: Troponin I: Initial 3.66 ng/ml (ULN 0.03 ng/ml). CRP 22.6 mg/L (<8.1 mg/L) ECG with repolarization anomaly. Echo with no pericardial effusion and normal heart function. Troponins slowly resolving over 24 hours: 3.53; 2.62; 2.01
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1377815

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NY
Alter: 23,0
Geschlecht: F
Eingang: 07.06.2021
Impfdatum: 07.06.2021
Beginn: 07.06.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Asthenia Dehydration Feeling cold Heart rate increased Loss of consciousness Presyncope

Symptomtext

Patient ,, was vaccinated at approximately 2:15pm today at Vaccine Clinic. While in the observation area post-vaccine, patient lost consciousness at approximately 2:20pm for 60-90 seconds. Patient was not nervous, did not feel dizzy, nauseous, or feel she had an allergic reaction to the vaccine. Patient is an employee of Environmental and was accompanied by a co-worker. PA evaluated the patient, initial pulse rate was 104, a few minutes later was 87, then rose again to 97.BP was 125/78. Patient reported feeling weak and cold, has not eaten or had anything to drink today except a cup of coffee and cookies in the morning. PA assessed the patient vasovagaled due to dehydration, not due to a reaction from the vaccine. Patient drank 3 small bottles of water, ate saltine crackers and a granola bar. EMS was called and we attempted to cancel as the nurse was going to take the patient to ED, but EMS arrived on site already, assessed the patient and the patient refused to go to the ED by nurse or EMS. Patient was observed until 3:12pm and went home in an Uber. Patient info: Appointment #D11KA5Q

Weitere VAERSDATA-Felder

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

VAERS 1376975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: OK
Alter: 15,0
Geschlecht: F
Eingang: 07.06.2021
Impfdatum: 05.06.2021
Beginn: 05.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Dizziness Hypotension Loss of consciousness Syncope

Symptomtext

Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Hypotension-Severe

Weitere VAERSDATA-Felder

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

VAERS 1373725

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MD
Alter: 50,0
Geschlecht: F
Eingang: 04.06.2021
Impfdatum: 15.05.2021
Beginn: 16.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Dizziness Nausea Syncope

Symptomtext

Fainted; Feeling very light-headed; Slightly nauseous; This is a spontaneous report from a non-contactable consumer (patient). A 50-year-old female patient received 2nd dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, LOT number: EW0179, expiration date unknown) via unspecified route of administration on left arm on 15May2021 at 12:00 PM at age of 50-year-old at single dose for COVID-19 immunization. Patient was not pregnant at time of vaccination and events onset. Medical history included back pain. Patient had no known allergies. Patient previously received 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, LOT number: EW0171, expiration date unknown) on 24Apr2021 at 12:00 PM at age of 50-year-old via unspecified route of administration on left arm for COVID-19 immunisation. Concomitant medications included cyclobenzaprine, gabapentin, both administered within 2 weeks of vaccination. Patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient wasn't diagnosed with COVID-19. Since the vaccination, patient hasn't been tested for COVID-19. In the morning after the injection on 16May2021 at 09:30 AM, patient was in the kitchen and started feeling very light-headed and slightly nauseous. Patient sat in a chair but still felt the same. She got up to go lie down and fainted. After crawling to the couch and lying down for a few minutes, she felt better. The events didn't result in emergency room visit or physician office visit. Outcome of the events was recovered. No treatment received for the events. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Back pain
Andere Medikamente: CYCLOBENZAPRINE; GABAPENTIN
Allergien: -
Vorherige Impfungen: -

VAERS 1371569

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MO
Alter: 13,0
Geschlecht: M
Eingang: 03.06.2021
Impfdatum: 20.05.2021
Beginn: 23.05.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Chest pain Dyspnoea Electrocardiogram Loss of consciousness

Symptomtext

Sharp chest pains, difficulty breathing and passed out for about 30 seconds.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: EKG on 4/24/21. Low resting heart rate of 57 bpm. Has an appointment with a cardiologist to follow up.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Zyrtec, Singular, D3 Vitamin, Omega 3 Vitamin
Allergien: Azythromycin
Vorherige Impfungen: -

VAERS 1370586

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0179

schwer

Staat: MD
Alter: 32,0
Geschlecht: F
Eingang: 03.06.2021
Impfdatum: 13.05.2021
Beginn: 19.05.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: - / LA

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

Aphasia Migraine Myoclonus Paralysis Seizure

Symptomtext

Nightly sleep seizures/spastic seizure lasting 5 minutes of uncontrollable myoclonus only of the left leg; Temporary, passing paralysis; spastic seizure lasting 5 minutes of uncontrollable myoclonus only of the left leg; longer aphasia (inability to speak); severe migraines; This is a spontaneous report from a contactable consumer. This 32-year-old female consumer reported that she received 2nd dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot Ew0179) on 13May2021 at 02:45 PM into left arm for COVID-19 immunisation. Medical history included Hypermobile Ehlers-danlos syndrome, non-epileptic seizures, migraines, mild traumatic brain injury, intractable pain, severe food allergies. Known allergies: Wheat, gluten, eggs, soy, estrogens. Historical vaccine included 1st dose of BNT162B2 (lot Ew0171) on 22Apr2021 at 02:45 PM into left arm for COVID-19 immunisation. Concomitant drugs included Morphine, hydrocodone bitartrate, paracetamol (NORCO), diazepam (VALIUM), Propranolol, Hydroxyzine. The patient had a non-epileptic seizure disorder that was well controlled. After the second dose she began to have nightly sleep seizures, severe migraines, but am writing because of a spastic seizure lasting 5 minutes of uncontrollable myoclonus only of the left leg, with longer aphasia (inability to speak) and temporary, passing paralysis. The symptoms passed in an hour but an epileptic patient could have died. Event onset time was 19May2021 06:30 PM. No treatment was received. The outcome of the event was resolving.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Egg allergy; Ehlers-Danlos syndrome; Food allergy; Intractable pain; Migraine; Non-epileptic seizure; Soy allergy; Traumatic brain injury
Andere Medikamente: MORPHINE; NORCO; VALIUM; PROPRANOLOL; HYDROXYZINE
Allergien: -
Vorherige Impfungen: -

VAERS 1369331

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: IL
Alter: 61,0
Geschlecht: M
Eingang: 02.06.2021
Impfdatum: 12.05.2021
Beginn: 28.05.2021
Tage bis Beginn: 16,0
Dosis: 2
Route/Site: SYR / AR

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

Computerised tomogram Dyspnoea Pulmonary thrombosis Ultrasound Doppler

Symptomtext

Dose #1 received on 4/21/21. Dose #2 received on 5/12/21. Difficulty breathing beginning on 5/5/28/21. Diagnosed with multiple blood clots in right lung on 5/30/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 3,0
Labordaten: CT scan 5/30/21 Ultrasound of legs 5/30/21
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1368050

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: NY
Alter: 23,0
Geschlecht: F
Eingang: 02.06.2021
Impfdatum: 02.06.2021
Beginn: 02.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Chills Confusional state Dizziness Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Chills-Mild, Systemic: Confusion-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Shakiness-Mild, Systemic: Weakness-Medium, Additional Details: EMT and paramedics came

Weitere VAERSDATA-Felder

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

VAERS 1365315

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: AZ
Alter: 13,0
Geschlecht: M
Eingang: 01.06.2021
Impfdatum: 01.06.2021
Beginn: 01.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hyperhidrosis Loss of consciousness

Symptomtext

13 year old patient became diaphoretic and lost consciousness. He immediately woke up and vitals were normal. Parent denies any previous health conditions or syncopal episodes.

Weitere VAERSDATA-Felder

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

VAERS 1364930

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NJ
Alter: 43,0
Geschlecht: M
Eingang: 01.06.2021
Impfdatum: 22.05.2021
Beginn: 27.05.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Chest X-ray Chest discomfort Dyspnoea Electrocardiogram Pericarditis Pyrexia

Symptomtext

Pericarditis. Pressure in upper chest, trouble breathing, slight fever, rapid heartbeat. Given 800mg Ibuprofen 3 times a day for 5 days and doing much better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Hospital blood work, chest X-ray EKG completes on 5/28/21
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1362386

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NY
Alter: 14,0
Geschlecht: F
Eingang: 31.05.2021
Impfdatum: 30.05.2021
Beginn: 30.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Confusional state Dizziness Flushing Hyperhidrosis Nausea Syncope

Symptomtext

Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Nausea-Mild

Weitere VAERSDATA-Felder

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

VAERS 1361498

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: TX
Alter: 34,0
Geschlecht: F
Eingang: 31.05.2021
Impfdatum: 28.05.2021
Beginn: 28.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Confusional state Seizure Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Confusion-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Seizure-Mild, Additional Details: Pt was unresponsive approximately 5 mins after recieving COVID vax. Pt was sitting next to husband and husband called for help. Upon viewing the pt, pt appeared unconscious and possibly seizing. EMS (911) was called and in the mean time Rph attended to pt. By the time EMS arrived pt was starting to respond and gradually aware of environment and self . Pt was reccommended to visit hospital for further check up, but pt and husband declined. said shes doing fine and much better and husband agreed.

Weitere VAERSDATA-Felder

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

VAERS 1361707

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NY
Alter: 12,0
Geschlecht: F
Eingang: 30.05.2021
Impfdatum: 30.05.2021
Beginn: 30.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Feeling abnormal Hyperhidrosis Loss of consciousness Syncope

Symptomtext

After receiving vaccination, syncopal episode while sitting in the chair. Mom held child from falling to the ground and slowly placed her on the floor. LOC for less than 2 minutes. Alert and talking, ice pack to forehead and fluids offered. Placed in wheelchair and sent to med evaluation for further evaluation. Mom present at all times. VS taken 104/80 HR 72 Resp 16, diaphoretic with c/o's of lightheaded and foggy feeling. Lying on cot with Gatorade/water offered. Pt has never passed out with a vaccination in the past, had carrots for breakfast and little fluid intake. Very anxious with getting the shot. Discussion with mom & pt. importance of hydration eating when the next dose given, it will be in the med evaluation area lying down. Pt alert an ambulatory with 1/2 Gatorade and 1/2 eater prior to discharge with mom. Discussed s/s of reaction and call pediatrician with any further concerns. Verbalized understanding, discharged ambulatory with mom.

Weitere VAERSDATA-Felder

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

VAERS 1361484

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NC
Alter: 24,0
Geschlecht: M
Eingang: 30.05.2021
Impfdatum: 29.05.2021
Beginn: 29.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Confusional state Dizziness Flushing Hyperhidrosis Hyperventilation Hypoaesthesia Hypotension Injection site pain Syncope Tachycardia Tremor Unresponsive to stimuli Visual impairment

Symptomtext

Site: Pain at Injection Site-Medium, Systemic: Confusion-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Medium, Systemic: Hyperventilation-Severe, Systemic: Hypotension-Severe, Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Shakiness-Medium, Systemic: Tachycardia-Medium, Systemic: Visual Changes/Disturbances-Medium, Additional Details: Pt has history of vaso vagal syncope. Patient entered an episode of syncope and quickly recovered. Paramedics arrived to futher consult patient to recovery.

Weitere VAERSDATA-Felder

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

VAERS 1361179

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NY
Alter: 12,0
Geschlecht: F
Eingang: 29.05.2021
Impfdatum: 28.05.2021
Beginn: 28.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Syncope

Symptomtext

5 mins after being on the observation area patient experienced a feeling of dizziness while being with her mother, she fainted but didnt fall as she supported her body, mother expresses that something similar happened recently when she went to obtain blood work for her ab test. Also fx hx of vasovagal sx as per discussion. Denies any chest pain, no sob, no HA, no palpitations. Pt was transfered via wheelchair to the medical stretcher area and was observed and lie down in supine position with elevation of her legs for 30 mins. Patient left home without further episodes and stable, VS at time were 100/64 HR 67 Dr and EMS were at the site. Medical Advised provided

Weitere VAERSDATA-Felder

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

VAERS 1360490

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CO
Alter: 48,0
Geschlecht: F
Eingang: 29.05.2021
Impfdatum: 07.05.2021
Beginn: 07.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Dizziness Loss of consciousness Nausea Road traffic accident Sluggishness

Symptomtext

blacked out; lost control of the car and had an accident; I felt sluggish/dizzy and a bit nauseous/It was the same dizzy and nauseous feeling but more intense; I felt sluggish/dizzy and a bit nauseous/It was the same dizzy and nauseous feeling but more intense; I felt sluggish/dizzy and a bit nauseous/It was the same dizzy and nauseous feeling but more intense; This is a spontaneous report from a contactable consumer (patient). A 48-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in Arm Left on 07May2021 08:30 (Batch/Lot Number: EW0179) as 2nd dose, single for covid-19 immunization at a hospital. Medical history included allergy to some animal. Prior to vaccination, the patient was not diagnosed with COVID-19. There were no concomitant medications. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine and has no other medications received within 2 weeks of vaccination. The patient had the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot: EN6199) on 16Apr2021 at 08:30 in the left arm for COVID-19 immunization. The patient felt sluggish/dizzy and a bit nauseous the evening of the vaccine (07May2021). The next day (08May2021 08:00), the patient felt the same way while driving. It was the same dizzy and nauseous feeling but more intense. Then a few seconds later, she blacked out, lost control of the car and had an accident. The events resulted in emergency room/department or urgent care. The patient was treated with stitches and painkillers for the injuries. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the events was recovered on May2021. Information on Lot/Batch number was available. Additional information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to animal
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1358197

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MI
Alter: 45,0
Geschlecht: M
Eingang: 28.05.2021
Impfdatum: 28.05.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Hyperhidrosis Loss of consciousness Pallor Seizure Unresponsive to stimuli

Symptomtext

Approximately 5 minutes after administering the vaccine, he was waiting in his car with a friend, He became unresponsive and appeared to have lost consciousness. Upon arrival to the vehicle he looked to be having a seizure. Did not respond to verbal commands but did respond to sternal rub. EMS called. BP 118/58 and pulse 60. He was diaphoretic and pale. EMS arrived and during their interview he had another more intense and longer seizure. Transported to the Emergency Room.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None. History of Seizure Disorder
Vorgeschichte: History of Seizures
Andere Medikamente: None
Allergien: NKA
Vorherige Impfungen: -

VAERS 1357744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: IL
Alter: 17,0
Geschlecht: M
Eingang: 28.05.2021
Impfdatum: 27.05.2021
Beginn: 27.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Fall Loss of consciousness

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Nausea-Mild, Systemic: Vomiting-Mild, Additional Details: AFTER GETTING PFIZER COVID VACCINES,PATIENT GIVEN INSTRUCTIONS TO SIT DOWN FOR 15 MIN TO MONITOR,AFTER 2 MIN,PHARMACITS (MYSELF) OBSERVED THAT HE IS FALLING DOWN,HE FELT DIZZINESS,I WAS ABLE TO REVIVE HIM IN 3O SEC,HE WAS RESPONSE AND TALKING,I LET HIM SIT DOWN ON A CHAIR,HE ASKED FOR WATER,GAVE WATER,HE FELT VERY GOOD,HE LEFT THE PHARMACY AFTER 40 MINUTES,THEY DIDNT HAVE A PRIMARY CARE DR YET,BUT SPOKE WITH DAD,AFTER 6 HRS,PATIENT DOING VERY WELL,DIDNT HAVE TO GO TO HOPSPITAL!

Weitere VAERSDATA-Felder

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

VAERS 1357269

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: IL
Alter: 35,0
Geschlecht: F
Eingang: 28.05.2021
Impfdatum: 11.05.2021
Beginn: 13.05.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: - / LA

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

Thrombosis

Symptomtext

I am feeling a clot in my left armpit after 1 day of having 2nd dose of COVID19 Pfizer; This is a spontaneous report from a contactable consumer (patient). A 35-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration and administered in left arm at age of 35-years, on 11May2021 18:00 (Lot Number: EW0179) as single dose for covid-19 immunization. The patient medical history was not reported. The patient was not pregnant at time of vaccination. Concomitant medications were none (the patient did not receive any other medications within 2 weeks of vaccination). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Historical vaccine included the first dose of BNT162B2 on an unknown date for covid-19 immunization. The patient reported that she was feeling a clot in her left armpit at 08:00 on 13May2021 (reported as after 1 day of having 2nd dose of COVID19 Pfizer). The patient was not diagnosed with COVID-19 prior to vaccination and had not been tested for COVID-19 since the vaccination. Event outcome was not recovered. No follow-up attempts needed. No further information expected.

Weitere VAERSDATA-Felder

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

VAERS 1351706

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NC
Alter: 16,0
Geschlecht: M
Eingang: 26.05.2021
Impfdatum: 26.05.2021
Beginn: 26.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Fall Feeling abnormal Head injury Loss of consciousness Unresponsive to stimuli

Symptomtext

Patient received the Pfizer COVID vaccine at 1745. Patient states he didn't feel right but stood up to go to the observation area and lost consciousness causing him to fall backwards to the floor where he was witnessed hitting his head on the gym floor. Patient was unresponsive for approximately one minute and was then alert and oriented but c/o dizziness. VS at 1756 BP 137/63 HR 85 and O2 Sat 98%. Patient remained in the supine position for approximately 10 minutes and was then aided into a sitting position on the floor and then assisted into a chair. Patient was then observed for 30 minutes by staff where he continued to c/o lightheadedness and dizziness. VS at 1806 BP 115/68 HR 84 O2 Sat 97%. EMS was then called to assess patient for continued dizziness. VS by EMS sitting BP 122/77 and standing 117/70. Patient was offered to be taken by EMS for further assessment but patient and grandfather both declined further care at this time. Patient and grandfather were instructed to call 911 immediately for any change in mental status, nausea/vomiting, or any other reaction symptoms with verbalization of understanding and agreement. Patient was advised upon discharge to stay hydrated and rest for the remainder of the evening. Patient and grandfather were also encouraged to discuss reaction with patient's PCP prior to receiving second dose.

Weitere VAERSDATA-Felder

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

VAERS 1348276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: IL
Alter: 19,0
Geschlecht: F
Eingang: 25.05.2021
Impfdatum: 25.05.2021
Beginn: 25.05.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Fall Loss of consciousness

Symptomtext

Client 2-5 minutes after vaccine fell out of her chair and hit her head on the ground. Client attended to immediately, when she was rolled over she was unconscious. Epi 0.3 mg im given, feet elevated as she laid on the ground. Client awoke. 911 called and client sent to ED.

Weitere VAERSDATA-Felder

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

VAERS 1348054

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: TX
Alter: 61,0
Geschlecht: F
Eingang: 25.05.2021
Impfdatum: 11.05.2021
Beginn: 13.05.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

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

Bell's palsy Facial asymmetry Facial pain Feeling abnormal Flushing Headache Hypoaesthesia Laboratory test Limb discomfort Muscle spasms Neck pain Pain Paraesthesia Peripheral coldness Rash

Symptomtext

Patient has had Bells Palsy 2 times prior. 1976 H1N1 vaccine / 2009 after having been infected with H1N1. No Fever at all during 14 days May 12- facial pain, body aches, head aches. May 15- all symptoms continued facial swelling, loss of feeling to touch of face. Pain traveling down neck. Left side of face dropping. Hands very cold and cramping. May 17 - body aches and headaches leave. All other symptoms and facial pain continues. Tingling of skin on knees begins. May 21 - knees and thighs begin to feel numb and tingly. This feeling of not right continues to increase and spread. May 24 - all facial pain increased. Legs and arms tingly and numbing feeling unsteady. May 25- flushing and rash appears. Arms are heavy and all other symptoms continue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: 5/25/2021- ordered tests for 5/26/2021 - 34429 / 37859 / 39820 / 433 / 6399 / 7788 / 866 / 90839
Aktuelle Erkrankungen: Hashimotos Thyroidism, seasonal allergies.
Vorgeschichte: Hashimotos Thyroidism, Lichen Sclerosis, Rosacea.
Andere Medikamente: Thyroid NP 90 mg per day. Multi vitamin, Benadryl 2mg
Allergien: Penicillin, Sulfa drugs
Vorherige Impfungen: 1976 - H1N1

VAERS 1344080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: OH
Alter: 17,0
Geschlecht: F
Eingang: 24.05.2021
Impfdatum: 21.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Body temperature increased Breast pain Chest discomfort Dyskinesia Hypoaesthesia oral Presyncope Taste disorder

Symptomtext

After receiving dose, pt experienced Vasovagal response which she never had before when receiving a shot. When they woke her she had a lot of jerky arm movement. About half an hour to 1hr after injection she said she had an odd taste in her mouth and her tongue was numb. Her chest felt tight but was not wheezing. About an hour later when she was home (~6pm) gave her "click it albuterol" and it relieved the tightness in the chest. She had pain in her left breast area. Around 6:30pm she continued to comment about her tongue being numb and pain in her breasts. She fell asleep right away and the next afternoon around 1pm she had a temperature of 99F. After motrin the temperature went back to normal and she felt better. No further chest tightness after that and she is feeling normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: pre-existing asthma
Vorgeschichte: -
Andere Medikamente: probiotic, multi vitamin
Allergien: sulfa drugs, amoxicillin
Vorherige Impfungen: January 2019 after a flu shot she had asthma flare up 3 days later with a strong cough and no fever or other symptoms. She need

VAERS 1343830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: TX
Alter: 13,0
Geschlecht: M
Eingang: 24.05.2021
Impfdatum: 22.05.2021
Beginn: 22.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Syncope

Symptomtext

Patient (13 years old) fainted at the vaccination table after receiving his first dose of the Pfizer vaccine, while waiting for his mother as she was getting vaccinated. Patient saw his mother bleed after the vaccine and fainted in the chair, as he began to fall, the vaccinator was able to catch him and assist him to the floor. Patient was turned on his side. EMS was called at 0912 and arrived at 0919. Patient was assessed by paramedics and found to be stable. Patient?s mother reported no PMH and the he doesn?t usually faint after injections. Patient left accompanied by his mother.

Weitere VAERSDATA-Felder

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

VAERS 1343714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: PA
Alter: 20,0
Geschlecht: M
Eingang: 24.05.2021
Impfdatum: 23.05.2021
Beginn: 23.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

Systemic: Fainting / Unresponsive-Medium, Additional Details: Patient fainted approximately 5 minutes after administration. Did not hit floor, was caught by father. Paramedics came and toook him to hospital. Report given by mom later in the night said he was stable, vitals were fine and he was discharged to home.

Weitere VAERSDATA-Felder

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

VAERS 1341937

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: IL
Alter: 15,0
Geschlecht: F
Eingang: 23.05.2021
Impfdatum: 22.05.2021
Beginn: 22.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Loss of consciousness

Symptomtext

Passed out about 5 minutes after receiving the shot. Was sitting in a chair and collapsed to the ground. She regained consciousness within 30 seconds and was sitting in a chair again 5 minutes later

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Amoxicilin allergy
Vorherige Impfungen: -

VAERS 1341604

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: PA
Alter: 54,0
Geschlecht: M
Eingang: 23.05.2021
Impfdatum: 22.05.2021
Beginn: 22.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Headache Hypotension Syncope

Symptomtext

Systemic: Dizziness / Lightheadness-Severe, Systemic: Headache-Severe, Systemic: Hypotension-Severe, Additional Details: patient fainted 7-10 minutes after vaccination. He felt when tried to stand up so he layed down until the help arrives. Patient mentioned about having history of fainting whne he had blood draw years back. Never received any vaccinations. EMS took him to hospital for check up. No allergic reactons noted no breathing issues as well.

Weitere VAERSDATA-Felder

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

VAERS 1341420

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 14,0
Geschlecht: M
Eingang: 22.05.2021
Impfdatum: 22.05.2021
Beginn: 22.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Loss of consciousness

Symptomtext

The client was accompanied by his mother. Staff vaccinated the client. When filling out the consent form, the client started looking pale and was about to pass out. Staff caught the client before falling off the chair. They laid him down and put a cool pack on his neck. Called 911 to scene at 1731. EMT arrived at the scene at 1740. The client passed out for a minute but was still breathing. Vitals BP, 124/66, HR 56, Pulse Ox, 98%. Vaccinated lot num Pfizer EW0179 exp. 08/2021. EMT Transported client at 06:05pm

Weitere VAERSDATA-Felder

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

VAERS 1341253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 28,0
Geschlecht: M
Eingang: 22.05.2021
Impfdatum: 22.05.2021
Beginn: 22.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Feeling hot Syncope

Symptomtext

Patient observed at 1442 sliding down in his observation chair. Observation nurse helped lower patient to the floor. Patient had a syncopal episode for a few seconds. Patient woke up, assisted into wheelchair, and taken to private room for further assessment. Full set of vitals obtained as follows: O2 sat 99% RA, HR 66, BP 138/80, RR 18. Patient stated he was feeling fine and that he previously was outside today and was very hot before receiving his vaccine. Patient also stated he had a historyof syncopal episodes from being over heated. Monitored pt for another 10 minutes and took another set of vitals at 1452 as follows: O2 sat 99% RA, HR 83, BP 135/85, RR 17. Assessed patient vitals 10 minutes later at 1502...

Weitere VAERSDATA-Felder

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

VAERS 1341016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 22,0
Geschlecht: M
Eingang: 22.05.2021
Impfdatum: 22.05.2021
Beginn: 22.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Feeling hot Hypotension Syncope Vital signs measurement Wheelchair user

Symptomtext

Patient observed at 10:49 sliding down in his observation chair. On assessment pt had a syncopal episode. Assisted to wheel chair and taken to private observation area with supplies to lay on cot. Full set of vitals obtained as follows: O2 sat 98% RA, HR 59, RR 15, BP 100/85. Pt stated he was dizzy and hot. Fanned pt, further observed, vitals taken at 10:59 as follows: O2 sat 99% RA, HR 62, RR 14, BP 118/75. Assisted pt to drink water, stated no PMH, no current medications, and stated he was nervous. Vitals taken at 11:09 as follows: O2 sat 99%, HR 65, RR 12, BP 122/76. Pt stated he was feeling better. Assisted pt to sit up and took a full set of vitals as follows: O2 sat 99% RA, HR 80, RR 15, BP 115/60. Vitals....

Weitere VAERSDATA-Felder

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

VAERS 1340967

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: IL
Alter: 13,0
Geschlecht: F
Eingang: 22.05.2021
Impfdatum: 22.05.2021
Beginn: 22.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Confusional state Dizziness Syncope

Symptomtext

Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild

Weitere VAERSDATA-Felder

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

VAERS 1340929

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0179

schwer

Staat: IL
Alter: 16,0
Geschlecht: M
Eingang: 22.05.2021
Impfdatum: 22.05.2021
Beginn: 22.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Syncope

Symptomtext

patient slumped, syncopal episode for less than 2 seconds. Awakened stating "I feel light headed". Site staff reported event to NP right way, at 10:30am, BP 120/80 pulse of 58, Patient's mother came to patient's side, repeat BP 120/78, pulse 58; , repeat again at 11:20 116/80, pulse 60. Mother declines EMS. Patient in good spirits, A&ox4, and left site with mother normal gait and affect.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: BP 10:30 = 120/80; HR 58 BP 10:40 = 120/78 BP 11:20 = 116/80 HR 60
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: n/a
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1338604

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: FL
Alter: 32,0
Geschlecht: M
Eingang: 21.05.2021
Impfdatum: 17.05.2021
Beginn: 17.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Impaired driving ability Loss of consciousness

Symptomtext

Patient fianc?e stated patient passed out while driving, but regained consciousness. Patient was advised to go to nearest urgent clinic or call 911.

Weitere VAERSDATA-Felder

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

VAERS 1338399

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: PA
Alter: 12,0
Geschlecht: F
Eingang: 21.05.2021
Impfdatum: 14.05.2021
Beginn: 15.05.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Cold sweat Dizziness Fall Limb discomfort Malaise Pallor Palpitations Presyncope Pulse abnormal Vomiting

Symptomtext

On 5/15, at 4:00pm while in the shower, patient had a pre-syncopal episode with dizziness, and heaviness in her arms and legs. Before she fell I was able to assist her to a sitting position. Her skin was pale and clammy, pulse thready 90bpm, bp 80/50. Symptoms improved after 15 minutes. On 5/21, at 10:00am was outside at a school sports activity. She began to feel slightly dizzy. She ran a short race and the dizziness was worse. She was pale, hr 120, bp 100/60. She drank fluids and rested but still felt unwell and a headache started so she came home. The headache evolved into a severe migraine with several episodes of vomiting. She also felt heart palpitations, which is unusual with her migraines. Hr was 100 and regular. Bp 100/60. Discussed with pediatrician, who patient had seen 5/20. Appointment scheduled with cardiology 5/26

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Migraine headaches
Andere Medikamente: Migrelief supplement, occasional Tylenol
Allergien: None
Vorherige Impfungen: -

VAERS 1337139

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: SC
Alter: 46,0
Geschlecht: M
Eingang: 21.05.2021
Impfdatum: 29.04.2021
Beginn: 09.05.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: IM / RA

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

Bell's palsy

Symptomtext

10 days post vaccine patient was diagnosed with Bells Palsy at the local ER. No hospitalization required.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: DBM 1, CAD, HTN
Andere Medikamente: -
Allergien: MIralax
Vorherige Impfungen: -

VAERS 1337085

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: IL
Alter: 43,0
Geschlecht: F
Eingang: 21.05.2021
Impfdatum: 17.05.2021
Beginn: 20.05.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Blood thyroid stimulating hormone Computerised tomogram thorax Differential white blood cell count Dizziness Dyspnoea Fibrin D dimer Full blood count Glomerular filtration rate Metabolic function test Palpitations Pregnancy test urine Prothrombin time Syncope Troponin I Urine analysis

Symptomtext

Shortness of Breath Feeling Dizzy/Faint Heart Palpitations

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: COMPLETE BLOOD COUNT WITH AUTO DIFF COMPREHENSIVE METABOLIC PANEL D DIMER ESTIMATED GLOMERULAR FILTRATION RATE IP POCT URINE PREGNANCY PROTHROMBIN TIME (PTINR) THYROID STIMULATING HORMONE TROPONIN I, HIGHT SENSITIVITY y URINALYSIS URINE MIRCROSCOPIC EXAM CR CHEST CT ANGIO PULMONARY EMBOLISM W AND/OR WO CONTRAST LOPAMIDOL
Aktuelle Erkrankungen: No known illnesses at time of vaccination
Vorgeschichte: No current health issues. DVT over 10 years ago.
Andere Medikamente: Multivitamins
Allergien: Possible shriimp
Vorherige Impfungen: POSSIBLE EVENT, AFTER FLU VACCINE +10 YEARS AGO

VAERS 1336924

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: DE
Alter: 36,0
Geschlecht: M
Eingang: 21.05.2021
Impfdatum: 20.05.2021
Beginn: 20.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Flushing Hyperhidrosis Loss of consciousness Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Mild, Additional Details: patient received 1st pfizer vaccine and after 10 min he felt light headed and passed out. He layed on the ground and was responsive and was able to communicate. He did not have any injuries after passing out. He remained laying down for about 15 min until his pressure came back up and he said he felt ok. He asked for a glucose tablet which we administered. He said he has had this type of reaction before to receiving vaccines but did not indicate that ahead of time. He did not want ambulance.

Weitere VAERSDATA-Felder

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

VAERS 1334085

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: UT
Alter: 39,0
Geschlecht: F
Eingang: 20.05.2021
Impfdatum: 13.05.2021
Beginn: 13.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Anaphylaxis prophylaxis Asthenia Chest discomfort Electrocardiogram normal Headache Hypoaesthesia Neurological examination normal Throat tightness Vision blurred

Symptomtext

About 5 minutes after she received her vaccine, she developed a posterior headache, worsening numbness and weakness, a sensation of tightness in her throat, blurred vision, and some chest pressure. Patient was transferred to the ED for observation. She was normotensive and saturating well on room air. Neurologic exam was performed and and EKG, both were within normal limits. The patient was administered 25 mg diphenhydramine and throat tightness symptoms improved. The patient was discharged to home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylaxis prophylaxis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Muscle weakness
Andere Medikamente: None
Allergien: Gadolinium. PCN
Vorherige Impfungen: -

VAERS 1331020

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: RI
Alter: 17,0
Geschlecht: M
Eingang: 19.05.2021
Impfdatum: 12.05.2021
Beginn: 15.05.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: SYR / -

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

Chest pain Echocardiogram normal Electrocardiogram ST segment elevation Electrocardiogram abnormal Myocarditis Troponin increased

Symptomtext

Patient developed severe chest pain and was found to have myopericarditis. This occurred 3 days after receiving his 2nd Pfizer covid vaccine. Prior to this event, he was in his usual state of health and denied any viral prodrome or illness. In the hospital, he received NSAIDs and supportive care with significantly clinical improvement. He was discharged with cardiology follow up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 3,0
Labordaten: EKG: diffuse ST elevation Troponin 22.813 (Reference range: 0.006 - 0.060 NG/ML ) 5/16/21 0857 Troponin 29.2 (Reference range: 0.006 - 0.060 NG/ML ) 5/16/21 1302 Troponin 7.528 (Reference range: 0.006 - 0.060 NG/ML ) 5/18/21 0731 Echo: normal 5/16/21
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1330599

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: WI
Alter: 44,0
Geschlecht: F
Eingang: 19.05.2021
Impfdatum: 05.05.2021
Beginn: 05.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Cold sweat Dizziness Dyskinesia Fatigue Loss of consciousness Mobility decreased Nausea Presyncope Tunnel vision

Symptomtext

Patient had received her 2nd COVID vaccine and was about 10 minutes into her post vaccination waiting when she began feeling lightheaded, clammy, and nauseated. She got up and walked over to the staff desk where she continued to feel lightheaded and developed tunnel vision. Staff got her into a wheelchair and she subsequently lost consciousness. They noticed brief arm and leg jerking motions. She had no bowel or bladder incontinence or tongue bite. There was no postictal period. She is brought to the ED. She has had minimal to eat or drink today. She does note that she has had multiple syncopal episodes in the past including with blood draws and at the dentist. She currently feels fatigued and slightly nauseated. She was lightheaded and had difficulty standing after the episode so she was brought to the ED The episode sounds more consistent with syncope than seizure given the lack of postictal period, no tongue bite, bowel or bladder incontinence. She likely had some myoclonic jerks due to syncope in an upright position. EKG shows normal sinus rhythm without evidence acute ischemia or infarct, low suspicion for ACS or malignant dysrhythmia as cause for syncope, particularly since she had a clear prodrome prior to syncope. Symptoms appear most consistent with vasovagal syncope related to vaccination. Patient feeling improved after rest and p.o. intake. Able to ambulate steadily in ED. Appears appropriate for outpatient follow-up.

Weitere VAERSDATA-Felder

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

VAERS 1328503

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: AZ
Alter: 14,0
Geschlecht: F
Eingang: 18.05.2021
Impfdatum: 16.05.2021
Beginn: 16.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Presyncope

Symptomtext

Patient complained of dizziness about 5 minutes after vaccination. Patient was sitting at the clinic lobby with her mother. I assisted the patient inside the exam room to lay down on the exam table. Patients was so dizzy and about to faint. She could hardly get up to the exam table. I instructed her to get up to the exam table one more time. She was able to get up and lay down on the table. Patient did not lose consciousness. Vitals were taken and were stable. Mother gave patient gatorade to drink. Patient stayed laid down on the table for about 10-15 minutes. Mother was watching the patient. Patient was fully alert and no longer feeling dizzy. Patient walked with her mother. My assistant walked them outside our facility.

Weitere VAERSDATA-Felder

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

VAERS 1327426

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 38,0
Geschlecht: F
Eingang: 18.05.2021
Impfdatum: 18.05.2021
Beginn: 18.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Hyperhidrosis Loss of consciousness Nausea Pallor Syncope Vision blurred

Symptomtext

Patient received in RN triage area, post-COVID vaccination administration. Patient being observed for 15 minutes as recommended per CDC guidelines on post-vaccination RN monitoring. Patient approached nurses stating that she felt nauseous and lightheaded. Patient noted diaphoretic, and pale in color; while helping patient to the wheelchair the patient fainted and was completed unconscious. Patient guided to floor by staff. Patient was unconscious for about a minute while on floor. RRT called. When patient came to patient reporting lightheadedness, blurred vision. Vitals 09:11: BP: 103/62, HR: 63, O2: 96%. Patient denies any history of syncope or fainting. Patient stated that she had not had anything to eat this morning. Denies any Hx of anaphylactic reaction to vaccines. Patient denies adverse reactions to vaccinations in past. Tolerated injection well. Patient sent to ER with RRT . All questions and concerns addressed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Patient sent to ER.
Aktuelle Erkrankungen: none
Vorgeschichte: anxiety/depression
Andere Medikamente: denies
Allergien: Pseudoephedrine Hcl
Vorherige Impfungen: -

VAERS 1326654

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: PR
Alter: 15,0
Geschlecht: M
Eingang: 18.05.2021
Impfdatum: 17.05.2021
Beginn: 17.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Seizure Tonic convulsion

Symptomtext

Systemic: Seizure-Mild, Additional Details: AFTER 5 MINUTES OF ADMINISTARTION VACCINE PATIENT BEGIN A SEIZURE OF LESS 1 MINUTE MOTHER DESCRIBED TONIC SEIZURE PATIENT NOT HAD PAST HISTORY OF SEIZURE

Weitere VAERSDATA-Felder

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

VAERS 1326629

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MI
Alter: 15,0
Geschlecht: M
Eingang: 18.05.2021
Impfdatum: 17.05.2021
Beginn: 17.05.2021
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 Dyspnoea Hyperhidrosis Hypotension Syncope Unresponsive to stimuli

Symptomtext

Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Confusion-Medium, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Hypotension-Severe, Additional Details: sweating profusely, EMS called and came to pharmacy, checked on pt and all clear for him to leave, parents had no problem and said they didnt need anything before they leave

Weitere VAERSDATA-Felder

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

VAERS 1326481

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW-0179

schwer

Staat: PA
Alter: 23,0
Geschlecht: M
Eingang: 18.05.2021
Impfdatum: 14.05.2021
Beginn: 14.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Cold sweat Headache Seizure like phenomena Vomiting

Symptomtext

Patient presented @ 1356 hrs in observation area. Patient was sitting in chair. Observed patients' head tilt backwards. Care initiated with head/neck support. Patient began seizure like activity lasting approx. 1 minute. Patient transferred to floor for protection. Upon exam Patient was AAO x 2, skin: cool/clamy. Patient began c/o headache and denied any past medical history. Transferred patient to cot for evaluation. VS: HR:92,RR:20,BP:106/64. Patient began vomiting during evaluation. Post vomiting patient said he felt fine. EMS on scene and care transferred to ED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure like phenomena
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Negative
Vorgeschichte: Negative
Andere Medikamente: Zertec
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 1326225

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: -
Alter: 30,0
Geschlecht: F
Eingang: 18.05.2021
Impfdatum: 29.04.2021
Beginn: 30.04.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Diarrhoea Dizziness Fatigue Influenza like illness Nasopharyngitis Pain Pain in extremity Sinus pain Syncope

Symptomtext

fainting; Severe stomach-flue like symptoms with diarrhea; Severe stomach-flue like symptoms with diarrhea; Aches/Body aches in core; Head-cold like symptoms with sinus pain; Head-cold like symptoms with sinus pain; fatigue; Wooziness; Body aches in core and legs; This is a spontaneous report received from a non-contactable consumer (patient). A 30-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EW0179), via an unspecified route of administration on 29Apr2021 (at age of 30 years old) as single dose for COVID-19 immunization. Medical history included known allergies: Sulfa drugs. There were no concomitant medications. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. No COVID prior vaccination. No COVID tested post vaccination. The patient experienced Severe stomach-flue like symptoms with diarrhea, fainting, aches. Head-cold like symptoms with sinus pain, fatigue, wooziness. Body aches in core and legs. All events on 30Apr2021. No treatment received for all events. The outcome of the events was recovered in 2021. No follow-up attempts are Possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1323709

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NC
Alter: 17,0
Geschlecht: M
Eingang: 17.05.2021
Impfdatum: 05.05.2021
Beginn: 08.05.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / RA

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

Angiotensin converting enzyme Antineutrophil cytoplasmic antibody Antinuclear antibody Antiphospholipid antibodies Aphasia Asthenia Bacterial test Beta-2 glycoprotein antibody Brain oedema C-reactive protein normal Confusional state Drooling Dysarthria Electroencephalogram normal Facial paralysis CSF cell count CSF culture CSF test abnormal

Symptomtext

Pt was seen at ED on5/8 for L sided weakness in the setting of a headache. Pt?s mother reports that these symptoms began 2 days after receiving second dose of Pfizer COVID-19 vaccination in R deltoid. She says that on 5/6, pt complained of L arm weakness during cooking class at school, which was followed by a mild L sided headache later in the day. Symptoms resolved without intervention but recurred on 5/8 with associated L sided facial droop, slurred speech, L arm spasms, and L foot drag. Pt was seen at ED for this and had a HA (5/10 in severity) at that time -- workup was unremarkable with a normal head CT, laboratory workup, and resolution of symptoms. Pediatric Neurology evaluated the pt, deemed no further workup necessary, and advised outpatient follow up. Pt presented again to the ED on 5/10 with concern for full tonic/clonic seizure, witnessed by pt?s mother. Mother reports that she heard pt fall and went upstairs to find pt seizing on his bed -- says that pt had shaking of bilateral upper extremities (in flexed position close to chest) and symmetric lower extremity shaking; eyes were closed without clear focality or eye deviation. Also some drooling, though no incontinence or tongue biting. Episode lasted for approximately 2 minutes; pt was confused and did not recall what happened immediately afterwards but improved within the next 8 minutes. He was taken to the ED by EMS. By the time he arrived in the ED, he had left sided weakness again. He was given Keppra 1g, placed on EEG, and was admitted. EEG overnight was read "normal" and additional workup was unremarkable. Pt had MRI brain completed showing cortical abnormalities in the R parietal lobe, suspected to be related to recent seizure. MRA showed patent intracranial cerebral vasculature. MRV showed no evidence of dural venous sinus thrombosis. Weakness resolved by the morning and pt was back to baseline on morning of 5/11/21. However, around 9 AM, L sided weakness (face, arm>leg) with associated headache recurred. Mom says that this event was captured on EEG. He was then transferred to our facility. He was placed on pEEG and had repeat labs, imaging completed. Pt did have L sided facial droop, L arm weakness, and slurred speech on arrival, but this resolved within 24 hours. Pt had one additional episode of "wave" of L sided weakness including L sided facial droop and slurred speech at one other time during the hospitalization, but no additional seizure like activity. He was discharged on 5/14 with a normal neuro exam-- some labs (including labs of Rheum and Id workup were pending at time of discharge.) Primary and consulting teams elected to forgo steroids but reconsider should symptoms worsen or return. Pt was readmitted on 5/16-- had an episode of expressive aphasia + headache while at a social gathering; states that he became overwhelmed by the noise. No additional seizure like activity.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: 4,0
Labordaten: MRI 5/11: 1. Area of cortically based FLAIR/DWI hyperintensity in the right parietal lobe. There appear to be some areas of subtle associated restricted diffusion. In the setting of recent seizure activity, this is favored to represent cytoxic edema (due to recent seizure activity). Alternative consideration would be a focal encephalitis, which is felt less likely. No abnormal enhancement is seen in this region. Consider repeat MRI upon resolution of seizure activity to document resolution of imaging findings. MRI 5/16: 1. Asymmetric, subtle right cerebral gyral swelling and increased signal. In the associated regions there is prominent sulcal enhancement which may be due to secondary vascular changes (slow flow or hyperemia) versus leptomeningeal enhancement. Findings are more prominent on the prior and favored to reflect encephalitis; autoimmune or infective. Postictal MRI changes remain a possibility, but are felt to be less likely in the absence of more robust seizure activity. 5/11- CRP, ESR, ANA, anti-DNA ds, angiotensin converting enzyme , lupus anticoagulant panel, anti-cardiolipin, anti-beta 2 glycoprotein, CMP, ANCA, anti-Sm, RNP, Ro, La, C3/C4 unremarkable. 5/12 CSF significant for pleocytosis. Meningitis PCR panel, CSF cx, West Nile virus, Respiratory Virus Extended panel, Syphilis, HIV unremarkable. 5/14 quant TB gold pending, anti microsomal thyroid, thyroglobulin pending. 5/16 CBC ESR, CRP, CMP unremarkable.
Aktuelle Erkrankungen: none
Vorgeschichte: Raynaud's
Andere Medikamente: tylenol
Allergien: none
Vorherige Impfungen: -

VAERS 1323375

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NC
Alter: 14,0
Geschlecht: M
Eingang: 17.05.2021
Impfdatum: 14.05.2021
Beginn: 14.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood glucose normal Contusion Dizziness Electrocardiogram normal Eye injury Fall Joint injury Loss of consciousness Nasal injury Presyncope Syncope

Symptomtext

59kg 14 yo M with NKDA and PMH of headaches had a syncopal episode after receiving first Covid19 vaccination in left deltoid at 1458 5/14/21 (lot # EW0179) . Patient described feeling light headed and does not recall losing consciousness. Fell face side down and had trauma of right knee and nose and above the left eye. Bruising on his nose. Reportedly hit the metal base of the curtain that separated the vaccination area from the observation area. EMS called for concern of facial fractures. BG 98/48 and HR 75 with O2 sats 99% post event. EKG negative. BG within normal limits. Patient did have sustained loss of consciousness. Followup BP 101/69 with HR 77. Event attributed to vasovagal reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: EKG; BG check; physical exam
Aktuelle Erkrankungen: None
Vorgeschichte: Headaches
Andere Medikamente: None
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1323080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: IL
Alter: 20,0
Geschlecht: M
Eingang: 17.05.2021
Impfdatum: 08.05.2021
Beginn: 08.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Aortic stenosis Back pain Blood creatine phosphokinase increased Chest X-ray normal Chest pain Computerised tomogram head normal Computerised tomogram thorax normal Dilatation ventricular ECG P wave inverted Echocardiogram abnormal Ejection fraction decreased Electrocardiogram Electrocardiogram ST segment depression Electrocardiogram ST segment elevation Electrocardiogram T wave peaked Electrocardiogram abnormal Epstein-Barr virus antibody positive Fatigue

Symptomtext

20 YO patient with no significant PMH who presents with headache, back pain, and chest pain. He received 2nd Pfizer COVID19 vaccine dose 5/8/21. Later that day he felt very tired. On 5/9/21, he developed a headache that worsened throughout the day, was felt over whole head, but more painful in temporal areas, and he became nauseous. On 5/11/21, he developed back and chest pain and had 2 episodes of NBNB emesis. The chest pain is sharp, located over the whole chest and extends to axillae. The back pain is worse in the right shoulder. The back and chest pain are worse with inspiration, movement, and supination. CMR confirmed myopericarditis. Patient treated with colchicine and NSAIDs and IVF, has cardiology f/u on

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 3,0
Labordaten: see below
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: escitalopram 10mg daily
Allergien: vancomycin - anaphylaxis/angioedema
Vorherige Impfungen: -

VAERS 1321311

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: -
Alter: 17,0
Geschlecht: M
Eingang: 15.05.2021
Impfdatum: 15.05.2021
Beginn: 15.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hypotension Oxygen saturation decreased Presyncope

Symptomtext

Near fainting, low blood pressure and low oxygen saturation

Weitere VAERSDATA-Felder

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

VAERS 1321068

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: NY
Alter: 20,0
Geschlecht: F
Eingang: 15.05.2021
Impfdatum: 15.05.2021
Beginn: 15.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Loss of consciousness

Symptomtext

Patient became light headed after walking to the waiting area and passed out. Mom stated that this typically happens after receiving vaccines. She laid on the floor for 5 minutes prior to coming to an upright position.

