VAERS Reports : EN6208

VAERS 2710784

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

kritisch

Staat: -
Alter: 86,0
Geschlecht: F
Eingang: 07.11.2023
Impfdatum: 17.03.2021
Beginn: 05.11.2023
Tage bis Beginn: 963,0
Dosis: 2
Route/Site: SYR / -

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

Acute respiratory failure Alanine aminotransferase increased Anion gap Aspartate aminotransferase increased Bacterial test negative Basophil count decreased Basophil percentage decreased Bilirubin urine Blood albumin normal Blood alkaline phosphatase increased Blood bilirubin normal Blood calcium normal Blood chloride normal Blood creatinine increased Blood glucose normal Blood lactic acid Blood lactic acid normal Blood potassium normal

Symptomtext

Document Type: History and Physical Document Subject: History & Physical Note Performed By: MD on November 05, 2023 05:09 EST Verified By: MD on November 05, 2023 05:09 EST Encounter Info: Hospital, Inpatient, 11/05/23 - * Final Report * Document Has Been Revised Chief Complaint Cough History of Present Illness/Subjective This is an 88-year-old female with advanced Parkinson's disease with dementia, history of CHF, chronic atrial fibrillation, chronic anticoagulation on Eliquis, stage III chronic disease, hypertension, hyperlipidemia, presents with complaint of cough and generalized malaise and myalgias over about the past 24 hours. The daughter described the patient's cough as productive of clear sputum. Also some diarrhea reportedly. Episode of emesis earlier in the day, nonbloody and nonbilious. Blood pressure elevated at 153/119 and heart rate up around 115-120 which concerned the daughter as well. The daughter is from state but has been living with her mother lately to provide care as her Parkinson's disease advances. Patient was treated for urinary tract infection last week with Keflex, today was to be the final dose. White blood cell count normal,absent lymphocyte count 900.Creatinine 1.29, glucose 128, alkaline phosphatase 258, AST 311 and ALT 47. BNP is 500, troponin 56 initially, 124 on repeat.Serum lactate 1.6. Urine is bland. COVID-19 positive. Chest x-ray shows no acute cardiopulmonary abnormality. Moderate hiatal hernia on CT but otherwise nothing acute. Blood pressure labile, room systolic ranging from 86-1 59, likely some of that reactive, patient with dementia, her sleep-wake cycles of disturbed, is poor in the morning, etc.That being said, the patient does experience sleep disturbances as expected with Parkinson's disease, sometimes with insomnia, sometimes prolonged sleeping. Incomplete voiding. No history of significant constipation. Chronic tremor. The patient is pleasant and cooperative, however, the patient's daughter does describe progressive dementia. Review of Systems Unable to obtain outside of what was provided by the daughter as noted above. Physical Exam/Objective Vitals & Measurements most recent past 24 hours Hemodynamics Neurologic Patient Weight Patient Height None Reported Constitutional: No acute distress, well-nourished Eyes: PERRLA, normal conjunctiva ENMT: Moist oral mucosa Neck: Supple, non-tender, intact range of motion Respiratory: Lungs CTAB, good airflow Cardiovascular: Regular rate and rhythm no peripheral edema Gastrointestinal: Soft, non-tender, non-distended Musculoskeletal: No joint swelling, no deformity, intact ROM Integumentary: Intact, warm, dry no rashes Neurologic: Alert, moves all extremities, chronic pill-rolling tremor and masked facies. Assessment/Plan 1. COVID-19 U07.1 Chest x-ray clear. Will check inflammatory markers, started on Dex and remdesivir as she is requiring supplemental oxygen. Check procalcitonin levels, no antibiotics indicated at this time however. 2. Acute respiratory failure with hypoxia J96.01 Mild, in fact, no lower than 89% in the emergency department. This was in the middle of the night and she does have a history of sleep apnea, could be related to that. RT and OT protocol, wean as able. 3. Atrial fibrillation I48.91 Continue propranolol. Monitor. May need to add and/or titrate additional AV nodal blocking medication. Monitor electrolytes. Check thyroid function. 4. Elevated troponin R79.89 No distress, not a great historian but does not appear to be in any discomfort of any kind. Likely supply demand ischemia in the setting of tachycardia, COVID-19 infection, and delayed renal clearance. Trend until stable and flat. 5. Elevated brain natriuretic peptide (BNP) level R79.89 Exacerbated most likely by kidney disease and chronic diastolic heart failure. Continue the patient's home diuretic. 6. Elevated LFTs R79.89 Uncertain what to make of this, isolated elevation of AST and minimal elevation of alkaline phosphatase with normal total bilirubin and prior cholecystectomy. Suspect this is secondary to viral infection. Monitor during hospitalization. 7. CAD (coronary artery disease) I25.10 Continue aspirin and long-acting nitrate. 8. COPD mixed type J44.9 Overall good airflow, does not appear to be on home respiratory medication, will add as needed nebulizers. 9. Urinary retention R33.9 Monitor for retention 10. Stage 3a chronic kidney disease (CKD) N18.31 At or near baseline, continue diuretic, monitor 11. Parkinson disease G20 Continue carbidopa levodopa 12. Diastolic heart failure I50.30 Continue home diuretic, monitor intake and output, low-sodium diet 13. Hx of long-term (current) use of anticoagulants Z92.29 Age-adjusted Eliquis 14. Hypertension I10 Coreg, isosorbide 15. Hyperlipemia E78.5 Noted Full code Eliquis Code Status Full Code Chronic Problem List Anxiety Atrial fibrillation Bilateral bunions Bunion of right foot CAD (coronary artery disease) Chronic diarrhea Chronic rhinitis COPD mixed type Depression Diastolic heart failure Goiter Gout Hammertoes of both feet Hernia, hiatal Hx of long-term (current) use of anticoagulants Hyperlipemia Hypertension Long term use of drug Mixed conductive and sensorineural hearing loss of both ears Neck pain Onychogryphosis OSA on CPAP Parkinson disease Peripheral vascular disease Plantar callus Sensorineural hearing loss, bilateral Stage 3a chronic kidney disease (CKD) Thrush Type 2 diabetes mellitus with peripheral neuropathy Urinary retention Procedure/Surgical History ?Cholecystectomy Laparoscopic (08/31/2010) ?Colonoscopy (08/28/2008) ?Cataract ?exploratory laparotomy ?Hysterectomy Surgical History Internal 10/06/2017 EGD Bx MD Medications Home Medications (18) Active acetaminophen 325 mg oral tablet 650 mg = 2 Tablet, PRN, Orally, Q4H aspirin 81 mg oral tablet 81 mg = 1 Tablet, Orally, Daily carbidopa-levodopa 25 mg-100 mg oral tablet 1 Tablet, Orally, TID cloNIDine 0.1 mg oral tablet 0.1 mg = 1 Tablet, Orally, QHS Eliquis 2.5 mg oral tablet 2.5 mg = 1 Tablet, Orally, BID febuxostat 40 mg oral tablet 40 mg = 1 Tablet, Orally, QAM Fish Oil 1000 mg oral capsule 1,000 mg = 1 Capsule, Orally, BID gabapentin 100 mg oral capsule 100 mg = 1 Capsule, Orally, At Bedtime isosorbide mononitrate 60 mg oral tablet, extended release 60 mg = 1 Tablet, Orally, QAM Keflex 500 mg oral capsule 500 mg = 1 Capsule, Orally, BID, for UTI levothyroxine 50 mCg (0.05 mg) oral tablet 50 mCg = 1 Tablet, Orally, Daily Lipitor 40 mg oral tablet 40 mg = 1 Tablet, Orally, At Bedtime memantine 5 mg oral tablet 5 mg = 1 Tablet, Orally, Daily multivitamin 1 Tablet, Orally, QAM PARoxetine 20 mg oral tablet 20 mg = 1 Tablet, Orally, Daily propranolol 80 mg oral tablet 80 mg = 1 Tablet, Orally, BID Protonix 40 mg oral delayed release tablet 40 mg = 1 Tablet, Orally, BID spironolactone 25 mg oral tablet 25 mg = 1 Tablet, Orally, QAM Active Scheduled Inpatient Medications None Reported One-Time Medications Given 11/04/23 00:00:00 TO 11/05/23 05:09:14 None Reported PRN Medications (0600 - 0559) from 11/04 - 11/05 None Reported Allergies Benadryl (Confusion) Social History Alcohol Past, 1-2 times per year Electronic Cigarette/Vaping E-Cigarette Use Never. Home/Environment Lives in state 5 months out of the year starting in Nov., Lives with Alone. Substance Abuse Denies Tobacco Tobacco Use: Never (less than 100 in lifetime). Family History DM - Diabetes mellitus: Mother. Heart disease: Mother and Father. Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 8.1 k/cumm (11/04/23 21:51:00) RBC: 4.9 million/cumm (11/04/23 21:51:00) Hgb: 15.4 GM/dL High (11/04/23 21:51:00) Hct: 45.3 % (11/04/23 21:51:00) MCV: 92 fL (11/04/23 21:51:00) MCH: 31.4 pg (11/04/23 21:51:00) MCHC: 34 GM/dL (11/04/23 21:51:00) RDW: 14.5 % (11/04/23 21:51:00) Platelet: 249 k/cumm (11/04/23 21:51:00) MPV: 8.2 fL (11/04/23 21:51:00) Neutrophils %: 84 % (11/04/23 21:51:00) Lymphocytes %: 11 % (11/04/23 21:51:00) Monocytes %: 4 % (11/04/23 21:51:00) Eosinophils %: 0 % (11/04/23 21:51:00) Basophils %: 0 % (11/04/23 21:51:00) Absolute Neutrophil: 6.8 k/cumm (11/04/23 21:51:00) Absolute Lymphocyte: 0.9 k/cumm Low (11/04/23 21:51:00) Absolute Monocyte: 0.3 k/cumm (11/04/23 21:51:00) Absolute Eosinophil: 0 k/cumm (11/04/23 21:51:00) Absolute Basophil: 0 k/cumm (11/04/23 21:51:00) Chemistry: Sodium SerPl QN: 139 mmol/L (11/04/23 21:51:00) Potassium SerPl QN: 4 mmol/L (11/04/23 21:51:00) Chloride SerPl QN: 105 mmol/L (11/04/23 21:51:00) Carbon Dioxide SerPl QN: 25 mmol/L (11/04/23 21:51:00) Anion Gap: 9 mmol/L (11/04/23 21:51:00) BUN SerPl QN: 14 mg/dL (11/04/23 21:51:00) Creatinine SerPl QN: 1.29 mg/dL High (11/04/23 21:51:00) Estimated GFR (CKD-EPI, no race): 40 mL/min/1.73m2 Low (11/04/23 21:51:00) Estimated CRCL (CG): 33 mL/min Low (11/04/23 21:51:00) Glucose SerPl QN: 128 mg/dL High (11/04/23 21:51:00) Calcium Total SerPl QN: 9.9 mg/dL (11/04/23 21:51:00) Alkaline Phos SerPl QN: 258 Units/L High (11/04/23 21:51:00) ALT SerPl QN: 47 Units/L (11/04/23 21:51:00) AST SerPl QN: 311 Units/L High (11/04/23 21:51:00) Bilirubin Total SerPl QN: 0.9 mg/dL (11/04/23 21:51:00) Total Protein SerPl QN: 7.3 GM/dL (11/04/23 21:51:00) Albumin SerPl QN: 4.6 GM/dL (11/04/23 21:51:00) Lipase SerPl QN: 14 Units/L (11/04/23 21:51:00) Troponin-I High Sensitivity: 124 ng/L High (11/04/23 23:46:00) BNP Pl QN: 505 pg/mL High (11/04/23 21:51:00) Lactate Venous Pl QN: 1.6 mmol/L (11/04/23 21:51:00) Urine Studies: Color: Yellow (11/05/23 00:51:00) Clarity: Clear (11/05/23 00:51:00) Specific Gravity: 1.018 (11/05/23 00:51:00) pH: 5.5 (11/05/23 00:51:00) Protein: 100 Abnormal (11/05/23 00:51:00) Glucose: Normal (11/05/23 00:51:00) Ketones: NEGATIVE (11/05/23 00:51:00) Bilirubin: NEGATIVE (11/05/23 00:51:00) Hgb Ur: NEGATIVE (11/05/23 00:51:00) Nitrite: NEGATIVE (11/05/23 00:51:00) Urobilinogen: Normal (11/05/23 00:51:00) Leukocyte Esterase Ur: NEGATIVE (11/05/23 00:51:00) WBC: 0-5 (11/05/23 00:51:00) RBC: 0-2 (11/05/23 00:51:00) Bacteria: NONE (11/05/23 00:51:00) Squamous Epithelial: Few (11/05/23 00:51:00) Hyaline Casts: 3-5 (11/05/23 00:51:00) All Other Labs: COVID 19 Specimen Source: Nasopharyngeal (11/04/23 22:18:00) Coronavirus SARS-CoV2 Rapid: Detected Abnormal (11/04/23 22:18:00) Micro - Last 7 days Rapid Influenza Method: PCR - Liat (11/04/23 22:18:00) Rapid Influenza A PCR: Not Detected (11/04/23 22:18:00) Rapid Influenza B PCR: Not Detected (11/04/23 22:18:00) Diagnostics Radiology Results - Last 24 hours Across Visits 11/04/2023 23:10 - XR Chest PA or AP Portable IMPRESSION: 1. No obvious infiltrate or effusion.2. Mild cardiomegaly.3. Moderate hiatal hernia.Template Version: IUHPR_STRThank you for consulting our team of subspecialty radiologists at Physicians Radiology. 11/04/2023 23:11 - CT Abd/Pelvis W/O IV Contrast IMPRESSION: 1. There is a normal appendix.2. Moderate hiatal hernia.3. Status post hysterectomy.4. No suspicious adnexal mass.5. No nephrolith, ureterolith or hydronephrosis.6. Status post cholecystectomy.7. No evidence of calcified choledocholithiasis or acutepancreatitis.Template Version: IUHPR_STRThank you for consulting our team of subspecialty radiologists at Physicians Radiology. Signature Line Electronically Signed on 11/05/23 05:09 EST ________________________________________________________ MD Electronically Signed on 11/05/23 05:12 EST ________________________________________________________ MD

Weitere VAERSDATA-Felder

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

VAERS 2645187

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

kritisch

Staat: FL
Alter: 77,0
Geschlecht: M
Eingang: 14.06.2023
Impfdatum: 26.02.2021
Beginn: 19.08.2022
Tage bis Beginn: 539,0
Dosis: 2
Route/Site: - / -

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

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

Symptomtext

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

Weitere VAERSDATA-Felder

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

VAERS 2639045

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: TN
Alter: 68,0
Geschlecht: F
Eingang: 31.05.2023
Impfdatum: 23.03.2021
Beginn: 01.04.2023
Tage bis Beginn: 739,0
Dosis: 2
Route/Site: IM / -

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

Bacteraemia Death Debridement Decubitus ulcer Encephalopathy Food refusal General physical health deterioration Haemodialysis Hypophagia Hyporesponsive to stimuli Malnutrition Necrotising soft tissue infection Refusal of treatment by patient Ventricular tachycardia

Symptomtext

She was admitted as above. She was severely encephalopathic throughout her hospital stay. She often refused food and therapies. She was maintained on hemodialysis. Because of her developing malnutrition from lack of oral intake, she developed a severe sacral decubitus ulcer with necrotic and infected tissue and bacteremia. Efforts to prevent this were unsuccessful as the patient steadfastly refused to allow a feeding tube and refused to take more nutrition. She was seen by Dr. and taken to the operating room for debridement. Unfortunately, she remained poorly responsive. I discussed extensively with her sons over the last few hospital days. They agreed that she would not want heroic measures to keep her alive. She deteriorated further with an episode of ventricular tachycardia, and the family decided to pursue comfort measures only. She passed away peacefully.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension Type 2 diabetes CVA x2 with difficulty speaking and walking Chronic kidney disease stage 3 Diastolic CHF Renal carcinoma, probably post partial nephrectomy, details unclear Hypothyroidism Dementia
Andere Medikamente: -
Allergien: Codeine Sulfa
Vorherige Impfungen: -

VAERS 2624226

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 01.05.2023
Impfdatum: 22.03.2021
Beginn: 08.10.2021
Tage bis Beginn: 200,0
Dosis: 2
Route/Site: IM / -

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

Acute respiratory failure Aortic arteriosclerosis Chronic respiratory failure Obstructive sleep apnoea syndrome Respiratory failure Sleep apnoea syndrome

Symptomtext

G47.30 SLEEP APNEA 9/13/2021 ATHEROSCLEROSIS OF AORTA G47.33 OBSTRUCTIVE SLEEP APNEA 10/7/2021 ATHEROSCLEROSIS OF AORTA J96.00 ACUTE RESPIRATORY FAILURE 10/7/2021 ATHEROSCLEROSIS OF AORTA J96.02 ACUTE HYPERCAPNIC RESPIRATORY FAILURE 10/11/2021 ATHEROSCLEROSIS OF AORTA J96.10 CHRONIC RESPIRATORY FAILURE 9/13/2021 ATHEROSCLEROSIS OF AORTA G47.30 SLEEP APNEA 9/13/2021 ATHEROSCLEROSIS OF AORTA G47.33 OBSTRUCTIVE SLEEP APNEA 10/7/2021 ATHEROSCLEROSIS OF AORTA J96.00 ACUTE RESPIRATORY FAILURE 10/7/2021 ATHEROSCLEROSIS OF AORTA J96.02 ACUTE HYPERCAPNIC RESPIRATORY FAILURE 10/11/2021 ATHEROSCLEROSIS OF AORTA J96.10 CHRONIC RESPIRATORY FAILURE 9/13/2021 ATHEROSCLEROSIS OF AORTA

Weitere VAERSDATA-Felder

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

VAERS 2623158

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 88,0
Geschlecht: M
Eingang: 28.04.2023
Impfdatum: 17.03.2021
Beginn: 02.06.2021
Tage bis Beginn: 77,0
Dosis: 2
Route/Site: IM / LA

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

Acute myocardial infarction Acute respiratory failure Aortic arteriosclerosis Hyperlipidaemia Hypotension Joint effusion Transitional cell cancer of the renal pelvis and ureter Type 2 diabetes mellitus

Symptomtext

I21.4 ACUTE NON ST ELEVATION MI 6/2/2021 ATHEROSCLEROSIS OF AORTA I95.9 HYPOTENSION 6/2/2021 ATHEROSCLEROSIS OF AORTA J96.00 ACUTE RESPIRATORY FAILURE 6/24/2021 ATHEROSCLEROSIS OF AORTA I21.4 ACUTE NON ST ELEVATION MI 6/2/2021 TRANSITIONAL CELL CARCINOMA, LEFT URETER I95.9 HYPOTENSION 6/2/2021 TRANSITIONAL CELL CARCINOMA, LEFT URETER J96.00 ACUTE RESPIRATORY FAILURE 6/24/2021 TRANSITIONAL CELL CARCINOMA, LEFT URETER I21.4 ACUTE NON ST ELEVATION MI 6/2/2021 DM 2 W HYPERLIPIDEMIA EFFUSION OF RIGHT WRIST I95.9 HYPOTENSION 6/2/2021 DM 2 W HYPERLIPIDEMIA EFFUSION OF RIGHT WRIST J96.00 ACUTE RESPIRATORY FAILURE 6/24/2021 DM 2 W HYPERLIPIDEMIA EFFUSION OF RIGHT WRIST

Weitere VAERSDATA-Felder

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

VAERS 2584254

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: NY
Alter: 87,0
Geschlecht: F
Eingang: 20.02.2023
Impfdatum: 15.09.2022
Beginn: 22.01.2023
Tage bis Beginn: 129,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure Atelectasis Blood gases Blood lactic acid Body temperature decreased COVID-19 Cerebral haemorrhage Cerebral mass effect Chest X-ray abnormal Computerised tomogram head abnormal Endotracheal intubation Fall Fraction of inspired oxygen Lactic acidosis Leukocytosis Mechanical ventilation SARS-CoV-2 test positive Sepsis

Symptomtext

1/22/2023-Brought in EMS, presents to ED, had been found unresponsive at bottom of stairs. HR in 60, while obtaning CT dropped to 30's, 1 amp Atropine given. Temp-85.8, BP 194/91.Covid + test. Intubated. CT- LArge intraparenchymal Hemmorhage R cerebral hemisphere, centered R temporal and occipital lobes .2x5.9 cm. 1.9cm r to L midline shift. Evidence of impending transtentorial herniation and brainstem deviation to the left. CXR-small desnity upper left lung, atelectasis. Admit to trauma, acute hypoxic resp failure s/t fall, intraparencymal hemorrhage. WBC 18.4 1/23/2023- Vent-AC VC 400/14/100 Fio2/5 Peep. Comfort care patient has been made DNR. Sepsis d/t Covid leukocytosis 18.4, lactic acidosis 2.4. 1/23/2023-Levophed to keep MAP above 65 WBC 13.2. ABG 7.353/43.4/24.1 on 100% Fio2 AC VC vent. 1/24/2023-Terminal exubation @1257.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroidism and HTN
Andere Medikamente: -
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2566908

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MN
Alter: 72,0
Geschlecht: M
Eingang: 24.01.2023
Impfdatum: 12.11.2021
Beginn: 14.11.2022
Tage bis Beginn: 367,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 Chills Confusional state Cough Dyspnoea Influenza like illness Lower urinary tract symptoms Micturition urgency Oropharyngeal pain Pollakiuria Pyrexia Rhinorrhoea SARS-CoV-2 test positive Urinary incontinence Urinary tract infection

Symptomtext

Patient brought to the ED by EMS on 11/14 for urinary symptoms (urinary incontinence, frequency, urgency) and flu-like symptoms (chills, subjective fever, sore throat, rhinorrhea, cough, and shortness of breath). Patient's family also notes patient has been more confused. He required 4L O2 and is on RA at baseline. He was tested for COVID-19 by PCR and was positive. Ultimately patient was admitted 11/14/22 - 11/17/22 for UTI, acute hypoxic respiratory failure, COVID-19, among other problems. He initially required supplemental O2, however was able to be weaned off. Patient has received the COVID primary vaccine series and one booster.

Weitere VAERSDATA-Felder

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

VAERS 2562294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 18.01.2023
Impfdatum: 19.03.2021
Beginn: 06.12.2022
Tage bis Beginn: 627,0
Dosis: 2
Route/Site: - / -

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

Acute respiratory failure Aneurysm ruptured Anxiety Atelectasis Atrial fibrillation COVID-19 Chronic obstructive pulmonary disease Cough Depression Dyspnoea Intensive care Mechanical ventilation Physical deconditioning Pneumonia bacterial Pyrexia Respiratory failure SARS-CoV-2 test positive Superinfection

Symptomtext

Patient is a 73 y.o. female who was referred to the ED on 12/6/2022 with concern for pneumonia after presenting with 2 day complaint of cough, shortness of breath, and fevers. She was found to be SARS-C0V2 positive with admission requested with concern for associated pneumonia. She was admitted to the ICU with acute on chronic hypoxemic, hypercapnic respiratory failure. COPC assumed care with transferr out of the ICU 12/11/2022. Acute on chronic hypoxemic, hypercapnic respiratory failure COVID 19 with superimposed bacterial pneumonia Tracheostomy present Baseline respiratory status includes tracheostomy placement in May 2022 following a prolonged hospitalization for a ruptured splenic aneurysm -She is maintained at 5-6 L/min via trach mask at home, she weaned to a FiO2 of 30% at 6-7 L from earlier need for ventilatory support via an exchanged her cuffless tracheostomy with a cuffed 6 shiley tracheostomy -Acute decompensation was believed multifactorial related to COVID-19, deconditioning , atelectasis and bacterial pneumonia -Treatment included dexamethasone and 7 days of antibiotics. Enterococcus UTI Possible asymptomatic bacteruria, she received nitrofurantoin x 5 days given the nature of her acute presentation COPD Continue inhaled bronchodilator therapy Paroxysmal atrial fibrillation Rate controlled; continue diltiazem and apixaban Anxiety and depression Continue buspirone

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 25,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2560328

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: NV
Alter: 79,0
Geschlecht: F
Eingang: 15.01.2023
Impfdatum: 13.03.2021
Beginn: 15.05.2021
Tage bis Beginn: 63,0
Dosis: 2
Route/Site: SYR / AR

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

Anticoagulant therapy Dyspnoea Pulmonary embolism

Symptomtext

I started experiencing breathing difficulties in May, 2021, which increased in severity until, on 06/29/2021, were so bad I had to see a doctor. I went to a clinic, was sent to ER, admitted to hospital, & a large pulmonary embolism was found. A blood thinner (Eliquis) & high blood pressure meds were prescribed. On 07/07/2021, I was transferred to a rehab center to rebuild strength & breathing endurance. I was discharged on 07/27/2021 with supplemental O2 required for any exertion. To date I still require prescribed meds & supplemental O2 for exertion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: Contact the local Medical Center for records regarding my hospitalization on 06/29?07/07/2021.
Aktuelle Erkrankungen: None
Vorgeschichte: COPD,asthma,cancer survivor (breast & lung)
Andere Medikamente: Levothyroxine,Advair,Letrozole,Latanoprost,Prolia,Proventil
Allergien: Sulfa, codeine
Vorherige Impfungen: -

VAERS 2559529

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 13.01.2023
Impfdatum: 11.03.2021
Beginn: 01.08.2022
Tage bis Beginn: 508,0
Dosis: 2
Route/Site: - / -

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

Accident Burns third degree COVID-19 Death Endotracheal intubation General physical health deterioration Hypotension Intensive care Loss of consciousness Mechanical ventilation Pulse absent Pulseless electrical activity Respiratory fume inhalation disorder Resuscitation SARS-CoV-2 test positive Skin wound Thermal burn

Symptomtext

3rd dose PFIZER COVID VACCINE GIVEN 10/12/21, LOT #FH8020; EMS called to house fire; pt found unconscious without a pulse; CPR and medications started; continued to be PEA; intubated; pt regained pulse, placed on a ventilator; grade III inhalation injury; 4% TBSA partial and full thickness burns to head, bilateral arms, back; pt tested positive for COVID; taken to Burn ICU; pt's condition worsened; hypotensive requiring vasopressors; vital signs began to trend downward; family transitioned pt to comfort measures and she expired in the hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: hx of CVA
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2545812

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

kritisch

Staat: MN
Alter: 75,0
Geschlecht: F
Eingang: 29.12.2022
Impfdatum: 18.05.2022
Beginn: 28.12.2022
Tage bis Beginn: 224,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

Patient expired 12/28/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown
Vorgeschichte: PMH CAD, STEMI, CKD Stage 3, HTN, hyperlipidemia, asthma, baseline dementia, epilepsy.
Andere Medikamente: Unknown
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2508620

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 66,0
Geschlecht: F
Eingang: 15.11.2022
Impfdatum: 16.03.2021
Beginn: 01.01.2022
Tage bis Beginn: 291,0
Dosis: 2
Route/Site: - / -

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

Anaemia COVID-19 Chronic obstructive pulmonary disease Death Endotracheal intubation General physical health deterioration Respiratory distress SARS-CoV-2 test positive

Symptomtext

Pt to hospital and found to be positive for COVID; severe anemia and underlying COPD; pt had a long hospitalization; began to decline clinically and required intubation; no improvement; pt continued to worsen; family decided on de-escalation and comfort measures; pt remained GIP at hospital due to respiratory distress; pt passed away in the hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 33,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2490319

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MN
Alter: 87,0
Geschlecht: M
Eingang: 26.10.2022
Impfdatum: 27.09.2022
Beginn: 06.10.2022
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: IM / RA

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

Angiopathy Chest tube insertion Computerised tomogram thorax abnormal Death Depressed level of consciousness Dyspnoea Fatigue Haemothorax Hypopnoea Intrapericardial thrombosis Pericardial effusion Pericardial haemorrhage Pleural effusion Productive cough Pulse absent Red blood cell transfusion Resuscitation Sputum discoloured

Symptomtext

Patient previously tested positive on 8/13/22. Patient was brought to local Hospital ED on 10/6 with unknown onset of shortness of breath and productive cough with yellow sputum. He also reported feeling "very very tired". During this visit, CT scan showed concern for blood and blood clots in the pericardium, and the patient was found to have a systolic blood pressure in the 100s. Bedside ultrasound showed fluid around the heart. He was given a unit of blood and started on Levophed, and was transferred to alternate Hospital ED. Within minutes of arrival, the patient became obtunded and unresponsive with shallow respirations. The provider was unable to palpate a pulse so CPR was started immediately. Patient was given multiple rounds of epinephrine, bicarb, calcium and volume resuscitation with IV fluid and packed red blood cells. The provider was concerned for aortic dissection or other catastrophic vascular cause for the patient's presentation. Further ultrasound revealed an apparent pleural effusion on the left. Needle thoracostomy and tube thoracostomy was performed with a large volume of blood from the left hemithorax. Early in the resuscitation, ready pulses were felt with rhythm checks, however pulses were lost and were not regained. per the provider, given the prolonged downtime, likely catastrophic vascular event and the patient's advanced age, further resuscitation efforts appeared futile. Patient passed on 10/6 at 2:28pm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Pt history of asthma, type II diabetes, ESRD, dementia.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2480449

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: NY
Alter: 59,0
Geschlecht: F
Eingang: 17.10.2022
Impfdatum: 17.11.2021
Beginn: 24.04.2022
Tage bis Beginn: 158,0
Dosis: 2
Route/Site: IM / RA

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

Acute respiratory distress syndrome Acute respiratory failure Anticoagulant therapy Blood gases COVID-19 Cardiac failure Cardiomegaly Cerebral haemorrhage Chest X-ray abnormal Computerised tomogram abnormal Computerised tomogram head abnormal Computerised tomogram thorax abnormal Confusional state Crepitations Death Dysphagia Echocardiogram abnormal Endotracheal intubation

Symptomtext

4/24/2022-Presented to ED, unwitnessed fall states hit head large hematoma on L eye, admitted to drinking alcohol daily. Confused. CT Had, R parafalcine subdural and L frontal/parietal subdural hygroma. CT-sacral fracture and L subtrochanteric femur fx. Covid -test. Baseline 02 use 2L NC. Increased to 3L intermittently desat to mid 80's.Admit intraparenchymal hemorrhage with subdural hematoma s/t to fall. 4/25/2022-Left subtrochanteric hip fracture repair. R occiptal intraparenchymal hemorrhage inceased to 1.5cm L anterior frontal intraparenchymal hemorrhage increased to 5mm. No surgical intervention. BP controlled less then 140/80 currently 104/62, o2 sat 90's on 3L NC. Keppra 750mg BID. ST eval clear liquids, swallowing difficulties. 4/26/2022- R occipital intraparenchymal hemorrhage stable on f/u CT. 4/27/2022-On NRB, sat in mid 70's, o2 changed to 5L sata now 88-92%. 4/28/2022-AM-Mentation decline, desat 70-80 becoming more altered, fine wheezes bilateral and creptation on R side. Placed on NRB 15L. CXR-mod airpace disease/infiltrates LAsix IV and levaquin , CT no evidence of PE. IVC filter placed to prevent PEd/t recent surgery and immobility. PM-Sats in high 90's with NRB, but patient would not keep on, desatting to 70's. 5L NC was placed so suctioning could occur, sats would not maintain over 70%, thick yellow sputum obtained by suction. Became tachy and transfered to ICU and intubated. Acute on chronic hypoxemic resp failure s/t to ARDS d/t pneumonia vs pulm edema in setting of HFrEF and AMS. Current bilevel setting FiO2 60%. 4/29/2022-Bilevel 16 25/10 35%. WBC and h&h stable. On Vanco cefepime and flagyl. 4/30/2022- recent echo showed severe L ventricular dilatation with moderate miral regurg EF 20%. Continue entresto hold toresemide 5/2/2022- Exubated on 2L NC. Continue cefepime and flagyl. 5/3/2022- WBC 15.4 from 13.3 ABG 7.453/31.9/66/22.3/90 cxr-pulmonary vascular congestion and cardiomegaly. Cont digoxin and metoprolol 5/5/2022- Transfered to ICU. Wears bipap at HS. o2 sat on 2L stable. 5/13/2022- Rapid response called Acute RF, hypoxic 80's on sat , tachypneic using resp muscles. BP 154/104 RR 24 ABG 7.45/25/97/18/ on NRB worsening CT chest -pulmonary infiltrates and b/l pleural effusion. Bipap with PEEP 8. Continued distress, intubated and transfered to ICU. Chest Ct consisten with b/l diffuse groundglass opacities/ Covid + test. Ferritin 535.0. Started on steroids, barcitinib, remdesivir, vitamins and heparin. Cefepime and Vanco. 5/15/2022- Vent 12 22/6 60% 5/17/2022-Palliative orders placed d/t severe HF and mitral valve issues, fluid is in lungs and she is at high risk for reintubation if extubation is attempted. Terminally exubated. Morphine increased. WBC 15.5 5/19/2022- Time of death 1003.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 25,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: ETOH abuse, COPED, Afib, CAD. HLD and post CABG ICD placement
Andere Medikamente: -
Allergien: Aspirin, PCN and adhesive
Vorherige Impfungen: -

VAERS 2462519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge En6208

kritisch

Staat: FL
Alter: 32,0
Geschlecht: M
Eingang: 27.09.2022
Impfdatum: 01.03.2021
Beginn: 17.11.2021
Tage bis Beginn: 261,0
Dosis: 1
Route/Site: - / -

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

Cerebrovascular accident Intracardiac thrombus Ventricular septal defect

Symptomtext

On 11-17-21, suffered stroke caused by a blood clot that went thru a hole in the heart

Weitere VAERSDATA-Felder

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

VAERS 2442760

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: TX
Alter: 80,0
Geschlecht: F
Eingang: 13.09.2022
Impfdatum: 08.10.2021
Beginn: 07.09.2022
Tage bis Beginn: 334,0
Dosis: 2
Route/Site: IM / LA

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

Acute myocardial infarction Asthenia COVID-19 Cachexia Death General physical health deterioration Pallor Pneumonia Respiratory failure SARS-CoV-2 test positive

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization/Death. Patient received Pfizer-BioNTech on 3/1/21, 3/22/21 and 10/8/21. Presented to ED c/o generalized weakness progressing over the past 6 days. Pale, ill appearing, and cachectic, admitted for respiratory failure related to PNA, nstemi, and covid 19. Cont'd to worsen, transiitioned to comfort care. Expired 09/07/22. Pt treated with cefepime, and decadron.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 7,0
Labordaten: COVID+ 8/31/22 - This sample was analyzed using the Biofire Torch system using PCR or equivalent Nucleic Acid Amplification (NAA) technology.
Aktuelle Erkrankungen: -
Vorgeschichte: GERD
Andere Medikamente: vitamin d3, clobetasol, estradiol
Allergien: Penicillins
Vorherige Impfungen: -

VAERS 2440817

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: NY
Alter: 85,0
Geschlecht: F
Eingang: 12.09.2022
Impfdatum: 22.02.2021
Beginn: 14.02.2022
Tage bis Beginn: 357,0
Dosis: 2
Route/Site: IM / LA

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

Acute kidney injury Aortic stenosis Asthenia Blood creatinine increased Blood gases Blood urea increased Bronchitis COVID-19 COVID-19 pneumonia Cardiac arrest Cardiac failure Cardiac failure acute Chest X-ray abnormal Creatinine renal clearance decreased Death Dyspnoea Glomerular filtration rate decreased Haemoglobin decreased

Symptomtext

2/14/2022-Presents to weakness and SOB. Covid + test. Recently treated for bronchitis Jan 2022 with amox. 2L NC 95% sat. Afebrile. CXR: Mod right pleural effusion. Hgb 7.1 dropped to 6.5 1 unit PRBC. Admit acute decompensated HF with preserved EF in setting of severe aortic stenosis Covid 19 pneumonia. 2/15/2022- Remdesivir, Decadron and azithromycin started. Ferritin 12.5 iron supplements started. Troponinemia (downtrending) s/t demand ischemia Trop:0.053,0.059 and 0.069. 2/17/2022-AKI worsening, BUN was 71 and 1.4 (baseline creatnine 0.7-1) remdesivir d/c low creatnine clearance. 2/19/2022-AKI worsening with diuresis. Lasix held. Placed on Bipap 16/6 45%. CXR:Worsening bilateral infiltrates 2/19/2022- ABG: 7.154/85.6/73/30.1/95. Need for TAVR held due to acuity. 2/21/2022-Started baricitinib, aztreonam and Vanco continue decadron. 2/21/2022-Sating WDL on Bipap 45%. expiratory wheeze and rhonci noted through night r lung. 2/22/2022-Continues on Bipap, BP range -110/60-118/71 sattng 95% HR range 110-150 a fib. WBC-21.3. TPN started. DNR/DNI on file. Creatnine of 1.3, BUN 105 EGFR 41. Platelets decrease to 50 from 60. ABG: 7.34/60.8/88/33/98 on bipap 2/24/2022- Amiodarone dtt running @ 16.67 ml~/hr HR 60-80's. Continues in Bipap tolerates short period of HFNC. Palliative following family wishes to continue aggressive care. 3/1/2022- WBC-9.4. Platelets 100. BUN 82. Went into sinus brady due to worsening hypoxia leading to asystole. DNR/DNI. Time of death 1941.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 15,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, CHR, A fib, HTN, hx of strokes and Restless leg syndrome,
Andere Medikamente: -
Allergien: alendronate Sodium, Doxycycline, Iodine, gabapentin, Keflex an
Vorherige Impfungen: -

VAERS 2118705

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: PA
Alter: -
Geschlecht: U
Eingang: 16.08.2022
Impfdatum: 24.02.2021
Beginn: 20.03.2021
Tage bis Beginn: 24,0
Dosis: 2
Route/Site: - / LA

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

Acne Ageusia Amnesia Anosmia Cellulitis Arthralgia Condition aggravated Dry mouth Food intolerance Deafness Economic problem Glossodynia Gynaecomastia Immune system disorder Insomnia Laboratory test Male sexual dysfunction Muscle atrophy

Symptomtext

I was compelled to receive a COVID vaccine priiior to my knee surgery in May 2021. I received two doses of the Pfizer BioNtech vaccine on 02/24/2021 and 03/18/2021. On 03/20/2021 began to develop immune system issues. It began with the total disappearance of my seasonal allergies that I have had for over 50 years. I received allergy shots for approximately 10 years from age 7 through age 16. On 03/21/2021 I developed severe Xerostomia and Glossodynia. Ove the next 16 months I developed numerous disorders including...tinnitus and hearing loss..acne..morbilliform rash..trigger finger..sleeplessness (the first incident lasted 91 hours and then 28 hours, after sleeping for 2 hours and I've had dozens of recurrances)..loss of sense of taste..loss of sense of smell..headaches (I never had a headache until October 2021, then I developed blinding headaches, everyday from the beginning of October 2021 to the middle of January 2022)..severe nausea every morning (with dry heaves until my eyes are black and blue, several times week)..pneumonia (3 times in 6 weeks)..cellulitis..vasculitis..memory loss (my short term memory is nonexistent)..loss of sexual function..gynecomastia..severe muscle loss..loss of income..physical disability. As a result of my layers of disorders, I have been recruited to participate in the FDA-authorized vaccine injury study. I am barely able to make enough money to support myself.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Gynaecomastia
Hospital-Tage: -
Labordaten: I've had numerous tests run by MDs
Aktuelle Erkrankungen: -
Vorgeschichte: High blood pressure, low testosterone; clean life
Andere Medikamente: Testosterone Cypionate Bystolic Multivitamin and minerals
Allergien: Pollen and mold
Vorherige Impfungen: -

VAERS 2370274

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 14.07.2022
Impfdatum: 10.02.2021
Beginn: 03.03.2022
Tage bis Beginn: 386,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Death

Symptomtext

Narrative: PATIENT PASSED AWAY DUE TO COVID-19. PT WAS HOSPTILIZED AND FULLY VACCINATED AT THE TIME OF HIS DEATH.

Weitere VAERSDATA-Felder

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

VAERS 2368823

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: TN
Alter: 86,0
Geschlecht: M
Eingang: 14.07.2022
Impfdatum: 23.03.2021
Beginn: 11.06.2022
Tage bis Beginn: 445,0
Dosis: 1
Route/Site: IM / -

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Death from COVID-19 S/p Vaccination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 19,0
Labordaten: Positive covid-19 test
Aktuelle Erkrankungen: -
Vorgeschichte: CAD A fib Hypertension Gout Chronic Kidney Disease Stage 3
Andere Medikamente: Pradaxa Amiodarone Atorvastatin Carvedilol Entresto Spironolactone Vitamin C Multivitamin Allopurinol
Allergien: None
Vorherige Impfungen: -

VAERS 2364430

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: IL
Alter: 67,0
Geschlecht: F
Eingang: 11.07.2022
Impfdatum: 07.04.2021
Beginn: 29.01.2022
Tage bis Beginn: 297,0
Dosis: 2
Route/Site: IM / -

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

Anticoagulant therapy COVID-19 Dyspnoea Enteral nutrition Hypoxia Inappropriate schedule of product administration Oxygen saturation decreased Pulmonary embolism SARS-CoV-2 test positive

Symptomtext

Pfizer Dose 1 3/10/21 (EN6205 Pfizer Dose 2 4/7/21 (EN6208) COVID Positive 1/29/22 1/29/22: Patient is a 68-year-old female who presents from the nursing home with increasing shortness of breath, hypoxia and COVID positive. A full history of present illness could not be had as the patient is nonverbal since having a hemorrhagic stroke with resultant left-sided hemiplegia and the past patient also is NPO and has a G-tube. Patient was found to be having hypoxia at the nursing home with O2 saturations in the 80% range, it is believed that the patient is chronically on supplemental O2 via nasal cannula. EMS were notified who did give the patient a nebulizer treatment and increased her oxygen which improved her saturations into the low 90s. No further information could be had from the patient. The patient's medical history, current medications, imaging studies, vital signs, laboratory studies and agency room records were personally reviewed. Case was also discussed directly with the emergency room provider. 2/2/22: Patient is a 68-year-old female who presents from the nursing home with increasing shortness of breath, hypoxia and COVID positive. A full history of present illness could not be had as the patient is nonverbal since having a hemorrhagic stroke with resultant left-sided hemiplegia and the past patient also is NPO and has a G-tube. Patient was found to be having hypoxia at the nursing home with O2 saturations in the 80% range, it is believed that the patient is chronically on supplemental O2 via nasal cannula. EMS were notified who did give the patient a nebulizer treatment and increased her oxygen which improved her saturations into the low 90s. No further information could be had from the patient. The patient's medical history, current medications, imaging studies, vital signs, laboratory studies and agency room records were personally reviewed. Case was also discussed directly with the emergency room provider. Patient is mostly nonverbal as above. She had a new PE, currently was on Xarelto past. She was initially started on a IV heparin, subsequently Lovenox. Will change her to Eliquis at discharge. Patient was also continued on Decadron Levaquin. The she will be continued on tube feeds as instructed. Accu-Cheks q.6 hours with basal Lantus and a sliding scale insulin coverage with Humalog. Patient was weaned off of oxygen. She is hemodynamically stable, medically stable to be discharged back to skilled nursing facility today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CKD HTN intracerebral hemorrhage left sided hemiplegia
Andere Medikamente: albuterol 2 inh Q4h PRN apixaban 5 mg PO BID atorvastatin 20 mg PO HS bisacodyl 10 mg PR QD PRN carvedilol 6.25 mg PO BID guaifenesin 10 mL PO Q4h PRN insulin glargine 35 units SQ QD insulin lispro sliding scale SQ ACHS lisinopril 40 mg PO
Allergien: sulfa drugs - unknown
Vorherige Impfungen: -

VAERS 2329028

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MI
Alter: 79,0
Geschlecht: M
Eingang: 23.06.2022
Impfdatum: 24.02.2021
Beginn: 22.01.2022
Tage bis Beginn: 332,0
Dosis: 2
Route/Site: IM / UN

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

Atrial fibrillation COVID-19 Cardio-respiratory arrest Condition aggravated Death Hypotension Respiratory distress SARS-CoV-2 test positive Unresponsive to stimuli

Symptomtext

Pt to ED 1/22 for hypotension, respiratory distress and AFib, upon arrival pt is not alert to any stimuli. COVID+ 1/22, on Vancomycin. Pt coded twice, first time for 5 minutes second for 1 minute, pt received antibiotics and multiple boluses. Family changed code status to comfort care, pt expired 1/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: 1,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: Pulmonary emphysema (CMS/HCC) ... Pulmonary emphysema (CMS/HCC) Obstructive sleep apnea syndrome C. difficile colitis, 11/26/21 Endocrine Hypothyroidism Diabetes mellitus (CMS/HCC) Chronic pulmonary embolism (CMS/HCC) Renal failure Lymphedema of both lower extremities BMI 50.0-59.9, adult (CMS/HCC) Debility General weakness AKI (acute kidney injury) (CMS/HCC) Chronic atrial fibrillation (CMS/HCC) Atrial fibrillation (CMS/HCC) Essential hypertension Mixed hyperlipidemia Venous insufficiency, peripheral Xerosis of skin Traumatic hematoma of left lower leg Ulcer of left lower extremity with fat layer exposed (CMS/HCC) Leg edema Chronic venous hypertension with ulcer involving left side Venous ulcer of left leg (CMS/HCC) Varicose veins of l low extrem w ulcer oth part of lower leg (CMS/HCC) Macrocytic anemia Inability to walk Acute bilateral ankle pain CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min (CMS/HCC) Closed fracture of multiple ribs of right side with routine healing Hypertensive heart disease without heart failure At risk for falls At risk for impaired skin integrity Pulmonary nodule Venous stasis Acute on chronic congestive heart failure (CMS/HCC) CKD (chronic kidney disease) Recurrent cellulitis of right lower extremity Urinary retention Swelling Gluteal abscess Supratherapeutic INR Necrotizing soft tissue infection Paroxysmal atrial fibrillation (CMS/HCC) Functional quadriplegia (CMS/HCC) Left wrist sprain Respiratory distress
Andere Medikamente: atorvastatin (LIPITOR) 10 MG PO Tab ... atorvastatin (LIPITOR) 10 MG PO Tab colchicine (COLCRYS) 0.6 MG PO Tab collagenase (SANTYL) 250 UNIT/GM EXTERNAL Ointment fluticasone (FLONASE) 50 MCG/ACT NASAL Suspension levothyroxine (SYNTHROID, LE
Allergien: hydrochlorothiazide, sulfa antibiotics
Vorherige Impfungen: -

VAERS 2311618

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 97,0
Geschlecht: F
Eingang: 07.06.2022
Impfdatum: 24.03.2021
Beginn: 01.09.2021
Tage bis Beginn: 161,0
Dosis: 2
Route/Site: - / -

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

Asthenia COVID-19 Cough Death Failure to thrive Feeding disorder Gastrostomy SARS-CoV-2 test positive

Symptomtext

9/12/21 Pt had a hospital admission for a positive COVID test; was treated with ABX; dc'd to SNF for continued care; pt admitted to hosp on 9/28/21 via ambulance with weakness, FTT, coughing, difficulty eating; PEG tube placed; dc'd back to SNF for continued care where she passed away on 11/16/21

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: dementia, CKD, first degree atrioventricular block
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2241249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: IA
Alter: 73,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 18.03.2021
Beginn: 28.10.2021
Tage bis Beginn: 224,0
Dosis: 2
Route/Site: IM / -

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

Acute respiratory failure Ageusia Anosmia Asthenia COVID-19 COVID-19 pneumonia Cellulitis Chills Computerised tomogram thorax abnormal Decreased appetite Dyspnoea Feeling abnormal Fibrin D dimer increased General physical health deterioration Pneumonia Pyrexia Retching SARS-CoV-2 test positive

Symptomtext

COVID Vaccine Breakthrough Case Pfizer Dose 1 2/24/21 (EN6200) Pfizer Dose 2 3/18/21 (EN6208) COVID Positive 11/3/21 11/3/21: Patient is a 74 year old female with past history of diabetes mellitus, obesity, hyperlipidemia, and hypertension was admitted with 1 week duration of worsening weakness and shortness of breath and found to have COVID-19 pneumonia. History is obtained from chart review as well as discussion with the patient and the ED provider. Patient's chart notes a history of obstructive sleep apnea although the patient denies and states she does not use a CPAP or BiPAP. She was admitted in September with lower extremity cellulitis. She has been vaccinated for COVID-19 earlier this year with to shots. States she started feeling poorly about 5-6 days ago. She has had worsening weakness as well as decreased appetite with a loss of taste and smell. Also had some associated fevers and chills and did have some dry heaving but no current nausea or vomiting. Also denies any diarrhea. Continued to worsen and presented to the ER today by EMS. COVID-19 rapid antigen test was performed which returned positive. D-dimer was elevated and underwent CT chest which did show bilateral pneumonia with no PE. Currently she is resting comfortably on 3 L of oxygen. She would like something to eat. She denies a known history of lung disease and does not use any oxygen at baseline. 11/8/21: The patient is a 74 year old female with obstructive sleep apnea, diabetes mellitus, obesity, hyperlipidemia, and hypertension admitted with 1 week duration of worsening weakness and shortness of breath and found to have COVID-19 pneumonia. She has been vaccinated for COVID-19 earlier this year with 2- shots. States she started feeling poorly about 5-6 days before her current admission. She has had worsening weakness as well as decreased appetite with a loss of taste and smell. Also had some associated fevers and chills and did have some dry heaving but no current nausea or vomiting. Also denies any diarrhea. Continued to worsen and presented to the ER today by EMS. COVID-19 rapid antigen test was performed which returned positive. D-dimer was elevated and underwent CT chest which did show bilateral pneumonia with no PE. She was admitted for acute hypoxemic respiratory failure due to COVID-19 infection. Treated with oxygen, levofloxacin, dexamethasone She continued to have improvement in her oxygen requirement and today she was doing okay on 1 L NC. She will have home oxygen walk and patient will be discharged back on her home medications She will follow with her primary care provider for further directions

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: HLD OSA DM Type 2 multiple personality disorder osteopenia
Vorgeschichte: HLD OSA DM Type 2 multiple personality disorder osteopenia
Andere Medikamente: aspirin 81 mg PO QD bupropion ER 150 mg PO QD clacium carbonate 600 mg PO 2xweek citalopram 20 mg PO QD cyanocobalamin 1 tab PO 2xweek empagliflozin 25 mg PO QD ferrous gluconate 240 mg PO 3xweek furosemide 80 mg PO QD glimepiride 2 mg PO Q
Allergien: amitriptyline - loopy codeine - confusion demerol - slow to awake erythromycin - shakes latex - rash liraglutide - headache lisinopril - dizzy, cough penicillins - dyspnea shellfish - dyspnea trioxzalen - localized reaction, erythema
Vorherige Impfungen: -

VAERS 2235932

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MN
Alter: 63,0
Geschlecht: M
Eingang: 15.04.2022
Impfdatum: 08.04.2021
Beginn: 11.04.2022
Tage bis Beginn: 368,0
Dosis: 1
Route/Site: SYR / LA

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Influenza A virus test Intensive care Positive airway pressure therapy SARS-CoV-2 test positive

Symptomtext

Received Pfizer vaccines on 3/18/21, 4/8/21 Tested positive for COVID-19 (and Influenza A) by PCR on 4/11/22. Admitted to Hospital on 4/14/22 d/t acute hypoxemic respiratory failure, in ICU on BiPAP, diagnosed w/ pneumonia d/t COVID-19. Underlying Type 2 DM, CAD, asthma.

Weitere VAERSDATA-Felder

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

VAERS 2201503

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: TN
Alter: 66,0
Geschlecht: M
Eingang: 28.03.2022
Impfdatum: 24.03.2021
Beginn: 23.12.2021
Tage bis Beginn: 274,0
Dosis: 2
Route/Site: SYR / -

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

Acute kidney injury Acute respiratory failure Anticoagulant therapy COVID-19 Cerebrovascular accident Death Endotracheal intubation Fibrin D dimer Intensive care Lung infiltration Mental status changes Respiratory failure Septic shock Shock haemorrhagic

Symptomtext

Admitted to CCU with CVA, altered mental status, respiratory failure related to Covid. Covid 19 status post dexamethasone until 01/10/2021, did not receive remdesivir secondary to AKI Quantitative D dimer was 16.72 on 01/11/2022, anticoagulated held d/t concern for GI bleed on 01/08/2022. Acute respiratory failure with hypoxemia, intubated 01/04/2022, Pulmonary infiltrates present on admission, consistent with with Covid-19. Treated with six days of meropenem, transitioned to cefepime and vancomycin on 01/09/2022. Developed septic shock on 01/16/2022, requiring 4 pressors. Both septic shock and hemorrhagic shock contributing to his death.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Coronary artery disease, HTN, hyperlipidemia, Type 2 Diabetes
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 2173476

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: FL
Alter: 83,0
Geschlecht: F
Eingang: 11.03.2022
Impfdatum: 26.03.2021
Beginn: 28.01.2022
Tage bis Beginn: 308,0
Dosis: 2
Route/Site: IM / UN

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

Death

Symptomtext

ADMITTED TO HOSPITAL

Weitere VAERSDATA-Felder

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

VAERS 2173272

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: FL
Alter: 64,0
Geschlecht: F
Eingang: 11.03.2022
Impfdatum: 12.03.2021
Beginn: 09.03.2022
Tage bis Beginn: 362,0
Dosis: UNK
Route/Site: - / -

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

Acute myocardial infarction Angiogram pulmonary abnormal Anticoagulant therapy COVID-19 COVID-19 pneumonia Chest pain Cough Electrocardiogram abnormal Lung disorder Lung opacity Myocardial ischaemia Myocardial necrosis marker increased SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st Vaccine received on 02/19/2021. 65y/o with PMHX of Type2 DM, Chronic Bronchitis, HTN, HLD presents to ED with 1 month c/o cough and 1 week c/o chest pain. Pt originally saw her PCP where she tested positive for Covid. PCP referred pt to ED for Imaging and f/u of CP. CTA Chest with LLL opacities and small patches groundglass airspace disease RUL. Room air sat 99%, pt afebrile. Cardiac enzymes positive and EKG with ischemic changes. Pt diagnosed with Covid PNA and NSTEMI. Started on Steroids and Heparin gtt. Plan heart cath once respiratory status improves.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19- Detected on 03/09/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: DM2, Chronic Bronchitis, HTN, HLD
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2157920

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: OH
Alter: 90,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 06.04.2021
Beginn: 08.01.2022
Tage bis Beginn: 277,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Cerebrovascular accident Chest X-ray abnormal Pneumonia SARS-CoV-2 test positive

Symptomtext

Patient admitted to the hospital on 01/08/2022 . Daughter interviewed on 01/14, said mother was still in the hospital, she had a stroke on 01/01/22 and contracted the virus at the hospital. Patient was still in the hospital on 01/14/2022. No underlying health conditions charted in System, nor the symptoms patient was experiencing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: Abnormal chest xray, patient had developed pneumonia. 2019 Novel Coronavirus RNA on 01/08/2022 positive.
Aktuelle Erkrankungen: -
Vorgeschichte: System has charted she has underlying health condition but not specific.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2155142

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: KY
Alter: 60,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 15.04.2021
Beginn: 11.01.2022
Tage bis Beginn: 271,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory distress syndrome Acute respiratory failure COVID-19 COVID-19 pneumonia Cardiac arrest Cardiomegaly Chest X-ray abnormal Chronic obstructive pulmonary disease Dyspnoea Dyspnoea exertional Dysstasia Fall Hypertension Intensive care Life support Liver function test abnormal Multiple organ dysfunction syndrome Pain

Symptomtext

1/7/22 60 yr/o female with a history of COPD, morbidly obese, who presents to the emergency department complaining of 2-week history of leg pain and swelling. She states she started having swelling in her left leg about 2 weeks ago she notified her PCP and they placed her on a water pill. She states last week she was walking from the bedroom to the kitchen with her cane and she had fallen landing on her abdomen. She denies any injury from the fall and states the fire department had to help and come pick her up. She states she thinks she might of fallen because of her left leg. The pain is a sharp pain located in her left thigh that radiates down to her left. She states she feels like her left foot is swollen She states she feels like her left foot is swollen like there is a balloon in her foot she states yesterday evening she went to get ready for bed and she felt like her left leg was "locking up" and she could not get into the bed and that her significant other had to help push her into the bed. The pain is persistent despite attempts of relief with 50 mg tramadol. There are no associated symptoms of chest pain, worsening shortness of breath, abdominal pain, numbness/tingling or weakness to lower extremities. She states she has been having issues with shortness of breath for a while and that is why her PCP placed her on oxygen several months ago. 2100-patient was seen walking out of the bathroom in the back hallway with a walker. She appeared in acute respiratory distress, tachypneic, with pursed lip breathing and was not wearing her required daily oxygen. I brought a wheelchair and had the patient sit in the wheelchair and hooked her up to the pulse oximeter, grabbed an oxygen tank and placed her on 4 L via nasal cannula, oxygen sats were 83% on room air. After about 10 minutes oxygen saturations maintained at 87% on 6 L and was increased to 10 L. Patient wheeled back to the bed and was placed in the room on a monitor. After about 2-3 minutes on 10 L her oxygen increased to 92%. RT arrived at bedside. Patient's husband states that she has been running low on her home oxygen tanks, and that she has an issue with the insurance. He states they will only allow her to have several small oxygen tanks. He states she was placed on the oxygen about 6 months ago due to persistent dyspnea with exertion but feels as if the oxygen is not helping. She is to wear 2L of oxygen continuously. Review of Systems Constitutional: Negative for chills, diaphoresis, fatigue and fever. HENT: Negative for facial swelling. Eyes: Negative for redness. Respiratory: Negative for cough and shortness of breath. Cardiovascular: Negative for chest pain and leg swelling. Gastrointestinal: Negative for abdominal pain, constipation, diarrhea, nausea and vomiting. Genitourinary: Negative for dysuria and flank pain. Musculoskeletal: Negative for back pain and arthralgias. Left leg pain Skin: Negative for pallor and rash. Neurological: Negative for speech difficulty. Hematological: Negative for adenopathy. Psychiatric/Behavioral: Negative for confusion. The patient is not nervous/anxious. 1/23/22 Discharge Diagnoses/Reason for Hospitalization: Principal Problem: Acute respiratory failure with hypoxia Active Problems: Obesity hypoventilation syndrome COPD (chronic obstructive pulmonary disease) Hypertension Abnormal LFTs Left leg pain COVID-19 PNA, Hospital Course: 61 yo F admitted with acute respiratory failure due to COVID-19 pneumonia. Despite aggressive treatment, we reached the point of being unable to successfully oxygenate and ventilate patient, with SpO2 persistently in low 80s despite high vent settings, inhaled nitric oxide, sedatives, paralytics. She began developing multiorgan system failure due to hypoxia. Patient's long time significant other stated that patient would not want prolonged mechanical ventilation if there was no hope for recovery. Unfortunately, they were not married and she has no children. Attempted to obtain emergency guardianship for S.O. with no success, so ICU care was continued. Patient ultimately suffered cardiac arrest, ACLS was performed with no return of spontaneous circulation on 1/22/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 15,0
Labordaten: 1/11/22 COVID-19 Result Detected Abnormal XR Chest 1 Vw 1/7/22 IMPRESSION: Cardiomegaly and pulmonary vascular congestion
Aktuelle Erkrankungen: -
Vorgeschichte: COPD (chronic obstructive pulmonary disease) o DVT (deep venous thrombosis) 2011 o Emphysema of lung o Hyperglycemia 2014 o Hyperlipidemia LDL goal <100 5/22/2017 o Hypertension o Hypothyroidism o Influenza A o Morbid obesity with BMI of 70 and over, adult o Obesity hypoventilation syndrome 12/20/2013 o Pneumonia o Snoring o Vulvar lesion
Andere Medikamente: acetaminophen 325 MG tablet Take 2 tablets by mouth every 6 (six) hours as needed for Pain for up to 15 doses. methocarbamol 500 MG tablet Take 1 tablet by mouth 3 (three) times daily for 15 doses. albuterol (2.5 MG/3ML) 0.083% nebuli
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2155088

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: CA
Alter: 64,0
Geschlecht: M
Eingang: 03.03.2022
Impfdatum: 18.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / UN

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

Cerebrovascular accident Laboratory test Thrombosis

Symptomtext

I had a stroke ON 10/21/21. I had no risk factors for stroke up until this point. They are calling this an unprovoked /paradoxical clot. This means that they do not know what caused the clot And given that there were no recent risk factors other than the vaccine booster I got A few days before, they could not prove or rule out that was the risk factor

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: TOO MANY TEST RESULTS TO LIST HERE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2150943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 69,0
Geschlecht: M
Eingang: 01.03.2022
Impfdatum: 22.03.2021
Beginn: 01.07.2021
Tage bis Beginn: 101,0
Dosis: 2
Route/Site: - / -

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

Acute respiratory failure Atrial fibrillation COVID-19 Cardiac arrest Chronic obstructive pulmonary disease Condition aggravated Death Emphysema Endotracheal intubation General physical health deterioration Hypoxia Post-acute COVID-19 syndrome Pulmonary fibrosis Resuscitation SARS-CoV-2 test positive

Symptomtext

pt had recent hosp admission with positive COVID test, was improved and dc'd to home; back to hosp again with severe hypoxemia; COVID test negative this time; O2 sats 71% on RA; placed on 15L High-flow O2; AHRF, post acute sequelae of COVID infection; pulmonary fibrosis; emphysema COPD, paroxysmal A Fib; required intubation due to failing condition; suffered cardiac arrest and despite resuscitation efforts the pt died in the hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, COPD, DMT2, CAD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2085481

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MN
Alter: 84,0
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: 03.11.2021
Beginn: 02.02.2022
Tage bis Beginn: 91,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure

Symptomtext

Patient had 3 doses of Pfizer COVID vaccine on 11/3/21, 3/10/21, and 2/17/21, and was hospitalized on 2/2/22 for acute hypoxic respiratory failure and is still hospitalized today, 2/3/22

Weitere VAERSDATA-Felder

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

VAERS 2085362

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: KY
Alter: 49,0
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: 13.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 15,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Acute respiratory failure Alanine aminotransferase normal Albumin globulin ratio Angiogram Anion gap Aspartate aminotransferase normal Atypical pneumonia Basophil count Basophil percentage decreased Blood albumin decreased Blood alkaline phosphatase normal Blood bilirubin normal Blood calcium decreased Blood chloride normal Blood creatinine normal Blood glucose normal Blood lactic acid

Symptomtext

49 yr/o female with a history of HTN, obesity, Graves' disease, asthma, T2DM, HLD, heroin abuse, hep C, MRSA, IVDU, COPD pancreatitis who presents to the emergency department complaining of abdominal pain with associated symptoms of nausea and vomiting. She was very flat affect and not very forthcoming with information at this time. She endorses a history of pancreatitis. She endorses a history of IVDU, and states she last used heroin this morning. Patient stated " I just feel crappy". Limited HPI due to patients unwillingness to provide detail information. She reported to the triage nurse that she recently tested positive for Covid 19. Pt denies headache, chest pain, shortness of breath. Review of Systems Constitutional: Negative for chills, diaphoresis, fatigue and fever. HENT: Negative for facial swelling. Eyes: Negative for redness. Respiratory: Positive for shortness of breath. Negative for cough. Cardiovascular: Positive for chest pain. Negative for leg swelling. Gastrointestinal: Positive for abdominal pain, nausea and vomiting. Negative for constipation and diarrhea. Genitourinary: Negative for dysuria and flank pain. Musculoskeletal: Negative for back pain and arthralgias. Skin: Negative for pallor and rash. Neurological: Negative for speech difficulty. Hematological: Negative for adenopathy. Psychiatric/Behavioral: Negative for confusion. The patient is not nervous/anxious. History of Present Illness: 49 year old F with history of tobacco/substance abuse, HTN, grave's disease with severe exopthalmos, NIDDM, hep C, chronic pancreatitis. She presented to Er with complaints of abdominal pain, n/v, with recent coid + test. ER evaluation revealed wbc 10.58, BNP 7.91, troponin <0.01, BP 210/86. - CTA chest: No obvious source for the acute abdominal discomfort. The preliminary report by the VRad radiologist described "significant gastritis." However, these findings are felt to be artifactual due to suboptimal distention of the stomach, and are grossly stable when compared to multiple prior exams over the past 3 years. 2. Groundglass nodular infiltrates involving the right middle and lower lobes, indicating an atypical pneumonia. - CXR; Rounded airspace opacity in the right lower lung likely representing pneumonia or residual pneumonitis as seen on prior chest CT dated 12/12/2021 Onset: several days Location: abd pain Duration: constant Characteristics: sharp Radiation: none Alleviating factors: none Aggravating factors: none Severity: moderate Associated symptoms: n/v, headache, chest pain, soa Patient admitted for further evaluation and treatment. 1/31/22Discharge Diagnoses: Covid 19 pneumonia, acute resp failure with hypoxia Abdominal pain with intractable nausea and vomiting Hypertensive urgency IVDU Diabetes melliuts Grave's disease

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: COVID-19 Result Not Detected Detected Abnormal 1/28/22 CBC w/Diff Collection Time: 01/28/22 12:28 AM Result Value Ref Range White Blood Count 10.58 4.5 - 11.0 10*3/uL Red Blood Count 4.32 4.0 - 5.2 10*6/uL Hemoglobin 11.9 (L) 12.0 - 16.0 g/dL Hematocrit 36.9 36.0 - 46.0 % Mean Corpuscular Volume 85.4 80.0 - 100.0 fL Mean Corpuscular Hemoglobin 27.5 26.0 - 34.0 pg Mean Corpuscular HGB Conc 32.2 31.0 - 37.0 g/dL Red Cell Distribution Width-CV 12.6 12.0 - 16.8 % Platelet Count 230 140 - 440 10*3/uL Mean Platelet Volume 12.3 8.4 - 12.4 fL Diff Type Hospital CBC w/AutoDiff (arb'U) Neutrophils % 73.3 45 - 80 % Lymphocyte % 14.6 (L) 15 - 50 % Monocyte % 5.9 0 - 15 % Eosinophil% 5.0 0 - 7 % BASO% 0.3 0 - 2 % Immature Granulocyte% 0.9 0.0 - 1.0 % Nucleated RBC % 0 0 /100(WBC) Neutrophil Abs 7.76 2.0 - 8.8 10*3/uL Lymphocyte-Absolute 1.54 0.7 - 5.5 10*3/uL Monocyte Absolute 0.62 0.0 - 1.7 10*3/uL EOS-Absolute 0.53 0.0 - 0.8 10*3/uL Basophil Abs 0.03 0.0 - 0.2 10*3/uL Immature Granulocyte Abs 0.10 0.00 - 0.10 10*3/uL Comprehensive Metabolic Panel(CMP) Collection Time: 01/28/22 12:28 AM Result Value Ref Range Sodium 135 (L) 136 - 145 mmol/L Potassium 3.5 3.5 - 5.1 mmol/L Chloride 104 98 - 107 mmol/L Carbon Dioxide 22 22 - 29 mmol/L Anion Gap 9 5 - 13 (arb'U) Glucose 200 (H) 74 - 99 mg/dL Blood Urea Nitrogen (BUN) 11 7 - 19 mg/dL Creatinine-Blood 1.01 0.55 - 1.02 mg/dL BUN/Creatinine Ratio 10.9 RATIO Estimated GFR 58 (L) >60 /1.73 m2 Estimated GFR if >60 >60 /1.73 m2 Total Protein 7.5 6.4 - 8.2 g/dL Albumin 3.1 (L) 3.5 - 5.2 g/dL Globulin 4.4 1.5 - 4.5 g/dL Albumin/Globulin Ratio 0.7 (L) 1.1 - 2.5 RATIO Calcium 8.6 8.4 - 10.2 mg/dL Total Bilirubin 0.5 0.2 - 1.2 mg/dL AST/SGOT 14 5 - 34 U/L ALT/SGPT 8 0 - 55 U/L Alkaline Phosphatase 118 40 - 150 U/L Lipase Collection Time: 01/28/22 12:28 AM Result Value Ref Range Lipase 4 4 - 39 U/L Troponin Collection Time: 01/28/22 2:03 AM Result Value Ref Range Troponin <0.010 0.000 - 0.034 ng/mL B-Type Natriuretic Peptide Collection Time: 01/28/22 2:03 AM Result Value Ref Range B-Type Natriuretic Peptide 79.1 1 - 87 pg/mL Glucose-Glucometer Collection Time: 01/28/22 6:16 AM Result Value Ref Range Glucose Glucometer 196 (H) 74 - 99 mg/dL Troponin Collection Time: 01/28/22 10:56 AM Result Value Ref Range Troponin 0.012 0.000 - 0.034 ng/mL B-Type Natriuretic Peptide Collection Time: 01/28/22 10:56 AM Result Value Ref Range B-Type Natriuretic Peptide 196.1 (H) 1 - 87 pg/mL Lactic Acid Collection Time: 01/28/22 10:56 AM Result Value Ref Range Lactic Acid 2.3 (H) 0.7 - 2.0 mmol/L
Aktuelle Erkrankungen: -
Vorgeschichte: Anxiety Arthritis o Asthma o Colon polyp COPD (chronic obstructive pulmonary disease) Depression DM (diabetes mellitus) INSULIN SINCE 2009 Fibroids Gout Grave's disease Hepatitis C NO SYMPTOMS Hepatitis C without mention of hepatic coma Hyperlipidemia Hypertension IBS (irritable bowel syndrome) Knee pain MRSA (methicillin resistant Staphylococcus aureus) Neuropathy Obesity Pancreatitis Pancreatitis, chronic PTSD (post-traumatic stress disorder) Seasonal allergies Seizures LAST SZ 2003 Sleep apnea Snoring STD (sexually transmitted disease) Tobacco abuse Torn rotator cuff Vitamin D deficiency
Andere Medikamente: albuterol HFA 108 (90 Base) MCG/ACT inhalerCommonly known as: buterol HFA 108 (90 Base) MCG/ACT inhaler Inhale 2 puffs into the lungs every 4 (four) to 6 (six) hours as needed for Wheezing or Shortness of Air (And or cough). ALPRAZolam
Allergien: Ibuprofen, Darvocet, Strawberry extract,
Vorherige Impfungen: -

VAERS 2079374

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MI
Alter: 81,0
Geschlecht: M
Eingang: 01.02.2022
Impfdatum: 02.04.2021
Beginn: 05.01.2022
Tage bis Beginn: 278,0
Dosis: 2
Route/Site: - / -

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

Acute myocardial infarction Anticoagulant therapy Blood creatinine increased COVID-19 COVID-19 pneumonia Cardiac failure congestive Chest X-ray abnormal Dyspnoea Fibrin D dimer Hypoxia Respiratory distress SARS-CoV-2 test positive Troponin increased

Symptomtext

Patient is fully vaccinated. DX: SoB, hypoxia, respiratory distress, pneumonia due to COVID.Pt tested positive for COVID on home test on 1/4. EMS reported that he was hypoxic at 79% on initial arrival. Placed on non-rebreather with improvement. ER workup showed NSTEMI with troponins elevated at 0.22. Pt started on Heparin gtt. Pt started on empiric antibiotics. CXR showed mild CHF. D dimer 1226.Cr 2.72. Patient seen by cardio and ID. Placed on remdesivir and decadron. Oxygen weaned down and discharged.

Weitere VAERSDATA-Felder

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

VAERS 2079128

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: WI
Alter: 86,0
Geschlecht: M
Eingang: 01.02.2022
Impfdatum: 23.11.2021
Beginn: 30.01.2022
Tage bis Beginn: 68,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Death

Symptomtext

Death related to COVID-19 infection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: OSC: Hypertensive heart disease; CKD stage 3; HLD; dementia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2075933

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: IL
Alter: 74,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 11.03.2021
Beginn: 03.10.2021
Tage bis Beginn: 206,0
Dosis: 2
Route/Site: IM / -

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

Acute kidney injury Acute respiratory failure Asthenia Balance disorder Blood creatinine increased Blood culture Blood pressure increased Blood sodium decreased Blood test COVID-19 COVID-19 pneumonia Chronic kidney disease Condition aggravated Culture urine positive Escherichia infection Eye contusion Fall Fibrin D dimer increased

Symptomtext

COVID Vaccine Breakthrough Case Pfizer Dose 1 2/17/21 (EN6200) Pfizer Dose 2 3/11/21 (EN6208) COVID Positive 10/4/21 10/4/21: Patient is a direct admit from ER. A past medical history is significant with diabetes, CKD , CAD with stents, and deficiency anemia sleep apnea, hypertension. She presented to the ER with complaints of losing balance, generalized weakness and frequent falls at home. She is from home with her husband who called EMS services. Upon arrival to the ER she was noted with a black left eye and has been reporting she fell out of the bed. Blood work was completed at ER was significant with sodium 129, creatinine 2.3, D-dimer 1.21. She also has a positive urine and a positive COVID 19 test positive. Due to her elevated creatinine a CTA was not done. The patient was noted hypoxia requiring 2 L nasal cannula. Upon arrival to medical unit the patient was noted with SpO2 86% on 12 L oxygen. Respiratory eval and treat was ordered. She was then transferred to ICU for close monitoring. Pulmonology consultation initiated. For transferring to ICU I addressed patient's goals of care and she was to continue with full treatment. She refused to to be intubated if needed. I discussed the plan of care with the patient and she is agreeable to stay in hospital for further management 10/9/21: Patient is a 74-year-old female who was admitted on 10/4/2021 with acute hypoxic respiratory failure, secondary to bilateral COVID pneumonia, elevated LFTs, secondary to COVID, AKI on CKD, and E coli UTI. She was noted to be very weak and has been suffering frequent falls. This is thought to be complicated by excessive amounts of lorazepam at home (3mg @hs). She was admitted to the ICU. Critical care intensivist was consulted. She was started on IV Levaquin, IV corticosteroids, and supplemental oxygen. Blood cultures and sputum culture were ordered. Lorazepam was discontinued. Her urine culture showed positive for E coli, resistant to Levaquin. Levaquin was discontinued and Rocephin and Azithromycin were started. The patient has slowly improved. She is currently only requiring 4 L of supplemental oxygen by nasal cannula. Physical therapy evaluated her and recommended SNF placement. Her vitals have been stable otherwise. Blood pressures were mildly elevated, so the patient's amlodipine was increased to 10 mg p.o. daily. Labs have been unremarkable. Patient is being discharged to swing bed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: see above
Aktuelle Erkrankungen: h/o aspiration HTN chronic gastritis chronic gout CAD diabetic nephropathy diabetic neuropathy diverticulitis gastroparesis GAD intraductal papillary mucinous neoplasm HLD monoclonal gammopathy of unknown significance obesity OSA DM type 2
Vorgeschichte: h/o aspiration HTN chronic gastritis chronic gout CAD diabetic nephropathy diabetic neuropathy diverticulitis gastroparesis GAD intraductal papillary mucinous neoplasm HLD monoclonal gammopathy of unknown significance obesity OSA DM type 2
Andere Medikamente: acetaminophen 650 mg PO Q4h PRN allopurinol 450 mg PO QD amlodipine 10 mg PO QD vitamin C 500 mg PO QD atenolol 25 mg PO BID atorvastatin 10 mg PO HS probiotic 1 cap PO QD clopidogrel 75 mg PO QD duloxetine DR 60 mg PO QD furosemide 40 mg P
Allergien: GoLYTELY - vomiting
Vorherige Impfungen: -

VAERS 2058551

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge : EN6208

kritisch

Staat: MN
Alter: 71,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 14.03.2021
Beginn: 13.01.2022
Tage bis Beginn: 305,0
Dosis: 2
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure Ammonia decreased Asthma Bladder catheterisation Blood creatinine increased Blood sodium increased Brain natriuretic peptide normal C-reactive protein increased COVID-19 pneumonia Cerebral haematoma Cerebral mass effect Cerebral small vessel ischaemic disease Cerebral ventricular rupture Cerebrovascular accident Chest X-ray abnormal Cheyne-Stokes respiration Computerised tomogram head abnormal

Symptomtext

HOSPITAL COURSE: 72-year-old female (refused an interpreter) with history of hepatitis C cirrhosis, pancytopenia, hypertension, CKD stage IV, insulin-dependent type 2 diabetes, GERD, history of CVA resulting in a seizure disorder admitted for acute hypoxemic respiratory failure due to COVID-19 pneumonia. Tenuous respiratory status - on continuous BiPAP with multi-organ failure. Acute hypoxemic respiratory failure due to COVID-19 pneumonia/ possible superimposed bacterial infection Neutropenia, resolved Afebrile/sats 70s on RA initially/placed on 15L NRB. Rapidly escalating oxygen requirements, now has been on continuous BiPAP since 1/17. As of the last 2 days (1/18 and 1/19), encephalopathic and less interactive with increased accessory muscle usage. Neutropenia has resolved, remains on cefepime and doxycycline. High risk of pulmonary edema given need to correct free water deficit but this is likely contributing to her encephalopathy. D-dimer is elevated, but in the setting of thrombocytopenia, holding heparin. pulmonlogy signed off 1/19 Pt requiring 100%FI02 this am. Got 40mg IV lasix x1 by XC MD. Able to wean back to 70%FI02. 1/21: Pt stable on Bipap, 50%FI02, satting 100%. CRP trending down to 2.5. Procalc 0.35-improved from prior Lungs sound clear. However pt is unresponsive to pain and pupils are sluggish/minimally reactive if at all. Unclear etiology of her worsening neurological state. Reviewed MAR, no sedating meds on board in last 24hours to explain unresponsive state. Pts ammonia yesterday was <10, however LFTs have worsened suggesting possibility of worsening hepatic encephalopathy. Did not have any prolonged periods of hypoxia to suggest acute hypoxic brain injury. A stat CT head to r/o ICH was ordered but not obtained until 8pm on 1/21. Per XC MD note from 1/21: "Received page from radiology regarding CT head results. CT: Large intraparenchymal hemorrhage centered in the right thalamus/posterior basal ganglia, measuring approximately 5 x 5 x 4 cm cm. Rupture into the ventricles with hydrocephalus. Significant mass effect from the large intraparenchymal hematoma, with deviation of the third ventricle to the left of midline by about 11 mm, and extensive effacement of sulci in the cerebral hemispheres, and partial effacement of the sylvian fissure on the right. This is most likely a hypertensive hemorrhage. Extensive, marked changes of presumed chronic small vessel ischemia in cerebral white matter. I called and spoke with Dr. of neurology to discuss the case. He felt that her chance of recovery was negligible, especially considering she is on BiPAP for CAP and COVID pneumonia and has liver failure. Should the family desire to pursue aggressive measures, the patient would likely need to be intubated given the severity of the hemorrhage and she would need platelets to maintain Plt >50 (currently 34). I then spoke with Dr. of neurosurgery. He received the images as well and feels this is a massive hemorrhage. There are no surgical recommendations and this stroke is likely unsurvivable. I called the patients daughter to update her on the changes. I explained that regardless of further interventions, her stroke is likely unsurvivable and if she were to survive, her deficits would be catastrophic. Given her other medical issues and prior discussions of limited further aggressive care, I recommended we focus on her comfort. I explained that could mean taking her off the BiPAP, stopping any unnecessary medications, and stopping her artifical nutrition. During this, we would provide her with medications to keep her comfortable, such as morphine for air hunger. I also explained that if we removed her BiPAP, I suspect she would likely pass within hours but that healthy family can come to her bedside. She did have questions regarding her will which was not completed before she became unresponsive and I directed her to obtain legal counsel to discuss financial issues as this is not my area of practice. She requested to reach out to her siblings before any changes were made. Update 2245: Spoke with patients son. He indicated he was the patients hcPOA. I explained the current situation and he is understandably upset. At this time, he wants to continue her current plan of care. I explained in depth that this is not likely a survivable event and that she could pass tonight regardless of ongoing BiPAP use. I also explained that in situations like this, BiPAP and tube feeds can prolong the dying process and suffering. He is trying to reach back out to his sisters to discuss further. He had hoped they could all be present when his mother passes, though daughter is COVID+ so I explained she would not be able to be here, though his mother could have 4 healthy visitors at her bedside. He will call again after speaking with family further. Update 0200: Met with the family at bedside (6 people as well as daughter via video conference) multiple times after their arrival. Extensive discussion with everyone about her diagnosis and poor prognosis. Questions answered. After further discussion, family decided to proceed with comfort care orders given her current interventions will not improve her outcome and they continue to decline intubation which would likely be necessary for her survival. Comfort care orders placed. Recommended RN give morphine for comfort before removing BiPAP. OK to remove feeding tube as well for comfort but leave foley and IV in. I discontinued all unnecessary medications at end of life including antibiotics. I did choose to leave her Keppra as the risk of seizure is high and could cause discomfort for both the patient and her family. I advised that I remain available to further discuss with them if needed. Update 0600: re-evaluated patient. Most of family still present at bedside. She is having cheyne-stokes breathing and I educate the family that death is likely imminent. She has been requiring a significant amount of ativan and narcotics to remain comfortable, though there is concern her PIV may have been leaking. Now that we are using PO liquid she is much more comfortable." The pt passed peacefully at 0633 on 1/22 with family at bedside. GOC Multiple conversations with family with different Hospitalist providers this week. Decision-makes are daughter, son and his wife. They continue to understand severity of patients illness and declining trajectory with multiorgan system failure. Today (01/19), explained to daughter that patient remains incredibly sick and she is unlikely to survive if needing intubation, recommended DNI which she was understanding. She agreed that intubation would not be within patients goals of care. Discussed continuous BiPAP use and that this can be very uncomfortable. Currently, she is tolerating this however with non-violent restraints, ativan and 1:1 at bedside. Daughter is still hopeful to continue BiPAP, but also understands that this is not sustainable. Other concern is nutrition as patient has not been fed. Previous discussions have been to initiate NG tube, but this is not currently possible given continuous BiPAP. 1/20 Discussed with admin, who agreed to make exception to allow son to come to bedside to aid family decisions re nutrition, comfort care, etc. After numerous conversations and meetings facilitated by medicine and palliative, Family agreed that they want to attempt tube feeds per NG, continue bipap for now to give pt opporunity to improve clinically, however if further deteriorates would want to withdraw cares with family visitation at bedside. AKI on CDK Hypernatremia Hypokalemia Baseline Cr around 2.0, which has been up-trending. Additionally, further worsening hypernatremia despite D5. Very tenuous respiratory status given HF and cirrhosis, but as encephalopathy will only worsen with deranged Na, will need to increase D5 rate. 1/20 creat at 2.57, NA 151. Got 40mg lasix overnight per XC MD for increasing hypoxia. Hx of acute decompensate heart failure Hx of CHF. Last TTE 1/20/21 with normal EF. Repeat echo on 1/17/22 appears wnl. Does not appear volume overloaded at present but does have worsening 02 requirement, increasing infiltrates on CXR. BNP on 1/17 WNL. Sounds dry on my exam on 1/20, however did get lasix 40meq by XC MD overnight. -careful monitoring of fluid status Acute metabolic encephalopathy Has been worsening since 1/14. Likely d/t hypernatremia, however other considerations include hepatic encephalopathy. Pt injured left posterior wrist when attempting to get out of restraint causing a hematoma to form. Started 1:1 on 1/14 overnight. 1/21 unresponsive as above. Hep C Cirrhosis Had been stable on torsemide po and spinolactone. LFTs baseline on admission. -hold torsemide and spironolactone at this time due to worsening renal function Hx of CVA: Thrombocytopenia Chronically her plts run 60-100. PLTs have been variable, currently 37. PTA plavix and heparin were held given worsening thrombocytopenia IDDMII: Fasting glucose 103 on 1/19 when received lantus 18 units evening of 1/18. Increased to 372 on 1/21, pharmD adjusting regimen and adding NPH. Seizure disorder: resuming keppra IV while NPO Asthma: albuterol PRN GERD: famotidine held as NPO, on PPI IV for PPX HTN: Hold PTA amlodipine and toprol XL, continue IV metoprolol PRN and monitor for b-blocker withdrawal

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 10,0
Labordaten: COVID PCR POSITIVE 1/13/2022
Aktuelle Erkrankungen: -
Vorgeschichte: 72-year-old Cambodian female (refused an interpreter) with history of hepatitis C cirrhosis, pancytopenia, hypertension, CKD stage IV, insulin-dependent type 2 diabetes, GERD, history of CVA resulting in a seizure disorder Past Medical History: Diagnosis Date ? ADHF (acute decompensated heart failure) (HCC) 11/15/2016 ? Anxiety 06/22/2011 ? Cirrhosis (HCC) ? Clostridium difficile colitis 07/2008 hospitalized ? CVA (cerebral infarction) (HCC) ? Depressive disorder, not elsewhere classified ? Diabetes type 2, glucose range 89-108 ? Edema of both legs ? Encephalopathy acute 8/24/2012, 1/2/2013 ? ESBL (extended spectrum beta-lactamase) producing bacteria infection 09/17/2012 CLEARED by protocol 1/24/21 ? hepatitis c ? Hyperlipidemia LDL goal <70 06/26/2017 ? Hypertension 02/05/2010 ? Malaria ? Pancytopenia s/p bone marrow biopsy 7/1/08 ? PFO (patent foramen ovale) ? Positive PPD, treated Treated with 12 months of INH after having a positive ppd when she immigrated ? Renal failure ? Schwannoma of spinal cord (HCC) L1 level. ? Seizure disorder - dx @ hospital 10/2012 11/01/2012 ? Seizure disorder - dx @ hospital 10/2012 ? Severe malnutrition (HCC) ? TIA (transient ischemic attack)
Andere Medikamente: -
Allergien: Mirtazapine
Vorherige Impfungen: -

VAERS 2055442

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: WA
Alter: 72,0
Geschlecht: M
Eingang: 21.01.2022
Impfdatum: 24.03.2021
Beginn: 14.01.2022
Tage bis Beginn: 296,0
Dosis: 2
Route/Site: IM / RA

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

Acute kidney injury Acute respiratory failure COVID-19 Endotracheal intubation Intensive care Metabolic encephalopathy Pneumonia SARS-CoV-2 test positive Seizure Sepsis

Symptomtext

Patient received Pfizer COVID vaccine on 3/3/21 and 3/24/21. On 1/14/22, patient admitted to our CCU with acute respiratory failure with hypoxia (intubated) and sepsis due to bilateral pneumonia, acute kidney injury, acute metabolic encephalopathy, and COVID-19 positive status. As of today (1/21/22), patient is still intubated in CCU.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 7,0
Labordaten: COVID status positive 1/14/22.
Aktuelle Erkrankungen: -
Vorgeschichte: MMP including history of right pontine CVA stroke in 2020 with residual left-sided weakness with slurred speech along with occipital and right frontal encephalomalacia, coronary artery disease status post CABG in 2008 with ischemic cardiomyopathy, chronic kidney disease stage III, hypertension, dyslipidemia, complete heart block status post pacemaker placement, BPH, sleep apnea both central and obstructive (does use CPAP) and seizure d/o diagnosed in 6/2021 maintained on 3 antiepileptics.
Andere Medikamente: acetaminophen PRN, allopurinol, amlodipine, atorvastatin, carvedilol, vitamin d3, clopidogrel, divalproex, ferrous sulfate, icosapent ethyl, lacosamide, levetiracetam, losartan, potassium chloride
Allergien: indomethacin
Vorherige Impfungen: -

VAERS 2047464

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: TN
Alter: 67,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 30.03.2021
Beginn: 18.01.2022
Tage bis Beginn: 294,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Death Vaccine breakthrough infection

Symptomtext

COVID RELATED DEATH/ BREAKTHROUGH CASE

Weitere VAERSDATA-Felder

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

VAERS 2046294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: NY
Alter: 57,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 17.02.2021
Beginn: 14.07.2021
Tage bis Beginn: 147,0
Dosis: 2
Route/Site: - / -

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

Arterial stent insertion Myocardial infarction

Symptomtext

Not sure if this is related. I had a Heart Attack July 14, 2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: Stent placed in artery.
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: Levothyroxine Bupropion Hydrochoride XL Ubrelvy Myrbetiq Vitamin D Vitamin B12 Multivitamin
Allergien: Pencillian Codeine Amoxicillian Banana
Vorherige Impfungen: -

VAERS 2551134

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 89,0
Geschlecht: M
Eingang: 06.01.2022
Impfdatum: 18.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / -

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

Anaemia Anaemia splenic Cardioversion Condition aggravated Death Dysphagia Renal impairment Splenic haemorrhage Transfusion Urinary retention Ventricular tachycardia

Symptomtext

Narrative: Patient was not previously Covid psitive and did not have any predisposing factors(PMH, allergies, etc.) for experiencing and adverse drug event. The ADR did not occur at the time of the administration of the vaccine nor was there and ADR that occurred between the observation period and the date of death. Patient presented to ED on 3/16/21 adter his ICD activated due to an episode of vtach. His hospital stay progressed to an inability to void urine, worsening renal function, dysphagia, and anemia and anemia from a splenic bleed requiring blood transfusions requiring a transition to palliative care before he deceased on 3/26/21. Patient had a PMH significant for HFrEF w/ICD, CAD s/p CABGx5, HTN, Afib, and vtach.

Weitere VAERSDATA-Felder

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

VAERS 2006015

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MI
Alter: -
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 25.03.2021
Beginn: 03.11.2021
Tage bis Beginn: 223,0
Dosis: 2
Route/Site: - / -

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

Acute kidney injury Acute myocardial infarction Anticoagulant therapy Arterial therapeutic procedure Asthenia COVID-19 Dehydration Diarrhoea Dyspnoea Fibrin D dimer increased Nausea Platelet count decreased Renal haematoma SARS-CoV-2 test positive Thrombocytopenia Vomiting

Symptomtext

COVID+ on 11/3/2021. Indication for admission was SOB. 83-year-old gentleman with significant past medical history known for abdominal aortic aneurysm/COPD not on O2/hypertension, who presented initially to his primary care physician yesterday for generalized weakness and was asked to present to the ER. Admission dx: dehydration, nausea/vomiting, loose stools, acute kidney injury and COVID-19 virus infection. D-dimer 3303--2280-- 3211. NSTEMI. Thrombocytopenia Platelet 89--111--125--improving. Hx of Right renal hematoma Early 6/2021, s/p coiling 6/1/21. Completed 3 days of decadron and remdesivir. Lovenox and eliquis. Pt discharged

Weitere VAERSDATA-Felder

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

VAERS 2541681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 93,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 11.03.2021
Beginn: 03.05.2021
Tage bis Beginn: 53,0
Dosis: 2
Route/Site: IM / RA

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

Death

Symptomtext

Narrative: Patient was not previously COVID-19 positive and did not have any predisposing factors(PMH, allergies, etc.) for experiencing an adverse drug event. The ADR did not occur at the time of the administration of the vaccine nor was there an ADR that occurred between the observation period and the date of death. PMh significant for CKD, Glaucoma, bradycardia, vitamin d deficiency, hyperlipidemia, basal cell carcinoma of skin, peripheral vascular disease. Diabetes Mellitus. Carotid Artery stenosis, HTN, advanced age. Per note, patient deceased on 5/3/2021. No cause of death noted.