Weitere VAERSDATA-Felder

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

VAERS 1320893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: IA
Alter: 15,0
Geschlecht: F
Eingang: 15.05.2021
Impfdatum: 15.05.2021
Beginn: 15.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Eye movement disorder Loss of consciousness Vomiting

Symptomtext

Patient went to sit 15 minutes for recovery post-vaccine with her mom. All of a sudden she said "My arm feels funny," then laid her head on her mom. Her mom said her eyes rolled back and she passed out and slid down the chair onto the floor. 911 was called, pharmacist ran to scene. Patient remained on floor, started puking. Told her to breath deep, offered water. She slowly started feeling better. Paramedics arrived and examined her. After about 30 minutes, patient left with mom. No ER needed.

Weitere VAERSDATA-Felder

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

VAERS 1320835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: -
Alter: 15,0
Geschlecht: M
Eingang: 15.05.2021
Impfdatum: 15.05.2021
Beginn: 15.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Dizziness Headache Hyperhidrosis Loss of consciousness Pallor

Symptomtext

Patient brought to medical tent after collapsing after he got vaccinated. Nursing reports he has been unconscious for 2 minutes after standing up and was caught by nurse. Pt was sweaty which got better when supine. Pt felt weak, headache, dizziness and pale. no difficulty swallowing. attempted to sit up and dizziness worsened. Pt's symptoms did not improve so EMS initiated.

Weitere VAERSDATA-Felder

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

VAERS 1319609

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: UT
Alter: 19,0
Geschlecht: F
Eingang: 15.05.2021
Impfdatum: 12.05.2021
Beginn: 12.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Loss of consciousness

Symptomtext

Called and asked to assist in the vaccine clinic. Patient vaccinated at approximately 1620, reaction at 1630 Patient sitting on the floor complaining of being light headed. Patient reports feeling better and is able to converse without difficulty. Patient moved to a chair on her own accord and after approximately one minute patient began to lose consciousness. BP taken and was reported at 56/35 and was placed on 4L of O2. Patient did not respond well and was transitioned to O2 per facemask at 10 L and paramedics called. Patient transferred to stretcher and patient regained consciousness. Patient able to speak. VS taken by team and BS taken and was WNL. Patient declined ER visit, but remained in vaccine clinic for additional 30 minutes until 1715. Patient left clinic ambulatory in stable condition without incident.

Weitere VAERSDATA-Felder

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

VAERS 1318533

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: OH
Alter: 27,0
Geschlecht: M
Eingang: 14.05.2021
Impfdatum: 14.05.2021
Beginn: 14.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Loss of consciousness Syncope

Symptomtext

I had just returned to the pharmacy and I heard shouting. I looked and saw that the patient was on the floor. I grabbed our emergency kit and went to patient's aid. He was on the floor with his head against the shelving. He was not conscious. I instructed a staff member to call 911. I put my hand on his arm and the other on his chest and asked several times if he was ok. After approximately 30 seconds he looked at me and regained consciousness. He knew where he was and recognized his wife in the immediate vicinity. He said that he has a history of fainting and he thought maybe seeing his wife get vaccinated and seeing a small amount of blood on her arm before I put a band-aid on her arm triggered his fainting spell. EMS arrived after about 10 minutes and shortly thereafter he fainted again.

Weitere VAERSDATA-Felder

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

VAERS 1318037

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 15,0
Geschlecht: F
Eingang: 14.05.2021
Impfdatum: 14.05.2021
Beginn: 14.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Syncope

Symptomtext

Patient felt dizzy and fainted after 4 minutes of receiving the Pfizer COVID-19 vaccine. Pt immediately woke up, no change in level of consciousness. Patient awake, alert, and oriented to name, place, time, and situation. Vital signs were within normal limits. BP 96/54, HR 71, SpO2 99% in RA. Patient left ambulatory with mother in stable condition after 40 minutes of monitoring and observation.

Weitere VAERSDATA-Felder

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

VAERS 1317740

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: IA
Alter: 31,0
Geschlecht: M
Eingang: 14.05.2021
Impfdatum: 14.05.2021
Beginn: 14.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Computerised tomogram head Fall Head injury Skin laceration Syncope

Symptomtext

Patient received vaccine and was standing in waiting area and had witnessed syncopal episode and fall. Hit back of head and had laceration. Patient slow to arose and provider from urgent care called to evaluate. Awakened and able to answer questions. Appeared laceration would need sutures/staples. Ambulance called for and transported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Head CT completed and negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1317332

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NC
Alter: 18,0
Geschlecht: F
Eingang: 14.05.2021
Impfdatum: 14.05.2021
Beginn: 14.05.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Anaphylactic reaction Pruritus

Symptomtext

Patient received her 1st Covid vaccine today, with a known history of anaphylaxis to the flu shot 6 months prior. She was assigned a 30 minute wait time. She received her vaccine at 1225 on 14May2021, and approximately 15 minutes later developed itchiness around her mouth and face. She reported this felt similar to the beginning of her prior episode. Physician and nurse were notified, who evaluated patient. Patient?s airway was clear, respirations unlabored and normal to auscultation. Vitals were within normal limits. EMS was notified, and 50mg Benadryl was given at 1255. At this time patient?s reaction appeared minor and stable, so epipen was at patient?s side however not given yet. EMS arrived rapidly, and repeated eval, confirming same evaluation and history. Patient was transferred in stable condition to the ER for extended monitoring.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Nortriptyline
Allergien: History of flu shot allergy
Vorherige Impfungen: Flu

VAERS 1317024

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NC
Alter: 13,0
Geschlecht: F
Eingang: 14.05.2021
Impfdatum: 14.05.2021
Beginn: 14.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Loss of consciousness Nausea Syncope

Symptomtext

My daughter passed out 2 times within 5 minutes of receiving her first dose. She complained of being nauseous after both fainting episodes. We gave her water and orange juice and she ultimately felt better after about 25 minutes of resting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: 50mg Zoloft
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 1316517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: TX
Alter: 35,0
Geschlecht: M
Eingang: 14.05.2021
Impfdatum: 13.05.2021
Beginn: 13.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Syncope Unresponsive to stimuli

Symptomtext

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 1315651

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 22,0
Geschlecht: F
Eingang: 13.05.2021
Impfdatum: 13.05.2021
Beginn: 13.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Heart rate decreased Loss of consciousness Somnolence

Symptomtext

Patient with complaints of lightheadedness 30 minutes after receiving vaccination. Patient stated that she did not eat today, powerade and a lollipop provided. Shortly after, patient with complaints of dizziness and slow heart rate. Vitals at 1546: HR 65 BP 90/62 and RR 20. At 1605, patient with increased drowsiness, dizziness and a brief moment of lapse in consciousness. Evaluated by paramedics on scene and declined transport to ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None reported
Vorgeschichte: Anxiety
Andere Medikamente: None
Allergien: History of anaphylaxis to unknown agent.
Vorherige Impfungen: -

VAERS 1314819

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 26,0
Geschlecht: F
Eingang: 13.05.2021
Impfdatum: 28.04.2021
Beginn: 28.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenopia Chest discomfort Chest pain Loss of consciousness Nausea Throat tightness Unresponsive to stimuli Vaccination complication

Symptomtext

After receiving the vaccine about five minutes later my Chest became very heavy and painful my throat felt like I?m knot closing and I passed out I was woken up at the site but I was unresponsive all I remember was them telling me to stay awake the ambulance is on the way I became very nauseous

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: I was rushed by ambulance to hospital. Doctor said I had a reaction to the vaccine it was very hard to open my eyes they felt really heavy but not swollen
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin Clindamycin
Vorherige Impfungen: -

VAERS 1312485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MN
Alter: 61,0
Geschlecht: F
Eingang: 12.05.2021
Impfdatum: 10.05.2021
Beginn: 10.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Back pain Cerebral disorder Cough Decreased appetite Discomfort Fatigue Headache Nausea Pain Paraesthesia oral Seizure

Symptomtext

slight cough, lips tingling right after shot, then back pain and discomfort, headache 4 hours later, then next morning - extreme fatigue, nausea, then through the day - brain shut down, slept all day, extreme pains throughout body like being stabbed and twisting the knife, convulsion like movements from pain, couldn't eat or drink. Didn't feel better until next morning. That was the worse experience I've ever been through. This was my second vaccine. I reacted to the first vaccine also, but not with such pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: asthma
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: similar reaction but lesser degree, 61 years old, covid 19 pfizer

VAERS 1312242

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: GA
Alter: 12,0
Geschlecht: M
Eingang: 12.05.2021
Impfdatum: 11.05.2021
Beginn: 11.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Anaphylactic reaction Chest discomfort Cyanosis Erythema Lip swelling Peripheral swelling

Symptomtext

Vaccine was given at 3pm. At 4:30pm patient had a tight chest so he used his inhaler. At 8:30pm he went into anaphylaxis---red from head to toe, swollen hands and feet, could not move fingers or toes, lips blue and swollen. He was transported to the ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: asthma
Andere Medikamente: none
Allergien: allergic to peanuts, penicillin, rocephin
Vorherige Impfungen: rash after flu vaccine at age 3

VAERS 1310340

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: IL
Alter: 17,0
Geschlecht: M
Eingang: 12.05.2021
Impfdatum: 12.05.2021
Beginn: 12.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Head injury Headache Syncope

Symptomtext

patient was found to have fainted in the waiting area. Reports hitting his head, but was conscious by the time we examined him. A+Ox3, vision intact, speaking normally, complaining of slight pain where he hit his head

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: denies fever/cold within two weeks of getting this vaccine
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: Denies
Vorherige Impfungen: felt lightheaded, but symptoms resolved after stepping outside after the first COVID vaccine

VAERS 1309971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NY
Alter: 22,0
Geschlecht: M
Eingang: 12.05.2021
Impfdatum: 11.05.2021
Beginn: 11.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Flushing Heart rate increased Hyperhidrosis Hypotension Nausea Presyncope Syncope Tachycardia Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Hypotension-Medium, Systemic: Nausea-Severe, Systemic: Tachycardia-Severe, Additional Details: Pt has vaso-vagal reaction: syncope, low blood pressure, increased pulse, profuse sweating

Weitere VAERSDATA-Felder

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

VAERS 1306598

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: IL
Alter: 16,0
Geschlecht: M
Eingang: 12.05.2021
Impfdatum: 06.05.2021
Beginn: 07.05.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / RA

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

Bilevel positive airway pressure Dyspnoea Fatigue Hypotension Intensive care Cardiogenic shock Electrocardiogram ST segment elevation Haemoptysis Hypoxia Laboratory test Oxygen saturation decreased Pain Pericarditis Myocarditis Nausea Respiratory failure Troponin increased Vomiting

Symptomtext

Youth had his second dose of Pfizer COVID vaccine on 5/6/21. On 5/7/21 he woke up reporting body ache and fatigue. Treated with Tylenol and rest. On 5/9/21 he was reporting that he felt short of breath, blood pressure and 02 sats were low. He was taken to the ER for evaluation. Determined he had pericarditis and was flown via helicopter to ER Hospital where he remains in the PICU on bipap and cardiac IV drips.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiogenic shock
Hospital-Tage: -
Labordaten: Labs per at Hospital
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: VYVANSE 40 MG QAM CLONIDINE 0.2 MG QHS ABILIFY 15 MG QAM
Allergien: NKA
Vorherige Impfungen: -

VAERS 1308686

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NC
Alter: 38,0
Geschlecht: F
Eingang: 11.05.2021
Impfdatum: 11.05.2021
Beginn: 11.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Hyperhidrosis Syncope

Symptomtext

At approximately 4:41 PM, patient sustained episode of syncope with seizure activity. Patient regained consciousness and then had additional episode of syncope. At 4:45 PM, VITALS BP 98/42, HR 60, RR 20, O2 99%. EMS called, HR 50, O2 97% with persistent diaphoresis without nausea. Patient A&O x4 and conversant with staff. EMS arrived at 5:00 PM and assumed care, Patient declined EMS visit and significant other took her home. Significant other on scene reports that patient has history of syncope with blood drawns

Weitere VAERSDATA-Felder

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

VAERS 1307800

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

schwer

Staat: MA
Alter: 15,0
Geschlecht: M
Eingang: 11.05.2021
Impfdatum: 11.05.2021
Beginn: 11.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Pallor Swelling face Syncope Visual impairment

Symptomtext

pt found by ems crew incomapny of mother in vaccine booth after having recieved vaccine. pt appeared to have suffered a syncapo episode due to a vaso vagal response. pt mother had consented to all ems evaluation and treatment. pt was assessed on scene and pt wa then transfered to hall way for further evaluation. original vitals at vaccine booth was bp63/42 hr 46 rr 18 spo2 99 ra. pt had perspiration on forehead and pale skin and mild visual disturbances. pt improved once in hallw ay. vitals bp 87/59 hr 52 rr 18 spo2 99 RA. pt began to "feel better" PTs mother denied any allergies or pmhx. pt care was released and pt was escorted out of center by staff with mother

Weitere VAERSDATA-Felder

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

VAERS 1303602

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 17,0
Geschlecht: F
Eingang: 10.05.2021
Impfdatum: 10.05.2021
Beginn: 10.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Syncope

Symptomtext

Pt felt like she was going to vomit 2 mins after administration, then fainted as being assisted to gurney to lie down.

Weitere VAERSDATA-Felder

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

VAERS 1303262

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MI
Alter: 45,0
Geschlecht: F
Eingang: 10.05.2021
Impfdatum: 06.05.2021
Beginn: 09.05.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / RA

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

Angiogram pulmonary abnormal Anion gap Blood albumin decreased Blood triglycerides increased C-reactive protein increased Chest X-ray normal Chest pain Echocardiogram normal Electrocardiogram ST segment elevation Electrocardiogram T wave inversion Hepatic lesion High density lipoprotein decreased International normalised ratio normal Lymphadenopathy Myocarditis Nausea Pain in extremity Pericardial effusion

Symptomtext

Pt presented to Urgent Care on the third day after vaccine (5/9) with chest pain, left arm pain, nausea and vomiting. EKG showed T-wave inversion on V2 and pt was sent to the ED for further evaluation. At the ED, bloodwork showed a significantly elevated troponin level. Pt was admitted for a possible NSTEMI and placed on a heparin gtt, diagnosis changed to myocardial injury within the setting of myo/pericarditis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: In ED: WBC 11.09, initial troponin 345, anion gap 8, 2-hour troponin 365, CRP 107, PT/INR normal, chest xray normal. Echo and EKG with no acute changes, but EKG showed "diffuse ST elevation without reciprocal changes". After admission: 6-hour troponin 402, CT angio of thorax with "no pulmonary embolism, trace pericardial and small bilateral pleural effusions, indeterminate liver lesion, nonspecific mild bilateral axillary lymphadenopathy suggest possibly being reactive"; 5/10 0800 troponin 351, albumin 2.7, triglycerides 241, HDL cholesterol 39
Aktuelle Erkrankungen: -
Vorgeschichte: N/A
Andere Medikamente: Balziva, cetirizine
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 1302966

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MO
Alter: 49,0
Geschlecht: F
Eingang: 10.05.2021
Impfdatum: 08.05.2021
Beginn: 09.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Headache Loss of consciousness Myalgia Nausea Tinnitus

Symptomtext

at 4:20am - Severe headache, nausea, deafening high pith noise in both ears, lost consciousness. The next morning - muscle and joint pains, headache only in the left half of the body. I am healthy, exercise regularly, eat a healthy diet and have no prior chronic health conditions. This is highly usual for me.

Weitere VAERSDATA-Felder

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

VAERS 1301313

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CO
Alter: 18,0
Geschlecht: F
Eingang: 09.05.2021
Impfdatum: 09.05.2021
Beginn: 09.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Loss of consciousness

Symptomtext

Patient passed out after receiving second Pfizer vaccine

Weitere VAERSDATA-Felder

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

VAERS 1296377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: WI
Alter: 17,0
Geschlecht: F
Eingang: 07.05.2021
Impfdatum: 07.05.2021
Beginn: 07.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Hypoacusis Nausea Pallor Syncope

Symptomtext

Immediately after giving the injection, patient felt lightheaded, nauseated, had a decrease in her hearing and became pale. She slumped down in her chair and became limp and was carried to a reclining chair where her legs were elevated. Ice packs were placed on her neck. Her pulse was 70 and a few minutes after this her BP was 100/60. Dr. and an EMT were onsite and did help to monitor her status.She drank water and ate some food and by 10:25 was feeling well enough to return to her classes. She was escorted to class by a teachers aide.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: No She did not eat breakfast or any food before vaccination
Vorgeschichte: No
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 1293672

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 36,0
Geschlecht: F
Eingang: 07.05.2021
Impfdatum: 06.05.2021
Beginn: 06.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Acute respiratory distress syndrome Chest discomfort Dysphagia Dyspnoea Endotracheal intubation Pharyngeal swelling Respiratory distress Urticaria Extubation General physical health deterioration Hypersensitivity Intensive care Sedation Hyperventilation Pruritus Stridor Throat irritation Wheezing

Symptomtext

Itching of chest and throat then laryngeal stridor - Like she was hyperventilating O2 via Mask Sat 99 PO Benadryl 50 mg EMS contact and transported to ED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory distress
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: Bronchitis (Discharge Diagnosis) - 5/4/21 Allergic rhinitis (Discharge Diagnosis) - 5/4/21 Discharge Disposition: Discharge to Home (Routine) Attending Physician: PA-C, Upon admission to ED, Patient + Drug screen
Vorgeschichte: Allergic asthma(Confirmed) Active Allergic rhinitis(Confirmed) Active Anxiety about health(Confirmed) Active Chronic laryngitis(Confirmed) Active Female cystocele(Confirmed) Active Lumbar degenerative disc disease(Confirmed) Active Muscle tension dysphonia(Confirmed)1 Active Bulging lumbar disc(Confirmed) Active Multiple environmental allergies(Confirmed) Active Fibromyalgia(Confirmed) Active Chronic GERD(Confirmed) Active History of cervical cancer(Confirmed) Active Lumbar disc disease with radiculopathy(Confirmed)2 Active L-S radiculopathy(Confirmed) Active Neck pain(Confirmed) Active Central stenosis of spinal canal(Confirmed) Active 1UCI voice therapy start 10/7/19 2PMR
Andere Medikamente: Azithromycin Flonase GuaiFenesin ibuprofen loratadine proair hfa Promethazine DM Sudafed 24 hour
Allergien: Ativan Latex
Vorherige Impfungen: Rash from the neck down with first dose

VAERS 1294124

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 22,0
Geschlecht: M
Eingang: 06.05.2021
Impfdatum: 06.05.2021
Beginn: 06.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Feeling cold Hypoaesthesia Immediate post-injection reaction Pallor Paraesthesia Syncope

Symptomtext

At around 4:30 PM patient had a syncope episode immediately after receiving first Covid dose of Pfizer. Vaccinating nurse guided patient from chair to the floor with legs elevated, as patient verbalized feeling he was going to pass out. Patient verbalized he had both hands tingling and feeling numb. Patient also stated he was cold and appeared pale. Patient vitals b/p 140/92, pulse 89, O2 sat 100%. Patient was provided sweater and started to feel warm per patient. Symptoms began to resolve naturally and patient stated he was ready to sit up. Patient sat up against wall, and 5 minutes later sat up and transferred back into chair. Patient verbalized feeling well and no longer experiencing tingling/numbness in both hands. Pale skin was no longer observed.

Weitere VAERSDATA-Felder

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

VAERS 1293447

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 26,0
Geschlecht: F
Eingang: 06.05.2021
Impfdatum: 06.05.2021
Beginn: 06.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Nausea Syncope Vomiting

Symptomtext

Within minutes of vaccine, had syncopal episode for approx. 30 seconds. When she regained consciousness, c/o nausea and had emesis. Vital Signs WNL

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: unknown but was advised to consult with an allergist
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: Yaz (birth control)
Allergien: unknown
Vorherige Impfungen: -

VAERS 1293419

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 16,0
Geschlecht: M
Eingang: 06.05.2021
Impfdatum: 06.05.2021
Beginn: 06.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Loss of consciousness Pallor

Symptomtext

Approximately 5 minutes after receiving his vaccine, pt started to feel light headed on his way to the observation area, and sat on the ground. As Medic approached, I helped patient to his feet and walked him over to a chair and sat him down, about 10 seconds after sitting him down he stated he was going to pass out, medic immediately braced patient and held him up and pt did go unconscious for about 15 seconds. Pt quickly regained consciousness and was alert and oriented but still feeling light headed, he was helped to a wheel chair and taken to the cot area for eval. Pt skins pale, cool, moist, pupils perrl, lungs clear bilaterally, vitals: BP 120/84, HR 52, RR16, SPO295%, pt asked if he has a slow heart rate and he declined, HR did return to normal at 82 BPM approximately 10 minutes later. PT kept on cot for 30 minutes, and felt much better after. Pt released to his father who stated that everyone in the family always passes out when they get shots.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: None
Allergien: none
Vorherige Impfungen: -

VAERS 1292972

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 17,0
Geschlecht: F
Eingang: 06.05.2021
Impfdatum: 06.05.2021
Beginn: 06.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Gait disturbance Syncope

Symptomtext

Client received her second dose of the Pfizer COVID-19 vaccine (Lot #EW0179 Exp. 8/2021) at 10:03 AM. EMT saw client stand in observation area. Client appeared "unsteady on her feet". EMT rushed to patient and guided her slowly to the ground while protecting her head. Patient then fainted. EMTs assisted patient to gravity bed where patient regained consciousness. Patient was alert and oriented to person, place, time, and event (AAO x 4) immediately following the incident. Client's vitals were assessed every 5 minutes. They were recorded as follows 10:19- Blood Pressure (BP) 100/74, Heart Rate (HR) 86, Oxygen Saturation (SPO2) 99%, and Respiratory Rate (RR) 18; 10:24- BP 100/72, HR 81, SPO2 99% RR 18; 10:29- BP 100/76, HR 82, SPO2 99% RR 16; 10:34- BP 102/74, HR 84, SPO2 99% RR 18; 10:39- BP 100/72, HR 82, SPO2 99% RR 18; 10:44- BP 110/76, HR 86, SPO2 99% RR 18. Client was given a bottle of water and instructed to remain in a semi-fowler's (45 degree) position until vitals stabilized. Patient remained on vaccination site for 30 minutes following the episode of fainting. EMT obtained orthostatic vital signs (vital trend from lying down, to sitting, to standing). Patient was negative for orthostatic hypotension. Symptoms resolved as indicated above in vital signs. Patient stated she was "feeling better" and declined EMS transport. Patient and father were educated by RN on home care (rest and fluids) and to seek emergency medical attention if symptoms persisted or worsened. Patient left the vaccination site at 10:45 with father and sister with steady gait and in no change in status.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: History of anaphylactic reaction to bananas
Vorherige Impfungen: -

VAERS 1291422

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge EW0179

schwer

Staat: TX
Alter: 31,0
Geschlecht: F
Eingang: 05.05.2021
Impfdatum: 03.05.2021
Beginn: 04.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Anaphylactic reaction Angioedema Blood test Chills Hyperhidrosis Lip swelling Muscle spasms Myalgia Pyrexia Vomiting

Symptomtext

10 hours after vaccination, began fever, sweating, muscle aches and cramping, chills, and vomiting. 30 hours after vaccine lips swelled and began experiencing angioedema and anaphylaxis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Not released by hospital, but blood was drawn.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lithium Lamotrigine Klonopin Ambien Doxycycline Trifluoperazine Birth control pill
Allergien: None
Vorherige Impfungen: -

VAERS 1290667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NH
Alter: 18,0
Geschlecht: F
Eingang: 05.05.2021
Impfdatum: 05.05.2021
Beginn: 05.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Presyncope

Symptomtext

Who: What: Vasovagel Where: Observation When: 5/5/2021 @ 1700 How: Response to second vaccine Pt was taken by EMS and was only able to get mothers information which is listed above. Pt is 18, email and phone number are posted. 911 called by medic, taken to ER on request of mother. Pt stable at time of transfer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: Anxiety, Depression
Vorgeschichte: Anxiety/Depression
Andere Medikamente: Adderall, Prozac, Topamax
Allergien: NKA
Vorherige Impfungen: -

VAERS 1290346

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 16,0
Geschlecht: F
Eingang: 05.05.2021
Impfdatum: 05.05.2021
Beginn: 05.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

Client received the Pfizer Covid-19 Vaccine (Lot #EW0167 Exp. 08/2021) at 1:51 PM. Approximately 10 minutes after receiving her first dose the patient fainted from her chair in the observation area. Patient did not strike her head. EMT and other nurses responded and sat the patient upright and began treatment. Patient was A&O X3, immediately after fainting. Patient was assisted to the gravity bed and vitals were taken, see below. Patient stated that she felt better almost immediately after laying in the gravity bed. Vital signs are as follows: 1400- BP: 100/80, O2: 98%, P: 80, Res: 18; 1405- BP: 106/74, O2: 98%, P:96, Res: 18; 1410- BP: 110/70, O2: 99%, P: 90, Res: 18; 1415- BP: 110/70, O2: 99%, P: 87, Res: 18; 1420- BP: 112/70, O2: 99%, P: 86, Res: 18; 1425- BP: 110/70, O2: 99%, P: 96, Res: 18.Patient's vitals improved over time after laying down. Patient was accompanied by her mother who was outside at the time of her fainting. Patient has a history of fainting after injections and getting blood drawn. Patient and Patient's mother felt comfortable after 30 minutes of observation to leave the vaccination site and return home. Client declined EMS transport. Patient and Patient's mother were instructed to seek medical attention if symptoms worsened or if symptoms returned. Patient left the facility in good condition with a steady gait.

Weitere VAERSDATA-Felder

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

VAERS 1289912

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: -
Alter: 41,0
Geschlecht: F
Eingang: 05.05.2021
Impfdatum: 05.05.2021
Beginn: 05.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Hyperhidrosis Muscular weakness Pallor Presyncope

Symptomtext

PALE, DIAPHORETIC, LIMB BUT RESPONSIVE, NEAR SYNCOPE, CODE GREEN CALLED, BP 85/55 HR 70, IVF STARTED, TRANSPORTED TO HOSPITAL.

Weitere VAERSDATA-Felder

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

VAERS 1288756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 53,0
Geschlecht: M
Eingang: 05.05.2021
Impfdatum: 04.05.2021
Beginn: 04.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Blood glucose normal Dizziness Excessive eye blinking Hyperhidrosis Syncope

Symptomtext

DIZZY, DIAPHORETIC, EYES FLUTTERING, SYNCOPE, SEEN BY PARAMEDICS, BP 171/90 HR 97, BS: 99. PT HAS NO HX OF SYNCOPE, REFUSED TRANSPORT, AMA SIGNED.

Weitere VAERSDATA-Felder

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

VAERS 1287363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: VA
Alter: 32,0
Geschlecht: M
Eingang: 04.05.2021
Impfdatum: 04.05.2021
Beginn: 04.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Hyperhidrosis Pallor Syncope

Symptomtext

5 minutes after receiving the vaccine, during the 15 minutes observation time, patient had a syncopal episode that lasted for less than 1 minute. Patient did not loss consciousness, he was alert and oriented to person, place, time and event but he was diaphoretic and pale, BP: 100/70, HR: 58, O2 sat: 98, RR: 18. Patient was then observed for another 30 minutes in the clinic, at which time HR: 88, O2 Sat: 98, BP: 110/76, he was no longer diaphoretic or pale. Patient was discharged home and advised to follow up with his PCP.

Weitere VAERSDATA-Felder

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

VAERS 1287100

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 33,0
Geschlecht: M
Eingang: 04.05.2021
Impfdatum: 04.05.2021
Beginn: 04.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Head injury Syncope

Symptomtext

Patient fainted and bumped/scraped his head in the process. He came to quickly and was alert and oriented. His physical exam was normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Physical Exam only
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported
Andere Medikamente: Not reported
Allergien: Not reported
Vorherige Impfungen: -

VAERS 1285519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MI
Alter: 52,0
Geschlecht: F
Eingang: 04.05.2021
Impfdatum: 04.05.2021
Beginn: 04.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Dizziness Drug hypersensitivity Loss of consciousness Syncope

Symptomtext

Patient received her second dose of her vaccine and during her 15 minute observation period the patient passed out and struck her head on the floor. She did take a minute to respond to the nurse at her side and has no recollection of the event or hitting her head. She was moved in to an observation area and she reported feeling dizzy and lightheaded prior to her syncopal episode. Because she struck her head directly on the floor EMS was called to the clinic. She refused EMS transportation to the hospital. Her husband arrived to the clinic and reported he would be transporting her for further evaluation.

Weitere VAERSDATA-Felder

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

VAERS 1279951

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NY
Alter: 18,0
Geschlecht: F
Eingang: 02.05.2021
Impfdatum: 02.05.2021
Beginn: 02.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Condition aggravated Syncope Unresponsive to stimuli

Symptomtext

Patient; writer was called by family member, patient observed sitting in chair with episode of unresponsiveness. No head trauma, No SOB, No respiratory distress. Paramedic notified. Patient had episode of fainting lasting about 30secs then returned to baseline mental status post covid vaccination. MD notified. Family member present stated that she history of fainting. Patient discharged home, in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: see above
Aktuelle Erkrankungen: Seasonal Allergies
Vorgeschichte: fainting after injections
Andere Medikamente: claritin, singular
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1278326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: NY
Alter: 18,0
Geschlecht: M
Eingang: 01.05.2021
Impfdatum: 01.05.2021
Beginn: 01.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal discomfort Fall Postictal state Seizure

Symptomtext

% minutes after the patient was vaccinated he c/o abdominal discomfort, he told his mother that he felt like he was falling. Patient the fell to the floor and had a seizure the lasted approximately 5-10 seconds. Pt awoke postictal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: pt was sent to hospital for evaluation.
Aktuelle Erkrankungen: DENIES
Vorgeschichte: Patient has a history of a seizure as a child after being vaccinated ( was afebrile)
Andere Medikamente: denies
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1278163

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: MO
Alter: 42,0
Geschlecht: F
Eingang: 01.05.2021
Impfdatum: 01.05.2021
Beginn: 01.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Dizziness Loss of consciousness

Symptomtext

The patient received their vaccination then they waited outside the pharmacy for 15 minutes then went to eat within the store. After eating while walking around the store, the patient felt dizzy and began to pass out. The husband who was walking with her helped her to the ground. The patient remained unconscious for a couple minutes. Breathing and pulse were noted. 911 was called and paramedics examined the patient after she awoke. She was unable to establish place and time upon examination. She was then taken by paramedics to the hospital.

Weitere VAERSDATA-Felder

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

VAERS 1271436

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: WI
Alter: 30,0
Geschlecht: M
Eingang: 29.04.2021
Impfdatum: 29.04.2021
Beginn: 29.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Headache Immediate post-injection reaction Loss of consciousness Musculoskeletal stiffness Syncope

Symptomtext

Approximately 3-5 minutes post-vaccination, patient was seated, texting a message on cell phone, and fainted. Slumped out of chair face down. Witnessed by several volunteer employees. Not witnessed by pharmacist who had administered the vaccine. Volunteers called for help. Immediately pharmacist responded to patient. Loss of conscious noted. Patient was assessed and gently rolled to back with head support and began to regain consciousness, stiffened arms and legs noted. Patient asked, "Do you have a history of seizure disorder?" Initially unable to respond. Pharmacist requested 911 be called as is looked like a seizure. Asked again, and then patient shook head no and then verbal no. Muscles more relaxed. Stroke assessment performed with arms and legs equal to weight, no facial droop, verbal back to normal. Patient asked if he would like to sit up in chair after about 5 minutes on back. Patient complained of headache but no other injuries. Stated he had no bump on his head. Paramedics arrive in less than 10 minutes from call. Assessed patient. Vitals normal. Skin color normal from pale. Paramedics assumed vasovagal fainting episode. Pharmacist agreed. Patient offered water and consumed 12 ounces. Stayed additional 30 minutes. Stood and sit tested for balance. Left without complaint.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown, no history of seizure disorder
Vorgeschichte: History of light-headedness when exposed to blood or needles.
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1263710

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 34,0
Geschlecht: M
Eingang: 27.04.2021
Impfdatum: 27.04.2021
Beginn: 27.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

fainted

Weitere VAERSDATA-Felder

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

VAERS 1259580

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: -
Alter: 49,0
Geschlecht: F
Eingang: 26.04.2021
Impfdatum: 26.04.2021
Beginn: 26.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Syncope

Symptomtext

Syncopal episode after second Pfizer injection. Refused 911. Ambulatory in no distress. See IR form

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure
Andere Medikamente: Metoprolol, "Dizziness" meds, Ibuprofen
Allergien: NKDa
Vorherige Impfungen: Syncopal episode. Dislikes needles

VAERS 1256874

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 17,0
Geschlecht: M
Eingang: 25.04.2021
Impfdatum: 25.04.2021
Beginn: 25.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Nausea Paraesthesia Syncope

Symptomtext

Tingly, Dizzy, nausea , fainted

Weitere VAERSDATA-Felder

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

VAERS 1252691

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 19,0
Geschlecht: M
Eingang: 24.04.2021
Impfdatum: 24.04.2021
Beginn: 24.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Hyperhidrosis Hypotension Nausea Seizure like phenomena Syncope

Symptomtext

SEVERAL MINUTES AFTER GETTING THE VACCINE THE PATIENT FAINTED AND SEEMED TO BE HAVING A SEIZURE. THIS HAPPENED 4 TIMES AND EACH EPISODE LASTED ABOUT 10 SECONDS. AMBULANCE CAME RIGHT AWAY. PT HAD SEVERLY LOW BLOOD PRESSURE, SWEATING, NAUSEA. MOM CAME AND PICKED UP PATIENT, HE REFUSED TO GO TO HOSPITAL.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure like phenomena
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NO
Vorgeschichte: NO
Andere Medikamente: -
Allergien: NO
Vorherige Impfungen: -

VAERS 1252652

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

schwer

Staat: CA
Alter: 18,0
Geschlecht: F
Eingang: 24.04.2021
Impfdatum: 24.04.2021
Beginn: 24.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cyanosis Dry skin Feeling abnormal Food craving Loss of consciousness Pallor Peripheral coldness Pulse abnormal

Symptomtext

Patient is a 18-year-old, female. No known medical history. No known allergies. At 3:18 pm, the patient received her first dose of Pfizer vaccine (lot number EW0179, expires on 08/2021) on left deltoid, given by RN. Patient informed RN that she has a history of fainting after vaccines. RN recommended the patient wait in the zero-gravity chair. Patient continued to be A&Ox3, walked herself over to the EMT waiting area with a steady, balanced, and sat down in zero-gravity chair. At 3:20 pm, patient checked in with EMT and stated she feels "fine". At 3:27 pm, while waiting in observation area, patient stated "I don't feel good" and went unconscious. EMT reclined patient into supine position. Patient remained unconscious for approximately 10 seconds. RN called 9-1-1 at 3:28 pm. Patient regained consciousness at 3:28 pm and stated "I need something sweet". At 3:30 pm, the patient's BP 69/44, RR 8/min, HR 63 bpm and weak, skin dry and cold to touch, lips pale and cyanotic. At 3:33 pm, the patient's BP was 87/60. Fire Department arrived on site at 3:34 pm. Patient was transferred to gurney by FD. Patient left facility at 3:34 pm .