Weitere VAERSDATA-Felder

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

VAERS 2536334

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 81,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 15.03.2021
Beginn: 02.05.2021
Tage bis Beginn: 48,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Bedridden Death Hyponatraemia Loss of personal independence in daily activities Malaise Nausea Small intestinal obstruction Vomiting

Symptomtext

Narrative: Patient was not previously COVID-19 positive and did not have any predisposing factors(PMH, allergies, etc.) for experiencing an adverse drug event. The ADR did not occur at the time of the administration of the vaccine nor was there an ADR that occurred between the observation period and the date of death. PMH significant for antineoplastic chemotherapy hx, htn, tobacco use, neoplasm of left upper lobe of lung, hypertriglyceridemia, htn, hypercholesterolemia, malignant neoplasm of intrathoracic lymph nodes. Per note 4/20/2021 "is a 79 y/o MALE is here for follow-up. He is not doing well. He was recently admitted to the hospital with small bowel obstruction and hyponatremia. No etiology was disocevered for his SBO. Hyponatremia improved with urea powder. Patient was discharfged to rehab on 4/15/21. He reports continuing to feel weak and also admits nausea and vomiting. Overall, he is bed-bound most of the day and requires assistance with all ADLs. He states he wishes to go home." patient deceased 5/2/2021 while under care of hospice.

Weitere VAERSDATA-Felder

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

VAERS 2536326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 61,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 10.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

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

Death

Symptomtext

Narrative: Patient received two doses of covid vaccine. Found deceased in home nearing one month after second vaccination. PMH included GAD/depression, ETOH/cannabis abuse, COPD, tobacco dependence, LE PVD, AAA (3.5 cm), colonic polyp, and hyperlipidemia. No further evaluation of death documented.

Weitere VAERSDATA-Felder

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

VAERS 2536222

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 63,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 12.03.2021
Beginn: 06.04.2021
Tage bis Beginn: 25,0
Dosis: 2
Route/Site: IM / LA

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

Death

Symptomtext

Narrative: Patient was not previously COVID-19 positive and did not have any predisposing factors(PMH, allergies, etc.) for experiencing an adverse drug event. The ADR did not occur at the time of the administration of the vaccine nor was there an ADR that occurred between the observation period and the date of death. Patient was hospitalized on 3/8/21 at hospital for a severe COPD exacerbation. In February 2021 he was diagnosed with lung cancer that could not be treated surgically. On 3/29/21 he was admitted to hospital with his second MI in 5 months. He later passed away there on 4/6/21. Other comorbidities include COPD requiring oxygen, MI, HTN, HLD, smoking, polysubstance abuse, homelessness.

Weitere VAERSDATA-Felder

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

VAERS 2532977

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 64,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 19.04.2021
Beginn: 23.04.2021
Tage bis Beginn: 4,0
Dosis: UNK
Route/Site: IM / LA

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

Acute respiratory failure Death Dyspnoea Dyspnoea exertional Dyspnoea paroxysmal nocturnal Haemoglobin decreased Oedema peripheral Orthopnoea Respiratory failure

Symptomtext

Narrative: 62 yo male with PMH of COPD, not on home oxygen, HFpEF, chronic IDA, HTN, hep C, hx of prostate CA s/p radical prostatectomy, was found dead in his home on 04/23/2021. Prior to his death, patient left AMA on 4/19/2021. Pt was admitted on 4/18/2021 for shortness of breath/acute on chronic hypoxic respiratory failure. Per discharge summary on 4/19/21, patient had increasing SOB for past 2 weeks, unable to walk 10 feet without become SOB. He was found to have orthopnea, PND, and bilateral pedal edema. Records also showed that patinet left AMA on 3/30/21 at the ED. It was recommended that he went to ED due to low hemoglobin of 7.2 (trending downward).

Weitere VAERSDATA-Felder

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

VAERS 2529727

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 79,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 15.03.2021
Beginn: 14.04.2021
Tage bis Beginn: 30,0
Dosis: 2
Route/Site: IM / LA

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

Death

Symptomtext

Narrative: Patient was not previously COVID-19 positive and did not have any predisposing factors(PMH, allergies, etc.) for experiencing an adverse drug event. The ADR did not occur at the time of the administration of the vaccine nor was there an ADR that occurred between the observation period and the date of death. PMH significant for AF, HF, t2dm, sleep apnea, obesity, htn, hospitalized 3/2/2021 for chf, worsening kidney function and end stage liver disease. discharged to hospice care. Deceased 4/14/2021

Weitere VAERSDATA-Felder

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

VAERS 2540349

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 12.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

Narrative: Patient received one dose of covid vaccine. PMH included ETOH abuse, CVA, afib on xarelto, CAD s/p MI, hyperlipidemia, chronic LE lymphedema, gout, Vit D deficiency, and colonic polyps (patient refuses colonoscopy). No documentation relating to cause of death. Reporting per instruction.

Weitere VAERSDATA-Felder

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

VAERS 1999538

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MI
Alter: 79,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 27.03.2021
Beginn: 31.12.2021
Tage bis Beginn: 279,0
Dosis: 2
Route/Site: - / -

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

Death Dyspnoea General physical health deterioration

Symptomtext

atient with past medical history significant for liver cancer, hypertension, hyperlipidemia, type 2 diabetes, CKD stage III who presents to ED complaining of dyspnea. Patient reports that she has been experiencing worsening shortness of breath over the past few days. placed on 15 L of high flow nasal cannula. She was evaluated by infectious disease and treated with remdesivir, baricitinib and steroids. Per patient wishes she was made DNR comfort. Patient steadily declined and expired on 12/31

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: past medical history significant for liver cancer, hypertension, hyperlipidemia, type 2 diabetes, CKD stage III
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2500242

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 79,0
Geschlecht: M
Eingang: 02.01.2022
Impfdatum: 17.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

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

Death

Symptomtext

Narrative: Patient received two doses of covid vaccine. Patient was in LTC/hospice for end stage dementia. No further evaluation of death noted. Reporting per facility instructions.

Weitere VAERSDATA-Felder

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

VAERS 2498949

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 84,0
Geschlecht: M
Eingang: 02.01.2022
Impfdatum: 15.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

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

Death

Symptomtext

Narrative: Patient received two doses of covid vaccine. Unclear if patient had any changed medical history or if this outcome was related at all to vaccination. No details reported of death. Reporting per facility instruction.

Weitere VAERSDATA-Felder

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

VAERS 1958832

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: FL
Alter: 81,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 17.03.2021
Beginn: 29.11.2021
Tage bis Beginn: 257,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure COVID-19

Symptomtext

Hospitalized for acute hypoxemic respiratory failure, COVID19 11/29/21-12/10/21. Treated with dexamethasone IV and Remdesivir. Discharged to hospice.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 12,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1958665

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN 6208

kritisch

Staat: ME
Alter: 67,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 13.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: SYR / LA

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

Acute myocardial infarction Asthenia Blood test C-reactive protein abnormal Carditis Cerebral thrombosis Cerebrovascular accident Computerised tomogram Cough Dyspnoea Electrocardiogram Embolism Histamine abnormal Impaired work ability Inflammation Magnetic resonance imaging Malaise Nasal polyps

Symptomtext

Within 4 days after Pfizer #1 (March 13, 2021) sneezing and dry coughing fits lasting for up to several hours at a time ensued - flaring up sporadically for many months following the shot, having to leave work and events due to extreme nature of symptoms. Had a phone appointment with doctor on 3/17 to discuss issues. After shot #2 (April 3, 2021) inflamed sinuses caused complete blockage of nasal cavity and couldn't breathe through the nose (on April 22, 2021). Nasal polyps eventually formed and surgery is now recommended. General malaise and lack of energy continued throughout the year. Inflammation and exasperated histamines made the year miserable. Hospitalized with nstemi heart attack, blood clots and stroke on 11/29/2021. Off the charts inflammation (CRP test) , EKGs, CtScan, and MRIs (11/29/2021-12/3/2021) showed massive inflammation of heart and multiple blood clots in the brain - "a shower of emboli".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 5,0
Labordaten: MRI, ctscan ekg , crp, blood tests 11/29-12/3 Then 10days of rehabilitation.
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure
Andere Medikamente: olmesartan medoxomil 40-25 mg
Allergien: None known
Vorherige Impfungen: -

VAERS 1939760

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MI
Alter: 88,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 25.03.2021
Beginn: 30.10.2021
Tage bis Beginn: 219,0
Dosis: 2
Route/Site: UN / UN

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

Acute respiratory failure Asthenia Atrial fibrillation COVID-19 Cough Death Essential hypertension Gastrointestinal haemorrhage Hypotension Influenza A virus test negative Influenza B virus test Normocytic anaemia Positive airway pressure therapy Respiratory syncytial virus test negative SARS-CoV-2 test positive Type 2 diabetes mellitus Upper respiratory tract infection

Symptomtext

88-year-old female with a history of hypertension, diabetes presents with generalized weakness. Patient has had cough, progressive weakness for the past 9 days. Patient presented to the primary care office 6 days ago and was diagnosed with a upper respiratory infection and given a Z-Pak. Patient has been taking this for the past 5 days with no improvement. Overnight patient has significant worsening of her weakness. Patient not initially complaining of any shortness of breath. On EMS arrival patient found to be 39% on room air. Patient is placed on 15 L nonrebreather O2 improved to 77%. Patient has no other complaints. Patient is vaccinated with Pfizer vaccine ?2. o New-onset atrial fibrillation; CHADS2Vasc =5. ? Repeat limited 2D echo unchanged from 11/19/21 echo o DCCV 12/1 due to afib RVR with hypotension o Essential hypertension; BP labile, currently requiring vasopressors o DMII o Acute hypoxic respiratory failure secondary to COVID on CPAP o NC anemia 2/2 suspected GIB patient expired 12/7/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: Covid-19, Flu, RSV by NAA Order: 1265949960 Status: Final result Visible to patient: No (inaccessible in myBeaumontChart) Next appt: None Specimen Information: Nasopharyngeal; Swab 0 Result Notes 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)
Aktuelle Erkrankungen: Diabetes mellitus (CMS/HCC) ? Hyperlipidemia ? Hypertension
Vorgeschichte: Diabetes mellitus (CMS/HCC) ? Hyperlipidemia ? Hypertension
Andere Medikamente: amLODIPine (NORVASC) 10 MG PO Tab take 10 mg by mouth once daily. Med Note (Wed Nov 17, 2021 3:32 PM) Filled 08/23/21 x 90 days via pharmacy azithromycin (Zithromax Z-Pak) 250 MG PO Tab Take 2 tablets by mouth on day 1 then 1 daily
Allergien: none
Vorherige Impfungen: -

VAERS 2568425

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 02.12.2021
Impfdatum: 02.04.2021
Beginn: 14.08.2021
Tage bis Beginn: 134,0
Dosis: 2
Route/Site: IM / LA

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

Death Lung neoplasm malignant Lymphoedema

Symptomtext

Narrative: Hospice patient death with progressive lung cancer, severe lymphedema and other complications over 4 months since 2nd vaccine dose. Pfizer

Weitere VAERSDATA-Felder

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

VAERS 1916357

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: TN
Alter: 83,0
Geschlecht: M
Eingang: 02.12.2021
Impfdatum: 24.03.2021
Beginn: 01.12.2021
Tage bis Beginn: 252,0
Dosis: 2
Route/Site: SYR / -

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

COVID-19 Death Vaccine breakthrough infection

Symptomtext

COVID-19 RELATED DEATH; BREAKTHROUGH CASE

Weitere VAERSDATA-Felder

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

VAERS 1912668

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MI
Alter: 74,0
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: 04.03.2021
Beginn: 20.11.2021
Tage bis Beginn: 261,0
Dosis: 2
Route/Site: - / -

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

Agonal respiration COVID-19 COVID-19 pneumonia Cough Death Fatigue Hypoxia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Pt received Pfizer vaccines on 03/04/2021 and 03/25/2021. Pt presented to the ED with complaints of cough, congestion, and generalized fatigue. Pt was found to be COVID positive and diagnosed with COVID-19 pneumonitis. Pt was hypoxic requiring 5L of oxygen. Pt began experiencing agonal breathing and was a DNR/DNI status. Pt died on 11/24/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: SARS-COV-2 by NAA, POC positive for SARS
Aktuelle Erkrankungen: -
Vorgeschichte: Parotid cancer with chemotherapy, Friedreich's ataxia, HLD, paraplegia
Andere Medikamente: -
Allergien: none
Vorherige Impfungen: -

VAERS 1890024

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MN
Alter: 74,0
Geschlecht: M
Eingang: 22.11.2021
Impfdatum: 12.03.2021
Beginn: 20.11.2021
Tage bis Beginn: 253,0
Dosis: 2
Route/Site: - / -

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

Cardiac arrest Death

Symptomtext

Dose 1 Pfizer given 2/19/2021 lot # EN6203 Patient had a cardiac arrest at home and died in the emergency room.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Metastatic melanoma, CAD, afib, hyperlipidemia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1876660

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: KY
Alter: 87,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 17.03.2021
Beginn: 21.09.2021
Tage bis Beginn: 188,0
Dosis: 2
Route/Site: IM / -

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

Craniocerebral injury Death

Symptomtext

Pt deceased r/t closed head injury

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Cardiovascular and Mediastinum Hypertension Hypertension, benign essential, goal below 140/90 Other Hyperlipidemia Glaucoma Hyperglycemia
Andere Medikamente: latanoprost (XALATAN) 0.005 % ophthalmic solution simvastatin (ZOCOR) 10 MG tablet triamcinolone (KENALOG) 0.1 % cream Vitamin D, Cholecalciferol, 400 units CAPS
Allergien: NKA
Vorherige Impfungen: -

VAERS 1857973

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: CA
Alter: 79,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 13.03.2021
Beginn: 25.10.2021
Tage bis Beginn: 226,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure Alanine aminotransferase normal Anion gap Aspartate aminotransferase normal Basophil percentage Blood bilirubin normal Blood chloride normal Blood creatinine normal Blood culture positive Blood glucose increased Blood glucose normal Blood lactic acid Blood potassium normal Blood sodium normal Blood urea normal COVID-19 COVID-19 pneumonia Carbon dioxide increased

Symptomtext

80 yof with HTN, HLD, DM2, CKD3, Alzheimer dementia, CAD ( PCI in 2002), s/p fall in 4/2021 resulting in subdural hematoma and T8 vertebral fx requiring hospitalization 4/20-5/2/2021, who was transferred from her SNF residence with shortness of breath and hypoxia and was found to have COVID-19 PNA. CORONAVIRUS COVID-19 PNEUMONIA (10/25/2021) ACUTE HYPOXEMIC RESPIRATORY FAILURE (10/25/2021) Mildly elevated Troponin. Assessment: Pt has completed 2 doses of COVID vaccine. Initially required 2lit of supplemental O2 to keep sat>90. She was started on Remdesivir and 3 doses of decadron and with improving oxygenation medications were discontinued. She has been able to transition to room air At rest and work with PT with no supplemental O2 needs. Mildly elevated D dimer is likely secondary to COVID infection. And she had Mildly elevated troponin (0.07-0.1-0.06) likely due to demand ischemia from COVID pneumonia. Incentive spirometry encouraged. IMPROVE VTE SCORE D-dimer > 2x Upper Limit of Normal - 2 POINTS Immobilization for at least 7 days - 1 POINTS Age more than 60 years. - 1 POINTS She was not on chemical DVT prophylaxis while in house given hx of prior SDH hx and noted down trending WBC and PLT counts. As the counts seems steady to improved, I discussed the case with neurology on call, given no symptoms and absence of blood in last CT head in 4/202, it would be ok to treat with chemical DVT prophylaxis. I will also request for a repeat CBC in a week. HTN / CAD s/p stents She was initially started on half dose of her BP meds and as BP started to increase, PTA dose of BP meds were resumed, however metoprolol was kept at half dose with noted resting HR of 50's-60's on current dose. - continue PTA lasix 10 mg daily DM 2. Hba1c 7.6 4/2021. Fasting glucose was 200s. Pt was on NPH 40 mg qam and 10 mg qpm at SNF+ glipizide per PTA meds. Glipizide was on hold in the hospital and While on decadron pm dose of NPH was increased in house, however with discontinuation of decadron and 50-60% of meal intake, I am holding off glipizide upon discharge. Thrombocytopenia sec to COVID pneumonia: platelet 130's also is leukopenic ?COVID related. Levels better today. Will arrange for follow up CBC in a week. 1/2 positive blood cx with GPC in clusters from admission with no fever and overall improvement and coag negative staph growth suspect contaminant. Primary Procedures: None Secondary Procedures: None Reason for Hospital Admission (Admitting Diagnosis): Hypoxic respiratory failure, COVID-19 disease

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: Results for patient as of 11/10/2021 11:20 10/26/2021 06:20 NA: 144 K: 3.7 CL: 107 CO2: 34 (H) BUN: 19 CREAT: 0.71 ANION GAP4 SERPL: 3 (L) GLUC: 90 ALT: 10 AST: 15 ALKP: 55 TBILI: 0.4 COMMENT, GLOMERULAR FILTRATION RATE: SEE NOTE WBC: 3.2 (L) RBC'S: 3.69 HGB: 10.4 (L) HCT: 33.5 (L) MCV: 91 RDW, RBC: 14.1 PLT: 122 (L) IMMAT GRANULO % AUTO: 0 NRBC: 0 NEUTROPHILS % AUTO: 60 ANC: 1.9 LYMPHS % AUTO: 29 MONOS % AUTO: 10 EOS % AUTO: 1 BASO'S % AUTO: 0 Results for patient as of 11/10/2021 11:20 10/25/2021 02:40 LACTATE: 0.4 (L) 10/25/2021 03:03 XR CHEST: Rpt (A) 10/25/2021 08:54 GLUC BLD GLUCOMETER: 214 (H) 10/25/2021 09:33 HGBA1C %: 6.8 (H) ESTIMATED AVERAGE GLUCOSE: 148 (H) TROPONIN I: 0.10 (H)
Aktuelle Erkrankungen: -
Vorgeschichte: pmhx of HTN, HLD, DM2 (Hba1c 7.6 4/2021), CKD3 (baseline Cr 0.8), Alzheimer dementia, CAD/perioperative MI 6/2002 s/p MV-PCI, a recent hospitalization for subdural hematoma/nondisplaced T8 vertebral body fracture after a mechanical fall 4/20-5/2/2021
Andere Medikamente: Outpatient Home Medications Taking? Acetaminophen (TYLENOL) 325 mg Oral Tab Takes Occasionally Sig: Give 2 tablets every 8 hours orally round the clock for 7 days and then as needed . Do not exceed 10 tablets in 24 hours Aspirin (ECOTRIN LO
Allergien: Allergies Allergen Reactions ? Codeine Patient Reports, Reaction Unknown 2000-02-07 ? Morphine Hallucinations 2004-01-29 per pt ? Sulfa (Sulfonamide Antibiotics) 2000-02-07;rash
Vorherige Impfungen: -

VAERS 2596725

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 09.03.2021
Beginn: 02.09.2021
Tage bis Beginn: 177,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Chronic respiratory failure Vaccine breakthrough infection

Symptomtext

Narrative: Breakthrough covid-19 infection: Admitted with acute chronic hypoxic respiratory failure COVID-19 pneumonia

Weitere VAERSDATA-Felder

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

VAERS 1833690

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: NY
Alter: 62,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 31.03.2021
Beginn: 16.04.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: IM / RA

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

Aphasia Cerebrovascular accident Computerised tomogram head abnormal MELAS syndrome Magnetic resonance imaging head abnormal Neurological symptom

Symptomtext

MELAS stroke-like episode with Broca aphasia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 7,0
Labordaten: Brain CT right anterior temporal stroke Brain MRI right anterior temporal stroke
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes and deafness due to the m.3243A>G mitochondrial DNA mutation
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1827494

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: PA
Alter: 69,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 13.03.2021
Beginn: 19.04.2021
Tage bis Beginn: 37,0
Dosis: 2
Route/Site: - / LA

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

Blood test Blood test abnormal Chest pain Colon cancer Dyspnoea Echocardiogram Muscle strain Myalgia Myocardial infarction

Symptomtext

had high levels of Topamine in her blood; was having chest pain; shortness of breath; colon cancer; heart attack; it wasn't her heart it was muscular strain; muscle pain; This is a spontaneous report from a contactable consumer (patient). A 70-year-old female patient received the second dose of bnt162b2 on 13Mar2021 at 13:00 (at the age of 69-years-old) (lot number: EN6208) via unknown route of administration in left arm at single dose for COVID-19 immunization. Medical history was not reported. Concomitant medications were reported as none. Historical vaccine included the first dose of BNT162B2 on 20Feb2021 (at the age of 69-years-old) (lot number: EN6201) in her left arm for covid 19 immunization. Patient did not have additional Vaccines Administered on Same Date of the Pfizer Suspect. Patient did not have any other vaccination within 4 weeks. Family Medical History Relevant to AE was reported as None. She started having chest pain and shortness of breath on 30Sep2021 and was admitted to the hospital on 04Oct2021. While at the hospital they found high levels of topamine in her blood which may have indicated a slight heart attack. She was calling today to see if it was safe for her to get the booster. Her son was an antivaxxer and told her not to get it because it may have caused that increased level. She did not think that though because the shots were 6 months before this happened. Patient stated that nothing was wrong with her heart now, but she did have colon cancer. She was calling about the Pfizer Covid vaccine and has a question about the booster and got the 1st and 2nd doses and then last Monday she was telling her doctor she was having chest pain and shortness of breath and so he told her to go to the emergency room and she went to the emergency room. Stated they did blood work and she had high levels of Topamine in her blood and said that could be a signal a slight heart attack and they admitted her to the hospital and did the echo and it was ok stated she told her son about the enzyme Topamine and he said the shot caused high levels of Topamine and she also saw that information on the website also. Her son was anti-vaxxer but she was looking up this herself and now she wanted to ask about the booster because of this and she saw her heart doctor but did not think to ask him about this and she wanted to ask if it is safe to get the booster. The reported events occurred after the 2nd dose but it was a good while from the dosage and did not happen right after the dosage; stated the photo of her patient card did not have the expiry date or NDC numbers written on it. The chest pain began she would say on 30Sep2021 but it wasn't her heart it was muscular strain and her heart WAs fine; stated the shortness of breath began the same day on 30Sep2021 and the shortness of breath was ongoing and about the same; stated the muscle pain was gone and resolved she would say on 11Oct2021. She had colon cancer and did not know it at the time but was diagnosed with that on 19Apr2021. Lab data included: blood test in 2021: she had high levels of Topamine in her blood; echo in 2021: normal. The events shortness of breath, chest pain, muscle pain, high levels of Topamine, heart attack, muscular strain were required to visit Emergency Room and Physician Office, but was admitted to the hospital from 04Oct2021 to 06Oct2021 because of the high level of Topamine. The outcome of the events heart attack was recovered in 2021. The outcome of the event shortness of breath was not recovered. The outcome of the event was having chest pain; muscle pain was recovered on 11Oct2021. The outcome of other events was unknown.

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Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 2,0
Labordaten: Test Date: 2021; Test Name: blood test; Result Unstructured Data: Test Result:she had high levels of Topamine in her blood; Comments: she had high levels of Topamine in her blood; Test Date: 2021; Test Name: echo; Result Unstructured Data: Test Result:normal
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1808100

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MA
Alter: 79,0
Geschlecht: M
Eingang: 22.10.2021
Impfdatum: 16.03.2021
Beginn: 07.09.2021
Tage bis Beginn: 175,0
Dosis: 2
Route/Site: UN / UN

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

Acidosis Acute respiratory distress syndrome Blood culture negative Blood lactic acid increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cholelithiasis Condition aggravated Cough Death Dyspnoea Endotracheal intubation Enteral nutrition Extubation Fatigue Hyperglycaemia Hypoxia

Symptomtext

Brief Summary/Assessment: 80M with a history of NSVT, type 2 diabetes mellitus, gout, BPH, HLD, HTN, GERD, admitted for COVID-19 pneumonia, s/p intubation on 9/11/21 now s/p remdes, dex, and Baricitinib; paralysis stopped 9/21, reparalyzed 9/22 with new consolidations c/f aspiration PNA. Hospital Course Hospital Course: Updated as of 9/24 ============== HPI ============== Patient is a 80 y.o. male with a history of NSVT, type 2 diabetes mellitus, gout, BPH, HLD, HTN, GERD, who presented as a transfer from with hypoxia in the setting of COVID-19 infection. The patient states that he had attended a party/"feast," where he believes is the event at which he contracted COVID-19. On 8/27, he called his ambulatory practice, where he noted rhinorrhea, rhinitis, post-nasal drip, and cough. He has a history of rhinosinusitus (followed by Dr.), treated with nasal lavage and ipratropium spray TID, though he only uses it once a day or less. He had received 2 doses of Pfizer vaccination earlier this year. Given his history, vaccination status, and otherwise non-concerning symptoms, he was advised to restart the nasal lavage and ipratropium sprays. He was seen on 8/31 and noted to have a cough over the last few months and a tickle in his throat. A CXR was ordered, which showed no evidence of PNA or pulmonary edema. On 9/2, he presented to urgent care for worsening symptoms and was started on doxycycline 100mg BID for 7 days and given medication for cough. A COVID test was obtained. The patient tested positive for COVID and was found to be hypoxic to 70% on RA. EMS placed him on 10L NC with improvement to 80%. He was transferred to ICU on HFNC. CT surgery Course Course was notable for increased O2 requirement, FiO2 increased to 80% on HFNC (60-70L), with SpO2 >85%. Desaturation to the 70%s when coughing. He was tachypneic over the past 3-4 days, with RR in the 50s. He occasionally felt that he was tiring out. FiO2 was weaned from 80% to 70%, with goal O2 of 85-88%. He was continued on remdesivir (planned 5-day course), dexamethasone 6mg daily (planned 10-day course), baricitinib 4mg daily (planned 14-day course). ========== MICU COURSE (09/11 - 9/24 ) ========== (By problem) # COVID-19 c/b PNA+severe ARDS, with possible superinfection/sepsis When PT was admitted to the medical facility, he was on HFNC of 60L/min and FiO2 80%. He was working hard to breathe, with more frequent desaturations and longer recovery times despite being maxed on HFNC. He was started on and completed a 5-day course of cefepime and doxycycline for possible bacterial superinfection. After a lengthy discussion with the patient (and daughter + son on the phone), he was intubated. He was paralyzed, proned, and began Veletri with improvement in his oxygenation. He was diuresed generally with net goal even. He was unparalyzed after 2 days and stopped proning given only mild improvement in oxygenation upon proning. He developed a pressor requirement originally thought to be due to sedation; however, early sepsis also on the differential due to ongoing pressor needs. Despite trying to avoid paralysis, he developed worsening oxygenation with vent dyssynchrony, and so he was re-paralyzed and re-proned on 9/17. Oxygenation and pressor requirements continued to worsen despite AC/VC settings of 420/30/12/90%, with PaO2 in the 50s. The patient was started on cefepime (switched to ceftazidime), vancomycin, and fluconazole (switched to micafungin). Blood cultures were negative. RUQUS showed a contracted gallbladder with stones. He was able to wean down on the RR, FiO2, and pressor requirements, so he was un-paralyzed on 9/21. Restarted paralysis 9/23 after oxygen requirements increased, patient's MAP started to drop to the 50s, and fever spiked on 9/22 c/f septic shock. Patient was broadened to meropenem on 9/22. CXR 9/23 showed worsening lower lobe haziness and consolidation c/f aspiration pneumonia with residual volumes in stomach of up to 1.8 L (likely cause of pneumonia). Patient's condition continued to decline with renal failure likely in setting of septic shock with decreased/minimal urine output. Patient was started on CVVH on 9/23 and continued to worsen on 9/24 with increased acidosis (likely metabolic) in setting of sepsis. He was given a dose of vancomycin on 9/24. Lactate continued to increase rapidly at a peak of 7.1 on 9/24. At that time, the medical team contacted the family to provide further insight into the poor clinical trajectory at which time, the HCP made the decision to change the patient's code status to DNR/OK to intubate and later to comfort measures as nothing more medically could be done. The patient was extubated and passed peacefully with family surrounding him. # Nutrition # Hyperglycemia He was started on tube feeds with insulin to manage hyperglycemia (in the setting of a 10-day course of dexamethasone). Tube feeds were then stopped on 9/22 evening as team was concerned that patient was aspirating. Patient was started on D5 on 9/24 to provide some nutrition. # Goals of Care Several conversations took place with the patient (prior to intubation) and family (once oxygenation status worsened despite near-maximized ventilation/oxygenation with re-paralysis, re-proning). The family ultimately decided to change the person's code status to DNR/OK to intubate and ultimately to comfort care.

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Praegender Schweregrund: Death
Hospital-Tage: 14,0
Labordaten: Covid positive 9/23/21, 9/21/21, 9/20/21, 9/17/21 9/16/21, 9/14/21, 9/14/21, 9/13/21, 9/10/21
Aktuelle Erkrankungen: unk
Vorgeschichte: Allergic rhinitis ? Anxiety 6/14/1993 On chronic lorazepam. ? Atherosclerosis of native coronary artery of native heart with angina pectoris ? Benign prostatic hyperplasia 6/6/2016 has persistent nocturia, some frequency, and a history of elevated PSA levels in the 4-6 range. has seen Dr in past. last visit with him was 2/7/2013 with PSA at that time of 5.24 and PVR of 54cc. He was going to f/u with him after a trip but this never happened. No discussion of elevated PSA's in EMR with Dr but PSA was checked in 2/4/14 4.91, up from 3.86 in 5/8/13. does not take flomax as previously prescribed. does still take saw palmetto. No new change in sypmtoms. was given Bactrim in 2013 for prostatities, developed hyponatremia and then switch to quinolone (per Dr. notes) but I don't see any follow up in EMR. 12/15: saw Dr in July was contemplating epididymal cyst resection but no longer bothering him. didn't feel prostate bx was necessary. ? Chronic coronary artery disease 6/6/2016 CABG x 4 in 1986 after he "took a heart attack", 2008 coronary angiogram-: LIMA open LAD. LAD small and diffusely diseased. V open to D1 and OM1. Native CX-branch disease only. RCA 90%-90% amenable to possible stent in future if needed. PLV 90%. LAD cause of new ischemia and not amenable to intervention. 16 beat run of SVT. Atenolol 25 mg switched to nadolol 40 mg. 2/21/08 Holter monitor NSR 44-73 averaging 53. Rare VPB. No couplets and no NSVT. 11/09 increasing angina-dull substernal chest pressure/squeezing. 11/19/09 exercise sestamibi-anterior-TNG-bradycardia and hypotension-EW. 11/20/09 catheterization. 75% mid RCA, 95% RCA and PDA. Two DES Xience Stents. Remained bradycardic and therefore beta blocker stopped. F/by Dr. Last stress test 2013 with excellent exercise capacity 10 minutes, ECG negative for ischemia. Perfusion images with incomplete scarring in the inferior, inferolateral wall and distal anterolateral apex. Mild distal anterolateral and mild distal inferolateral ischemia. Compare ? Dry eyes ? Dry skin dermatitis ? Dyslexia Graduated junior year high school ? Elevated prostate specific antigen (PSA) 6/6/2016 see notes under BPH. noted elevated PSA in past. former PCP with PSA 4.9 > 1 yr ago. repeat yesterday 4.6. no prior bx. prostate u/s by Dr in 12/2012 showed enlarged heterogeneous prostate. we discussed lab findings on phone and I recommend that he see Dr. in follow up for ?prostate biopsy. he will call his office, and i've placed CRMS referral. he saw Dr. in July 2015 -- no prostate bx planned. considered epid cyst resection but sx's resolved. Lab Results Component Value Date PSA 4.60* 06/18/2015 PSA 4.91* 02/04/2014 PSA 3.86 05/08/2013 ? Gastroesophageal reflux disease ? Gout ? H/O coronary artery bypass surgery 06/13/2016 CABG x 4 followed by 2 stents ? Herpes simplex 6/6/2016 ? Hip pain 6/6/2016 Seen by an orthopedist-had an MRI of left hip, most recently seen by anesthesiologist who recommended steroid injection. pt would like to discuss if this is the best choice for pain control, he is faxing us the results of MRI and sched to discuss this virtually with dr., on the 16th.: 3/16/16: he's presently at the race track. Had an MRI of his L hip. went to PT -- was told by ortho to get a steroid injection in L hip. PT recommending a 2nd opinion. at this point not hurting too much. some soreness but manageable. told him ok to get 2nd opinion for a firmer dx. 4+ wks of PT hasn't helped. ok to consider steroid injection. ? History of coronary artery bypass surgery ? Hyperlipidemia 6/6/2016 On Zetia and statin Lab Results Component Value Date CHOL 173 11/30/2015 HDL 63 11/30/2015 LDL 84 11/30/2015 TRIG 132 11/30/2015 CHOLHDL 2.7 11/30/2015 ? Hypertension 6/6/2016 BP Readings from Last 3 Encounters: 12/01/15 128/60 11/23/15 133/84 09/23/15 134/68 ? Lightheadedness ? Lip swelling ? Motion sickness ? Old myocardial infarction ? Onychocryptosis ? Overweight (BMI 25.0-29.9) ? Pain in joint, ankle and foot ? PCO (posterior capsule opacification), right ? Plantar fasciitis ? Prediabetes ? Rotator cuff syndrome of left shoulder ? Shoulder pain 6/6/2016 Right shoulder, Status post steroid injection 2015 December ? Sinusitis ? Sleep disorder 6/6/2016 prior h/o of mild to mod OSA (no record of the study in our EMR) but he'd refused CPAP at the time. He's gained weight over the years, partly due to inc'd regular wine intake (1 bottle/day). sleeps well w/o much snoring but reports often nappingin mid/late morning after waking and having light breakfast. I suggested, esp in light of his cardiac disease, that he should consider repeat sleep study for re-assessment, but he'd prefer to hold off on scheduling b/c he's up in another state for the summer. encouraged him to get this scheduled at his earliest convenience and he knows he can call the office to have it scheduled. ? Status post insertion of drug eluting coronary artery stent 6/13/2016 ? Tubular adenoma 6/6/2016 history of TA in 8/14/2000 and TA and HP on colonoscopy from March 2007 (GI Dr). needs updated colonoscopy. Had repeat in 2011 with no polyps and was recommended to have repeat again in 5-7 years -- DUE 2016 (earliest). ? Type 2 diabetes mellitus without complication, without long-term current use of insulin ? Viral upper respiratory tract infection with cough and Past Surgical History: Procedure Laterality Date ? CATARACT EXTRACTION s/p YAG OS ? CORONARY ARTERY BYPASS GRAFT S/P CORONARY ARTERY BYPASS GRAFT x 4 ? KNEE ARTHROPLASTY ? KNEE ARTHROSCOPY Left spur ? LAPAROSCOPIC CHOLECYSTECTOMY N/A 7/12/2021 Procedure: LAPAROSCOPIC CHOLECYSTECTOMY; Surgeon: MD; Location: OR; Service: General Surgery ? UNCODED SURGICAL HISTORY S/P Decompression of median nerve
Andere Medikamente: EPINEPHrine 0.3 mg/0.3 mL auto-injector Sig: INJECT 0.3 ML (0.3 MG TOTAL) INTO THE SHOULDER, THIGH, OR BUTTOCKS ONCE FOR 1 DOSE. SAW PALMETTO ORAL Sig: Take by mouth. UBIDECARENONE (COENZYME Q10) 100 mg Tab Note (11/23/2015): Needs MD Verif
Allergien: Ace Inhibitors Cough ? Atorvastatin Myalgia ? Budesonide ? Sulfa (Sulfonamide Antibiotics) BACTRIM (TRIMETHOPRIM/SULFAMETHOXAZOLE) - PHS Allergy Remediation ? Penicillins Rash
Vorherige Impfungen: -

VAERS 1700097

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 21.10.2021
Impfdatum: 22.03.2021
Beginn: 06.09.2021
Tage bis Beginn: 168,0
Dosis: 2
Route/Site: - / -

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

Acute respiratory failure COVID-19 pneumonia Cardio-respiratory arrest Death Endotracheal intubation COVID-19 General physical health deterioration Resuscitation

Symptomtext

pt brought to hospital via EMS post cardiopulmonary arrest; CPR and intubation performed; acute respiratory failure with hypoxia, COVID pneumonia; pt's condition worsened; pt was made a DNR and expired in the hospital

Weitere VAERSDATA-Felder

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

VAERS 1700097

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 21.10.2021
Impfdatum: 22.03.2021
Beginn: 06.09.2021
Tage bis Beginn: 168,0
Dosis: 2
Route/Site: SYR / -

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

Acute respiratory failure COVID-19 pneumonia Cardio-respiratory arrest Death Endotracheal intubation COVID-19 General physical health deterioration Resuscitation

Symptomtext

pt brought to hospital via EMS post cardiopulmonary arrest; CPR and intubation performed; acute respiratory failure with hypoxia, COVID pneumonia; pt's condition worsened; pt was made a DNR and expired in the hospital

Weitere VAERSDATA-Felder

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

VAERS 1790842

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: IN
Alter: 52,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: 02.04.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Asthenia Computerised tomogram Cough Decreased appetite Depression Dyspnoea Migraine Pulmonary embolism Pulmonary thrombosis

Symptomtext

pulmonary embolism; two blood clots in her lungs; she was depressed about that,; migraine; cough; pretty weak; shortness of breath; has a low appetite; This is a spontaneous report from a contactable consumer (patient herself) via a Pfizer-sponsored program, Support. A 52-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/Lot Number: EN6208) via an unspecified route of administration on 02Apr2021 (at the age of 52 years old) as dose 2, single for COVID-19 immunisation. Medical history included blood clot and deep vein thrombosis (DVT) back in 2012 that broke off and it did go to her lungs. Patient had a pulmonary embolism and pneumonia with the last blood clot 9 years ago, and high blood pressure which puts the patient more at risk. The patient also experienced a COVID in Oct2020 wherein she had brain fog and loss of taste and sense of smell. Patient stated that she was curious as to how this happens again. The patient's concomitant medications were not reported. Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot: EN6198) on 10Mar2021 (at the age of 52 years old) as dose 1 for COVID-19 immunisation. On unspecified date in 2021, it was reported that the patient experienced two blood clots in her lungs and pulmonary embolism (hospitalization). The patient just got released from the hospital yesterday evening and they found that she has blood clots; she had gotten the blood clots in the lungs and experienced other side effects, shortness of breath, so she will have to take blood thinners to the rest of her life and she was depressed about that, so she wanted to know if that could be related to the COVID-19 vaccine. She stated that this was a second blood clot, and that she had a blood clot back in 2012, and even though it was a 9 years ago she was wondering if this time it could be related to the vaccine. Patient was totally shocked as this was her second one, she clarified her second blood clot. The patient thought maybe the first time was because she was on birth control pills and that may have accelerated it and the first time she had them, she had a warning, stated her leg like her calf was hurting but this time there was no leg pain, and it was automatically in her lungs; she had a cough and shortness of breath. Patient stated that she did not want to get Covid, stated that she already had Covid last October, stated that she did not want to get it again that it was terrible. Initially she thought she had Covid again last Oct2021 (as reported; pending clarification), and has had some long-hauler symptoms and this was prior to the vaccines. The patient also stated that she thought she got Covid again because of the shortness of breath and cough, and cannot imagine how she would have gotten Covid again, she had been wearing a mask everywhere since the other variants have picked up. The patient clarified that she went to the ER Sunday night, 26Sep2021, stated it was because she got scared, she had called the telehealth doc and they immediately said she had a blood clot. The patient had symptoms for a while, unknown exact date symptoms started, went to ER, and they did a CT scan, which showed blood clots on each side of lungs seen. The patient was admitted for one night, discharged yesterday 27Sep2021, and it was reported that the symptoms last week was a bad week and she started with a migraine on Wednesday last week, short of breath and then Thursday evening the cough came along with the shortness of breath. Patient thought maybe this really started before this, maybe in Jul or Aug2021, two different nurse practitioners mentioned her shortness of breath at that time. They thought it may be allergies or something, states they kept blowing her off. Patient stated she asked to see a specialist to check heart and lungs after recovering from Covid and see about those long-haul symptoms. The first time she had blood clots, she was in the hospital for 5-6 days, states this time she was only there for one night, she was treated with blood thinner, first started her with an IV drip bag, unknown name of medication, then gave her one dose of Eliquis and has to pick up prescription for Eliquis, has missed a dose of the Eliquis because it was not ready at the pharmacy. Stated it was serious, she has come close to death twice, should be ready to pick up around 6 PM and she really needs that medication. No further details provided. States her symptoms are not as bad as they were, and she still was pretty weak and has a low appetite, she was eating but just not very hungry. The outcome of the event pulmonary embolism and thrombosis pulmonary was recovering, while for the other events was unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 1,0
Labordaten: Test Date: 20210926; Test Name: CT scan; Result Unstructured Data: Test Result:showed blood clots on each side of lungs seen
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Birth control pill; Blood pressure high; Clot blood; COVID-19 (loss of taste and sense of smell); DVT; Foggy feeling in head (from Covid in Oct2020.); Pneumonia; Pulmonary embolism
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1785328

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: TN
Alter: 80,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 20.03.2021
Beginn: 06.10.2021
Tage bis Beginn: 200,0
Dosis: 2
Route/Site: IM / -

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

Anticoagulant therapy COVID-19 pneumonia Computerised tomogram thorax abnormal Electrocardiogram ST-T segment abnormal Pulmonary embolism Sepsis

Symptomtext

Hospitalized for7 days for severe sepsis secondary to COVID 19 pneumonia. Received IV Rocephin, azithromycin,oxygen, remdesivir, decadron, albuterol, encouraged to self prone. Acute ulmonary emboli on lovenox. Discharged on home health

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 7,0
Labordaten: RV strain on CT 10/6; pulmonary embolism
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Dementia, osteoporosis, depression
Andere Medikamente: Unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 1782406

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: IN
Alter: 52,0
Geschlecht: F
Eingang: 13.10.2021
Impfdatum: 10.03.2021
Beginn: 26.09.2021
Tage bis Beginn: 200,0
Dosis: 2
Route/Site: - / -

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

Chest pain Dyspnoea Pulmonary embolism

Symptomtext

began having shortness of breath and chest pain in September 2021. Went to ER and had both lungs with Pulmonary Emboli. Client had covid virus October 2020.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: Hospital has all records.
Aktuelle Erkrankungen: -
Vorgeschichte: high blood pressure. Had another blood clot in 2012 in her leg.
Andere Medikamente: multivitamins, vitamin B 3, fish oil, probiotics, vitamin c, Allegra, Flonase, Pepcid, Eliquis, lisinopril
Allergien: Erythromycin
Vorherige Impfungen: -

VAERS 1782381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: AR
Alter: 75,0
Geschlecht: F
Eingang: 13.10.2021
Impfdatum: 10.03.2021
Beginn: 01.10.2021
Tage bis Beginn: 205,0
Dosis: 1
Route/Site: IM / UN

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Chronic obstructive pulmonary disease Condition aggravated Cough Dyspnoea Escherichia infection Glycosylated haemoglobin decreased Hepatic enzyme increased Hyperglycaemia Hypertension Hypokalaemia Hypoxia Leukopenia Obesity Oedema Oedema peripheral

Symptomtext

75-year-old female presents to the emergency room with complaint of cough fever shortness of breath. It is difficult to tell exactly how long symptoms have been present. She states 2 weeks off and on but at other times states that most of her symptoms have really only been worse for the past for 5 days. No diarrhea. Patient lives alone. She has tested positive for COVID tonight. She has had the vaccination. She knows of no exposure. Review of Systems Constitutional: [Patient denies fever, chills, sweats, and weight changes.] Eyes: [Patient denies any visual symptoms] ENT: [No difficulties with hearing. No symptoms of rhinitis or sore throat.] Cardiovascular: [Patient denies any chest pain, palpitations, orthopnea, or PND.] Pulmonary: As in HPI Gastrointestinal: [No nausea, vomiting, diarrhea, constipation, abdominal pain, hematochezia, or melena.] GU: [No urinary hesitancy or dribbling. No nocturia or urinary frequency. No abnormal urethral discharge.] Musculoskeletal: [No myalgias or arthralgias. No hot, swollen joints.] Neurologic: [No headaches, no seizures. Patient denies numbness, tingling, or weakness on either side of the body. There are no visual symptoms.] Psychiatric: [Patient denies problems with mood disturbance or anxiety.] Endocrine: [No excessive urination or excessive thirst noted. No heat or cold intolerance. No weight gain or changes in skin or hair.] Dermatologic: [Patient denies any rashes or skin changes.] Physical Exam Vitals & Measurements HR: 89(Peripheral) HR: 90(Monitored) RR: 17 BP: 155/80 SpO2: 95% WT: 114.9 kg VITAL SIGN LAST CHARTED MINIMUM MAXIMUM Blood Pressure 155/80 (10/01 21:15) 120/62 (10/01 20:15) 156/80 (10/01 19:15) Heart Rate 89 (10/01 21:15) 86 (10/01 20:45) 101 (10/01 18:20) Respirations 17 (10/01 21:15) 16 (10/01 20:30) 21 (10/01 19:10) Temperature 99.0 (10/01 18:20) 99.0 (10/01 18:20) 99.0 (10/01 18:20) SpO2 95 (10/01 21:15) 86 (10/01 19:10) 97 (10/01 20:30) O2 Flow Rate 2 (10/01 19:56) 2 (10/01 19:56) 2 (10/01 19:56) Weight 114.9 (10/01 18:20) 114.9 (10/01 18:20) 114.9 (10/01 18:20) General: Alert and oriented, No acute distress. Eye: Extraocular movements are intact. HENT: Normocephalic, Atraumatic. Neck: No jugular venous distention. Respiratory: Crackles bilaterally Cardiovascular: Normal rate, Regular rhythm. Gastrointestinal: Soft, Non-tender, Non-distended, Normal bowel sounds. Obesity Musculoskeletal: 4+ pitting pedal edema bilaterallyAdmitted with Principal Diagnosis of COVID-19 pneumonia, Hypoxemia, Acute on Chronic hypoxemic respiratory failure. Plan: Vaccinated: Yes Symptom onset: 9/17/21 Diagnosis: 10/1/21 Dexa day: 4 - wil complete 10 days at dc Symptom duration likely too long to benefit from remdesivir. She is on home oxygen 2 liters/minute while sleeping only, but she does not have tanks at home, will arrange home oxygen continuously at least for a few weeks... Diagnosis: COPD. Plan: No active wheezing. On Advair. Quit smoking in 1991 Diagnosis: Obesity. Diagnosis: E. coli UTI. Plan: Empiric ceftriaxone appropriate based on culture sensitivities, complete 3rd day here before dc. Diagnosis: Hypokalemia. Course: Improving. Diagnosis: Leukopenia. Plan: Likely from virus, monitor. Diagnosis: Hypertension. Course: Well controlled. Diagnosis: Elevated liver enzymes. Plan: Likely from virus Diagnosis: Type 2 diabetes mellitus with hyperglycemia. Plan: She says she has been diabetic for 15 years but has never required medicine, always controlled with lifestyle. Current flare likely from corticosteroid effect. Checked A1c. 6.2, will be off Dex in a week so will not rx further insulin at dc.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: Positive for COVID-19 on 10/01/2021
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1778922

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MI
Alter: 63,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 16.04.2021
Beginn: 07.10.2021
Tage bis Beginn: 174,0
Dosis: 1
Route/Site: IM / UN

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

Acidosis Arterial catheterisation Auscultation Breath sounds abnormal COVID-19 Cardio-respiratory arrest Central venous catheterisation Computerised tomogram thorax abnormal Condition aggravated Death Dyspnoea Endotracheal intubation General physical health deterioration Hyperkalaemia Hypoxia Intensive care Intestinal ischaemia Lung infiltration

Symptomtext

9/24 PMHx of COPD, pneumonia, pulm HTN, Anxiety who presents for SOB w/ wheezing x 3 days. Diag. w/ Pneumonia upon assessment. 9/25 CT suspicious for small pulmonary emboli. Examination of the lungs reveals numerous groundglass airspace opacities throughout the upper lobes and lower lobes bilaterally. 9/28 Lungs reduced to auscultation bilaterally. Right lower lobe crackles. On CT There is interval worsening in aeration with development of bilateral infiltrates diffusely throughout both lungs. The pleural spaces remain clear. 10/4 patient currently requiring warmed high flow oxygen at 45L. Overnihgt desaturations into 10/5 10/6 pt desat to 62%, pt pale, tachypenic, tachycardic. Rapid response called to aid 10/6 Again RRT was called due to hypoxia Osat was in mid 80s%, pt was on high flow 10/6 She has been transferred to the ICU due to worsening respiratory status. Discussed plan for EGD tomorrow with patient and her daughter at the bedside. 10/6 Called to ICU patient showing signs of respiratory fatigue, requested to intubate patient. Patient oxygenated with ambu bag and mask with FiO2 100%. Intubation followed. 10/7 Central Line Placement - Right Internal Jugular 10/7 COIVD+ Result 10/7 Discussed with family poor prognosis, and clinical deterioration, will remain full code 10/8 CRITICAL CARE PROCEDURE NOTE - ARTERIAL CATHETER INSERTION 10/8 Septic shock with multiple organ failure, suspect ischemic bowel 10/8 Code blue called at 05:31 pm. On arrival to room, patient had achieved ROSC. Per nursing staff patient has been severely acidotic throughout the day with pH<7. Patient is on multiple pressors. Renal failure with hyperkalemia. There was suspicion for possible ischemic bowel however CT of abdomen could not be obtained as patient is too unstable. Patient had coded again while I was at rapid response. Per nurse staff ED doctor present for the code and pronounced patient

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Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: 14,0
Labordaten: SARS-COV-2 (COVID-19) by NAA, Micro (See Responses to 18)
Aktuelle Erkrankungen: N/A
Vorgeschichte: COPD, ARF, esophageal obstruction, major depressive disorder, coagulopathy, Drug-induced hypokalemia, pulmonary emboli
Andere Medikamente: acyclovir, amylase-lipase-protease, Biotin 2500, buPROPion, ca, Caffeine calCITriol copper gluconate Cyanocobalamin cyclobenzaprine ferrous sulfate furosemide HYDROcodone-acetaminophen latanoprost multivitamin olanzapine omeprazole
Allergien: N/A
Vorherige Impfungen: -

VAERS 1749730

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: WA
Alter: 53,0
Geschlecht: M
Eingang: 10.10.2021
Impfdatum: 02.09.2021
Beginn: 03.09.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Death Decreased appetite Dizziness Fall Dialysis Discomfort Feeling abnormal Head injury Headache Hypotension Immunisation Off label use Oedema peripheral SARS-CoV-2 test negative Syncope

Symptomtext

My husband got his first shot and ever since he gained edema on his leg, to the extent he had to receive his first emergent dialysis on May. Doctor also thought something was wrong about his condition. At the day of his booster shot on Sep 2, he felt dizzy, low-pressure, and fainted on stairs when he walked down in the morning at home. Dr. did not recommend any procedure to take. My Husband felt really bad and uncomfortable during Sep 5-6. He passed away in the morning on Sep 16. We also requested private autopsy for him. He was a infection disease medical Doctor.

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: three PCR tests were negative on May, July, Sep 2021
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetic, Hypertension
Andere Medikamente: insulin , D3, Calcium
Allergien: no fresh sea food
Vorherige Impfungen: -

VAERS 1772066

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: TN
Alter: 70,0
Geschlecht: M
Eingang: 08.10.2021
Impfdatum: 22.03.2021
Beginn: 14.09.2021
Tage bis Beginn: 176,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Case fully vaccinated with Pfizer. Second dose received on 3/22/2021. Tested positive for COVID on 9/14/2021. Admitted to Medical Center on 9/20/2021. Expired on 9/27/2021 while still hospitalized.

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

VAERS 1768588

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 07.10.2021
Impfdatum: 10.03.2021
Beginn: 01.10.2021
Tage bis Beginn: 205,0
Dosis: UNK
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Death

Symptomtext

death N17.9 - AKI (acute kidney injury) (CMS/HCC) J96.01 - Acute respiratory failure with hypoxia (CMS/HCC)

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

VAERS 1768157

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: WV
Alter: 54,0
Geschlecht: M
Eingang: 07.10.2021
Impfdatum: 01.04.2021
Beginn: 11.06.2021
Tage bis Beginn: 71,0
Dosis: 1
Route/Site: SYR / LA

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

Arterial occlusive disease Atrioventricular block complete Chest pain Coronary angioplasty Coronary arterial stent insertion Coronary artery occlusion Dyspnoea Electrocardiogram Hyperhidrosis Myocardial infarction Ultrasound scan

Symptomtext

On 06/11/2021 had heart attack complete blockage on RCA which resulted in chest pains, shortness of breath, profuse sweating. Was admitted to a local hospital and procedure through the right arm was used to clear blockage and place a stent at the site of blockage. This occurred even being completely healthy and with no history of heart disease of under laying condition, and very minimal blockages in other part of this artery and others, less than 20% blockage. Recovered and sent home day later with lifetime of medications.

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Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 1,0
Labordaten: EKG and ultrasounds performed on 06/11/2021 and 06/12/2021
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: Celiac
Vorherige Impfungen: -

VAERS 1759327

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: PA
Alter: 69,0
Geschlecht: F
Eingang: 04.10.2021
Impfdatum: 12.03.2021
Beginn: 06.09.2021
Tage bis Beginn: 178,0
Dosis: 1
Route/Site: IM / LA

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

Acquired diaphragmatic eventration Acute respiratory failure Adenovirus test Angiogram pulmonary Anticoagulant therapy Anticoagulation drug level above therapeutic Anxiety Arteriosclerosis coronary artery Asthenia Bladder disorder Bordetella test negative Breath sounds abnormal COVID-19 COVID-19 pneumonia Chlamydia test negative Computerised tomogram abdomen abnormal Computerised tomogram thorax abnormal Coronavirus test negative

Symptomtext

ED to Hosp-Admission Discharged 9/13/2021 - 9/18/2021 (5 days) Hospital Problems * (Principal) COVID-19 Yes Rheumatoid arthritis Yes RHEUMATOID ARTHRITIS; Current use of long term anticoagulation Not Applicable Supratherapeutic INR Yes Acute hypoxemic respiratory failure Yes Encephalopathy Yes Poor prognosis Yes Immunosuppressed status Yes Presenting Problem/History of Present Illness/Reason for Admission Acute hypoxemic respiratory failure Hospital Course 1. Acute hypoxic respiratory failure secondary to COVID-19 pneumonia: Patient has been continued on remdesivir IV, Decadron 6 mg IV, infectious disease consultation appreciated patient is not a candidate for baricitinib as she has immunosuppression. 2. Supratherapeutic INR: Patient got a dose of vitamin K 3. Known rheumatoid arthritis on multiple immunosuppressive medications including prednisone methotrexate and rinvoq , hold on medications until she recovers from COVID-19 pneumonia. 4. Hypothermia likely related to severe infection with COVID: resolved Because of the comorbidities, patient was extremely sick and was requiring very high oxygen she decided to change her CODE STATUS to comfort care, patient will be changed to hospice. Operative Procedures Performed Treatments: treated for Covid, changed to comfort care Procedures: none Consults: none Pertinent Test Results:none Physical Exam at Discharge Heart Rate: (!) 104 Resp: (!) 24 BP: 119/84 Temperature: 36.6 ?C (97.8 ?F) Weight: 71.9 kg (158 lb 8.2 oz) General: Patient seems very sick, seems anxious HEENT: Atraumatic normocephalic Neck supple CVs: S1-S2 regular rate and rhythm Respiratory: Patient has bilateral coarse breath sounds, requiring supplemental oxygen with nasal cannula Abdomen: Soft nontender bowel sounds present Neurologically: seems restless Patient has right BKA Discharge Instructions Condition at Discharge Discharge Condition: very sick Chief Complaint Patient presents with ? Shortness of Breath 1. Acute hypoxemic respiratory failure 2. COVID-19 3. Current use of long-term anticoagulation 4. Supratherapeutic INR 5. Poor prognosis 6. Encephalopathy Plan: Pulse oximetry continuously - high flow nasal cannula. Consult pulmonology. Decadron 6mg IV daily Remdesevir IV full course guidelines advise AGAINST routine plasma use in hospitalized patients. I do not believe benefits > risks. Spoke to ED physician personally Given vitamin K to reverse INR > 9.8 Critical care time spent 60 minutes o Nutrition: heart healthy if passes dysphagia screen o VTE prophylaxis: heparin o Full Code History of Present Illness a 69 y.o. female. I personally interviewed patient, reviewed chart, and reviewed emergency room resident history and agree with it in its following entirety unless otherwise noted below. " a 69 y.o. female w h/o DVT on coumadin, vaccinated against covid. presenting to the ED with weakness and fatigue for the past 2 weeks. Patient is not able to provide much history. Per her sister she has been ill for the past 2 weeks symptoms including weakness, fatigue, shortness of breath. She is normally alert and oriented x3, no history of dementia. She was seen in urgent care and prescribed antibiotics and steroids but she did not receive a Covid test. She continued to worsen on the next couple days and her neighbors who checked on her, and she was not very responsive so they called EMS. Per EMS patient was satting approximately 50% on room air and she was put on nonrebreather at 15 L and had improvement in saturation." Patient is on high flow nasal cannula saturating in the upper 90s. She has a very poor historian. Not coughing just short of breath. No edema No rashes Principal problem Acute hypoxic respiratory failure Covid pneumonia Rheumatoid arthritis-immunocompromised state Patient was admitted to Hospital on 9/13 with Covid pneumonia and acute hypoxic respiratory failure. She was requiring high flow nasal cannula at the time of admission. She was started on Decadron and IV remdesivir. Due to the requirement of high flow nasal cannula pulmonology was consulted and also infectious disease was also consulted. Per infectious disease immunomodulators are contraindicated in this immunosuppressed patient. Due to patient worsening respiratory state patient opted for comfort care and hospice. Patient was changed to comfort care and was consulted on 9/17. Patient is continued on comfort care medications with the help of the hospice Patient died on 9/21 at 2320

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: 09/21/21 1830 COVID-19 (SARS CoV-2,RNA Molecular Amplification) Collected: 09/21/21 1706 | Final result | Specimen: Swab from Nasopharynx COVID-19 SARS-CoV-2 Overall Result Detected Critical 09/21/21 1830 COVID-19 PCR - Pre-Procedure Screening (Asymptomatic) Collected: 09/21/21 1706 | Final result | Specimen: Swab from Nasopharynx 09/13/21 0332 Respiratory virus detection panel Collected: 09/13/21 0205 | Final result | Specimen: Swab from Nasopharynx Adenovirus Not Detected Mycoplasma pneumoniae Not Detected Chlamydophila pneumoniae Not Detected Parainfluenza Not Detected COVID-19 SARS-CoV-2 Overall Result Detected Critical Enterovirus/Rhinovirus Not Detected Coronavirus Not Detected Respiratory Syncytial Virus Not Detected Influenza A Not Detected Bordetella pertussis Not Detected Influenza B Not Detected Bordetella parapertussis Not Detected Metapneumovirus Not Detected I have personally reviewed the radiology image CT abdomen pelvis with contrast Result Date: 9/13/2021 PROCEDURE INFORMATION: Exam: CT Abdomen And Pelvis With Contrast Exam date and time: 9/13/2021 3:27 AM Age: 69 years old Clinical indication: Other: N/a; Additional info: AMS, SOB TECHNIQUE: Imaging protocol: Computed tomography of the abdomen and pelvis with contrast. Radiation optimization: All CT scans at this facility use at least one of these dose optimization techniques: automated exposure control; mA and/or kV adjustment per patient size (includes targeted exams where dose is matched to clinical indication); or iterative reconstruction. Contrast material: OMNI 350; Contrast volume: 80 ml; Contrast route: INTRAVENOUS (IV); COMPARISON: CT ABDOMEN PELVIS W CONTRAST 2/14/2019 3:12 PM FINDINGS: Lungs: Bilateral diffuse infiltrates are noted as described in the chest CT report. Mediastinal space: A large hiatal hernia is present. Liver: Normal. No mass. Gallbladder and bile ducts: Pneumobilia is again noted as previously described. Pancreas: Normal. No ductal dilation. Spleen: Normal. No splenomegaly. Adrenal glands: Normal. No mass. Kidneys and ureters: Multiple bilateral renal cysts are unchanged, the largest measuring 4.8 cm in the lower pole on the right. Stomach and bowel: Unremarkable. No obstruction. No mucosal thickening. Appendix: No evidence of appendicitis. Intraperitoneal space: Unremarkable. No free air. No significant fluid collection. Vasculature: IVC filter is present. Lymph nodes: Unremarkable. No enlarged lymph nodes. Urinary bladder: The bladder is decompressed. Reproductive: Fibroid uterus is noted. This has a low-density portion to it centrally which may represent distended endometrium, this is new from the prior study. Bones/joints: Patient is status post ORIF left hip fracture. Soft tissues: Unremarkable. IMPRESSION: 1. No acute process identified. 2. New hypodensity within the uterus, this could represent distended endometrium, correlation with pelvic sonography recommended. 3. IVC filter. 4. Stable renal cysts. 5. Large hiatal hernia. 6. Bilateral pulmonary infiltrates consistent with probable viral pneumonia. COMMENTS: For patients with an IVC filter, recommend assessment for a management plan for the patient's IVC filter. If there is no established management plan, recommend referral to an interventional clinician on a nonemergent basis for evaluation. THIS DOCUMENT HAS BEEN ELECTRONICALLY SIGNED CT angiogram chest pulmonary embolism with and without contrast Result Date: 9/13/2021 PROCEDURE INFORMATION: Exam: CTA Chest Without And With Contrast Exam date and time: 9/13/2021 3:27 AM Age: 69 years old Clinical indication: Other: N/a; Additional info: SOB. Covid positive ? pe TECHNIQUE: Imaging protocol: Computed tomographic angiography of the chest without and with contrast. 3D rendering (Not supervised by radiologist): MIP and/or 3D reconstructed images were created by the technologist. Radiation optimization: All CT scans at this facility use at least one of these dose optimization techniques: automated exposure control; mA and/or kV adjustment per patient size (includes targeted exams where dose is matched to clinical indication); or iterative reconstruction. Contrast material: OMNI 350; Contrast volume: 80 ml; Contrast route: INTRAVENOUS (IV); COMPARISON: CT ABDOMEN PELVIS W CONTRAST 2/14/2019 3:12 PM FINDINGS: Pulmonary arteries: Normal. No pulmonary emboli. Aorta: Unremarkable. No aortic aneurysm. No aortic dissection. Lungs: Extensive patchy ground-glass infiltrates are seen bilaterally involving all lung segments. Pleural spaces: Unremarkable. No pneumothorax. No pleural effusion. Heart: Coronary atherosclerosis is present. Lymph nodes: Unremarkable. No enlarged lymph nodes. Diaphragm: Elevation of the left hemidiaphragm is noted. Stomach and bowel: A large paraesophageal hernia is present most of the stomach resides in the lower thorax. Bones/joints: Unremarkable. No acute fracture. Soft tissues: Unremarkable. IMPRESSION: 1. No evidence of pulmonary embolus. 2. Extensive bilateral patchy ground-glass infiltrates.Commonly reported imaging features of COVID-19 pneumonia are present. Other processes such as influenza pneumonia and organizing pneumonia, as can be seen with drug toxicity and connective tissue disease, can cause a similar imaging pattern. (Reference:) 3. Large hiatal hernia. 4. Coronary atherosclerosis. Medical Decision Making/ Level of Risk: high
Aktuelle Erkrankungen: -
Vorgeschichte: Nervous Chronic pain syndrome Peripheral neuropathy Phantom limb pain Generalized pain Encephalopathy Respiratory Acute hypoxemic respiratory failure Circulatory Chronic deep vein thrombosis (DVT) of proximal vein of left lower extremity Benign essential hypertension Digestive Adenomatous polyp of colon Vitamin B12 deficiency Genitourinary Hyperactivity of bladder Renal cyst Acute cystitis without hematuria Musculoskeletal Complete below knee amputation of right lower extremity DDD (degenerative disc disease), lumbar Degeneration, intervertebral disc, thoracic Facet arthropathy, lumbar Osteoarthritis of right shoulder Osteoporosis Thoracic spondylosis Primary osteoarthritis involving multiple joints Intertrigo Endocrine/Metabolic Hyperlipidemia Hematologic Supratherapeutic INR Infectious/Inflammatory COVID-19 Immune Immunosuppressed status Rheumatoid arthritis Other Abdominal adhesions Incisional hernia Lymphedema Spinal stenosis of lumbar region Controlled substance agreement signed Current use of long term anticoagulation Ambulatory dysfunction Medication management Long term (current) use of anticoagulants Poor prognosis
Andere Medikamente: UNKNOWN
Allergien: CefuroximeChest Pain / Tightness AdhesiveRash AspirinOther (document details in comments) DoxycyclineNausea Only Nsaids (Non-steroidal Anti-inflammatory Drug)Other (document details in comments)
Vorherige Impfungen: -

VAERS 1758709

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: PA
Alter: 62,0
Geschlecht: M
Eingang: 04.10.2021
Impfdatum: 11.03.2021
Beginn: 14.09.2021
Tage bis Beginn: 187,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Acute respiratory failure Adenovirus test Alpha 1 foetoprotein Angiogram pulmonary abnormal Appendicolith Arthralgia Atrial fibrillation Barrett's oesophagus Blood culture negative Bordetella test negative COVID-19 COVID-19 pneumonia Cardiac failure Cardiac failure chronic Cerebrovascular accident Chest X-ray abnormal Chlamydia test negative

Symptomtext

ED to Hosp-Admission Discharged 9/14/2021 - 9/19/2021 (5 days) Hospital Presenting Problem/History of Present Illness/Reason for Admission Shortness of breath [R06.02] Acute on chronic respiratory failure with hypoxia Hospital Course 63 y.o. male with a PMHx of COPD not on home O2, HFpEF, A. fib on anticoagulation, hyperlipidemia, hypertension, GERD, anxiety presented on 9/14/2021 to Hospital because of shortness of breath. Patient was recently admitted to Hospital on 8/9 for multifocal pneumonia, respiratory failure requiring intubation for 5 days, complicated by CVA and A. fib with RVR, completed IV antibiotics and course of steroids and discharged on 9/12. Patient was diagnosed with COVID-19, with supporting CXR and CTA Chest findings, no PE was found. He was placed on 6L O2 NC. Patient also met severe sepsis criteria, and was empirically started on Vancomycin and Cefepime. He was started on a 10-day course of Decadron, 5-day course of Remdesivir. Vancomycin and Cefipime were discontinued once blood cultures were negative at 48 hours. Patient completed 5-day course of Remdesivir, IV Decadron was transitioned to PO Decadron to be completed outpatient by 9/23/21. Patient was weaned off oxygen and breathing well on room air. PT recommended home with home health. He will need follow up with the Heart Failure team, for which an appointment is already made for 10/15/21. He will also need follow up with Pulmonology to set up PFTs in 4-6 weeks. He will also need follow up with Gastroenterology to manage his untreated Hepatitis C and Barrett's Esophagus found on previous EGD. He has an AFP lab pending to screen. Hospital Problems POA * (Principal) Acute respiratory failure with hypoxia Yes Mixed anxiety depressive disorder Yes Chronic hepatitis C virus infection Yes Chronic obstructive pulmonary disease Yes Severe sepsis Yes COVID-19 virus infection Yes Leukocytosis Yes Demand ischemia Yes Left shoulder pain Yes Fracture of left humerus Yes Gastroesophageal reflux disease without esophagitis Yes Microcytic anemia Yes Hx of gout Yes Paroxysmal atrial fibrillation Yes On apixaban therapy Not Applicable Essential hypertension Yes Mixed hyperlipidemia Yes Chronic heart failure with preserved ejection fraction Yes Barrett's esophagus Yes Other cirrhosis of liver Yes Smoker unmotivated to quit Yes Esophageal thickening Yes Hilar lymphadenopathy Yes Mediastinal lymphadenopathy Yes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: Updated Procedure 09/14/21 1653 Respiratory virus detection panel Collected: 09/14/21 1553 | Final result | Specimen: Swab from Nasopharynx Adenovirus Not Detected Mycoplasma pneumoniae Not Detected Chlamydophila pneumoniae Not Detected Parainfluenza Not Detected COVID-19 SARS-CoV-2 Overall Result Detected Critical Enterovirus/Rhinovirus Not Detected Coronavirus Not Detected Respiratory Syncytial Virus Not Detected Influenza A Not Detected Bordetella pertussis Not Detected Influenza B Not Detected Bordetella parapertussis Not Detected Metapneumovirus Not Detected Imaging Results Procedure Component Value Ref Range Date/Time Ultrasound renal complete [3303071895] Resulted: 09/15/21 1701 Order Status: Completed Updated: 09/15/21 1701 Narrative: US RENAL COMPLETE IMPRESSION: Unremarkable renal ultrasound. No evidence of mass or hydronephrosis. END OF IMPRESSION: INDICATION: Proteinuria. TECHNIQUE: Ultrasound evaluation of the kidneys and bladder performed. Permanently recorded images were obtained and stored. COMPARISON: CT of the abdomen and pelvis performed September 14, 2021. FINDINGS: Right Kidney: 10.1 cm. Normal size and appearance. No mass or hydronephrosis. Simple renal cysts are identified, the largest along the upper pole measuring up to 2.9 cm. Left Kidney: 10.1 cm. Normal size and appearance. No mass or hydronephrosis. Bladder: Normal in appearance. Ureteral Jets: Seen bilaterally. This report was created using software. Thank you for allowing us to participate in the care of your patient. CT angiogram chest pulmonary embolism with and without contrast [3303016960] Resulted: 09/14/21 2004 Order Status: Completed Updated: 09/14/21 2004 Narrative: CTA CHEST PULMONARY EMBOLISM W WO CONTRAST IMPRESSION: Pulmonary-parenchymal infiltrates, likely consistent with COVID-19 pneumonia. Extensive mediastinal and hilar adenopathy. Underlying infectious or inflammatory or infiltrative process is to be considered. No evidence of aortic aneurysmal dilatation or obvious dissection. No evidence of pulmonary artery embolism appreciated to the second, and most third order branches. Thickening of the middle and distal esophagus appreciated on this examination. Underlying infectious or inflammatory or infiltrative process is to be considered. Underlying, more worrisome process must also be considered and excluded. Concurrent CT of the abdomen was evaluated and reported separately. Findings, as discussed in the body of the report. Appropriate followup, as clinically directed. Pulmonary Artery Embolism: None. Cardiomegaly: None. RV/LV Ratio: N/A END OF IMPRESSION: INDICATION: Hypoxia. Assess for pulmonary artery embolism. TECHNIQUE: Enhanced helical CTA scan of the chest was performed from the lung apices to below the diaphragm, including the pulmonary artery. 2 mm axial reconstructions with MPR coronal, oblique and sagittal images were created. 3D post processing imaging was obtained and stored. CONTRAST: 80 mL of IOHEXOL 350 MG IODINE/ML INTRAVENOUS SOLUTION administered INTRAVENOUS. Quality of contrast opacification was adequate. COMPARISON: None. FINDINGS: CT of the Chest: CT of the chest revealing extensive bilateral pulmonary-parenchymal infiltrates, worrisome for COVID-19 pneumonia. There is no definite evidence of pleural effusion. No evidence of pneumothorax identified. Heart size is within normal limits. There is no evidence of pericardial effusion noted. There appears to be hiatus hernia with thickening of the esophagus from the level of the carina to the gastroesophageal junction. Underlying infectious or inflammatory or infiltrative process is to be considered. Followup is recommended to exclude an underlying, more worrisome process. Significant mediastinal adenopathy is identified on this examination. In the subcarinal region measuring approximately 1.7 cm. At the right hilum measuring approximately 1.3 cm in short axis, and within the left hilum measuring approximately 1 cm in short axis. The thyroid gland is unremarkable. The aorta is without evidence of aneurysmal dilatation or obvious dissection. There is no definite evidence of pulmonary artery embolism appreciated to the second, and most third order branches. Concurrent CT of the abdomen will be evaluated and reported separately. Thoracic spine revealing intervertebral disc space narrowing is appreciated. Vacuum disc formation is noted. Facet alignment is maintained. Facet arthropathy is appreciated. This report was created using software. Thank you for allowing us to participate in the care of your patient. CT abdomen pelvis with contrast [3302996573] Resulted: 09/14/21 1938 Order Status: Completed Updated: 09/14/21 1938 Narrative: CT ABDOMEN PELVIS W CONTRAST IMPRESSION: There are no inflammatory changes, focal enhancing collection or mass in the abdomen or pelvis. There is small tiny 2 mm calcific density at the tip of appendix may suggest appendicolith. There is no evidence of acute appendicitis. END OF IMPRESSION: INDICATION: Fever, abdominal pain, Covid positive.. TECHNIQUE: Sequential axial 3 mm collimated images are obtained through the abdomen and pelvis after the administration of IV contrast. Sagittal and coronal 3 mm collimated 2D reformats are included. CONTRAST: 80mL of IOHEXOL 350 MG IODINE/ML INTRAVENOUS SOLUTION administered INTRAVENOUS. COMPARISON: 8/10/2021 FINDINGS: CT abdomen: The evaluation of pulmonary bases reveals multiple small patchy infiltrates central and peripheral distribution both lower lobes consistent with Covid infection. The liver, gallbladder, pancreas, spleen, adrenal glands and kidneys are unremarkable. There is small cortical cyst in the upper to midpole of right kidney medially measuring 3.2 cm. The portal vein and hepatic vein are patent. Abdominal aorta and IVC are patent. The kidneys demonstrate symmetric enhancement and no evidence of hydronephrosis. There is no enlarged mesenteric or retroperitoneal lymphadenopathy. The stomach and duodenum are unremarkable. The small bowel loops are normal with no dilatation or bowel wall thickening. No free air or free fluid is seen. CT Pelvis: Urinary bladder and sigmoid colon demonstrate no acute abnormality. There is no evidence of sigmoid diverticulitis. The cecum, and terminal ileum are normal. There is small tiny 2 mm calcific density at the tip of appendix may suggest appendicolith. There is no evidence of acute appendicitis. No pelvic free air or fluid is seen. No pathologic pelvic adenopathy is detected. Evaluation of bone windows reveals no acute osseous abnormality. None This report was created using software. Thank you for allowing us to participate in the care of your patient. X-ray chest 1 view, Portable [3302996941] Resulted: 09/14/21 1919 Order Status: Completed Updated: 09/14/21 1919 Narrative: XR CHEST 1 VW PORT IMPRESSION: Sensitive bilateral pulmonary parenchymal infiltrates. Underlying infectious or inflammatory or infiltrative process is to be considered. Findings, as discussed in the body of the report. Appropriate followup, as clinically directed. END OF IMPRESSION: INDICATION: Shortness of breath. TECHNIQUE: AP semierect portable examination of the chest. COMPARISON: Prior examination of August 17, 2021. FINDINGS: The heart size is within normal limits. There are extensive bilateral pulmonary parenchymal infiltrates identified on this examination. Underlying infectious or inflammatory infiltrative process is to be considered. Underlying congestion must also be considered. Osseous skeleton is grossly intact. No evidence of pleural effusion or pneumothorax is noted. This report was created using software. Thank you for allowing us to participate in the care of your patient.
Aktuelle Erkrankungen: -
Vorgeschichte: Nervous Carpal tunnel syndrome Lumbar radiculopathy Nicotine dependence Right hip pain Chronic pain of right hip Left shoulder pain Respiratory Hilar lymphadenopathy Chronic obstructive pulmonary disease Acute respiratory failure with hypoxia Circulatory Chronic heart failure with preserved ejection fraction Mediastinal lymphadenopathy Demand ischemia Paroxysmal atrial fibrillation Essential hypertension Digestive Barrett's esophagus Other cirrhosis of liver Esophageal thickening Chronic hepatitis C virus infection Chronic viral hepatitis C Obese Upper GI bleed Gastroesophageal reflux disease without esophagitis Musculoskeletal Arthritis of knee Closed compression fracture of L4 lumbar vertebra Compression deformity of vertebra Disc degeneration, lumbar Eczema Edema, lower extremity Fracture of bone Hemarthrosis, lower leg Osteoarthritis of knee Osteoarthritis Osteoarthrosis, localized, primary, knee Plantar fasciitis Primary osteoarthritis of both knees Pseudogout Arthritis of right hip Fracture of left humerus Endocrine/Metabolic Mixed hyperlipidemia Hematologic Microcytic anemia Leukocytosis Infectious/Inflammatory COVID-19 virus infection Immune Psoriasis Severe sepsis Other Smoker unmotivated to quit Controlled substance agreement signed Adjustment insomnia Mixed anxiety depressive disorder Depression Ganglion cyst Lumbar canal stenosis Lumbar stenosis Psychoactive substance abuse Substance abuse Hx of gout On apixaban therapy
Andere Medikamente: acetaminophen (TYLENOL) 325 mg tablet albuterol HFA (VENTOLIN HFA) 90 mcg/actuation inhaler allopurinol (ZYLOPRIM) 300 mg tablet amiodarone (PACERONE) 200 mg tablet amLODIPine (NORVASC) 5 mg tablet apixaban (ELIQUIS) 5 mg tablet atorv
Allergien: BlackberryHives / Urticaria MeloxicamHives / Urticaria, Other (document details in comments) Sulfa (Sulfonamide Antibiotics)Hives / Urticaria Sulfamethoxazole-trimethoprimHives / Urticaria, Other (document details in comments)
Vorherige Impfungen: -

VAERS 1747982

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: NJ
Alter: 56,0
Geschlecht: F
Eingang: 30.09.2021
Impfdatum: 16.03.2021
Beginn: 30.04.2021
Tage bis Beginn: 45,0
Dosis: 2
Route/Site: - / RA

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

Cerebrovascular accident Hypotension

Symptomtext

cryptogenic stroke; low blood pressure; This is a spontaneous report from a contactable consumer (patient). A 56-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in arm right on 16Mar2021 16:00 (Batch/Lot Number: EN6208) as single dose for covid-19 immunisation (age at vaccination was 56-year-old). Medical history included hashimotos. Patient was non-smoker and daily exerciser. Patient received other medications in two weeks. Historical vaccine included 1st dose of BNT162B2 (Lot number: EN6203) on 23Feb2021 at 16:00 for Covid-19 immunisation (age at vaccination was 55-year-old). The patient experienced acryptogenic stroke 4 weeks following 2nd vaccination. No reason found. Normal BMI, no blockages, non-smoker, low blood pressure, daily exerciser. Onset date of acryptogenic stroke was 30Apr2021 at 18:30. Treatment for acryptogenic stroke was unknown. Patient was hospitalized for acryptogenic stroke for 3 days. Outcome of acryptogenic stroke was resolving. Outcome of low blood pressure was unknown. Patient had Nasal Swab Covid test date: 05Jul2021: Negative. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: Test Name: Blood pressure; Result Unstructured Data: Test Result:Low; Comments: low blood pressure; Test Name: BMI; Result Unstructured Data: Test Result:Normal; Comments: Normal BMI; Test Name: investigation; Result Unstructured Data: Test Result:no blockages; Test Date: 20210705; Test Name: Covid test; Test Result: Negative ; Comments: Covid test type post vaccination: Nasal Swab Covid test date: 05Jul2021 Covid test result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Exercise adequate; Hashimoto's disease (Other medical history: Hashimotos); Non-smoker
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1745656

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: CA
Alter: 67,0
Geschlecht: M
Eingang: 29.09.2021
Impfdatum: 16.03.2021
Beginn: 25.09.2021
Tage bis Beginn: 193,0
Dosis: 2
Route/Site: IM / RA

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

Acute respiratory failure C-reactive protein increased COVID-19 pneumonia Cough Dyspnoea Pain Pyrexia

Symptomtext

Admitted 9/25 for SOB, sx onset 9/15 Reports fever, body aches, cough; home sats readings 88-89% for 3 days prior to admission 67 Y male with a h/o smoking ( 10 pack years, quit last year), metastatic rectal cancer, claustrophobia, h/o post-polio syndrome admitted for acute hypoxemic respiratory failure 2/2 to COVID-19 PNA. Pt. being treated in the hospital x5 days w/ remdesivir and decadron x10days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: Results as of 9/29/2021 14:43 3/14/2020 12:06 CRP, SER QL: 20.6 (H) 9/26/2021 06:40 CRP, SER QL: 16.1 (H) 9/27/2021 06:45 CRP, SER QL: 10.3 (H) 9/28/2021 06:22 CRP, SER QL: 4.6 (H)
Aktuelle Erkrankungen: ADENOCARCINOMA, RECTUM (Chronic)
Vorgeschichte: Hx of metastatic rectal cancer on Xeloda oral regimen; post-poliomyelitis syndrome
Andere Medikamente: Atorvastatin (LIPITOR) 20 mg Oral Tab ; Desipramine (NORPRAMIN) 100 mg Oral Tab; Gas Relief 80 simethicone, 80 mg Oral Chew Tab ; HYDROcodone-Acetaminophen (NORCO) 7.5-325 mg Oral Tab; Ibuprofen (MOTRIN) 600 mg Oral Tab; Lisinopril-hydroCHL
Allergien: Gabapentin
Vorherige Impfungen: -

VAERS 1734641

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: FL
Alter: 72,0
Geschlecht: F
Eingang: 25.09.2021
Impfdatum: 28.03.2021
Beginn: 31.08.2021
Tage bis Beginn: 156,0
Dosis: 2
Route/Site: IM / RA

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

Anaemia Aphasia Breath sounds absent COVID-19 Cardiac arrest Cardio-respiratory arrest Death Encephalopathy Endotracheal intubation Endotracheal intubation complication Extubation Facial paralysis Haemorrhage Heart sounds abnormal Hemiparesis Infection Intensive care Mydriasis

Symptomtext

Patient required hospitalization due to breakthrough infection. Patient received Pfizer vaccine (2nd dose in series) on 03/28/2021. Patient was hospitalized from 08/31/21 - 09/24/21. Below is copied from patients discharge (death) summary: Patient is a 73 y.o. female with PMH of RA/PMR and hypothyroidism who was initially admitted to the hospital on 8/31 for stroke like symptoms (left sided weakness, right facial droop and aphasia) for which she recieved TNK and had neuro ICU admission. MRI and stroke workup was unrevealing how patient remained enephalopathic with development of hypoxic respiratory failure requiring intubation from 9/5-9/14. Following extubation, patient was downgraded to hospitalist serevice for further management on 9/16. On 9/24, patient was admitted to MICU following cardiac arrest with asystole noted on telemetry. Patient recieved 6 rounds of CPR, epix3, bicarbx2, and calcium. She was intubated at that time and ROSC was achieved with post-resuscitation BP 100/50. Epi gtt was started and patient was admitted to MICU service. Immediately upon arrival to patient coded again at 4:21 AM with PEA arrest. She recieved Epix5, bicarbx3 with ROSC at 4:36. Upon achieving ROSC, patient again became pulseless with PEA arrest at which time an additional 3 rounds of CPR were performed however patient did not achieve ROSC and began to have copious blood return from ETT. Given patients anemia and active bleed, TNK was not administered as risks overweighed benefits. No further rounds of CPR performed. No Subsequent spontaneous movements were present. There was no response to verbal or tactile stimuli. Pupils were dilated and fixed. No breath sounds were appreciated over either lung field. No carotid pulses or peripheral pulses were palpable. No heart sounds were auscultated over entire precordium. Patient pronounced dead at 5:16 AM. Family was notified and condolensces were offered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 24,0
Labordaten: SARS-COV-2, NAA, Detected 09/15/21.
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, hypothyroidism, polymyalgia RA
Andere Medikamente: albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulizer solution Take by nebulization every 6 hours as needed for Wheezing. Information, Historical aspirin 81 MG tablet Take by mouth daily. Information, Historical docusate sodium
Allergien: Amlodipine
Vorherige Impfungen: -

VAERS 1734167

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: CO
Alter: -
Geschlecht: F
Eingang: 25.09.2021
Impfdatum: -
Beginn: 07.08.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Artery dissection Cerebrovascular accident SARS-CoV-2 test

Symptomtext

2 strokes in occipital lobe and dissection of artery; 2 strokes in occipital lobe and dissection of artery; This is a spontaneous report from a contactable consumer (patient) A 49-year-old female patient (not pregnant) received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EN6208) via an unspecified route of administration in Arm Left on 2021 as single dose for covid-19 immunisation. Medical history included lupus, aplastic anemia (apls) and Raynauds; patient had unspecified allergies. Previously on 09Mar2021 (at 49 years) the patient took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: En6203) in Right arm for covid-19 immunisation.Concomitant medications included hydroxychloroquine; escitalopram oxalate (LEXAPRO); rivaroxaban (XARELTO) and vitamis, all taken for unspecified indication, start and stop date were not reported. Nasal Swab on 02Sep2021 was negative. The patient experienced 2 strokes in occipital lobe and dissection of artery on 07Aug2021 at 08:00 am. Patient was treated with Lovenox.Events results in Emergency room/department or urgent care and hospitalization for 4 days in Aug2021.Patient recovered with lasting effects on an unknown date in 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: Test Date: 20210902; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy (unspecified); Aplastic anemia; Lupus erythematosus; Raynauds
Andere Medikamente: HYDROXYCHLOROQUINE; LEXAPRO; XARELTO
Allergien: -
Vorherige Impfungen: -

VAERS 1719423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 21.09.2021
Impfdatum: 11.03.2021
Beginn: 26.08.2021
Tage bis Beginn: 168,0
Dosis: 2
Route/Site: - / -

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Confusional state Death Dyspnoea Endotracheal intubation General physical health deterioration Oxygen saturation decreased SARS-CoV-2 test positive

Symptomtext

presented to ED confused, O2 saturation decreased, hx of COVID positive for approximately 1 week; hx of COPD; dyspnea; intubated, acute hypoxemic respiratory failure, COVID pneumonia; pt's condition deteriorated where he died in the hospital

Weitere VAERSDATA-Felder

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

VAERS 1719277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: HI
Alter: 61,0
Geschlecht: M
Eingang: 21.09.2021
Impfdatum: 17.03.2021
Beginn: 22.06.2021
Tage bis Beginn: 97,0
Dosis: 2
Route/Site: IM / LA

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

Anticoagulant therapy Computerised tomogram Decreased activity Deep vein thrombosis Pulmonary embolism Ultrasound scan abnormal

Symptomtext

I noticed that my endurance was diminished for two weeks and when I when I went to the hospital on 07/06/2021. I was diagnosed with multiple bilateral Pulmonary Emboli confirmed by ultrasound. I also had a DVT in my right leg slightly to the medial side of my knee. It was treated with anticoagulants. Currently I have no symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: CT Scan 07/06/2021 Ultrasound 07/06/2021
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension
Andere Medikamente: Lisinopril 20mg; Loratadine 10mg
Allergien: Bactrim-hives; Seasonal Allergies
Vorherige Impfungen: -

VAERS 1718958

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: PA
Alter: 58,0
Geschlecht: M
Eingang: 21.09.2021
Impfdatum: 02.04.2021
Beginn: 12.04.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: SYR / RA

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

Cardiomegaly Feeling abnormal Sudden cardiac death

Symptomtext

Patient passed away on May 29th due to "Sudden Cardiac Death due to Cardiomegaly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Sudden cardiac death
Hospital-Tage: -
Labordaten: He never had an enlarged heart before per an XRAY. He also never felt right after having the Vaccine
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lasartin, Colace,
Allergien: None
Vorherige Impfungen: -

VAERS 1694583

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: PA
Alter: 59,0
Geschlecht: F
Eingang: 13.09.2021
Impfdatum: 31.03.2021
Beginn: 18.07.2021
Tage bis Beginn: 109,0
Dosis: 1
Route/Site: SYR / LA

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

Anticoagulant therapy Back pain Chest pain Computerised tomogram thorax abnormal Echocardiogram Pericardial effusion Pulmonary embolism Pulmonary mass Ultrasound scan abnormal

Symptomtext

I went to the emergency room with chest and back pain. A CT scan of my chest revealed a pulmonary embolism in my right lung. It also showed a small amount of fluid around my heart and a mass on the right side of my lung. an ultrasound of my heart showed minimal fluid around my heart and that my heart was pumping normally. a PET-CT ordered to better define the lung mass. Given blood thinner by stomach injection and placed on apixaban on July 22, 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Zyrtec
Allergien: Shellfish
Vorherige Impfungen: -

VAERS 1101594

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: ND
Alter: 36,0
Geschlecht: M
Eingang: 10.09.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Apnoea Blood glucose decreased Confusional state Fall Feeling hot Head injury Hyperhidrosis Loss of consciousness Pallor Posture abnormal Respiratory arrest Seizure Skin warm Syncope Urinary incontinence

Symptomtext

About 10 minutes post shot while sitting in waiting area I fainted. Once I came to they checked vitals and got me into a wheelchair. When moving to a private area I felt warm, that was when I fainted again, locked up and slid out of the wheelchair and had a seizure. I also stopped breathing for 5-10 seconds and urinated myself. I was covered in blankets and ice packs upon regaining consciousness and was tested by the nursing staff and EMTs. No abnormalities found in heart rate or blood drawn or blood pressure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Allergic to Penicillin and Sulfa
Vorherige Impfungen: -

VAERS 1101594

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: ND
Alter: 36,0
Geschlecht: M
Eingang: 10.09.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Apnoea Blood glucose decreased Confusional state Fall Feeling hot Head injury Hyperhidrosis Loss of consciousness Pallor Posture abnormal Respiratory arrest Seizure Skin warm Syncope Urinary incontinence

Symptomtext

About 10 minutes post shot while sitting in waiting area I fainted. Once I came to they checked vitals and got me into a wheelchair. When moving to a private area I felt warm, that was when I fainted again, locked up and slid out of the wheelchair and had a seizure. I also stopped breathing for 5-10 seconds and urinated myself. I was covered in blankets and ice packs upon regaining consciousness and was tested by the nursing staff and EMTs. No abnormalities found in heart rate or blood drawn or blood pressure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Allergic to Penicillin and Sulfa
Vorherige Impfungen: -

VAERS 1679141

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: WI
Alter: 73,0
Geschlecht: M
Eingang: 07.09.2021
Impfdatum: 11.03.2021
Beginn: 29.08.2021
Tage bis Beginn: 171,0
Dosis: 1
Route/Site: IM / -

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Patient was taken with the ER, tested positive for COVID-19 upon admission. He passed away on 9/01/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1675019

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: FL
Alter: 81,0
Geschlecht: M
Eingang: 05.09.2021
Impfdatum: 14.04.2021
Beginn: 31.07.2021
Tage bis Beginn: 108,0
Dosis: 1
Route/Site: IM / RA

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

Acute kidney injury Atrial fibrillation Bilevel positive airway pressure Blood creatine phosphokinase increased COVID-19 Computerised tomogram abdomen Computerised tomogram head abnormal Computerised tomogram thorax abnormal Death Dyspnoea Endotracheal intubation Enterococcal bacteraemia Hypernatraemia Hypotension Intensive care Lethargy Lung opacity Mechanical ventilation

Symptomtext

Patient required hospitalization due to breakthrough infection. He received the Pfizer vaccine (2nd dose in series) on 04/14/21. Patient was hospitalized from 07/31/21 - 08/31/21. Below is copied from discharge summary: Discharged Condition: deceased Hospital Course: Patient is a 82 y.o. male with a PMH of recurrent UTIs, BPH, COPD, bicytopenia (leukopenia and erythropenia), DDM2, HTN, and HLD who presented to the ED on 7/31 for AMS. He was found down by family and EMS was called. SpO2 was 68% and pt was placed on NRB. He was brought to the ED and was COVID + (despite previous Pfizer vaccination on 3/24 & 4/14). CT C/A/P showed bilateral opacities. He also had a brief episode of afib RVR treated w/ metoprolol w/ subsequent hypotension requiring levophed gtt. He later was intubated d/t hypercapnic respiratory failure and admitted to the MICU. His course was complicated by hypernatremia elevated CK, AKI, PSAR UTI and enterococcus bacteremia. Abx were de-escalated to levoflaxacin and ampicillin.Of note he did not receive Remdesivir or Toclilizumab d/t bacteremia. He completed a 7 day course of solumedrol. He was extubated to HFNC on 8/6 and was transferred to the floor on 8/8 and only requiring 5L NC at the time. While on the floor pt had increased lethargy. On the evening of 8/11 pt was noted to have tachypnea and use of accessory muscles. Pt was placed on a VM and on the morning of 8/12 placed on BIPAP.CTH was obtained and showed new bilateral SDH/hygromas. IM team spoke with team and they recommended MRI brain stroke protocol. Patient continued to have respiratory decline remain on ventilator his symptoms continue to escalate was shortness of breath desaturation to patient was ventrally placed on 100 percent was on flow land saturation still remains low family meeting with palliative Care patient was made DNR with no escalation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 31,0
Labordaten: SARS-COV-2, NAA, Detected: 07/31/21.
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma ? BPH with urinary obstruction ? CAD (coronary artery disease) Echo Dobutamine Stress Test 01/16/20 ? Chronic kidney disease Creatinine NL (0.86) on 04/20/20 ? COPD (chronic obstructive pulmonary disease) severe, PFT 2011 ? Coronary artery calcification seen on CAT scan ? Diabetes mellitus A1C 7.3 01/23/20 ? Dysphonia 2010 chronic ? Elevated PSA per notes ? GERD (gastroesophageal reflux disease) ? Hiatal hernia Small, per 05/22/19 EGD ? History of chronic cough ? Hypercholesterolemia ? Hypertension ? Kidney stones ? Osteoarthritis ? Schatzki's ring per 05/22/19 EGD ? Snores ? Unspecified gastritis and gastroduodenitis without mention of hemorrhage ? Urinary retention with CIC twice daily
Andere Medikamente: ACCU-CHEK AVIVA PLUS VI STRIP USE ONE STRIP TO CHECK BLOOD SUGAR THREE TIMES DAILY BEFORE MEALS ACCU-CHEK AVIVA PLUS W/DEVICE DOES NOT APPLY KIT 3 times daily. AMLODIPINE (NORVASC) 10 MG ORAL TABLET TAKE ONE TABLET BY MOUTH ON
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1916104

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: FL
Alter: 61,0
Geschlecht: M
Eingang: 30.08.2021
Impfdatum: 16.03.2021
Beginn: 09.04.2021
Tage bis Beginn: 24,0
Dosis: 1
Route/Site: IM / RA

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

Angiogram pulmonary abnormal Anticoagulant therapy Cardiac failure Inappropriate schedule of product administration Orthopnoea Pulmonary embolism Wheezing

Symptomtext

Pt admitted on 4/19/21-4/15/21 bilateral pulmonary emboli & heart failure. Currently on Eliquis, carvedilol, Entresto. No prior pulm or cardiac history. Pt received Pfizer dose #1 on 3/16/21 + dose #2 4/21/2021. Of note pt seen in office 11/2020 with ongoing symptoms of wheezing, orthopnea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 7,0
Labordaten: CT angio 4/9/21 Bilat. PE with bifurcations of main pulm arteries
Aktuelle Erkrankungen: ongoing cough/SOB
Vorgeschichte: Meralgia paresthetica - intermittent MVP
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1542059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: CA
Alter: 85,0
Geschlecht: M
Eingang: 30.08.2021
Impfdatum: 20.03.2021
Beginn: 10.08.2021
Tage bis Beginn: 143,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 Infection Respiratory disorder SARS-CoV-2 test positive

Symptomtext

Breakthrough Covid infection, acute respiratory failure

Weitere VAERSDATA-Felder

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

VAERS 1542059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

kritisch

Staat: CA
Alter: 85,0
Geschlecht: M
Eingang: 30.08.2021
Impfdatum: 20.03.2021
Beginn: 10.08.2021
Tage bis Beginn: 143,0
Dosis: 2
Route/Site: SYR / LA

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

Acute respiratory failure COVID-19 Infection Respiratory disorder SARS-CoV-2 test positive

Symptomtext

Breakthrough Covid infection, acute respiratory failure

Weitere VAERSDATA-Felder

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

VAERS 1646251

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: FL
Alter: 48,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 19.03.2021
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / RA

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

Anaphylactic shock Choking Drooling Dysphagia Oropharyngeal spasm Skin discolouration Throat irritation

Symptomtext

choking; scratchy throat; the muscles in her throat started seizing up completely within minutes; couldn't swallow whatsoever/no muscle control with swallowing; she couldn't control her spit; fingertips started turning blue; anaphylactic shock; This is a spontaneous report from a contactable consumer from a Pfizer sponsored program. A 48-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EN6208), via an unspecified route of administration, administered in right arm (reported: right upper arm) on 19Mar2021 12:30 (at the age of 48 years old) as dose 1, single for COVID-19 immunization. Medical history included triple negative breast cancer from 2017 to an unknown date, CREST (an autoimmune disorder that affects the scleroderma), and asthma from an unknown date. Concomitant medications include unspecified blood pressure and asthma medications. The patient received her 1st dose of COVID vaccine on 19Mar2021 and on the same day had anaphylactic shock. She reported she got the shot and within 10 minutes she had a really scratchy throat and she reported it to the nurse. The muscles in her throat started seizing up completely within minutes. She stated she did not have trouble breathing but she couldn't swallow whatsoever, she couldn't control her spit, when she tried to swallow, she was choking as she had no muscle control with swallowing. She also relayed her fingertips started turning blue. She was given an epi pen for the events. She was transported in the emergency room (ER) for 8 hours but was not admitted. The outcome of the events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic shock
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthmatic; CREST syndrome (an autoimmune disorder that affects the scleroderma); Triple negative breast cancer
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1641591

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: FL
Alter: 68,0
Geschlecht: M
Eingang: 27.08.2021
Impfdatum: 19.03.2021
Beginn: 24.08.2021
Tage bis Beginn: 158,0
Dosis: UNK
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 Diarrhoea Dyspnoea Nausea Pneumonia Pneumonia viral SARS-CoV-2 test positive

Symptomtext

Patient admitted 8/24/21 for nausea, diarrhea, and shortness of breath. History of non-Hodgkin's lymphoma and chemotherapy given 8/9. Resulted positive for COVID on 8/24. Diagnosed with COVID 19, bilateral viral pneumonia and acute hypoxi respiratory failure. Patient received Pfizer vaccination on 3/19/21 and 4/10/2021. Patient is still hospitalized. Hospital Name City State

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: non-Hodgkin's lymphoma, DVT
Andere Medikamente: simvastatin, Eliquis, allopurinol, ondansetron, calcium
Allergien: Smoke
Vorherige Impfungen: -

VAERS 1632255

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: VT
Alter: 56,0
Geschlecht: F
Eingang: 25.08.2021
Impfdatum: 09.04.2021
Beginn: 11.05.2021
Tage bis Beginn: 32,0
Dosis: 1
Route/Site: IM / AR

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

Activated partial thromboplastin time normal Computerised tomogram thorax abnormal Condition aggravated Cough Dyspnoea Fibrin D dimer increased Full blood count normal Prothrombin time normal Pulmonary embolism Ultrasound Doppler normal

Symptomtext

Approximately a week after first vaccine, began to experience SOB, cough which persisted through 2nd vaccine. She finally presented to the ED on 5/11/21 and was found to have bilateral PEs. No recent travel, surgery, trauma or immobility. Not on hormones. Normal BMI. Non-smoker. No prior hx venous thromboembolism.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: D-Dimer 2527 (normal < 230) CT PE protocol - bilateral PEs with evidence of right heart strain Normal PT, PTT Normal CBCD Negative LE ultrasounds
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: melatonin multivitamin
Allergien: beta blockers PCN sulfonamide antibiotics
Vorherige Impfungen: -

VAERS 1623587

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: WI
Alter: 94,0
Geschlecht: F
Eingang: 23.08.2021
Impfdatum: 10.03.2021
Beginn: 29.07.2021
Tage bis Beginn: 141,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 Chest pain Confusional state Death Pneumonia SARS-CoV-2 test positive

Symptomtext

Client received Pfizer Dose 1 on 2/16/21 and Dose 2 on 3/10/21. On 7/29/21 she had chest pain and confusion. She was taken to the ER - diagnosed w/ "little pneumonia." While still in the hospital, she wasn't tested for COVID until 8/2 when she tested positive. Client passed away on 8/8 with "Acute Hypoxemic Respiratory Failure due to COVID-19."