Weitere VAERSDATA-Felder

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

VAERS 2711979

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: GA
Alter: 24,0
Geschlecht: F
Eingang: 09.11.2023
Impfdatum: 04.08.2021
Beginn: 06.08.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Cardiac monitoring abnormal Chest X-ray normal Electrocardiogram normal Fatigue Feeling jittery Heart rate increased Hypertension Laboratory test normal Tachycardia

Symptomtext

On the Friday after I got the vaccine I started having tachycardia when standing. I would feel very tired and jittery while standing. I went to the ER on 8/14/23 for high heart rate (180's) and high blood pressure. I have never recovered and now have to take medication everyday.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: 1,0
Labordaten: EKG - normal chest xray - normal labs work - normal Heart monitor for a month - Tachycardia
Aktuelle Erkrankungen: high cholesterol
Vorgeschichte: -
Andere Medikamente: Crestor
Allergien: -
Vorherige Impfungen: -

VAERS 2677739

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: NY
Alter: 45,0
Geschlecht: F
Eingang: 29.08.2023
Impfdatum: 22.06.2021
Beginn: 20.09.2021
Tage bis Beginn: 90,0
Dosis: 1
Route/Site: UN / LA

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

Acoustic stimulation tests Angiocardiogram Angiogram Asthenia Bradycardia Dyspnoea Echocardiogram Electrocardiogram Electroencephalogram Electronystagmogram Fatigue Gait disturbance Heart rate increased Hypertension Left atrial enlargement Magnetic resonance imaging head Migraine Muscular weakness

Symptomtext

Symptoms: Onset of neuropathy hand tremors and weakness in lower extremities. Onset of pulsatile tinitus Onset cardiac symptoms: left atrial enlargement; tachycardia and bradycardia; heart palpitations; high blood pressure; elevated heart rate; Onset Right-sighted migraines/headaches Onset Edema (right foot) Onset Difficulty walking (use cane for support) Onset Extreme debilitating fatigue, including dyspnea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 4,0
Labordaten: Treatment for pulsatile tinitus (12/21/2021) CT Angiogram of the heart (4/14/2022) EKGs: 1. 12/30/21 2. 01/12/2022 3.01/15/2022 4. 4/25/2022 5. 07/13//2022 Echocardiogram (1/12/2022) EKGs: 11/09/2021 12/07/2021 12/09/2021 12/30/2021 02/04/2022 02/23/2022 03/12/2022 03/13/2022 08/26/2023 (2) Echocardiogram Transthoraciac (1.12.22) December 2021 Hearing test (Dec. 21) (2) Nuclear stress test (3/15/2022) Doppler ultrasound examination of cerebral blood flow (12/21/21) Transcranial doppler (3/22/22) Sonogram and ENG of lower extremities MR Angiography (3/24/22) & MRI of the brain (4/1/22) Electroencephalogram (3/1/22)
Aktuelle Erkrankungen: Hypothyroidism
Vorgeschichte: Lymphedema (in left foot); History of thyroid cancer; Bilateral renal cysts; Lumbar radiculopathy
Andere Medikamente: Levothyroxine, Calcitriol
Allergien: N/A
Vorherige Impfungen: -

VAERS 2630480

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 38,0
Geschlecht: F
Eingang: 11.05.2023
Impfdatum: 18.01.2023
Beginn: 10.02.2023
Tage bis Beginn: 23,0
Dosis: 2
Route/Site: IM / LA

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

Hypotension

Symptomtext

HYPOTENSION

Weitere VAERSDATA-Felder

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

VAERS 2614070

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: CO
Alter: 83,0
Geschlecht: F
Eingang: 12.04.2023
Impfdatum: 03.08.2021
Beginn: 08.08.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: - / LA

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

Gait disturbance Hypoaesthesia Myalgia Pain Paraesthesia Sciatica

Symptomtext

developed pain; numbness; tingling from her hips all the way to her feet; Sciatica; she is feeling is muscle pain up on her knee.; she had trouble walking; 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 84-year-old female patient received BNT162b2 (BNT162B2), on 03Aug2021 as dose 2, single (Lot number: EW0179) at the age of 83 years, in left arm for covid-19 immunization. The patient had no relevant medical history. The patient took concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot: EW0179, Expiry: Unknown, Site: Left arm), administration date: 08Jul2021, when the patient was 83-year-old, for COVID-19 immunization, reaction(s): "No problem". The following information was reported: SCIATICA (non-serious) with onset 08Aug2021, outcome "recovering"; PAIN (non-serious) with onset 08Aug2021, outcome "recovering", described as "developed pain"; HYPOAESTHESIA (non-serious) with onset 08Aug2021, outcome "recovering", described as "numbness"; GAIT DISTURBANCE (non-serious) with onset 08Aug2021, outcome "not recovered", described as "she had trouble walking"; MYALGIA (non-serious) with onset 08Aug2021, outcome "recovering", described as "she is feeling is muscle pain up on her knee."; PARAESTHESIA (non-serious) with onset 08Aug2021, outcome "recovering", described as "tingling from her hips all the way to her feet". Therapeutic measures were taken as a result of pain, hypoaesthesia, paraesthesia. Additional information: The patient received her 2nd dose of the Pfizer covid vaccine back on 03Aug2021, on 08Aug2021 (also reported as 5 days after) she developed pain, numbness, and tingling from her hips all the way to her feet. The patient says it was first diagnosed as sciatica. The patient was asking if there is any way we can help her for the situation. She also says later on that what she was feeling was muscle pain up on her knee. She said that the 'sciatica' did not work and she went to 4 doctors and found out what it was. She heard it was a reaction to the second shot. She said that she went back and looked and she said that 5 days after receiving the shot, she had trouble walking. She takes no other medications just some Vitamins.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2613410

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0179

moderat

Staat: GA
Alter: 36,0
Geschlecht: F
Eingang: 07.04.2023
Impfdatum: 04.08.2021
Beginn: 04.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood pressure increased Dizziness postural Dyspnoea Hypoaesthesia Throat irritation

Symptomtext

Presented and given Pfizer vaccine approximately 9:30am. Approximately 9:37 am was asked how she was feeling and she complained throat feeling itchy and having trouble taking a deep breath. Complained of numbness in the fingers of the right hand. Blood pressure taken in the right arm at 9:48 am 193/108. EMS called at approximately 9:55 am. Client was taken out to the ambulance with EMT's at each side. Client complained of dizziness upon standing. Client transported by ambulance to Hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Not Applicable
Aktuelle Erkrankungen: None Known
Vorgeschichte: None Known
Andere Medikamente: None Known
Allergien: None Known other than condoms - itching
Vorherige Impfungen: -

VAERS 2593203

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: WI
Alter: 52,0
Geschlecht: M
Eingang: 08.03.2023
Impfdatum: 21.04.2021
Beginn: 02.05.2021
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Autoimmune thyroiditis Chest pain Dizziness Dry skin Dyspepsia Dyspnoea Erythema Heart rate irregular Laboratory test abnormal Massage Muscle spasms Muscle tightness Myalgia Pain in extremity Palpitations Skin exfoliation Tendon pain

Symptomtext

Initially muscle tightness, cramping and painful tendons from wrist through shoulder. All muscle groups. That never completely subsided but was able to recover with massage. A few months later, started having irregular heart beats. Heart was racing when I was falling asleep. Had shortness of breath, difficult to describe chest pain, dizziness, digestion issues and skin issues (dry, flaky and red).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Checked with ER and found nothing irregular with heart. Went to clinic and was tested for thyroid issues. Was diagnosed with a thyroid disorder. Began taking medication. Later, was tested to determine what type of thyroid disorder I have. Found it was an auto immune disorder (Hashimotos disease).
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2576391

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 81,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 17.09.2022
Beginn: 04.01.2023
Tage bis Beginn: 109,0
Dosis: 1
Route/Site: - / -

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

Back pain COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

01/04/23 presents to ED for "low back pain" "shortness of breath". PMHx of "hyperlipidemia, depression, and chronic back pain"

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 2576391

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 81,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 17.09.2022
Beginn: 04.01.2023
Tage bis Beginn: 109,0
Dosis: 3
Route/Site: - / -

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

Back pain COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

01/04/23 presents to ED for "low back pain" "shortness of breath". PMHx of "hyperlipidemia, depression, and chronic back pain"

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 2563524

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: PA
Alter: 14,0
Geschlecht: F
Eingang: 19.01.2023
Impfdatum: 01.07.2021
Beginn: 15.07.2021
Tage bis Beginn: 14,0
Dosis: 2
Route/Site: SYR / AR

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

Anxiety Blood test Computerised tomogram Condition aggravated Dizziness Fatigue Feeling abnormal Hyperhidrosis Laboratory test Loss of personal independence in daily activities Magnetic resonance imaging Memory impairment Migraine Nausea New daily persistent headache Palpitations Pollakiuria Postural orthostatic tachycardia syndrome

Symptomtext

After the vaccine in July 2021 pt. has had a daily migraine/headache every day and has developed Inappropriate Sinus Tachycardia and POTS. She has been seeing multiple specialists, Neurologist, Cardiologist, ENT, Allergist/Immunologist, GI, Psychology, Psychiatry and there is still no resolution to her problems. She has had to leave school and was in a Mental Health Partial Hospitalization Program and Intensive Outpatient program for 6 months. She now homeschools and in addition to traditional medicine we have tried chiropractor, acupuncture, nutritional supplements, individual therapy, group therapy, physical therapy looking for a solution to these medical problems. She has been on lots and lots of medications but none will stop the daily migraine. Symptoms have gone on for 19 months. They include: daily migraine, fatigue, brain fog, memory problems, dizziness, lightheadedness, racing heart, excessive sweating, anxiety, nausea, vision problems, excessive urination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: She has had multiple medical tests at a local Hospital, where she was diagnosed after 8 months with no answers. Also seen at different health care facilities. She has been referred to a doctor by her cardiologist to the clinic there but appointment isn't until June 2023. She has had an MRI, CT scan, tilt table test, blood work
Aktuelle Erkrankungen: none
Vorgeschichte: Migraines once or twice/month
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2562585

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0179

moderat

Staat: CO
Alter: 34,0
Geschlecht: F
Eingang: 18.01.2023
Impfdatum: 05.05.2021
Beginn: 05.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Abdominal distension Decreased appetite Fatigue Heavy menstrual bleeding Migraine Weight increased

Symptomtext

Daily since vax: Migraines Lack of appetite Constant bloating Extreme weight gain Fatigue Menstrual cycle now extremely heavy Diagnosed as exaggerated immune response to vax

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/a
Vorgeschichte: Daily Migraines Constant Bloating Extreme weight gain in just a few months Daily Lack of appetite Chronic fatigue
Andere Medikamente: N/a
Allergien: N/a
Vorherige Impfungen: -

VAERS 2565366

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 91,0
Geschlecht: M
Eingang: 17.01.2023
Impfdatum: 18.05.2021
Beginn: 15.12.2022
Tage bis Beginn: 576,0
Dosis: 2
Route/Site: UN / UN

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

Alanine aminotransferase normal Allen's test Anion gap Aspartate aminotransferase normal Asthenia Base excess decreased Basophil count decreased Benign prostatic hyperplasia Bilirubin urine Blood albumin decreased Blood alkaline phosphatase normal Blood bicarbonate decreased Blood bilirubin increased Blood calcium decreased Blood chloride normal Blood creatinine normal Blood glucose normal Blood magnesium normal

Symptomtext

Narrative: 12/15/22 - Pt with a medical history of hyperlipidemia, history of TIA, spinal stenosis, suspected GCA (negative biopsy, on steroids), plantar fascial fibromatosis, tobacco abuse who presents to the ED complaining of increased fatigue, weakness x 1 week, decline in appetite, and purulent draining hand wound. Chills noted today. Pt also reports left sided chest pain. Wife noted Pt had acute onset of congestion, he is pale, and not performing his ADLs as usual (onset within past 24hrs). Pt tested COVID+ and was admitted to hospital 12/15/22 (with discharge on 12/29/22). PRINCIPAL DIAGNOSIS (Reason for admission after study): covid 19 with hypoxia ADDITIONAL DIAGNOSES: dementia ,chronic benign prostatic hypertrophy hyperlipidemia mild normocytic anemia mild hyponatremia hard of hearing. HOSPITAL COURSE: Pt admitted to the floor. dx covid with hypoxia. pt started on steroids. cont supplemental oxygen. pt monitored. did not need oxygen the next day. pt hearing aids and glasses at home. PT eval done and recs were 24/7 care at home. wife currently on chemo and unable to provide this. ppd placed. pt started on remdesivir by pharm d on 12/22. pt also restarted on steroids. pt completed 3 days of remdesivir and 7 days of dexamethasone. pt tolerated medications. pt communication improved with use of amplifyer. pt completed 10 days of isolation. sws working on STR for pt. due to abnormal imaging pulm consulted - will try wixella and triotropium due concern for underlying pulm ds. pt stable for discharged 12/29/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Pt tested COVID+ on 12/15/2022 Vital Signs *Temperature 99.4 F (37.4 C) Pulse 87 Respirations 18 Blood Pressure 165/72 Pain scale recorded: 1 Pulse Oximetry 94 Room Air 12/15/22 LABS: APPEARANCE: Clear UR COLOR: Yellow SPECIFIC GRAVITY: 1.016 UROBILINOGEN: 2 UR KETONES: TRACE UR GLUCOSE: Normal UR PROTEIN: NEGATIVE UR PH: 6.5 WBC/HPF: 2 RBC/HPF: 4 NITRITE, URINE: NEGATIVE LEUKOCYTE ESTERASE, URINE: Negative URINE BLD: TRACE URINE BILI: NEGATIVE COVID-19 PCR (FLUVID)(CEPHEID): POSITIVE H* FLU A PCR (FLUVID)(CEPHEID): NEGATIVE FLU B PCR (FLUVID)(CEPHEID): NEGATIVE RSV PCR (FLUVID)(CEPHEID): NEGATIVE pHEPOC: 7.470 H pCO2EPOC: 26.1 L* pO2EPOC: 67.5 L* pCO2(T)EPOC: 25.7 L* pO2TEPOC: 66.0 L* HCO3ARTEPOC: 19.0 L BEEPOC: -3.5 L O2SATEPOC: 94.7 cTCO2EPOC: 19.8 L* TESTCOMMENTEPOC: SATS 94# ALLENTESTEPOC: Positive DRAWSITEepoc: R Radial PTTEMPepoc: 98 PEEPEPOC: pending NOTIFYDATEEPOC: 20221215181000 READBACKEPOC: Yes SAMPLETYPEEPOC: Arterial CRITICALPRESENTEPOC: Yes CRITICALACTION: Repeated test CRITICALNOTIFYEPOC: DR WBC: 7.1 RBC: 4.12 L HGB: 12.0 L HCT: 35.0 L MCV: 84.9 MCH: 29.1 MCHC: 34.2 RDW: 15.4 PLT: 274 MPV: 8.0 EOSINO, ABSOLUTE: 0.0 BASO, ABSOLUTE: 0.0 GRAN % (SS): 75.1 H LYMPH % (SS): 12.8 L MONO % (SS): 11.1 EOS% (SS): 0.3 BASO% (SS): 0.7 GRAN# (SS): 5.4 LYMPH# (SS): 0.9 L MONO# (SS): 0.8 TOTAL BILIRUBIN: 1.4 H ASAT: 12 ALKALINE PHOSPHATASE: 66 TOTAL PROTEIN: 5.9 L ALBUMIN: 2.8 L SODIUM: 136 POTASSIUM: 4.0 CHLORIDE: 106 CO2: 21 L ANION GAP (CALCULATED): 9 GLUCOSE: 105 H CREATININE: 0.9 CALCIUM: 8.9 MAGNESIUM: 1.8 ALT: 6 EGFR: 81 UREA, BUN: 10 TROP-I iSTAT: 0.02
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2557457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 81,0
Geschlecht: M
Eingang: 11.01.2023
Impfdatum: 22.01.2021
Beginn: 13.12.2022
Tage bis Beginn: 690,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Tachycardia

Symptomtext

12/13/22 presents to ED for "tachycardia". PMHx of "CLL, history of breast cancer s/p mastectomy"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: 12/13/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2557457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 81,0
Geschlecht: M
Eingang: 11.01.2023
Impfdatum: 22.01.2021
Beginn: 13.12.2022
Tage bis Beginn: 690,0
Dosis: 4
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Tachycardia

Symptomtext

12/13/22 presents to ED for "tachycardia". PMHx of "CLL, history of breast cancer s/p mastectomy"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: 12/13/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2555876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 50,0
Geschlecht: F
Eingang: 10.01.2023
Impfdatum: 24.04.2021
Beginn: 12.12.2022
Tage bis Beginn: 597,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

12/12/22 presents to ED for "shortness of breath, cough". PMHx of "DM and HTN"

Weitere VAERSDATA-Felder

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

VAERS 2550055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW 0179

moderat

Staat: WA
Alter: 13,0
Geschlecht: M
Eingang: 04.01.2023
Impfdatum: 10.06.2021
Beginn: 01.06.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / AR

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

Headache Migraine

Symptomtext

Starting the week after the second dose persistent migraine headaches that are not relieved with over the counter pain medications. Experiences headache every day. Nothing helps to relieve the headaches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: All Cephalosporin antibiotics Bactrim
Vorherige Impfungen: -

VAERS 2542810

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0179

moderat

Staat: AR
Alter: 35,0
Geschlecht: F
Eingang: 24.12.2022
Impfdatum: 05.06.2021
Beginn: 04.09.2021
Tage bis Beginn: 91,0
Dosis: UNK
Route/Site: SYR / AR

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

Cardiac ablation Cardiac electrophysiologic study abnormal Dizziness Electrocardiogram abnormal Palpitations Retained products of conception Supraventricular tachycardia Uterine dilation and curettage Valsalva maneuver Visual impairment

Symptomtext

On 9/4/21, she was relaxing when she suddenly began to experience palpitations, lightheadedness, and fading vision. Her palpitations persisted until she arrived in the ED and was found to have a heart rates around 200 bpm and SVT on initial EKG. Valsalva was then performed and she converted to sinus rhythm. 10/29/2021 EP study + AVNRT ablation slow pathway modification

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Suction D&C for Retained POC on 7/20/2021 15 days postpartum at time of vaccination
Vorgeschichte: None
Andere Medikamente: Prenatal vitamins Fish oil albuterol PRN
Allergien: None
Vorherige Impfungen: -

VAERS 2539131

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge EW0179

moderat

Staat: MI
Alter: 75,0
Geschlecht: M
Eingang: 21.12.2022
Impfdatum: 10.02.2021
Beginn: 10.10.2022
Tage bis Beginn: 607,0
Dosis: 3
Route/Site: - / -

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

Blood cortisol Blood sodium decreased COVID-19 Dyspnoea Fatigue Hypotension Inflammatory marker test Oxygen saturation decreased SARS-CoV-2 test positive White blood cell count decreased

Symptomtext

The patient is a 76-year-old male, who presented from home to the emergency room for more shortness of breath and fatigue and his pulse ox dropping. In the emergency room, he was positive for active COVID (he has 2 immunizations from "Evusheld." He is an ex-smoker with a history of non-Hodgkin's lymphoma, diagnosed 6 years ago and his last chemotherapy was about 6 months ago. He denies chest pain and his blood pressure is low, though he has a history of hypertension. His sodium was low as was his white blood count. He has a history of coronary artery disease with prior myocardial infarction, gastrointestinal bleeding, and hyperlipidemia. Additional information for Item 18: HOSPITAL COURSE: The patient was seen in consultation by Dr. from Infectious Disease and Dr. from Pulmonary. The patient was treated initially with his usual medications including intravenous fluids, electrolytes, oxygen, respiratory bronchodilators, and was started on dexamethasone and Remdesivir. Dr. directed COVID therapy. Dr. requested a TSA and cortisol level, which was drawn. He improved symptomatically. His inflammatory markers improved significantly and he was subsequently discharged home on 10/14/2022 to follow up with Dr. from Oncology and Dr., his primary care doctor.

Weitere VAERSDATA-Felder

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

VAERS 2539131

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 75,0
Geschlecht: M
Eingang: 21.12.2022
Impfdatum: 10.02.2021
Beginn: 10.10.2022
Tage bis Beginn: 607,0
Dosis: 4
Route/Site: - / -

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

Blood cortisol Blood sodium decreased COVID-19 Dyspnoea Fatigue Hypotension Inflammatory marker test Oxygen saturation decreased SARS-CoV-2 test positive White blood cell count decreased

Symptomtext

The patient is a 76-year-old male, who presented from home to the emergency room for more shortness of breath and fatigue and his pulse ox dropping. In the emergency room, he was positive for active COVID (he has 2 immunizations from "Evusheld." He is an ex-smoker with a history of non-Hodgkin's lymphoma, diagnosed 6 years ago and his last chemotherapy was about 6 months ago. He denies chest pain and his blood pressure is low, though he has a history of hypertension. His sodium was low as was his white blood count. He has a history of coronary artery disease with prior myocardial infarction, gastrointestinal bleeding, and hyperlipidemia. Additional information for Item 18: HOSPITAL COURSE: The patient was seen in consultation by Dr. from Infectious Disease and Dr. from Pulmonary. The patient was treated initially with his usual medications including intravenous fluids, electrolytes, oxygen, respiratory bronchodilators, and was started on dexamethasone and Remdesivir. Dr. directed COVID therapy. Dr. requested a TSA and cortisol level, which was drawn. He improved symptomatically. His inflammatory markers improved significantly and he was subsequently discharged home on 10/14/2022 to follow up with Dr. from Oncology and Dr., his primary care doctor.

Weitere VAERSDATA-Felder

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

VAERS 2539088

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 82,0
Geschlecht: F
Eingang: 21.12.2022
Impfdatum: 18.01.2021
Beginn: 03.10.2022
Tage bis Beginn: 623,0
Dosis: 3
Route/Site: - / -

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

Bladder catheterisation Blood sodium abnormal COVID-19 Dehydration Fall Fluid intake restriction Fractured sacrum Hyponatraemia Imaging procedure abnormal SARS-CoV-2 test positive Urinary retention

Symptomtext

This is a 84y.o. female with a PMH significant for hypertension, CKD stage II, neurogenic bladder and osteoperosis presented to hospital on 10/3/2022 after a mechanical fall. Was found to be hyponatremic. Imaging showed nondisplaced fracture of right sacrum and comminuted right fracture. Patient was seen and evaluated by ortho and no intervention was indicated beside PT/OT. Fall was attributed to hyponatremia, excess fluid intake escitalopram and dehydration from recent illness . Pt was put on fluid restriction with improvement in Sodium. She was also given one dose of tolvaptan to bring sodium to higher normal level. Sodium was normal Upon discharge and she will f/u with nephrology. She also had covid and completed 5 days of paxlovid op that was started 9/30. Urology saw pt due to urinary retention. Pt had 3 days of urinary cath for decompression of the bladder after which TOV was attempted with success. She will follow up with urology for further eval of possible neurogenic bladder Pt was discharged to sar. She was encouraged to f/u with colorectal surgery for evaluation of fecal incontinence although not observed during admission. Her gabapentin frequency was increased to 4 times daily for pelvic pain. She will follow up with neurosurgery for further eval. She has an mri that she will get outpatient. Patient was discharged in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: 10/3 SARS-CoV-2 -COVID-19 by NAA, Micro -- detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2539036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 70,0
Geschlecht: F
Eingang: 21.12.2022
Impfdatum: 14.04.2021
Beginn: 26.09.2022
Tage bis Beginn: 530,0
Dosis: 2
Route/Site: - / -

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

Abdominal lymphadenopathy COVID-19 Cardiac stress test normal Computerised tomogram thorax abnormal Cough Dyspnoea Echocardiogram normal Ejection fraction normal Hilar lymphadenopathy Hypertension Lymph node calcification Oesophagram Procalcitonin SARS-CoV-2 test positive Troponin normal

Symptomtext

This is a 72y.o. female with PMHx significant for CAD prior PCI, HTN, sarcoidosis, CHF diastolic dysfunction who presented for shortness of breath progressively worsening over the last few weeks. She endorses mild SOB at baseline and does not use supplemental O2 or CPAP at home. Endorses a dry cough. She is vaccinated against COVID and did not test positive in the past until 9/26. Recently hospitalized for HTN. States she has a hx Pulmonary embolism from early 2000s. Denies chest pain, abdominal pain, nausea, vomiting, paresthesia, fever, chills. During ED eval, chest CT showed no PE, but a bulky calcified lymphadenopathy in the hila and upper abd. Trop negative, COVID positive. procalcitonin 7.32. Admit for further eval and management. covid precautions removed 10/6 and sats stable on RA now. She completed IV decadron and Remdesivir 10/1. ID was following and completed ceftin . She has hx of Dysphagia S/p dilation on 7/21 via EGD. Esophagram showing no evidence of obstruction and Esophageal dysmotility and she is tolerating reg diet. Per cardio, CP likely due to MS in nature. ECHO with EF 55% and stress test neg with EF 70%. Psych was following and trazadone increased, continue xanax. PT/OT recommending SAR and pt agreeable. She is stable for d/c with close Op follow up

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 10,0
Labordaten: 9/26 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2199201

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 92,0
Geschlecht: F
Eingang: 21.12.2022
Impfdatum: 19.04.2021
Beginn: 27.09.2022
Tage bis Beginn: 526,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Chills Fatigue Pyrexia SARS-CoV-2 test positive Cough Dyspnoea Full blood count

Symptomtext

94y.o. male with a past medical history of AML with last round of chemo the day before admission, hypertension, hypercholesterolemia, and OSA. He presented to the emergency room with cough, difficulty breathing, and fever. Fever was noted during chemotherapy session. He was noted to be COVID-19 positive He was on Nc oxygen and able to be weaned. He was ofllowed by ID and had 5 days of remdesivir with clinical improvement On discharged he Continued acyclovir, cipro and diflucan He was followed by oncology for his history of AML and cbc was monitored He had CKD3 and we Monitored renal function. He was ambulatory and improved to room air Leukopeni improved and after discussing with ID , we felt stable for discharge home with a short course of steroids

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 6,0
Labordaten: 9/27 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2199201

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 92,0
Geschlecht: F
Eingang: 21.12.2022
Impfdatum: 19.04.2021
Beginn: 27.09.2022
Tage bis Beginn: 526,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Chills Fatigue Pyrexia SARS-CoV-2 test positive Cough Dyspnoea Full blood count

Symptomtext

94y.o. male with a past medical history of AML with last round of chemo the day before admission, hypertension, hypercholesterolemia, and OSA. He presented to the emergency room with cough, difficulty breathing, and fever. Fever was noted during chemotherapy session. He was noted to be COVID-19 positive He was on Nc oxygen and able to be weaned. He was ofllowed by ID and had 5 days of remdesivir with clinical improvement On discharged he Continued acyclovir, cipro and diflucan He was followed by oncology for his history of AML and cbc was monitored He had CKD3 and we Monitored renal function. He was ambulatory and improved to room air Leukopeni improved and after discussing with ID , we felt stable for discharge home with a short course of steroids

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 6,0
Labordaten: 9/27 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2507258

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 79,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 24.02.2021
Beginn: 19.09.2022
Tage bis Beginn: 572,0
Dosis: 3
Route/Site: - / -

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

Anxiety COVID-19 Confusional state Dyspnoea SARS-CoV-2 test positive

Symptomtext

09/19/22 presents to ED for "anxiety, confusion, SOB". PMHx of "anxiety, depression, and a colon cancer treated in 1998 with surgery and chemotherapy, and recently diagnosed with breast CA on Letrozole"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 09/20/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2484263

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: NC
Alter: 32,0
Geschlecht: F
Eingang: 20.10.2022
Impfdatum: 30.09.2021
Beginn: 23.05.2022
Tage bis Beginn: 235,0
Dosis: 3
Route/Site: IM / RA

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

Blood test Computerised tomogram normal Dyspnoea Dyspnoea exertional Electrocardiogram normal Fibrin D dimer Heart rate increased X-ray normal

Symptomtext

I went to walk around the neighborhood and I relieved that I was out of breath. I checked my apple watch and my heart rate was elevated more than usual. When I sat down it was a little bit better. It got to the point when I was changing my clothes I had shortness of breath. I went to the ER and they checked the see if I had blood clots. I did not have blood clots. I have been seeing several different doctors and specialist. Nobody can explain what is going on with me. I have been doing IBS treatment and I still have the shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Bloodwork, D-dimer; X-ray , Normal; CT- Scan, normal; EKG, normal
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Unknown
Allergien: N/A
Vorherige Impfungen: HPV Gardasil,02/19/2007, Passed out; Hepatitis B 04/19/2010, Passed out

VAERS 2478468

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

moderat

Staat: MI
Alter: 42,0
Geschlecht: F
Eingang: 14.10.2022
Impfdatum: 28.12.2021
Beginn: 05.01.2022
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: SYR / RA

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

Abdominal pain upper Back pain Chest pain Computerised tomogram abdomen Differential white blood cell count Dysstasia Eating disorder Electrocardiogram Full blood count Lipase Metabolic function test Scan with contrast Ultrasound abdomen

Symptomtext

A week or so after the booster shot I start getting pain in my stomach. I assumed it was heartburn issues this continued to get worse and the pain escalated. By the end of the month I was in the hospital. I could not eat without pain, I should not sit/stand/lay without immense pain. The pain was from front to back in the center of my body right underneath my sternum.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 4,0
Labordaten: Lipase COMPREHENSIVE METABOLIC PANEL CBC w/differential EKG 12-Lead US RIght Upper Quadrant Ultrasound CT Abdomen Pelvis - w contrast
Aktuelle Erkrankungen: none
Vorgeschichte: Mitral valve prolapse, Bi-cuspid Triscuspid valve
Andere Medikamente: B6, Mag. Oxide, Iron supplements, Claritin, Tylenol (500mg), Benadryl (1 tablet)
Allergien: Turmeric , Cefaclor, Ciprofloxacin, Erythromycin, Hydrocodone-Acetaminophen, Latex, Penicillins, Potassium Clavulanate, Tramadol Hcl, Azithromycin, Hydromorphone, Adhesive Tape-Silicones
Vorherige Impfungen: -

VAERS 2467308

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 03.10.2022
Impfdatum: 30.11.2021
Beginn: 23.09.2022
Tage bis Beginn: 297,0
Dosis: 3
Route/Site: - / -

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

Asthenia Blood sodium decreased COVID-19 Dyspnoea Hyperkalaemia Hyponatraemia Respiratory symptom

Symptomtext

Discharge Provider: DO Primary Care Provider: MD Admission Date: 9/23/2022 Discharge Date: 9/28/2022 PRESENTING PROBLEM: Hyperkalemia [E87.5] Hyponatremia [E87.1] Difficulty breathing [R06.89] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 73 years old male with history of squamous cell cancer of epiglottis status post total laryngectomy and partial pharyngectomy and bilateral neck dissection with cricophyargeal myotomy, hypothyroidism, chronic bronchitis on 2L oxygen at home, On salt tabs who presented to the hospital with weakness and shortness of breath with URI symptoms. He was found to have covid infection and severe hyponatremia, Na 120. He was treated with antibiotics, steroid and breathing treatment. He was back to baseline on home oxygen at discharge. He was evaluated by PT, and OT, recommended for home with home health services. This was changed to subacute as PT and OT agreed with patient that he was too weak to be discharge home. He was discharged on salt tabs three times per day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Tobacco abuse Hypothyroidism Dysphagia Weight loss Weakness SIADH (syndrome of inappropriate ADH production) (HCC) Squamous cell cancer of epiglottis (HCC) Chronic hypoxemic respiratory failure (HCC) Chronic low back pain Decreased hearing History of malignant neoplasm of thyroid Postinflammatory pulmonary fibrosis (HCC) Pressure injury, stage 2 (HCC) Chronic obstructive lung disease (HCC) Underweight Tobacco dependence syndrome Pure hypercholesterolemia Laryngeal cancer (HCC) Pleural effusion Pulmonary nodule Non-healing surgical wound Atopic dermatitis Pituitary adenoma (HCC) Tracheostomy present (HCC) Hyponatremia COVID-19 Chronic bronchitis (HCC)
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler aspirin 325 MG tablet docusate 100 MG capsule Emollient (MOISTURIZING LOTION) LOTN hydrocortisone (HYTONE) 2.5 % lot
Allergien: Breo Ellipta [Fluticasone Furoate-vilanterol]Other, Dizziness UmeclidiniumOther, Dizziness
Vorherige Impfungen: -

VAERS 2452341

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 74,0
Geschlecht: M
Eingang: 20.09.2022
Impfdatum: 26.10.2021
Beginn: 13.09.2022
Tage bis Beginn: 322,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Asthenia COVID-19 Cough Dyspnoea Fibrin D dimer increased Hiccups Nausea Oesophagram Regurgitation Ultrasound Doppler Vomiting

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 9/13/2022 Discharge Date: Sep 15, 2022 PRESENTING PROBLEM: Generalized weakness [R53.1] COVID-19 virus infection [U07.1] HOSPITAL COURSE: patient presented with shortness of breath after being diagnosed with COVID six days prior; he was found to be weak so was admitted for this. patient had a cough, nausea, vomiting, and hiccups as well. he was treated conservatively and PT/OT as well as SLP were asked to see him. SLP recommended GI evaluation as patient c/o of food being regurgitated or sticking in his chest; esophogram was normal and GI signed-off recommending PRN follow-up. patient's hiccups improved with thorazine and after a d/w pharmacy protonix was added (to be taken for 30 days) as an adjunct to treat said hiccups. patient had a bit of an AKI (he has a solitary kidney and CKD with baseline of 2.2) which improved with IVF. d-dimer elevation attributed to COVID as his symptoms improved without VTE intervention and a BLLE venous doppler was negative. patient was amenable for discharge citing that he felt less short of breath, was coughing less, and had less hiccups. he was still feeling a bit weak. all questions and concerns addressed, all meds and follow-ups reviewed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Complete tear of right rotator cuff;OSA (obstructive sleep apnea); HTN (hypertension); Pneumonia; Lumbar radiculopathy; Cardiac pacemaker in situ; Lumbar stenosis; Solitary kidney; CKD (chronic kidney disease) stage 4, GFR 15-29 ml/min (HCC); Type 2 diabetes mellitus with diabetic polyneuropathy, without long-term current use of insulin (HCC); Poor venous access; Other hyperlipidemia; Migraine headache; Malignant melanoma of right upper extremity including shoulder (HCC); Hypogonadism male; Depressive disorder Thrombocytopenia (HCC); Degenerative tear of medial meniscus of right knee; OSA on CPAP Class 1 obesity with body mass index (BMI) of 32.0 to 32.9 in adult, unspecified obesity type, unspecified whether serious comorbidity present; Essential hypertension; Polycythemia, secondary; Sick sinus syndrome (HCC); Generalized weakness; Intractable hiccups.
Andere Medikamente: Acetaminophen (TYLENOL); Albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA); Amlodipine (NORVASC); Atorvastatin (LIPITOR); Chlorpromazine (THORAZINE); Citalopram (CELEXA); Dapagliflozin (FARXIGA); Guaifenesin (MUCINEX); Guaifenesin-Dex
Allergien: AcyclovirHives; Ace Inhibitors: Other; Contrast Dye [Ivp Dye, Iodine Containing] NSAIDS
Vorherige Impfungen: -

VAERS 2430996

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 86,0
Geschlecht: M
Eingang: 07.09.2022
Impfdatum: 13.03.2021
Beginn: 03.08.2022
Tage bis Beginn: 508,0
Dosis: 3
Route/Site: - / -

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

Angiogram pulmonary abnormal Asthenia Atelectasis B-cell small lymphocytic lymphoma COVID-19 Chest X-ray abnormal Chronic lymphocytic leukaemia Cough Dyspnoea Infection Lung consolidation Lung infiltration Neutropenia Neutrophil count decreased Pyrexia SARS-CoV-2 test positive

Symptomtext

87y.o. male known to our office for management of CLL/SLL who completed 6 cycles of RminiCHOP on 7/27/2022. Pt was admitted to hospital on 8/3/2022 for SOB, cough, and subjective fevers. Pt was found to be covid19 positive in the ED. CXR with infiltrate vs atelectasis in right midlung and bilateral bases. CTA Chest PE protocol 8/4 negative for PE, showed multifocal areas of consolidation. Pt was started on empiric vanoc/cefepime on admit. ID and pulmonology were consulted. Vanco stopped. Pt remained on Cefepime x 7 days total, completed on 8/10/22. Pt was also treated with remdesivir 8/5/2022-8/8/22, and started on Decadon 6mg daily x 10 days. Pt will complete last two days as OP, course will complete on 8/13/22. Pt will also remain on PPI ppx x 1 week at discharge. Pt was neutropenic on admit. He received Neulasta on 7/27/2022, Granix started on admission due to persistent neutropenia and acute infection. Discontinued Granix 8/5 given ANC >1.0. Patient was able to be weaned back to room air on 8/11/22. PT/OT evaluated patient and recommended SAR at discharge. Patient's wife was very adamant that patient was discharged home with home care. Patient became very weak during hospitalization and requires two person assist to stand. His wife remained insistent patient be discharged to her care. Exception made to have wife come to hospital while patient in isolation so she was able to visualize patient and better understand recommendations for SAR. Wife submitted written documentation that she understands the risks of being patient home and prefers patient be discharged to her care with home care. Patient has two son's that are also available to help patient as needed. After long deliberation with patient's wife, will agreed to have patient discharged with home skilled nursing, PT, and OT. Patient's wife is an RN and was well educated on the risk she is taking on by bringing patient home. Patient will follow up in our office in 2 weeks after he is cleared from COVID 19 isolation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 7,0
Labordaten: 8/3 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2420998

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 66,0
Geschlecht: M
Eingang: 26.08.2022
Impfdatum: 04.05.2021
Beginn: 21.08.2022
Tage bis Beginn: 474,0
Dosis: 1
Route/Site: IM / UN

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

Body temperature increased COVID-19 Chest pain Dyspnoea Fatigue SARS-CoV-2 test positive Tachycardia

Symptomtext

Pt to ED 8/21 for fatigue x3 days. Pt tachy in triage at 115 with low grade temp. Pt reporting intermittent CP/shortness of breath. COVID+ 8/21. 8/23 bed without any gait disturbances. Pt denies any CP, nausea, vomitng and SOB. Pt discharged 8/23.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: Gastroesophageal reflux disease ... Gastroesophageal reflux disease Chronic idiopathic constipation Weight loss Hematochezia Abdominal bloating General weakness
Andere Medikamente: Acetaminophen 500 MG PO Cap ... Acetaminophen 500 MG PO Cap Alendronate Sodium 70 MG PO Effer Tab aspirin 81 MG PO Chew Tab atorvastatin (LIPITOR) 20 MG PO Tab hydrocortisone (CORTEF) 10 MG PO Tab Levothyroxine Sodium (SYNTHROID PO) lisinop
Allergien: Penicillins
Vorherige Impfungen: -

VAERS 2417740

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: OH
Alter: 16,0
Geschlecht: F
Eingang: 22.08.2022
Impfdatum: 18.05.2021
Beginn: 18.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal pain Abnormal faeces Angiogram Anti-transglutaminase antibody Antinuclear antibody positive Arthralgia Blood immunoglobulin A C-reactive protein normal Choking sensation Cough Diarrhoea Dysphonia Dyspnoea Ear swelling Electrocardiogram normal Endoscopy upper gastrointestinal tract Faecal calprotectin Full blood count normal

Symptomtext

Approximately 8-9 hours after receiving her first Pfizer COVID vaccination (around 9 or 9:30pm on May 18, 2021), the patient developed facial swelling and red, blotchy rashes around the bridge of her nose, between her eyebrows, on the top of her right ear, and on her eyelids. She wanted to see what her symptoms would do so we waited 24 hours from her vaccination time before giving her one dose of Benadryl (50 mg) at 1:30pm on Wednesday May 19. The first dose of Benadryl did help her eyelids appear better. However, by the evening of Wednesday May19, 2021, we noticed a "whistling" sound to her voice when she would try to talk. By Thursday May 20, 2021, she began to struggle some and cough while eating around 3 or 4pm. By 9:30pm that night (5/20/21), she was experiencing a tight/choking feeling in her throat and was having enough trouble breathing that we went to a the Hospital ER. While at the ER, they tried to give her a shot of epinephrine, but unfortunately the epinephrine did not help improve her symptoms of the tight, choking feeling in her throat and the struggle to breath. In the ER, she was advised to take Zyrtec instead of Benadryl because Zyrtec has less side effects. She took her first dose of Zyrtec on Friday May 21, 2021, at 12:30pm. Around 10pm on Saturday May 22, 2021, she noticed decreased swelling in the top of her right ear and bridge of her nose, less of a tight feeling in her throat, and she was having a "louder" more normal sounding voice. By Monday May 24, 2021, her face was back to it normal appearance and her throat was doing better. Yet her throat has never returned to 100% since her first COVID vaccination. Beyond that, this event has seemed to initiate a wave of issues and symptoms that continue to this day. We began with the allergy clinic and saw a doctor after receiving the COVID vaccination. The doctor referred us to the GI clinic where we saw another doctor. That doctor ordered an esophagram to determine if any reflux or long-term damage of the patient's esophagus was evident, but a cricopharyngeal bar was discovered through this procedure. The doctor referred us to the ENT clinic where we met with another doctor. That doctor performed a FEES exam in her office and noted that she witnessed food getting stuck in the patient's throat and lateral sidewall squeezing with swallowing. On August 13, 2021, the patient had surgery at the Hospital that included a botox injection by ENT for her cricopharyngeal bar and an upper endoscopy for GI. In November 2021, she began to experience abdominal pain, loose stools, and occasional oily residue in her stool. In January 2022, she has begun to have daily headaches which cause her to be sensitive to light. We made an appointment with her regular optometrist, she ruled out any eye issues as being the cause for the patient's headaches. In April 2022, the patient has begun to have join pain and swelling particularly in her knees and hands. She has had bright red patches appear on her knees that are warm to the touch and the back bend of her knees appears swollen. Her hand joints can feel stiff and sore to her at times and have developed small bumps at the knuckles. She will occasionally now struggle with mouth sores as well. For her headaches, we were sent to the Neurology clinic. For her joint issues, we were seen by the Rheumatology clinic. We have also had a virtual appointment with the Psychology department to help the patient find coping mechanisms for the pain. We have had ongoing tests and lab work as detailed below. At this point, we believe that rheumatology is considering the patient to have fibromyalgia as they have allowed her to join a study for patients dealing with fibromyalgia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: June 2021: lab work for Hospital Allergy clinic. Labs normal other than slightly low WBC Esophagram June 15, 2021: cricopharyngeal bar At the advice of allergy clinic received her second dose of Pfizer COVID vaccine on 6-16-21 Lot EW0183 Surgery: Botox injection with ENT for cricopharyngeal bar and Upper endoscopy with GI clinic on August 13, 2021 Labs for GI Clinic January 4, 2022: IGA and tissue transglutaminase AB IGA. Both normal Labs for GI Clinic January 6, 2022: Calprotectin (fecal). Normal Third booster for Pfizer Covid 1-10-22 Lot FJ1611 Labs for pediatrician April 5, 2022: CBC, comprehensive metabolic panel, C-reative protein, sedimentation rate, thyroid profile, ANA. All normal, ANA positive at 40 EKG for NCH Neurology May 24, 2022: Normal MRI Head angiography without contrast and MRI Head without contrast for Neurology June 23, 2022: Both normal
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: OTC multivitamin Doxycycline Hyclate 50 mg Low-Ogestrel 28 tablet
Allergien: Varicella vaccine
Vorherige Impfungen: Varicella vaccine reaction at 12 months of age on November 1, 2005. The patient became extremely swollen in her face to the poi

VAERS 2414666

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MA
Alter: 28,0
Geschlecht: M
Eingang: 18.08.2022
Impfdatum: 05.05.2021
Beginn: 06.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Fatigue Injection site pain Rash

Symptomtext

Moderate to severe chest pain for 3 days after injection. Chest rash for 3 days after injection. Injection site pain for 2 days after injection. Severe fatigue for 3 days after injection.

Weitere VAERSDATA-Felder

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

VAERS 2393230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: IA
Alter: 39,0
Geschlecht: F
Eingang: 27.07.2022
Impfdatum: 15.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: UN / UN

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

Abdominal distension Abdominal pain upper Allergy test Anxiety Blood test Cold sweat Cortisol increased Decreased appetite Disturbance in attention Dizziness Fatigue Feeling abnormal Gastrointestinal disorder Gastrooesophageal reflux disease Gingival swelling Headache Hot flush Hyperhidrosis

Symptomtext

Acid Reflux. Chronic Fatique. Dizzy. Headache. Hot Flashes. Loss of Appetite. Aniexty. Memory Problems. Muscle cramps. Nauseous. Sweaty/clamy hands. Swollen gums - mouth raw. Bloating. Stomach & upper right quadrant pain. Blurred vision - trouble focusing. Hand Tremors. Bowel-GI trouble Brain Fog - trouble concentrating Fatique.High Cortisol/Edgy. Frequent Falling asleep in office/car/at table.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: 2021-2022 I've had way too many Blood tests, scans, tests to recollect. 9/13/21 Celiac Disease Comp. Food Allergy Blood Test. My doctors have all that on file.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Zryetc, Flonase. Benedryl As needed
Allergien: Eggs, Reglan
Vorherige Impfungen: -

VAERS 1832139

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 26.07.2022
Impfdatum: 04.01.2021
Beginn: 06.05.2021
Tage bis Beginn: 122,0
Dosis: 3
Route/Site: - / -

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

Chest discomfort Cough Dyspnoea COVID-19 SARS-CoV-2 test positive

Symptomtext

PMhx of moderate persistent asthma, Hx of provoked DVT 10 yrs ago was admitted for worsening dyspnea, cough and chest heaviness over last wk

Weitere VAERSDATA-Felder

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

VAERS 1832139

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 26.07.2022
Impfdatum: 04.01.2021
Beginn: 06.05.2021
Tage bis Beginn: 122,0
Dosis: UNK
Route/Site: - / -

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

Chest discomfort Cough Dyspnoea COVID-19 SARS-CoV-2 test positive

Symptomtext

PMhx of moderate persistent asthma, Hx of provoked DVT 10 yrs ago was admitted for worsening dyspnea, cough and chest heaviness over last wk

Weitere VAERSDATA-Felder

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

VAERS 2357623

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 31,0
Geschlecht: F
Eingang: 05.07.2022
Impfdatum: 11.05.2021
Beginn: 11.05.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chest X-ray normal Dyspnoea Electrocardiogram abnormal Feeling jittery Nervousness Pharyngeal paraesthesia Sinus tachycardia Visual impairment

Symptomtext

Presents to ED after reaction to Covid vaccine. Patient states she received her injection and was waiting up between 5 to 10 minutes after the injection. She acutely felt tingling in her throat short of breath and describes "wave of purple halos around lights". She had 2 significant episodes of this and was provided epinephrine injection at the vaccine facility and sent to ED for further evaluation. She is still feeling extremely shaky and jittery and is complaining of mild dyspnea. Patient provided Benadryl, fluids, Pepcid. Chest x-ray is unremarkable and EKG is sinus tachycardia. Patient observed for several hours without recurrence or worsening of symptoms. Patient stable for discharge home and close follow-up with PCP in the next 1 to 2 days. Patient discharged with steroids, Benadryl and EpiPen and counseled regarding biphasic reaction precautions. Treating physician was (withheld).

Weitere VAERSDATA-Felder

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

VAERS 2338849

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: NJ
Alter: 68,0
Geschlecht: F
Eingang: 28.06.2022
Impfdatum: 11.05.2021
Beginn: 01.06.2021
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: SYR / LA

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

Arthralgia Grip strength decreased Hypoaesthesia Joint swelling Mobility decreased Paraesthesia Peripheral swelling Swelling

Symptomtext

Symptoms started in June, slowly worsening, and continued until Booster in January. I had swollen fingers and wrists, pain in the fingers, and went to the doctor on October about it. She thought maybe Rheumatoid Arthritis but comprehensive blood test came back "perfect" and with no RA. This continued until my BOOSTER on 01/12/2022, Pfizer-BioNTech Lot FJ6369, when all of the previous symptoms quickly escalated into very restricted finger movements,tingling, exteme swelling, numbness, loss of hand strength, and barely able to bend fingers. Then it also caused swelling of area around the knees and knee joint pain, swelling of feeet/ankles/toes and ankle joint pain, and now near elbows too. It is the end of June 2022 and I still have all of these issues - and I was in PERFECT HEALTH prior to two vaccines and booster - pain free walking five miles a day. (First vaccine 04/20/2021 at 4:40 PM Pfizer-BioNTech Lot EW0172)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Bloodwork Oct. 2021
Aktuelle Erkrankungen: None
Vorgeschichte: None. I was in great shape and good health, exercising and walking daily
Andere Medikamente: Levothyroxine 25mg and Restasis eyedrops
Allergien: Penicillin allergy, and sensitivity to: cow dairy products, soy, gluten
Vorherige Impfungen: -

VAERS 2328822

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 37,0
Geschlecht: F
Eingang: 23.06.2022
Impfdatum: 17.06.2021
Beginn: 12.06.2022
Tage bis Beginn: 360,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

6/12 38y.o. female presented with sob

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 6/12 Sars-Cov-2.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2319038

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 19,0
Geschlecht: M
Eingang: 14.06.2022
Impfdatum: 04.05.2021
Beginn: 22.05.2022
Tage bis Beginn: 383,0
Dosis: 1
Route/Site: - / -

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

Cough Dyspnoea SARS-CoV-2 test negative

Symptomtext

5/23 20y.o. male with history of asthma (intubation x4), eosinophilic esophagitis, lumbar laminectomy, obesity, HTN, bipolar disorder who presents for cough and dyspnea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 5/22 SARS-CoV-2 by NAA, Not Detected 5/23 SARS-CoV-2 by NAA, Detected 5/25 SARS-CoV-2 by NAA, Not Detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2310580

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: OR
Alter: 36,0
Geschlecht: F
Eingang: 06.06.2022
Impfdatum: 05.05.2021
Beginn: 05.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Chills Dehydration Fatigue Feeling cold Feeling hot Hyperhidrosis Mobility decreased Pain Pyrexia

Symptomtext

I had the normal symptoms like they said to expect, I had body aches, chills, fever, I would get really hot and would sweat, and then I would got freezing cold. Then the next day my fever kept rising and it was up to 103.4, and it would not go down with any medicine that I was taking. I was very fatigue during this time and felt like I could not move. I called my Dr. and she advised that I was very dehydrated and that I needed to take sips of water, or Gatorade, or other fluids to help keep myself hydrated. She also advised to take certain amounts of Tylenol for up to an hour and if it did not go down then I would have to go to the emergency room, It began to finally drop to 103.0 then slowly to 100.00, I was just very very tired and fatigue. My first dose was very hard as well I just did not need to go the the Dr. for that one.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Prenatal Vitamin, Pro-Biotic, Magnesium, Sertraline
Allergien: Shellfish, Mold, Latex
Vorherige Impfungen: -

VAERS 2301573

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: ME
Alter: 25,0
Geschlecht: M
Eingang: 29.05.2022
Impfdatum: 23.04.2021
Beginn: 01.07.2021
Tage bis Beginn: 69,0
Dosis: UNK
Route/Site: SYR / LA

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

Antinuclear antibody Blood immunoglobulin G Blood iron Disturbance in attention Inflammation Iron binding capacity total Memory impairment Mobility decreased Mood altered Morose Muscle rigidity Pica Transferrin saturation decreased

Symptomtext

Within weeks my special needs son started having memory issues and concentration issues. He went from a vibrant, social, young man to a sullen, moody individual who couldn't get out of bed. He then started having pica issues that increased as time went on. It wasn't until psychiatric hospitalizations with no improvement led me to insist that his iron levels be taken because of the pica. It was found that his iron number were off. He also became very rigid and displayed full body inflammation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: 22,0
Labordaten: Iron 50 ug/dL Iron Binding Capacity 416 ug/dL H Percent Saturation 12 % L General Information Ordered by DO Collected on 02/21/2022 3:46 PM (Blood) Resulted on 02/22/2022 7:46 PM RNP Ab IgG 2.7 U U H Ordered by MD Collected on 04/04/2022 8:06 AM Resulted on 04/06/2022 4:28 PM
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Escitalopram, clonidine
Allergien: Allergy to tetanus shot
Vorherige Impfungen: Tetanus

VAERS 2298690

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: OH
Alter: 47,0
Geschlecht: F
Eingang: 27.05.2022
Impfdatum: 20.05.2021
Beginn: 01.05.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: SYR / AR

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

Abdominal discomfort Asthma Fatigue Feeling cold Paraesthesia Pyrexia Rash Urticaria Vaccination site pain

Symptomtext

Three weeks after my vaccination, I had fever, chills, upset stomach, and tingling sensation all over my body. I had pain in my arm where I had the vaccination. I had overwhelming fatigue for a few days after the other symptoms subsided. I cannot recall if I had lost my sense of taste and smell; but I did have COVID-19 prior to the vaccination being available. I was diagnosed with Asthma after the vaccination, but I am not sure if it is related. I also developed a rash, I had hives all over my body. I was prescribed prednisone and referred to an Allergist. Now, I get hives on my left foot and left arm. I did not have allergies prior to the vaccination. I do plan on receiving the third shot, as recommended by my Physician, once my allergies and Asthma are under control.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: Grapeseed extract; vitamin D; ibuprofen
Allergien: Cephalexin
Vorherige Impfungen: -

VAERS 2294353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 23,0
Geschlecht: U
Eingang: 25.05.2022
Impfdatum: 15.04.2021
Beginn: 20.05.2022
Tage bis Beginn: 400,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Palpitations SARS-CoV-2 test positive

Symptomtext

5/20 24y.o. adult with a medical history significant for obesity, obstructive sleep apnea, hypertension, gestational diabetes, factor V leiden mutation, bipolar disorder, SVT, tobacco abuse, who presented to Hospital on 5/20/2022 from home with a chief complaint of palpitations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: 1,0
Labordaten: 5/20 SARS-CoV-2 Detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2290479

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: NJ
Alter: 55,0
Geschlecht: M
Eingang: 23.05.2022
Impfdatum: 17.05.2021
Beginn: 01.07.2021
Tage bis Beginn: 45,0
Dosis: 2
Route/Site: SYR / RA

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

Blood test Hypertension Magnetic resonance imaging Neuralgia

Symptomtext

Starting in 01/2022 I have had high blood pressure. I never had it before getting the vaccine. My doctor prescribed me valsartan 80mg. It has been keeping me under control so far. Also, more recently I am having severe sciatic nerve pain again in my entire right leg. It has lasted about 7 weeks. I am in physical therapy but the pain is still pretty bad. This pain started in the summer of 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Leg MRI 07/30/2022 and 04/19/2022. Multiple rounds of blood work.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multivitamin; Bayer aspirin; Lipitor; zinc; vitamin C; vitamin D; vitamin B; alprazolam as needed
Allergien: Penicillin; shellfish
Vorherige Impfungen: Pfizer dose 1 (04/28/2021) my blood pressure dropped right after the vaccine and I almost passed out. I was given orange juice a

VAERS 2287054

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: IL
Alter: 37,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 18.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal distension Abdominal pain Alopecia Blood test Computerised tomogram Cyanosis Diabetes mellitus Diarrhoea Diplopia Dizziness Fatigue Feeling abnormal Gait disturbance Headache Heart rate increased Hypertension Hypoaesthesia Hypotonia

Symptomtext

I had a lot of fatigue and numbness in the leg, I couldn't hardly walk, my nose and arms. I couldn't even sleep, from my neck into my back. I had a really bad headache. I have a lot of cramping in my gut. I felt swollen, bloating and I had Tinnitus in both ears along with dizziness. I had brain fog, high blood pressure an high heart rate for about 3 weeks. I had diarrhea, vomiting, I had double vision with the left eye and slow vision in both eyes. I had tingling all over my body, it not as worse now. My muscles is very loose. Even in my throat was hurting, my feet got swollen and turned blue. I even had a rash on my arms, chest and abdomen. I am still having these issue. I am even experiencing hair lost.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Blood Panel; Thyroid; Diabetes; CT Scan; MRI; Eye exam
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Magnesium and Vitamin D
Allergien: No
Vorherige Impfungen: -

VAERS 2283151

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

moderat

Staat: FL
Alter: 63,0
Geschlecht: F
Eingang: 18.05.2022
Impfdatum: 02.07.2021
Beginn: 13.05.2022
Tage bis Beginn: 315,0
Dosis: UNK
Route/Site: - / -

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

Chest pain Dyspnoea

Symptomtext

presented to the ed with chest pain and shortnes of breath

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Copd osteo arthritis right lung cancer radiation
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2278852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MN
Alter: 65,0
Geschlecht: F
Eingang: 16.05.2022
Impfdatum: 11.05.2021
Beginn: 12.01.2022
Tage bis Beginn: 246,0
Dosis: 2
Route/Site: SYR / AR

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

Blood calcium increased Cataract Hypertension Ultrasound kidney Ultrasound thyroid Urine calcium increased Vomiting

Symptomtext

Starting early January of 2022, I developed 2 days of explosive vomiting resolved by fluid and bed rest. Next episode, 02/13/2022 2 days of explosive vomiting resolved by drinking fluids, bed rest and the "BRAT" diet. 03/09/2022: I was seen for high calcium in blood and urine labs, and high blood pressure. Resolution still pending as I am undergoing more tests. 04/12/2022: seen for cataract evaluation, unresolved and more exams pending. 05/02/2022: Seen by endocrinology again for high blood pressure and calcium in urine, more tests pending. 05/04/2022: prescribed amlodipine for high blood pressure. 05/16/2022: underwent tests for high calcium levels and possibly due to a thyroid condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Numerous urine and blood tests for calcium levels, ultrasound of kidneys, nuclear scan of thyroid area, ultrasound of thyroid.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes type II; Depression
Andere Medikamente: Metformin ER 500mg 4 per day; women's 50+ multivitamin daily; levothyroxine 75mcg daily; atorvastatin 40mg daily; baby aspirin 81mg daily; sertraline 100mg daily and calcium citrate 630mg + D3 daily
Allergien: None
Vorherige Impfungen: -

VAERS 2278544

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 32,0
Geschlecht: M
Eingang: 16.05.2022
Impfdatum: 15.05.2021
Beginn: 16.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Anxiety Inappropriate schedule of product administration Inflammation Loss of personal independence in daily activities Mobility decreased Pain Posture abnormal Sensory disturbance

Symptomtext

I got the second shot and I waited the recommended 15 minutes. I felt a sensation of what I thought may be an onset of a back spasm, but it didn't go any further so I attributed it to anxiety over the vaccine itself. When I returned home, I was doing some things around the house when the pain really started to set in, around 3-4 hours later. By the next morning, it had gotten to the point where I could hardly move without pain. I had to move around hunched over and could really only lay on the couch. I went to my doctor who refilled my prescription for 5 mg cyclobenzaprine (1 tablet twice daily.) He also advised that I could take ibuprofen for inflammation. It took the rest of the week before I was able to return to normal activity.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Torn Meniscus
Andere Medikamente: None
Allergien: Prednisone; certain dairy products
Vorherige Impfungen: -

VAERS 2271086

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 56,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 20.04.2021
Beginn: 07.02.2022
Tage bis Beginn: 293,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Chest pain Dyspnoea

Symptomtext

02/07/22 presents to ED for "covid infection that was discovered 1-27 -22 with worsening shortness of breath and chest pain". PMHx of "ILD, multisystem sarcoidosis, PBC, DM2, GERD, and glaucoma"

Weitere VAERSDATA-Felder

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

VAERS 2270882

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 17,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 09.05.2021
Beginn: 08.05.2022
Tage bis Beginn: 364,0
Dosis: 2
Route/Site: SYR / LA

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

COVID-19 Chills Cough Decreased appetite Oropharyngeal pain Pain Paraesthesia Productive cough Pyrexia SARS-CoV-2 test positive Skin discomfort Tremor Vaccine breakthrough infection

Symptomtext

Breakthrough case of COVID-19: She had a fever of 101.1, body aches, shaking, chills, and felt like pins and needles were poking her body. She did not have an appetite, coughing, sore throat, and coughing up phlegm. She was prescribed benzonatate 200mg and Flonase.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: COVID-19 test positive.
Aktuelle Erkrankungen: No
Vorgeschichte: Seizures; ADHD; obesity; prediabetic; mood disorder.
Andere Medikamente: Prozac 10mg; Briviact 25mg; Lamictal 50mg; melatonin 5mg; Zyrtec 10mg; vitamin D 25mg; Benadryl 25mg; Larin-24; multivitamin.
Allergien: No
Vorherige Impfungen: -

VAERS 2270866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 37,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 21.04.2021
Beginn: 16.02.2022
Tage bis Beginn: 301,0
Dosis: UNK
Route/Site: - / -

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

Acute kidney injury COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

02/16/22 presents to ED for "AKI and shortness of breath". PMHx of "IgA nephropathy s/p renal transplant, HTN, and hypothyroidism"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 02/17/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2270809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 27.04.2021
Beginn: 23.02.2022
Tage bis Beginn: 302,0
Dosis: UNK
Route/Site: - / -

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

Haemodialysis Hypotension

Symptomtext

02/23/22 presents as transfer "from her LTAC due to hypotension during hemodilaysis". PMHx of "ESRD (Started dialysis on 11/10/21), obesity, CHF, chronic afib (on eliquis), TIIDM, and HTN"

Weitere VAERSDATA-Felder

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

VAERS 2269073

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: CA
Alter: 42,0
Geschlecht: M
Eingang: 10.05.2022
Impfdatum: 06.05.2021
Beginn: 01.01.2022
Tage bis Beginn: 240,0
Dosis: 2
Route/Site: SYR / RA

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

Asthma exercise induced Blood test Condition aggravated Dyspnoea Headache Laboratory test normal Magnetic resonance imaging Nasal congestion Pain Pyrexia

Symptomtext

It started around Jan/2022. I started going back to the gym. I participate in a exercise program. I noticed that I would get a headache in the back lower part of head. It would happen even after less intense workouts. My doctor ran some test given my heart condition. They came back normal. She thinks it might exercise induced asthma. I was given an inhaler and when I use it during exercise it goes away. I had COVID-19 as well in Jan/2022. The symptoms started and stayed mild the whole time. I didn't consider it as much more than a cold. I had a stuffy nose, body aches, mild fever, trouble breathing. The symptoms lasted for about a week, but they did start to dissipate as time went on.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: MRI Blood Test
Aktuelle Erkrankungen: None
Vorgeschichte: Congenital corrected transposition of the greater vessel in heart
Andere Medikamente: Acyclovir Levothyroxine Calcitriol Calcium Carbonate Escitalopram
Allergien: None
Vorherige Impfungen: -

VAERS 2268782

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 62,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 21.04.2021
Beginn: 11.03.2022
Tage bis Beginn: 324,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

03/11/22 presents to ED for "Shortness of breath". PMHx of "htn, hypothyroidism, breast cancer recurrence and metastasis".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 03/11/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267427

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: OH
Alter: 42,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 04.05.2021
Beginn: 08.11.2021
Tage bis Beginn: 188,0
Dosis: 2
Route/Site: SYR / RA

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

COVID-19 Dyspnoea Malaise Mobility decreased Oropharyngeal pain Parosmia Pyrexia Rash SARS-CoV-2 test positive

Symptomtext

After the vaccine by May 7th, I had a rash from my collar bone to my belly button and all over my back as well, I also had a fever. On Nov 6th, I started to have symptoms of COVID-19 with a minor sore throat, and the next day I almost vomited because of the smells I was smelling and tested positive on Nov. 8, 2021. On the 9th, I received the anti-bodies and I started feeling better, I had a fever of about 101 for about 5 days, and I chills and body aches. I was having a lot of fatigue for at least 13 days, I was also in quarantine for 13 days, COVID-19 and shortness of breathe for up to six weeks after COVID-19. I could not do my normal duties. I tried to get an inhaled steroid from my Dr. but it took a while for me to receive it. The first inhaler given did not work Nov 19 it was albuterol but it did not help, and then a different Dr. prescribed Flovent on Dec 16, I used that for a few weeks and the shortness of breath started to get better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypermobility Spectrum Disorder Dysautonomia Raynaud's Syndrome
Andere Medikamente: Cetirizine 10 mg 2x daily Norvasc 5mg 1x daily Glycopyrrolate 1mg 1x daily Naltrexone 4.5mg 1x daily Baclofen 10mg 2x daily Cimetidine 400mg 1x daily Fish oil 300 mg 2x daily Vitamin D 1000mg 2xdaily Turmeric 2 tablets 2x daily Natural D-Hi
Allergien: N/A
Vorherige Impfungen: Rash for the Flu Vaccine

VAERS 2267410

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 54,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 11.10.2021
Beginn: 08.05.2022
Tage bis Beginn: 209,0
Dosis: 3
Route/Site: IM / -

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

COVID-19 COVID-19 pneumonia SARS-CoV-2 test positive

Symptomtext

covid pneumonia 5/8/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: SARS cov 2 by PCR positive on 5/8/22
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension and chronic myeloid leukemia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267110

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: OH
Alter: 44,0
Geschlecht: F
Eingang: 08.05.2022
Impfdatum: 21.05.2021
Beginn: 22.05.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Chest pain Echocardiogram Electrocardiogram ambulatory Injection site pain Musculoskeletal pain Palpitations

Symptomtext

Stabbing Chest Pain (Ice Pick like) in my heart, Over all Chest Pain - had to put a warm compress on my chest for many days. Severe heart palpitations that were painful. Pain in left shoulder and shoulder blade. All of this occurred off and on for about 6 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: ER visit on 5/24/21. Echo cardiogram 6/11/2021. Wore a heart monitor to check my heart beats - 5 days - 6/1 - 6/6. I am still being monitored and may need a cardia MRI as I continue to have symptoms off and on.
Aktuelle Erkrankungen: None
Vorgeschichte: Lyme Disease
Andere Medikamente: IC Progesterone 200mg, Magnesium Taurate - 100mg, Primrose Oil Metagenics SPM, Acetyl L Carnitine, Vitamin C Crystals, Vitamin D3 - 2000IU, Ox Bile - 500mg, Meriva, Tudca, Liposomal Glutathione, Gallbladder Nutrients, Supreme Binder, Axis E
Allergien: None
Vorherige Impfungen: -

VAERS 2263354

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 33,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 06.05.2021
Beginn: 27.04.2022
Tage bis Beginn: 356,0
Dosis: 2
Route/Site: - / -

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

Abdominal pain Chest X-ray normal Chest pain Chills Cough Dizziness Electrocardiogram normal Headache Nausea Occupational exposure to SARS-CoV-2 Pain Pyrexia Respiratory tract congestion Vomiting

Symptomtext

Patient is fully vaccinated. 34-year-old female with no significant past medical history who presents with complaints of body aches, chest pain, generalized abdominal pain, fever/chills, nausea/vomiting, headaches, dizziness, cough, and congestion that started about 3 days ago. Patient states that her coworker tested positive for COVID and she was exposed to him on 4 days ago. BP 115/68 | Pulse 58 | Temp 98.4 ?F (36.9 ?C) (Oral) | Resp 16 | Ht 157.5 cm (5' 2") | Wt 68 kg (150 lb) | SpO2 97% chest x ray: No acute intrathoracic process. EKG normal sinus rhythm. Started patient on a 1 L bolus of fluids and Toradol for pain.Gave her a dose of Norco. Discharged home.

Weitere VAERSDATA-Felder

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

VAERS 2260246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: UT
Alter: 16,0
Geschlecht: M
Eingang: 02.05.2022
Impfdatum: 01.05.2021
Beginn: 01.09.2021
Tage bis Beginn: 123,0
Dosis: 2
Route/Site: IM / -

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

Abdominal discomfort Ageusia Anosmia COVID-19 Chest discomfort Chest pain Cough Diarrhoea Dyspnoea Fatigue Hypogeusia Malaise Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Patient contracted COVID-19 with symptoms of body aches, fever, cough, loss of taste and smell, diarrhea, stomach upset, chest pain/tightness, shortness of breathe, fatigue, and was ill for 7 days. His loss of taste and smell has not fully returned, he can taste some items but has not fully recovered those senses.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: COVID-19 Rapid nasal swab and PCR were both positive.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2254672

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: TX
Alter: 52,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 30.04.2021
Beginn: 01.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test Dizziness Electrocardiogram Fatigue Headache Pain Pain in extremity Palpitations Swelling Ultrasound scan

Symptomtext

I was just tired, I think my legs ached and heart racing. My head also felt dizzy. I also had swelling and pain and a headache. After the 3rd shot, the heart palpitations became concerning. I had an EKG and sonogram performed and wore a heart monitor for 7 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Blood work for follow up on diabetes; EKG and ECG; Sonogram
Aktuelle Erkrankungen: None
Vorgeschichte: Pre diabetic
Andere Medikamente: Dexilant Zetia Ozempic
Allergien: None
Vorherige Impfungen: -

VAERS 2252336

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MN
Alter: 59,0
Geschlecht: M
Eingang: 26.04.2022
Impfdatum: 21.04.2021
Beginn: 19.04.2022
Tage bis Beginn: 363,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Dyspnoea Hypoxia SARS-CoV-2 test positive

Symptomtext

SOB, AND HYPOXIA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: POSITIVE COVID TEST 4/19/2022
Aktuelle Erkrankungen: -
Vorgeschichte: COPD (chronic obstructive pulmonary disease) (HCC
Andere Medikamente: dexAMETHasone (DECADRON) tablet 6 mg (6 mg oral Given 4/25/22 1001) POTASSIUM REPLACEMENT ORAL - NOT FOR DOCUMENTATION PURPOSES (has no administration in time range) POTASSIUM REPLACEMENT INTRAVENOUS - NOT FOR DOCUMENTATION PURPOSES (has no
Allergien: -
Vorherige Impfungen: -

VAERS 2243187

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 99,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 13.04.2021
Beginn: 04.07.2021
Tage bis Beginn: 82,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Cough Dyspnoea Fatigue SARS-CoV-2 test positive

Symptomtext

7/4/21 hx of PE in past, hx of gastric ulcer not on AC, hx of CHF presented with chief c.o cough, SOB and fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 7/4/21 SARS-CoV-2 (COVID-19) by NAA Detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2220295

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 90,0
Geschlecht: F
Eingang: 07.04.2022
Impfdatum: 30.09.2021
Beginn: 03.01.2022
Tage bis Beginn: 95,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cyanosis Dyspnoea Gait disturbance Oxygen saturation decreased SARS-CoV-2 test positive

Symptomtext

Starting in Jan she started to have a hard time walking and breathing from COVID. I noticed when I went over there that her feet were blue. I took her to the ER and her O2 was at 82. They put her on oxygen and tested her for COVID. They put her on an inhaler which has helped and a walker.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Diarrhea problem
Andere Medikamente: Prilosec, Eliquis, Metoprolol Tartrate, Magnesium Oxide, Multivitamin, Iron
Allergien: None
Vorherige Impfungen: -

VAERS 2214192

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 60,0
Geschlecht: M
Eingang: 04.04.2022
Impfdatum: 10.04.2021
Beginn: 25.01.2022
Tage bis Beginn: 290,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

01/25/22 presents to ED for "cough and shortness of breath". PMHx of "Non insulin dependent type 2 diabetes, HTN, Dyslipidemia"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 01/25/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2214173

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 04.04.2022
Impfdatum: 23.04.2021
Beginn: 18.01.2022
Tage bis Beginn: 270,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

01/18/22 presents to EC ED for "SOB". PMHx of "recent MI and CABG"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 01/18/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2214164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 04.04.2022
Impfdatum: 17.05.2021
Beginn: 22.01.2022
Tage bis Beginn: 250,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Chest pain Dizziness Dyspnoea SARS-CoV-2 test positive

Symptomtext

01/22/22 presents to EC ED for "chest pain, SOB, and lightheadedness". PMHx of "hypertension, hyperlipidemia CKD, and BPH"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 01/22/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2198971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 62,0
Geschlecht: F
Eingang: 25.03.2022
Impfdatum: 28.04.2021
Beginn: 07.01.2022
Tage bis Beginn: 254,0
Dosis: UNK
Route/Site: - / -

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

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

Symptomtext

01/07/22 presents to ED for "chest pain". PMHx of "CAD s/p stenting, HTN, HLD"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 01/07/22 SARS-CoV-2 (COVID-19) by regulatory authority detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2196927

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 44,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 24.04.2021
Beginn: 14.01.2022
Tage bis Beginn: 265,0
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 Speech disorder

Symptomtext

01/14/22 presents to ED for "speech problem, chest pain and shortness of breath". PMHx of "GERD, DM, hypertension, hypothyroidism, scoliosis, sleep apnea on C-PAP, bipolar disorder, ADHD, depression, and anxiety"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 01/14/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2196379

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 86,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 24.09.2021
Beginn: 21.03.2022
Tage bis Beginn: 178,0
Dosis: 3
Route/Site: IM / -

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

Anion gap Arthralgia Basophil count decreased Basophil percentage decreased Blood bicarbonate normal Blood calcium normal Blood chloride normal Blood creatinine normal Blood glucose normal Blood potassium normal Blood sodium normal Blood urea normal C-reactive protein increased COVID-19 COVID-19 pneumonia Cardiac failure acute Cardiac failure congestive Chest X-ray abnormal

Symptomtext

Hospitalized (3.21.22 - 3.23.22); COVID-19 positive (3.21.22); fully vaccinated PLUS Booster -pfizer x3 D/c Summary:Discharge Summary BRIEF OVERVIEW: Discharge Provider: withheld Primary Care Provider at Discharge: withheld Admission Date: 3/21/2022 Discharge Date: 3/23/2022 Active Hospital Problems Diagnosis Date Noted POA ? COVID-19 virus infection 03/21/2022 Yes ? COPD (chronic obstructive pulmonary disease) 09/24/2015 Yes ? Sarcoidosis- Stage II 03/20/2015 Yes Resolved Hospital Problems Diagnosis Date Noted Date Resolved POA ? Chronic respiratory failure with hypoxia 05/27/2020 03/23/2022 Yes ? Acute on chronic diastolic congestive heart failure Active Issues Requiring Follow-up Issue: COVID-19 infection Recommended follow-up provider/specialty: PCP What is needed: Follow-up to ensure resolution of symptoms DISCHARGE DISPOSITION: Home without services DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: COVID-19 virus infection COVID-19 Acute respiratory disease due to COVID-19 virus HOSPITAL COURSE: Patient is a 86 y.o. female who presents today for COIVD 19 brought in by her daughter. She did not want to come in but her daughter found that she was significantly hypoxic at home and insisted she come in. She has had these symptoms for the last 3 days getting significantly worse in the past 24hours. In the ED she was positive for COVID 19 and persistently hypoxic so she was started on O2 and our service was contacted for admission.. Patient was admitted and started on dexamethasone therapy. Renal function precluded the use of remdesivir. She stabilized and we were able to wean her off supplemental oxygen over the next 2 days. She was able to ambulate without the need for supplemental oxygen on the day of discharge. She was subsequently discharged home to complete a Medrol Dosepak and isolate until 10 days from the 1st day of symptoms. She can then return to activity as tolerated. She is to resume her regular medications as previously ordered. She can return to diet and activity as tolerated. She is recommended to follow up with her primary care provider in the next 10-14 days to ensure complete resolution of her symptoms. She understood all these instructions and was discharged home in stable condition. CONSULTS / RECOMMENDATION: None INPATIENT PROCEDURES: None BP 131/84 | Pulse 93 | Temp 36.6 ?C (Oral) | Resp 18 | Ht 1.549 m | Wt 63 kg | SpO2 96% | BMI 26.24 kg/m? Physical Exam Vitals and nursing note reviewed. Constitutional: General: She is not in acute distress. Appearance: She is well-developed and well-nourished. HENT: Head: Normocephalic and atraumatic. Right Ear: External ear normal. Left Ear: External ear normal. Nose: Nose normal. Mouth/Throat: Mouth: Oropharynx is clear and moist. Mucous membranes are moist. Pharynx: Oropharynx is clear. Eyes: Extraocular Movements: Extraocular movements intact and EOM normal. Conjunctiva/sclera: Conjunctivae normal. Pupils: Pupils are equal, round, and reactive to light. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Pulses: Intact distal pulses. Heart sounds: Normal heart sounds. No murmur heard. Pulmonary: Effort: Pulmonary effort is normal. Breath sounds: Normal breath sounds. Chest: Breasts: No tenderness. Abdominal: General: Bowel sounds are normal. Palpations: Abdomen is soft. Tenderness: There is no guarding or rebound. Hernia: There is no hernia in the right inguinal area. Musculoskeletal: General: Normal range of motion. Cervical back: Normal range of motion and neck supple. Lymphadenopathy: Cervical: No cervical adenopathy. Lower Body: No right inguinal adenopathy. No left inguinal adenopathy. Skin: General: Skin is warm and dry. Findings: No rash. Neurological: Mental Status: She is alert and oriented to person, place, and time. Deep Tendon Reflexes: Reflexes are normal and symmetric. Psychiatric: Mood and Affect: Mood and affect normal. Behavior: Behavior normal. Thought Content: Thought content normal. Judgment: Judgment normal 3/21/22 H&P: CHIEF COMPLAINT: COVID-19 virus infection ASSESSMENT / PLAN: * COVID-19 virus infection Assessment & Plan Patient is an 86-year-old female with past medical history of CHF, chronic obstructive pulmonary disease, sarcoidosis, hypertension, hyperlipidemia who presented to the emergency department with 3 days of worsening shortness of breath especially worse over the past 24 hours. Her daughter was concerned about her breathing and brought for evaluation. The patient states that she would not have sought medical care if her daughter had not insisted she come here. She denies any chest pain, fever, productive cough, leg swelling, numbness, tingling, weakness. Her work up in the ED was positive for COVID 19 pneumonitis. She did not have fever. Her CXR showed bilateral infiltrates. She required 2L nc O2 and I was contacted by the ED staff for admission. We are admitting her for respiratory support, remdesivir and steroid therapy. Chronic respiratory failure with hypoxia Assessment & Plan Patient on 2L as needed at home and requiring 2L continuously now. Acute on chronic diastolic congestive heart failure Assessment & Plan Patient is euvolemic. Will monitor fluid status keeping her overall negative. Will limit Na to 2000mg and fluids to 2000ml. COPD (chronic obstructive pulmonary disease) Assessment & Plan Not currently exacerbated. Will continue inhalers as at home. Steroids for COVID/COPD Sarcoidosis- Stage II Assessment & Plan Stable. Chronic HISTORY OF PRESENT ILLNESS: Patient is a 86 y.o. female who presents today for COIVD 19 brought in by her daughter. She did not want to come in but her daughter found that she was significantly hypoxic at home and insisted she come in. She has had these symptoms for the last 3 days getting significantly worse in the past 24hours. In the ED she was positive for COVID 19 and persistently hypoxic so she was started on O2 and our service was contacted for admission.. Review of Systems Constitutional: Positive for chills and fatigue. Negative for fever and unexpected weight change. HENT: Negative for hearing loss, sore throat and trouble swallowing. Eyes: Negative for pain and visual disturbance. Respiratory: Positive for cough and shortness of breath. Negative for wheezing and sputum production. Cardiovascular: Negative for chest pain, palpitations and leg swelling. Gastrointestinal: Negative for nausea, vomiting, diarrhea, blood in stool and trouble swallowing. Genitourinary: Negative for dysuria, frequency, urgency, vaginal bleeding and vaginal discharge. Musculoskeletal: Positive for joint pain. Negative for muscle pain. Neurological: Negative for headaches, dizziness, light-headedness, speech difficulty, numbness/tingling and weakness. Endo/Heme/Allergy: Negative for adenopathy. Psychiatric/Behavioral: Negative for depression and anxiety. Skin: Negative for itching, rash, wound and breast changes. Breast: Negative for breast changes. OBJECTIVE: BP 101/53 | Pulse 91 | Temp 36.3 ?C (Oral) | Resp 18 | Ht 1.549 m | Wt 63 kg | SpO2 95% | BMI 26.24 kg/m? Physical Exam Vitals and nursing note reviewed. Constitutional: General: She is not in acute distress. Appearance: She is well-developed. Interventions: Nasal cannula in place. HENT: Head: Normocephalic and atraumatic. Right Ear: External ear normal. Left Ear: External ear normal. Nose: Nose normal. Mouth/Throat: Mouth: Mucous membranes are moist. Pharynx: Oropharynx is clear. Eyes: Extraocular Movements: Extraocular movements intact. Conjunctiva/sclera: Conjunctivae normal. Pupils: Pupils are equal, round, and reactive to light. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Heart sounds: Normal heart sounds. No murmur heard. Pulmonary: Effort: Pulmonary effort is normal. Breath sounds: Normal breath sounds. Abdominal: General: Bowel sounds are normal. Palpations: Abdomen is soft. Tenderness: There is no guarding or rebound. Hernia: There is no hernia in the right inguinal area. Musculoskeletal: General: Deformity present. Normal range of motion. Cervical back: Normal range of motion and neck supple. Lymphadenopathy: Cervical: No cervical adenopathy. Skin: General: Skin is warm and dry. Findings: No rash. Neurological: Mental Status: She is alert and oriented to person, place, and time. Deep Tendon Reflexes: Reflexes are normal and symmetric. Psychiatric: Behavior: Behavior normal. Thought Content: Thought content normal. Judgment: Judgment normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 2,0
Labordaten: Basic Metabolic Panel (BMP) Collected: 03/23/22 0419 Order Status: Completed Specimen: Blood, Venous Updated: 03/23/22 0552 Sodium Level 142 134 - 146 mmol/L Potassium Level 3.6 3.4 - 5.0 mmol/L Chloride 105 98 - 112 mmol/L HCO3 27 21 - 29 mmol/L Anion Gap 10 9 - 18 mmol/L Glucose Level 98 70 - 99 mg/dL Blood Urea Nitrogen 17 8 - 20 mg/dL Creatinine 0.51 0.50 - 1.10 mg/dL MDRD eGFR >60 >=60 mL/min/1.73 CG eCrCl 60 mL/min/1.73 m2 Calcium Level Total 9.0 8.6 - 10.4 mg/dL C Reactive Protein (CRP), Blood Level (Abnormal) Collected: 03/23/22 0419 Order Status: Completed Specimen: Blood, Venous Updated: 03/23/22 0552 C-Reactive Protein 25.1 High <=5.0 mg/L D-Dimer [375792447] (Abnormal) Collected: 03/23/22 0419 Order Status: Completed Specimen: Blood, Venous Updated: 03/23/22 0543 D-Dimer Quant 3,290 High 0 - 500 ng/mL FEU Complete Blood Count w/Differential (Abnormal) Collected: 03/23/22 0419 Order Status: Completed Specimen: Blood, Venous Updated: 03/23/22 0530 White Blood Cell 9.06 4.00 - 10.80 x10*3/uL Red Blood Cell 3.97 Low 4.20 - 5.40 x10*6/uL Hemoglobin 12.0 12.0 - 16.0 g/dL Hematocrit 36.9 Low 37.0 - 47.0 % Mean Cell Volume 92.9 80.0 - 100.0 fL Mean Cell Hemoglobin 30.2 27.0 - 33.0 pg Mean Cell Hemoglobin Concentration 32.5 32.0 - 37.0 g/dL Red Cell Diameter Width 14.9 11.0 - 16.0 % NRBC Absolute Count 0.00 0.00 - 0.01 x10*3/uL NRBC Automated 0.0 0.0 - 0.1 %WBC Platelet 263 140 - 400 x10*3/uL Mean Platelet Volume 10.7 7.4 - 11 fL Neutrophil Automated 81.0 High 35.0 - 80.0 % Immature Granulocyte Automated 0.3 0.0 - 0.6 % Lymphocyte Automated 10.9 Low 20.0 - 50.0 % Monocytes Automated 7.5 2.0 - 12.0 % Eosinophil Automated 0.0 0.0 - 6.0 % Basophil Automated 0.3 0.0 - 2.0 % Neutrophil Absolute Count 7.33 1.80 - 7.80 x10*3/uL Immature Granulocyte Absolute Count 0.03 0.00 - 0.05 x10*3/uL Lymphocyte Absolute Count 0.99 Low 1.00 - 4.00 x10*3/uL Monocyte Absolute Count 0.68 0.00 - 0.90 x10*3/uL Eosinophil Absolute Count 0.00 0.00 - 0.50 x10*3/uL Basophil Absolute Count 0.03 0.00 - 0.20 x10*3/uL
Aktuelle Erkrankungen: -
Vorgeschichte: Left-sided weakness 02/02/2022 Unknown ? COVID-19 02/02/2022 Unknown ? Chronic pain 12/15/2021 Unknown ? Macular degeneration 06/29/2021 Unknown ? Osteoporosis 02/25/2021 Unknown ? Abnormal finding on CT scan 02/25/2021 Unknown ? History of diabetes mellitus 12/09/2020 Unknown ? S/P TAVR (transcatheter aortic valve replacement) 03/07/2020 Unknown ? GERD (gastroesophageal reflux disease) 08/20/2019 Unknown ? Diabetic peripheral neuropathy 08/15/2018 Unknown ? Aortic valve sclerosis 03/19/2018 Unknown ? Moderate mitral regurgitation by prior echocardiogram 03/19/2018 Unknown ? Squamous cell skin cancer 10/12/2017 Unknown ? Essential hypertension 11/14/2016 Unknown ? HLD (hyperlipidemia) 11/14/2016 Unknown ? History of CVA (cerebrovascular accident) 08/01/2016 Unknown ? Mediastinal adenopathy 09/24/2015 Unknown ? Depression 09/18/2015 Unknown ? Hypothyroidism 09/18/2015 Unknown ? Actinic keratosis 09/18/2015
Andere Medikamente: Acetaminophen 650 mg Oral Every 6 hours PRN Albuterol Sulfate 2.5 mg Nebulization Every 4 hours PRN, Dx:J44.1-Acute exacerbation of COPD 108 (90 Base) MCG/ACT Aers, 2 puffs Inhalation Every 6 hours PRN Aspirin 81 mg Oral Every morning Atorv
Allergien: demerol - skin rash/hives, nausea & vomiting morphine - skin rash/hives, nausea & vomiting penicillin - skin rash/hives tramadol - skin rash/hives, nausea & vomiting
Vorherige Impfungen: -

VAERS 1540566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 39,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 10.08.2021
Beginn: 10.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Hypersensitivity Hypoaesthesia oral Oral pruritus Paraesthesia Paraesthesia oral SARS-CoV-2 test Throat irritation Throat tightness

Symptomtext

Allergic Reaction; Numbness and tingling of mouth, lips and tongue; tingling of mouth, lips and tongue; Itching in throat; tingling in face; itchy mouth; throat was tight; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 39-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in deltoid left, administration date 10Aug2021 12:20 (Lot number: EW0179) at the age of 39 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Known allergies: Milk containing products" (unspecified if ongoing); "allergies" (ongoing). Concomitant medication(s) included: ALLEGRA taken for hypersensitivity (ongoing); PROZAC; FLEXERIL [CYCLOBENZAPRINE HYDROCHLORIDE]. Past drug history included: Vicodin, reaction(s): "Known allergy: vicodin"; Percocet, reaction(s): "Known allergies: percocet"; Tylenol, reaction(s): "Known allergies: tylenol". Vaccination history included: Pneumonia vaccine, reaction(s): "Known allergies: Pneumonia vaccine". The following information was reported: HYPERSENSITIVITY (medically significant) with onset 10Aug2021 12:40, outcome "recovered" (13Aug2021), described as "Allergic Reaction"; HYPOAESTHESIA ORAL (non-serious) with onset 10Aug2021 12:40, outcome "recovered", described as "Numbness and tingling of mouth, lips and tongue"; PARAESTHESIA ORAL (non-serious) with onset 10Aug2021 12:40, outcome "recovered", described as "tingling of mouth, lips and tongue"; THROAT IRRITATION (non-serious) with onset 10Aug2021 12:40, outcome "recovered", described as "Itching in throat"; PARAESTHESIA (non-serious) with onset 10Aug2021 12:40, outcome "recovered", described as "tingling in face"; ORAL PRURITUS (non-serious) with onset 10Aug2021 12:40, outcome "recovered", described as "itchy mouth"; THROAT TIGHTNESS (non-serious) with onset 10Aug2021 12:40, outcome "recovered", described as "throat was tight". The events "allergic reaction", "numbness and tingling of mouth, lips and tongue", "tingling of mouth, lips and tongue", "itching in throat", "tingling in face", "itchy mouth" and "throat was tight" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test unknown results, notes: Nasal Swab. Therapeutic measures were not taken as a result of hypersensitivity. Therapeutic measures were taken as a result of hypoaesthesia oral, paraesthesia oral, throat irritation with 25 mg of Benadryl x2, continued Benadryl every 4hrs for 3 days per vaccine nurse Instruction. Clinical course: Onset 20 minutes after vaccine administered: Itching in throat for 24 hours. Numbness and tingling of mouth, lips and tongue for 3 days. Developed itchy mouth, tingling in lips, tongue and face, throat was tight. Took 25 mg of Benadryl x2, continued Benadryl every 4hrs for 3 days per vaccine nurse Instruction. Symptoms resolved 72 hrs later. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient not diagnosed with covid-19 prior to vaccination and patient tested for COVID-19 post vaccination. Specific Relevant Test for Thromboembolic Events with Thrombocytopenia reported as none.; Sender's Comments: Based on available information, a possible contributory role of BNT162B2 vaccine cannot be excluded for the reported events due to temporal relationship. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Name: Nasal Swab; Result Unstructured Data: Test Result:Unknown results; Comments: Nasal Swab
Aktuelle Erkrankungen: Allergy
Vorgeschichte: Medical History/Concurrent Conditions: Dairy intolerance
Andere Medikamente: ALLEGRA; PROZAC; FLEXERIL [CYCLOBENZAPRINE HYDROCHLORIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 1540566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 39,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 10.08.2021
Beginn: 10.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Hypersensitivity Hypoaesthesia oral Oral pruritus Paraesthesia Paraesthesia oral SARS-CoV-2 test Throat irritation Throat tightness

Symptomtext

Allergic Reaction; Numbness and tingling of mouth, lips and tongue; tingling of mouth, lips and tongue; Itching in throat; tingling in face; itchy mouth; throat was tight; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 39-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in deltoid left, administration date 10Aug2021 12:20 (Lot number: EW0179) at the age of 39 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Known allergies: Milk containing products" (unspecified if ongoing); "allergies" (ongoing). Concomitant medication(s) included: ALLEGRA taken for hypersensitivity (ongoing); PROZAC; FLEXERIL [CYCLOBENZAPRINE HYDROCHLORIDE]. Past drug history included: Vicodin, reaction(s): "Known allergy: vicodin"; Percocet, reaction(s): "Known allergies: percocet"; Tylenol, reaction(s): "Known allergies: tylenol". Vaccination history included: Pneumonia vaccine, reaction(s): "Known allergies: Pneumonia vaccine". The following information was reported: HYPERSENSITIVITY (medically significant) with onset 10Aug2021 12:40, outcome "recovered" (13Aug2021), described as "Allergic Reaction"; HYPOAESTHESIA ORAL (non-serious) with onset 10Aug2021 12:40, outcome "recovered", described as "Numbness and tingling of mouth, lips and tongue"; PARAESTHESIA ORAL (non-serious) with onset 10Aug2021 12:40, outcome "recovered", described as "tingling of mouth, lips and tongue"; THROAT IRRITATION (non-serious) with onset 10Aug2021 12:40, outcome "recovered", described as "Itching in throat"; PARAESTHESIA (non-serious) with onset 10Aug2021 12:40, outcome "recovered", described as "tingling in face"; ORAL PRURITUS (non-serious) with onset 10Aug2021 12:40, outcome "recovered", described as "itchy mouth"; THROAT TIGHTNESS (non-serious) with onset 10Aug2021 12:40, outcome "recovered", described as "throat was tight". The events "allergic reaction", "numbness and tingling of mouth, lips and tongue", "tingling of mouth, lips and tongue", "itching in throat", "tingling in face", "itchy mouth" and "throat was tight" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test unknown results, notes: Nasal Swab. Therapeutic measures were not taken as a result of hypersensitivity. Therapeutic measures were taken as a result of hypoaesthesia oral, paraesthesia oral, throat irritation with 25 mg of Benadryl x2, continued Benadryl every 4hrs for 3 days per vaccine nurse Instruction. Clinical course: Onset 20 minutes after vaccine administered: Itching in throat for 24 hours. Numbness and tingling of mouth, lips and tongue for 3 days. Developed itchy mouth, tingling in lips, tongue and face, throat was tight. Took 25 mg of Benadryl x2, continued Benadryl every 4hrs for 3 days per vaccine nurse Instruction. Symptoms resolved 72 hrs later. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient not diagnosed with covid-19 prior to vaccination and patient tested for COVID-19 post vaccination. Specific Relevant Test for Thromboembolic Events with Thrombocytopenia reported as none.; Sender's Comments: Based on available information, a possible contributory role of BNT162B2 vaccine cannot be excluded for the reported events due to temporal relationship. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Name: Nasal Swab; Result Unstructured Data: Test Result:Unknown results; Comments: Nasal Swab
Aktuelle Erkrankungen: Allergy
Vorgeschichte: Medical History/Concurrent Conditions: Dairy intolerance
Andere Medikamente: ALLEGRA; PROZAC; FLEXERIL [CYCLOBENZAPRINE HYDROCHLORIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 2181728