Weitere VAERSDATA-Felder

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

VAERS 1554304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 82,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 31.03.2021
Beginn: 02.08.2021
Tage bis Beginn: 124,0
Dosis: UNK
Route/Site: - / -

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

Cerebrovascular accident

Symptomtext

Cerebrovascular accident (CVA), unspecified mechanism

Weitere VAERSDATA-Felder

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

VAERS 1549566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: NY
Alter: 42,0
Geschlecht: M
Eingang: 12.08.2021
Impfdatum: 15.03.2021
Beginn: 05.04.2021
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: SYR / LA

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

Anticoagulant therapy Anxiety Basedow's disease Blood test Chest scan Deep vein thrombosis Echocardiogram Hyperhidrosis Nervousness Pain in extremity Palpitations Pulmonary embolism Pulmonary imaging procedure abnormal Ultrasound Doppler abnormal Ultrasound thyroid Weight decreased

Symptomtext

Heart palpitations; anxiety and nervousness; weight loss; and sweating excessively. I ultimately got diagnosed Grave's Disease which is an autoimmune disorder of Thyroid. Currently on treatment for that: Medication - Methimazole; Propranolol for that. Also I have been diagnosed with a Deep Vein Thrombosis and Pulmonary Embolism. 24th of June, I went to the ER. I was having leg pain and they did a chest scan and found a Pulmonary Embolism as well. I am currently on a blood thinner Xarelto. I was admitted to the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: Around May 26 - They did ultrasound of thyroid and some other tests and a number of blood tests (my doctor) at a few different facilities. June 24th - chest scan, ultrasound of leg; echo-cardiogram and a number of blood tests.
Aktuelle Erkrankungen: No
Vorgeschichte: Hypertension; HIV
Andere Medikamente: Lisinopril; Viktardy; Vit D; Vit B; Flax Seed
Allergien: No
Vorherige Impfungen: -

VAERS 1540347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

kritisch

Staat: NJ
Alter: 92,0
Geschlecht: M
Eingang: 10.08.2021
Impfdatum: 10.03.2021
Beginn: 02.08.2021
Tage bis Beginn: 145,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory distress syndrome COVID-19 pneumonia Death Dyspnoea SARS-CoV-2 test positive Urinary tract infection

Symptomtext

I am the epidemiologist reporting on behalf of patient. Case was admitted after daughter found Dad on the floor was previously being treated for a UTI -- Transported to the ED as he had Difficulty breathing -- during hospital start was treated for COVID Pneumonia -- was treatment at hospital and discharged 8/6 -- 8/7 Returned to ED w/Acute Respiratory Distress -- Daughter was by bedside declined Mechanical Inc -- pt. expired 3 hrs later. Patient was fully vaccinated with Pfizer on 2/17 and 3/10.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 3,0
Labordaten: + Rapid Test on 8/3/21
Aktuelle Erkrankungen: MENTAL,OTHER CHRONIC DISEASES, CARDIOVASCULAR DISEASE, IMMUNOCOMPROMISED CONDITION, CHRONIC LUNG DISEASE (ASTHMA/EMPHYSEMA/COPD)
Vorgeschichte: MENTAL,OTHER CHRONIC DISEASES, CARDIOVASCULAR DISEASE, IMMUNOCOMPROMISED CONDITION, CHRONIC LUNG DISEASE (ASTHMA/EMPHYSEMA/COPD)
Andere Medikamente: UNKNOWN
Allergien: UNKNOWN
Vorherige Impfungen: -

VAERS 1512787

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 29.07.2021
Impfdatum: 17.03.2021
Beginn: 31.05.2021
Tage bis Beginn: 75,0
Dosis: UNK
Route/Site: - / -

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

Cerebrovascular accident Trigeminal neuralgia

Symptomtext

Stroke (cerebrum) Trigeminal neuralgia

Weitere VAERSDATA-Felder

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

VAERS 1509756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: ND
Alter: 54,0
Geschlecht: M
Eingang: 28.07.2021
Impfdatum: 12.03.2021
Beginn: 21.05.2021
Tage bis Beginn: 70,0
Dosis: 1
Route/Site: IM / UN

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

Death

Symptomtext

Patient was hospitalized and passed away. 2nd vaccine given 4/6/2021

Weitere VAERSDATA-Felder

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

VAERS 1502285

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 86,0
Geschlecht: F
Eingang: 26.07.2021
Impfdatum: 09.04.2021
Beginn: 12.05.2021
Tage bis Beginn: 33,0
Dosis: UNK
Route/Site: - / -

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

Acute kidney injury Death Gastrointestinal haemorrhage

Symptomtext

death - Gastrointestinal hemorrhage, unspecified - Acute kidney failure, unspecified

Weitere VAERSDATA-Felder

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

VAERS 1502042

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 60,0
Geschlecht: M
Eingang: 26.07.2021
Impfdatum: 01.04.2021
Beginn: 26.03.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Acute kidney injury Death Gastrointestinal haemorrhage

Symptomtext

Death 7/25/21 N17.9 - AKI (acute kidney injury) K92.2 - Gastrointestinal hemorrhage, unspecified gastrointestinal hemorrhage type

Weitere VAERSDATA-Felder

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

VAERS 1464361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: OR
Alter: 77,0
Geschlecht: F
Eingang: 12.07.2021
Impfdatum: 13.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Angiogram Blood magnesium Cerebrovascular accident Computerised tomogram head Computerised tomogram neck Echocardiogram Magnetic resonance imaging head Metabolic function test

Symptomtext

Stroke

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 2,0
Labordaten: CTA head/neck 03/13/2021, MR head 03/14, Emboli monitoring... 03/14/2021, /2021, Echocardiogram complete 03/14/2021, comprehensive metabolic panel 03/13/2021, comprehensive metabolic panel plus magnesium 03/14/202, 1basic metabolic panel 03/15/2021
Aktuelle Erkrankungen: Sciatica
Vorgeschichte: Hypercholesteremia, osteopenia, prolapsed bladder, occasional fecal intolerance
Andere Medikamente: Atorvastatin, Clopidogrel, calcium, vitamin C, vitamin D, vitamin & mineral complex, NeoLife Tre-En-En (grain lipids), NeoLife carotenoid complex, salmon oil, Lactobacillus
Allergien: Lactose intolerance
Vorherige Impfungen: -

VAERS 1453749

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: FL
Alter: 82,0
Geschlecht: M
Eingang: 07.07.2021
Impfdatum: 22.03.2021
Beginn: 11.04.2021
Tage bis Beginn: 20,0
Dosis: 2
Route/Site: - / RA

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

Cerebrovascular accident Dermatitis Pruritus Rash morbilliform Scratch

Symptomtext

Rash: all over his body, like measles, on his back, arms, and legs/ terrible measle like rash all over my body except for my face; The itching was so bad that I scratched myself to the point of drawing blood; Itching, worse itching he ever experienced/ intense itching all over my body/worse itching/ itching was so bad; they called it, Dermatitis.; he thought he was having a stroke.; This is a spontaneous report from a contactable consumer (patient). This is report 1 of 2. An 82-years-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/Lot Number: EN6208; NDC/expiration: unknown) via an unspecified route of administration, administered at arm right on 22Mar2021 at 10:00 (at the age of 82-years-old) as dose 2, single for covid-19 immunization. Medical history included ongoing high blood pressure diagnosed many years ago, ongoing high cholesterol which was diagnosed around the same that his high blood pressure, ongoing type 2 diabetes mellitus diagnosed when he was in his 20's and he does not take any medications for his type 2 diabetes. The patient did not receive other products. No investigation assessment was reported. He stated several family members had the Moderna Covid vaccine, and they had some negative reactions. There were no additional vaccines administered on same date of the Pfizer suspect. The patient did not receive any prior vaccinations (within 4 weeks prior to the COVID vaccine) and no adverse events were reported following prior vaccinations. Family medical history relevant to adverse event was not provided. His other family members had flu like symptoms, and they were all females. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Concomitant medications received within 2 weeks of vaccination included rosuvastatin calcium (CRESTOR); losartan (LOSARTAN); propranolol; primidone (MYSOLINE) and acetylsalicylic acid (ASPIRIN (E.C.)) all taken for an unspecified indication, start and stop date were not reported. He had been taking the same medications for years and never had any negative reactions. Patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot: EN6200; expiry date: unknown), via unspecified route of administration, administered on right arm on 01Mar2021 at 10:00 for COVID-19 immunization. The patient experienced terrible reaction 3 weeks after the second vaccine. He woke up in the morning, turned on light and saw that he had rash all over his body (except for face), like measles, on his back, arms, and legs, intense itching all over body, worse itching he ever experienced in his life on 11Apr2021. The itching was so bad that he scratched himself to the point of drawing blood. He thought he was having a stroke. When he went to urgent care, he was treated with 2 injections Benadryl and steroid (Lot or expiration date was unknown). He was also treated with Pepcid. The injections did not help his symptoms. In the urgent care they didn't knew what the rash was and later clarified that they called it dermatitis. He stated that the staff did not thought that it was not related to the vaccine. He reclarified that when he was at urgent care, the staff told him that he should feel better in the evening, but by midnight, he decided to go to the emergency room. In the emergency room, he was given Tagamet, Hydroxyzine, and Prednisone. The rash went away and reported that itching was present, but not as bad as it was before. He reported that he took Hydroxyzine as prescribed, and after about 20 minutes, his itching diminishes but then in the evening he started to itch again. Later in the report it was mentioned that for some days he only has to take it once a day and sometimes he can skip a day when he was not itching. He was treated and released from the emergency room. The patient went to dermatologist and neurologist and no one could tell him why he had itching, no one had come up with a treatment as he was still itching. The patient stated that he called because he was reading information about the side effects and learned that the vaccine may cause a rash. Relevant tests were reported as none. Device date was reported as 22Jun2021. The outcome of the rash was recovered completely in 2021, for scratch and pruritus was not resolved and for stroke and dermatitis was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Blood pressure high (diagnosed many years ago); High cholesterol (around the same that his high blood pressure was diagnosed); Type 2 diabetes mellitus (diagnosed when he was in his 20's and he does not take any medications for his Type 2 diabetes)
Vorgeschichte: -
Andere Medikamente: CRESTOR; LOSARTAN; PROPRANOLOL; MYSOLINE; ASPIRIN (E.C.)
Allergien: -
Vorherige Impfungen: -

VAERS 1450601

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 78,0
Geschlecht: F
Eingang: 06.07.2021
Impfdatum: 02.04.2021
Beginn: 13.06.2021
Tage bis Beginn: 72,0
Dosis: UNK
Route/Site: - / -

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

Cerebral haemorrhage Death

Symptomtext

death I61.9 - Nontraumatic intracerebral hemorrhage, unspecified

Weitere VAERSDATA-Felder

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

VAERS 1450341

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 75,0
Geschlecht: F
Eingang: 06.07.2021
Impfdatum: 08.04.2021
Beginn: 08.05.2021
Tage bis Beginn: 30,0
Dosis: UNK
Route/Site: - / -

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

Cerebral haemorrhage Cerebrovascular accident Death Facial paresis

Symptomtext

death I61.9 - Nontraumatic intracerebral hemorrhage, unspecified R29.810 - Facial weakness I63.9 - Cerebrovascular accident (CVA), unspecified mechanism (CMS/HCC)

Weitere VAERSDATA-Felder

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

VAERS 1446385

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: IN
Alter: 64,0
Geschlecht: F
Eingang: 03.07.2021
Impfdatum: 15.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / -

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

Abnormal behaviour Death Malaise

Symptomtext

She started to feel very sick almost immediately after taking it. She wasn't herself (according to her husband, aka my girlfriend's dad) and she died on March 20th, 2021. Yet somehow the EMT had the nerve to try and pretend it wasn't because of the experimental mRNA thing you guys call a Vaccine.

Weitere VAERSDATA-Felder

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

VAERS 1440889

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: PA
Alter: 78,0
Geschlecht: M
Eingang: 01.07.2021
Impfdatum: 24.02.2021
Beginn: 22.06.2021
Tage bis Beginn: 118,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 Endotracheal intubation Intra-aortic balloon placement

Symptomtext

Patient was Positive for Covid-19 in September 2020, repeat testing in October showed negative result. Patient was vaccinated on 2/24/21 and 3/17/21 with Pfizer-BioNTech COVID-19 vaccine. Patient developed COVID 19 on 6/20/21, and was hospitalized for acute respiratory failure. Patient was intubated and required pressor support with norepinephrine and an IABP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Potassium, Telmisartan/HCTZ
Allergien: Contrast dye, latex, PCN
Vorherige Impfungen: -

VAERS 1437651

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: KY
Alter: 68,0
Geschlecht: M
Eingang: 30.06.2021
Impfdatum: 03.03.2021
Beginn: 03.06.2021
Tage bis Beginn: 92,0
Dosis: 2
Route/Site: IM / RA

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

Acute respiratory failure COVID-19 Chest X-ray abnormal Computerised tomogram spine Muscular weakness SARS-CoV-2 test false positive SARS-CoV-2 test positive

Symptomtext

Patient admitted 6/3/2021 found to be COVID-19 positive Event Description: Allergies (drug/food and reaction):__cephalosporine, clarithromycin Date of Vaccination 1 :__2/23/2021- Pfizer-Lot EN6198- uk- Left arm Date of Vaccination 2 :__3/23/2021- Pfizer ?lot EN6208- UK- right arm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 16,0
Labordaten: 6/4/2021 0513 COVID-19 by PCR Detected 6/6/2021 1700 COVID-19 by PCR Not Detected 6/7/2021 1412 COVID-19 by PCR Not Detected
Aktuelle Erkrankungen: Chief Concern, Brief History of Present Illness, and Hospital Course 68yo M with PMH including Parksinson's disease, oligodendroglioma (s/p chemo, radiation, resection), seizure disorder 2/2 brain cancer, BPH, CKD who presents for evaluation of progressively worsening weakness in lower extremities . Was evaluted by Neurology on presentation and dose of Sinemet updated. CT lumbar/Thoracic spine without acute abnormality. Was COVID + initially, but repeat test negative x 2, was not treated with Dexamethasone. This was likely a false positive. Plan for discharge to acute rehab which was denied by insurance and which wife is appealing. Pt has been finally accepted to a rehab facility and has an ambulance set for 1 pm today. Has CKD with Cr stable On room air Rest of the hospital course is as follows: ACUTE: #Acute hypoxic respiratory failure: resolved #Possible obstructive sleep apnea: -pt was hypoxic overnight at sleep on 6/15-6/16. Doesn't use oxygen at home -CXR on 6/16 was stable in comparison to CXR from 6/5. Changes in CXR likely represent old COVID exposure. As he is no longer hypoxic, and has no other evidence of pneumonia, further imaging is not pursued.
Vorgeschichte: Parkinson's, oligodendroglioma, seizure disorder 2/2 brain cancer, BPH, CKD,
Andere Medikamente: acetaminophen PRN, aspirin, atorvastatin, carbiopd-levodopa, certirizine, cholecalciferol, lamotrigine, levetiracetam, levothyroxine, mirabegron, multi-vitamin, phenyleprhrine-mineral oil, Miralax, tamsulosin
Allergien: ceftriaxone (anaphylaxis), cefuroxime (SOB, Swelling, rash), cephalosporins (anaphylaxis) , Clarithromycin (anaphylaxis), bactrim (rash)
Vorherige Impfungen: -

VAERS 1437462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 80,0
Geschlecht: U
Eingang: 30.06.2021
Impfdatum: 06.04.2021
Beginn: 25.06.2021
Tage bis Beginn: 80,0
Dosis: UNK
Route/Site: - / -

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

Cerebrovascular accident

Symptomtext

I63.9 - Acute CVA (cerebrovascular accident) (CMS/HCC)

Weitere VAERSDATA-Felder

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

VAERS 1433809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: IN
Alter: 71,0
Geschlecht: F
Eingang: 29.06.2021
Impfdatum: 17.03.2021
Beginn: 09.05.2021
Tage bis Beginn: 53,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Condition aggravated Death Nucleic acid test

Symptomtext

Death 5/19/2021 Causes of death listed on death certificate: 1) COVID 19

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: RT-PCR or other NAAT test
Aktuelle Erkrankungen: 1) COVID 19
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1433253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 90,0
Geschlecht: F
Eingang: 29.06.2021
Impfdatum: 05.04.2021
Beginn: 11.05.2021
Tage bis Beginn: 36,0
Dosis: UNK
Route/Site: - / -

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

Acute myocardial infarction

Symptomtext

I21.4 - Non-ST elevation (NSTEMI) myocardial infarction

Weitere VAERSDATA-Felder

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

VAERS 1433148

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 50,0
Geschlecht: F
Eingang: 29.06.2021
Impfdatum: 01.04.2021
Beginn: 13.06.2021
Tage bis Beginn: 73,0
Dosis: UNK
Route/Site: - / -

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

Acute myocardial infarction Gastrointestinal haemorrhage Pneumonia

Symptomtext

J18.9 - Pneumonia I21.4 - NSTEMI (non-ST elevated myocardial infarction) (CMS/HCC) K92.2 - GI bleed

Weitere VAERSDATA-Felder

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

VAERS 1432917

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 73,0
Geschlecht: F
Eingang: 29.06.2021
Impfdatum: 12.03.2021
Beginn: 17.05.2021
Tage bis Beginn: 66,0
Dosis: UNK
Route/Site: - / -

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

Acute myocardial infarction

Symptomtext

NSTEMI (non-ST elevated myocardial infarction)

Weitere VAERSDATA-Felder

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

VAERS 1429845

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: PA
Alter: 37,0
Geschlecht: F
Eingang: 26.06.2021
Impfdatum: 19.05.2021
Beginn: 11.06.2021
Tage bis Beginn: 23,0
Dosis: 1
Route/Site: SYR / LA

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

Exposure during pregnancy Foetal death Foetal heart rate abnormal Ultrasound foetal Uterine dilation and evacuation

Symptomtext

Received 2nd dose at end of first trimester. Had healthy pregnancy with weekly scans. Strong growth and heart rate. No abnormalities detected during ultrasound on June 2nd (when I was 13.5 weeks pregnant). NIPT showed no abnormalities and they considered viable pregnancy. 2 1/2 weeks after vaccine, I went for routine doctor visit and baby had no heart beat. I STRONGLY believe this was the result of the Covid vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Foetal death
Hospital-Tage: -
Labordaten: June 2nd (NIPT ultrasound and blood work) where pregnancy confirmed as viable, strong heartbeat and no abnormalities detected. No trisomy or downs. This was the last ultrasound before we learned on June 11th (at a regular doctors visit) that the baby died. Went to the hospital on June 14th for a D&E surgery.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Pre natal vitamins
Allergien: None
Vorherige Impfungen: -

VAERS 1423397

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: IN
Alter: 66,0
Geschlecht: M
Eingang: 24.06.2021
Impfdatum: 16.03.2021
Beginn: 14.04.2021
Tage bis Beginn: 29,0
Dosis: 2
Route/Site: - / LA

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

Blood pressure increased Blood test Catheter placement Echocardiogram Myocardial infarction Urine analysis

Symptomtext

Heart attack, Elevated blood pressure

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: heart cath, blood, urine, ecko, cardiac unltra sound.
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NARCO
Allergien: NONE
Vorherige Impfungen: -

VAERS 1420505

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: ND
Alter: 65,0
Geschlecht: F
Eingang: 23.06.2021
Impfdatum: 11.03.2021
Beginn: 22.04.2021
Tage bis Beginn: 42,0
Dosis: 2
Route/Site: IM / LA

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

Pulmonary embolism

Symptomtext

Patient presented to the ED and was subsequently hospitalized for pulmonary embolism within 6 weeks of receiving COVID vaccination.

Weitere VAERSDATA-Felder

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

VAERS 1419908

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: IN
Alter: 64,0
Geschlecht: M
Eingang: 23.06.2021
Impfdatum: 16.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Acute respiratory failure Asthenia Biopsy Computerised tomogram Cough Dyspnoea Hypoxia Investigation Laboratory test Pneumonia staphylococcal Pyrexia SARS-CoV-2 test Weight decreased X-ray

Symptomtext

Acute respiratory failure with hypoxia; Acute respiratory failure with hypoxia; Couldn't breathe; Pneumonia due to MRSA/Ground glass pneumonia; weak; lost 20 pounds; fever; Cough; This is a spontaneous report from a contactable consumer (the patient himself). A 64-year-old male patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number EN6208, Exp 30Jun2021) via an unspecified route of administration in arm left on 16Apr2021 11:00AM (at the age of 64-year-old) at single dose for COVID-19 immunisation. Relevant medical history included heart disease ongoing from 1997 (this happened in 1997 and the patient had been living with it for a little while), heart attack, pacemaker defibrillator because of cardiac arrest (in 2011), atrial fibrillation (diagnosed a little while, he was not sure and had been in and out of the hospital and to heart doctor quite a bit) and hypertension. The patient was administered with first shot of BNT162b2 (Lot number EW0153) in left shoulder on 16Mar2021 11:00AM (at the age of 64-year-old). Concomitant medications were not reported. On 16Apr2021 after the second dose, the patient was fine. There were no reactions after the first dose, but the second dose two days after he started developing a cough and fever. He thought it was a side effect but then ended up in the ER with pneumonia. They gave him antibiotics and sent him home. He went through the antibiotics and went back because he was still sick and not responding. They gave him more antibiotics and sent him home. He went through that batch and ended up really bad so he had to call an ambulance a few weeks later. He was diagnosed with MRSA Pneumonia and stayed in the hospital for 5 days. Then, he was discharged. He went back to the ER again a few days later because he did not seem to be improving. He was coughing and was weak. He was given another batch of antibiotics. He did not know if it was from the shot or what - he was healthy until then. The patient added that she lost 20 pounds and confirmed that it was following the vaccine. Two days after the vaccine, maybe it was 19Apr2021, he had a fever and it was now gone (exact dates were unknown). Cough happened at the same time of the fever but it was not as bad, and then progressively got worse. His lungs started filling up. They thought it was COVID. by the x-rays it looked like COVID lung but they took a sample and it was MRSA (exact dates were unknown). His admission was 18May2021 and was for acute respiratory failure with hypoxia. Discharge paperwork said acute chronic combined systolic diastolic congestive heart failure but he has had that for many years. It also stated primary hypertension but he has had that. The paperwork sayid pneumonia due to MRSA and pneumonia due to unspecified organism. He was hospitalized 18May2021 through 23May2021 with pneumonia and the reason he was hospitalized was because he could not breathe. Lost 20 pounds: after he started getting sick from the beginning of it all, he was coughing and losing weight and all that. It may not be quite 20 pounds, maybe 17, but he just knew that he was down quite a bit. He was 160s now, he was high 170s before (as reported). Treatment included Lasix and all kinds of different antibiotics. They were giving him, he did not know what it was, at first. Then, they narrowed it down and once they found out it was MRSA they gave him Clindamycin he believes. Investigations: they did CT scans, chest X-rays, and labs but he does not know any information. Each time they did a chest x-ray, when he went to get a chest x-ray, each one was worse all the way up to when he was admitted. When he went, they did a bronchial scope or whatever, he was not sure, and they saw lots of swelling and infiltrate. He did not know what this meant, stuff was infiltrating into the tissue and it was not just in the airways. He added it looked like ground glass pneumonia is what they said. The patient added that he was usually pretty active and cannot do anything anymore. He had three or four Covid tests, all negative, no additional details provided. Outcome of the events was unknown. Follow-up attempts are needed. Further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: Test Name: Sample; Result Unstructured Data: Test Result:MRSA; Test Date: 202105; Test Name: CT scans; Result Unstructured Data: Test Result:Unknown; Test Date: 202105; Test Name: bronchial scope; Result Unstructured Data: Test Result:they saw lots of swelling and infiltrate; Test Date: 202105; Test Name: Labs; Result Unstructured Data: Test Result:Unknown; Test Date: 202105; Test Name: X-ray; Result Unstructured Data: Test Result:Looked like COVID; Test Name: COVID test; Result Unstructured Data: Test Result:Negative; Comments: Three or four tests
Aktuelle Erkrankungen: Heart disease, unspecified (Verbatim: heart disease)
Vorgeschichte: Medical History/Concurrent Conditions: AFib (Verbatim: afib); Cardiac arrest; Defibrillator/pacemaker insertion (Verbatim: pacemaker defibrillator because of cardiac arrest); Heart attack (Verbatim: heart attack); Hypertension
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1414511

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: FL
Alter: 70,0
Geschlecht: M
Eingang: 21.06.2021
Impfdatum: 18.03.2021
Beginn: 26.04.2021
Tage bis Beginn: 39,0
Dosis: 2
Route/Site: IM / RA

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

Basophil count increased Blood albumin normal Blood cholesterol normal Blood phosphorus normal Blood triglycerides increased Cerebrovascular accident Dysstasia Eosinophil count increased Fall Grip strength decreased Haemoglobin decreased Hemiplegia High density lipoprotein normal Low density lipoprotein normal Magnetic resonance imaging head Mean cell haemoglobin concentration normal Movement disorder Nucleated red cells

Symptomtext

Ok on 4/26/2021 at 10:00PM I was going to bed and I had some water and I dropped it and I had a bottle of medication and I dropped that as well. I went to pick it up and I could not pick it up, I fell onto the bed and I could not get up. My left leg and left arm were paralyzed and I could barely speak. I could tell I could was having a stroke and I called my wife in as best I could and they called 911. They determined yes it was a stroke and they took me to the ambulance. When I was in the ambulance it went away, it only lasted about 15 minutes. I was taken to the hospital and stayed there for three days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: MRI without contrast 4/27/2021 Phosphorous 3.2, albumin 3.8, Triglycerides 169H, Cholesterol 170, LDL chol 97, HDL chol 39, HDL risk factoer 4.4 WBC 4.2, RBC 4.23 L, HGB 13.1 L, MCHC 32.4, RDW 13.4 EOS 5.2, BASO 1.0, Nucleated RBC 0
Aktuelle Erkrankungen: n/a
Vorgeschichte: Pre diabetic type 2, low thyroid, asthma
Andere Medikamente: Advair 2x daily, Pioglitazone, Levothyroxine, Antihistamine as needed
Allergien: N/a
Vorherige Impfungen: -

VAERS 1388607

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MN
Alter: 38,0
Geschlecht: M
Eingang: 10.06.2021
Impfdatum: 26.03.2021
Beginn: 06.04.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: IM / LA

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

Blood cholesterol normal Cardiac arrest Chest pain Electrocardiogram normal Stent placement Thrombectomy Thrombosis

Symptomtext

Chest pains while working out since receiving the vaccine. Ultimately, two blood clots were formed and caused a cardiac arrest May 25th, 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 3,0
Labordaten: May 25, 2021: Two blood clots were removed, and two stents were placed in the arteries. EKG after the stents show normal heart operation. No significant plaque buildup in arteries. Cholesterol is in good range.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: daily multi vitamin, magnesium
Allergien: N/A
Vorherige Impfungen: -

VAERS 1384625

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: AR
Alter: 56,0
Geschlecht: M
Eingang: 09.06.2021
Impfdatum: 26.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Cerebral haemorrhage

Symptomtext

brain bleed; This is a spontaneous report from a contactable consumer (patient's wife) via Pfizer sponsored program support. This is the first report of 2 reports, for the first dose. A 56-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration at age of 56-years, administered in left upper bicep on 26Mar2021 (Lot Number: EN6208) as single dose for COVID-19 immunisation. Medical history included ongoing diabetes and the patient had it for 10 years or so and was diet controlled, his blood sugars was good. And ongoing supraventricular tachycardia (SVT) for about 4 years and was medication control. And patient was an amputee from an accident many years ago. Concomitant medications included ongoing carvedilol (COREG) taken for SVT. It was reported that the patient had a brain bleed after the first dose that might be but probably wasn't related to the vaccine. Event outcomes was unknown. No follow-up attempts needed. No further information expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021596614 same reporter/patient/drug, different event/dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Diabetes (the patient had it for 10 years or so and was diet controlled, his blood sugars was good); Supraventricular tachycardia (He hd this diagnoses for about 4 years and was medication control.)
Vorgeschichte: Medical History/Concurrent Conditions: Amputee (from an accident many years ago.)
Andere Medikamente: COREG
Allergien: -
Vorherige Impfungen: -

VAERS 1378788

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 61,0
Geschlecht: M
Eingang: 07.06.2021
Impfdatum: 05.04.2021
Beginn: 17.05.2021
Tage bis Beginn: 42,0
Dosis: UNK
Route/Site: - / -

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

Acute kidney injury Acute myocardial infarction

Symptomtext

I21.4 - Non-ST elevation (NSTEMI) myocardial infarction N17.9 - Acute kidney failure, unspecified

Weitere VAERSDATA-Felder

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

VAERS 1218667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: NY
Alter: 87,0
Geschlecht: F
Eingang: 07.06.2021
Impfdatum: 16.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Amyotrophic lateral sclerosis Headache Hypertension Cerebral haemorrhage Computerised tomogram Death Electrocardiogram Magnetic resonance imaging

Symptomtext

First Vaccine March 26, 2021 -individual received the vaccine approximately 8 15 AM, for the better part of the day was was tired, uncoordinated and disorientated. Upon waking from a nap, speech was slurred and was brought immediately to Hospital ER, diagnosed with a CVA (Cerebral Vascular Accident)/ Stroke and a non ST elevated myocardial infarction. Individual was admitted for 5 days and released on March 31. She was then under care of her primary doctor and a neurologist. Both doctors were aware that she received the vaccine, and were aware that she was to receive the second vaccine. (Dates of those appointments April 5th and 7th. Second Vaccine April 16, 2021 - individual received the vaccine approximately 8:20 AM. I accompanied my Mother to both appointments) and we advised of the prior incident CVA and NSTEMI and hospital stay, and not further action or discussion was initiated. We were given at tag to say we had to wait 30 minutes post the vaccine. Less than a few minutes in the waiting room, my Mother complained of a severe headache, and we immediately advised the paramedic in the room and immediately they took her into a private medical room,, EMS attached EKG's along with cuffs for blood pressure. The head pain was severe and they immediately transferred her to an ambulance and brought to Hospital Emergency Room, She suffered a cerebral hemorage and it was non recoverable, and she died approx 3 30 that afternoon

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: -
Labordaten: MRI, CAT SCANS
Aktuelle Erkrankungen: Yes, On the day of the first vaccine March 26, 2021 that afternoon admitted to the hospital that evening with a stroke and a non-ST elevated myocardial infarction. Was admitted to the hospital for 5 days, released on March 31st.
Vorgeschichte: Atrial fibrillation, High Blood Pressure, UTI. High Blood Pressure
Andere Medikamente: Eliquis 5 mg, 2 x per day total 10 mg Lisinopril 10 mg 1 x per day Toprol 25 mg, 2 x per day Prilosec 20 mg 1 x per day Ferrous Sulfate (Iron) 25 Mg 2x per day Aspirin 81 mg Tablet, 1 x per day Vitamin C 250 mg, 2x per day, total 500 mg Vit
Allergien: Penicillin, Nitrofurantoin, Azithromycin
Vorherige Impfungen: -

VAERS 1374122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 75,0
Geschlecht: F
Eingang: 04.06.2021
Impfdatum: 17.03.2021
Beginn: 17.05.2021
Tage bis Beginn: 61,0
Dosis: UNK
Route/Site: - / -

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

Death Pneumonia

Symptomtext

death J18.9 - Pneumonia, unspecified organism

Weitere VAERSDATA-Felder

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

VAERS 1369067

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: FL
Alter: 68,0
Geschlecht: M
Eingang: 02.06.2021
Impfdatum: 16.03.2021
Beginn: 30.05.2021
Tage bis Beginn: 75,0
Dosis: 2
Route/Site: SYR / RA

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

Angiogram pulmonary abnormal Pulmonary embolism

Symptomtext

30 May 2021 I was diagnosed as an otherwise healthy male with pulmonary embolism in the lower right lung. No predispositions to blood clots.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: CT Angiogram of the chest. Final report available at Hospital
Aktuelle Erkrankungen: None
Vorgeschichte: Mild hypertension (8 years)
Andere Medikamente: Amlodipine 10mg
Allergien: None
Vorherige Impfungen: -

VAERS 1368164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 66,0
Geschlecht: F
Eingang: 02.06.2021
Impfdatum: 01.04.2021
Beginn: 26.05.2021
Tage bis Beginn: 55,0
Dosis: UNK
Route/Site: - / -

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

Gastrointestinal haemorrhage Pulmonary embolism

Symptomtext

K92.2 - GI bleed I26.99 - Acute pulmonary embolism without acute cor pulmonale, unspecified pulmonary embolism type (CMS/HCC)

Weitere VAERSDATA-Felder

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

VAERS 1367744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MI
Alter: 80,0
Geschlecht: M
Eingang: 02.06.2021
Impfdatum: 27.03.2021
Beginn: 04.05.2021
Tage bis Beginn: 38,0
Dosis: 2
Route/Site: IM / AR

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

Angiogram pulmonary abnormal Anticoagulant therapy Deep vein thrombosis Dyspnoea Pulmonary embolism Ultrasound Doppler abnormal

Symptomtext

Patient presented to the ED on 5/5 after being sent by his PCP after an ultrasound in the office showed a DVT along with patient's complaint of shortness of breath. Patient denied history of DVT/PE. In the ED, CTA-PE showed bilateral pulmonary embolic disease and Ultrasound confirmed acute right lower extremity DVT. Patient was started on a heparin drip and then switched to enoxaparin 1 mg/kg every 12 hours per pulmonary. Hematology/Oncology was consulted and determined that acute bilateral PE likely provoked by recent vaccination with the second dose of the Pfizer vaccine. Patient was switched to rivaroxaban 20 mg daily prior to discharge for planned duration of 3 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 4,0
Labordaten: 5/4/21 CTA PE: Bilateral pulmonary embolic disease, right more extensive than left 5/7/21 Vasc Bilateral Lower Extremity Venous Duplex: Deep venous thrombosis involving the right lower extremity predominantly the mid and distal femoral vein and right popliteal vein.
Aktuelle Erkrankungen: None
Vorgeschichte: Arthritis, CHF, T2DM, GERD, Hypercholesteremia, sleep apnea, TIA, ulcer
Andere Medikamente: aspirin 81 mg daily, celecoxib 100 mg twice daily, docusate 10, docusate 100 mg twice daily, emagliflozin 25 mg once daily, gabapentin 300 mg every 12 hours, norco 5-325 mg every 4 hours as needed for pain, pitavastatin 2 mg once daily
Allergien: Erythromycin (GI distress, N/V)
Vorherige Impfungen: -

VAERS 1366598

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MN
Alter: 86,0
Geschlecht: F
Eingang: 02.06.2021
Impfdatum: 24.03.2021
Beginn: 09.05.2021
Tage bis Beginn: 46,0
Dosis: 2
Route/Site: SYR / LA

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

Blood loss anaemia Blood test Computerised tomogram intestine Death Electrocauterisation Endoscopy gastrointestinal abnormal Haemoglobin decreased Internal haemorrhage Intestinal mucosal tear Rectal examination Upper gastrointestinal haemorrhage

Symptomtext

Onset acute blood loss due to internal bleeding on approximately 05/09/21, upper GI bleeding and anemia. Hemoglobin dropped to 5.2 resulting in death. Hospitalization on 05/12/21 discharged to Hospice Care 05/15/21 loss of life on 05/22/21.

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Praegender Schweregrund: Death
Hospital-Tage: 3,0
Labordaten: 05/12/21 lab (blood) tests hemoglobin 5.6 and rectal exam to determine source of bleeding. CT Scan, Endoscopy resulting in cauterization of tear in lower intestine. Unable to view all tears. Next blood test shows hemoglobin 5.2.
Aktuelle Erkrankungen: Congestive heart failure Atrial fibrillation Lymphadema
Vorgeschichte: Congestive heart failure Atrial fibrillation Previous replacement of aortic valve
Andere Medikamente: Furosemide, acidophilus, allopurinol, ferrous sulfate, latanaprost, levothyroxine, magnesium oxide, multivitamin, potassium chloride. ascorbic acid. B complex, diltiazem, metoprolol succinate, vitamin D-3, warfarin
Allergien: Erythromycin
Vorherige Impfungen: -

VAERS 1362402

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 90,0
Geschlecht: M
Eingang: 31.05.2021
Impfdatum: 15.03.2021
Beginn: 05.05.2021
Tage bis Beginn: 51,0
Dosis: 2
Route/Site: IM / LA

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

Acute kidney injury Death Hyponatraemia Hypoosmolar state

Symptomtext

death N17.9 - Acute kidney failure, unspecified E87.1 - Hypo-osmolality and hyponatremia

Weitere VAERSDATA-Felder

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

VAERS 1361104

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge En6208

kritisch

Staat: MD
Alter: 56,0
Geschlecht: M
Eingang: 29.05.2021
Impfdatum: 26.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain upper Burning sensation Chest pain Computerised tomogram thorax abnormal Flank pain Hypoaesthesia Pain Paraesthesia Pulmonary embolism Scan with contrast abnormal

Symptomtext

Within a week after first vaccine dose, burning in legs from above the knee to feet. Numbness and tingling in fingers and feet. Symptoms continue. Within a week after second vaccine, onset of bilateral upper quadrant pain, thoracic and flank pain that worsened over time. Unable to lie down due to sharp pain. Reached out to Oncology and PCP offices after symptoms of both vaccines for awareness and guidance. 5/4/21 - Emergency and inpatient visit - diagnosed with bilateral pulmonary emboli.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: CT scan with contrast - Bilateral PE
Aktuelle Erkrankungen: None
Vorgeschichte: Diffuse Large B-Cell Lymphoma, Acid Reflux
Andere Medikamente: Vitamin D, Omeprazole
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1358345

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: IN
Alter: 59,0
Geschlecht: M
Eingang: 28.05.2021
Impfdatum: 10.04.2021
Beginn: 01.05.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: IM / LA

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

Death Pulmonary embolism

Symptomtext

My husband died May 1st, 3 weeks after his last vaccine April 10 . He had a saddle pulmonary emboli. He did not have any symptoms that I knew of prior to May 1st. Entering info for research data.

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: na
Aktuelle Erkrankungen: none
Vorgeschichte: Diabetes, 7- CABG, veracious veins, Hx of Kidney stones , HTN, Hx of gastric bypass, Hx of stroke (L Basilar) with hearing loss in L ear, Orchiectomy due to veracious vein,
Andere Medikamente: Vit. C, ASA 81mg, Calcium Carbonate with Vit. D, Clopidogrel 75mg, Iron, Folic acid, Gabapentin 900mg bid, HCTZ 25mg, Lisinopril 20mg, Magnesium, Metformin 500mg bid, Metoprolol XL 100mg, astrostatin 40mg, Tylenol 500mg , Wellbrutin 300mg,
Allergien: NKMA
Vorherige Impfungen: -

VAERS 1357369

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: VA
Alter: 39,0
Geschlecht: M
Eingang: 28.05.2021
Impfdatum: 11.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: - / -

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

Pulmonary embolism

Symptomtext

Passed away from a Pulmonary Embolism; This is a spontaneous report from a contactable consumer. A 39-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration at the age of 39 years old, on 11Mar2021 (Lot Number: EN6208) as single dose for covid-19 immunisation. Medical history included wolff-parkinson-white syndrome from an unknown date to 15Mar2021. The patient was diagnosed with this later in life, but was told he probably had it his entire life it just hadn't caused any issues for him. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient's concomitant medications were not reported. The patient previously got the flu vaccine for immunization every year with no issues. The patient passed away from a pulmonary embolism on 15Mar2021. The patient was not hospitalized prior to his death. He died from the pulmonary embolism in his sleep. The reporter denied any medications, labs, testing, or treatments for her husband relevant to these events. The patient died on 15Mar2021. There was a private autopsy performed and they said that the Pfizer Covid Vaccine was one of the contributing factors to the patient's death. The autopsy said the vaccine was a contributing factor. The reporter stated she told them since they said it was the pulmonary embolism that killed him, then that's what it should say. The Medical Examiner was saying that the science for the vaccine is so new, they just don't have the data that they need.; Reported Cause(s) of Death: Pulmonary embolism

Weitere VAERSDATA-Felder

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

VAERS 1338605

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 80,0
Geschlecht: F
Eingang: 21.05.2021
Impfdatum: 12.03.2021
Beginn: 21.03.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: IM / LA

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

Acute kidney injury Death

Symptomtext

Death Acute kidney injury

Weitere VAERSDATA-Felder

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

VAERS 1338394

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 39,0
Geschlecht: M
Eingang: 21.05.2021
Impfdatum: 07.04.2021
Beginn: 07.05.2021
Tage bis Beginn: 30,0
Dosis: 1
Route/Site: IM / LA

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

Acute kidney injury Chest pain Death Fatigue Nausea

Symptomtext

Death N17.9 - Acute kidney failure, unspecified FATIGUE CHEST PAIN NAUSEA

Weitere VAERSDATA-Felder

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

VAERS 1331545

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: PA
Alter: 78,0
Geschlecht: M
Eingang: 19.05.2021
Impfdatum: 12.03.2021
Beginn: 28.03.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: IM / LA

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

Acute myocardial infarction Acute respiratory failure Adenovirus test Anticoagulant therapy Atrial fibrillation Blood test Bordetella test negative COVID-19 COVID-19 pneumonia Cardiomyopathy Chronic kidney disease Coronavirus test negative Enterovirus test negative Essential hypertension Human rhinovirus test Influenza A virus test negative Influenza B virus test Pneumonia

Symptomtext

ED to Hosp-Admission Discharged 3/28/2021 - 4/2/2021 (5 days) Treatment team. Acute hypoxemic respiratory failure due to COVID-19 Principal problem Discharge Summary (Physician) Internal Medicine Discharge Summary Hospitalist Medicine Admission Date: 3/28/2021 PCP: (doctor) Length of Stay: 5 Days Discharging provider: (doctor) Discharge Date: 4/2/2021 Admission Diagnosis Hospital Problems POA * (Principal) Acute hypoxemic respiratory failure due to COVID-19 Yes Cardiomyopathy Yes Obstructive sleep apnea syndrome Yes Essential hypertension Yes Type 2 diabetes mellitus Yes Presence of automatic (implantable) cardiac defibrillator Unknown Pneumonia due to 2019 novel coronavirus Yes Stage 4 chronic kidney disease Yes Pneumonia of both lungs due to infectious organism, unspecified part of lung Yes Atrial fibrillation with rapid ventricular response Yes NSTEMI (non-ST elevated myocardial infarction) Yes Hospital Course: Patient is a pleasant 79-year-old male admitted due to acute hypoxic respiratory secondary COVID-19 pneumonia. He was continued on dexamethasone for the COVID-19 pneumonia however the medicine was relatively contraindicated due to renal failure. Patient was seen by cardiology continued on aspirin beta-blocker and statin for non-STEMI and already was anticoagulated with Xarelto which is continued. Patient's oxygenation requirements did improve and he was set up for home oxygen prior to discharge. Patient was continue with PT and OT and slowly did well he was doing well clinically at this time may be discharged home for convalescence as per protocol. Patient may follow-up with PCP and specialist as noted

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 5,0
Labordaten: 03/28/21 2220 Respiratory virus detection panel Collected: 03/28/21 2114 | Final result | Specimen: Swab from Nasopharynx Adenovirus Not Detected Mycoplasma pneumoniae Not Detected Chlamydophila pneumoniae Not Detected Parainfluenza Not Detected COVID-19 SARS-CoV-2 Overall Result DetectedCritical Enterovirus/Rhinovirus Not Detected Coronavirus Not Detected Respiratory Synctial Virus Not Detected Influenza A Not Detected Bordetella pertussis Not Detected Influenza B Not Detected Bordetella parapertussis Not Dete
Aktuelle Erkrankungen: -
Vorgeschichte: Respiratory Obstructive sleep apnea syndrome Pneumonia due to 2019 novel coronavirus Acute hypoxemic respiratory failure due to COVID-19 Pneumonia of both lungs due to infectious organism, unspecified part of lung Circulatory Cardiomyopathy Essential hypertension Atrial fibrillation with rapid ventricular response NSTEMI (non-ST elevated myocardial infarction) Digestive Obesity, morbid Genitourinary Stage 4 chronic kidney disease Endocrine/Metabolic Insulin dependent type 2 diabetes mellitus, uncontrolled Other Implantable defibrillator reprogramming/check Central sleep apnea syndrome Presence of automatic (implantable) cardiac defibrillator
Andere Medikamente: allopurinoL (ZYLOPRIM) 100 mg tablet aspirin 81 mg tablet BYDUREON 2 mg/0.65 mL pen injector calcitrioL (ROCALTROL) 0.25 mcg capsule furosemide (LASIX) 40 mg tablet gabapentin (NEURONTIN) 100 mg capsule HumuLIN 70/30 U-100 KwikPen 100 unit/
Allergien: Prednisone
Vorherige Impfungen: -

VAERS 1331259

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: PA
Alter: 81,0
Geschlecht: F
Eingang: 19.05.2021
Impfdatum: 10.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / RA

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

Acute respiratory failure Atrial fibrillation Bilevel positive airway pressure Bladder catheterisation COVID-19 pneumonia Chills Dyspnoea Ejection fraction Endotracheal intubation Hypotension Intensive care International normalised ratio increased Oxygen saturation decreased Pain Pneumonia aspiration Pulmonary congestion Pyrexia SARS-CoV-2 test positive

Symptomtext

Office Visit 3/20/2021 Urgent Care PA-C Family Medicine COVID-19 +1 more Dx Fever Reason for Visit Progress Notes PA-C (Physician Assistant) ? ? Family Medicine ? ? Encounter Date: 3/20/2021 ? ? Signed Cosigned by: MD at 3/29/2021 9:22 AM Expand AllCollapse All 1. Viral URI 2. Chest congestion MDM Number of Diagnoses or Management Options Viral URI: new, needed workup Diagnosis management comments: The patient's current medications, allergies, problem list, and family history were reviewed. Please see the physical exam. The patient See HPI and physical exam to review pertinent information regarding visit. Images available were reviewed by me and reviewed with pt/family. Prescription medication recommendations were reviewed in light of the patient's age, past medical history and comorbidities.Plan of care reviewed; patient agrees with plan. See patient discharge instructions for more details. Follow up with PCP if symptoms do not improve or go to ER if symptoms worsen. Patient was seen today for fever. Diagnoses and all orders for this visit: Viral URI Chest congestion - POCT COVID-19 Antigen There are no Patient Instructions on file for this visit. History Chief Complaint Patient presents with ? Fever Fever 101 this morning.chest congstion, body aches, chills since Thursday. HPI Patient is a 81 y.o. female presents complaining of chest congestion, cough, body aches and pain in her chest with breathing for the past 2 or 3 days. She denies any loss of taste/smell, sore throat, shortness of breath, vomiting or diarrhea. ED to Hosp-Admission Discharged 3/22/2021 - 4/18/2021 (27 days) Hospital MD Last attending ? Treatment team Acute hypoxemic respiratory failure due to COVID-19 Principal problem Discharge Summary MD (Physician) ? ? Internal Medicine Discharge Summary Hospitalist Medicine Date: 4/18/2021 Admission Date: 3/22/2021 PCP: CRNP Length of Stay: 27 Days Discharging provider: MD Discharge Date: 4/18/2021 Admission Diagnosis Medical Problems Hospital Problems POA * (Principal) Acute hypoxemic respiratory failure due to COVID-19 Yes Myasthenia gravis without exacerbation Yes Toxic diffuse goiter without crisis Yes Long term current use of anticoagulant therapy Not Applicable Hashimoto's thyroiditis Yes Persistent atrial fibrillation Yes Aspiration into airway Yes COVID-19 Yes Anemia, normocytic normochromic Unknown HPI: 81-year-old female with reported myasthenia gravis diagnosed with myasthenia gravis in 2016 noted 5 weeks after finding to have difficulty swallowing and breathing requiring intubation had Plex during admission she was subsequently placed on CellCept and prednisone for long-term but was subsequently weaned off and now follows with neurology Dr., history of thoracic stenosis neck arthritis, Hashimoto's thyroiditis hyperthyroidism on methimazole, heart failure with LVEF of 45%, and atrial fibrillation on Coumadin and rate control agents following with Cardiology who presented to the Hospital on 03/22/2021 with acute hypoxic respiratory failure. The patient reportedly received her Pfizer first vaccine [per patient's son unclear date-but was reported to be due for her second vaccine at the end of this month] and subsequently was found to have fevers and chills on Saturday for which she went to urgent care and was found to be COVID-19 positive for which she was recommended for Tylenol and supportive care. On 03/22/2021 it was reported that she was found by EMS to have acute hypoxic respiratory failure with oxygen saturation in the 50s unclear for how long this had occurred for for which patient was emergently intubated. There was a concern for possible aspiration as as well given unclear how long she was hypoxic for for which she was started on cefepime and vancomycin protocol. Procalcitonin level was ordered. Hospital Course: Please see in details from H&P initially from critical care since patient was being they are almost 22 days. There is multiple consult including cardiologist palliative care note as well as urologist consult note In briefly this is a very pleasant 81-year-old female she had a history of myasthenia gravis currently treated with Dr. not in medication now for myasthenia gravis chronic atrial fibrillation long-term use of anticoagulation Coumadin history of toxic goiter currently on methimazole she was admitted initially on March 22 because she was having chills fever shortness of breath and EMS found that she is having acute hypoxic respiratory failure oxygen saturation is only 50% and emergently intubated admitted in critical care unit. Patient was intubated on March 22 meanwhile patient has a complicated series whilst she was in ICU. She was treated twice for septic shock she was treated first Covid pneumonia respiratory failure with possible aspiration. She was unable to extubate almost 19 days. Eventually she was extubated on 1 April 9. After that patient initially on BiPAP and then she tolerated nasal cannula successfully currently 3 L of oxygen. Meanwhile because of sepsis aspiration pneumonia COVID-19 pneumonia respiratory failure patient was treated with and also urinary tract infection patient was treated with multiple antibiotic vancomycin and Maxipime. For COVID-19 pneumonia she also was treated for tract residual normal. And also Decadron. Patient was not a candidate for remdesivir at that point. After extubation patient, up very slowly patient was transferred to PCU because of tachycardia and hypotension unable to thread beta-blocker digoxin and Cardizem the medication was adjusted pretty slowly patient was started Lovenox injection for bridging Coumadin Coumadin was initially hold been longtime and then after Lovenox injection and Coumadin was started patient currently INR is 1.9 today. She was Coumadin been longtime because her Chad vascular score was high she also had a history of congestive heart failure in addition of chronic atrial fibrillation heart rate is fluctuated in the range of 80-120. She is currently on digoxin we will continue digoxin she is currently on Toprol which started 50 mg and currently 100 mg Toprol she also have a Cardizem with splitting the medication 120 mg p.o. twice daily. Heart rate is better controlled today blood pressure is low borderline this patient need to be watched even in the nursing home for further evaluation of medication adjustment. She also mentioned that she is having chronic hypokalemia potassium was replaced alert here and so then started potassium 20 M EQ p.o. twice daily may need to further adjustment and follow-up potassium in the nursing she she was tachycardic heart rate in module was started recently as 7 days ago now her heart rate is much better now this patient need to see endocrinologist also to follow-up. Patient was complicated with urinary retention and continue straight cath and finally ended up with Foley's catheter this patient must need to evaluate by urology for further evaluation of chronic urinary retention. Meanwhile patient clinically stable vitals are good she does not have any fever shortness of breath tolerable with 3 L of oxygen now she does not have any chest pain she is not in any myasthenia gravis medication this patient will benefit to see follow-up with pulmonary group for post Covid pneumonia require long-term intubation and also neurology for myasthenia gravis Dr. This patient will benefit to a urologist outpatient and also physician to nursing home need to adjust medication in the setting of hypotension tachycardia we will continue Coumadin current dose 7.5 mg and may need to further adjustment slowly. She is currently on 3 L of oxygen we will continue and titrate down slowly. Discharge disposition is nursing home Condition upon discharge patient is awake alert oriented no chest pain still 3 L of oxygen tolerable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 27,0
Labordaten: COVID-19: History Infection Status Resolved 4/18/2021 Probable COVID-19 (Resolved) Specimen information: Swab / Nares Added: 3/20/2021 by POCT COVID-19 Antigen (Collected 03/20/21) Onset date: 3/20/2021 Resolved: 4/18/2021 (Expired) Add: Rule-Out COVID-19 and Respiratory Viruses Add: SARS-CoV-2 (related to COVID-19) Add: Rule-Out SARS-CoV-2 (related to COVID-19) Add: Probable COVID-19
Aktuelle Erkrankungen: -
Vorgeschichte: Nervous Myasthenia gravis without exacerbation Eaton-Lambert syndrome Respiratory Acute hypoxemic respiratory failure due to COVID-19 Aspiration into airway Circulatory Essential hypertension Persistent atrial fibrillation Musculoskeletal Disorder of bone Endocrine/Metabolic Toxic diffuse goiter without crisis Hyperlipidemia Impaired fasting glucose Hashimoto's thyroiditis Hematologic Anemia, normocytic normochromic Infectious/Inflammatory COVID-19 Other Spinal stenosis Long term current use of anticoagulant therapy Insomnia Anxiety state
Andere Medikamente: acetaminophen 325 mg oral tablet digoxin (LANOXIN) 125 mcg (0.125 mg) tablet dilTIAZem CD (CARDIZEM CD) 120 mg 24 hr capsule(Expired) gabapentin (NEURONTIN) 600 mg tablet LORazepam (ATIVAN) 0.5 mg tablet methIMAzole (TAPAZOLE) 5 mg tablet m
Allergien: Immune Globulin,gamma (Igg) Human Amiodarone Analogues Atorvastatin Iodinated Contrast Media Lisinopril
Vorherige Impfungen: -

VAERS 1327468

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MD
Alter: 63,0
Geschlecht: F
Eingang: 18.05.2021
Impfdatum: 29.03.2021
Beginn: 30.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / -

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

Anal incontinence Death Dyspnoea Pain Pneumonia

Symptomtext

She did not have control of her bowels when sneezed or coughing. She complained of trouble breathing and in a lot of pain. She passed away on April 3 with pneumonia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Copd
Vorgeschichte: Copd Heart condition
Andere Medikamente: Albuterol Fluticasone Prednisone Advair Hydrochlorothazide Theophylline Amolodipine besylate Baby aspirin Clopidoqrel Cetirizine Metoprolol tartrate Gabapentin Atorvastatin Incruse Famotidine Montelulcast
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1317378

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 99,0
Geschlecht: F
Eingang: 14.05.2021
Impfdatum: 09.04.2021
Beginn: 08.05.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: IM / LA

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

Agitation Asthenia Bedridden Cachexia Cognitive disorder Confusional state Death Dyspnoea Hallucination Incontinence Livedo reticularis Loss of personal independence in daily activities Mobility decreased Patient uncooperative Respiratory rate decreased Restlessness Skin wound Unresponsive to stimuli

Symptomtext

This 99 year old female received the Covid shot on 4/9/21 and died on 5/8/21.

Weitere VAERSDATA-Felder

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

VAERS 1311448

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 83,0
Geschlecht: F
Eingang: 12.05.2021
Impfdatum: 29.03.2021
Beginn: 09.04.2021
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: IM / LA

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

Pulmonary embolism

Symptomtext

I26.99 - Acute pulmonary embolism, unspecified pulmonary embolism type, unspecified whether acute cor pulmonale present

Weitere VAERSDATA-Felder

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

VAERS 1310470

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MA
Alter: 76,0
Geschlecht: F
Eingang: 12.05.2021
Impfdatum: 12.03.2021
Beginn: 12.05.2021
Tage bis Beginn: 61,0
Dosis: 2
Route/Site: IM / -

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

Angiogram pulmonary abnormal Deep vein thrombosis Dyspnoea Fibrin D dimer increased Pulmonary embolism Ultrasound scan abnormal

Symptomtext

DVT and PE, pt p/w progresssive SOB 2nd dose recieved on 3/12/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: CTA of chest and LE ultrasound, positive D-dimer blood test
Aktuelle Erkrankungen: None
Vorgeschichte: Hx breast CA HTN HLD
Andere Medikamente: anastrozole 1mg PO daily HCTZ 12.5mg PO daily lisinopril 20mg PO daily Pravastatin 10mg PO daily
Allergien: Doxycycline
Vorherige Impfungen: -

VAERS 1285757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: PA
Alter: 40,0
Geschlecht: M
Eingang: 12.05.2021
Impfdatum: 28.04.2021
Beginn: 28.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain lower Computerised tomogram abdomen abnormal Renal infarct Urogram Abdominal pain Blood creatine phosphokinase normal Blood lactic acid Blood test C-reactive protein increased Cerebrovascular accident Computerised tomogram Decreased appetite Computerised tomogram abdomen Computerised tomogram head Computerised tomogram pelvis Echocardiogram Computerised tomogram abnormal Electrocardiogram normal

Symptomtext

part of my left kidney was no longer receiving blood; blood clot; placed on stroke protocols.; I developed severe abdominal pain in my left side during the evening; lack of appetite; bouts of severe discomfort; This is a spontaneous report from a contactable consumer (patient). A 40-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; Batch/Lot Number: EW0167) via an unspecified route of administration, administered in Arm Left on 28Apr2021 12:15 (40-years-old) as 2nd dose, single for COVID-19 immunization. The patient medical history was not reported. Vaccination Facility Type was clinic. Concomitant medications included ibuprofen (ADVIL); desloratadine (CLARINEX). The patient previously took first dose of BNT162B2 (lot number=EN6208) on 07Apr2021 01:15 PM (40-years-old) on Left arm for COVID-19 immunization. It was reported that the patient developed severe abdominal pain in my left side during the evening of Wednesday, 28Apr2021 19:00. The pain appeared sporadically throughout the evening and continued through Friday, April 30. During this time, he experienced a lack of appetite and bouts of severe discomfort. Tried treating with GasX and Tylenol. Duration of Hospitalization reported as 3 days. On Saturday, 01May2021, starting around 10:30 a.m., the pain in his left-side abdominal area intensified and did not diminish. After 6 hours, he visited the ER at hospital. After being admitted to the ER, a series of blood, urine and imaging tests were performed on me. The doctor on duty reported that a CT scan showed that part of my left kidney was no longer receiving blood (disability). He was placed on Heparin and admitted to the hospital. He was diagnosed with a blood clot and placed on stroke protocols. The adverse event result in Emergency room/department or urgent care. Treatment received for the adverse events was Heparin, fluids, blood work, urine analysis. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the events abdominal pain, lack of appetite, and bouts of severe discomfort was recovering; while other events was unknown. Events reported as serious due to hospitalization and life threatening.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: Test Date: 20210501; Test Name: Blood test; Result Unstructured Data: Test Result:Unknown; Test Date: 20210501; Test Name: CT scan; Result Unstructured Data: Test Result:CT scan showed that part of my left kidney was no; Comments: CT scan showed that part of my left kidney was no longer receiving blood.; Test Date: 20210501; Test Name: imaging test; Result Unstructured Data: Test Result:Unknown; Test Date: 20210501; Test Name: Urine test; Result Unstructured Data: Test Result:Unknown
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ADVIL; CLARINEX [DESLORATADINE]
Allergien: -
Vorherige Impfungen: -

VAERS 1307748

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 11.05.2021
Impfdatum: 22.03.2021
Beginn: 12.04.2021
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: IM / RA

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

Acute myocardial infarction

Symptomtext

NSTEMI (non-ST elevated myocardial infarction)

Weitere VAERSDATA-Felder

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

VAERS 1307366

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 75,0
Geschlecht: F
Eingang: 11.05.2021
Impfdatum: 24.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: IM / RA

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

Pulmonary embolism

Symptomtext

I26.99 - Pulmonary embolism

Weitere VAERSDATA-Felder

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

VAERS 1307334

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 53,0
Geschlecht: M
Eingang: 11.05.2021
Impfdatum: 12.04.2021
Beginn: 23.04.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: IM / RA

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

Acute myocardial infarction Myocardial infarction

Symptomtext

I21.4 - Non-ST elevation (NSTEMI) myocardial infarction

Weitere VAERSDATA-Felder

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

VAERS 1307313

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 11.05.2021
Impfdatum: 01.04.2021
Beginn: 05.04.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: UN / UN

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

Acute myocardial infarction Gastrointestinal haemorrhage Myocardial infarction

Symptomtext

I21.4 - NSTEMI (non-ST elevated myocardial infarction) K92.2 - Gastrointestinal hemorrhage, unspecified gastrointestinal hemorrhage type

Weitere VAERSDATA-Felder

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

VAERS 1303031

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 10.05.2021
Impfdatum: 17.03.2021
Beginn: 01.05.2021
Tage bis Beginn: 45,0
Dosis: 2
Route/Site: IM / RA

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

Death

Symptomtext

This 68 year old male received the Covid shot on 3/17/21 and died 5/21.

Weitere VAERSDATA-Felder

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

VAERS 1302683

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 10.05.2021
Impfdatum: 17.03.2021
Beginn: 01.05.2021
Tage bis Beginn: 45,0
Dosis: 2
Route/Site: IM / LA

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

Death

Symptomtext

This 70 year old female received the Covid shot on 3/17/21 and died on 5/1/21.

Weitere VAERSDATA-Felder

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

VAERS 1302224

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: NY
Alter: 59,0
Geschlecht: F
Eingang: 10.05.2021
Impfdatum: 15.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: IM / RA

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

Computerised tomogram thorax abnormal Condition aggravated Dyspnoea Fibrin D dimer increased Heart rate increased Oxygen saturation decreased Pain in extremity Pulmonary embolism SARS-CoV-2 test Scan with contrast abnormal Ultrasound Doppler normal

Symptomtext

I was hospitalized for bilateral pulmonary embolism 4/18/2021 at hospital. I think I had symptoms for over 3 weeks prior to hospitalization. I was rapid COVID tested on 3/26/2021 the nurse at CVS asked why my blood oxygen was low. I did not know but had me pant and move my fingers and it went up to 96. I also remember severe leg pain on a drive 3/25/21. I noticed shortness of breath 4/5/21 and fast pulse but didnot go to hospital until 4/18/21. I previously had a PE 7/2009 and also had it for ~2 weeks before going to hospital. I was not on blood thinner since 2015. The doctors at the hospital and primary care doctor did not seem to think the PE was vaccine related but they also do not believe I had symptoms for over 3 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: blood test showed elevated dimer, CT scan with contrast showed bilateral pulmonary embolism, leg ultra sound scan did not show blood clots in legs.
Aktuelle Erkrankungen: none
Vorgeschichte: high blood pressure, obesity
Andere Medikamente: 25 mg Atenolo, 50 mg HCT, 300 mg Allopurinol, multi-vitamin, folgard equivalent
Allergien: none
Vorherige Impfungen: -

VAERS 1293462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 64,0
Geschlecht: M
Eingang: 06.05.2021
Impfdatum: 29.03.2021
Beginn: 29.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cerebral haemorrhage Death

Symptomtext

This 64 year old male received the Covid shot on 3/29/21 and went to the ED on 3/29/21 and was admitted for left-sided nontraumatic intracerebral hemorrhage and died on 5/4/21. Please refer to the other details submitted within this report and contact the person who submitted this report via email for additional follow up details and investigation.

Weitere VAERSDATA-Felder

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

VAERS 1293194

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 86,0
Geschlecht: M
Eingang: 06.05.2021
Impfdatum: 07.04.2021
Beginn: 28.04.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: IM / LA

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

Cerebrovascular accident

Symptomtext

I63.9 - Acute CVA (cerebrovascular accident) (CMS/HCC) I63.9 - Cerebrovascular accident (CVA), unspecified mechanism (CMS/HCC)

Weitere VAERSDATA-Felder

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

VAERS 1289422

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MD
Alter: 71,0
Geschlecht: M
Eingang: 05.05.2021
Impfdatum: 24.03.2021
Beginn: 01.05.2021
Tage bis Beginn: 38,0
Dosis: 2
Route/Site: IM / LA

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

Acute coronary syndrome Acute myocardial infarction Angiogram abnormal Anticoagulant therapy Coronary arterial stent insertion Coronary artery stenosis Percutaneous coronary intervention

Symptomtext

Patient is a 71 yr. old male admitted for Hospital (non-ST elevated myocardial infarction) [I21.4], ACS (acute coronary syndrome) [I24.9, Please refer to the History and Physical report for information on presentation. The patient was admitted. He ruled in for myocardial infarction and cardiology was consulted. He was started on beta-blocker and statin and aspirin and anticoagulated. Subsequently he was taken for angiography. The following results were found: Right dominant coronary anatomy. Left main-0%. LAD-mid 90% stenosis with plaque extending up to the diagonal bifurcation. Distal 30% narrowing. TIMI-3 flow. D1-small with proximal 40% narrowing. D2-medium size vessel with mid 30% narrowing. Circumflex-proximal 30% supplying a large branching OM. OM1-luminal irregularities up with up to mid 20% narrowing. RCA-dominant vessel with slight luminal irregularity distally. Right PDA-20% narrowing proximally. Right PLB-30% narrowing proximally. The patient underwent PCI with stent to the LAD and transferred to the floor. I discussed him with Dr. who recommended discharge to home this afternoon. ACE inhibitor

Weitere VAERSDATA-Felder

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

VAERS 1269763

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: NC
Alter: 47,0
Geschlecht: F
Eingang: 05.05.2021
Impfdatum: 02.04.2021
Beginn: 14.04.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: IM / LA

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

Death Inappropriate schedule of product administration Off label use Pulse absent Sudden death Unresponsive to stimuli

Symptomtext

My wife (age 47) died on 14Apr2021 of a sudden death. She was found at home unresponsive and pulseless. Her medical history is non-contributory for a sudden cardiac death. A full autopsy is pending.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: n/a; My wife was declared dead at the home. Toxicology is pending.
Aktuelle Erkrankungen: Occasional migraines
Vorgeschichte: Anxiety
Andere Medikamente: L-Thyroxine (Synthroid) 50 mcg PO, daily Lexapro 20 mg PO, daily Sumatriptan 100 mg PO, PRN (may take a 2nd dose after 2 hours if needed), PRN Clonazepam 0.5 - 1.0 mg PO, PRN as needed for anxiety
Allergien: NKDA No food allergies
Vorherige Impfungen: -

VAERS 1286232

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

kritisch

Staat: MI
Alter: 70,0
Geschlecht: M
Eingang: 04.05.2021
Impfdatum: 04.05.2021
Beginn: 25.03.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / UN

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

Death

Symptomtext

patient passed away before second dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: na
Vorgeschichte: diabetes, post MI
Andere Medikamente: cardiac medications
Allergien: na
Vorherige Impfungen: -

VAERS 1285673

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 79,0
Geschlecht: F
Eingang: 04.05.2021
Impfdatum: 15.03.2021
Beginn: 29.04.2021
Tage bis Beginn: 45,0
Dosis: 2
Route/Site: IM / LA

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

Aphasia Cerebrovascular accident

Symptomtext

Aphasia CVA (cerebral vascular accident)

Weitere VAERSDATA-Felder

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

VAERS 1281561

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MN
Alter: 39,0
Geschlecht: F
Eingang: 03.05.2021
Impfdatum: 11.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / RA

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

Cerebrovascular accident

Symptomtext

Patient presented to the ED and was subsequently hospitalized within 6 weeks of receiving COVID vaccination. Patient suffered a stroke. She was then admitted for rehab on 3/18/21 for 7 days.

Weitere VAERSDATA-Felder

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

VAERS 1272049

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

kritisch

Staat: FL
Alter: 41,0
Geschlecht: F
Eingang: 29.04.2021
Impfdatum: 01.04.2021
Beginn: 05.04.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

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

Cerebrovascular accident Computerised tomogram Dizziness Hypoaesthesia Lumbar puncture Magnetic resonance imaging Reversible cerebral vasoconstriction syndrome Speech disorder Syncope Vomiting X-ray

Symptomtext

vomting, collapsing, dizzy, couldn't feel hands, speech impaired, small stroke

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: x-ray, cat scan, mri, spinal tap, pulled fluid from spine, diagnosed wit rcvs
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: vitamin d3, fishoil, multivitamin
Allergien: -
Vorherige Impfungen: -

VAERS 1270832

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: CA
Alter: 72,0
Geschlecht: M
Eingang: 29.04.2021
Impfdatum: 22.03.2021
Beginn: 23.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Death Dyspnoea Syncope

Symptomtext

Beginning the day after the inoculation, my husband began feeling worse in terms of his difficulty in breathing. He used the Albuterol inhaler more than usual. It progressively got worse over the next 2 weeks, ending with my husband?s sudden collapse and death exactly 2 weeks later on April 5, 2021. The inoculation may or may not have been directly linked to his unexpected death, but I feel it may have exasperated his condition, which led to his death. And I feel it is important to report this to you. I later heard that he should not have been using his Albuterol inhaler one week prior to receiving the Pfizer vaccine. I don?t know if that is true, but that information was never told to my husband, if it is.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Diagnosed in February 2021 with severe COPD overlapped with Asthma
Vorgeschichte: Controlled hypertension & cholesterol
Andere Medikamente: Wixela Inhub 500 Albuterol HFA90 Amlodipine 10mg Lisinopril 20mg (half) Rosuvastatin 20 mg Brimonidine 0.2 Latanoprost 0.005
Allergien: -
Vorherige Impfungen: -

VAERS 1217275

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 96,0
Geschlecht: F
Eingang: 29.04.2021
Impfdatum: 15.03.2021
Beginn: 29.03.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Blood urine present Death Femur fracture Pain in extremity

Symptomtext

This 96 year old female received the Covid shot on 3/15/21 and went to the ED on 3/29/21 and again on 4/22/21 and was admitted on 4/22/21 with weakness, leg pain, blood in urine, displaced transverse fracture of shaft of right femur and died on 4/23/21 . Please refer to the other details submitted within this report and contact the person who submitted this report via email for additional follow up details and investigation.

Weitere VAERSDATA-Felder

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

VAERS 1176003

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MN
Alter: 65,0
Geschlecht: M
Eingang: 29.04.2021
Impfdatum: 11.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: - / -

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

Death

Symptomtext

Patient presented to the ED and was subsequently hospitalized within 6 weeks of receiving COVID vaccination.

Weitere VAERSDATA-Felder

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

VAERS 1176003

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MN
Alter: 65,0
Geschlecht: M
Eingang: 29.04.2021
Impfdatum: 11.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

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

Death

Symptomtext

Patient presented to the ED and was subsequently hospitalized within 6 weeks of receiving COVID vaccination.

Weitere VAERSDATA-Felder

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

VAERS 1268064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 28.04.2021
Impfdatum: 19.03.2021
Beginn: 25.04.2021
Tage bis Beginn: 37,0
Dosis: 2
Route/Site: IM / RA

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

Death

Symptomtext

This 76 year old female received the 2nd Covid shot on 3/19/21 and died on 4/25/21. Please refer to the other details submitted within this report and contact the person who submitted this report via email for additional follow up details and investigation.

Weitere VAERSDATA-Felder

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

VAERS 1266615

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 81,0
Geschlecht: M
Eingang: 28.04.2021
Impfdatum: 18.03.2021
Beginn: 24.04.2021
Tage bis Beginn: 37,0
Dosis: 2
Route/Site: IM / RA

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

Death

Symptomtext

Death

Weitere VAERSDATA-Felder

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

VAERS 1239231

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: FL
Alter: 54,0
Geschlecht: M
Eingang: 27.04.2021
Impfdatum: 07.04.2021
Beginn: 17.04.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: - / RA

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

Laboratory test Near death experience Pulmonary embolism Pulmonary thrombosis SARS-CoV-2 test

Symptomtext

had pulmonary embolism in both lungs; blood clots/blood clots in the lungs; This is a spontaneous report from a contactable consumer (patient). A 54-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 2 via an unspecified route of administration administered in arm right on 07Apr2021 at vaccination age of 54 years old (Lot Number: EN6208; Expiration Date: Jun2021) as single dose for covid-19 immunisation. There was no medical history. No known allergies. No Covid prior vaccination. The patient's concomitant medications were not reported. The patient previously took BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration administered in arm left on 08Mar2021 14:00 at vaccination age of 54 years old (Lot Number: EN6205; Expiration Date: 30Jun2021) as single dose for covid-19 immunisation. No other vaccine in four weeks. No other medications in two weeks. The patient experienced had pulmonary embolism in both lungs on 17Apr2021 13:00, blood clots/blood clots in the lungs on 17Apr2021 13:00. Events resulted in emergency room/department or urgent care, hospitalization, life threatening illness (immediate risk of death from the event), disability or permanent damage. The patient had pulmonary embolism in both lungs. He was in the hospital for 3 days and now he will have to take blood thinners in definitely. He was admitted 17Apr2021 and discharged home 19Apr2021. He did not have history of blood clots and zero risk factors. Two doctors blamed the vaccine. He did not want to take blood thinners forever. He needed help figuring out how to determine if this was related to the vaccine. He had a reaction to the second shot and he had been in the hospital the last 3 days and the 2 different doctors that saw him said the only thing that was different was that he had received the COVID vaccine. He had blood clots in both of his lungs, he was in serious condition for a couple days there but his biggest concern now was that they were telling him that he will have to take medication forever to thin his blood because they didn't think there was a genetic reason it happened and that was the protocol that healthcare providers have to follow. They were telling him that he might contact a hematologist and do a blood study but they said they were certain that it came from the vaccine because there was no history of this in his family or himself. He said the condition's medical term was pulmonary embolism but he just said blood clots in the lungs because he thought he would make it easier to explain. Both doctors that saw him felt it was brought on the by the vaccine. He was not looking to sue or anything, he didn't want to be taking a blood thinner for the rest of life. He was not doing this for any reason other than to get well. He realized this situation was very rare with Pfizer, it was like 4 in 1 million with Pfizer according to his physicians. Covid tested post vaccination: Nasal Swab on 17Apr2021 with negative result. Therapeutic measures were taken as a result of had pulmonary embolism in both lungs, blood clots/blood clots in the lungs. The outcome of events was recovered with sequelae.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Near death experience
Hospital-Tage: 2,0
Labordaten: Test Date: 20210417; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1239231

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: FL
Alter: 54,0
Geschlecht: M
Eingang: 27.04.2021
Impfdatum: 07.04.2021
Beginn: 17.04.2021
Tage bis Beginn: 10,0
Dosis: UNK
Route/Site: SYR / RA

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

Laboratory test Near death experience Pulmonary embolism Pulmonary thrombosis SARS-CoV-2 test

Symptomtext

had pulmonary embolism in both lungs; blood clots/blood clots in the lungs; This is a spontaneous report from a contactable consumer (patient). A 54-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 2 via an unspecified route of administration administered in arm right on 07Apr2021 at vaccination age of 54 years old (Lot Number: EN6208; Expiration Date: Jun2021) as single dose for covid-19 immunisation. There was no medical history. No known allergies. No Covid prior vaccination. The patient's concomitant medications were not reported. The patient previously took BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration administered in arm left on 08Mar2021 14:00 at vaccination age of 54 years old (Lot Number: EN6205; Expiration Date: 30Jun2021) as single dose for covid-19 immunisation. No other vaccine in four weeks. No other medications in two weeks. The patient experienced had pulmonary embolism in both lungs on 17Apr2021 13:00, blood clots/blood clots in the lungs on 17Apr2021 13:00. Events resulted in emergency room/department or urgent care, hospitalization, life threatening illness (immediate risk of death from the event), disability or permanent damage. The patient had pulmonary embolism in both lungs. He was in the hospital for 3 days and now he will have to take blood thinners in definitely. He was admitted 17Apr2021 and discharged home 19Apr2021. He did not have history of blood clots and zero risk factors. Two doctors blamed the vaccine. He did not want to take blood thinners forever. He needed help figuring out how to determine if this was related to the vaccine. He had a reaction to the second shot and he had been in the hospital the last 3 days and the 2 different doctors that saw him said the only thing that was different was that he had received the COVID vaccine. He had blood clots in both of his lungs, he was in serious condition for a couple days there but his biggest concern now was that they were telling him that he will have to take medication forever to thin his blood because they didn't think there was a genetic reason it happened and that was the protocol that healthcare providers have to follow. They were telling him that he might contact a hematologist and do a blood study but they said they were certain that it came from the vaccine because there was no history of this in his family or himself. He said the condition's medical term was pulmonary embolism but he just said blood clots in the lungs because he thought he would make it easier to explain. Both doctors that saw him felt it was brought on the by the vaccine. He was not looking to sue or anything, he didn't want to be taking a blood thinner for the rest of life. He was not doing this for any reason other than to get well. He realized this situation was very rare with Pfizer, it was like 4 in 1 million with Pfizer according to his physicians. Covid tested post vaccination: Nasal Swab on 17Apr2021 with negative result. Therapeutic measures were taken as a result of had pulmonary embolism in both lungs, blood clots/blood clots in the lungs. The outcome of events was recovered with sequelae.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Near death experience
Hospital-Tage: 2,0
Labordaten: Test Date: 20210417; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1134110

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: AR
Alter: 48,0
Geschlecht: F
Eingang: 25.04.2021
Impfdatum: 23.03.2021
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Anaphylactic reaction Anaphylactic shock Blister Illness Oral discomfort Burning sensation Cardiac monitoring Intensive care Laboratory test Oral disorder Paraesthesia oral Pharyngeal swelling Respiratory disorder Swollen tongue Tongue disorder Tongue discomfort

Symptomtext

anaphylactic reaction; anaphylactic shock; my tongue first tingling; burning all over my tongue; massive and dangerous swelling of my tongue; an intense burning on the roof of my mouth; there were bumps forming all over the back of my tongue; blisters forming on the back of my throat; She has been very very sick; This is a spontaneous report from a contactable consumer (patient), other healthcare professional, and a physician. A 48-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EN6208), dose 1 via an unspecified route of administration, administered in Arm Left on 23Mar2021 16:00 (at the age of 48years) as single dose for Covid-19 immunization. Medical history included known allergies: mild allergy to sulfa as a child that resulted in a rash; mild allergy to Crestor that resulted in extreme gas and bloating; other medical history: type 2 diabetic that has been controlled for 8 years with no A1C higher than 7.0. The patient is not pregnant at the time of vaccination. Concomitant medications included metformin, glipizide, bupropion hydrochloride (WELLBUTRIN), lovastatin, and other unspecified medication; 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 reported that on 23Mar2021, she received her vaccine at 4 p.m. and experienced an anaphylactic reaction within 5 minutes, by 4:10 she was taken to the ER (emergency room) attached to the clinic due to her tongue first tingling, then burning all over her tongue, and then massive and dangerous swelling of her tongue and an intense burning on the roof of her mouth. The attending physician noted there were bumps forming all over the back of her tongue and blisters forming on the back of her throat. She was admitted for anaphylactic shock and kept at the ER for 2 hours before being transferred via ambulance to other hospital and she was admitted to the ICU (intensive case unit). She spent the next day in the ICU then 2 days in Cardiac Care, another day back in the ICU, with a 5th and final day back in the Cardiac care. All 5 days were spend trying to get her anaphylactic shock under control. She had numerous doses of EpiPen, steroids, Benadryl, and Pepcid. Her tongue never did completely stop swelling and the burning sensation has never stopped. The patient was hospitalized for 5 days. It was reported further reported that the patient was hospitalized for 6 days (also initially reported as 5 days-pending clarification) and was sent home with medications but was back in the hospital yesterday (unspecified date) because of another big blow up. She has had 2 stays in the ICU, 4 days in cardiac care and is now back in cardiac care again because of yesterday. It has been 2 weeks since she received the vaccine and it is now day 12 but it keeps coming back and she just cannot stop it. She has been very very sick, in a very severe, very rare, extreme, constant state of anaphylactic shock. She has had many Epi (Epinephrine) and is on strong steroids but it has not subsided. She mentioned that their lead pharmacist called last week but never heard any response back. Her doctor told her that they accessed a website from Pfizer which allowed them to search for adverse reactions and they mentioned to her that most of these reactions subside within 24-48 hours. She mentioned that she has no food allergies, no allergies to vaccines, and has only had minor drug reactions. This is the 1st time that this has happened to her and it is getting serious. The events 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). The patient has not been tested for COVID-19 since the vaccination. The outcome of events was not recovered. The reporter (consumer) assessed the events as non-serious. Information on lot/batch number was available. Additional information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic shock
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sulfonamide allergy (Mild allergy to sulfa as a child that resulted in a rash); Type 2 diabetes mellitus (That has been controlled for 8 years with A1C higher than 7.0)
Andere Medikamente: METFORMIN; GLIPIZIDE; WELLBUTRIN; LOVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 1245985

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 80,0
Geschlecht: M
Eingang: 23.04.2021
Impfdatum: 08.04.2021
Beginn: 20.04.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

This 80 year old white male received the Covid shot on 4/8/21 and died on 4/18/21. Please refer to the other details submitted within this report and contact the person who submitted this report via email for additional follow up details and investigation.

Weitere VAERSDATA-Felder

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

VAERS 1238276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 58,0
Geschlecht: M
Eingang: 21.04.2021
Impfdatum: 22.03.2021
Beginn: 15.04.2021
Tage bis Beginn: 24,0
Dosis: 1
Route/Site: IM / LA

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

Death

Symptomtext

This 58 year old white male hospice patient received the Covid shot on 3/22/21 and died on 4/15/21. Please refer to the other details submitted within this report and contact the person who submitted this report via email for additional follow up details and investigation.