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: TX
Alter: 47,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 29.04.2021
Beginn: 29.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Hypoaesthesia Paraesthesia

Symptomtext

they must have hit a nerve or something because she immediately developed numbness and tingling in her fingers for several hours; they must have hit a nerve or something because she immediately developed numbness and tingling in her fingers for several hours; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 48 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 29Apr2021 (Lot number: EW0179) at the age of 47 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Overweight" (unspecified if ongoing), notes: She states she is definitely overweight. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, Vaccine Name: First dose , Lot Number / Expiry Date: EW0162/ Unknown, Route, Anatomical Location: Left arm , No. of Previous Doses: This was dose 1, Date: 07Apr2021), administration date: 07Apr2021, when the patient was 47 years old, for COVID-19 immunization. The following information was reported: PARAESTHESIA (non-serious), HYPOAESTHESIA (non-serious) all with onset 29Apr2021, outcome "recovered" and all described as "they must have hit a nerve or something because she immediately developed numbness and tingling in her fingers for several hours". The event "they must have hit a nerve or something because she immediately developed numbness and tingling in her fingers for several hours" and "they must have hit a nerve or something because she immediately developed numbness and tingling in her fingers for several hours" was evaluated at the emergency room visit. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Overweight (She states she is definitely overweight)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2179408

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: NY
Alter: 35,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 12.08.2021
Beginn: 01.09.2021
Tage bis Beginn: 20,0
Dosis: 2
Route/Site: - / RA

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

Central nervous system lesion Dizziness Fatigue Feeling abnormal Magnetic resonance imaging head Muscular weakness Myalgia Pain Pain in extremity Paraesthesia Tenderness

Symptomtext

Lesions found on MRI on her brain; Dizziness; Exhaustion; Brain fog; Pins and needles; Muscle pain; has aches, tenderness, soreness all over her body; has aches, tenderness, soreness all over her body; she feels like a punching bag; hands hurt, aches, weak in both hands; hands hurt, aches, weak in both hands; stabbing pain in both thumbs; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 35 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 12Aug2021 (Lot number: EW0179) at the age of 35 years as dose 2, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (First Dose, Lot: EW0179, Administered in right arm), administration date: 21Jul2021, when the patient was 35 years old, for Covid-19 Immunization. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 01Sep2021, outcome "recovering", described as "stabbing pain in both thumbs"; MYALGIA (non-serious) with onset 02Sep2021, outcome "not recovered", described as "Muscle pain"; PARAESTHESIA (non-serious) with onset 03Sep2021, outcome "not recovered", described as "Pins and needles"; DIZZINESS (non-serious) with onset 04Sep2021, outcome "not recovered", described as "Dizziness"; FATIGUE (non-serious) with onset 04Sep2021, outcome "not recovered", described as "Exhaustion"; FEELING ABNORMAL (non-serious) with onset 04Sep2021, outcome "not recovered", described as "Brain fog"; CENTRAL NERVOUS SYSTEM LESION (non-serious) with onset 11Oct2021, outcome "not recovered", described as "Lesions found on MRI on her brain"; PAIN IN EXTREMITY (non-serious), MUSCULAR WEAKNESS (non-serious) all with onset 01Sep2021, outcome "recovering" and all described as "hands hurt, aches, weak in both hands"; PAIN (non-serious), TENDERNESS (non-serious) all with onset 02Sep2021, outcome "not recovered" and all described as "has aches, tenderness, soreness all over her body"; FEELING ABNORMAL (non-serious) with onset 02Sep2021, outcome "not recovered", described as "she feels like a punching bag". The events "stabbing pain in both thumbs", "muscle pain", "pins and needles", "dizziness", "exhaustion", "brain fog", "lesions found on mri on her brain", "hands hurt, aches, weak in both hands", "hands hurt, aches, weak in both hands", "has aches, tenderness, soreness all over her body", "has aches, tenderness, soreness all over her body" and "she feels like a punching bag" were evaluated at the physician office visit and emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional Information: Patient got vaccine about 5 months ago but did not report the adverse event then. She is still dealing with the adverse events. They found lesions on her brain on an MRI. She started to have side effects 3 weeks to the day she got the second dose. She got the second dose on 12Aug2021. On the evening of 01Sep2021 she started to have stabbing pain both of her thumbs of her hands. She was in bed. On 01Sep2021 in evening stabbing pain in her both thumbs in hands, bed disregard, woke up morning. Lesions found on MRI on brain: This was like shortly after her attack. Five months since having events she is still experiencing them. They have not all subsided. When she had the MRI, they said it was not demyelinating. At the time they did not believe it was MS, but now since she is still experiencing symptoms it's pointing to that. The MRI was on 11Oct2021. Patient said that she is a mom of three boys and is distraught about this. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20211011; Test Name: MRI brain; Result Unstructured Data: Test Result:lesions on brain
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 2168202

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: TX
Alter: 90,0
Geschlecht: M
Eingang: 09.03.2022
Impfdatum: 14.05.2021
Beginn: 23.08.2021
Tage bis Beginn: 101,0
Dosis: 2
Route/Site: IM / OT

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

COVID-19 pneumonia Hypoxia

Symptomtext

COVID-19 pneumonia with hypoxia: improving, completed remdesivir. Doing well today on day of DC

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2162509

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 64,0
Geschlecht: M
Eingang: 07.03.2022
Impfdatum: 08.10.2021
Beginn: 23.01.2022
Tage bis Beginn: 107,0
Dosis: 3
Route/Site: UN / UN

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

Cough Debridement Dyspnoea Hypoxia Incisional drainage Influenza A virus test negative Influenza B virus test Osteomyelitis acute Oxygen saturation decreased Respiratory syncytial virus test negative SARS-CoV-2 test negative

Symptomtext

Attending Physician: Date of Admission: 1/23/2022 Chief Complaint: Shortness of breath Source of Information: Patient and available chart review History of Present Illness: This is a 64y.o. male with a PMHx of essential hypertension, type II diabetes mellitus, osteomyelitis of LLE, right BKA, PVD, and DVT who presents to the hospital with a chief complaint of shortness of breath and hypoxia. Patient was found to have low SpO2 at his ECF this morning and states he had an acute onset of shortness of breath that started to occur last night. He states his SOB was present at rest. He is currently denying any active chest pain, palpitations, n/v/d, fever, chills, abdominal pain, lower extremity pain, headache, lightheadedness, dizziness. He does admit to a non-productive cough, which started yesterday. Patient was placed on 4L NC at that time with improvement of SpO2 to 97% per EMS. Patient does not require any oxygen at baseline. Patient denies any recent travel or sick contacts. He is vaccinated x3 for COVID-19 with his booster completed in October 2021. Of note, patient was recently seen at our facility and discharged on 1/14/22 for acute osteomyelitis of his left lower extremity. He underwent debridement on 1/3/22 and incision and drainage on 1/7/22. He was discharged on 1/14 to ECF with wound VAC changes every other day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: HEALTH SYSTEM LABORATORY Chart Review Copy (64 yrs) PT CLASS: Inpatient PATIENT STATUS: Discharged GENDER: male Results Covid-19, Flu, RSV by NAA Contains abnormal data Covid-19, Flu, RSV by NAA Status: Final result Next appt: None Specimen Information: Nasopharyngeal; Swab 0 Result Notes Component Ref Range & Units Influenza A Not Detected Not Detected Influenza B Not Detected Not Detected RSV Not Detected Not Detected SARS-CoV-2 (COVID-19) by NAA, Micro Not Detected Detected Abnormal Narrative Methodology: Nucleic Acid Amplification(NAA)/Polymerase Chain Reaction(PCR) The SARS-CoV-2 (COVID-19) test is for in vitro diagnostic use under the FDA Emergency Use Authorization (EUA) for laboratories certified to perform high complexity testing. This test has not been FDA cleared or approved. Specimen Collected: 01/23/22 7:37 AM Last Resulted: 01/23/22 8:32 AM Order Details View Encounter Lab and Collection Details Routing Result History Result Care Coordination Patient Communication Released Not seen Back to Top Result Comments Released Not seen Covid-19, Flu, RSV by NAA on 1/23/22 Order Covid-19, Flu, RSV by NAA Reports Transmitted at Order Entry Transmitted to: Order Details Open Order Details Specimen Collection Record Collection: Date/Time: Jan 23, 2022 7:37 AM Specimen Received Record Received: Date/Time: Jan 23, 2022 7:51 AM Order Requisition Covid-19, Flu, RSV by NAA on 1/23/22
Aktuelle Erkrankungen: Diabetes mellitus
Vorgeschichte: -
Andere Medikamente: ACETAMINOPHEN (TYLENOL) 325 MG PO TAB take 650 mg by mouth every 6 hours as needed for FOR MILD PAIN, FOR FEVER or FOR HEADACHE. ASPIRIN 81 MG PO CHEW TAB take 81 mg by mouth once daily. ATORVASTATIN (LIPITOR) 20 MG PO TAB tak
Allergien: Penicillins Rash/Itching
Vorherige Impfungen: -

VAERS 2161044

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0179

moderat

Staat: NY
Alter: 43,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 21.05.2021
Beginn: 04.06.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: - / LA

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

Hypoaesthesia Meralgia paraesthetica Paraesthesia

Symptomtext

Meraglia paraesthica; tingling and a numbness in my right thigh. It feels similar to your foot "falling asleep". It happens while standing or lying down.; tingling and a numbness in my right thigh. It feels similar to your foot "falling asleep". It happens while standing or lying down.; 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 (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 21May2021 18:00 (Lot number: Ew0179) at the age of 43 years as dose 1, single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: VIT D; VITAMIN C; IRON. The following information was reported: MERALGIA PARAESTHETICA (non-serious) with onset 04Jun2021 12:00, outcome "not recovered", described as "Meraglia paraesthica"; PARAESTHESIA (non-serious), HYPOAESTHESIA (non-serious) all with onset 04Jun2021 12:00, outcome "not recovered" and all described as "tingling and a numbness in my right thigh. It feels similar to your foot "falling asleep". It happens while standing or lying down.". Therapeutic measures were not taken as a result of meralgia paraesthetica, paraesthesia, hypoaesthesia. Additional Information: Seriousness criteria reported as no. List of any other medications the patient received within 2 weeks of vaccination: Multi vitamin, vitamin d, vitamin c, iron supplement. The patient did not receive any vaccines within four weeks prior to the vaccination. Meraglia paraesthica, tingling and a numbness in right thigh. It feels similar to your foot falling asleep. It happens while standing or lying down. It has begun to subside over the past 2 weeks but not gone completely. Prior to vaccination patient was not diagnosed with covid-19. since the vaccination the patient had not been tested for COVID-19. No known allergies. Other medical history: N/A Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: VIT D; VITAMIN C; IRON
Allergien: -
Vorherige Impfungen: -

VAERS 2154606

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 23,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 04.05.2021
Beginn: 05.02.2022
Tage bis Beginn: 277,0
Dosis: 2
Route/Site: - / -

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

Arthralgia COVID-19 Chest pain Computerised tomogram normal Electrocardiogram normal Fatigue Myalgia Tachycardia Troponin normal

Symptomtext

Patient is fully vaccinated and boosted. COVID + at ED visit on 2/5/2022. 24-year-old female presents to the ED complaining of chest pain. Patient states that she has been experiencing intermittent substernal chest pain for the past 2 days. She does admit to intermittent associated shortness of breath. Positive for fatigue, myalgias, arthralgias. Tachycardia present. No CT evidence for central or segmental Pulmonary Embolism. Troponin normal. EKG: Normal sinus rhythm. Cannot rule out Anterior infarct. Iopamidol given, zofran and fluid. Discharged home.

Weitere VAERSDATA-Felder

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

VAERS 2151077

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: IL
Alter: 39,0
Geschlecht: M
Eingang: 01.03.2022
Impfdatum: 13.05.2021
Beginn: 13.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Distraction osteogenesis Injection site reaction Mobility decreased Musculoskeletal stiffness

Symptomtext

A growth of bone appeared visible to the naked eye (it was noticed by my girlfriend) on the top of my left shoulder above the injection site. Palpation confirmed its existence as bone. I googled the side-effect and it said bone growths were often a side effect of vaccines, and since there were not adverse effects and I didn't have a doctor, I didn't report it. I just went to urgent care yesterday and mentioned it to the doctor who told me to report it to the CDC. The lasting effects have been a small decrease in mobility, stiffness and slight soreness in that shoulder.

Weitere VAERSDATA-Felder

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

VAERS 2150758

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: LA
Alter: 58,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 29.07.2021
Beginn: 30.07.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / RA

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

Hypoaesthesia Pain in extremity Paraesthesia

Symptomtext

Numbness and tingling in fingers on the right hand; Numbness and tingling in fingers on the right hand; Soreness on wrist and in right hand; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 59 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 29Jul2021 13:00 (Lot number: EW0179) at the age of 58 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Hbp" (unspecified if ongoing), notes: Other medical history: Hbp. Concomitant medication(s) included: DILTIAZEM. The following information was reported: HYPOAESTHESIA (non-serious), PARAESTHESIA (non-serious) all with onset 30Jul2021 06:30, outcome "not recovered" and all described as "Numbness and tingling in fingers on the right hand"; PAIN IN EXTREMITY (non-serious) with onset 30Jul2021 06:30, outcome "not recovered", described as "Soreness on wrist and in right hand". The events "numbness and tingling in fingers on the right hand", "numbness and tingling in fingers on the right hand" and "soreness on wrist and in right hand" were evaluated at the physician office visit. It was unknown if therapeutic measures were taken as a result of hypoaesthesia, paraesthesia, pain in extremity. Additional information: Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, patient had not tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (Other medical history: Hbp)
Andere Medikamente: DILTIAZEM
Allergien: -
Vorherige Impfungen: -

VAERS 2140359

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: TX
Alter: 69,0
Geschlecht: M
Eingang: 25.02.2022
Impfdatum: 23.08.2021
Beginn: 22.12.2021
Tage bis Beginn: 121,0
Dosis: 3
Route/Site: SYR / RA

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

Ageusia Anosmia Asthenia COVID-19 Cardiac disorder Cough Decreased appetite Diarrhoea Dyspnoea Fatigue Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Shortness of breath, lost of taste-smell-appetite, sore throat cough, diarrhea, weakness, fatigue, fever, heart disease and Contracted Covid 19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 6,0
Labordaten: Covid 19.
Aktuelle Erkrankungen: N/A
Vorgeschichte: HIV positive; diabetes; reno deficiency
Andere Medikamente: JULUCA
Allergien: N/A
Vorherige Impfungen: -

VAERS 2137671

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge EW0179

moderat

Staat: MI
Alter: 32,0
Geschlecht: F
Eingang: 24.02.2022
Impfdatum: 03.08.2021
Beginn: 21.09.2021
Tage bis Beginn: 49,0
Dosis: 1
Route/Site: IM / -

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

Burning sensation Chiropractic Electromyogram Hypoaesthesia Insomnia Magnetic resonance imaging Magnetic resonance imaging neck Muscle spasms Nerve conduction studies Paraesthesia Sleep disorder Spinal X-ray

Symptomtext

After patient's 2nd COVID vaccine she had symptoms of stabbing, burning and cramping. Patient has undergone many tests and has worked with a chiropractor, pain management. She does report intermittent tingling, numbness and burning. She has had difficulty with sleeping through the night as symptoms do wake her up in the middle the night. She does find it hard to fall sleep after waking up due to the symptoms. She has tried multiple medications including tramadol, Flexeril, ibuprofen, Tylenol and naproxen. Patient has also been referred to specialists including neurology. She does continue to follow with Psychiatry for history of anxiety and depression. She did recently start working with occupational therapy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: 12/17/2021 x-ray of her cervical spine 12/27/2021 MRI of her right elbow without contrast 1/26/2022 MRI of her cervical spine without contrast 11/10/2021 electromyogram and nerve conduction test
Aktuelle Erkrankungen: none
Vorgeschichte: Depression, anxiety
Andere Medikamente: none
Allergien: penicillins
Vorherige Impfungen: -

VAERS 2137355

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: KS
Alter: 60,0
Geschlecht: M
Eingang: 24.02.2022
Impfdatum: 02.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Abdominal discomfort Blood test Dizziness Dyspnoea Echocardiogram Fatigue Feeling abnormal Head discomfort Headache Nausea Pain Palpitations Tinnitus Transient ischaemic attack Ultrasound Doppler

Symptomtext

He got his vaccine, he started having severe headaches, throbbing/stabbing type. A lot of dizziness and head pressure, brain fog. He also had heart palpitations, sometimes ringing in the ears, lots of fatigue, lots of pain all over his body. He had a lot of shortness of breath, nausea and sometimes stomach discomfort. He had a TIA on 12/3/2021 which his doctor does not feel it was related to the vaccine. His Cardiologist couldn't say whether he felt it was or not either. His symptoms are progressively getting worse. He saw an interview by Dr regarding this and realized that he had this condition. He got his first vaccine and had some headaches at times, lots of heart palpitations and shortness of breath. He saw his cardiologist who did an Echocardiogram, and some blood work and he didn't think that it was related to his heart. He wasn't sure until he had the 3rd one. His saw his PCP since the TIA and also his cardiologist who did a sonogram of his carotid arteries. He is scheduled to see a neurologist on 4/27/22. He is still having all of these symptoms since having the vaccine. He has been wanting to go to the hospital for the dizziness and the shortness of breath and is avoiding that due to fear of dying from COVID he may catch in the ER. When he had the 2nd vaccine the headaches got worse, not as much dizziness, but the brain fog started about that time, the fatigue, head pressure, shortness of breath continued, nausea continued and heart palpitations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Echo, blood work and carotid artery sonogram.
Aktuelle Erkrankungen: None.
Vorgeschichte: Diabetes, asthma.
Andere Medikamente: Hydrocodone, Glimepiride.
Allergien: Propofol.
Vorherige Impfungen: -

VAERS 2127419

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: CA
Alter: -
Geschlecht: M
Eingang: 19.02.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Axillary mass Blood test Lymphadenopathy Pain Paraesthesia Urine analysis

Symptomtext

Its swollen lymph node; I have it like mass forming under in my armpit; I just got my first dose of the vaccine its pretty painful; getting like tingly feelings in my finger tips on my left arm; I just got my first dose of the vaccine its pretty painful; getting like tingly feelings in my finger tips on my left arm; Its swollen lymph node; I have it like mass forming under in my armpit; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 25 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 2021 (Lot number: EW0179) as dose 1, single for covid-19 immunisation. Relevant medical history included: "Major depressive disorder" (unspecified if ongoing); "Anxiety" (unspecified if ongoing); "Migraine" (unspecified if ongoing). Concomitant medication(s) included: METOPROLOL TARTRATE; ELETRIPTAN taken for migraine; VENLAFAXINE taken for depression. The following information was reported: LYMPHADENOPATHY (non-serious), AXILLARY MASS (non-serious) all with onset 2021, outcome "unknown" and all described as "Its swollen lymph node; I have it like mass forming under in my armpit"; PARAESTHESIA (non-serious), PAIN (non-serious) all with onset 2021, outcome "unknown" and all described as "I just got my first dose of the vaccine its pretty painful; getting like tingly feelings in my finger tips on my left arm". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of lymphadenopathy, paraesthesia, pain, axillary mass. Additional information: Its swollen lymph node or what should be going on, but the patient had it like mass forming under in armpit. The patient just got first dose of the vaccine on Saturday but it was pretty painful and getting like tingly feelings in finger tips on left arm and got the arm the vaccine. The patient stated that he had just been resting pretty much and drinking water. When probed for any medication, the patient took for treatment, the patient stated as no. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Name: Blood test; Result Unstructured Data: Test Result:unknown; Comments: haven't got those result back; Test Name: Urine analysis; Result Unstructured Data: Test Result:unknown; Comments: haven't got those result back
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Major depressive disorder; Migraine
Andere Medikamente: METOPROLOL TARTRATE; ELETRIPTAN; VENLAFAXINE
Allergien: -
Vorherige Impfungen: -

VAERS 2116472

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: CA
Alter: 86,0
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 14.02.2022
Beginn: 14.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Anxiety Blood pressure increased Condition aggravated Dizziness Nausea

Symptomtext

86 year old client came in and received Pfizer (LOT # FK9895) COVID Vaccine Booster on 2/14/2022. After receiving booster at 1635, client reported feeling dizzy, anxious, and "a little bit of Nausea" in observation room and had a BP of 178/ 98. Client reported her normal BP is usually in the 150's at 1635. Client reported she has a history of hypertension and anxiety. Client took her own PRN Ativan at 1642 for anxiousness and reported that she has "not taken her blood pressure medication today". 1702 Clients BP was 184/82 RR 14, HR 91, 02 96% RA. 1718 Clients BP was 180/90, P81, and O2 96% on RA. At 1720 Client and Client's Son was educated by lead nurse to take Client's BP before giving her prescription BP Medication by PCP (Conidine) at home and if signs and symptoms continue to persist and not improve son is advised to call 9-1-1. Client was Wheelchaired out by Observation Site EMT back to car and accompanied by Client's Son.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Hypertension Anxiety
Andere Medikamente: Ativan Conidine
Allergien: NKA
Vorherige Impfungen: -

VAERS 2116387

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0179

moderat

Staat: PA
Alter: 25,0
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: 13.09.2021
Beginn: 16.09.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Chest pain Electrocardiogram normal

Symptomtext

About 24 hours after the first dose, I started feeling pain in my chest. This pain has never been preset before. It went away after about 3 days. About 36 hours after the second dose, the pain returned and was worse than the first time. I assumed it would go away on its own, but it did not. On 9/21/2021 I went to the urgent care. They performed an EKG, told me it was normal, and then told me to go to the nearest ER if the pain got worse. I did not go to the ER as I did not feel as though the pain was bad enough. On 11/17/2021 I went to the cardiovascular medicine provider. They also performed an EKG, gave the same results as the urgent care, but also instructed me to get a blood test to check for inflammation. On 12/1/2021 I got a blood test. The results show an average "risk for future cardiovascular event" according to the data sheet. These results were sent to the medical center. I called them to find out their interpretation of the results. They informed me that there is no risk and to go to the ER if the pain continues. I did not go to the ER due to the high expense. The pain is continuing.

Weitere VAERSDATA-Felder

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

VAERS 2113086

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: KY
Alter: 60,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 07.10.2021
Beginn: 21.01.2022
Tage bis Beginn: 106,0
Dosis: 2
Route/Site: IM / RA

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

Albumin globulin ratio Anaemia Anion gap Blood creatinine increased Blood glucose normal Blood lactic acid Blood magnesium normal Blood phosphorus Blood potassium decreased Blood urea increased Brain natriuretic peptide increased COVID-19 COVID-19 pneumonia Cardiac flutter Chest X-ray abnormal Chest pain Differential white blood cell count abnormal Dyspnoea

Symptomtext

1/21/22 61 yr/o female who presents with right sided pleuritic chest pain. Symptoms have been present for the past 2 days. The patient has history of asthma, acute on chronic respiratory failure, is on 3 L/min oxygen via nasal cannula at baseline. States she has increased her oxygen use to 4 L/min when active but has maintained her baseline oxygen rate while at rest. Reports productive cough since onset of symptoms.. No fevers or chills. Patient has been compliant with her dialysis schedule. Patient arrives via EMS. Vital stable during transport per EMS. Patient reports sharp pain in her right lower chest which is worse with deep breaths. Reports associated dyspnea. Denies any abdominal pain Review of Systems Constitutional: Negative for chills and fever. Respiratory: Positive for shortness of breath. Negative for cough. Cardiovascular: Positive for chest pain. Negative for leg swelling. Gastrointestinal: Negative for abdominal pain, nausea and vomiting. Skin: Negative for rash. Neurological: Negative for dizziness and headaches. All other systems reviewed and are negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 8,0
Labordaten: 1/21/22 COVID-19 Result Detected Abnormal CBC W/DIFF - Abnormal; Notable for the following components: Result Value White Blood Count 15.25 Red Blood Count 3.04 Hemoglobin 8.6 (*) Hematocrit 28.9 (*) Mean Corpuscular HGB Conc 29.8 (*) Neutrophils % 89.0 (*) Lymphocyte % 1.9 (*) Neutrophil Abs 13.58 (*) Lymphocyte-Absolute 0.29 (*) Immature Granulocyte Abs 0.11 (*) All other components within normal limits COMPREHENSIVE METABOLIC PANEL (CMP) - Abnormal; Notable for the following components: Potassium 3.4 (*) Anion Gap 16 (*) Glucose 182 (*) Blood Urea Nitrogen (BUN) 22 (*) Creatinine-Blood 3.81 (*) Estimated GFR 12 (*) Estimated GFR if race 15 (*) Albumin/Globulin Ratio 0.9 (*) All other components within normal limits PROCALCITONIN - Abnormal; Notable for the following components: Procalcitonin 7.14 (*) All other components within normal limits B-TYPE NATRIURETIC PEPTIDE - Abnormal; Notable for the following components: B-Type Natriuretic Peptide 343.6 (*) All other components within normal limits COVID-19, NOVEL CORONAVIRUS + FLU A/B PCR TROPONIN MAGNESIUM PHOSPHORUS LACTIC ACID 1/21/22 XR Chest 2Vw: IMPRESSION: 1.Acute right midlung and left infrahilar pulmonary infiltrates concerning for pneumonia superimposed on chronic interstitial lung disease with associated moderately severe cylindrical and cystic bronchiectasis 61 yr/o with PMH PAF, ESRD, DM, chronic respiratory failure, CHF, COPD, anemia who presented with dyspnea and was found to have PNA due to COVIVD19. She was treated for following: COVID-19 pneumonia: Scheduled + as needed albuterol. Vitamin C. Symbicort. Delsym. Mucinex. Remdesivir x5d. ZnSO4. Incentive spirometry. Flutter. Supplemental oxygen as needed. Daily inflammatory markers.flutter, IS, mucinex, delsym, ZnSO4, vit C - on 3L NC (her home O2) Acute on chronic anemia: Hemoglobin 6.8 1/28 and got PRBC. Gradual decrease noted over the last few days, suspect iatrogenic etiology. Stable after transfusion N/V: continue zofran, compazine, scopolamine patch ESRD: nephrology following. Outpatient arrangements are made. COPD: continue inhaled medications Hypoglycemia: Resolved -Remains off lantus, actos, tradjenta, starlix. Continue SSI (if needed at discharge Hypotension: midodrine Discharge Diagnoses:Principal Problem: Multifocal pneumonia (6/11/2019) Active Problems: Diabetes mellitus (3/31/2015) End-stage renal disease on hemodialysis (9/23/2018) Chronic anticoagulation (8/17/2020) Chronic respiratory failure with hypoxia (12/2/2020) Chronic diastolic (congestive) heart failure (12/24/2020) COPD (chronic obstructive pulmonary disease) (12/24/2020) PAF (paroxysmal atrial fibrillation) (1/11/2021) Intractable vomiting with nausea (5/26/2021) Hypotension (6/18/2021) Pneumonia due to COVID-19 virus (1/24/2022)
Aktuelle Erkrankungen: -
Vorgeschichte: Acute and chronic respiratory failure with hypoxia 08/2020 requiring intubation and mechanical ventilatio Acute and chronic respiratory failure with hypoxia 08/2020 requiring intubation and mechanical ventilation o Anxiety o Asthma o Atrial fibrillation o Atrial flutter o Bacteremia due to Staphylococcus 8/18/2015 o Breast cancer, left Dx 12/2014 had lumpectomy and chemo and radiation o CAP (community acquired pneumonia) 1/1/2017 o Cardiomegaly o CHF (congestive heart failure) o COPD (chronic obstructive pulmonary disease) chronic resp failure with hypoxia o DDD (degenerative disc disease), lumbar o Depression o Diabetes mellitus, type II o Dialysis (juvenile) of retina (with detachment) o ESRD on hemodialysis o Fe deficiency anemia o Fibromyalgia o GERD (gastroesophageal reflux disease) o Healthcare associated bacterial pneumonia 11/4/2017 o Hypercholesterolemia o Hyperlipidemia o Hypertension o Intracranial hypertension o Necrotizing fasciitis 08/2020 of left groin o Neuropathy o NSVT (nonsustained ventricular tachycardia) o Obesity o On home oxygen therapy 02/02/2018 o Pancytopenia due to chemotherapy 7/15/15 o Pneumonia of both lower lobes due to infectious organism 6/11/2019 o Pulmonary HTN 02 dependent o Restless leg syndrome o Sarcoidosis of lung o Sleep apnea wears bipap o Syncope and collapse o V-tach o Vision abnormalities
Andere Medikamente: albuterol-ipratropium (DUO-NEB) 0.5-2.5 mg/3 mL nebulizer Take 1 ampule by nebulization every 4 (four) hours as needed for Wheezing for up to 30 days. o amikacin sulfate (AMIKIN) 500 MG/2ML SOLN injection Take 1 mL by nebulization Twice a
Allergien: Adhesive
Vorherige Impfungen: -

VAERS 2110246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: WI
Alter: 59,0
Geschlecht: M
Eingang: 14.02.2022
Impfdatum: 06.05.2021
Beginn: 03.02.2022
Tage bis Beginn: 273,0
Dosis: 2
Route/Site: IM / LA

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

Atrial fibrillation Brain natriuretic peptide increased COVID-19 Condition aggravated Cough Dyspnoea Electrocardiogram abnormal Influenza Influenza A virus test positive Orthopnoea SARS-CoV-2 test positive Tachycardia Wheezing

Symptomtext

The patient is a 59 y.o. male with PMH of afib not currently on anticoag (s/p successful DCCV in May 2021 and has been on off DOAC since that time), non-ischemic CMP w/ improved LVEF w/ medical therapy, CKD3a, HTN, valvular disease that improved w/ medical therapy and LVEF who presents with wheezing and dyspnea. Patient felt in his normal state of health this past week (recently recovered from PCR proven influenza A infection). He awoke this morning and felt like he couldn't catch his breath. Felt audibly wheezy. Called family for a ride to the ER, but they were taking too long so he called EMS instead for concern of worsening respiratory status. Came in to the ED for evaluation. Upon arrival, he was tachycardic and EKG showed afib w/ RVR. Vitals otherwise stable. Given neb with improvement in respiratory status. Labs w/ mildly elevated BNP, so he was also given lasix 60 mg IV alongside methylpred IV given his wheezing. Stable on RA. His viral panel screen did return w/ a positive COVID PCR. Started on a dilt gtt as well for his RVR and admitted to the GM service. Patient tells me that he has been compliant with his meds. Weight stable, but does endorse more orthopnea. No fevers, chills, sweats, n/v/d, change in taste/smell. No recent travel. No cp or palpitations. Has been coughing today which is new. Never smoker. No hx of asthma either.

Weitere VAERSDATA-Felder

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

VAERS 2109051

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: TX
Alter: 57,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 29.07.2021
Beginn: 01.07.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Dyspnoea Fatigue Gait inability Grip strength decreased Hypoaesthesia Magnetic resonance imaging Nodule Pain in extremity Peripheral swelling Vomiting X-ray

Symptomtext

she had a huge knot in her arm and it has grown to 3 places in her left arm; had problems that night; I almost stop breathing; I had not been able to walk; without having to sit down and rest; I had not been able to walk; without having to sit down and rest; taken her feeling out of her left hand; When the pain gets so bad I wanna throw up; big knot that came up on my arm and it was really swollen, really sore; her grip has become weak; fatigue; big knot that came up on my arm and it was really swollen, really sore; 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 57-year-old female patient received bnt162b2 (BNT162B2), via an unspecified route of administration, administered in arm left, administration date 29Jul2021 (Lot number: EW0179) at the age of 57 years as dose 1, single for covid-19 immunization. Relevant medical history included: "Asthma" (unspecified if ongoing). The patient took concomitant medication for asthma. The following information was reported: NODULE (medically significant) with onset 29Jul2021, outcome "not recovered", described as "she had a huge knot in her arm and it has grown to 3 places in her left arm"; GRIP STRENGTH DECREASED (non-serious) with onset 2021, outcome "unknown", described as "her grip has become weak"; FATIGUE (non-serious) with onset 2021, outcome "unknown", described as "fatigue"; PAIN IN EXTREMITY (non-serious), PERIPHERAL SWELLING (non-serious) all with onset 2021, outcome "unknown" and all described as "big knot that came up on my arm and it was really swollen, really sore"; DYSPNOEA (non-serious) with onset 29Jul2021, outcome "recovered" (Oct2021), described as "had problems that night; I almost stop breathing"; GAIT INABILITY (non-serious) with onset Jul2021, outcome "recovered" (Oct2021), described as "I had not been able to walk; without having to sit down and rest"; VOMITING (non-serious) with onset 2021, outcome "unknown", described as "When the pain gets so bad I wanna throw up"; HYPOAESTHESIA (non-serious) with onset 2021, outcome "unknown", described as "taken her feeling out of her left hand". The event "she had a huge knot in her arm and it has grown to 3 places in her left arm" resulted in physician office visit. The patient underwent the following laboratory tests and procedures: magnetic resonance imaging (MRI): (2021) looks normal; x-ray (x-rays): (2021) looks normal. Therapeutic measures were taken as a result of nodule, pain in extremity, peripheral swelling. Additional information: After the patient received the Pfizer COVID-19 vaccine last 29Jul2021, the patient had a huge knot in her arm and it has grown to 3 places in her left arm, and it has also appeared in her left leg last week. It is also appearing in her right arm now. It has cut of her circulation in her hand and her grip has become weak. She said that she now has limited use in her left hand and arm. She also said that she has a high level of fatigue. She said that she basically had to rest while walking from her kitchen to her bedroom. She used to run 9 miles before. She also used to carry 15lbs now she can only carry a carton of milk. She wanted to know if those have been reported as adverse events for the vaccine and what to do to treat her adverse events. It was also reported that since the vaccination, there was a big knot that came up on her arm and it was really swollen, really sore. The patient had problems that night where she was 'later', where she almost stopped breathing and that went from 29Jul2021 until Oct2021 where I could not lift anything with my arm. On the patient's left side, she could not carry anything over a like a gallon of milk and she was carrying 50 pounds sac of dog food 3 days before the injection on her shoulder. She was walking 9 miles a week 'as unlike' and had not been able to walk to her bedroom and to the kitchen without having to sit down and rest and this was from Jul2021 until the end of Oct2021. Since that time, the patient's left arm has 3 huge knots in it now and they are growing almost 6-8 inches long and she should say that each one has taken her feeling out of her left hand where the more she uses her arm, the less she can hold, can grip, can grasp, and can lift her arm up. There is a place, that started at Christmas (25Dec2021) behind her left leg and this last week there is three places in her right arm that is starting to grow. So, the patient had X-rays and MRIs and they say that it looks normal. The patient is being scheduled for an EMG. The patient asks how to treat it because it is getting worse. The knots were growing all over her body. The patient has lost the use of her right arm now. Since Thursday of last week, the places started growing in her right arm and the patient believes that she was losing the feeling in it. The patient was losing stability to grasp and hold pencils or pen. The patient is in fear now due to the events. The patient saw her doctors because of the knots in her arm and the doctors saw that there was a deformity in the patient's arm. The patient's doctors have no clue on what this was. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: MRI; Result Unstructured Data: Test Result:looks normal; Test Date: 2021; Test Name: X-rays; Result Unstructured Data: Test Result:looks normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2105916

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 64,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 26.05.2021
Beginn: 01.07.2021
Tage bis Beginn: 36,0
Dosis: 1
Route/Site: - / LA

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

Palpitations Sleep disorder

Symptomtext

In the months of July, August, and September, several nights/week, heart would pound very rapidly as fast as you can say 1,2,3,4,5,6,7,8,9.10 within 5 seconds in chest upon during the night while sleeping, waking me, and it would last up to 20 seconds before stopping. Never have had this before. Not like palpitations at all. Informed doctor. They didn?t know what to do except to get an EKG. I did not get one. After three months, it went away. I am convinced it was from the two vaccines. Why am I reporting this now? Because of a news story that aired today in which another person told her similar story to the news. I know of others who have had cardiac experiences.

Weitere VAERSDATA-Felder

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

VAERS 2105025

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: OR
Alter: 29,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 29.04.2021
Beginn: 30.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Fatigue Mobility decreased Pain

Symptomtext

I felt exhausted, and had body aches all over. For the next 3 days I was mainly in bed sleeping.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: Diabetes- Type 2, PCOS
Andere Medikamente: duloxetine- 40mg
Allergien: none
Vorherige Impfungen: flu vaccine- I experience body aches.

VAERS 2095447

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 85,0
Geschlecht: F
Eingang: 08.02.2022
Impfdatum: 25.05.2021
Beginn: 28.01.2022
Tage bis Beginn: 248,0
Dosis: 2
Route/Site: IM / -

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

Abdominal infection Abdominal pain Abdominal pain upper Acute kidney injury Anaemia Anal incontinence Aspartate aminotransferase increased Asthenia Back pain Blood alkaline phosphatase increased Blood creatinine increased Blood culture Blood lactic acid Blood phosphorus decreased Blood potassium increased Blood test abnormal C-reactive protein increased COVID-19