Weitere VAERSDATA-Felder

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

VAERS 1171204

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: IN
Alter: -
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 24.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / -

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

Death Dysarthria Fall Impaired driving ability Posture abnormal Life support Laboratory test Pulmonary embolism

Symptomtext

Pulmonary embolism/ blood clot/ passed out; This is a spontaneous report from a contactable consumer (patient's daughter). A male patient of an unspecified age received BNT162B2 (Pfizer COVID-19 vaccine), dose 1 via an unspecified route of administration, administered in arm, side unknown, on 24Mar2021 14:30 (Lot Number: EN6208) as single dose for COVID-19 immunisation. Vaccination facility type was clinic. Medical history included colon cancer in 2011. He had cancer in 2011 but resolved that year without chemotherapy or radiation. His lab work was good. There were no concomitant medications. No prior vaccinations (within 4 weeks). No family medical history relevant to AE. The patient experienced pulmonary embolism on 26Mar2021 with fatal outcome. The reporter was reporting on the Pfizer COVID vaccine that her father received. She stated he died from a blood clot after receiving the first dose. Stated she needs help because he had no health issues and he died. She just wanted this information to be out there and for people to be aware. This morning they had been reading on the news that the Johnson and Johnson vaccine is on hold. It seems to be put on the market without research. She felt like her father was a guinea pig. Her mother didn't want to get her second dose. Stated there seems to be an issue with Pfizer too. Her father had no issues whatsoever. His death certificate stated the cause of death was a pulmonary embolism, but he had no history of blood clots. Passed away Friday 26Mar2021 at 11:33 am. The reporter stated when he went to Emergency Room they thought he was having a heart attack. All physicians were wondering what happened because he had no health issues. The event required a visit to the emergency room that day because he passed out at his job. The patient underwent lab tests and procedures which included lab work: good in 2011. The patient died on 26Mar2021. An autopsy was performed that revealed pulmonary embolism.; Reported Cause(s) of Death: Pulmonary embolism; Autopsy-determined Cause(s) of Death: Pulmonary embolism

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Test Date: 2011; Test Name: lab work; Result Unstructured Data: Test Result:Good
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Colon cancer
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1171204

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: IN
Alter: -
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 24.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: ID / AR

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

Death Dysarthria Fall Impaired driving ability Posture abnormal Life support Laboratory test Pulmonary embolism

Symptomtext

Pulmonary embolism/ blood clot/ passed out; This is a spontaneous report from a contactable consumer (patient's daughter). A male patient of an unspecified age received BNT162B2 (Pfizer COVID-19 vaccine), dose 1 via an unspecified route of administration, administered in arm, side unknown, on 24Mar2021 14:30 (Lot Number: EN6208) as single dose for COVID-19 immunisation. Vaccination facility type was clinic. Medical history included colon cancer in 2011. He had cancer in 2011 but resolved that year without chemotherapy or radiation. His lab work was good. There were no concomitant medications. No prior vaccinations (within 4 weeks). No family medical history relevant to AE. The patient experienced pulmonary embolism on 26Mar2021 with fatal outcome. The reporter was reporting on the Pfizer COVID vaccine that her father received. She stated he died from a blood clot after receiving the first dose. Stated she needs help because he had no health issues and he died. She just wanted this information to be out there and for people to be aware. This morning they had been reading on the news that the Johnson and Johnson vaccine is on hold. It seems to be put on the market without research. She felt like her father was a guinea pig. Her mother didn't want to get her second dose. Stated there seems to be an issue with Pfizer too. Her father had no issues whatsoever. His death certificate stated the cause of death was a pulmonary embolism, but he had no history of blood clots. Passed away Friday 26Mar2021 at 11:33 am. The reporter stated when he went to Emergency Room they thought he was having a heart attack. All physicians were wondering what happened because he had no health issues. The event required a visit to the emergency room that day because he passed out at his job. The patient underwent lab tests and procedures which included lab work: good in 2011. The patient died on 26Mar2021. An autopsy was performed that revealed pulmonary embolism.; Reported Cause(s) of Death: Pulmonary embolism; Autopsy-determined Cause(s) of Death: Pulmonary embolism

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Test Date: 2011; Test Name: lab work; Result Unstructured Data: Test Result:Good
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Colon cancer
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1171204

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: IN
Alter: -
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 24.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Death Dysarthria Fall Impaired driving ability Posture abnormal Life support Laboratory test Pulmonary embolism

Symptomtext

Pulmonary embolism/ blood clot/ passed out; This is a spontaneous report from a contactable consumer (patient's daughter). A male patient of an unspecified age received BNT162B2 (Pfizer COVID-19 vaccine), dose 1 via an unspecified route of administration, administered in arm, side unknown, on 24Mar2021 14:30 (Lot Number: EN6208) as single dose for COVID-19 immunisation. Vaccination facility type was clinic. Medical history included colon cancer in 2011. He had cancer in 2011 but resolved that year without chemotherapy or radiation. His lab work was good. There were no concomitant medications. No prior vaccinations (within 4 weeks). No family medical history relevant to AE. The patient experienced pulmonary embolism on 26Mar2021 with fatal outcome. The reporter was reporting on the Pfizer COVID vaccine that her father received. She stated he died from a blood clot after receiving the first dose. Stated she needs help because he had no health issues and he died. She just wanted this information to be out there and for people to be aware. This morning they had been reading on the news that the Johnson and Johnson vaccine is on hold. It seems to be put on the market without research. She felt like her father was a guinea pig. Her mother didn't want to get her second dose. Stated there seems to be an issue with Pfizer too. Her father had no issues whatsoever. His death certificate stated the cause of death was a pulmonary embolism, but he had no history of blood clots. Passed away Friday 26Mar2021 at 11:33 am. The reporter stated when he went to Emergency Room they thought he was having a heart attack. All physicians were wondering what happened because he had no health issues. The event required a visit to the emergency room that day because he passed out at his job. The patient underwent lab tests and procedures which included lab work: good in 2011. The patient died on 26Mar2021. An autopsy was performed that revealed pulmonary embolism.; Reported Cause(s) of Death: Pulmonary embolism; Autopsy-determined Cause(s) of Death: Pulmonary embolism

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Test Date: 2011; Test Name: lab work; Result Unstructured Data: Test Result:Good
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Colon cancer
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1224541

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: FL
Alter: -
Geschlecht: F
Eingang: 18.04.2021
Impfdatum: -
Beginn: 26.03.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Cerebrovascular accident Fatigue Headache Myalgia Rash Seizure Urticaria

Symptomtext

fatigue; felt like she was going to have a stroke; hives; two seizures; rash from head to toe; wrap around headache; sore muscles; This is a spontaneous report from a contactable other healthcare professional (patient). A 66-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EN6208), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunisation. The patient's medical history included seizure, high blood pressure, and atrial fibrillation with rapid ventricular response on 03Feb2021, all ongoing. The patient's concomitant medications included metoprolol tartrate (LOPRESSOR) taken for blood pressure measurement, lisinopril taken for an unspecified indication, valproate semisodium (DEPAKOTE) taken for seizure from 2017 to an unspecified stop date, and hydrochlorothiazide, lisinopril (LISINOPRIL HCTZ) taken for an unspecified indication. The patient experienced two seizures on 27Mar2021. Patient felt like she was going to have a stroke on an unspecified date. The patient experienced hives on 27Mar2021, fatigue on an unspecified date, rash from head to toe on 27Mar2021, wrap around headache on 26Mar2021, and sore muscles on 26Mar2021. The outcome of the events wrap around headache and sore muscles was recovered on 28Mar2021, for hives and rash from head to toe was recovering, and the outcome of the rest of the events was unknown. Events relatedness was reported as related.; Sender's Comments: Other than a close temporal association, there was no other evidence or argument in support to causality for BNT162B2 in the serious events, Seizure and Cerebrovascular accident. Seizure was consistent with underlying medical condition, still on treatment with VALPROATE SEMISODIUM. Chronic hypertension may have increased the risk of vascular accident, despite the poly-medication with different type of antihypertensive agents. 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: Cerebrovascular accident
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Atrial fibrillation with rapid ventricular response; Blood pressure high; Seizures
Vorgeschichte: -
Andere Medikamente: LOPRESSOR; LISINOPRIL; DEPAKOTE; LISINOPRIL HCTZ
Allergien: -
Vorherige Impfungen: -

VAERS 1224523

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: FL
Alter: 66,0
Geschlecht: F
Eingang: 18.04.2021
Impfdatum: 22.03.2021
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Arthralgia Back pain Chest pain Crying Dyspnoea Heart rate abnormal Myocardial infarction Pain Pain in extremity Panic attack Panic reaction Paraesthesia Stress

Symptomtext

Soreness to left arm, hurts in chest around breast, back, shoulder blade; Soreness to left arm, hurts in chest around breast, back, shoulder blade; Soreness to left arm, hurts in chest around breast, back, shoulder blade; Soreness to left arm, hurts in chest around breast, back, shoulder blade; Unable to lift arm, pain makes her catch her breath/ Difficult to take a deep breath; Thought she was having a heart or panic attack; Stress, heart rate, panic; soreness from the shot; Stress, heart rate, panic; Stress, heart rate, panic; Stress, heart rate, panic; Tingling in hands and down the arm; crying; This is a spontaneous report received from contactable consumer (patient). A 66-year-old female patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration at the age of 66-years-old on 22Mar2021 13:57 (Lot Number: EN6208) as single dose for COVID-19 immunization. Medical history included migraine. Concomitant medication included topiramate taken for migraine from 15Mar2021 and ongoing. The patient had her shot last Monday afternoon and had some soreness from the shot on Mar2021. On Tuesday, 23Mar2021, it began getting sore back behind her shoulder blade; it has gotten progressively worse, and now she can barely lift her arm. She does not know if it's a muscle or has to do with the vaccine, or if she pulled a muscle although she has not done anything. It's difficult to take a deep breath, she can't lift her arm, it is sore. It hurts down into her chest and around her breast; also, hurts around on her back where her shoulder blade is. She has tried heat compress, cold compress, and massage the area. It seems like the pain will ease up but then it starts again. She becomes stressed about it and her heart rate starts panicking. She gets tingles down the arm. Thought she was having a heart or panic attack. It has gotten worse as the week has progressed. It was worse on Sunday; even worse on Monday; worse yesterday and she was crying. She has also been stressed at work. Doesn't know whether to go to the doctor or an urgent care, or if she needs to. The patient is 66 years old and says she is in fairly good health. Right now she is unable to lift her arm and has tingles in the hand and down the arm. The pain makes her catch her breath. If this gets much worse she is going to go have it checked out. Again mentions that she has been having stress. It does seem to be a little worse. The patient experienced thought she was having a heart or panic attack on Mar2021, stress, heart rate, panic on Mar2021, soreness from the shot on Mar2021, soreness to left arm, hurts in chest around breast, back, shoulder blade on 23Mar2021, unable to lift arm, pain makes her catch her breath/ difficult to take a deep breath on Mar2021, tingling in hands and down the arm on Mar2021, and crying on Mar2021. The outcome of the event Soreness to left arm, hurts in chest around breast, back, shoulder blade was not recovered while for the rest of the events was unknown. Prior Vaccinations (within 4 weeks) was None. She had an unspecified shot but reiterated no vaccines. No AEs following prior vaccinations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Migraine
Andere Medikamente: TOPIRAMATE
Allergien: -
Vorherige Impfungen: -

VAERS 1139553

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: FL
Alter: 68,0
Geschlecht: M
Eingang: 18.04.2021
Impfdatum: 26.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Hyperhidrosis Myalgia Nausea Malaise Myocardial infarction SARS-CoV-2 test

Symptomtext

admitted to ER Saturday morning with massive heart attack; feeling unwell Friday evening; This is a spontaneous report from a contactable consumer (patient). A 68-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), Batch/Lot Number: EN6208), dose 2 via an unspecified route of administration, administered in Arm Left on 26Mar2021 13:30 (at the age of 68years) as single dose for Covid-19 immunization. The patient received the first dose of BNT162B2 (lot number: EN6200) on 02Mar2021 (at the age of 68years) for Covid-19 immunization. The patient's medical history was not reported, no known allergies. Concomitant medications included rosuvastatin taken for an unspecified indication, start and stop date were not reported. The patient was not diagnosed with COVID-19 prior to vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. It was reported that the patient was feeling unwell on Friday evening (as reported); patient admitted to ER (emergency room) Saturday morning with massive heart attack. Onset date for both events was reported as 26Mar2021 21:45. The events resulted in Emergency room/department or urgent care, Hospitalization, Life threatening illness (immediate risk of death from the event), Disability or permanent damage. The patient was hospitalized for both events from 27Mar2021 to 01Apr2021 (as reported duration of hospitalization: for 5 days). Treatment of events included 2 Stents. The patient had Covid test post vaccination on an unspecified date: Nasal Swab =Negative. The outcome of events was recovering. The outcome of events was recovering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 5,0
Labordaten: Test Name: COVID-19 Virus test; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ROSUVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 1214304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 15.04.2021
Impfdatum: 11.03.2021
Beginn: 05.04.2021
Tage bis Beginn: 25,0
Dosis: 1
Route/Site: UN / UN

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

Acute myocardial infarction Blood loss anaemia Dyspnoea End stage renal disease Gastrointestinal haemorrhage Hyperkalaemia Pulmonary oedema

Symptomtext

K92.2 - Gastrointestinal hemorrhage, unspecified gastrointestinal hemorrhage type R06.02 - Shortness of breath N18.6 - End stage renal disease E87.5 - Hyperkalemia D50.0 - Blood loss anemia J81.1 - Pulmonary edema I21.4 - NSTEMI (non-ST elevated myocardial infarction)

Weitere VAERSDATA-Felder

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

VAERS 1208744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 81,0
Geschlecht: M
Eingang: 14.04.2021
Impfdatum: 02.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

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

Death

Symptomtext

Death

Weitere VAERSDATA-Felder

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

VAERS 1207286

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 14.04.2021
Impfdatum: 17.03.2021
Beginn: 29.03.2021
Tage bis Beginn: 12,0
Dosis: 2
Route/Site: IM / RA

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

Death

Symptomtext

Death

Weitere VAERSDATA-Felder

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

VAERS 1201793

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: AL
Alter: 49,0
Geschlecht: M
Eingang: 13.04.2021
Impfdatum: 12.04.2021
Beginn: 12.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Acute myocardial infarction Catheterisation cardiac Chest discomfort Chest pain Coronary artery bypass

Symptomtext

He had been experiencing chest discomfort after eating and activity for a month, that resolved with rest. Family history of ischemic heart disease. Pt is a smoker, HTN and dyslipidemia. I was just informed a patient received the Pfizer vaccine yesterday @ 1129. Arrived to ER @1700 with a STEMI. He went for a heart cath yesterday and CABG this morning. Per the cath report his LAD was occluded. I believe he was more aware of his symptoms after receiving the vaccine and that is why he finally came in.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 1,0
Labordaten: Heart cath 04/12; CABG 04/13
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1200619

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 74,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 29.03.2021
Beginn: 02.04.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain Death Sepsis

Symptomtext

Death Sepsis abdominal pain

Weitere VAERSDATA-Felder

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

VAERS 1191960

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: FL
Alter: 49,0
Geschlecht: F
Eingang: 10.04.2021
Impfdatum: 20.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Acute myocardial infarction SARS-CoV-2 test Thrombosis

Symptomtext

Blood clot in LAD which caused a STEMI; Blood clot in LAD which caused a STEMI; This is a spontaneous report received from a contactable consumer (female). A 49-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot Number: EN6208), first dose via an unspecified route of administration, administered in Arm Left on 20Mar2021 08:15 (at the age of 49 years old), single dose for covid-19 immunisation. Medical history included hypothyroidism, Penicillin allergy, both from an unknown date. The patient was taking unspecified concomitant medications within 2 weeks of vaccination. The patient experienced blood clot in lad which caused a STEMI on an unspecified date (reported as 03Mar2021 15:15, for clarification since before vaccination date). The outcome of the events was unknown. The events was assessed as serious, causing hospitalization, disability and was life-threatening. Treatment for the events were Balloon in LAD / clot buster. The patient underwent lab tests and procedures which included COVID-19: negative on 03Mar2021. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Information on Lot/Batch number was available. Additional information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 3,0
Labordaten: Test Date: 20210303; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism; Penicillin allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1180894

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 92,0
Geschlecht: M
Eingang: 08.04.2021
Impfdatum: 11.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Cardiac arrest Death Respiratory arrest

Symptomtext

respiratory arrest, cardiac arrest Narrative: Patient died 1 day after receiving 2nd dose of COVID vaccine in his bed at home. Paramedics arrived but were not able to resuscitate.

Weitere VAERSDATA-Felder

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

VAERS 1179310

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: CA
Alter: 38,0
Geschlecht: F
Eingang: 08.04.2021
Impfdatum: 14.03.2021
Beginn: 25.03.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: - / LA

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

Myocardial infarction SARS-CoV-2 test

Symptomtext

I had heart attack about 2 weeks after the 1st dose. I was almost lost my life. Doctor still could not diagnose the cause because I am a healthy women; This is a spontaneous report from a contactable consumer (patient). A 38-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EN6208), dose 1 via an unspecified route of administration at the age of 38-years, administered in arm left on 14Mar2021 15:15 as single dose for covid-19 immunisation. The patient medical history was not reported. There were no concomitant medications. The patient had heart attack about 2 weeks after the 1st dose (25Mar2021 09:00). I was almost lost my life. Doctor still could not diagnose the cause because I am a healthy women. I will provide more detail if you need them for research. The patient did not receive other vaccine in four weeks, did not receive other medications in twoweeks, she received treatment (Emergency room, hospitalized, cardiac procedure) for the event. The patient did not received Covid prior vaccination, she tested Covid post vaccination (Covid-19 PCR test) via Nasal Swab on 28Mar2021, Covid test result was negative. There is no known allergies. The outcome of the event was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: Test Date: 20210328; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1175526

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: FL
Alter: 74,0
Geschlecht: F
Eingang: 07.04.2021
Impfdatum: 11.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: SYR / LA

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

Pulmonary embolism

Symptomtext

PATIENT DEVELOPED PULMONARY EMBOLISM FOLLOWING THE VACCINE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: DM2, Rheumatoid arthritis, athrosclerosis of aorta, hypothyroidism, CKD3, psoriatic arthritis, PVD, hyperlipidemia
Andere Medikamente: Vit d3, coq10, lansoprazole, gabapentin, Januvia, metformin, Synthroid, ropinirole, spironolactone, tramadol
Allergien: clindamycin, erythromycin
Vorherige Impfungen: -

VAERS 1165904

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: NM
Alter: 89,0
Geschlecht: M
Eingang: 04.04.2021
Impfdatum: 19.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Asthenia Blood test Cerebrovascular accident Chest X-ray Computerised tomogram Disorientation Dysstasia Feeling abnormal Gait disturbance Glassy eyes Investigation Urine analysis

Symptomtext

The way he is acting is more like he had a stroke; eyes glazed over; disoriented; felt funny; very weak; can barely stand and barely walk without human assistance and his walker; can barely stand and barely walk without human assistance and his walker; This is a spontaneous report from a contactable consumer. An 89-year-old male patient received bnt162b2 (Pfizer-BioNTech COVID 19), dose 2 via an unspecified route of administration, administered in left arm on 19Mar2021 12:15 (Batch/Lot Number: EN6208) as single dose for COVID-19 immunisation. Medical history included vascular dementia; hypertension; hypothyroidism; malignant melanoma of back (resected/in remission); bladder cancer (surgery in Nov2018/in remission); prediabetic; chronic kidney disease stage 3 due to hypertension; and sleep related hypoxia. No known allergies. Concomitant medications included donepezil taken for an unspecified indication, start and stop date were not reported; memantine taken for an unspecified indication, start and stop date were not reported; levothyroxine taken for an unspecified indication, start and stop date were not reported; lisinopril taken for an unspecified indication, start and stop date were not reported; lovastatin taken for an unspecified indication, start and stop date were not reported; fluoxetine taken for an unspecified indication, start and stop date were not reported; cyanocobalamin (VITAMIN B-12) taken for an unspecified indication, start and stop date were not reported; aspirin [acetylsalicylic acid] taken for an unspecified indication, start and stop date were not reported; and unspecified multivitamin tablet. The patient previously received 1st dose of bnt162b2 (Pfizer-BioNTech COVID 19) on 26Feb2021 07:45 PM in the left arm for Covid-19 immunization. The patient has not received other vaccine in four weeks. The first day after the shot, there were not any adverse reactions. The next morning at approximately 11:00 am, the reporter found patient laying on the floor next to his bed, eyes glazed over, disoriented, and he said "he felt funny". The reporter got him sitting up leaning on the side of the bed and called. The EMT's came and checked his vitals. Within half an hour from finding the patient laying on the floor, he seemed almost back to normal. However, since he is 89 years old, the patient was transported by ambulance. Blood was drawn, a urine sample was taken, a chest Xray, and a CT scan of his head and his spine were the labs that were run. All the labs came back normal. However, once patient got home after being in the ER for 5 hours, he is very weak, can barely stand and barely walk without human assistance and his walker. The way he is acting is more like he had a stroke. Onset of the events reported as 20Mar2021 11:15 AM. The events resulted in emergency room/department or urgent care. Outcome of the events was not recovered. The patient used walker due to can barely stand and barely walk; for other events, there was no treatment given. The patient was not diagnosed of Covid prior vaccination and has not been tested for Covid post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: Test Date: 20210320; Test Name: Blood; Result Unstructured Data: Test Result:normal; Test Date: 20210320; Test Name: chest Xray; Result Unstructured Data: Test Result:normal; Test Date: 20210320; Test Name: CT scan of his head and his spine; Result Unstructured Data: Test Result:normal; Test Date: 20210320; Test Name: vitals; Result Unstructured Data: Test Result:Unknwon Results; Test Date: 20210320; Test Name: urine sample; Result Unstructured Data: Test Result:normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bladder cancer; Bladder neoplasm surgery; Chronic kidney disease stage 3; Hypertension; Hypothyroidism; Hypoxia; Malignant melanoma; Malignant melanoma excision; Pre-diabetic; Vascular dementia
Andere Medikamente: DONEPEZIL; MEMANTINE; LEVOTHYROXINE; LISINOPRIL; LOVASTATIN; FLUOXETINE; VITAMIN B-12; ASPIRIN [ACETYLSALICYLIC ACID]
Allergien: -
Vorherige Impfungen: -

VAERS 1162930

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 02.04.2021
Impfdatum: 14.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / UN

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

Cerebral haemorrhage Death

Symptomtext

Patient died of a cerebral hemorrhage on 3/15/2021 at 11:30 AM.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None known.
Vorgeschichte: At the time of vaccination, the patient did not have any known chronic or long-standing health conditions. After death, the autopsy report said the patient had heart disease, but this was not known prior. The patient did not exhibit any symptoms of heart disease. I do not believe she had high blood pressure.
Andere Medikamente: Unsure of all supplements taken. However, these were recently purchased. Rosas Raw Hibiscus Concentrate, NOW NAC N-Acetyl Cystine, Solgar Melatonin Liquid, Host Defense Fungi Perfect Chaga Extract, Mother's Irish Moss, Lifeextension Echnc
Allergien: None known.
Vorherige Impfungen: -

VAERS 1116604

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: WI
Alter: 63,0
Geschlecht: M
Eingang: 02.04.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Balance disorder Fatigue Headache Movement disorder Cerebral haemorrhage Dizziness Gait disturbance Intensive care Pain Surgery Syncope

Symptomtext

The patient stated he felt fine the day he received the vaccine. However, starting the day after, he developed dizziness, achiness and a headache. These symptoms progressively worsened over the course of several days. On day 6 after receiving the vaccine, the patient stated his right leg started dragging and he had a difficult time functioning. The patient drove himself to the ER where he collapsed. A bleed in the brain was subsequently discovered and the patient underwent surgery, where he spent 3 days in the ICU. The patient was later discharged. As of today, the patient states he has resumed normal function

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None reported by patient
Vorgeschichte: Patient stated he has history of gout, high blood pressure and diabetes. He has also had a stent put in place several years ago
Andere Medikamente: Patient stated he is on a blood thinner (patient would not specify which one), metformin, atorvastatin and "blood pressure" medications
Allergien: No Known Drug allergies per patient
Vorherige Impfungen: -

VAERS 1156042

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: NY
Alter: 68,0
Geschlecht: M
Eingang: 01.04.2021
Impfdatum: 05.03.2021
Beginn: 05.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Blindness Cerebrovascular accident Computerised tomogram head abnormal Magnetic resonance imaging head abnormal

Symptomtext

Pfizer-BioNTECH Covid 19 vaccine EUA , side effect was a stroke affecting loss of vision in both eyes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: Cat Scan, MRI
Aktuelle Erkrankungen: -
Vorgeschichte: sarcoidiosis
Andere Medikamente: amolodopine, baby aspirin
Allergien: bee stings, shellfish
Vorherige Impfungen: -

VAERS 1155752

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MN
Alter: 73,0
Geschlecht: F
Eingang: 01.04.2021
Impfdatum: 10.03.2021
Beginn: 29.03.2021
Tage bis Beginn: 19,0
Dosis: 1
Route/Site: - / -

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

Death

Symptomtext

Patient death within 60 days of receiving a COVID vaccine

Weitere VAERSDATA-Felder

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

VAERS 1153547

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: WA
Alter: 77,0
Geschlecht: M
Eingang: 31.03.2021
Impfdatum: 12.02.2021
Beginn: 18.02.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal discomfort Abdominal pain lower Abdominal tenderness Biopsy lymph gland abnormal Cough Computerised tomogram Infection Leukaemia Lymphoma SARS-CoV-2 test Death Diarrhoea Diffuse large B-cell lymphoma Faeces discoloured Fluorescent in situ hybridisation negative Immunohistochemistry Nausea Weight decreased

Symptomtext

Diffuse large B cell lymphoma. Died 03/25/2021. See item 11 for additional details. We became aware of the situation via a post on our social media page placed by the patient's daughter-in-law on or about 03/22/2021. I reached the patient's son on 03/25/2021, and then we pursued information from the hospital. The initial social media post suggested that the onset of cervical lymphadenopathy followed dose 1, but the hospitalist's history suggests it predated that ("8-10 weeks" prior to 03/18/2021 admission).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: See item 11. Cervical LN bx 03/22/2021: Diffuse large B-cell lymphoma, activated B-cell phenotype (Hans Classification). Positive for double expression (BCL-2 80-90%, c-MYC 50-60%) by immunohistochemistry. EBV-EBER is negative by in situ hybridization.
Aktuelle Erkrankungen: Upon admission to hospital on 03/18/2021, he reported, "...for the last month or so he has had 'really bad cough,' nausea and abdominal pain but no vomiting. Abdominal pain is in lower abdomen, pressure-like, non-radiating, hurts more when moves onto left side and better laying down and on right side. Has watery diarrhea, non-bloody, 'yellow water' having several episodes per day over this time as well. Has lost nearly 30 pounds with weight down to 260 from 288 pounds over this period of time. Has noticed lymph node swelling in neck 8 to 10 weeks ago, generally nonpainful unless lays on eat wrong way. Has been evaluated as an outpatient with reported multiple negative COVID-19 tests. Had recent labs with elevated WBC and liver function tests with CT neck,chest/abdomen/pelvis recently showing diffuse adenopathy concerning for lymphoma for which he underwentFNA the other day which was non-diagnostic. He was scheduled for lymph node biopsy today but when he woke up felt poorly and had wife call 911." Left cervical lymph node biopsy of 03/22/2021 revealed a diffuse large B-cell lymphoma, activated B-cell phenotype.
Vorgeschichte: Aortic regurgitation, diabetes mellitus type 2, hypertension, hyperlipidemia, obesity
Andere Medikamente: Pfizer dose 1: 02/12/2021 (left deltoid) Pfizer dose 2: 03/09/2021 (left deltoid) No other known medications.
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1095221

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MD
Alter: 66,0
Geschlecht: M
Eingang: 31.03.2021
Impfdatum: 09.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: IM / RA

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

Acute myocardial infarction Chest pain Stent placement Angina unstable Condition aggravated Dyspnoea Hypertensive urgency Pain in jaw

Symptomtext

3/17/21: patient presented and was admitted through ED for chest pain. Patient had recent event of NSTEMI and stent was placed last Friday. Per the EUA, hospitalizations are to be reported irrespective of attribution to vaccine.

Weitere VAERSDATA-Felder

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

VAERS 1144851

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 80,0
Geschlecht: F
Eingang: 29.03.2021
Impfdatum: 16.03.2021
Beginn: 21.03.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Cerebral infarction Cerebrovascular accident Hypertension Nervous system disorder

Symptomtext

Acute CVA (cerebrovascular accident) Focal neurological deficit Uncontrolled hypertension Cerebral infarction, unspecified

Weitere VAERSDATA-Felder

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

VAERS 1144648

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 99,0
Geschlecht: F
Eingang: 29.03.2021
Impfdatum: 05.02.2021
Beginn: 24.02.2021
Tage bis Beginn: 19,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Pulmonary embolism

Symptomtext

Pulmonary embolism (CMS/HCC) COVID-19

Weitere VAERSDATA-Felder

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

VAERS 1143277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 84,0
Geschlecht: F
Eingang: 29.03.2021
Impfdatum: 10.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: IM / RA

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

Cerebral haemorrhage Haemorrhage intracranial Hypertension Mental status changes

Symptomtext

Altered mental status Intracranial hemorrhage (CMS/HCC) Hypertension Cerebral brain hemorrhage (CMS/HCC

Weitere VAERSDATA-Felder

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

VAERS 1143254

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 29.03.2021
Impfdatum: 17.03.2021
Beginn: 24.03.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

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

Death

Symptomtext

Death

Weitere VAERSDATA-Felder

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

VAERS 1139491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: NY
Alter: 45,0
Geschlecht: F
Eingang: 27.03.2021
Impfdatum: 22.03.2021
Beginn: 25.03.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test Chest X-ray Chest pain Chills Computerised tomogram Dyspnoea Electrocardiogram Hyperhidrosis Immune system disorder Pulmonary embolism

Symptomtext

I had my second vaccine on Monday, 3/22, and woke up at 1am on Thursday 3/25 with extreme chest pain, shortness of breath, sweating and chills. I went to the ER, and they discovered two blood clots in my lungs. I've never had pulmonary embolisms before, so this is a very strange coincidence. I am in cancer treatment, so my risk of PEs is higher, but the timing is too close for me not to think that the second vaccine traumatized my immune system, causing the PEs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: EKG, Chest x-ray, blood work and CT scan.
Aktuelle Erkrankungen: Stage 4 breast cancer
Vorgeschichte: Stage 4 breast cancer
Andere Medikamente: Levothyroxine, Vit D, Vit B, Iron supplement, and in my off-week from taking Xeloda for stage 4 breast cancer.
Allergien: none
Vorherige Impfungen: -

VAERS 1134477

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: VA
Alter: 78,0
Geschlecht: F
Eingang: 25.03.2021
Impfdatum: 23.03.2021
Beginn: 24.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Death Resuscitation Unresponsive to stimuli

Symptomtext

Resident found unresponsive found at 1545, CPR done, EMS responded and resident Pronounced Dead at 1615

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Diabetes type2, CVA, Hyperlipidemia, Hypokalemia, Schizophrenia, Anemia
Vorgeschichte: Same as #11
Andere Medikamente: Risperidone 0.25mgmat bedtime Risaqurad Capsule 1 PO Morning and night Potassium chloride 20MEQ/16ml (10%) 16 ml QAM Norvasc Tab 6mg 1tab QAM Mirtazapine Tab 7.5mg I tab PO at night Metformin HCL tab 600mg 2 tab AM
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1131328

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: MA
Alter: 69,0
Geschlecht: F
Eingang: 24.03.2021
Impfdatum: 18.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Death Gastrointestinal disorder

Symptomtext

Severe GI symptoms followed by death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: bronchitis, seasonal allergies
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 1124121

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: FL
Alter: 62,0
Geschlecht: M
Eingang: 22.03.2021
Impfdatum: 19.03.2021
Beginn: 21.03.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / RA

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

Cough Death

Symptomtext

DECEDENT WAS NOTED TO BE COUGHING FOLLOWING THE ADMINISTERING OF THE VACCINE. FAMILY INTERVIEWED COULD NOT RECALL WHETHER THE DECEDENT WAS COUGHING PRIOR TO RECEIVING THE VACCINE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: NONE REPORTED.
Aktuelle Erkrankungen: NONE REPORTED.
Vorgeschichte: DM, CHF, HTN, MORBID OBESITY
Andere Medikamente: LASIX, INSULIN
Allergien: SEASONAL ALLERGIES
Vorherige Impfungen: -

VAERS 1123532

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: FL
Alter: 101,0
Geschlecht: F
Eingang: 22.03.2021
Impfdatum: 20.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Death Diarrhoea Headache Respiratory arrest Unresponsive to stimuli

Symptomtext

Dose given at 1649hrs. At 2030hrs, complaints of headache and diarrhea. At 0100hrs on 03/21, family noticed patient unresponsive and not breathing. Fire rescue called out and pronounced her at 0210hrs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, Hyperlipidemia, Stroke
Andere Medikamente: Lipitor, Furosemide, Metoprolol
Allergien: None
Vorherige Impfungen: -

VAERS 1121906

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: PA
Alter: 90,0
Geschlecht: F
Eingang: 22.03.2021
Impfdatum: 18.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Death Dizziness Injection site pain Nausea

Symptomtext

Site: Pain at Injection Site-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Nausea-Medium, Additional Details: Coroners Office contacted Pharmacy on 3/21/21 to report a patient who had recieved a dose of the covid vaccine on 3/18/21 and was founded deceased on 3/20/2021

Weitere VAERSDATA-Felder

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

VAERS 1118914

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: CA
Alter: 84,0
Geschlecht: F
Eingang: 20.03.2021
Impfdatum: 11.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: IM / LA

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

Angiogram Blood pressure abnormal Brain natriuretic peptide increased Chest X-ray normal Dyspnoea Ischaemia Lung consolidation Myocardial strain Oxygen saturation decreased Pneumothorax Pulmonary embolism Pulmonary hypertension Respiratory rate increased

Symptomtext

SHORTNESS OF BREATH PT bibm c/o sob, per medics new afib rvr with elevated respirations and low et02 and bp. patient had a recent covid vaccine last week. Chest x-ray is normal but her BNP is elevated which may be related to her underlying ischemia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: CT angio Chest: Large right main pulmonary artery emboli, with essentially complete obstruction of right pulmonary arteries. Additional left segmental and subsegmental pulmonary emboli at upper and lower lobes. Probable resulting pulmonary hypertension and right heart strain. Complete collapse and consolidation left lower lobe
Aktuelle Erkrankungen: ESSENTIAL HYPERTENSION AORTIC VALVE STENOSIS ATRIAL FIBRILLATION W RAPID VENTRICULAR RESPONSE PULMONARY HTN PULMONARY EMBOLISM ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN HYPERGLYCEMIA ACUTE HYPOXEMIC RESPIRATORY FAILURE ABNL LUNG IMAGING ELEVATED TROPONIN I NONTRAUMATIC ACUTE KIDNEY INJURY
Vorgeschichte: OSTEOPOROSIS HYPOTHYROIDISM COLON POLYP PREDIABETES DIVERTICULOSIS OF COLON THROMBOCYTOPENIA, UNSPECIFIED HYPERLIPIDEMIA SCREENING COLONOSCOPY FHX OF COLON CANCER
Andere Medikamente: Hydrochlorothiazide, Losartan, Metoprolol, Levothyroxine, Timolol, Atorvastatin, latanoprost
Allergien: Lisinopril, Keflex, Cipro, Bactrim, Nickel, Nitrofurantoin, aspirin
Vorherige Impfungen: -

VAERS 1118702

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: TN
Alter: 66,0
Geschlecht: M
Eingang: 20.03.2021
Impfdatum: 15.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Aphasia Blood cholesterol increased Blood triglycerides increased Cerebrovascular accident Computerised tomogram abnormal Echocardiogram normal Magnetic resonance imaging normal Thrombosis Ultrasound scan normal Urine analysis normal Visual impairment

Symptomtext

Had a stroke 36 hours after getting second vaccine. Lost ability to speak and see clearly, had word salad. Was identified quickly by my wife and was taken by ambulance to hospital where they gave me TPA clot buster infusion after identifying a clot in my left back side of brain and luckily I responded well and have all speech function back we believe so far.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: Ct scan- showed clot in left back Brain. neck scan - no clots in neck arteries. echo gram was negative. Mri was negative- no damage. Pulmonary ultrasound for extremities was negative. Blood pressure was high end of normal range. cholesterol blood work, triglycerides and cholesterol were initially high. Urinalysis was clear and negative.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1105193

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: IA
Alter: 83,0
Geschlecht: M
Eingang: 16.03.2021
Impfdatum: 12.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / UN

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

Death Pulmonary fibrosis

Symptomtext

Death due to pulmonary fibrosis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Patient was hospitalized from 1/31- 2/4 with SARS- COVID-19 pneumonia.
Vorgeschichte: chronic hypoxemic respiratory failure, pulmonary fibrosis, coronary artery disease, diastolic heart failure, ALS, type 2 diabetes, obesity, hypothyroidism, BPH, anemia, degenerative lumbar disc disease, diverticulosis, gout, hyperlipidemia, ocular hypertension, orthostatic hypotension, sleep apnea
Andere Medikamente: acetaminophen, benzonatate, clopidogrel, cyclobenzaprine, docusate-senna prn, doxylamine, escitalopram, fluticasone topical, furosemide, hydrocortisone topical, latanoprost ophthalmic, levothyroxine, metformin, midodrine, nitroglycerin prn,
Allergien: celebrex, penicillin, sulfa drugs, tramadol
Vorherige Impfungen: -

VAERS 1103970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

kritisch

Staat: WV
Alter: 66,0
Geschlecht: M
Eingang: 16.03.2021
Impfdatum: 11.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Death Illness Pallor Peripheral coldness Pulse absent

Symptomtext

Reported by EMS per report from wife that he was "sick after shot" and got worse during the night. Wife found him the following morning cold and pale, pulseless. Dispatch called at 719AM. Pt pronounced on the scene and taken to Funeral Home. Uncertain if Medical Exam is planned

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: no
Vorherige Impfungen: -

VAERS 2725913

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: VA
Alter: 59,0
Geschlecht: F
Eingang: 20.12.2023
Impfdatum: 12.03.2021
Beginn: 01.05.2021
Tage bis Beginn: 50,0
Dosis: 1
Route/Site: IM / LA

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

Myoclonic epilepsy Seizure

Symptomtext

event: myoclonic epilepsy (seizures) 10 to 15 seizures each day since vaccine. never had seizures prior to vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: anxiety
Andere Medikamente: zoloft 50mg daily
Allergien: -
Vorherige Impfungen: frozen shoulder from tetanus shot in 2020

VAERS 2713930

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: WA
Alter: 28,0
Geschlecht: F
Eingang: 14.11.2023
Impfdatum: 18.03.2021
Beginn: 18.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Blood pressure decreased Blood pressure increased Blood pressure measurement Condition aggravated Diplopia Dizziness postural Dystonia Fibromyalgia Headache Heart rate Heart rate abnormal Illness Migraine Muscle spasms Pain Postural orthostatic tachycardia syndrome Presyncope SARS-CoV-2 test

Symptomtext

severe dystonia, doesn't allow me to use my feet or hands.; Immediately sick; headache; I have had a migraine since and it will not go away.; POTS; Fibromyalgia; BVD; my health worsened; My vision has decreased and is blurry; My vision has decreased and is blurry; My vision over lapping, or double.; I am constantly dizzy and cannot tolerate being upright.; My body is in constant pain; muscle spasms; issues with my heart rate; Blood pressure increases; Blood pressure decreases; Fall risk, prone to fainting; This is a spontaneous report received from a contactable reporter (Consumer or other non HCP). The reporter is the patient. A 28-year-old female patient received bnt162b2 (BNT162B2), on 18Mar2021 at 10:30 as dose 1, single (Lot number: EN6208) at the age of 28 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "iih" (unspecified if ongoing); "depression" (unspecified if ongoing). Concomitant medication(s) included: PROZAC; POTASSIUM; DIAMOX [ACETAZOLAMIDE]; VIT D [VITAMIN D NOS]; MAGNESIUM; RIBOFLAVIN. Past drug history included: Amoxicillin, reaction(s): "known allergies". The following information was reported: VISUAL IMPAIRMENT (hospitalization, disability) with onset 18Mar2021 at 10:30, outcome "not recovered", described as "BVD"; BLOOD PRESSURE DECREASED (hospitalization, disability) with onset 18Mar2021 at 10:30, outcome "not recovered", described as "Blood pressure decreases"; BLOOD PRESSURE INCREASED (hospitalization, disability) with onset 18Mar2021 at 10:30, outcome "not recovered", described as "Blood pressure increases"; PRESYNCOPE (hospitalization, disability) with onset 18Mar2021 at 10:30, outcome "not recovered", described as "Fall risk, prone to fainting"; FIBROMYALGIA (hospitalization, disability) with onset 18Mar2021 at 10:30, outcome "not recovered"; DIZZINESS POSTURAL (hospitalization, disability) with onset 18Mar2021 at 10:30, outcome "not recovered", described as "I am constantly dizzy and cannot tolerate being upright."; MIGRAINE (hospitalization, disability) with onset 18Mar2021 at 10:30, outcome "not recovered", described as "I have had a migraine since and it will not go away."; ILLNESS (hospitalization, disability) with onset 18Mar2021 at 10:30, outcome "not recovered", described as "Immediately sick"; PAIN (hospitalization, disability) with onset 18Mar2021 at 10:30, outcome "not recovered", described as "My body is in constant pain"; VISUAL IMPAIRMENT (hospitalization, disability), VISION BLURRED (hospitalization, disability) all with onset 18Mar2021 at 10:30, outcome "not recovered" and all described as "My vision has decreased and is blurry"; DIPLOPIA (hospitalization, disability) with onset 18Mar2021 at 10:30, outcome "not recovered", described as "My vision over lapping, or double."; POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME (hospitalization, disability) with onset 18Mar2021 at 10:30, outcome "not recovered", described as "POTS"; HEADACHE (hospitalization, disability) with onset 18Mar2021 at 10:30, outcome "not recovered"; HEART RATE ABNORMAL (hospitalization, disability) with onset 18Mar2021 at 10:30, outcome "not recovered", described as "issues with my heart rate"; MUSCLE SPASMS (hospitalization, disability) with onset 18Mar2021 at 10:30, outcome "not recovered"; CONDITION AGGRAVATED (hospitalization, disability) with onset 18Mar2021 at 10:30, outcome "not recovered", described as "my health worsened"; DYSTONIA (hospitalization, disability, medically significant) with onset 18Mar2021 at 10:30, outcome "not recovered", described as "severe dystonia, doesn't allow me to use my feet or hands.". The patient was hospitalized for dystonia, illness, headache, migraine, postural orthostatic tachycardia syndrome, fibromyalgia, visual impairment, condition aggravated, visual impairment, vision blurred, diplopia, dizziness postural, pain, muscle spasms, heart rate abnormal, blood pressure increased, blood pressure decreased, presyncope (hospitalization duration: 4 day(s)). The events "severe dystonia, doesn't allow me to use my feet or hands.", "immediately sick", "headache", "i have had a migraine since and it will not go away.", "pots", "fibromyalgia", "bvd", "my health worsened", "my vision has decreased and is blurry", "my vision over lapping, or double.", "i am constantly dizzy and cannot tolerate being upright.", "my body is in constant pain", "muscle spasms", "issues with my heart rate", "blood pressure increases", "blood pressure decreases" and "fall risk, prone to fainting" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: Blood pressure measurement: (unspecified date) decreases, notes: Blood pressure increases and decreases to dangerous levels; (unspecified date) increases, notes: Blood pressure increases and decreases to dangerous levels; Heart rate: (unspecified date) issues with my heart rate; SARS-CoV-2 test: (01Oct2021) Inconclusive, notes: Nasal Swab. It was unknown if therapeutic measures were taken as a result of dystonia, illness, headache, migraine, postural orthostatic tachycardia syndrome, fibromyalgia, visual impairment, condition aggravated, visual impairment, vision blurred, diplopia, dizziness postural, pain, muscle spasms, heart rate abnormal, blood pressure increased, blood pressure decreased, presyncope. Clinical course: immediately sick and had headache. Patient have had a migraine since and it will not go away. Caused POTS, Fibromyalgia, BVD, and other Illnesses. After the vaccine, patient went to the ER 4 times before being admitted into the hospital for an intractable migraine and was released still in pain and sick. For over 2 years after the vaccine patient continued to collect symptoms and her health worsened. Her vision had decreased and was blurry, over lapping, or double. Patient was constantly dizzy and cannot tolerate being upright. Her body was in constant pain and the severe dystonia did not allow her to use her feet or hands. Constant muscle spasms and issues with heart rate. Blood pressure increases and decreases to dangerous levels. Fall risk, prone to fainting. Patient had dose 2 (lot number: ER8729) on 09Apr2021 at 04:30 PM on right arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: 4,0
Labordaten: Test Name: Blood pressure; Result Unstructured Data: Test Result:decreases; Comments: Blood pressure increases and decreases to dangerous levels.; Test Name: Blood pressure; Result Unstructured Data: Test Result:increases; Comments: Blood pressure increases and decreases to dangerous levels.; Test Name: Heart rate; Result Unstructured Data: Test Result:issues with my heart rate; Test Date: 20211001; Test Name: Nasal Swab; Test Result: Inconclusive ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Depression; Idiopathic intracranial hypertension
Andere Medikamente: PROZAC; POTASSIUM; DIAMOX [ACETAZOLAMIDE]; VIT D [VITAMIN D NOS]; MAGNESIUM; RIBOFLAVIN
Allergien: -
Vorherige Impfungen: -

VAERS 2685696

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MN
Alter: 40,0
Geschlecht: F
Eingang: 24.09.2023
Impfdatum: 22.02.2021
Beginn: 15.03.2021
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: UN / LA

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

Blindness Dyskinesia Dyspnoea Dyspnoea exertional Electric shock sensation Exercise tolerance decreased Facial pain Herpes simplex test positive Hypoaesthesia Impaired work ability Laboratory test normal Loss of personal independence in daily activities Muscle spasms Muscle twitching Pain in extremity Palpitations Screaming Skin swelling

Symptomtext

I received the vaccine in Feb. and March of 2021. That summer, I climbed a flight of stairs and noticed my heart was pounding and I was out of breath. After this continued, I asked doctors about it and I was dismissed. Within several more months I started twitching involuntarily. Even my eye balls would twitch in their sockets. I could visually see my muscles having spasms throughout my body. My skin would raise up and down. My feet and hands began to fall asleep on their own accord. I would get zaps in my face and feet so painful I would yell out in pain. I lost vision and have lived with a significant reduction in my vision. The overall impact on my body took away my ability to work out like I used to. Just the other day I gasped for air and almost threw up after just a short workout trying to push it like I used to. My life got taken away from me. I "all of a sudden" tested positive for herpes two. EVEN THOUGH I was negative (I have the test) when I got the vaccine and I had NO new partners. The stupid thing triggered my T cells to malfunction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: Like the majority of people, my tests come back normal. But, my history before and after speaks for itself. So do my medical charts that prove this.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Buproprion XL 150 mg every other day.
Allergien: -
Vorherige Impfungen: -

VAERS 2618955

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 21.04.2023
Impfdatum: 27.10.2021
Beginn: 31.05.2022
Tage bis Beginn: 216,0
Dosis: 3
Route/Site: - / -

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

Hypoxia Lacunar stroke Symptom recurrence Thalamic stroke

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE LACUNAR STROKE, UNSPECIFIED TYPE AND ARTERY ACUTE STROKE OF THALAMUS, UNSPECIFIED TYPE AND ARTERY HYPOXEMIA 6/1/2022, 6/29/2022, 6/30/2022. & 2/8/2023 - RECURRENCE OF SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2610194

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

schwer

Staat: -
Alter: 65,0
Geschlecht: F
Eingang: 05.04.2023
Impfdatum: 23.02.2021
Beginn: 03.04.2023
Tage bis Beginn: 769,0
Dosis: 2
Route/Site: IM / AR

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

Laboratory test Myocarditis

Symptomtext

myocarditis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: MCG 4/3/23
Aktuelle Erkrankungen: na
Vorgeschichte: na
Andere Medikamente: na
Allergien: na
Vorherige Impfungen: -

VAERS 2584074

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: AR
Alter: 62,0
Geschlecht: F
Eingang: 19.02.2023
Impfdatum: 25.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Abdominal pain upper Choking Colon operation Decreased appetite Dizziness Dyspnoea Immediate post-injection reaction Intestinal mass Mass excision Nausea Pancreatitis Pancreatitis chronic Pancreatitis necrotising Peripheral artery thrombosis Peripheral swelling Swelling Vomiting

Symptomtext

Instant trouble breathing, feet swelled within 24 hours from first dose, stayed swollen, second dose extreme breathing choking trouble, dizzy light headed. Notified nurse immediately. Extreme swelling persisted for months, stomach aches trouble eating vomiting nausea. Continued for over one year. Doctors dismissed any discussion regarding COVID shot,symptoms worsened to several hospital procedures emergency room care and more surgery. Sudden onset of pancreatitis attack. Never had any pancreas issue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Peripheral artery thrombosis
Hospital-Tage: 20,0
Labordaten: Both leg artery reduction clots and blockage, removal of large masses in colon, urgent surgery removed large colon mass, mass still in colon. Severe sudden pancreas attack has left me with necrosis of pancreas and chronic pancreatitis. Waiting on another surgery. I have no history of and alcohol intake. Never had alcohol
Aktuelle Erkrankungen: None
Vorgeschichte: Back surgery, knee surgery, shoulder surgery
Andere Medikamente: None
Allergien: Sulfa, iodine, cefalix
Vorherige Impfungen: -

VAERS 2560227

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: FL
Alter: 50,0
Geschlecht: F
Eingang: 15.01.2023
Impfdatum: 24.03.2021
Beginn: 24.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Antiacetylcholine receptor antibody Arthralgia Blood copper Blood test Borrelia test Cardiac stress test Chest X-ray Chest pain Cognitive disorder Computerised tomogram abdomen Computerised tomogram head Computerised tomogram spine Confusional state Diplegia Dysphemia Electric shock sensation Electrocardiogram

Symptomtext

After 1st and 2nd doses of Pfizer COVID vaccine I experienced ringing in ears, joint pain, headache, fatigue, swollen joints, and nausea that never went away. After Booster shot I experienced all of the above plus additional symptoms that have slowly added over time. My symptoms are constantly changing and now include but are not limited to: Widespread debilitating burning and aching pain in my arms, legs, neck and chest. Weight Loss, Cognitive issues, brain fog and confusion. Abdominal pain, pain in jaw and all teeth. Left side face paralysis of eye and mouth causing a sneering look. In June 2022 I began stuttering when I talk and starting having seizure like myoclonic jerking of both arms, legs and neck. New symptoms since include: Tremors, falling, intermittent paralysis of arms. Tingling, numbness, electric shocks throughout body. muscle twitching and spasms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: 2022 CT and MRI of brain and spinal cord CT scan of abdomen Heart stress test EKG EEG Chest xrays spine xrays sleep test Multiple blood panels repeated throughout the year: CBC Thyroid Metabolic panel Hepatitis HIV STD Rheumatoid factors SED rate Iron, TIBC Hemoglobin D-Dimer Hepatic HLA-B27 DNA typing Lyme screen Celiac Heavy Metal Copper Acetylcholine receptor binding
Aktuelle Erkrankungen: none
Vorgeschichte: psoriasis and psoriatic arthritis
Andere Medikamente: Cosentyx
Allergien: none
Vorherige Impfungen: -

VAERS 2553618

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

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

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

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

Symptomtext

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

Weitere VAERSDATA-Felder

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

VAERS 2539118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MI
Alter: 89,0
Geschlecht: F
Eingang: 21.12.2022
Impfdatum: 04.03.2021
Beginn: 07.10.2022
Tage bis Beginn: 582,0
Dosis: 2
Route/Site: - / -

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

Computerised tomogram normal Confusional state Coronary arterial stent insertion Coronary artery disease Fall COVID-19 Cardiac pacemaker evaluation Catheterisation cardiac abnormal Chest X-ray normal Computerised tomogram head normal Implantable defibrillator insertion Percutaneous coronary intervention Post procedural complication Pyrexia SARS-CoV-2 test positive Skin laceration Syncope Troponin increased

Symptomtext

90y.o. male with multiple medical problems including CAD, dementia, paroxysmal atrial fibrillation, sick sinus syndrome status post permanent pacemaker who presented to ED on 10/7/2022 from a local hospital for cardiology consultation. Patient was evaluated at the hospital after sustaining a fall/syncopal episode. Per notes his wife heard a noise and found patient on the floor. He had a scalp laceration that was repaired at a facility. His PPM was interrogated and showed a 2-minute run of V. tach. Troponin was elevated (175, 378, 504, 663). He underwent cardiac cath on 10/9 which showed multivessel disease, successful PCI and stent placement. Family requested transfer to our facility as this is where he receives most of his care. Patient was placed on IV heparin drip. CT head/cervical spine negative, chest x-ray, pelvic x-ray negative. He is now S/P post pacemaker upgrade to ICD implant by Dr. on 10/11/22. Pts post-operative course was complicated by confusion, fevers due to COVID-19 infection. He is s/p remdesivir and dexamethasone and has since been removed from isolation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: 10/13 SARS-CoV-2 -COVID-19 by NAA, Micro -- detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2518386

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IL
Alter: 38,0
Geschlecht: F
Eingang: 28.11.2022
Impfdatum: 07.04.2021
Beginn: 08.04.2022
Tage bis Beginn: 366,0
Dosis: 1
Route/Site: IM / AR

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

Arrhythmia Blood catecholamines normal Catecholamines urine normal Diagnostic procedure Echocardiogram normal Electrocardiogram Electrocardiogram ambulatory Electroencephalogram normal Electromyogram normal Fatigue Feeling abnormal Heart rate abnormal Heart rate decreased Hypotension Immediate post-injection reaction Magnetic resonance imaging head normal Muscle twitching Presyncope

Symptomtext

Began with muscle twitches and tremors, brain fog and exhaustion immediately following vaccination. Drop in heart rate observed between doses 1-2. Cardiac symptoms developed over time, including rapid swings in heart rate, sudden onset hypotension, and severe episodes of full body tremors presenting alongside full body tremors, pre-syncope and tinnitus. Sudden onset of new arrthymias, specifically runs of non-sustained ventricular tachycardia (NSVT). Symptoms similar to dysautonomia but does not meet full clinical criteria. Patient had no prior medical history and diagnostic testing has found no common cause, even as symptoms persisted. Patient sought medical care, did not initially suspect vaccine understanding it to be safe and effective. Patient received booster shot in December 2021 and began to suspect vaccine involvement when symptoms worsened after booster. The more time that passes since the last dose, patient is gradually improving but still struggles with arrythmias and tachycardia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: 1,0
Labordaten: Numerous ECGs and Holter monitors Echocardiogram, November 2021 - normal EEG, EMG, Brain MRI, June 2022 - normal Catecholamines, plasma and urine- November 2021, January 2022, August 2023 - normal Tilt table test - January 2022 - inconclusive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D; Excedrin (as needed)
Allergien: None
Vorherige Impfungen: -

VAERS 2513929

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MI
Alter: 83,0
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 19.03.2021
Beginn: 14.11.2022
Tage bis Beginn: 605,0
Dosis: 1
Route/Site: IM / UN

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

COVID-19 Confusional state Cough Oropharyngeal pain Productive cough Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Syncope

Symptomtext

Pt transfer to facility 11/11 from previous facility for syncope. 11/14 pt with sore throat, pt COVID+ 11/14. 11/15 pt with fever on and off, complaining of congested cough. 11/16 pt aox2-3, confused, denies pain, non-productive cough, on room air, afebrile. 11/17 Pt a&ox3, denies any distress. Pt discharged on 11/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 11,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: OSA (obstructive sleep apnea) Digestive Fatty liver Endocrine Acquired hypothyroidism Syncope Multiple-type hyperlipidemia Stage 3a chronic kidney disease Acquired hammer deformity of great toe Osteitis of pelvic region Complex renal cyst Essential hypertension Anxiety and depression Vasovagal syncope History of loop recorder Orthostatic hypotension Paroxysmal A-fib History of colonoscopy Cognitive deficits SSS (sick sinus syndrome) Syncope, unspecified syncope type Angina of effort Syncope S/P cardiac catheterization
Andere Medikamente: aspirin 81 MG PO Chew Tab atorvastatin (LIPITOR) 40 MG PO Tab escitalopram (LEXAPRO) 10 MG PO Tab levothyroxine (Synthroid) 75 MCG PO Tab lisinopril (PRINIVIL, ZESTRIL) 40 MG PO Tab metoprolol (TOPROL XL) 50 MG PO TABLET SR 24 HR ticagrelor
Allergien: Amoxicillin Celecoxib Clavulanic Acid Cox-2 Inhibitors Morphine And Related Sulfanilamide Tetanus Toxoids
Vorherige Impfungen: -

VAERS 2472653

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MD
Alter: 60,0
Geschlecht: F
Eingang: 08.10.2022
Impfdatum: 15.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Fatigue Nausea Syncope Tilt table test positive

Symptomtext

Fainting syncope??Severe fatigue, dizziness, light-headedness, nausea Stadium was site of initial vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Tilt table test 11 months later which revealed fainting syncope at hospital with my cardiologist. In city
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Synthroid, Rousuvastatin, Paroxetine, lisinipril
Allergien: None
Vorherige Impfungen: -

VAERS 2453564

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MI
Alter: 75,0
Geschlecht: F
Eingang: 21.09.2022
Impfdatum: 03.03.2021
Beginn: 24.08.2022
Tage bis Beginn: 539,0
Dosis: 2
Route/Site: IM / UN

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

Asthenia COVID-19 Cardiac monitoring Chest pain Confusional state Cough Dialysis Hypophagia Intensive care Lethargy SARS-CoV-2 test positive

Symptomtext

Patient to ED 8/24 ED for Dialysis from Nursing home. Patient COVID+ 8/24. 8/25 patient remains very weak with infrequent non productive cough. 8/26 Patient A0X4, denies any complaints of CP/SOB. 8/29 patient is resting with no dyspnea, poor oral intake, on nasal cannula. 8/31 patient respirations even and unlabored and chest expansion is symmetrical. Patient placed on cardiac monitor, denies shortness of breath or chest pain. 9/3 patient is A&Ox4, on RA, no signs of respiratory distress noted. 9/7 transferred out of the ICU, is resting and weak. 9/8 patient is A&O x 2-3 with periods of confusion, lethargic, denies any SOB/chest pain, no S/S of acute distress. Patient complaining of chest pain, worsened by cough. 9/14 patient discharged.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 15,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: Bronchospasm with bronchitis, acute Pulmonary emphysema (CMS/HCC), Acute exacerbation of chronic obstructive pulmonary disease (COPD) (CMS/HCC), Bilateral pleural effusion Adynamic ileus (CMS/HCC), Carotid stenosis, Subclavian artery stenosis, left Subclavian steal syndrome, Claudication of right lower extremity, SOB (shortness of breath), Coronary artery disease of native artery of native heart with stable angina pectoris (CMS/HCC), Mixed hyperlipidemia, Essential hypertension, Mitral valve insufficiency, Aortic ectasia (CMS/HCC), PAD (peripheral artery disease) (CMS/HCC), Obesity (BMI 30-39.9), CKD (chronic kidney disease), stage IV (CMS/HCC), Hyperkalemia Edema of both legs, Pericardial effusion, Paroxysmal atrial fibrillation (CMS/HCC), Iron deficiency anemia due to chronic blood loss A-fib (CMS/HCC), Persistent atrial fibrillation (CMS/HCC), Septic shock (CMS/HCC), Acquired thrombocytopenia (CMS/HCC), Acute urinary retention, Hydronephrosis, right Hypothermia, Atrial fibrillation with RVR (CMS/HCC), ESRD (end stage renal disease) (CMS/HCC)
Andere Medikamente: albuterol (PROVENTIL, VENTOLIN, PROAIR) HFA 108 (90 Base), MCG/ACT INHAL Aero Soln, amiodarone (CORDARONE, PACERONE) 200 MG PO Tab, aspirin (ECOTRIN) 81 MG PO Tablet Delayed Response, atorvastatin (LIPITOR) 40 MG PO Tab, B complex-vitamin c
Allergien: Iodinated Diagnostic Agents, Sulfa Antibiotics, Codeine, Meperidine HCL
Vorherige Impfungen: -

VAERS 2433424

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 02.03.2021
Beginn: 14.08.2022
Tage bis Beginn: 530,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Confusional state Cough Diabetic ketoacidosis Dyspnoea Intensive care Nausea Respiratory distress SARS-CoV-2 test positive Vomiting

Symptomtext

66-year-old female brought into the emergency room history of diabetes difficulty with breathing, nausea and vomiting last 2 to 3 days. Patient a little more awake and alert than on admission. Patient is still confused about how long she has been in the hospital. History of camping with their motor home in Park the week of 24 July. There for 3 to 4 days with her grandchildren. Apparently one of the grandchildren started to feel ill on the way home 27th 28th. Patient has been home with some respiratory distress. Patient was tested at home 8/10 tested positive they called primary care and was given a prescription for Paxlovid. Patient states she took it on the 10th 11th and 12th and on the morning of admission here. Patient had progressive nausea and vomiting over the last 2 to 3 days. Patient was noted to require O2 in the ER placed on 2 L with progression over the next 24 hours. Patient has been evaluated by MICU, currently on 6 to 7 L. Breathing better. Patient maintained on the floor. Infectious diseases been asked to assist. Patient able to call her husband to verify dates. Infectious disease has been asked to assist. Patient has cough shortness of breath does not require home O2 normally. She was found to have COVID and was in DKA. She received dexamethasone 6 mg daily, now complete.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 10,0
Labordaten: 8/14 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC-- detected
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2359772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: FL
Alter: 52,0
Geschlecht: M
Eingang: 06.07.2022
Impfdatum: 29.04.2022
Beginn: 26.05.2022
Tage bis Beginn: 27,0
Dosis: 1
Route/Site: SYR / LA

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

Angiogram cerebral Computerised tomogram abdomen Computerised tomogram head Computerised tomogram thorax Jugular vein thrombosis Magnetic resonance imaging head abnormal Scan with contrast Scan with contrast abnormal Sigmoid sinus thrombosis Transverse sinus thrombosis Vascular occlusion

Symptomtext

MRI Brain w/wo 5/27/22 Acute thrombosis of the proximal right IJ vein and right sigmoid and transverse sinuses, nearly completely occlusive at the sigmoid sinus.

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Praegender Schweregrund: Jugular vein thrombosis
Hospital-Tage: -
Labordaten: MRI Brain w/wo 5/27/22, CT head with IV contrast- 5/30/22, MRA head 5/31/22, MRA head 6/2/22, CT C/A/P
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, MS
Andere Medikamente: Vitamin D3 125mcg, Amlodapine 10mg, Losartan 100mg
Allergien: NKA
Vorherige Impfungen: -

VAERS 2320663

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 56,0
Geschlecht: M
Eingang: 15.06.2022
Impfdatum: 19.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Dyspnoea Intensive care SARS-CoV-2 test positive

Symptomtext

Narrative: Hospitalization, COVID positive and fully vaccinated upon admission, critical care admit for shortness of breath and COVID positive

Weitere VAERSDATA-Felder

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

VAERS 2318980

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MI
Alter: 86,0
Geschlecht: M
Eingang: 14.06.2022
Impfdatum: 09.03.2021
Beginn: 07.06.2022
Tage bis Beginn: 455,0
Dosis: 1
Route/Site: - / -

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

Asymptomatic COVID-19 SARS-CoV-2 test positive Syncope

Symptomtext

6/7 87y.o. male admitted through the emergency room when he had a syncopal episode on the morning of presenting the ER via EMS; he was COVID-positive and epidemiology has seen him and he was positive back in April he is asymptomatic at this time and he is not in isolation as they feel this is resolved COVID

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Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: 6/7 SARS-Cov-2 Detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267711

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CO
Alter: 27,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 31.03.2021
Beginn: 10.05.2021
Tage bis Beginn: 40,0
Dosis: 1
Route/Site: SYR / LA

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

Bell's palsy Eyelid function disorder Facial paralysis

Symptomtext

Bells Palsy - lasted approximately 10 days. Facial drooping, incapable of closing eye, inability to move right side of face

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2248005

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208)

schwer

Staat: IA
Alter: 71,0
Geschlecht: F
Eingang: 22.04.2022
Impfdatum: 08.04.2021
Beginn: 07.12.2021
Tage bis Beginn: 243,0
Dosis: 2
Route/Site: IM / -

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

Acute kidney injury Acute respiratory distress syndrome Anticoagulant therapy Aphasia Asthenia Atrial fibrillation COVID-19 COVID-19 pneumonia Cough Decreased appetite Dyspnoea Dyspnoea exertional Endotracheal intubation Fatigue Gastrostomy General physical health deterioration Hyporesponsive to stimuli Hypoxia

Symptomtext

COVID Breakthrough Case Pfizer Dose 1 3/18/21 (ER2613) Pfizer Dose 2 4/8/21 (EN6208) COVID Positive 12/8/2021 12/10/21:Patient is a 72-year-old female patient comes to the hospital with complaints of extreme generalized weakness and shortness of breath which have been getting worse in the last few days. Patient has been vaccinated along with her husband for the COVID-19 infection. She was in a gathering with friends on third of December and was possibly exposed to the infection. Since then patient has been progressively feeling very weak, fatigue, decreased appetite and has had dry cough which is not resolving. She has no fever/chills. Patient was seen as an outpatient in the clinic but was discharged home for conservative treatment at home. She came to the emergency room as she was getting progressively worse. Patient is being admitted for further care. She has history of type 2 diabetes, depression, fibromyalgia, hypertension, GERD and asthma. Shortness of breath present with minimal ambulation and dry cough present. 1/3/22: Patient presented with hypoxia COVID pneumonia on admission as noted. Was intubated from outside facility and transferred secondary to ICU bed availability. Patient was intubated on arrival, pulmonology was consulted. Patient was started on course of remdesivir, pr sit to neb, Decadron, empiric antibiotics. Pulmonary critical care assisted during admission, developed severe ARDS had to be prolonged and placed on Flolan, finish multiple course of antibiotics ceftaz, Zosyn, vancomycin. Due to develop AFib was on metoprolol, Eliquis. AKI resolved. Did develop edematous tongue suspected secondary to prolonged pronating. Unfortunately patient was not able to be weaned off vent and after prolonged intubation. A decision was made to trach and PEG patient. This was done on 12/29. Sedation was gradually weaned off patient had some minimal response f opens eyes however not verbal and tracking, retracts to pain. Considering condition request was made transfer to select Specialty facility for ongoing care and management.

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Praegender Schweregrund: Acute respiratory distress syndrome
Hospital-Tage: 25,0
Labordaten: -
Aktuelle Erkrankungen: asthma HTN CFS depression anxiety diverticulosis DM type II fibromyalgia GERD knee osteoarthritis obesity myalgias HLD
Vorgeschichte: asthma HTN CFS depression anxiety diverticulosis DM type II fibromyalgia GERD knee osteoarthritis obesity myalgias HLD
Andere Medikamente: APAP 325 mg PO Q4h PRN albuterol 2 puffs Q6h PRN apixaban 5 mg PO BID vitamin D 500 mg PO QD aspirin 81 mg PO QD magnesium oxide 400 mg PO QD metoprolol 25 mg PO BID venlafaxine 37.5 mg PO BID
Allergien: Benylin - swelling, mouth Lyrica - unknown
Vorherige Impfungen: -

VAERS 2214482

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: KY
Alter: 73,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 01.04.2021
Beginn: 03.04.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Cardiac ablation Cardiac monitoring abnormal Extrasystoles Fear Heart rate increased Inappropriate schedule of product administration Palpitations Thrombosis Ventricular extrasystoles

Symptomtext

After 2nd dose, rapidness came with the skipped heart beats. I had skipped beats, pounding, and rapid heart rate kept getting worse. After a month, I went to the doctor because I was scared and she sent me to the heart doctor and they put a monitor on me and then put me on medication to try and control it, and then I had a Cardiac Ablation. I had the surgery at a local hospital and I had a blood clot when they did the surgery. I was having 24000 a day on PVC and now I'm having 1200 a day and still have the rapid heart rate like it was. I can't think of anything else that happened. I had a vascular check up 2 months prior to 1st dose and they found nothing abnormal.

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Praegender Schweregrund: Thrombosis
Hospital-Tage: 1,0
Labordaten: Heart monitor, Cardiac Ablation (April 2021).
Aktuelle Erkrankungen: None
Vorgeschichte: Bad Kidneys; Acid Reflux; Sleep Apnea; High Blood Pressure.
Andere Medikamente: High Blood Pressure Medicine; Acid Reflux Medicine; Vitamin D; D3; B.
Allergien: Iodine; Cipro; Z-Pak; Latex.
Vorherige Impfungen: Pfizer Dose 1 2021, E#823847

VAERS 2213078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: TX
Alter: -
Geschlecht: U
Eingang: 02.04.2022
Impfdatum: 01.03.2021
Beginn: 01.06.2021
Tage bis Beginn: 92,0
Dosis: 2
Route/Site: - / LA

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

Alopecia areata Deep vein thrombosis

Symptomtext

DVT in upper left arm; Alopecia Areata - sudden loss of patches of hair; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 50 year-old patient received bnt162b2 (BNT162B2), administered in arm left, administration date Mar2021 (Lot number: EN6208) as dose 2, single for covid-19 immunisation. Relevant medical history included: "Hashimotos" (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXINE; ALLEGRA. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Batch/Lot No: EN6202, Location of injection: Arm Left), administration date: Feb2021, for COVID-19 Immunization. The following information was reported: DEEP VEIN THROMBOSIS (disability, life threatening) with onset Jun2021, outcome "not recovered", described as "DVT in upper left arm"; ALOPECIA AREATA (disability, life threatening) with onset Jun2021, outcome "not recovered", described as "Alopecia Areata - sudden loss of patches of hair". The events "dvt in upper left arm" and "alopecia areata - sudden loss of patches of hair" were evaluated at the physician office visit and emergency room visit. Therapeutic measures were taken as a result of deep vein thrombosis, alopecia areata and included treatment with steroid shots for alopecia and apixaban (ELIQUIS Rx) for DVT (deep vein thrombosis). The patient had not received any other vaccines within 4 weeks. Prior to vaccination, the patient was not diagnosed as COVID-19. The facility type vaccine was Pharmacy or Drug Store. It was unknown whether the patient had been tested for COVID-19 since the vaccination. Follow-up attempts are completed. No further information is expected.

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Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hashimoto's disease
Andere Medikamente: LEVOTHYROXINE; ALLEGRA
Allergien: -
Vorherige Impfungen: -

VAERS 2178300

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CO
Alter: 65,0
Geschlecht: F
Eingang: 14.03.2022
Impfdatum: 30.03.2021
Beginn: 26.12.2021
Tage bis Beginn: 271,0
Dosis: 2
Route/Site: IM / LA

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

Chest X-ray abnormal Dyspnoea Pulmonary oedema

Symptomtext

Patient vaccinated with Pfizer on 3/9/21 and 3/30/21. Presented to ED with complaints of worsening shortness of breath. Previous medical history of type 2 diabetes, urinary incontinence, spinal stenosis, emphysema, and RLS. Chest x-ray showed pulmonary edema. Patient admitted for further workup. Admitted 12/26/21, discharged 12/28/21.

Weitere VAERSDATA-Felder

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

VAERS 2176365

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IN
Alter: 64,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 20.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Diarrhoea Dizziness Presyncope Vertigo positional

Symptomtext

A week of positional vertigo.; Second shot...day of felt like cloud lifted. 20 after shot...almost blacked out,; Dizzy; Diarrhea; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 64 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 20Mar2021 14:00 (Lot number: EN6208) at the age of 64 years as dose 2, single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Past drug history included: Known allergies: compazine for vomiting, reaction(s): "Known Allergies: Compazine", notes: Known Allergies: Compazine; Known allergies: tyramine, reaction(s): "Known Allergies: Tyramine", notes: Known Allergies: Tyramine. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6200, Location of injection: Arm Left, Vaccine Administration Time: 10:00 AM), administration date: 26Feb2021, when the patient was 64 years old, for COVID-19 immunization. The following information was reported: VERTIGO POSITIONAL (non-serious) with onset 20Mar2021, outcome "unknown", described as "A week of positional vertigo."; PRESYNCOPE (non-serious) with onset 20Mar2021, outcome "unknown", described as "Second shot...day of felt like cloud lifted. 20 after shot...almost blacked out,"; DIZZINESS (non-serious) with onset 20Mar2021, outcome "unknown", described as "Dizzy"; DIARRHOEA (non-serious) with onset 20Mar2021, outcome "unknown", described as "Diarrhea". The events "a week of positional vertigo.", "second shot...day of felt like cloud lifted. 20 after shot...almost blacked out,", "dizzy" and "diarrhea" were evaluated at the physician office visit. Therapeutic measures were not taken as a result of vertigo positional, presyncope, dizziness, diarrhoea. Additional information included: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not received other medications within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2132201

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: KY
Alter: 73,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 29.09.2021
Beginn: 04.02.2022
Tage bis Beginn: 128,0
Dosis: 2
Route/Site: IM / LA

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

Activated partial thromboplastin time shortened Alanine aminotransferase normal Albumin globulin ratio normal Angiogram pulmonary abnormal Anion gap Arteriogram coronary abnormal Aspartate aminotransferase normal Basophil count normal Basophil percentage Blood albumin normal Blood alkaline phosphatase increased Blood bilirubin normal Blood calcium normal Blood chloride normal Blood creatinine normal Blood glucose normal Blood magnesium normal Blood potassium normal

Symptomtext

2/4/22 74-year-old white female who presents to the emergency department with a chief complaint of "having all the symptoms of a heart attack". The patient has a history of prior myocardial infarction and states she began having all the same symptoms tonight. She complains of left-sided chest pressure that radiates to the left side of the neck and left shoulder region that began around 12:30 AM tonight while working as a cashier. The pain is resolved at the time of my evaluation, lasting roughly an hour. The pain was associated with shortness of breath, nausea, and diaphoresis. She had no vomiting. She felt lightheaded and near syncopal but did not lose consciousness. She denies any exacerbating or relieving She denies any exacerbating or relieving factors, stating that her relief was spontaneous. She denies any recent fever, sore throat, or runny nose. She states she has a chronic cough. She denies lower extremity pain and swelling. She denies abdominal pain, diarrhea, and bloody stools. Review of Systems Constitutional: Negative for chills and fever. HENT: Negative for congestion, sore throat and sinus pressure. Eyes: Negative for redness and itching. Respiratory: Positive for cough (Chronic) and shortness of breath. Cardiovascular: Positive for chest pain. Negative for leg swelling. Gastrointestinal: Negative for abdominal pain, diarrhea, nausea and vomiting. Genitourinary: Negative for dysuria and hematuria. Musculoskeletal: Negative for back pain. Skin: Negative for rash. Neurological: Positive for light-headedness. Negative for syncope and headaches. Hematological: Negative for adenopathy. Psychiatric/Behavioral: Negative for confusion. All other systems reviewed and are negative. Discharged Condition: stable Hospital Course: 74-year-old female presented to emergency department with complaint of chest pain and shortness of breath that began while she was at work as a cashier at a convenience store. She endorsed associated nausea, diaphoresis, and lightheadedness. She has a history of myocardial infarction and was concerned symptoms were that of another MI. Vital signs on presentation were unremarkable: Temp 97.7, pulse 88, BP 145/91, respiratory rate 20, SPO2 100%. Laboratory studies were unremarkable. Troponins were flat x4. Covid testing is positive and CTA chest did reveal extensive bilateral groundglass opacities typical of COVID-19 virus infection. Following presentation she required supplemental O2 to maintain oxygen saturation greater than 90%. Respiratory status is stable on 2 L O2 BNC, SPO2 96%. No increased work of breathing conversational dyspnea. She was started on dexamethasone and vitamin supplementation. Initial CRP was 0.4. We suspect presenting chest pain and shortness of breath are related to COVID. The patient was monitored with continuous telemetry following her admission and no arrhythmias were detected. Fortunately the patient's respiratory status remained stable for her brief hospital course. She was maintaining adequate oxygen saturations on 2 L O2. She will be set up for supplemental O2 BNC, to be delivered to her room prior to her discharge today. She will be followed on an ongoing basis by the hospital. She already has a pulse oximeter at home and she will be provided with a BP cuff.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: 1,0
Labordaten: 2/4/22 COVID-19 Result Detected Abnormal CBC w/Diff Collection Time: 02/04/22 1:48 AM Result Value Ref Range White Blood Count 7.97 4.5 - 11.0 10*3/uL Red Blood Count 4.57 4.0 - 5.2 10*6/uL Hemoglobin 14.2 12.0 - 16.0 g/dL Hematocrit 43.6 36.0 - 46.0 % Mean Corpuscular Volume 95.4 80.0 - 100.0 fL Mean Corpuscular Hemoglobin 31.1 26.0 - 34.0 pg Mean Corpuscular HGB Conc 32.6 31.0 - 37.0 g/dL Red Cell Distribution Width-CV 13.5 12.0 - 16.8 % Platelet Count 274 140 - 440 10*3/uL Mean Platelet Volume 11.6 8.4 - 12.4 fL Diff Type Hospital CBC w/AutoDiff (arb'U) Neutrophils % 68.9 45 - 80 % Lymphocyte % 21.6 15 - 50 % Monocyte % 7.2 0 - 15 % Eosinophil% 1.5 0 - 7 % BASO% 0.5 0 - 2 % Immature Granulocyte% 0.3 0.0 - 1.0 % Nucleated RBC % 0 0 /100(WBC) Neutrophil Abs 5.50 2.0 - 8.8 10*3/uL Lymphocyte-Absolute 1.72 0.7 - 5.5 10*3/uL Monocyte Absolute 0.57 0.0 - 1.7 10*3/uL EOS-Absolute 0.12 0.0 - 0.8 10*3/uL Basophil Abs 0.04 0.0 - 0.2 10*3/uL Immature Granulocyte Abs 0.02 0.00 - 0.10 10*3/uL Comprehensive Metabolic Panel(CMP) Collection Time: 02/04/22 1:48 AM Result Value Ref Range Sodium 138 136 - 145 mmol/L Potassium 3.5 3.5 - 5.1 mmol/L Chloride 102 98 - 107 mmol/L Carbon Dioxide 19 (L) 22 - 29 mmol/L Anion Gap 17 (H) 5 - 13 (arb'U) Glucose 175 (H) 74 - 99 mg/dL Blood Urea Nitrogen (BUN) 15 10 - 20 mg/dL Creatinine-Blood 0.95 0.55 - 1.02 mg/dL BUN/Creatinine Ratio 15.8 RATIO Estimated GFR 58 (L) >60 /1.73 m2 Estimated GFR if African-American >60 >60 /1.73 m2 Total Protein 7.4 6.2 - 8.0 g/dL Albumin 3.8 3.2 - 4.6 g/dL Globulin 3.6 1.5 - 4.5 g/dL Albumin/Globulin Ratio 1.1 1.1 - 2.5 RATIO Calcium 9.7 8.4 - 10.2 mg/dL Total Bilirubin 0.9 0.2 - 1.2 mg/dL AST/SGOT 28 5 - 34 U/L ALT/SGPT 32 0 - 55 U/L Alkaline Phosphatase 135 40 - 150 U/L B-Type Natriuretic Peptide Collection Time: 02/04/22 1:48 AM Result Value Ref Range B-Type Natriuretic Peptide 38.2 3 - 160 pg/mL Magnesium Collection Time: 02/04/22 1:48 AM Result Value Ref Range Magnesium 1.8 1.6 - 2.6 mg/dL Troponin Collection Time: 02/04/22 1:48 AM Result Value Ref Range Troponin 0.018 0.000 - 0.034 ng/mL D-Dimer,Quantitative Collection Time: 02/04/22 2:25 AM Result Value Ref Range D-DIMER 982 (H) <500 ng/mL FEU Protime-INR Collection Time: 02/04/22 2:25 AM Result Value Ref Range Prothrombin Time 11.7 10.3 - 13.3 s INR 1.0 INR Partial Thromboplastin Time Collection Time: 02/04/22 2:25 AM Result Value Ref Range Partial Thromboplastin Time 29.0 25.1 - 36.5 s Repeat Troponin 2 Hours after the Initial Troponin is drawn Collection Time: 02/04/22 4:13 AM Result Value Ref Range Troponin 0.022 0.000 XR Chest 1 Vw 2/4/22 IMPRESSION: Cardiomegaly CT Angiogram Chest For PE 2/4/22 IMPRESSION: 1. No pulmonary embolism. 2. Cardiomegaly. 3. Heterogeneous groundglass opacities are seen, correlate with edema. Infectious process not excluded.
Aktuelle Erkrankungen: -
Vorgeschichte: Anxiety o Asthma o Benign essential HTN o COPD (chronic obstructive pulmonary disease) o Coronary artery disease o Heart attack o Hyperlipidemia o Myocardial infarction 6/18/14 Anterior o Obstructive sleep apnea o Pneumonia o Stroke o Urinary tract infection
Andere Medikamente: albuterol (ACCUNEB) 1.25 MG/3ML nebulizer solution, Take 1 ampule by nebulization every 4 (four) to 6 (six) hours as needed for Wheezing or Shortness of Air. o albuterol (ACCUNEB) 1.25 MG/3ML nebulizer solution, Take 3 mLs by nebulization
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1258291

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IN
Alter: 64,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 20.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Diarrhoea Dizziness Pain Presyncope Vaccination site pain Injection site pain Nodule Vein disorder

Symptomtext

pain in my arm where they gave me the shot; diarrhea; dizzy spells; almost fainted; I have been experiencing severe pain.; my vein is bends all like pop out early you know get real noticeable; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 64 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 20Mar2021 (Lot number: EN6208) at the age of 64 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Blood pressure" (unspecified if ongoing), notes: Verbatim: Blood pressure. Concomitant medication(s) included: METOPROLOL taken for blood pressure measurement, start date: 2018 (ongoing). The following information was reported: VACCINATION SITE PAIN (non-serious), outcome "unknown", described as "pain in my arm where they gave me the shot"; DIARRHOEA (non-serious), outcome "unknown", described as "diarrhea"; DIZZINESS (non-serious), outcome "unknown", described as "dizzy spells"; PRESYNCOPE (non-serious), outcome "unknown", described as "almost fainted"; PAIN (non-serious), outcome "unknown", described as "I have been experiencing severe pain."; VEIN DISORDER (non-serious), outcome "unknown", described as "my vein is bends all like pop out early you know get real noticeable". Therapeutic measures were taken as a result of vaccination site pain. Additional information: The patient has been experiencing severe pain for a like a week after she got her first shot in arm. That was setting a quality of her life. She cannot really use her left arm very much at all. She has a knot that was own one of her veins was bend all like pop out early got real noticeable. She had pain in her arm where they gave her the shot. She had diarrhoea for six days, a couple of weeks ago. She had experienced dizzy spells where she almost fainted there. Everything she did not know anything else that it could be a tribute to other than the shot because she was basically a healthy person. That was the first dose, on 20Mar2021 when she have it and has suffered terribly, almost every second was like a equator after she was having problems. The patient was still taking Tylenol, she has tried ice, heating pad and did anything to just ease it as much as she can. She don't remember when she first started taking Tylenol, that was when she was in pain almost constantly ever since about a week after so. When probed for any Treatment for the adverse event, all she has taken was Tylenol when she hurt. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure (Verbatim: Blood pressure)
Andere Medikamente: METOPROLOL
Allergien: -
Vorherige Impfungen: -

VAERS 2098834

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 82,0
Geschlecht: M
Eingang: 09.02.2022
Impfdatum: 25.02.2021
Beginn: 08.02.2022
Tage bis Beginn: 348,0
Dosis: 2
Route/Site: IM / RA

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

Acute pulmonary oedema Body temperature increased COVID-19 pneumonia Diarrhoea Dyspnoea Fatigue

Symptomtext

Admitted to hospital on 2/8 with COVID-19 pneumonia. Patient is a 83 y.o. never smoker with a history of ESRD, hypertension, BPH who presents to a local ER chief complaint of fatigue and admitted for acute pulmonary edema. Patient severely hard of hearing; however, answering questions appropriately including orientation reports recent diarrhea for approximately 3 weeks and reportedly noted improvement prior to hospital evaluation. Developed fatigue and shortness of breath beginning 2/8/2022 with reported elevated temperature 99; therefore, sought ER for evaluation.

Weitere VAERSDATA-Felder

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

VAERS 2079570

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MA
Alter: 21,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 28.05.2021
Beginn: 07.12.2021
Tage bis Beginn: 193,0
Dosis: 1
Route/Site: IM / LA

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

C-reactive protein increased Chest discomfort Chest pain Ejection fraction decreased Left atrial enlargement Left ventricular dilatation Magnetic resonance imaging heart Myocarditis Pyrexia Right ventricular ejection fraction decreased Troponin increased

Symptomtext

Patient received 1st covid vaccine on 5/6/21 and 2nd dose on 5/28/21. Patient had a urgent care visit on 11/23/21 for evaluation of fever, chest pain , chest tightness and then patient presented to outside hospital ED. According to cardiology follow up note on 11/30/21, patient was diagnosed with myopericarditis 1 week prior with TnT 0.79 to 0.97, no rise and fall, CRP 144. Patient got mri cardiac non stress imaging on 12/7/21 and the conclusion was that it was consistent with healing phase of myocarditis with normal left ventricular function. Patient was treated with ibuprofen, indomethacin and colchicine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: mri cardiac non stress imaging on 12/7/21: 1. The left ventricular size is mildly dilated. The left ventricular ejection fraction is 61 % by Simpson's method. Global left ventricular function is normal. There are no regional wall motion abnormalities of the left ventricular wall. The left ventricular mass is normal. 2. There are multiple foci of subepicardial late gadolinium enhancement in the inferior and inferolateral walls of the left ventricle extending from the basal to apical levels, which represents residual myocardial inflammation or scar. There is no evidence of myocardial edema by T2 weighted imaging. 3. The right ventricular size is normal. The right ventricular ejection fraction is 57 % by Simpson's method. Global right ventricular function is normal. There are no regional wall motion abnormalities of the right ventricular wall. There is no late gadolinium enhancement of the right ventricle. 4. Left atrial size is mildly enlarged. Right atrial size is normal. 5. There is no pericardial thickening, edema or inflammation by late gadolinium enhancement imaging to suggest pericarditis.
Aktuelle Erkrankungen: N/A
Vorgeschichte: mid intermittent asthma
Andere Medikamente: cetirizine, vitamin d3, epinephrine, mirena
Allergien: tree nuts, coconut, sulfamethoxazole-trimethoprim, soy, sulfa, shellfish containing products
Vorherige Impfungen: -

VAERS 2079570

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MA
Alter: 21,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 28.05.2021
Beginn: 07.12.2021
Tage bis Beginn: 193,0
Dosis: 2
Route/Site: IM / LA

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

C-reactive protein increased Chest discomfort Chest pain Ejection fraction decreased Left atrial enlargement Left ventricular dilatation Magnetic resonance imaging heart Myocarditis Pyrexia Right ventricular ejection fraction decreased Troponin increased

Symptomtext

Patient received 1st covid vaccine on 5/6/21 and 2nd dose on 5/28/21. Patient had a urgent care visit on 11/23/21 for evaluation of fever, chest pain , chest tightness and then patient presented to outside hospital ED. According to cardiology follow up note on 11/30/21, patient was diagnosed with myopericarditis 1 week prior with TnT 0.79 to 0.97, no rise and fall, CRP 144. Patient got mri cardiac non stress imaging on 12/7/21 and the conclusion was that it was consistent with healing phase of myocarditis with normal left ventricular function. Patient was treated with ibuprofen, indomethacin and colchicine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: mri cardiac non stress imaging on 12/7/21: 1. The left ventricular size is mildly dilated. The left ventricular ejection fraction is 61 % by Simpson's method. Global left ventricular function is normal. There are no regional wall motion abnormalities of the left ventricular wall. The left ventricular mass is normal. 2. There are multiple foci of subepicardial late gadolinium enhancement in the inferior and inferolateral walls of the left ventricle extending from the basal to apical levels, which represents residual myocardial inflammation or scar. There is no evidence of myocardial edema by T2 weighted imaging. 3. The right ventricular size is normal. The right ventricular ejection fraction is 57 % by Simpson's method. Global right ventricular function is normal. There are no regional wall motion abnormalities of the right ventricular wall. There is no late gadolinium enhancement of the right ventricle. 4. Left atrial size is mildly enlarged. Right atrial size is normal. 5. There is no pericardial thickening, edema or inflammation by late gadolinium enhancement imaging to suggest pericarditis.
Aktuelle Erkrankungen: N/A
Vorgeschichte: mid intermittent asthma
Andere Medikamente: cetirizine, vitamin d3, epinephrine, mirena
Allergien: tree nuts, coconut, sulfamethoxazole-trimethoprim, soy, sulfa, shellfish containing products
Vorherige Impfungen: -

VAERS 2069051

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 12.03.2021
Beginn: 21.01.2022
Tage bis Beginn: 315,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Intensive care

Symptomtext

Admitted to hospital with COVID on 1/21/22 requiring ICU admission

Weitere VAERSDATA-Felder

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

VAERS 2067955

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: ME
Alter: 62,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 17.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Blood glucose Dizziness Presyncope

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 62 year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), administered in arm left, administration date 17Mar2021 (Lot number: EN6208, Expiration Date: 30Jun2021) at the age of 62 years as dose 1, single for COVID-19 immunisation. Relevant medical history included: "Asthma" (unspecified if ongoing); "Fibromyalgia" (unspecified if ongoing). The patient took concomitant medications. Past drug history included: Tylenol, reaction(s): "it makes me go to sleep". The following information was reported: DIZZINESS (non-serious), PRESYNCOPE (non-serious) all with onset 17Mar2021, outcome "not recovered" and all described as "had several dizzy stuff where I almost passed out". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of dizziness, presyncope. Additional information: The patient take tonic medications and free to susceptible when she take medications. When she tool Tylenol, it made her to go to sleep. Her body did not do well with stuff. Anyways, since she had her COVID shot, she had several dizzy stuff where she almost passed out. The event was persisting. It was not constant but it happens 2 -3 times a day and she was trying to make herself very aware what she was doing when it happens and what was happening to her while it was going on. The patient had not taken anything for it other than she was making herself drink more water but that did not feel to making a difference. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Test Date: 202012; Test Name: diabetic test; Result Unstructured Data: Test Result:Unknown Result
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Fibromyalgia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2056640

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CO
Alter: 35,0
Geschlecht: M
Eingang: 22.01.2022
Impfdatum: 12.03.2021
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Body temperature increased Disorientation Fatigue Headache Hyperhidrosis Impaired driving ability Memory impairment Nausea Presyncope SARS-CoV-2 test negative Speech disorder Visual impairment

Symptomtext

Felt over heated/three to five minutes he felt a rush; Sweating through my clothes; Black vision; Very close to passing out/he felt like fainting; I couldn't form a sentence to come out of my mouth to ask for water from him; Very fatigued; Nausea; Headache/pressure at the crown of his head; Felt disoriented like super forgetful; Felt disoriented like super forgetful; His motor functions not on point like trying to operate electronics; 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 35-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injcetion), administered in arm left, administration date 12Mar2021 13:30 (Lot number: EN6208) at the age of 35 years as dose 1, single for COVID-19 immunisation. Relevant medical history included: "Oral surgery" (unspecified if ongoing). There were no concomitant medications. The following information was reported: BODY TEMPERATURE INCREASED (non-serious) with onset 12Mar2021, outcome "not recovered", described as "Felt over heated/three to five minutes he felt a rush"; HYPERHIDROSIS (non-serious) with onset 12Mar2021, outcome "recovered" (14Mar2021), described as "Sweating through my clothes"; VISUAL IMPAIRMENT (non-serious) with onset 12Mar2021, outcome "unknown", described as "Black vision"; PRESYNCOPE (non-serious) with onset 12Mar2021, outcome "not recovered", described as "Very close to passing out/he felt like fainting"; SPEECH DISORDER (non-serious) with onset 12Mar2021, outcome "not recovered", described as "I couldn't form a sentence to come out of my mouth to ask for water from him"; FATIGUE (non-serious) with onset 12Mar2021, outcome "not recovered", described as "Very fatigued"; NAUSEA (non-serious) with onset 12Mar2021, outcome "not recovered", described as "Nausea"; HEADACHE (non-serious) with onset 12Mar2021, outcome "not recovered", described as "Headache/pressure at the crown of his head"; MEMORY IMPAIRMENT (non-serious), DISORIENTATION (non-serious) all with onset 12Mar2021, outcome "not recovered" and all described as "Felt disoriented like super forgetful"; IMPAIRED DRIVING ABILITY (non-serious) with onset Mar2021, outcome "not recovered", described as "His motor functions not on point like trying to operate electronics". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The events did not require a visit to emergency room (ER) and physician. The patient had no prior vaccinations within 4 weeks. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Test Name: COVID test; Result Unstructured Data: Test Result:Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Oral surgery
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2045485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN 6208

schwer

Staat: WA
Alter: 62,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 02.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 20,0
Dosis: 2
Route/Site: IM / RA

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

Burning sensation Impaired work ability Laboratory test Memory impairment Pain in extremity Peripheral swelling Skin discolouration Thrombosis

Symptomtext

Shortly after my second shot I developed clotting and swelling in my legs'. My feet started to feel like they were Burning, and my toes turned dark!!!! and painful. I started to forget many simple things, like how to make my reports in Excel, something I have been doing for years. I almost quit my job due to poor memory. My Memory is some what better. but my legs still swell, and my toed are still dark, and my feet are very uncomfortable. My doctor In another country said he has had (MANY) cases like my case, and told me I was a super dumb, for getting the vaccine after I had already had and recovered from COVID 19. which by the way was a nothing sickness for me and my family. we just took out Protocol vitamins. I won't be taking any more Vaccines of any kind EVER!!!!!

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: My Doctor took several blot Chemical test you can ask him.
Aktuelle Erkrankungen: no
Vorgeschichte: none
Andere Medikamente: None
Allergien: no
Vorherige Impfungen: -

VAERS 2039365

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: KY
Alter: 92,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 18.11.2021
Beginn: 15.01.2022
Tage bis Beginn: 58,0
Dosis: 2
Route/Site: IM / RA

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

Acute respiratory distress syndrome COVID-19 SARS-CoV-2 test positive

Symptomtext

COVID-19 infection resulting in hospitalization, ARDS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory distress syndrome
Hospital-Tage: 3,0
Labordaten: COVID-19 PCR (+) 1/13/22
Aktuelle Erkrankungen: NONE
Vorgeschichte: Chest pain ? Coronary artery disease involving native coronary artery of native heart with unstable angina pectoris ? Difficulty walking ? Elevated troponin ? Hyperlipidemia ? Hypothyroidism ? Lightheadedness ? Pulmonary edema ? Third degree AV block
Andere Medikamente: acetaminophen (TYLENOL) 325 MG tablet Nursing Home Yes Yes Take 650 mg by mouth Every 4 (Four) Hours As Needed for Mild Pain . aluminum-magnesium hydroxide-simethicone (Antacid) 200-200-20 MG/5ML suspension Nursing Home Yes Yes T
Allergien: Shellfish-derived products, Shrimp flavor, Azithromycin, and Codeine
Vorherige Impfungen: -

VAERS 1753380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MI
Alter: 80,0
Geschlecht: M
Eingang: 14.01.2022
Impfdatum: 25.03.2021
Beginn: 25.11.2021
Tage bis Beginn: 245,0
Dosis: 2
Route/Site: - / -

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

Acute kidney injury Anaemia COVID-19 Hypotension Mental status changes Anticoagulant therapy Atelectasis Bladder catheterisation Chest X-ray abnormal Deep vein thrombosis Dyspnoea Haematuria Hip surgery Oedema peripheral Pyrexia SARS-CoV-2 test positive White blood cell count increased Respiratory failure

Symptomtext

Patient is fully vaccinated including a booster on 11/18/2021. COVID + on 11/25/2021. Hospitalized 11/25-12/09/2021. Admitting dx: altered mental status, hypotension, sepsis, COVID-19 , acute kidney injury. Treatment: broad-spectrum IV antibiotics with IV vancomycin pharmacy dose and IV cefepime. Respiratory failure is related to COVID-19. supplemental oxygen. Patient will continue on Breo inhaler daily. Patient will continue on albuterol nebulizer p.r.n.. HYdration and monitoring for AKI. 2 units blood for anemia. Discussed the case with the family who made the patient DNR comfort but they declined hospice care at this point. Plan for the patient be discharged to go to subacute rehab and to consider hospice care and comfort care at the rehab. Discharged to skilled nursing home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 15,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1753380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MI
Alter: 80,0
Geschlecht: M
Eingang: 14.01.2022
Impfdatum: 25.03.2021
Beginn: 25.11.2021
Tage bis Beginn: 245,0
Dosis: 2
Route/Site: SYR / -

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

Acute kidney injury Anaemia COVID-19 Hypotension Mental status changes Anticoagulant therapy Atelectasis Bladder catheterisation Chest X-ray abnormal Deep vein thrombosis Dyspnoea Haematuria Hip surgery Oedema peripheral Pyrexia SARS-CoV-2 test positive White blood cell count increased Respiratory failure

Symptomtext

Patient is fully vaccinated including a booster on 11/18/2021. COVID + on 11/25/2021. Hospitalized 11/25-12/09/2021. Admitting dx: altered mental status, hypotension, sepsis, COVID-19 , acute kidney injury. Treatment: broad-spectrum IV antibiotics with IV vancomycin pharmacy dose and IV cefepime. Respiratory failure is related to COVID-19. supplemental oxygen. Patient will continue on Breo inhaler daily. Patient will continue on albuterol nebulizer p.r.n.. HYdration and monitoring for AKI. 2 units blood for anemia. Discussed the case with the family who made the patient DNR comfort but they declined hospice care at this point. Plan for the patient be discharged to go to subacute rehab and to consider hospice care and comfort care at the rehab. Discharged to skilled nursing home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 15,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1992193

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MD
Alter: 66,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 14.03.2021
Beginn: 02.04.2021
Tage bis Beginn: 19,0
Dosis: 1
Route/Site: - / -

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

Ischaemic stroke

Symptomtext

Ischemic brain stroke in mid brain region; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). A 66 year-old male patient received bnt162b2 (BNT162B2), administration date 14Mar2021 09:00 (Lot number: EN6208) at the age of 66 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Open heart by pass surgery" (unspecified if ongoing); "knee replacement surgery" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: ISCHAEMIC STROKE (caused and prolonged hospitalization, disability, medically significant) with onset 02Apr2021 14:00, outcome "recovered with sequelae", described as "Ischemic brain stroke in mid brain region". The patient was hospitalized and prolonged hospitalization for ischaemic stroke (hospitalization duration: 47 day(s)). The event "ischemic brain stroke in mid brain region" was evaluated at the emergency room visit. Therapeutic measures were taken as a result of ischaemic stroke.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: 47,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bypass surgery; Knee surgery NOS
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1992193

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MD
Alter: 66,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 14.03.2021
Beginn: 02.04.2021
Tage bis Beginn: 19,0
Dosis: 1
Route/Site: IM / UN

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

Ischaemic stroke

Symptomtext

Ischemic brain stroke in mid brain region; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). A 66 year-old male patient received bnt162b2 (BNT162B2), administration date 14Mar2021 09:00 (Lot number: EN6208) at the age of 66 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Open heart by pass surgery" (unspecified if ongoing); "knee replacement surgery" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: ISCHAEMIC STROKE (caused and prolonged hospitalization, disability, medically significant) with onset 02Apr2021 14:00, outcome "recovered with sequelae", described as "Ischemic brain stroke in mid brain region". The patient was hospitalized and prolonged hospitalization for ischaemic stroke (hospitalization duration: 47 day(s)). The event "ischemic brain stroke in mid brain region" was evaluated at the emergency room visit. Therapeutic measures were taken as a result of ischaemic stroke.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: 47,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bypass surgery; Knee surgery NOS
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2013933

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: OH
Alter: 61,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 01.04.2021
Beginn: 05.01.2022
Tage bis Beginn: 279,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Dizziness Hypotension Loss of consciousness SARS-CoV-2 test positive Syncope

Symptomtext

Patient was seen at the PCP office on 1/5/2021 for dizziness, hypotension, and syncope. He did report these been having 6 to 7 weeks of low blood pressure and passing out. Patient was fully vaccinated with Pfizer (3/11/21 & 4/1/21). Patient is still admitted with COVID

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 2,0
Labordaten: + COVID 19 on 1/5/21
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2659175

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 40,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 13.04.2021
Beginn: 13.04.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Anaphylactic reaction Dysphagia Throat tightness

Symptomtext

Narrative: 39 yo female with PMH GERD, depression, anxiety, migraine and PTSD was observed to have an anaphylactic reaction after her second dose of COVID19 Pfizer vaccine on 4/13/2021. Patient was sent to the ED 30 minutes after receiving the second dose of the vaccine. Pt denied SOB but had throat tightness and difficulty swallowing. Pt denied SOB, lip swelling or tongue swelling. Pt had a similar reaction with the first COVID-1 vaccine on 2/22/2021 and was treated with epinephrine. According to COVID-19 vaccine notes, patient was treated with epi 0.3mg, decadron 10 mg IV, Benadryl 50mg IV, famotidine 20mg PO with resolution of all symptoms prior to leaving ED. Patient was instructed not to receive COVID19-vaccine in the future. Per progress notes, patient was seen in same day asking whether or not she should have received the second dose of COVID19. Provider stated that patient left before he could make the recommendation that she shouldn't get it again.

Weitere VAERSDATA-Felder

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

VAERS 2001841

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MI
Alter: 91,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 27.03.2021
Beginn: 29.10.2021
Tage bis Beginn: 216,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Fall Mental status changes Pyrexia SARS-CoV-2 test positive Syncope

Symptomtext

Pt COVID + on 10/29/2021. Admitted with syncope, fall, fever, altered mental status changes and COVID-19. Treatment: IV decadron, Breo inhaler, albuterol nebulizer. Family took patient home.

Weitere VAERSDATA-Felder

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

VAERS 2001827

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 54,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 01.04.2021
Beginn: 01.05.2021
Tage bis Beginn: 30,0
Dosis: 1
Route/Site: SYR / LA

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

Back pain Breast cancer Deep vein thrombosis

Symptomtext

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

Weitere VAERSDATA-Felder

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

VAERS 1981558

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MD
Alter: 68,0
Geschlecht: M
Eingang: 27.12.2021
Impfdatum: 18.03.2021
Beginn: 01.07.2021
Tage bis Beginn: 105,0
Dosis: 2
Route/Site: IM / AR

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

Condition aggravated Superficial vein thrombosis Thrombophlebitis Vascular pain

Symptomtext

Not sure if attributable to this injection, but in July, as indicated in earlier section, developed a clot in right leg, great saphenous. Worth noting that this is the same leg in which I had a DVD in 2017 following emergency surgery for a broken hip. (Fun times.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Superficial vein thrombosis
Hospital-Tage: -
Labordaten: End of July through September, a series of ultrasound studies following initial visit to ER at which time I had a painful, bulging vein in the right leg. Positive for blockage from knee to ankle. Was put on blood thinner for approximately six weeks. Blockage stabilized but did not recede.
Aktuelle Erkrankungen: None
Vorgeschichte: Elevated cholesterol and blood pressure. Barrett's esophagus. Seizures dating back to 1968, but without seizures for more than 30 years and still taking Dilantin for the condition.
Andere Medikamente: Dilantin, Rosuvastatin, Levothyroxine, Finasteride, Gabapentin, Tamsulosin, Ezetimibe, Atenolol, Vitamin C, Vitamin D3, Calcium, Magnesium, Vitamin B12, Zinc
Allergien: None
Vorherige Impfungen: -

VAERS 1944644

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: VA
Alter: 37,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 13.03.2021
Beginn: 13.04.2021
Tage bis Beginn: 31,0
Dosis: 1
Route/Site: SYR / LA

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

Arthritis Back pain Chest pain Laboratory test Loss of personal independence in daily activities Magnetic resonance imaging Myocarditis Pain X-ray

Symptomtext

A few days after my second shot, I had severe chest pain that felt like I was having a heart attack. I went to the er a few hours later, and they said the heart was fine, but I had inflammation in the area near the heart and that it was going to feel like I was having a heart attack until it healed. A few weeks after that, I still was not feeling better but the pain also moved to my back, I went to the dr where they did lab tests and said that I may have inflammatory arthritis. While waiting to see an arthritis dr, the pain went to my big toe on my left foot, right elbow, left knee, neck, and middle back. It was about 8 out of ten on the pain scale with severe morning stiffness. I went to the arthritis dr, and she said it was likely caused by the vaccine as it happened right after and it was more severe and sudden onset than arthritis would normally present. The pain has been ongoing since that time. I?ve had to alter my whole life to deal with it. I eat a strict anti inflammatory diet, and I have to work out all the time and apply heat and cold packs. With that, I have lessened the pain and it is only in my back. I?ve spent every last penny I had this year trying to get this under control, and even maxed out my credit card. Since my second vaccine, I?ve been struggling to keep my inflammatory response under control, and it moved to my stomach recently. It?s been miserable, and I?ve always been very healthy until this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Tons of labs at unknown dates from the start date until a few weeks ago Mri a few months ago X-ray sometime this summer
Aktuelle Erkrankungen: None
Vorgeschichte: Migraine, and premature ovarian failure.
Andere Medikamente: Multi vitamin, progesterone, estrogen.
Allergien: Sunflower seeds, penicillin, doxycycline.
Vorherige Impfungen: -

VAERS 1929093

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 23.03.2021
Beginn: 06.12.2021
Tage bis Beginn: 258,0
Dosis: 2
Route/Site: - / -

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

Fall Syncope

Symptomtext

patient had syncope and witnessed fall. she was treated in the EC of hospital where she was tested. She was discharged on 12/7 from the EC.

Weitere VAERSDATA-Felder

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

VAERS 1921154

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 01.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / AR

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

Ear discomfort Feeling hot Flushing Headache Hyperhidrosis Loss of consciousness Tinnitus

Symptomtext

Woke up morning after vaccination went to use bathroom and start usual routine. Suddenly felt very hot, flush, and sweaty (while sitting bathroom). Decided to go lay down in bed again. Passed out walking back to bed. Recovered within a few minutes, but with headache persisting throughout day. Day 2 post, woke up with fullness in left ear (same side as shot) and mild tinnitus. Headache was still present but alleviated with analgesic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None.
Vorgeschichte: Hypothyroidism
Andere Medikamente: Synthroid, Liothyronine, Duloxetine, Magnesium Complex, Zyrtec, Pepsid
Allergien: NKA
Vorherige Impfungen: -

VAERS 1905340

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MN
Alter: 72,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 12.03.2021
Beginn: 28.11.2021
Tage bis Beginn: 261,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Intensive care Vaccine breakthrough infection

Symptomtext

Fully vaccinated with COVID breakthrough and inpatient admit to an ICU unit. Chronic underlying lung disease with home oxygen

Weitere VAERSDATA-Felder

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

VAERS 1876793

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MI
Alter: 81,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 17.03.2021
Beginn: 15.11.2021
Tage bis Beginn: 243,0
Dosis: 2
Route/Site: IM / -

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

Abdominal pain Asthenia COVID-19 Diarrhoea Fall SARS-CoV-2 test positive Syncope

Symptomtext

symptoms of covid include weakness leading to syncope/fall; abdominal pain, diarrhea since about 11/15/21, then tested positive for covid

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: SARS-CoV-2 (COVID-19) by NAA, Micro detected on 11/17/21
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes, claudication, aortic valve stenosis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1403597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MI
Alter: 52,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 30.03.2021
Beginn: 15.11.2021
Tage bis Beginn: 230,0
Dosis: 2
Route/Site: - / -

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

Blindness unilateral Eye pain Pain in extremity Pyrexia Thrombosis COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough Case

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Covid + in 11/15
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1815443

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NY
Alter: 37,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 16.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Burning sensation Erythema Thrombosis X-ray limb

Symptomtext

That evening on my right calf was red and burning feeling in my calf, It felt like I had a blood clot. Symptoms remain for a week, My docor though it was a side effect of the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Send to the emergency room and I had an X-Ray on your right calf up to my leg. No labs were done.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Elevated Blood pressure
Andere Medikamente: Amlodipine 10MG a day for blood pressure and pindolol 1/2 of 5MG A day
Allergien: N/A
Vorherige Impfungen: -

VAERS 1795048

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MI
Alter: 53,0
Geschlecht: M
Eingang: 18.10.2021
Impfdatum: 09.03.2021
Beginn: 29.08.2021
Tage bis Beginn: 173,0
Dosis: 2
Route/Site: SYR / LA

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

Back pain Bladder catheter temporary Computerised tomogram kidney abnormal Condition aggravated Lithotripsy Mobility decreased Muscle injury Nephrolithiasis Post procedural complication Renal colic Renal stone removal Thrombosis Urethral obstruction Vomiting

Symptomtext

Multiple kidney stone events during the month of August, 2021. Worst attack began 8/29/21, lasting 10+hours. Vomiting for 8+ hours. Muscular injury of lower back as a result of severe vomiting. Could not get out of bed morning of 8/31, due to severe back pain and kidney stone attack beginning. Transported to hospital ER and was admitted 8/31/21. Laser Lithotripsy was performed to break up kidney stones in left kidney. Kidney stone still present in the right kidney. Urethra was blocked by post-op clotting, requiring temporary catheterization.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 4,0
Labordaten: CT scan 8/31/21
Aktuelle Erkrankungen: None
Vorgeschichte: Kidney Stones
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1793634

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NY
Alter: 64,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: 19.03.2021
Beginn: 29.03.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: IM / RA

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

Computerised tomogram thorax Diplopia Facial paralysis Laboratory test Magnetic resonance imaging Magnetic resonance imaging head Myasthenia gravis Viral titre Vision blurred

Symptomtext

Onset of Myesthenia Gravis 10 days after first vaccine. Blurry vision then became Double vision, Diplopia, droopy eye Treated with mestinon 120mg every 4 hours to normalize vision. dosage has been reduced to 60 mg twice a day currently.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: MRI brain 3/23/21 MRI Orbits only 3/23/21 Musk antibody titer 4/2/21 Acetycholine Recep Mod 4/2/21 Aceltylcholine recep block 4/2/21 Acelcholine recap bindere 4/2/21 CT Chest 4/2/21
Aktuelle Erkrankungen: asthma, Lyme disease,
Vorgeschichte: asthma, Lyme disease,
Andere Medikamente: Albuterol, Budesonide, Omeprozole, exemestane, aspirin, antihistamine, Singulair, multi vitamin, vit D, magn?sium and calcium and D, zyflamend, Curcumin, Co Q 10, multi mineral,
Allergien: Tree nuts, Bactrim
Vorherige Impfungen: -

VAERS 1792267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 75,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: 10.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: - / LA

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

Electric shock sensation

Symptomtext

Electricity in my legs; This is a spontaneous report from a contactable consumer, the patient. A 75-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EN6208) via an unspecified route of administration in the left arm on 10Mar2021 at 14:30 (at the age of 75-years-old) as a single dose for COVID-19 immunisation. The patient did not have any medical history. The patient had no known allergies to medications, food, or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included amlodipine (MANUFACTURER UNKNOWN), losartan (MANUFACTURER UNKNOWN), vitamin d nos (VIT D) and zinc (MANUFACTURER UNKNOWN); all for unknown indications from unknown dates and unknown if ongoing. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 14Mar2021 at 09:00, the patient experienced electricity in legs. The event 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 event. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event electricity in legs was unknown at the time of this report. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: AMLODIPINE; LOSARTAN; VIT D [VITAMIN D NOS]; ZINC
Allergien: -
Vorherige Impfungen: -

VAERS 1780107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: KY
Alter: 81,0
Geschlecht: M
Eingang: 12.10.2021
Impfdatum: 12.04.2021
Beginn: 12.10.2021
Tage bis Beginn: 183,0
Dosis: UNK
Route/Site: IM / LA

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

Aortic arteriosclerosis Arteriosclerosis coronary artery Atelectasis Breath sounds abnormal COVID-19 pneumonia Cardiomegaly Cerebral atrophy Chest X-ray abnormal Computerised tomogram head normal Computerised tomogram thorax Computerised tomogram thorax abnormal Dysphagia Dyspnoea Facial paralysis Feeding disorder Feeling abnormal General physical condition abnormal Goitre

Symptomtext

He has been feeling bad for about one week. States his shortness of breath has progressively gotten worse. He also complains of difficulty swallowing. He has been unable to eat for about two weeks. He says that water just runs out of his mouth when he takes a sip. General Appearance: Appears thin. Head: Normocephalic, atraumatic Eyes: PERRL, conjunctiva/corneas clear, EOM's intact, sclera anicteric Ears: TMs not observed Nose: Patent without discharge Throat: No erythema or exudate Neck: Supple, without thyromegaly or masses. Trachea is midline. Back: Straight, no CVA tenderness Lungs: Decreased breath sounds Chest wall: No tenderness Heart: Regular rate and rhythm, S1 and S2 normal, no murmur, rub or gallop Abdomen: Soft, non-tender, non-distended, bowel sounds active all four quadrants, no masses, no organomegaly Extremities: Extremities normal, atraumatic, no cyanosis or edema Pulses: 2+ and symmetric all extremities Skin: Warm, dry, no rashes or lesions Lymph nodes: No adenopathy in the neck, axilla, or groin Neurologic: No focal deficits. CNII-XII intact. Speech is fluent. Conversation is coherent. Admitted to hospital, started on nasal O2 at 4lpm. MEDICATIONS GIVEN IN THE ER Medications Ampicillin/Sulbactam 3 gm/100 mL in NS (has no administration in time range) Azithromycin 500 mg/250 mL in D5W (has no administration in time range) fluconazole (DIFLUCAN) tablet 200 mg (has no administration in time range) iohexol (OMNIPAQUE) 300 MG/ML injection 60 mL (60 mLs Intravenous Given 10/12/21 1414)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: 2,0
Labordaten: CT Head wo contrast: Brain Parenchyma: No acute intracranial hemorrhage, CT evidence of acute territorial infarct, mass, mass effect or midline shift. Patchy areas of white matter hypoattenuation are nonspecific but are most typical of chronic microvascular change. Ventricles/Extra-axial Spaces:No hydrocephalus or extra-axial fluid collection. There is generalized cerebral volume loss. Extracranial Structures:Visualized orbits are unremarkable. Paranasal sinuses and mastoids are clear. Calvarium is unremarkable. IMPRESSION: No acute CT abnormality. XR Chest: IMPRESSION: Mild infrahilar opacities bilaterally likely represent atelectasis. CT Angiogram Chest For PE IMPRESSION: 1. No pulmonary embolism or aortic dissection. 2. Bilateral groundglass infiltrates in a pattern most suggestive of Covid 19 pneumonitis though other forms of pneumonia are also in the differential diagnosis. 3. Cardiomegaly with coronary artery and aortic atherosclerotic calcification. 4. Multinodular enlargement of the thyroid consistent with goiter. Right lobe involved more than left
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 diabetes, GERD
Andere Medikamente: ? aspirin EC EC tablet 81 mg, 81 mg, Oral, Daily, ? citalopram (CeleXA) tablet 20 mg, 20 mg, Oral, Daily, ? famotidine (PEPCID) tablet 20 mg, 20 mg, Oral, BID, ? fluconazole (DIFLUCAN) tablet 200 mg, 200 mg, Oral, Q24H,
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1756862

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NY
Alter: 64,0
Geschlecht: F
Eingang: 02.10.2021
Impfdatum: 12.03.2021
Beginn: 25.06.2021
Tage bis Beginn: 105,0
Dosis: 2
Route/Site: IM / LA

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

Abnormal involuntary movement scale Bell's palsy Blood test Computerised tomogram Craniotomy Drain placement Facial paralysis Lacrimation increased Magnetic resonance imaging Spontaneous haematoma Subdural haematoma

Symptomtext

Discovered drooping face on right side about two hours after noting watering right eye. Immediately went to Emergency Dept. Diagnosed BOTH Bell's Palsy as well as Acute Spontaneous Subdural Hematoma in Fronto/Parietal Area

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: 5,0
Labordaten: Muscle movement observational tests, taste test, blood work, CT scan, MRI scan on 6/25/2021 upon admission to E.D. CT scans daily for next 3 days to watch for more bleeding. Neurosurgery (craniotomy with drain insertion) on 6/26/2021.
Aktuelle Erkrankungen: NONE
Vorgeschichte: Hypertension GERD Arthritis
Andere Medikamente: Losartan 50mg qd Dexilant 60 mg qd Multi-Vit one qd Vit D 5000mg qd Vit C 1000mg qd MSM 1000mg qd Tumeric 1000mg qd
Allergien: Codeine Oxycodones Outdoor seasonal allergies
Vorherige Impfungen: Shingles 2nd shot - body aches, headache; Exact date, brand unknown to me, but was within last 4 yrs, when I was over 60 yrs old

VAERS 1753319

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 29,0
Geschlecht: M
Eingang: 01.10.2021
Impfdatum: 24.03.2021
Beginn: 28.03.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: SYR / LA

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

Anhedonia Anxiety Asthenia Blood pressure decreased Chest discomfort Chest pain Computerised tomogram thorax normal Condition aggravated Crying Decreased appetite Delirium Depersonalisation/derealisation disorder Depression Derealisation Disorientation Dissociation Disturbance in attention Dizziness

Symptomtext

05/2020 - Umbilical hernia repair (no mesh) and appendectomy. Smooth surgery, smooth recovery, no issues at all except hernia recurring 6 weeks later. 12/2020 - Covid. I had fever, cough, horrible headache, loss of taste/smell, etc. Negative covid test, wife tested positive. I?m 100% sure I had it and I had a false negative. Recovered fully from what I could tell in about 2-4 wks. Mid 03/2021 - 2nd Pfizer vaccination. A few days later - playing tennis with a friend. Not overly warm out (maybe 80-85 degrees no humidity). Had to stop mid game because i felt like I absolutely could not catch my breath and i felt like a slight pain in my chest. Had an EKG done a week later and it was fine. Early 04/2021 - Step-father inlaw passed away pretty unexpectedly. 04/13/2021 - Hernia repair (mesh used). I was totally fine, not concerned at all before the surgery. Woke up in the recovery room in a panic, couldn?t breathe. I remember gasping for air. They were able to stabilize me I guess? Sent me home that day and I only really remember a couple things the rest of that day, and I think I was fairly normal. 04/14/2021 - When everything really went to shit. Every 6 hours after the 10am surgery the previous day I was taking 5mg of oxycodone. On the 5th and final dose that I took at around 4:30p, I went into a serious panic attack with horrible like air hunger/shortness of breath. Went to the ER said all my vitals and stuff were fine and sent me home. Had another panic attack I think later that night. I remember like my head just feeling like immense pressure, and my mind doing/seeing things it never had before. Like I was just seeing stars and I for sure felt like I was going to die. Eventually I was able to fall asleep around 3am. Had continued air hunger/shortness of breath every day around the clock for the next two months. Constantly felt like I wasn?t getting enough air. I think the lowest my O2 went to was 90 or 91. Another panic attack early May. Which was when I stopped working. Late 05/2021 - Went to a psychiatrist and was given Zoloft. Took for 4 or 5 days. Didn?t sleep for 4 days straight. Early 06/2021 - Between the insomnia and suicidal thoughts I asked my family to get me some help. I was tired and delirious and having some intense frequent thoughts about hurting myself. I?ve never had thoughts like these ever before. Discontinued Zoloft while I was in the ER. Early 06/2021 - ER sent me to a mental hospital for a 72 hour hold. This was hands down the worst experience and time of my life. I received no help at all while I was there and it felt like I was in prison. They tried giving me a few different pills and none helped. I got about 12 hours combined of sleep while I was there. 06/10/2021 - Went to this mental health outpatient treatment facility. Was absolutely reeling at the time. Most of the people there were nice but had radically different backgrounds I had (abusive or completely dysfunctional home), and it was obvious that all of their problems were rooted in their families. Now my family isn?t perfect, but I?ve always had 100% loving parents. Didn?t find the program very helpful. 6/15/2021 - Started on Prozac 10mg, went up to 20mg. At this time I absolutely couldn?t do anything (most days for the previous 2 weeks prior to this I sat in one spot and had no desire to do anything, it was the worst feeling ever). Late 06/2021 - Psych told me to go up to 40mg of Prozac. Nearly got serotonin syndrome, went to urgent care and went back down to 20mg. Mid 07/2021 - Went back to home with my mom and wife. Late 07/2021 - titrated up to 30mg because 20mg didn?t seem to be doing much. Early 08/2021 - Stumbled upon a r/covidlonghaulers sub-Reddit and discovered that all this shit seems to be covid related. The only differences between my surgery last year and this year from a biological standpoint was the mesh and having gotten covid in 12/2020. Early 08/2021 - moved to the mountains with my wife and her mom. A week later - evacuated from our house for 3 weeks because of wildfires. Mid 09/2021 - evac lifted went back to our house. Late 09/2021 - family decided I should come back home for a little while. List of symptoms throughout all of this (bolded are the ones still lingering to this day): Constant headaches. Sleep problems / chronic insomnia (never had a problem with sleeping in my life prior to all of this). Earlier on in April, May, June I?d get either brain zap feelings or a shot of adrenaline that would jolt me awake when I was trying to fall asleep. For a long time it was hard to get to sleep and stay asleep. Thankfully now it?s easier to fall asleep, but I usually wake up 3-6x per night. Difficulty Breathing (this mostly went away in June). Dissociation/Derealization/Depersonalization; Dizziness; Hand Tremors (I have a video I can text if you?d like); Anhedonia; General brain fog; Difficulty thinking; reading; concentrating; forgetfulness; nausea and appetite loss; Acid Reflux; Chest pain/tightness/discomfort (few EKG?s, a CT of my chest and an echo done. All show my heart/lungs are fine) Palpitations every so often Orthostatic / Tachycardia problems (BP drops 20-30 systolic when I go from laying down to standing and 10-15 diastolic). Heart rate usually goes up by 25+, (usually from 70 ish to 100ish); Disorientation (especially after sleep) Low energy most of the time, but I can do almost all tasks without any physical inabilities; Difficulty exercising and honestly maybe PEM; Exercising makes me feel shitty. I recently (late september) did a kind of test where I cycled for 30 mins one day. The next day I felt horrible. A little over 24 hours later I was absolutely balling for about 20-30 mins. Muscle twitches; Anxiety/PTSD/Depression/Intrusive thoughts; Body aches; Muscle soreness or stiffness with minimal activity; No pre-existing physical or mental health issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: All tests coming back mostly normal
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1741997

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NY
Alter: 43,0
Geschlecht: M
Eingang: 28.09.2021
Impfdatum: 21.03.2021
Beginn: 31.03.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: SYR / RA

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

Blood test Chest pain Dizziness Dyspnoea Electrocardiogram ambulatory Loss of consciousness Renal scan

Symptomtext

I first noticed getting light-headed and a week after that my chest started killing me. I passed out and I ended up in ER. They couldn't find anything wrong with me. Two weeks after that, I was getting off of a plane and passed out again and went back to the hospital. I still have symptoms, it's about twice a week, I still pass out about twice a week. I feel it coming my chest, starts hurting, and I get really short of breath, and I pass out. I am seeing a cardiologist for it, Internal Medicine. The cardiologist thought I had high blood pressure but the next day he checked it and said that isn't, but no treatment yet as they don't know what to give me.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Hospital (two ER visits) did bloodwork to check on heart attack; did a kidney something scan. They made me wear a Holter device it monitors my EKG for a month. They didn't find anything. They didn't find anything heart attack related. The doctor sees something going on but does not what it is that is causing it. Was in the ER overnight both times.
Aktuelle Erkrankungen: No
Vorgeschichte: I have never been to a doctor before this
Andere Medikamente: TYLENOL
Allergien: Aspirin; penicillin
Vorherige Impfungen: -

VAERS 1735630

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: WA
Alter: 63,0
Geschlecht: F
Eingang: 26.09.2021
Impfdatum: 01.03.2021
Beginn: 23.09.2021
Tage bis Beginn: 206,0
Dosis: 1
Route/Site: SYR / LA

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

Balance disorder Electrocardiogram Hyperhidrosis Magnetic resonance imaging Migraine Nausea Seizure Vertigo Vomiting

Symptomtext

Seizure whole body seized Obsessive vomiting Sweats Vertigo no balance Migraine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Mri- 09-23-21 EKG. X3 NAUSEA MEDS WALKER
Aktuelle Erkrankungen: None
Vorgeschichte: High BP Bi polar disorder Hypothyroidism Barrettes esophagus
Andere Medikamente: Lovoxcil Lispearanol Nexium Trazadone Quiepine
Allergien: Sun Bee wasps
Vorherige Impfungen: -

VAERS 1723069

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: PA
Alter: 52,0
Geschlecht: F
Eingang: 22.09.2021
Impfdatum: 21.03.2021
Beginn: 23.03.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain upper Anticoagulant therapy Cholecystectomy Computerised tomogram abdomen Computerised tomogram abdomen abnormal Fatigue Gallbladder disorder Headache Impaired work ability Influenza Musculoskeletal chest pain Pain Thrombosis

Symptomtext

On March 22 I had flu symptoms headache achy and tired the next day on the 23rd I was at work teaching an exercise class I got a severe stomach pain and was unable to continue working this lasted for 11 days and it lasted 7-9 hours everyday and every time I ate it got worse I got an appointment was in April but my husband took me to the ED and because of the location of the pain between my ribs they wanted to rule out a heart attack. When that was ruled out they did a CT of the abdomen and they saw 4 inch blood clot I was transferred to a different hospital better equipped I was hospitalized there and later sent me home on blood thinners. At home the pain continue and on April 9th my husband took me to the clinic and they said the medicine needs time and to give it time but on April 13 my doctor sent me again to the ED and they did a angio CT and found my gallbladder is very bad and needs to come out but it has to take 3 months of blood thinners now the blood clots are gone and now my gallbladder was removed and everything is going back to normal. In November I have anther angio CT to make sure everything is still normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Infertility
Andere Medikamente: Multivitamin; Nexium; Restasis eye drops
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1666815

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: FL
Alter: 54,0
Geschlecht: F
Eingang: 02.09.2021
Impfdatum: 15.03.2021
Beginn: 21.03.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: SYR / LA

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

Angiocardiogram Blood test Chest X-ray Chest pain Computerised tomogram thorax Dyspnoea Echocardiogram Electrocardiogram Electrocardiogram ambulatory Heart rate increased Laboratory test Lipids Pain Painful respiration Pericarditis Urine analysis

Symptomtext

Chest pain, shortness of breath, rapid heart rate, painful breathing, symptoms developed 6 days after vaccine on 3/21/2021 and progressed rapidly. 3/22/2021 I was sent to ER by my PCP. My condition had worsened, I was in a lot of pain with difficulty breathing and a very rapid heart rate. I was admitted to Hospital through the ER after they diagnosed my condition as pericarditis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 3,0
Labordaten: 3-22-2021 to 3-24-2021; Chest X-ray; EKG; Echocardiogram; Chest CT scan; Coronary CTA Scan; Blood tests/Count; Hematology; Routine Coagulation; Routine Chemistry; Lipids CV Risks; Urine Chemistry; Urinalysis Autoimmune; General Serology; Molecular Infections; April and May 2021 Holter Scan; Echocardiogram; September 1, 2021; EKG
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Amlodipine 10 mg; Levothyroxine 100 mcg
Allergien: None known
Vorherige Impfungen: -

VAERS 1666576

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 02.09.2021
Impfdatum: 11.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Bradycardia Dizziness Intensive care

Symptomtext

Two hours after vaccination, I went into heart bradycardia. My HR went down to 38. I felt as if I was going to pass out. My husband helped to keep me safe and alert.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: Monitored in CCU
Aktuelle Erkrankungen: Lupus / AIH / Hashimotos /Heart - LBBB, small vessel / Iron deficiency anemia /osteoporosis / osteoarthritis
Vorgeschichte: See 11
Andere Medikamente: Synthroid/ plaquenil/ tagamet/ Vit D3/ B complex/ Magnesiu,/ valtrex
Allergien: penicillin/ erythromycin /cephalosporin /ciprofloxacin /Celebrex /clindamycin / Bactrim / Keflex /Raloxifene /benzonatate
Vorherige Impfungen: -

VAERS 1658618

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 61,0
Geschlecht: M
Eingang: 31.08.2021
Impfdatum: 24.03.2021
Beginn: 06.08.2021
Tage bis Beginn: 135,0
Dosis: 1
Route/Site: SYR / RA

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

VIth nerve paralysis

Symptomtext

Diagnosed with sixth-nerve palsy in left eye. I have been receiving shots every 6 weeks or so in my left eye to reduce fluid, with no adverse affects over the past 12 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: VIth nerve paralysis
Hospital-Tage: -
Labordaten: Examination
Aktuelle Erkrankungen: none
Vorgeschichte: DIabetes
Andere Medikamente: Metformin, Insulin type R, insulin type n, Atorvastatin, lisinopril, Levothyroxine, Tramadol, gabapentin
Allergien: None
Vorherige Impfungen: -

VAERS 1641230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: VA
Alter: 65,0
Geschlecht: F
Eingang: 27.08.2021
Impfdatum: 13.03.2020
Beginn: 14.03.2020
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Cold sweat Ear disorder Loss of consciousness Tinnitus

Symptomtext

Cold sweat and blacked out at home next day after 1st shot. Husband witnessed. After 2nd shot both my husband and myself had ear issues like ringing in ears.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Diverticulitis
Andere Medikamente: Losarton pot/hydrochlorothiazide, esomeprazole magnesium, lovastatin, mature multi vitamin, vitamin D, mega red
Allergien: Oxicotin
Vorherige Impfungen: -

VAERS 1633021

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

schwer

Staat: PA
Alter: 79,0
Geschlecht: F
Eingang: 25.08.2021
Impfdatum: 01.04.2021
Beginn: 01.05.2021
Tage bis Beginn: 30,0
Dosis: 2
Route/Site: SYR / LA

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

Syncope

Symptomtext

fainted in May and again in July. none of the tests that have been taken have found anything wrong that would cause me to faint. that is why i am reporting this to see if anyone else has experienced an issue like this.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: fish oil, calcium citrate, multi-vitamin, lisinopril, simvastatin, low dose aspirin
Allergien: morphine
Vorherige Impfungen: -

VAERS 1591671

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MD
Alter: 68,0
Geschlecht: F
Eingang: 20.08.2021
Impfdatum: 17.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 15,0
Dosis: 1
Route/Site: IM / AR

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

Anaphylactic reaction Blood pressure decreased Blood test abnormal Breast swelling Cold sweat Dizziness Eosinophil count increased Fear Feeling cold Nausea Vomiting

Symptomtext

2 weeks after each COVID vaccine, I experienced sudden drop in BP. First vaccine on 3/17 was followed 2 weeks later with BP drop. First BP reading on 4/1 was 88/58. Minutes later, I double-checked & BP reading was 72/53. Was cold and clammy; felt faint. Grew nauseous and threw up. Had no EPI pen. Feared this was anaphylaxsis & took the most logical thing I could think of ? 37.5 mg phentermine. Symptoms subsided in about 20 minutes(?) 2d Covid shot received 4/7. 2 weeks later ? nearly identical reaction occurred: BP plummeted, cold clammy. Did not throw up this time. I took 37.5 mg phentermine right away - and was OK. Also, significant breast swelling (from C to D), which has NOT gone away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Had bloodwork done several months later - - eosinophils were still elevated (
Aktuelle Erkrankungen: hives of unknown origin - for approx 30 days prior to vax
Vorgeschichte: fatigue & moderate impairment of certain executive function following concussion/TBI
Andere Medikamente: 18.75 g phentermine HCI - 4 days per week for fatigue
Allergien: sensitive to codeine, percocet
Vorherige Impfungen: -

VAERS 1582969

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: FL
Alter: 67,0
Geschlecht: M
Eingang: 18.08.2021
Impfdatum: 16.02.2021
Beginn: 16.08.2021
Tage bis Beginn: 181,0
Dosis: 2
Route/Site: IM / -

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

COVID-19 Condition aggravated Neurological symptom SARS-CoV-2 test positive Seizure

Symptomtext

Presents with Seizure this morning. Per EMS, Pt was increased on Depakote, and hadn't gotten a refill on his prescription which caused back-to-back seizures, each lasting approx 30 seconds and entire episode lasting 3-5 minutes. Pt who has a hx of seizures currently is back to normal and has no complaints or pain at this time. Patient was recently hospitalized at our MC for concerns of possible CVA. He and his wife report that he had a full inpatient workup, including MRI and ultrasounds which were negative for acute stroke. Patient was determined to have had seizure activity leading to his neurological symptoms, and he was increased on his Depakote to 500 mg b.i.d.. Patient's wife states that they have not

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: SARS COV2 COVID 19 PCR 08/16/2021 (INCIDENTAL FINDING)
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Anxiety, back pain, Brain injury with open intracranial wound, CABG, Carotid stenosis, Claudication, Dyslipidemia
Andere Medikamente: Hydralazine, Carvedilol, Divalproex, ASA, Jevity, Multivit
Allergien: Lisinopril, Statins, PCN
Vorherige Impfungen: -

VAERS 1139541

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IA
Alter: 41,0
Geschlecht: F
Eingang: 05.08.2021
Impfdatum: 23.03.2021
Beginn: 06.05.2021
Tage bis Beginn: 44,0
Dosis: 1
Route/Site: - / LA

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

Anaphylactic reaction Anxiety Burning sensation Dizziness Electric shock sensation Bell's palsy Blood pressure increased Blood test Hypoaesthesia Dry mouth Panic attack Paraesthesia oral Swelling face Feeling abnormal Head discomfort Headache Hypoacusis Inflammation

Symptomtext

Mild anaphylactic throat swelling at clinic; Mild anaphylactic throat swelling at clinic; left side head nerve inflammation; ear muffled- no infection; head twitching/spasm, dull, burning, sharp, neddle; head twitching/spasm, dull, burning, sharp, neddle; head twitching/spasm, dull, burning, sharp, neddle/head pressure; head twitching/spasm, dull, burning, sharp, neddle/head pressure; head twitching/spasm, dull, burning, sharp, neddle; migraine line pains; sinus pressure; tinnitus; heightened anxiety; nerve zaps in brain, toes and tooth; dizziness; bdain fog; speech problem; mini stroke like symptoms; insomnia; base skull feels swollen; High inflammation markers; This is a spontaneous report from a contactable consumer (patient). This 41-year-old female patient received bnt162b2 (Brand: Pfizer), dose 2 via an unspecified route of administration, administered in arm right on 23Mar2021 (Batch/Lot Number: ER781) as dose 2, single at the age of 41-year-old for covid-19 immunisation. Medical history included high bp and known allergies penicillin. Concomitant medications included hydroxyzine hydrochloride (HYDROXIZINE) taken for an unspecified indication, start and stop date were not reported; hydrochlorothiazide, losartan potassium (LOSARTAN HCTZ) taken for an unspecified indication, start and stop date were not reported. No other vaccine in four weeks. Facility where the most recent COVID-19 vaccine was administered: Other. First dose was received on 23Mar2021 08:30 am in arm left at the age of 41-year-old with Batch/lot number: EN6208 and experienced all Left side - Face numbness, mild inner mouth swelling, ER visit, went away after 2 weeks, and very heavy legs. Adverse event 2nd dose: mild anaphylactic throat swelling at clinic, doubled on hydroxyzine per nurse. 10 days post (as reported): left side head nerve inflammation, ear muffled- no infection, head twitching/spasm, dull, burning, sharp needle, migraine line pains, sinus pressure, head pressure, tinnitus, heightened anxiety, nerve zaps in brain, toes and tooth, dizziness, brain fog, speech problem, mini stroke like symptoms, insomnia, base skull feels swollen. ER, primary doc, neurons and physical therapists being seen. No treatments avail...VAX reaction confirmed. High inflammation markers. Adverse event start date reported as 06May2021 08:00 am. Events resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Life threatening illness (immediate risk of death from the event), Disability or permanent damage. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19. Covid test post vaccination covid test type post vaccination: Nasal Swab on 11Jul2021: Negative. Treatment was unknown. The patient was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Test Date: 20210506; Test Name: inflammation markers; Result Unstructured Data: Test Result:High; Test Date: 20210711; Test Name: Covid test; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Penicillin allergy
Andere Medikamente: HYDROXIZINE; LOSARTAN HCTZ
Allergien: -
Vorherige Impfungen: -

VAERS 1139541

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IA
Alter: 41,0
Geschlecht: F
Eingang: 05.08.2021
Impfdatum: 23.03.2021
Beginn: 06.05.2021
Tage bis Beginn: 44,0
Dosis: 1
Route/Site: IM / -

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

Anaphylactic reaction Anxiety Burning sensation Dizziness Electric shock sensation Bell's palsy Blood pressure increased Blood test Hypoaesthesia Dry mouth Panic attack Paraesthesia oral Swelling face Feeling abnormal Head discomfort Headache Hypoacusis Inflammation

Symptomtext

Mild anaphylactic throat swelling at clinic; Mild anaphylactic throat swelling at clinic; left side head nerve inflammation; ear muffled- no infection; head twitching/spasm, dull, burning, sharp, neddle; head twitching/spasm, dull, burning, sharp, neddle; head twitching/spasm, dull, burning, sharp, neddle/head pressure; head twitching/spasm, dull, burning, sharp, neddle/head pressure; head twitching/spasm, dull, burning, sharp, neddle; migraine line pains; sinus pressure; tinnitus; heightened anxiety; nerve zaps in brain, toes and tooth; dizziness; bdain fog; speech problem; mini stroke like symptoms; insomnia; base skull feels swollen; High inflammation markers; This is a spontaneous report from a contactable consumer (patient). This 41-year-old female patient received bnt162b2 (Brand: Pfizer), dose 2 via an unspecified route of administration, administered in arm right on 23Mar2021 (Batch/Lot Number: ER781) as dose 2, single at the age of 41-year-old for covid-19 immunisation. Medical history included high bp and known allergies penicillin. Concomitant medications included hydroxyzine hydrochloride (HYDROXIZINE) taken for an unspecified indication, start and stop date were not reported; hydrochlorothiazide, losartan potassium (LOSARTAN HCTZ) taken for an unspecified indication, start and stop date were not reported. No other vaccine in four weeks. Facility where the most recent COVID-19 vaccine was administered: Other. First dose was received on 23Mar2021 08:30 am in arm left at the age of 41-year-old with Batch/lot number: EN6208 and experienced all Left side - Face numbness, mild inner mouth swelling, ER visit, went away after 2 weeks, and very heavy legs. Adverse event 2nd dose: mild anaphylactic throat swelling at clinic, doubled on hydroxyzine per nurse. 10 days post (as reported): left side head nerve inflammation, ear muffled- no infection, head twitching/spasm, dull, burning, sharp needle, migraine line pains, sinus pressure, head pressure, tinnitus, heightened anxiety, nerve zaps in brain, toes and tooth, dizziness, brain fog, speech problem, mini stroke like symptoms, insomnia, base skull feels swollen. ER, primary doc, neurons and physical therapists being seen. No treatments avail...VAX reaction confirmed. High inflammation markers. Adverse event start date reported as 06May2021 08:00 am. Events resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Life threatening illness (immediate risk of death from the event), Disability or permanent damage. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19. Covid test post vaccination covid test type post vaccination: Nasal Swab on 11Jul2021: Negative. Treatment was unknown. The patient was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Test Date: 20210506; Test Name: inflammation markers; Result Unstructured Data: Test Result:High; Test Date: 20210711; Test Name: Covid test; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Penicillin allergy
Andere Medikamente: HYDROXIZINE; LOSARTAN HCTZ
Allergien: -
Vorherige Impfungen: -

VAERS 1139541

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IA
Alter: 41,0
Geschlecht: F
Eingang: 05.08.2021
Impfdatum: 23.03.2021
Beginn: 06.05.2021
Tage bis Beginn: 44,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Anxiety Burning sensation Dizziness Electric shock sensation Bell's palsy Blood pressure increased Blood test Hypoaesthesia Dry mouth Panic attack Paraesthesia oral Swelling face Feeling abnormal Head discomfort Headache Hypoacusis Inflammation

Symptomtext

Mild anaphylactic throat swelling at clinic; Mild anaphylactic throat swelling at clinic; left side head nerve inflammation; ear muffled- no infection; head twitching/spasm, dull, burning, sharp, neddle; head twitching/spasm, dull, burning, sharp, neddle; head twitching/spasm, dull, burning, sharp, neddle/head pressure; head twitching/spasm, dull, burning, sharp, neddle/head pressure; head twitching/spasm, dull, burning, sharp, neddle; migraine line pains; sinus pressure; tinnitus; heightened anxiety; nerve zaps in brain, toes and tooth; dizziness; bdain fog; speech problem; mini stroke like symptoms; insomnia; base skull feels swollen; High inflammation markers; This is a spontaneous report from a contactable consumer (patient). This 41-year-old female patient received bnt162b2 (Brand: Pfizer), dose 2 via an unspecified route of administration, administered in arm right on 23Mar2021 (Batch/Lot Number: ER781) as dose 2, single at the age of 41-year-old for covid-19 immunisation. Medical history included high bp and known allergies penicillin. Concomitant medications included hydroxyzine hydrochloride (HYDROXIZINE) taken for an unspecified indication, start and stop date were not reported; hydrochlorothiazide, losartan potassium (LOSARTAN HCTZ) taken for an unspecified indication, start and stop date were not reported. No other vaccine in four weeks. Facility where the most recent COVID-19 vaccine was administered: Other. First dose was received on 23Mar2021 08:30 am in arm left at the age of 41-year-old with Batch/lot number: EN6208 and experienced all Left side - Face numbness, mild inner mouth swelling, ER visit, went away after 2 weeks, and very heavy legs. Adverse event 2nd dose: mild anaphylactic throat swelling at clinic, doubled on hydroxyzine per nurse. 10 days post (as reported): left side head nerve inflammation, ear muffled- no infection, head twitching/spasm, dull, burning, sharp needle, migraine line pains, sinus pressure, head pressure, tinnitus, heightened anxiety, nerve zaps in brain, toes and tooth, dizziness, brain fog, speech problem, mini stroke like symptoms, insomnia, base skull feels swollen. ER, primary doc, neurons and physical therapists being seen. No treatments avail...VAX reaction confirmed. High inflammation markers. Adverse event start date reported as 06May2021 08:00 am. Events resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Life threatening illness (immediate risk of death from the event), Disability or permanent damage. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19. Covid test post vaccination covid test type post vaccination: Nasal Swab on 11Jul2021: Negative. Treatment was unknown. The patient was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Test Date: 20210506; Test Name: inflammation markers; Result Unstructured Data: Test Result:High; Test Date: 20210711; Test Name: Covid test; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Penicillin allergy
Andere Medikamente: HYDROXIZINE; LOSARTAN HCTZ
Allergien: -
Vorherige Impfungen: -

VAERS 1524949

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: AL
Alter: 65,0
Geschlecht: F
Eingang: 04.08.2021
Impfdatum: 05.04.2021
Beginn: 05.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Chest X-ray Computerised tomogram Headache Magnetic resonance imaging Reaction to preservatives Throat tightness Thrombosis Ultrasound scan

Symptomtext

Second dose: when admitted to hospital, found out had blood clots in legs and lungs; Second dose: Developed from that a severe headache; Second dose: Had a more severe reaction after receiving second dose; Second dose: Throat was going to close up; This is a spontaneous report from a contactable consumer. This 65-Year-old female consumer (Patient) reported that: A 65-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: solution for injection, Batch/Lot Number: EN6208), via an unspecified route of administration, administered in Arm Left on 05Apr2021 at 09:05 (at the age of 65-year-old) as single dose for covid-19 immunisation. The patient had a steroid injection, has allergies to medication, and had a reaction occurred a couple of years ago. Patient had no family history, and no relevant test was performed. Concomitant medication(s) included paracetamol (TYLENOL) taken for an unspecified indication from 04Apr2021 to an unspecified stop date. Patient was not administered any vaccine on same day. The patient was not received any other vaccine four weeks prior vaccination. The patient's historical vaccine included first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: solution for injection, Batch/Lot Number: EN6200), via an unspecified route of administration, administered in Arm Left on 15Mar2021 (at the age of 65-year-old) as single dose for covid-19 immunisation and experienced the events Had a severe reaction from first dose, Was sick for about a week behind the first dose with slight headache, Just weak and tired. The patient was taken to the emergency room. The paramedics had to come to the vaccination site and give the caller mediations there. The patient needed more done and was taken to the hospital. The patient stated she was in bed for about what seemed like a month or at least three weeks until she went to get the second dose Pfizer Covid Vaccine. On 05Apr2021 the patient received the second dose Pfizer Covid Vaccine. The caller's primary care doctor said it should be okay and told the patient to take Tylenol. The patient took Tylenol the night prior and the morning of the second dose Pfizer Covid Vaccine on 05Apr2021. The caller shared with the persons at the vaccination site what occurred after the caller received the first dose Pfizer Covid Vaccine and the caller was taken to a cot to lay down on just in case. The patient had a more severe reaction with the second dose Pfizer Covid Vaccine on 05Apr2021. The patient's throat was going to close up on 05Apr2021 patient can't remember the name of the reaction that the persons at the site specifically called the reaction. The paramedics came and gave the patient an epi pen and Benadryl and all of that, even when fire department got there, nothing used worked. Took the patient to the hospital for the night and the next day the caller came home. She developed from that a severe headache the patient was sick with severe headache ever since 05Apr2021. When admitted to the hospital is when the patient found out she had blood clots in her legs and lungs on unspecified date. If the caller had not been admitted to the hospital, she would probably not be here. The caller was in the hospital from 22Apr2021 to 15May2021, about three weeks. Dates documented as provided by patient. The patient states the hospital was trying to dos something to help the patient with the headaches and get the blood clots under control. Got the blood clots somewhat under control but nothing helped the headaches. Today, the caller is still suffering from severe headaches, debilitating and can't really do anything 24/7. When the patient received the second dose Pfizer Covid Vaccine the headache was more intense, it worsened. patient clarified date of hospitalization was 29Apr2021 to either 13May2021 or 15May2021. The caller states the headache is the major thing. The headache is limited to what the caller can do. The caller has physical therapy coming in twice a week. The patient underwent lab tests and procedures which included chest x-ray: unknown result on unspecified date, computerised tomogram: unknown result on unspecified date, magnetic resonance imaging: unknown result on unspecified date, ultrasound scan: unknown result on unspecified date, ultrasound scan: unknown result on unspecified date. Therapeutic measures were taken as a result of the events Had a more severe reaction after receiving second dose and Throat was going to close up with epi pen and Benadryl. The outcome of the events Had a more severe reaction after receiving second dose and Second dose: Throat was going to close up was unknown, Second dose: when admitted to hospital, found out had blood clots in legs and lungs was recovering and Second dose: Developed from that a severe headache was not recovered. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 16,0
Labordaten: Test Name: Chest X-ray; Result Unstructured Data: Test Result:UNKNOWN RESULT; Test Name: CT scan; Result Unstructured Data: Test Result:UNKNOWN RESULT; Test Name: MRI; Result Unstructured Data: Test Result:UNKNOWN RESULT; Test Name: echogram; Result Unstructured Data: Test Result:UNKNOWN RESULT; Test Name: Ultrasound of heart, legs and lungs; Result Unstructured Data: Test Result:UNKNOWN RESULT
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Drug allergy (couple of years ago.)
Andere Medikamente: TYLENOL
Allergien: -
Vorherige Impfungen: -

VAERS 1334627

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: FL
Alter: 64,0
Geschlecht: F
Eingang: 31.07.2021
Impfdatum: 30.03.2021
Beginn: 30.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Atrial fibrillation Loss of consciousness Lung disorder Nausea Renal disorder Cardiac failure Dehydration Echocardiogram Intensive care Mental status changes Renal failure Vomiting

Symptomtext

She confirms she passed out.; She ended up in the hospital with lots of vomiting and nausea.; She ended up in the hospital with lots of vomiting and nausea.; her heart started with Afib; her kidneys shut down; her lungs were affected; This is a spontaneous report from a contactable consumer (patient) via sponsored program. A 64-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number and Expiration date was not reported), dose 1 via an unspecified route of administration on 30Mar2021 (at the age of 64-year-old) as DOSE 1, SINGLE for covid-19 immunisation; morphine (MORPHINE), route of administration, start and stop date, batch/lot number and dose were not reported for an unspecified indication; gabapentin (GABAPENTIN), route of administration, start and stop date, batch/lot number and dose were not reported for an unspecified indication. The patient medical history and concomitant medications was not reported. The patient experienced she confirms she passed out. (medically significant) on 31Mar2021, she ended up in the hospital with lots of vomiting and nausea. She had to get rehydrated. On 30Mar2021, she ended up in the hospital with lots of vomiting and nausea. on 30Mar2021, her heart started with afib (medically significant) in 2021, her kidneys shut down in 2021, her lungs were affected in 2021. The patient was hospitalized for she confirms she passed out and she ended up in the hospital with lots of vomiting and nausea from 31Mar2021 to 07Apr2021. The reporter also stated that her kidneys shut down, her lungs were affected, her heart started with Afib. She takes lots of medications and wasn't getting them because of the vomiting. She states she takes Gabapentin and when she suddenly stops it she goes into a coma. She says that did not happen however she was "in an altered state of consciousness for 5 days and then in a couple of days I got to go home." She was in the hospital for a week. She also takes Morphine, and "this relates to the stopping of the gabapentin": "it looks like you've taken more morphine that you have" since the kidney's stopped working. She says the doctors feel that's what happened. She says its not an allergic reaction. If she can stop the nausea and vomiting "is it too risky to take the second dose?" Her doctor said she is "lucky to be alive" and not to take the second dose. Caller states she filed a VAERS report but the report number is not handy. She said she takes a lot of different medications and because of all of the vomiting, she really wasn't getting all of those medications, 2 of which were Gabapentin and Morphine. She said when she stops the Gabapentin suddenly, she goes into a coma. However, that didn't happen while she was in the hospital, but she says she was in an altered state of consciousness for 5 days while being in the hospital. She was in the hospital for a week, and for 5 days, she was in that altered state of consciousness, and then a couple of days later, she got to go home. In regards to the Morphine, she stated because of the vomiting, which she believes is also related to the stopping of the Gabapentin, it looked like she had taken more Morphine than she actually had because of her kidneys not working properly. The doctors feel that is what happened. Her question for the agent was that she knows it is not an allergic reaction but, if she can't stop the nausea and vomiting, is it too risky to get the second dose? She said that her doctor told her she was lucky to be alive and should not take the second dose. She also filed a report through VAERS but does not have the report number handy. Agent states that the agent stated she was going to fax an AE report to the regulatory authority. Agent stated that she told the caller to talk to her physician because Pfizer cannot determine if she should take the next dose or make a recommendation to stop the nausea and vomiting- this all has to be discussed with the physician. States that she put him down on the report she filed. She was very surprised the doctors at the hospital were all about the Morphine and it wasn't about the Morphine. States that she filed a report with VAERS but this is the first time speaking with Pfizer. The only reason she called Pfizer is that her doctor said that its up to her if she wanted to get the second shot. The vaccine would give her protection but he couldn't guarantee that the kidneys wouldn't shut down just because of the vomiting. She thought maybe there was an injection they could give her if she went to the hospital to have the vaccine. She confirms she passed out. They made her wait an hour after the shot because of her history. After about 2 hours of getting home, she started throwing up. She thought well the paperwork said nausea, and it did not occur that it would get as bad it did. She states she didn't realized it was that bad, and when she doesn't get Gabapentin after so many hours, her brain starts getting fuzzy, and she was saying she was fine, but wasn't. She has had comas before because she didn't keep her Gabapentin down. She clarifies she has been in a coma 3 times be before in the hospital because she was not keeping the Gabapentin down. That is why she felt that it was more from the Gabapentin and not from the morphine. She mentions she was given her Narcan 3 times and it didn't do anything. She mentions she wrote this all down in the report and didn't hide the fact had that she took Morphine. They counted the pills and the pills were all there, but it turns out, when her kidneys shuts down and she stopped taking certain drugs, the morphine elevates she guesses. She confirms she was in an altered state for 5 days. Clarified that it was 30Mar2021 that she got the vaccine and has this reaction. Her breathing shut down, her lungs were bad and she started going into A-fib which she never had A-fib before. Clarified that the vaccine facility had kept her there for one hour and then 2 hours later, she started throwing up. The next morning 31Mar2021, she passed out and she was taken to the hospital. She got out of the hospital on 07Apr2021. She states she was out of it for 5 days. She confirms she takes many medications. She knows that she didn't keep anything down on 30Mar2021, but she does not know what she kept down on 31Mar2021. Obviously, she kept the Morphine down otherwise it wouldn't have been in her system, but she was just out of it. That is how bad the nausea and vomiting was. The paperwork said nausea, but she wasn't warned about extreme vomiting. She states she was taken off of everything. The only thing she knows she was given was Narcan. She was told until she could wake up and swallow, they wouldn't give her any medication. She had to go cold turkey on everything. She was on IV's, but she really doesn't know what they were doing because she was unconscious. Caller states that she has another call and requests someone to call her back. Caller advised that Pfizer would contact her if in need of further information. She states she is on many medications, including Gabapentin and Morphine. She was told until she could wake up and swallow, they wouldn't give her any medication. No further details were provided or obtained. The action taken for morphine and gabapentin was unknown. Therapeutic measures were taken as a result of she confirms she passed out, she ended up in the hospital with lots of vomiting and nausea, her heart started with afib, her kidneys shut down, her lungs were affected. The outcome of the events was unknown. Information on the Batch/lot number has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Coma
Andere Medikamente: morphine; gabapentin
Allergien: -
Vorherige Impfungen: -

VAERS 1515789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 30.07.2021
Impfdatum: 13.03.2021
Beginn: 23.07.2021
Tage bis Beginn: 132,0
Dosis: 1
Route/Site: IM / LA

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

Antiphospholipid syndrome Axillary pain Back pain Blood test Chest X-ray Chills Eye pain Fatigue Headache Hypoaesthesia Musculoskeletal stiffness Neck pain Pain Pain in extremity Pyrexia Skin discolouration Thrombosis Ultrasound Doppler abnormal

Symptomtext

I awoke @ 7:45 AM with an extremely painful, stiff, sore left arm. Bicep ached near vaccination entry point. Bicep, elbow, forearm and hand were stiff and painful. Left hand was numb and slightly discolored. Soreness in left armpit and neck as well. Called and described symptoms. Advised to g immediately to ER. I did. Doctor saw me. Did ultrasound of left upper body from neck down to shoulder, bicep, forearm and hand. Chest xray. Blood work. Diagnosis: blood clot. Waited for complete blood work results; not available until Wednesday 7/28. On 7/23 PM fever, chills and body aches throughout. Increased fatigue. Slept 11 hours on 7/23. Bed rest on 7/24. Lower back pain and pain in left arm remained. Slept 10 hours. Diagnosis: antiphosphal lipid syndrome. No personal history of blood clots or family history of such. I was prescribed Xarelto, 15 mg. X twice a day. Also taking Tylenol 3 times a day as safe. Left arm pain has lessened. Still slight. Also pain in low back (kidneys?) eye sockets and temples.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Ultrasound of left upper body Chest Xray Blood panel
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None
Allergien: Unknown. Undiagnosed.
Vorherige Impfungen: -

VAERS 1512849

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 29.07.2021
Impfdatum: 01.04.2021
Beginn: 28.06.2021
Tage bis Beginn: 88,0
Dosis: UNK
Route/Site: - / -

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

Ischaemic stroke

Symptomtext

I63.9 - Acute ischemic stroke

Weitere VAERSDATA-Felder

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

VAERS 1512831

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 71,0
Geschlecht: M
Eingang: 29.07.2021
Impfdatum: 02.04.2021
Beginn: 06.07.2021
Tage bis Beginn: 95,0
Dosis: UNK
Route/Site: - / -

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

Facial paresis Ischaemic stroke

Symptomtext

I63.9 - Acute ischemic stroke (CMS/HCC) R29.810 - Facial weakness

Weitere VAERSDATA-Felder

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

VAERS 1512671

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN-6208

schwer

Staat: VA
Alter: 50,0
Geschlecht: M
Eingang: 29.07.2021
Impfdatum: 18.03.2021
Beginn: 18.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Blood test normal Chest pain Diarrhoea Dizziness Dyspnoea Echocardiogram normal Electrocardiogram normal Eyelid irritation Immediate post-injection reaction Injection site pain Muscle spasms Pain Pericarditis Throat tightness Vomiting

Symptomtext

Immediately after receiving the injection, I felt pain/sore that traveled from the injection site, went through and across my left pectoral and ended at center of my chest/heart area. I waited 15 minutes in the observation area to see if symptoms would get worse, but they did not; and so I left the facility and drove home. On my way home, about 45 minutes after receiving the shot, I felt my throat tightening up a bit, and my left hand and eyelids began to cramp up. I stopped at a pharmacy and bought some Benadryl. After 30 minutes, the pain in my chest began to feel better, and the cramping had disappeared. At about 6 pm that same day, my chest pain returned; and so I took one more Benadryl. The pain/soreness began to disappear after about 30 minutes. I felt fine for exactly two weeks. On Thursday, April 1st, I woke up with severe abdominal pain, diarrhea, and constant vomiting for about 12 hours. Went to urgent care and received an anti-nausea shot. The vomiting stopped, but the abdominal pain continued until the next morning. The weekend of April 10th, I experienced the chest pain again. This time it was very concerning because I felt very lightheaded, short of breath and faint. I checked myself into ER two days after.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 2,0
Labordaten: ECG, blood work and tests all showed normal. Heart ultrasound showed normal. The diagnosis was presumptive pericarditis. I was in the hospital overnight and discharged the following day. Followed up with my PCP, cardiologist, and allergist. The allergist recommended that I opt out of receiving a second dose of the mRNA COVID-19 vaccine.
Aktuelle Erkrankungen: persistent, recurring vertigo since Aug 2020
Vorgeschichte: rhinitis
Andere Medikamente: fenofibrate, pravastatin, Nexium, meclizine, multivitamins
Allergien: none
Vorherige Impfungen: -

VAERS 1511838

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: FL
Alter: 24,0
Geschlecht: M
Eingang: 29.07.2021
Impfdatum: 30.04.2021
Beginn: 01.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Electric shock sensation Headache Hypokinesia Pain Pyrexia Tremor

Symptomtext

Violent uncontrollable shaking; Loss of motor control; Sensations of electricity shooting; Shooting through my body; High fever; Headache; This is a spontaneous report from a contactable consumer, the patient. A 24-year-old male patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EN6208) via an unspecified route of administration in the arm left on 30Apr2021 at 12:30 (at the age of 24-years-old) as a single dose for COVID-19 immunisation. Medical history included COVID-19. Concomitant medications were not reported. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EN6206) via an unspecified route of administration in the arm left on 09Apr2021 at (at the age of 24-years-old) as a single dose for COVID-19 immunisation. Prior to the vaccination, the patient diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 01May2021 at 02:45, the patient experienced violent uncontrollable shaking that occurred in waves and patterns for approximately 1 hour, loss of motor control and sensations of electricity shooting through his body, high fever and headache for the next two days. The clinical outcomes of violent uncontrollable shaking, loss of motor control and sensations of electricity shooting through his body, high fever and headache were recovering. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19:Yes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1508800

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NY
Alter: -
Geschlecht: F
Eingang: 28.07.2021
Impfdatum: 19.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Allergy to vaccine Electric shock

Symptomtext

Experienced an electric shock; She thinks she has an allergy to the vaccine since she had three marks on her back like on the skin; This is a spontaneous report from a contactable consumer or other non-hcp (Patient). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation solution for injection; Lot Number: EN6208, Expiration date: Unknown) via an unspecified route of administration on 19Mar2021 as dose 1, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. It was reported that she received the second dose on 07Apr2021; the lot number is EW0153, unknown NDC number and expiry. In 2021 the patient experienced an electric shock, and she thinks she has an allergy to the vaccine since she had three marks on her back like on the skin. Caller stated she got the vaccine the first and second dose and on the first dose, she had experienced an electric shock, but she thinks she has an allergy to the vaccine since she had three marks on her back like on the skin. Caller stated Pfizer should send her straight to the doctor since the marks happened after the second vaccine. There was no product complaint to this report. A medical information request was there. The clinical outcome of the events was unknown. follow-up attempts are possible, additional information has been requested.

Weitere VAERSDATA-Felder

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

VAERS 1495705

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: WA
Alter: 82,0
Geschlecht: M
Eingang: 22.07.2021
Impfdatum: 19.03.2021
Beginn: 24.04.2021
Tage bis Beginn: 36,0
Dosis: 2
Route/Site: IM / RA

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

Blood creatine phosphokinase MB abnormal Brain natriuretic peptide abnormal Brain natriuretic peptide increased C-reactive protein abnormal Cardiac failure congestive Chest X-ray abnormal Chills Communication disorder Dyspnoea Dyspnoea exertional Echocardiogram abnormal Ejection fraction Electrocardiogram abnormal Fibrin D dimer increased Heart valve incompetence Left ventricular dysfunction Left ventricular hypertrophy Oedema

Symptomtext

Dx: Pericarditis s/s: Dyspnea on exertion, edema, fever/chills unknown symptom onset date, patient poor historian. diagnosed with pericardial effusion, suspect pericarditis. viral panel negative. etiology not defined defined as acute on chronic dyspnea and acute CHF

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 1,0
Labordaten: Vitals: Temp: 37.4C Resp: 20 HR: 89 BP: 127/79 O2: 94 CXR: Abnormal 04/24/2021- no description in report EKG: EKS showed sinus tachycardia with PAC's most likely secondary, cautious with metroprolol 04/24/2021 ECHO:mild concentric left ventricular hypertrophy and mildly reduced systolic function. normal right ventricular size borderline reduced systolic function. mild to moderate regurgitation. moderate size pleural effusion . not evidence of tamponade. rhythm is tachycardia. Ejection fraction 50. 04/26/2021 Resp Panel: neg 04/24/2021 CKMB: abnormal 04/25/2021 D-dimer: abnormal 04/24/2021 CRP: abnormal 04/25/2021 ESR: abnormal 04/25/2021 BNP: abormal 180 reference range: <100 pg/mL date highest level: 04/25/2021 Troponin: normal COVID-19: negative 04/28/2021 ECHO:
Aktuelle Erkrankungen: NA: Data received from the report pulled at State level with limited details.
Vorgeschichte: NA: Data received from ESSENCE report pulled at State level with limited details. Report indicates patient has chronic lung disease, HTN
Andere Medikamente: NA: Data received from the report pulled at State level with limited details.
Allergien: NA: Data received from the report pulled at State level with limited details.
Vorherige Impfungen: -

VAERS 1490625

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NV
Alter: 61,0
Geschlecht: F
Eingang: 21.07.2021
Impfdatum: 08.04.2021
Beginn: 07.05.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: IM / LA

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

Deep vein thrombosis Thrombophlebitis superficial Ultrasound Doppler abnormal Venogram

Symptomtext

Developed a blood clot in my left leg.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Ultrasound done in Primary Physicians office, who then said it was a superficial clot and referred me to as since done a more indepth ultrasound and found in addition to the superficial clot there is a deep vein clot in my left calf and they have ordered a Venogram Cat Scan.
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroidism, Fibromyalgia, Morbid Obesity
Andere Medikamente: RX: Synthroid, cytomel, paxil, flexeril, calcitrol, Vitamin D OTC: Multi Vitamin, Calcium Citrate, Iron, Vit D3, Magnesioum, Vit B Complex, D-Mannose, Cranberry supplement
Allergien: -
Vorherige Impfungen: -

VAERS 1479071

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: WA
Alter: 49,0
Geschlecht: F
Eingang: 16.07.2021
Impfdatum: 25.03.2021
Beginn: 25.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / LA

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

Dysphemia Fatigue Feeling abnormal Feeling cold Hypothermia Mental impairment Muscle tightness Pain Seizure Tremor

Symptomtext

12 hours later almost exactly, I started to feel hypothermic, my brain became foggy, I started shaking uncontrollably, could not think straight, stuttered, repeated saying how cold I was, temp 97 deg. Ended up falling asleep from exhaustion. Later was told it was likely seizures and should have sought treatment but couldn?t think straight to make that decision. Next day my body was extremely sour and tight from the convulsions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: None as I didn?t know to do that
Aktuelle Erkrankungen: None
Vorgeschichte: None really
Andere Medikamente: B12, C, D3, Biotin, multi bite, Busbarone, singular, trazadone, lovastatin, turmeric, probiotic
Allergien: Pecaset
Vorherige Impfungen: Left arm soreness, neck pain and tiredness. Arm felt like some nerve issues make arm feel heavy and tingly. Still feels that way

VAERS 1465585

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NY
Alter: 44,0
Geschlecht: F
Eingang: 12.07.2021
Impfdatum: 02.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: SYR / LA

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

Anxiety Arthralgia Axillary pain Blood test normal Breast pain Burning sensation Echocardiogram Electric shock sensation Electrocardiogram Fatigue Heart rate increased Herpes zoster Insomnia Joint noise Lymphadenopathy Muscle twitching Musculoskeletal chest pain Neck pain

Symptomtext

Had very bad lymph swelling after the initial dose on day 10. Breast pain and lumps under left arm, vaccine side, running down into my ribs and up into my neck. Random migratory pain in joints along with Muscle twitching, headache over right eye, almost felt like a shingles attack. Increased heart rate, fatigue, anxiety, insomnia. Did not seek medical care as was told that those were normal reactions. Symptoms settled day before second shot on March 23. Felt okay for a week then they started back up again but even more pronounced. Have had armpit, breast, back, rib pain that feel like burning and electrical currents, heart palpitations. Random muscle twitching. Joints have been aching and cracking. Had blood work done for lymes disease in April. Negative. In May saw an obgyn who deemed it vaccine related but could offer no treatment after testing negative to RA, Lupus, Lymes. June 14th presented to urgent care as rib and back pain had intensified. They ran an ecg. Ecg was abnormal and was transferred to ER. June 15 Went to hospital where ekg was again abnormal, lengthened qt and st segments which indicate STEMI but clinically I didn?t present any symptoms. Was referred to cardiologist for heart issues. Still suffering back, rib, underarm pain and breast swelling with sensitivity along with random muscle twitching in various areas multiple times a day. Doctors cannot figure out what is cause and say vaccine related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: Lymes blood panel 03/23/21 Complete blood panel 04/29/22 RA, lupus, Lymes panel 05/20/21 EKG 06/14/21 EKG 06/15/21 Blood panel for Heart attack 06/15/21 Stress echo & echocardiogram 07/09/20
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Zyrtec, Flonase, magnesium, quercetin, curcurmin.
Allergien: Crustaceans.
Vorherige Impfungen: -

VAERS 1463249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 53,0
Geschlecht: F
Eingang: 11.07.2021
Impfdatum: 17.03.2021
Beginn: 06.04.2021
Tage bis Beginn: 20,0
Dosis: 1
Route/Site: OT / -

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

Back pain Loss of personal independence in daily activities Memory impairment Peripheral venous disease Post procedural contusion Postoperative thrombosis Procedural pain Tooth disorder Ultrasound scan Vascular procedure complication

Symptomtext

Intraoperative venous injury; Memory impaired; dental issues; Activities of daily living impaired; Back pain; Postoperative bruise; Procedural site pain; Postoperative thrombosis; Venous peripheral insufficiency; This is a solicited report based on the information received by Pfizer. Solicited report by a consumer (patient) of a 53-year-old female with events of surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising and non-serious surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising, bad memory, dental issues and hard time putting on stockings because of pain in back with humira (adalimumab) and humira 40mg/0.4ml (adalimumab). The patient (262 lb 66 in) had a relevant medical history of smoker: ten sticks of cigarettes per day, leg surgery, fibromyalgia and high cholesterol. The patient has other concomitant therapy of tylocorpine and viscus. On unknown dates, the patient experienced surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising, bad memory, dental issues and hard time putting on stockings because of pain in back. On 06Apr2021, the patient experienced surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising. In May2021, the patient experienced surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising and surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising. In 2021, the surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising resolved. Pfizer biontech covid-19 vaccine (tozinameran) was also considered suspect. The patient had a vein inside of her leg that she had to have a surgery on. Glue was used to close it up but she was concerned that the vein moved or it was a blood clot because she could feel it. So, she was told that an ultrasound could be done on it to make sure that it was taken care of. A month ago, in may 2021, it was painful and was bruising but as of 15jun2021, it was not and was thought that it was possibly there. The patient was supposed to get a second ultrasound on it after the summer of 2021 because she did not think that the first one was right. She started to experience leg pain after she had the covid-19 vaccine shots. She stated that the pain was caused by the clot in her vein due to insufficiency. She was told that if she would have worn the stockings more, it would not have been as bad, but she was having a hard time putting them on because of the pain in her back. The patient also stated that her memory was bad and so, she had to look up the lot number. It was unknown if the patient was enrolled in a covid-19 vaccine trial. On 17Mar2021, the patient received first dose of covid-19 vaccine manufactured by Pfizer, lot number en6208, expiration date 30Jun2021. On 07Apr2021, the patient received second dose of covid-19 vaccine manufactured by Pfizer, lot number aw0151, expiration date 31Jul2021. The patient was treated with Cyclobenzaprine. Causality for Humira(Adalimumab) The reporter's causality for the event(s) of surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising onset 06Apr2021, surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising onset 06apr2021, surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising onset in may2021, surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising unknown onset, surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising onset in may2021, dental issues, hard time putting on stockings because of pain in back unknown onset and hard time putting on stockings because of pain in back unknown onset was not provided. The reporter's causality for the event(s) of surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising unknown onset and bad memory with humira(adalimumab) was no reasonable possibility. There is no reasonable possibility that the events of surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising onset 06apr2021, surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising onset 06apr2021, surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising unknown onset, surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising onset in may2021, surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising unknown onset, surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising onset in may 2021, bad memory, dental issues, hard time putting on stockings because of pain in back unknown onset and hard time putting on stockings because of pain in back unknown onset are related to humira(adalimumab). Causality for HUMIRA 40mg/0.4ml(adalimumab) The reporter's causality for the event(s) of surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising onset 06apr2021, surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising onset 06apr2021 and surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising onset in may2021 with humira 40mg/0.4ml(adalimumab) was no reasonable possibility. The reporter's causality for the event(s) of surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising unknown onset, surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising unknown onset, surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising onset in may2021, bad memory, dental issues, hard time putting on stockings because of pain in back unknown onset and hard time putting on stockings because of pain in back unknown onset was not provided. There is no reasonable possibility that the events of surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising onset 06apr2021, surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising onset 06apr2021, surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising unknown onset, surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising onset in may2021, surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising unknown onset, surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising onset in may2021, bad memory, dental issues, hard time putting on stockings because of pain in back unknown onset and hard time putting on stockings because of pain in back unknown onset are related to humira 40mg/0.4ml(adalimumab). Relevant laboratory & other diagnostic tests May2021 ultrasound: insufficient vein Change history On 17Jun2021, received updates to patient demographics, medical history, event information, reporter opinion of causality, company opinion of causality, company alternative etiology, suspect drug information, concomitant drug information, treatment drug information, laboratory/diagnostic procedures and narrative description. The event of "surgery on vein of leg/concerned that vein moved or was a blood clot/could feel it, was possibly there/was painful and bruising" was amended to "surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising". The event of "surgery on vein of leg/concerned that vein moved or was a blood clot/could feel it, was possibly there/was painful and bruising" was amended to "surgery on vein of leg/vein moved or was a blood clot/ leg pain caused by clot in vein due to insufficiency /was painful and bruising". Reaction information: The events were considered serious, other medically important condition. Suspect drug information: Adalimumab (HUMIRA), solution for injection in pre-filled syringe, at an unknown daily dose from an unspecified date to an unspecified date (discontinued causality) subcutaneous for moderate to severe hidradenitis suppurativa moderate to severe rheumatoid arthritis; adalimumab (HUMIRA) 40 mg/0.4 ml (40 milligram, solution for injection in pre-filled pen) at daily dose of (40 mg, 1 in 1 wk), subcutaneous for rheumatoid arthritis hidradenitis suppurativa from 10Jul2020 to an unspecified date. Product-reaction level: Seq.no.:1 adalimumab (HUMIRA, solution for injection in pre-filled syringe) subcutaneous, unknown to discontinued: The action taken in response to the events for adalimumab (HUMIRA, solution for injection in pre-filled syringe) was unknown. The causality by the reporter was not reported for postoperative thrombosis, venous peripheral insufficiency, procedural site pain, intraoperative venous injury, postoperative bruise, dental disorder NOS, activities of daily living impaired and back pain; while for venous operation and memory impaired was no reasonable possibility. The causality as per manufacturer was no reasonable possibility. Seq.no.:2 HUMIRA 40mg/0.4ml (40 milligram, solution for injection in pre-filled pen) (adalimumab) at 40 mg, 1 in 1 wk, subcutaneous from 10Jul2020 to an unspecified date: The action taken in response to the events for HUMIRA 40mg/0.4ml was unknown. The causality by the reporter for the events postoperative thrombosis, venous peripheral insufficiency and procedural site pain was unrelated, while for the remaining events was not reported. The reported causality as per manufacturer for all events was no reasonable possibility. Seq. no.:3 Pfizer Biontech covid-19 vaccine(tozinameran)(injection)(tozinameran), first dose on 17Mar2021 (lot number: EN6208) and second dose on 07Apr2021 (lot number: AW0151) both at dose of 1 in 1 once, intramuscular for COVID-19 vaccination (at the age of 53-years-old). Causality as per reporter for the events postoperative thrombosis, venous peripheral insufficiency and procedural site pain was probable, while for the remaining event was not reported. Concomitant medications included paracetamol (TYLENOL) montelukast; omeprazole; vitamin d3; loratadine; folic acid; pregabalin (LYRICA); fluticasone propionate, salmeterol xinafoate (ADVAIR); methotrexate sodium; ibuprofen (MOTRIN CHILDREN); albuterol [salbutamol] (ALBUTEROL [SALBUTAMOL]); all taken for an unspecified indication, start and stop date were not reported. Patient medical history included the patient started smoking when she was in middle school: smoker ten sticks of cigarettes per day, abstains from alcohol, leg surgery, fibromyalgia, high cholesterol, penicillin allergy manifested by hives. Lab result included an ultrasound in May2021. The outcome of the events postoperative thrombosis, venous peripheral insufficiency, venous operation, intraoperative venous injury, memory impaired, dental disorder NOS was not recovered/not resolved; procedural site pain improved; postoperative bruise recovered/resolved in 2021; while the outcome of the remaining events was unknown. The reporter's assessment of the causal relationship of the events intraoperative venous injury, postoperative bruise, memory impaired, dental issues, activties of daily living impaired and back pain with BNT162B2 was not provided at the time of this report. Since no determination has been received, the case is managed based on the company causality assessment. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on the information currently available (considering the patient's medical and personal history and patient demographics), the reported events postoperative thrombosis, venous peripheral insufficiency, intraoperative venous injury, postoperative bruise, memory impaired, dental issues, activities of daily living impaired and back pain are likely intercurrent conditions unrelated to suspect product BNT162B2. Case will be reassessed upon receipt of additional information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Postoperative thrombosis
Hospital-Tage: -
Labordaten: Test Date: 202105; Test Name: ULTRASOUND; Result Unstructured Data: Test Result:insufficient vein
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Abstains from alcohol (Verbatim: Abstains from alcohol); Fibromyalgia (Verbatim: Fibromyalgia); High cholesterol (Verbatim: High cholesterol); Penicillin allergy (Verbatim: Penicillin allergy manifested by hives); Smoker (Verbatim: Smoker: ten sticks of cigarettes per day); Surgery (Verbatim: Leg surgery)
Andere Medikamente: TYLENOL; MONTELUKAST; OMEPRAZOLE; VITAMIN D3; LORATADINE; FOLIC ACID; LYRICA; ADVAIR; METHOTREXATE SODIUM; MOTRIN CHILDREN; ALBUTEROL [SALBUTAMOL]
Allergien: -
Vorherige Impfungen: -

VAERS 1459227

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 53,0
Geschlecht: F
Eingang: 09.07.2021
Impfdatum: 17.03.2021
Beginn: 06.04.2021
Tage bis Beginn: 20,0
Dosis: 1
Route/Site: OT / -

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

Back pain Loss of personal independence in daily activities Memory impairment Peripheral venous disease Post procedural contusion Postoperative thrombosis Procedural pain Tooth disorder Ultrasound scan Vascular procedure complication

Symptomtext

Intraoperative venous injury; Memory impaired; Dental disorder NOS; back pain; Loss of personal independence in daily activities; Postoperative bruise; Procedural site pain; Postoperative thrombosis; Venous peripheral insufficiency; This is a Solicited report from a non-contactable consumer (patient) based on the information received by Pfizer from AbbVie (MFR Control No: 21K-163-3951457-00). A 53-year-old female patient received bnt162b2 (BNT162B2), dose 1 intramuscular on 17Mar2021 (Lot Number: EN6208) as single dose, dose 2 intramuscular on 07Apr2021 (Lot Number: AW0151) as single dose for covid-19 immunisation; adalimumab (HUMIRA), subcutaneous from an unspecified date to an unspecified date, at UNK, Discontinued, subcutaneous from unknown date (reported as 10Jul2021 which is a future date) to an unspecified date, at 0.4 mL, weekly(40mg, weekly) for Moderate to severe Hidradenitis suppurativa and Moderate to severe Rheumatoid arthritis. Medical history included abstains from alcohol, leg surgery, fibromyalgia, high cholesterol, penicillin allergy manifested by hives, smoker (smoker-ten sticks of cigarettes per day). Concomitant medications included paracetamol (TYLENOL); montelukast (MONTELUKAST); omeprazole (OMEPRAZOLE); vitamin d3 (VITAMIN D3); loratadine (LORATADINE); folic acid (FOLIC ACID); pregabalin (LYRICA); fluticasone propionate, salmeterol xinafoate (ADVAIR); methotrexate (METHOTREXATE); ibuprofen (MOTRIN CHILDREN); salbutamol (ALBUTEROL HFA). The patient experienced postoperative thrombosis on 06Apr2021 with outcome of not recovered , venous peripheral insufficiency on 06Apr2021 with outcome of not recovered , venous operation on an unspecified date with outcome of not recovered, procedural site pain on May2021 with outcome of recovering, intraoperative venous injury on an unspecified date with outcome of not recovered , postoperative bruise on May2021 with outcome of recovered in 2021, memory impaired on an unspecified date with outcome of not recovered , dental disorder nos on an unspecified date with outcome of not recovered , back pain on an unspecified date with outcome of unknown , loss of personal independence in daily activities on an unspecified date with outcome of unknown. The patient underwent lab tests and procedures which included ultrasound: Insufficient Vein on May2021. The action taken in response to the event for bnt162b2 was not applicable, for adalimumab was unknown. The reporter's assessment of the causal relationship of the events with the suspect product was not provided at the time of this report. Since no determination has been received, the case is managed based on the company causality assessment. No follow-up attempts are possible. No further information is expected.; Sender's Comments: There is no reasonable possibility that reported events Postoperative thrombosis, Venous peripheral insufficiency, Procedural site pain, Intraoperative venous injury, Postoperative bruise, Memory impaired, dental disorder, back pain and loss of personal independence are related to BNT162B2. The events are likely intercurrent conditions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Postoperative thrombosis
Hospital-Tage: -
Labordaten: Test Date: 202105; Test Name: ultrasound; Result Unstructured Data: Test Result:Insufficient Vein
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Abstains from alcohol; Fibromyalgia; High cholesterol; Penicillin allergy (NOTE: PENICILLIN ALLERGY MANIFESTED BY HIVES); Smoker (NOTE: SMOKER-TEN STICKS OF CIGARETTES PER DAY); Surgery (NOTE: LEG SURGERY)
Andere Medikamente: TYLENOL; MONTELUKAST; OMEPRAZOLE; VITAMIN D3; LORATADINE; FOLIC ACID; LYRICA; ADVAIR; METHOTREXATE; MOTRIN CHILDREN; ALBUTEROL HFA
Allergien: -
Vorherige Impfungen: -

VAERS 1457109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 08.07.2021
Impfdatum: 17.03.2021
Beginn: 01.07.2021
Tage bis Beginn: 106,0
Dosis: UNK
Route/Site: - / -

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

Bell's palsy

Symptomtext

G51.0 - Bell palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1135580

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 48,0
Geschlecht: F
Eingang: 05.07.2021
Impfdatum: 17.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Anaphylactic reaction Arthropod bite Blood test Condition aggravated Hypersensitivity Blood pressure decreased Blood pressure increased Blood pressure measurement Chest discomfort Heart rate Cough Dizziness Dysphonia Dyspnoea Ear swelling Heart rate increased Full blood count normal Intensive care

Symptomtext

Anaphylaxis immediately following vaccine. Taken to ER from clinic. Released from ER. Two days later on March 19 I was taken back to ER after 2 additional anaphylaxis episodes. I was administered epipen twice in ER on the 19th and was admitted into hospital in the CCU as ICU patient. Released on March 23. Since release from hospital I have had 6 cases of anaphylaxis requiring epipen since the vaccine- each in response to bug bites. I have never used epipen for bug bites prior to vaccine- it was manageable through Benadryl previously. I am now on 200 milligrams of Benadryl per day, 15 milligrams of prednisone. Pepcid AC twice a day. Advair once a day. This is all to keep my system from experiencing anaphylaxis. My allergies are much worse since the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: 4,0
Labordaten: Blood panels
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma Allergies History of anaphylaxis
Andere Medikamente: Singular Flovent
Allergien: Sulfa Bug bites (mosquito and ant)
Vorherige Impfungen: -

VAERS 1135580

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 48,0
Geschlecht: F
Eingang: 05.07.2021
Impfdatum: 17.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Anaphylactic reaction Arthropod bite Blood test Condition aggravated Hypersensitivity Blood pressure decreased Blood pressure increased Blood pressure measurement Chest discomfort Heart rate Cough Dizziness Dysphonia Dyspnoea Ear swelling Heart rate increased Full blood count normal Intensive care

Symptomtext

Anaphylaxis immediately following vaccine. Taken to ER from clinic. Released from ER. Two days later on March 19 I was taken back to ER after 2 additional anaphylaxis episodes. I was administered epipen twice in ER on the 19th and was admitted into hospital in the CCU as ICU patient. Released on March 23. Since release from hospital I have had 6 cases of anaphylaxis requiring epipen since the vaccine- each in response to bug bites. I have never used epipen for bug bites prior to vaccine- it was manageable through Benadryl previously. I am now on 200 milligrams of Benadryl per day, 15 milligrams of prednisone. Pepcid AC twice a day. Advair once a day. This is all to keep my system from experiencing anaphylaxis. My allergies are much worse since the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: 4,0
Labordaten: Blood panels
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma Allergies History of anaphylaxis
Andere Medikamente: Singular Flovent
Allergien: Sulfa Bug bites (mosquito and ant)
Vorherige Impfungen: -

VAERS 1135580

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 48,0
Geschlecht: F
Eingang: 05.07.2021
Impfdatum: 17.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Anaphylactic reaction Arthropod bite Blood test Condition aggravated Hypersensitivity Blood pressure decreased Blood pressure increased Blood pressure measurement Chest discomfort Heart rate Cough Dizziness Dysphonia Dyspnoea Ear swelling Heart rate increased Full blood count normal Intensive care

Symptomtext

Anaphylaxis immediately following vaccine. Taken to ER from clinic. Released from ER. Two days later on March 19 I was taken back to ER after 2 additional anaphylaxis episodes. I was administered epipen twice in ER on the 19th and was admitted into hospital in the CCU as ICU patient. Released on March 23. Since release from hospital I have had 6 cases of anaphylaxis requiring epipen since the vaccine- each in response to bug bites. I have never used epipen for bug bites prior to vaccine- it was manageable through Benadryl previously. I am now on 200 milligrams of Benadryl per day, 15 milligrams of prednisone. Pepcid AC twice a day. Advair once a day. This is all to keep my system from experiencing anaphylaxis. My allergies are much worse since the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: 4,0
Labordaten: Blood panels
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma Allergies History of anaphylaxis
Andere Medikamente: Singular Flovent
Allergien: Sulfa Bug bites (mosquito and ant)
Vorherige Impfungen: -

VAERS 1446446

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: OH
Alter: 37,0
Geschlecht: M
Eingang: 03.07.2021
Impfdatum: 01.04.2021
Beginn: 05.04.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: SYR / RA

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

Blood test Electromyogram abnormal Guillain-Barre syndrome Hypoaesthesia Immunoglobulin therapy Lumbar puncture Magnetic resonance imaging Muscular weakness Neuropathy peripheral X-ray

Symptomtext

Four days following first dose, sudden numbness developed followed by weakness in right leg. Initially attributed to peroneal neuropathy and did not seek medical help. Second dose was received and left foot numbness developed followed by weakness. Symptoms ascended to knees the next few days and was admitted to the hospital. MRI's, x-rays, blood work, lumbar puncture were performed. Treated with 4 days of IVIG. EMG performed to diagnose with Guillain-Barre Syndrome.