Symptomtext

Hospitalized (1.28.22 - 1.31.22 - RE-ADMITTED 2.5.22 - still inpt with neck pain & AMS); COVID-19 positive (1.28.22); Fully vaccinated 1/28/22 H&P: CHIEF COMPLAINT Nausea ASSESSMENT AND PLAN Covid pneumonia - patient presenting with complaints of fever, nausea, vomiting, diarrhea and increased confusion which started yesterday. Also having minor dry cough. She is vaccinated but not boosted. - currently stable on RA - CXR showing findings consistent with Covid pneumonitis - not currently a candidate for interventions as stable on RA - consider starting Dexamethasone is becomes hypoxic - prn supportive care - monitor on pulse ox Lactic acidosis, resolved - likely 2/2 dehydration, vomiting and diarrhea - LA 2.3 -> 1.2, WBC WBL - given 2L NS bolus - given Vanc, cefepime, flagyl for empiric sepsis tx in ED, holding off on further Abx - CT A/P negative for acute process - UA negative - stool studies pending - blood cultures pending AKI on CKD 3 - Cr 2.36, baseline around 1.9 - given 2L NS in ED, will continue with gentile IVF for a few more hours - holding Lasix - avoid nephrotoxins and renally dose medications - continue to monitor Hypophosphatemia - phos 1.9 - given 15 mmol Kphos - continue to monitor and replace as needed Chronic HFpEF, stable Essenital HTN - most recent echo showing EF 58% - holding home Lasix with AKI - continue home Norvasc and metoprolol - daily weights, strict I/Os NIDDM - A1c pending - not currently on medications at home - will place on 24 hour coreective for now - continue to monitor and adjust as needed HDL CVA - continue home statin GERD - PPI Chronic anemia - hgb 10.8 which is baseline Rheumatoid arthritis Chronic immunosuppression - continue home 5mg Prednisone daily Vascular Dementia Depression - slightly more altered than normal per daughter at bedside but was started on Tramadol yesterday by PCP for chronic back pain. Daughter would like assistance with official DPOA designation - will stop tramadol - continue home Remeron Diet: DM liberal VTE Prophylaxis: Lovenox Code status: Full Code per daughter at bedside HISTORY OF PRESENT ILLNESS Patient is a 85 y.o. female with past medical history significant for CVA, vascular dementia, CHF diabetes, depression, hypertension presented to the emergency department complaints of fever, nausea/vomiting and diarrhea. With patient's dementia, most of history is obtained through daughter a who is at bedside. Per daughter, patient began having symptoms of fever/chills, nausea/vomiting and diarrhea beginning yesterday 1/27. Notes that she has been having decreased appetite. Patient has been complaining intermittently of abdominal pain but denies any pain on admission. Daughter notes that she does have a minor dry the last few days. She also notes increased confusion over the last few days with acute worsening yesterday. Of note, patient did go see PCP yesterday and was started on tramadol for chronic back pain. Confusion worsened after starting this medication. Daughter notes that she currently lives with patient. Patient is ambulatory but uses walker/cane to get around. Denies any recent falls. Notes compliance with her medications. Believes that her sister may have been COVID positive but was never tested. Patient is vaccinated but not boosted. Upon arrival to emergency department, patient was febrile, tachycardic. She was stable on room air. Baseline blood work was obtained which was remarkable for AKI, hypophosphatemia lactic acid 2.1 and stable chronic anemia. Sepsis workup was initiated and blood cultures were obtained. He was negative for acute infection. COVID PCR was positive. CXR was obtained consistent with bilateral COVID pneumonitis. CT abdomen and pelvis was obtained which was negative for acute process. Patient was empirically started on vanc, cefepime and Flagyl for suspected intra-abdominal infection. She was also given a 2 L NS bolus. Repeat lactic acid normalized. Patient was then transferred to Hospital and admitted to General Medicine for further evaluation and management. Patient Active Problem List Diagnosis ? Abnormal CT of the abdomen ? Acute kidney injury ? Alcohol abuse ? Anorexia ? Bilateral cataracts ? Cerebrovascular accident ? Chronic combined systolic and diastolic heart failure ? Coronary arteriosclerosis ? Dehydration ? Dementia with behavioral disturbance ? Diabetic nephropathy ? Dyslipidemia ? Elevated lipase ? Epigastric abdominal pain ? Hypertension ? General weakness ? Gout ? Non-ST elevation (NSTEMI) myocardial infarction ? Type 2 diabetes mellitus ? Community acquired pneumonia, bilateral ? Intractable back pain ? Physical deconditioning ? Protein-calorie malnutrition, moderate ? COVID-19 Review of Systems Unable to perform ROS: Dementia Constitutional: Positive for appetite change, chills and fever. HENT: Negative for congestion and trouble swallowing. Respiratory: Positive for cough. Negative for shortness of breath. Gastrointestinal: Positive for abdominal pain, diarrhea, nausea and vomiting. Negative for abdominal distention. Neurological: Positive for weakness. Psychiatric/Behavioral: Positive for confusion. BJECTIVE BP 136/55 | Pulse 91 | Temp 98.8 ?F (37.1 ?C) (Oral) | Resp 25 | Wt 66 kg (145 lb 8.1 oz) | SpO2 94% | BMI 28.42 kg/m? Physical Exam Constitutional: General: She is not in acute distress. HENT: Head: Normocephalic and atraumatic. Mouth/Throat: Mouth: Mucous membranes are dry. Pharynx: Oropharynx is clear. Eyes: Extraocular Movements: Extraocular movements intact. Pupils: Pupils are equal, round, and reactive to light. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Pulmonary: Effort: Pulmonary effort is normal. No respiratory distress. Breath sounds: Normal breath sounds. No wheezing. Abdominal: General: Bowel sounds are normal. There is no distension. Palpations: Abdomen is soft. Tenderness: There is no abdominal tenderness. Musculoskeletal: General: No swelling or tenderness. Skin: General: Skin is warm and dry. Neurological: Mental Status: She is alert. Mental status is at baseline. Comments: A&O 1-2 Psychiatric: Mood and Affect: Mood normal. Behavior: Behavior normal Discharge Summary MD (Physician) ? ? General Medicine BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider: MD Admission Date: 1/28/2022 Discharge Date: Jan 31, 2022 Resolved Hospital Problems Diagnosis Date Noted Date Resolved POA ? AKI (acute kidney injury) 01/29/2022 02/02/2022 Unknown ? Encephalopathy Sepsis due to COVID pneumonia with possible secondary bacterial infection 01/29/2022 02/02/2022 Yes ? Acute kidney injury Discharge Disposition: home health care svc Active Issues Requiring Follow-up: COVID pneumonia with secondary bacterial infection - follow-up with primary care Dementia - follow-up with primary care, recommend formal neurocognitive evaluation, family to work on guardianship Type 2 diabetes with hyperglycemia - follow-up with primary care DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Severe sepsis [A41.9, R65.20] COVID-19 virus infection [U07.1] COVID-19 [U07.1] AKI (acute kidney injury) N17.9] HOSPITAL COURSE: 85 y.o. female with past medical history significant for CVA, vascular dementia, CHF diabetes, depression, hypertension presented to the emergency department complaints of fever, nausea/vomiting and diarrhea. Upon arrival to emergency department, patient was febrile, tachycardic. She was stable on room air. Baseline blood work was obtained which was remarkable for AKI, hypophosphatemia lactic acid 2.1 and stable chronic anemia. Sepsis workup was initiated and blood cultures were obtained. He was negative for acute infection. COVID PCR was positive. CXR was obtained consistent with bilateral COVID pneumonitis. CT abdomen and pelvis was obtained which was negative for acute process. Patient was empirically started on vanc, cefepime and Flagyl for suspected intra-abdominal infection. She was also given a 2 L NS bolus. Repeat lactic acid normalized. Patient was then transferred to Hospital and admitted to General Medicine for further evaluation and management. Patient stayed in hospital for 3 days. Patient were monitored for her COVID pneumonia and has not needed any oxygen support. She did not have any fever episodes. After 1st 24 hours of stay patient has been tolerating diet. During her monitoring, she had a saturation of 90% but continues to be at room air, she was given a dose of dexamethasone 6 mg once. The following day, she did pretty well maintaining saturations around 97 to 99% on room air. Had hyperglycemia that she was given corrective doses of insulin and Decadron discontinued. Patient remained to be at her baseline mentation and had been engaging to care team. Her CRP was also monitored and showed down trending. D-dimers were elevated but were stable. Lovenox prophylaxis had been given throughout stay. She was started on antibiotics for possible secondary bacterial infection with Rocephin and doxycycline. Patient's renal function was also monitored and her AKI had resolved. Her electrolyte imbalances were corrected. Her hyperglycemia episode had improved and had shown stability. PTOT evaluation were completed and recommended home health care with assist provided that caregivers are there 24/7. This was ensured by family, patient was then discharged home stable. During stay, attempted completion of DPOA, but patient incapacitated to do this. Family then informed on accomplishing guardianship after this hospitalization. Was informed of daughter that they are already in process of doing this. INPATIENT PROCEDURES: BP 128/64 | Pulse 78 | Temp 37.1 ?C (Oral) | Resp 16 | Wt 63.8 kg | SpO2 98% | BMI 27.47 kg/m? Physical Exam Vitals and nursing note reviewed. Constitutional: General: She is not in acute distress. Appearance: She is well-developed. HENT: Head: Normocephalic and atraumatic. Eyes: Conjunctiva/sclera: Conjunctivae normal. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Heart sounds: No murmur heard. Pulmonary: Effort: Pulmonary effort is normal. No respiratory distress. Breath sounds: Normal breath sounds. Abdominal: Palpations: Abdomen is soft. Tenderness: There is no abdominal tenderness. Musculoskeletal: Cervical back: Neck supple. Skin: General: Skin is warm and dry. Neurological: Mental Status: She is alert. Comments: Oriented only to self Psychiatric: Cognition and Memory: Cognition is impaired 2/5/22 H&P:CHIEF COMPLAINT: Neck pain, AMS ASSESSMENT / PLAN: COVID 19 -COVID 19 PCR positive: 1/28/2022 (consider clearing from severe respiratory precautions 2/7 pending clinical course) -vaccinated, but not boosted -on RA -CXR with bilateral infiltrates that are stable compared to recent hosptialization -supportive care -tylenol PRN for fever -repeat labs in am SIRS -ongoing fevers, tachycardia, WBC 12.51 -suspect secondary to above, CXR stable -procal/LA WNL -UA unremarkable -blood Cx pending -possibly secondary to above (unclear onset of symptoms) -no worsening respiratory symptoms per family -follow labs -completed course of doxycycline outpatient Acute Hyperkalemia -K=5.6 on admission -cardiac monitoring -will start Lokelma -repeat labs in am Generalized Weakness -PT/OT -nutrition consult Neck Pain -CT C spine negative -lidoderm patch -Tylenol PRN Vascular Dementia Depression -continue home meds, med rec pending -increased confusion noted at home per family, oriented to self on admission -will need care management input regarding dispo planning, family reported to ED they can no longer care for patient at home Chronic Anemia -check Fe studies -Hgb at baseline Chronic Diastolic HF -echo 11/23: EF=58%, LA mildly dilated -hold LAix, suspect patient dry CKD Stage III, stable -baseline around 1.2 -follow daily labs -avoid nephrotoxins, renally dose medications DM Type II, non-insulin dependent -HgbA1c=7.1 -24 hour corrective insulin HTN -continue home meds CVA HLD -continue statin RA Chronic immunosuppression -continue 5mg Prednisone daily GERD -PPI DVT PPX: Lovenox SubQ FULL CODE, discussed with daughter over the phone on admission. HISTORY OF PRESENT ILLNESS: Patient is a 85 y.o. female with HX of Vascular Dementia, CVA, DM type II, CKD, HTN, diastolic HF, RA, and Depression who presents today with increased confusion and neck pain. The patient was recently admitted to the hospitalist service 1/28/2022 to 1/31/2022 with sepsis, COVID 19, and AKI. There was initially concern for possible intra-abdominal infection in the setting of N/V/D, but CT imaging was negative. She remained on RA over the course of the hospitalization. The patient's AKI improved. She received ABx for possible bacterial PNA. She was discharged home in stable condition. She was prescribed doxycycline at DC. The patient's daughters live with her. I am unable to obtain Hx from the patient on admission. She is oriented to self only. She denies pain. I reached out to daughter oer the the phone. Who states the pt has had difficulty ambulating for the past 3 days. She was previously able to walk without a walker/cane. No falls/trauma that they are aware of. She has been complaining of neck pain. The patient has been drinking liquids, but not eating her usual amount. She one incontinent stool within the past three days. Otherwise she has not noted any cough/shortness of breath. She reports that her mother is more confused than her baseline. Per notes from most recent admission family to pursue guardianship. The patient has 9 children. In the ED the patient was febrile with Tmax of 38.7 degrees C. HR was in the 120s. K 5.6. Cr 1.3. Alk phos 232. AST 52. WBC 12.51. Hgb 10.6 and Hct 32.6. Plt 423. CRP 61.4. LA 1.3. Troponin was indeterminate, but flat. UA was negative. EKG with sinus tachycardia. CXR with bilateral infiltrates (stable/mildly improved). CT C spine without contrast without evidence of Fx or traumatic malalignment. OBJECTIVE: BP 167/81 | Pulse 105 | Temp 100.9 ?F (38.3 ?C) (Oral) | Resp 16 | Wt 65.4 kg (144 lb 2.9 oz) | SpO2 97% | BMI 28.16 kg/m? Physical Exam Vitals reviewed. Constitutional: General: She is not in acute distress. Appearance: She is not ill-appearing. HENT: Head: Normocephalic and atraumatic. Right Ear: Hearing normal. Left Ear: Hearing normal. Mouth/Throat: Mouth: Mucous membranes are moist. Pharynx: Oropharynx is clear. Eyes: Extraocular Movements: Extraocular movements intact. Conjunctiva/sclera: Conjunctivae normal. Pupils: Pupils are equal, round, and reactive to light. Neck: Vascular: No JVD. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Heart sounds: Normal heart sounds. No murmur heard. No gallop. Pulmonary: Effort: Pulmonary effort is normal. No respiratory distress. Breath sounds: Normal breath sounds. No wheezing, rhonchi or rales. Abdominal: General: Bowel sounds are normal. There is no distension. Palpations: Abdomen is soft. Tenderness: There is no abdominal tenderness. There is no guarding. Musculoskeletal: General: Normal range of motion. Cervical back: Normal range of motion and neck supple. Right lower leg: No edema. Left lower leg: No edema. Skin: General: Skin is warm and dry. Neurological: Mental Status: She is alert. She is disoriented. Comments: Oriented to self only Spontaneously moving all extremities Following basic commands Psychiatric: Comments: Flat affect, cooperative

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Past Medical History: Diagnosis Date ? Alcohol abuse ? Anemia ? Arthritis ? CAD (coronary artery disease) ? Chronic combined systolic and diastolic CHF (congestive heart failure) ? CKD (chronic kidney disease) ? CVA (cerebral vascular accident) ? Dementia with behavioral disturbance ? Depression ? Diabetes mellitus ? Gout ? Hyperlipemia ? Hypertension ? Hypothyroidism ? NSTEMI (non-ST elevated myocardial infarction 02/25/2018 ? Pancreatic pseudocyst ? Portal vein thrombosis ? PVD (posterior vitreous detachment)
Andere Medikamente: acetaminophen (TYLENOL) 500 mg capsule, Take 1 capsule by mouth 3 (three) times a day if needed., ? acetaminophen (TYLENOL) 500 mg tablet, every 12 hours., ? amLODIPine (NORVASC) 5 mg tablet, TAKE 1 TABLET BY MOUTH EVERY MORNING, ? atorv
Allergien: penicillins - hives
Vorherige Impfungen: -

VAERS 2092226

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: FL
Alter: 71,0
Geschlecht: F
Eingang: 07.02.2022
Impfdatum: 10.07.2021
Beginn: 26.01.2022
Tage bis Beginn: 200,0
Dosis: 1
Route/Site: - / -

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

Asthenia COVID-19 Confusional state Fall Hypercalcaemia Hyperparathyroidism Mobility decreased SARS-CoV-2 test positive

Symptomtext

Patient presented to the hospital after falling, confusion, weakness and trouble getting around. She was admitted for severe hypercalcemia with suspected hyperparathyroidism. Patient was tested as part of a discharge plan to an ECF and found to be positive for COVID-19 on 1/26/22. Previously vaccinated with Pfizer 6/18/21 & 7/10/21. Discharged from the hospital 2/3/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: 13,0
Labordaten: COVID-19 PCR 1/26/22.
Aktuelle Erkrankungen: -
Vorgeschichte: GERD, Hypertension, hyperparathyroidism
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2091567

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: NM
Alter: 24,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 26.05.2021
Beginn: 01.07.2021
Tage bis Beginn: 36,0
Dosis: 2
Route/Site: SYR / AR

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

Amnesia Anxiety Asthenia Decreased appetite Depression Diplopia Dizziness Dyspnoea Fatigue Headache Heart rate increased Hot flush Hyperacusis Hypoaesthesia Migraine Muscle spasms Muscle twitching Nausea

Symptomtext

numbness, tingles, twitching, tremors, spasms, fatigue, weakness, heart palpitations, increased heart rate, pain in limbs, shortness of breath, body aches, sensitivity to light, vision problems, double vision, sensitivity to sounds, light headed, headaches, migraines, loss of appetite, nausea, vomiting, heat flashes, short term memory loss, severe anxiety, panic attacks, severe depression

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: nausea/upset stomach
Vorgeschichte: asthma
Andere Medikamente: progesterone mp thyroid spironolactone
Allergien: -
Vorherige Impfungen: -

VAERS 2090807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: FL
Alter: 96,0
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 21.05.2021
Beginn: 03.02.2022
Tage bis Beginn: 258,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Diarrhoea SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st vaccine received on 04/30/2021. 97 y/o PMHx HTN, COPD, HLD, CHF presents to ED with 1 week history of diarrhea and cough. Pt has been on hospice x2 years at home. Afebrile, Room air sat 96%, CXR indicative of Covid PNA. Started on IV ABX.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19 -Detected on 02/03/2022
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, CHF, HLD, HTN
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2090045

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 20,0
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 15.05.2021
Beginn: 15.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Dyspnoea Palpitations

Symptomtext

heart palpitations; short of breath; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 20 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 15May2021 19:30 (Lot number: EW0179) at the age of 20 years as dose 2, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, Batch/lot number: EW0161 , left arm), administration date: 26Apr2021, when the patient was 20 years old, for Covid-19 immunization. The following information was reported: PALPITATIONS (non-serious) with onset 15May2021, outcome "unknown", described as "heart palpitations"; DYSPNOEA (non-serious) with onset 15May2021, outcome "recovering", described as "short of breath". Therapeutic measures were not taken as a result of palpitations, dyspnoea. Additional Information: Patient did not receive any other vaccines within 4 weeks prior to the Covid vaccine. He states he received the Covid 19 vaccine because his mother was a doctor and she advised him to get the vaccine. If it wasn't for her telling him to get the vaccine he would not have gotten it. Patient got his second dose and it gave him side effects like heart palpitations and he was short of breath. When probing if the caller is still experiencing side effects he states when he exercises he feels like short of breath a little bit. When he does hard exercises he is still short of breath. His side effects started about 25 minutes after he received the Covid 19 vaccine. He states he has no medical history and he does not take any medications. He does not do drugs and he does not smoke. He doesn't do anything. When probing for his date of birth he said first 1998, then 1999, and then 2000. He said he was 20 years old. This is discrepant but documented as provided by patient. He declines to provide the day and month. He did not have to see a doctor or go to the emergency room for treatment. No adverse events reported following prior vaccinations. No relevant tests reported. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient's Medical History :None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2089875

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: AZ
Alter: 37,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 27.06.2021
Beginn: 27.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Dizziness Dyspnoea Feeling hot Nausea

Symptomtext

Warm feeling; dizziness; shortness of breath; nausea; This is a spontaneous report from a contactable Nurse. This 37-year-old Female Nurse (Patient) reported for herself that: A 37 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 27Jun2021 16:00 (Lot number: EW0179) at the age of 37 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Hypothyroidism" (unspecified if ongoing); "Gastritis" (unspecified if ongoing). Concomitant medication(s) included: SYNTHROID; SPIRONOLACTONE; MULTIVITAMINS [VITAMINS NOS]. The following information was reported: FEELING HOT (non-serious) with onset 27Jun2021 16:15, outcome "recovered" (2021), described as "Warm feeling"; DIZZINESS (non-serious) with onset 27Jun2021 16:15, outcome "recovered" (2021), described as "dizziness"; DYSPNOEA (non-serious) with onset 27Jun2021 16:15, outcome "recovered" (2021), described as "shortness of breath"; NAUSEA (non-serious) with onset 27Jun2021 16:15, outcome "recovered" (2021), described as "nausea". Therapeutic measures were not taken as a result of feeling hot, dizziness, dyspnoea, nausea. Additional information: Patient did not had covid prior vaccination or tested for covid post vaccination. Patient did not had any other vaccine in four weeks. Follow-up (10Sep2021): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Gastritis; Hypothyroidism
Andere Medikamente: SYNTHROID; SPIRONOLACTONE; MULTIVITAMINS [VITAMINS NOS]
Allergien: -
Vorherige Impfungen: -

VAERS 1715127

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: NJ
Alter: 41,0
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 31.08.2021
Beginn: 01.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Chest pain

Symptomtext

felt minor chest pains/the 2nd week he felt like a heavy strong chest pain; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 41 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 31Aug2021 (Lot number: EW0179) at the age of 41 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "cholesterol is a little high", start date: 2021 (unspecified if ongoing), notes: did bloodwork back in Jun2021 or Jul2021 and was told his cholesterol was a little high; "Covid", start date: Mar2021 (unspecified if ongoing), notes: had Covid in Mar2021. There were no concomitant medications. Vaccination history included: Tb shot (got the TB shot and it left a mark). The following information was reported: CHEST PAIN (non-serious) with onset Sep2021, outcome "recovered" (Sep2021), described as "felt minor chest pains/the 2nd week he felt like a heavy strong chest pain". Additional information: HCP occupation/specialty was pediatrician. Caller states that the 2nd or 3rd day after the shot he felt minor chest pains and the 2nd week he felt like a heavy strong chest pain that he did not go to the ER or doctor for. Caller relays that it went away after 2-3 minutes, that it seemed longer to him but it was probably like 2-3 minutes. No investigation assessment. States that after that 1st week on the 2nd or 3rd day it went away and did not happen again until the middle of the 2nd week it happened again and went away and he hopes it does not come again. Caller states he had Covid in Mar2021 and did not get that strong chest pain then. Time the vaccination was given around 12-1pm. No history of previous immunization with the Pfizer vaccine considered as suspect. No additional vaccines administered on same date of the pfizer suspect. No prior vaccinations (within 4 weeks). Caller was asking should he take the 2nd shot. No follow-up attempts are possible. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cholesterol high (did bloodwork back in Jun2021 or Jul2021 and was told his cholesterol was a little high); COVID-19 (had Covid in Mar2021)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1715127

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: NJ
Alter: 41,0
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 31.08.2021
Beginn: 01.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Chest pain

Symptomtext

felt minor chest pains/the 2nd week he felt like a heavy strong chest pain; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 41 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 31Aug2021 (Lot number: EW0179) at the age of 41 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "cholesterol is a little high", start date: 2021 (unspecified if ongoing), notes: did bloodwork back in Jun2021 or Jul2021 and was told his cholesterol was a little high; "Covid", start date: Mar2021 (unspecified if ongoing), notes: had Covid in Mar2021. There were no concomitant medications. Vaccination history included: Tb shot (got the TB shot and it left a mark). The following information was reported: CHEST PAIN (non-serious) with onset Sep2021, outcome "recovered" (Sep2021), described as "felt minor chest pains/the 2nd week he felt like a heavy strong chest pain". Additional information: HCP occupation/specialty was pediatrician. Caller states that the 2nd or 3rd day after the shot he felt minor chest pains and the 2nd week he felt like a heavy strong chest pain that he did not go to the ER or doctor for. Caller relays that it went away after 2-3 minutes, that it seemed longer to him but it was probably like 2-3 minutes. No investigation assessment. States that after that 1st week on the 2nd or 3rd day it went away and did not happen again until the middle of the 2nd week it happened again and went away and he hopes it does not come again. Caller states he had Covid in Mar2021 and did not get that strong chest pain then. Time the vaccination was given around 12-1pm. No history of previous immunization with the Pfizer vaccine considered as suspect. No additional vaccines administered on same date of the pfizer suspect. No prior vaccinations (within 4 weeks). Caller was asking should he take the 2nd shot. No follow-up attempts are possible. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cholesterol high (did bloodwork back in Jun2021 or Jul2021 and was told his cholesterol was a little high); COVID-19 (had Covid in Mar2021)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2085493

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: KY
Alter: 58,0
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: 17.04.2021
Beginn: 02.02.2022
Tage bis Beginn: 291,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 pneumonia

Symptomtext

Pt admitted w/ covid pna, requiring o2. on remdesivir/dexamethasone

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: has a past medical history of Asthma, CHF (congestive heart failure) (HCC), COPD (chronic obstructive pulmonary disease) (HCC), Diabetes mellitus (HCC), Fibromyalgia, Hypertension, Kidney stones, Obesity with body mass index greater than 30, Pneumonia, and Renal disorder.
Vorgeschichte: has a past medical history of Asthma, CHF (congestive heart failure) (HCC), COPD (chronic obstructive pulmonary disease) (HCC), Diabetes mellitus (HCC), Fibromyalgia, Hypertension, Kidney stones, Obesity with body mass index greater than 30, Pneumonia, and Renal disorder.
Andere Medikamente: Insulin Glargine, albuterol, aspirin EC, budesonide-formoterol, cyclobenzaprine, insulin lispro, lisinopril, and metFORMIN
Allergien: codeine, naproxen,. penicillin, vancomycin
Vorherige Impfungen: -

VAERS 2085101

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 57,0
Geschlecht: M
Eingang: 03.02.2022
Impfdatum: 02.05.2021
Beginn: 10.01.2022
Tage bis Beginn: 253,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Chest X-ray normal Chest pain Computerised tomogram normal Cough Dyspnoea Myalgia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Patient is fully vaccinated. 58-year-old male who presents emergency center for evaluation of chest pain shortness of breath, and myalgias. Patient states that he has a history of deep venous thrombosis and Manera embolism. Patient states that he has been having congestion, cough, shortness of breath has been going for the past 3 days. Patient states that he went to his primary care provider today and was tested for COVID. Patient states that his COVID test was positive. BP 154/72 | Pulse 62 | Temp 98.3 ?F (36.8 ?C) (Oral) | Resp 18 | Ht 188 cm (6' 2") | Wt 101 kg (222 lb) | SpO2 97% | BMI 28.50 kg/m? CXR: No evidence of an acute process.No CT evidence of acute pulmonary emboli. Patient stable and discharged.

Weitere VAERSDATA-Felder

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

VAERS 2082462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: GA
Alter: 75,0
Geschlecht: F
Eingang: 02.02.2022
Impfdatum: 21.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Lymphadenopathy Myalgia Paraesthesia Ultrasound scan normal

Symptomtext

Swollen Lymph Node under left arm. Currently causing muscle tenderness and tingling in left arm. I had an Ultrasound, and no evidence of breast cancer was found. I am currently scheduled to see a breast specialist on 2/23/2022 and may have to have a biopsy performed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: I had an Ultrasound on 11/8/21, and no evidence of breast cancer was found.
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 Diabetes, Stage 2 Kidney-Disease
Andere Medikamente: Cartia, Vitamin D3, Tart Cherry Supplement
Allergien: Morphine, Lipitor
Vorherige Impfungen: -

VAERS 2080347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: NC
Alter: 34,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 21.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / -

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

Dyspnoea Heart rate increased Palpitations

Symptomtext

I've noticed that my heart rate has been elevated since my booster shot given on 12/21. I experience breathlessness, heart palpitations, and high heart rate when completing normal, every day activities. My smart watch has noted that my heart rate has been trending higher for 7 weeks, starting 2 days after my booster shot. My resting heart rate has increased by 11 beats per minute.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: My smart watch has noted that my heart rate has been trending higher for 7 weeks, starting 2 days after my booster shot. My resting heart rate has increased by 11 beats per minute.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: ibuprofen, tylenol
Allergien: none
Vorherige Impfungen: -

VAERS 2074405

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 44,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 06.05.2021
Beginn: 26.06.2021
Tage bis Beginn: 51,0
Dosis: 2
Route/Site: - / LA

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

Condition aggravated Inflammation Pain Polymenorrhoea SARS-CoV-2 test

Symptomtext

Full body inflammatory response with old injuries (bone and soft tissue) being so inflamed and painful as to be debilitating; Full body inflammatory response with old injuries (bone and soft tissue) being so inflamed and painful as to be debilitating.; Menstrual period was very early for 2 cycles (16-day cycle followed by a 9-day cycle. Normal cycle length 24 28 days); Full body inflammatory response with old injuries (bone and soft tissue) being so inflamed and painful as to be debilitating; This is a spontaneous report received from contactable reporter (Consumer or other non-HCP). The reporter is the patient. A 44-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 06May2021 (Lot number: EW0179) at the age of 44 years as dose 2, single for COVID-19 immunisation. Relevant medical history included: "Celiac disease" (unspecified if ongoing); "Gluten intolerance" (unspecified if ongoing), notes: known allergies: gluten and "Injury" (unspecified if ongoing), notes: Full body inflammatory response with old injuries (bone and soft tissue). Concomitant medication included unspecified supplements. Past drug history included: Fentanyl, reaction: "Drug allergy", notes: known allergies: fentanyl. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: EW0161; Anatomical Location: Right arm; Route of Administration: unspecified), administration date: 15Apr2021, when the patient was 44 years old, for COVID-19 immunisation. The following information was reported: INFLAMMATION (non-serious), CONDITION AGGRAVATED (non-serious) and PAIN (non-serious), all with onset 26Jun2021, outcome "recovered with sequelae", and all described as "Full body inflammatory response with old injuries (bone and soft tissue) being so inflamed and painful as to be debilitating", POLYMENORRHOEA (non-serious) with onset 26Jun2021, outcome "recovered with sequelae" described as "Menstrual period was very early for 2 cycles (16-day cycle followed by a 9-day cycle. Normal cycle length 24 28 days)". The events "Full body inflammatory response with old injuries (bone and soft tissue) being so inflamed and painful as to be debilitating" and "Menstrual period was very early for 2 cycles (16-day cycle followed by a 9-day cycle. Normal cycle length 24 28 days)" were evaluated at the emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of inflammation, condition aggravated, polymenorrhoea and pain. Additional Information: Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. The patient had no history of abnormal menstrual cycles and has not had any additional abnormal cycles since then. Since the vaccination, the patient had been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 20211223; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Celiac disease; Gluten intolerance (known allergies: gluten); Injury (Full body inflammatory response with old injuries (bone and soft tissue))
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2071619

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 31,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 06.05.2021
Beginn: 30.12.2021
Tage bis Beginn: 238,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Chills Cough Headache Migraine Pyrexia

Symptomtext

Patient is fully vaccinated. COVID positive at ED visit on 12/30/2021. 32-year-old female presenting with concern for Covid and also a migraine. Patient is positive for cough, chills, fever (101) and headache. No real shortness of breath. Denies chest pain. BP 132/83 | Pulse 89 | Temp 99.6 ?F (37.6 ?C) | Resp 18 | Ht 172.7 cm (5' 8") | Wt 118 kg (260 lb) | LMP 11/30/2021 | SpO2 96% | BMI 39.53 kg/m? IV established. Headache cocktail ordered. Patient was feeling much better. Headache significantly improved. Discharged from ED.

Weitere VAERSDATA-Felder

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

VAERS 2067855

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: OH
Alter: 73,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 06.08.2021
Beginn: 01.08.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Asthenia Blood test Chest X-ray Cough Dysgeusia Dyspnoea Electrocardiogram Headache Pain in extremity Rash

Symptomtext

I tasted the vaccine but it tasted like metal; it made me have a coughing spell; Rash; weakness for almost 2 months; Shortness of breath; Headache; my arm had soreness it's like somebody beat me up on my arm; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 73 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 06Aug2021 14:00 (Lot number: EW0179) at the age of 73 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Blood pressure management" (unspecified if ongoing). Concomitant medication(s) included: HYDROCHLOROTHIAZIDE taken for blood pressure management. The following information was reported: DYSGEUSIA (non-serious) with onset 06Aug2021, outcome "unknown", described as "I tasted the vaccine but it tasted like metal"; COUGH (non-serious) with onset 06Aug2021, outcome "unknown", described as "it made me have a coughing spell"; RASH (non-serious) with onset 06Aug2021, outcome "unknown", described as "Rash"; ASTHENIA (non-serious) with onset Aug2021, outcome "not recovered", described as "weakness for almost 2 months"; DYSPNOEA (non-serious) with onset Aug2021, outcome "unknown", described as "Shortness of breath"; HEADACHE (non-serious) with onset Aug2021, outcome "unknown", described as "Headache"; PAIN IN EXTREMITY (non-serious) with onset Aug2021, outcome "unknown", described as "my arm had soreness it's like somebody beat me up on my arm". The events "I tasted the vaccine but it tasted like metal", "it made me have a coughing spell", "rash", "weakness for almost 2 months", "shortness of breath", "headache" and "my arm had soreness it's like somebody beat me up on my arm" were evaluated at the emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of headache, pain in extremity. Additional information: The patient stated the vaccine was received at Pharmacy/drug store in the early afternoon and she did not remember the exact time so it's may 2'clock(06Aug2021). The patient was still in the store and she tasted the vaccine but it tasted like metal and it made her had a coughing spell then she had a rash and then she was still having weakness for almost 2 months. The patient went to the ER on the 20th and did blood work, EKG, chest x-ray then patient had a doctor appointment this past week. The patient was worry about the weakness and she had shortness of breath. She was checked for heart issues. For events worsened, improved and persisting, patient stated that the weakness, yeah she did not know it just didn't go away it's just she forced myself to get stuff done because she didn't want to lay around and wasted away so the doctor also told her keep moving around drink lots of fluid till they found out what's going on. For treatment, the patient she first had usual symptoms of side effects like headache she took Tylenol (treatment) for that for several days her arm had soreness it's like somebody beat her up on her arm after work, so it's mostly like the weakness brothering her and the shortness of the breath, she didn't know. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Blood work; Result Unstructured Data: Test Result:Unknown results; Test Date: 2021; Test Name: Chest x-ray; Result Unstructured Data: Test Result:Unknown results; Test Date: 2021; Test Name: EKG; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure management
Andere Medikamente: HYDROCHLOROTHIAZIDE
Allergien: -
Vorherige Impfungen: -

VAERS 2065386

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 49,0
Geschlecht: M
Eingang: 26.01.2022
Impfdatum: 06.05.2021
Beginn: 20.01.2022
Tage bis Beginn: 259,0
Dosis: 2
Route/Site: IM / -

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

Dyspnoea Hypoxia SARS-CoV-2 test

Symptomtext

Shortness of breath and hypoxic to the 60%.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: SARS-CoV-2 (COVID-19), point-of-care, antigen - office.
Aktuelle Erkrankungen: -
Vorgeschichte: Anemia; diabetes mellitus, type II; esophageal reflux; kidney stone; OSA (obstructive sleep apnea); hyperlipidemia; unspecified essential hypertension
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2062962

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 62,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 10.05.2021
Beginn: 21.01.2022
Tage bis Beginn: 256,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 Chills Cough Dyspnoea Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

chills, fever, congestion, cough, short of breath

Weitere VAERSDATA-Felder

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

VAERS 2059327

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: TX
Alter: 42,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 18.05.2021
Beginn: 23.08.2021
Tage bis Beginn: 97,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 pneumonia Dyspnoea Fatigue Pain Productive cough Pyrexia

Symptomtext

Presented with SOB, fever, body aches, fatigue, productive cough x 2 days; admit with Covid 19 PNA; tx with remdesivir, maxipime, steroids, doxycycline, zinc, Vit C, Vit D

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2057527

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: PA
Alter: 37,0
Geschlecht: M
Eingang: 22.01.2022
Impfdatum: 21.12.2020
Beginn: 01.02.2021
Tage bis Beginn: 42,0
Dosis: 3
Route/Site: IM / RA

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

Blood test Bronchoscopy Cardiac stress test Chest X-ray Chest discomfort Chest pain Dyspnoea Echocardiogram Granuloma Lung opacity Palpitations Paranasal sinus discomfort Sinusitis Tachycardia

Symptomtext

A few weeks after my second dose I began to feel slight chest pain/pressure discomfort in the mediastinal area in different spots. The symptoms progressively got worse as time went on. By 06/01/2021 my symptoms included strong heart palpitations, irregular beat tachycardic episodes, chest pressure/pain mediatinally and chest area surrounding my lungs mostly anteriorly and slightly posteriorly. My breathing also began to feel different as I felt I was unable to take deep breaths feeling SOB. After my third vaccine dose my symptoms worsen severly. Eventually, a CT of my lungs showed bilateral distal ground glass infiltration and granuloma formation which previous CXR failed to show. Since the CT scan a bronchoscopy was performed and treatment plan was started after all results came back from procedure. Steroid and antibiotic was perscribed. Treatment showed evidence of positive progresssion, but not complete recovery. Symptoms are not as severe which include heart palpitations, lower chest pressure and slight SOB. Any exertion and my symptoms worsen, mostly SOB. Trying to take very deep breaths very often and severe sinus pressure/inflammation (more left sided) has also been symptoms throughout this entire process.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Blood tests, Chest X-Rays, Transthoracic Echo, Stress test, Bronchoscopy all after 08/01/2021
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2051361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: NJ
Alter: 61,0
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: 15.06.2021
Beginn: 28.07.2021
Tage bis Beginn: 43,0
Dosis: 2
Route/Site: IM / AR

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

Headache Migraine Ophthalmic migraine

Symptomtext

7/28/2021: Ocular migraine lasted approximately 30 minutes. 7/29/2021: Ocular migraine lasted approximately 60 minutes followed by a migraine headache, which I never experienced previously. 7/29/2021: Seen by eye doctor and advised it was not my eyes. It was recommended to see a neurologist if it happens again. 11/6/2021: Ocular migraine lasted approximately 15 minutes. 11/8/2021: Ocular migraine lasted approximately 15 minutes and I had a headache for the remainder of the day. 12/6/2021: Headache all day. 12/30/2021: Headache developed at 1:00 pm and lasted the remainder of the day. 01/11/2022: Ocular migraine lasted approximately 2 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Examined by eye doctor.
Aktuelle Erkrankungen: None
Vorgeschichte: Acid reflux
Andere Medikamente: Restasis; Omeprazole; Vitamin D3; Multivitamin
Allergien: Sulfa drugs; Sardines
Vorherige Impfungen: -

VAERS 2051220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: KY
Alter: 64,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 12.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: IM / RA

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

Chills Cough Dyspnoea Fatigue Illness Nausea Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

1/20/22 65 yr/o female who presents with cough congestion with associated sore throat nausea fatigue. The patient recently had a COVID booster 3 days ago however has been gradually getting more sick over the last several days with associated fever at home. Also has had some mild shortness of breath today as well. Review of Systems Constitutional: Positive for chills, fatigue and fever. Respiratory: Positive for cough and shortness of breath. Cardiovascular: Negative for chest pain. Gastrointestinal: Negative for abdominal pain, nausea and vomiting. Genitourinary: Negative for dysuria. Musculoskeletal: Negative for back pain. Skin: Negative for rash. Neurological: Negative for dizziness and headaches. Review of Systems Neurological: Negative for dizziness and headaches. Psychiatric/Behavioral: The patient is not nervous/anxious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 1/17/22 COVID-19 Result Detected Abnormal
Aktuelle Erkrankungen: -
Vorgeschichte: Arthritis o Benign essential HTN o Chronic kidney disease o Coronary artery disease o Diabetes mellitus o Diabetes mellitus o Glaucoma o Hyperlipidemia o Hyperthyroidism o Nonsenile cataract
Andere Medikamente: aspirin 81 MG tablet Take 81 mg by mouth daily 1/17/2022 o atorvastatin (LIPITOR) 40 MG tablet Take 40 mg by mouth daily . o benazepril (LOTENSIN) 20 MG tablet Take 20 mg by mouth daily. o clopidogrel (PLAVIX) 75 MG tablet Take 75
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2047961

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 51,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 06.05.2021
Beginn: 09.01.2022
Tage bis Beginn: 248,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 Dyspnoea Headache Myalgia SARS-CoV-2 test positive

Symptomtext

short of breath, myalgias, headache

Weitere VAERSDATA-Felder

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

VAERS 2046407

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: OH
Alter: 61,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 20.05.2021
Beginn: 15.01.2022
Tage bis Beginn: 240,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 COVID-19 pneumonia Dyspnoea SARS-CoV-2 test positive

Symptomtext

Patient fully vaccinated with Pfizer on 4/29/21 and 5/20/21. Patient admitted with COVID PNA on 1/16/22 and is still admitted. Had increased SOB and O2 sats 85% on admission

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 3,0
Labordaten: + 1/16/22 COVID
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1278091

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

moderat

Staat: MI
Alter: 36,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 01.05.2021
Beginn: 26.12.2021
Tage bis Beginn: 239,0
Dosis: 2
Route/Site: IM / AR

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

Abdominal pain Abdominal pain lower Abdominal pain upper Abdominal rebound tenderness Chills Fatigue Hypertension Nausea Pelvic pain Pyrexia Injection site erythema Pruritus

Symptomtext

? Abdominal Pain "It feels like my stomach just hit a wall and I had instant pain, I think I popped a cyst or something" RLQ and pelvis, fever and nausea x2 days, +rebound tenderness ? Pelvic Pain HPI Pt is a 37-year-old female presenting to our ED with chief complaint of right lower quadrant abdominal pain. Past medical history significant for endometriosis, right sided ovarian torsion, left-sided ectopic pregnancy. Past surgical history significant for left sided oophrectomy, hysterectomy, laparoscopic cyst removal of right ovary with torsion. Patient reports earlier today she was having intercourse with her husband approximately an hour prior to arrival, when suddenly she began to have sharp stabbing right lower quadrant pain. Patient went to the ER right away, stating symptoms are similar to prior ovarian torsion, similar presentation too. Patient denies history of appendectomy. Over the past few days she has had nausea, chills, fatigue and temp of 99?F. Denies taking any medications for her symptoms. Pt further denies any vaginal bleeding, changes in vaginal discharge, urinary sx, flank pain. Review of Systems Constitutional: Negative for fever, + chills HEENT: Negative for recent URI symptoms Respiratory: Negative for shortness of breath Cardiovascular: Negative for chest pain Gastrointestinal: + abdominal pain, + nausea Genitourinary: Negative for urinary symptoms Musculoskeletal: Negative for trauma Skin: Negative for rash Neurological: Negative for weakness or paresthesias Psychiatric/Behavioral: Negative for agitation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: ? Abdominal Pain "It feels like my stomach just hit a wall and I had instant pain, I think I popped a cyst or something" RLQ and pelvis, fever and nausea x2 days, +rebound tenderness ? Pelvic Pain HPI Pt is a 37-year-old female presenting to our ED with chief complaint of right lower quadrant abdominal pain. Past medical history significant for endometriosis, right sided ovarian torsion, left-sided ectopic pregnancy. Past surgical history significant for left sided oophrectomy, hysterectomy, laparoscopic cyst removal of right ovary with torsion. Patient reports earlier today she was having intercourse with her husband approximately an hour prior to arrival, when suddenly she began to have sharp stabbing right lower quadrant pain. Patient went to the ER right away, stating symptoms are similar to prior ovarian torsion, similar presentation too. Patient denies history of appendectomy. Over the past few days she has had nausea, chills, fatigue and temp of 99?F. Denies taking any medications for her symptoms. Pt further denies any vaginal bleeding, changes in vaginal discharge, urinary sx, flank pain. Review of Systems Constitutional: Negative for fever, + chills HEENT: Negative for recent URI symptoms Respiratory: Negative for shortness of breath Cardiovascular: Negative for chest pain Gastrointestinal: + abdominal pain, + nausea Genitourinary: Negative for urinary symptoms Musculoskeletal: Negative for trauma Skin: Negative for rash Neurological: Negative for weakness or paresthesias Psychiatric/Behavioral: Negative for agitation
Aktuelle Erkrankungen: Anemia ? Ectopic pregnancy 2009 s/p MTXx2 with Lap salpingectomy ? Endometriosis stage IV ? Endometriosis ? History of DVT (deep vein thrombosis) provoked after surgeries ? Hypertension 12/26/2021 ? Kidney stones ? Ovarian torsion 2008? s/p lap detorsion ? PID (pelvic inflammatory disease) 2006 ? Pulmonary embolism (CMS/HCC) ? Syphilis 2003 ? Trichomonas infection 2004 Pertinent Negatives - Past Medical History Diagnosis Date Noted ? Asthma 12/11/2016 ? CAD (coronary artery disease) 12/11/2016 ? Cancer 12/11/2016 ? Chronic obstructive pulmonary disease (CMS/HCC) 12/11/2016 ? CVA (cerebrovascular accident) (CMS/HCC) 12/11/2016 ? Diabetes mellitus (CMS/HCC) 12/11/2016 ? Dialysis patient 12/11/2016 ? Fibromyalgia 12/11/2016 ? Hypothyroidism 12/11/2016 ? Immune disorder (CMS/HCC) 12/11/2016 ? Restrictive lung disease 12/11/2016 ? Vascular disease
Vorgeschichte: Anemia ? Ectopic pregnancy 2009 s/p MTXx2 with Lap salpingectomy ? Endometriosis stage IV ? Endometriosis ? History of DVT (deep vein thrombosis) provoked after surgeries ? Hypertension 12/26/2021 ? Kidney stones ? Ovarian torsion 2008? s/p lap detorsion ? PID (pelvic inflammatory disease) 2006 ? Pulmonary embolism (CMS/HCC) ? Syphilis 2003 ? Trichomonas infection 2004 Pertinent Negatives - Past Medical History Diagnosis Date Noted ? Asthma 12/11/2016 ? CAD (coronary artery disease) 12/11/2016 ? Cancer 12/11/2016 ? Chronic obstructive pulmonary disease (CMS/HCC) 12/11/2016 ? CVA (cerebrovascular accident) (CMS/HCC) 12/11/2016 ? Diabetes mellitus (CMS/HCC) 12/11/2016 ? Dialysis patient 12/11/2016 ? Fibromyalgia 12/11/2016 ? Hypothyroidism 12/11/2016 ? Immune disorder (CMS/HCC) 12/11/2016 ? Restrictive lung disease 12/11/2016 ? Vascular disease
Andere Medikamente: Patient's Medications New Prescriptions No medications on file Previous Medications DIPHENHYDRAMINE (BENADRYL) 25 MG PO TAB take 1 Tab by mouth every 6 hours as needed for FOR ITCHING or FOR RASH. METOPROLOL (LOPRESSOR) 25 MG PO T
Allergien: Imported_Misc_Allergy D limonene flavor- unknown rx- listed on allergy list from HOSPITAL ? Codeine Hives and Hives ? Ibuprofen Itching and Hives ? Iodinated Diagnostic Agents Hives, Itching and Hives Patient had a breakthrough reaction on 1/28/20 after being premedicated for CT Abdomen Pelvis. Severe itching and Radiologist administered Benadryl. ? Ketorolac Tromethamine Hives ? Metoclopramide In outside record from another facility - doesn't know reaction ? Metrizamide Other Comment from MD in CT note states possible anaphylaxis reaction to iodine ? Nsaids Told due to ketoralac allergy
Vorherige Impfungen: -

VAERS 1278091

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 36,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 01.05.2021
Beginn: 26.12.2021
Tage bis Beginn: 239,0
Dosis: 2
Route/Site: UN / UN

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

Abdominal pain Abdominal pain lower Abdominal pain upper Abdominal rebound tenderness Chills Fatigue Hypertension Nausea Pelvic pain Pyrexia Injection site erythema Pruritus

Symptomtext

? Abdominal Pain "It feels like my stomach just hit a wall and I had instant pain, I think I popped a cyst or something" RLQ and pelvis, fever and nausea x2 days, +rebound tenderness ? Pelvic Pain HPI Pt is a 37-year-old female presenting to our ED with chief complaint of right lower quadrant abdominal pain. Past medical history significant for endometriosis, right sided ovarian torsion, left-sided ectopic pregnancy. Past surgical history significant for left sided oophrectomy, hysterectomy, laparoscopic cyst removal of right ovary with torsion. Patient reports earlier today she was having intercourse with her husband approximately an hour prior to arrival, when suddenly she began to have sharp stabbing right lower quadrant pain. Patient went to the ER right away, stating symptoms are similar to prior ovarian torsion, similar presentation too. Patient denies history of appendectomy. Over the past few days she has had nausea, chills, fatigue and temp of 99?F. Denies taking any medications for her symptoms. Pt further denies any vaginal bleeding, changes in vaginal discharge, urinary sx, flank pain. Review of Systems Constitutional: Negative for fever, + chills HEENT: Negative for recent URI symptoms Respiratory: Negative for shortness of breath Cardiovascular: Negative for chest pain Gastrointestinal: + abdominal pain, + nausea Genitourinary: Negative for urinary symptoms Musculoskeletal: Negative for trauma Skin: Negative for rash Neurological: Negative for weakness or paresthesias Psychiatric/Behavioral: Negative for agitation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: ? Abdominal Pain "It feels like my stomach just hit a wall and I had instant pain, I think I popped a cyst or something" RLQ and pelvis, fever and nausea x2 days, +rebound tenderness ? Pelvic Pain HPI Pt is a 37-year-old female presenting to our ED with chief complaint of right lower quadrant abdominal pain. Past medical history significant for endometriosis, right sided ovarian torsion, left-sided ectopic pregnancy. Past surgical history significant for left sided oophrectomy, hysterectomy, laparoscopic cyst removal of right ovary with torsion. Patient reports earlier today she was having intercourse with her husband approximately an hour prior to arrival, when suddenly she began to have sharp stabbing right lower quadrant pain. Patient went to the ER right away, stating symptoms are similar to prior ovarian torsion, similar presentation too. Patient denies history of appendectomy. Over the past few days she has had nausea, chills, fatigue and temp of 99?F. Denies taking any medications for her symptoms. Pt further denies any vaginal bleeding, changes in vaginal discharge, urinary sx, flank pain. Review of Systems Constitutional: Negative for fever, + chills HEENT: Negative for recent URI symptoms Respiratory: Negative for shortness of breath Cardiovascular: Negative for chest pain Gastrointestinal: + abdominal pain, + nausea Genitourinary: Negative for urinary symptoms Musculoskeletal: Negative for trauma Skin: Negative for rash Neurological: Negative for weakness or paresthesias Psychiatric/Behavioral: Negative for agitation
Aktuelle Erkrankungen: Anemia ? Ectopic pregnancy 2009 s/p MTXx2 with Lap salpingectomy ? Endometriosis stage IV ? Endometriosis ? History of DVT (deep vein thrombosis) provoked after surgeries ? Hypertension 12/26/2021 ? Kidney stones ? Ovarian torsion 2008? s/p lap detorsion ? PID (pelvic inflammatory disease) 2006 ? Pulmonary embolism (CMS/HCC) ? Syphilis 2003 ? Trichomonas infection 2004 Pertinent Negatives - Past Medical History Diagnosis Date Noted ? Asthma 12/11/2016 ? CAD (coronary artery disease) 12/11/2016 ? Cancer 12/11/2016 ? Chronic obstructive pulmonary disease (CMS/HCC) 12/11/2016 ? CVA (cerebrovascular accident) (CMS/HCC) 12/11/2016 ? Diabetes mellitus (CMS/HCC) 12/11/2016 ? Dialysis patient 12/11/2016 ? Fibromyalgia 12/11/2016 ? Hypothyroidism 12/11/2016 ? Immune disorder (CMS/HCC) 12/11/2016 ? Restrictive lung disease 12/11/2016 ? Vascular disease
Vorgeschichte: Anemia ? Ectopic pregnancy 2009 s/p MTXx2 with Lap salpingectomy ? Endometriosis stage IV ? Endometriosis ? History of DVT (deep vein thrombosis) provoked after surgeries ? Hypertension 12/26/2021 ? Kidney stones ? Ovarian torsion 2008? s/p lap detorsion ? PID (pelvic inflammatory disease) 2006 ? Pulmonary embolism (CMS/HCC) ? Syphilis 2003 ? Trichomonas infection 2004 Pertinent Negatives - Past Medical History Diagnosis Date Noted ? Asthma 12/11/2016 ? CAD (coronary artery disease) 12/11/2016 ? Cancer 12/11/2016 ? Chronic obstructive pulmonary disease (CMS/HCC) 12/11/2016 ? CVA (cerebrovascular accident) (CMS/HCC) 12/11/2016 ? Diabetes mellitus (CMS/HCC) 12/11/2016 ? Dialysis patient 12/11/2016 ? Fibromyalgia 12/11/2016 ? Hypothyroidism 12/11/2016 ? Immune disorder (CMS/HCC) 12/11/2016 ? Restrictive lung disease 12/11/2016 ? Vascular disease
Andere Medikamente: Patient's Medications New Prescriptions No medications on file Previous Medications DIPHENHYDRAMINE (BENADRYL) 25 MG PO TAB take 1 Tab by mouth every 6 hours as needed for FOR ITCHING or FOR RASH. METOPROLOL (LOPRESSOR) 25 MG PO T
Allergien: Imported_Misc_Allergy D limonene flavor- unknown rx- listed on allergy list from HOSPITAL ? Codeine Hives and Hives ? Ibuprofen Itching and Hives ? Iodinated Diagnostic Agents Hives, Itching and Hives Patient had a breakthrough reaction on 1/28/20 after being premedicated for CT Abdomen Pelvis. Severe itching and Radiologist administered Benadryl. ? Ketorolac Tromethamine Hives ? Metoclopramide In outside record from another facility - doesn't know reaction ? Metrizamide Other Comment from MD in CT note states possible anaphylaxis reaction to iodine ? Nsaids Told due to ketoralac allergy
Vorherige Impfungen: -

VAERS 2039116

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 51,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 12.05.2021
Beginn: 28.11.2021
Tage bis Beginn: 200,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Cough Electrocardiogram Fibrin D dimer increased Pain Respiratory tract congestion SARS-CoV-2 test positive Sinus tachycardia

Symptomtext

Patient fully vaccinated. COVID + on 11/28/2021. ED visit on 11/28/2021. 52-year-old male presents complaining of cough, congestion, and body aches that began approximately 4 days ago. The patient's wife is having similar symptoms. He denies any fevers or chills. Denies any nausea or vomiting.He denies any shortness of breath. Patient has a history of tachycardia at baseline, evaluated by cardio. BP 149/80 | Pulse 108 | Temp 98.4 ?F (36.9 ?C) (Oral) | Resp 22 | Ht 182.9 cm (6') | Wt 113 kg (250 lb) | SpO2 99% | BMI 33.91 kg/m? EKG Final interpretation: sinus tachycardia, no signs of ischemia and no infarction. d-dimer the patient but it was elevated (507). CTA ordered. No evidence of PE. Patient does have right-sided consolidation.He was given steroids. He'll be referred to Dr clinic for infusion. Discharged.