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Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 5,0
Labordaten: MRI - 5/7/21 Lumbar Puncture - 5/10/21 EMG - 6/17/21
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Erythromycin
Vorherige Impfungen: -

VAERS 1437476

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

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Staat: -
Alter: 86,0
Geschlecht: F
Eingang: 30.06.2021
Impfdatum: 23.03.2021
Beginn: 26.06.2021
Tage bis Beginn: 95,0
Dosis: UNK
Route/Site: - / -

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

Ischaemic stroke

Symptomtext

I63.9 - Acute ischemic stroke (CMS/HCC)

Weitere VAERSDATA-Felder

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

VAERS 1224918

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: PA
Alter: 67,0
Geschlecht: F
Eingang: 30.06.2021
Impfdatum: 09.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: SYR / RA

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

Atrioventricular block Syncope Bradycardia Headache Inappropriate schedule of product administration Neck pain Off label use

Symptomtext

Started fainting in morning . By afternoon I had fainted 4 times. Went to ER and said it was a heart block and I needed a pacemaker. Never had trouble before.

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Praegender Schweregrund: Syncope
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Psoriasis-high blood pressure-
Andere Medikamente: Atovaston -synthroid- atenolol-Stelara- potassium-sertraline-chlorthalidone
Allergien: No
Vorherige Impfungen: -

VAERS 1433146

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 49,0
Geschlecht: M
Eingang: 29.06.2021
Impfdatum: 07.05.2021
Beginn: 24.06.2021
Tage bis Beginn: 48,0
Dosis: UNK
Route/Site: - / -

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

Pericarditis

Symptomtext

I30.9 - Acute pericarditis, unspecified

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

VAERS 1426506

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: AL
Alter: 43,0
Geschlecht: F
Eingang: 25.06.2021
Impfdatum: 16.03.2021
Beginn: 30.04.2021
Tage bis Beginn: 45,0
Dosis: 2
Route/Site: IM / LA

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

Angiogram normal Blood test Computerised tomogram Electrocardiogram Headache Intensive care Magnetic resonance imaging head abnormal Nausea Scan with contrast abnormal Subarachnoid haemorrhage Ultrasound Doppler Vomiting

Symptomtext

Sudden onset headache accompanied with nausea and vomiting around noon. ER visit MRI showed grade 1 SAH at basilar artery. Transported to ICU. Angiogram negative, nonaneurysmal unknown cause. No history of high cholesterol or high BP or trauma to head.

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Praegender Schweregrund: Intensive care
Hospital-Tage: 8,0
Labordaten: Angiography, MRI with and without contrast, CT scan, ECG, blood work, transcranial doppler
Aktuelle Erkrankungen: None
Vorgeschichte: PCOS
Andere Medikamente: Multivitamin Vitamin D Berberine 1200mg
Allergien: None
Vorherige Impfungen: -

VAERS 1424584

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NJ
Alter: 63,0
Geschlecht: M
Eingang: 24.06.2021
Impfdatum: 04.04.2021
Beginn: 28.05.2021
Tage bis Beginn: 54,0
Dosis: 2
Route/Site: IM / LA

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

Blood test Cardiac monitoring Dizziness Syncope Urine analysis

Symptomtext

Syncope (1 event), dizziness when walking has persisted since syncope on 05/28/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Complete physical 06/08/2021 Complete blood work & urinalysis 06/10/2021 EKG 06/10/2021 Heart monitor began 06/15/2021
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure
Andere Medikamente: Amlodipine (5mg), multi-vitamin, B12, biotin
Allergien: None
Vorherige Impfungen: -

VAERS 1412898

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN 6208

schwer

Staat: CA
Alter: 24,0
Geschlecht: M
Eingang: 19.06.2021
Impfdatum: 02.04.2021
Beginn: 04.04.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / RA

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

Asthenia Blood test Chest pain Chills Myocarditis Pericarditis Pyrexia Troponin increased

Symptomtext

I felt the typical symptoms after dose #2 the following day (Saturday, April 3rd, 2021) These symptoms included fever, feeling weak and having chills at night. However, those symptoms subsided by Sunday, April 4th, 2021. Instead, I began to have very odd chest pains that I have never had before. I went to the ER and they believed it was due to me taking too much ibuprofen for my fever symptoms which would give me heart burn and said it could be a symptom from the vaccine. The night thereafter I woke up due to an earthquake and felt the chest pain only much worse. I immediately went to the ER again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Whilst at the ER on Monday evening, April 5, 2021, blood tests were ran and I had a troponin level of 12. I was diagnosed with pericarditis/myocarditis.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1412440

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: FL
Alter: 64,0
Geschlecht: F
Eingang: 19.06.2021
Impfdatum: 06.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: - / LA

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

Chest pain Myocarditis

Symptomtext

Myocarditis; strong pain/pangs in chest at middle of the night; This is a spontaneous report received from a contactable consumer (patient). A non-pregnant 64-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 at the age of 64-years-old via an unspecified route of administration, administered in Arm Left on 06Apr2021 (Lot Number: EN6208) as 2nd dose, single for covid-19 immunisation. Medical history included mitral valve prolapse, seasonal allergy, hypotension. No other vaccine in four weeks. No covid prior vaccination. No covid tested post vaccination. The patient's concomitant medications were not reported. The patient previous took fist dose of BNT162B2 on 16Mar2021 at the age of 64-years-old administered in Left arm (Lot number: EL9262) for covid-19 immunisation and experienced chest pains/soreness/pangs. The patient experienced strong pain/pangs in chest at middle of the night of the vaccine. Since then she still had chest pains/soreness/pangs, what she now think is myocarditis. Adverse event start date was 16Apr2021. No treatment was received. The event outcome was not recovered.

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Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Low blood pressure; Mitral valve prolapse; Seasonal allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1407084

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 61,0
Geschlecht: F
Eingang: 17.06.2021
Impfdatum: 18.03.2021
Beginn: 16.06.2021
Tage bis Beginn: 90,0
Dosis: 2
Route/Site: IM / RA

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

Acute kidney injury Anticoagulant therapy Atrial fibrillation Blood chloride decreased Blood creatinine increased Blood sodium decreased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Deep vein thrombosis Diarrhoea Dyspnoea Electrocardiogram normal Fatigue Glycosylated haemoglobin increased Hypertension Hypertrophic cardiomyopathy

Symptomtext

Component Results: Component Your Value Standard Range Flag; Troponin T, 2 hr., 5th gen 1923 ng/L<=10 ng/L<=10 ng/L H; Consider acute myocardial injury 2H Delta 862 ng/L ng/Lng/L;2H Delta Interp Changing Evaluate for acute myocardial injury; Troponin T, 6 hr., 5th gen; 2104 ng/L; <=10 ng/L<=10 ng/L H; Consider acute myocardial injury; 6H Delta SEE COMMENT ng/L ng/Lng/L; Test cancelled. Specimen not received within delta timeframe.; 6H Delta Interp SEE COMMENT; Test cancelled. Specimen not received within delta timeframe. General Information-Ordered by, M.D., Ph.D._____________________________________________________ Your Admission - 03/30/21Printer friendly page--New window will open-Admission Summary-Notes-Clinical Notes H&P by M.D., Ph.D. at 3/30/2021 3:55 AM-Status: Signed-CARD 3 Admission Note-SUBJECTIVE- CHIEF COMPLAINT= Chest pain. HISTORY OF PRESENT ILLNESS Patient is a 56 y.o. female who presented to the Emergency Department due to chest pain. She has experienced this pain each evening for the past 3 evenings, and states that it starts in her right arm then migrates through her shoulder and across to her chest. The pain can last for anywhere from 5 minutes to 4 hours. This has come on at rest, but in the setting increased personal life stressors as well as uncontrolled hypertension. She states that she is normally on hydrochlorothiazide for hypertension, but ran out of this medication about a week ago. When she checked her blood pressure at home it was in the 230s/120s, therefore she presented to the emergency department locally. Her medical comorbidities are notable for poorly controlled hypertension, mixed hyperlipidemia that is untreated, current tobacco use (1-2 packs per day for 40 years), and medically complicated obesity. In the emergency department she was found to have mild polycythemia with hemoglobin of 15.2 and leukocytosis of 13.7. INR, D-dimer, and BMP were normal. High sensitivity troponin T was found to be 770 ng/L. ECG showed normal sinus rhythm with T-wave inversion in aVL that was not present on 08/25/2004. Chest x-ray was largely unremarkable. Her chest pain resolved, but given the elevated troponin ECG changes she was treated for NSTEMI with heparin infusion, and loaded with aspirin and clopidogrel and directly admitted to the Hospital Cardiology service. Upon arrival she remained free of chest pain but continued to have significant hypertension. I have reviewed and updated the following: Past Medical History, Family History, Social History, and Allergies. Current Outpatient Medications on File Prior to Encounter: hydrochlorothiazide (HYDRODIURIL) 25 mg tablet, Take 1 tablet (25 mg total) by mouth daily., Past Week at Unknown time; Lorazepam (ATIVAN) 0.5 mg tablet, Take 0.5 mg by mouth daily as needed for anxiety., More than a month at Unknown time. REVIEW OF SYSTEMS Pertinent items are noted in HPI; all other review of systems was negative. OBJECTIVE VITAL SIGNS Temperature: [36.8 ?C-36.9 ?C] 36.9 ?C; Heart Rate: [83-117] 83; Resp Rate: [20-26] 22; Blood Pressure: (164-195)/(81-129) 164/106; SpO2:[92 %-97 %] 95 %;Weight: [104 kg-106 kg] 104 kg; Pulse Rate: [90-109] 94. PHYSICAL EXAM General: Alert, oriented, no acute distress; HEENT: Mucous membranes moist, JVP difficult to assess due to body habitus; CV: Regular rate and rhythm without murmur; Lungs: Clear to auscultation bilaterally; Abdomen: Obese, soft, nontender, nondistended, normoactive bowel sounds; Extremities: No peripheral edema appreciated; Neuro: No focal deficits appreciated. DIAGNOSTICS I have reviewed labs and imaging from the past 24 hours. ASSESSMENT / PLAN Patient is a 56 y.o. female who was directly admitted to the Cardiology Service from Emergency Department due to NSTEMI and poorly controlled hypertension. She also has untreated mixed hyperlipidemia and is a current smoker. We will continue to trend troponins and treat NSTEMI was heparin infusion, aspirin, and clopidogrel. I will start a statin and initiate low-dose lisinopril and carvedilol for blood pressure control with plans to up titrate as tolerated. I will update a lipid panel in checked for diabetes. I will obtain a TTE in the morning and keep her NPO for probable coronary angiogram pending negative COVID swab. #1 Non-ST Elevation Myocardial Infarction; #2 Poorly controlled systemic hypertension; #3 Mixed hyperlipidemia, previously untreated; #4 Medically complicated obesity (BMI 38-trend troponin- loaded with aspirin and clopidogrel- Aspirin 81 mg daily- clopidogrel 75 mg daily- moderate intensity heparin infusion- rosuvastatin 20 mg daily- lisinopril 2.5 mg daily, up titrate as tolerated- carvedilol 6.25 mg twice daily, up titrate as tolerated- holding home hydrochlorothiazide in lieu of lisinopril and carvedilol- lipid panel - hemoglobin A1c- TTE- NPO for probable angiogram (not-ordered)- cardiac rehab consult ordered;#5 Abuse Tobacco Smoking- nicotine patch- nicotine inhaler as needed- nicotine cessation consult; #6 Anxiety She is prescribed lorazepam 0.5 mg which she takes when she has a panic attack which only occurs a couple times per year. For now we will just monitor. Diet: NPO; Tubes/lines: PIV; VTE prophylaxis: heparin infusion; Code status: Full Code; Disposition: anticipate discharge to home when clinically stable. Counseling was provided face-to-face at bedside regarding the plan of care as stated above. I personally spent over half of a total 70 minutes in counseling and coordination of care as documented above. M.B.B.S. at 3/30/2021 10:58 AM Status: Signed. SUBJECTIVE HISTORY OF PRESENT ILLNESS Patient is a very pleasant 56-year-old female who is owner of multiple nursing facilities who presented with chest pain and hypertensive emergency. She ran out of her hydrochlorothiazide last week, was fairly busy managing all her nursing homes with COVID pandemic and vaccination program. She was having intermittent chest pain, chest pressure radiating to the right arm. In this setting she checked her blood pressure, and it was noted to be 240 systolic over 140 diastolic. In this setting was sent to the ER and subsequently sent here. Initial troponin was 770. Subsequently, it went up to 1923. Delta was 862. ECG showed sinus rhythm with clear ST depression in the inferolateral leads. Patient currently is chest pain-free. She was initiated on carvedilol and restarted her home hydrochlorothiazide. Blood pressure is better. She had a good night's sleep. OBJECTIVE PHYSICAL EXAMINATION; Vital Signs: Noted.; General: Alert and oriented x3. Cardiac: S1, S2 normal.; Lungs: Clear.; Abdomen: Soft.; Extremities: No edema of feet.; Vessels: Peripheral pulses well-felt.; DIAGNOSTICS Creatinine is 0.7. Bicarb is 30. ASSESSMENT / PLAN Patient, is a 56-year-old female with obesity, hypertension, smoking, presented with hypertensive emergency. Blood pressure is better controlled now. She did have clear ST-T changes with troponin elevation, and we will treat it as NSTEMI at this point. Certainly, this can be demand ischemia in setting of hypertensive emergency, but she has multiple risk factors which would warrant coronary artery disease evaluation. We will plan for an angiogram today. We will get an echo today. Post that, we will reassess and see how things go. It appears that this was in setting of medication noncompliance. However, if this happens again, we may also look for other secondary causes of hypertension, especially with the fact that her bicarbonate was 30. All her questions were answered. DIAGNOSES: #1 Hypertensive emergency; #2 NSTEMI; #3 Obesity. M.B.B.S. DD: 03/30/2021 08:54:32 CT; DT: 03/30/2021 09:13:15 CT; Job ID: 914158020/mjb. Sedation Note by HCP at 3/30/2021 10:22 AM Status: Signed. INTERVAL HISTORY AND PHYSICAL PRE-PROCEDURE UPDATE H&P reviewed. The patient was examined and there are no significant changes to the H&P. PRE-SEDATION ASSESSMENT Consent Consents Obtained: written. The benefits, risks and alternatives to the procedure and the potential need for sedation or anesthesia as well as the names, roles, and responsibilities of healthcare team members performing significant interventional tasks were discussed with the patient and/or decision maker: yes. Indications / Reason for Visit. Procedure / Reason for Visit: coronary angiogram with possible intervention. Presedation Assessment. The following portions of the patient's history were reviewed and updated as appropriate: allergies, current medications, family history, medical history, social history and problem list: Yes. Review of Symptoms pertinent ROS negative. Physical Exam Mallampati: II - soft palate, uvula, fauces visible. Assessment Plan ASA Physical Status: class 3 - patient with severe systemic disease Sedation Plan: moderate sedation. Patient seen, evaluated, and approved for sedation: yes. Cardiology Fellow 11053 Discharge Instr - Referrals / Follow-Ups by HCP at 3/30/2021 11:18 AM Status: Written Take a copy of this after visit summary to your appointment(s).---------------------------------------------------- Monday, April 5th, 2021:-- 12:30 p.m. -- Hospital follow-up with Dr. primary care provider, at Medical Center------------------------------ --------------------------- You may have outpatient appointments at Clinic that changed during your hospitalization. Refer to your Clinic Patient Visit Guide (PVG) for the most current schedule of appointments and detailed instructions of tests/procedures. Call, if you did not receive an PVG or need to CANCEL any Clinic appointment(s). H&P by HCP at 3/30/2021 12:33 PM; Status: Signed; CARDIOLOGY 3 H&P HISTORY OF PRESENT ILLNESS; Patient is a 56 yo F with history of hypertension, dyslipidemia, smoking history, and obesity who presents with chest pain, found to have NSTEMI. She owns and runs 4 assisted living facilities. In the past three days, she has had chest pain at rest following dinner, while sitting in the living room. It has lasted from minutes to hours and was relieved on its own. Yesterday she was prompted by her husband to present for medical attention. She has smoked 1-2 packs daily for the past 40 years. She is on hydrochlorothiazide 25mg daily for her blood pressure. Blood pressure was 171/129 here in the ED. Troponins rose from 770 to 1061 to 1923. Current Medications: [MAR Hold] acetaminophen tablet 1,000 mg (TYLENOL), Q6H PRN; acetaminophen tablet 1,000 mg (TYLENOL), TID PRN; [START ON 3/31/2021] aspirin chewable tablet 81 mg, Daily; [MAR Hold] aspirin DR tablet 81 mg, Daily; atropine injection 0.5 mg, Q5 Min PRN; bisacodyl suppository 10 mg (DULCOLAX), Daily PRN; [MAR Hold] calcium carbonate chewable tablet 400 mg of calcium (TUMS), Q2H PRN; carvedilol tablet 25 mg (COREG), BID with meals; [MAR Hold] Clopidogrel tablet 75 mg (PLAVIX), Daily; [START ON 3/31/2021] Clopidogrel tablet 75 mg (PLAVIX), Daily; docusate sodium capsule 100 mg (COLACE), BID PRN; fentanyl injection 25 mcg (SUBLIMAZE), Q2 Min PRN; fentanyl injection 25 mcg (SUBLIMAZE), Once PRN; flumazenil injection 0.2 mg (ROMAZICON), Once PRN; heparin (porcine) 1,000 unit/mL injection 3,200 Units, PRN **OR** heparin (porcine) 1,000 unit/mL injection 6,400 Units, PRN; heparin (porcine) 100 Units/mL in NaCl 0.45% 250 mL infusion, Continuous; [MAR Hold] lisinopril tablet 2.5 mg (PRINIVIL,ZESTRIL), Daily; Lorazepam injection 1 mg (ATIVAN), Once PRN; midazolam (PF) injection 0.25 mg (VERSED), Q2 Min PRN; midazolam (PF) injection 0.5 mg (VERSED), Once PRN; midazolam (PF) injection 0.5 mg (VERSED), Q2 Min PRN; midazolam (PF) injection 1 mg (VERSED), Q2 Min PRN; NaCl 0.9 % bolus 250 mL, Once; NaCl 0.9% infusion, Once PRN; naloxone injection 0.2 mg (NARCAN), Once PRN; naloxone injection 0.2 mg (NARCAN), PRN; MAR Hold] nicotine 10 mg inhaler 1 puff (NICOTROL), PRN [MAR Hold] nicotine 21 mg/24 hr. 1 patch (NICODERM CQ), Daily; ondansetron (PF) injection 4 mg (ZOFRAN), Once PRN;[MAR Hold] polyethylene glycol powder packet 1 packet (MIRALAX), Daily PRN; promethazine injection 6.25 mg (PHENERGAN), Q6H PRN; [MAR Hold] rosuvastatin tablet 20 mg (CRESTOR), Daily at bedtime; sodium chloride 0.9 % injection 10 mL, PRN; sodium chloride 0.9 % injection 3 mL, PRN; sodium chloride 0.9 % injection 3 mL, Q12H SCH. OBJECTIVE BP 143/83 | Pulse 71 | Temp 36.6 ?C (Oral) | Resp 21 | Ht 165.1 cm | Wt 104 kg | SpO2 94% | BMI 38.19 kg/m?. Intake/Output Summary (Last 24 hours) at 3/30/2021 1212. Last data filed at 3/30/2021 1130. Gross per 24 hour Intake 323.71 ml; Output 700 ml; Net-376.29 ml; GEN: Pleasant, no distress CV: Regular, no extra heart sounds, JVP is flat; PULM: Clear bilaterally; EXTR: No edema, strong R radial pulse ; ;EKG: NSR, nonspecific changes. ASSESSMENT / PLAN NSTEMI, s/p PCI to circumflex 3/30/21; Hypertension, uncontrolled; Nicotine dependence; Dyslipidemia; Obesity. She has an NSTEMI with significant elevation in her troponin. We will proceed with coronary angiography for this and anticipate PCI. We will intensify her antihypertensive regimen. Nicotine cessation is critical and we will consult our cessation specialists. We will refer her to cardiac rehab. DAPT for 1 year. Plan:1. Coronary angiography with intervention today; 2. High intensity statin, uptitrate carvedilol, keep lisinopril 2.5mg, restart hctz later this evening.; 3. Nicotine cessation referral. Cardiac rehab referral; 4. F/u TTE. Addendum: Angiography demonstrated her culprit lesion to be in the circumflex for which she received a 2.5 x 16 mm synergy stent. Mild disease elsewhere. She will require DAPT for one year. The patient was seen and discussed with the attending consultant, Dr. and PA. M.D. Cardiology fellow 3/30/2021 Consults by HCP at 3/30/2021 1:51 PM Status: Signed Consult Orders 1. Cardiac Rehabilitation consult (hospital) [2222776702510] ordered by M.D. at 03/30/21 1136; 2. Cardiac Rehabilitation consult (hospital) [2222776391034] ordered by M.D., Ph.D. at 03/30/21 0343 Cardiac Rehabilitation Referral. Reason for Visit: Cardiac Health Clinic consultation for referral to cardiac rehabilitation. Liaison met with the patient/family to discuss cardiac rehabilitation referral. Patient/family was provided with progressive verbal and printed home-going exercise guidelines. Patient/family understands and agrees with the exercise guidelines.1. Participation in a Phase II cardiac rehabilitation program is recommended. Patient was informed about what cardiac rehabilitation has to offer and why it is beneficial. The plan of care for the rehabilitation program consists of risk factor modification, monitored and supervised exercise and assistance in the recovery process with ongoing education and support. Patient is interested in attending a cardiac rehabilitation program.; 2. Eligibility: MI and PCI; 3. Exceptions/exclusions: None;.4. Referral: Patient agreed with referral to a cardiac rehabilitation program. Please see discharge order and/or letter for program details. Clinic Health System Phone:; 5. Appropriate referral information will be sent to the receiving cardiac rehabilitation program as applicable. Patient provided verbal authorization to send relevant materials to the cardiac rehab program. Recommend that the patient check with insurance company to verify coverage of the cost of cardiac rehabilitation program visits. Discharge Summary by PA at 3/31/2021 10:20 AMStatus: Addendium CARDIOLOGY HOSPITAL DISCHARGE SUMMARY DATE OF ADMISSION: 3/30/2021 DATE OF DISCHARGE: 3/31/2021 Discharge Provider: M.B.B.S. Discharge Provider Team: RST CARD 3 PRINCIPAL DIAGNOSIS Non-ST Elevation Myocardial Infarction. DISMISSAL DIAGNOSES #1 Non-ST Elevation Myocardial Infarction; #2 Poorly controlled systemic hypertension; #3 Mixed hyperlipidemia, previously untreated;#4 Medically complicated obesity (BMI 38); #5 Abuse Tobacco Smoking, Nicotine Dependence; #6 Anxiety. RECOMMENDATIONS FOR FOLLOW-UP APPOINTMENTS CBC and Basic metabolic panel; Cardiovascular risk factor modification; Cardiac rehabilitation participation (set up); Nicotine cessation; Blood pressure monitoring and management; Plavix for one year, aspirin lifelong; Assess right radial access site. *Statin Therapy Initiated: *A fasting lipid profile showed: Total Cholesterol 173 mg/dL, Triglycerides 218 mg/dL, HDL 39 mg/dL, LDL 90 mg/dL. *Baseline LDL is [ ] mg/dl. Please titrate to meet goal lipid levels.*Please recheck lipids and ALT/AST in 6 to 8 weeks.*Goal of statin therapy is a LDL less than 70 mg/dl or a 50% reduction in LDL. FOLLOW-UP APPOINTMENTS For appointment details refer to your Patient Appointment Guide. HOSPITAL COURSE Admission Weight: 104 kg; Dismissal Weight: 103 kg; BMI: Body mass index is 37.82 kg/m?.Patient is a 56 y.o. female who presented to the Emergency Department due to chest pain. She has experienced this pain each evening for the past 3 evenings, and states that it starts in her right arm then migrates through her shoulder and across to her chest. The pain can last for anywhere from 5 minutes to 4 hours. This has come on at rest, but in the setting increased personal life stressors as well as uncontrolled hypertension. She states that she is normally on hydrochlorothiazide for hypertension, but ran out of this medication about a week ago. When she checked her blood pressure at home it was in the 230s/120s, therefore she presented to the emergency department locally. Her medical comorbidities are notable for poorly controlled hypertension, mixed hyperlipidemia that is untreated, current tobacco use (1-2 packs per day for 40 years), and medically complicated obesity(BMI 38.19 kg/m2). Intravenous heparin was initiated for the heparin nomogram. She was Plavix loaded and received aspirin. Carvedilol, lisinopril and Rosuvastatin were initiated. She proceeded to coronary angiogram with drug-eluting stent to the left distal circumflex artery. Transthoracic echocardiogram demonstrated ejection fraction 63%. Nicotine dependence was consulted and provided cessation information and prescriptions for nicotine replacement therapy. TEST RESULTS PENDING AT DISCHARGE :Pending Labs; None; DISCHARGE DISPOSITION: Home or Self Care [1]; CONDITION ON DISCHARGE: Stable. DIET AT DISCHARGE: Cardiac diet consisting of low sodium (1500 mg to 2000 mg per day), low cholesterol, low fat. No alcohol, (or discuss with physician).PRIMARY PROVIDER Patient Care Team:D.O. as External Primary Care Physician (Family Medicine) Primary Care Providers: Pcp (General); No address on file Primary Care Provider Phone Number: None Primary Care Provider Fax Number: None MARGIN CODE Operative Note Report Case/Log ID: 1507626443 Case Time: 10:44 AM Procedure Information CORONARY ANGIOGRAPHY Laterality N/A; Left Heart Catheterization Laterality N/A; Percutaneous Coronary Angioplasty Laterality N/A; Stent Placement Laterality N/A. Surgeons Surgeon Role M.D. Primary M.D. First Assistant, M.D. First Assistant, Diagnosis. Pre-op diagnosis: Non-ST Elevation Myocardial Infarction , Morbid Obesity Body Mass Index >= 35 with Comorbid Condition. Post-op diagnosis: Non-ST Elevation Myocardial Infarction , Morbid Obesity Body Mass Index >= 35 with Comorbid Condition. Anesthesia Type Moderate sedation (rn). Surgeon Documentation. No notes of this type exist for this encounter. Specimens None. Implants Implant Name LRB; Site No. Used; Manufacturer Mfr No.; Serial No.; Status; Type STNT SYNERGY XD DE 2.50X16 - LOG1507626443 N/A; Coronary Scientific H7493941816250 Implanted Cardiac Stent; Drains None Estimated Blood Loss None. Worsening shortness of breath COVID-19 positive on 06/06, Sxs started on 06/01 HPI: This is a 61 year old female who presents with complain of worsening Shortness of breath, COVID-19 positive PMHx Kidney transplant for glomerulonephritis, 1998, 2nd transplant in 2009 on Cellcept and prednisone and recurrent UTIs since then and since then when she gets UTI, she starts Cipro or Keflex HOCM myectomy 2009. Just saw yesterday. Denied CP/ SOB/ orthopnea/ cough/ leg swelling/ syncope/ PND. stated " no gradients across LVOT. At acceptable risk for planned procedure. Afib in 2009, Legally blind, Gout, Hand amputation 2017 at work , Hip replacement Ventriculostomy - cyst removed 1999] Pt completed COVID vaccination series (Pfizer 2/25/21, 3/18/21) but has been on immunosuppression 2/2 renal tx. Her symptoms have been persistent since 6/1. She states that she has been having fever morning and evening, cough, fatigue. She states that over the past 1-2 days prior to presentation to the ED she has had hypoxia to 85-89% on home pulse ox and intermittent episodes of fever, pt reports worse dyspnea w/ ambulation. Pt called her nephrologist on 06/01 and recommended course of Amoxicillin w/out improved, given worsening and not improving sxs her nephrollogist recommended to presented to the ED, On arrival to the ED she was initially tachypnic with ambulation to the bed, but has since improved. On initial exam she is not in any acute respiratory distress. CXR showed finding of viral PNA, Creatinine 1.17 baseline < 1.0 Sodium 126 This is a 61 year old female who presents with complain of worsening Shortness of breath, COVID-19 positive PMHx Kidney transplant for glomerulonephritis, 1998, 2nd transplant in 2009 on Cellcept and prednisone and recurrent UTIs since then and since then when she gets UTI, she starts Cipro or Keflex HOCM myectomy 2009. Just saw Physician yesterday. Denied CP/ SOB/ orthopnea/ cough/ leg swelling/ syncope/ PND. Physician stated " no gradients across LVOT. At acceptable risk for planned procedure. Afib in 2009, Legally blind, Gout, Hand amputation 2017 at work , Hip replacement Ventriculostomy - cyst removed 1999] Worsening shortness of breath COVID-19 positive on 06/06, Sxs started on 06/01 On arrival to the ED she was initially tachypnic with ambulation to the bed, but has since improved. On initial exam she is not in any acute respiratory distress. CXR showed finding of viral PNA, Creatinine 1.17 baseline < 1.0 Sodium 126 Active Problems: Active respiratory failure dute to COVID-19 Hypoxia Symptomatic 6/1, tested positive for COVID infection 6/6. Currently sat 93-95% on RA; States she sats down to 85% at night. Short of breath on ambulation Xray findings suggestive of atypical viral/Covid 19 pneumonia. Plan: - dexamethasone, remdesivir, mucinex - Oxygen NC to keep SpO2 >94% - IS q1h - ID consult appreciate recommendations - Mucinex,Sch, robitussin PRN and albuterol PRN - Incentive spirometry Kidney replaced by transplant Aki Increased creatinine 1.77 baseline Hyponatremia Hypochloremia - Creatinine 1.17 from 0.95 possible d/t dehydration. - Na 126, Cl 94 Plan: - Normal saline bolus - Hold cellcep - Continue tacrolimus - Prednisone hold, due dexamethasone for tx of COVID infection - Hold lasix, allopurinol, lisinopril - Continue valgancclovir - Avoid Nephrotoxic agent - renally dose meds - Gentle IVF NS 75 ml/hr - Usodium and Uosm Hypertension Hypertrophic obstructive cardiomyopathy (HOCM) (HCC) Atrial fibrillation (HCC) DVT prophylaxis - Normal sinus rhythm on EKG Plan: - Heparin - Continue atorvastatin, ASA, coreg - Monitor for palpitations, dizziness, headache, SOB - Holding Lisinopril and Lasix in setting of Aki - Continue Coreg Gastritis - currently asymptomatic Plan: - Protonix while on Steroids Prediabetes - Hgb A1C 6.1 4/3 Plan: - Low carb diet Legally blind - Patient moves about room without difficulty

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Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 2,0
Labordaten: I have reviewed the progress note obtained and documented by the PA and I personally participated in the key components of care. I have discussed the case and management of the patient's care. The following comments revise or confirm relevant key components of the note. -COVID 19 with hypoxia diagnosed 6/6. Failed outpatient therapy. 88% O2 at home. Has had relentless cough, some diarhea - Renal transplant for glomerulonephritis, 1998, 2nd transplant in 2009-Cellcept and prednisone and recurrent UTIs since then and since then when she gets UTI, she starts Cipro or Keflex. Follows with Physician here. Baseline cr 0.88-1.01. 1.17 here Pancytopenia Hyponatremia HOCM myectomy 2009. Denied CP or orthopnea or leg swelling, syncope or PND. Dr. saw 3/2021 who noted No gradients across LVOT Afib in 2009 Stage I left breast cancer (pT1miNx), s/p RT 30 Gy in 5 Fx completed 5/20/20 Legally blind Gout Hand amputation 2017 at work Hip replacement Ventriculostomy - cyst removed 1999 Numerous drug allergies Moderate to severe LEFT Mastodynia, likely radiation effect diagnosed 4/7/21 Osteopenia Mild protein calorie manlutrition -Started Decadron and Remdesevir today for COVID-19 with hypoxia in renal transplant patient who had received Pfizer COVID vaccine several months ago -Intensify supportive care: I/S q 1, ambulate, schedule Mucinex, schedule Albuterol MDI -Monitor renal and hepatic labs and the pancytopenia -Heparin started for DVT prophylaxis -Hold Cellcept -gentle hydration -Renal transplant team and ID consulted -Hyponatremia in setting of volume depletion, COVID, decreased oral solute. Work up ordered and IVFs started.
Aktuelle Erkrankungen: CMV colitis
Vorgeschichte: Hospital Kidney replaced by transplant UTI (urinary tract infection) Hypertrophic obstructive cardiomyopathy (HOCM) (HCC) Atrial fibrillation (HCC) Prediabetes Legally blind Anxiety COVID-19 virus infection Blood creatinine increased compared with prior measurement Hypoxia Acute respiratory failure due to COVID-19 (HCC) Gastritis Non-Hospital Hyperlipidemia Benign hypertensive kidney disease with chronic kidney disease stage V or end stage renal disease (HCC) Unspecified vitamin D deficiency Retention of urine, unspecified Acute idiopathic gout of right foot Gout Amputation of hand with complication, right, initial encounter (HCC) Exposure keratoconjunctivitis of both eyes Dyslipidemia Muscle weakness Breast neoplasm, Tis (DCIS), left Traumatic amputation of hand (HCC) Encounter for coordination of complex care
Andere Medikamente: Amoxicillin 500 mg tablet mycophenolate mofetil (CELLCEPT) 250 mg capsule predniSONE (DELTASONE) 5 mg tablet calcitriol (ROCALTROL) 0.25 mcg capsule furosemide (LASIX) 20 mg tablet POLY-IRON 150 FORTE 150-25-1 mg-mcg-mg cap lisinopril (ZEST
Allergien: Codeine: Swelling, GI Upset, Vomiting Chlorhexidine: Rash Ranitidine: Intolerance Cimetidine: GI Upset Cozaar: GI Upset Flonase: Bloody Nose Levofloxacin: muscle pain
Vorherige Impfungen: -

VAERS 1402261

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IN
Alter: 51,0
Geschlecht: F
Eingang: 16.06.2021
Impfdatum: 24.04.2021
Beginn: 06.06.2021
Tage bis Beginn: 43,0
Dosis: 2
Route/Site: IM / LA

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

Blood test Chest pain Dizziness Echocardiogram abnormal Electrocardiogram QT prolonged Electrocardiogram abnormal Fatigue Microcytic anaemia Nausea Pericarditis

Symptomtext

Chest Pain, Nausea, Fatigue, Dizziness, Diagnosed with Pericarditis, Prolonged QT Interval, Microcytic anemia. Visit to the cardiologist to occur for a follow up on 6/22/2021. Reporting due to news reports about Pericarditis being linked to Pfizer vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 2,0
Labordaten: EKG, Echocardiogram, Blood Work all done in the emergency room on 6/7/2021
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, High Blood Pressure
Andere Medikamente: Amlodipine 10 mg, once daily
Allergien: Penecillin, Morphone
Vorherige Impfungen: -

VAERS 1399832

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: RI
Alter: 55,0
Geschlecht: M
Eingang: 15.06.2021
Impfdatum: 13.03.2021
Beginn: 27.03.2021
Tage bis Beginn: 14,0
Dosis: UNK
Route/Site: - / LA

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

Amnesia Angiogram cerebral abnormal Aphasia Computerised tomogram head abnormal Drain of cerebral subdural space Fatigue Headache Intensive care Magnetic resonance imaging head abnormal Pain Photophobia Subarachnoid haemorrhage

Symptomtext

I suffered a Subarchnoid brain hemorrhage. The was bleed in the subarachnoid space surrounding the brain. I went to emergency at hospital with worst headache of my life. After a brain hemorrhage was confirmed by CT-scan, I was rush to hospital were I was treated in the Cerebral critical unit. I suffered through the worst pain of my life for 10 days as the blood from the hemorrhage drained. It 2.5 months later and I am still dealing with the effects of the hemmorhage (headaches, exhaustion, light sensitivity, short term memory loss and speech issues,

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Praegender Schweregrund: Intensive care
Hospital-Tage: 4,0
Labordaten: 3/27/2021 CT-scan of brain at Hospital - Subarachnoid hemorrhage detected 3/28/2021 Cerebral angiogram at Hospital - Subarchnoid hemorrhage confirmed - no anyurism or cause found 3/31/2021 MRI of brain - confirmed
Aktuelle Erkrankungen: Diabetes
Vorgeschichte: Diabetes
Andere Medikamente: Insulin (Humolog) short acting Insulin (Lantus) Long lasting Multi-vitamin vitamin D
Allergien: No
Vorherige Impfungen: -

VAERS 1396729

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MN
Alter: 62,0
Geschlecht: F
Eingang: 14.06.2021
Impfdatum: 11.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: IM / LA

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

Activated partial thromboplastin time Blood electrolytes C-reactive protein Chest X-ray Dyspepsia Electrocardiogram Full blood count Metabolic function test Myalgia Pericarditis Prothrombin time Sleep disorder Troponin T

Symptomtext

I started having what I thought was indigestion about 4:30 pm. on March 31st. During that night I could not lay down without pain and had to sleep in a recliner. I thought it might be muscle pain because I had exercised that day. I did not want to take Motrin since I was getting my second Covid 19 shot the next day and it said not to take Motrin before getting the shot. At about 3:00 am I couldn't take the pain any longer and told my husband to take me to the emergency room. While I was there they did many tests and finally said I had pericardiatis. They told me that I could not get my second Covid 19 shot that day. I was very disappointed. I was able to leave the hospital at about noon on April 1st. I was told to go to a cardiologist and have an echo done. I went to the cardiologist on

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: 4/1/21: ECG 7:20am, C-reactive protein Level, APTT (Clotting Factor TEST), Prothrombin Time, Complete Blood Count, Troponin T, Baseline - 14, 5th Gen P, Metabolic/Electrolyte Panel, DX Chest Portable, Troponin t 2H/6H, (10 Result) P, ECG, ECG.
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure
Andere Medikamente: hudroCHLOROthiazide 12.5mg, amLoDIPine 5mg tablet, letrozole 2.5mg, levothyrozine 88mcg, Vitamin D3 2000mcg, Calcium 1,200.
Allergien: none
Vorherige Impfungen: -

VAERS 1387735

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

schwer

Staat: VA
Alter: 53,0
Geschlecht: F
Eingang: 10.06.2021
Impfdatum: 12.03.2021
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Bell's palsy Blood pressure abnormal Blood pressure measurement Computerised tomogram Diabetes mellitus Dizziness Dysarthria Headache Hypersensitivity Magnetic resonance imaging head abnormal Paraesthesia Swelling face Vaccination site swelling

Symptomtext

Bells Palsy/ little bit more droopier than usual/facial droop; allergic reaction; blood pressure went up to normal, which was not normal for her, as its very low/ 120/70, which was normal, but not great for her and was high for her; dizziness; headaches; tingly feelings/still just felt a little tingling still; got the shot in her left arm and it was swollen; slurring of speech; face got swollen and definitely impacted her speech; This is a spontaneous report from the contactable consumer (patient herself) and physician via Medical Information. A 53-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), via an unspecified route of administration, administered in the left arm on 12Mar2021 at 10:30 at the age of 53 years old (Batch/Lot Number: en6208, Expiration date: unknown) as the 1st dose, single dose for COVID-19 immunization. Relevant medical history included brain surgery in 2014 and facial reconstruction in 2015, further reported as transplant or transfer from her thigh in 2015 for her left cheek, so her face after brain surgery in 2014 was reconstructed in 2015 and she could have a symmetrical face; and vestibular condition from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. The patient was asking for accommodations Pfizer would provide to advocate for people working from home to minimize their risk of exposure to COVID-19. The patient was a teacher, who taught languages and she often had students with hearing disabilities and had to take her mask down so they could see her lips. She reported that she was fully vaccinated but was concerned about being exposed to people who haven't been vaccinated and asked if there were any recommendations or accommodations being offered by Pfizer to assist her with trying to work from home. The patient received her second vaccine dose on 02Apr2021 at 10:30 AM with lot number: ep7533. The patient reported experiencing Bells Palsy after being vaccinated on an unspecified date in Mar2021 and was asking how long or much protection she had against COVID-19, because her understanding was that because she reacted to the vaccine in this way, if she got COVID-19, she might experience the same type of reaction to COVID-19 and she didn't want to experience Bells Palsy again. The patient reported that she had "distinct reactions" to both the first and second doses and was told by her neurologist that because its a live virus and she had a reaction to it, she had the potential to get the same symptoms from COVID-19. The patient further asked if the Pfizer-BioNTech COVID-19 vaccine could shed the virus and was provided with references. Upon follow up, the patient stated that she was one of those people who had an allergic reaction to Pfizer, she had both doses. The patient stated she thought she was better off vaccinated. After the first dose, she did have the characteristic symptoms and people thought she was having a stroke; she was fine, but it freaked out her husband. She stated she should know as she has had facial reconstruction and did have it in the left arm. The patient got vaccinated at a clinic in a neighboring area and called her primary care doctor. The patient stated her blood pressure went up to normal on an unspecified date in Mar2021, which was not normal for her, as its very low. She stated she had the characteristic dizziness, headaches, tingly feelings, and Bells palsy on an unspecified date in Mar2021. She stated her primary care doctor asked her where she got the shot, she said in her left arm and it was swollen on an unspecified date in Mar2021. The patient stated she did go to the emergency room, which was scary. She stated she spent a year and a half trying to stay away and stated everybody got to see her at her baseline, which was a semi-symmetrical face. The patient stated after a while, the doctor said yes the patient might want to consider getting the second dose. The patient stated that because of the brain surgery, she was able to quickly write an email to many doctors who could weigh in. The patient stated that the doctor said the benefits outweighed the risk, but the other recommendation, which was brilliant, they said to get it in her leg. The patient stated she did have an allergic reaction to the second one, but not the same way and stated it was the characteristic tiredness on an unspecified date. The patient stated her husband got Moderna and was out a whole day. The patient also stated she had the slurring of speech, the face, and it took a couple of days to go away, but it did and then she was back to her as-symmetrical face as she could have. The patient stated the second time though she went a week and a half later, she thought it was too much zoom fatigue, but the doctor said it sounded like annular fissures. The doctor then asked if she did get her vaccine and she told the doctor she did. The patient didn't know if that's a thing; she thought she would bring that up, because her back became inflamed. The patient further stated that for the first dose, her face got swollen and definitely impacted her speech, which promoted her to go to the emergency room. She stated she felt dizziness, headaches, she knew what to expect, but she got worried when she was getting a little bit more droopier than usual. The patient stated that for the second time (dose), it took about 12 weeks to recover and she had been able to recover; she stated her back was inflamed and fortunately, there was no slipped disc or bulging discs, it was just annular fissures. The patient stated that a doctor in the area said that it made sense; it was locally the right thigh (second dose) - lower back, left arm (first dose) - left side of the face, and its kind of thematically and spatially related. The patient stated she got this at the hospital way back in Mar2021. The patient stated they did a brain magnetic resonance imaging (MRI), computerized axial tomography (CAT) scan, and diabetes test. The patient stated that to live the pandemic, she was worried that she had eaten too many cookies, but everything came back normal, as normal for her. She stated clearly she had got issues, but they were issues long before the vaccine. The patient was one of those people who definitely had something happening and people were saying no that can't be. She stated it was evident that yes, it was Bells palsy, she had never had. She stated she had had facial paralysis that was taken care of by Gracilis surgery. She stated it was experimental when she did it, but it's not so experimental anymore after her brain surgery. The patient stated Pfizer might want to hear her happy ending. The patient stated her daughter got Pfizer a few weeks prior reporting, so she's fully vaccinated and they had their first hug since 2020 and it was just an emotional thing. The patient stated she followed up with a neurologist and she was going to see him in the middle of June, she sees him every couple of months, mostly for work accommodations. The patient stated that the idea being if Bell's plays was her reaction from a dead form of the virus, even getting sick with it would indicate that this could happen to her in a different context. She stated that since she's a teacher, it's a good thing for her to know as she went back to work, she'd been able to work online, she'd probably not going to be able to argue for that unless her doctor argued for her. She stated her neurologist would know more of the story. She stated she saw her primary care doctor for her annual physical after she was fully vaccinated. She stated the follow-up was with a neurologist. The patient further stated she was fine and was not fine at the time of the reported events, but it was better to get the vaccine than to get COVID-19. She stated her mother and sister were all vaccinated. The patient further stated that on her 1st dose, she felt like someone had taken a hammer to her head and was headachy and not feeling great and was taken to room to wait; stated her blood pressure was taken and it was 120/70, which was normal, but not great for her and was high for her as she normally had a very low blood pressure. She went home and might be an hour after getting home, she realized her face was swelling and got the 1st dose of the vaccine to the left side of her upper arm and her face started to swell and she did have brain surgery in 2014 and stated in 2015, she had Gracilis free flap of her right thigh and had a new cheek and had calf nerves grow back together again and had to learn to walk again at that time, because they spliced the nerves, which was not a transplant but a transfer. The patient stated the flap made her face back symmetrical as possible and used her face and able to drink coffee, smile and keep food in her mouth; stated her face kind of drooped anyway, but this was more than that. The patient stated her husband said she had been traumatized and just to relax and she kind of got Bell's Palsy, which she had never had before and got diagnosed with it and was swollen and started having slurred speech; stated she had facial droop and got to the hospital, which was emotional and getting the Pfizer COVID vaccine was emotional and she was trying not to add to her issues. The patient stated was able to see formal field and everyone thought she was having a stroke, but she was not having a stroke and everybody said it couldn't be the Pfizer vaccine; it had to be something else. The patient stated her healthcare professional (HCP) asked about her baseline and her husband had photos of her and she was not normally symmetrical in her face. They did scans, MRI brain and everything checked out normal, which was a blessing and several HCPs were getting results and she did not have diabetes. The patient stated she was trying to be careful during the pandemic with her health and they kept her in the emergency room from 11-12 pm to 8:00 pm and she was saying she was hungry and thirsty and did not know they did not want her to eat or drink and wanted to make sure she could swallow and she was ok swallowing, but had dribble on the left side of her face with the drooping. She stated she saw her primary HCP before she went to the emergency room and he asked which side she got the Pfizer COVID vaccine on and that was kind of where he had the idea that this could be related to the vaccine and the reported events occurred so close to when the vaccine was administered and the reported events occurred immediately after the vaccine; she stated her blood pressure was ok and she ate a cookie and maybe had not enough breakfast and got worse. The patient stated her slurred speech and Bell's palsy lasted a day or two and everything went back to normal, stated because she had brain surgery, which saved her life; the HCP said maybe she should rethink going for the 2nd dose of the Pfizer COVID Vaccine; she followed-up with her neurologist and everybody weighed in the benefits outweigh the risk and she got the 2nd dose. She did the 2nd dose of the Pfizer COVID Vaccine in her right thigh and had inflammation in her lower spine after that; stated how the shot felt like a shot in the arm or a horse kicked you; stated she felt like the Pfizer COVID vaccine felt like a shot in the arm, but never felt that pain and had swelling and had a half an apple sized swelling in her leg for a couple of days; stated she also did not feel the face drooping, because the 2nd dose of the vaccine was done in her leg. With the second dose, she started to get really bad lower back pain and went to the HCP and was maybe sitting down too much; stated she did not have proper posture sometimes and did not want to stand. She stated she saw a holistic HCP, which was a chiropractor and that HCP did not touch her spine; stated she saw that HCP on 14Apr2021 and she was diagnosed with annular fissures and they thought she had a slipped bulging disc and never had that before, but had a tingling sensation and they said to take a few weeks to recover. She stated she kept seeing her HCP and had recovered and had to say as soon as they said this was probably related, because she thought the Pfizer COVID vaccine targeted places that were weak and that was the weak part in her body regarding her spine; stated her left side arm was weak and the weak side of her face that was where the transfer of nerves was and that had gotten swollen and did not work. She stated she was fine and would say she was better and thought she was completely recovered and from time to time still just felt a little tingling still and did not have that before; stated because of her brain surgery, the neurologist said she could tingle independently and she did not normally tingle in that area, but she was better and 90 percent better; stated the HCP said to give 12 weeks to recover and she would see her again next week and would see the HCP every 2-3 weeks so this; said they needed the discs to get fluid in them so they were healing; stated her daughter got the Pfizer COVID Vaccine and is doing well. The patient underwent further lab tests and procedures, which included Brain MRI, CAT scans, and diabetes test, which were all normal on an unspecified date. The patient was recovering from the event "tingly feelings/still just felt a little tingling still," while she recovered from the rest of the events on an unspecified date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Test Name: blood pressure; Result Unstructured Data: Test Result:normally had a very low blood pressure; Test Date: 202103; Test Name: blood pressure; Result Unstructured Data: Test Result:120/70; Comments: normal; Test Name: CAT Scans; Result Unstructured Data: Test Result:normal; Test Name: diabetes test; Result Unstructured Data: Test Result:normal; Test Name: Brain MRI; Result Unstructured Data: Test Result:normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Brain operation; Facial reconstructive surgery (transplant/transfer from her thigh for her left cheek,so she could have a symmetrical face); Vestibular abnormalities
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1227954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NY
Alter: 56,0
Geschlecht: F
Eingang: 08.06.2021
Impfdatum: 25.03.2021
Beginn: 25.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Abdominal pain lower Asthenia Body temperature Diplopia Fatigue Blood test Chronic inflammatory demyelinating polyradiculoneuropathy Computerised tomogram normal Condition aggravated Dysphagia Feeling abnormal Guillain-Barre syndrome Hemiparesis Hypoaesthesia Pain in extremity Malaise Pyrexia Swallow study

Symptomtext

It started with feeling run down, are started hurting, started running fever, so then it proceeded to feel nothing on my left side, feeling like with no strength at all. My left side start going down with no feeling. It stated with CIDP. GBS. Then I was admitted into the hospital on Sunday 03/28/2021. I was there for four days. Discharged on 03/31/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 4,0
Labordaten: They did a CAT Scan and it was negative. Blood test was done but I don't if it was negative or positive. Swallening test was done, because I was having difficulties. Physical Therapy was done to see if I needed a walker.
Aktuelle Erkrankungen: I have Cidp. A nerve condition.
Vorgeschichte: I have a really bad nerve condition.
Andere Medikamente: Over the counter meds allergy cetirizine tabs 10mg. Baby aspirin. I also take, Montelukast, Amlodipine, Befylate, Advair, Hydrochlorothiazide, Gabapenpin, and Gammagaid monthly.
Allergien: I am allergic to Shellfish.
Vorherige Impfungen: -

VAERS 1227954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NY
Alter: 56,0
Geschlecht: F
Eingang: 08.06.2021
Impfdatum: 25.03.2021
Beginn: 25.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Abdominal pain lower Asthenia Body temperature Diplopia Fatigue Blood test Chronic inflammatory demyelinating polyradiculoneuropathy Computerised tomogram normal Condition aggravated Dysphagia Feeling abnormal Guillain-Barre syndrome Hemiparesis Hypoaesthesia Pain in extremity Malaise Pyrexia Swallow study

Symptomtext

It started with feeling run down, are started hurting, started running fever, so then it proceeded to feel nothing on my left side, feeling like with no strength at all. My left side start going down with no feeling. It stated with CIDP. GBS. Then I was admitted into the hospital on Sunday 03/28/2021. I was there for four days. Discharged on 03/31/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 4,0
Labordaten: They did a CAT Scan and it was negative. Blood test was done but I don't if it was negative or positive. Swallening test was done, because I was having difficulties. Physical Therapy was done to see if I needed a walker.
Aktuelle Erkrankungen: I have Cidp. A nerve condition.
Vorgeschichte: I have a really bad nerve condition.
Andere Medikamente: Over the counter meds allergy cetirizine tabs 10mg. Baby aspirin. I also take, Montelukast, Amlodipine, Befylate, Advair, Hydrochlorothiazide, Gabapenpin, and Gammagaid monthly.
Allergien: I am allergic to Shellfish.
Vorherige Impfungen: -

VAERS 1378100

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 73,0
Geschlecht: F
Eingang: 07.06.2021
Impfdatum: 22.03.2021
Beginn: 20.04.2021
Tage bis Beginn: 29,0
Dosis: UNK
Route/Site: - / -

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

Acute kidney injury Fall Seizure

Symptomtext

N17.9 - Acute kidney injury (CMS/HCC) SEIZURES FALL

Weitere VAERSDATA-Felder

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

VAERS 1375097

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 04.06.2021
Impfdatum: 12.04.2021
Beginn: 26.05.2021
Tage bis Beginn: 44,0
Dosis: UNK
Route/Site: - / -

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

Bell's palsy

Symptomtext

G51.0 - Bell's palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1370642

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: OR
Alter: 71,0
Geschlecht: M
Eingang: 03.06.2021
Impfdatum: 06.04.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Myocarditis

Symptomtext

I'm curious about this condition called Myocarditis, and I think I'm experiencing symptoms of this conditions'; This is a spontaneous report from a contactable consumer (patient). A 71-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 06Apr2021 (Batch/Lot Number: EN6208) as 2nd dose, single for covid-19 immunisation. No patient history. No other medical conditions. Concomitant medications included periodically thyroid medication. The patient received first dose of BNT162B2 on 11Mar2021 (lot number: EN6202) at age of 71 years old for covid-19 immunisation. Patient was curious about this condition called myocarditis and he think he was experiencing symptoms of this conditions, this kind brought on his Pfizer vaccine and so Pfizer was his first contact right now and there was couple of numbers on the sheet when he got his second vaccine shot. The outcome of event was unknown.

Weitere VAERSDATA-Felder

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

VAERS 1356323

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: LA
Alter: 29,0
Geschlecht: M
Eingang: 27.05.2021
Impfdatum: 31.03.2021
Beginn: 26.04.2021
Tage bis Beginn: 26,0
Dosis: 2
Route/Site: SYR / LA

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

Chest pain Echocardiogram abnormal Electrocardiogram abnormal Myocarditis Pericarditis Pyrexia

Symptomtext

Pericarditis and subsequent myopericarditis. Intense chest pain that worsened upon lying down and a low grade fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: 2 ECGs from 2 separate doctors that both diagnosed pericarditis. Followed up with cardiologist who agreed and ordered an echocardiogram where the subsequent myopericarditis was noted.
Aktuelle Erkrankungen: None
Vorgeschichte: ADHD
Andere Medikamente: Vyvanse (60mg), Lactase supplement (lactose intolerance), men?s multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1205145

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: FL
Alter: 53,0
Geschlecht: M
Eingang: 27.05.2021
Impfdatum: 13.03.2021
Beginn: 24.03.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: - / LA

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

Bell's palsy Computerised tomogram Ear pain Headache Magnetic resonance imaging Neck pain Tongue paralysis

Symptomtext

Bell paulsy left side of my face paralized

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: 1,0
Labordaten: Cat scan MRI
Aktuelle Erkrankungen: Diabetis2 high blood pressure
Vorgeschichte: -
Andere Medikamente: Januvia100mg rosuvastatin10mg atenolol 25mg amladipine 10/40 metformin1000 jardiance 10mg aspirin 325mg
Allergien: No
Vorherige Impfungen: -

VAERS 1350545

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 81,0
Geschlecht: F
Eingang: 26.05.2021
Impfdatum: 30.03.2021
Beginn: 30.04.2021
Tage bis Beginn: 31,0
Dosis: 2
Route/Site: IM / LA

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

Anticoagulant therapy Asthenia Brain compression Cardiac stress test abnormal Fall General physical health deterioration Head injury Hyponatraemia Loss of consciousness Myocardial ischaemia Percutaneous coronary intervention Skin laceration Stent placement Troponin Vomiting

Symptomtext

Patient brought to the ED with generalized weakness worsening over prior 2-3 days, states she started experiencing after receiving 2nd dose of Covid vaccine. Found to have a positive troponin, hyponatremia. Stress test revealed reversible myocardial ischemia of the inferior and lateral walls of left ventricle with a large defect size but mild defect severity. Patient underwent PCI with DES placement and was placed on triple therapy with aspirin, clopidogrel and eliquis. Patient presented to ED again on 5/23/21 outcome: patient is brought to ED after a fall and loss of unconsciousness, hit her head with large laceration at back of head, 2 episodes of vomiting, leading to terminal events: brainstem compression and rapid deterioration and CS of 2T preclude meaningful survival

Weitere VAERSDATA-Felder

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

VAERS 1343267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MN
Alter: 78,0
Geschlecht: M
Eingang: 24.05.2021
Impfdatum: 24.03.2021
Beginn: 03.04.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: UN / LA

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

Haemorrhagic stroke Hypoaesthesia Intensive care Paraesthesia

Symptomtext

Stroke, Hemmoragic Numbness, tingling on left side Went to emergency room at the Hospital Forwarded by ambulance to different Hospital Placed in Nuerology Intensive Care Unit (ICU) at hospital Released from ICU to Nuerology ward Released from Nuerology ward to Rehab Unit Released from Rehab to home for outpatient rehab

Weitere VAERSDATA-Felder

Praegender Schweregrund: Haemorrhagic stroke
Hospital-Tage: 13,0
Labordaten: Numerous - see Emergency Room at Hospital in Hospital Emergency Room
Aktuelle Erkrankungen: -
Vorgeschichte: Sinus Drip
Andere Medikamente: Amlodipine, Atorvaststin, Gabapentin, Montelukast, Propranolol, Omeprazole, Xaralto, Aller-tec, Multivitamin, Naicin, AREDS Multivitamin, Pseudoepherin (sp?), CoQ10, Fish oil
Allergien: Coumadin
Vorherige Impfungen: -

VAERS 1340853

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: DC
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 / LA

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

Dizziness Fall Feeling hot Loss of consciousness Syncope

Symptomtext

After 3 minutes of observation in a chair, he got up to move to the observation area in clinic and then fainted. He fell backward against a closed door and slid down. He quickly regained consciousness and his vitals were stable. within 10 minutes he was no longer dizzy or hot. He was able to sit up right without issues. Per dad, this is the same reaction he had to the flu vaccine in fall of 2020.

Weitere VAERSDATA-Felder

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

VAERS 1334016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

schwer

Staat: ND
Alter: 50,0
Geschlecht: M
Eingang: 20.05.2021
Impfdatum: 10.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 22,0
Dosis: 1
Route/Site: IM / RA

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

Bell's palsy Computerised tomogram Headache Laboratory test Magnetic resonance imaging

Symptomtext

Bellls Palsey and headaches developed 21 days after administration

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: CT scan and MRI, and lad work 04-01-2021
Aktuelle Erkrankungen: -
Vorgeschichte: diabetes type 2
Andere Medikamente: tylenol, metformin,
Allergien: -
Vorherige Impfungen: -

VAERS 1329458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: FL
Alter: -
Geschlecht: F
Eingang: 19.05.2021
Impfdatum: 14.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: - / -

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

Blood alcohol Blood alcohol increased Disturbance in attention Feeling abnormal Loss of consciousness Malaise Weight

Symptomtext

Blacked out / Unconscious; Not able to concentrate very well; Brain fog; I do not feel well; Alcohol level was elevated; This is a spontaneous report from a contactable consumer (patient). A 64-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration on 14Apr2021 (Batch/Lot Number: EN6208) as a single dose for COVID-19 immunisation. Medical history was not reported. Alcohol use after vaccination was reported. Concomitant medications included vitamins. The patient got the vaccine on the 14Apr2021 (also reported as 15Apr2021), but she guesses it was on Wednesday (14Apr2021). On 16Apr2021 (also reported as 17Apr2021), "two days later or in those 2 days", she experienced a brain fog. She was not able to concentrate very well. She didn't feel physically bad just not being able to concentrate. On Friday (16Apr2021), she went to a friend's home and had 2 glasses of wine and she also tasted a cocktail. She didn't have the cocktail, she just tasted a little bit of her cocktail. Something happened, she doesn't know, she was sitting there, having a telephone conversation. All of a sudden she told her friend that she did not feel well and apparently she kind of blacked out. The ambulance came. She doesn't remember any of this because apparently she was unconscious. The ambulance took her to the hospital. Her alcohol level was elevated and this was the part that she doesn't understand because she didn't remember that much. She only had the wine. She was wondering what effect the vaccine had with alcohol because she was not abusing the alcohol. This was very distressful for her because nothing like this has ever happened before. She thinks they treated her with fluids and some kind of a vitamin package like 'banana packer'. The patient stated she was hospitalized from 16Apr2021 to 17Apr2021. The outcome of the events blacked out / unconscious, brain fog, not being able to concentrate, did not feel well and alcohol level was elevated was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 1,0
Labordaten: Test Name: Alcohol level; Result Unstructured Data: Test Result:elevated; Test Name: Weight; Result Unstructured Data: Test Result:About 128
Aktuelle Erkrankungen: Alcohol use (She had two glasses of wine and she also tasted a cocktail on 16Apr2021)
Vorgeschichte: -
Andere Medikamente: VITAMINS NOS
Allergien: -
Vorherige Impfungen: -

VAERS 1328956

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN 6208

schwer

Staat: MO
Alter: 37,0
Geschlecht: F
Eingang: 19.05.2021
Impfdatum: 15.04.2021
Beginn: 29.04.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / RA

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

Asthenia Back pain Neck pain Pain in extremity Paraesthesia Shock symptom Vaccine positive rechallenge

Symptomtext

36 days after the first dose and 2 weeks after second dose I began to feel a shock feeling from my fingers up my arms. I also had sore and weak legs shortly after that. Knees and ankles hurt after that and by May 3rd I was weak all over and then I started to have tingling feeling on my toes legs fingers and arms. I also have back and neck pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Shock symptom
Hospital-Tage: -
Labordaten: I went to a walk in clinic and I was told that I could be sore from the prednisone that I had just got done taking for my poison ivy. Also the Dr. said to take ibuprofen. He said to go to the hospital if I do not get any better. I plan to go to ER Thursday morning.
Aktuelle Erkrankungen: No
Vorgeschichte: I have asthma and allergies.
Andere Medikamente: No
Allergien: Pinnicillin and flu shot
Vorherige Impfungen: Gillian Barre Syndrome

VAERS 1286499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: FL
Alter: 61,0
Geschlecht: F
Eingang: 15.05.2021
Impfdatum: 09.04.2021
Beginn: 30.04.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: - / LA

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

Anticoagulant therapy Blood test Computerised tomogram Pulmonary thrombosis X-ray Laboratory test SARS-CoV-2 test

Symptomtext

Numerous blood clots in both lungs; This is a spontaneous report from a contactable consumer (patient reported for herself). A 61-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection, Lot Number: ER8730, expiry date not reported), via an unspecified route of administration, administered in left arm on 09Apr2021 09:00 AM as 2ND DOSE, SINGLE for covid-19 immunization. Medical history included degenerative disc disease, fibromyalgia, hypothyroidism, migraines, known allergies to tape and anise allergy. The patient had negative nasal swab on 07Nov2020. The patient had no covid prior to vaccination. Concomitant medications included morphine at 15 mg, twice a day; oxycodone (XTAMPZA ER) at 36 mg; and heparin; all taken for an unspecified indication, start and stop date were not reported. The patient received the first dose of BNT162B2 as COVID-19 immunization on 19Mar2021 09:00 AM (at the age of 61 years old) (brand Pfizer, lot en6208) administered on the left arm. The patient had no other vaccine in four weeks. On 30Apr2021 09:00 AM, patient had numerous blood clots in both lungs. On 01May2021 to May2021, she was admitted to the hospital for 2 days with numerous blood clots in both lungs. After several tests (May2021), they could not find any reason for getting these clots. So, thinking the only other thing patient did different was get the covid vaccine. The event was reported as serious medically significant, life threatening, and had caused hospitalization from 01May2021 to an unspecified date in May2021. It resulted to emergency room/department or urgent care, hospitalization, life threatening illness (immediate risk of death from the event). Therapeutic measures were taken as a result of the event which included Heparin IV. The patient had not recovered from the event numerous blood clots in both lungs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 2,0
Labordaten: Test Date: 202105; Test Name: tests; Result Unstructured Data: Test Result:they could not find any reason for getting these c; Comments: they could not find any reason for getting these clots; Test Date: 20201107; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Adhesive tape allergy; Degenerative disc disease (other_medical_history : Degenerative Disc disease); Fibromyalgia (other_medical_history: Fibromyalgia); Food allergy; Hypothyroidism (other_medical_history : Hypothyroidism); Migraine (other_medical_history : Migraines)
Andere Medikamente: MORPHINE; XTAMPZA ER
Allergien: -
Vorherige Impfungen: -

VAERS 1316029

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: HI
Alter: 70,0
Geschlecht: M
Eingang: 14.05.2021
Impfdatum: 30.03.2021
Beginn: 05.04.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: SYR / RA

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

Acoustic shock Condition aggravated Tinnitus

Symptomtext

After 7-10 days after the second Pfizer shot, my existing Tinnitus worsened in my left ear. The ringing grew louder and I felt a shock if someone yelled or if there was a loud noise.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acoustic shock
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: High blood pressure. High cholesterol.
Andere Medikamente: Atorvastatin Calcium, Bisoprolol Fumarate, Amlodipine Besylate BioAstin, Fish Oil supplement, Multi-vitamin, minoxidil
Allergien: none
Vorherige Impfungen: Temporary back pain after flu shot in Oct 2020. 69 years old.

VAERS 1310246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 53,0
Geschlecht: M
Eingang: 12.05.2021
Impfdatum: 12.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / RA

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

Acute kidney injury Hyponatraemia Hypoosmolar state Seizure

Symptomtext

Hypo-osmolality and hyponatremia Acute kidney failure, unspecified Unspecified convulsions Hyponatremia

Weitere VAERSDATA-Felder

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

VAERS 1307856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 72,0
Geschlecht: F
Eingang: 11.05.2021
Impfdatum: 25.02.2021
Beginn: 08.03.2021
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: IM / RA

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

Seizure

Symptomtext

R56.9 - Seizure

Weitere VAERSDATA-Felder

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

VAERS 1306576

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 71,0
Geschlecht: M
Eingang: 11.05.2021
Impfdatum: 11.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Facial paralysis Facial paresis Muscular weakness

Symptomtext

R29.810 - Facial droop EXTREMITY WEAKNESS CHEST PAIN R29.810 - Facial weakness

Weitere VAERSDATA-Felder

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

VAERS 1299651

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MS
Alter: 43,0
Geschlecht: F
Eingang: 08.05.2021
Impfdatum: 07.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: SYR / LA

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

Imaging procedure abnormal Intensive care Subarachnoid haemorrhage

Symptomtext

Subarachnoid hemorrhage. Was in icu from 4/8/2021 until 4/15/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 7,0
Labordaten: In icu from 4/9/2021 until 4/15/2021
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Nine
Vorherige Impfungen: -

VAERS 1297806

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 86,0
Geschlecht: M
Eingang: 07.05.2021
Impfdatum: 16.03.2021
Beginn: 19.04.2021
Tage bis Beginn: 34,0
Dosis: 2
Route/Site: IM / LA

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

Bell's palsy

Symptomtext

This 86 year old male received the Covid shot on 3/16/21 and went to the ED on 04/19/21 and was admitted on 4/21/21 with the following diagnoses listed below. G51.0 - Bell's palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1291116

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MO
Alter: 65,0
Geschlecht: F
Eingang: 05.05.2021
Impfdatum: 09.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: - / -

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

Arteriospasm coronary Chills Contusion Diarrhoea Dizziness Myalgia Pain in extremity Palpitations Phlebitis Ultrasound scan Peripheral swelling Thrombosis

Symptomtext

leg was bruised; heart spasms; Diarrhea; inflammation along the major vein in her leg; heart palpitation; light headed/dizzy; severe muscle pain; tenderness and soreness in her inner thigh of the left leg/throbbing pain; Chills; This is a spontaneous report from a contactable consumer (patient, self-reported). A 65-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EN6208), via an unspecified route of administration in unspecified arm on 09Mar2021 (12:00) at single dose for Covid-19 immunization. The patient's medical history included ongoing hypothyroidism. Concomitant medication included levothyroxine been taking for 10-11 years for hypothyroidism. On 17Mar2021, Wednesday, the patient received the vaccine and had chills. On 18Mar2021, the patient had tenderness and soreness in her inner thigh of the left leg. On 19Mar2021, the patient had severe muscle pain on her calf of leg to inner thigh and it was throbbing so bad behind her knee on her left leg that she called her physician, and a sonogram was performed on 23Mar2021 which had found there was not a blood clot but there was severe inflammation along the major vein in her leg. On 20Mar2021, the patient had heart palpitation, her doctor told her to drink water and propel, she had heart spasms for 6 hours and felt lightheaded and dizzy. she thought she would go to the hospital, but she lives in a rural community and felt it did not make sense to go to the hospital. Palpitations and tenderness recovering. Her doctor and she was put on a heart monitor for her heart palpitations. She had heart palpitations with her hypothyroid but, this was totally different when she has had heart palpitations in the past. On an unknown date in Apr2021, the patient had diarrhea for 6 days. Patient had not been back to the doctor, but the nurse thought it was ok for her to take the second vaccine, but the patient was not comfortable with it. No prior vaccinations within the week. The patient never taken the flu shot. She had never received the flu vaccine or pneumonia nothing, so this was new for her getting the COVID vaccine. Caller clarified the chills started the week after she received the vaccine on Wednesday 17Mar2021. Severe muscle pain: Caller stated this happened on the 19, 20, 21, and 22 as well as the throbbing pain and then the next day on Monday 22Mar2021 she went to call her doctor and had a sonogram that next day on Tuesday (23Mar2021). Caller stated she still had the muscle pain in her left leg on the inner thigh but it was more so when she was active and once in a while she felt like her leg was bruised for a day or two but then it went away and she did not have a blood clot. Left leg throbbing: Caller stated this continually got worse and then on Sunday she felt so bad she laid in bed with her knee up and it throbbed like crazy. Caller stated this stopped about 2 days after she got the sonogram and it was not that severe it was just really tender and sore. Heart palpitation: Caller clarified that the heart murmurs she referred to earlier was actually heart palpitations. Caller stated this started at 8 in the morning and then at 10 in the morning she started getting light-headed and thought about going to the emergency room and figured no she will get through this. Caller stated she called her physician for the heart palpitations on Monday and she saw her doctor the following Tuesday and that is when her doctor had given her the heart monitor. Caller stated for 6 hours she felt horrible on Saturday since she knows the difference from her normal heart palpitations from her thyroid. Diarrhea: Caller stated this last for 6 days and was last week or so. Treatment: Caller stated no she is not a medicine taker she does not even take Tylenol or Advil unless it is a necessity. Outcome of the event chills recovered on 18Mar2021, tenderness and soreness in her inner thigh of the left leg/throbbing pain was resolving, severe muscle pain and inflammation along the major vein in her leg was not resolved, heart palpitation was resolving, light headed/dizzy was resolved on 20Mar2021, diarrhea was resolved on Apr2021, leg was bruised was resolved, heart spasms was unknown. No follow-up attempts are needed. No further information is expected. follow up(20Apr2021): New information was reported from a contactable consumer (patient) included: new events (coronary spasm, pain in extremity, phlebitis lower limb and bruising of leg) and event details. Case is upgraded to serious upon this follow up. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Date: 20210323; Test Name: sonogram; Result Unstructured Data: Test Result:0; Comments: had found there was not a blood clot but there was severe inflammation along the major vein in her leg.
Aktuelle Erkrankungen: Hypothyroidism
Vorgeschichte: -
Andere Medikamente: LEVOTHYROXINE
Allergien: -
Vorherige Impfungen: -

VAERS 1287041

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 04.05.2021
Impfdatum: 21.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: SYR / RA

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

Deep vein thrombosis Thrombosis Ultrasound scan

Symptomtext

Blood Clot Deep Vein Thrombosis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Ultra sound
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure
Andere Medikamente: Levothyroxine 0.150 mg Hydrochlorothiazide 1. 25 mg Losartan 25 mg Sertaline 50 mg
Allergien: None
Vorherige Impfungen: -

VAERS 1282317

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 53,0
Geschlecht: M
Eingang: 03.05.2021
Impfdatum: 16.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Fall Loss of consciousness Malaise

Symptomtext

Patient received PFIZER vaccine and was in waiting room. He came up to nurse and stated that he was not feeling well as he was stating this, he began leaning over table, then began to fall to floor but was assisted to floor by nurse. Medical alert called. Patient did not bump his head. Patient loss consciousness for about 3-5 seconds, and then began to open his eyes. Patient was able to answer questions regarding his name, the date, and place. Initial vitals (10:00 AM), BP 102/51, HR 55, O2- 96. 2nd set of vitals (10:03 AM) 120/58, HR 84, O2-99. Patient stable and taken to ED via wheelchair.

Weitere VAERSDATA-Felder

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

VAERS 1281021

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 54,0
Geschlecht: M
Eingang: 03.05.2021
Impfdatum: 16.04.2021
Beginn: 29.04.2021
Tage bis Beginn: 13,0
Dosis: 2
Route/Site: IM / -

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

Bell's palsy Hypoaesthesia Swelling face

Symptomtext

COVID 19 Pfizer vaccine dose#1 given 3/24/2021. COVID 19 Pfizer vaccine dose#2 given 4/16/2021. Developed puffiness and numbness on R side of face 4/29/2021. Evaluated on 5/2/2021 and diagnosed with Bell's Palsy. Will complete a four day course of steroid treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Atorvastatin
Allergien: -
Vorherige Impfungen: -

VAERS 1279373

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: AR
Alter: 52,0
Geschlecht: M
Eingang: 01.05.2021
Impfdatum: 26.03.2021
Beginn: 31.03.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy Blood test Computerised tomogram Deafness Ear discomfort Ear pain Eyelid ptosis Feeling abnormal Headache Hypoaesthesia Metabolic function test Oropharyngeal pain Vertigo Vomiting

Symptomtext

3/31: earache, headache 4/1 ? 4/4: earache, headache, sore throat, vertigo, vomiting, brain fog. On 4/4, doctor prescribed Amoxicillin 125 MG 2x/day 4/5 ? 4/7: sharp earache with pressure, loss of hearing in left ear, sore throat, brain fog, headache 4/8 ? 4/11: noticed Ptosis, numbness left side of face, persistent headache. Went to Emergency Room, performed CT scan, blood test, confirmed there is no stroke, DIAGNOSED FOR BELLS PALSY. Prescribed Prednisone and Valacyclovir for 7 days. 4/12 ? 4/22: Treated by NP for Bells Palsy, referred for rehab/therapy. 4/23: symptoms clear, Bells Palsy 95% return to normal 4/30 : received 2nd Pfizer vaccine dose Lot # ER8737

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: fOn 4/9 Emergency Room Basic Metabolic Panel and CBC With Differential
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1208416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: WA
Alter: 33,0
Geschlecht: M
Eingang: 01.05.2021
Impfdatum: 25.03.2021
Beginn: 25.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Blood electrolytes normal Blood pressure decreased Computerised tomogram normal Condition aggravated Dizziness Blood pressure measurement Feeling abnormal Loss of consciousness Electrocardiogram normal Impaired driving ability Injury Nausea Presyncope Road traffic accident Troponin normal Tinnitus

Symptomtext

Passed out; Felt strange/weird; Nauseous; Dizzy; ears rang; Blood pressure drop; This is a spontaneous report from a contactable consumer, reporting for himself. A 33-year-old male patient received the first dose of the bnt162b2 (BNT162B2; Lot Number: EN6208), via an unspecified route of administration in the left arm on 25Mar2021 at 11:00 at a single dose for covid-19 immunisation. The patient received the vaccination in the pharmacy. There was no medical history or concomitant medications. There were no other vaccines administered in the last four weeks. On 25Mar2021 at 23:30, the patient experienced passed out, felt strange/weird, nauseous, dizzy, ears rang, and blood pressure drop. The clinical course was as follows: the patient was advised to wait 15 minutes before leaving. He set an alarm. He bought some food to eat (potatoes and jerky) and waited to leave the site until 11:22. He felt strange/weird, but this was not an unusual feeling after receiving any kind of shot/vaccine for the patient. He was driving to work and started to get a little nauseous but nothing too bad. Thirty seconds later, he started to get dizzy, ears rang, felt blood pressure drop, and passed out going freeway speeds. He was treated in the emergency department and released the same day. There was no treatment given in response to the events. There was no covid prior to or post vaccination. The clinical outcome of the events was recovering. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 20210325; Test Name: Blood pressure; Result Unstructured Data: Test Result:Drop
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: NONE
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1208416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: WA
Alter: 33,0
Geschlecht: M
Eingang: 01.05.2021
Impfdatum: 25.03.2021
Beginn: 25.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Blood electrolytes normal Blood pressure decreased Computerised tomogram normal Condition aggravated Dizziness Blood pressure measurement Feeling abnormal Loss of consciousness Electrocardiogram normal Impaired driving ability Injury Nausea Presyncope Road traffic accident Troponin normal Tinnitus

Symptomtext

Passed out; Felt strange/weird; Nauseous; Dizzy; ears rang; Blood pressure drop; This is a spontaneous report from a contactable consumer, reporting for himself. A 33-year-old male patient received the first dose of the bnt162b2 (BNT162B2; Lot Number: EN6208), via an unspecified route of administration in the left arm on 25Mar2021 at 11:00 at a single dose for covid-19 immunisation. The patient received the vaccination in the pharmacy. There was no medical history or concomitant medications. There were no other vaccines administered in the last four weeks. On 25Mar2021 at 23:30, the patient experienced passed out, felt strange/weird, nauseous, dizzy, ears rang, and blood pressure drop. The clinical course was as follows: the patient was advised to wait 15 minutes before leaving. He set an alarm. He bought some food to eat (potatoes and jerky) and waited to leave the site until 11:22. He felt strange/weird, but this was not an unusual feeling after receiving any kind of shot/vaccine for the patient. He was driving to work and started to get a little nauseous but nothing too bad. Thirty seconds later, he started to get dizzy, ears rang, felt blood pressure drop, and passed out going freeway speeds. He was treated in the emergency department and released the same day. There was no treatment given in response to the events. There was no covid prior to or post vaccination. The clinical outcome of the events was recovering. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 20210325; Test Name: Blood pressure; Result Unstructured Data: Test Result:Drop
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: NONE
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1274784

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: TX
Alter: 63,0
Geschlecht: M
Eingang: 30.04.2021
Impfdatum: 16.03.2021
Beginn: 23.04.2021
Tage bis Beginn: 38,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Chest X-ray Computerised tomogram head Computerised tomogram neck Dysarthria Echocardiogram Electrocardiogram Facial paralysis Feeling abnormal Magnetic resonance imaging Ultrasound scan

Symptomtext

Slurred speech, drooping left upper lip, feeling funny. One episode at @ 9:00 am, second episode @ 3:00 pm on the same day. Treatments at ER: Plavix, IV fluids

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: 2,0
Labordaten: April 23rd - Blood work, EKG, chest X-ray, CT scan April 24th -Additional blood work, chest x-ray, MRI, Echo cardiogram, CT scan of head and neck, ultrasound of arteries..
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1270419

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: PA
Alter: 68,0
Geschlecht: M
Eingang: 29.04.2021
Impfdatum: 13.03.2021
Beginn: 12.04.2021
Tage bis Beginn: 30,0
Dosis: 2
Route/Site: - / 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: Confirmed by visual exam at my private doctor?s office.
Aktuelle Erkrankungen: I got Bell?s palsy one month after my second vaccine. I had seen other reports of this happening on the internet on my local tv news. Although Pfizer claims this happens at approximately the same rate as the generaL population, I don?t feel this should be dismissed by Pfizer and should be studied more to alleviate this reaction to their vaccine.
Vorgeschichte: Diabetes, Neuropathy, High Blood Pressure,
Andere Medikamente: Amlodipine, Atorvastin, Celecoxib, Doxycycline Hyclate, Finasteride, Gabapentin, Glipizide, Losartan-Hydrochlorothiazide, Metformin, Metroprolol Succinate
Allergien: None
Vorherige Impfungen: -

VAERS 1269743

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: PA
Alter: 67,0
Geschlecht: F
Eingang: 29.04.2021
Impfdatum: 19.03.2021
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / LA

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

Contusion Eye contusion Head injury Headache Magnetic resonance imaging head Nausea Pain Syncope

Symptomtext

collapsed, head hit the tile floor of bathroom; collapsed, head hit the tile floor of bathroom; right arm was bruised; corner of her eye was purple/bruised; feeling nauseated; Headaches off and on; pain; This is a spontaneous report from a contactable consumer (patient). A 67-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; Lot Number: EN6208) intramuscular, administered in Arm Left, at the age of 67-year-old, on 19Mar2021 11:00, as SINGLE DOSE for covid-19 immunisation. Medical history included asthma and Allergies. The patient's concomitant medications were not reported. The patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number EN6203) single dose, at the age of 67-year-old, on 26Feb2021, for covid-19 immunisation and experienced slight ache in her left arm, headaches, and mitral valve disease. On 20Mar2021, the patient had headaches off and on and the patient mostly woke up with them. The patient doesn't know if the headaches were from pollen in the air since it is Spring time or mold. On 24Mar2021 at 4am, the patient got out of bed because she had to use the restroom. As soon as the patient took the first step into the tile floor of the bathroom, the patient collapsed. The patient didn't fall, the patient collapsed on the file floor. Her head hit the floor. Her head was killing her when she was laying there. The patient used the restroom and went back to bed. The patient got out of bed because her head was killing her. The patient guesses she threw her right arm out to brace herself, because she noticed her right arm was bruised the morning of 24Mar2021 when she went to shower. The patient took Equate 500MG for the events head hit the tile floor of bathroom, headache, and right arm was bruised and used a wash cloth with cold water as a cold compress and applied it by her eyebrow, the corner of her eye was purple/bruised. It looked like she had eyeshadow on. On 24Mar2021, she was feeling nauseated. Thankfully, she had the next 2 days off (Thursday and Friday) because she didn't feel so hot. On 26Mar2021, the patient called her PCP and was asked if she wanted to come in/ make an appointment. Since, the caller was planning to meet with the surgeon about her upcoming surgery on 29Mar2021, it didn't really fit into her schedule. She was undergoing all these tests, etc. It was determined her surgery was going to happen after receiving the second vaccine. The surgery is hopefully a mitral valve repair. The patient mentioned that her provider is aware of her experience with the COVID vaccine. The patient saw the surgeon on 29Mar2021, and she told him all about her experience. He advised the patient to call her PCP and schedule an appointment with them. She saw her PCP on 01Apr2021. She told her PCP what happened and her PCP asked why she didn't go to urgent care. The patient doesn't really know why she didn't, she just thought she was going to feel better. The patient thought she would work through the pain since Mar2021. Plus, she had everything going on with her surgery- like finding out she had to have the surgery and going under other tests. Her PCP wanted her to go to radiology to have a MRI of the head/brain done. She had the MRI done at 3:00PM on 06Apr2021 and the results were negative. Up until last weekend, she still felt "headachy". The patient has headaches too because of stress knowing her surgery was scheduled in a matter of 2 weeks, so she didn't know if the headaches she was experiencing was because of the COVID vaccine, stress, allergies, etc. The patient was certain the headache she experienced the day after she collapsed, was due to the collapse. The patient clarified that she knew it was more of a "collapse" instead of a fall because all the furniture leading to the bathroom, like the loveseat, lamp, cedar chest, etc, were all intact with no marks. It was like all of a sudden she collapsed. Her bruising is all gone, but there might be a slight mark that is like yellow and green (because the bruising changes colors) on her arm. Her eye was okay. The patient will have her planned surgery on 15Apr2021. The events required physician office visit. The patient underwent unspecified lab test and procedures relevant to her upcoming surgery but no other testing in regards to her symptoms after the COVID vaccine. Outcome of headache was not recovered, the events corner of her eye was purple/bruised and right arm was bruised recovered in 2021, while it was unknown for the other events.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Date: 20210406; Test Name: MRI brain; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Asthma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1269723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CT
Alter: 58,0
Geschlecht: M
Eingang: 29.04.2021
Impfdatum: 10.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: - / LA

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

Deep vein thrombosis International normalised ratio Limb discomfort Peripheral swelling Ultrasound scan

Symptomtext

DVT in right leg; Swelling in right leg; Discomfort in right leg while walking; This is a spontaneous report from a contactable consumer (patient). A 58-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), first dose via an unspecified route of administration, administered in the left arm on 10Mar2021 at 16:30 (batch/lot number: EN6208) as a single dose for COVID-19 immunisation (wanted the protection). Medical history included deep vein thrombosis (DVT) from Jul2018 and ongoing. No family medical history relevant to the adverse events. Concomitant medication included warfarin taken for maintenance level for history of DVT from Aug2020 and ongoing. The patient experienced DVT in right leg on 02Apr2021, swelling in right leg on 15Mar2021 and discomfort in right leg while walking on 15Mar2021. The patient reported that he had a reaction to the COVID-19 vaccine and he believes that it was directly related to the COVID-19 vaccine. He reported that he has a history of blood clots in his right leg going back to 2018. He reported that his most recent DVT was in Aug2020 and he was cleared in Nov2020. He reported that he received the COVID-19 vaccine on 10Mar2021. He reported that on 15Mar2021, he started to notice his right leg swelling. He reported that he called his physician on 29Mar2021 and that his physician ordered an ultrasound. He reported that he had the ultrasound on 02Apr2021 and a deep vein thrombosis was found again. Swelling in right leg: he reported that the swelling has gone down. He reported that the reason that he mentioned that he has a history of blood clots was because of his warfarin dosage. He reported that he was first diagnosed with a deep vein thrombosis in Jul2018. He reported that he went through that cycle and that his maintenance level of warfarin was maybe 10 or 12 mg of warfarin per day. He reported that he had another deep vein thrombosis in Aug2020, and since Aug2020 he has been on 17 mg of warfarin daily. He reported that the blood level on warfarin maintenance was supposed to be between 2 and 2.5. He reported that now because of the deep vein thrombosis he experienced in Aug2020, his doctor wanted his level to be at 2.5 to 3.5. He stated that he doesn't think that at that blood level for his warfarin that he should have gotten a blood clot. He reported that something compromised or interfered with the warfarin, resulting in a deep vein thrombosis. Discomfort when walking: he reported that it feels like his leg was compressing. He reported that the discomfort seems to have gotten better. He was queried for details of warfarin prescription. He reported that the 10 or 12 mg warfarin tablets that he had been taking when the blood clot was diagnosed in Aug2020 have been consumed and he no longer has the bottle. He reported that he did not have the bottle with him for his current warfarin prescription. He reported that the warfarin was not auto-refilled by the pharmacy. He reported that the warfarin was only prescribed a week or two at a time. Investigations: he reported that since Aug2020 when the deep vein thrombosis returned, he started doing self INR tests at home. He reported that he constantly self-monitors his INR at home and his levels were consistently at 3.0 to 3.1. He reported that he monitors his INR at least once a week, sometimes twice a week depending on how he feels. He reported that sometimes his INR goes over 4 and he can feel it. He reported that his system was a little off when it feels too high so he knows how to adjust. He reported that he last checked his INR today, 15Apr2021, and that it was 4.0. He reported that he typically checks his INR on Wednesday. He reported that he keeps a log of his INR levels. He reported that he did not see his physician on 29Mar2021, but that he called his physician and his physician wrote a prescription for the caller to get an ultrasound. Vaccination facility type was pharmacy. Vaccine was not administered at military facility. The adverse events did not require a visit to the emergency room and physician office. No prior vaccinations (within 4 weeks). He reported that he doesn't usually get vaccines. BNT162B2 second dose (lot number: ER5729) was administered on an unspecified date; anatomical location: left arm. The outcome of the events was recovering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Test Date: 20210415; Test Name: INR; Result Unstructured Data: Test Result:4.0; Test Date: 20210402; Test Name: ultrasound; Result Unstructured Data: Test Result:deep vein thrombosis was found
Aktuelle Erkrankungen: DVT
Vorgeschichte: -
Andere Medikamente: WARFARIN
Allergien: -
Vorherige Impfungen: -

VAERS 1103094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: PA
Alter: 54,0
Geschlecht: F
Eingang: 28.04.2021
Impfdatum: 10.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Anaphylactic reaction Chest discomfort Dyspnoea Feeling hot Injection site bruising Cough Immediate post-injection reaction Paraesthesia oral Respiratory distress Vaccination site pain Wheezing Throat tightness

Symptomtext

Felt funny in her chest, like a really weird, really warm and heavy feeling, almost like she couldn't breathe; almost like she couldn't breathe/Difficulty Breathing; Felt funny in her chest, like a really weird, really warm and heavy feeling/ warm feeling in the chest; having an anaphylactic reaction from the vaccine; Respiratory, Wheezing, Difficulty Breathing and Respiratory Distress; Respiratory, Wheezing, Difficulty Breathing and Respiratory Distress; Very sore right arm where she was given the injection; felt like she was punched several times in her arm; Injection site bruising; This is a spontaneous report from a contactable nurse(patient). The nurse reported similar events for herself and her husband. This is the first of two reports. A 54-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) (at 54 years of age), dose 1 intramuscular, administered in arm right on 10Mar2021 16:00 (Batch/Lot number was not reported) as a single dose for COVID-19 immunisation. Medical history included severe asthma which started as a child and then it went away and then as an adult it got severe around 2010 and ongoing, she was an asthmatic and would panic and start feeling worse. She had ongoing chronic obstructive pulmonary disease (COPD), brain surgery in 2007, low immune system, allergies to cephalosporins, pulmonary and stomach issues; and bradycardia (as her BP usually runs 90/45 and she is bradycardic). Concomitant medications included tiotropium bromide (SPIRIVA RESPIMAT), salbutamol sulfate (PROAIR HFA), fluticasone propionate, salmeterol xinafoate (ADVAIR HFA), salbutamol (VENTOLIN [SALBUTAMOL]), and montelukast (MONTELUKAST), all taken for asthma, chronic obstructive pulmonary disease from an unspecified start date and ongoing; clarithromycin (CLARITIN [CLARITHROMYCIN], omeprazole, phenytoin sodium, azelastine, ipratropium bromide, fluticasone propionate (FLONASE [FLUTICASONE PROPIONATE]), and ipratropium bromide, salbutamol sulfate (DUONEB), all taken for an unspecified indication from an unspecified start date and ongoing; prednisone taken for an unspecified indication from 2021 and ongoing as she was on this steroid 2 weeks before the vaccine; and azithromycin which she takes prophylactically for her low immune system from an unspecified start date and ongoing. She was on a lot of medications period and most are for her pulmonary and stomach issues. The patient previously took propofol, Versed, Nitrous Oxide, and Percocet wherein the patient had drug hypersensitivity and anaphylactic shock with these; adhesive from nicotine patch made her arm to get red and swollen (Dermatitis contact). She previously took EpiPen for anaphylaxis. It was reported that on 10Mar2021, the patient had the first dose of the vaccine and it felt funny in her chest, like a really weird, really warm and heavy feeling, almost like she couldn't breathe. She got her vaccine at a hospital in their clinic and she was transferred from the vaccine clinic to the ER. Stated she was given a shot with an Epi-pen in her thigh at the clinic and transferred to the ER. In the ER, she was given Benadryl and watched for 4 hours. She would state this was medically significant because of airway, breathing, circulation and she felt like she couldn't breathe. She added that it was kind of weird and freaky. She mentioned that along with that, shortly before she was released from the ER, she experienced a very sore arm where she was given the injection. She heard that was very common so she dealt with it. However as the night progressed, it got increasingly worse, it almost felt like she was punched several times in her arm. It probably started between hour 3 and 4 after receiving the vaccine. She added that she had a very sore right arm where she was given the injection; felt like she was punched several times in her arm. It was not serious, just annoying and it was gone 3 days later. She had injection site bruising on 10Mar2021. She stated that she knows this because she was a nurse, but a lot of times, people experienced this reaction when they are given Dilaudid wherein they get a warm feeling in their chest, so they push it really slow and dilute it with saline so it doesn't have the respiratory factor. She stated that this was kind of what the feeling was like for her and it was scary because she didn't expect it. She stated that the ER team that assessed her said, because she wasn't used to that feeling, she may have had a panic attack and that may have made it worse. After she was treated, she spoke with her husband and he had the shot two minutes before her and he had the same feeling but he didn't freak out and didn't want to appear weak. Stated he told her he had the same feeling and it lasted 5 minutes and then it went away. Stated since she got scared, it made it worse. She doesn't know if she had a panic attack that made it worse. She stated that of course her husband didn't tell her that until she was out of the ER, that it does go away. That made her feel better because she wasn't the only one that experienced that. States he didn't say anything about it, because he was worried about her, he said it was a warm feeling in the chest and not being able to breathe but he didn't want to say anything because she was an asthmatic and would panic and start feeling worse. She mentioned that they weren't going to let her get the second dose, so she went to an allergy doctor and told them what happened and about her husband having the same reaction and because she was severely immunocompromised. Stated the hospital said they were not giving her the second dose unless an allergist says it is safe and sets a protocol and he had to write a letter to the hospital. Stated she was pre-medicated 24 hours before the vaccine with 50mg Benadryl, 50mg Benadryl the day of the shot and 50mg of Benadryl two days after the shot. Stated she will have full immunity on 14Apr2021. She added that she had a pulmonary doctor, brain cancer doctor, ENT doctor, stated they don't know if it was caused by the vaccine, but they are pretty sure she had a reaction but they can handle it with pre-medicating her. She received the second vaccine on 31Mar2021. She mentioned that she was happy to be able to get her second shot. She stated that at first they didn't want to give it to her because of her reaction but she kept calling. So she went to a hospital to saw an allergist and he had to sign off that it was safe to give her the second shot and under what circumstances. Stated she had the letter from the hospital that she was seen by them and she needed to be pre-medicated and it had to be given at a hospital that had the ability to intervene quickly and she needed to be watched for at least 30 minutes after the vaccine. She mentioned that to go through what she went though, and not be able to get would have been disappointing. Because of her immune system, it is important to get the shot and there was a way around the reaction which worked for her. She added that even having an anaphylactic reaction from the vaccine, she was able to recover quickly. Stated with having asthma, COPD and a low immune system, she may not recover from Covid. It makes sense they evaluated it and came up with a solution and a pre medication protocol and when and how long and she was still able to get the shot because it is important. Answers to follow up questions indicated that on 10Mar2021, the patient had the first dose of the vaccine and it felt funny in her chest, like a really weird, really warm and heavy feeling, almost like she couldn't breathe. She was given the shot and getting ready to get out of the chair and her husband was about to sit down for his shot. Stated she would say the time of the course of the reaction was within under 5 minutes of her injection. The patient required medical intervention with Epi-Pen, Benadryl, and Duo-Neb. The patient was not hospitalized because she was immunocompromised, it was better to watch herself at home and because she had an Epi Pen at home in case she has that sort of reaction returning over a 72 hour period. Stated they instructed her husband and told them if she felt any different to come back to ER. She was not admitted to the ICU. Organ involvement included: Respiratory, Wheezing, Difficulty Breathing and Respiratory Distress. The event required initiation of new medication or other treatment or procedure including Epi-Pen, Benadryl, DuoNeb. Patient have a history of previous allergies: Medication Allergies to Cephalosporins, Anesthesia medications: Propofol, Versed, Nitrous Oxide, Percocet: Anaphylactic shock; Adhesive from nicotine patch, caused her arm to get red and swollen. She takes EpiPen as she had previous history of allergies and since she had multiple medication allergies and had a history of quickly going into anaphylaxis, stated her BP usually runs 90/45 and she was Bradycardic. She did not receive any recent vaccines for any other conditions prior to the events being reported. She did not receive any recent vaccines for SARS-CoV2 other than Pfizer-BioNTech COVID-19 Vaccine prior to the event being reported. She has not received any other vaccines around the time of the Pfizer-BioNTech COVID-19 Vaccine vaccination. The patient recovered from 'felt funny in her chest, like a really weird, really warm and heavy feeling, almost like she couldn't breathe', Difficulty breathing, and 'warm feeling in the chest' on 10Mar2021; while having an anaphylactic reaction from the vaccine, Respiratory, Wheezing, Difficulty Breathing and Respiratory Distress were recovered on an unknown date; Vaccination site pain recovered on 13Mar2021 and Injection site bruising recovered on 18Mar2021. Therapeutic measures were taken as a result of all events except Vaccination site pain and Injection site bruising. Relatedness of drug to reactions/events: Reaction assessed for events "felt funny in her chest, like a really weird, really warm and heavy feeling, almost like she couldn't breathe", 'very sore right arm where she was given the injection; felt like she was punched several times in her arm.' and Injection site bruising: Method of assessment: Global Introspection: Drug result: Related. Information on the lot/batch number has been requested.; Sender's Comments: Based on available information, the Company considered all serious and non-serious events as possibly associated to BNT162B2 injection, due to a plausible chronological sequence. Current patient conditions of asthma, chronic obstructive pulmonary disease and allergic diathesis may have been considered as favoring factors in development of reported events. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate,Linked Report(s) : US-PFIZER INC-2021406773 same reporter and drug, similar events, different patient

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Asthma (it got severe around 2010 and ongoing, she was an asthmatic and would panic and start feeling worse); COPD
Vorgeschichte: Medical History/Concurrent Conditions: Abdominal disorder; Asthma (started as a child and then it went away and then as an adult); Bradycardia (States her BP usually runs 90/45 and she is Bradycardic.); Brain operation; Drug allergy; Immune system disorder; Pulmonary disorder
Andere Medikamente: SPIRIVA RESPIMAT; PROAIR HFA; ADVAIR HFA; VENTOLIN [SALBUTAMOL]; MONTELUKAST; CLARITIN [CLARITHROMYCIN]; OMEPRAZOLE; PHENYTOIN SODIUM; AZELASTINE; IPRATROPIUM BROMIDE; FLONASE [FLUTICASONE PROPIONATE]; DUONEB; PREDNISONE; AZITHROMYCIN
Allergien: -
Vorherige Impfungen: -

VAERS 1261789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NY
Alter: -
Geschlecht: F
Eingang: 27.04.2021
Impfdatum: 26.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / RA

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

Chills Dizziness Muscular weakness Nausea SARS-CoV-2 test Syncope

Symptomtext

Fainted; Sudden light nausea; Full body chills; Muscle weakness in legs; Lightheadedness; This is a spontaneous report from a contactable consumer (the patient). A 70-year-old female patient received the first dose and second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), on 26Feb2021 12:15 (lot number EN6203) and on 19Mar2021 12:00 (lot number EN6208), respectively, both via an unspecified route of administration in the right arm (age at vaccination unknown), as a single dose for COVID-19 immunization. The patient's medical history was not reported. The patient was not pregnant at the time of vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included: fluoxetine hydrochloride (PROZAC), lorazepam, and pantoprazole. The patient had an allergy to contrast dye. The patient did not receive any other vaccines within four weeks prior to the vaccination. On an unspecified date, the patient experienced sudden light nausea, then full body chills, followed by muscle weakness in legs, and lightheadedness, then she fainted. Then she was fine. This whole reaction progression took place within 60 seconds, plus about 2 minutes for full leg muscle strength to return. No treatment was received for the events. The patient had a negative nasal swab COVID test on 04Mar2021. The outcome of the events was recovered on an unspecified date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Date: 20210304; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: PROZAC; LORAZEPAM; PANTOPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 1258807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CO
Alter: 65,0
Geschlecht: F
Eingang: 26.04.2021
Impfdatum: 11.03.2021
Beginn: 16.04.2021
Tage bis Beginn: 36,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain Anticoagulant therapy Computerised tomogram abdomen Gastrointestinal oedema Gastrointestinal wall thickening Haematocrit decreased Haemoglobin decreased Intestinal congestion Mesenteric vein thrombosis Nausea Peritoneal adhesions Platelet count decreased Pyrexia Thrombocytopenia Thrombophlebitis superficial White blood cell count normal

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA: patient presented with abdominal pain and nausea and admitted for anticoagulation (heparin) and monitoring for SMV thrombus. Patient developed fever to 40 degrees Celsius and underwent diagnostic laparoscopy with evidence of recovering ischemia of the jejunum and omental adhesion along the left abdomen. Found to have left upper extremity superficial thrombophlebitis concerning for early suppurative complications in setting of persistent fevers and mild thrombocytopenia. Heparin discontinued when thrombocytopenia developed and platelet counts have increased.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mesenteric vein thrombosis
Hospital-Tage: -
Labordaten: Platelets: initially 227 10*9/L on arrival, five days later 131 10*9/L (lowest point), most recent count 183 10*9/L; also that day WBC 5.0 10*9/L, hemoglobin 9.4 g/dL, hematocrit 28.7% Vaccine-induced (VITT) HIT Elisa with reflex SRA (detects the presence for IgG antibodies to heparin-platelet factor 4 (PF4) complexes: 0.496 OD CT abdomen/pelvis: occlusive thrombus in the superior mesenteric vein and multiple tributaries, with associated central mesenteric congestion; wall thickening and submucosal edema predominantly involving the proximal jejunum and less so the distal duodenum
Aktuelle Erkrankungen: superior mesenteric vein thrombosis, ischemic bowel, superficial thrombophlebitis, gastric sleeve and hiatal hernia repair
Vorgeschichte: hypertension, hyperlipidemia, obesity, gastrectomy, breast cancer, osteoarthritis, sleep apnea
Andere Medikamente: alprazolam, docusate, duloxetine, esomeprazole, lisinopril, sucralfate, ondansetron, oxycodone, simvastatin, tamoxifen, venlafaxine
Allergien: none reported
Vorherige Impfungen: -

VAERS 1255692

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: WV
Alter: 60,0
Geschlecht: F
Eingang: 25.04.2021
Impfdatum: 11.03.2021
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / RA

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

Thrombosis

Symptomtext

Blood Clot; This is a spontaneous report from a contactable nurse. A 60-year-old female patient (no pregnant) received her second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EN6208), intramuscular at the age 60-year-old at arm right on 11Mar2021 at single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. The patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EN6200), intramuscular at the 60-year-old at right arm on 19Feb2021 for COVID-19 immunisation and experienced pneumonia. There was no other vaccine in four weeks. Facility type vaccine was reported as public health clinic/administration facility. The patient experienced blood clot on Mar2021 after 2nd. The patient was hospitalized for event for 5 days. Adverse event resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care, hospitalization, life threatening illness. The patient received the treatment for event. The outcome of event was unknown.; Sender's Comments: Based on information available, a possible contribution role of the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) to the onset of event clot blood cannot be completely excluded. The case will be reassessed should additional information become available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics committees and Investigators, as appropriate.,Linked Report(s) : US-PFIZER INC-2021422806 same patient/product, different dose and event

Weitere VAERSDATA-Felder

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

VAERS 1255361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

schwer

Staat: CA
Alter: 61,0
Geschlecht: F
Eingang: 25.04.2021
Impfdatum: 12.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / RA

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

Blood pressure increased Blood pressure measurement Chest pain Dizziness Headache Heart rate Heart rate increased Insomnia Nausea Palpitations Syncope Tremor

Symptomtext

felt like she was going to faint; Chest pain; rapid heartbeat; high blood pressure; dizziness; Headache; nausea; could not sleep for 6 days; Heart Racing; Body shaking; This is a spontaneous report from a contactable consumer (patient) reported that a 61-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: en6208), via an unspecified route of administration, administered in arm right on 12Mar2021 09:30 (at the age of 61-years-old) as a single dose for covid-19 immunisation. The patient was not pregnant at the time of vaccination. The patient medical history included asthma, blood pressure and cholesterol; all from an unknown date. The patient had known allergies. No covid prior vaccination. No other vaccines in four weeks. Concomitant medications included fluticasone propionate, salmeterol xinafoate (ADVAIR); chlorphenamine maleate, phenylpropanolamine hydrochloride (NASAMEX); simvastatine; ibuprofen; losartan; and furosemide (FUROSE); all were taken for an unspecified indication, start and stop date were not reported. On 13Mar2021 10:00, the patient experienced chest pain, rapid heartbeat, high blood pressure, dizziness, felt like she was going to faint and couldn't walk so dizzy. Her heart raced/heart racing for 5 days, headache, nausea and could not sleep for 6 days and body shaking. The events resulted in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. The patient received treatment for the events. Double the dose of losartan for blood pressure. Not tested covid post vaccination. The outcome of the events was recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Date: 20210313; Test Name: blood pressure; Result Unstructured Data: Test Result:high; Test Date: 20210313; Test Name: heartbeat; Result Unstructured Data: Test Result:Rapid
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Asthma; Blood pressure abnormal; Cholesterol
Andere Medikamente: ADVAIR; NASAMEX; SIMVASTATINE; IBUPROFEN; LOSARTAN; FUROSE
Allergien: -
Vorherige Impfungen: -

VAERS 1255105

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MA
Alter: 74,0
Geschlecht: F
Eingang: 25.04.2021
Impfdatum: 20.03.2021
Beginn: 21.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Abdominal pain upper Chills Diarrhoea Head injury Loss of consciousness Syncope

Symptomtext

I fainted and hit my head.; I fainted and hit my head.; passing out; stomach cramps; diarrhea; chills; This is a spontaneous report from a contactable consumer. A 74-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 2 via an unspecified route of administration, administered in Arm Left on 20Mar2021 12:45 (Batch/Lot Number: EN6208) as SINGLE DOSE for covid-19 immunisation. Medical history included Thyroidectomy. Concomitant medications included pravastatin sodium (PRAVASTATIN SODIUM); levothyroxine sodium (SYNTHROID); aspirin [acetylsalicylic acid] (ASPIRIN [ACETYLSALICYLIC ACID]). The patient received first dose of BNT162B2 on 27Feb2021 at 74-years-old for COVID-19 immunization: lot number=EN6203, lot unknown=False, administration date=27Feb2021, vaccine location=Left arm, dose number=1. On 22Mar2021 16:00, the patient fainted and hit her head. On 21Mar2021, the patient had stomach cramps, diarrhea and chills. I was wondering if passing out was an uncommon side effect. The outcome of the events was recovered. The patient received treatment for the events.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Thyroidectomy
Andere Medikamente: PRAVASTATIN SODIUM; SYNTHROID; ASPIRIN [ACETYLSALICYLIC ACID]
Allergien: -
Vorherige Impfungen: -

VAERS 1242361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: PA
Alter: 33,0
Geschlecht: M
Eingang: 22.04.2021
Impfdatum: 14.04.2021
Beginn: 14.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Amnesia Blood pressure measurement Bradycardia Fall Heart rate Hypotension Loss of consciousness Nausea

Symptomtext

Patient recieved his immunization and after walking from the immunization area to the seated waiting area, he suddently lost consciousness and fell to the floor from standing . Upon falling, his face and jaw line were the first part of his body to make contact with the ground. Immdiate examiation post-fall was completed to ensure his spinal column was un-harmed prior to lifting him to a sitting position. He became nauseated, along with amnesia and EMS was immediately called to the scene for further evaluation and to take him to a hospital for routine testing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: After falling, we took his blood pressure & heart rate (while lying down). He was hypotensive and bradycardic (90/46 mmHg and 46 bpm). After he reached a sititng position, his blood pressure and heart rate remained unchanged for the next 5-10 minutes before EMS took him to the local ER.
Aktuelle Erkrankungen: None per patient
Vorgeschichte: None per patient
Andere Medikamente: None per patient
Allergien: None per patient
Vorherige Impfungen: -

VAERS 1239431

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IL
Alter: 71,0
Geschlecht: M
Eingang: 21.04.2021
Impfdatum: 12.03.2021
Beginn: 15.04.2021
Tage bis Beginn: 34,0
Dosis: 2
Route/Site: IM / LA

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

Blood test normal Computerised tomogram head Facial paralysis Ocular discomfort

Symptomtext

On day 32 (April 15, 2021) post second COVICD- 19 vaccination patient started to develop slight paralysis of the left side of his face ( mouth, cheek) and eye was also feeling heavy/fatigued. On April 21, 2021 patient was directed to go to local ER for examination to rule out stroke.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: On April 21, 2021 patient had a head CT scan and multiple blood analysis done. All were in normal parameters.
Aktuelle Erkrankungen: None
Vorgeschichte: Stage 4 Hodgkin's lymphoma
Andere Medikamente: Losartan, 81 mg aspirin, simvastatin, multi-vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1238513

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: WA
Alter: 37,0
Geschlecht: M
Eingang: 21.04.2021
Impfdatum: 10.03.2021
Beginn: 16.04.2021
Tage bis Beginn: 37,0
Dosis: 1
Route/Site: IM / LA

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

Computerised tomogram abdomen Computerised tomogram thorax Pulmonary thrombosis

Symptomtext

Bilateral pulmonary thrombosis; hospitalized 2 day, given IV anticoagulant;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 2,0
Labordaten: Abdominal and thoracic CT 4/20/2021 and 4/21/2021
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1237232

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NE
Alter: 35,0
Geschlecht: M
Eingang: 21.04.2021
Impfdatum: 20.03.2021
Beginn: 28.03.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: SYR / LA

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

Computerised tomogram Scan with contrast Splenic infarction Splenic thrombosis Swelling

Symptomtext

Swollen spleen, blood clot in spleen, splenal infarct.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Splenic thrombosis
Hospital-Tage: 6,0
Labordaten: Ct scan with and with out contrast 04/01/21. In hospital. Too many test ran between 04/01-04/06 while in hospital to put on here.
Aktuelle Erkrankungen: -
Vorgeschichte: High blood pressure High triglycerides High cholesterol
Andere Medikamente: Fenofibrate 54 mg Bupropion XL 150mg Rosuvastatin 10mg Lisinopril-HCTZ 20/12.5mg
Allergien: None
Vorherige Impfungen: -

VAERS 1234190

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CO
Alter: 60,0
Geschlecht: F
Eingang: 20.04.2021
Impfdatum: 11.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RA

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

Atrioventricular block Blood thyroid stimulating hormone Bradycardia Electrocardiogram Full blood count abnormal Haematocrit decreased Haemoglobin decreased Hypotension Liver function test normal Nodal rhythm Platelet count normal QRS axis abnormal Sinus bradycardia Syncope Troponin increased White blood cell count

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA: patient presents to emergency department (ED) bradycardic and hypotensive three days after vaccination and immediately following a syncopal episode. Found to have high grade AV block while on metoprolol and verapamil. Patient admitted and symptoms improved with glucagon administration and medication dose adjustments. Discharged to home medically stable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: In the ED: ECG: sinus bradycardia with junctional rhythm, abnormal R-wave progression early transition, abnormal T CBC: Hemoglobin: 9.2 g/dL, Hematocrit 29.2%, WBC andplatelets within normal ranges Electrolytes, TSH, LFTs within normal ranges Initial troponin elevated, rest within normal ranges
Aktuelle Erkrankungen: allergic rhinitis; hypothyroid medication dose adjustments for low TSH; nasal obstruction; nasal polyps; shortness of breath; tachycardia
Vorgeschichte: asthma; COPD; GERD; hyperlipidemia; hypertension; MRSA; sleep apnea; syncope; thyroid disease; TIA; cerebral artery occlusion with cerebral infarction; hypertrophic cardiomyopathy
Andere Medikamente: albuterol; atorvastatin; azelastine; baclofen; cetirizine; chlorthalidone; diphenhydramine; doxycycline; duloxetine; vitamin D2; estradiol; fluticasone inhaler and nasal; gemfibrozil; guaifenesin; lamotrigine; levothyroxine; meloxicam; meto
Allergien: cats; hydrocodone-acetaminophen; sulfa
Vorherige Impfungen: -

VAERS 1233502

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CO
Alter: 63,0
Geschlecht: M
Eingang: 20.04.2021
Impfdatum: 12.03.2021
Beginn: 10.04.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Hepatic vein thrombosis Mesenteric vein thrombosis Portal vein thrombosis Splenic vein thrombosis

Symptomtext

Abdominal pain, Portal Vein Thrombosis (Blood clots in veins to the Liver, Spleen and Large Intestine) Treatment - Heparin drip and then converted over to the blood thinner Xarelto Recommended that I follow up with my primary care physician and seek the advice of a Hematologist

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hepatic vein thrombosis
Hospital-Tage: 2,0
Labordaten: I do not have this information. I will see if I can get it and get back to you.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, High Cholesterol
Andere Medikamente: Levothyroxine 0.100mg, Atorvastatin 80mg, Losartan Potassium 50mg, Tamsulosin HCL 0.4mg, Fluticasone Propionate, Vitamins, Ubiquinol, Probiotic Formula, Low Dose Aspirin
Allergien: Sulfa drugs, Eliquis
Vorherige Impfungen: -

VAERS 1093681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 26,0
Geschlecht: F
Eingang: 20.04.2021
Impfdatum: 11.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Chest discomfort Dizziness Dyspnoea Nausea Paraesthesia oral Throat tightness Urticaria Vaccination complication

Symptomtext

ED visit within 6 weeks of COVID vaccination - Epinephrine and benadryl administered

Weitere VAERSDATA-Felder

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

VAERS 1093681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 26,0
Geschlecht: F
Eingang: 20.04.2021
Impfdatum: 11.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Anaphylactic reaction Chest discomfort Dizziness Dyspnoea Nausea Paraesthesia oral Throat tightness Urticaria Vaccination complication

Symptomtext

ED visit within 6 weeks of COVID vaccination - Epinephrine and benadryl administered

Weitere VAERSDATA-Felder

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

VAERS 1093681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 26,0
Geschlecht: F
Eingang: 20.04.2021
Impfdatum: 11.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: UN / UN

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

Anaphylactic reaction Chest discomfort Dizziness Dyspnoea Nausea Paraesthesia oral Throat tightness Urticaria Vaccination complication

Symptomtext

ED visit within 6 weeks of COVID vaccination - Epinephrine and benadryl administered

Weitere VAERSDATA-Felder

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

VAERS 1229501

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: VA
Alter: 19,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: 26.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Syncope

Symptomtext

Syncope - two episodes after vaccine administration. Transported to local hospital for evaluation.

Weitere VAERSDATA-Felder

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

VAERS 1229253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: AL
Alter: 18,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: 07.04.2021
Beginn: 07.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Malaise Skin discolouration Syncope

Symptomtext

1328 - Father stated daughter didn't feel well - walked to stretcher and fainted. 1330 - Patient awake, VS taken, on stretcher, color improved, talking. BP = 98/53, HR = 74, RR = 22, O2 Sat = 100% 1335 - Patient sitting up. 1340 - Patient talking, drinking soda. BP = 117/76, HR = 80, RR = 22, O2 Sat = 100% 1350 - Patient's color pink, in no apparent distress. BP = 129/71, Hr = 83, RR = 16, O2 Sat = 98% 1351 - Patient ambulated out of clinic with father.

Weitere VAERSDATA-Felder

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

VAERS 1228182

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 47,0
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 17.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Erythema Flushing Hyperhidrosis Loss of consciousness Rash macular

Symptomtext

Systemic: After patient was directed to sit down for 15 min to be observed. A few min after patient sat down in chair he passed out and fell off his chair. Nurse gave epipen called 911. Had scrape on R front scalp and some blood on nostril.-Medium, Systemic: Flushed / Sweating-Mild, Additional Details: Patient reported that he had a phobia of needles prior to vaccination. Vaccine was given at approximately 2:50pm. After he fell, the nurse noted he was face down. The nurse asked him to roll on his back and he responded after a few moments. His skin was red, blotchy, and sweaty. Patient said that he was ok and didn't want to get sent to ER. Epipen was administered at 3:02pm on 3/17/21 and ambulance arrived 3:07pm. The nurse noted some improvement but pt was complaining of hand and arm pain.

Weitere VAERSDATA-Felder

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

VAERS 1227193

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 78,0
Geschlecht: M
Eingang: 18.04.2021
Impfdatum: 01.04.2021
Beginn: 12.04.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: IM / -

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

Bell's palsy Facial paralysis Oropharyngeal pain

Symptomtext

Pt is GCS 15 and A&Ox4. Skin is P/W/D to pt ethnicity. Neuro intact and PERRLA. Respirations are regular/equal and non-labored. pt states he's had left sided facial droop for 2 days and a sore throat for 5 days. pt denies any other symptoms at this time. pt appears to have bells palsy. Dr. was contacted and she ruled out a stroke. Symptoms started 1 week after the completion of vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1227152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge En6208

schwer

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 18.04.2021
Impfdatum: 15.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Bell's palsy

Symptomtext

Bells Palsy right side of face; This is a spontaneous report from a contactable consumer (patient). This 60-year-old female patient (patient was not pregnant at the time of vaccination) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number En6208), via an unknown route on 15Mar2021 at 12:00 pm (at the age of 60-years-old) at single dose on the left arm for COVID-19 immunization. Medical history was none. The patient did not have allergies to medications, food, or other products. Relevant concomitant medications patient received within 2 weeks of vaccination included pantoprazole 40mg. On 15Mar2021 at 12:00, the patient had Bells Palsy right side of face. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. No treatment received for the event. Outcome of the event Bells Palsy right side of face was recovered in 2021. Follow up attempts are needed. Information on the lot/batch number has been requested.

Weitere VAERSDATA-Felder

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

VAERS 1224537

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: FL
Alter: 66,0
Geschlecht: F
Eingang: 18.04.2021
Impfdatum: 26.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Blood pressure measurement Headache Heart rate Human rhinovirus test Muscle fatigue Myalgia Rash Seizure Urticaria

Symptomtext

seizures; muscle fatigue; hives; rash from head to toe; sore muscles; wrap around headache; This is a spontaneous report received from a contactable healthcare professional (patient herself). A 66 -year-old female patient received her second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 26Mar2021 (Batch/Lot Number: EN6208; Expiration Date: 30Jun2021) as a single dose for COVID-19 immunisation. She provided a brief history from 2017. She was walking her dog and she fell and suffered a concussion, she had a seizure, then she developed bipolar disorder. She's been taking sodium valproate (DEPAKOTE) for her seizures since 2017. She reports she's very active. She's not an old lady. She can run circles around some 22 year old's. In September of 2017, she had a concussion and had seizures. She's been on sodium valproate (DEPAKOTE) since that time. She's not mentally ill, the concussion she got in 2017 caused her brain to turn bipolar. It's hard for people to understand that. Sodium valproate (DEPAKOTE) was 500mg. She takes 1 tablet in the morning and 2 tablets at night because it can make you sleepy. She reports she was recently hospitalized in Feb2021 for atrial fibrillation with rapid ventricular rate (RVR). Her heartrate was 181 beats per minute, her blood pressure was dropping, she tested positive for rhinovirus and the doctor thinks the atrial fibrillation with RVR was caused from the rhinovirus. She was allergic to bee venom and carries an EPI PEN. Medical history also included ongoing high blood pressure from an unspecified date (controlled with medication). Concomitant medications included ongoing metoprolol tartrate (LOPRESSOR) taken for blood pressure; ongoing lisinopril; ongoing valproate semisodium (DEPAKOTE) taken for seizure from 2017; ongoing hydrochlorothiazide, lisinopril (LISINOPRIL HCTZ) taken for blood pressure; paracetamol (TYLENOL) from an unspecified date in 2021. The patient received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 05Mar2021 (Batch/Lot Number: EM9810; Expiration Date: 30Jun2021). The patient did not receive any recent vaccines for any other conditions or any recent vaccines for any other conditions prior to the event being reported; or any other vaccines around the time of Pfizer-BioNTech COVID-19 Vaccine vaccination. The patient reported that with the second Covid 19 vaccine she had two seizures on 27Mar2021. The seizures were back to back. The seizures resolved within 2 minutes. She had fatigue from an unspecified date, sore muscles and a wrap around headache on 26Mar2021. The wrap around headache felt like she was going to have a stroke even though her blood pressure was fine. She monitored her blood pressure at her home. She feels it's weird that they publish that the second Covid 19 vaccine is going to be worse. She thought she'd have muscle soreness and fatigue but not seizures. She looked it up and the wrap around headache and seizure are the rarest things that can happen after receiving the Covid 19 vaccine. She stayed in bed from Friday afternoon after she received the second Covid 19 vaccine on 26Mar2021 and started to feel better Sunday afternoon, 28Mar2021. Her blood pressure and pulse were both fine with her wrap around headache. She had fatigue with both Covid 19 vaccines. She also developed hives, which she still has. She has a rash from her head to her toes. It looked like she rolled around in an ant bed. The hives were clearing up. She was using an anti-itch cream. The hives and the rash started midday on Saturday, 27Mar2021. She only has around 5 hives now on her chest. She hasn't taken Benadryl. She doesn't like to take it. Her doctor didn't want her to open the hives and cause impetigo. She never had any soreness in her arm. She doesn't think the headache was serious because she had a blood pressure cuff at home. She just knew the hives and the rash were a reaction to the Covid 19 vaccine. She didn't go to the hospital for her seizures. She was not seen in the Emergency Department, hospitalized, or admitted to an Intensive Care Unit. She tries to do holistic medicines and treatments. She doesn't run to the hospital every time something happens. She tries to stay out of the hospital. She's fine now and she loves Pfizer. If she can get a medicine she needs that Pfizer makes she tries to get it. She tries to see every side of things. Outcome of seizures was recovered on 27Mar2021 and sore muscles was recovered on 28Mar2021; of remaining events was recovering. Follow-up attempts are completed. No further information is expected.; Sender's Comments: A causal association between BNT162B2 and seizure cannot be excluded based on a compatible temporal relation. 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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Test Name: blood pressure; Result Unstructured Data: Test Result:fine.; Test Name: blood pressure; Result Unstructured Data: Test Result:was dropping; Test Name: heart rate; Result Unstructured Data: Test Result:181 beats per minute,; Test Name: pulse; Result Unstructured Data: Test Result:fine; Test Name: rhinovirus; Result Unstructured Data: Test Result:positive
Aktuelle Erkrankungen: Atrial fibrillation (181 beats per minute); Blood pressure high (Controlled with medication); Seizures
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to venom (Carries an Epi pen); Bipolar disorder; Concussion; Fall
Andere Medikamente: LOPRESSOR; LISINOPRIL; DEPAKOTE; LISINOPRIL HCTZ; TYLENOL
Allergien: -
Vorherige Impfungen: -

VAERS 1224436

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NE
Alter: 72,0
Geschlecht: M
Eingang: 18.04.2021
Impfdatum: 17.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / LA

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

Deep vein thrombosis Fatigue

Symptomtext

deep vein thrombosis on Sunday; Extreme fatigue on Friday; This is a spontaneous report received from a contactable consumer. A 72-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EN6208) via unspecified route on left arm single dose for COVID-19 immunization on 17Mar2021, 10:45 AM, at 72-year-old. Medical history was not reported. The patient had not had COVID prior vaccination. Concomitant medications in two weeks included: fluoxetine 20 mg; atorvastatin 10 mg. The patient had not had other vaccine in four weeks. The patient previously took morniflumate (FLOMAX) and had allergy to it. The patient was extreme fatigue on Friday 19Mar2021 and deep vein thrombosis on Sunday 21Mar2021 06:00 PM. I was hospitalized for two days including a veinogram to remove the blood clots from my left leg. I'm now taking rivaroxaban (XARELTO) 15 mg twice a day and were wearing a compression sock for my left leg. Treatment also received as IV heparin. Emergency room/department or urgent care involved and reported as serious due to hospitalization for 2 days. The patient had not had COVID tested post vaccination. Outcome of the events was resolving.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: FLUOXETINE; ATORVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 1219720

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: OH
Alter: 58,0
Geschlecht: M
Eingang: 18.04.2021
Impfdatum: 07.04.2021
Beginn: 10.04.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal pain upper Anticoagulant therapy Blood test Computerised tomogram abnormal Portal vein thrombosis Nausea Vomiting

Symptomtext

I was having severe stomach pains. A CT scan showed a blood clot in the portal vein. I?ve been hospitalized now for four days administering Heperin. No history or risk factors for blood clotting. Could this be vaccine related?

Weitere VAERSDATA-Felder

Praegender Schweregrund: Portal vein thrombosis
Hospital-Tage: 4,0
Labordaten: Blood testing - 4/13/31 CT Scan - 4:15/31
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Flomax
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1169389

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge En6208

schwer

Staat: CT
Alter: 56,0
Geschlecht: M
Eingang: 18.04.2021
Impfdatum: 15.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Bell's palsy Facial pain Facial paralysis Incomplete course of vaccination Herpes zoster SARS-CoV-2 test

Symptomtext

bell palsy; Got shingles; This is a spontaneous report from a contactable consumer (patient). A 56-year-old male patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration, administered in Arm Left on 15Mar2021 12:00 (Lot Number: En6208), at the age of 56-years at vaccination, as SINGLE DOSE for covid-19 immunisation. Medical history was none. The patient previously took Advil and experienced allergy. Prior to vaccination, the patient was not diagnosed with COVID-19. Concomitant medication included vitamins nos and 'Acid pill' taken for an unspecified indication, start and stop date were not reported. On 2021, the patient experienced bell palsy and shingles. The event involved physician office visit. The patient underwent lab tests and procedures which included sars-cov-2 test (Nasal Swab): inconclusive on 31Mar2021. The outcome of the events was not recovered. Therapeutic measures were taken as a result of the events which includes viral pill and strides. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Test Date: 20210331; Test Name: SARS-CoV-2 test (Nasal Swab); Result Unstructured Data: Test Result:Inconclusive; Comments: Inconclusive
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: VITAMINS NOS
Allergien: -
Vorherige Impfungen: -

VAERS 1169389

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CT
Alter: 56,0
Geschlecht: M
Eingang: 18.04.2021
Impfdatum: 15.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: IM / LA

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

Bell's palsy Facial pain Facial paralysis Incomplete course of vaccination Herpes zoster SARS-CoV-2 test

Symptomtext

bell palsy; Got shingles; This is a spontaneous report from a contactable consumer (patient). A 56-year-old male patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration, administered in Arm Left on 15Mar2021 12:00 (Lot Number: En6208), at the age of 56-years at vaccination, as SINGLE DOSE for covid-19 immunisation. Medical history was none. The patient previously took Advil and experienced allergy. Prior to vaccination, the patient was not diagnosed with COVID-19. Concomitant medication included vitamins nos and 'Acid pill' taken for an unspecified indication, start and stop date were not reported. On 2021, the patient experienced bell palsy and shingles. The event involved physician office visit. The patient underwent lab tests and procedures which included sars-cov-2 test (Nasal Swab): inconclusive on 31Mar2021. The outcome of the events was not recovered. Therapeutic measures were taken as a result of the events which includes viral pill and strides. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Test Date: 20210331; Test Name: SARS-CoV-2 test (Nasal Swab); Result Unstructured Data: Test Result:Inconclusive; Comments: Inconclusive
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: VITAMINS NOS
Allergien: -
Vorherige Impfungen: -

VAERS 1214380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NY
Alter: 51,0
Geschlecht: M
Eingang: 15.04.2021
Impfdatum: 26.03.2021
Beginn: 13.04.2021
Tage bis Beginn: 18,0
Dosis: UNK
Route/Site: SYR / RA

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

Bell's palsy Facial paralysis Nasopharyngitis

Symptomtext

DEVELOPED BELL?S PALSY - DIAGNOSED 4/14/2021 COLD SYMPTOMS DEVELOPED 8 DAYS AFTER SECOND SHOT (4/3//2021), AND THEN FACIAL PARALYSIS WITH BELL?S DIAGNOSED ON 4/14

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: JUST OBSERVATIONS BY 911 FOLKS AND AT URGENT CARE
Aktuelle Erkrankungen: NONE
Vorgeschichte: MILD HYPERTENSION
Andere Medikamente: LOSARTAN POTASSIUM D3 MAGNESIUM CITRATE COQ10 B12 VITAMIN C
Allergien: SHELL FISH
Vorherige Impfungen: -

VAERS 1205170

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: OH
Alter: 36,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 21.03.2021
Beginn: 23.03.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: - / LA

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

Chills Confusional state Dizziness Fatigue Headache Musculoskeletal stiffness Nausea Neck pain Oropharyngeal pain Pain in extremity Pyrexia Seizure Tinnitus Vaccination site discomfort

Symptomtext

increased seizure activity; I had the normal yet severe side effects of sore arm & neck; I had the normal yet severe side effects of sore arm & neck; stiffness behind the ear, stiffness of the neck; stiffness of the neck and injection site arm; fatigue; fever; headache; sore throat; chills; I started suffering from tinnitus; dizziness; nausea; confusion; This is a spontaneous report from a contactable consumer (patient). A 36-year-old female patient received the second dose of BNT162B2 (Lot Number: EN6208) via an unspecified route of administration, administered in left arm on 21Mar2021 14:45 (at the age of 36-year-old) as single dose for COVID-19 immunization. Medical history included epilepsy and asthma. The patient is not pregnant. Concomitant medication included levetiracetam. No other vaccine in four weeks. The patient previously received the first dose of BNT162B2 (Lot Number: EN6203) administered in left arm on 28Feb2021 14:30 (at the age of 36-year-old) as single dose for COVID-19 immunization. The patient had the normal yet severe side effects of sore arm & neck, stiffness behind the ear, stiffness of the neck and injection site arm, fatigue, fever, headache, sore throat, chills, for the first few days her 2nd dose. But on day 2, she started suffering from tinnitus, dizziness, nausea, confusion in both ears and increased seizure activity. The events started about 2 days after the second shot on 23Mar2021 12:00 PM; its been a week now and it still hasn't gotten better or gone away. She had an appointment with her pcp tomorrow but so far nothing has helped. Its debilitating and extremely hard to focus & function. She mainly just wanted to know if any other vaccine trial participant/recipients have reported anything similar & if so, how long can she expect this to last. The adverse events resulted in Doctor or other healthcare professional office/clinic visit. It was unknown if treatment was received for the events. No COVID prior vaccination. No COVID tested post vaccination. The outcome of the events was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Epilepsy
Andere Medikamente: LEVETIRACETAM
Allergien: -
Vorherige Impfungen: -

VAERS 1205034

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

schwer

Staat: FL
Alter: 51,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 11.04.2021
Beginn: 11.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Fall Headache Syncope Unresponsive to stimuli

Symptomtext

51 y/o female with syncopal episode following vaccination. Per witness pt suddenly fell out of the chair. Pt unresponsive about 15-20 secs. Per pt she started to have headache and suddenly fell to the floor. Pt has Hx of hypotension and depression. VS stable writer called emergency transport and husband. Pt requested to be sent to ER. Nurse attempted to get pt med list from husband and he was unable to locate it at the time but stated that he would bring list to ER. EMS present at the time of incident, monitored pt until Fire & Rescue arrived.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: VS 137165 991.14
Aktuelle Erkrankungen: none
Vorgeschichte: depression, hypotension
Andere Medikamente: Heart medication this morning. Med unknown-per pt
Allergien: nka
Vorherige Impfungen: -

VAERS 1204377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: OR
Alter: 33,0
Geschlecht: M
Eingang: 13.04.2021
Impfdatum: 13.04.2021
Beginn: 13.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Blood pressure decreased Decreased appetite Heart rate decreased Hyperhidrosis Loss of consciousness Nausea Pallor

Symptomtext

Loss of consciousness, low BP, low HR (40s), profuse sweating, loss of color/appetite, nausea within 3 minutes of injection. Was treated by EMTs, HR and BP monitored for about 30 minutes until within normal range and pt could sit unassisted and felt "normal". Pt was given water and food and released.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Cold symptoms within month prior. no symptoms within 1 week of vaccine.
Vorgeschichte: -
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1203462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CO
Alter: 66,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 21.03.2021
Beginn: 24.03.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / LA

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

Deep vein thrombosis Diarrhoea Dizziness Headache Pain in extremity Ultrasound Doppler abnormal

Symptomtext

On 3/24/21, just three days after receiving my second Pfizer vaccine, I started noticing excruciating pain in my left calf. I managed the pain with Tylenol, but as it continued to get worse and debilitating, I saw my doctor on 3/30/21 who immediately scheduled an ultra sound. On 3/31/21 at 9:00 am, I had the ultra sound and the results were DVT (BLOOD CLOT). SEE DETAILED RESULTS IN ITEM 19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: On 3/31/21 reported critical results to Dr. at 10:32 am, then she reported to me the FINDINGS (see pg 2)...
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Levothyroxine .075 mg/day
Allergien: none
Vorherige Impfungen: -

VAERS 1201081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NC
Alter: 21,0
Geschlecht: M
Eingang: 13.04.2021
Impfdatum: 13.04.2021
Beginn: 13.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Loss of consciousness

Symptomtext

Patient was in the health COVID 19 clinic for his 1st dose Pfizer vaccine. Vaccine was administered and patient was sent to the observation area for a 15 minute wait. Upon arrival to the observation area he sat down in a chair and states that he " begin to feel dizzy and then blacked out". Patient was found on the floor by observation nursing staff. He was alert and oriented x4 and vitals were with in normal range. Vitals were as followed: BP 118/74, Heart rate: 79 and regular, 02 98 on room air. Patient was assisted to the emergency pod and he stated that "this happens all the time with needles, and plus I haven't had anything to eat this morning." Gave the patient crackers and a coke monitored for 35 Minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: UNKNOWN
Allergien: UNKNOWN
Vorherige Impfungen: -

VAERS 1191637

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CO
Alter: 54,0
Geschlecht: F
Eingang: 10.04.2021
Impfdatum: 11.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / LA

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

Seizure

Symptomtext

Seizure

Weitere VAERSDATA-Felder

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

VAERS 1190650

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge EN6208

schwer

Staat: FL
Alter: 18,0
Geschlecht: F
Eingang: 10.04.2021
Impfdatum: 10.04.2021
Beginn: 10.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Nausea Presyncope

Symptomtext

Nausea, vasovagal

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1186459

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MN
Alter: 16,0
Geschlecht: F
Eingang: 09.04.2021
Impfdatum: 09.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Pallor Syncope

Symptomtext

Pt was vaccinated. She said she felt fine. Pt walked 15 feet then fainted. Her mom was able to catch her. We moved her to a cot. She slowly regained consciousness. She had no signs of anaphylaxis. She was breathing fine. Her mother states she has fainted during blood draws in the past and her daughter hadn't eaten this morning. We monitored pt for 30 minutes. Her color and smile came back. Pt was able to walk out on her own. Her mother will monitor her today.

Weitere VAERSDATA-Felder

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

VAERS 1183938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NJ
Alter: 32,0
Geschlecht: F
Eingang: 09.04.2021
Impfdatum: 11.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / LA

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

Thrombosis Vaginal haemorrhage

Symptomtext

I began to bleed and pass blood clots from my vagina; I began to bleed and pass blood clots from my vagina; This is a spontaneous report from a contactable consumer (patient). A 32-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in the left arm on 11Mar2021 01:15 (at the age of 32 years) (Batch/Lot Number: EN6208) as a single dose for COVID-19 immunisation. Medical history included birth control. Concomitant medications were not reported. The patient is not pregnant. On 13Mar2021 04:00, the patient began to bleed and pass blood clots from her vagina. The event blood clots was assessed as serious (medically significant). The patient visited the doctor for the events and the events were given treatment. The outcome of the events was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Birth control
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1181254

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: OR
Alter: 79,0
Geschlecht: F
Eingang: 08.04.2021
Impfdatum: 13.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 13,0
Dosis: 2
Route/Site: IM / LA

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

Activated partial thromboplastin time Arterial stent insertion Blood creatine phosphokinase Chest X-ray Computerised tomogram thorax Condition aggravated Echocardiogram Full blood count International normalised ratio Lymphatic mapping Metabolic function test Pain in extremity Peripheral artery occlusion Peripheral artery thrombosis Renal function test Troponin Ultrasound Doppler

Symptomtext

03-26-2021 patient developed LLE pain, progressively worsened. Admitted to hospital on 03/29 and discharged 04/01. Pt diagnosed with superficial femoral artery occlusion and popliteal artery thrombosis. Left femoral artery stent placed 03/31/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Peripheral artery thrombosis
Hospital-Tage: 4,0
Labordaten: Imaging: Chest Xray, Arterial duplex lower extremity ultrasound, transthoracic echo, lower extremity vein mapping, chest CT Labs: Troponin, PTT, INR, CPK, CBC, Renal Function, BMP
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, PAD, hypothyroidism, hyperlipidemia
Andere Medikamente: Amlodipine, ASA, Biotin, Vitamins, Zyrtec, Plavix, COQ10, COSOPT, Cardura, Collagen Ex, Repatha, Atrovent, Synthroid, Fish Oil, Protonix, Metamucil, Valtrex
Allergien: Ezetimibe, Pravastatin, Rosuvastatin, Hydralazine, Vicodin, Zetia
Vorherige Impfungen: -

VAERS 1175865

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IA
Alter: 57,0
Geschlecht: M
Eingang: 07.04.2021
Impfdatum: 19.03.2021
Beginn: 27.03.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

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

Activated partial thromboplastin time Blood glucose Blood pressure increased Blood test Chest X-ray Computerised tomogram Dysarthria Electrocardiogram Facial paralysis Haemoglobin Hypoaesthesia International normalised ratio Metabolic function test Troponin

Symptomtext

About 7 - 8 days after the vaccination, the patient began experiencing numbness in his chin that came and went. By Friday, April 2, the patient began experiencing left side numbness and droopiness in his face, had slurred speech and increased blood pressure. Patient thought he was having a stroke, so wife took him to the ER. All lab work and medical tests came back normal. The patient has an appointment with their family doctor on 4/8 and an appointment with a neurologist next month.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: Per the patient's wife, the patient had a CAT Scan, Chest X-ray, EKG, and various blood work including aPTT, BMP, hemoglobin, POCT glucose, troponin and protamine-INR.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1173016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NC
Alter: 54,0
Geschlecht: F
Eingang: 06.04.2021
Impfdatum: 15.03.2021
Beginn: 15.03.2021
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 Fatigue Loss of consciousness Palpitations

Symptomtext

Zero pain with injection. Immediately upon the needle leaving my arm I began to feel dizzy and really weak. Thought I was going to pass out but didn?t . My tongue felt funny almost electric. Then my heart took off and raced for a good bit. Just felt really washed out. It was a drive through clinic we did not alert anyone. Felt my husband would get someone if I passed out. Felt really tired for the rest of the day and had heart palpitations throughout the following week. I?m now fine. Called in to my primary and they advised I should report

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None SVT and AV node rentry, but has not been an issue for years
Andere Medikamente: None
Allergien: Have experienced a similar reaction to lidocaine with epinephrine.
Vorherige Impfungen: -

VAERS 1165894

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 49,0
Geschlecht: U
Eingang: 04.04.2021
Impfdatum: 17.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Anaphylactic reaction

Symptomtext

anaphylaxis; This is a spontaneous report from a contactable consumer (patient). A 49-year-old patient of an unspecified gender received the first dose of bnt162b2 (BNT162B2rpeorted as PFIZER BIONTECH COVID-19 VACCINE), via an unspecified route of administration in the left arm on 17Mar2021 09:30 (lot number: EN6208) as a single dose for covid-19 immunisation. Medical history included covid-19 prior vaccination. The patient has known allergies. The patient did not receive other vaccine in four weeks. There were no concomitant medications. On 17Mar2021 09:30, the patient had anaphylaxis which resulted in a doctor or other healthcare professional office/clinic visit. The adverse event required treatment which included diphenhydramine (BENADRYL). The patient has not been COVID tested post vaccination. The outcome of the event was recovered in Mar2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (prior vaccination)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1162062

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MN
Alter: 32,0
Geschlecht: F
Eingang: 02.04.2021
Impfdatum: 13.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Arthralgia Bell's palsy Ear pain Neck pain Otorrhoea Pain in extremity

Symptomtext

left eye and left side of mouth was not working/Bell's palsy.; left ear was hurting all day; drainage in patient left ear; neck down to elbow was sore; neck down to elbow was sore/soreness on arm; neck down to elbow was sore; This is a spontaneous report from a contactable consumer. This 32-year-old female consumer (non-pregnant) reported for herself that she received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in arm left on 13Mar2021 10:00 (Batch/Lot Number: EN6208) as single dose for covid-19 immunisation. Medical history was none. Concomitant medications included metformin and prenatal vitamin. Patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. About 30 mins after the shot patient neck down to elbow was sore. On 14Mar2021 the soreness on arm went away but patient neck was still sore. 14Mar2021 night there was drainage in patient left ear. On 15Mar2021 patient left ear was hurting all day. 16Mar2021 morning (07: 45 am) patient woke up with no more pain in left ear, but left eye and left side of mouth was not working. Patient went to ER and they said patient have Bell's palsy. Patient had no control of the left side of face by 18Mar2021. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, patient had not been tested for COVID-19. Event Bell's palsy resulted in emergency room/department or urgent care, disability or permanent damage, and patient received unspecified medications as treatment for the event. Outcome of events pain in arm/elbow was recovered on 14Mar2021, outcome of event left ear was hurting was recovered on 16Mar2021, outcome of events Bell's palsy and neck pain was not recovered, and outcome of event drainage in patient left ear was unknown.

Weitere VAERSDATA-Felder

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

VAERS 1160145

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IN
Alter: 58,0
Geschlecht: M
Eingang: 02.04.2021
Impfdatum: 02.04.2021
Beginn: 02.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest pain Seizure

Symptomtext

1st dose Pfizer administered at 0940 at clinic. patient experienced no reactions or symptoms during observation period at the clinic. Patient had been home for approximately 2 hours when he started experiencing some chest pain prior to his seizures around 1210. He does have a history of seizures which are uncontrolled ranging from having them twice a week to twice a month. patient reports the seizures were no worse than any other seizure he has had in the past. The seizures lasted periodically for approximately 20 minutes. patient reports he didn't consult with his PCP or neurologist prior to the vaccine. The patient was encouraged to seek medical treatment if symptoms persist or worsen over the next hours. He was also encouraged to reach out to his neurologists prior to the second dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: epilepsy
Andere Medikamente: seizure meds
Allergien: none indicated
Vorherige Impfungen: -

VAERS 1159107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CO
Alter: 59,0
Geschlecht: F
Eingang: 02.04.2021
Impfdatum: 15.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Balance disorder Dizziness Headache Loss of consciousness Vomiting

Symptomtext

Slight ha when woke up on 16th. Within 15 min dizzy and passed out. Heavy vomiting and no strength. Bone crushing pain, Laid on floor, partner called 1-800 suggested pepto mismol. Vommitted that. Called EMS to help Get. Me to bathroom and back laid down. No fever. Took other vs . Next thing I know I was in bed eating toast and cola. Left me still weak and trouble keeping balane. Should I get 2nd shot?

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Osteoporosis and sarcoidosis
Vorgeschichte: Osteoporosis and sarcoidosis
Andere Medikamente: Prednisone, folic acid, mestinon, hctz, multi vit, calcium vit d, methotrexate, Tylenol x stench that, remicsde iv
Allergien: None
Vorherige Impfungen: -

VAERS 1158978

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: KS
Alter: 62,0
Geschlecht: M
Eingang: 02.04.2021
Impfdatum: 31.03.2021
Beginn: 31.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chills Hallucination Headache Influenza like illness Loss of consciousness Tremor

Symptomtext

I began shaking violently and severe cold chills. I began hallucinating and felt like I was turning inside out. I blacked out and woke 2 hours later with severe flu like pain in my entire body and a severe headache. I do not do drugs and I had no alcohol in the 3 days before I wa vaccinated. It is now 47 hours after the vaccination and I have moderate flu like symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none I am aware of
Vorgeschichte: Asthma since childhood
Andere Medikamente: Turmeric, glucosamine and multi vitamin
Allergien: none
Vorherige Impfungen: -

VAERS 1158158

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 54,0
Geschlecht: F
Eingang: 01.04.2021
Impfdatum: 18.03.2021
Beginn: 18.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Abdominal pain upper Blood cholesterol increased Blood potassium decreased Blood sodium decreased Blood test abnormal Diarrhoea Electrocardiogram normal Face injury Fall Hypotension Syncope Tooth fracture Vomiting White blood cell count increased

Symptomtext

Thursday, March 18, 2021, 11:00 pm Around 12 hours after the vaccine, I started having stomach cramps and began having diarrhea. About an hour later (around midnight), I fainted while seated on the toilet and fell face first into the tiled floor. My forehead and mouth/teeth apparently broke my fall and I realized when I came to, I had chipped my two front teeth. There was a good amount of blood and soon after my house mates came to find me, they got me up to lean over the toilet as then I began getting sick and throwing up. They called the paramedics as I kept throwing up. The paramedics tended to me and after two does of an anti-nausea pill, I was able to at least keep a bit of water down. ....

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: 3/19 - blood work; EKG fine; low BP. Blood work showed high white blood cell count and low potassium and sodium. 3/20 in ER - blood work showed fine white blood cell count but...
Aktuelle Erkrankungen: sinus infection 2 weeks prior and took doxycycline for it
Vorgeschichte: asthma since age 4; had some basil cell and surface melanoma removed over the last 5 years
Andere Medikamente: Hydrochlorothiazide 50 mg; Ventolin; Singular; Benzonatate; Zy
Allergien: sulfa drug allergy; shellfish allergy
Vorherige Impfungen: -

VAERS 1156359

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IN
Alter: 47,0
Geschlecht: F
Eingang: 01.04.2021
Impfdatum: 30.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / RA

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

Dizziness Syncope

Symptomtext

Dizzy and fainted at 6:00am on April 1, 2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Ortho-Cyclen, Singulair, Zyrtec, Spironolactone
Allergien: -
Vorherige Impfungen: -

VAERS 1156175

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: FL
Alter: 59,0
Geschlecht: F
Eingang: 01.04.2021
Impfdatum: 26.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Asthenia Bradycardia Chest X-ray normal Dizziness Electrocardiogram Full blood count Hypertension Hypotension Loss of consciousness Metabolic function test Presyncope Sinus bradycardia

Symptomtext

Within 15-minutes of vaccination, the patient reported feeling near-syncopal. EMS evaluated the patient on-site. The patient was hypotensive (93/63) and bradycardic (56bpm) with a FSBG of 91mg/dl. EKG demonstrated sinus brady, rate 50bpm, no ST elevation. EMS administered 4mg Ondansetron PO. EMS transported the patient to Hospital Emergency Department. In the ED, the patient reported they felt weak, dizzy, and briefly lost consciousness. The patient was not in any acute distress, but was hypertensive (141/78). The patient left AMA without a diagnosis after "waiting too long" and was informed of the risks of leaving the ED prior to complete evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: EKG (3/26): Sinus bradycardia, rate 59bpm CBC/CMP (3/26): Unremarkable CXR (3/26): No radiographic evidence of acute cardiopulmonary disease.
Aktuelle Erkrankungen: None reported
Vorgeschichte: HTN
Andere Medikamente: None reported
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1156150

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: FL
Alter: 56,0
Geschlecht: F
Eingang: 01.04.2021
Impfdatum: 26.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Bradycardia Electrocardiogram Hypertension Sinus bradycardia Syncope Troponin

Symptomtext

Within 15-minutes of vaccination, the patient had a syncopal event. EMS evaluated the patient on-site. The patient reported a history of syncope with the sight of needles and blood. EKG demonstrated sinus brady, rate 48 bpm, no ST elevation. The patient was hypertensive (155/88) and bradycardic. EMS administered 4mg Ondansetron PO. EMS transported the patient to Hospital Emergency Department. In the ED, the patient reported that they were currently asymptomatic after suffering a syncopal event following vaccination. The patient was normotensive (121/80). Given the patient's improvement in transit to the ED, the physician discharged the patient with a diagnosis of syncope.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EKG (3/26): NSR, rate 70bpm, no ST-T changes, no ectopy, normal PR & QRS intervals POC BMP (3/26): Unremarkable POC Troponin (3/26): 0.00 ng/dL
Aktuelle Erkrankungen: None reported
Vorgeschichte: Hypothyroidism, Arthritis
Andere Medikamente: Levaquin, Plaquinel
Allergien: Estrogen
Vorherige Impfungen: -

VAERS 1155172

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NY
Alter: 61,0
Geschlecht: F
Eingang: 01.04.2021
Impfdatum: 10.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / LA

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

Diarrhoea Dizziness Dyspnoea Feeling hot Hyperhidrosis Loss of consciousness Mobility decreased

Symptomtext

Woke up very dizzy, light headed, felt like diarrhea, hot, sweaty, passed out approximately 4 times, had a harder time breathing, than normal being on oxygen. Stayed in bed for approximately 27 hours, just couldnt function well. Didnt contact Dr. About it, had family stay with me for couple days. I know it was from the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Didnt go
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic COPD
Andere Medikamente: Deliresp, Ipratropium Bromide and albuterol sulfate inhalation. Budesonide inhalation
Allergien: Morphine
Vorherige Impfungen: -

VAERS 1142781

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: VT
Alter: 52,0
Geschlecht: F
Eingang: 01.04.2021
Impfdatum: 25.03.2021
Beginn: 25.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Asthenia Chest discomfort Headache Muscle spasms Dyspnoea Feeling abnormal Hallucination Loss of consciousness Movement disorder Pain in extremity Restlessness Oxygen saturation decreased Presyncope Tremor

Symptomtext

Patient reports symptoms starting a few hours after vaccination, started with chest heaviness, then severe joint pain, O2 sat 91-94% on Room air, Went to bed, the next AM same symptoms but also experienced increased weakness unable to stand feeling like she was blacking out, almost had a fall, layed down then had involuntary muscle spasms, very weak and then headache. This lasted through the day 3/26/2021. Better the following day 3/27 but still felt some weakness through 3/28.

Weitere VAERSDATA-Felder

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

VAERS 1154533

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 30,0
Geschlecht: M
Eingang: 31.03.2021
Impfdatum: 31.03.2021
Beginn: 31.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Hyperhidrosis Loss of consciousness Pallor

Symptomtext

patient was given the vaccine and then went to observation room. While there, he complained of dizziness and became diaphoretic and passed out for about 10 seconds. Vitals were taken and a rapid response was called for the team to come. He came back and felt thirsty and was pale. He was then transferred to Urgent Care to be observed before being discharged.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Glucose 84 Vitals stable
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 1153381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: VA
Alter: 39,0
Geschlecht: M
Eingang: 31.03.2021
Impfdatum: 11.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Abdominal pain Chills Constipation Dizziness Facial paralysis Fatigue Heart rate abnormal Hypoaesthesia Lymphadenopathy Pain Pyrexia

Symptomtext

left-side facial drooping began within 8 hours; feeling dizzy; ntense fatigue; full body aches; Facial numbness; Low fever; chills; heavy heart beat; intermittent cramps of the abdomen and on the left side (between hip and rib cage); Swollen lymph nodes in the neck; constipation; This is a spontaneous report from a contactable consumer (patient). A 39-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 1 via an unspecified route of administration, administered in left arm on 11Mar2021 12:15 (lot number: EN6208) as single dose at the age of 39 years old for COVID-19 immunisation. Medical history included allergies: minor reaction to iodine CT contrast. Concomitant medications included fish oil, turmeric [curcuma longa rhizome] (TURMERIC), and xantofyl (LUTEIN); all taken for an unspecified indication, start and stop date were not reported. The patient previously took iodine and experienced allergies (minor reaction to iodine CT contrast). On 11Mar2021 12:45 PM, within an hour of the shot, the patient started feeling dizzy. Intense fatigue and full body aches set in within 3 hours. Facial numbness and left-side facial drooping began within 8 hours. Low fever, chills, heavy heartbeat, and intermittent cramps of the abdomen and on the left side (between hip and rib cage) began within 18 hours. Swollen lymph nodes in the neck and constipation began within 48 hours. Facial numbness, heavy heartbeat, and fatigue persist, though drooping has become less pronounced and the other symptoms have largely resolved at 100 hours since the first shot. Seeking guidance on whether further medical help should be sought (did nurse line call with insurance company) and whether the booster shot should be administered. The AEs resulted in doctor or other healthcare professional office/clinic visit. No treatment was given for the adverse events. The patient has not been tested for COVID post vaccination. The patient was not diagnosed with COVID prior to vaccination. No other vaccines received four weeks prior to COVID vaccination. Outcome of the events was recovered with sequelae.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Contrast media allergy
Andere Medikamente: FISH OIL; TURMERIC [CURCUMA LONGA RHIZOME]; LUTEIN
Allergien: -
Vorherige Impfungen: -

VAERS 1153312

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MN
Alter: 68,0
Geschlecht: F
Eingang: 31.03.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Blood test Dermatitis Facial paralysis Hypoaesthesia Mass Pain of skin Swelling

Symptomtext

Her left arm and face were numb; mass/swelling on her face; The left side of her face is drooping; face became swollen; face became swollen and inflamed; face was still swollen and sore; This is a spontaneous report from a contactable consumer (patient) and a contactable nurse. This 68-year-old female patient received the 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EN6208, expiration date: 30Jun2021) via intramuscular in the left arm on 12Mar2021 at 14:10 at single dose for COVID-19 immunisation. Medical history included hyperlipidemia, pneumonia and flu. The patient had family medical history of diabetes. Concomitant medications included estrogens conjugated (PREMARIN) ongoing. The patient was not pregnant. The patient no other vaccine in four weeks or other medications in two weeks. The left side of the patient's face became swollen and inflamed. Five days later the left side of her face was still swollen and sore. The left side of her face was drooping. Events started date was 12Mar2021 at 15:00 PM. No treatment for AE was received, except events "mass/swelling on her face" and "Her left arm and face were numb". The patient had no COVID prior vaccination, no COVID tested post vaccination. A nurse reported that the 2nd dose was scheduled for 05Apr2021. The patient had last blood work (reported as BW) on Sep2020 with comments: normal. The left side of patient's face was drooping on 14Mar2021. The nurse stated patient went to ER. Her left arm and face were numb. They noticed a mass/swelling on her face. Outcome of the events "mass/swelling on her face", "Her left arm and face were numb" was unknown, of the other events was not recovered.; Sender's Comments: A contributory role of BNT162B2 to event the left side of her face is drooping is considered possibly based on temporal association and known safety profile. 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: Facial paralysis
Hospital-Tage: -
Labordaten: Test Date: 202009; Test Name: Last BW; Result Unstructured Data: Test Result:normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Flu; Hyperlipidemia; Pneumonia
Andere Medikamente: PREMARIN
Allergien: -
Vorherige Impfungen: -

VAERS 1152688

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: TN
Alter: 42,0
Geschlecht: F
Eingang: 31.03.2021
Impfdatum: 22.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Chest pain Ear pain Electrocardiogram normal Fatigue Headache Malaise Nausea Periorbital pain Pyrexia SARS-CoV-2 test Seizure

Symptomtext

Vaccine 3/22/21, started with fatigue/generally feeling unwell 3/25/21, fever. Received Tdap vaccine 3/26/21. Persistent fever, pain around eye, ear and radiating into her head, nausea. Symptoms continued to worsen, developed chest pain and new onset seizure 3/31/21- Sent to ER for evaluation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Sars-cov results pending; EKG normal- sent to ER for further evaluation
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, Chronic allergic rhinitis, Depression/anxiety, Asthma, Food allergies
Andere Medikamente: Mirena, Lisinopril-Hydrochlorothiazide, Qvar, Proair, Fexofenadine, Nasonex, Ergocalciferol, Cyanocobalamin
Allergien: Doxycycline, Almond, Shellfish, Sesame Seeds
Vorherige Impfungen: -

VAERS 1152509

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: -
Geschlecht: U
Eingang: 31.03.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Seizure

Symptomtext

4 seizures were documented and EMS and 911 was called, O2 given by nasal cannula

Weitere VAERSDATA-Felder

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

VAERS 1150381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: PA
Alter: 72,0
Geschlecht: M
Eingang: 31.03.2021
Impfdatum: 10.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Diplopia VIth nerve paralysis

Symptomtext

Suspect 6th Nerve Palsy; Double Vision; This is a spontaneous report from a contactable consumer (patient). A 72-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), second dose via an unspecified route of administration, administered in Arm Left on 10Mar2021 10:30 AM (Batch/Lot Number: EN6208) as SINGLE DOSE for covid-19 immunization. Medical history included High Blood Pressure (controlled by medication) from an unknown date and unknown if ongoing. The patient had no known allergies. The patient has no COVID prior to vaccination, and not COVID tested post vaccination. No other vaccine in four weeks. Other medication in two weeks was noted (reported as yes) but it was unspecified. The patient previously vaccinated of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) first dose, lot number: EN6200 on 17Feb2021 12:30 PM at the left arm single dose for COVID-19 immunization. It was reported that the patient experienced Double Vision and Suspect 6th Nerve Palsy on 11Mar2021 at 08:00 AM. The outcome of the events was recovering. There was no treatment for the event.

Weitere VAERSDATA-Felder

Praegender Schweregrund: VIth nerve paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (Controlled by medication)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1128154

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 64,0
Geschlecht: M
Eingang: 31.03.2021
Impfdatum: 12.03.2021
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Blood pressure decreased Blood pressure measurement Chills Cold sweat Computerised tomogram Computerised tomogram head Computerised tomogram spine Computerised tomogram thorax Dehydration Disease recurrence Dizziness Hyperhidrosis Nausea SARS-CoV-2 test Electrocardiogram Fatigue Rib fracture Skin laceration

Symptomtext

Fainted; Fainted; lightheadedness; drop in blood pressure; sweats; clammyness; major chills; shaking; nausea; vomiting; This is a spontaneous report from a contactable consumer reporting for himself. A 64-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EN6208) via an unspecified route of administration, administered in the left arm on 12Mar2021 15:45 (at the age of 64-years-old) as single dose for COVID-19 immunisation. Medical history included minor history of fainting (4x in 15 years). The patient had no known allergies. Concomitant medications included ibuprofen (ADVIL [IBUPROFEN]); omeprazole; fish oil, vitamins etc. The patient had no COVID prior to vaccination. The patient felt great initially. Fainted in response to lightheadedness (drop in blood pressure) 4 hours later on 12Mar2021 at 07:30 PM - on a hardwood floor. 7 stitches after an ambulance ride and multiple CT scans. Also had sweats/clammyness, major chills (shaking), and nausea and vomiting over the next 12 hours or so. Spent 2 nights in the hospital to rule out other causes for fainting. The received the following as treatment for the events: stitches, IV to rehydrate and anti-nausea meds. The events resulted to doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care and hospitalization. The patient was hospitalized for two days. The patient tested negative on a COVID-19 test via nasal swab on 12Mar2021. The patient was recovering from the events.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 2,0
Labordaten: Test Date: 20210312; Test Name: blood pressure; Result Unstructured Data: Test Result:drop; Test Date: 20210312; Test Name: COVID-19 test (Nasal Swab); Test Result: Negative ; Test Date: 20210312; Test Name: CT scans; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fainting (4x in 15 years)
Andere Medikamente: ADVIL [IBUPROFEN]; OMEPRAZOLE; FISH OIL
Allergien: -
Vorherige Impfungen: -

VAERS 1128154

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 64,0
Geschlecht: M
Eingang: 31.03.2021
Impfdatum: 12.03.2021
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Blood pressure decreased Blood pressure measurement Chills Cold sweat Computerised tomogram Computerised tomogram head Computerised tomogram spine Computerised tomogram thorax Dehydration Disease recurrence Dizziness Hyperhidrosis Nausea SARS-CoV-2 test Electrocardiogram Fatigue Rib fracture Skin laceration

Symptomtext

Fainted; Fainted; lightheadedness; drop in blood pressure; sweats; clammyness; major chills; shaking; nausea; vomiting; This is a spontaneous report from a contactable consumer reporting for himself. A 64-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EN6208) via an unspecified route of administration, administered in the left arm on 12Mar2021 15:45 (at the age of 64-years-old) as single dose for COVID-19 immunisation. Medical history included minor history of fainting (4x in 15 years). The patient had no known allergies. Concomitant medications included ibuprofen (ADVIL [IBUPROFEN]); omeprazole; fish oil, vitamins etc. The patient had no COVID prior to vaccination. The patient felt great initially. Fainted in response to lightheadedness (drop in blood pressure) 4 hours later on 12Mar2021 at 07:30 PM - on a hardwood floor. 7 stitches after an ambulance ride and multiple CT scans. Also had sweats/clammyness, major chills (shaking), and nausea and vomiting over the next 12 hours or so. Spent 2 nights in the hospital to rule out other causes for fainting. The received the following as treatment for the events: stitches, IV to rehydrate and anti-nausea meds. The events resulted to doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care and hospitalization. The patient was hospitalized for two days. The patient tested negative on a COVID-19 test via nasal swab on 12Mar2021. The patient was recovering from the events.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 2,0
Labordaten: Test Date: 20210312; Test Name: blood pressure; Result Unstructured Data: Test Result:drop; Test Date: 20210312; Test Name: COVID-19 test (Nasal Swab); Test Result: Negative ; Test Date: 20210312; Test Name: CT scans; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fainting (4x in 15 years)
Andere Medikamente: ADVIL [IBUPROFEN]; OMEPRAZOLE; FISH OIL
Allergien: -
Vorherige Impfungen: -

VAERS 1097835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IL
Alter: 44,0
Geschlecht: F
Eingang: 31.03.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Anaphylactic reaction Hypertension Pharyngeal swelling Swollen tongue Throat irritation Tongue pruritus

Symptomtext

Anaphylaxis; This is a spontaneous report from a two contactable consumer (patient and office assistant). A 44-year-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EN6208), via an unspecified route of administration in left arm on 12Mar2021 at 18:30 as a single dose for COVID-19 immunization. Medical history included hypothyroidism, bipolar and high blood pressure. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. It was unknown if patient had covid prior vaccination. Concomitant medication included lamotrigine (LAMICTAL), levothyroxine (MANUFACTURER UNKNOWN), amlodipine (MANUFACTURER UNKNOWN) and glucosamine (MANUFACTURER UNKNOWN). On 12Mar2021 at 18:45, the patient experienced anaphylaxis. It was reported that patient visited emergency room/department or urgent care. The patient took Benadryl and 2 epinephrine shots as a treatment. It was reported that COVID test was not done after post vaccination. The outcome of the event was resolved on Mar2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bipolar disorder; Blood pressure high; Hypothyroidism
Andere Medikamente: LAMICTAL; LEVOTHYROXINE; AMLODIPINE; GLUCOSAMINE
Allergien: -
Vorherige Impfungen: -

VAERS 1097835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IL
Alter: 44,0
Geschlecht: F
Eingang: 31.03.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Anaphylactic reaction Hypertension Pharyngeal swelling Swollen tongue Throat irritation Tongue pruritus

Symptomtext

Anaphylaxis; This is a spontaneous report from a two contactable consumer (patient and office assistant). A 44-year-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EN6208), via an unspecified route of administration in left arm on 12Mar2021 at 18:30 as a single dose for COVID-19 immunization. Medical history included hypothyroidism, bipolar and high blood pressure. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. It was unknown if patient had covid prior vaccination. Concomitant medication included lamotrigine (LAMICTAL), levothyroxine (MANUFACTURER UNKNOWN), amlodipine (MANUFACTURER UNKNOWN) and glucosamine (MANUFACTURER UNKNOWN). On 12Mar2021 at 18:45, the patient experienced anaphylaxis. It was reported that patient visited emergency room/department or urgent care. The patient took Benadryl and 2 epinephrine shots as a treatment. It was reported that COVID test was not done after post vaccination. The outcome of the event was resolved on Mar2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bipolar disorder; Blood pressure high; Hypothyroidism
Andere Medikamente: LAMICTAL; LEVOTHYROXINE; AMLODIPINE; GLUCOSAMINE
Allergien: -
Vorherige Impfungen: -

VAERS 1148571

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

schwer

Staat: WA
Alter: 54,0
Geschlecht: F
Eingang: 30.03.2021
Impfdatum: 30.03.2021
Beginn: 30.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Cold sweat Diarrhoea Dizziness Loss of consciousness Nausea Syncope

Symptomtext

fainted a couple of mins, regained consciousness but feeling light headed, nauseated reported a cold sweat. had diarrhea. was not still feeling well so 911 called and was taken to a hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no known medical conditions
Vorgeschichte: n/a
Andere Medikamente: no medications
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1148313

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MA
Alter: 53,0
Geschlecht: F
Eingang: 30.03.2021
Impfdatum: 18.03.2021
Beginn: 18.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Dizziness Flushing Presyncope

Symptomtext

dizziness, lightheadedness, flushing to chest and face, pre-syncope, BP 190/100

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hx of HTN - on lisinopril
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1146401

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN-6208

schwer

Staat: VA
Alter: 54,0
Geschlecht: F
Eingang: 30.03.2021
Impfdatum: 29.03.2021
Beginn: 30.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Headache Injection site pain Insomnia Nasopharyngitis Pain Peripheral coldness Syncope

Symptomtext

12:30 AM - minor headache, body aches, trouble sleeping, pain at injection site 2:30 AM - freezing cold hands, cold feet and body, minor headache, body aches, trouble sleeping, pain at injection site 6:30 AM - minor headache, body aches, trouble sleeping, fainting, pain at injection site

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Sudden hearing loss in right ear, vertigo
Vorgeschichte: N/A
Andere Medikamente: Fish oil, Vitamin D
Allergien: N/A
Vorherige Impfungen: -

VAERS 1141189

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: ME
Alter: 56,0
Geschlecht: F
Eingang: 28.03.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Blood test normal Confusional state Electrocardiogram normal Fatigue Head discomfort Impaired driving ability Loss of consciousness Mental impairment Road traffic accident Somnambulism

Symptomtext

blacked out or fell asleep while driving to work the next morning which resulted in a car accident; no recall of driving; extreme confusion during the day. Heaviness in head for several days; fatigue for several days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 1,0
Labordaten: taken by ambulance to the emergency room where I received an EKG and blood work and monitoring; results were fine and I was released
Aktuelle Erkrankungen: no
Vorgeschichte: chronic migraines
Andere Medikamente: Relpax topiramate Lexapro
Allergien: no
Vorherige Impfungen: -

VAERS 1140955

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: WA
Alter: 68,0
Geschlecht: F
Eingang: 27.03.2021
Impfdatum: 20.03.2021
Beginn: 21.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Arthralgia Erythema Headache Monoplegia Pain in extremity Paralysis

Symptomtext

Paralysis of arm and hand on side (L) where vaccine was administered. Extreme pain (Fire -like) shooting up and down the leg on the opposite side (R) with very bad joint pain. This went off & on through the night/early morning in the first 22 hrs after vaccination. Woke with most pain gone, L hand red and sore, minor headache. Through out the following week I have experienced difficult pain and instability of some joints.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paralysis
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Diagnosed with a connective tissue disorder years ago, EDS, probably Raynauds too Symptomatic PVC?s Varicose Veins
Andere Medikamente: Vitamin C, D, B complex, zinc Diosmin, Nattokinnase Prozac 20mg
Allergien: Penicillin, seemingly react to supplements that are not yeast free, vitamin K causes circulatory problems
Vorherige Impfungen: -

VAERS 1139570

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IA
Alter: 61,0
Geschlecht: F
Eingang: 27.03.2021
Impfdatum: 23.03.2021
Beginn: 23.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Aphasia Asthenia Chest X-ray normal Computerised tomogram head normal Electrocardiogram QT prolonged Electrocardiogram abnormal Feeling abnormal Nervousness Paralysis Rash Similar reaction on previous exposure to drug Sinus arrhythmia Syncope

Symptomtext

Pfizer COVID-19 Vaccine EUA Patient presents 3/23/21 for medical monitoring of syncopal episode s/p COVID - 19 vaccine # 2. Lowered to the floor by vaccine staff. Patient reports symptoms of weakness, other wise states she ""feels fine"". Two additional syncopal episodes witnessed by myself when patient attempts to change position. Past medical history is significant for mild persistent allergic asthma, pre-diabetes, OSA, obesity and BPPV. Patient reports history of same reaction s/p previous vaccine. At a approximately 0837 patient was noted to have a worsening rash present to her face. EpiPen administered via left lateral thigh at 0838. EMS called to transport patient the ED for further evaluation. Treatment administered: epipen (lot 0FM406, exp 02/22) left lateral thigh at 0838. Upon arrival to the ED, patient's temperature is 98.8? F, heart rate 92-103, respiratory rate 30, saturating 99% on room air with blood pressure 164/91. The patient's laboratory studies were largely unremarkable. While in the ED, the nurse was getting ready to get the patient up to the commode when the patient started to ""not feel right again."" She asked her to administer the medications for allergic reaction and reports wall the 2nd medication was being infused, she felt paralyzed and unable to talk, although she was able to hear everything and was aware, she was unable to move or speak for a short amount of time. CT head with completed at this time and showed no acute intracranial findings. Chest x-ray unremarkable. EKG showed normal sinus rhythm with sinus arrhythmia, heart rate 80 and prolonged QT at 470. The patient was administered Solu-Medrol 125 mg IV, Pepcid 20 mg IV, Benadryl 50 mg IV, normal saline 1 L IV. Pt was admitted to hospital for observation. The patient was seen on the unit laying in bed with her husband at the bedside. She reports that she is feeling slightly better and hungry and has never felt at paralyzed/unable to speak feeling before and is very nervous about this. She was wondering if she had a seizure, although she reports feeling aware the entire time and did not lose bowel or bladder function. We discussed that that is not typical for a seizure, but even if we did an EEG at this time, it would not be able to tell us what occurred in the past. We discussed continue the Benadryl, Pepcid, and IV steroids for today and likely decreasing them tomorrow. We discussed the workup of syncopal episodes as well. The patient and her husband were agreeable to this plan. Patient was discharged from the hospital on 03/24/2021 in a stable medical condition. Patient was instructed to follow-up with her PCP in 1 week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paralysis
Hospital-Tage: 1,0
Labordaten: See above
Aktuelle Erkrankungen: -
Vorgeschichte: Allerghic rhinitis Benign paroxysmal positional vertigo GERD Obesity OSA Osteoarthritis of hip Prediabetes Asthma
Andere Medikamente: Albuterol 2 puffs inh PRN Azelastine 2 sprays BID Symbicort inh BID Clonazepam 0.5 mg TID PRN Diphenhydramine 25 mg PO PRN Meclizine 25 mg PO TID PRN Montelukast 10 mg PO QHS Omeprazole 20 mg PO BID
Allergien: Formaldehyde topical - unknown Sulfa drugs - unknown
Vorherige Impfungen: -

VAERS 1138535

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CO
Alter: 54,0
Geschlecht: M
Eingang: 26.03.2021
Impfdatum: 26.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Dizziness Hyperhidrosis Loss of consciousness

Symptomtext

Light headed and dizzy, sweating, passed out briefly. 15 seconds. This was 45 minutes after getting injection. I did not have trouble breathing or swallowing. Very similar to what has happened to me sometimes getting blood drawn but happens at time of appointment not after. Reclined, deep breaths and started to feel better within 10 minutes. An hour later feeling much better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: High Cholesterol
Andere Medikamente: Fluoxetine, Simvastatin
Allergien: Sumac
Vorherige Impfungen: -

VAERS 1137985

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: WI
Alter: 52,0
Geschlecht: M
Eingang: 26.03.2021
Impfdatum: 11.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

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

Ageusia Bell's palsy Ear discomfort Eyelid disorder Facial paralysis Headache Hyperacusis Lacrimation increased Sensory loss

Symptomtext

Patient was diagnosed with Bells Palsy. On 3/15/21, patient noticed loss of taste and a sensation in his tongue. On 3/16/21, patient had right sided facial paralysis with some right ear discomfort, right eyelid drooping, right upper temple headache, sensitivity to sounds, and right eye only able to be open halfway. Patient also states that his right eye was watery. He denies a mouth droop. Patient went to urgent care on 3/16 and he was prescribed Prednisone. On 3/18, patient went to see his primary care physician and was prescribed an antiviral. He has not had any new or worsening symptoms since 3/18 pm, but he has not seen much improvement in symptoms either. He describes a small improvement in taste.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1137745

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 39,0
Geschlecht: M
Eingang: 26.03.2021
Impfdatum: 11.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal pain Blood test normal Chills Constipation Dizziness Facial paralysis Fatigue Flank pain Heart rate irregular Hypoaesthesia Lymphadenopathy Magnetic resonance imaging head Pain Pyrexia

Symptomtext

Within an hour of the shot, started feeling dizzy. Intense fatigue and full body aches set in within 3 hours. Facial numbness and left-side facial drooping began within 8 hours. Low fever, chills, heavy heart beat, and intermittent cramps of the abdomen and on the left side (between hip and rib cage) began within 18 hours. Swollen lymph nodes in the neck and constipation began within 48 hours. At ~4 days since the first shot, the facial numbness, heavy heart beat, and fatigue persisted, though the drooping became less prominent and the other symptoms have largely resolved. At ~2 weeks since the first shot, the facial numbness has been constant, but varying in intensity, and the left-side facial drooping has returned multiple times.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: MRI of the head and blood work were ordered and performed. Given no prior history with these issues, the timing relative to the administration of the first vaccine shot, and the lack of findings from imaging and blood work, the symptoms appear to be vaccine-related.
Aktuelle Erkrankungen: None
Vorgeschichte: Moderate-high cholesterol
Andere Medikamente: Fish Oil, Turmeric, Lutein
Allergien: CT iodine contrast
Vorherige Impfungen: -

VAERS 1137006

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IN
Alter: -
Geschlecht: U
Eingang: 26.03.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: SYR / LA

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

Decreased appetite Dizziness Fatigue Rhinorrhoea Thrombosis

Symptomtext

Extreme fatigue, dizziness, lack of appetite increase in mucus, some blood clotting in mucus

Weitere VAERSDATA-Felder

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

VAERS 1136954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 26.03.2021
Impfdatum: 18.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Dizziness Face injury Loss of consciousness Nausea

Symptomtext

Awoke approx 6AM. Took daily synthroid went back to sleep woke up feeling nauseous and dizzy went to bathroom felt like I needed to sit down next I remember I woke up on the floor with cut over my left eye.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoporosis Hypothyroidism
Andere Medikamente: Synthroid Calcium + minerals Joint supplement Collagen Cranberry Probiotics
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1135872

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 17,0
Geschlecht: M
Eingang: 25.03.2021
Impfdatum: 25.03.2021
Beginn: 25.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Fall Syncope

Symptomtext

17 year old male had syncope episode with fall from seated position to floor with spontaneous regain of consciousness. 911 was called. Normal vital signs. Legs were elevated. Patient assessed by paramedics, PA and NP. Patient declined transport to hospital for further medical evaluation and was encouraged to seek medical care if symptoms worsened. Yes

Weitere VAERSDATA-Felder

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

VAERS 1134282

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: FL
Alter: 36,0
Geschlecht: M
Eingang: 25.03.2021
Impfdatum: 20.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Syncope

Symptomtext

Client had a syncope episode after receiving the vaccine. Client states he has a history of syncope after vaccination. 97.9 degrees, HR 68, BP 127/72. 1:30 pm asst. to BR, gait steady, no c/o dizziness, continued to wait in observation area. Allowed to leave at 2pm.

Weitere VAERSDATA-Felder

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

VAERS 1133338

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: FL
Alter: 62,0
Geschlecht: F
Eingang: 25.03.2021
Impfdatum: 23.03.2021
Beginn: 23.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Asthenia Atrioventricular block first degree Bacterial test positive Blood glucose normal Condition aggravated Dizziness Electrocardiogram abnormal Fatigue Full blood count normal Headache Hypertension Metabolic function test normal Pain Presyncope Protein urine present Urine analysis abnormal Vaccination complication

Symptomtext

Within 15-minutes of vaccination, the patient reported dizziness. EMS evaluated the patient on-site. The patient was hypertensive (175/97) with a FSBG of 152 mg/dl. EKG demonstrated NSR, rate 86bpm, no ST elevation. EMS transported the patient toEmergency Department for further evaluation. In the ED, the patient reported dizziness, lightheadedness, near-syncope, aching headache, generalized fatigue, and weakness. Physician administered 25mg PO Meclizine. Upon reevaluation, the patient reported improvement and was discharged with diagnoses of Vaccine reaction and Dizziness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: CBC/CMP (3/23): Unremarkable UA (3/23): 100 Protein, Few Bacteria EKG (3/23): NSR, rate 88bpm, 1st Degree AV block
Aktuelle Erkrankungen: None reported.
Vorgeschichte: Anemia, Anxiety, COPD, Asthma, DMII, CKD, Vertigo, HTN, HLD, Migraines, DJD, IBS
Andere Medikamente: Meclizine, Metoprolol, Gabapentin, Verapamil, Gabitril, Wellbutrin, Levalbuterol Tartrate, Dicyclomine, Advair, Simvastatin, Furosemide, Fioricet, Levothyroxine, Clonidine, Aspirin, Fenofibrate, Metoclopramide, Tramadol
Allergien: Tetracycline, Albuterol, Cleomycin, Clindaymycin, Spiria, Bleach, Gadolinium Contrast Medium, Cortisone, Iodine Contrast Medium
Vorherige Impfungen: -

VAERS 1131948

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: FL
Alter: 39,0
Geschlecht: M
Eingang: 25.03.2021
Impfdatum: 18.03.2021
Beginn: 18.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

Client passed out-Syncopal episode. Going to Hospital. BS-96, BP 80/40, HR 58, O2 97%.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: Passes out whenever he gets a shot.

VAERS 1417394

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 36,0
Geschlecht: F
Eingang: 24.03.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Electrocardiogram normal Nausea Opisthotonus Pallor Presyncope

Symptomtext

nausea, syncope sent to ED, not admitted Narrative: 35 yo FEMALE with a history of anaphylaxis to penicillin in her younger years, received her first shot of the Pfizer vaccine earlier today. Approximately 10 minutes after receiving the injection, she felt a sense of lightheadedness, associated with mild nausea, but no shortness of breath or difficulty swallowing. The next thing she knows, the nurses were standing at her side and she was on the floor. she was seen by the attending staff to look somewhat pale, and have a brief episode of arching of her back before she was lowered to the ground. She did not fall out of the chair onto the ground. There was no subsequent tonic-clonic activity, and the patient did not lose consciousness per the nursing staff in attendance. Concern for the possibility of anaphylaxis the staff administered epinephrine 0.3 mL intramuscular. Upon ED evaluation, the patient appeared to have had a mild vasovagal reaction to her injection. No evidence this was anaphylaxis. A 12-lead EKG was performed which revealed a normal sinus rhythm, with a ventricular rate of 69bpm. Intervals, durations and QRS axis were normal, with no diagnostic ST segments. With further observation there was no concerning symptoms and was discharged home.

Weitere VAERSDATA-Felder

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

VAERS 1131469

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NV
Alter: 46,0
Geschlecht: M
Eingang: 24.03.2021
Impfdatum: 17.03.2021
Beginn: 18.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Bell's palsy Laboratory test

Symptomtext

Bell's palsy predniSONE 20MG vaiACYclovir HCL 1GM Artifitial Tears Erythomycin

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: LABS
Aktuelle Erkrankungen: HIV/ DIABETES
Vorgeschichte: NONE
Andere Medikamente: PREZISTA/ RETONAVIR/ DESCOVY/ metFORMIN/ TORVASTATIN/ MULTIVATAMINS/ COLLAGEN
Allergien: NONE
Vorherige Impfungen: -

VAERS 1130782

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IA
Alter: 56,0
Geschlecht: M
Eingang: 24.03.2021
Impfdatum: 10.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Chest discomfort Cough Palpitations Pulmonary oedema Pyrexia

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA On 3/11/21, ran fever 103 to 104.5, coughing, some fluid in lungs, around evening time started heart palpitations and tightness pain in chest. As of 3/24/21 still have heart palpitations when doing yard work or light exercise. Tightness pain in chest area has gone away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: -
Labordaten: None, was told was normal for some patients who had covid prior.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Fluticasone Propionate Nasal Spray 50 mcg, Pravastatin 20mg, Montelukast Sodium 10mg, Losartan Potassium 50mg, Glucosamine HCI 1500 mg and 1200mg Chondroitin Sulfate (Cosamin DS), D3 5000 IU.
Allergien: None
Vorherige Impfungen: -

VAERS 1130378

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: OH
Alter: 46,0
Geschlecht: F
Eingang: 24.03.2021
Impfdatum: 19.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Syncope Unresponsive to stimuli

Symptomtext

This was this person's second dose. She had episode of syncope following the first dose that required prolonged monitoring in the EC. Patient was laid down on stretcher prior to vaccine administration. Patient immediately went syncopal following injection and became unresponsive. Breathing remained even and nonlabored with good pulse. Patient remained lying down for about 30 minutes before she sat in a chair for approximately 15 minutes. Attempt to have patient leave but patient became syncopal again in bathroom and needed to be assisted into wheelchair and brought back to observation area where she laid down for another 15 minutes. Patient was alternating back and forth between being alert and unresponsive. Patient was finally able to leave area with mother at 1719. Refused to be transferred to the Emergency Room for evaluation.

Weitere VAERSDATA-Felder

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

VAERS 1128477

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IN
Alter: 64,0
Geschlecht: M
Eingang: 24.03.2021
Impfdatum: 17.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: - / -

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

Abdominal discomfort Chills Hyperhidrosis Influenza like illness Loss of consciousness Nausea Vomiting

Symptomtext

Flu-like symptoms, sweating, chills, nausea, passed out twice during the first few hours after the onset of symptoms. Upset stomach, vomiting in the night. Felt better the next day and by the third day after the onset of symptoms felt recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Amlodipine 5 mg. daily
Allergien: None
Vorherige Impfungen: Shingrix vaccine, flulike symptoms but much, much milder. Age 64

VAERS 1128283

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 33,0
Geschlecht: M
Eingang: 24.03.2021
Impfdatum: 16.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Seizure

Symptomtext

Systemic: Seizure-Mild, Additional Details: Minor seizure lasted only briefly. Patient seemed unconcerned afterwards and informed pharmacy staff that he goes through this outcome after getting any type of vaccine.

Weitere VAERSDATA-Felder

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

VAERS 1128260

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

schwer

Staat: MA
Alter: 71,0
Geschlecht: M
Eingang: 24.03.2021
Impfdatum: 23.03.2021
Beginn: 23.03.2021
Tage bis Beginn: 0,0
Dosis: 2
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 1127584

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MD
Alter: 51,0
Geschlecht: F
Eingang: 23.03.2021
Impfdatum: 23.03.2021
Beginn: 23.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Paralysis

Symptomtext

Paralysis to bilateral hands for 2-3minutes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paralysis
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: Auto immune disorder Scleraderma
Andere Medikamente: Vitamin D, Vitamin C, Plaquenil Sulfasalazine
Allergien: NKA
Vorherige Impfungen: -

VAERS 1123633

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

schwer

Staat: -
Alter: 62,0
Geschlecht: F
Eingang: 22.03.2021
Impfdatum: 22.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Syncope

Symptomtext

syncopal episode shortly after receiving vaccine.