Weitere VAERSDATA-Felder

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

VAERS 2032377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: IA
Alter: 40,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 18.08.2021
Beginn: 27.08.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: IM / -

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

Alanine aminotransferase increased Aspartate aminotransferase increased Asthenia Blood chloride decreased Blood creatinine increased Blood glucose normal C-reactive protein increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram thorax abnormal Decreased appetite Diarrhoea Dyspnoea Fatigue Feeling abnormal Fibrin D dimer increased Hypoxia

Symptomtext

COVID Vaccine Breakthrough Case Pfizer Dose 1 8/18/21 (EW0179) COVID Positive 8/30/21 Presented to and discharged from ED 8/31/21 Discharged to home 8/31/21 9/6/21: Patient is a 40-year-old male who presents to the ED today for worsening COVID-19 symptoms. The patient tested positive for COVID-19 on 08/30/2021. The patient complains of fevers, body aches, fatigue, shortness of breath that have been worsening. The patient has been taking Tylenol and ibuprofen for relief of symptoms with minimal relief. Patient also reports diarrhea and decreased appetite. Patient has a past medical history significant for generalized anxiety, aortic stenosis, tachycardia. Upon arrival to ED patient's O2 saturation was 88% on room air, patient was placed on 4 L nasal cannula with resolution of hypoxia. Chest x-ray was performed and revealed marked interval increase in bilateral pneumonia concerning for atypical infection. Patient's vital signs were as follows temperature 102?, heart rate 116, respirations 22, blood pressure 117/77. Patient's laboratory results were significant for ESR 32, D-dimer 0.51, CRP 15.3, chloride 96, glucose 150, creatinine 1.48, ALT 77, AST 67, lipase 92. Due to elevated D-dimer, CT angio of chest was ordered to rule out PE. Patient was seen and examined at the bedside in ED. Patient is lying in bed in no acute distress. Patient is currently on 4 L oxygen via nasal cannula and oxygen saturation is at 99%. Patient continues to complain of body aches, fatigue, weakness. Patient states he has been progressively feeling worse over the last couple of days despite taking Tylenol, ibuprofen for relief of symptoms. Patient denies any history of COPD, asthma. Patient denies any chest pain. Patient is being admitted for COVID pneumonia. 9/10/21: The patient, in fairly good health, tested positive for COVID-19 on 08/30/2021. He was given a pulse oximetry for home and home treatment plan, was noted to have 88% oxygenation on room air, and presented to the hospital for admission on 09/06/2021. He received IV CAP antibiotics, dexamethasone and remdesivir, and had gradual improvement with him able to get off oxygen. He did oxygen walk, did not require any supplemental oxygen with oxygenation 93% during ambulation. Blood pressure 130/80, pulse 74 and regular. He was afebrile. He has he had a CT scan of the chest showing no signs of pulmonary emboli. There were tiny bilateral pleural effusions and multifocal areas suggesting COVID-19 pneumonia. Since there has been such nice improvement, patient will go home with no new medications. Continue his activities of daily living. He may return to work next week for light duty and full duty on September 20th, if he continues to do well. Otherwise, follow up with doctor next week for re-evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 5,0
Labordaten: see above
Aktuelle Erkrankungen: HTN
Vorgeschichte: HTN
Andere Medikamente: metoprolol succinate 50 mg PO QD
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2031963

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: NY
Alter: 34,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 26.05.2021
Beginn: 26.06.2021
Tage bis Beginn: 31,0
Dosis: 2
Route/Site: SYR / LA

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

Anxiety Attention deficit hyperactivity disorder Condition aggravated Depression

Symptomtext

So a month after the vaccine, on 06/26/2021, I noticed my anxiety and it progressively got worse. At 1st I thought it was because I was cooped up in the house for so long, I was working from home since 03/2020. I did return back to the office 09/20/2021 for 3 days a week, but I could not go back because of my anxiety. After July I developed extreme depression. I reached out to an online app to a doctor and he diagnosed me with ADHD and I received online consultations. On 09/29/2021 I saw my doctor, because the anxiety became worse. He referred me to a neurologist and psychiatrist. Dr. mentioned he could not rule out the vaccine, but it could be that it is an after affect of having COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: He checked my lungs, reflexes and blood pressure.
Aktuelle Erkrankungen: I did have a mild cold 2 weeks before the vaccination.
Vorgeschichte: Severe migraines; IBS; fibromyalgia; PMDD; ADHD; tenderness on the top of my head like a headache it started when I got COVID-19 on 01/28/2021.
Andere Medikamente: None
Allergien: Dairy; red meat; onions; garli; broccoli; asparagus; peanuts; coconuts
Vorherige Impfungen: Pfizer Dose 1, 05/05/2021, I felt like I had COVID-19 all over again, bad headaches, chills, muscle soreness, GI issues.

VAERS 2028497

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: WI
Alter: 66,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 02.06.2021
Beginn: 05.01.2022
Tage bis Beginn: 217,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 COVID-19 pneumonia SARS-CoV-2 test positive

Symptomtext

Patient admitted as inpatient on 1/5/22 due to pneumonia due to COVID-19 virus. Patient was tested for COVID-19 and was positive on 1/5/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028202

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 63,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 01.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Herpes zoster

Symptomtext

Background info: about 25 years ago I had a classic case of shingles. I subsequently received two courses of shingles vaccines, the single vaccine and the more recent double vaccine. About a week after I received the booster COVID vaccine, I broke out on my upper back shoulder and around the top of my right shoulder. At first I thought it was an allergic reaction to something else but didn't know what it could be. Over the next week, the rash traveled across my back in a straight line. I took one leftover Valtrex pill that calmed the breakout and it was then I thought it could be a Shingles breakout. I scheduled a visit with my PCP. She had not seen any research on a relationship between the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Atorvastatin; Finasteride; Spironotactone; mirabegron; Flonase.
Allergien: Penicillin.
Vorherige Impfungen: -

VAERS 2027245

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: NC
Alter: 36,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 16.08.2021
Beginn: 16.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Paraesthesia Pruritus SARS-CoV-2 test Skin discolouration Vaccination site pruritus

Symptomtext

her arm immediately started itching, really badly/Just around the injection site.; maybe a little discoloration can't tell; injection site is itching; for felt like arm was falling asleep; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from medical information team. The reporter is the patient. Other Case identifier(s): US-PFIZER INC-202101057941. A 36 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 16Aug2021 (Lot number: EW0179) at the age of 36 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "COVID-19", start date: May2020 (unspecified if ongoing), notes: She had some weird side effects.; "Shingles" (unspecified if ongoing), notes: She has had shingles before. The patient's concomitant medications were not reported. The following information was reported: PRURITUS (non-serious) with onset 16Aug2021, outcome "not recovered", described as "her arm immediately started itching, really badly/Just around the injection site."; SKIN DISCOLOURATION (non-serious) with onset 16Aug2021, outcome "not recovered", described as "maybe a little discoloration can't tell"; VACCINATION SITE PRURITUS (non-serious) with onset 16Aug2021, outcome "not recovered", described as "injection site is itching"; PARAESTHESIA (non-serious) with onset 16Aug2021, outcome "recovering", described as "for felt like arm was falling asleep". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The patient did not have any family medical history relevant to adverse events. The facility where the most recent COVID-19 vaccine was administered was clinic. The vaccine was not administered at facility. No additional vaccines were administered on same date of the Pfizer suspect. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. It was reported that the patient received the first dose of the Pfizer COVID vaccine and her arm immediately started itching, really badly, maybe a little discoloration couldn't tell. It happened 10 minutes after the vaccination and it was an annoying itch. Just around the injection site. She felt itchiness. It was very itchy and she wanted to know if she could take Benadryl. The adverse event did not require a visit to Emergency Room or Physician Office. No relevant tests were done. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 202005; Test Name: COVID-19 test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (She had some weird side effects.); Shingles (She has had shingles before.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2024187

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: NC
Alter: 31,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 01.08.2021
Beginn: 03.08.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / LA

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

Dyspnoea Heart rate irregular

Symptomtext

Shortness of breath, irrational heartbeat; Shortness of breath, irrational heartbeat; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 31 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 01Aug2021 13:00 (Lot number: EW0179) at the age of 31 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: HEART RATE IRREGULAR (non-serious), DYSPNOEA (non-serious) all with onset 03Aug2021, outcome "not recovered" and all described as "Shortness of breath, irrational heartbeat". Therapeutic measures were not taken as a result of heart rate irregular, dyspnoea. Addition Information: No other vaccine in four weeks. No other medications in two weeks. She did not have Covid prior vaccination, She did not have Covid tested post vaccination. Patient had not any known allergies. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2019973

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: OR
Alter: 35,0
Geschlecht: M
Eingang: 09.01.2022
Impfdatum: 08.01.2022
Beginn: 09.01.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / AR

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

Angina pectoris Chest pain

Symptomtext

chest pain; left side; heart pain after 24 hours. contacted the doctor for more information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: asthma/bronchitis
Andere Medikamente: finasteride; escitalopram; albuterol; advair
Allergien: pineapple
Vorherige Impfungen: -

VAERS 2019811

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 46,0
Geschlecht: F
Eingang: 09.01.2022
Impfdatum: 04.05.2021
Beginn: 29.12.2021
Tage bis Beginn: 239,0
Dosis: 1
Route/Site: UN / UN

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

short of breath + COVID test

Weitere VAERSDATA-Felder

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

VAERS 2014796

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 50,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 13.05.2021
Beginn: 27.12.2021
Tage bis Beginn: 228,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 Cough Dyspnoea Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

congestion, cough, short of breath + COVID test

Weitere VAERSDATA-Felder

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

VAERS 2014769

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 52,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 07.05.2021
Beginn: 26.12.2021
Tage bis Beginn: 233,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 Dyspnoea Hypoxia SARS-CoV-2 test positive

Symptomtext

short of breath, hypoxia + COVID test

Weitere VAERSDATA-Felder

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

VAERS 2014445

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 51,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 16.05.2021
Beginn: 31.12.2021
Tage bis Beginn: 229,0
Dosis: UNK
Route/Site: - / -

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

Abdominal pain Abdominal pain upper Asthenia Condition aggravated Cough Dyspnoea Fatigue Nausea Pain Vomiting

Symptomtext

Pt presented to the ED on 12/31/21 Patient is a 52-year-old Caucasian female who presents to the emergency room with chief complaint of nausea and vomiting. She states that her whole body hurts. She states generalized weakness and fatigue. For the past 2-3 days she's had several episodes of nonbloody emesis to the point that she is not even able to keep down her usual home medications. She states that she has abdominal pain with shortness of breath. No chest pain. She has a reactive cough. She is fully vaccinated for coronavirus and received her second shot in April. Has not received a booster shot. She doesn't smoke. No alcohol or illicit drug use. Denies history of previous heart attacks...Pain in her stomach as an aching sensation in the periumbilical region. Constant nonradiating with no worsening or relieving factors. No sick contacts or recent travel. She's not home oxygen dependent and denies any chronic issues with her lungs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: Endocrine...Endocrine Type 2 diabetes mellitus Seizure disorder Migraine Acute chest pain Sepsis secondary to UTI Acute hypokalemia Leukocytosis Dilantin overdose Herniated nucleus pulposus Seizure Chronic low back pain Hypertension Shortness of breath Dyspnea Lumbago with sciatica S/P lumbar fusion Morbid obesity with BMI of 40.0-44.9, adult Lumbar radiculopathy Herniated nucleus pulposus of lumbosacral region Leg swelling Abdominal pain, RLQ (right lower quadrant) Acute abdominal pain Lumbar burst fracture COVID-19 Anemia, chronic disease
Andere Medikamente: amoxicillin-potassium...amoxicillin-potassium clavulanate (Augmentin) 500-125 MG PO Tab atenolol (TENORMIN) 25 MG PO Tab atorvastatin (LIPITOR) 80 MG PO Tab benzonatate (TESSALON) 200 MG PO Cap budesonide-formoterol (SYMBICORT) 160-4.5 MCG/
Allergien: Pregabalin
Vorherige Impfungen: -

VAERS 2000017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 01.02.2021
Beginn: 10.04.2021
Tage bis Beginn: 68,0
Dosis: 3
Route/Site: IM / LA

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

Atrial fibrillation Cardiac ablation Cardioversion Condition aggravated Echocardiogram abnormal

Symptomtext

Nothing until about May when the AFib became more prevalent resulting in Cardio Inversion in June. AFib condition reappeared in October that after attempt to control with medication, December 28, 2021, ablation was preformed. Booster given 9/29/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Cardio Inversion with echo cardiogram 6/2021. Ablation 12/28/2021 performed by Dr. 'PRIVATE'.
Aktuelle Erkrankungen: -
Vorgeschichte: Type 2 Diabetes, Sleep Apnea, high blood pressure, AFib - first diagnosed 1/2017 and no issues until afterwards.
Andere Medikamente: Sertraline HCl / Zoloft?, Spironolactone Tabs / Aldactone?, Biotin 10,000 mg / day- Hair and nail treatment, Eliquis 5 mg / 2-times daily Blood Thinner for AFib, Lamotrigine /Lamictal? 100 mg / twice daily- Depression, Metformin HCl XR / Gl
Allergien: Penicillin, Narcotic pain medication
Vorherige Impfungen: Beginning with the 2nd dosage.

VAERS 1998059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: NY
Alter: 41,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 02.05.2021
Beginn: 02.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / UN

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

Adverse reaction Decreased appetite Dyspnoea Fatigue Feeding disorder Gait disturbance Headache Impaired work ability Migraine Nausea Pyrexia Speech disorder Tremor Vomiting projectile

Symptomtext

Projectile vomiting, fever, difficulty speaking and breathing (needed to take gulps of air in order to speak), difficulty taking in air, shaking, fever, unable to walk unassisted, loss of appetite and extreme nausea, unable to eat solid food/ keep food down, extreme headache and migraine symptoms, extreme fatigue, unable to work for approx. 5 days after the 2nd dose due to battling the various symptoms over the course of the adverse reaction

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: None
Andere Medikamente: Daily vitamin
Allergien: No
Vorherige Impfungen: -

VAERS 1989358

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: NJ
Alter: 71,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 04.10.2021
Beginn: 18.12.2021
Tage bis Beginn: 75,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Impaired driving ability Mobility decreased Myalgia Pain in extremity

Symptomtext

Nearly 3 months after receiving the shot, and quite suddenly, I developed severe pain in my entire right arm. The shot was given quite high up on my arm, close to the shoulder. I commented about the height of the shot, and was told, "that is how we do it". The pain was in the muscles of my arm and the tissues that make up the shoulder. The pain was debilitating, making it difficult to put a shirt or coat on, drive a car, push a door open, etc. The pain, after 9 days has lessened and will hopefully go away so I don't need to see a doctor for treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None, just reviewed this with my primary care physician.
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure, under control. Non-contractile bladder, self cathertization. Hear patient.
Andere Medikamente: 1. Hiprex Tabs, 1 gm., 2X a day 2. Prinzide, 20/12.5 mg. 3. Amlodipine Besylate, 10 mg. 4. Ezetimide, 10 mg. 5. Toprol XL, 25 mg.
Allergien: Injected iodine for contrast.
Vorherige Impfungen: First Pfizer covid shot, arm pain for 7 days.

VAERS 1989274

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: GA
Alter: 39,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 29.06.2021
Beginn: 04.07.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: SYR / AR

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

Abdominal discomfort Antinuclear antibody Back pain Colonoscopy Computerised tomogram Constipation Dyskinesia Eructation Head discomfort Laparoscopy Migraine Neck pain Pain Pain in extremity Sensory disturbance Tremor Ultrasound pelvis

Symptomtext

GI issues within 5 days of 1st dose - (constipation and frequent burping) A few weeks later: Pulsating sensations in pelvic region, neck, ankles, and wrists Vibrating sensations/tremors in body and head Pressure in pelvis Lower back pain Stinging, burning pain in neck and arms Pressure in head Migraines/headaches Involuntary movements in arm, hand, face, and legs

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Colonoscopy - August 2021 CT scan - September 2021 Ultrasound and pelvic exam - September 2021 Laparoscopy - October 2021 ANA panel test - October 2021 CT scan - November 2021
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1975435

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: KY
Alter: 57,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 04.05.2021
Beginn: 20.12.2021
Tage bis Beginn: 230,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Chills Condition aggravated Decreased appetite Dyspnoea Head discomfort Headache Myalgia Pleurisy Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

12/20/21 presenting today for Chills (unable to cough/ runny nose/ stuffy head/ SOA / feels like pleurisy x 3 d ) and Covid-19 Positive 57 year old female presenting with chills, runny nose and congestion for 2 days. No sick contacts. 1/2021 had covid. Had 2 covid vaccines. Unsure of flu vaccine status. Non smoker. History HTN, allergies and pleurisy. Treating with nyquil with mild relief. Review of Systems Constitutional: Positive for appetite change, chills and fever. HENT: Positive for congestion and rhinorrhea. Negative for ear discharge, ear pain, sinus pain and sore throat. Eyes: Negative for redness. Respiratory: Positive for shortness of breath. Negative for cough and wheezing. 12/20/21 Gastrointestinal: Negative for diarrhea, nausea and vomiting. Musculoskeletal: Positive for myalgias. Allergic/Immunologic: Negative for environmental allergies. Neurological: Positive for headaches. Negative for dizziness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 12/20/21 COVID Result IPOC Detected Abnormal
Aktuelle Erkrankungen: -
Vorgeschichte: GERD, hypertension
Andere Medikamente: Aspirin 81 mg daily, Calcium carbonate antacid 1000mg daily Zaditor ophthalmic solution as needed
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1967802

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: TX
Alter: 37,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 11.05.2021
Beginn: 11.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Dyspnoea Headache Injection site erythema Injection site swelling Pyrexia Urticaria

Symptomtext

Fever of 103 for several days, swollen and deep red arm from injection site all the way down, extreme weakness headaches broke out in hives from my sculp all the way to my toes, trouble breathing. I took ibuprofen and Tylenol, OTC cold meds and pretty much just suffered for a good 7 days after both shots.

Weitere VAERSDATA-Felder

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

VAERS 1446358

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 42,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 12.06.2021
Beginn: 12.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Fatigue Feeling abnormal Headache Migraine Illness

Symptomtext

fatigue; brain fog; migraines; headaches; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 12Jun2021 (Lot number: EW0179) at the age of 42 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Endometriosis" (unspecified if ongoing); "But intolerant to many medications" (unspecified if ongoing): But intolerant to many medications; "But intolerant to many medications and foods" (unspecified if ongoing): But intolerant to many medications and foods; "I have long covid. It had improved significantly before I got the 2nd vaccine" (unspecified if ongoing). Concomitant medication(s) included: CLARITIN [CLARITHROMYCIN]. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0179, Location of injection: Left Arm), for COVID-19 immunization. The following information was reported: FATIGUE (disability) with onset 12Jun2021, outcome "not recovered", described as "fatigue"; FEELING ABNORMAL (disability) with onset 12Jun2021, outcome "not recovered", described as "brain fog"; MIGRAINE (disability) with onset 12Jun2021, outcome "not recovered", described as "migraines"; HEADACHE (disability) with onset 12Jun2021, outcome "not recovered", described as "headaches". The events "fatigue", "brain fog", "migraines" and "headaches" were evaluated at the physician office visit and emergency room visit. Therapeutic measures were not taken as a result of fatigue, feeling abnormal, migraine, headache. It was reported that patient was still not at the health baseline as she was at before the 2nd vaccine. Known allergies: Not fully allergic, but intolerant to many medications and foods. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19; Drug intolerance (But intolerant to many medications); Endometriosis; Food intolerance (But intolerant to many medications and foods)
Andere Medikamente: CLARITIN [CLARITHROMYCIN]
Allergien: -
Vorherige Impfungen: -

VAERS 1959385

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: TX
Alter: 53,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 04.11.2021
Beginn: 05.12.2021
Tage bis Beginn: 31,0
Dosis: 3
Route/Site: IM / RA

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

Arteriogram coronary abnormal Blood test normal Chest X-ray normal Chest discomfort Coronary arterial stent insertion Coronary artery occlusion Dyspnoea exertional Echocardiogram normal Electrocardiogram normal Loss of personal independence in daily activities Low density lipoprotein normal

Symptomtext

I have been a regular exercise and heart healthy man for several years. My cholesterol levels were not dangerously high and a recent LDL lab was 128. On 11/4/21, I got my Pfizer booster shot and developed shortness of breath and chest tightness on 12/05/21 while doing a physical workouts in our community gym and got better after I stopped my workout. The symptom started to show up during normal walk in next days and even got worse at showers as well. I went to a local health care facility and ended up with a stent in my right coronary artery. I strongly believe that this immediate episode happened due to my booster shot. Otherwise I was a roll model to our community youngsters for daily activities of workouts, playing soccer or basketball at least 3 to 4 days a week. I want CDC to do more studies even in the minority population who complains about complications of covid vaccinations. I will available on my phone (NUMBER) if anybody from CDC wants to talk with me regarding my case.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: 5,0
Labordaten: EKG, Chest xray at HCF EKG, chest xray, blood work, and echo are all normal CT Angio came with RCA block. Placed stent
Aktuelle Erkrankungen: None
Vorgeschichte: Slightly high BP
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1947834

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: WI
Alter: 27,0
Geschlecht: M
Eingang: 14.12.2021
Impfdatum: 28.04.2021
Beginn: 07.12.2021
Tage bis Beginn: 223,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Cough Dyspnoea Fatigue Hypophagia Malaise SARS-CoV-2 test positive

Symptomtext

Patient presents to ER with 6 days of feeling ill, and tested positive for COVID 12/1. Admitted on 12/08/21. Primarily has fatigue, nonproductive cough, mild sob; decreased oral intake. Patient has past medical history of end-stage renal disease due to medullary cystic disease (interstitial nephritis suggestive of nephrononopthisis and FSGS on June 2020 biopsy) status post kidney transplant December 2020.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: acetaminophen, acyclovir, calcium-cholecalciferol, mycophenolate sodium, predniSONE, sulfamethoxazole-trimethoprim , tacrolimus
Allergien: -
Vorherige Impfungen: -

VAERS 1947665

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: NJ
Alter: 55,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 11.05.2021
Beginn: 11.12.2021
Tage bis Beginn: 214,0
Dosis: 2
Route/Site: IM / -

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

COVID-19 pneumonia Chest pain Cough Dyspnoea Pain SARS-CoV-2 antibody test SARS-CoV-2 test positive

Symptomtext

56 yr old female with pmh of depression , anxiety , bipolar disorder presented to er c/o cough , sob and chest pain. she , works as a chef , denies any sick contacts . she tested positive for covid pneumonia . she reports her chest pain has been coming more frequently and more intensity and radiates to arm .

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 3,0
Labordaten: 12/11/2021 - SARS-COV-2 Antigen (++) 12/1/2021 - SARS-CoV-2 IgM 0.09; IgG 0.23, SARS-CoV-2 IgG2 QT-SPIKE 1773.20
Aktuelle Erkrankungen: -
Vorgeschichte: Bbipolar/ depression. L ovarary removed, carpral tunnel on L.
Andere Medikamente: lithium carbonate 600 mg Capsule Directions: 1 capsule oral twice a day every morning and at bedtime (Active) QUEtiapine 200 mg Tablet Extended Release 24 hr Directions: 1 tablet oral daily at bedtime (Active)
Allergien: IV Dye, shellfish, seafood
Vorherige Impfungen: -

VAERS 1944295

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 63,0
Geschlecht: U
Eingang: 13.12.2021
Impfdatum: 21.04.2021
Beginn: 03.12.2021
Tage bis Beginn: 226,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Dyspnoea exertional SARS-CoV-2 test positive Tachycardia

Symptomtext

12/03/21 presents to ED for "tachycardia and dyspnea w exertion ". PMHx of "Covid diagnosis last month".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: 12/03/21 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1944053

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 58,0
Geschlecht: M
Eingang: 13.12.2021
Impfdatum: 05.05.2021
Beginn: 02.12.2021
Tage bis Beginn: 211,0
Dosis: 2
Route/Site: UN / UN

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

Abdominal pain Abdominal pain upper Asymptomatic COVID-19 COVID-19 Computerised tomogram abdomen abnormal Condition aggravated Essential hypertension Flatulence Gastric dilatation Gastrointestinal tube insertion Ileus Intestinal dilatation Lactic acidosis Nausea Pain SARS-CoV-2 test positive Small intestinal obstruction Type 2 diabetes mellitus

Symptomtext

This is a 59y.o. male with significant past medical history of HTN, T2DM, S/P whipple procedure, dyslipidemia, anxiety, and depression that presented to the hospital with chief complaint of abdominal pain. He reports chronic abdominal pain over the past several years with abrupt worsening yesterday prompting ED evaluation. He admits to RUQ pain that radiates towards the left side of the abdomen. He admits to diffuse abdominal pain and cramping, nausea and vomiting. Denies any fever, chills, chest pain, shortness of breath. In the ED, patient normotensive, afebrile, stable SPO2 on room air. Coincidental finding of COVID+. CT AP concerning for SBO v ileus. NGT placed. Admitted for further evaluation and management with General surgery consultation. Patient seen and examined only by the attending physician. NP only responsible for chart review in an effort to limit exposure given the patient's COVID positive status.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 4,0
Labordaten: 1. Confirmed COVID-19. Incidental finding, asymptomatic. - Confirmed COVID positive on swab 12/2 - Respiratory status stable on room air - Not a candidate for Remdesivir or Decadron unless decompensation requiring supplemental oxygen - Supportive care - Enhanced Respiratory Isolation 2. SBO vs Ileus. - Abdominal KUB with gas and stool throughout the colon with a non specific bowel gas pattern - CT AP with dilated stomach and loops of small bowel with potential transition point in the RUQ region - Plan for conservative management; no acute surgical intervention needed at this time - NGT to LIS - management per surgery - IVF hydration - Antiemetics and Pain regimen PRN - General surgery evaluation and management 3. Lactic Acidosis. Resolved S/P IVF resuscitation. 4. Essential HTN. Normotensive. 5. Type 2 DM. Insulin sliding scale; hypoglycemic protocol. 6. HX Anxiety/MDD. SARS-COV-2 (COVID-19) by NAA, Micro Status: Final result Visible to patient: Yes (seen) Next appt: 12/23/2021 at 08:30 AM in Radiology (RADIOLOGY) Specimen Information: Nasopharyngeal; Swab 0 Result Notes Ref Range & Units SARS-CoV-2 (COVID-19) by NAA, Micro Not Detected Detected Abnormal Narrative The SARS-CoV-2 (COVID-19) by NAA test is for in vitro diagnostic use under the FDA Emergency Use Authorization (EUA) for laboratories certified to perform high complexity testing. This test has not been FDA cleared or approved. Methodology: Nucleic Acid Amplification (NAA)/Polymerase Chain Reaction (PCR). Specimen Collected: 12/02/21 12:50 AM Last Resulted: 12/02/21
Aktuelle Erkrankungen: Anxiety disorder ? Diabetes mellitus (CMS/HCC) ? Diabetes mellitus, type II (CMS/HCC) ? Dyslipidemia ? Hiatal hernia asymptomatic ? High cholesterol ? High triglycerides ? Hypertension ? Kidney stones ? Migraine ? Multiple renal cysts 4/12/17 Cluster of multiple cysts Left kidney - per MRI ? OSA on CPAP uses cpap ? Pancreatic mass 3/2017 incidenting finding w/ imaging for kidney stone ? Stomach pain 2006 ? Thyroid nodule 3/2017 Left, incidental finding per CT
Vorgeschichte: Anxiety disorder ? Diabetes mellitus (CMS/HCC) ? Diabetes mellitus, type II (CMS/HCC) ? Dyslipidemia ? Hiatal hernia asymptomatic ? High cholesterol ? High triglycerides ? Hypertension ? Kidney stones ? Migraine ? Multiple renal cysts 4/12/17 Cluster of multiple cysts Left kidney - per MRI ? OSA on CPAP uses cpap ? Pancreatic mass 3/2017 incidenting finding w/ imaging for kidney stone ? Stomach pain 2006 ? Thyroid nodule 3/2017 Left, incidental finding per CT
Andere Medikamente: ALPRAZolam (XANAX) 0.25 MG PO Tab take 0.25 mg by mouth twice daily as needed for FOR ANXIETY. Unknown Unknown time Aspirin 81 MG PO Tab take 81 mg by mouth once daily. 12/1/2021 Unknown time Med Note (Thu Dec 2, 2021 12:48 AM) ator
Allergien: Clindamycin Hives
Vorherige Impfungen: -

VAERS 1941891

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: NV
Alter: 36,0
Geschlecht: M
Eingang: 11.12.2021
Impfdatum: 03.05.2021
Beginn: 04.05.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / RA

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

Burning sensation Chills Cough Eye irritation Fatigue Insomnia Migraine Myalgia Oropharyngeal pain Pyrexia Rhinorrhoea

Symptomtext

Fever; chills; severe muscle pains; runny nose; severe migraine; fatigue; sore throat; burning; insomnia; coughing; burning eyes; This is a spontaneous report received from a contactable consumer. The reporter is the patient. A 36-year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 03May2021 16:30 (Lot number: EW0179) at the age of 36 years as dose 1, single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: PYREXIA (non-serious) with onset 04May2021 01:00, outcome "not recovered", described as "Fever"; CHILLS (non-serious) with onset 04May2021 01:00, outcome "not recovered", described as "chills"; MYALGIA (non-serious) with onset 04May2021 01:00, outcome "not recovered", described as "severe muscle pains"; RHINORRHOEA (non-serious) with onset 04May2021 01:00, outcome "not recovered", described as "runny nose"; MIGRAINE (non-serious) with onset 04May2021 01:00, outcome "not recovered", described as "severe migraine"; FATIGUE (non-serious) with onset 04May2021 01:00, outcome "not recovered", described as "fatigue"; OROPHARYNGEAL PAIN (non-serious) with onset 04May2021 01:00, outcome "not recovered", described as "sore throat"; BURNING SENSATION (non-serious) with onset 04May2021 01:00, outcome "not recovered", described as "burning"; INSOMNIA (non-serious) with onset 04May2021 01:00, outcome "not recovered", described as "insomnia"; COUGH (non-serious) with onset 04May2021 01:00, outcome "not recovered", described as "coughing"; EYE IRRITATION (non-serious) with onset 04May2021 01:00, outcome "not recovered", described as "burning eyes". Therapeutic measures were not taken as a result of pyrexia, chills, myalgia, rhinorrhoea, migraine, fatigue, oropharyngeal pain, burning sensation, insomnia, cough, eye irritation. Additional information: Most recent dose details: Product= COVID 19, brand= Pfizer, lot number=EW0170, administration date=24 May2021, administration time= 04:30 PM, dose number=2, vaccine location= Right arm. If other vaccine in four weeks: No. Other medications in two weeks: No. If Covid prior vaccination: Unknown. If Covid tested post vaccination: Unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1518374

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: GA
Alter: 41,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 01.05.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

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

Injection site pain Injection site swelling Pain in extremity Paraesthesia

Symptomtext

extreme arm pain; feels like there are needles; This is a spontaneous report received from a contactable Consumer or other non HCP from medical information team for a Pfizer sponsored program. The reporter is the patient. A 42-year-old female patient received bnt162b2 (BNT162B2), administration date May2021 (Batch/Lot number: unknown) at the age of 41 years as dose 2, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (First Dose), administration date: May2021, when the patient was 41 years old, for Covid-19 Immunization, reaction(s): "extreme arm pain", "needle in her arm". The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 2021, outcome "unknown", described as "extreme arm pain"; PARAESTHESIA (non-serious) with onset 2021, outcome "unknown", described as "feels like there are needles". The events "extreme arm pain" and "feels like there are needles" were evaluated at the physician office visit. Therapeutic measures were taken as a result of pain in extremity, paraesthesia. Additional Information: Caller would like to know if the pain will ever stop and any information that could be provided about that. Caller states that other family members have had the vaccine and they didn't have any issue. Caller states that she has taken Tylenol and Advil for the pain, and they both were not effective to help her pain. Caller does not have an NDC, Lot number, or expiration date to provide. Caller said after the first shot, her arm hurt and then she used the opposite arm for the second shot, and that probably was not a good idea. Caller confirms that she was fully vaccinated in May2021. Follow-up attempts completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1938962

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 88,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: 05.05.2021
Beginn: 06.12.2021
Tage bis Beginn: 215,0
Dosis: 2
Route/Site: UN / UN

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

Anticoagulant therapy Aortic arteriosclerosis Aortic valve incompetence Atelectasis Atrial fibrillation Blood alkaline phosphatase increased Blood bilirubin increased Blood sodium decreased COVID-19 Chest X-ray abnormal Condition aggravated Cough Diastolic dysfunction Dyspnoea Echocardiogram abnormal Ejection fraction normal Haemoglobin decreased Hypotension

Symptomtext

12/6/2021 - present (4 days) inpatient admission HCF - Hospital HISTORY OF PRESENT ILLNESS: Pt is a 89 y.o. male with past medical history of chronic diastolic HFpEF, Afib, restrictive lung disease and recent hospitalization for L1-L2 compression fracture and multiple rib fractures after ground level fall. Patient resides at (PRIVACY) where he recently tested positive for COVID-19 on 12/3. Patient presented to the ED with chief complaint of worsening hypoxia. Patient was reported to have oxygen saturations in the 80's. He wears 2L oxygen at baseline and reports having a new cough and intermittent SOB. He thinks his symptoms started 1 week ago but is unsure and tested positive on 12/3 for COVID. He is vaccinated with Pfizer although has not received his booster yet. He reportably had monoclonal abx infusion on 12/4. Patient does not recall the infusion and states he received 4 shots for COVID as treatment. He denies having any fever, chills, abdominal pain, vomiting or diarrhea. While in the ED, patient was noted to be in a-fib RVR thus, received cardizem 5mg IV and subsequently became hypotensive. Upon arrival to the ED, patient was afebrile, tachycardic HR 132bpm, otherwise hemodynamically stable on 4L oxygen. Labs were notable for Na 132, alk phos 145, bilirubin 1.2, wbc 3.29, hgb 9.9, plt 52. CXR showed bilateral pleural effusions slightly decreased in size compared to 11/20/21. No new or worsening opacity. No findings suspicious for overt heart failure. Patient received cardizem 5mg IV subsequently resulting in hypotension. His blood pressure improved with 2L IVF and home midodrine. Patient will be admitted to HCF for further treatment and evaluation. ASSESSMENT / PLAN: Iatrogenic hypotension, improving - secondary to IV cardizem - s/p 2L IVF and midodrine - check LA - will hold home lasix and aldactone for now and consider resuming tomorrow - continue BB and midodrine - monitor bp A-fib RVR- resolved - noted to be recurrent per previous hospitalization - continue BB - tele - keep Mg>2, K>4 COVID-19 infection - vaccinated, did not receive his booster - COVID + 12/3, symptom onset roughly 1 week ago per pt - reported to have had monoclonal abx infusion on 12/4, attempted to call facility to confirm but unable to reach staff - prone positioning daily, tele, continuous pulse ox - trend daily crp, d-dimer - consider monoclonal abx infusion pending discussion with facility Acute on chronic thrombocytopenia - suspect r/t COVID-19 - monitor cbc Right arm laceration - wound nurse consult Chronic diastolic HFpEF - not in acute exacerbation - 9/15/21 ECHO- EF 50-55%, grade 3 diastolic dysfunction, mod AR, mod to severe MR, mod-severe TR - holding lasix and aldactone d/t hypotension, resume when able - continue BB - daily wts, I&O's Chronic hypoxic respiratory failure Restrictive lung disease Bilateral pleural effusions, stable - stable, baseline 2L oxygen Deconditioning - lives at facility, own decision maker - PT/OT DVT prophylaxis: lovenox subq Code status: DNR/DNI Diet: general

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 4,0
Labordaten: DR CHEST SINGLE VIEW [356947569] Resulted: 12/07/21 0234 Order Status: Completed Updated: 12/07/21 0236 Narrative: EXAMINATION: Single View Chest EXAM DATE: 12/7/2021 1:21 AM TECHNIQUE: Single view chest INDICATION: cough COMPARISON: Chest radiograph on 11/20/2021 and 11/16/2021 ENCOUNTER: Not applicable _________________________ FINDINGS: The patient is slightly tilted and rotated to the left. The cardiomediastinal silhouette is enlarged but stable. The visualized pulmonary vascularity is noncongested. There is calcification at the aortic arch. There are small pleural effusions bilaterally, slightly decreased in size compared to radiograph dated 11/20/2021. There is atelectasis at the basilar regions bilaterally, similar to prior. Stable strandy opacification at the periphery of the right midlung, likely atelectasis. No evidence of lobar consolidation. No evidence of measurable pneumothorax. _________________________ Impression: Bilateral pleural effusions, slightly decreased in size compared to 11/20/2021. No new or worsening pulmonary opacity. No findings suspicious for overt failure. Collected: 12/07/21 0649 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 12/07/21 1630 COVID-19 PCR Detected
Aktuelle Erkrankungen: -
Vorgeschichte: permanent atrial fibrillation (HCC) Valvular heart disease Restrictive lung disease Edema Chronic diastolic congestive heart failure (HCC) Multiple fractures of ribs, bilateral, initial encounter for closed fracture Multiple comorbid conditions Counseling regarding advance care planning and goals of care Laceration of arm, right, complicated
Andere Medikamente: acetaminophen (TYLENOL) 325 MG tablet ascorbic acid (VITAMIN C) 1000 MG tablet aspirin 81 MG enteric coated tablet bisacodyl (DULCOLAX) 10 MG suppository cholecalciferol (VITAMIN D3) 25 MCG (1000 UT) capsule cyanocobalamin (B-12) 1000 MCG/M
Allergien: PenicillinsOther Sulfa DrugsRash
Vorherige Impfungen: -

VAERS 1909330

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: WI
Alter: 55,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 29.04.2021
Beginn: 25.11.2021
Tage bis Beginn: 210,0
Dosis: 2
Route/Site: IM / LA

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

Loss of personal independence in daily activities Mobility decreased

Symptomtext

Patient was admitted to Hospital admitted as observation on 11/24/21 due to impaired mobility and ADLs

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Tacrolimus, Cefdinir, Ciprofloxacin (Bulk), Cycloserine
Vorherige Impfungen: -

VAERS 1905571

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: IL
Alter: 72,0
Geschlecht: M
Eingang: 29.11.2021
Impfdatum: 06.07.2021
Beginn: 26.11.2021
Tage bis Beginn: 143,0
Dosis: 1
Route/Site: IM / UN

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

COVID-19 COVID-19 pneumonia Computerised tomogram thorax abnormal Cough Fatigue Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

73-year-old male past medical history of hypertension, high cholesterol, non-Hodgkin's lymphoma, CAD recent diagnosis of squamous cell carcinoma of the oropharynx who is here for evaluation of fever, congestion, cough and fatigue noted for last 2 weeks that exacerbated over the last few days. Patient states that he feels really tired. Patient denies any chest pain or shortness of breath. Patient has dry cough. Patient has been taking Tylenol as needed for fever. Patient denies any nausea, vomiting, abdominal pain, diarrhea. Patient requiring 15 L of oxygen nasal cannula

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: 11/26/2021 CT Chest : findings consistent with COVID19 pneumonia, no evidence of pulmonary embolism 11/26/2021 SARS COV2 COVID19 NAAT : Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension Hyperlipidemia Non-Hodgkin's lymphoma in remission coronary artery disease recent diagnosis of squamous cell carcinoma of the oropharynx
Andere Medikamente: aspirin (aspirin) 81 mg, EC Tablet, PO, Daily, 11/27/21 9:00:00 CST, 11/26/21 18:00:00 atorvastatin (atorvastatin) 80 mg, TAB, PO, Daily, 11/27/21 18:00:00 metoprolol (Metoprolol Tartrate) 12.5 mg, TAB, PO, BID (2 times a day), 11/
Allergien: Aleve
Vorherige Impfungen: -

VAERS 1904295

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: IL
Alter: 33,0
Geschlecht: M
Eingang: 28.11.2021
Impfdatum: 17.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: SYR / RA

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

Atrial fibrillation Blood magnesium normal Blood thyroid stimulating hormone normal Cardiac flutter Chest discomfort Drug screen negative Echocardiogram Echocardiogram normal Ejection fraction decreased Extrasystoles Fatigue Full blood count normal General physical health deterioration Heart rate increased Hypotension Metabolic function test normal

Symptomtext

2nd shot: woke up one night with heart fluttering for about 10-15 minutes. Went back to sleep without any further issues. 3rd shot: 11/21 woke up at 10:45pm with a rapid heartbeat and fluttering. I had my smartwatch with me and my heartbeat was at 160-180bpm. I waited about an hour and a half prior to checking myself into the hospital. I travel for work, working in a specific city that weekend and check myself into hospital around 12:30a.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: 1,0
Labordaten: Hospital notes: Attestation signed by MD at 11/26/2021 4:16 PM I saw and evaluated the patient. I have reviewed the resident's/fellow's findings and agree. Yes - I provided critical care for this patient. Critical care was necessary because there was a high probability of imminent or life-threatening deterioration and this patient required continuous observation and interventions to respond to emergent changes in their medical condition and prevent further deterioration in their clinical state. The critical care I provided included: managing hypotension or other hemodynamic instability, management of electrolyte/metabolic abnormalities, consultation with specialists, and review of medical records Critical Care Time: I spent a total of (30-74 minutes) 56 minutes personally providing critical care to patient. This does not include time spent teaching or performing any separately billable procedures. Patient is a 33-year-old male with no significant past medical history who presents to the ED in atrial fibrillation with rapid ventricular response. His initial HR was 181; he is hemodynamically stable with SBP in the 140s and is satting well on room air without other symptoms related to the fibrillation. Labwork including CBC, BMP, TSH, magnesium, utox sent. Labs all within normal limits and utox negative. No clear trigger for atrial fibrillation for this patient, given normal labs, no substance use. Patient given 5mg metoprolol initially with decrease in rates from 180s to 140s. Additional 5mg x2 metoprolol IV given without further significant response. Discussed cardioversion with patient; he prefers to avoid at this time and requests other pharmaceutical options. Patient given .0.25mg/kg diltiazem IV with good response with HR decrease to the 90s; patient remains in atrial fibrillation. Cardiology consulted for admission and recommend initiation of 5mg apixaban and 120mg ER diltiazem PO. At 4am, patient Hrs back between 130s and 150s and he was given an additional 0.35mg/kg diltiazem. TTE ordered. Patient was transferred to the inpatient floor in stable condition. (My notes) 7am converted to normal sinus rhythm was released at 10:30am on Monday 11/22 and traveled back home to another city that evening. (Post Hospital visit) Saw my personal doctor back in my city and as recommended by the cardiologists at the other city's hospital they recommended an Eco. My doctor order an Eco and it was performed at a local hospital on 11/24 notes are below. (Eco Results) PHYSICIAN INTERPRETATION: Left Ventricle: Normal LV systolic function. Left ventricular ejection fraction, by visual estimation, is 60 to 65%. Spectral Doppler shows normal pattern of LV diastolic filling. The left ventricular cavity size is normal. Right Ventricle: The right ventricular cavity is normal in size and structure. Global RV systolic function is normal. Left Atrium: The left atrium is normal in size and structure. Right Atrium: The right atrium is normal in size and structure. Mitral Valve: The mitral valve is structurally normal with normal leaflet excursion. Tricuspid Valve: The tricuspid valve is structurally normal with normal leaflet excursion. Aortic Valve: The aortic valve is trileaflet and structurally normal with normal leaflet excursion. The aortic valve is tricuspid. Pulmonic Valve: The pulmonic valve is trileaflet without evidence of stenosis or insufficiency. Aorta: The aortic root and ascending aorta are structurally normal with no evidence of dilitation. Pericardium: No evidence of pericardial abnormalities. There is no pleural effusion in either the left or right lateral region. In comparison to the previous echocardiogram(s): There are no prior studies on this patient for comparison purposes. ECHO/TEE --- Final --- 11/28- still feeling very tired and experiencing chest tightness at times especially when laying down when trying to sleep. Have had a few skipped beats/flutters in the past week but nothing more than a couple of beats and not for an extended period of time.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Azelastine, Benadryl, Claritin D
Allergien: Tree nuts, sesame seeds, Aleve, Advil, NSAIDs
Vorherige Impfungen: Pfizer 5/3

VAERS 1897420

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 59,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 15.04.2021
Beginn: 20.11.2021
Tage bis Beginn: 219,0
Dosis: 2
Route/Site: - / -

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

Dyspnoea

Symptomtext

dyspnea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: POS on admission 11.20.21
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1894814

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: 92,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 23.04.2021
Beginn: 09.11.2021
Tage bis Beginn: 200,0
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

11/9/21 presents to EC ED "reports left sided chest pain and SOB". PMH "A fib on coumadin, CHF, CKD, CAD, CVA, GERD, HTN, hx of NHL, pulmonary HTN".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 11/09/21 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1894295

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge EW0179

moderat

Staat: MI
Alter: 89,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 16.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Pneumonia SARS-CoV-2 test positive

Symptomtext

CAP

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: 2,0
Labordaten: 11.16.21 positive on admission
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1889616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: KS
Alter: 31,0
Geschlecht: M
Eingang: 22.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dyspnoea exertional Headache Muscle spasticity Muscle twitching Palpitations SARS-CoV-2 test Sleep disorder

Symptomtext

Within 6 hours began to experience heart palpitations. When attempting to excercise later that night, severe dyspnea and palpitations occurred with light movement. Palpitations continued into the night with new onset spastic muscle twitching and headache. Palpitations: frequency decreased through days 2-3. They do continue to occur between two and three times daily Spastic Movement: still continues to awaken at night and occurs a minimum of 2 times daily Dyspnea: appears to have subsided after the third day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: Rapid antigen tests at least one time per week since Covid began. Working as an RN have cared for an uncountable number of proven and suspected covid positive patients.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Wellbutrin
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1885487

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 73,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 04.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Condition aggravated Fatigue Musculoskeletal stiffness Osteoarthritis

Symptomtext

On November, 4th, I received a COVID booster shot. The reaction to shot number 3 was less than expected on the day of the shot and for the next two days. I did not feel ill, just very tired. Although, I was not as tired as with shot number 2. About a week after receiving the COVID booster shot, I noticed that the the pain and stiffness I have from osteoarthritis was getting worse. I have flare up pain and stiffness occasionally so I did not think much of it and it only lasts a few days. However, this time the pain flare up kept getting worse and is still ongoing. I contacted my Primary Care Doctor and asked her advice on 11/15. She indicated that to her knowledge, arthritis flare up from COVID vaccination occurred within a couple days of the injection. She advised that I wait another week and take the maximum amount of Tylenol per day to relieve some of the pain. If there was no improvement in the pain and stiffness, to come in to see if something else was going wrong. I have been taking the maximum safe amount of Tylenol since then and I do have less pain and stiffness, but I cannot tell if the reduced pain is a result of gradual improvement or from taking the Tylenol. I don't know for sure that the increased pain and stiffness is a result of the COVID vaccine or not. The vaccine injection is the only thing that I have done differently than my routine activities for the past three weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: high blood pressure, migraines, obesity, previous prostate cancer, blockage of artery in right eye, osteoarthritis
Andere Medikamente: Lisinopril, atorvastatin, hydrochlorothiazide, propranolol, aspirin, fenofibrate, folic acid, vitamin D3, magnesium, glucosamine, B-complex,
Allergien: None
Vorherige Impfungen: -

VAERS 1876851

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 52,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 16.04.2021
Beginn: 10.11.2021
Tage bis Beginn: 208,0
Dosis: 2
Route/Site: - / -

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

Dyspnoea

Symptomtext

SOB,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: 11.10.21
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, A fib with RVR, CHF, PAF, hypothyroidism type 2 diabetes,
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1874647

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: FL
Alter: 31,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 01.05.2021
Beginn: 01.06.2021
Tage bis Beginn: 31,0
Dosis: 1
Route/Site: SYR / AR

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

Alopecia Alopecia universalis Blood test Condition aggravated Immediate post-injection reaction Madarosis

Symptomtext

Took 1st and 2nd Pfizer vaccine in May 2021 and immediately patches on the sides of my head started to get bigger and bigger, until I was completely bald and now I have alopecia universalis! No hair, eyebrows or lashes. No supplements, steroids, or medication helps with help growth.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Blood test
Aktuelle Erkrankungen: N/A
Vorgeschichte: None
Andere Medikamente: N/a
Allergien: N/a
Vorherige Impfungen: -

VAERS 1872814

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: KY
Alter: 68,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 31.03.2021
Beginn: 15.11.2021
Tage bis Beginn: 229,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 pneumonia

Symptomtext

Given monoclonal antibody infusion 3 days prior to admission. Now with covid PNA and admitted to the hospital. On room air right now dexamethasone started,

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1872671

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 20,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 05.05.2021
Beginn: 07.11.2021
Tage bis Beginn: 186,0
Dosis: 2
Route/Site: IM / AR

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

Abdominal pain COVID-19 Complication of device insertion Computerised tomogram abdomen abnormal Condition aggravated Food intolerance Gastrointestinal tube insertion Intestinal obstruction Laboratory test Nausea SARS-CoV-2 test positive Small intestinal obstruction Vomiting

Symptomtext

Hospitalized 11/7/2021; COVID-19 positive 11/7/2021; fully vaccinated Discharge Summary MD (Physician) Surgery BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider: MD Admission Date: 11/7/2021 Discharge Date: 11/08/2021 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Small bowel obstruction (HCC) [K56.609] HOSPITAL COURSE: Patient was seen at the emergency department for crampy abdominal pain, nausea and vomiting. CT showed a chronic bowel obstruction and patient was transferred to hospital for further management. Patient was incidentally found to be COVID positive and the monoclonal antibody infusion clinic was contacted. Patient met criteria and was given the monoclonal antibody during her inpatient stay. Patient was unable to tolerate placement of an NG tube but was still having bowel movements. A gastrografin challenge was performed which showed passage of the contrast into the colon. Her pain improved and she was able to tolerate regular food prior to discharge. Although she has a known history of Crohn's disease, patient had no leukocytosis or signs of active crohn's disease on CT. Given the chronic nature of the obstruction with evidence of fecalization expect an acute on chronic exacerbation of a possible crohn's stricture which should be investigated further.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Crohn's disease Small bowel obstruction
Andere Medikamente: acetaminophen (TYLENOL) 325 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler cetirizine (ZYRTEC) 10 MG tablet guaiFENesin (MUCINEX) 600 MG 12 hr tablet ibuprofen (MOTRIN) 600 MG tablet Multiple
Allergien: NKA
Vorherige Impfungen: -

VAERS 1869235

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: NJ
Alter: 65,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 29.04.2021
Beginn: 22.10.2021
Tage bis Beginn: 176,0
Dosis: 2
Route/Site: IM / -

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

COVID-19 Confusional state Exposure to SARS-CoV-2 Hypotension Lethargy SARS-CoV-2 antibody test SARS-CoV-2 test positive

Symptomtext

Admitted with lethargy, hypotension, confusion on 10/23. Long standing placement issues. then became COVID-19 POS after employee exposure at hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: 23,0
Labordaten: 10/27/2021 - SARS-COV-2 PCR (-); also NEGATIVE on 10/22. 9/12 11/13/2021 - SARS-CoV-2 PCR (++) 11/13/2021 - SARS-COV-2 IgM 0.04; IgG 0.01
Aktuelle Erkrankungen: -
Vorgeschichte: ESRD on PD, Type II Diabetes, Diabetes insipidus, breast CA with mastectomy and LN Dissection, depression, anxiety, peripheral neuropathy
Andere Medikamente: Unknown
Allergien: Iodine, Benadryl, Furosemide, Pregabalin, Sulfa
Vorherige Impfungen: -

VAERS 1868326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: KS
Alter: 43,0
Geschlecht: M
Eingang: 14.11.2021
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Pain

Symptomtext

Intermittent dull pain in chest lasting for a few minutes each time. This occurred for the two days after vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Calcium, Glucosamine, Vitamin D, Allegra, Fish Oi, Vitamin B Complex
Allergien: -
Vorherige Impfungen: -

VAERS 1867229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: IL
Alter: 61,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 07.05.2021
Beginn: 07.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Dysgeusia Fatigue Paraesthesia oral Pyrexia Vaccination site discomfort Vaccination site reaction

Symptomtext

tiredness; slight fever; 20 minutes after felt tingle at injection site and front of tongue shortly thereafter then had metallic taste for a couple of days. Then expected tiredness slight fever 24 hours later not lasting lon; 20 minutes after felt tingle at injection site and front of tongue shortly thereafter then had metallic taste for a couple of days. Then expected tiredness slight fever 24 hours later not lasting lon; 20 minutes after felt tingle at injection site and front of tongue shortly thereafter then had metallic taste for a couple of days. Then expected tiredness slight fever 24 hours later not lasting lon; metallic taste; This is a spontaneous report from a contactable consumer. A 61-years-old non pregnant female patient received second dose of bnt162b2 (BNT162B2, Solution for injection, Batch/Lot Number: EW0179), via an unspecified route of administration, administered in Arm Left on 07May2021 08:00 as dose 2, single for covid-19 immunisation. The patient medical history was not reported. Concomitant medication(s) included magnesium (MAGNESIUM) taken for an unspecified indication, start and stop date were not reported; probiotics (PROBIOTICS) taken for an unspecified indication, start and stop date were not reported. The patient previously took first dose of bnt162b2 (BNT162B2, Solution for injection, Batch/Lot Number: EW0169), via an unspecified route of administration, administered in Arm Left on 16Apr2021 04:00 pm as dose 1, single for covid-19 immunisation. On 07May2021, the patient experienced 20 minutes after felt tingle at injection site and front of tongue shortly thereafter then had metallic taste for a couple of days, then expected tiredness slight fever 24 hours later not lasting lon, metallic taste. On 08May2021, the patient experienced tiredness, slight fever. No treatment was received for the events. On the unspecified date, the outcome of events was recovered. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: MAGNESIUM; PROBIOTICS
Allergien: -
Vorherige Impfungen: -

VAERS 1853704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 35,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 10.05.2021
Beginn: 07.10.2021
Tage bis Beginn: 150,0
Dosis: 2
Route/Site: SYR / LA

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

Anxiety COVID-19 Cardiac disorder Chest discomfort Depression Heart rate increased Palpitations SARS-CoV-2 test positive

Symptomtext

Flare up heart issues, anxiety and depression. chest tightness - racing and increased heart rate, palpitations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: COVID -19 Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Cholesterol Fibromyalgia Arthritis Herniated Disc Nerve Damage Ovarian Cysts Seizures Migraines Overweight
Andere Medikamente: N/A
Allergien: Shellfish Astral Haldol Capra
Vorherige Impfungen: -

VAERS 1853379

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: IL
Alter: 17,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 10.05.2021
Beginn: 12.05.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: - / LA

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

Body temperature Malaise Pyrexia Tremor

Symptomtext

Didn't feel well; can't stop shaking and feels like something wrong; Fever being so high and temperature is 102.7; Didn't feel well; can't stop shaking and feels like something wrong; This is a spontaneous report from a contactable consumer (patient mother). A 17-year-old Female patient received BNT162B2(PFIZER BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EW0179), dose 2 via an unspecified route of administration, administered in Arm Left on 10May2021 03:00 (At the age of 17-year-old) as dose 2, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported.The patient previously received BNT162B2(PFIZER BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EW0179), dose 1 via an unspecified route of administration on 11Apr2021 (At the age of 17-year-old) as dose 1, single for covid-19 immunization.On 12May2021 the patient experienced didn't feel well; can't stop shaking and feels like something wrong, fever being so high and temperature is 102.7.The reporter stated, her daughter (consumer) who is a minor had her second dose (Covid) vaccine at 3-o-clock. She woke up this morning and did not feel well. She took two ibuprofen (treatment) and she came home from school in noon she did not feel good and went to bed. She texts me about 45 min ago and said she cannot stop shaking that she feels like something is wrong, so patient mother took her temperature it said 102.7, patient mother called her paediatrician and they said to call this number and very concerned about her fever being so high. If it was infant that is not high but she is (17 years) old an adult that is high. The patient mother would like a medical advice and she do not want to take her to the ER (not clarified) and expose her and I am very concerned about as we have a history of epilepsy in our family, so that is why patient mother worried about high fever. The patient underwent lab tests and procedures which included body temperature: 102.7 on Fever being so high and temperature is 102.7. Therapeutic measures were taken as a result with ibuprofen (400 mg) at 8 am in the morning and 400 mg at 5 PM in the evening after measuring the temperature. Outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Name: Fever; Result Unstructured Data: Test Result:102.7; Comments: Fever being so high and temperature is 102.7
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Epilepsy (have a history of epilepsy in our family, so that is why patient mother)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1850832

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 05.05.2021
Beginn: 05.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Chest pain Injection site pain Pain in extremity

Symptomtext

Severe pain all down injection arm and spread to right arm and upper chest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Seasonal Allergies
Vorherige Impfungen: -

VAERS 1845337

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: -
Alter: -
Geschlecht: U
Eingang: 05.11.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Hypoaesthesia Paraesthesia

Symptomtext

Hand was tingling and numb like I had slept on it and it is still like that; My fingers on my right hand; Hand was tingling and numb like I had slept on it and it is still like that; My fingers on my right hand; This is a spontaneous report from a contactable consumer or other non hcp (patient). A patient of unspecified age and gender received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; formulation: Solution for injection, Batch/Lot Number: EW0179), via an unspecified route of administration on an unspecified date as DOSE 1, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. It was reported that patient was calling because patient took the Pfizer vaccine on the 29th (not clarified) and on the 30th, patient woke up and hand was tingling and numb like, patient had slept on it and it was still like that, today was the 8th. Patient stated that fingers on right hand, was that one of the side effect. Patient wanted to know that how long is it supposed to last. The Outcome of the events was unknown. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1843475

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: CA
Alter: 38,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 22.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Anaemia Balance disorder Blood test abnormal Condition aggravated Dizziness Dysstasia Fatigue Feeling abnormal Gait disturbance Injection site pain Memory impairment Muscular weakness Neck pain Pain Pain in extremity Pyrexia Tremor

Symptomtext

Short Term: Pain at the injection site that went up to my neck and down to my fingers lasting over a week. Starting the next day 24 hours of fever, fatigue etc. Long Term: Constant muscle weakness and dizziness. I now stumble and lose my balance a lot. Standing up with my eyes closed is extremely difficult. I lose my balance constantly and my legs and arms always feel shaky and weak, like I?ve just been lifting heavy weights when I have not. I?ve always had a little bit of brain fog, but now it?s exponentially worse. My memory has gotten oddly bad. I forget things I?m talking about or in the middle of doing now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: On October 21, 2021, my doctor did a general blood test after I complained about these symptoms. I told the appointment center this all started after I was vaccinated. My doctor said the test results showed I was still slightly anemic (I have been for years). He suggested iron supplements and did not follow-up on any of the other symptoms, nor did he order any other tests.
Aktuelle Erkrankungen: Possible mild anemia
Vorgeschichte: Mild Anemia
Andere Medikamente: Wellbutrin
Allergien: -
Vorherige Impfungen: -

VAERS 1842981

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Nausea Tachycardia

Symptomtext

Tachycardia (HR140-150), Nausea and dizziness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: None
Allergien: Benadryl-Hives and swelling in throat Morphine- Rash and swelling in throat
Vorherige Impfungen: -

VAERS 1840345

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: IL
Alter: 77,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 27.05.2021
Beginn: 26.10.2021
Tage bis Beginn: 152,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain COVID-19 Chest X-ray abnormal Chest pain Diarrhoea Dysuria Hypophagia Lung opacity Nausea Oropharyngeal pain Pyrexia SARS-CoV-2 test positive Vomiting

Symptomtext

11/02/2021 ED physician's note: "Patient states that she has had diffuse abdominal pain associated with nausea and vomiting has been constant in nature over the past x1 week after getting her flu shot. She also reports dysuria and diarrhea as well as sore throat and chest pain. She has not been eating well since her sx onset. No shortness of breath or lightheadedness noted. Noted to have fever but denies any ill contacts. States she is fully vaccinated for Covid. No modification factors of her symptoms". Treatment: decadron, duo-nebs. Pt is still hospitalized.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 11/02/2021 Covid positive CXR: Hazy bilateral patchy groundglass opacities noted throughout both lungs. The pattern is nonspecific, however, in the appropriate clinical setting this is consistent with atypical/viral pneumonia.
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, diabetes, hyperlipidemia, CKD
Andere Medikamente: -
Allergien: Acarbose, Levaquin [Levofloxacin]
Vorherige Impfungen: -

VAERS 1840014

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MI
Alter: 87,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 12.05.2021
Beginn: 22.10.2021
Tage bis Beginn: 163,0
Dosis: 2
Route/Site: IM / UN

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

Abdominal pain Chest X-ray Condition aggravated Cough Electrocardiogram Fatigue Pyrexia Respiratory tract congestion SARS-CoV-2 test

Symptomtext

Signs and symptoms: cough, congestion, fever, fatigue, and abdominal pain. Treatment:Cefepime IV adjusted to renal functions plus Linezolid 600 mg PO/IV every 12 hrs for total of 7 days with last doses on 11/5/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: COVID test. Chest x-ray. EKG.
Aktuelle Erkrankungen: Toe MSSA infection, , abdominal pain.
Vorgeschichte: A-fib. Acidic reflux. Arthritis, Diverticulitis, Hiatal hernia. nitrostat ypertension. Polio. Seizures.
Andere Medikamente: levocetirizine, amiodarone , vitamin D. mesalamine , omeprazol
Allergien: Penicillin, sulfa antibiotics, wheat extract
Vorherige Impfungen: -

VAERS 1839304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MA
Alter: 46,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 10.05.2021
Beginn: 10.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Chills Dizziness Dyspnoea Ear discomfort Fatigue Head discomfort Headache Insomnia Neck pain Pain Pyrexia Vomiting

Symptomtext

For a second she couldn't breathe; Threw up; Chills; Dizziness; Headache; Body ache; High fever; Neck hurting; Head exploding; Ears popping; Exhausted all night; Did not sleep; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 46-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EW0179 and expiry date was unknown) via an unspecified route of administration in left arm on 10May2021 09:13 (at the age of 46-years-old) as dose 2, single for covid-19 immunization. Patient medical history included reaction to penicillin from 2002 (Had the Penicillin pills from; back home-there they just gave penicillin shot in leg; they just gave Penicillin pill, and the reaction was hives). Patient had ongoing food allergy. It was reported that patient had these from many years ago. Patient concomitant medications included vitamin d nos as the patient has low vitamin D (had been taking for may be 4-5 years or more, from a long time). The patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EW0170) via an unspecified route of administration in left arm on 19 Apr 2021 around 13:15-13:30 (at the age of 46-years-old) as dose 1, single for covid-19 immunization. No additional vaccines administered on same date of the Pfizer Suspect. Patient had no family medical history relevant to adverse events. Patient had not received any other vaccines (within 4 weeks) prior to the first administration date of the suspect vaccine other than dose 1 of 2 of Pfizer Covid-19 Vaccine. No adverse events following prior vaccinations. Patient stated that she received the first dose of Pfizer Covid-19 Vaccine on 19Apr2021, and she did not have any adverse events after the first dose. On 10May2021 19:00, patient reported that after receiving the second dose she experienced chills, dizziness, headache, body ache, high fever, neck hurting, head exploding, ears popping, exhausted all night because she did not sleep; could not breathe for a second, threw up on 11May2021around 00:00 or before 00:30. Patient reported on 11May2021 morning around 10:30 she kind of left the bed, decided was going to do something, moved around and felt a little better. Around 13:00 she took a Tylenol, which she waited until over 24 hours after she got the Pfizer Covid-19 Vaccine to take. Patient stated she was doing much better now. It was reported that the adverse event did not require an emergency room or physician office visit. There were no relevant tests. Outcome of the events exhausted all night, did not sleep was recovered on an unspecified date in 2021, and the rest events were recovering at the time of report. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Food allergy (It was reported that patient had these from many years ago.)
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy (Had the Penicillin pills from; back home.)
Andere Medikamente: VITAMIN D NOS.
Allergien: -
Vorherige Impfungen: -

VAERS 1839296

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: MO
Alter: 68,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 05.05.2021
Beginn: 06.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Abdominal pain upper Dyspnoea Fatigue Headache Illness

Symptomtext

Trouble breathingbut not enough to rush to the hospital. Her 02 didn't go below 93 percent; She had stomach problems and pain in stomach, and an over all feeling of being sick; Exhaustion; over all feeling of sick; headache; This is a spontaneous report from a contactable consumer (Patient). A 68-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EW0179), via an unspecified route of administration, administered in left arm on Monday 05May2021 (at the age of 68-year-old) as DOSE 2, SINGLE for COVID-19 immunization. The patient medical history included ongoing rheumatoid arthritis Diagnosed 16 years ago, ongoing systemic lupus erythematosus Diagnosed 15 years ago, influenza immunisation from an unknown date and unknown if ongoing. She stated she gets the flu shot every year she was fine. She was taking Remicade IV infusion at the hospital but had to stop because she had an allergic reaction to it. This was a few months ago. The patient concomitant medication(s) included ongoing methotrexate, ongoing prednisone and ongoing hydrochlorothiazide from unknown date. No other additional vaccines administered on same Date of the Pfizer suspect; no prior vaccinations received (within 4 weeks). She received at hospital and therefore, does not have a lot/exp. Historical Vaccine include bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EW0169), via an unspecified route of administration, administered in left arm on Monday 15Apr2021 at 12:15pm (at the age of 68-year-old) as DOSE 1, SINGLE for COVID-19 immunization. She states she went and had second shot Wednesday 05May2021 at noon and by midnight she was very very sick. On 06May2021 at 01:00am in the morning symptoms started, she was having trouble breathing, but not enough to rush to the hospital. Her 02 didn't go below 93 percent. She had stomach problems and pain in stomach, and an overall feeling of being sick. This went on 4 days. On the 3rd day she didn't have trouble breathing but her stomach and headache were still ongoing. She first thought maybe had some kind of sickness before she got the shot and it just appeared. Adverse Events does not require a visit to Emergency Room and Physician Office. Outcome of the event trouble breathing was recovered on 07May2021, while for all other events it was recovering. No follow-up attempts are needed. No further information is expected. ; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021527283 same reporter/drug/event, different patient

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Lupus syndrome (Diagnosed 15 years ago); Rheumatoid arthritis (Diagnosed 16 years ago).
Vorgeschichte: Medical History/Concurrent Conditions: Flu vaccination.
Andere Medikamente: METHOTREXATE; PREDNISONE; HYDROCHLOROTHIAZIDE
Allergien: -
Vorherige Impfungen: -

VAERS 1828816

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: WI
Alter: 67,0
Geschlecht: M
Eingang: 29.10.2021
Impfdatum: 28.09.2021
Beginn: 25.10.2021
Tage bis Beginn: 27,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal X-ray Abdominal pain Anaemia Aortic aneurysm rupture Blood creatinine normal Blood electrolytes normal Brain natriuretic peptide increased Chest X-ray normal Chest pain Computerised tomogram thorax Condition aggravated Electrocardiogram normal Fibrin D dimer Influenza virus test negative Musculoskeletal chest pain Pleuritic pain Pulmonary mass Respiratory syncytial virus test negative

Symptomtext

patient with atypical chest pain on 10/25/2021 & then with ruptured AAA on 10/28/2021. AAA is inoperable and patient has been admitted to the Palliative Care service. 10/28/2021: Patient is a 67 y.o. male who presents with abdominal pain that started earlier today. It was acute and severe in nature. Has a history of known AAA. He also has a history of COPD/CAD for which is he on home O2. He is received immunotherapy for NSCLC. 10/25/2021: 67-year-old male with past medical history notable for pulmonary hypertension, hyperlipidemia, CAD, atrial fibrillation on anticoagulation, COPD, NSCLC on immunotherapy, CKD 3 who presents with sudden onset of left-sided rib pain. Patient is non-toxic appearing. Hemodynamically stable and all other vital signs within normal limits. Differential includes rib fracture, intercostal muscle strain/sprain, pleurisy, pneumonia, PE. Workup is notable for stable anemia, no leukocytosis, normal electrolytes, baseline creatinine, negative COVID/flu/RSV, nonischemic EKG, baseline high sensitivity troponin 49 with stable to or delta troponin of 48, elevated BNP at 2800 similar to baseline. X-ray of the chest and left ribs did not reveal any focal infiltrate or rib fracture, or other definite etiology of patient's symptoms. Given this, as well as history of active malignancy with focal pleuritic pain, a D-dimer was obtained which was greater than 9000; a CT PE was then obtained, which showed no evidence of PE, but did unfortunately show interval development of a spiculated mass in the right lung concerning for tumor recurrence. Given negative workup as detailed above, suspect that patient's pain is related to an intercostal muscle strain/sprain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: CT angio - chest for PE, abdomen and plevis Xray - chest and ribs COVID PCR raid testing x2 (negative on 10/25/2021 & positive on 10/28/2021)
Aktuelle Erkrankungen: Illness: lung CA vaccination - 3rd COVID-19 vaccination
Vorgeschichte: -
Andere Medikamente: Unknown
Allergien: Niacin Prilosec [omeprazole]
Vorherige Impfungen: -

VAERS 1825292

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: GA
Alter: 38,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 30.06.2021
Beginn: 21.07.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: - / RA

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

Blood creatine phosphokinase increased Cardiac stress test Dyspnoea Laboratory test Pneumonia Polymyositis Troponin increased

Symptomtext

Shortness of breath developed to the point I could not breath and had to go to the ER First stay was 7 days and they were focused on my heart CK levels over 4,000 and troponin be really high Stress test and over 20 test were taken to try to find out what was going on and I had pneumonia on both lungs Medication* Mycophenolate mofetil 500mg (2times a day)/PredniSone 50mg (1time a day)/Colchicine 0.6 mg (1time a day) Famotidine 20m(2times a day)/ Albuterol HFA 90 mcg/actuation inhaler (2 puffs every 4 hours)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 15,0
Labordaten: Second stay two week later after going to primary care doctor and she sent me to the ER stayed 8 days and was put on oxygen Came home of oxygen and diagnosed me with POLYMYOSITIS AUTO IMMUNE DIEASESE All labs are available on system and test are still coming in my lungs were cleaned (Over 100 test were ran from both hospital stays) I can share all records if needed please jus contact me or my doctors at the Clinic or Hospital Doctors: Doctor 1 MD, Doctor 2 MD, Doctor 3 MD, Doctor 3 MD, Doctor 4 MD
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1824559

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: CO
Alter: 56,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 03.05.2021
Beginn: 04.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / RA

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

Chills Diarrhoea Dyspnoea Ear pain Fatigue Headache Lymphadenopathy Oropharyngeal pain Pain

Symptomtext

Headache; Body aches; Earache; Chills; Diarrhea; Fatigue; Trouble breathing; Sore throat; Swelled lymph nodes in neck; This is a spontaneous report from a contactable consumer, the patient. A 56-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0179) via an unspecified route of administration in the right arm on 03May2021 at 14:30 (at the age of 56-years old) as a single dose for COVID-19 immunisation. Medical history included hypothyroidism. The patient had no known allergies. Prior to vaccination, it was unknown whether the patient was diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. The patient did not receive any concomitant medications (reported as Na). The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EE0153) via an unspecified route of administration in the right arm on 12Apr2021 at 13:00 as a single dose for COVID-19 immunisation. On 04May2021 at 05:00, the patient experienced headache, body aches, earache, chills, diarrhea, fatigue, trouble breathing, sore throat and swelled lymph nodes in neck. These symptoms had not gone away for 10 days. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events headache, body aches, earache, chills, diarrhea, fatigue, trouble breathing, sore throat and swelled lymph nodes in neck was not resolved at the time of this report. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1823575

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: TX
Alter: 82,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Chills Fatigue Myalgia Tremor Vaccination site erythema Vaccination site pain

Symptomtext

chills really bad; he was shaking all over; Muscle pain across two shoulders and arms; tired; Injection site redness; injection site pain; This is a spontaneous report from a contactable consumer (patient). An 82-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE Solution for injection), via an unspecified route of administration, in the left arm, on 12Oct2021 (Lot number: EW0179), at age 82 years old, as dose 3 (booster), single, for COVID-19 immunisation. Relevant medical history included diabetic, heart problems, and lymphoedema all from unknown date, not reported if ongoing or not, and flu on an unknown date. Concomitant medications included unspecified products. Historical vaccines included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) received on 21Feb2021 (lot number: EN6203), at age 81 years old, as dose 1, single; and BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) received on 14Mar2021 (lot number: EN6204), at age 81 years old, as dose 2, single, for COVID-19 immunisation. The patient did not receive prior vaccinations within 4 weeks. On 12Oct2021, the patient experienced injection site pain and injection site redness. On 13Oct2021 at 08:00, the patient started to have chills really bad, he was shaking all over. On 13Oct2021, the patient experienced muscle pain across two shoulders and arms and was tired. The patient had the shot on 12Oct2021 at noon and had no problems with it from noon until this morning. This morning at about 8:00 the caller started to have chills really bad, he was shaking all over. The caller put a heating pad on this body to warm himself up. The patient's injection site had pain but not too bad, but there was pain. The patient has taken 2 Tylenols in order to ease the pain a little bit. The caller was tired and fell asleep once he put the heating pad on him and woke up about 5 minutes ago and slept for 3 hours. The patient also had muscle pain across his two shoulders and arms. The patient had injection site redness. The patient stated it was nothing is too serious except the chills and the patient has never had anything like that not even when he had the flu. The events did not result to emergency room and physician's room visits. The outcome of the event injection site redness was not resolved. The patient was recovering from the remaining events. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetic; Flu; Heart disorder; Lymphoedema
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1821573

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: WI
Alter: 68,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 02.05.2021
Beginn: 26.10.2021
Tage bis Beginn: 177,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 Condition aggravated Follicular lymphoma SARS-CoV-2 test positive

Symptomtext

Pt was admitted to the hospital due to complications of known Follicular lymphonma. She tested positive for COVID on routine admission testing. She had history of previous COVID positive with monoconal antibody treatment

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 10/27/2021 ARS Coronavirus-2, PCR detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1817849

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: KY
Alter: 67,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 01.05.2021
Beginn: 30.08.2021
Tage bis Beginn: 121,0
Dosis: 1
Route/Site: IM / UN

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

Ageusia Anosmia Asthenia COVID-19 Chills Cough Diarrhoea Dyspnoea Headache Myalgia Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Wheezing

Symptomtext

She developed a fever, chills, rigors, muscle aches , lost taste and smell ,headache runny nose, cough, wheezing ,shortness of breath diarrhea and congestion and felt weak.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: POSITIVE Antigen test on 08/30/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension and Current Smoker
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1817849

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: KY
Alter: 67,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 01.05.2021
Beginn: 30.08.2021
Tage bis Beginn: 121,0
Dosis: 2
Route/Site: IM / UN

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

Ageusia Anosmia Asthenia COVID-19 Chills Cough Diarrhoea Dyspnoea Headache Myalgia Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Wheezing

Symptomtext

She developed a fever, chills, rigors, muscle aches , lost taste and smell ,headache runny nose, cough, wheezing ,shortness of breath diarrhea and congestion and felt weak.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: POSITIVE Antigen test on 08/30/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension and Current Smoker
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1812778

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: TX
Alter: 69,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 30.04.2021
Beginn: 15.05.2021
Tage bis Beginn: 15,0
Dosis: 2
Route/Site: - / LA

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

Chills Dyspnoea Nausea Pain in extremity Pyrexia

Symptomtext

chills; fever; nausea; sore arm; shortness of breath, along with sob on my daily morning walks; This is a spontaneous report from a contactable consumer (patient). A 69-years-old female non-pregnant patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Lot Number: EW0179), via an unspecified route of administration in the left arm on 30Apr2021 as dose 2, single for COVID-19 immunization (at the age of 69-years-old). The patient medical history and concomitant medications were not reported, patient was a healthy woman. There were no known allergies. Historical vaccine included first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Lot Number: EW0162), via an unspecified route of administration in the left arm on 09Apr2021 14:00 as dose 1, single for COVID-19 immunization (at the age of 69-years-old). The patient did not receive any other medications within 2 weeks of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Patient stated that she received her second dose of Pfizer Covid vaccine on 30Apr2021. On 15May2021, she did have the side effects of chills, fever, nausea for 24 hours along with a sore arm. Two weeks after the vaccine she noticed shortness of breath while climbing stairs in her apartment along with sob on her daily morning walks with her dog. Then (30) days later she noticed it getting worse, she had no underlying conditions, she did not suffer from this prior to the vaccine. She was not on any prescription meds. She was a reformed smoker, she quit 28Apr1998. The patient did not receive any treatment for the events. The clinical outcome for events was not recovered except recovered for chills, fever and nausea on 16May2021. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1395121

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: GA
Alter: 34,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 11.05.2021
Beginn: 12.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Abdominal pain Back pain Blood test Chest pain Computerised tomogram Dyspnoea Costochondritis Dizziness Fibrin D dimer increased Headache Hypoaesthesia Loss of personal independence in daily activities Paraesthesia Troponin I Vision blurred

Symptomtext

Shortness of breath with chest pain; Shortness of breath with chest pain; abdominal pain; Shortness of breath with back pain; This is a spontaneous report from a contactable consumer (patient). A 34-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot Number: EW0179), via an unspecified route of administration, administered in Left arm on 11May2021 15:15 at the age of 34-years-old as dose 2, single for covid-19 immunisation at Public Health Clinic/facility. Medical history included vertigo from an unknown date and supplements (supplementation therapy) on an unknown date. Concomitant medications included colecalciferol (VITAMIN D [COLECALCIFEROL]) taken as supplement, start and stop date were not reported and iron (IRON) taken as supplement, start and stop date were not reported received within 2 weeks of vaccination. The patient previously took first dose of historical vaccine, bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot Number: EW0169), via an unspecified route of administration, administered in Left arm on 20Apr2021 17:00 (at the age of 34-years-old) as single dose for covid-19 immunisation. The 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. Device Date: 19May2021. On 12May2021 at 04:00, the patient experienced Shortness of breath with chest pain, abdominal pain and back pain. Adverse events resulted Doctor or other healthcare professional office/clinic visit and Emergency room/department or urgent care. Treatment received for the adverse events included Emergency treatment- medicine prescribed (steroids). The outcome of events was not recovered. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Supplementation therapy; Vertigo
Andere Medikamente: VITAMIN D [COLECALCIFEROL]; IRON
Allergien: -
Vorherige Impfungen: -

VAERS 1395121

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: GA
Alter: 34,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 11.05.2021
Beginn: 12.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Abdominal pain Back pain Blood test Chest pain Computerised tomogram Dyspnoea Costochondritis Dizziness Fibrin D dimer increased Headache Hypoaesthesia Loss of personal independence in daily activities Paraesthesia Troponin I Vision blurred

Symptomtext

Shortness of breath with chest pain; Shortness of breath with chest pain; abdominal pain; Shortness of breath with back pain; This is a spontaneous report from a contactable consumer (patient). A 34-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot Number: EW0179), via an unspecified route of administration, administered in Left arm on 11May2021 15:15 at the age of 34-years-old as dose 2, single for covid-19 immunisation at Public Health Clinic/facility. Medical history included vertigo from an unknown date and supplements (supplementation therapy) on an unknown date. Concomitant medications included colecalciferol (VITAMIN D [COLECALCIFEROL]) taken as supplement, start and stop date were not reported and iron (IRON) taken as supplement, start and stop date were not reported received within 2 weeks of vaccination. The patient previously took first dose of historical vaccine, bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot Number: EW0169), via an unspecified route of administration, administered in Left arm on 20Apr2021 17:00 (at the age of 34-years-old) as single dose for covid-19 immunisation. The 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. Device Date: 19May2021. On 12May2021 at 04:00, the patient experienced Shortness of breath with chest pain, abdominal pain and back pain. Adverse events resulted Doctor or other healthcare professional office/clinic visit and Emergency room/department or urgent care. Treatment received for the adverse events included Emergency treatment- medicine prescribed (steroids). The outcome of events was not recovered. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Supplementation therapy; Vertigo
Andere Medikamente: VITAMIN D [COLECALCIFEROL]; IRON
Allergien: -
Vorherige Impfungen: -

VAERS 1806179

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: KS
Alter: 51,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 01.10.2021
Beginn: 03.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Acquired diaphragmatic eventration Chest X-ray abnormal Chest pain Dyspnoea Full blood count normal Metabolic function test Pleuritic pain

Symptomtext

Severe pleuritic chest pain., shortness of breath,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 10/4/21 - CBC, CMP - both normal 10/4/21 - CXR - elevated right hemidiaphragm.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Dyazide, levothyroxine, Calcitriol, calcium, Effexor
Allergien: Naproxen - hematuria Augmentin - rash
Vorherige Impfungen: -

VAERS 1804164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: GA
Alter: 77,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 26.08.2021
Beginn: 12.10.2021
Tage bis Beginn: 47,0
Dosis: 3
Route/Site: IM / LA

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

Adverse event Asthenia Condition aggravated Dyspnoea Pneumonia SARS-CoV-2 test negative Urinary tract infection

Symptomtext

So the whole adverse event would have started around the 13th of October and I felt a little weak to begin with. I am low on iron so I just figured it was that, I get weak sometimes easier than other days. Meanwhile, I did forget to tell you, I did have an infection - a UTI, I had went to the Clinic and they did give me antibiotics for that but that was unrelated it seems. So anyways I just was getting weaker and weaker and thought I would go to the ER, and I went there on 10/17/2021 and that was it. The outcome was pneumonia, that is why I had the shortness of breath. I was there for a few hours anyway. I went home with my treatment, antibiotics and I have been feeling better every day. I was given Albuterol, Dextral Methorphan, Doxycycline, Prednisone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Covid test - negative - 10/17/2021
Aktuelle Erkrankungen: N/a
Vorgeschichte: N/a
Andere Medikamente: Lisinopril, B12 vitamin, D3 vitamin, iron supplement
Allergien: N/a
Vorherige Impfungen: -

VAERS 1804136

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0179

moderat

Staat: TX
Alter: 41,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 01.09.2021
Beginn: 01.10.2021
Tage bis Beginn: 30,0
Dosis: 2
Route/Site: IM / LA

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

Dysgeusia Injection site pain Mobility decreased Pain Pain in extremity Tinnitus

Symptomtext

metallic taste began within the hour and has lasted for weeks with no relief ringing in both ears and began hours later after injection and comes and goes, have not had this until the injection pain along entire left arm where it was painful to lift arm and perform much movement

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: -
Vorherige Impfungen: Tetnus booster at age 30, injection site swelled to larger than softball size and was warm to touch

VAERS 1800878

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: KS
Alter: 62,0
Geschlecht: F
Eingang: 20.10.2021
Impfdatum: 15.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test Chest X-ray normal Chest pain Condition aggravated Dizziness Electrocardiogram normal Extra dose administered Full blood count normal Nausea Troponin

Symptomtext

Excruciating chest pain, nausea and lightheaded beginning at 6:00 pm on the day following the covid booster. Went to Emergency room at 6:30 10/16/2021. Blood tests, EKG, and chest xray. No heart related issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Chest xray 10/16/2021 EKG 10/16/2021 Triponin test 10/16/2021 CBC 10/16/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, high cholesterol, GERD, migraines
Andere Medikamente: Albuterol, zocor, Detrol LA, Claritin, Symbicort, Aimovig, Rabeprazole, Nurtec, multivitamin.
Allergien: Penicillin, Codeine, Maxalt, Sulfa
Vorherige Impfungen: Excruciating chest pain after 2nd dose Pfizer covid 04/13/2021. Age 62

VAERS 1800819

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0179

moderat

Staat: GA
Alter: 60,0
Geschlecht: F
Eingang: 20.10.2021
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Balance disorder Erythema Migraine Muscular weakness Pain Swelling

Symptomtext

Patient email reads, " area is reddened swollen with some pain. My legs feel wobbly and weak at times. In addition she has a migraine that her regular medication is not helping. Attempted to follow up with email employee not responding to call or email.

Weitere VAERSDATA-Felder

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