Weitere VAERSDATA-Felder

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

VAERS 1122587

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

schwer

Staat: KY
Alter: 50,0
Geschlecht: F
Eingang: 22.03.2021
Impfdatum: 22.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal discomfort Anxiety Dizziness Loss of consciousness Vomiting

Symptomtext

anxiety before receiving vaccine, received vaccine, felt sick to her stomach, lightheaded, passed out and vomited while unconscious and very diaphoretic

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Benadryl Claritin Flonase aspirin calcium tumriac fish oil
Allergien: sulfa antibiotics
Vorherige Impfungen: -

VAERS 1122548

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: KY
Alter: 34,0
Geschlecht: F
Eingang: 22.03.2021
Impfdatum: 12.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Deep vein thrombosis Limb discomfort Peripheral swelling

Symptomtext

Saturday night (3/13/21) and into Sunday morning (3/14/21), patient began feeling discomfort in lower right leg. Discomfort and feeling of swelling continued through Sunday evening. Monday (3/15/21) patient began using compression stocking and elevating leg, which eased some discomfort. Slight swelling, discomfort, and heat in the leg continued throughout entire week. DVT presumed. Contacted physician. Treatment for DVT and treatment dosage (Fondaparinux 7.5mg) commenced Wednesday (3/17/21) through to date. Discomfort has dissipated but slight swelling still remains. Appears to be getting better each day, although a very slow progression. Patient history of antiphospholipid syndrome has been managed for over fifteen years with blood thinners. Onset of a clotting event always followed a justifiable cause. No spontaneous/unexplainable clotting events to date. Patient otherwise healthy without any other current event which could explain a blood clot following vaccination. Reporting this information as it may be helpful in determining whether persons with APS or similar condition should receive Covid-19 vaccination. Note: this information being provided by patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Visual exam
Aktuelle Erkrankungen: -
Vorgeschichte: Antiphospholipid Syndrome
Andere Medikamente: Eliquis 5mg tablet
Allergien: Heparin
Vorherige Impfungen: -

VAERS 1120928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge En6208

schwer

Staat: CA
Alter: 47,0
Geschlecht: F
Eingang: 21.03.2021
Impfdatum: 19.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Anaphylactic reaction Condition aggravated Parosmia Pharyngeal swelling Swollen tongue

Symptomtext

Prior to the shot, my idiopathic anaphylaxis has been in remission. Since the shot, my throat and tongue have been swollen. I cannot be around certain smells because my tongue and throat start to swell.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Non
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma; celiacs disease; idiopathic anaphylaxis;
Andere Medikamente: Allegra (4 180 MG); montelukast (10 MG); Focalin XR 10 MG; probiotic; multivitamin
Allergien: Sesame, NSAIDS; Flaxseed; quinoa; almond, cloves; radishes; avocado, peanuts
Vorherige Impfungen: -

VAERS 1120294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: LA
Alter: 51,0
Geschlecht: F
Eingang: 21.03.2021
Impfdatum: 11.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / RA

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

Blood magnesium normal Blood phosphorus normal Cold sweat Computerised tomogram head Diarrhoea Fatigue Feeling abnormal Feeling cold Full blood count normal Head injury Hypotension Leukocytosis Loss of personal independence in daily activities Metabolic function test Nausea Pallor Pyrexia Skin laceration

Symptomtext

The day after the vaccine, pt experienced typical side effects of fatigue and fever that was controlled by Tylenol. The fatigue was extreme and has continued to present day. Also, she has inability to focus and concentrate. She is nauseated daily intermittently. The main complication was in post vaccination day 5, she felt worse than before. Vertigo, nausea, extreme fatigue and inability to perform ADLs and spent most of the day in bed. Approximately 1 am the next morning she woke me, cold, clammy and pale collapsing on the side of the bed with a feeling of impending doom after having diarrhea saying ?something is really wrong.? She went back to the toilet, but had a syncopal episode from standing where she fell straight and flat on her back with no attempt to break her fall. She hit her head on the marble floor and shoe molding. She was unresponsive for 10-20 seconds with no palpable pulse or visible respiratory effort before becoming arousable. She was groggy, but oriented to person and place. She was amnestic for the event. She had an approximately 6 inch full thickness laceration to her posterior scalp that required staples. I took her BP- 85/56, pulse 50, respirations were normal. Ambulance called. Mild hypotension that responded to fluid bolus. CT of head was negative and other than non-specific leukocytosis, labs were normal (CBC, CMP, TFTs, Mg and PO4).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: 3/17/21- see above
Aktuelle Erkrankungen: Hypertension Peri menopausal
Vorgeschichte: Hypertension Peri menopause Anxiety
Andere Medikamente: Losartan 100 mg, Amlodipine 5 mg, Toprol XL 25 mg- all of these are daily. Takes Toprol as needed. Standard women?s MVI Sumatriptan 25 mg as needed- none in several months. Fiorcet as needed- none recently Alprazolam- 0.25 mg as needed. Tak
Allergien: Reglan- dysphoria NSAIDS- hives
Vorherige Impfungen: -

VAERS 1118510

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 29,0
Geschlecht: M
Eingang: 20.03.2021
Impfdatum: 20.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Dizziness Heart rate increased Pallor Syncope Visual impairment

Symptomtext

Patient reported fast heartbeat, sweating. Patient was pale, HR 112, O2Sat 96%, BP 108/60, reported feeling dizzy, vision changes, had brief moment of syncope, then aroused, Oxygen applied at 2l via NC, patient continued with sweating, HR now 78, EMS called, patient continued with sweating and feeling weak gradual improvement, EMS arrived, patient evaluated and did not want to go to ER for eval. Vitals rechecked and patient ambulated to private vehicle with no further difficulty.

Weitere VAERSDATA-Felder

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

VAERS 1117478

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

schwer

Staat: CA
Alter: 63,0
Geschlecht: F
Eingang: 19.03.2021
Impfdatum: 12.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Bell's palsy Blood test Computerised tomogram head Facial paralysis Hypoaesthesia oral Hypoaesthesia teeth Lagophthalmos Mastication disorder

Symptomtext

I was vaccinated on Friday morning. Everything seemed OK. On the next day Saturday, I felt some numbness on me left upper lip and right tooth. The numbness increased and changed to my left face paralysis. I could not chew or close my left eye totally. My husband brought me to the ER on Tuesday morning. They diagnosed that I had peripheral Bell's palsy and gave prescription to me with antivirus medicine, prednison, eye oilment and eye drops, and shield to cover my left eye while I go to sleep. Today is Friday, one week after I got vaccinated. I also go to get acupuncture.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: CT of the brain. Blood work (at ER on Tuesday 03/16/2021
Aktuelle Erkrankungen: none
Vorgeschichte: Diabetes, Hypertension, Obesisty, Insomia.
Andere Medikamente: Metformin 1000 mg bid. Januvia 100 mg qd, Propanolol 20 mg bid, Olmesartan 40 mg qd.
Allergien: none
Vorherige Impfungen: -

VAERS 1117259

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MA
Alter: 29,0
Geschlecht: F
Eingang: 19.03.2021
Impfdatum: 15.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Hyperhidrosis Hypotension Incontinence Loss of consciousness Nausea Syncope

Symptomtext

Patient reported history of queasiness after injection. Patient fell weak, diaphoretic after injection. Patient was escorted to a chair when she fainted and became unconscious for approximately 1 minute, had an episode of incontinence. EMS service was ordered. Patient's BP was recorded by the EMS and was hypotensive. Patient refused to go to ER and was escorted to the car where her family member was waiting to take her home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Unknown
Allergien: No
Vorherige Impfungen: -

VAERS 1114415

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

schwer

Staat: CA
Alter: 21,0
Geschlecht: M
Eingang: 19.03.2021
Impfdatum: 14.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Fall Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Medium, Additional Details: patient fainted and fell from the chair he was sitting while being obeserved. after a few minutes, he woke up by him self and got up by himself.when i (rph at the store) got there,he was awake and able to talk to me .i took his blood pressure and it was normal and oxygen sat was also normal.we advised him to contact his pcp asap and fainted again and go to er.

Weitere VAERSDATA-Felder

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

VAERS 1112723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: ME
Alter: 24,0
Geschlecht: F
Eingang: 18.03.2021
Impfdatum: 18.03.2021
Beginn: 18.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Syncope

Symptomtext

Patient fainted after immunization.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: BP after 20 minutes 110/70
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1112167

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN 6208

schwer

Staat: -
Alter: 36,0
Geschlecht: M
Eingang: 18.03.2021
Impfdatum: 18.03.2021
Beginn: 18.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood glucose normal Dizziness Dyspnoea Hyperhidrosis Loss of consciousness Somnolence Unresponsive to stimuli Visual impairment

Symptomtext

Pt. Found unresponsive in observation chair. Attempted sternal rub. Pt. Unconscious ~ 30 seconds, disoriented when finally awoke. Within 1-2 minutes, pt. was able to be re-oriented. EMS called. Pt. Became diaphoretic, stating that he was having a hard time getting air. Pt. Placed on 6L non-rebreather. Pt. Transferred to stretcher without issue. Pt. Able to have normal conversation. Per pt, he often faints when having blood drawn. Pt. Only ate a banana prior to getting his vaccine, pt. Normally has a more robust breakfast. After EMS arrival, VS remained stable. Per EMS BG normal. EMS attempted to get patient to sit up, pt again became increasingly diaphoretic and less responsive/drowsy. Pt. Stated he felt dizzy and was seeing white spots. Pt. Transferred to EMS stretcher and taken to ED. 1009: HR 56, RR 18, BP 129/83, SpO2 93% 1015: HR 59, RR 20, BP 115/80, SpO2 98%

Weitere VAERSDATA-Felder

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

VAERS 1110716

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NY
Alter: 47,0
Geschlecht: M
Eingang: 18.03.2021
Impfdatum: 18.03.2021
Beginn: 18.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chest discomfort Hyperhidrosis Syncope

Symptomtext

Pt. was monitored for 15 minutes after receiving the first dose of the COVID-19 vaccine, Pfizer. Complained of chest discomfort, tightness, diaphoresis, and syncope when attempting to stand. HR was 166 at initial presentation, BP was 117/75, SPO2 98% on room air, R 18 equal and unlabored.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hypertension
Vorgeschichte: Chronic Hypertension
Andere Medikamente: Norvasc, Lopressor, Lisinopril, Nexium, Naltrexone
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1110043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: FL
Alter: 49,0
Geschlecht: M
Eingang: 18.03.2021
Impfdatum: 16.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Fear of injection Hyperhidrosis Syncope

Symptomtext

11:06 am Experience syncope episodes after receiving vaccine. Vital signs BP 102/55, HR 65. Sweaty and dizzy (afraid of needles). BP 127/75, HR 73, O2 sat 99 RA Accucheck 103. Client request to go home w/ spouse. Cleared by EMT.

Weitere VAERSDATA-Felder

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

VAERS 1107510

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: PA
Alter: 47,0
Geschlecht: M
Eingang: 18.03.2021
Impfdatum: 13.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Bell's palsy Dysarthria Eye disorder Facial paralysis Headache Hypoaesthesia Swelling face Swollen tongue

Symptomtext

Patient presented tot he hospital Emergency Department with right side facial numbness and drooping. Patient was initially screened as a stroke patient but it was ultimately diagnosed as Bell's Palsy. Patient was treated and discharged home.

Weitere VAERSDATA-Felder

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

VAERS 1109064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: ME
Alter: 31,0
Geschlecht: F
Eingang: 17.03.2021
Impfdatum: 17.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

No pain at the time of injection, but fainted after returning to sit outside. After about twenty minutes, with fluids and a snack kindly provided by the pharmacy staff, recovered quickly.

Weitere VAERSDATA-Felder

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

VAERS 1108460

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IN
Alter: 67,0
Geschlecht: F
Eingang: 17.03.2021
Impfdatum: 16.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Anaphylactic reaction Cough Pruritus Wheezing

Symptomtext

67 year old female with PMH of HTN, HFpEF, history of DVT, obesity, migraines, gastroparesis, Sicca symptoms, asthma, chronic bronchitis, and GERD who presents with anaphylactic reaction s/p COVID vaccine administration. Received COVID vaccine across the street (<1 minute EMS ride) C/o itching, cough, and wheezing shortly after No respiratory distress or hypoxia en route Received IM epi (2 weeks expired) and Benadryl PTA Symptoms improving now Has extensive allergy list Review of Systems 10 point ROS completed and negative except noted in HPI above Physical Exam/Objective Vitals & Measurements last 24 hours VITAL SIGNS Temp C: 36.3 DegC Heart Rate: 87 bpm Resp Rate: 16 br/min BP #1: 139 / 59 mmHg SpO2 (%): 99 % O2 Device: Room air Height CM: 152.4 cm Ideal Body Weight: 45.5 kg General: NAD, well-nourished Eyes: No scleral icterus, EOMI HENT: Normocephalic, atraumatic, no airway edema Neck: Supple, intact range of motion Respiratory: Lungs CTAB, symmetric chest wall expansion, no wheezes, speaking in full sentences Cardiovascular: RRR, no murmur, +2 peripheral pulses Abdomen: Soft, NTTP, non-distended Musculoskeletal: No gross deformity Integumentary: Intact, warm, dry, no rashes Neurologic: A&O x 3, no focal deficits Psychiatric: Cooperative, appropriate mood and affect Medical Decision Making 67 year old female with extensive PMH including asthma, chronic bronchitis, and GERD who presents with anaphylactic reaction s/p COVID vaccine administration. Has long list of allergies. On exam, airway intact, no respiratory distress, no wheezing, speaking in full sentences, C/o subjective itching and cough that is starting back up. IV methylprednisone IV famotidine Albuterol PRN Benadryl PRN Observe Rx EpiPen upon discharge Re-Assessment Observed for >4 hours Symptoms resolved Counseled patient on EpiPen use and gave strict return precautions Has albuterol and Benadryl in her purse Has had many reactions in the past and is very familiar with how to manage them Discharge home with daughter

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: see above
Aktuelle Erkrankungen: see ED notes
Vorgeschichte: see ED notes
Andere Medikamente: Abaloparatide, aspirin, cevimeline, cholecalciferol, clonazepam, cyanocobalamin, cyclosporine opthalmic, diltiazem, duloxetine, erenumab, famotidine, furosemide, levealbuterol, metoprolol, multivitamin, pantoprazole, potassium chloride, pra
Allergien: "artificial sweetners", Avelox, azithromycin, baclofen, Bextra, Ceftin, codeine, Compazine, contrast dye, Darvocet N, Duricef, Forradil,erythromycin, Keflex, latex, lisinopril, Lorcet, NSAIDS, nuts, peanuts, penicillin, povidone iodine, Prnivil, shellfish, Skelzsin, sulfa, Toradol, Ultram, vancomycin, Vicodin, Xolair, Zestril
Vorherige Impfungen: -

VAERS 1107927

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: VA
Alter: 67,0
Geschlecht: M
Eingang: 17.03.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
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

Member had a syncope episode/ vasovagal immediately following the vaccine administration while sitting in the chair. He immediately recovered after the episode and was AAOx3 when transferred to urgent care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: CAD and high cholesterol
Vorgeschichte: -
Andere Medikamente: unknown
Allergien: PCN
Vorherige Impfungen: -

VAERS 2554306

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 50,0
Geschlecht: M
Eingang: 16.03.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
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 abnormal Dizziness Hyperhidrosis Presyncope Pruritus

Symptomtext

diaphoretic Narrative: Pt received 1st dose of Pfizer COVID-19 vaccine on 3/12/21 at 10:15 AM. Within 12 mins, the pt c/o feeling diaphoretic, dizzy, itchy. Pt does not have HX of allergic reaction previously. On exam: SLBP is 83/53, HR=54. alert, awake, orientated. Given Epi Pen 2 dose IM, Benadryl IM injection, Famotidine IM. Called 911 to transfer pt to ED at Emergency Room. When rechecking BP before transfer was BP 106/62 P-59 - at the recheck pt states he felt better. Per the ED note: The medics find him with stable vital signs and he arrives here otherwise asymptomatic. No wheezing. No tongue swelling. No drooling. No other recent active illness. Does not routinely take other medications and is unaware of other allergic reaction history. The ED provider stated "This patient presents with a brief bout of diaphoresis and change of blood pressure approximate 30 minutes after receiving his Covid vaccination. I believe this to be less likely an acute allergic reaction more likely to be some type of vagal event. He is remain stable throughout his stay here and is currently stable for outpatient management. No evidence of anaphylaxis or other emergent allergic issue."

Weitere VAERSDATA-Felder

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

VAERS 1106432

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 25,0
Geschlecht: M
Eingang: 16.03.2021
Impfdatum: 16.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Immediate post-injection reaction Limb injury Seizure Syncope

Symptomtext

10:00 am client received his COVID19 vaccination. Immediately the client fainted and fell out of his chair on his left shoulder. He did not hurt his head. Client was lying flat on the floor and then started having seizures and was placed on his left side. Episode lasted 3 seconds. Client was able to answer questions and alert and oriented x 4 and no complaints of pain or discomfort. 10:07 1st vitals taken. 10:09 am client stood up and walked to observation area. Client was under observation for 30 minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: 1st Vitals taken at 10:07 am - BP 134/80, HR 90, and O2 - 98% 2nd Vitals taken at 10:15 am. - BP - 124/82, HR 65, and O2 - 99%
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: No. However, client stated he took 2 CBD gummies to calm him, and taken a few sips of Monster energy drink of white color with no color and no carbs.
Allergien: None.
Vorherige Impfungen: -

VAERS 1105906

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN 6208

schwer

Staat: CA
Alter: 21,0
Geschlecht: F
Eingang: 16.03.2021
Impfdatum: 16.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Dizziness Electrocardiogram Fear of injection Syncope

Symptomtext

Pt with mom states she feels dizzy and faint. While with EMS on site, pt states her chest felt tight. Mom at beside with pt.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: BP 89/49 HR 55 02% 100 on RA Pt placed on gurney from wheelchair. BP 94/54 HR 73, O2 100% on RA Pt talking and laughing. Said she was very nervous and afraid of needles. 13:00 BP 95/62 HR 66 98% RA 12 Lead EKG NSR
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: Pt's mom states she sometimes takes and anxiety med that was prescribed to her when her grandma died. She doesnt have name.
Allergien: NONE
Vorherige Impfungen: -

VAERS 1105597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN 6208

schwer

Staat: CA
Alter: 35,0
Geschlecht: F
Eingang: 16.03.2021
Impfdatum: 13.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Presyncope

Symptomtext

Slumped over after receiving vaccine. Hx vasovagal with previous vaccines. Pt evaluated by MD & EMTs, DC home in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: None
Vorgeschichte: rNone
Andere Medikamente: None
Allergien: NONE
Vorherige Impfungen: unknown, provides history after the fact.

VAERS 1105476

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 24,0
Geschlecht: M
Eingang: 16.03.2021
Impfdatum: 16.03.2021
Beginn: 16.03.2021
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 Loss of consciousness

Symptomtext

Client stated that he was waiting in observation and told his father he felt dizzy at which time he closed his eyes and passed out per his father for approximately ten seconds. Onsite paramedics responded and evaluated client. Client released to go AMA and advised to go emergency services.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: BP: 111/71 HR: 77 RR:17 glucose: 113
Aktuelle Erkrankungen: none
Vorgeschichte: asthma
Andere Medikamente: none
Allergien: peanuts and hydroxyzine injection
Vorherige Impfungen: -

VAERS 1104787

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: PA
Alter: 27,0
Geschlecht: F
Eingang: 16.03.2021
Impfdatum: 12.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / LA

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

Blood pressure decreased Dizziness Erythema Nausea Ocular hyperaemia Skin discolouration Skin warm Syncope

Symptomtext

Warm and red skin, bloodshot eyes, dropping blood pressure, fainting, dizziness, nausea, purple feet

Weitere VAERSDATA-Felder

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

VAERS 1104041

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: PA
Alter: 22,0
Geschlecht: M
Eingang: 16.03.2021
Impfdatum: 13.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Alanine aminotransferase increased Anion gap normal Aphasia Aspartate aminotransferase normal Basophil count decreased Blood albumin decreased Blood alkaline phosphatase normal Blood bilirubin decreased Blood calcium normal Blood chloride increased Blood creatinine increased Blood glucose normal Blood lactic acid normal Blood magnesium normal Blood phosphorus normal Blood potassium normal Blood sodium increased Blood urea decreased

Symptomtext

SARS-CoV-2 / COVID-19 mRNA IM (Pfizer-BioNTech) Date Status Dose VIS Date Route Site Manufacturer Lot# Given By Verified By 3/13/2021 Given 0.3 mL EUA 12/2020 IM RD Pfizer, Inc EN6208 RN --

Weitere VAERSDATA-Felder

Praegender Schweregrund: Psychogenic seizure
Hospital-Tage: -
Labordaten: POC Glucose 98 POC Glucose CHEM PROFILE Sodium 141 147 Sodium Potassium 3.6 3.5 Potassium Chloride 108 122 Chloride CO2 16 19 CO2 Anion Gap 17 6 Anion Gap BUN 8 8 BUN Creatinine 1.27 0.79 Creatinine Glucose, Random 105 86 Glucose, Random Calcium 9.2 8.8 Calcium CORRECTED CALCIUM 9.3 CORRECTED CALCIUM AST 11 AST ALT 41 ALT Alkaline Phosphatase 76 Alkaline Phosphatase Total Protein 6.3 Total Protein Albumin 3.4 Albumin TOTAL BILIRUBIN 0.28 TOTAL BILIRUBIN eGFR 80 127 eGFR Phosphorus 3.7 Phosphorus Magnesium 2.0 Magnesium OTHER CHEM LACTIC ACID 6.4 1.5 LACTIC ACID CBC WBC 12.30 14.11 WBC Red Blood Cell Count 5.37 4.36 Red Blood Cell Count Hemoglobin 16.7 13.7 Hemoglobin HCT 51.0 40.7 HCT MCV 95 93 MCV MCH 31.1 31.4 MCH MCHC 32.7 33.7 MCHC RDW 11.9 11.9 RDW Platelet Count 324 232 Platelet Count MPV 10.6 10.8 MPV nRBC 0 nRBC DIFFERENTIAL Neutrophils % 79 Neutrophils % Immat GRANS % 0 Immat GRANS % Lymphocytes Relative 19 Lymphocytes Relative Monocytes Relative 2 Monocytes Relative Eosinophils 0 Eosinophils Basophils Relative 0 Basophils Relative Immature Grans Absolute 0.05 Immature Grans Absolute Absolute Neutrophils 9.64 Absolute Neutrophils Lymphocytes Absolute 2.32 Lymphocytes Absolute Absolute Monocytes 0.26 Absolute Monocytes Absolute Eosinophils 0.01 Absolute Eosinophils Basophils Absolute 0.02 Basophils Absolute OTHER DRUGS TOPIRAMATE LEVEL 7.4 TOPIRAMATE LEVEL DIABETES POC Glucose 98 POC Glucose T& B LYMPHOCYTES nRBC 0 nRBC EEG Video Monitoring 24 Hour Status: Final result EEG Video Monitoring 24 Hour Status: Final result Visible to patient: Yes Next appt: 04/03/2021 at 01:40 PM in Family Medicine (COVID VACCINE RESOURCE) Details Reading Physician Reading Date Result Priority MD 3/14/2021 Routine Narrative & Impression Continuous Video EEG Long Term Monitoring Date performed: 3/13-3/14/2021 Referring Provider: DO Report date: 3/14/2021 Study type: Continuous video EEG, up to 24 hours ICD 10 diagnosis: Spells/Fit NOS, Seizures R56.9 and Functional neurological symptoms disorder, with seizure F44.5 Start time: 3/13/2021 23:49 End time: 3/14/2021 15:07 Patient History: Patient is 22 y.o. male on continuous video EEG monitoring for the assessment of seizures, characterization of events, and effect of treatment. Patient has presumed epilepsy and nonepileptic psychogenic seizures. He started to have a cluster of seizures after getting COVID19 vaccine. Current AEDs: Medications include: Facility-Administered Medications Ordered in Other Visits Medication Dose Route Frequency Provider Last Rate ? acetaminophen 650 mg Oral Q6H PRN, DO ? fluticasone 1 spray Nasal Daily PRN, DO ? gabapentin 400 mg Oral TID, DO ? hydrOXYzine HCL 25 mg Oral Q6H PRN, DO ? ibuprofen 800 mg Oral Q8H PRN, DO ? levETIRAcetam 1,500 mg Oral Q12H SCH, DO ? sertraline 50 mg Oral Daily, DO ? topiramate 150 mg Oral TID, DO Description of Procedure: A 24 hours continuous video EEG was performed with electrodes applied using the International 10-20 System at least 16 channels are reviewed and formatted into longitudinal bipolar, transverse bipolar, and referential (to common reference or calculated common reference) montages. Additional electrodes used included T1, T2, and extraocular electrodes, and ECG, along with video recording. The EEG was recorded with the patient awake, drowsy, and asleep state. This study was intermittently monitored by a monitoring technologist. The physician interpreting the study had access to the data throughout the recording. The recording was technically satisfactory. Findings: Background Activity: The background is grossly symmetric with respect to voltages and activities. During wakefulness, the background is extremely low voltage, but appears to be organized with diffuse extremely low amplitude beta and alpha activity. There is a symmetric very low voltage 8-8.5 Hz posterior dominant rhythm. Drowsiness is characterized by attentuation of the alpha rhythm, prominent anterior beta activity, central theta activity, roving eye movements, positive occipital sharp transients of sleep (POSTS) and vertex waves. Stage 2 sleep is characterized by symmetric sleep spindles and K-complexes. Other findings: The single lead ECG shows a regular and sinus rhythm. Events: Event 1 - nonepileptic 10:07 - patient was receiving routine nursing care. He is looking for the event button. Then he asked the nurse if she could push the event button because he feels that he is about to have a seizure. (he has a child-like prosody.) He leans back on his left side, becomes very stiff, hands go into a "claw-like" position and rigid with rapid low amplitude shaking of his arms. There is shaking in his legs but to a lesser extent. He unable to speak. He is in a stiff rigid posture with hands shaking for about 30 seconds, he relaxes and stiffens and relaxes for a couple of cycles. Then he is unresponsive until 10:08:25. There is tremor artifact on the EEG but no evolving ictal activity or epileptiform discharges. Interpretation: This is a normal more than 15 hours continuous video EEG recording. The episode of arms and hands clenching and extremity rigidity and shaking is a psychogenic nonepileptic event. MD Last Resulted: 03/14/21 16:23 Order Details View Encounter Lab and Collection Details Routing Result History Ordered On 3/13/2021 9:28 PM Ordering Provider Authorizing Provider Ordering User Ordering Department DO Study Result Continuous Video EEG Long Term Monitoring Date performed: 3/13-3/14/2021 Referring Provider: DO Report date: 3/14/2021 Study type: Continuous video EEG, up to 24 hours ICD 10 diagnosis: Spells/Fit NOS, Seizures R56.9 and Functional neurological symptoms disorder, with seizure F44.5 Start time: 3/13/2021 23:49 End time: 3/14/2021 15:07 Patient History: Patient is 22 y.o. male on continuous video EEG monitoring for the assessment of seizures, characterization of events, and effect of treatment. Patient has presumed epilepsy and nonepileptic psychogenic seizures. He started to have a cluster of seizures after getting COVID19 vaccine. Current AEDs: Medications include: Facility-Administered Medications Ordered in Other Visits Medication Dose Route Frequency Provider Last Rate ? acetaminophen 650 mg Oral Q6H PRN, DO ? fluticasone 1 spray Nasal Daily PRN, DO ? gabapentin 400 mg Oral TID, DO ? hydrOXYzine HCL 25 mg Oral Q6H PRN, DO ? ibuprofen 800 mg Oral Q8H PRN, DO ? levETIRAcetam 1,500 mg Oral Q12H SCH , DO ? sertraline 50 mg Oral Daily, DO ? topiramate 150 mg Oral TID, DO Description of Procedure: A 24 hours continuous video EEG was performed with electrodes applied using the International 10-20 System at least 16 channels are reviewed and formatted into longitudinal bipolar, transverse bipolar, and referential (to common reference or calculated common reference) montages. Additional electrodes used included T1, T2, and extraocular electrodes, and ECG, along with video recording. The EEG was recorded with the patient awake, drowsy, and asleep state. This study was intermittently monitored by a monitoring technologist. The physician interpreting the study had access to the data throughout the recording. The recording was technically satisfactory. Findings: Background Activity: The background is grossly symmetric with respect to voltages and activities. During wakefulness, the background is extremely low voltage, but appears to be organized with diffuse extremely low amplitude beta and alpha activity. There is a symmetric very low voltage 8-8.5 Hz posterior dominant rhythm. Drowsiness is characterized by attentuation of the alpha rhythm, prominent anterior beta activity, central theta activity, roving eye movements, positive occipital sharp transients of sleep (POSTS) and vertex waves. Stage 2 sleep is characterized by symmetric sleep spindles and K-complexes. Other findings: The single lead ECG shows a regular and sinus rhythm. Events: Event 1 - nonepileptic 10:07 - patient was receiving routine nursing care. He is looking for the event button. Then he asked the nurse if she could push the event button because he feels that he is about to have a seizure. (he has a child-like prosody.) He leans back on his left side, becomes very stiff, hands go into a "claw-like" position and rigid with rapid low amplitude shaking of his arms. There is shaking in his legs but to a lesser extent. He unable to speak. He is in a stiff rigid posture with hands shaking for about 30 seconds, he relaxes and stiffens and relaxes for a couple of cycles. Then he is unresponsive until 10:08:25. There is tremor artifact on the EEG but no evolving ictal activity or epileptiform discharges. Interpretation: This is a normal more than 15 hours continuous video EEG recording. The episode of arms and hands clenching and extremity rigidity and shaking is a psychogenic nonepileptic event. , MD Imaging EEG Video Monitoring 24 Hour - 3/13/2021 Result History EEG Video Monitoring 24 Hour on 3/14/2021 - Order Result History Report Order Report Order Details Study Summary Priority Study Status Reading Physician Reading Date Routine MD 3/14/2021 Lead Tech Supporting Staff Ordered On 3/13/2021 9:28 PM Ordering Provider Authorizing Provider Ordering User Order Details Exam Details Patient Details Encounter Medications Study Note Reading Physician Reading Date Result Priority 3/14/2021 Routine Narrative & Impression Continuous Video EEG Long Term Monitoring Date performed: 3/13-3/14/2021 Referring Provider:, DO Report date: 3/14/2021 Study type: Continuous video EEG, up to 24 hours ICD 10 diagnosis: Spells/Fit NOS, Seizures R56.9 and Functional neurological symptoms disorder, with seizure F44.5 Start time: 3/13/2021 23:49 End time: 3/14/2021 15:07 Patient History: Patient is 22 y.o. male on continuous video EEG monitoring for the assessment of seizures, characterization of events, and effect of treatment. Patient has presumed epilepsy and nonepileptic psychogenic seizures. He started to have a cluster of seizures after getting COVID19 vaccine. Current AEDs: Medications include: Facility-Administered Medications Ordered in Other Visits Medication Dose Route Frequency Provider Last Rate ? acetaminophen 650 mg Oral Q6H PRN, DO ? fluticasone 1 spray Nasal Daily PRN, DO ? gabapentin 400 mg Oral TID, DO ? hydrOXYzine HCL 25 mg Oral Q6H PRN, DO ? ibuprofen 800 mg Oral Q8H PRN, DO ? levETIRAcetam 1,500 mg Oral Q12H SCH, DO ? sertraline 50 mg Oral Daily , DO ? topiramate 150 mg Oral TID , DO Description of Procedure: A 24 hours continuous video EEG was performed with electrodes applied using the International 10-20 System at least 16 channels are reviewed and formatted into longitudinal bipolar, transverse bipolar, and referential (to common reference or calculated common reference) montages. Additional electrodes used included T1, T2, and extraocular electrodes, and ECG, along with video recording. The EEG was recorded with the patient awake, drowsy, and asleep state. This study was intermittently monitored by a monitoring technologist. The physician interpreting the study had access to the data throughout the recording. The recording was technically satisfactory. Findings: Background Activity: The background is grossly symmetric with respect to voltages and activities. During wakefulness, the background is extremely low voltage, but appears to be organized with diffuse extremely low amplitude beta and alpha activity. There is a symmetric very low voltage 8-8.5 Hz posterior dominant rhythm. Drowsiness is characterized by attentuation of the alpha rhythm, prominent anterior beta activity, central theta activity, roving eye movements, positive occipital sharp transients of sleep (POSTS) and vertex waves. Stage 2 sleep is characterized by symmetric sleep spindles and K-complexes. Other findings: The single lead ECG shows a regular and sinus rhythm. Events: Event 1 - nonepileptic 10:07 - patient was receiving routine nursing care. He is looking for the event button. Then he asked the nurse if she could push the event button because he feels that he is about to have a seizure. (he has a child-like prosody.) He leans back on his left side, becomes very stiff, hands go into a "claw-like" position and rigid with rapid low amplitude shaking of his arms. There is shaking in his legs but to a lesser extent. He unable to speak. He is in a stiff rigid posture with hands shaking for about 30 seconds, he relaxes and stiffens and relaxes for a couple of cycles. Then he is unresponsive until 10:08:25. There is tremor artifact on the EEG but no evolving ictal activity or epileptiform discharges. Interpretation: This is a normal more than 15 hours continuous video EEG recording. The episode of arms and hands clenching and extremity rigidity and shaking is a psychogenic nonepileptic event. , MD Signed Electronically signed by , MD on 3/14/21 at 1625 Questions Order Question Answer Reason for Exam: Seizures vs pseudoseizures Additional Information Specimen ID Bill Type Client ID Specimen Date Taken Specimen Time Taken Specimen Received Date Specimen Received Time Result Date Result Time Mar 14, 2021 4:23 PM Lab Component SmartPhrase Guide EEG Video Monitoring 24 Hour on 3/13/21 Results RouContinuous Video EEG Long Term Monitoring Date performed: 3/13-3/14/2021 Referring Provider:, DO Report date: 3/14/2021 Study type: Continuous video EEG, up to 24 hours ICD 10 diagnosis: Spells/Fit NOS, Seizures R56.9 and Functional neurological symptoms disorder, with seizure F44.5 Start time: 3/13/2021 23:49 End time: 3/14/2021 15:07 Patient History: Patient is 22 y.o. male on continuous video EEG monitoring for the assessment of seizures, characterization of events, and effect of treatment. Patient has presumed epilepsy and nonepileptic psychogenic seizures. He started to have a cluster of seizures after getting COVID19 vaccine. Current AEDs: Medications include: Facility-Administered Medications Ordered in Other Visits Medication Dose Route Frequency Provider Last Rate ? acetaminophen 650 mg Oral Q6H PRN, DO ? fluticasone 1 spray Nasal Daily PRN, DO ? gabapentin 400 mg Oral TID, DO ? hydrOXYzine HCL 25 mg Oral Q6H PRN, DO ? ibuprofen 800 mg Oral Q8H PRN, DO ? levETIRAcetam 1,500 mg Oral Q12H SCH, DO ? sertraline 50 mg Oral Daily, DO ? topiramate 150 mg Oral TID, DO Description of Procedure: A 24 hours continuous video EEG was performed with electrodes applied using the International 10-20 System at least 16 channels are reviewed and formatted into longitudinal bipolar, transverse bipolar, and referential (to common reference or calculated common reference) montages. Additional electrodes used included T1, T2, and extraocular electrodes, and ECG, along with video recording. The EEG was recorded with the patient awake, drowsy, and asleep state. This study was intermittently monitored by a monitoring technologist. The physician interpreting the study had access to the data throughout the recording. The recording was technically satisfactory. Findings: Background Activity: The background is grossly symmetric with respect to voltages and activities. During wakefulness, the background is extremely low voltage, but appears to be organized with diffuse extremely low amplitude beta and alpha activity. There is a symmetric very low voltage 8-8.5 Hz posterior dominant rhythm. Drowsiness is characterized by attentuation of the alpha rhythm, prominent anterior beta activity, central theta activity, roving eye movements, positive occipital sharp transients of sleep (POSTS) and vertex waves. Stage 2 sleep is characterized by symmetric sleep spindles and K-complexes. Other findings: The single lead ECG shows a regular and sinus rhythm. Events: Event 1 - nonepileptic 10:07 - patient was receiving routine nursing care. He is looking for the event button. Then he asked the nurse if she could push the event button because he feels that he is about to have a seizure. (he has a child-like prosody.) He leans back on his left side, becomes very stiff, hands go into a "claw-like" position and rigid with rapid low amplitude shaking of his arms. There is shaking in his legs but to a lesser extent. He unable to speak. He is in a stiff rigid posture with hands shaking for about 30 seconds, he relaxes and stiffens and relaxes for a couple of cycles. Then he is unresponsive until 10:08:25. There is tremor artifact on the EEG but no evolving ictal activity or epileptiform discharges. Interpretation: This is a normal more than 15 hours continuous video EEG recording. The episode of arms and hands clenching and extremity rigidity and shaking is a psychogenic nonepileptic event. ting Details
Aktuelle Erkrankungen: Digestive Chronic constipation Pharyngitis Cardiovascular and Mediastinum Chronic migraine Nervous and Auditory Seizure disorder Musculoskeletal and Integument Atypical nevi Acne vulgaris Contact dermatitis Other Ambulatory dysfunction Speech abnormality Abdominal pain Hx of tonic-clonic seizures Conversion disorder with seizures or convulsions Right facial numbness history of Asperger's syndrome Psychogenic nonepileptic seizure Medical clearance for psychiatric admission Current severe episode of major depressive disorder without psychotic features without prior episode Generalized anxiety disorder Psychophysiological insomnia Anxiety and depression Seizure Autism disorder Lactic acidosis Leukocytosis
Vorgeschichte: Digestive Chronic constipation Pharyngitis Cardiovascular and Mediastinum Chronic migraine Nervous and Auditory Seizure disorder Musculoskeletal and Integument Atypical nevi Acne vulgaris Contact dermatitis Other Ambulatory dysfunction Speech abnormality Abdominal pain Hx of tonic-clonic seizures Conversion disorder with seizures or convulsions Right facial numbness history of Asperger's syndrome Psychogenic nonepileptic seizure Medical clearance for psychiatric admission Current severe episode of major depressive disorder without psychotic features without prior episode Generalized anxiety disorder Psychophysiological insomnia Anxiety and depression Seizure Autism disorder Lactic acidosis Leukocytosis
Andere Medikamente: albuterol (ProAir HFA) 90 mcg/act inhaler diazepam (VALIUM) 10 mg tablet fluticasone (FLONASE) 50 mcg/act nasal spray gabapentin (NEURONTIN) 400 mg capsule hydrOXYzine HCL (ATARAX) 25 mg tablet ibuprofen (MOTRIN) 400 mg tablet l
Allergien: Lorazepam]Shortness Of Breath, Anaphylaxis Dilantin [Phenytoin]Other (See Comments) Pollen ExtractItching
Vorherige Impfungen: -

VAERS 1103896

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

schwer

Staat: IN
Alter: 31,0
Geschlecht: F
Eingang: 16.03.2021
Impfdatum: 15.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Lethargy Syncope

Symptomtext

Patient was at check out. She told that she felt faint. Check out woman went around and caught her before she hit the floor and lowered her down. Patient was out for about 10 seconds. Patient reports a hx of fainting with vaccines. She has no hx of HTN. Her bp was 90/50 at 4:13 pm when she was assessed. Her oxygen was 97% and pulse was 60. 5 minutes later she was assessed again. bp was 100/60 oxygen 98% and HR 70. At 4:25pm her bp was 104/62. oxygen 99% and pulse 69. She was still lethargic from the event. We had her picked up.

Weitere VAERSDATA-Felder

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

VAERS 2552218

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 36,0
Geschlecht: F
Eingang: 15.03.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Confusional state Hyperhidrosis Loss of consciousness Opisthotonus Pallor Throat tightness Unresponsive to stimuli

Symptomtext

pale, diaphoresis, tightness in throat Narrative: Patient lost consciousness for ~2 minutes ~11 mins after covid vaccination. Witness observed patient arching her back and non responsive. patient was safely lowered to floor. vitals BP 99/52 HR 62 R 18 97RA. patient was pale and diaphoretic. code team was called at 11:42 epi pen was administered. as patient began to come to she was very confused. code team arrived to transfer patient to ED.

Weitere VAERSDATA-Felder

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

VAERS 1102827

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: AL
Alter: 35,0
Geschlecht: F
Eingang: 15.03.2021
Impfdatum: 14.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Limb discomfort Muscle tightness Syncope

Symptomtext

Patient rec'd 2nd dose at 1217, had syncopal episode x 3 in observation area. Patient evaluated by Dr . We layed patient supine. Patient became more alert. Attempted to sit patient up after 10 minutes, had syncopal episode again. Patient c/o left arm and chest heaviness, left neck tightness, and left sided facial tingling. BP remained 130-150/60's and HR in the 60's. EMS was called at 1301. Transported to HH ED with belongings. Patient's mother notified.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EKG- Sinus Bradycardia Chest Xray: No acute cardiopulmonary findings. SAO2= 97-100% CBC, Cardiac Enzymes: No findings
Aktuelle Erkrankungen: Hypothyroidism, Sacroiliac joint pain
Vorgeschichte: -
Andere Medikamente: Zofran, Ibuprofen, Liothyronine
Allergien: Morphine
Vorherige Impfungen: -

VAERS 1101843

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NJ
Alter: 74,0
Geschlecht: M
Eingang: 15.03.2021
Impfdatum: 11.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Drooling Faecal vomiting Hypotension Loss of consciousness Unresponsive to stimuli Vomiting

Symptomtext

During observation period (15 minutes) patient became unresponsive. Maintained airway and stayed upright in chair but began drooling and did not respond to Dr. or nurse. Patient was unresponsive for approximately 5 minutes, during which time 911 was called and patient became conscious. Patient vomitted upon becoming responsive, scant amount. Patient was hypotensive during episode and at arrival of medics (90/50 approx.). Patient with recent history of hypotension and per spouse patient was due for his Midodrine. Patient was taken to local hospital for evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Active problems - Computerized Problem List is the source for the following: 1. Bilateral age-related nuclear cataracts 2. Hematuria 3. Proteinuria 4. Primary malignant neoplasm of base of tongue 5. Systolic heart failure 6. Anxiety 7. Pulmonary venous thrombosis 8. CVA - Cerebrovascular accident 9. Polycythemia 10. Vitamin D deficiency 11. Hyponatremia 12. Dyslipidemia 13. Primary malignant neoplasm of colon 14. Coronary arteriosclerosis (SNOMED CT 53741008) 15. Peripheral vascular disease 16. Hypertension 17. Malignant neoplasm of skin 18. Other Hemochromatosis
Vorgeschichte: Active problems - Computerized Problem List is the source for the following: 1. Bilateral age-related nuclear cataracts 2. Hematuria 3. Proteinuria 4. Primary malignant neoplasm of base of tongue 5. Systolic heart failure 6. Anxiety 7. Pulmonary venous thrombosis 8. CVA - Cerebrovascular accident 9. Polycythemia 10. Vitamin D deficiency 11. Hyponatremia 12. Dyslipidemia 13. Primary malignant neoplasm of colon 14. Coronary arteriosclerosis (SNOMED CT 53741008) 15. Peripheral vascular disease 16. Hypertension 17. Malignant neoplasm of skin 18. Other Hemochromatosis
Andere Medikamente: ALOH/DIPH/MAG/LIDO/SIMET 1:1:1 MOUTHWASH Sig: TAKE 2.5ML BY MOUTH EVERY FOUR HOURS AS NEEDED , SWISH AND SPIT AMIODARONE HCL (PACERONE) 200MG TAB Sig: TAKE ONE-HALF TABLET BY MOUTH ONCE DAILY APIXABAN 5MG TAB (CPC)
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1101737

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IN
Alter: 56,0
Geschlecht: M
Eingang: 15.03.2021
Impfdatum: 11.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Pallor Syncope

Symptomtext

Pt felt lightheaded once in parking lot after receiving vaccine around noon. Beeped horn at 12:10pm. Fainted and reports possible stiffening of limbs/seizure activity. Hx of fainting with needles. Pt was pale and lightheaded when nurse arrived to car at 12:11pm. 911 called immediately due to possible seizure. BP 90/50, unable to obtain pulse and O2 sats. Ambulance on scene at 12:17pm and patient transported to hospital via ambulance at 12:30pm. Pt was feeling better and responsive when he left scene.

Weitere VAERSDATA-Felder

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

VAERS 1101702

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 27,0
Geschlecht: F
Eingang: 15.03.2021
Impfdatum: 15.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

Patient with syncope a few minutes after vaccination. Able to keep patient upright in chair until able to get in wheelchair. After a minute or two, patient was alert again. Given juice. Vitals stable. Able to discharge home with boyfriend.

Weitere VAERSDATA-Felder

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

VAERS 1101449

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NJ
Alter: 33,0
Geschlecht: F
Eingang: 15.03.2021
Impfdatum: 13.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Loss of consciousness

Symptomtext

Pfizer-BioNTech COVID- 19 Vaccine EUA: Vaccine recipient has a history of vasovagal reaction when getting injections or blood. Her mother was holding the patient, assisted her to the floor, protecting her head, turned her to the side to protect her airway. Patient experienced loss of consciousness for a few seconds and then came back. Her mother described this as "normal" and patient had many work ups. EMS came to assess the patient and patient was placed in wheelchair and taken to observation.

Weitere VAERSDATA-Felder

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

VAERS 1100789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NY
Alter: 44,0
Geschlecht: M
Eingang: 15.03.2021
Impfdatum: 14.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Dizziness Headache Loss of consciousness Syncope

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Patient was feeling paralized. However, we can cleary see the patient moving all his extremities-Mild, Systemic: Headache-Mild, Systemic: Weakness-Mild

Weitere VAERSDATA-Felder

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

VAERS 1100772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: OH
Alter: 64,0
Geschlecht: M
Eingang: 15.03.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
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 Dizziness Electrocardiogram Hyperhidrosis Irritability Loss of consciousness

Symptomtext

Patient was in recovery area per protocol. Patient developed light headedness, diaphoresis, irritability and then collapsed into chair and then floor (helped by nursing staff) patient appeared unconscious but was breathing, oxygen applied, emergency response initiated

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Head CT, EKG, Basic laboratory in emergency department same date and time as event.
Aktuelle Erkrankungen: None
Vorgeschichte: none
Andere Medikamente: omeprazole
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1098906

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 20,0
Geschlecht: M
Eingang: 14.03.2021
Impfdatum: 14.03.2021
Beginn: 14.03.2021
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 Somnolence Tremor

Symptomtext

Patient passed out or fell asleep. Once approached he woke up and was shaking for a bit. He had no issues breathing, no hives, or rash. Upon awakening he was given some water and quickly recovered. After a few minutes the patient seemed normal. We observed him for about another 30 minutes and he continued to be fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None other than blood pressure which was normal
Aktuelle Erkrankungen: None, however patient was tired from a party the night before
Vorgeschichte: No known health conditions
Andere Medikamente: Patient was drinking a "red bull" energy drink and had nothing to eat that morning
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1097911

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NC
Alter: 52,0
Geschlecht: F
Eingang: 14.03.2021
Impfdatum: 12.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Head injury Loss of consciousness Syncope

Symptomtext

I had a sudden syncope episode with LOC as I walked to my bedroom. Didn't wake up until my head hit door jam and I was on the floor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Adderall, effexor, women's daily gummy, cranberry gummy
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1097822

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NY
Alter: 59,0
Geschlecht: F
Eingang: 13.03.2021
Impfdatum: 12.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Chills Head injury Headache Myalgia Syncope

Symptomtext

During the night following the vaccination, I had chills, muscle aches and a headaceh. I got up to go the batheroom and on the way back to bed I fainted and hit head on the floor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: Hashimotos
Andere Medikamente: Levoxyl Citalporam Zyrtec Multivitamin Vitamin D Calcium
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 1097227

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

schwer

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 13.03.2021
Impfdatum: 13.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Presyncope

Symptomtext

vasovagal response, monitored, cool packs, sx resolved

Weitere VAERSDATA-Felder

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

VAERS 1097122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IA
Alter: 50,0
Geschlecht: M
Eingang: 13.03.2021
Impfdatum: 10.03.2021
Beginn: 10.03.2021
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

Symptomtext

Patient had anaphylaxis to first dose of Pfizer vaccine - Epipen used

Weitere VAERSDATA-Felder

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

VAERS 1097083

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 61,0
Geschlecht: M
Eingang: 13.03.2021
Impfdatum: 13.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Electrocardiogram Loss of consciousness

Symptomtext

Patient was driving into holding/observation post vaccination and complained of dizziness and then had a brief syncopal episode losing consciousness for a few seconds as reported by his wife.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: EKG done by ALS which showed abnormal sinus rhythm with no ectopy
Aktuelle Erkrankungen: No illnesses or medical conditions per wife
Vorgeschichte: None noted by wife
Andere Medikamente: None
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1097070

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: IA
Alter: 53,0
Geschlecht: M
Eingang: 13.03.2021
Impfdatum: 10.03.2021
Beginn: 10.03.2021
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

Symptomtext

Patient had 1st dose of pfizer and 45-60 minutes later had anaphylaxis in which an epipen was administered. Patient was taken via ambulance to The hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: unsure - patient left via ambulance
Aktuelle Erkrankungen: Unsure
Vorgeschichte: Unsure
Andere Medikamente: Epipen as needed for bee stings Unsure of other meds
Allergien: Bee Sting
Vorherige Impfungen: -

VAERS 1096942

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

schwer

Staat: RI
Alter: 33,0
Geschlecht: M
Eingang: 13.03.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Flushing Hyperhidrosis Hypotension Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Hypotension-Severe, Additional Details: Patient had short fainting spell post vaccination while seated, immunizer was a registered nurse who provided immediate care, checked blood pressure, 100/60 then 125/90 10 minutes later, patient was upright and responsive after being assisted. after observation period left on own ability with mother. left message with pcp office post event, spoke with patient following morning, no issues feeling fine.

Weitere VAERSDATA-Felder

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

VAERS 1096885

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 22,0
Geschlecht: F
Eingang: 13.03.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Syncope

Symptomtext

syncope, hx of syncope with immunizations

Weitere VAERSDATA-Felder

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

VAERS 1096817

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: -
Alter: 22,0
Geschlecht: F
Eingang: 13.03.2021
Impfdatum: 13.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Loss of consciousness

Symptomtext

Patient stated she passes out after shots, so RN got her a wheelchair to sit in while the shot was being administered. The vaccine was administered and she felt fine. While sitting for another minute she passed out in the wheelchair and the RN called for help. The patient came too. The patient was assessed by paramedics on scene and stayed an extra 30 minutes. She knew she blacked out and she went home with her mother.

Weitere VAERSDATA-Felder

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

VAERS 1096741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MN
Alter: 50,0
Geschlecht: M
Eingang: 13.03.2021
Impfdatum: 13.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Seizure

Symptomtext

Had seizure in car when leaving the facility, about 1/2 hour after the vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Anxiety, depression
Vorgeschichte: Anxiety, depression, Hypothyroidism, fibromyalgia, obesity, ETOH disorder in remission, panic disorder, tobacco abuse, ICD, crhonic neck and back pain, restless legs.
Andere Medikamente: not specified
Allergien: NKA
Vorherige Impfungen: -

VAERS 1096301

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

schwer

Staat: FL
Alter: 38,0
Geschlecht: M
Eingang: 13.03.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Presyncope Syncope

Symptomtext

Systemic: Fainting / Unresponsive-Medium, Additional Details: Patient fainted, was given EPI then came back, EMTs came and said it was a vagal response. Patient recovered, but was taken to ER by ambulance because EPI was given.

Weitere VAERSDATA-Felder

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

VAERS 1095640

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: WA
Alter: 47,0
Geschlecht: F
Eingang: 12.03.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hypotension Presyncope Tremor

Symptomtext

near syncope, hypotension, shaking. Lasted 20 minutes in clinic with stable BP, HR, and SpO2 mostly >96%. Dipped to 88% a few times. no respiratory symptoms, rash, or throat swelling. transferred from clinic to ED via ambulance

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: none in clinic. see hospital records
Aktuelle Erkrankungen: none known
Vorgeschichte: none known
Andere Medikamente: none
Allergien: acetaminophen, diphenhydramine. one prior food anaphylactic episode (unk what food)
Vorherige Impfungen: -

VAERS 1095624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: NV
Alter: 64,0
Geschlecht: M
Eingang: 12.03.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Blood glucose normal Generalised tonic-clonic seizure

Symptomtext

Client had clonic/tonic seizures x2 within one minute of receiving the COVID-19 vaccine, first dose. Within 3-4 minutes of the seizure activity, client was awake, alert, oriented x3. Client was placed on a stretcher by paramedics and transferred via a stretcher to the observation area. Client remained awake, alert, oriented x3. No incontinence noted. Client was transferred to the hospital by the paramedics to the hospital within 10-15 minutes after seizure activity. No other family members were present with client.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Generalised tonic-clonic seizure
Hospital-Tage: -
Labordaten: 3/12/2021 2:26pm BP: 173/94 Pulse: 93 Respiration: 24 Blood Sugar: 96
Aktuelle Erkrankungen: Diverticulitis, Enlarged Prostate, denies any cardiac disease or diabetes
Vorgeschichte: History of seizure disorder. Last seizure activity reported 4 years ago. No recent changes in seizure medication Keppra (750mg BID).
Andere Medikamente: Keppra 750mg BID
Allergien: Penicillin, Dilaudid, Morphine
Vorherige Impfungen: -

VAERS 1093031

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 31,0
Geschlecht: F
Eingang: 11.03.2021
Impfdatum: 11.03.2021
Beginn: 11.03.2021
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 Dizziness Nausea Paraesthesia Syncope

Symptomtext

Patient felt dizzy, fainted, nauseous and tingling sensation all over her body. Allowed to rest with feet higher than her head, 911 called, water given. Refused to go to the hospital. Her friend took her home with no symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Blood pressure: 100/65 - 129/85, HR: 55-61, O2 sat 99-100%, Blood sugar 92
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1092624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: CA
Alter: 54,0
Geschlecht: M
Eingang: 11.03.2021
Impfdatum: 11.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

Patient experienced a syncopal episode two minutes after receiving Pfizer vaccine. While paramedics were assessing him he had another syncopal episode. He was transported to Northridge hospital for evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: per patient, "no"
Vorgeschichte: per patient, "no"
Andere Medikamente: per patient, "no"
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1092279

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MD
Alter: 26,0
Geschlecht: M
Eingang: 11.03.2021
Impfdatum: 10.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hypotension Loss of consciousness Oxygen saturation decreased Seizure

Symptomtext

About 30 minutes after dose he passed out and had a seizure that lasted 10 -15 seconds. This happened a couple times. He went to hospital had low blood pressure and oxygen. He stabilized and was released. He has a follow up appointment with his primary care doctor.

Weitere VAERSDATA-Felder

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

VAERS 1091848

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MA
Alter: 67,0
Geschlecht: F
Eingang: 11.03.2021
Impfdatum: 11.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Chest X-ray Condition aggravated Cough Dyspnoea Electrocardiogram

Symptomtext

increased cough, difficulty breathing, anaphylaxis; received IM EpiPen, IM Benadryl, and IV Solumedrol 125mg Symptoms improved; did not need repeat Epi dosing. did not receive Famotidine because has documented allergy to Ranitidine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: 3/11/21 CXR: interstitial disease EKG non ischemia
Aktuelle Erkrankungen: COPD exacerbation
Vorgeschichte: urticaria, hyperlipidemia, acquired hypothyroidism, COPD, Hashimoto's thyroiditis, allergic rhinitis to pollen, animal hair and dander and Dermatophagiodes, Prediabetes, Obesity, Glaucoma suspected, Sigmoid diverticulitis, colonic polyps, diverticulitis, partial small bowel obstruction
Andere Medikamente: Advair HFA 115/21, Albuterol, Flonsae, Synthroid, Prilosec, Zocor, Trazodone, Venlafaxine ER, EpiPen, Tylenol.
Allergien: Aleve, Chantix, Erythromycin, Macrolide antibiotics, Ciprofloxacin, Wellbutrin, Zantac
Vorherige Impfungen: -

VAERS 1091214

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: ND
Alter: 27,0
Geschlecht: M
Eingang: 11.03.2021
Impfdatum: 10.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Fall Head injury Immediate post-injection reaction Seizure

Symptomtext

Immediately after he said he was dizzy. I had him remove his mask and take some deep breaths. He did. I called for help from other nurses in the room. He had seizure activity and fell from the chair to the floor. In the process he hit his head on the table. He had his stocking hat on. The other nurses were there immediately. Talking to him, reassuring the mom, BP, pulse oximeter, ice pack, privacy curtains in place. He was offered food and drink. Other staff removed others from the room. The ambulance was called. And arrived. The ambulance assessed him. Education and instruction were given. They asked him to go to ER. He refused. They advised him to see his Doctor. The ambulance had him sign their needed paperwork. Helped him to his feet, he refused to use their cart provided. He said, I am fine. He was strongly encouraged to follow up with his Doctor. He walked out of the room with ambulance personal and his mom.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: None listed.
Vorgeschichte: None listed.
Andere Medikamente: None listed.
Allergien: None listed.
Vorherige Impfungen: Pt denied any previous issues. Mother reported "this happened last time." Mother had no further details.

VAERS 1089650

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6208

schwer

Staat: IA
Alter: 45,0
Geschlecht: M
Eingang: 10.03.2021
Impfdatum: 10.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Loss of consciousness

Symptomtext

patient was sitting after the shot in the waiting area for 15 min after the shot and one of his college who is sitting near by called me and said he passed out twice but when I went with the nurse he was ok and he said he did not. but his friend said no he did. we kept watch him closely for one hour. no symptoms observed. no sob , we offer him epipen or bendryl but he refused. I asked to call his family dr of pcp he said he does not have one. I called the patient on his sell phone after 6 hr of incident and he said he had no issue after that

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: na
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: no Rx drugs or otc
Allergien: No allergy
Vorherige Impfungen: -

VAERS 1085809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

schwer

Staat: MO
Alter: 61,0
Geschlecht: M
Eingang: 09.03.2021
Impfdatum: 09.03.2021
Beginn: 09.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope Unresponsive to stimuli

Symptomtext

Patient had a syncopal episode

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None. Patient denied care after regaining responsiveness
Aktuelle Erkrankungen: None
Vorgeschichte: HTN, GERD, Radiculopathy, Anxiety, Asthma
Andere Medikamente: Gabapentin, Methocarbamol, Buspiron, HCTZ/Lisinopril
Allergien: Amlodipine, Hyoscyamine, Flunisolide, Fluticason
Vorherige Impfungen: Syncopal events

VAERS 2707360

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: MN
Alter: 79,0
Geschlecht: M
Eingang: 31.10.2023
Impfdatum: 26.10.2022
Beginn: 23.10.2023
Tage bis Beginn: 362,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

Pt presents in ED 10/23/23 for weakness and SOB. Pt is vaccinated against COVID with 5 previous shots. He tested positive for COVID on 10/23 and was admitted to the hospital.

Weitere VAERSDATA-Felder

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

VAERS 2707352

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: MN
Alter: 59,0
Geschlecht: F
Eingang: 31.10.2023
Impfdatum: 19.10.2021
Beginn: 26.10.2023
Tage bis Beginn: 737,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

PT ARRIVED IN THE ED ON 10/26/23 COMPLAINING OF SHORTNESS OF BREATH STARTING 10/24. COVID TEST WAS POSITIVE. SHE ADMITTED TO THE HOSPTIAL AND WAS DISCHARGED HOME 10/28.

Weitere VAERSDATA-Felder

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

VAERS 2700694

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: TX
Alter: 60,0
Geschlecht: F
Eingang: 24.10.2023
Impfdatum: 20.03.2021
Beginn: 02.02.2022
Tage bis Beginn: 319,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Chest X-ray abnormal Chills Cough Culture urine positive Diarrhoea Dyspnoea Fibrin D dimer increased Inflammatory marker increased Klebsiella test positive Lung infiltration Pain Pyrexia

Symptomtext

presented to the ED complaining of worsening cough and shortness of breath on 2/3. Patient started to have intermittent fever, chills, body aches and diarrhea since last week; Chest x-ray showed bilateral lung infiltrates consistent with COVID-19 disease. ID was consulted and she was started on Veklury along with Rocephin 1gm daily, Azithromycin 500mg daily, steroids and lovenox. HD #3, she required 4L NC but was stable. Her urine culture grew Klebsiella and she was started on Nitrofurantoin. Her inflammatory markers fell nicely. HD #4, her ddimer has a slight elevation and her 02 requirement fell to 2L NC; home on O2

Weitere VAERSDATA-Felder

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

VAERS 1276898

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN 6208

moderat

Staat: FL
Alter: 61,0
Geschlecht: M
Eingang: 23.10.2023
Impfdatum: 16.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / -

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

Angiogram Computerised tomogram head Headache Magnetic resonance imaging head Migraine Fatigue Feeling abnormal General symptom Immunisation reaction Laboratory test New daily persistent headache Scan with contrast

Symptomtext

New daily persistent headache

Weitere VAERSDATA-Felder

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

VAERS 2643804

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: MD
Alter: 69,0
Geschlecht: F
Eingang: 11.06.2023
Impfdatum: 11.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Acoustic stimulation tests abnormal Deafness Migraine Nausea Tinnitus

Symptomtext

The morning after the injection I woke up with nausea followed by an all-day migraine ending in the evening. Then on the 4th day after the injection, I began to hear electrical noises. I was then diagnosed with Tinnitus and hearing loss by an Ear Nose & Throat Specialist in 3/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Hearing test 3/2021
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Vitamin D, Multivitamin 50+
Allergien: Allergic to Advil, Cipro, Doxy.
Vorherige Impfungen: Flu Oct. 2020 - Extreme nerve pain on left side of head and face

VAERS 2638353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: FL
Alter: 29,0
Geschlecht: F
Eingang: 30.05.2023
Impfdatum: 16.03.2021
Beginn: 23.06.2022
Tage bis Beginn: 464,0
Dosis: 1
Route/Site: - / -

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

Arthralgia COVID-19 Chest pain Computerised tomogram abdomen abnormal Computerised tomogram thorax normal Diarrhoea Fibrin D dimer increased Fibromyalgia Hypertension Hypothyroidism Myxoedema Pelvic fluid collection Pleurisy Rectal haemorrhage SARS-CoV-2 test positive Vaccine breakthrough infection Vaginal haemorrhage

Symptomtext

BREAKTHROUGH COVID: FULLY VACCINATED WITH HISTORY OF COVID 19. Monitor off Rocephin, Zithromax --stable, No treatment indicated for COVID-19 at this time as she is on room air. PT TESTED POSITIVE 2 WEEKS EARLIER, CONTINUED TO TEST POSITIVE. PT ADMITTED FOR Chest Pain, COVID19, Pleurisy, Diarrhea,Arthralgia, Hypertension, Hypothyroidism, Fibromyalgia, Myxedema, rectal bleeding and vaginal bleeding.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: CT CHEST: NEGATIVE, CT ABDOMEN Small volume pelvic free fluid, likely physiologic for patient age. Positive D-Dimer - Negative for PE
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: Lupus, Ehlers-Danlos syndrome
Andere Medikamente: UNKNOWN
Allergien: INJECTABLE MAGNESIUM SULFATE, REGLAN, VACOMYCIN
Vorherige Impfungen: -

VAERS 2635526

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: FL
Alter: 86,0
Geschlecht: F
Eingang: 23.05.2023
Impfdatum: 22.02.2021
Beginn: 13.07.2022
Tage bis Beginn: 506,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Chest X-ray normal Computerised tomogram head normal Dyspnoea Electrocardiogram abnormal Gait inability Laboratory test abnormal Lethargy Metabolic acidosis Metabolic encephalopathy QRS axis abnormal SARS-CoV-2 test positive Sinus rhythm Upper respiratory tract infection Urinary tract infection Vaccine breakthrough infection Wheezing

Symptomtext

Breakthrough COVID: Fully vaccinated. Patient is an 87 year-old female , She took 4 rapid antigen covid tests at home which were all positive. Due to worsening lethargy to the point where patient was unable to ambulate, she was brought to the ED. No shortness of breath, chest pain, fevers, nausea, vomiting, abdominal pain, or dysuria. In the ED, her vitals were stable and she was saturating 90-98% on room air. She was placed on 2 L nasal cannula for comfort. Labs were notable for mild metabolic acidosis and UTI. She had no leukocytosis. Chest x-ray did not show consolidation or infiltrates. She was given 1 g Rocephin in the ED as well as decadron for dyspnea/wheezing. She was admitted for acute metabolic encephalopathy, UTI, and covid-19 upper respiratory infection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: CT head was negative for acute abnormality. EKG showed normal sinus rhythm with left axis deviation.
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: advanced dementia, CAD s/p CABG, HTN, HLD
Andere Medikamente: UNKNOWN
Allergien: NKA
Vorherige Impfungen: -

VAERS 2621221

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: WA
Alter: 72,0
Geschlecht: F
Eingang: 11.04.2023
Impfdatum: 17.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Condition aggravated Laboratory test normal Neck pain Pain Pain in extremity

Symptomtext

Sudden onset of multiple painful joints without swelling or redness. Pain level 7-8 out of 10. Joints included bilateral mid foot and ankles, base of both thumbs and R shoulder and neck. I have had pain with osteoarthritis with a rheumatoid factor for many years but this pain was very intense and occurred in multiple joints. Saw my functional medicine Nurse Practitioner after 2 months of putting up with pain and not getting any relief - she treated me with low dose Naltroxone and Boswellia and symptoms started to resolve after 1 week and then resolved back to usual aches and pains after 3 weeks of treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Multiple labs all negative
Aktuelle Erkrankungen: Rheumatoid Arthritis
Vorgeschichte: Osteoarthritis, Rheumatoid arthritis
Andere Medikamente: -
Allergien: None known
Vorherige Impfungen: -

VAERS 2595514

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: FL
Alter: 49,0
Geschlecht: F
Eingang: 13.03.2023
Impfdatum: 17.03.2021
Beginn: 25.03.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

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

Atrial fibrillation Blood test normal Palpitations

Symptomtext

On 03/25/2021, I drank an herbal tea, Tension Tamer Tea, Celestial Seasonings brand, about 01:30 AM. I went to lie down and within 20 minutes, I started feeling heart palpitations. It lasted a half hour. I woke my husband and told him I needed to go to the hospital. There, they gave me an IV, and my heart rate was 107 beats per minute. My heartrate finally corrected after medication. I stayed overnight in the hospital. The tea has an ingredient that is a form of Ginseng. I now have AFIB.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: 1,0
Labordaten: 25MAR2021 - Bloodwork- Normal
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Vitamin D; Iron
Allergien: Hazelnut; Hay Fever
Vorherige Impfungen: -

VAERS 2577363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: MN
Alter: 92,0
Geschlecht: F
Eingang: 07.02.2023
Impfdatum: 05.05.2022
Beginn: 02.12.2022
Tage bis Beginn: 211,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia COVID-19 COVID-19 pneumonia Dementia Fatigue Gait inability Productive cough SARS-CoV-2 test positive

Symptomtext

Patient with history of dementia and brought to the ED on 12/2/22 by her family. Family reports for the past two days, patient has become increasingly weak to the point where she is no longer able to walk with her walker. Additionally reports new and worsening productive cough and fatigue. COVID PCR test performed in the ED resulted positive. Ultimately, patient admitted 12/2/22 - 12/4/22 for COVID-19 pneumonia, among other problems. She did not require supplemental O2.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2560674

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: FL
Alter: 24,0
Geschlecht: M
Eingang: 16.01.2023
Impfdatum: 30.04.2021
Beginn: 07.05.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: SYR / LA

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

Angina pectoris Anxiety Cardiac flutter Chest discomfort Chest pain Feeling cold Heart rate irregular Inflammation Painful respiration Palpitations Peripheral coldness Sleep disorder Social anxiety disorder Weight decreased Weight gain poor

Symptomtext

May 2021 One week after the second and final dose of Pfizer: My heart was fluttering irregularly and pounding heart beat. Over the next year and half I noticed myself experiencing extreme anxiety as well as social anxiety when around people. I lost weight and can?t gain any weight. My body is always cold. My hands and feet are always ice cold. I can?t sleep on my left side without waking up in the middle of the night with pains coming from my heart that?s beating against my rib bones. (Probably inflammation) Sept 2022: At work I was climbing down a ladder from a hot attic and experienced super sharp pains in my heart with each beat for a couple of minutes straight. My chest was very tight and anytime I would breath it felt very sore. I felt the soreness for the next 2 weeks into October 2022. Jan 1st 2023: I received my health coverage from PRIVATE Blue. Now I?m able to have this issue addressed and that is what I?m trying to start here now. Please and thank you

Weitere VAERSDATA-Felder

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

VAERS 2548999

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: NY
Alter: 54,0
Geschlecht: M
Eingang: 03.01.2023
Impfdatum: 07.04.2022
Beginn: 21.08.2022
Tage bis Beginn: 136,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Chest X-ray normal Cough Dyspnoea Haematochezia Haemoglobin decreased SARS-CoV-2 test positive White blood cell count normal

Symptomtext

8/21/2022- Presents to ED form group home, covid + h. Covid + home test and feels SOB and cough. Also noted blood in stool, pmh of GI bleeds, 2 units ordered HGb 6.8. currently on Protonix, f/u with GI outpatient UTD with colonoscopy.Covid + test. CXr-no acute pulmonary disease. Afebrile, BP-87/54. O2 sat WNL. WBC-5.5 8/22/2022-Hgb 8.2, VSS , o2 sat WNL. D/C home with Paxlovid.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CP, GI Bleeds, DVT, HLD, seizures and OSA.
Andere Medikamente: -
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2537710

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: -
Alter: 37,0
Geschlecht: F
Eingang: 20.12.2022
Impfdatum: 07.04.2021
Beginn: 07.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Arrhythmia Echocardiogram Electrocardiogram Electrocardiogram ambulatory Heart rate increased Supraventricular tachycardia

Symptomtext

Rapid Heart Rate the evening after the vaccination. I have since been diagnosed with Supraventricular Tachycardia (SVT) and have continuing problems with heart rate and occasional arrhythmia.

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Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: Heart Monitor worn. Multiple EKG's taken. Echocardiogram done as well last fall.
Aktuelle Erkrankungen: Diabetes
Vorgeschichte: Diabetes
Andere Medikamente: Fiasp Insulin, Toujeo Insulin
Allergien: None
Vorherige Impfungen: -

VAERS 2525193

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 23.02.2021
Beginn: 24.09.2022
Tage bis Beginn: 578,0
Dosis: 2
Route/Site: IM / LA

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

Acute kidney injury Asthenia COVID-19 COVID-19 pneumonia Cough Dyspnoea Faeces discoloured SARS-CoV-2 test positive

Symptomtext

Narrative: Patient received three COVID 19 Vaccine in Feb/Mar 2021 and Feb 2022. The patient tested positive for COVID 19 on 24 Sep 2022. The patient presented to the ED with generalized weakness, cough, sob with any activity, and black stool. The patient was admitted to the hospital with covid pneumonia and acute kidney injury. The patient was treated with oxygen and antibiotics. The patient was discharged on a 27 Sep 2022 in stable condition. Reported per EUA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2316590

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: CA
Alter: 74,0
Geschlecht: M
Eingang: 27.09.2022
Impfdatum: 15.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Blood glucose abnormal Blood glucose decreased Electrocardiogram Blood urea COVID-19 Drug ineffective Dyspnoea Cardiac flutter Nasopharyngitis SARS-CoV-2 test

Symptomtext

Cardiac flutter; short of breath; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. Other Case identifier(s): 2022SA211752. A 76-year-old male patient received BNT162b2 (BNT162B2), on 15Mar2021 as dose 1, single (Lot number: EN6208) at the age of 74 years for covid-19 immunisation; insulin glargine (LANTUS), (Lot number: IF034A, Expiration Date: 31May2024) at daily (100 iu/ml 15 u daily) for type 1 diabetes mellitus. The patient's relevant medical history included: "Diabetic", start date: 1982 (ongoing), notes: At the time of the event, the patient had ongoing Diabetic in 1982.; "Road traffic accident" (unspecified if ongoing), notes: Road traffic accident with while driving and had an accident. Concomitant medication(s) included: HUMALOG taken for type 1 diabetes mellitus; NOVOLOG taken for type 1 diabetes mellitus; RAMIPRIL; ATORVASTATIN; LEVEMIR, start date: 2011. The following information was reported: CARDIAC FLUTTER (medically significant), outcome "unknown"; DYSPNOEA (non-serious), outcome "unknown", described as "short of breath". The action taken for insulin glargine was unknown. Therapeutic measures were taken as a result of cardiac flutter. Follow-Up (26Sep2022): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Diabetic (At the time of the event, the patient had ongoing Diabetic in 1982.)
Vorgeschichte: Medical History/Concurrent Conditions: Road traffic accident (Road traffic accident with while driving and had an accident)
Andere Medikamente: HUMALOG; NOVOLOG; RAMIPRIL; ATORVASTATIN; LEVEMIR; LANTUS
Allergien: -
Vorherige Impfungen: -

VAERS 2433814

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: MN
Alter: 86,0
Geschlecht: M
Eingang: 08.09.2022
Impfdatum: 13.03.2021
Beginn: 06.08.2022
Tage bis Beginn: 511,0
Dosis: 1
Route/Site: IM / RA

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

Asthenia COVID-19 Cough Dyspnoea Pyrexia SARS-CoV-2 test positive

Symptomtext

SOB, COUGH, WEAKNESS, FEVER

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 4,0
Labordaten: POSITIVE COVID TEST 8/13/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Acute on chronic diastolic ACC/AHA stage C congestive heart failure Aftercare following organ transplant AKI (acute kidney injury) Anemia in chronic renal disease ARF (acute renal failure) Asthma Atherosclerosis of coronary artery Cataract Chronic edema Dyslipidemia EBV (Epstein-Barr virus) viremia Elevated lactic acid level Elevated troponin ESRD (end stage renal disease) Gastroesophageal reflux disease with esophagitis and hemorrhage GI bleed HHS (hypothenar hammer syndrome) Hyperglycemia Hyperlipidemia Hypertension due to kidney transplant Hypertensive urgency Immunosuppression Iron deficiency anemia secondary to blood loss (chronic) Lactic acidosis MGUS (monoclonal gammopathy of unknown significance) Multifactorial gait disorder Neoplasm of uncertain behavior of skin Pancytopenia Pneumonia Presbyopia Proteinuria Severe malnutrition Superficial keratitis Syncope and collapse Type II diabetes mellitus with ophthalmic manifestations Vascular dementia without behavioral disturbance Vitamin B12 deficiency Vitamin D deficiency
Andere Medikamente: amLODIPine (NORVASC) 10 mg oral tablet azaTHIOprine (IMURAN) 50 mg Oral Tab Calcium Carbonate-Vit D3-Min 600 mg calcium- 400 unit oral Tab cholecalciferol, Vitamin D3, 1,000 unit Oral Tab cyanocobalamin 100 mcg oral Tab ferrous sulfate (FER
Allergien: -
Vorherige Impfungen: -

VAERS 2433018

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: -
Alter: 70,0
Geschlecht: M
Eingang: 08.09.2022
Impfdatum: -
Beginn: 15.06.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

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

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

Symptomtext

Narrative: Fully vaccinated, admitted for chest pain, incidentally COVID positive

Weitere VAERSDATA-Felder

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

VAERS 2439961

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 27.08.2022
Impfdatum: 18.02.2021
Beginn: 27.04.2022
Tage bis Beginn: 433,0
Dosis: 2
Route/Site: IM / RA

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

Arthralgia Asthenia COVID-19 COVID-19 pneumonia Chest pain Cough Myalgia Productive cough Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Narrative: Patient received four doses of Pfizer COVID 19 Vaccine. Pt had his 4th shot booster for COVID 19 with the Pfizer vaccine in April 2022 at an outside facility. About 1-2 days after that, he started developing some generalized weakness, cough with white phlegm, runny nose/congestion, myalgias and arthralgias. The patient tested positive for COVID 19 on 27 April 2022. The patient presented to the ED with symptoms above and was admitted with COVID pneumonia, cough, and chest pain. The patient was treated with iv antibiotics. The patient was discharged on 29 April 2022 in stable condition. Reported per EUA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2420890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: -
Alter: 46,0
Geschlecht: M
Eingang: 26.08.2022
Impfdatum: 25.02.2021
Beginn: 01.06.2021
Tage bis Beginn: 96,0
Dosis: 2
Route/Site: UN / AR

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

Cardiac stress test abnormal Chest discomfort Dyspnoea exertional

Symptomtext

Three months after receiving the second dose of the Covid 19 vaccine, he began complaining of chest tightness and also had difficulty catching his breath after participating in strenuous activity. He initially believed he was experiencing Exercise-induced asthma, which he had experienced in the past. He was prescribed an Albuterol Sulfate HFA inhaler. He believed he felt some relief while using the inhaler; however, at some point, it was no longer helping.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: abnormal stress test (June 2021)
Aktuelle Erkrankungen: -
Vorgeschichte: high blood pressure
Andere Medikamente: Escitalopram, Lisinopril
Allergien: -
Vorherige Impfungen: -

VAERS 2415997

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: MN
Alter: 45,0
Geschlecht: M
Eingang: 19.08.2022
Impfdatum: 11.10.2021
Beginn: 19.07.2022
Tage bis Beginn: 281,0
Dosis: 1
Route/Site: IM / RA

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

Acute kidney injury COVID-19 Chest pain Chills Cough Dizziness Fatigue Orthostatic hypotension Pain Pneumonia Pneumonia bacterial Pyrexia SARS-CoV-2 test positive Troponin increased Vaccine breakthrough infection

Symptomtext

Patient seen in the ED on 7/19 for cough, fever, chills, lightheadedness, fatigue, chest pain, and body aches. COVID PCR swab taken in the ED was positive. Patient ultimately was admitted from 7/19-7/21 under observation status . Discharge diagnoses include probable left lower lobe bacterial CAP, COVID-19 infection, elevated 2 hours delta troponin, orthostatic hypotension, and AKI resolved. Patient has been vaccinated against COVID-19. This meets criteria for vaccine breakthrough case review.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Patient with history of type II diabetes
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2415713

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: FL
Alter: 49,0
Geschlecht: F
Eingang: 19.08.2022
Impfdatum: 30.03.2021
Beginn: 01.05.2021
Tage bis Beginn: 32,0
Dosis: 2
Route/Site: - / RA

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

Carpal tunnel syndrome Condition aggravated Magnetic resonance imaging head Myelitis Nerve conduction studies Peripheral sensory neuropathy Peroneal nerve palsy Polyneuropathy

Symptomtext

inflammatory polyneuropathy with sensory neuropathyin both legs minor motor deficits (comments: worsening neuropathy/carpal tunnel in both hands despite decrease in activity and regular arm bracing); inflammatory polyneuropathy with sensory neuropathyin both legs minor motor deficits (comments: worsening neuropathy/carpal tunnel in both hands despite decrease in activity and regular arm bracing); Possible myelitis in thoracic; Condition aggravated; peroneal palsy (comment: carpal tunnel in both hands prior injury, symptoms worsened significantly after vaccination); peroneal palsy (comment: carpal tunnel in both hands prior injury, symptoms worsened significantly after vaccination); This is a spontaneous report received from a contactable reporter (Consumer or other non-HCP). The reporter is the patient. A 49-year-old female patient received BNT162b2 (BNT162B2), on 30Mar2021 at 14:40 as dose 2, single (Lot number: EN6208) at the age of 49 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Epilepsy" (ongoing), notes: Diagnosed almost 5 years earlier; "Seizures" (unspecified if ongoing); "Carpal tunnel in both hands prior injury" (unspecified if ongoing), notes: Carpal tunnel in both hands prior injury; "Carpal tunnel in both hands" (unspecified if ongoing). Concomitant medication included: VIMPAT oral taken for seizure, start date: Sep2020, stop date: 21Sep2021. Vaccination history included: BNT162b2 (Dose: 1st, Date: 09Mar2021, Time: 03:30 PM, Anatomical Site of injection: Left arm, upper, Route of administration: Intramuscular, Batch/Lot number: EN6198), administration date: 09Mar2021, when the patient was 49-year-old, for COVID-19 Immunization, reactions: "transverse myelitis", "Guillain Barre resulting in myeltitis small fiber and sensory neuropathy with sensory involvement with mitochondiral disease", "Sensory neuropathy", "Small fiber neuropathy", "cheeks felt warm", "rash on her neck and cheeks", "numbness in her feet, especially the left foot/ It is affecting her entire body, face, tongue, and mouth", "transient mouth/tongue tingling", "fasciculations", "mouth burning". The following information was reported: CONDITION AGGRAVATED (medically significant) with onset May2021, outcome "unknown"; PERONEAL NERVE PALSY (non-serious), CARPAL TUNNEL SYNDROME (non-serious) all with onset May2021, outcome "unknown" and all described as "peroneal palsy (comment: carpal tunnel in both hands prior injury, symptoms worsened significantly after vaccination)"; MYELITIS (medically significant) with onset Jul2021, outcome "unknown", described as "Possible myelitis in thoracic"; POLYNEUROPATHY (medically significant), PERIPHERAL SENSORY NEUROPATHY (non-serious) all with onset Nov2021, outcome "unknown" and all described as "inflammatory polyneuropathy with sensory neuropathyin both legs minor motor deficits (comments: worsening neuropathy/carpal tunnel in both hands despite decrease in activity and regular arm bracing)". The patient underwent the following laboratory tests and procedures: Magnetic resonance imaging head: (May2020) Possible myelitis in thoracic; (Jul2021) Possible myelitis in thoracic; Nerve conduction studies: (May2021) Peroneal palsy, notes: Carpal tunnel in both hands prior injury. symptoms worsened significantly after vaccination; (Nov2021) Inflammatory polyneuropathy with sensory neuropath, notes: Worsening neuropathy carpal tunnel in both hands despite decrease in activity and regular arm bracing. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 202005; Test Name: MRI (Brain curvical thoracic lumber); Result Unstructured Data: Test Result:Possible myelitis in thoracic; Test Date: 202107; Test Name: MRI (Brain curvical thoracic lumber); Result Unstructured Data: Test Result:Possible myelitis in thoracic; Test Date: 202105; Test Name: Nerve conduction emg; Result Unstructured Data: Test Result:Peroneal palsy; Comments: Carpal tunnel in both hands prior injury. symptoms worsened significantly after vaccination; Test Date: 202111; Test Name: Nerve conduction emg; Result Unstructured Data: Test Result:Inflammatory polyneuropathy with sensory neuropath; Comments: Worsening neuropathy carpal tunnel in both hands despite decrease in activity and regular arm bracing
Aktuelle Erkrankungen: Epilepsy (Diagnosed almost 5 years earlier)
Vorgeschichte: Medical History/Concurrent Conditions: Carpal tunnel syndrome; Injury (Carpal tunnel in both hands prior injury); Seizures
Andere Medikamente: VIMPAT
Allergien: -
Vorherige Impfungen: -

VAERS 2401710

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: HI
Alter: 34,0
Geschlecht: M
Eingang: 04.08.2022
Impfdatum: 10.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Blood glucose normal Eosinophil percentage increased Hypertension Rash Urticaria

Symptomtext

urticarial rash over bilateral upper and lower extremities, waistline, back and bilateral ears

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: hypertension 179/93 glucose 153 mg/dl eosinophil 10%
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2372018

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: CO
Alter: 29,0
Geschlecht: F
Eingang: 17.07.2022
Impfdatum: 25.03.2021
Beginn: 29.03.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / RA

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

Condition aggravated Herpes zoster Pruritus Rash

Symptomtext

Monday around lunch I began to notice an inching feeling in my midsection. When I got home that afternoon I was reasonably certain it was shingles. The rash looked and felt consistent with a previous course of shingles about 18 years ago. I set up an appointment the next morning. Course was short due to starting antivirals within about 30 hours of first symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None. Based on description and past experience, MD believed the rash was consistent with shingles via telahealth.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Women's multi vit
Allergien: Gluten
Vorherige Impfungen: -

VAERS 2366185

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: IL
Alter: 78,0
Geschlecht: M
Eingang: 12.07.2022
Impfdatum: 06.04.2021
Beginn: 21.12.2021
Tage bis Beginn: 259,0
Dosis: 2
Route/Site: IM / -

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

Alcohol abuse Angiogram pulmonary abnormal Atelectasis COVID-19 COVID-19 pneumonia Chest X-ray normal Chronic obstructive pulmonary disease Computerised tomogram abdomen normal Computerised tomogram thorax abnormal Condition aggravated Cough Dyspnoea Inappropriate schedule of product administration Laboratory test Lung consolidation Lung infiltration Pneumonia Pneumonia bacterial

Symptomtext

Pfizer Dose 1 3/9/21 (EN6205) Pfizer Dose 2 4/6/21 (EN6208) COVID Positive 1/21/22 1/21/22: Patient is a 79-year-old male with history of generalized anxiety, COPD, CVA, and HTN. He also reports chronic alcohol abuse. Reports he drinks 3 cans of beer daily. Reports he woke up suddenly at 01:30 today with cough, shortness of breath, and chest congestion. He denies fever, chills, nausea, vomiting, diarrhea, recent exposure to COVID. He is fully vaccinated for COVID, but has not gotten his booster. Patient's vitals have been stable in the ED. He was placed on supplemental oxygen at 2L for comfort, but has no documented hypoxia. Labs were fairly unremarkable, aside from a WBC count of 32.23. CXR showed no acute processes, however, CTA chest showed a persistent right middle lobe infiltrate/consolidation with milder bilateral lower lobe infiltrate or atelectasis. They recommended follow-up CT in 6-8 weeks and pulmonology follow-up at discharge to ensure resolution of right middle lobe consolidation and to exclude an underlying malignancy or endobronchial obstructing process. CT of abdomen showed no acute processes. In the ED, the patient received 125 mg Solu-Medrol, 750 mg Levaquin, and a DuoNeb. 1/24/22: Patient is a 79-year-old male with history of COPD, HTN, CVA, and anxiety disorder who was admitted on 1/21/2022 with acute COPD exacerbation, bilateral COVID pneumonia, likely superimposed bacterial pneumonia, and sepsis. He was admitted to the medical floor and was started on IV antibiotics, IV steroids, and remdesivir. On admission, his CT chest showed persistent right middle lobe infiltrate/consolidation, and the radiologist recommended follow-up CT in 6-8 weeks as well as Pulmonary consult to ensure the resolution of the right middle lobe consolidation and to exclude an underlying malignancy or endobronchial obstructing process. I discussed this with the patient, and he tells me he will follow-up with his PCP. The patient has slowly improved over the last several days. His WBCs are trending down, and today are at 13k. He denies shortness of breath at rest, dyspnea on exertion, chest pain, palpitations. He is requesting to go home today. As he is not requiring supplemental oxygen, he will be discharged home on dexamethasone and Levaquin. I explained to him the importance of finishing both of these medications, even if he feels like he does not need them. He verbalized understanding.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CoPD HTN CVA anxiety
Andere Medikamente: albuterol-ipratroium 2 puffs Q4h PRN alprazolam 0.5 mg PO PRN amlodipine 5 mg PO QD aspirin 325 mg Po qD carvedilol 6.25 mg Po BID clopidogrel 75 mg PO QD multivitami n1 tab PO QD prostate prohealth 1 tab PO BID fish oil 1200 mg PO QD panto
Allergien: codeine - hot flashes, chills, syncope
Vorherige Impfungen: -

VAERS 2347383

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: AR
Alter: 68,0
Geschlecht: F
Eingang: 01.07.2022
Impfdatum: 02.12.2021
Beginn: 30.06.2022
Tage bis Beginn: 210,0
Dosis: 1
Route/Site: IM / LA

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

Atrial fibrillation COVID-19 Condition aggravated Hypoglycaemia SARS-CoV-2 test positive

Symptomtext

The patient was admitted on 6-30-22 to our Medical/Surgical unit at 1724 from the ER department with hypoglycemia and atrial fibrillation. Patient was tested for covid-19 on arrival and was confirmed positive for covid-19 at 2353 the same day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes, hypoglycemia, Atrial Fibrillation
Andere Medikamente: Allopurinol 100mg po daily. Amlodipine Besylate/hctz 5-10mg po daily Eliquis 5 mg po bid Glimepiride 4mg po bid Jardiance 25mg po daily Levothyroxine 75 mg po daily Metoprolol 100 mg po daily
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2327056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: MI
Alter: 74,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 03.03.2021
Beginn: 15.06.2022
Tage bis Beginn: 469,0
Dosis: 2
Route/Site: IM / UN

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

COVID-19 Cough Dizziness Dyspnoea Laboratory test Positive airway pressure therapy Productive cough SARS-CoV-2 test positive Sepsis

Symptomtext

Pt to ED 6/15 for cough and sob, positive at home COVID test. COVID+ upon admission 6/15, maintained on Decadron. 6/16 pt reporting SOB and dizziness. Sepsis BPA fired score of 5. RRT not activated. VSS on 2L NC. ID on consult. Started on remdesivir. 6/18 pt remains A&Ox4 and showing no s/s of distress. Oxygen remains at 2L via NC and patient using home CPAP machine. Productive cough noted overnight. 6/19 pt remains A&Ox4 and showing no s/s of distress. 6/19 pt discharged.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: OSA (obstructive sleep apnea) Chronic obstructive pulmonary disease Chronic respiratory failure with hypoxia, on home O2 therapy Rhinitis, chronic IFG (impaired fasting glucose) Secondary hyperparathyroidism Lymphedema S/P splenectomy Nocturnal enuresis Pulmonary hypertension Occlusion of celiac artery CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min Seborrheic eczema Varicose veins of lower extremity Right ureteral calculus Peripheral vascular disease Venous ulcer History of colonoscopy Ureteral stone with hydronephrosis Gout Right nephrolithiasis Venous insufficiency of both lower extremities Onychomycosis Cellulitis of right lower leg Cellulitis of leg Obesity (BMI 35.0-39.9 without comorbidity) Leg pain, bilateral Celllitis and abscess of left leg Cellulitis of right lower extremity Bilateral renal cysts Wound infection COVID-19 Cellulitis of right lower extremity Polycythemia
Andere Medikamente: albuterol (PROVENTIL, VENTOLIN, PROAIR) HFA 108 (90 Base) MCG/ACT INHAL Aero Soln amoxicillin-potassium clavulanate (AUGMENTIN) 875-125 MG PO Tab budesonide-formoterol (Symbicort) 160-4.5 MCG/ACT INHAL inhaler bumetanide (Bumex) 1 MG PO Tab
Allergien: Adhesive tape
Vorherige Impfungen: -

VAERS 2325669

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: MA
Alter: 48,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 15.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Condition aggravated Cystitis interstitial Dysuria Feeling cold Micturition urgency Myalgia Pain in extremity Pelvic pain Pollakiuria Pyrexia Sleep disorder

Symptomtext

About two weeks after the 2nd dose I woke up with fever and chills around 1AM. I stayed home with muscle aches and joint paint. Around 11PM that night I had a flare up of my interstitial cystitis. This causes pain and urgency while I urinate and I have constant frequency. I had a lot of pelvic. I was still having pain on April 2nd and honestly had bilateral foot and hand pain and knee pain down into my ankles and feet. I had hip pain start as well and just pain in my joints which lasted about eight weeks where it was severe and then it has gotten better but has not gone away completely. I had a telehealth appointment with my urologist and we set up an instillation because we had upped my medication for my Interstitial cystitis flare up. However I did not get the instillation because the pain had gotten better and I was able to return to the medication two times a day rather than taking that extra third dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Interstitial Cystitis
Andere Medikamente: SINGULAIR; antihistamine; nasal spray; steroid inhaler; ELMIRON
Allergien: Walnuts; codeine; sulfur
Vorherige Impfungen: -

VAERS 2320314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6208

moderat

Staat: -
Alter: 56,0
Geschlecht: M
Eingang: 15.06.2022
Impfdatum: 10.03.2021
Beginn: 19.12.2021
Tage bis Beginn: 284,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 COVID-19 pneumonia SARS-CoV-2 test positive

Symptomtext

Narrative: Admission: Fully vaccinated, COVID positive admitted for COVID pneumonia

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -